6294 NP_109597 S188F not found in SNVbox database
9603 NP_705833 S82F not found in SNVbox database
204 NP_705833 E405K not found in SNVbox database
905 NP_705833 S146L not found in SNVbox database
1357 NP_001070868 H143D not found in SNVbox database
1969 NP_001070868 P206L not found in SNVbox database
2578 NP_705833 L754F not found in SNVbox database
4141 NP_705833 E710K not found in SNVbox database
4164 NP_001070868 P366S not found in SNVbox database
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr10:52575823 G>A maps to NM_138932.2 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:52573625 G>A maps to NM_138932.2 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr10:52580389 C>T maps to NM_138932.2 K263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:52580382 G>A maps to NM_138932.2 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:52595993 C>T maps to NM_138932.2 K148K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:52603816 G>A maps to NM_138932.2 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr10:52566489 C>T maps to NM_138932.2 *595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:52619603 G>A maps to NM_138932.2 Q33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr10:52596008 G>A maps to NM_138932.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:52619640 G>A maps to NM_138932.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:52580395 C>T maps to NM_138932.2 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:52587969 C>T maps to NM_138932.2 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:52595972 C>T maps to NM_138932.2 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:52603783 G>A maps to NM_138932.2 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:52573618 G>A maps to NM_138932.2 Q449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:52573619 G>A maps to NM_138932.2 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr16:7645561 C>T maps to NM_145891.2 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:7760623 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr16:7629798 G>A maps to NM_145891.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr16:7383010 G>C maps to NM_145891.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:7645594 G>A maps to NM_145891.2 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr16:7680644 C>T maps to NM_145891.2 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:7680635 G>A maps to NM_145891.2 E256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr16:7721557 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:7629891 C>T maps to NM_145891.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr16:7568234 C>T maps to NM_145891.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr16:7645561 C>T maps to NM_145891.2 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr12:9246084 C>T maps to NM_000014.4 W739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr12:9265008 G>A maps to NM_000014.4 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr12:9262478 G>A maps to NM_000014.4 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:9265964 G>A maps to NM_000014.4 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:9230415 G>A maps to NM_000014.4 R1053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr12:9262529 G>A maps to NM_000014.4 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr12:9242530 C>T maps to NM_000014.4 R895R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr12:9243922 A>G maps to NM_000014.4 S781S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr12:9265129 G>A maps to NM_000014.4 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:9230359 G>A maps to NM_000014.4 S1071S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:9223140 C>T maps to NM_000014.4 A1379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr12:9264766 G>A maps to NM_000014.4 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:9262610 G>A maps to NM_000014.4 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:9243045 G>A maps to NM_000014.4 F834F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:9248272 C>T maps to NM_000014.4 K625K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:9248139 G>A maps to NM_000014.4 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr12:9265096 G>A maps to NM_000014.4 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:9265988 C>T maps to NM_000014.4 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr12:8982356 C>T maps to NM_144670.3 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:8982356 C>T maps to NM_144670.3 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:8994107 G>A maps to NM_144670.3 W408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr12:9013765 G>A maps to NM_144670.3 K1125K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:8995902 T>A maps to NM_144670.3 Y474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:9009928 G>A maps to NM_144670.3 L1006L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:8994113 G>A maps to NM_144670.3 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:8998760 T>C maps to NM_144670.3 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:9010679 C>T maps to NM_144670.3 L1082L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr12:8995863 C>T maps to NM_144670.3 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:8988119 G>A maps to NM_144670.3 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:9008103 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:8993993 C>T maps to NM_144670.3 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr12:8990162 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:9000233 C>T maps to NM_144670.3 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:9009895 G>A maps to NM_144670.3 T995T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr12:9016487 T>C maps to NM_144670.3 L1201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr12:9016585 G>A maps to NM_144670.3 G1233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:8976443 G>A maps to NM_144670.3 Q125Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr12:8994056 G>A maps to NM_144670.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:8988875 G>T maps to NM_144670.3 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr12:8991814 G>A maps to NM_144670.3 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr22:43089291 G>A maps to NM_017436.4 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:43089081 C>T maps to NM_017436.4 W292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr22:43088979 G>A maps to NM_017436.4 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr22:43089081 C>T maps to NM_017436.4 W292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr22:43089246 G>A maps to NM_017436.4 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr22:43089714 G>A maps to NM_017436.4 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:43089246 G>A maps to NM_017436.4 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:43089885 G>A maps to NM_017436.4 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr3:137843165 C>T maps to NM_016161.2 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr3:137843129 C>T maps to NM_016161.2 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:137843429 C>T maps to NM_016161.2 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr3:137849888 G>A maps to NM_016161.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:137843678 C>G maps to NM_016161.2 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr3:137849912 C>T maps to NM_016161.2 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:53715135 G>A maps to NM_015665.5 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr12:53702560 G>A maps to NM_015665.5 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr12:53702565 G>A maps to NM_015665.5 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr12:53703002 G>A maps to NM_015665.5 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr12:53703019 G>A maps to NM_015665.5 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr12:53703479 G>A maps to NM_015665.5 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr12:53715135 G>A maps to NM_015665.5 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:53708083 G>A maps to NM_015665.5 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr12:53709123 G>A maps to NM_015665.5 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:53708590 G>A maps to NM_015665.5 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr12:53715135 G>A maps to NM_015665.5 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:125558420 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:125609553 C>T maps to NM_023928.3 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr12:125621226 G>A maps to NM_023928.3 V566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:125599087 C>T maps to NM_023928.3 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:125621385 C>T maps to NM_023928.3 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:151545383 C>T maps to NM_001086.2 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:151535365 G>A maps to NM_001086.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr3:151535167 G>A maps to NM_001086.2 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr3:151545927 C>T maps to NM_001086.2 Q390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:151535329 G>A maps to NM_001086.2 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:151542594 G>A maps to NM_001086.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:151545474 C>T maps to NM_001086.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:151474811 C>T maps to NM_207365.3 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr3:151451939 C>T maps to NM_207365.3 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:151474778 G>A did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr1:12785266 C>T maps to NM_001103170.1 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:12785501 C>T maps to NM_001103170.1 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:12785266 C>T maps to NM_001103170.1 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:12785761 C>T maps to NM_001103170.1 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:12785398 G>A maps to NM_001103170.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:12785392 G>A maps to NM_001103170.1 Q161Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr1:12785953 G>A maps to NM_001103170.1 K348K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12785746 C>T maps to NM_001103170.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:12785515 C>T maps to NM_001103170.1 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:12785809 G>A maps to NM_001103170.1 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:12726172 T>C maps to NM_001013630.1 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:12704714 C>T maps to NM_001013630.1 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:12704573 C>T maps to NM_001013630.1 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr1:12726436 C>T maps to NM_001013630.1 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr1:12711317 C>T maps to NM_001013630.1 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:12704612 C>T maps to NM_001013630.1 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:12711284 G>A maps to NM_001013630.1 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:12726700 C>T maps to NM_001013630.1 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:12704612 C>T maps to NM_001013630.1 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12704714 C>T maps to NM_001013630.1 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12711221 G>A maps to NM_001013630.1 K83K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12711242 C>T maps to NM_001013630.1 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12725998 C>T maps to NM_001013630.1 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr4:171008296 G>A maps to ENST00000509167 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr4:170994382 G>A maps to ENST00000509167 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr15:67524188 C>T maps to NM_024666.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr15:67501877 C>T maps to NM_024666.3 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:69708037 G>A maps to NM_014911.3 P841P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:69736436 G>A maps to NM_014911.3 V644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr2:69734625 G>A maps to NM_014911.3 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr2:69754440 C>T maps to NM_014911.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:69736496 G>A maps to NM_014911.3 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr2:69748026 G>A maps to NM_014911.3 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:219130369 G>A maps to ENST00000444053 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:74465772 G>A maps to NM_001166579.1 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:74464833 C>T maps to NM_001166579.1 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:74464884 G>A maps to NM_001166579.1 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:70292954 G>A maps to ENST00000418685 A648A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:70286800 G>A maps to ENST00000418685 A934A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:70311042 G>A maps to ENST00000418685 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:44268343 G>A maps to NM_020745.2 S966S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr6:44274092 G>A maps to NM_020745.2 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:44269817 G>A maps to NM_020745.2 I859I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:44269120 G>A maps to NM_020745.2 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:44272222 G>A maps to NM_020745.2 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:44278885 G>A maps to NM_020745.2 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr6:44274083 G>A maps to NM_020745.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr6:44272528 C>T maps to NM_020745.2 V535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:41108280 G>A maps to NM_001136042.2 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:57215959 G>A maps to NM_181806.2 Q653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr4:57209808 G>A maps to NM_181806.2 V898V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr4:57216217 G>A maps to NM_181806.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:121726101 A>G maps to NM_005763.3 S716S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:121755207 G>A maps to NM_005763.3 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:121719730 G>A maps to NM_005763.3 P772P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:121773726 C>T maps to NM_005763.3 K18K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr17:35376338 C>T maps to NM_012138.3 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:35345952 C>T maps to NM_012138.3 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:79094801 C>T maps to NM_001080395.2 R978R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:79095359 G>A maps to NM_001080395.2 P792P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr17:79094849 G>A maps to NM_001080395.2 A962A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr16:8829604 C>T maps to NM_001127448.1 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:8866689 C>T maps to NM_001127448.1 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:8839921 G>A maps to NM_001127448.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr16:8862081 C>T maps to NM_001127448.1 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr16:8862721 C>T maps to NM_001127448.1 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr9:107589321 G>A maps to NM_005502.3 A748A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr9:107599323 C>T maps to NM_005502.3 W416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:107568611 G>A maps to NM_005502.3 N1458N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:107555132 C>T maps to NM_005502.3 R1897R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr9:107568637 G>A maps to NM_005502.3 Q1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr9:107568638 G>A maps to NM_005502.3 F1449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:107578465 C>G maps to NM_005502.3 L1232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr9:107594983 G>A maps to NM_005502.3 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr17:67187419 G>A maps to NM_080282.3 I636I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr17:67170828 G>A maps to NM_080282.3 F989F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:67210938 C>T maps to NM_080282.3 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr17:67197774 G>A maps to NM_080282.3 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr17:67148206 G>A maps to NM_080282.3 F1458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:67212387 G>A maps to NM_080282.3 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr17:67149477 G>A maps to NM_080282.3 T1368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:67189322 G>A maps to NM_080282.3 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr17:67190037 G>A maps to NM_080282.3 Q480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr17:67145058 A>C maps to NM_080282.3 L1514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr2:215854086 G>A maps to NM_173076.2 F1265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr2:215831614 G>A maps to NM_173076.2 F1947F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr2:215890503 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:215914478 A>G maps to NM_173076.2 Y188Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr2:215855671 G>A maps to NM_173076.2 I1126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr2:215843181 C>T maps to NM_173076.2 L1662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:215928820 C>T maps to NM_173076.2 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:215855734 C>T maps to NM_173076.2 V1105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:215872516 C>T maps to NM_173076.2 W842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:215865484 G>A maps to NM_173076.2 S1041S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:215872483 G>A maps to NM_173076.2 F853F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:215845305 G>A maps to NM_173076.2 I1547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr2:215845257 G>A maps to NM_173076.2 Y1563Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:215851396 G>A maps to NM_173076.2 V1344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:215840561 C>T maps to NM_173076.2 E1776E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:215851369 C>T maps to NM_173076.2 K1353K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:215820085 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:215821457 C>T maps to NM_173076.2 A2054A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:215839502 G>A maps to NM_173076.2 L1823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:215862523 G>A maps to NM_173076.2 T1063T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:215868951 C>T maps to NM_173076.2 L888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:215866416 G>A maps to NM_173076.2 Q910*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:215914409 G>A maps to NM_173076.2 C211C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr2:215809795 C>T maps to NM_173076.2 S2424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr2:215809774 G>A maps to NM_173076.2 I2431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:215919360 C>T maps to NM_173076.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr2:215914451 G>A maps to NM_173076.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:215896554 G>A maps to NM_173076.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr2:215823760 G>A maps to NM_173076.2 Q1976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:215809780 C>T maps to NM_173076.2 W2429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:215843680 G>A maps to NM_173076.2 L1608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:215833509 C>T maps to NM_173076.2 G1904G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:215845251 C>T maps to NM_173076.2 K1565K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:215872483 G>A maps to NM_173076.2 F853F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr2:215914375 G>A maps to NM_173076.2 Q223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr7:48547536 C>T maps to NM_152701.3 S4472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:48431661 G>A maps to NM_152701.3 R3933R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:48314303 C>T maps to NM_152701.3 Q1681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr7:48559845 C>T maps to NM_152701.3 L4669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr7:48316015 G>A maps to NM_152701.3 R2251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:48273741 G>A maps to NM_152701.3 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:48563984 C>T maps to NM_152701.3 F4731F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr7:48450123 G>A maps to NM_152701.3 T4026T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:48411913 C>T maps to NM_152701.3 F3651F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr7:48392066 C>T maps to NM_152701.3 P3557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:48318428 C>T maps to NM_152701.3 S2546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:48451958 C>T maps to NM_152701.3 L4080L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr7:48559845 C>T maps to NM_152701.3 L4669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr7:48278968 C>T maps to NM_152701.3 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr7:48316081 C>T maps to NM_152701.3 S2273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr7:48431652 C>T maps to NM_152701.3 L3930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr7:48547506 C>T maps to NM_152701.3 I4462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr7:48411913 C>T maps to NM_152701.3 F3651F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr7:48550792 C>T maps to NM_152701.3 F4546F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr7:48556371 G>A maps to NM_152701.3 S4564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:48311533 C>T maps to NM_152701.3 F757F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:48556383 C>T maps to NM_152701.3 F4568F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:48356766 G>A maps to NM_152701.3 L3291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr7:48391835 G>T maps to NM_152701.3 L3480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:48443294 G>A maps to NM_152701.3 V3963V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:48619945 G>A maps to NM_152701.3 G4827G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr7:48312946 C>T maps to NM_152701.3 F1228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr7:48547506 C>T maps to NM_152701.3 I4462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:48288032 C>T maps to NM_152701.3 V619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:48318308 G>A maps to NM_152701.3 L2506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:48318380 G>A maps to NM_152701.3 K2530K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:48391895 G>A maps to NM_152701.3 V3500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:48506594 G>A maps to NM_152701.3 R4286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:48547611 G>A maps to NM_152701.3 R4497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:48556365 C>T maps to NM_152701.3 S4562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr7:48316105 G>A maps to NM_152701.3 E2281E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:48273744 G>A maps to NM_152701.3 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:139911055 G>A maps to ENST00000355090 Q995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr9:139903068 G>A maps to ENST00000355090 F2388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr9:139915192 G>A maps to ENST00000355090 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr9:139905885 G>A maps to ENST00000355090 F1954F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr9:139912063 G>A maps to ENST00000355090 S794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:139905528 G>A maps to ENST00000355090 F2014F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:139911794 G>A maps to ENST00000355090 F832F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:139915990 G>A maps to ENST00000355090 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:139917472 G>C maps to ENST00000355090 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:139913673 G>A maps to ENST00000355090 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr9:139910780 G>A maps to ENST00000355090 S1052S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr9:139905119 G>A maps to ENST00000355090 L2072L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr9:139905465 G>A maps to ENST00000355090 L2035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr9:139910618 G>A maps to ENST00000355090 L1068L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr9:139908776 G>A maps to ENST00000355090 A1391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr9:139904054 G>A maps to ENST00000355090 F2254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr9:139906600 G>A maps to ENST00000355090 T1801T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr9:139906978 G>A maps to ENST00000355090 A1745A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:139910619 G>A maps to ENST00000355090 I1067I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr9:139906451 G>A maps to ENST00000355090 V1823V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr9:139906957 G>A maps to ENST00000355090 I1752I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr9:139905957 G>A maps to ENST00000355090 V1930V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:139905713 G>A maps to ENST00000355090 F1979F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:139907192 G>A maps to ENST00000355090 L1714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr16:2345601 C>T maps to NM_001089.2 E801E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr16:2369794 C>T maps to NM_001089.2 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr16:2376020 G>A maps to NM_001089.2 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr16:2338045 C>T maps to NM_001089.2 Q995Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr16:2367651 G>A maps to NM_001089.2 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:2347480 C>T maps to NM_001089.2 W704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:2373620 G>A maps to NM_001089.2 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr16:2333204 G>A maps to NM_001089.2 L1339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr16:2376239 G>A maps to NM_001089.2 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr16:2369590 C>T maps to NM_001089.2 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:2333216 G>A maps to NM_001089.2 I1335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:2376254 C>T maps to NM_001089.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:2333321 G>A maps to NM_001089.2 A1300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr16:2376428 C>T maps to NM_001089.2 K13K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr16:2369608 G>A maps to NM_001089.2 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:2331153 G>A maps to NM_001089.2 C1411C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr16:2373617 C>G maps to NM_001089.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:2342195 G>A maps to NM_001089.2 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:2336705 G>A maps to NM_001089.2 D1089D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:2350131 C>T maps to NM_001089.2 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr16:2334957 G>A maps to NM_001089.2 D1175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr1:94586583 C>T maps to NM_000350.2 Q6Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr1:94485299 C>T maps to NM_000350.2 V1678V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:94506905 C>T maps to NM_000350.2 G1127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:94495989 C>T maps to NM_000350.2 W1449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:94548949 A>G maps to NM_000350.2 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr1:94480119 C>T maps to NM_000350.2 L1813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:94466456 G>A maps to NM_000350.2 T2138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44Q-06A-11D-A25O-08 chr1:94471025 G>A maps to NM_000350.2 R2040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:94564544 G>A maps to NM_000350.2 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:94543443 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr1:94463527 G>A maps to NM_000350.2 L2206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:94486959 C>T maps to NM_000350.2 W1618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:94474330 G>A maps to NM_000350.2 I1937I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:94471032 G>T maps to NM_000350.2 A2037A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:94564364 G>A maps to NM_000350.2 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr1:94568627 G>A maps to NM_000350.2 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:94471041 G>A maps to NM_000350.2 Y2034Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:94476399 G>A maps to NM_000350.2 F1890F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:94502304 G>A maps to NM_000350.2 L1285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:94514480 T>A maps to NM_000350.2 K896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr1:94564544 G>A maps to NM_000350.2 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:94467527 C>T maps to NM_000350.2 K2056K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:94502344 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:94463551 C>T maps to NM_000350.2 Q2198Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:94481368 G>A maps to NM_000350.2 F1746F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:94495006 G>A maps to NM_000350.2 P1511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:94502337 G>A maps to NM_000350.2 L1274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:94508332 G>A maps to NM_000350.2 L1104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:94574246 G>A maps to NM_000350.2 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:94586592 G>A maps to NM_000350.2 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:94474305 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:94512509 G>A maps to NM_000350.2 F961F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:94526104 C>T maps to NM_000350.2 T716T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr17:67302981 G>A maps to ENST00000392677 Y224Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:67249975 G>A maps to ENST00000392677 Q1428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:67247925 G>A maps to ENST00000392677 V1500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:67260956 A>G maps to ENST00000392677 F1079F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:67283853 G>A maps to ENST00000392677 P647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:67293375 A>G maps to ENST00000392677 I464I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:67129867 T>C maps to NM_080284.2 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr17:67075407 T>G did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:67103945 G>A maps to NM_080284.2 F760F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:67101642 G>A maps to NM_080284.2 P900P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr17:67092927 G>A maps to NM_080284.2 S1045S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr17:67094153 G>A maps to NM_080284.2 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:67080472 C>T maps to NM_080284.2 L1428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:67084375 G>A maps to NM_080284.2 F1210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr17:67083502 G>A maps to NM_080284.2 I1270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:67079069 C>T maps to NM_080284.2 V1520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr17:67079154 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:67075143 C>T maps to NM_080284.2 W1608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:67110992 G>A maps to NM_080284.2 F564F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr17:67129903 A>G maps to NM_080284.2 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr17:67129876 G>A maps to NM_080284.2 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:67101750 G>A maps to NM_080284.2 I864I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr19:1051464 C>T maps to NM_019112.3 L948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr19:1054603 C>T maps to NM_019112.3 L1254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:1046381 C>T maps to NM_019112.3 P533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:1055315 C>T maps to NM_019112.3 L1391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:1041404 C>T maps to NM_019112.3 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr19:1047196 C>T maps to NM_019112.3 F629F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:1042380 G>A maps to NM_019112.3 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:1046243 C>T maps to NM_019112.3 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:1047172 C>T maps to NM_019112.3 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:1058698 C>T maps to NM_019112.3 F1744F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:1062200 C>T maps to NM_019112.3 L1867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr19:1063640 C>T maps to NM_019112.3 A1937A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:1049424 G>A maps to NM_019112.3 K847K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr17:66883623 C>T maps to NM_007168.2 R1016R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr17:66873811 C>T maps to NM_007168.2 L1309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr17:66917521 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr17:66925339 C>T maps to NM_007168.2 K325K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:66938078 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:66871837 C>T maps to NM_007168.2 R1429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:66883512 G>A maps to NM_007168.2 F1053F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:66871528 G>A maps to NM_007168.2 S1461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:66925718 G>A maps to NM_007168.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:66871423 G>A maps to NM_007168.2 F1496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:66878040 C>T maps to NM_007168.2 K1263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:66883608 G>A maps to NM_007168.2 S1021S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:66898965 C>T maps to NM_007168.2 V844V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:66928583 G>A maps to NM_007168.2 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr17:66871522 T>C maps to NM_007168.2 Q1463Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr17:66902221 G>A maps to NM_007168.2 F747F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr17:66903959 G>A maps to NM_007168.2 I693I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:66925359 A>G maps to NM_007168.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:66873805 C>T maps to NM_007168.2 G1311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:66879960 C>T maps to NM_007168.2 K1186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:66883548 G>A maps to NM_007168.2 F1041F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:66929359 C>T maps to NM_007168.2 W173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr17:66938085 G>A maps to NM_007168.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:66928481 C>T maps to NM_007168.2 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:67020376 C>T maps to NM_080283.3 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:66986041 C>T maps to NM_080283.3 R1289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:67016590 G>C maps to NM_080283.3 V846V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:67012495 C>T maps to NM_080283.3 R979R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:66981226 G>C maps to NM_080283.3 P1417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr17:66987028 C>T maps to NM_080283.3 Q1262Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr17:67047175 A>T maps to NM_080283.3 L31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr17:66980285 C>T maps to NM_080283.3 T1470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:66980195 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr7:87180058 G>A maps to NM_000927.3 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr7:87144651 C>T maps to NM_000927.3 E1059E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr7:87144603 C>T maps to NM_000927.3 G1075G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:87179313 G>A maps to NM_000927.3 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:87170678 G>A maps to NM_000927.3 F771F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr7:87196207 T>C maps to NM_000927.3 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:87179524 G>A maps to NM_000927.3 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:87179797 G>A maps to NM_000927.3 R404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:87138734 G>A maps to NM_000927.3 I1115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:87150164 G>T maps to NM_000927.3 R905R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr7:87144570 G>A maps to NM_000927.3 F1086F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:229665972 G>A maps to NM_012089.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr1:229676462 G>A maps to NM_012089.2 R365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr1:229661689 G>A maps to NM_012089.2 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:169792775 G>A maps to NM_003742.2 A926A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:169791713 G>A maps to NM_003742.2 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:169874613 G>A maps to NM_003742.2 R8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr2:169833116 G>C maps to NM_003742.2 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:169780290 G>A maps to NM_003742.2 T1269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:169828505 G>A maps to NM_003742.2 Q497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:169780206 C>T maps to NM_003742.2 K1297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:169781286 C>T maps to NM_003742.2 Q1215Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr2:169780143 G>A maps to NM_003742.2 S1318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:169828371 G>A maps to NM_003742.2 I541I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:169780257 G>A maps to NM_003742.2 I1280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:169825917 G>A maps to NM_003742.2 F651F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:169826676 G>A maps to NM_003742.2 Q563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr2:169792880 G>A maps to NM_003742.2 I891I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:169783742 T>A maps to NM_003742.2 K1181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:169801119 G>A maps to NM_003742.2 Q869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:169826713 G>A maps to NM_003742.2 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:169842718 G>A maps to NM_003742.2 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:169792789 A>G maps to NM_003742.2 L922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr2:169788942 G>A maps to NM_003742.2 Q1053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:87035666 C>T maps to NM_018849.2 Q1148Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr7:87041263 G>A maps to NM_018849.2 R957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:87038586 G>A maps to NM_018849.2 L1016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:87053296 G>A maps to NM_018849.2 V712V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:87101969 C>T maps to NM_018849.2 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:87060830 G>A maps to NM_018849.2 V594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr7:87056158 G>A maps to NM_018849.2 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:87069661 G>A maps to NM_018849.2 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:87101969 C>T maps to NM_018849.2 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:87101969 C>T maps to NM_018849.2 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:87082365 G>A maps to NM_018849.2 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:87031441 G>A maps to NM_018849.2 V1277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:87041246 G>A maps to NM_018849.2 L962L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:87092146 G>A maps to NM_018849.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:87051438 G>A maps to NM_018849.2 Q772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr7:87076520 C>T maps to NM_018849.2 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:20738085 G>A maps to NM_001163941.1 W689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr7:20795138 G>A maps to NM_001163941.1 L1222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr7:20785054 C>T maps to NM_001163941.1 L1141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr7:20721150 C>T maps to NM_001163941.1 I577I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:20721138 T>G maps to NM_001163941.1 G573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr7:20739545 C>T maps to NM_001163941.1 F751F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr7:20725383 A>C maps to NM_001163941.1 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:20766724 C>T maps to NM_001163941.1 F896F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:20725317 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:20685682 C>T maps to NM_001163941.1 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:20721178 C>T maps to NM_001163941.1 R587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:20782639 G>A maps to NM_001163941.1 G1055G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:20766721 C>T maps to NM_001163941.1 A895A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr7:20778752 G>A maps to NM_001163941.1 G1005G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:20778752 G>A maps to NM_001163941.1 G1005G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:20762823 A>G maps to NM_001163941.1 E869E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr7:20766712 G>A maps to NM_001163941.1 R892R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr7:20706380 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr7:20683155 G>A maps to NM_001163941.1 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:20682905 G>A maps to NM_001163941.1 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:220081122 G>A maps to NM_005689.2 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:220080738 G>A maps to NM_005689.2 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr23:74296470 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:74318807 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:74332751 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:74288866 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:74282184 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:74284973 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:150731373 G>A maps to ENST00000297504 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:150732714 C>T maps to ENST00000297504 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr7:150737980 C>T maps to ENST00000297504 I502I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:150733721 C>T maps to ENST00000297504 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr7:150725643 A>C maps to ENST00000297504 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr7:150739163 C>A maps to ENST00000297504 T595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:150733219 C>T maps to ENST00000297504 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:150737980 C>T maps to ENST00000297504 I502I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150731894 C>T maps to ENST00000297504 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:123433227 G>A maps to NM_203444.2 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:123444422 G>A maps to NM_203444.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:123419894 G>A maps to NM_203444.2 F609F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr16:16110415 C>T maps to ENST00000399408 Q185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr16:16215893 C>T maps to ENST00000399408 V1161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr16:16162083 C>T maps to ENST00000399408 F583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr16:16138471 C>T maps to ENST00000399408 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:16177347 C>T maps to ENST00000399408 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:16139752 C>T maps to ENST00000399408 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:16177242 A>T maps to ENST00000399408 P712P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr16:16215944 C>T maps to ENST00000399408 F1178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:16138456 C>T maps to ENST00000399408 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:16177227 C>T maps to ENST00000399408 S707S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:16230361 C>T maps to ENST00000399408 R1395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr16:16130355 C>T maps to ENST00000399408 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr16:16177254 G>A maps to ENST00000399408 W716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr16:16225792 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:16126991 C>T maps to ENST00000399408 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr16:16225749 C>T maps to ENST00000399408 F1318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr16:16162101 C>T maps to ENST00000399408 F589F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr16:16215848 C>T maps to ENST00000399408 S1146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:16138399 C>T maps to ENST00000399408 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr16:16150145 C>T maps to ENST00000399408 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr6:43400804 C>T maps to NM_033450.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr6:43416633 C>T maps to NM_033450.2 I1297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr6:43406445 C>T maps to NM_033450.2 I652I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:43400950 C>T maps to NM_033450.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:43403586 C>T maps to NM_033450.2 D526D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:43413383 C>T maps to NM_033450.2 N998N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr6:43402441 C>T maps to NM_033450.2 C445C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:43412652 C>T maps to NM_033450.2 L911L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr6:43399894 C>T maps to NM_033450.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:43403496 G>T maps to NM_033450.2 T496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr6:43412967 C>T maps to NM_033450.2 T954T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:43401061 C>T maps to NM_033450.2 N405N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr6:43413674 C>T maps to NM_033450.2 T1095T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr6:43414038 C>A maps to NM_033450.2 L1105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:43400227 C>T maps to NM_033450.2 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:43413569 C>T maps to NM_033450.2 S1060S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:43412874 C>T maps to NM_033450.2 F923F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr16:48221215 G>A maps to NM_032583.3 V943V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:48201472 G>A maps to NM_032583.3 L1330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr16:48227837 C>T maps to NM_032583.3 T820T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr16:48234261 C>T maps to NM_032583.3 G669G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:48231936 C>T maps to NM_032583.3 K753K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr16:48226484 G>A maps to NM_032583.3 F884F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:48245041 G>A maps to NM_032583.3 V475V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:48261815 C>T maps to NM_032583.3 W99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr16:48244969 C>T maps to NM_032583.3 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:48250033 G>A maps to NM_032583.3 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr16:48244996 G>A maps to NM_032583.3 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:48258240 G>A maps to NM_032583.3 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr16:48204117 G>A maps to NM_032583.3 F1263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:48201472 G>A maps to NM_032583.3 L1330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:48248803 G>A maps to NM_032583.3 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:48258240 G>A maps to NM_032583.3 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:48261856 G>A maps to NM_032583.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr16:48244996 G>A maps to NM_032583.3 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr16:48174783 C>T maps to NM_033226.2 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr16:48142408 G>A maps to NM_033226.2 S771S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr16:48167669 G>A maps to NM_033226.2 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr16:48121874 C>T maps to NM_033226.2 V1199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:48119551 C>T maps to NM_033226.2 G1260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr16:48174678 G>A maps to NM_033226.2 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr16:48173145 C>T maps to NM_033226.2 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:48130779 C>T maps to NM_033226.2 W1024*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:48162522 C>T maps to NM_033226.2 K454K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr16:48151210 C>T maps to NM_033226.2 Q582Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr16:48167669 G>A maps to NM_033226.2 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr16:48145686 C>T maps to NM_033226.2 K708K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:48117822 C>T maps to NM_033226.2 G1330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:48119605 G>A maps to NM_033226.2 L1242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:48139139 G>A maps to NM_033226.2 F861F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:48164722 C>T maps to NM_033226.2 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr16:48173133 G>A maps to NM_033226.2 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:101601753 G>A maps to NM_000392.3 G1215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr10:101578581 C>T maps to NM_000392.3 I769I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:101590173 C>T maps to NM_000392.3 R911*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:101544501 G>A maps to NM_000392.3 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr10:101590580 T>A maps to NM_000392.3 I952I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:101590502 C>T maps to NM_000392.3 S926S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:101606800 G>A maps to NM_000392.3 L1410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr10:101557015 C>T maps to NM_000392.3 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr17:48734091 C>T maps to NM_003786.3 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:48741435 C>T maps to NM_003786.3 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr17:48755253 T>C maps to NM_003786.3 T1176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:48745354 C>T maps to NM_003786.3 I589I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:48746587 G>A maps to NM_003786.3 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr17:48746560 G>A maps to NM_003786.3 G666G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr17:48757160 G>A maps to NM_003786.3 V1236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr17:48746223 C>T maps to NM_003786.3 I627I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:48755477 C>T maps to NM_003786.3 F1201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr17:48741197 C>T maps to NM_003786.3 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr17:48733369 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr17:48734504 C>T maps to NM_003786.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:48764953 C>T maps to NM_003786.3 I1446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:48741447 C>T maps to NM_003786.3 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr17:48746817 C>T maps to NM_003786.3 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr17:48757214 C>T maps to NM_003786.3 I1254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr17:48734525 C>T maps to NM_003786.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:48734525 C>T maps to NM_003786.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:48746743 G>A maps to NM_003786.3 W699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:48753419 G>A maps to NM_003786.3 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:48755477 C>T maps to NM_003786.3 F1201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:48762083 C>T maps to NM_003786.3 F1376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:48735492 C>T maps to NM_003786.3 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:48761317 C>T maps to NM_003786.3 I1321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr13:95822791 C>T maps to NM_005845.3 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr13:95861830 G>A maps to NM_005845.3 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr13:95858839 G>A maps to NM_005845.3 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr13:95858787 G>A maps to NM_005845.3 Q387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr13:95816739 C>T maps to NM_005845.3 E689E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:95735478 G>A maps to NM_005845.3 P867P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr13:95847188 G>A maps to NM_005845.3 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr13:95816658 G>A maps to NM_005845.3 F716F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr13:95830016 G>A maps to NM_005845.3 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr13:95829961 G>A maps to NM_005845.3 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr13:95861830 G>A maps to NM_005845.3 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr3:183667836 G>A maps to NM_005688.2 I1007I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:183646564 A>G maps to NM_005688.2 D1301D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:183707069 G>A maps to NM_005688.2 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:183700570 G>A maps to NM_005688.2 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr3:183639171 G>A maps to NM_005688.2 T1410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:183655756 G>A maps to NM_005688.2 G1262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr16:16284137 C>T maps to NM_001171.5 W506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr16:16259671 C>T maps to NM_001171.5 R1038R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:16302616 C>T maps to NM_001171.5 K254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr16:16251660 G>A maps to NM_001171.5 P1247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:16263548 C>T maps to NM_001171.5 Q983Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr16:16256935 G>A maps to NM_001171.5 F1140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr16:16276349 C>T maps to NM_001171.5 L722L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:16291898 G>A maps to NM_001171.5 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:16286740 G>A maps to NM_001171.5 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:16297331 G>A maps to NM_001171.5 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:16315559 G>A maps to NM_001171.5 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:16269829 C>T maps to NM_001171.5 G868G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:16282689 G>A maps to NM_001171.5 Q593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:16297280 G>A maps to NM_001171.5 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr16:16282689 G>A maps to NM_001171.5 Q593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:16282696 G>A maps to NM_001171.5 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:16297343 G>A maps to NM_001171.5 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:16267253 T>A maps to NM_001171.5 K892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:16259566 G>A maps to NM_001171.5 L1073L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr16:16296028 G>A maps to NM_001171.5 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr16:16267236 C>T maps to NM_001171.5 K897K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr16:16256869 G>A maps to NM_001171.5 F1162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr16:16272783 G>A maps to NM_001171.5 S762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:16284022 G>A maps to NM_001171.5 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:16248636 G>A maps to NM_001171.5 F1352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr16:16284038 G>A maps to NM_001171.5 F539F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr16:16253383 G>A maps to NM_001171.5 I1230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr16:16282828 G>A maps to NM_001171.5 V546V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:16276672 G>A maps to NM_001171.5 F686F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:16282771 C>T maps to NM_001171.5 E565E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr16:16255421 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:17416775 C>A maps to ENST00000302539 E1453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr11:17496473 G>A maps to ENST00000302539 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr11:17482076 G>A maps to ENST00000302539 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr11:17414564 G>A maps to ENST00000302539 F1574F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:17428581 G>A maps to ENST00000302539 S1006S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:17430031 C>T maps to ENST00000302539 R910R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:17452409 G>A maps to ENST00000302539 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:17452500 G>A maps to ENST00000302539 F559F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr11:17452440 G>A maps to ENST00000302539 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:17482076 G>A maps to ENST00000302539 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:17464408 C>T maps to ENST00000302539 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:17483348 C>G maps to ENST00000302539 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr11:17419936 G>A maps to ENST00000302539 N1235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:17426126 G>A maps to ENST00000302539 F1164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:17418803 C>T maps to ENST00000302539 L1309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr11:17426144 G>A maps to ENST00000302539 S1158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr11:17438481 G>A maps to ENST00000302539 D751D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr11:17427100 C>T maps to ENST00000302539 E1114E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr11:17427102 C>A maps to ENST00000302539 E1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:17482079 C>T maps to ENST00000302539 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr11:17483243 G>A maps to ENST00000302539 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr11:17483186 G>A maps to ENST00000302539 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:17414624 C>T maps to ENST00000302539 R1554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr11:17483345 C>T maps to ENST00000302539 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr11:17419305 C>T maps to ENST00000302539 V1265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:17417236 G>A maps to ENST00000302539 I1410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:17449874 G>A maps to ENST00000302539 V667V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:17496473 G>A maps to ENST00000302539 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr11:17485032 G>A maps to ENST00000302539 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr11:17434946 C>T maps to ENST00000302539 G824G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr11:17491663 G>A maps to ENST00000302539 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr11:17483186 G>A maps to ENST00000302539 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:17418474 G>A maps to ENST00000302539 A1370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:17483174 G>A maps to ENST00000302539 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:17415848 G>A maps to ENST00000302539 I1504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:17464351 C>T maps to ENST00000302539 E515E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:17449879 G>A maps to ENST00000302539 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:17464324 C>T maps to ENST00000302539 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:17482037 G>A maps to ENST00000302539 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:17483288 G>A maps to ENST00000302539 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:17496473 G>A maps to ENST00000302539 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:17498203 G>A maps to ENST00000302539 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr11:17483186 G>A maps to ENST00000302539 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:17414612 A>C maps to ENST00000302539 L1558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:17418546 C>T maps to ENST00000302539 Q1346Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:17438478 G>A maps to ENST00000302539 P752P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:17428443 G>A maps to ENST00000302539 S1052S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr11:17449859 G>A maps to ENST00000302539 G672G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr12:21964987 G>A maps to NM_005691.2 S1402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr12:22046964 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr12:22025664 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr12:21997801 G>A maps to NM_005691.2 F1048F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:21981963 C>T maps to NM_005691.2 L1199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:22086768 G>A maps to NM_005691.2 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr12:22001150 C>T maps to NM_005691.2 E933E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:22078975 G>A maps to NM_005691.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:22001164 G>A maps to NM_005691.2 Q929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:21965020 G>A maps to NM_005691.2 I1391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:21998656 G>A maps to NM_005691.2 F992F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:21997801 G>A maps to NM_005691.2 F1048F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr12:21971125 C>T maps to NM_005691.2 S1243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:21960390 C>T maps to NM_005691.2 G1446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr12:21962819 C>T maps to NM_005691.2 L1427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:21997801 G>A maps to NM_005691.2 F1048F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:21967626 C>T maps to NM_005691.2 G1351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:22028660 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:21970175 C>T maps to NM_005691.2 V1279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:21965080 G>A maps to NM_005691.2 V1371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:22078906 G>A maps to NM_005691.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:22012525 G>A maps to NM_005691.2 V833V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:22059213 G>A maps to NM_005691.2 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr12:21997415 C>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr12:21954096 G>A maps to NM_020297.2 L1511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:21965020 G>A maps to NM_005691.2 I1391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:22025611 G>A maps to NM_005691.2 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:22061091 G>A maps to NM_005691.2 V458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr12:22005153 G>A maps to NM_005691.2 I882I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:21970221 C>T maps to NM_005691.2 W1264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr12:21971125 C>T maps to NM_005691.2 S1243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:153001938 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:153001939 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:153008674 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:152994742 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:152991602 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr12:39967591 G>A maps to NM_005164.3 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr12:39994470 C>T maps to NM_005164.3 G516G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:39973388 G>A maps to NM_005164.3 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:39998562 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:39997779 A>G maps to NM_005164.3 I478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr12:40012940 G>A maps to NM_005164.3 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:39947730 C>A maps to NM_005164.3 E736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:39947933 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr12:40001421 C>T maps to NM_005164.3 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr1:94964160 C>T maps to ENST00000454898 R488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:94982684 G>C maps to ENST00000454898 *684Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:94964160 C>T maps to ENST00000454898 R488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr14:74756198 G>A maps to NM_005050.3 V481V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr14:74759504 G>A maps to NM_005050.3 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:74762642 G>A maps to NM_005050.3 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:74766261 G>A maps to NM_005050.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr14:74759017 G>A maps to NM_005050.3 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr14:74759018 G>A maps to NM_005050.3 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr4:146044171 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:146044632 C>T maps to NM_002940.2 F507F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:146031359 C>T maps to NM_002940.2 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr4:146032130 C>T maps to NM_002940.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:146029174 C>T maps to NM_002940.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr6:30551479 C>T maps to NM_001025091.1 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:30557644 G>A maps to NM_001025091.1 E709E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr6:30557593 C>T maps to NM_001025091.1 F692F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:30551996 C>T maps to NM_001025091.1 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr7:150905162 C>T maps to NM_005692.3 R633R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:150912051 G>A maps to NM_005692.3 I549I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150915700 G>A maps to NM_005692.3 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:183908822 C>T maps to NM_018358.2 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:183911236 C>T maps to NM_018358.2 F656F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr3:183906716 G>A maps to NM_018358.2 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:183910649 C>T maps to NM_018358.2 V572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr21:43645803 G>A maps to NM_004915.3 E22E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr21:43645803 G>A maps to NM_004915.3 E22E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr21:43711741 C>T maps to NM_004915.3 I555I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:43704777 C>T maps to NM_004915.3 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr21:43711711 C>T maps to NM_004915.3 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr21:43702475 C>T maps to NM_004915.3 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr21:43646013 G>A maps to NM_004915.3 W92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr21:43704786 C>T maps to NM_004915.3 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr21:43710227 G>A maps to NM_004915.3 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr21:43714761 C>T maps to NM_004915.3 S600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr21:43702514 C>T maps to NM_004915.3 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr21:43711711 C>T maps to NM_004915.3 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr21:43711738 G>A maps to NM_004915.3 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:43716294 C>T maps to NM_004915.3 I610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:89022422 A>C maps to NM_004827.2 V442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:89052263 C>T maps to NM_004827.2 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:89061117 G>A maps to NM_004827.2 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr4:89034568 C>T maps to NM_004827.2 K360K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:89036160 G>A maps to NM_004827.2 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:119031007 C>T maps to NM_001142505.1 F503F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr11:119029406 C>T maps to NM_001142505.1 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:119029361 C>T maps to NM_001142505.1 F421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr11:119029560 C>T maps to NM_001142505.1 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:119031752 C>T maps to NM_001142505.1 F626F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:119025266 G>A maps to NM_001142505.1 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:119025517 C>T maps to NM_001142505.1 C193C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:119031617 G>A maps to NM_001142505.1 T581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:119020881 C>T maps to NM_001142505.1 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:119031617 G>A maps to NM_001142505.1 T581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr2:44065036 C>T maps to NM_022436.2 Q67Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:44059133 C>T maps to NM_022436.2 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:44064985 G>A maps to NM_022436.2 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:44041706 A>T maps to NM_022436.2 I557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr2:44053606 G>A maps to NM_022436.2 Q230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:44050042 C>T maps to NM_022436.2 E452E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:44052127 G>A maps to NM_022436.2 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr2:44049979 G>A maps to NM_022436.2 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr2:44073391 C>T maps to NM_022437.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:44079491 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr2:44102552 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:44099244 G>A maps to NM_022437.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:44079831 G>A maps to NM_022437.2 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:44102517 G>A maps to NM_022437.2 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:44102391 C>T maps to NM_022437.2 F532F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:44073308 C>T maps to NM_022437.2 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:44079741 C>T maps to NM_022437.2 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:44079891 C>T maps to NM_022437.2 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:44079587 G>A maps to NM_022437.2 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:44102412 C>T maps to NM_022437.2 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:27353479 G>A maps to NM_032604.3 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:27346827 C>A maps to NM_032604.3 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr7:73150987 G>A maps to NM_148912.2 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr7:73151383 G>A maps to NM_148912.2 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:25300862 G>A maps to NM_015600.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr20:25282880 C>T maps to NM_015600.3 K377K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:52003558 C>T maps to NM_032750.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr17:27893339 G>A maps to NM_198147.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:27889812 G>A maps to NM_198147.2 H391H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:27889806 G>A maps to NM_198147.2 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:89738512 C>T maps to NM_152924.4 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:89738533 C>T maps to NM_152924.4 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr18:19239240 A>C maps to NM_138340.4 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr14:23072901 A>C maps to NM_022060.2 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr14:23072910 C>T maps to NM_022060.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr14:23078743 C>T maps to NM_022060.2 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr14:23070652 C>T maps to NM_022060.2 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr3:43753261 C>T maps to NM_016006.4 Q190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr3:43759318 C>T maps to NM_016006.4 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:43744061 G>A maps to NM_016006.4 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:43753251 C>T maps to NM_016006.4 D186D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:43756496 C>T maps to NM_016006.4 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:58271158 C>T maps to NM_020676.5 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:58271158 C>T maps to NM_020676.5 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:17412215 C>T maps to NM_024527.4 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:17403475 C>T maps to NM_024527.4 K438K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:17412092 C>T maps to NM_024527.4 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr2:204231697 C>T maps to ENST00000295851 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:204231652 C>T maps to ENST00000295851 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr17:47295183 G>A maps to NM_016428.2 K123K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:47299474 G>A maps to NM_016428.2 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr17:47294029 G>A maps to NM_016428.2 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr17:47296975 C>T maps to NM_016428.2 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr17:47299495 C>T maps to NM_016428.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:47295228 G>A maps to NM_016428.2 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:47299582 G>A maps to NM_016428.2 E311E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr17:47295174 C>T maps to NM_016428.2 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:100527068 C>T maps to ENST00000471714 Q1213Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr3:100621519 C>T maps to ENST00000471714 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr3:100497218 C>T maps to ENST00000471714 G1405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr3:100595386 C>T maps to ENST00000471714 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr3:100469404 A>G maps to ENST00000471714 G1756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:100570745 C>A maps to ENST00000471714 E449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr3:100527029 G>A maps to ENST00000471714 R1226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:100508334 C>T maps to ENST00000471714 V1341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr9:133759736 G>A maps to NM_007313.2 W706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr9:133760199 C>T maps to NM_007313.2 A860A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr9:133760067 C>T maps to NM_007313.2 V816V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr9:133755521 C>T maps to NM_007313.2 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr9:133755497 C>T maps to NM_007313.2 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr9:133755917 C>T maps to NM_007313.2 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr9:133755917 C>T maps to NM_007313.2 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr1:179100500 G>A maps to NM_007314.3 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:179084118 T>C maps to NM_007314.3 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:179077359 G>A maps to NM_007314.3 S1014S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:179078466 G>A maps to NM_007314.3 T645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:179095613 G>A maps to NM_007314.3 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:179095763 C>T maps to NM_007314.3 W145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:179076996 G>A maps to NM_007314.3 A1135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr10:116207723 G>A maps to ENST00000277895 F618F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr10:116213207 G>A maps to ENST00000277895 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:116417947 G>A maps to ENST00000277895 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:116213219 C>T maps to ENST00000277895 R556R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr10:116213213 G>A maps to ENST00000277895 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr10:116251619 G>A maps to ENST00000277895 Y304Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr4:8055965 G>A maps to NM_001130083.1 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:7985002 C>T maps to NM_001130083.1 R604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:8009774 G>A maps to NM_001130088.1 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:8089971 C>T maps to NM_001130083.1 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr4:8009852 G>A maps to NM_001130083.1 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:8009921 C>T maps to NM_001130083.1 K494K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:148627397 G>A maps to NM_014945.2 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr5:148596538 C>T maps to NM_014945.2 Y229Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:148630941 C>T maps to NM_014945.2 F603F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr5:148632324 C>T maps to NM_014945.2 Y621Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr9:136131229 G>A maps to NM_020469.2 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:136137529 G>A maps to NM_020469.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:136131694 G>A maps to NM_020469.2 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr9:136131067 C>T maps to NM_020469.2 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:150558185 C>T maps to ENST00000416793 I734I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:150554733 G>A maps to ENST00000416793 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr7:150555992 G>A maps to ENST00000416793 R571R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr7:150556124 C>T maps to ENST00000416793 I615I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr7:150553641 G>A maps to ENST00000416793 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:150558146 C>T maps to ENST00000416793 F721F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:150553893 C>T maps to ENST00000416793 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr7:150556109 G>A maps to ENST00000416793 Q610Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:150555986 C>T maps to ENST00000416793 F569F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:150554580 C>T maps to ENST00000416793 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr7:150553698 C>T maps to ENST00000416793 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:150553944 C>T maps to ENST00000416793 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:150556124 C>T maps to ENST00000416793 I615I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:150554206 C>T maps to ENST00000416793 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:150554424 G>A maps to ENST00000416793 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr7:150553713 G>A maps to ENST00000416793 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr7:150554433 C>T maps to ENST00000416793 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr17:914038 C>T maps to NM_021962.2 K722K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr17:962062 C>T maps to NM_021962.2 K409K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr17:912971 G>A maps to NM_021962.2 S763S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:1012281 G>A maps to NM_001092.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr17:1012269 C>T maps to NM_001092.3 K13K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:107782364 C>T maps to NM_139166.4 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:107782249 G>A maps to NM_139166.4 Q57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr8:107781755 G>A maps to NM_139166.4 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr8:107782307 C>T maps to NM_139166.4 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:107773265 C>T maps to NM_139166.4 *382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr6:26597287 G>A maps to NM_013375.2 E26E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:26598803 G>A maps to NM_013375.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:26598587 C>T maps to NM_013375.2 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:26598509 C>T maps to NM_013375.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:127396526 C>T maps to NM_172027.2 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr3:127399302 C>T maps to NM_172027.2 I474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr3:127395237 G>A maps to NM_172027.2 W148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:34194757 G>A maps to NM_145804.2 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:34192557 G>A maps to NM_145804.2 F486F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:34181822 C>T maps to NM_145804.2 E825E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:34218897 G>A maps to NM_145804.2 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr3:38167343 G>A maps to NM_001607.3 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:38169314 C>T maps to NM_001607.3 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:47317849 G>A maps to NM_006111.2 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr18:47317896 G>A maps to NM_006111.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr18:47329068 G>T maps to NM_006111.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:35634797 G>A maps to NM_198834.1 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr17:35468499 C>T maps to NM_198834.1 V2177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:35620617 A>G maps to NM_198834.1 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr17:35615256 G>A maps to NM_198834.1 I513I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr17:35549192 T>C maps to NM_198834.1 L1418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:35609885 A>G maps to NM_198834.1 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:35640207 G>A maps to NM_198834.1 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:35548084 G>A maps to NM_198834.1 P1516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr17:35445883 C>T maps to NM_198834.1 K2339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:35640207 G>A maps to NM_198834.1 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:35578712 G>A maps to NM_198834.1 H1205H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr17:35478400 C>T maps to NM_198834.1 Q2050Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:35538186 G>A maps to NM_198834.1 S1629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr17:35538294 G>A maps to NM_198834.1 I1593I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:35470111 G>A maps to NM_198834.1 P2121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr17:35601575 G>A maps to NM_198834.1 F890F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:35557126 C>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:35640207 G>A maps to NM_198834.1 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr12:109629447 C>T maps to NM_001093.3 S725S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr12:109629451 C>T maps to NM_001093.3 R727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:109698355 C>T maps to NM_001093.3 L2190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:109577350 C>T maps to NM_001093.3 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr12:109677679 C>T maps to NM_001093.3 L1570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr12:109610099 C>T maps to NM_001093.3 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:109696851 C>T maps to NM_001093.3 N2145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr12:109703000 C>T maps to NM_001093.3 I2343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:109629450 C>T maps to NM_001093.3 I726I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:109631488 C>T maps to NM_001093.3 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:109639469 C>A maps to NM_001093.3 A959A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:109694020 C>T maps to NM_001093.3 T2081T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr12:109673143 C>T maps to NM_001093.3 L1458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:109692059 C>T maps to NM_001093.3 P2029P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:109605747 C>T maps to NM_001093.3 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:109684048 C>T maps to NM_001093.3 I1789I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr12:109623460 C>T maps to NM_001093.3 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr12:109650723 C>T maps to NM_001093.3 I1111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr12:109634838 C>T maps to NM_001093.3 F836F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr12:109702049 C>T maps to NM_001093.3 L2267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:109629447 C>T maps to NM_001093.3 S725S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:109677759 C>T maps to NM_001093.3 F1596F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:109685437 C>T maps to NM_001093.3 Q1867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:109631464 C>T maps to NM_001093.3 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr12:109605813 C>T maps to NM_001093.3 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr12:112182657 T>C maps to NM_001136538.1 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr12:112187044 C>T maps to NM_001136538.1 R936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:112174776 C>T maps to NM_001136538.1 I592I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr12:112186238 C>T maps to NM_001136538.1 I899I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr12:112182516 T>C maps to NM_001136538.1 D626D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NF-06A-11D-A19A-08 chr12:112153652 C>T maps to NM_001136538.1 H324H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr12:112130548 C>T maps to NM_001136538.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr12:112130533 C>T maps to NM_001136538.1 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr12:112194135 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:112167653 C>T maps to NM_001136538.1 R461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:112185103 C>T maps to NM_001136538.1 A831A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:134131178 C>T maps to NM_014384.2 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:128598593 G>A maps to NM_014049.4 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:128627104 C>T maps to NM_014049.4 I452I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:211082804 T>A maps to NM_001608.3 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:211070511 G>A maps to NM_001608.3 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:76190486 C>T maps to ENST00000370834 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:121177151 G>A maps to NM_000017.2 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:121176361 C>G maps to NM_000017.2 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr12:121175679 G>A maps to NM_000017.2 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr17:7124307 C>T maps to ENST00000356839 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr15:89400693 C>T maps to NM_013227.3 P1626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr15:89392753 C>T maps to NM_013227.3 A606A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr15:89381921 C>T maps to NM_013227.3 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr15:89388802 G>A maps to NM_013227.3 Q373Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr15:89395184 C>T maps to NM_013227.3 I729I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr15:89400534 G>A maps to NM_013227.3 R1573R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr15:89398251 C>T maps to NM_013227.3 F812F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr15:89403578 G>A maps to NM_013227.3 E2285E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr15:89381942 G>A maps to NM_013227.3 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr15:89403629 C>T maps to NM_013227.3 C2302C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr15:89382239 C>T maps to NM_013227.3 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr15:89401743 G>A maps to NM_013227.3 G1976G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:89381933 C>T maps to NM_013227.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:89381984 C>T maps to NM_013227.3 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr15:89402193 C>T maps to NM_013227.3 S2126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:89398539 G>A maps to NM_013227.3 V908V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:89400744 C>T maps to NM_013227.3 P1643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:89398587 G>A maps to NM_013227.3 E924E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr15:89401230 C>T maps to NM_013227.3 F1805F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:89400783 C>T maps to NM_013227.3 F1656F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr15:89401899 C>T maps to NM_013227.3 A2028A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr15:89401707 C>T maps to NM_013227.3 L1964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr15:89401191 C>T maps to NM_013227.3 V1792V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr15:89398548 C>T maps to NM_013227.3 G911G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:89416117 G>T maps to NM_013227.3 E2399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr15:89402334 C>T maps to NM_013227.3 T2173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr15:89398206 G>A maps to NM_013227.3 E797E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr15:89402419 C>T maps to NM_013227.3 L2202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr15:89398702 C>T maps to NM_013227.3 L963L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr15:89388937 C>T maps to NM_013227.3 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:89398296 G>A maps to NM_013227.3 K827K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:89398392 G>A maps to NM_013227.3 E859E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:89400018 G>A maps to NM_013227.3 E1401E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:89400655 C>T maps to NM_013227.3 L1614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:89401878 C>T maps to NM_013227.3 A2021A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr15:89392936 C>T maps to NM_013227.3 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:89400291 T>C maps to NM_013227.3 S1492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:89400801 G>A maps to NM_013227.3 V1662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:89401938 C>T maps to NM_013227.3 F2041F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr15:89400084 C>T maps to NM_013227.3 A1423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:7247223 C>T maps to NM_014716.3 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr17:7247259 G>A maps to NM_014716.3 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr17:7245640 C>T maps to NM_014716.3 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:7240654 C>A maps to NM_014716.3 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:7251240 G>A maps to NM_014716.3 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:7240681 G>A maps to NM_014716.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:7240681 G>A maps to NM_014716.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:7251513 G>A maps to NM_014716.3 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:7247254 C>T maps to NM_014716.3 R217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:7245289 C>T maps to NM_014716.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr17:7246847 G>A maps to NM_014716.3 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr3:195009892 A>G maps to NM_012287.5 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr3:195022714 G>A maps to NM_012287.5 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:195028037 C>T maps to NM_012287.5 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:195063201 G>A maps to NM_012287.5 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr3:195102637 G>A maps to NM_012287.5 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr3:195000118 G>A maps to NM_012287.5 Q759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:1233951 C>T maps to NM_030649.2 W286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:1237423 G>A maps to NM_030649.2 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:1231241 G>A maps to NM_030649.2 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:1231242 G>A maps to NM_030649.2 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:1236056 G>A maps to NM_030649.2 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:1229501 G>A maps to NM_030649.2 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:1230857 G>A maps to NM_030649.2 F594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:226349292 G>A maps to NM_022735.3 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:226334325 G>A maps to NM_022735.3 V524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr17:43220920 C>T maps to NM_001135706.1 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:43216424 G>A maps to NM_001135706.1 W242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr17:43216449 C>T maps to NM_001135706.1 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:27497366 C>T maps to ENST00000375888 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:180382606 C>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr1:180461442 G>A maps to NM_032360.3 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:15121002 G>A maps to NM_001039844.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr17:31355371 G>A maps to NM_183377.1 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:31343036 T>C maps to NM_183377.1 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:31438944 C>T maps to NM_183377.1 W283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:32483155 G>A maps to NM_001094.4 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr17:31350946 C>T maps to NM_183377.1 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:31350946 C>T maps to NM_183377.1 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr17:31350958 C>T maps to NM_183377.1 E423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:31351015 C>T maps to NM_183377.1 K404K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr17:32483089 C>T maps to NM_001094.4 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr17:31415946 G>A maps to NM_183377.1 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:31352992 G>A maps to NM_183377.1 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:31415910 G>A maps to NM_183377.1 F319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:32483452 G>A maps to NM_001094.4 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:32483452 G>A maps to NM_001094.4 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr12:50471846 C>T maps to NM_020039.2 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:50453674 C>T maps to NM_020039.2 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:50474933 G>A maps to NM_020039.2 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr12:50471138 G>A maps to NM_020039.2 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr12:50471885 C>T maps to NM_020039.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:50474460 C>T maps to NM_020039.2 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:150746352 C>T maps to NM_020321.2 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:150745995 G>A maps to NM_020321.2 E8E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr7:150748968 T>C maps to NM_020321.2 Y429Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:150746439 C>T maps to NM_020321.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:220396750 G>A maps to NM_018674.4 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:220396586 C>T maps to NM_018674.4 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr2:220396801 C>T maps to NM_018674.4 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:220396616 G>A maps to NM_018674.4 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:220402442 G>A maps to NM_018674.4 Q624Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:220396517 G>A maps to NM_018674.4 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr2:220399908 C>T maps to NM_018674.4 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr2:220399923 C>T maps to NM_018674.4 C496C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr4:156784841 C>T maps to NM_017419.2 K35K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:44105062 C>T maps to NM_032592.3 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr16:67694174 C>T maps to NM_001082486.1 W69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr16:67694175 C>T maps to NM_001082486.1 W69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr16:67694228 G>A maps to NM_001082486.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr16:67694228 G>A maps to NM_001082486.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr16:67694252 C>T maps to NM_001082486.1 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr17:61568323 G>A maps to NM_000789.3 W884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr17:61568583 G>A maps to NM_000789.3 R918R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr17:61571325 C>T maps to NM_000789.3 I1060I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:61571731 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:61566317 G>A maps to NM_000789.3 G822G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:61571792 G>A maps to NM_000789.3 G1114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:61568381 G>A maps to NM_000789.3 S903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:61557232 G>A maps to NM_000789.3 E205E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:61557815 C>T maps to NM_000789.3 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:61558930 G>A maps to NM_000789.3 W317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:61568706 C>T maps to NM_000789.3 A959A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:61568712 C>T maps to NM_000789.3 A961A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:61570795 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:61571733 C>T maps to NM_000789.3 L1095L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:61557833 C>T maps to NM_000789.3 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr17:61557803 C>T maps to NM_000789.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:61559940 G>A maps to NM_000789.3 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr17:61560516 C>T maps to NM_000789.3 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr17:61568743 T>C did not map to a codon.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr17:61571325 C>T maps to NM_000789.3 I1060I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr17:61558976 C>T maps to NM_000789.3 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr17:61566099 C>T maps to NM_000789.3 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:61562317 G>A maps to NM_152830.2 E30E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:61574597 C>T maps to NM_000789.3 F1264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:15582304 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr23:15609835 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:15582235 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:15605945 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:15618903 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:15610378 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:15603684 C>G did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:15610442 C>A did not map to a codon.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr23:15580107 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:6309841 G>A maps to NM_133492.2 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:6312489 G>A maps to NM_133492.2 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:6312489 G>A maps to NM_133492.2 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:6307228 C>T maps to NM_133492.2 W187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:6309786 G>A maps to NM_133492.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:6309799 G>A maps to NM_133492.2 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:6309835 G>A maps to NM_133492.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:6312194 G>A maps to NM_133492.2 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A264-06A-11D-A196-08 chr19:6307273 C>T maps to NM_133492.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr9:19435067 C>T maps to NM_001010887.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:19446395 C>T maps to NM_001010887.2 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr9:19450563 G>A maps to NM_001010887.2 W253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr9:19450564 G>A maps to NM_001010887.2 W253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:19423879 C>T maps to NM_001010887.2 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:76709842 C>T maps to NM_018367.5 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:76701611 C>T maps to NM_018367.5 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:100490863 G>A maps to NM_000665.3 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:100491646 C>T maps to NM_000665.3 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:100491718 C>T maps to NM_000665.3 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:23551019 C>T maps to NM_014977.3 E212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:23530346 G>A maps to NM_014977.3 F1215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr14:23549484 C>T maps to NM_014977.3 E411E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr17:40063733 G>A maps to ENST00000401700 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:40070072 G>A maps to ENST00000401700 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:40042509 G>A maps to ENST00000401700 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:40042417 G>A maps to ENST00000401700 I717I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr17:40070006 C>T maps to ENST00000401700 W94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr17:40025765 G>A maps to ENST00000401700 L1048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:40065272 C>T maps to ENST00000401700 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:135621047 C>T maps to NM_138326.2 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:135659391 C>T maps to NM_138326.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:135616889 G>A maps to NM_138326.2 W54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:135630211 G>A did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:135625234 G>A maps to NM_138326.2 W191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr9:32419033 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:32419039 C>T maps to NM_002197.2 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:32407273 C>A maps to NM_002197.2 S38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr9:32449070 C>T maps to NM_002197.2 Q850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr9:32419073 C>T maps to NM_002197.2 Q233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:32405518 C>T maps to NM_002197.2 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr22:41895782 C>A maps to ENST00000396512 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr22:41913585 C>T maps to ENST00000396512 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:41895767 C>T maps to ENST00000396512 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr22:41913579 C>T maps to ENST00000396512 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:74004355 C>T maps to NM_001037161.1 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr14:74009758 A>G maps to NM_001037161.1 K222K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:74009848 C>T maps to NM_001037161.1 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:55070050 G>A maps to NM_015547.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr1:55062986 G>A maps to NM_015547.3 E221E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:55072899 C>T maps to NM_015547.3 F488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:55063088 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:55069585 C>T maps to NM_015547.3 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:55059615 G>C maps to NM_015547.3 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:55072899 C>T maps to NM_015547.3 F488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:55059687 C>T maps to NM_015547.3 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:55069579 C>T maps to NM_015547.3 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:55070822 C>T maps to NM_015547.3 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:80641771 G>A maps to NM_130767.2 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:80628363 A>T maps to NM_130767.2 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:80643675 G>A maps to NM_130767.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:80628306 G>A maps to NM_130767.2 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:80626662 G>A maps to NM_130767.2 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr5:80638514 C>T maps to NM_130767.2 W368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:74036060 G>A maps to NM_006821.4 K39K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:6453327 G>A maps to NM_007274.3 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr20:44485897 G>A maps to NM_005469.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:23722030 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:23723116 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:23722058 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:73947503 G>A maps to NM_004035.6 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:73945887 G>A maps to NM_004035.6 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr17:73945303 G>A maps to NM_004035.6 F574F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:73951754 G>C maps to NM_004035.6 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:73945586 G>A maps to NM_004035.6 R525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:73949572 G>A maps to NM_004035.6 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:58519226 C>T maps to NM_003500.3 Q176Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:58510268 G>A maps to NM_003500.3 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:58519829 G>A maps to NM_003500.3 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:58520701 G>A maps to NM_003500.3 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:58512242 G>A maps to NM_003500.3 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:58520250 T>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr4:8416600 G>A maps to NM_003501.2 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr4:8411950 G>A maps to NM_003501.2 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:8390951 G>A maps to NM_003501.2 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:8394117 G>A maps to NM_003501.2 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr4:8383293 G>A maps to NM_003501.2 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:8383292 G>A maps to NM_003501.2 R527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:8383293 G>A maps to NM_003501.2 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr2:111559250 G>A maps to NM_001142807.1 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr2:111666434 G>A maps to NM_001142807.1 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:111666389 C>T maps to NM_001142807.1 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:111666392 G>A maps to NM_001142807.1 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:111542358 C>T maps to NM_001142807.1 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr2:111666449 G>A maps to NM_001142807.1 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr2:111789238 G>A maps to NM_001142807.1 W439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:111666425 G>A maps to NM_001142807.1 Q283Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:111556266 C>T maps to NM_001142807.1 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:111789229 C>T maps to NM_001142807.1 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:111556242 C>T maps to NM_001142807.1 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr2:111789214 G>A maps to NM_001142807.1 K431K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:111562932 G>A maps to NM_001142807.1 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:111666452 C>T maps to NM_001142807.1 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:111789229 C>T maps to NM_001142807.1 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:111789271 C>T maps to NM_001142807.1 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:111850536 G>A maps to NM_001142807.1 R512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:111551741 C>T maps to NM_001142807.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:271864 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr2:277291 G>A maps to NM_004300.3 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:47264355 C>T maps to NM_001610.2 Q352Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:47270235 G>A maps to NM_001610.2 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:147120146 A>G maps to NM_016361.3 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:147120213 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:147131764 C>T maps to NM_016361.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:147122010 G>A maps to NM_016361.3 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr3:141011958 T>A maps to NM_001037172.1 L452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:141006221 C>T maps to NM_001037172.1 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr3:141011641 C>T maps to NM_001037172.1 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:141011446 C>T maps to NM_001037172.1 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr3:141011770 G>A maps to NM_001037172.1 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:132071616 C>T maps to NM_001134194.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:132063784 C>T maps to NM_001134194.1 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr3:132061481 T>G maps to NM_001134194.1 Y214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:132071589 G>A maps to NM_001134194.1 Q297Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:132071616 C>T maps to NM_001134194.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:132061442 C>T maps to NM_001134194.1 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:132036381 C>T maps to NM_001134194.1 R28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:51295409 G>A maps to NM_033068.2 E177E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:51297145 G>A maps to NM_033068.2 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr19:51298159 G>A maps to NM_033068.2 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr22:51178265 C>T maps to NM_001097.2 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr22:51182621 C>T maps to NM_001097.2 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr22:51178326 C>T maps to NM_001097.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr12:6752785 G>A maps to NM_032489.2 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr12:6753340 A>C maps to NM_032489.2 Y302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:6749306 C>T maps to NM_032489.2 T448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6748161 G>A maps to NM_032489.2 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6749240 C>T maps to NM_032489.2 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6749667 C>T maps to NM_032489.2 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6752833 G>A maps to NM_032489.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:70824015 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:70817801 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:70817802 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:70823770 C>T did not map to a codon.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr23:70823685 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:70823865 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:70823895 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:70823745 G>A did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr23:70823611 A>G did not map to a codon.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr11:125547953 C>T maps to NM_001612.5 E97E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr15:78485845 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:78486326 G>A maps to NM_015162.4 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:78487012 G>A maps to NM_015162.4 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:78466726 C>T maps to NM_015162.4 K614K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:6147629 C>T maps to NM_030924.3 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr19:6183196 G>A maps to NM_030924.3 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr19:6165877 G>A maps to NM_030924.3 W197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:6165908 C>T maps to NM_030924.3 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:6183238 G>A maps to NM_030924.3 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:6187639 C>T maps to NM_030924.3 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:6147619 G>A maps to NM_030924.3 K77K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:6156555 C>T maps to NM_030924.3 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr19:6156555 C>T maps to NM_030924.3 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr19:6183188 C>T maps to NM_030924.3 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr19:6185473 G>A maps to NM_030924.3 K450K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr19:6147544 C>T maps to NM_030924.3 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:48503747 C>T maps to ENST00000427954 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:48551588 C>T maps to ENST00000427954 I611I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr17:48538184 C>T maps to ENST00000427954 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:48551880 C>T maps to ENST00000427954 R631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr17:48549853 C>T maps to ENST00000427954 I488I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr17:48540790 C>T maps to ENST00000427954 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:48551588 C>T maps to ENST00000427954 I611I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:48538679 C>T maps to ENST00000427954 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:48541211 C>T maps to ENST00000427954 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr17:48539888 C>T maps to ENST00000427954 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr16:89199644 C>T maps to NM_174917.2 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr16:89167526 C>T maps to NM_174917.2 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr4:185684407 G>A maps to NM_001995.2 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr4:185698107 A>G maps to NM_001995.2 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr4:185678842 G>A maps to NM_001995.2 I634I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:185687119 G>T maps to NM_001995.2 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:185698092 G>A maps to NM_001995.2 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr4:185678860 C>A did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr4:185687871 G>A maps to NM_001995.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr4:185694279 G>A maps to NM_001995.2 H290H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:223773637 G>T maps to NM_203372.1 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:223795393 C>T maps to NM_203372.1 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:108926537 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:108902615 T>A did not map to a codon.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr23:108926079 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:108902600 G>A did not map to a codon.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr23:108925959 A>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr10:114136198 C>T maps to NM_016234.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:114158656 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:114169358 C>T maps to NM_016234.3 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:114176674 G>A maps to NM_016234.3 K427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:114168235 T>A maps to NM_016234.3 Y219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr10:114169400 G>A maps to NM_016234.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:114136162 C>T maps to NM_016234.3 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:114154742 G>A maps to NM_016234.3 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:114171664 T>C maps to NM_016234.3 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:114169280 G>A maps to NM_016234.3 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:114176734 C>T maps to NM_016234.3 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr10:114158690 C>T maps to NM_016234.3 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr5:131326617 G>A maps to NM_001009185.1 Q105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr5:131305828 C>T maps to NM_001009185.1 W500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr5:131303686 G>A maps to NM_001009185.1 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr5:131323770 C>T maps to NM_001009185.1 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:131308512 G>A maps to NM_001009185.1 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:131310624 G>A maps to NM_001009185.1 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:131290046 G>A maps to NM_001009185.1 I683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:131308970 C>T maps to NM_001009185.1 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr5:131308458 C>T maps to NM_001009185.1 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr16:20638542 C>A maps to NM_052956.2 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr16:20696605 C>T maps to NM_052956.2 Q104Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr16:20696611 G>A maps to NM_052956.2 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr16:20648725 G>A maps to NM_052956.2 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr16:20673126 C>T maps to NM_052956.2 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr16:20651902 G>A maps to NM_052956.2 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:20638538 T>G maps to NM_052956.2 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:20638539 C>T maps to NM_052956.2 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr16:20638572 C>T maps to NM_052956.2 K455K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr16:20702489 G>A maps to NM_052956.2 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr16:20638584 C>T maps to NM_052956.2 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:20693666 G>A maps to NM_052956.2 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr16:20673120 G>A maps to NM_052956.2 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr16:20638545 G>A maps to NM_052956.2 F464F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:20648725 G>A maps to NM_052956.2 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:20696536 C>T maps to NM_052956.2 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr16:20682983 G>A maps to NM_052956.2 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr16:20673120 G>A maps to NM_052956.2 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:20648147 C>T maps to NM_052956.2 K404K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:20702342 C>T maps to NM_052956.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr16:20681187 G>A maps to NM_052956.2 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr16:20702390 C>T maps to NM_052956.2 W40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:20702471 G>A maps to NM_052956.2 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr16:20681304 C>T maps to NM_052956.2 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:20634825 C>T maps to NM_052956.2 K572K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:20636756 C>T maps to NM_052956.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr16:20681187 G>A maps to NM_052956.2 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr16:20494400 C>T maps to NM_001010845.2 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr16:20494420 C>T maps to NM_001010845.2 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr16:20497955 C>T maps to NM_001010845.2 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:20476865 C>T maps to NM_001010845.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr16:20476960 C>T maps to NM_001010845.2 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr16:20487037 G>A maps to NM_001010845.2 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:20471531 C>T maps to NM_001010845.2 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:20494414 C>T maps to NM_001010845.2 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:20476978 G>A maps to NM_001010845.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr16:20481026 C>T maps to NM_001010845.2 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr16:20494444 G>A maps to NM_001010845.2 K525K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr16:20471448 C>T maps to NM_001010845.2 R5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr16:20481026 C>T maps to NM_001010845.2 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:20486980 C>T maps to NM_001010845.2 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr16:20492170 G>A maps to NM_001010845.2 E479E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:20477026 G>A maps to NM_001010845.2 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:20480945 G>A maps to NM_001010845.2 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:20486980 C>T maps to NM_001010845.2 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr16:20476951 C>T maps to NM_001010845.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr16:20497933 G>A maps to NM_001010845.2 G556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr16:20477030 C>T maps to NM_001010845.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:20497972 G>A maps to NM_001010845.2 K569K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr16:20476978 G>A maps to NM_001010845.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:20482499 C>T maps to NM_001010845.2 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:20489921 C>T maps to NM_001010845.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:20492234 C>T maps to NM_001010845.2 R501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr16:20563564 C>T maps to NM_182617.3 W265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr16:20548645 C>T maps to NM_182617.3 G556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:20576145 G>A maps to NM_182617.3 Q8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr16:20570741 G>A maps to NM_182617.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr16:20563564 C>T maps to NM_182617.3 W265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:20559467 C>T maps to NM_182617.3 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:20548645 C>T maps to NM_182617.3 G556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:20563564 C>T maps to NM_182617.3 W265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:20548645 C>T maps to NM_182617.3 G556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:20559467 C>T maps to NM_182617.3 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:20548623 G>A maps to NM_182617.3 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr16:20570655 G>A maps to NM_182617.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr16:20563465 C>T maps to NM_182617.3 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:20548669 C>T maps to NM_182617.3 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:20556493 G>A maps to NM_182617.3 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr16:20566694 G>A maps to NM_182617.3 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr16:20793094 G>A maps to NM_005622.3 Q335Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:7469804 G>A maps to NM_001080454.1 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:7463135 G>A maps to NM_001080454.1 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:7463327 C>T maps to NM_001080454.1 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:7480884 G>A maps to NM_001080454.1 V553V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr12:7477097 C>T maps to NM_001080454.1 Y480Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr12:7476954 C>T maps to NM_001080454.1 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:7475909 G>A maps to NM_001080454.1 Q402Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:7457121 G>A maps to NM_001080454.1 K65K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:7473343 G>A maps to NM_001080454.1 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr16:20448598 C>T maps to NM_017888.2 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:20430622 C>T maps to NM_017888.2 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:20442627 C>T maps to NM_017888.2 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:20422919 C>T maps to NM_017888.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr16:20422910 C>T maps to NM_017888.2 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr16:20451667 G>A maps to NM_017888.2 V553V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:20442539 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:20422862 C>T maps to NM_017888.2 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:20439147 C>T maps to NM_017888.2 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr16:20429463 G>A maps to NM_017888.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr16:20448486 G>A maps to NM_017888.2 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr16:20429439 C>T maps to NM_017888.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:20422910 C>T maps to NM_017888.2 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr16:20439126 G>A maps to NM_017888.2 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr20:24994653 G>A maps to NM_032501.2 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr20:25000664 G>A maps to NM_032501.2 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr20:24994175 G>A maps to NM_032501.2 Y525Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr20:25002055 A>T maps to NM_032501.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:24993468 G>A maps to NM_032501.2 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:25003623 G>A maps to NM_032501.2 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr20:25003715 C>A maps to NM_032501.2 E274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:24994250 G>A maps to NM_032501.2 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:33500979 C>T maps to NM_001076552.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr20:33500926 C>T maps to NM_001076552.2 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:33509147 C>T maps to NM_001076552.2 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr12:81568679 C>T maps to NM_024560.2 D404D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr12:81528707 G>A maps to NM_024560.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:81627163 G>T maps to NM_024560.2 E545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:81647090 C>T maps to NM_024560.2 I575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr12:81627141 C>T maps to NM_024560.2 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:81472120 G>A maps to NM_024560.2 E74E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:81568676 G>A maps to NM_024560.2 Q403Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:81647353 C>T maps to NM_024560.2 R634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:229568805 C>T maps to NM_001100.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:229568050 G>A maps to NM_001100.3 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:229567635 C>A maps to NM_001100.3 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:229568552 G>A maps to NM_001100.3 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:90695040 C>T maps to NM_001141945.1 W358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:5567918 G>A maps to NM_001101.3 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:5568197 G>A maps to NM_001101.3 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr7:5568830 G>A maps to NM_001101.3 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:5567912 C>T maps to NM_001101.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr7:5567492 G>A maps to NM_001101.3 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr7:5569225 G>A maps to NM_001101.3 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr5:56778120 C>T maps to NM_001017992.2 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:56778063 C>T maps to NM_001017992.2 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:56778201 C>T maps to NM_001017992.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr5:56778078 G>A maps to NM_001017992.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:56777744 G>A maps to NM_001017992.2 Q264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:56777622 G>A maps to NM_001017992.2 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:56778486 C>T maps to NM_001017992.2 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr15:35085668 G>A maps to NM_005159.4 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:35085665 G>A maps to NM_005159.4 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:35084717 C>T maps to NM_005159.4 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:35084684 C>T maps to NM_005159.4 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr17:79478024 G>A maps to NM_001614.2 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr17:79478220 G>A maps to NM_001614.2 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:79478940 C>T maps to NM_001614.2 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr17:79478970 C>T maps to NM_001614.2 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr17:79478514 C>T maps to NM_001614.2 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:79478250 G>A maps to NM_001614.2 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr2:74135894 G>A maps to NM_001615.3 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr2:74128494 G>A maps to NM_001615.3 K19K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:74129554 C>T maps to NM_001615.3 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr2:74128539 C>T maps to NM_001615.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:74140693 C>T maps to NM_001615.3 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:179292228 C>T maps to NM_004301.3 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:179287618 T>C maps to NM_004301.3 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:100244236 C>T maps to NM_016188.4 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:100244203 G>A maps to NM_016188.4 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr7:100246253 G>A maps to NM_016188.4 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:100245114 C>T maps to NM_016188.4 K237K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:100245156 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr7:100243895 G>A maps to NM_016188.4 I392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr7:100244708 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:111624688 G>A maps to NM_006687.2 Q29Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr9:111625525 G>A maps to NM_006687.2 E308E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:111625831 G>A maps to NM_006687.2 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr9:111618036 G>A maps to NM_006686.3 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr9:111617139 C>T maps to NM_006686.3 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:111618189 G>A maps to NM_006686.3 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ES-06A-11D-A20D-08 chr9:111617775 G>A maps to NM_006686.3 H145H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr1:18149838 G>A maps to NM_030812.2 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr1:18152482 G>A maps to NM_030812.2 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:18152296 C>T maps to NM_030812.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:18152344 C>T maps to NM_030812.2 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:18152803 C>T maps to NM_030812.2 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:8808103 G>A maps to NM_178525.3 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr19:8807851 C>T maps to NM_178525.3 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr19:8807923 C>T maps to NM_178525.3 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:8807959 G>C maps to NM_178525.3 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:8808175 C>T maps to NM_178525.3 K292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:8808604 G>A maps to NM_178525.3 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:8808550 G>A maps to NM_178525.3 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:8807914 G>A maps to NM_178525.3 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:8808424 G>A maps to NM_178525.3 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:8808058 G>A maps to NM_178525.3 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr19:8807892 G>A maps to NM_178525.3 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:8807923 C>T maps to NM_178525.3 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr19:8808457 C>T maps to NM_178525.3 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:8808448 C>A maps to NM_178525.3 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr19:8808814 C>T maps to NM_178525.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:8807883 G>A maps to NM_178525.3 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:8809027 G>A maps to NM_178525.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr14:69341638 G>A maps to NM_001130004.1 S894S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:69347700 G>A maps to NM_001130004.1 I653I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr14:69371393 G>A maps to NM_001130004.1 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:69352140 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr14:69346819 G>A maps to NM_001130004.1 I713I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr14:69371390 G>A maps to NM_001130004.1 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr14:69358904 C>T maps to NM_001130004.1 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:69352209 G>A maps to NM_001130004.1 A439A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:69376694 G>A maps to NM_001130004.1 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:69387774 G>A maps to NM_001130004.1 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr1:236925828 G>A maps to NM_001103.2 R865R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:236914939 C>T maps to NM_001103.2 T609T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:236923025 G>A maps to NM_001103.2 R768R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:236890998 C>T maps to NM_001103.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A6L9-06A-11D-A32N-08 chr1:236910964 A>G did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:236908052 C>T maps to NM_001103.2 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:236902627 C>T maps to NM_001103.2 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:236898938 C>T maps to NM_001103.2 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:236912518 G>A maps to NM_001103.2 E537E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:236902832 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:236881216 C>T maps to NM_001103.2 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:236914813 G>A maps to NM_001103.2 E567E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:236924439 C>T maps to NM_001103.2 V831V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:236881273 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:236925805 C>T maps to NM_001103.2 Q858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr1:236923028 G>A maps to NM_001103.2 K769K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:236914837 C>T maps to NM_001103.2 I575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:236902624 G>A maps to NM_001103.2 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:236908010 C>T maps to NM_001103.2 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr1:236889311 C>T maps to NM_001103.2 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:236918446 C>T maps to NM_001103.2 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr11:66322679 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr11:66322818 C>T maps to NM_001104.1 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:66321561 C>T maps to NM_001104.1 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:66322806 C>T maps to NM_001104.1 Y229Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr19:39191311 C>T maps to NM_004924.3 R79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr19:39215190 C>T maps to NM_004924.3 Q666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:104248025 G>A maps to NM_005736.3 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:104248026 G>A maps to NM_005736.3 H65H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:104241782 G>A maps to NM_005736.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:98275433 G>A maps to NM_005735.3 N116N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:98274436 G>A maps to NM_005735.3 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr2:98275373 G>A maps to NM_005735.3 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:114670796 C>T maps to NM_005721.3 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr7:152497739 G>A maps to NM_020445.4 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:152551574 G>A maps to NM_020445.4 K398K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:152551616 C>T maps to NM_020445.4 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:152550595 C>T maps to NM_020445.4 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr7:149981868 G>T maps to NM_001164458.1 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:149983536 G>A maps to NM_001164458.1 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:37400290 C>T maps to NM_024855.3 I552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr20:37400314 G>A maps to NM_024855.3 K560K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr3:53907081 G>A maps to NM_022899.4 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:53912392 G>A maps to NM_022899.4 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr23:127186129 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:127185187 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:127186096 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:127186017 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:127185519 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:127186075 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:127185460 C>T did not map to a codon.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr23:127185815 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:127186074 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:127185269 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:127185195 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:127185251 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:127185092 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:127185416 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr23:127186106 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:127185267 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:127185391 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:127185836 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:127185106 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr23:127186091 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:127185850 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:127186105 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:127185836 C>T did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:127185214 T>C did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:2939041 C>T maps to NM_080431.4 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:2939173 C>T maps to NM_080431.4 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr1:2938343 C>A maps to NM_080431.4 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:2938861 C>T maps to NM_080431.4 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:2939041 C>T maps to NM_080431.4 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:2938964 C>T maps to NM_080431.4 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:2939143 G>A maps to NM_080431.4 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:2939048 C>T maps to NM_080431.4 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:2939080 G>A maps to NM_080431.4 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:2939041 C>T maps to NM_080431.4 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:2939041 C>T maps to NM_080431.4 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:2938363 C>T maps to NM_080431.4 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:2939140 G>A maps to NM_080431.4 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:2938636 G>A maps to NM_080431.4 E129E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:2938642 C>T maps to NM_080431.4 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr2:158637083 G>A maps to NM_001111067.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:158617437 G>T maps to NM_001111067.2 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:158634708 G>A maps to NM_001111067.2 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:158636951 C>T maps to NM_001111067.2 Q76Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr12:52374762 C>T maps to NM_020328.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr12:52369268 C>T maps to NM_020328.3 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr12:52377936 C>T maps to NM_020328.3 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:52370316 C>T maps to NM_020328.3 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr2:158395119 G>A maps to NM_145259.2 R441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:158399336 C>T maps to NM_145259.2 K327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:158406692 G>A maps to NM_145259.2 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr2:158395119 G>A maps to NM_145259.2 R441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:158443810 G>A maps to NM_145259.2 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:148654053 G>A maps to NM_001616.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:148653909 C>T maps to NM_001616.3 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:148683721 A>T maps to NM_001616.3 K447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:38523741 C>T maps to NM_001106.3 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:38523756 C>T maps to NM_001106.3 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:38524762 C>T maps to NM_001106.3 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:38519381 C>G maps to NM_001106.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38520722 C>T maps to NM_001106.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr12:52306946 G>A maps to NM_001077401.1 K42K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr12:52309988 G>A maps to NM_001077401.1 W406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:52309150 C>T maps to NM_001077401.1 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr12:52312838 G>A maps to NM_001077401.1 K439K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr12:52312850 T>A maps to NM_001077401.1 C443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:52312865 C>T maps to NM_001077401.1 T448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:52307412 C>T maps to NM_001077401.1 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:52309925 C>T maps to NM_001077401.1 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:52312853 G>A maps to NM_001077401.1 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:52306892 G>A maps to NM_001077401.1 V24V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D3-A51R-06A-11D-A25O-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr3:52020303 G>A maps to ENST00000463937 E232E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:67410209 C>T maps to NM_080658.1 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr20:43251472 G>A maps to NM_000022.2 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr20:43251571 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:43257797 G>A maps to NM_000022.2 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:43257722 G>A maps to NM_000022.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr20:43251686 G>A maps to NM_000022.2 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr4:123317443 C>T maps to NM_139243.3 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr4:123301319 G>A maps to NM_139243.3 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr4:123301319 G>A maps to NM_139243.3 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:123301331 C>T maps to NM_139243.3 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr4:123301319 G>A maps to NM_139243.3 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:123301319 G>A maps to NM_139243.3 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr4:123317410 G>A maps to NM_139243.3 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr4:123314756 C>T maps to NM_139243.3 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:84230342 C>T maps to NM_139174.3 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr16:84229645 C>T maps to NM_139174.3 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr16:84229829 C>T maps to NM_139174.3 V542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:84229034 C>T maps to NM_139174.3 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:84224961 C>T maps to NM_139174.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr16:84230549 G>A maps to NM_139174.3 S656S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:84230519 G>A maps to NM_139174.3 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:43639245 T>A maps to ENST00000422466 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr15:58957324 G>A maps to NM_001110.2 Q186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:58936117 G>A maps to NM_001110.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr17:42855101 C>T maps to NM_002390.4 S647S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr17:42854277 C>G maps to NM_002390.4 Y543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr17:42849141 G>A maps to NM_002390.4 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:42849669 C>T maps to NM_002390.4 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr10:127753537 G>A maps to NM_003474.4 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:127737932 G>A maps to NM_003474.4 I605I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:127782639 G>A maps to NM_003474.4 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr10:127738158 C>T maps to NM_003474.4 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:127755327 C>T maps to NM_003474.4 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:127967521 C>T maps to NM_003474.4 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr10:127824172 G>T maps to NM_003474.4 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr1:155028321 C>T maps to NM_207197.1 H223H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:155030484 C>T maps to NM_207197.1 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:155028557 C>T maps to NM_207197.1 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:155028638 C>T maps to NM_207197.1 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:155032807 C>T maps to NM_207197.1 T732T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:155029729 A>C maps to NM_207197.1 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr1:155025183 C>T maps to NM_207197.1 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:155028618 C>T maps to NM_207197.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr8:39506006 T>C maps to NM_014237.2 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr8:39442146 C>T maps to NM_014237.2 F2F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr8:39468071 C>T maps to NM_014237.2 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:39581303 G>A maps to NM_014237.2 W685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:39505983 C>T maps to NM_014237.2 Q390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr8:39466602 A>G maps to NM_014237.2 E77E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:39468046 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:39535043 T>G maps to NM_014237.2 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr8:39495126 C>T maps to NM_014237.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:39442146 C>T maps to NM_014237.2 F2F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:39564382 C>T maps to NM_014237.2 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr8:39564382 C>T maps to NM_014237.2 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr8:39495135 G>A maps to NM_014237.2 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr8:39564370 C>T maps to NM_014237.2 F655F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:39525701 G>A maps to NM_014237.2 K504K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr8:39564370 C>T maps to NM_014237.2 F655F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr8:39587458 A>T maps to NM_014237.2 *740Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:39564413 C>T maps to NM_014237.2 Q670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr8:39495989 G>A maps to NM_014237.2 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr8:39502951 T>A maps to NM_014237.2 C335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr8:39581319 C>T maps to NM_014237.2 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:39495177 G>A maps to NM_014237.2 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr5:156915475 G>A maps to ENST00000430702 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr5:156940500 G>A maps to ENST00000430702 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:156921774 G>A maps to ENST00000430702 F543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:156921747 G>A maps to ENST00000430702 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:156915374 C>T maps to ENST00000430702 R818R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:156924096 G>A maps to ENST00000430702 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:156946918 G>A maps to ENST00000430702 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr5:156920178 C>T maps to ENST00000430702 A572A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr5:156918647 G>A maps to ENST00000430702 I692I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:156915383 C>T maps to ENST00000430702 R815R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:156929951 C>T maps to ENST00000430702 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:156907965 C>T maps to ENST00000394020 S918S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:156940504 C>T maps to ENST00000430702 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:156964929 C>T maps to ENST00000430702 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr8:39604025 C>T maps to NM_001464.3 R713R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:39604025 C>T maps to NM_001464.3 R713R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:39626973 C>T maps to NM_001464.3 Q383Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:39679181 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr8:39624427 C>T maps to NM_001464.3 W482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr8:39626979 G>A maps to NM_001464.3 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr8:39606960 A>G maps to NM_001464.3 N628N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:39604031 G>A maps to NM_001464.3 F711F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:39682403 G>A maps to NM_001464.3 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr8:39626979 G>A maps to NM_001464.3 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:39644531 C>T maps to NM_001464.3 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:39646226 G>A maps to NM_001464.3 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:39691491 C>T maps to NM_001464.3 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr8:39626919 C>T maps to NM_001464.3 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr8:39634659 C>T maps to NM_001464.3 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr8:39604025 C>T maps to NM_001464.3 R713R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:39604030 G>A maps to NM_001464.3 Q712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr8:39604025 C>T maps to NM_001464.3 R713R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr8:39624517 G>T maps to NM_001464.3 C452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr8:39646193 C>T maps to NM_001464.3 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:39606905 G>A maps to NM_001464.3 Q647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr8:39604025 C>T maps to NM_001464.3 R713R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr14:70990373 A>G maps to NM_003814.4 H417H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr14:70990606 G>A maps to NM_003814.4 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr14:70990898 G>A maps to NM_003814.4 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:70991578 G>A maps to NM_003814.4 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr14:70926273 G>A maps to NM_003813.2 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:70925169 A>G maps to NM_003813.2 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:70925424 C>T maps to NM_003813.2 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr14:70924299 C>T maps to NM_003813.2 Y28Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr14:70925586 C>T maps to NM_003813.2 F457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr14:70925725 C>T maps to NM_003813.2 Q504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:70924998 G>A maps to NM_003813.2 W261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:70924527 C>T maps to NM_003813.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:70924275 G>A maps to NM_003813.2 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:70924605 G>A maps to NM_003813.2 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:70926081 G>A maps to NM_003813.2 K622K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:70926126 G>A maps to NM_003813.2 E637E. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D3-A51E-06A-11D-A25O-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr7:87785276 C>T maps to NM_021723.3 I621I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:87763711 A>G maps to NM_021723.3 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr7:87792380 G>A maps to NM_021723.3 G654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr7:87774727 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:87795235 G>A maps to NM_021723.3 K722K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:87774471 C>T maps to NM_021723.3 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:87792380 G>A maps to NM_021723.3 G654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:207432006 G>A maps to NM_003812.2 Q485Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:207345993 C>T maps to NM_003812.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr2:207426989 C>T maps to NM_003812.2 Q440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr2:207459550 G>A maps to NM_003812.2 R723R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr8:24167699 G>A maps to NM_014265.4 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr8:24207458 C>A maps to NM_014265.4 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr8:24199185 C>T maps to NM_014265.4 F582F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr8:24181447 G>A maps to NM_014265.4 E274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr8:24188791 G>A maps to NM_014265.4 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr8:24181438 C>T maps to NM_014265.4 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:24167675 G>A maps to NM_014265.4 K76K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr8:24207383 C>T maps to NM_014265.4 S666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr8:24199185 C>T maps to NM_014265.4 F582F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:24170909 C>T maps to NM_014265.4 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr8:24197051 G>A maps to NM_014265.4 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr8:24170960 G>A maps to NM_014265.4 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr8:24193158 G>A maps to NM_021777.3 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr8:24167678 C>T maps to NM_014265.4 N77N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr8:24208804 G>A maps to NM_014265.4 K720K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr8:24201062 C>T maps to NM_014265.4 I652I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr8:24201092 C>T maps to NM_014265.4 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr8:24167699 G>A maps to NM_014265.4 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr8:24177769 C>T maps to NM_014265.4 Q200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr8:24193107 G>A maps to NM_014265.4 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr8:24193056 C>T maps to NM_014265.4 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr8:24193089 G>A maps to NM_014265.4 K501K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:24196977 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:24181423 C>T maps to NM_014265.4 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr8:24188791 G>A maps to NM_014265.4 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:24201062 C>T maps to NM_014265.4 I652I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr8:24209516 C>T maps to NM_014265.4 P732P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr8:24201062 C>T maps to NM_014265.4 I652I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:24188791 G>A maps to NM_014265.4 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr8:24199164 G>A maps to NM_014265.4 W575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr8:24188791 G>A maps to NM_014265.4 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr8:24181447 G>A maps to NM_014265.4 E274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr8:24187610 G>A maps to NM_014265.4 V362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:24170930 C>T maps to NM_014265.4 Y138Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:24181468 G>A maps to NM_014265.4 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:24181411 G>A maps to NM_014265.4 K262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr8:24188830 G>A maps to NM_014265.4 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:175898019 C>T maps to NM_014269.4 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr4:175898196 G>A maps to NM_014269.4 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:175898710 C>T maps to NM_014269.4 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr4:175896840 C>T maps to NM_014269.4 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr4:175898196 G>A maps to NM_014269.4 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr4:175898196 G>A maps to NM_014269.4 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr4:175898163 G>A maps to NM_014269.4 K496K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:175897248 G>A maps to NM_014269.4 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:175898964 G>A maps to NM_014269.4 V763V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:175897464 G>A maps to NM_014269.4 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr4:175898637 G>A maps to NM_014269.4 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr4:175896840 C>T maps to NM_014269.4 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr4:175898955 A>G maps to NM_014269.4 Q760Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr4:175897257 G>A maps to NM_014269.4 W194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:175896747 C>T maps to NM_014269.4 H24H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:175897905 G>A maps to NM_014269.4 E410E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:175896789 G>A maps to NM_014269.4 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J6-06A-11D-A19A-08 chr1:120436619 G>T maps to NM_021794.2 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:120437027 G>A maps to NM_021794.2 C644C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:120436813 A>G maps to NM_021794.2 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:120438356 G>A maps to NM_021794.2 H201H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:120437738 C>T maps to NM_021794.2 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:120437243 C>T maps to NM_021794.2 T572T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:120438485 G>A maps to NM_021794.2 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:120438380 C>T maps to NM_021794.2 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:120438566 C>T maps to NM_021794.2 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr1:120438380 C>T maps to NM_021794.2 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:120437708 G>A maps to NM_021794.2 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:120437335 G>A maps to NM_021794.2 R542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:120438509 C>T maps to NM_021794.2 K150K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:39079205 C>T maps to NM_145004.5 C437C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr8:39089650 G>A maps to NM_145004.5 W544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr8:39114850 C>T maps to NM_145004.5 F717F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:39091501 C>T maps to NM_145004.5 F573F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr8:39091416 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr8:39080725 C>T maps to NM_145004.5 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr8:39091501 C>T maps to NM_145004.5 F573F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:39114781 C>T maps to NM_145004.5 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr20:3652868 G>A maps to NM_025220.2 D503D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr20:3652110 G>T maps to NM_025220.2 A646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:3650191 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr20:3652876 G>A maps to NM_025220.2 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr20:3651786 G>A maps to NM_025220.2 F702F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:3654065 G>A maps to NM_025220.2 D356D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:3655673 C>T maps to NM_025220.2 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr8:24300034 G>A maps to ENST00000380789 K34K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr8:24304748 C>T maps to ENST00000380789 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:24350573 G>A maps to ENST00000380789 K558K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr8:24339713 A>G maps to ENST00000380789 E255E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr8:24321469 C>T maps to ENST00000380789 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr8:24300053 C>T maps to ENST00000380789 R41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:24342867 C>T maps to ENST00000380789 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr8:24342867 C>T maps to ENST00000380789 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:24350606 C>T maps to ENST00000380789 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:24344782 C>T maps to ENST00000380789 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:24350738 A>G maps to ENST00000380789 G613G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:24299995 C>T maps to ENST00000380789 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr8:24324356 G>A maps to ENST00000380789 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr8:24359082 C>T maps to ENST00000380789 F734F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NF-06A-11D-A19A-08 chr8:24358348 C>T maps to ENST00000380789 I683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr8:24349414 G>A did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr8:24324356 G>A maps to ENST00000380789 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr8:24357707 C>T maps to ENST00000380789 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr8:24365021 C>T maps to ENST00000380789 I768I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr8:24324425 T>C maps to ENST00000380789 Y168Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:135085326 G>A maps to NM_001109.4 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr10:135083962 C>T maps to NM_001109.4 G562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr8:38913097 C>T maps to NM_003816.2 F466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr8:38879212 C>T maps to NM_003816.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:38880704 C>T maps to NM_003816.2 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr8:38947605 C>T maps to NM_003816.2 F703F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr8:24254781 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:24254923 G>A maps to NM_014479.3 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:24256962 C>T maps to NM_014479.3 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:24261523 C>T maps to NM_014479.3 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr8:24250836 C>T maps to NM_014479.3 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr8:24259436 C>T maps to NM_014479.3 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:24256962 C>T maps to NM_014479.3 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr8:24251644 G>A maps to NM_014479.3 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:24256526 G>A maps to NM_014479.3 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr8:24256385 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr8:24255245 G>A maps to NM_014479.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:24251641 C>T maps to NM_014479.3 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:24251644 G>A maps to NM_014479.3 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:24250803 G>A maps to NM_014479.3 Q79Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:24256962 C>T maps to NM_014479.3 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr8:24259436 C>T maps to NM_014479.3 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:24250827 C>T maps to NM_014479.3 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr8:24256407 C>T maps to NM_014479.3 Q262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:24255194 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:24256520 G>A maps to NM_014479.3 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr8:24254923 G>A maps to NM_014479.3 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr8:24256520 G>A maps to NM_014479.3 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr8:24242034 C>T maps to NM_014479.3 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr8:24257732 G>C maps to NM_014479.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr8:24254939 C>T maps to NM_014479.3 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr8:24261598 C>T maps to NM_014479.3 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:24251644 G>A maps to NM_014479.3 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:24256501 G>A maps to NM_014479.3 W293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:24256520 G>A maps to NM_014479.3 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:24251644 G>A maps to NM_014479.3 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr8:24259436 C>T maps to NM_014479.3 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr21:28211920 G>A maps to NM_006988.3 F671F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr19:8661000 G>A maps to NM_030957.2 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr19:8661063 C>T maps to NM_030957.2 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:8661036 G>A maps to NM_030957.2 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:8670022 G>A maps to NM_030957.2 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:8651588 C>T maps to NM_030957.2 Q752Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:8661989 G>A maps to NM_030957.2 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:8645812 G>A maps to NM_030957.2 F1092F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:8651600 C>T maps to NM_030957.2 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr19:8670019 C>T maps to NM_030957.2 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:8645835 G>A maps to NM_030957.2 Q1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:8668756 G>A maps to NM_030957.2 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr19:8661231 G>A maps to NM_030957.2 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:8651533 G>A maps to NM_030957.2 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr19:8654803 C>T maps to NM_030957.2 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:8654207 C>T maps to NM_030957.2 E692E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr19:8651733 G>A maps to NM_030957.2 F735F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:8665874 C>T maps to NM_030957.2 K249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:8651447 G>A maps to NM_030957.2 I799I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:8654159 G>A maps to NM_030957.2 I708I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:8669950 G>A maps to NM_030957.2 H127H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:8660771 G>A maps to NM_030957.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:8645835 G>A maps to NM_030957.2 Q1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr19:8665928 C>T maps to NM_030957.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:8661986 C>T maps to NM_030957.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:8668756 G>A maps to NM_030957.2 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr19:8651600 C>T maps to NM_030957.2 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr19:8661947 G>A maps to NM_030957.2 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:8656695 G>A maps to NM_030957.2 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:8670541 G>A maps to NM_030957.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr19:8670571 G>A maps to NM_030957.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr5:33527454 C>T maps to NM_030955.2 K1541K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:33576785 C>T maps to NM_030955.2 S1115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr5:33658434 C>T maps to NM_030955.2 K348K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:33576176 G>A maps to NM_030955.2 I1318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:33616043 G>A maps to NM_030955.2 I759I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr5:33751617 G>A maps to NM_030955.2 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:33881472 C>T maps to NM_030955.2 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:33576383 G>A maps to NM_030955.2 L1249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:33576467 G>A maps to NM_030955.2 L1221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:33751617 G>A maps to NM_030955.2 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:33588886 G>A maps to NM_030955.2 C894C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:33561137 C>T maps to NM_030955.2 W1373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A197-06A-32D-A197-08 chr5:33631007 A>G maps to NM_030955.2 C633C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr5:33881304 G>A maps to NM_030955.2 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:33576176 G>A maps to NM_030955.2 I1318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:33881334 G>A maps to NM_030955.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:33891922 G>A maps to NM_030955.2 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:33616127 C>T maps to NM_030955.2 V731V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr9:136320567 C>T maps to NM_139025.3 S1137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr9:136302869 G>A maps to NM_139025.3 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:136320537 T>C maps to NM_139025.3 A1127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr9:136287655 C>T maps to NM_139025.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:136302971 C>T maps to NM_139025.3 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:136320463 C>T maps to NM_139025.3 Q1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr9:136321695 C>T maps to NM_139025.3 T1249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr9:136302908 G>A maps to NM_139025.3 E492E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr9:136307759 C>T maps to NM_139025.3 C710C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr9:136305489 C>T maps to NM_139025.3 V604V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:136305465 G>A maps to NM_139025.3 A596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:136289453 C>T maps to NM_139025.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr9:136314963 C>T maps to NM_139025.3 I974I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:136320417 C>T maps to NM_139025.3 S1087S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:136320691 C>T maps to NM_139025.3 L1179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr10:72468533 C>T maps to NM_139155.2 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:72493730 C>T maps to NM_139155.2 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:72509662 G>A maps to NM_139155.2 L786L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr10:72500918 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr10:72509716 C>T maps to NM_139155.2 P804P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:72509680 G>A maps to NM_139155.2 V792V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:72509737 C>T maps to NM_139155.2 I811I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:72511376 C>T maps to NM_139155.2 A860A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr11:130339293 G>A maps to NM_139055.2 V560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:130343514 C>T maps to NM_139055.2 P884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:130342956 C>T maps to NM_139055.2 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:130332500 C>T maps to NM_139055.2 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:130332675 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr11:130342956 C>T maps to NM_139055.2 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:130342956 C>T maps to NM_139055.2 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:130341140 C>T maps to NM_139055.2 S647S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:130319455 G>A maps to NM_139055.2 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:130318951 C>T maps to NM_139055.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr11:130343085 C>T maps to NM_139055.2 F741F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr11:130319380 C>T maps to NM_139055.2 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:130319506 C>T maps to NM_139055.2 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:130343085 C>T maps to NM_139055.2 F741F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr11:130332554 C>T maps to NM_139055.2 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr5:5191843 G>A maps to NM_139056.2 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr5:5186195 C>T maps to NM_139056.2 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:5242221 G>A maps to NM_139056.2 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44Q-06A-11D-A25O-08 chr5:5182345 C>T maps to NM_139056.2 Q231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:5242224 G>A maps to NM_139056.2 G861G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:5242221 G>A maps to NM_139056.2 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:5186171 C>T maps to NM_139056.2 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:5239923 G>A maps to NM_139056.2 V803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:5190094 G>A maps to NM_139056.2 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:5306726 G>A maps to NM_139056.2 P1099P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr5:5146390 C>T maps to NM_139056.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr5:5191879 C>T maps to NM_139056.2 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr5:5146400 C>T maps to NM_139056.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr5:5209250 G>A maps to NM_139056.2 K499K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr5:5242239 C>T maps to NM_139056.2 P866P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:5235147 C>T maps to NM_139056.2 F624F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr15:100821445 G>A maps to NM_139057.2 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr15:100537691 G>A maps to NM_139057.2 V898V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr15:100537733 C>T maps to NM_139057.2 R884R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr15:100692896 G>A maps to NM_139057.2 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr15:100591906 T>C maps to NM_139057.2 G775G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr16:77317855 G>A maps to NM_199355.2 I1221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr16:77398171 C>T maps to NM_199355.2 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr16:77396149 C>T maps to NM_199355.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr16:77317861 C>T maps to NM_199355.2 R1219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr16:77389946 C>T maps to NM_199355.2 G450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr16:77398162 G>A maps to NM_199355.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:77401557 G>A maps to NM_199355.2 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:77353903 G>A maps to NM_199355.2 R792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:77359785 C>T maps to NM_199355.2 W670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr16:77369750 G>A maps to NM_199355.2 P587P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr16:77387704 C>T maps to NM_199355.2 Q513Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr16:77369678 G>A maps to NM_199355.2 F611F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:77465431 C>T maps to NM_199355.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr16:77468356 A>G maps to NM_199355.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr16:77354997 G>A maps to NM_199355.2 Y755Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:77353841 G>A maps to NM_199355.2 F812F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:77356334 C>T maps to NM_199355.2 K687K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:77359871 G>A maps to NM_199355.2 N641N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:77353910 G>A maps to NM_199355.2 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr16:77323239 G>A maps to NM_199355.2 S1157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr16:77325336 C>T maps to NM_199355.2 E1076E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:77356241 C>T maps to NM_199355.2 G718G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr16:77328903 G>A maps to NM_199355.2 L974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr16:77387752 C>T maps to NM_199355.2 E497E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr16:77353835 G>A maps to NM_199355.2 F814F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:77317853 C>T maps to NM_199355.2 *1222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:77389841 G>A maps to NM_199355.2 F485F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr16:77465338 C>T maps to NM_199355.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr16:77465431 C>T maps to NM_199355.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr16:77401383 G>A maps to NM_199355.2 H244H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr16:77325264 C>T maps to NM_199355.2 K1100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr16:77327116 T>C maps to NM_199355.2 E1015E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:77353841 G>A maps to NM_199355.2 F812F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:77353847 C>T maps to NM_199355.2 G810G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:77389847 C>T maps to NM_199355.2 K483K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:77401431 G>A maps to NM_199355.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr16:77465431 C>T maps to NM_199355.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr16:77387773 C>T maps to NM_199355.2 Q490Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr5:129037263 G>A maps to NM_133638.3 W1040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr5:129037111 C>T maps to NM_133638.3 R990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:128983558 G>A maps to NM_133638.3 G652G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:128862022 G>A maps to NM_133638.3 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:128984508 G>A maps to NM_133638.3 R668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr5:128990051 C>T maps to NM_133638.3 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr5:128983523 C>T maps to NM_133638.3 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:129030500 G>A maps to NM_133638.3 K963K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:128958001 C>T maps to NM_133638.3 I571I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:128990080 T>C maps to NM_133638.3 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:129037188 C>T maps to NM_133638.3 A1015A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:129037189 C>T maps to NM_133638.3 R1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:129072802 C>T maps to NM_133638.3 Y1172Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:129030434 C>T maps to NM_133638.3 S941S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:128956391 G>A maps to NM_133638.3 Q514Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:128864229 G>A maps to NM_133638.3 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr5:178579178 C>T maps to NM_014244.4 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:178552072 G>A maps to NM_014244.4 S953S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr5:178541287 C>T maps to NM_014244.4 R1072R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:178552027 C>T maps to NM_014244.4 R968R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:178580518 G>A maps to NM_014244.4 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr5:178770911 G>A maps to NM_014244.4 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:178559291 C>T maps to NM_014244.4 E743E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:178634555 C>T maps to NM_014244.4 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:178555047 G>A maps to NM_014244.4 V843V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:178555116 G>A maps to NM_014244.4 V820V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:178564818 G>A maps to NM_014244.4 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:178585871 G>A maps to NM_014244.4 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:178541002 G>A maps to NM_014244.4 I1167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr12:43777627 C>T maps to ENST00000389420 G1535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr12:43777752 G>A maps to ENST00000389420 Q1494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr12:43777752 G>A maps to ENST00000389420 Q1494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr12:43944828 C>T maps to ENST00000389420 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr12:43770450 T>G maps to ENST00000389420 S1667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:43822139 C>T maps to ENST00000389420 T1283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:43822169 G>A maps to ENST00000389420 S1273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr12:43822443 C>T maps to ENST00000389420 W1216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:43860459 G>A maps to ENST00000389420 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:43777711 C>T maps to ENST00000389420 Q1507Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:43945673 G>A maps to ENST00000389420 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr12:43833461 G>A maps to ENST00000389420 P852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:43821131 C>T maps to ENST00000389420 W1362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:43895990 C>T maps to ENST00000389420 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr12:43896071 C>T maps to ENST00000389420 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr12:43826507 G>A maps to ENST00000389420 Q943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr12:43777645 G>A maps to ENST00000389420 D1529D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:43771280 G>A maps to ENST00000389420 R1628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:43777405 C>T maps to ENST00000389420 R1584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:43777459 C>T maps to ENST00000389420 V1566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:43822139 C>T maps to ENST00000389420 T1283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:43846451 G>A maps to ENST00000389420 R603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:43862494 T>C maps to ENST00000389420 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:43862508 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr4:73148984 T>G maps to NM_014243.1 S1162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3BZ-06A-12D-A196-08 chr4:73280627 G>A maps to NM_014243.1 Q189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr4:73149254 G>A maps to NM_014243.1 V1072V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:73148897 G>A maps to NM_014243.1 I1191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr4:73175216 T>C maps to NM_014243.1 E692E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:73185050 G>A maps to NM_014243.1 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:73149395 G>A maps to NM_014243.1 S1025S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:161161901 C>T maps to NM_005099.4 G680G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:161166388 C>T maps to NM_005099.4 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:161161967 G>A maps to NM_005099.4 I658I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:161167979 C>T maps to NM_005099.4 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:161166021 C>T maps to NM_005099.4 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:161166529 G>A maps to NM_005099.4 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr21:28338242 G>A maps to NM_007038.3 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr21:28327190 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr21:28338410 C>T maps to NM_007038.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr21:28338311 C>T maps to NM_007038.3 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr21:28296629 G>A maps to NM_007038.3 V845V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr21:28337648 G>A maps to NM_007038.3 D354D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr21:28296914 C>T maps to NM_007038.3 R750R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr21:28296686 C>T maps to NM_007038.3 T826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:28305320 G>A maps to NM_007038.3 Q578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:64766844 G>A maps to NM_197941.2 D74D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr5:64625227 G>A maps to NM_197941.2 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:64595870 C>T maps to NM_197941.2 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:64747381 G>A maps to NM_197941.2 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr5:64748620 C>T maps to NM_197941.2 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:64595810 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:64748575 G>A maps to NM_197941.2 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:64769443 C>T maps to NM_197941.2 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr5:64747411 G>A maps to NM_197941.2 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr5:64748638 C>T maps to NM_197941.2 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr15:79056046 C>T maps to ENST00000258883 W1581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr15:79059039 A>G maps to ENST00000258883 N1071N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr15:79083115 G>A maps to ENST00000258883 H308H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr15:79069869 C>T maps to ENST00000258883 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr15:79083523 G>A maps to ENST00000258883 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr15:79056995 G>A maps to ENST00000258883 S1443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr15:79080694 T>G maps to ENST00000258883 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:79058732 G>A maps to ENST00000258883 L1174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr15:79064127 G>A maps to ENST00000258883 I725I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:79058664 G>A maps to ENST00000258883 F1196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr15:79064055 G>A maps to ENST00000258883 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:79064032 C>T maps to ENST00000258883 W757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr15:79092797 G>A maps to ENST00000258883 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr15:79059078 C>G maps to ENST00000258883 V1058V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr15:79059039 A>G maps to ENST00000258883 N1071N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr15:79059831 C>T maps to ENST00000258883 Q916Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:79051843 G>A maps to ENST00000258883 I1663I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:79058001 C>T maps to ENST00000258883 A1417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:79059006 C>T maps to ENST00000258883 E1082E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:79066541 G>A maps to ENST00000258883 A659A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:79067089 G>A maps to ENST00000258883 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:79092620 G>A maps to ENST00000258883 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr15:79058877 C>T maps to ENST00000258883 L1125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr15:79058877 C>A maps to ENST00000258883 L1125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr15:79064070 C>G maps to ENST00000258883 P744P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:130284446 C>T maps to NM_007037.4 E515E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:130288956 G>A maps to NM_007037.4 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:130289091 G>A maps to NM_007037.4 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr11:130275830 C>T maps to NM_007037.4 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:130278668 C>T maps to NM_007037.4 E639E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:130275641 G>A maps to NM_007037.4 I827I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:130275704 G>A maps to NM_007037.4 F806F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:130289091 G>A maps to NM_007037.4 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:130275788 G>A maps to NM_007037.4 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:130281489 C>T maps to NM_007037.4 V524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:130286133 G>A maps to NM_007037.4 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:130286859 C>T maps to NM_007037.4 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr11:130275728 G>A maps to NM_007037.4 F798F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr3:64536711 G>A maps to NM_182920.1 S1575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:64532453 T>G maps to NM_182920.1 R1682R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:64601032 G>A maps to NM_182920.1 F1051F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:64666918 G>A maps to NM_182920.1 Q213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:64627542 G>A maps to NM_182920.1 R613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:64589968 G>A maps to NM_182920.1 A1171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:64527204 C>T maps to NM_182920.1 L1763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:64582640 G>A maps to NM_182920.1 S1348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:64619150 G>A maps to NM_182920.1 C724C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr3:64601032 G>A maps to NM_182920.1 F1051F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:64527201 C>T maps to NM_182920.1 K1764K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr3:64532454 C>T maps to NM_182920.1 W1681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr9:18657707 G>A maps to NM_001040272.4 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:18889746 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:18770619 G>A maps to NM_001040272.4 G746G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:18707035 C>A maps to NM_001040272.4 S622S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:18888041 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr9:18753298 G>A maps to NM_001040272.4 W670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:18504888 G>A maps to NM_001040272.4 W42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr9:18892395 G>A maps to NM_001040272.4 V1551V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr9:18721636 C>T maps to NM_001040272.4 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr9:18657719 C>T maps to NM_001040272.4 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr9:18777007 C>T maps to NM_001040272.4 A927A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr9:18680361 C>T maps to NM_001040272.4 Q397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:18777259 G>A maps to NM_001040272.4 R1011R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:18657707 G>A maps to NM_001040272.4 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:18657713 G>A maps to NM_001040272.4 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:18770673 C>T maps to NM_001040272.4 F764F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:18777013 C>T maps to NM_001040272.4 F929F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:18829901 G>A maps to NM_001040272.4 P1392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:18889627 C>T maps to NM_001040272.4 Q1509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:18892398 C>T maps to NM_001040272.4 T1552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:136402602 G>A maps to ENST00000393061 W165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr9:136402627 G>A maps to ENST00000393061 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:136401899 G>A maps to ENST00000393061 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr15:84611350 G>A maps to NM_207517.2 W707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr15:84705530 C>T maps to NM_207517.2 T1587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr15:84651196 C>T maps to NM_207517.2 F939F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr15:84690342 G>A maps to NM_207517.2 A1485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr15:84553893 C>T maps to NM_207517.2 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr15:84582050 C>T maps to NM_207517.2 I636I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr15:84553917 G>A maps to NM_207517.2 Q342Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr15:84561640 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr15:84651196 C>T maps to NM_207517.2 F939F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr15:84581952 C>T maps to NM_207517.2 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:84561588 A>G maps to NM_207517.2 Q472Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr15:84690204 C>T maps to NM_207517.2 T1439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:84651028 C>T maps to NM_207517.2 I883I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:84694115 C>T maps to NM_207517.2 A1528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:84611434 G>A maps to NM_207517.2 E735E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:84651512 C>T maps to NM_207517.2 L1045L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr15:84373226 G>A maps to NM_207517.2 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:84553915 C>T maps to NM_207517.2 Q342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:84690160 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:84700163 C>T maps to NM_207517.2 S1578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr15:84582035 C>T maps to NM_207517.2 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:84639262 C>T maps to NM_207517.2 Q840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr15:84561483 G>A maps to NM_207517.2 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:150531496 G>A maps to ENST00000369039 G896G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:150526423 G>A maps to ENST00000369039 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:150525072 G>A maps to ENST00000369039 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:150526210 C>T maps to ENST00000369039 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr1:150525994 G>A maps to ENST00000369039 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:150528642 C>T maps to ENST00000369039 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:150525645 G>A maps to ENST00000369039 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr1:150527965 T>C maps to ENST00000369039 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:150525594 G>A maps to ENST00000369039 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:1507246 G>A maps to NM_213604.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:1507327 G>A maps to NM_213604.2 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:1506655 G>A maps to NM_213604.2 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr7:939097 G>A maps to NM_006869.2 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:938709 C>T maps to NM_006869.2 Q352Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:938748 C>T maps to NM_006869.2 E339E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:959656 C>T maps to NM_006869.2 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr17:29272070 G>A maps to ENST00000394782 K225K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr17:29283284 T>C maps to ENST00000394782 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:29283461 C>T maps to ENST00000394782 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr17:29261252 C>T maps to ENST00000394782 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr17:29283297 G>T maps to ENST00000394782 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr17:29283434 G>A maps to ENST00000394782 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:29280325 G>A maps to ENST00000394782 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr1:154557720 G>A maps to ENST00000292205 L1182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr1:154569429 G>A maps to ENST00000292205 S750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:154557500 G>A maps to ENST00000292205 S1197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:154573932 G>C maps to ENST00000292205 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:154570413 G>A maps to ENST00000292205 S651S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:154574583 G>A maps to ENST00000292205 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:154558738 G>A maps to ENST00000292205 I1083I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr1:154558738 G>A maps to ENST00000292205 I1083I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr1:154574655 C>T maps to ENST00000292205 K197K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:154574526 G>A maps to ENST00000292205 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr21:46624511 C>T maps to NM_015833.3 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr21:46596522 C>T maps to NM_015833.3 Q303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:1284255 C>G maps to NM_018702.2 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:1279771 G>A maps to NM_018702.2 D459D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:1405873 G>A maps to NM_018702.2 Y142Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr10:1313243 G>A maps to NM_018702.2 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr10:1406044 G>A maps to NM_018702.2 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr10:1284222 G>A maps to NM_018702.2 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr10:1405831 G>A maps to NM_018702.2 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:1313162 G>A maps to NM_018702.2 I393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr10:1262910 G>A maps to NM_018702.2 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:1230950 C>T maps to NM_018702.2 P631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:1279753 G>A maps to NM_018702.2 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr16:75646171 G>A maps to NM_012091.3 Q338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr16:75646172 G>A maps to NM_012091.3 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr16:75651151 G>A maps to NM_012091.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:1912831 C>T maps to NM_138422.1 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:33583598 C>T maps to ENST00000373441 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:33583690 C>T maps to ENST00000373441 I426I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr1:33583705 C>T maps to ENST00000373441 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:33562306 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:33558918 C>T maps to ENST00000373441 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:78399580 C>T maps to NM_020421.3 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:78365483 G>A maps to NM_020421.3 E208E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:78353447 C>T maps to NM_020421.3 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:78390840 C>T maps to NM_020421.3 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:78365595 T>C maps to NM_020421.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr14:78374166 C>T maps to NM_020421.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr7:140374463 G>A maps to NM_052853.3 K329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr7:140389515 C>T maps to NM_052853.3 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr19:41220504 C>T maps to NM_024876.3 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:41208506 G>A maps to NM_024876.3 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:41208577 G>A maps to NM_024876.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:41209631 G>A maps to NM_024876.3 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:41211271 G>A maps to NM_024876.3 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr7:45614654 C>T maps to NM_021116.2 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr7:45717848 C>T maps to NM_021116.2 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr7:45743039 C>T maps to NM_021116.2 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:45750247 C>T maps to NM_021116.2 I1018I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:45753423 C>T maps to NM_021116.2 Q1064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:45725733 C>T maps to NM_021116.2 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:45743272 C>T maps to NM_021116.2 I882I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr7:45717818 C>T maps to NM_021116.2 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:45650039 G>A maps to NM_021116.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr7:45744163 C>T maps to NM_021116.2 I922I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr7:45726196 C>T maps to NM_021116.2 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr7:45662342 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:45724597 G>A maps to NM_021116.2 T668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:45632474 C>T maps to NM_021116.2 R253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:45743206 C>T maps to NM_021116.2 Y860Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:45725583 G>A maps to NM_021116.2 W699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr7:45717628 C>T maps to NM_021116.2 T589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:45719388 C>T maps to NM_021116.2 V660V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:45725689 C>T maps to NM_021116.2 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:167792323 C>A maps to NM_018417.4 E1364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:167779005 C>T maps to NM_018417.4 W1581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:167830153 C>T maps to NM_018417.4 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:167870999 C>T maps to NM_018417.4 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr1:167839634 C>T maps to NM_018417.4 E492E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:167825449 C>T maps to NM_018417.4 K708K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:167802364 C>T maps to NM_018417.4 K1151K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:167825659 C>T maps to NM_018417.4 R638R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:167802295 G>A maps to NM_018417.4 L1174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:167798660 C>T maps to NM_018417.4 G1198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:167793931 G>A maps to NM_018417.4 F1304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:167865908 G>A maps to NM_018417.4 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:167798661 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:167849778 C>T maps to NM_018417.4 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:167793961 G>A maps to NM_018417.4 I1294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:167852752 G>A maps to NM_018417.4 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:167852751 G>A maps to NM_018417.4 Q315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr1:167852767 C>T maps to NM_018417.4 E309E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:167779025 C>T maps to NM_018417.4 T1574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:167805627 C>T maps to NM_018417.4 L1076L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:167802337 G>A maps to NM_018417.4 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:167814978 C>T maps to NM_018417.4 K943K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:167815250 G>A maps to NM_018417.4 S896S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr1:167794009 G>A maps to NM_018417.4 A1278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:167793727 G>A maps to NM_018417.4 L1346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr5:7414757 C>T maps to NM_020546.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:7817040 G>T maps to NM_020546.2 G982G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:7626296 C>T maps to NM_020546.2 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZG-06A-11D-A197-08 chr5:7789861 G>A maps to NM_020546.2 V859V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr2:25062746 G>A maps to NM_004036.3 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr2:25057784 G>A maps to NM_004036.3 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:25141757 G>A maps to NM_004036.3 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:25064517 G>A maps to NM_004036.3 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:25141244 G>A maps to NM_004036.3 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:25141685 G>A maps to NM_004036.3 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:25141595 G>A maps to NM_004036.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr2:25059845 G>A maps to NM_004036.3 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:25141451 G>A maps to NM_004036.3 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr2:25057469 G>A maps to NM_004036.3 D617D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr14:24800430 C>T maps to NM_139247.3 K267K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr14:24799091 G>A maps to NM_139247.3 N397N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:24793405 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr14:24799471 C>G maps to NM_139247.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr14:24803708 G>A maps to NM_139247.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr14:24787741 G>A maps to NM_139247.3 S1038S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:24791886 C>T maps to NM_139247.3 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:24798269 G>A maps to NM_139247.3 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr14:24787874 G>A maps to NM_139247.3 V1022V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:24789025 G>A maps to NM_139247.3 F885F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:24789025 G>A maps to NM_139247.3 F885F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:24794629 G>A maps to NM_139247.3 F592F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr14:24793395 G>A maps to NM_139247.3 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr3:123009974 G>A maps to NM_183357.2 I1104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr3:123014939 C>T maps to NM_183357.2 W1018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:123044255 G>A maps to NM_183357.2 I667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:123044258 G>A maps to NM_183357.2 S666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr3:123010055 G>A maps to NM_183357.2 I1077I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:123014945 G>A maps to NM_183357.2 F1016F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:123071316 G>A maps to NM_183357.2 Q416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:123014942 G>A maps to NM_183357.2 L1017L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:123023024 G>A maps to NM_183357.2 F816F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:123071389 G>A maps to NM_183357.2 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:123019093 G>A maps to NM_183357.2 L925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:123044288 G>A maps to NM_183357.2 I656I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr3:123023024 G>A maps to NM_183357.2 F816F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:123019001 G>A maps to NM_183357.2 F955F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:123019088 C>T maps to NM_183357.2 Q926Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:123022952 G>A maps to NM_183357.2 F840F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:123046464 C>T maps to NM_183357.2 R649R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:123046500 G>A maps to NM_183357.2 I637I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:123022946 G>A maps to NM_183357.2 I842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr12:49168220 G>A maps to NM_015270.3 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:49169184 G>A maps to NM_015270.3 F627F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:49169832 C>T maps to NM_015270.3 R573R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr12:49165663 G>A maps to NM_015270.3 F960F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:49162478 C>T maps to NM_015270.3 Q1134Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:49177037 G>A maps to NM_015270.3 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr12:49164629 G>A maps to NM_015270.3 L1059L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:49166089 G>A maps to NM_015270.3 L925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:49176533 G>A maps to NM_015270.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:49176653 G>A maps to NM_015270.3 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr16:50324450 C>T maps to NM_001114.3 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr16:50326618 G>A maps to NM_001114.3 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:50345623 G>A maps to NM_001114.3 W792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr16:50325717 C>T maps to NM_001114.3 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:50339720 C>T maps to NM_001114.3 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr16:50339412 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr16:50346814 G>A maps to NM_001114.3 Q873Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:50326720 C>T maps to NM_001114.3 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr16:50338389 C>T maps to NM_001114.3 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr16:50342696 C>T maps to NM_001114.3 I685I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr16:50335085 G>A maps to NM_001114.3 K443K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:50325657 C>T maps to NM_001114.3 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:50339720 C>T maps to NM_001114.3 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:50324450 C>T maps to NM_001114.3 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:50325801 G>A maps to NM_001114.3 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr8:131880138 G>A maps to NM_001115.2 I721I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr8:132052057 G>A maps to NM_001115.2 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3BZ-06A-12D-A196-08 chr8:131916182 G>A maps to NM_001115.2 I582I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr8:132051664 G>A maps to NM_001115.2 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr8:131916172 A>G maps to NM_001115.2 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr8:131949410 G>A maps to NM_001115.2 D463D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr8:131916173 G>A maps to NM_001115.2 Y585Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr8:131848632 G>A maps to NM_001115.2 S855S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr8:132051894 G>A maps to NM_001115.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:131861859 G>T maps to NM_001115.2 A800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:131880120 C>T maps to NM_001115.2 T727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:131812782 C>T maps to NM_001115.2 V983V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:131880138 G>A maps to NM_001115.2 I721I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr8:131859669 C>T maps to NM_001115.2 E834E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr8:131916125 G>A maps to NM_001115.2 I601I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:131826338 G>A maps to NM_001115.2 F963F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:132002650 C>T maps to NM_001115.2 E366E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:131955650 C>T maps to NM_001115.2 Q433Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr8:131922024 C>T maps to NM_001115.2 R523R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:131812689 G>A maps to NM_001115.2 I1014I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:131861883 G>A maps to NM_001115.2 S792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:131916125 G>A maps to NM_001115.2 I601I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:131848647 G>A maps to NM_001115.2 F850F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr8:131833659 G>A maps to NM_001115.2 F894F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr8:131916125 G>A maps to NM_001115.2 I601I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:131916182 G>A maps to NM_001115.2 I582I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr8:131861868 G>A maps to NM_001115.2 F797F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr8:132051910 C>T maps to NM_001115.2 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:131848632 G>A maps to NM_001115.2 S855S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr8:131812689 G>A maps to NM_001115.2 I1014I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:131880123 G>A maps to NM_001115.2 I726I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:131916161 C>T maps to NM_001115.2 Q589Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:132051922 G>A maps to NM_001115.2 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:131922024 C>T maps to NM_001115.2 R523R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:131949418 G>A maps to NM_001115.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:131922057 G>A maps to NM_001115.2 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:131861929 C>T maps to NM_001115.2 W777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:131964148 G>A maps to NM_001115.2 F402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr8:131916287 C>T maps to NM_001115.2 G547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr8:131848647 G>A maps to NM_001115.2 F850F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:131916287 C>T maps to NM_001115.2 G547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr8:131792713 G>A maps to NM_001115.2 N1226N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr8:131916200 G>A maps to NM_001115.2 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:131880138 G>A maps to NM_001115.2 I721I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr8:131861868 G>A maps to NM_001115.2 F797F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr8:131964220 G>A maps to NM_001115.2 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr8:132051984 G>A maps to NM_001115.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr8:131896896 G>A maps to NM_001115.2 T674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:131792973 G>A maps to NM_001115.2 L1140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:131792974 G>A maps to NM_001115.2 I1139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:131859668 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:131916026 C>T maps to NM_001115.2 G634G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:131792926 C>T maps to NM_001115.2 V1155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr8:131848647 G>A maps to NM_001115.2 F850F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr8:131955665 C>T maps to NM_001115.2 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:4042325 G>A maps to NM_001116.3 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr16:4016962 C>A maps to NM_001116.3 E959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:4016885 G>A maps to NM_001116.3 L984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:4027628 G>A maps to NM_001116.3 F894F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr16:4016396 G>A maps to NM_001116.3 R1147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr16:4043499 C>T maps to NM_001116.3 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr16:4164546 G>A maps to NM_001116.3 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr18:908328 G>A maps to NM_001117.3 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:905491 G>A maps to NM_001117.3 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr18:905425 C>T maps to NM_001117.3 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:909581 G>A maps to NM_001117.3 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:31146150 G>A maps to ENST00000409489 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr7:31124434 C>T maps to ENST00000409489 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:31124434 C>T maps to ENST00000409489 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:31123825 C>T maps to ENST00000409489 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:31102931 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:31117621 G>A maps to ENST00000409489 W58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:31121355 C>T maps to ENST00000409489 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:31125011 G>A maps to ENST00000409489 W208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:31120234 G>A maps to ENST00000409489 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:31142940 G>A maps to ENST00000409489 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:31124404 C>T maps to ENST00000409489 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr7:31146120 G>A maps to ENST00000409489 E466E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:31124948 C>T maps to ENST00000409489 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:31146147 G>A maps to ENST00000409489 K475K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr7:31124987 G>A maps to ENST00000409489 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr4:2927834 G>A maps to NM_014189.2 E650E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr4:2899945 C>T maps to NM_014189.2 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:2877716 C>T maps to NM_014189.2 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr4:2900017 A>G maps to NM_014189.2 K283K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr4:2896427 C>T maps to NM_014189.2 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:70919564 G>A maps to NM_001185054.1 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr2:70890594 G>A maps to NM_001185054.1 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr2:70900423 C>G maps to NM_017488.3 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:70931468 G>A maps to NM_001185054.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:70922897 G>A maps to NM_001185054.1 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:70917917 C>T maps to NM_001185054.1 K283K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:70906009 C>T maps to NM_001185054.1 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr2:70933405 G>A maps to NM_001185054.1 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:70923463 C>T maps to NM_001185054.1 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:70931507 C>T maps to NM_001185054.1 Q89Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr2:70933561 C>T maps to NM_001185055.1 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:70933561 C>T maps to NM_001185055.1 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:70903897 C>T maps to NM_001185055.1 G557G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:70922897 G>A maps to NM_001185054.1 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:70931582 C>T maps to NM_001185054.1 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr2:70923505 G>A maps to NM_001185054.1 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:70890625 C>T maps to NM_001185054.1 K704K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:70917959 G>A maps to NM_001185054.1 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:70933492 C>T maps to NM_001185054.1 Q16Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:111879042 C>T maps to NM_016824.3 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr10:111886189 C>T maps to NM_016824.3 R513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:111881986 C>T maps to NM_016824.3 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:111872536 C>T maps to NM_016824.3 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr10:111890218 C>T maps to NM_016824.3 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr4:100201388 G>A maps to NM_000667.3 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr4:100205880 C>T maps to NM_000667.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:100201356 G>T maps to NM_000667.3 S303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr4:100203745 G>A maps to NM_000667.3 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr4:100201319 C>T maps to NM_000667.3 W315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr4:100235016 C>T maps to NM_000668.4 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr4:100237183 G>A maps to NM_000668.4 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:100232726 G>A maps to NM_000668.4 N305N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr4:100231926 C>T maps to NM_000668.4 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:100231941 G>A maps to NM_000668.4 D361D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:100232052 C>T maps to NM_000668.4 K324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr4:100237234 C>T maps to NM_000668.4 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:100231989 C>T maps to NM_000668.4 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:100229017 G>T maps to NM_000668.4 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr4:100237177 G>A maps to NM_000668.4 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:100231926 C>T maps to NM_000668.4 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr4:100257909 C>T maps to NM_000669.3 *376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:100260828 A>G maps to NM_000669.3 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:100261798 G>A maps to NM_000669.3 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr4:100264167 G>A maps to NM_000669.3 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:100268229 C>T maps to NM_000669.3 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:100266093 G>A maps to NM_000669.3 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr4:100266219 C>T maps to NM_000669.3 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:100268181 C>T maps to NM_000669.3 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:100261750 C>T maps to NM_000669.3 W315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr4:100264206 G>A maps to NM_000669.3 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr4:100062755 G>A maps to ENST00000505590 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:100057637 C>T maps to ENST00000505590 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:100131639 G>A maps to NM_001102470.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr4:100131306 G>A maps to NM_001102470.1 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:100125386 G>A maps to NM_001102470.1 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:100129950 C>T maps to NM_001102470.1 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:100134802 G>A maps to NM_001102470.1 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr4:100134847 C>T maps to NM_001102470.1 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:100125396 G>A maps to NM_001102470.1 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:100349302 T>A maps to NM_000673.4 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:100341728 C>T maps to NM_000673.4 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:100341926 G>A maps to NM_000673.4 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr4:100349082 G>C maps to NM_000673.4 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:100349073 G>A maps to NM_000673.4 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr4:100349709 C>T maps to NM_000673.4 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr4:100341901 G>A maps to NM_000673.4 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr8:67372615 C>T maps to NM_144650.2 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:3504689 G>A maps to NM_018269.3 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:37214708 G>A maps to ENST00000416116 W35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:186572003 A>G maps to NM_004797.3 E82E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr3:186571029 C>T maps to NM_004797.3 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr3:186572327 G>A maps to NM_004797.3 Q190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr1:202915609 G>A maps to NM_015999.3 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:202911227 C>T maps to NM_015999.3 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr1:202915669 A>G maps to NM_015999.3 Y109Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:202911290 G>A maps to NM_015999.3 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr12:1893217 C>T maps to NM_024551.2 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:76154056 C>T maps to NM_006721.2 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:75960563 C>T maps to NM_006721.2 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr10:76468124 C>T maps to NM_006721.2 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr20:49509855 G>A maps to NM_181442.1 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:49509501 G>A maps to NM_181442.1 A583A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U9-06A-11D-A32N-08 chr20:49510899 G>A maps to NM_181442.1 D117D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr18:77895149 C>T maps to NM_014913.3 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr18:77895176 C>T maps to NM_014913.3 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr18:77895752 C>T maps to NM_014913.3 L819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr18:77894693 C>T maps to NM_014913.3 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr18:77896376 G>A maps to NM_014913.3 E1027E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:77896091 C>T maps to NM_014913.3 A932A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr1:203134703 C>T maps to NM_001048230.1 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:203134733 G>A maps to NM_001048230.1 E229E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr1:203134667 C>T maps to NM_001048230.1 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:203134559 C>T maps to NM_001048230.1 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:203134667 C>T maps to NM_001048230.1 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:203134931 C>T maps to NM_001048230.1 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr22:24837102 C>T maps to NM_000675.4 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr22:24836821 C>T maps to NM_000675.4 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:24837186 C>T maps to NM_000675.4 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:112043111 G>A maps to NM_000677.3 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:112031413 C>T maps to NM_020683.6 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:112043144 C>T maps to NM_000677.3 W128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:112106514 C>T maps to NM_001081976.1 W20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:112106515 C>T maps to NM_001081976.1 W20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:112031473 G>A maps to NM_020683.6 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:112043111 G>A maps to NM_000677.3 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:112042913 C>T maps to NM_000677.3 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:112045865 G>A maps to NM_020683.6 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:112031392 G>A maps to NM_020683.6 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:112033352 G>A maps to NM_020683.6 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:112042688 G>A maps to NM_000677.3 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:112042661 G>A maps to NM_000677.3 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:112043096 G>A maps to NM_000677.3 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:112028386 C>T maps to NM_020683.6 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:112026335 C>T maps to NM_020683.6 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:73052766 G>A maps to NM_031284.4 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr3:119306412 G>A maps to NM_001125.2 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:119306718 C>T maps to NM_001125.2 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr3:119301093 C>T maps to NM_001125.2 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:119301086 G>A maps to NM_001125.2 W24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:119305141 G>A maps to NM_001125.2 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr13:114107680 C>T maps to NM_138430.3 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr13:114083341 G>A maps to NM_138430.3 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr13:114098848 G>A maps to NM_138430.3 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr13:114107563 G>T maps to NM_138430.3 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:114107625 G>A maps to NM_138430.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr13:114098848 G>A maps to NM_138430.3 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:36557677 C>T maps to NM_017825.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:36558947 C>T maps to NM_017825.2 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:36557638 C>T maps to NM_017825.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:26722228 G>A maps to ENST00000356368 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr8:26722291 G>A maps to ENST00000356368 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:26627875 C>T maps to ENST00000356368 W397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:26628094 G>A maps to ENST00000356368 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr8:26623609 C>T maps to NM_033304.2 V442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr8:26627905 C>T maps to ENST00000356368 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr20:4228548 G>A maps to NM_000678.3 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:4228965 C>T maps to NM_000678.3 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:4229250 G>A maps to NM_000678.3 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:112838179 C>A maps to NM_000681.3 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:112838959 G>A maps to NM_000681.3 W402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr10:112838011 C>T maps to NM_000681.3 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr10:112838509 C>T maps to NM_000681.3 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr2:96781234 G>A maps to NM_000682.5 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr2:96780586 G>A maps to NM_000682.5 F434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:96781378 G>T maps to NM_000682.5 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr4:3769664 C>T maps to NM_000683.3 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr4:3769529 C>T maps to NM_000683.3 F399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:115804544 C>T maps to NM_000684.2 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:115804616 C>T maps to NM_000684.2 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr5:148207176 T>C maps to NM_000024.5 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:148207008 C>T maps to NM_000024.5 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr5:148207302 C>T maps to NM_000024.5 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:148207536 C>T maps to NM_000024.5 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr11:67049401 C>T maps to NM_001619.3 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr11:67050672 C>T maps to NM_001619.3 N434N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:67047158 G>A maps to NM_001619.3 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr11:67047098 C>T maps to NM_001619.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr22:26100116 C>T maps to NM_005160.3 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr22:26110409 C>T maps to NM_005160.3 F509F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr22:25961063 G>A maps to NM_005160.3 K19K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr20:60883137 C>T maps to NM_175573.1 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr20:60883138 C>T maps to NM_175573.1 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr20:60882795 C>T maps to NM_175573.1 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr22:40757275 G>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:40759029 G>A maps to NM_000026.2 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:40746002 C>T maps to ENST00000428371 H534H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:244583514 G>A maps to NM_001126.3 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:244601070 C>A did not map to a codon.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr14:105201409 C>T maps to NM_199165.1 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr14:105212675 G>A maps to NM_199165.1 Q468Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr14:105212582 G>A maps to NM_199165.1 E437E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:105207211 C>T maps to NM_199165.1 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr14:105205671 G>A maps to NM_199165.1 K165K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr7:44152206 C>T maps to NM_001129.3 F756F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr7:44151191 C>T maps to NM_001129.3 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:44146424 C>T maps to NM_001129.3 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:44151643 C>T maps to NM_001129.3 Q678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:89172530 C>T maps to NM_022767.3 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr15:89169880 C>T maps to NM_022767.3 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:3055715 G>A maps to NM_198969.1 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr4:7780516 G>A maps to NM_001134647.1 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:7787986 G>A maps to NM_001134647.1 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr4:7774672 C>T maps to NM_001134647.1 K709K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:7820862 G>A maps to NM_001134647.1 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:7844897 A>G maps to NM_001134647.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:7802240 G>A maps to NM_001134647.1 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:7811413 G>A maps to NM_001134647.1 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr4:7811422 G>A maps to NM_001134647.1 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr4:7774576 G>A maps to NM_001134647.1 I741I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:148715266 G>A maps to NM_152406.2 R755R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr10:116075333 C>T maps to NM_001001936.1 K199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:116067596 G>A maps to NM_001001936.1 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:116067597 T>A maps to NM_001001936.1 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr10:116075420 G>A maps to NM_001001936.1 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:116100455 G>A maps to NM_001001936.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:116055827 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:116073722 C>T maps to NM_001001936.1 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:116073767 C>T maps to NM_001001936.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr4:88052236 G>A maps to NM_001166693.1 T989T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:88055745 C>T maps to NM_001166693.1 T1145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:88035908 C>T maps to NM_001166693.1 R642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:88047466 C>T maps to NM_001166693.1 S930S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr4:88036096 C>T maps to NM_001166693.1 T704T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:88036195 C>T maps to NM_001166693.1 V737V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr23:148039954 C>A did not map to a codon.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr23:148044318 A>C did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:148037321 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:148037567 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:148038101 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:148037296 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:147743679 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:148044307 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:147733595 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:148068949 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:148037718 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:148044400 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:148069077 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr23:148038126 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:148037774 C>G did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:148038031 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr23:147985780 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr23:148037974 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:148037327 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:148037354 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:148062316 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:147744124 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:148037296 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:148037296 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:147743490 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:147743485 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr23:148068950 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:147744024 A>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:148044271 A>C did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:148037455 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:148059940 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:147743899 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:147985773 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:148037912 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:148055130 T>A did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:148037938 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:147967478 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:148044409 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:148055078 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:147743593 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:148037390 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:148072754 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr2:100199259 C>T maps to NM_001025108.1 T956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:100623279 C>T maps to NM_001025108.1 Q254Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:100210307 G>A maps to NM_001025108.1 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:100171179 G>A maps to NM_001025108.1 A1125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:100210136 G>A maps to NM_001025108.1 S687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:100623239 G>A maps to NM_001025108.1 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:100210262 G>A maps to NM_001025108.1 V645V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:100210148 G>A maps to NM_001025108.1 I683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr2:100199406 G>A maps to NM_001025108.1 P907P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:100210235 G>A maps to NM_001025108.1 P654P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:100210313 G>A maps to NM_001025108.1 H628H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr2:100623721 G>A maps to NM_001025108.1 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr2:100623279 C>T maps to NM_001025108.1 Q254Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:100199319 G>A maps to NM_001025108.1 A936A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr2:100623685 G>A maps to NM_001025108.1 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:100167980 G>A maps to NM_001025108.1 S1237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:100210085 G>A maps to NM_001025108.1 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:100623363 G>A maps to NM_001025108.1 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:100623646 C>T maps to NM_001025108.1 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr2:100209872 C>T maps to NM_001025108.1 R775R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:132269997 G>A maps to NM_014423.3 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:132227972 G>A maps to NM_014423.3 S840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr5:132270134 G>A maps to NM_014423.3 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr5:132270561 G>A maps to NM_014423.3 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:12356713 G>A maps to NM_006796.2 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr18:12367017 G>A maps to NM_006796.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A6L9-06A-11D-A32N-08 chr4:74364893 C>T maps to NM_001133.2 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:74352807 C>T maps to NM_001133.2 Q203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:74354355 G>A maps to NM_001133.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:74352707 G>A maps to NM_001133.2 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:74367530 G>A maps to NM_001133.2 K558K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr4:74354466 C>T maps to NM_001133.2 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:74354373 C>T maps to NM_001133.2 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:74365887 C>T maps to NM_001133.2 T530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr4:74347560 C>T maps to NM_001133.2 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:76202101 C>T maps to NM_001145526.1 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr17:76201791 C>T maps to NM_001145526.1 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:76201791 C>T maps to NM_001145526.1 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:76201791 C>T maps to NM_001145526.1 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr4:74315123 C>T maps to NM_001134.1 Y377Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr4:74315124 C>T maps to NM_001134.1 Q378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr4:74309108 C>T maps to NM_001134.1 Q221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr4:74318309 C>T maps to NM_001134.1 Q541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:74318254 C>T maps to NM_001134.1 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:74310739 C>T maps to NM_001134.1 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr4:74310727 T>C maps to NM_001134.1 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr2:64779312 C>T maps to ENST00000422803 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:64794824 A>C maps to ENST00000422803 R689R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:64819117 C>T maps to ENST00000422803 F921F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:236877163 C>T maps to NM_001037131.1 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A6L9-06A-11D-A32N-08 chr2:236708162 C>T maps to NM_001037131.1 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:236957794 C>T maps to NM_001037131.1 R662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:237032729 G>A maps to NM_001037131.1 R846R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:236817380 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:237028856 C>T maps to NM_001037131.1 I712I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:237028967 C>A maps to NM_001037131.1 I749I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:237028968 C>T maps to NM_001037131.1 L750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr2:237029027 C>T maps to NM_001037131.1 G769G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:236949459 C>T maps to NM_001037131.1 S622S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr10:88768278 C>T maps to NM_133447.1 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:88769256 G>A maps to NM_133447.1 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:88769433 C>T maps to NM_133447.1 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr10:88768936 C>T maps to NM_133447.1 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:88769010 C>T maps to NM_133447.1 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:88769358 C>T maps to NM_133447.1 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:88769358 C>T maps to NM_133447.1 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:88769433 C>T maps to NM_133447.1 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:88769040 G>A maps to NM_133447.1 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr10:88769289 G>A maps to NM_133447.1 K427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:88769256 G>A maps to NM_133447.1 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr10:88767441 T>C maps to NM_133447.1 D27D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:58135833 G>A maps to NM_014770.2 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:58129185 C>T maps to NM_001122772.1 W398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr7:150814261 C>T maps to NM_031946.4 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:150835374 C>T maps to NM_031946.4 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:150835375 C>T maps to NM_031946.4 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:150814530 C>T maps to NM_031946.4 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150835335 C>T maps to NM_031946.4 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr10:51769426 C>T maps to NM_001077665.2 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:51751482 C>T maps to NM_001077665.2 Q114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr10:51472634 G>A maps to ENST00000416142 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr10:51464850 G>A maps to ENST00000416142 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr10:51465642 C>T maps to ENST00000416142 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:51464850 G>A maps to ENST00000416142 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:51465495 C>T maps to ENST00000416142 K343K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr10:51464850 G>A maps to ENST00000416142 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:51465312 C>T maps to ENST00000416142 K404K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:51472604 T>A maps to ENST00000416142 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr15:86801225 G>A maps to NM_152336.2 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr15:86697659 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr15:86807790 G>A maps to NM_152336.2 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:87089342 C>T maps to NM_152336.2 I886I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr15:86809610 G>A maps to NM_152336.2 R512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr15:86807804 G>A maps to NM_152336.2 W422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr15:86686987 G>A maps to NM_152336.2 Q12Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr15:87531226 A>G maps to NM_152336.2 S1031S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr15:86687044 C>T maps to NM_152336.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr15:86807733 C>T maps to NM_152336.2 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr15:86790960 C>T maps to NM_152336.2 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr15:87531289 C>T maps to NM_152336.2 F1052F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:86697679 G>A maps to NM_152336.2 K48K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:86697751 C>T maps to NM_152336.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:86813152 C>T maps to NM_152336.2 F568F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:86940711 C>T maps to NM_152336.2 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr11:47684586 C>T maps to ENST00000357610 G844G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:47701581 G>A maps to ENST00000357610 S653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:47698905 G>A maps to ENST00000357610 I688I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr11:47726119 G>A maps to ENST00000357610 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:47711716 G>A maps to ENST00000357610 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:47681898 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:47689233 C>T maps to ENST00000357610 K745K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:49056531 G>A maps to NM_032785.3 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:49119052 G>A maps to NM_032785.3 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:49128875 G>A maps to NM_032785.3 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:49332875 C>T maps to NM_032785.3 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:49052745 G>A maps to NM_032785.3 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:49119121 C>T maps to NM_032785.3 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:27276420 C>T maps to NM_021831.5 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:27278043 C>T maps to NM_021831.5 A277A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A3AC-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr2:228401684 C>T maps to NM_001135187.1 Q476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:100159975 G>A maps to NM_006076.4 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:100153311 C>T maps to NM_006076.4 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:100151724 C>T maps to NM_006076.4 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr7:100151771 C>T maps to NM_006076.4 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr7:100160516 C>T maps to NM_006076.4 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:76357578 G>A maps to NM_018046.4 W632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:76359010 C>T maps to NM_018046.4 F693F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:76348589 C>A maps to NM_018046.4 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr7:141341052 G>A maps to NM_018238.3 W244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr1:100353539 C>T maps to ENST00000311030 A897A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:100379258 C>T maps to ENST00000311030 Q1377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:100340292 C>T maps to ENST00000311030 Q338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:100327055 T>A maps to NM_000645.2 L10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:100330032 C>T maps to ENST00000311030 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:100346233 C>T maps to ENST00000311030 Y595Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:15909808 G>A maps to NM_024758.3 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:15904239 C>A maps to NM_024758.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:15906599 C>T maps to NM_024758.3 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:15904212 C>T maps to NM_024758.3 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:15905398 C>T maps to NM_024758.3 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:15909808 G>A maps to NM_024758.3 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:15905503 C>T maps to NM_024758.3 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr6:32137187 C>A maps to NM_032741.4 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr6:32137788 G>A maps to NM_032741.4 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr9:139568308 G>A maps to NM_006412.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:139571923 G>A maps to NM_006412.3 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr21:45389064 C>T maps to NM_001037553.1 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr21:45390562 C>T maps to NM_001037553.1 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:161653067 G>A maps to NM_020133.2 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:161587426 C>T maps to NM_020133.2 W67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr6:161560466 G>A maps to NM_020133.2 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:6614770 G>A maps to NM_018361.3 K319K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr4:84519859 C>T maps to NM_032717.3 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:84516093 C>T maps to NM_032717.3 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:84519292 C>T maps to NM_032717.3 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr15:78819882 C>T maps to NM_001013619.2 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:78807358 C>T maps to NM_001013619.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:78819765 C>T maps to NM_001013619.2 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:178385995 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:178385996 G>A maps to NM_003659.3 R566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr7:16841420 G>A maps to ENST00000419572 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr7:16841387 G>T maps to ENST00000223274 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:16839433 C>T maps to ENST00000223274 K88K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:16902252 C>T maps to NM_176813.3 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:985854 C>T maps to NM_198576.2 G1675G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:983032 C>T maps to NM_198576.2 S1199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:989294 C>T maps to NM_198576.2 P1938P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44R-06A-41D-A25O-08 chr1:982065 C>T maps to NM_198576.2 S1067S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr1:981876 C>T maps to NM_198576.2 L1004L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:980619 C>T maps to NM_198576.2 I778I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:982005 C>T maps to NM_198576.2 S1047S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:981386 C>T maps to NM_198576.2 F908F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:984990 C>T maps to NM_198576.2 I1520I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:957748 C>T maps to NM_198576.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:983032 C>T maps to NM_198576.2 S1199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:979002 C>T maps to NM_198576.2 A563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:981128 C>T maps to NM_198576.2 P851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:957729 G>A maps to NM_198576.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:980797 C>T maps to NM_198576.2 Q811*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:230841680 G>A maps to NM_000029.3 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:230839075 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:230841824 C>T maps to NM_000029.3 Q326Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:230846179 G>A maps to NM_000029.3 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:230846194 G>A maps to NM_000029.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:88307706 G>A maps to ENST00000395847 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:88284437 G>A maps to ENST00000395847 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:88284476 G>A maps to ENST00000395847 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:88307706 G>A maps to ENST00000395847 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:148459571 C>T maps to NM_032049.2 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:148459739 G>A maps to NM_032049.2 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr3:148459397 G>A maps to NM_032049.2 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr3:148459236 C>T maps to NM_032049.2 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:148459446 C>T maps to NM_032049.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:148459739 G>A maps to NM_032049.2 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr3:148459739 G>A maps to NM_032049.2 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr23:115304183 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr23:115304507 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr23:115303704 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:115304403 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:115303763 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:115304183 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:115304599 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:115303751 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:115304403 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:115304027 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr23:115304557 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:115303710 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:115303631 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:115304601 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:115304174 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr23:115304210 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:115304076 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:115304183 C>T did not map to a codon.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr23:115303741 G>A did not map to a codon.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:11810167 C>T maps to NM_020350.4 Y133Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:11810168 C>T maps to NM_020350.4 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:241808721 C>T maps to NM_000030.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:241808729 G>A maps to NM_000030.2 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:241813429 C>T maps to NM_000030.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:241813425 G>A maps to NM_000030.2 K209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:241813455 C>T maps to NM_000030.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:241808434 G>A maps to NM_000030.2 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:241814561 C>T maps to NM_000030.2 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:241813461 C>T maps to NM_000030.2 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr2:241808651 C>T maps to NM_000030.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:241812410 C>T maps to NM_000030.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:241815372 C>T maps to NM_000030.2 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr5:35039543 G>A maps to NM_031900.3 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr5:35035370 C>T maps to NM_031900.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr5:35035328 G>A maps to NM_031900.3 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:109681428 G>A maps to NM_031279.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:109680995 G>A maps to NM_031279.3 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:177651731 T>A did not map to a codon.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr1:247040329 G>A maps to ENST00000428671 F991F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr1:247065862 G>A maps to ENST00000428671 R399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr1:247065862 G>A maps to ENST00000428671 R399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr20:32879331 G>A maps to NM_000687.2 R151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr20:32879332 G>A maps to NM_000687.2 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr20:32879290 G>A maps to NM_000687.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:110551661 C>T maps to NM_006621.4 Q43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:110561082 C>T maps to NM_006621.4 I404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr7:129046259 C>T maps to NM_015328.3 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr7:129046308 T>C did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:129046259 C>T maps to NM_015328.3 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:27876721 G>A maps to NM_001029882.2 P635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr1:27875199 G>A maps to NM_001029882.2 L1143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr1:27875200 G>A maps to NM_001029882.2 I1142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr1:27876231 G>T maps to NM_001029882.2 R799R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:27875277 G>A maps to NM_001029882.2 L1117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:27875278 G>T maps to NM_001029882.2 G1116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:27877701 G>A maps to NM_001029882.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:27877350 G>A maps to NM_001029882.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:135787208 G>C maps to NM_017651.4 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr6:135726088 T>C maps to NM_017651.4 K996K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:62288328 G>A maps to NM_001620.1 S4520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr11:62292210 G>A maps to NM_001620.1 L3226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr11:62300682 G>A maps to NM_001620.1 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr11:62290118 G>A maps to NM_001620.1 R3924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:62286123 G>A maps to NM_001620.1 V5255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr11:62284752 G>A maps to NM_001620.1 I5712I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr11:62289486 A>C maps to NM_001620.1 V4134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr11:62293839 A>T maps to NM_001620.1 I2683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr11:62299866 C>T maps to NM_001620.1 E674E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:62303491 G>A maps to NM_001620.1 Q27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr11:62298300 G>A maps to NM_001620.1 S1196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:62296502 T>A maps to NM_001620.1 K1796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr11:62292273 A>G maps to NM_001620.1 P3205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:62301155 G>A maps to NM_001620.1 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:62287734 G>A maps to NM_001620.1 A4718A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr11:62295852 G>T maps to NM_001620.1 P2012P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:62285730 G>T maps to NM_001620.1 S5386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:62288268 G>A maps to NM_001620.1 S4540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:62295954 C>T maps to NM_001620.1 K1978K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:62300403 A>T maps to NM_001620.1 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr11:62294595 T>C maps to NM_001620.1 G2431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:62291667 G>A maps to NM_001620.1 F3407F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:62298471 G>A maps to NM_001620.1 L1139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:62295534 G>A maps to NM_001620.1 S2118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr11:62287338 G>A maps to NM_001620.1 S4850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr11:62300295 G>A maps to NM_001620.1 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr11:62294949 G>A maps to NM_001620.1 S2313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:62295156 A>G maps to NM_001620.1 P2244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:62295270 A>C maps to NM_001620.1 V2206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:62288673 G>A maps to NM_001620.1 V4405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:62293077 A>G maps to NM_001620.1 V2937V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr11:62290458 G>A maps to NM_001620.1 P3810P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr11:62287509 G>A maps to NM_001620.1 F4793F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr14:105408641 C>T maps to NM_138420.2 P4382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr14:105418709 G>T maps to NM_138420.2 P1026P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr14:105410200 G>A maps to NM_138420.2 Q3863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr14:105405413 G>A maps to NM_138420.2 P5458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr14:105414308 G>A maps to NM_138420.2 F2493F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr14:105420994 G>A maps to NM_138420.2 Q265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr14:105411077 G>A maps to NM_138420.2 D3570D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:105411707 G>A maps to NM_138420.2 L3360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:105416015 G>A maps to NM_138420.2 P1924P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr14:105416204 G>A maps to NM_138420.2 S1861S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr14:105418241 G>A maps to NM_138420.2 I1182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:105419327 G>A maps to NM_138420.2 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr14:105410900 C>T maps to NM_138420.2 K3629K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr14:105410417 G>A maps to NM_138420.2 S3790S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:105410525 C>T maps to NM_138420.2 K3754K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:105409853 G>A maps to NM_138420.2 F3978F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:105414671 G>A maps to NM_138420.2 S2372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:105414779 G>A maps to NM_138420.2 S2336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr14:105418538 C>T maps to NM_138420.2 K1083K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr14:105420038 G>A maps to NM_138420.2 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:105410825 C>T maps to NM_138420.2 G3654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr14:105416318 G>A maps to NM_138420.2 F1823F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr14:105411656 C>T maps to NM_138420.2 P3377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:105410474 C>G maps to NM_138420.2 V3771V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr14:105419600 G>A maps to NM_138420.2 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:105418954 G>A maps to NM_138420.2 L945L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:105407009 C>A maps to NM_138420.2 V4926V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:105408932 G>A maps to NM_138420.2 S4285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:105421877 G>A maps to NM_138420.2 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr14:105418163 G>A maps to NM_138420.2 T1208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr14:105415877 C>T maps to NM_138420.2 L1970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr14:105413990 C>T maps to NM_138420.2 K2599K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:105406958 A>G maps to NM_138420.2 D4943D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:105410405 C>T maps to NM_138420.2 K3794K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr14:105418349 C>T maps to NM_138420.2 E1146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr14:105410204 C>T maps to NM_138420.2 T3861T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr14:105416894 C>G maps to NM_138420.2 P1631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr14:105407825 T>C maps to NM_138420.2 G4654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr14:105408779 G>A maps to NM_138420.2 S4336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr14:105413030 C>T maps to NM_138420.2 K2919K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr14:105420983 C>T maps to NM_138420.2 K268K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr14:105413480 G>A maps to NM_138420.2 A2769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:105404489 G>A maps to NM_138420.2 S5766S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:105409178 C>T maps to NM_138420.2 E4203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:105409274 G>A maps to NM_138420.2 S4171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:105414113 C>T maps to NM_138420.2 E2558E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:105415700 C>T maps to NM_138420.2 G2029G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:105415961 C>T maps to NM_138420.2 V1942V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr14:105409244 G>A maps to NM_138420.2 L4181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr14:105418442 C>T maps to NM_138420.2 A1115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr14:105416131 G>A maps to NM_138420.2 Q1886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr7:17379638 C>T maps to NM_001621.4 P730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr7:17373556 T>C maps to NM_001621.4 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr5:434651 G>A maps to NM_020731.3 R621R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:423969 C>T maps to NM_020731.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr5:354003 C>T maps to NM_020731.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr14:77929094 C>T maps to NM_012111.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:61412662 G>T maps to ENST00000389584 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr2:61413919 G>A maps to ENST00000389584 *333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:186333584 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr3:186330963 C>T maps to ENST00000273784 Q12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:186338547 G>A maps to ENST00000273784 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:186338622 C>T maps to ENST00000273784 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:186330938 C>T maps to ENST00000273784 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:186338391 C>T maps to ENST00000273784 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr16:31539883 C>T maps to NM_016633.2 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr16:31539906 G>A maps to NM_016633.2 Q68Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr16:31539945 C>T maps to NM_016633.2 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:31539474 G>A maps to NM_016633.2 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:31539876 G>A maps to NM_016633.2 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr16:31539945 C>T maps to NM_016633.2 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:31539876 G>A maps to NM_016633.2 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:8758051 G>A maps to NM_020661.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr12:8758051 G>A maps to NM_020661.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr12:8757937 C>T maps to NM_020661.2 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:8757985 C>T maps to NM_020661.2 W84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:31584595 C>T maps to NM_001623.3 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:129263944 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:129270668 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:129270669 G>A did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr23:129281737 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:71880916 G>A maps to NM_032797.5 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr10:71873972 G>A maps to NM_032797.5 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:71874718 G>A maps to NM_032797.5 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr10:71883675 G>A maps to NM_032797.5 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr10:71874038 G>A maps to NM_032797.5 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:71880334 G>A maps to NM_032797.5 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr22:21327629 G>A maps to NM_144704.2 K22K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr22:21330535 C>T maps to NM_144704.2 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr22:21328424 G>A maps to NM_144704.2 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:21329050 C>T maps to NM_144704.2 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr22:21332232 C>T maps to NM_144704.2 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:21327710 C>T maps to NM_144704.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr22:21328911 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:21329050 C>T maps to NM_144704.2 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:21328397 C>T maps to NM_144704.2 C134C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:21333928 C>T maps to NM_144704.2 G530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:106978145 T>C maps to NM_001624.2 F1150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:106987352 C>T maps to NM_001624.2 S1190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr6:107003645 G>A maps to NM_001624.2 W1455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:106967773 C>T maps to NM_001624.2 F489F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:106969054 G>A maps to NM_001624.2 L916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr6:106969109 C>T maps to NM_001624.2 L935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr6:107016345 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr6:106989480 C>T maps to NM_001624.2 F1214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr6:106968688 C>T maps to NM_001624.2 S794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr1:26669244 C>T maps to NM_001039775.3 W1068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:26664928 G>A maps to NM_001039775.3 P1128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:26669298 G>A maps to NM_001039775.3 T1050T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:26655268 C>T maps to NM_001039775.3 E1470E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:26664511 C>T maps to NM_001039775.3 G1166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:159043085 A>T maps to NM_004833.1 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:159035960 C>T maps to NM_004833.1 K185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:159035903 C>T maps to NM_004833.1 K204K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:67257812 C>T maps to NM_003977.2 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:67257813 C>T maps to NM_003977.2 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr11:67258442 C>T maps to NM_003977.2 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:67256781 C>T maps to NM_003977.2 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:6330368 G>A maps to NM_014336.3 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr17:6329136 G>A maps to NM_014336.3 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr21:45709621 G>A maps to NM_000383.2 K245K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CE-06A-11D-A19A-08 chr21:45706945 G>A maps to NM_000383.2 K131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr21:45711069 C>T maps to NM_000383.2 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr21:45712877 C>T maps to NM_000383.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YX-06A-11D-A197-08 chr21:45709923 C>T maps to NM_000383.2 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:45711069 C>T maps to NM_000383.2 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:45711087 C>T maps to NM_000383.2 I330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:4772262 C>T maps to NM_018836.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:4772460 G>A maps to NM_018836.3 E177E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:4772337 C>T maps to NM_018836.3 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:4772472 C>T maps to NM_018836.3 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:4772196 C>T maps to NM_018836.3 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:4772550 C>T maps to NM_018836.3 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:4832519 C>T maps to NM_018836.3 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:4832426 C>T maps to NM_018836.3 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:130630337 G>A maps to ENST00000223836 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:33478955 G>A maps to NM_001625.3 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:77806141 G>A maps to NM_174858.1 Q260Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:78001662 C>T maps to NM_174858.1 A520A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr1:77806156 C>T maps to NM_174858.1 D265D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:77987619 G>T maps to NM_174858.1 G474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr14:96917816 G>A maps to NM_152327.2 E336E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr14:96916164 G>A maps to NM_152327.2 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:96953233 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:96917829 C>T maps to NM_152327.2 R341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:96944949 G>A maps to NM_152327.2 E568E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:96875241 G>A maps to NM_152327.2 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:96904251 G>A maps to NM_152327.2 K230K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr17:55187449 C>T maps to ENST00000427138 F635F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:55183710 C>T maps to ENST00000427138 Q338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:55182887 C>T maps to ENST00000427138 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr17:55182892 G>A maps to ENST00000427138 W65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:55182851 C>T maps to ENST00000427138 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:55183953 C>T maps to ENST00000427138 Q419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:55184357 C>T maps to ENST00000427138 F553F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:42875716 T>A maps to NM_016248.2 S945S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr13:42874186 C>T maps to NM_016248.2 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr13:42891697 G>A maps to NM_016248.2 T1813T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr6:151670947 G>A maps to NM_005100.3 E474E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:151673659 G>A maps to NM_005100.3 V1378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:151672702 C>T maps to NM_005100.3 T1059T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:151672876 A>G maps to NM_005100.3 P1117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr6:151672174 G>A maps to NM_005100.3 E883E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:151671949 G>A maps to NM_005100.3 K808K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr15:86286970 C>A maps to NM_006738.4 A2773A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr15:86228061 C>T maps to NM_006738.4 F1753F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr15:86259046 C>T maps to NM_006738.4 S1880S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr15:86198667 C>T maps to NM_006738.4 A1465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:86278325 C>T maps to NM_006738.4 P2466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:86076915 G>T maps to NM_006738.4 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr15:86270680 C>T maps to NM_006738.4 A2362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:86124922 C>T maps to NM_006738.4 A1208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:86270674 C>T maps to NM_006738.4 T2360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:86123596 C>T maps to NM_006738.4 V766V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:119037547 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr23:119048715 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:119037501 G>A did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:119037260 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:112900289 C>T maps to NM_007203.4 S822S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:112900001 C>T maps to NM_007203.4 F726F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr9:112898772 C>T maps to NM_007203.4 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:112899020 C>T maps to NM_007203.4 F399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:112899266 C>T maps to NM_007203.4 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr12:4736420 G>A maps to NM_006422.2 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:4736882 C>T maps to NM_006422.2 R395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr12:4747273 C>T maps to NM_006422.2 W30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr12:4737407 G>A maps to NM_006422.2 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:4736474 G>T maps to NM_006422.2 A531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr12:4736483 G>A maps to NM_006422.2 I528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:4737889 G>T maps to NM_006422.2 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:4736645 G>A maps to NM_006422.2 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:4736483 G>A maps to NM_006422.2 I528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:4737029 C>T maps to NM_006422.2 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:4736417 G>A maps to NM_006422.2 F550F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr12:4736270 C>T maps to NM_006422.2 R599R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:4724928 C>T maps to NM_006422.2 L846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr23:49957641 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:49955651 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:49958743 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:49958046 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:49957223 A>G did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:49957434 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:49957174 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr23:49957271 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:49957960 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:49963309 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:49958660 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr23:49958742 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:49958064 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:49958661 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:49957282 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:49957300 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:49958710 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr23:49958325 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr23:49958118 C>T did not map to a codon.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr23:49958736 A>C did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:49958139 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:49957580 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:49957826 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:49958710 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:49958331 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:49957723 G>A did not map to a codon.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr23:49958660 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr14:33014962 C>T maps to NM_004274.4 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr14:33292160 G>A maps to NM_004274.4 S1714S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:33004899 A>G maps to NM_004274.4 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr14:33293837 C>T maps to NM_004274.4 A2273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr14:33014794 T>A maps to NM_004274.4 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:33016036 C>T maps to NM_004274.4 S726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr14:33201739 C>T maps to NM_004274.4 G1027G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:33015220 G>A maps to NM_004274.4 Q454Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr14:33069898 G>A maps to NM_004274.4 R877R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:33291509 C>T maps to NM_004274.4 P1497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr14:33293339 G>A maps to NM_004274.4 G2107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr14:33292790 G>A maps to NM_004274.4 G1924G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:33292868 G>A maps to NM_004274.4 K1950K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr14:33291017 C>T maps to NM_004274.4 T1333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr14:33292868 G>A maps to NM_004274.4 K1950K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:33165255 C>T maps to NM_004274.4 S980S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:33016186 C>T maps to NM_004274.4 A776A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:15484781 C>T maps to NM_005858.2 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:15483970 A>G maps to NM_005858.2 D184D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:15469801 C>T maps to NM_005858.2 V533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr19:15512298 G>A maps to NM_014371.2 Q160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr19:15511106 C>T maps to NM_014371.2 K349K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:15512026 G>A maps to NM_014371.2 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:15507969 C>T maps to NM_014371.2 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:15512188 G>A maps to NM_014371.2 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr7:91715707 T>A maps to NM_005751.4 L3064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:91631573 A>G maps to NM_005751.4 K781K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr7:91690669 C>T maps to NM_005751.4 R1900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr7:91631891 A>G maps to NM_005751.4 L887L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr7:91715657 G>A maps to NM_005751.4 T3047T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:91695829 C>T maps to NM_005751.4 F2100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:91731943 C>T maps to NM_005751.4 R3712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:91660863 C>T maps to NM_005751.4 I1428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:91708884 C>T maps to NM_005751.4 Q2480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:91730219 C>T maps to NM_005751.4 A3649A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:91718710 C>T maps to NM_005751.4 Q3076*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:91660863 C>T maps to NM_005751.4 I1428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr7:91630433 C>T maps to NM_005751.4 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr7:91631837 T>C maps to NM_005751.4 A869A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr7:91722538 G>T maps to NM_005751.4 E3163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:91709261 C>T maps to NM_005751.4 T2605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:91718796 G>A maps to NM_005751.4 R3104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr7:91714202 C>T maps to NM_005751.4 G2927G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr7:91727476 T>C maps to NM_005751.4 I3554I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr6:109850219 C>T maps to NM_001145128.2 R1209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:109962758 G>A maps to NM_001145128.2 Q299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr6:109871384 G>A maps to NM_001145128.2 R958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr9:117113182 T>C maps to NM_030767.4 P1059P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr9:117138748 G>A maps to NM_030767.4 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr9:117108287 A>G maps to NM_030767.4 S1172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:117139656 A>G maps to NM_030767.4 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:117106060 G>A maps to NM_030767.4 S1228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:117129924 G>A maps to NM_030767.4 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr9:117108960 G>T maps to NM_030767.4 R1168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr9:117108961 G>T maps to NM_030767.4 L1167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr9:117109057 G>A maps to NM_030767.4 S1135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr9:117121947 C>T maps to NM_030767.4 G806G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:117143570 G>A maps to NM_030767.4 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr9:117104354 G>A maps to NM_030767.4 Q1270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:117120289 G>A maps to NM_030767.4 Q884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:117122237 G>A maps to NM_030767.4 P743P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr1:109363228 C>T maps to NM_152763.3 R729R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:109395172 C>T maps to NM_152763.3 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:109366203 C>T maps to NM_152763.3 R681R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:109391554 C>T maps to NM_152763.3 Q387Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:46034622 C>T maps to NM_153326.1 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr7:134135573 C>A maps to NM_001628.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:134134531 G>A maps to NM_001628.2 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr7:134134531 G>A maps to NM_001628.2 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:134134531 G>A maps to NM_001628.2 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr7:134134531 G>A maps to NM_001628.2 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr7:134134531 G>A maps to NM_001628.2 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr7:134136346 G>A maps to NM_001628.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:134134531 G>A maps to NM_001628.2 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr7:134133182 G>A maps to NM_001628.2 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:134222965 C>T maps to NM_020299.4 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:134223736 C>T maps to NM_020299.4 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:134222353 C>T maps to NM_020299.4 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr7:134216694 G>A maps to NM_020299.4 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:134221439 C>T maps to NM_020299.4 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr7:134215552 C>T maps to NM_020299.4 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:134217799 C>T maps to NM_020299.4 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:134256360 G>A maps to ENST00000418096 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:134261722 C>T maps to ENST00000418096 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr10:5014476 C>T maps to NM_001353.5 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:5011069 C>T maps to NM_001353.5 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr10:5042640 C>T maps to NM_001135241.1 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr10:5037947 C>T maps to NM_001354.4 W227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr10:5144345 G>A maps to NM_003739.4 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr10:5144345 G>A maps to NM_003739.4 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:5141001 G>A maps to NM_003739.4 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr10:5238874 C>T maps to NM_001818.2 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr10:5258736 C>T maps to NM_001818.2 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:5258736 C>T maps to NM_001818.2 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr10:5248278 C>T maps to NM_001818.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr7:137776623 C>T maps to NM_005989.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr7:137792256 C>T maps to NM_005989.3 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:137801364 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:137776623 C>T maps to NM_005989.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:137790090 C>T maps to NM_005989.3 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:137791373 C>T maps to NM_005989.3 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:137792214 G>A maps to NM_005989.3 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr7:137798459 G>T maps to NM_005989.3 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:137773513 G>A maps to NM_005989.3 K87K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:137773514 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:137776629 G>A maps to NM_005989.3 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr7:137776575 C>T maps to NM_005989.3 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr7:137773459 G>A maps to NM_005989.3 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:4883991 G>A maps to NM_001040177.1 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:19632544 G>A maps to NM_003689.2 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:19634675 G>A maps to NM_003689.2 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:19609266 G>A maps to NM_012067.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:19611563 G>A maps to NM_012067.2 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:19610570 G>A maps to NM_012067.2 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:19595800 G>A maps to NM_201252.3 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr14:105241448 G>A maps to NM_001014432.1 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:105242063 G>A maps to NM_001014432.1 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:105241277 G>A maps to NM_001014432.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:105246460 G>A maps to NM_001014432.1 Q47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr14:105241328 G>A maps to NM_001014432.1 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:105239821 C>T maps to NM_001014432.1 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr19:50374973 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:40762862 G>A maps to NM_001626.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr19:40747871 G>A maps to NM_001626.3 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:40746008 G>A maps to NM_001626.3 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr1:243828126 G>A maps to NM_005465.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:116153159 G>A maps to ENST00000277315 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:52245536 C>T maps to ENST00000441729 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr3:52238817 C>T maps to ENST00000441729 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr3:52239920 C>T maps to ENST00000441729 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr23:55051267 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:55043922 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:55041297 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:55054204 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:55047647 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr23:55051222 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:55035749 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr4:74279342 C>T maps to NM_000477.5 F350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr4:74285295 C>T maps to NM_000477.5 F575F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr4:74270881 C>T maps to NM_000477.5 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:74280829 C>T maps to NM_000477.5 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr4:74280793 C>T maps to NM_000477.5 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr4:74282061 C>T maps to NM_000477.5 F427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:74277824 G>T maps to NM_000477.5 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr4:74274450 C>T maps to NM_000477.5 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr4:74274438 C>T maps to NM_000477.5 N133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr4:74274516 G>A maps to NM_000477.5 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:74275203 G>A maps to NM_000477.5 K205K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:74275204 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr4:74281998 A>G maps to NM_000477.5 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:74274417 C>T maps to NM_000477.5 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:74285295 C>T maps to NM_000477.5 F575F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:74279225 C>T maps to NM_000477.5 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr4:74270067 C>T maps to NM_000477.5 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr4:74279174 G>A maps to NM_000477.5 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr4:74272378 G>A maps to NM_000477.5 Q57Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr3:105271423 G>A maps to NM_001627.2 K553K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr3:105266007 C>T maps to NM_001627.2 R374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:105252523 C>T maps to NM_001627.2 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:105258924 G>A maps to NM_001627.2 E279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr19:49967974 C>T maps to NM_153329.3 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:49969057 C>T maps to NM_153329.3 S544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr19:49969018 C>T maps to NM_153329.3 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr19:49971807 C>T maps to NM_153329.3 A703A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:49965879 G>A maps to NM_153329.3 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr10:97397093 G>A maps to NM_002860.3 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:97371129 G>A maps to NM_002860.3 R665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr15:58285268 C>T maps to NM_003888.2 W186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr15:58285259 G>A maps to NM_003888.2 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:58253005 G>A maps to NM_003888.2 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:58258016 C>T maps to NM_003888.2 K269K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:58287302 G>A maps to NM_003888.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr15:58306085 G>A maps to NM_003888.2 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:58285268 C>T maps to NM_003888.2 W186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:58306079 C>T maps to NM_003888.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:101434166 C>T maps to NM_000693.2 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr9:38395819 C>T maps to NM_000692.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:38396090 C>T maps to NM_000692.3 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr9:38396623 C>T maps to NM_000692.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:38397256 G>A maps to NM_000692.3 E504E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:38395963 G>A maps to NM_000692.3 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr3:125844479 T>G maps to ENST00000273450 T603T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr3:125836891 G>A maps to ENST00000273450 I656I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr3:125879756 C>T maps to ENST00000273450 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr3:125877270 G>A maps to ENST00000273450 H123H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr3:125828934 C>T maps to ENST00000273450 K743K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:125876292 G>A maps to ENST00000273450 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:125874301 G>A maps to ENST00000273450 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:125833438 G>T maps to ENST00000273450 I691I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr3:125833480 C>T maps to ENST00000273450 V677V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr3:125824751 G>A maps to ENST00000273450 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:125836897 C>T maps to ENST00000273450 R654R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:125844542 G>A maps to ENST00000273450 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:125831636 G>A maps to ENST00000273450 F733F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:125833453 C>T maps to ENST00000273450 G686G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:125836935 G>A maps to ENST00000273450 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:125844485 C>T maps to ENST00000273450 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:125856769 G>A maps to ENST00000273450 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:125874325 G>A maps to ENST00000273450 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:125876305 C>T maps to ENST00000273450 W146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:125824731 C>T maps to ENST00000273450 T840T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:125850268 G>A maps to ENST00000273450 I537I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr12:105440678 G>A maps to NM_001034173.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:105454851 T>C did not map to a codon.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr12:105446670 T>G maps to NM_001034173.3 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr12:112221086 C>T maps to NM_000690.2 D115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr12:112219759 G>A maps to NM_000690.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:112228367 T>C did not map to a codon.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr12:112237855 G>A maps to NM_000690.2 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:112230429 C>T maps to NM_000690.2 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:112235943 G>A maps to NM_000690.2 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:112237855 G>A maps to NM_000690.2 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr12:112221089 G>A maps to NM_000690.2 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr12:112219759 G>A maps to NM_000690.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:112219819 G>A maps to NM_000690.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr17:19648409 G>A maps to NM_000691.4 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:19646599 G>A maps to NM_000691.4 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:19642819 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr17:19648364 C>T maps to NM_000691.4 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr17:19644443 G>A maps to NM_000691.4 Q257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr17:19648352 C>T maps to NM_000691.4 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:67789248 C>T maps to NM_001161473.1 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr11:67786691 C>T maps to NM_001161473.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:67431902 C>T maps to NM_001031615.1 K279K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:67430691 G>A maps to NM_001031615.1 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:67430835 G>A maps to NM_001031615.1 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:67432999 G>A maps to NM_001031615.1 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr11:67432807 G>A maps to NM_001031615.1 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:67433641 C>T maps to NM_001031615.1 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr11:67433011 G>A maps to NM_001031615.1 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:67430790 G>A maps to NM_001031615.1 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:67430796 G>A maps to NM_001031615.1 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:19216514 G>A maps to NM_003748.3 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr1:19204080 G>A maps to NM_003748.3 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:19203939 C>G maps to NM_003748.3 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:19204080 G>A maps to NM_003748.3 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr1:19201978 G>A maps to NM_003748.3 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:19199371 G>A maps to NM_003748.3 P553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:19209668 G>A maps to NM_003748.3 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:19204014 A>C maps to NM_003748.3 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:24505098 G>A maps to NM_170740.1 W204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:24515495 G>A maps to NM_170740.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:24505191 C>T maps to NM_170740.1 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:24503661 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:24533774 G>A maps to NM_170740.1 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr6:24502821 C>T maps to NM_170740.1 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr14:74538650 C>T maps to NM_005589.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr5:125896807 G>A maps to NM_001182.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr6:135264978 G>A maps to NM_022568.3 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:165634253 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:165652296 G>A maps to NM_000696.3 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:165652224 G>A maps to NM_000696.3 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr16:30080250 C>T maps to ENST00000395248 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr9:104187202 C>T maps to NM_000035.3 Q307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr9:104189763 C>T maps to NM_000035.3 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr9:104187159 C>A maps to NM_000035.3 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr9:104192063 C>T maps to NM_000035.3 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr9:104192120 G>A maps to NM_000035.3 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q3-06A-11D-A196-08 chr17:26901544 G>A maps to NM_005165.2 H197H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr17:26902185 G>A maps to NM_005165.2 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr17:26900871 G>A maps to NM_005165.2 R294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:5121917 G>A maps to NM_019109.4 W23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:5125426 C>T maps to NM_019109.4 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:5125426 C>T maps to NM_019109.4 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:38712070 C>T maps to NM_001013620.3 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:38714174 C>T maps to NM_001013620.3 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr13:52586553 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr22:50307356 G>A maps to NM_024105.3 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr22:50297902 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr23:110951457 C>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:110951409 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:110970245 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr23:110951567 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:110951285 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:110951450 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:110970076 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:110951443 T>C did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:110968238 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:110970086 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:110988107 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:110968172 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:95538397 G>A maps to NM_144988.3 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:95538397 G>A maps to NM_144988.3 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:125648251 C>T maps to NM_001195223.1 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr9:101980727 G>A maps to NM_033087.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr9:101980728 G>A maps to NM_033087.3 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr9:101980895 G>A maps to NM_033087.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:183961733 G>A maps to NM_005787.5 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr3:183962421 G>A maps to NM_005787.5 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr3:183961763 G>A maps to NM_005787.5 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr3:183960641 G>A maps to NM_005787.5 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:183961676 G>A maps to NM_005787.5 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr13:37573377 G>A maps to NM_013338.4 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr13:37569628 G>A maps to NM_013338.4 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr13:37559847 G>A maps to NM_013338.4 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr13:37539794 T>A maps to NM_013338.4 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:63868000 C>T maps to ENST00000263440 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr11:77835128 G>A maps to NM_024079.4 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:77812120 G>A maps to NM_024079.4 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr11:111707006 G>A maps to ENST00000428306 Q720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:111657225 C>T maps to ENST00000428306 R809R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:29917788 G>A maps to NM_004304.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr2:29455308 C>T maps to NM_004304.3 K831K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:29498004 C>T maps to NM_004304.3 G667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:29497986 C>T maps to NM_004304.3 Q673Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:29543704 G>A maps to NM_004304.3 F486F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:29450458 C>A maps to NM_004304.3 L965L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:29754788 C>T maps to NM_004304.3 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:29498285 G>A maps to NM_004304.3 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:29462668 C>T maps to NM_004304.3 G744G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:29543650 C>T maps to NM_004304.3 R504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:29498073 G>A maps to NM_004304.3 I644I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:29917857 G>A maps to NM_004304.3 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:29543647 G>A maps to NM_004304.3 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr2:29474029 C>T maps to NM_004304.3 G715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:29917848 C>T maps to NM_004304.3 E273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:29416374 C>T maps to NM_004304.3 E1526E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:29416608 G>A maps to NM_004304.3 S1448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:29432719 G>A maps to NM_004304.3 L1256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:29455287 C>T maps to NM_004304.3 L838L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:29498067 C>T maps to NM_004304.3 Q646Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:29754971 G>A maps to NM_004304.3 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr2:29451807 C>T maps to NM_004304.3 G919G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:29754809 G>A maps to NM_004304.3 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr14:78174242 G>T maps to NM_006020.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:78146284 G>A maps to NM_006020.2 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:78142162 G>A maps to NM_006020.2 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:109527986 G>A maps to NM_001145375.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr12:109527891 C>T maps to NM_001145375.1 W134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:102098209 C>T maps to NM_017621.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr7:102097861 G>A maps to NM_017621.3 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:36504284 G>A maps to ENST00000455847 D26D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr19:36505120 C>T maps to NM_032878.3 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr19:6374887 C>T maps to NM_032306.3 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:6374272 C>A maps to NM_032306.3 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:107403072 C>T maps to ENST00000417449 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:3726131 G>A maps to ENST00000403787 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:3726101 G>A maps to ENST00000403787 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:3750151 A>T maps to ENST00000403787 *410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:3727480 G>A maps to ENST00000403787 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:3727483 G>A maps to ENST00000403787 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:3744984 T>G maps to ENST00000403787 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr2:3729239 C>T maps to ENST00000403787 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr2:3743412 C>T maps to ENST00000403787 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr2:73717794 C>T maps to NM_015120.4 H2902H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr2:73718148 C>T maps to NM_015120.4 S3020S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr2:73716846 C>T maps to NM_015120.4 F2586F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:73675711 T>C maps to NM_015120.4 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:73677367 T>C maps to NM_015120.4 S1237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:73675292 C>T maps to NM_015120.4 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:73675189 C>T maps to NM_015120.4 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:73716846 C>T maps to NM_015120.4 F2586F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:73680577 C>A maps to NM_015120.4 S2307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:73799600 C>T maps to NM_015120.4 Q3532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:73677115 C>T maps to NM_015120.4 F1153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr2:73784357 C>T maps to NM_015120.4 Q3363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:73678099 C>T maps to NM_015120.4 P1481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:73682331 C>T maps to NM_015120.4 S2527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:73679774 C>T maps to NM_015120.4 Q2040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:73676434 C>T maps to NM_015120.4 F926F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr2:73676890 C>T maps to NM_015120.4 F1078F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:6902044 G>A maps to NM_000697.2 W144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr17:6905006 G>A maps to NM_000697.2 W346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr17:6909834 C>T maps to NM_000697.2 Y483Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr17:7979012 G>A maps to NM_001139.2 T518T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D9-A6EA-06A-11D-A30X-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EB-A44R-06A-41D-A25O-08 chr17:7990712 C>A maps to NM_001139.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr17:7989340 C>T maps to NM_001139.2 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:7990685 G>A maps to NM_001139.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:7976166 G>A maps to NM_001139.2 I676I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:7976250 G>A maps to NM_001139.2 F648F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:7984040 G>A maps to NM_001139.2 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:7989508 C>T maps to NM_001139.2 Q59Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:7980337 C>T maps to NM_001139.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:4540538 G>A maps to NM_001140.3 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:4536768 G>A maps to NM_001140.3 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:4541960 G>A maps to NM_001140.3 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:4542356 C>T maps to NM_001140.3 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:4542410 C>T maps to NM_001140.3 E118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr17:4540553 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:4536768 G>A maps to NM_001140.3 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:4536765 C>T maps to NM_001140.3 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr17:7945752 C>T maps to NM_001141.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:7942601 G>A maps to NM_001141.2 K43K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr17:7948632 C>T maps to NM_001141.2 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:7948189 C>T maps to NM_001141.2 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr17:7951772 C>T maps to NM_001141.2 Q641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:7948222 C>T maps to NM_001141.2 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr17:7950011 C>T maps to NM_001141.2 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr17:7942714 C>T maps to NM_001141.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr17:7950590 C>T maps to NM_001141.2 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr10:45920564 G>A maps to NM_000698.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr10:45924211 G>A maps to NM_000698.2 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr10:45938622 C>T maps to NM_000698.2 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr10:45940955 C>T maps to NM_000698.2 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr10:45869840 G>A maps to NM_000698.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr10:45935912 C>T maps to NM_000698.2 F339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:45924070 G>A maps to NM_000698.2 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:45877959 G>A maps to NM_000698.2 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:45936026 G>A maps to NM_000698.2 E377E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:45938941 G>T maps to NM_000698.2 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr13:31338125 C>T maps to NM_001629.2 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr13:31338101 G>A maps to NM_001629.2 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr13:31338173 C>T maps to NM_001629.2 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:31309783 C>T maps to NM_001629.2 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:31318245 G>A maps to NM_001629.2 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr13:31318200 C>T maps to NM_001629.2 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr17:8006772 G>A maps to ENST00000380149 S764S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr17:8006748 G>A maps to ENST00000380149 T772T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr17:8015462 C>T maps to ENST00000380149 K400K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:8015438 G>A maps to ENST00000380149 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr17:8015435 G>A maps to ENST00000380149 F409F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:8000064 G>A maps to ENST00000380149 I828I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:8007489 G>A maps to ENST00000380149 F732F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr17:8018371 C>T maps to ENST00000380149 W302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:233322372 G>A maps to NM_001631.3 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:233322729 G>A maps to NM_001631.3 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:233322372 G>A maps to NM_001631.3 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:233322729 G>A maps to NM_001631.3 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr2:233323357 G>A maps to NM_001631.3 K400K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:233322729 G>A maps to NM_001631.3 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:233322729 G>A maps to NM_001631.3 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:233322729 G>A maps to NM_001631.3 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:233322984 G>A maps to NM_001631.3 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:233323687 G>A maps to NM_001631.3 E473E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr4:113353726 C>T maps to NM_025144.3 H1008H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr4:113353727 C>A maps to NM_025144.3 R1009R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:113352338 C>T maps to NM_025144.3 R546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr4:113362184 C>T maps to NM_025144.3 F1217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:113346894 C>T maps to NM_025144.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:113303584 C>T maps to NM_025144.3 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr4:113353702 G>A maps to NM_025144.3 G1000G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr4:113346824 C>T maps to NM_025144.3 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:113348733 C>T maps to NM_025144.3 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:113352917 C>T maps to NM_025144.3 Q739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CC-06A-11D-A19A-08 chr18:56202519 C>T maps to NM_052947.3 E1633E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr18:56171358 G>A maps to NM_052947.3 I2017I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:56204102 G>A maps to NM_052947.3 L1106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr18:56205219 G>A maps to NM_052947.3 F733F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr18:56203077 G>A maps to NM_052947.3 I1447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr18:56184388 T>C maps to NM_052947.3 Q1897Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr18:56196447 G>A maps to NM_052947.3 I1792I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr18:56205026 T>A maps to NM_052947.3 R798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr18:56184166 G>A maps to NM_052947.3 I1971I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr18:56203320 C>T maps to NM_052947.3 K1366K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr18:56203767 G>A maps to NM_052947.3 I1217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr18:56246228 C>T maps to NM_052947.3 R593R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr18:56184325 G>A maps to NM_052947.3 I1918I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr18:56191278 G>A maps to NM_052947.3 S1839S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr18:56246909 G>A maps to NM_052947.3 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:56204424 G>A maps to NM_052947.3 C998C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr18:56149243 G>A maps to NM_052947.3 S2108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr15:85411374 C>T maps to NM_020778.4 A1804A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr15:85400629 G>A maps to NM_020778.4 P1089P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr15:85406064 C>T maps to NM_020778.4 I1645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:85406052 C>T maps to NM_020778.4 G1641G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr15:85411398 C>T maps to NM_020778.4 S1812S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:85407726 C>T maps to NM_020778.4 T1720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:85410591 C>T maps to NM_020778.4 R1792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr15:85411674 G>A maps to NM_020778.4 Q1904Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr15:85383850 G>A maps to NM_020778.4 K649K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:85382936 C>T maps to NM_020778.4 R345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:85399822 G>A maps to NM_020778.4 V820V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:85400659 C>T maps to NM_020778.4 F1099F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:85400660 C>T maps to NM_020778.4 L1100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:85383220 C>T maps to NM_020778.4 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:85399720 C>T maps to NM_020778.4 I786I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:21890666 G>A maps to NM_000478.4 K202K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr1:21887683 C>T maps to NM_000478.4 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:21900164 C>T maps to NM_000478.4 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:21890534 G>A maps to NM_000478.4 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:21894682 G>A maps to NM_000478.4 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:21889718 G>A maps to NM_000478.4 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:21894740 G>A did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr1:21900197 G>A maps to NM_000478.4 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:233246396 C>T maps to NM_001632.3 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr2:233244901 C>T maps to NM_001632.3 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr2:233245366 C>T maps to NM_001632.3 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr2:233272029 C>T maps to NM_031313.2 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:233274431 C>T maps to NM_031313.2 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:233272029 C>T maps to NM_031313.2 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:233274431 C>T maps to NM_031313.2 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:233272047 G>A maps to NM_031313.2 K79K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:202609104 G>A maps to NM_020919.3 A682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:202570175 C>T maps to NM_020919.3 W1530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:202589076 G>A maps to NM_020919.3 F1151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:202568856 G>A maps to NM_020919.3 F1641F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:202598154 G>A maps to NM_020919.3 F808F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:202619389 G>A maps to NM_020919.3 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:202569289 G>A maps to NM_020919.3 I1575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:202622464 T>C maps to NM_020919.3 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr2:202571690 G>A maps to NM_020919.3 Y1486Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:202617877 C>T maps to NM_020919.3 A576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:46716096 G>A maps to NM_147129.3 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:46717853 G>A maps to NM_147129.3 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr3:46723547 C>T maps to NM_147129.3 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:46718188 G>A maps to NM_147129.3 I657I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:46712536 G>A maps to NM_147129.3 I933I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr3:46718409 C>T maps to NM_147129.3 E620E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:46713052 C>T maps to NM_147129.3 E902E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:46713682 G>T maps to NM_147129.3 S827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:46718187 G>A maps to NM_147129.3 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:46727041 G>A maps to NM_147129.3 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:46727877 G>A maps to NM_147129.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:46712995 G>A maps to NM_147129.3 F921F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:202410311 C>T maps to NM_001168221.1 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr2:202466596 T>C maps to NM_001168221.1 Q127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:202469366 C>T maps to NM_001168221.1 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:202208900 G>A maps to NM_139163.2 Q152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr2:202492841 G>A maps to ENST00000409099 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:202494495 G>A maps to ENST00000409099 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:202492841 G>A maps to ENST00000409099 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr2:202494061 G>A maps to ENST00000409099 Q259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:203817286 C>T maps to NM_024744.14 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:203807617 C>T maps to NM_024744.14 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:203834640 G>A did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:203834747 C>T maps to NM_024744.14 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr12:85674155 C>T maps to NM_006982.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:110607307 C>T maps to NM_006492.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:110604122 C>T maps to NM_006492.2 E219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:110604185 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr1:110607256 G>A maps to NM_006492.2 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:44297125 C>T maps to NM_021926.3 K183K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr11:44297059 G>A maps to NM_021926.3 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr11:44286625 G>A maps to NM_021926.3 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr17:33521269 G>A maps to NM_152462.2 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:33520990 G>A maps to NM_152462.2 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:33520777 C>T maps to NM_152462.2 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:33520546 C>T maps to NM_152462.2 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:33520711 C>T maps to NM_152462.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:33520669 G>A maps to NM_152462.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:33520639 C>T maps to NM_152462.2 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr17:33520546 C>T maps to NM_152462.2 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:33520384 C>T maps to NM_152462.2 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:33520540 G>A maps to NM_152462.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:33521167 G>A maps to NM_152462.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr8:11188857 C>T maps to NM_054028.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr8:11188893 C>T maps to NM_054028.1 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr8:11188981 C>T maps to NM_054028.1 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr8:11188857 C>T maps to NM_054028.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr8:11189601 C>T maps to NM_054028.1 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:11189271 C>T maps to NM_054028.1 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:11189493 C>T maps to NM_054028.1 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:7386304 G>A maps to NM_001102614.1 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:34005932 G>A maps to NM_001167595.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20I-06A-11D-A196-08 chr5:33989590 A>T maps to NM_001167595.1 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr5:34007989 G>C maps to NM_001167595.1 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr4:71467325 G>A maps to NM_016519.4 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:71472125 C>T maps to NM_016519.4 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:71472212 G>A maps to NM_016519.4 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:71472008 C>T maps to NM_016519.4 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr4:71472161 C>T maps to NM_016519.4 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:71465308 C>T maps to NM_016519.4 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:116836409 G>A maps to NM_001633.3 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr9:116835232 C>T maps to NM_001633.3 E176E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr9:116840464 A>G maps to NM_001633.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:116837252 G>A maps to NM_001633.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr11:46564804 G>A maps to ENST00000458649 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr11:46564026 G>A maps to ENST00000458649 Q514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr11:46465036 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr11:46565584 C>T maps to ENST00000458649 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:46564471 C>T maps to ENST00000458649 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:46564443 G>A maps to ENST00000458649 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr11:46564803 G>A maps to ENST00000458649 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:46430161 G>A maps to ENST00000458649 Q1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:111196328 C>T maps to NM_001634.4 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr12:96361619 G>A maps to NM_152435.2 *427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr12:96356194 C>T maps to NM_152435.2 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr16:2578259 C>T maps to NM_001145815.1 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr16:2577837 C>T maps to NM_001145815.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr23:11312923 T>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:11316865 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:11316846 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr23:11316685 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:11317008 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:11316690 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:11316364 C>T did not map to a codon.
Sequencing variant TCGA-RP-A690-06A-11D-A30X-08 chr23:11316685 G>C did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:56397845 G>A maps to NM_001144.4 Q591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr16:56435649 G>A maps to NM_001144.4 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr16:56423199 C>T maps to NM_001144.4 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr12:53823688 C>T maps to NM_020547.2 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr12:53818186 C>T maps to NM_020547.2 C55C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:53819504 G>A maps to NM_020547.2 W218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:53823727 G>A maps to NM_020547.2 W418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:53818099 C>T maps to NM_020547.2 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:53824998 G>A maps to NM_020547.2 W488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:53823399 C>T maps to NM_020547.2 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:53818526 C>T maps to NM_020547.2 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:118081247 C>T maps to NM_001098526.1 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:118085556 G>A maps to NM_001098526.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:118067452 G>A maps to NM_001098526.1 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:118071225 G>A maps to NM_001098526.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:118071217 C>T maps to NM_001098526.1 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:118071268 G>A maps to NM_001098526.1 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:118074197 C>A maps to NM_001098526.1 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:110050283 G>A maps to NM_020703.2 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr1:110051030 G>A maps to NM_020703.2 N168N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:110050538 C>T maps to NM_020703.2 Q332Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:110051072 G>A maps to NM_020703.2 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr12:47471822 G>A maps to NM_001143668.1 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:47471828 C>T maps to NM_001143668.1 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:47472389 C>T maps to NM_001143668.1 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr12:47471959 G>A maps to NM_001143668.1 Q276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr12:47471279 C>T maps to NM_001143668.1 G502G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:47472503 C>T maps to NM_001143668.1 K94K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:47472494 G>A maps to NM_001143668.1 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:47472610 G>A maps to NM_001143668.1 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:47472611 G>A maps to NM_001143668.1 N58N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:47471888 C>T maps to NM_001143668.1 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:47472374 G>A maps to NM_001143668.1 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:47471411 C>T maps to NM_001143668.1 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:47471282 C>T maps to NM_001143668.1 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr3:49756664 G>A maps to NM_198722.2 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr3:49756439 G>A maps to NM_198722.2 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:49756835 C>T maps to NM_198722.2 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr23:109560937 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:128627088 G>A maps to NM_031445.2 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr14:103395161 G>A maps to NM_030943.3 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr14:103395161 G>A maps to NM_030943.3 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr12:31842013 C>T maps to NM_001113402.1 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr12:31862359 C>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:31850769 G>A maps to NM_001113402.1 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr23:112048228 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:112022743 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:112024184 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:112021850 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:112022751 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:112048296 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:112021839 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:112022405 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:112048314 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:112021839 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr23:112058648 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr23:112022804 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:112053138 G>A did not map to a codon.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr23:112024122 C>A did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:112033943 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:94533297 C>T maps to NM_130847.2 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:134085134 C>T maps to ENST00000514516 R450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr3:134077417 G>A maps to ENST00000514516 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:134085245 G>A maps to ENST00000514516 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:134089732 G>A maps to ENST00000514516 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:115229517 G>A maps to NM_000036.2 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:115221037 C>T maps to NM_000036.2 E369E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:115220123 C>T maps to NM_000036.2 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:115238104 C>T maps to NM_000036.2 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:115218599 G>A maps to NM_000036.2 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr1:115218563 G>A maps to NM_000036.2 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:115238085 G>A maps to NM_000036.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:115238104 C>T maps to NM_000036.2 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z4-06A-11D-A197-08 chr1:115221133 G>A maps to NM_000036.2 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:115238116 G>A maps to NM_000036.2 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:115223034 C>T maps to NM_000036.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:115220030 G>A maps to NM_000036.2 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:110171047 C>T maps to ENST00000393689 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:110163658 C>T maps to ENST00000393689 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:110169021 C>T maps to ENST00000393689 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:110163682 C>T maps to ENST00000393689 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:110168003 C>T maps to ENST00000393689 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:110168820 C>T maps to ENST00000393689 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:110163658 C>T maps to ENST00000393689 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:110163725 T>C maps to ENST00000393689 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:110168354 C>T maps to ENST00000393689 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:110170074 C>T maps to ENST00000393689 Y349Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr11:10516459 C>T maps to NM_000480.2 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:10515083 C>T maps to NM_000480.2 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:10518430 C>T maps to NM_000480.2 F510F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:10500129 G>A maps to NM_000480.2 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:10518397 G>A maps to NM_000480.2 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:10506365 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr7:38500903 G>A maps to NM_001635.3 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:38431534 C>T maps to NM_001635.3 E564E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:38500936 G>A maps to NM_001635.3 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:38433604 C>T maps to NM_001635.3 Q536Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:38429503 C>T maps to NM_001635.3 V627V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr7:38424483 G>A maps to NM_001635.3 Q675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:38433664 G>A maps to NM_001635.3 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:38433664 G>A maps to NM_001635.3 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr7:38574542 G>A maps to NM_001635.3 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:38431386 C>A maps to NM_001635.3 E614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:38424436 G>A maps to NM_001635.3 F690F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:71390639 C>T maps to NM_212557.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:71384526 A>G maps to NM_212557.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:104160223 G>A maps to NM_000699.2 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:104160211 G>A maps to NM_000699.2 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr1:104116493 G>A maps to NM_020978.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr7:2748314 G>A maps to NM_133463.1 W189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:2740288 G>A maps to NM_133463.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:2748706 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:2752418 G>A maps to NM_133463.1 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:2749362 G>A maps to NM_133463.1 E287E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr7:2752298 G>A maps to NM_133463.1 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr7:2740213 C>T maps to NM_133463.1 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:2752034 G>A maps to NM_133463.1 W340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:2740315 C>T maps to NM_133463.1 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:2740324 C>T maps to NM_133463.1 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:2752229 G>A maps to NM_133463.1 K405K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:66251902 C>T maps to NM_016627.4 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:112614444 C>T maps to NM_022662.2 E459E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr2:112582573 A>C maps to NM_022662.2 A927A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr2:112608457 T>G maps to NM_022662.2 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:112614390 C>T maps to NM_022662.2 K477K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:112620092 T>A maps to NM_022662.2 K379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr2:112622496 A>C maps to NM_022662.2 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:73983729 G>T maps to NM_173473.2 G20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:140075310 G>A maps to NM_013366.3 D513D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:140074635 G>A maps to NM_013366.3 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr9:140079371 G>A maps to NM_013366.3 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:140079371 G>A maps to NM_013366.3 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr9:140081952 G>A maps to NM_013366.3 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr4:25379078 C>T maps to ENST00000510092 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr4:25379078 C>T maps to ENST00000510092 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr4:25416219 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:25384967 G>A maps to ENST00000510092 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr4:25419868 C>T maps to ENST00000510092 A765A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:25379078 C>T maps to ENST00000510092 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr4:25379138 C>T maps to ENST00000510092 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:110812065 G>A maps to NM_016238.2 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr12:110841399 C>G maps to NM_016238.2 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr14:77269744 G>A maps to NM_015305.3 V529V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr14:77272971 T>C maps to NM_015305.3 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr14:77255600 G>A maps to NM_015305.3 A661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:77274303 G>A maps to NM_015305.3 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:213186678 C>T maps to NM_144567.3 W47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:213186684 A>G maps to NM_144567.3 C45C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:213178686 G>A maps to NM_144567.3 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:108264160 C>T maps to NM_001146.3 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:108334241 G>A maps to NM_001146.3 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr8:108264094 A>T maps to NM_001146.3 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr8:108334268 G>A maps to NM_001146.3 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr8:108264236 C>T maps to NM_001146.3 W448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr8:108334193 G>A maps to NM_001146.3 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr8:108296968 C>T maps to NM_001146.3 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:108297010 C>T maps to NM_001146.3 Q368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:108276554 C>T maps to NM_001146.3 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:108306174 C>A maps to NM_001146.3 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:108306175 C>T maps to NM_001146.3 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:6420386 C>T maps to NM_001147.2 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr8:6378861 C>T maps to NM_001147.2 E212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr20:860422 C>T maps to NM_015985.2 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr20:896764 C>T maps to NM_015985.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:858802 C>T did not map to a codon.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr20:858862 G>A maps to NM_015985.2 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:861900 G>A maps to NM_015985.2 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr20:896617 C>T maps to NM_015985.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr20:854936 C>T maps to NM_015985.2 V447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:896686 C>T maps to NM_015985.2 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr20:861924 G>A maps to NM_015985.2 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:861885 C>T maps to NM_015985.2 E293E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr20:896674 G>A maps to NM_015985.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr20:870941 G>A maps to NM_015985.2 Q127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr20:896815 A>C maps to NM_015985.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:861885 C>T maps to NM_015985.2 E293E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:896617 C>T maps to NM_015985.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:178822869 C>T maps to NM_004673.3 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:178834188 C>T maps to NM_004673.3 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr1:178821884 C>T maps to NM_004673.3 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr9:129851286 G>A maps to NM_012098.2 F471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr9:129870845 G>A maps to NM_012098.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:8436236 C>T maps to NM_139314.1 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr19:8430911 G>A maps to NM_139314.1 E131E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:8436278 C>T maps to NM_139314.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:8436015 G>A maps to NM_139314.1 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:101773423 G>A maps to NM_178127.4 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr11:101762114 A>T maps to NM_178127.4 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:101771206 G>A maps to NM_178127.4 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:101776578 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:101762309 G>T maps to NM_178127.4 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:101762198 G>A maps to NM_178127.4 H326H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:101765652 C>T maps to NM_178127.4 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:101765750 G>A maps to NM_178127.4 Q236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:101777978 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr19:10204223 C>T maps to NM_031917.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:11254941 C>T maps to NM_021146.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:11253758 G>A maps to NM_021146.2 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr1:11253758 G>A maps to NM_021146.2 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:41547831 G>A maps to ENST00000415018 S1339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr8:41585482 C>T maps to ENST00000415018 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr8:41566301 C>T maps to ENST00000415018 G664G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr8:41591587 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr8:41519034 C>T maps to ENST00000415018 R1966R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:41550195 G>A maps to ENST00000415018 F1276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr8:41543691 G>A maps to ENST00000415018 I1456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr8:41615577 C>T maps to ENST00000415018 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr8:41552190 G>A maps to ENST00000415018 S1082S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr8:41525790 C>T maps to ENST00000415018 V1796V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr8:41655035 G>A maps to ENST00000415018 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr8:41584782 C>T maps to ENST00000415018 Q137Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr8:41550297 G>A maps to ENST00000415018 F1242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:41577277 C>T maps to ENST00000415018 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr8:41547810 C>T maps to ENST00000415018 A1346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr8:41561627 G>A maps to ENST00000415018 A742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:41542161 G>A maps to ENST00000415018 I1479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr8:41655041 C>A maps to ENST00000415018 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr8:41530398 G>A maps to ENST00000415018 S1523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr8:41530089 C>T maps to ENST00000415018 V1626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:41522529 G>A maps to NM_020478.4 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:41552764 G>A maps to ENST00000415018 S1015S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr8:41548012 G>A maps to ENST00000415018 N1321N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr8:41519067 C>T maps to ENST00000415018 G1955G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:41566301 C>T maps to ENST00000415018 G664G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr8:41522451 C>T maps to NM_020478.4 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr8:41525853 C>T maps to ENST00000415018 R1775R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr8:41555584 C>T maps to ENST00000415018 V871V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr8:41550336 C>T maps to ENST00000415018 L1229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr8:41572528 G>A maps to ENST00000415018 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:41519016 C>T maps to ENST00000415018 V1972V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:41525799 G>A maps to ENST00000415018 F1793F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:41542136 G>A maps to ENST00000415018 R1488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:41545672 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:41550201 C>T maps to ENST00000415018 E1274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:41559077 C>T maps to ENST00000415018 S817S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:41582039 G>A maps to ENST00000415018 H215H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr8:41577322 G>A maps to ENST00000415018 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr8:41566358 C>T maps to ENST00000415018 E645E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:41566372 G>A maps to ENST00000415018 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:41566469 G>A maps to ENST00000415018 I608I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr4:114275701 C>T maps to NM_001148.4 S1976S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr4:114290801 C>T maps to NM_001148.4 S3817S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:114275900 C>T maps to NM_001148.4 Q2043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr4:114284611 G>A maps to NM_001148.4 G3625G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:114279694 G>A maps to NM_001148.4 R3307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:114208807 T>C maps to NM_001148.4 N709N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr4:114294454 C>T maps to NM_001148.4 I3903I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:114179524 C>T maps to NM_001148.4 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr4:114277366 A>G maps to NM_001148.4 S2531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:114277267 C>T maps to NM_001148.4 L2498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr4:114288884 G>A maps to NM_001148.4 E3732E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:114214639 C>T maps to NM_001148.4 I807I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:114275533 G>A maps to NM_001148.4 G1920G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr4:114161655 T>C maps to NM_001148.4 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:114120262 C>T maps to NM_001148.4 Q128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:114267165 G>A maps to NM_001148.4 P1453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:114276619 C>T maps to NM_001148.4 T2282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:114277054 C>T maps to NM_001148.4 D2427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:114277282 C>T maps to NM_001148.4 A2503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:114277762 C>T maps to NM_001148.4 S2663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:114279871 C>T maps to NM_001148.4 T3366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr4:114286225 C>T maps to NM_001148.4 I3640I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:114286204 C>T maps to NM_001148.4 L3633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr4:114170963 C>T maps to NM_001148.4 D312D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr10:61959949 G>A maps to NM_020987.2 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:61831287 G>A maps to NM_020987.2 I3117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr10:61802490 C>T maps to NM_020987.2 T4364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr10:61829547 G>A maps to NM_020987.2 S3697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr10:61932896 C>T maps to NM_020987.2 K744K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr10:61829988 C>T maps to NM_020987.2 G3550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr10:61830237 G>A maps to NM_020987.2 I3467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr10:61829427 G>A maps to NM_020987.2 G3737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr10:61958256 C>T maps to NM_020987.2 G510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr10:61830329 G>A maps to NM_020987.2 Q3437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr10:61831011 C>T maps to NM_020987.2 E3209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr10:61832292 T>C maps to NM_020987.2 K2782K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:61834251 G>A maps to NM_020987.2 G2129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:61834566 G>A maps to NM_020987.2 S2024S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr10:61831218 T>C maps to NM_020987.2 Q3140Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr10:61941145 G>A maps to NM_020987.2 R709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:61802490 C>T maps to NM_020987.2 T4364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:61802490 C>T maps to NM_020987.2 T4364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:61898738 G>A maps to NM_020987.2 L907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:61819669 G>A maps to ENST00000503366 I1618I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:61833786 C>T maps to NM_020987.2 R2284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:61833980 G>A maps to NM_020987.2 Q2220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:61834218 G>A maps to NM_020987.2 A2140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:61894073 C>T maps to NM_020987.2 R932R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:61832646 C>T maps to NM_020987.2 E2664E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:61932884 G>A maps to NM_020987.2 F748F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:61946556 G>A maps to NM_020987.2 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr10:61894131 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:62023646 C>T maps to NM_020987.2 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:61835055 C>T maps to NM_020987.2 T1861T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr10:61846546 G>A maps to NM_020987.2 F1212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr10:61955958 G>A maps to NM_020987.2 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr10:61834848 T>C maps to NM_020987.2 Q1930Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr10:61830300 C>T maps to NM_020987.2 W3446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr10:61846615 C>T maps to NM_020987.2 V1189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr10:61956323 G>A maps to NM_020987.2 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr10:61830990 G>A maps to NM_020987.2 T3216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr10:61832808 C>T maps to NM_020987.2 E2610E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:61829135 G>A maps to NM_020987.2 L3835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:61833993 C>T maps to NM_020987.2 K2215K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr10:61819110 G>A maps to NM_020987.2 R4225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr10:61834905 G>A maps to NM_020987.2 D1911D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr10:61831845 C>T maps to NM_020987.2 R2931R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:61828893 C>T maps to NM_020987.2 V3915V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr10:61802496 C>T maps to NM_020987.2 V4362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr10:61834620 C>T maps to NM_020987.2 A2006A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:61946493 C>T maps to NM_020987.2 A688A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:61835031 G>A maps to NM_020987.2 F1869F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:61932884 G>A maps to NM_020987.2 F748F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:62149191 C>T maps to NM_020987.2 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:61847918 G>A maps to NM_020987.2 R1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:62023727 G>A maps to NM_020987.2 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:61994535 G>A maps to NM_020987.2 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr10:61932689 G>A maps to NM_020987.2 Q784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr10:61835985 G>A maps to NM_020987.2 S1551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr10:61835610 C>T maps to NM_020987.2 K1676K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr10:61946487 C>T maps to NM_020987.2 V690V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr10:62029978 G>A maps to NM_020987.2 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr10:61830336 G>A maps to NM_020987.2 L3434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr10:61828506 A>C maps to NM_020987.2 G4044G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:61819110 G>A maps to NM_020987.2 R4225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:61898771 G>A maps to NM_020987.2 S896S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr10:61802490 C>T maps to NM_020987.2 T4364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr10:61831287 G>A maps to NM_020987.2 I3117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:61973198 G>A maps to NM_020987.2 R323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr10:61830300 C>T maps to NM_020987.2 W3446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr10:61847957 G>A maps to NM_020987.2 Q1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr10:61946646 G>A maps to NM_020987.2 I637I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:61802490 C>T maps to NM_020987.2 T4364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:61828485 C>T maps to NM_020987.2 T4051T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:61829394 C>T maps to NM_020987.2 V3748V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:61831245 G>A maps to NM_020987.2 T3131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:61831428 G>A maps to NM_020987.2 P3070P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:61831799 G>A maps to NM_020987.2 Q2947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:61832379 C>T maps to NM_020987.2 E2753E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:61832613 C>T maps to NM_020987.2 K2675K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:61833792 G>A maps to NM_020987.2 S2282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:61835771 G>A maps to NM_020987.2 R1623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:61844940 G>A maps to NM_020987.2 V1273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:61848063 C>T maps to NM_020987.2 T1127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:61848090 C>T maps to NM_020987.2 G1118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:61865749 G>A maps to NM_020987.2 R1081*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-FW-A3R5-06A-11D-A23B-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:61932086 G>A maps to NM_020987.2 T819T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:61941140 C>T maps to NM_020987.2 V710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:61962828 G>A maps to NM_020987.2 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr10:61847988 T>C maps to NM_020987.2 G1152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:61830465 G>A maps to NM_020987.2 S3391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:61831035 G>C maps to NM_020987.2 P3201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr10:62039363 G>A maps to NM_020987.2 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:61829253 G>A maps to NM_020987.2 S3795S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:61832649 C>T maps to NM_020987.2 E2663E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr10:61832814 G>A maps to NM_020987.2 S2608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:61830696 G>A maps to NM_020987.2 V3314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr2:190585359 C>T maps to NM_144708.3 L828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr2:190608179 G>A maps to NM_144708.3 L1330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr2:190557144 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:190597927 C>T maps to NM_144708.3 V1132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:190569914 G>A maps to NM_144708.3 K625K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr15:65226364 C>T maps to NM_182703.3 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr15:65219161 C>T maps to NM_182703.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr15:65208099 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr15:65239694 C>T maps to NM_182703.3 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr17:54431342 C>T maps to NM_153228.2 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr17:54558058 T>C maps to NM_153228.2 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:54450049 C>T maps to NM_153228.2 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:54428270 C>T maps to NM_153228.2 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr17:54428270 C>T maps to NM_153228.2 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:54403596 C>T maps to NM_153228.2 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr17:54555015 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:54450166 C>T maps to NM_153228.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:54535276 C>T maps to NM_153228.2 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:54559793 C>T maps to NM_153228.2 A726A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr17:54431396 A>G maps to NM_153228.2 E200E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr17:54543925 C>T maps to NM_153228.2 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:4111377 C>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:14751285 C>T maps to NM_054027.4 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr5:14758693 T>C maps to NM_054027.4 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr5:14758612 G>A maps to NM_054027.4 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:14756008 G>A maps to NM_054027.4 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:14716860 T>C maps to NM_054027.4 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr5:14749295 A>G maps to NM_054027.4 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:14751204 G>A maps to NM_054027.4 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:14758636 C>T maps to NM_054027.4 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:14751234 C>G maps to NM_054027.4 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:14746011 C>T maps to NM_054027.4 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:14751222 C>T maps to NM_054027.4 K214K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:14758678 G>A maps to NM_054027.4 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:14871550 C>T maps to NM_054027.4 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr5:14756008 G>A maps to NM_054027.4 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:139909124 G>A maps to ENST00000253810 K2198K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:139838839 T>C maps to ENST00000253810 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:139876129 C>T maps to ENST00000253810 S757S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:139866625 C>T maps to ENST00000253810 A742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:139917121 C>T maps to ENST00000253810 V2409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:139893012 A>T maps to ENST00000253810 A1422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:139908731 C>T maps to ENST00000253810 S2067S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr5:139906028 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:91924315 C>T maps to NM_019004.1 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:91936883 G>T maps to NM_019004.1 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:92027170 C>T maps to NM_019004.1 Q844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:92025741 C>T maps to NM_019004.1 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:113270851 C>T maps to NM_178510.1 Q721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:113270694 G>A maps to NM_178510.1 Q668Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:113264442 C>T maps to NM_178510.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:113268024 G>A maps to NM_178510.1 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:113265675 G>A maps to NM_178510.1 W169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:113265694 G>A maps to NM_178510.1 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:113270601 G>A maps to NM_178510.1 G637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr19:17394646 C>T maps to NM_152363.4 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:17397297 C>T maps to NM_152363.4 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:17397288 C>T maps to NM_152363.4 H592H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:17396326 C>T maps to NM_152363.4 G488G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr19:17393731 C>T maps to NM_152363.4 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:17394121 C>T maps to NM_152363.4 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:17394160 C>T maps to NM_152363.4 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:133306680 G>A maps to NM_015114.1 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:133313583 G>A maps to NM_015114.1 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr2:241448821 G>A maps to ENST00000401804 N779N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:241439871 G>A maps to ENST00000401804 F879F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:241463579 G>A maps to ENST00000401804 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:241463768 G>A maps to ENST00000401804 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:241492399 G>A maps to ENST00000401804 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:241421664 G>A maps to ENST00000401804 P940P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr2:241463383 A>G maps to ENST00000401804 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:241494456 G>A maps to ENST00000401804 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr10:92678944 C>T maps to NM_014391.2 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:92675308 G>A maps to NM_014391.2 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:92675337 G>A maps to NM_014391.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr10:92679961 C>T maps to NM_014391.2 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr13:111532019 G>A maps to NM_017664.2 A409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr16:89350630 G>A maps to NM_013275.4 P773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:89346523 G>A maps to NM_013275.4 P2142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:89357213 G>A maps to NM_013275.4 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:89347873 G>A maps to NM_013275.4 S1692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr16:89349763 G>T maps to NM_013275.4 T1062T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr16:89349480 C>A maps to NM_013275.4 E1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr16:89347447 G>A maps to NM_013275.4 P1834P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr16:89348233 G>A maps to NM_013275.4 L1572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:89351404 G>A maps to NM_013275.4 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:89347330 G>A maps to NM_013275.4 V1873V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:89351409 G>A maps to NM_013275.4 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr16:89348011 G>A maps to NM_013275.4 D1646D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr16:89357036 G>A maps to NM_013275.4 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:9255103 C>T maps to NM_015208.3 H613H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr18:9211729 A>G maps to NM_015208.3 Q200Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr18:9258619 G>T maps to NM_015208.3 R1785R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr18:9208709 C>T maps to NM_015208.3 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr18:9275538 C>T maps to NM_015208.3 S1927S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr18:9257665 C>T maps to NM_015208.3 S1467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr18:9257233 C>T maps to NM_015208.3 F1323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr18:9255100 C>T maps to NM_015208.3 F612F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr18:9258457 C>T maps to NM_015208.3 I1731I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:110450984 A>G maps to NM_033121.1 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:110463605 G>A maps to NM_033121.1 E287E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr1:70819824 G>A maps to NM_030816.4 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:67069776 C>T maps to NM_207354.2 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr11:67059549 A>T maps to NM_207354.2 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:67067322 C>T maps to NM_207354.2 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr10:5925961 G>A maps to NM_001009941.2 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr10:5922266 G>A maps to NM_001009941.2 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr10:5920176 A>T maps to NM_001009941.2 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr4:73956801 G>A maps to NM_032217.3 P2181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr4:74005788 G>A maps to NM_032217.3 I848I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:73944491 G>A maps to NM_032217.3 V2425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr4:73942767 G>A maps to NM_032217.3 I2547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:73942656 C>G maps to NM_032217.3 T2584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr10:99332523 C>T maps to NM_020349.2 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:99338082 G>A maps to NM_020349.2 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr10:99343349 G>A maps to NM_020349.2 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:99337562 C>T maps to NM_020349.2 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:69424031 C>T maps to NM_001098805.1 F776F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr9:69420402 G>A maps to NM_001098805.1 K431K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr9:69424031 C>T maps to NM_001098805.1 F776F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr10:90582745 C>T maps to NM_144590.2 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:90585809 A>G maps to NM_144590.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr10:90582775 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:90582745 C>T maps to NM_144590.2 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr10:90582745 C>T maps to NM_144590.2 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr10:90583081 G>A maps to NM_144590.2 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:90591669 G>A maps to NM_144590.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:90588375 G>A maps to NM_144590.2 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr19:4222680 C>T maps to ENST00000262970 S1152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:4219742 G>A maps to ENST00000262970 E1143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:4224188 G>A maps to ENST00000262970 Q1211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:4222713 G>A maps to ENST00000262970 K1163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:4210287 C>T maps to ENST00000262970 I416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:4217163 C>T maps to ENST00000262970 T759T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:4222755 C>T maps to ENST00000262970 L1177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:4216989 C>T maps to ENST00000262970 T701T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr10:27335336 G>A maps to NM_014915.2 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:27389210 G>A maps to NM_014915.2 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:27375501 C>T maps to NM_014915.2 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr10:27324072 G>A maps to NM_014915.2 S1102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:33098693 G>T maps to NM_032139.2 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:33130264 G>A maps to NM_032139.2 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:33119635 G>A maps to NM_032139.2 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:33135274 G>A maps to NM_032139.2 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:33135353 G>A maps to NM_032139.2 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr3:15711866 G>A maps to NM_015199.3 S1024S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr18:21218860 G>A maps to NM_173505.2 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr18:21229139 G>A maps to NM_173505.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr18:21181251 G>A maps to NM_173505.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr10:37508263 C>T maps to ENST00000374660 D1271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr10:37430973 C>T maps to ENST00000374660 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr10:37451750 G>A maps to ENST00000374660 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr10:37431075 C>T maps to ENST00000374660 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr10:37508365 G>A maps to ENST00000374660 T1305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr10:37442556 A>T maps to ENST00000374660 K533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr10:37508600 C>T maps to ENST00000374660 Q1384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr10:37433983 G>A maps to ENST00000374660 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr10:37508413 G>A maps to ENST00000374660 R1321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr10:37490167 C>T maps to ENST00000374660 L991L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:37430748 C>T maps to ENST00000374660 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr10:37506718 G>A maps to ENST00000374660 R1123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr10:37418872 C>T maps to ENST00000374660 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:37438751 G>A maps to ENST00000374660 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:37508413 G>A maps to ENST00000374660 R1321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:37478486 T>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:37505241 G>A maps to ENST00000374660 K1064K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr10:37421199 G>A maps to ENST00000374660 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:37438606 G>A maps to ENST00000374660 K468K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:37508086 C>T maps to ENST00000374660 T1212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:37508795 C>T maps to ENST00000374660 Q1449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:37442522 G>A maps to ENST00000374660 Q521Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:37486385 G>A maps to ENST00000374660 K961K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr10:37430898 T>G maps to ENST00000374660 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr10:37508192 A>T maps to ENST00000374660 K1248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr10:37430982 G>A maps to ENST00000374660 E330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr10:37505220 G>A maps to ENST00000374660 K1057K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr10:37430967 G>A maps to ENST00000374660 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr10:37508002 G>A maps to ENST00000374660 L1184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:37430973 C>T maps to ENST00000374660 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr10:37447440 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:37436351 C>T maps to ENST00000374660 Q448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:37490161 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:37508413 G>A maps to ENST00000374660 R1321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:37430874 C>T maps to ENST00000374660 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:37508065 G>A maps to ENST00000374660 K1205K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr10:37508413 G>A maps to ENST00000374660 R1321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr10:37419197 C>T maps to ENST00000374660 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr10:37506703 C>T maps to ENST00000374660 I1118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr10:37438603 C>T maps to ENST00000374660 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr10:37454073 G>A maps to ENST00000374660 W629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr10:37451601 C>T maps to ENST00000374660 F586F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr10:37508650 A>G maps to ENST00000374660 L1400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr10:37507987 G>A maps to ENST00000374660 L1179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr10:37436375 G>T maps to ENST00000374660 E456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr10:37506733 G>A maps to ENST00000374660 V1128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:37508426 C>T maps to ENST00000374660 L1326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:37436308 G>A maps to ENST00000374660 E433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr10:37419275 C>T maps to ENST00000374660 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr10:37430842 C>T maps to ENST00000374660 Q284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr10:37505241 G>A maps to ENST00000374660 K1064K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:37430805 G>A maps to ENST00000374660 E271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:37433932 C>T maps to ENST00000374660 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:37441018 G>A maps to ENST00000374660 K503K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:37447488 G>A maps to ENST00000374660 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:37451768 G>A maps to ENST00000374660 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:37486340 C>T maps to ENST00000374660 A946A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:37505220 G>A maps to ENST00000374660 K1057K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:37506751 G>A maps to ENST00000374660 Q1134Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:37508119 G>A maps to ENST00000374660 R1223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:37430874 C>T maps to ENST00000374660 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:37433932 C>T maps to ENST00000374660 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:37451750 G>A maps to ENST00000374660 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:37486385 G>A maps to ENST00000374660 K961K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr10:37454061 A>G maps to ENST00000374660 E625E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr10:37440997 C>T maps to ENST00000374660 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr18:14850211 G>T did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr18:14851566 G>A maps to NM_001145029.1 K1089K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr18:14796355 G>A maps to NM_001145029.1 R623R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:14851620 G>A maps to NM_001145029.1 V1107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr18:14752678 G>A maps to NM_001145029.1 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr18:14763874 G>A maps to NM_001145029.1 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr18:14763874 G>A maps to NM_001145029.1 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr18:14848842 C>T maps to NM_001145029.1 Q985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr18:14763874 G>A maps to NM_001145029.1 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:14752663 G>A maps to NM_001145029.1 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:14791398 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:14852239 C>T maps to NM_001145029.1 R1314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr18:14763883 G>A maps to NM_001145029.1 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr12:52282491 C>T maps to NM_182608.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:52282026 G>A maps to NM_182608.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:52284411 C>T maps to NM_182608.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:52284812 G>A maps to NM_182608.3 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:52283228 G>A maps to NM_182608.3 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:52284386 G>A maps to NM_182608.3 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:52284410 C>T maps to NM_182608.3 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:52284536 C>T maps to NM_182608.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:52284752 C>T maps to NM_182608.3 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr12:52282014 G>A maps to NM_182608.3 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr1:145474053 C>G maps to NM_001039888.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr5:79855004 G>A maps to NM_001004441.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr5:79855778 C>T maps to NM_001004441.2 Q20Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr5:79854511 G>A maps to NM_001004441.2 Q443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:79855154 G>A maps to NM_001004441.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:79854698 G>A maps to NM_001004441.2 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:145561655 G>A maps to NM_144698.3 G448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:145562033 C>T maps to NM_144698.3 A574A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:145561547 C>T maps to NM_144698.3 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:145561346 G>A maps to NM_144698.3 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:145555774 C>T maps to NM_144698.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:145561250 G>A maps to NM_144698.3 E313E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:145560239 G>A maps to NM_144698.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:145560116 G>A maps to NM_144698.3 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:145555702 G>A maps to NM_144698.3 W17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr1:145561323 C>T maps to NM_144698.3 R338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:145562486 C>T maps to NM_144698.3 S725S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:97862339 G>A maps to NM_001164315.1 Q854Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr2:97881265 C>T maps to NM_001164315.1 F1235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:97849223 G>A maps to NM_001164315.1 K622K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:97810276 C>T maps to NM_001164315.1 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr2:98165936 T>C maps to NM_025190.3 E474E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:98195376 C>T maps to NM_025190.3 E229E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:82936038 C>T maps to ENST00000260047 N507N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr5:132150809 G>T maps to NM_175873.4 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr2:197872648 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr2:197964577 C>T maps to NM_001195144.1 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr2:197990617 G>A maps to NM_001195144.1 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:198051773 G>A maps to NM_001195144.1 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:173596203 C>T maps to ENST00000367712 K213K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr1:173596224 C>T maps to ENST00000367712 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:173596224 C>T maps to ENST00000367712 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:173616141 G>A maps to ENST00000367712 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:173596224 C>T maps to ENST00000367712 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:173628332 G>A maps to ENST00000367712 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:173628281 C>T maps to ENST00000367712 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr1:173593968 C>T maps to ENST00000367712 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:173628410 C>T maps to ENST00000367712 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:173628476 G>A maps to ENST00000367712 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:173616057 G>A maps to ENST00000367712 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:101540167 G>A maps to NM_198401.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:94231317 C>T maps to NM_017704.2 R114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr11:94231574 C>T maps to NM_017704.2 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr20:10030293 C>T maps to NM_198798.1 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr20:10033911 A>T maps to NM_198798.1 K675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr20:10025098 C>T maps to NM_198798.1 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr20:10025187 C>T maps to NM_198798.1 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:10036271 G>A maps to NM_198798.1 E765E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr20:10036265 C>T maps to NM_198798.1 I763I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr20:10030779 G>A maps to NM_198798.1 K521K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr20:10030860 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr20:10023878 A>C maps to NM_198798.1 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr20:10019182 C>T maps to NM_198798.1 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr20:10030293 C>T maps to NM_198798.1 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr20:10035228 C>T maps to NM_198798.1 I718I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr20:10025187 C>T maps to NM_198798.1 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr20:10030639 G>T maps to NM_198798.1 E475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr20:10030497 G>A maps to NM_198798.1 G427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:10035156 G>A maps to NM_198798.1 K694K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr20:10023881 C>T maps to NM_198798.1 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr20:10036178 G>A maps to NM_198798.1 E734E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr4:125590849 A>G maps to NM_020337.2 T1194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr4:125593056 A>G maps to NM_020337.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:125592574 A>T maps to NM_020337.2 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr4:125591205 G>A maps to NM_020337.2 Q1076*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr4:125592976 G>A maps to NM_020337.2 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:125590234 G>A maps to NM_020337.2 S1399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr12:56639218 G>A maps to NM_173595.3 P782P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr12:56648424 G>A maps to NM_173595.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:56637081 G>A maps to NM_173595.3 D1025D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:56639293 G>A maps to NM_173595.3 P757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:71209715 G>A maps to NM_001115116.1 K264K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:55472047 C>T maps to NM_024669.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:55472068 C>T maps to NM_024669.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr5:55407473 C>T maps to NM_024669.2 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:55407154 G>A maps to NM_024669.2 R474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:77817706 C>T maps to NM_001029870.1 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:77816851 C>T maps to NM_001029870.1 G717G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:77816806 G>A maps to NM_001029870.1 F732F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr4:77816806 G>A maps to NM_001029870.1 F732F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr2:110373043 C>T maps to NM_023016.3 N326N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:118892653 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:118892683 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:90326360 G>A maps to ENST00000339746 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:117865009 G>A maps to ENST00000357099 K42K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:117876960 T>C maps to ENST00000357099 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr7:117865048 G>A maps to ENST00000357099 Q55Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr7:117864913 G>A maps to ENST00000357099 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr14:102973338 G>A maps to NM_152326.2 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr6:34937852 C>T maps to NM_015245.2 Y115Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:34950590 C>T maps to NM_015245.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:34985817 C>T maps to NM_015245.2 F664F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:34949601 C>T maps to NM_015245.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:34949645 C>T maps to NM_015245.2 H205H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:35048895 C>T maps to NM_015245.2 D890D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr6:34962098 G>A maps to NM_015245.2 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr12:100166804 C>T maps to NM_152788.3 K341K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr12:100200441 G>A maps to NM_152788.3 Q137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr12:99640265 C>T maps to NM_152788.3 E711E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr12:99145140 T>A maps to NM_152788.3 K1222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr12:99548137 A>G maps to NM_152788.3 L819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:99145162 G>A maps to NM_152788.3 P1214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:99548099 C>T maps to NM_152788.3 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:99201669 C>T maps to NM_181670.2 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr12:99837453 G>A maps to NM_152788.3 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr12:100166720 C>T maps to NM_152788.3 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr12:99640562 G>A maps to NM_152788.3 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:99145168 G>A maps to NM_152788.3 P1212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:99640631 G>A maps to NM_152788.3 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr16:4764058 C>T maps to NM_133450.2 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:4776691 G>A maps to NM_133450.2 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr16:4774807 G>C maps to NM_133450.2 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:21245186 G>A maps to NM_145865.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr16:21261291 G>A maps to NM_145865.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:21261429 C>T maps to NM_145865.2 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr16:21245097 C>T maps to NM_145865.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr9:101552821 C>T maps to ENST00000375018 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:101536358 G>A maps to ENST00000375018 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:101498824 G>A maps to ENST00000375018 A865A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:101546430 G>A maps to ENST00000375018 Q306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:220097913 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:220097336 C>T maps to NM_001042410.1 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:220098071 C>T maps to NM_001042410.1 Q246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:220098052 G>A maps to NM_001042410.1 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:220097336 C>T maps to NM_001042410.1 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:220099596 G>A maps to NM_001042410.1 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr7:36447419 T>C maps to NM_018685.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:36455449 C>A maps to NM_018685.2 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:36458934 C>T maps to NM_018685.2 V572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:36458935 C>T maps to NM_018685.2 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:36478868 G>A maps to NM_018685.2 V980V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:36483365 C>T maps to NM_018685.2 T991T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:36478814 C>T maps to NM_018685.2 V962V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr7:36450165 T>C maps to NM_018685.2 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr11:70007286 C>T maps to NM_018043.5 I533I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:69972295 C>T maps to NM_018043.5 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr11:70026113 C>T maps to NM_018043.5 I785I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:69934153 C>T maps to NM_018043.5 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:69972232 C>A maps to NM_018043.5 I343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:69951857 G>A maps to NM_018043.5 K237K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:70031743 C>T maps to NM_018043.5 I879I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr11:70007743 G>A maps to NM_018043.5 E599E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr11:69933964 G>A maps to NM_018043.5 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:70007352 C>T maps to NM_018043.5 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:69978114 C>T maps to NM_018043.5 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:70007779 C>T maps to NM_018043.5 F611F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:70007794 G>A maps to NM_018043.5 V616V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:70017032 C>T maps to NM_018043.5 F746F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:70017059 G>A maps to NM_018043.5 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:70031746 C>T maps to NM_018043.5 S880S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:69972244 C>T maps to NM_018043.5 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr3:43602867 G>A maps to NM_018075.3 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr3:43618397 C>T maps to NM_018075.3 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr3:43591316 A>G maps to NM_018075.3 V564V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr3:43618706 T>G maps to NM_018075.3 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:43618493 G>A maps to NM_018075.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:5687532 G>A maps to ENST00000356134 I796I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:5915238 C>T maps to ENST00000356134 E320E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:5915235 G>A maps to ENST00000356134 D321D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:5848554 G>A maps to ENST00000356134 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr12:5685009 G>A maps to ENST00000356134 Q872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr12:5687592 G>A maps to ENST00000356134 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:5841769 G>A maps to ENST00000356134 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr12:6030304 C>T maps to ENST00000356134 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:5860069 G>A maps to ENST00000356134 I371I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:5744480 C>T maps to ENST00000356134 V552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr12:5687640 G>A maps to ENST00000356134 P760P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr12:5756940 C>T maps to ENST00000356134 K525K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:5685148 G>A maps to ENST00000356134 I825I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:5860132 C>T maps to ENST00000356134 K350K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr12:5708725 C>T maps to ENST00000356134 S720S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr12:5708725 C>T maps to ENST00000356134 S720S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr12:5841762 G>A maps to ENST00000356134 R491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr12:5939636 C>T maps to ENST00000356134 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:5848554 G>A maps to ENST00000356134 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:5756931 G>A maps to ENST00000356134 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:5672725 C>T maps to ENST00000356134 V913V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:5841762 G>A maps to ENST00000356134 R491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:5939612 G>A maps to ENST00000356134 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:5963214 G>T maps to ENST00000356134 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:5685148 G>A maps to ENST00000356134 I825I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:5756943 C>T maps to ENST00000356134 W524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:5687655 G>A maps to ENST00000356134 F755F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr12:5939645 G>A maps to ENST00000356134 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr12:6030364 G>A maps to ENST00000356134 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr12:6030385 G>A maps to ENST00000356134 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:5848554 G>A maps to ENST00000356134 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr12:6030385 G>A maps to ENST00000356134 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:5848554 G>A maps to ENST00000356134 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:5724455 C>T maps to ENST00000356134 P609P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:5744378 G>A maps to ENST00000356134 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6030490 C>T maps to ENST00000356134 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:5744378 G>A maps to ENST00000356134 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:5722087 G>A maps to ENST00000356134 F656F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr12:5708725 C>T maps to ENST00000356134 S720S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr12:5744372 G>A maps to ENST00000356134 V588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr12:5941717 G>A maps to ENST00000356134 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:26656578 A>T maps to NM_031418.2 K669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:26664813 C>T maps to NM_031418.2 I787I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr11:26655832 C>T maps to NM_031418.2 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:26677681 G>T maps to NM_031418.2 G863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:26681951 G>A maps to NM_031418.2 R969R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:26620541 C>T maps to NM_031418.2 F556F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:26463552 T>C maps to NM_031418.2 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:26463525 C>T maps to NM_031418.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr11:26655802 C>T maps to NM_031418.2 F642F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:26655808 C>T maps to NM_031418.2 F644F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:26655802 C>T maps to NM_031418.2 F642F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:26681984 G>A maps to NM_031418.2 W980*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:26552784 G>A maps to NM_031418.2 W257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr12:101490386 G>A maps to ENST00000392977 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:101436177 C>T maps to ENST00000392977 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:101514366 C>T maps to ENST00000392977 V880V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:101480469 C>T maps to ENST00000392977 I523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:101520808 G>A maps to ENST00000392977 R943R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:101381319 C>T maps to ENST00000392977 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:101413817 C>T maps to ENST00000392977 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:101433755 C>T maps to ENST00000392977 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:101488062 G>A maps to ENST00000392977 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr12:101505386 C>T maps to ENST00000392977 I783I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:101333181 C>T maps to ENST00000392977 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:101436174 C>T maps to ENST00000392977 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr12:101488032 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:101520719 A>C maps to ENST00000392977 R914R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:101493364 G>A maps to ENST00000392977 Q672Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:101368622 G>A maps to ENST00000392977 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:101520725 C>T maps to ENST00000392977 R916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr12:101505377 C>T maps to ENST00000392977 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr12:101510496 C>T maps to ENST00000392977 R831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr12:101490416 C>T maps to ENST00000392977 F614F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:101480448 G>A maps to ENST00000392977 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:101488062 G>A maps to ENST00000392977 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:101493478 C>T maps to ENST00000392977 F710F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:101510474 G>A maps to ENST00000392977 V823V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:101510496 C>T maps to ENST00000392977 R831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:22257767 G>A maps to NM_213599.2 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:22301196 C>T maps to NM_213599.2 L876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:22301265 C>A maps to NM_213599.2 V899V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:22276937 G>A maps to NM_213599.2 W401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:22283727 C>T maps to NM_213599.2 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:22271782 G>A maps to NM_213599.2 K293K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:22242654 C>T maps to NM_213599.2 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:22283726 C>T maps to NM_213599.2 F561F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:22248888 C>T maps to NM_213599.2 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:22284556 G>A maps to NM_213599.2 Q622Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:22281075 C>T maps to NM_213599.2 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr11:22294507 A>T maps to NM_213599.2 G736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:22257815 C>T maps to NM_213599.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:22291882 C>T maps to NM_213599.2 R642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:45742407 C>T maps to NM_001142679.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:242155653 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr2:242142851 G>A maps to NM_001001891.3 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:242149040 C>T maps to NM_001001891.3 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:242151572 C>T maps to NM_001001891.3 F596F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr2:242151533 C>T maps to NM_001001891.3 F583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:242149040 C>T maps to NM_001001891.3 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:242149959 C>T maps to NM_001001891.3 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:242139640 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:17435526 T>C maps to NM_020959.2 S1110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:17434400 G>A maps to NM_020959.2 P1208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:430321 C>T maps to NM_001012302.2 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:428122 G>A maps to NM_001012302.2 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:428573 G>A maps to NM_001012302.2 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:420586 G>A maps to NM_001012302.2 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr11:433423 G>A maps to NM_001012302.2 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:69080188 C>A maps to NM_006305.3 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr12:48866515 C>T maps to NM_012404.2 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr12:48866488 G>A maps to NM_012404.2 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr12:48866515 C>T maps to NM_012404.2 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr15:90342540 G>A maps to NM_001150.2 I653I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr15:90349307 G>A maps to NM_001150.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr15:90349306 G>A maps to NM_001150.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:90335428 T>G maps to NM_001150.2 A830A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:90348320 G>A maps to NM_001150.2 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr15:90346520 G>A maps to NM_001150.2 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr15:90347173 G>A maps to NM_001150.2 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr15:90349754 C>T maps to NM_001150.2 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:90349784 G>A maps to NM_001150.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr15:90335398 G>A maps to NM_001150.2 I840I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr15:90328674 G>A maps to NM_001150.2 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:90340907 G>A maps to NM_001150.2 F685F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr15:90328729 C>T maps to NM_001150.2 L918L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr15:90335774 G>A maps to NM_001150.2 A756A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:69397420 G>A maps to NM_032208.2 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr2:69409719 C>T maps to NM_032208.2 F427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:69409764 C>T maps to NM_032208.2 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:69409767 C>T maps to NM_032208.2 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:69397402 C>T maps to NM_032208.2 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:69472589 C>T maps to NM_032208.2 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:69472544 C>T maps to NM_032208.2 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr4:80977167 C>A did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:80952846 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr10:46122250 C>T maps to NM_001128324.1 Q340Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:46159001 G>A maps to NM_001128324.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr4:169060730 G>A maps to NM_007193.3 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:169099069 G>A maps to NM_007193.3 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr4:169060655 G>A maps to NM_007193.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:169086396 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:81928874 T>C maps to NM_145869.1 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:81917755 G>A maps to NM_145869.1 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:124748069 C>T maps to NM_001003954.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr15:60646352 C>T maps to NM_001002858.2 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:60656651 G>A maps to NM_001002858.2 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr15:60653145 G>A maps to NM_001002858.2 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr4:79525460 C>T maps to NM_005139.2 R274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr4:79518494 C>T maps to NM_005139.2 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:122593727 G>A maps to NM_001154.3 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:150519720 C>T maps to NM_001155.4 K34K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr5:150518925 G>A maps to NM_001155.4 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr10:75143040 G>A maps to NM_004034.2 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr10:75135927 C>T maps to NM_004034.2 K464K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:150958815 C>T maps to NM_003568.2 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:150960768 C>T maps to NM_003568.2 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:150956526 C>T maps to NM_003568.2 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:150955860 C>T maps to NM_003568.2 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:150956827 C>T maps to NM_003568.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr7:36677508 C>T maps to NM_001177506.1 W133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr7:36552799 G>A maps to NM_001177506.1 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:36616195 C>T maps to NM_001177506.1 Q335Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr7:36570057 G>A maps to NM_001177506.1 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr7:36561713 C>T maps to NM_001177506.1 Q510Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:36580011 G>A maps to NM_001177506.1 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:36616229 C>T maps to NM_001177506.1 W324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:36726343 C>T maps to NM_001177506.1 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:36657924 T>A maps to NM_001177506.1 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr7:36552757 C>T maps to NM_001177506.1 K649K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:36677508 C>T maps to NM_001177506.1 W133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:36763690 G>A maps to NM_001177506.1 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr7:36552757 C>T maps to NM_001177506.1 K649K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr7:36588255 G>A maps to NM_001177506.1 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:36616206 T>G maps to NM_001177506.1 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:36580096 C>T maps to NM_001177506.1 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:36634027 G>A maps to NM_001177506.1 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr7:36763660 G>A maps to NM_001177506.1 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr7:36616229 C>T maps to NM_001177506.1 W324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:41001352 G>A maps to NM_009590.2 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:41001331 C>A maps to NM_009590.2 P606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr17:40997011 C>T maps to NM_009590.2 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr17:41002307 C>T maps to NM_009590.2 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:41002211 C>T maps to NM_009590.2 F706F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:40996858 C>G maps to NM_009590.2 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:40998145 C>T maps to NM_009590.2 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr17:41003656 G>A maps to NM_003734.2 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:41004742 C>T maps to NM_003734.2 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr17:41006660 C>T maps to NM_003734.2 H599H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr17:41004370 C>T maps to NM_003734.2 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:41004937 C>T maps to NM_003734.2 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr17:41004604 C>T maps to NM_003734.2 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:41006555 G>A maps to NM_003734.2 V564V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:41003626 C>T maps to NM_003734.2 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr17:41004295 C>T maps to NM_003734.2 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr17:41004592 G>A maps to NM_003734.2 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr17:41003773 G>A maps to NM_003734.2 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:41003707 G>A maps to NM_003734.2 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:201507520 G>A maps to NM_001159.3 E948E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr2:201507514 C>T maps to NM_001159.3 S946S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:201523928 C>T maps to NM_001159.3 H1071H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr2:201534341 C>T maps to NM_001159.3 F1281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:201460079 C>T maps to NM_001159.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:201501680 C>T maps to NM_001159.3 C798C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr2:201464441 C>T maps to NM_001159.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr2:201464353 C>T maps to NM_001159.3 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:201473809 C>T maps to NM_001159.3 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:201462152 C>T maps to NM_001159.3 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr2:201467037 C>T maps to NM_001159.3 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr2:201460034 C>T maps to NM_001159.3 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:201488606 C>T maps to NM_001159.3 V675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr2:201460031 A>T maps to NM_001159.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr2:201467061 C>T maps to NM_001159.3 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr22:29726638 G>A maps to NM_001127.3 Q862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr22:29745233 G>A maps to NM_001127.3 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr22:29750754 C>T maps to NM_001127.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr22:29727501 G>A maps to NM_001127.3 I820I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr22:29727459 G>A maps to NM_001127.3 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr22:29726375 G>T maps to NM_001127.3 P919P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr22:29759030 C>T maps to NM_001127.3 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:29752500 G>A maps to NM_001127.3 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:71807240 G>A maps to ENST00000423132 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr14:24036409 G>A maps to NM_003917.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr14:24033265 G>A maps to NM_003917.2 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr14:24033352 T>C maps to NM_003917.2 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:24035516 G>A maps to NM_003917.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr19:16337293 C>T maps to NM_001130524.1 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:16345233 C>T maps to NM_001130524.1 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr19:16318951 C>T maps to NM_001130524.1 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr19:16338470 C>T maps to NM_001130524.1 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NF-06A-11D-A19A-08 chr19:16345233 C>T maps to NM_001130524.1 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:16314425 C>T maps to NM_001130524.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:16344395 C>T maps to NM_001130524.1 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:10690439 G>A maps to ENST00000453102 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:10685606 G>A maps to ENST00000453102 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr19:10694661 C>A maps to ENST00000453102 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:10685645 C>T maps to ENST00000453102 E371E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:224642565 G>A maps to NM_001039569.1 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr19:50303022 C>T maps to NM_014203.2 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:50285960 C>T maps to NM_014203.2 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:50303355 C>T maps to NM_014203.2 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr11:984646 C>T maps to ENST00000332231 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:988673 C>T maps to ENST00000332231 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr11:993864 G>A maps to ENST00000332231 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:993823 C>T maps to ENST00000332231 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:1010582 C>T maps to ENST00000332231 A927A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:1009159 C>T maps to ENST00000332231 F828F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:1006570 C>T maps to ENST00000332231 F751F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr17:33984616 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr17:33951552 C>T maps to NM_001030006.1 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:33984728 C>T maps to NM_001030006.1 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:183899729 C>T maps to ENST00000411763 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:47342727 G>A maps to NM_004069.3 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr5:77334865 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:77385276 A>C maps to NM_003664.3 S839S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:77335071 C>T maps to NM_003664.3 T868T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr15:83333684 C>T maps to NM_004644.3 W661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr15:83346061 G>A maps to NM_004644.3 I484I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:83349687 G>A maps to NM_004644.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:83335592 G>A maps to NM_004644.3 I586I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr15:83349744 G>A maps to NM_004644.3 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:83334277 C>T maps to NM_004644.3 K634K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:83346865 C>T maps to NM_004644.3 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:83330663 G>A maps to NM_004644.3 R958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr15:83331463 G>A maps to NM_004644.3 Q920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr15:83345326 C>T maps to NM_004644.3 R517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr15:83332699 C>T maps to NM_004644.3 R744R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr15:83335673 C>T maps to NM_004644.3 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr15:83328415 G>A maps to NM_004644.3 L1049L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:2129388 G>A maps to ENST00000355272 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:2127178 G>A maps to ENST00000355272 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:2114267 C>T maps to ENST00000355272 Q819Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:2120979 G>A maps to ENST00000355272 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:2151281 G>A maps to ENST00000355272 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr19:2109957 C>T did not map to a codon.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr19:2115259 G>A maps to ENST00000355272 A769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr19:2115262 G>A maps to ENST00000355272 I768I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:75896459 G>A maps to NM_207012.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:42024822 C>T maps to NM_006803.3 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr8:42012426 C>T maps to NM_006803.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:42015559 C>T maps to NM_006803.3 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:115249168 C>T maps to NM_001284.2 N188N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr15:90378803 C>T maps to ENST00000398333 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr1:114442651 G>A maps to NM_006594.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:114437950 G>A maps to NM_006594.2 F652F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr1:114445306 G>A maps to NM_006594.2 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:114437755 C>T maps to NM_006594.2 T717T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr15:51221266 C>T maps to NM_007347.3 Q202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:51285608 G>A maps to NM_007347.3 G711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr15:51260512 G>A maps to NM_007347.3 Q635Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr15:51294750 G>A maps to NM_007347.3 L1102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr15:51293267 C>T maps to NM_007347.3 S1047S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:99700338 C>T maps to ENST00000429084 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:31535416 C>T maps to NM_007077.3 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr12:99126211 C>T maps to NM_181861.1 V1205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:99106140 T>C maps to NM_181861.1 A962A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr12:99053032 C>T maps to NM_181861.1 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr9:72064628 G>A maps to NM_001163.3 I684I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:72131526 C>T maps to NM_001163.3 E200E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr9:72131544 C>T maps to NM_001163.3 Q194Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr9:72067067 G>A maps to NM_001163.3 I646I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr9:72131835 G>A maps to NM_001163.3 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr9:72082852 G>A maps to NM_001163.3 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:72047481 G>A maps to NM_001163.3 I804I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:72055995 G>A maps to NM_001163.3 I739I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr9:72064562 G>A maps to NM_001163.3 I706I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr9:72055995 G>A maps to NM_001163.3 I739I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr9:72132045 G>A maps to NM_001163.3 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:72067052 C>T maps to NM_001163.3 S651S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr9:72064640 G>A maps to NM_001163.3 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:72071174 G>A maps to NM_001163.3 F592F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr9:72130977 C>T maps to NM_001163.3 Q383Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr15:29346944 C>T maps to NM_005503.3 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr15:29346533 C>T maps to NM_005503.3 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr15:29390742 C>T maps to NM_005503.3 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr15:29347004 C>T maps to NM_005503.3 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:29390736 C>T maps to NM_005503.3 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr15:29346356 C>T maps to NM_005503.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr19:3760156 G>A maps to NM_004886.3 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:3752967 G>A maps to NM_004886.3 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr19:3759740 G>A maps to NM_004886.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:6424401 G>A maps to ENST00000389906 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:6432346 G>A maps to ENST00000389906 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr10:26785231 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr10:26851354 G>A maps to NM_019043.3 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:26822438 G>A maps to NM_019043.3 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:26849065 C>T maps to NM_019043.3 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr10:26825082 G>A maps to NM_019043.3 W327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:26789787 C>T maps to NM_019043.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:26790012 A>G maps to NM_019043.3 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr10:26849068 G>A maps to NM_019043.3 K397K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr10:26849095 C>T maps to NM_019043.3 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:26800767 C>T maps to NM_019043.3 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:26800815 C>T maps to NM_019043.3 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:26781308 G>A maps to NM_019043.3 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:26802552 G>A maps to NM_019043.3 E259E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr4:40936677 T>C maps to NM_004307.1 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:40946956 G>A maps to NM_004307.1 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:41015684 G>A maps to NM_004307.1 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr4:40832535 G>A maps to NM_004307.1 R530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr4:40946980 C>T maps to NM_004307.1 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr4:41015684 G>A maps to NM_004307.1 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr4:40936493 G>A maps to NM_004307.1 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr4:40947068 G>T maps to NM_004307.1 S286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr5:139941689 C>T maps to ENST00000354402 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:139941204 G>A maps to ENST00000354402 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:139938379 G>A maps to ENST00000354402 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:139942060 G>A maps to ENST00000354402 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:112176282 C>T maps to NM_001127510.2 S1664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr5:112174606 G>T maps to NM_001127510.2 G1106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:112157647 T>G maps to NM_001127510.2 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:112175568 C>T maps to NM_001127510.2 S1426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:112178721 C>T maps to NM_001127510.2 S2477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr5:112179657 C>T maps to NM_001127510.2 S2789S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:112154985 C>T maps to NM_001127510.2 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr5:112176862 C>T maps to NM_001127510.2 R1858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:112178721 C>T maps to NM_001127510.2 S2477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:112175433 A>T maps to NM_001127510.2 P1381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr5:112174489 C>T maps to NM_001127510.2 Q1067*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr5:112174731 C>T maps to NM_001127510.2 Y1147Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr5:112175911 C>T maps to NM_001127510.2 Q1541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZG-06A-11D-A197-08 chr5:112173800 C>G maps to NM_001127510.2 S837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:112176168 C>T maps to NM_001127510.2 P1626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr19:1460849 C>T maps to NM_005883.2 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:1466296 T>A maps to NM_005883.2 Y999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:1453050 C>T maps to NM_005883.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:1465735 G>A maps to NM_005883.2 Q812Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr18:10471952 C>T maps to ENST00000423585 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:10471727 C>T maps to ENST00000423585 H199H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr20:57036199 G>A maps to NM_153360.1 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:57036094 G>A maps to NM_153360.1 D419D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr20:57042500 G>A maps to NM_153360.1 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:57035977 C>T maps to NM_153360.1 E458E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:159558146 C>T maps to NM_001639.3 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:159558416 C>T maps to NM_001639.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:159558227 G>A maps to NM_001639.3 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr1:159557900 G>A maps to NM_001639.3 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:159558179 G>A maps to NM_001639.3 E118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:159558476 C>T maps to NM_001639.3 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:159558470 C>T maps to NM_001639.3 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:159558293 G>A maps to NM_001639.3 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:159558341 G>A maps to NM_001639.3 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:49714100 C>T maps to ENST00000438011 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr3:49713213 C>T maps to ENST00000438011 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:49718604 C>T maps to ENST00000438011 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr3:49713331 G>A maps to ENST00000438011 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr3:49712679 C>T maps to ENST00000438011 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:55028766 G>A did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:55028745 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:43348115 C>T maps to NM_001142930.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:43342979 C>T maps to NM_001142930.1 N115N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:34909907 C>T maps to NM_015957.2 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:34916657 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:10500418 C>T maps to NM_198544.3 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:57004259 C>T maps to NM_005161.4 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr11:57003830 G>A maps to NM_005161.4 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr11:57003473 G>A maps to NM_005161.4 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr11:57003515 G>A maps to NM_005161.4 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:57003998 C>T maps to NM_005161.4 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:57003371 G>A maps to NM_005161.4 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:57003638 G>A maps to NM_005161.4 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:57003809 G>A maps to NM_005161.4 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:57003965 C>T maps to NM_005161.4 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:57003728 G>A maps to NM_005161.4 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr19:36365500 C>T maps to NM_001024807.1 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr19:36364606 C>T maps to NM_001024807.1 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr19:36369835 G>A maps to NM_001024807.1 E565E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:36370324 C>T maps to NM_001024807.1 F646F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:36364554 G>A maps to NM_001024807.1 W332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr19:36368999 C>T maps to NM_001024807.1 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:36365768 C>T maps to NM_001024807.1 Q448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr19:36362521 C>T maps to NM_001024807.1 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:36370055 C>T maps to NM_001024807.1 V598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr11:130005575 C>T maps to NM_001642.2 P601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr11:130013309 C>T maps to NM_001642.2 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:129999952 C>T maps to NM_001642.2 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:130011451 C>T maps to NM_001642.2 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:130011962 C>T maps to NM_001642.2 I728I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:130011905 C>T maps to NM_001642.2 I709I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:116707760 G>A maps to NM_000039.1 D52D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:116706541 C>T maps to NM_000039.1 K262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:156563764 C>T maps to ENST00000446584 T270T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D9-A3Z1-06A-11D-A23B-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:161193179 G>A maps to NM_001643.1 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:116691666 G>A maps to NM_000482.3 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr11:116691696 C>T maps to NM_000482.3 K359K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:116692125 C>T maps to NM_000482.3 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:116692203 G>A maps to NM_000482.3 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr11:116661593 C>A maps to NM_052968.4 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:116661392 G>A maps to NM_052968.4 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:116661635 C>T maps to NM_052968.4 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:21228807 G>A maps to NM_000384.2 F3644F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:21235059 G>A maps to NM_000384.2 S1560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr2:21247900 C>T maps to NM_000384.2 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:21230000 G>A maps to NM_000384.2 Q3247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:21229047 C>T maps to NM_000384.2 E3564E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:21236263 G>A maps to NM_000384.2 F1328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr2:21225555 G>A maps to NM_000384.2 F4246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:21230953 C>T maps to NM_000384.2 W2929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr2:21258487 C>T maps to NM_000384.2 K262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:21228840 C>T maps to NM_000384.2 W3633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:21225030 G>A maps to NM_000384.2 F4421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:21229593 C>T maps to NM_000384.2 E3382E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:21225801 G>A maps to NM_000384.2 F4164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:21260127 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr2:21229485 C>T maps to NM_000384.2 T3418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:21230372 G>A maps to NM_000384.2 L3123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:21230952 C>T maps to NM_000384.2 W2929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:21233505 T>C maps to NM_000384.2 Q2078Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:21230211 C>T maps to NM_000384.2 Q3176Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:21231942 G>A maps to NM_000384.2 A2599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:21225915 G>A maps to NM_000384.2 I4126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:21229419 G>A maps to NM_000384.2 F3440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:21228677 G>A maps to NM_000384.2 L3688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:21236095 G>A maps to NM_000384.2 S1384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:21249785 C>T maps to NM_000384.2 G706G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr2:21245743 G>A maps to NM_000384.2 I925I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:21225678 C>T maps to NM_000384.2 P4205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:21231903 G>A maps to NM_000384.2 F2612F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:21250806 T>A maps to NM_000384.2 K654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr2:21225675 C>T maps to NM_000384.2 G4206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr2:21235179 C>T maps to NM_000384.2 L1520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:21228678 G>A maps to NM_000384.2 F3687F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr2:21235347 C>T maps to NM_000384.2 Q1464Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:21230774 G>A maps to NM_000384.2 Q2989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:21230372 G>A maps to NM_000384.2 L3123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:21232289 G>A maps to NM_000384.2 L2484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:21238061 G>A maps to NM_000384.2 F1193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:21239330 G>A maps to NM_000384.2 V1104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:21225519 C>T maps to NM_000384.2 R4258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:21232761 C>T maps to NM_000384.2 G2326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:21234636 C>T maps to NM_000384.2 G1701G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:21234801 C>T maps to NM_000384.2 R1646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:21237348 G>A maps to NM_000384.2 F1271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:21260886 G>A maps to NM_000384.2 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:21233994 C>T maps to NM_000384.2 G1915G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:21227979 G>T maps to NM_000384.2 T3920T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:21233796 C>T maps to NM_000384.2 W1981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:21231267 C>T maps to NM_000384.2 L2824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:21255323 G>A maps to NM_000384.2 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:21231342 G>A maps to NM_000384.2 S2799S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:21234303 C>T maps to NM_000384.2 G1812G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:21226083 C>T maps to NM_000384.2 L4070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:21230628 A>T maps to NM_000384.2 L3037L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:21236167 C>T maps to NM_000384.2 T1360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr2:21229890 G>A maps to NM_000384.2 F3283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr2:21236326 G>T maps to NM_000384.2 S1307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr2:21229056 G>A maps to NM_000384.2 S3561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr2:21229305 G>A maps to NM_000384.2 D3478D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr2:21229950 G>A maps to NM_000384.2 F3263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr2:21228171 G>A maps to NM_000384.2 I3856I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr2:21247972 G>A maps to NM_000384.2 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr2:21232959 G>A maps to NM_000384.2 I2260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:21224982 T>G maps to NM_000384.2 S4437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:21236263 G>A maps to NM_000384.2 F1328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr2:21231816 G>A maps to NM_000384.2 I2641I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr2:21232370 G>A maps to NM_000384.2 L2457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:21227218 G>A maps to NM_000384.2 S4003S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:21228549 G>A maps to NM_000384.2 F3730F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:21230007 C>T maps to NM_000384.2 R3244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:21230571 C>T maps to NM_000384.2 L3056L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:21231372 G>A maps to NM_000384.2 I2789I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:21231576 G>A maps to NM_000384.2 F2721F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:21234549 C>T maps to NM_000384.2 K1730K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:21234768 C>T maps to NM_000384.2 T1657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:21235110 G>A maps to NM_000384.2 S1543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:21235485 G>A maps to NM_000384.2 F1418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:21245914 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:21249713 G>A maps to NM_000384.2 V730V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:21251344 G>A maps to NM_000384.2 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:21252799 C>T maps to NM_000384.2 G480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:21265244 C>T maps to NM_000384.2 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:21229844 G>A maps to NM_000384.2 L3299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:21234336 C>T maps to NM_000384.2 L1801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:21236259 G>A maps to NM_000384.2 L1330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:21247840 C>T maps to NM_000384.2 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:21252852 G>A maps to NM_000384.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:21265250 G>A maps to NM_000384.2 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr2:21235017 G>A maps to NM_000384.2 T1574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:21230013 G>A maps to NM_000384.2 L3242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:21234336 C>T maps to NM_000384.2 L1801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:21231651 C>T maps to NM_000384.2 L2696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr16:28506010 C>T maps to NM_018690.2 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:28507750 A>T maps to NM_018690.2 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:28507729 G>A maps to NM_018690.2 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr16:28508737 G>A maps to NM_018690.2 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr16:28507567 T>C maps to NM_018690.2 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr16:28508932 C>T maps to NM_018690.2 P848P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr12:7805421 G>A maps to NM_001644.3 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:7805349 G>A maps to NM_001644.3 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:7803717 C>T maps to NM_001644.3 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:7802202 C>T maps to NM_001644.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr12:7805349 G>A maps to NM_001644.3 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:7803717 C>T maps to NM_001644.3 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:7805370 C>T maps to NM_001644.3 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr6:41021142 G>A maps to NM_006789.3 E19E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:41029480 G>A maps to NM_006789.3 Q182Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr6:41029069 A>G maps to NM_006789.3 E45E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:41021151 G>A maps to NM_006789.3 E22E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr22:39357540 G>A maps to NM_001193289.1 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:39381962 C>T maps to ENST00000402182 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr22:39382369 C>T maps to ENST00000402182 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr22:39380205 C>T maps to ENST00000402182 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr22:39411752 C>T maps to ENST00000396762 N79N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr22:39413916 C>T maps to ENST00000396762 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr22:39411611 G>A maps to ENST00000396762 K32K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:39427709 G>A maps to NM_152426.3 E258E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:39427844 C>T maps to NM_152426.3 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr22:39427955 C>T maps to NM_152426.3 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:39421082 C>T maps to NM_152426.3 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:39440119 A>G maps to NM_001006666.1 Q68Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:39441499 C>T maps to NM_145298.5 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr22:39448128 C>T maps to NM_145298.5 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:39448344 C>T maps to NM_145298.5 I330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr22:39439040 G>A maps to NM_145298.5 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:39477500 C>T maps to NM_021822.3 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:39476999 G>A maps to NM_021822.3 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr22:39479783 T>C maps to NM_021822.3 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr22:39475065 G>A maps to NM_021822.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:39497336 G>A maps to NM_001166003.1 W82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:183617322 G>A maps to NM_203454.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:45422429 G>T maps to NM_001645.3 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr11:116703479 G>A maps to ENST00000360377 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:116701498 G>A maps to ENST00000360377 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:45448543 G>A maps to NM_001646.1 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:45448489 C>T maps to NM_001646.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:45448093 G>A maps to NM_001646.1 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:45411096 C>T maps to NM_000041.2 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr12:56755112 G>A maps to NM_001638.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:56755101 G>A maps to NM_001638.2 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:64219882 C>T maps to NM_000042.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr17:64219822 G>A maps to NM_000042.2 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:64210718 C>T maps to NM_000042.2 E278E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:64210748 C>T maps to NM_000042.2 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr17:64225467 C>T maps to NM_000042.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:64216855 G>A maps to NM_000042.2 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:64225434 C>T maps to NM_000042.2 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:36661670 C>T maps to NM_145343.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr22:36661835 G>A maps to NM_145343.2 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:36661377 C>T maps to NM_145343.2 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:36661520 G>A maps to NM_145343.2 E229E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:36661994 G>A maps to NM_145343.2 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:36661547 G>A maps to NM_145343.2 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:36623913 A>G maps to ENST00000451256 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr22:36627471 C>T maps to ENST00000451256 Q129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr22:36624019 G>A maps to ENST00000451256 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr22:36623629 G>A maps to ENST00000451256 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr22:36537304 C>T maps to NM_145640.2 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr22:36538009 C>T maps to NM_145640.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:36541576 G>A maps to NM_145640.2 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:36556777 C>T maps to NM_145640.2 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr22:36538009 C>T maps to NM_145640.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr22:36537751 G>A maps to NM_145640.2 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:36556852 G>A maps to NM_145640.2 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr22:36587425 C>T maps to ENST00000332987 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr22:36587482 A>G maps to ENST00000332987 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr22:36587653 C>A maps to ENST00000332987 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:36587387 C>T maps to ENST00000332987 W260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:36587446 C>T maps to ENST00000332987 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:36124911 G>A maps to NM_030642.1 K423K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr22:36123134 G>A maps to NM_030642.1 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F4-06A-12D-A25O-08 chr22:36116678 G>A maps to NM_030642.1 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:36055573 G>A maps to NM_030641.3 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:12940207 C>T maps to NM_001130415.1 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:31625492 G>A maps to NM_019101.2 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr6:31624325 C>T maps to NM_019101.2 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr23:23876822 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr23:23897031 C>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:23897067 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:23899058 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:84306434 T>C did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr21:27354659 G>A maps to NM_000484.3 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr21:27327991 G>A maps to NM_000484.3 F512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr17:58524994 C>A maps to NM_006380.2 E569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:58531839 C>T maps to NM_006380.2 E387E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:58529385 G>A maps to NM_006380.2 I453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:58539382 A>G maps to NM_006380.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:105582225 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:88876248 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:30951874 C>T maps to ENST00000509504 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr7:30951841 C>T maps to ENST00000509504 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:30951790 C>T maps to ENST00000509504 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr7:30961811 C>T maps to ENST00000509504 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr7:30963204 C>T maps to ENST00000509504 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:30961694 G>A maps to ENST00000509504 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:30961727 C>T maps to ENST00000509504 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:154295497 C>T maps to NM_080429.2 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:154295828 G>T maps to NM_080429.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr1:154295825 C>T maps to NM_080429.2 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:154296129 C>T maps to NM_080429.2 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:154296246 C>T maps to NM_080429.2 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr11:77301463 C>T maps to NM_173039.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr11:77301057 C>T maps to NM_173039.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:241631525 G>A maps to ENST00000429564 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:241631350 C>T maps to ENST00000429564 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:241621906 C>T maps to NM_001102467.1 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:241622143 G>A maps to NM_001102467.1 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:50349312 G>A maps to NM_000486.5 W246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:50344627 C>T maps to NM_000486.5 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:50344843 G>A maps to NM_000486.5 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:50349312 G>A maps to NM_000486.5 W246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr12:50347951 G>A maps to NM_000486.5 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:50344696 C>T maps to NM_000486.5 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:50344865 C>T maps to NM_000486.5 R85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:50344654 C>T maps to NM_000486.5 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr18:24440748 C>T maps to NM_001650.4 W227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr18:24440759 G>A maps to NM_001650.4 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:24436348 G>A maps to NM_001650.4 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:24442217 C>T maps to NM_001650.4 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:24442460 G>A maps to NM_001650.4 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr12:50357927 G>A maps to NM_001651.2 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr12:50355883 C>T maps to NM_001651.2 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr12:50355884 C>T maps to NM_001651.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:50358794 C>T maps to NM_001651.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr12:50368135 G>A maps to NM_001652.3 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:50366976 G>A maps to NM_001652.3 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:50367225 C>T maps to NM_001652.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr9:33395116 G>T maps to NM_001170.1 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr9:33386083 G>A maps to NM_001170.1 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:33385765 G>A maps to NM_001170.1 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:33385828 G>A maps to NM_001170.1 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr16:25235771 G>T maps to NM_001169.2 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr16:25228637 C>T maps to NM_001169.2 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr16:25239794 C>T maps to NM_001169.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr16:25232822 C>T maps to NM_001169.2 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr16:25228649 C>T maps to NM_001169.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:58467153 C>T maps to NM_020980.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr15:58467153 C>T maps to NM_020980.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr15:58467216 G>A maps to NM_020980.3 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:58471451 G>A maps to NM_020980.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr15:58465345 G>A maps to NM_020980.3 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:58430763 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:58430865 C>T maps to NM_020980.3 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr5:115351462 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:115338983 G>A maps to NM_173800.4 V648V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr5:115319053 C>T maps to NM_173800.4 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:115298573 G>A maps to NM_173800.4 W87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:115351417 C>T maps to NM_173800.4 V904V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:115335538 G>A maps to NM_173800.4 K485K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr5:115348084 G>A maps to NM_173800.4 K754K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr15:35176812 G>A maps to NM_014691.2 P980P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr23:66941764 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:66905909 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:66765995 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:66765852 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:66765699 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:66931341 G>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:66863241 C>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr23:66765794 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:66905895 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:66931290 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:66931443 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:66937360 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:66937410 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:66937440 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:66942706 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:66931362 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:66937342 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:66941749 C>T did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:66765647 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:47426120 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:47426162 A>T did not map to a codon.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr23:47428155 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:47426505 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:47426076 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:47426120 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:47426736 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:47424651 T>C did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:72409130 G>A maps to NM_001040118.2 A854A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr11:72412699 G>T maps to NM_001040118.2 R766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr11:72406139 G>A maps to NM_001040118.2 V1193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:72416852 G>A maps to NM_001040118.2 I602I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr11:72408488 A>G maps to NM_001040118.2 G944G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:72404459 G>A maps to NM_001040118.2 S1288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:72404815 G>A maps to NM_001040118.2 P1243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:72423532 G>A maps to NM_001040118.2 D276D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:72423290 G>A maps to NM_001040118.2 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:72410592 G>A maps to NM_001040118.2 F769F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:72421434 G>A maps to NM_001040118.2 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:72397145 G>A maps to NM_001040118.2 R1426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:72407607 G>A maps to NM_001040118.2 I1086I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:72423499 G>A maps to NM_001040118.2 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:72437978 G>A maps to NM_001040118.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:36134887 G>A maps to NM_015230.2 P1129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr4:36163140 G>A maps to NM_015230.2 S735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr4:36152535 G>A maps to NM_015230.2 F961F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr4:36212303 G>A maps to NM_015230.2 R399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:36230270 G>A maps to NM_015230.2 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr4:36130311 T>C maps to NM_015230.2 E1161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr4:36122869 C>T maps to NM_015230.2 T1275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:36230379 G>A maps to NM_015230.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:36069744 G>A maps to NM_015230.2 F1633F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr4:36230835 C>T maps to NM_015230.2 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:36162208 G>A maps to NM_015230.2 Q772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:36214079 G>A maps to NM_015230.2 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr4:36179538 C>T maps to NM_015230.2 E589E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr4:36069773 G>A maps to NM_015230.2 R1624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr4:36069786 C>T maps to NM_015230.2 K1619K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:36231066 G>A maps to NM_015230.2 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:36189152 G>T maps to NM_015230.2 S533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr4:36115826 C>T maps to NM_015230.2 W1374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:36069801 G>A maps to NM_015230.2 H1614H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:36122869 C>T maps to NM_015230.2 T1275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:36130236 C>T maps to NM_015230.2 T1186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:36149242 G>A maps to NM_015230.2 S1042S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:36150107 G>A maps to NM_015230.2 I973I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:36166572 G>A maps to NM_015230.2 S712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:36166614 C>T maps to NM_015230.2 R698R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr5:141059842 G>A maps to NM_022481.5 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr5:141059843 G>A maps to NM_022481.5 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr5:141051753 G>A maps to NM_022481.5 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:141035195 G>A maps to NM_022481.5 Q1368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr5:141059914 A>G maps to NM_022481.5 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:141036103 A>G maps to NM_022481.5 R1252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr5:141041667 A>C maps to NM_022481.5 R985R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:141051139 G>A maps to NM_022481.5 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:141052691 G>A maps to NM_022481.5 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:141033692 G>A maps to NM_022481.5 Q1487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr5:141051858 G>T maps to NM_022481.5 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:141046036 G>A maps to NM_022481.5 P842P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:141044606 C>T maps to NM_022481.5 W894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:141052201 G>A maps to NM_022481.5 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:141059161 G>A maps to NM_022481.5 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr5:141039040 G>A maps to NM_022481.5 I1090I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:143694447 G>A maps to NM_015193.3 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:143694972 G>A maps to NM_015193.3 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:143694849 C>T maps to NM_015193.3 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:228285395 C>T maps to NM_001024228.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:228284826 C>T maps to NM_001024228.1 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr12:49334740 G>A maps to NM_001659.2 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:57570188 C>A maps to NM_001660.3 G24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr7:127229593 G>T maps to NM_001662.3 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr7:127230118 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr7:127229611 T>A maps to NM_001662.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr14:50360930 G>A maps to NM_001663.3 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:50360696 C>T maps to NM_001663.3 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr14:50360477 C>A maps to NM_001663.3 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:61908561 C>T maps to NM_175609.1 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:47187860 C>T maps to NM_032389.3 G501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr22:43243590 G>A maps to NM_014570.4 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr22:43218306 G>A maps to NM_014570.4 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:43195137 G>A maps to NM_014570.4 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:43243539 A>C maps to NM_014570.4 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr22:43218406 G>A maps to NM_014570.4 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr22:43206868 C>T maps to NM_014570.4 E382E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr8:68115389 A>G maps to NM_006421.3 L1686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:68165839 T>C maps to NM_006421.3 T848T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr8:68188299 G>A maps to NM_006421.3 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:68179590 C>T maps to NM_006421.3 T553T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:68139384 G>A maps to NM_006421.3 T1301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr8:68113760 C>T maps to NM_006421.3 R1736R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr8:68111237 A>G maps to NM_006421.3 F1827F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:47601350 C>T maps to NM_006420.2 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:47615006 C>T maps to NM_006420.2 R1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr20:47621704 C>T maps to NM_006420.2 F1177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr20:47558508 C>T maps to NM_006420.2 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:47633840 C>T maps to NM_006420.2 S1457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:47612359 C>T maps to NM_006420.2 A1054A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19T-06A-11D-A19A-08 chr20:47592646 C>T maps to NM_006420.2 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr20:47626918 C>T maps to NM_006420.2 F1245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr20:47570301 C>T maps to NM_006420.2 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:153809444 C>T maps to NM_001025595.1 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr6:131904497 G>A maps to ENST00000356962 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr6:131894454 T>A maps to ENST00000356962 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:68117432 G>C maps to NM_001172.3 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:121304900 G>A maps to NM_001012659.1 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:121305434 G>A maps to NM_001012659.1 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr3:121305188 C>T maps to NM_001012659.1 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:121289613 G>A maps to NM_001012659.1 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:121304942 C>T maps to NM_001012659.1 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr3:121289565 G>A maps to NM_001012659.1 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:121303896 G>A maps to NM_001012659.1 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:121305239 C>T maps to NM_001012659.1 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:121305071 G>A maps to NM_001012659.1 W191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:121304942 C>T maps to NM_001012659.1 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:121305408 C>T maps to NM_001012659.1 Q304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:46702862 G>A maps to NM_004308.2 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:46702649 G>A maps to NM_004308.2 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:148887968 C>T maps to NM_024605.3 I565I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:148743938 C>T maps to NM_024605.3 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:148744080 G>A maps to NM_024605.3 K95K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr15:32928920 G>A maps to NM_014783.3 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr10:32197516 A>G maps to NM_018287.5 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr10:32150513 G>A maps to NM_018287.5 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:32096681 T>C maps to NM_018287.5 P815P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:32132465 G>A maps to NM_018287.5 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:32120667 G>A maps to NM_018287.5 R483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:143959719 G>A maps to NM_018460.3 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:143986230 C>T maps to NM_018460.3 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr16:24942648 T>A maps to NM_001006634.1 S657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr16:24946941 G>A maps to NM_001006634.1 D581D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:24942240 G>A maps to NM_001006634.1 T793T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr16:24958884 G>A maps to NM_001006634.1 Q387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:129921870 G>A maps to NM_033515.2 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:99025842 G>A maps to NM_032900.4 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr10:99003877 G>A maps to NM_032900.4 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:110450792 C>T maps to NM_020809.2 Q959Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:110482074 C>T maps to NM_020809.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:110451158 C>T maps to NM_020809.2 K837K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:110451632 G>A maps to NM_020809.2 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:110485296 C>T maps to NM_020809.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr11:110454424 G>A maps to NM_020809.2 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:110477347 G>A maps to NM_020809.2 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:110477351 G>A maps to NM_020809.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr11:110462841 G>A maps to NM_020809.2 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr10:24884676 G>A maps to NM_020824.3 F1227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr10:24873719 G>T maps to NM_020824.3 S1833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr10:24874254 G>A maps to NM_020824.3 R1655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:24889826 C>T maps to NM_020824.3 Q960Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:24874768 G>A maps to NM_020824.3 P1483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr10:24874691 G>C maps to NM_020824.3 S1509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr10:24908777 G>A maps to NM_020824.3 S682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:24873955 G>A maps to NM_020824.3 S1754S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr10:24873481 G>A maps to NM_020824.3 S1912S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:24909487 G>A maps to NM_020824.3 R446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr10:24896492 G>A maps to NM_020824.3 N873N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr10:49658806 G>A maps to ENST00000417912 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr10:49658878 G>A maps to ENST00000417912 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr10:49658878 G>A maps to ENST00000417912 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:49687742 G>A maps to ENST00000417912 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:49654618 A>G maps to ENST00000417912 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:49791075 C>T maps to ENST00000417912 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:49663143 C>T maps to ENST00000417912 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr10:49667781 G>A maps to ENST00000417912 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:49687790 C>T maps to ENST00000417912 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:49654523 C>T maps to ENST00000417912 R685R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:49663134 G>A maps to ENST00000417912 Y250Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:49812808 C>T maps to ENST00000417912 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr4:86844905 G>A maps to NM_001025616.2 W125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:86491736 C>T maps to NM_001025616.2 Q15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr4:86916054 C>A maps to NM_001025616.2 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr4:86852175 G>A maps to NM_031305.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:86863240 G>A maps to NM_001025616.2 E138E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr4:86921784 G>A maps to NM_001025616.2 Q719Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:69046382 C>T maps to NM_001007231.2 R378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:68962351 G>A maps to NM_001007231.2 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:69046309 C>T maps to NM_001007231.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:69049500 C>T maps to NM_001007231.2 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:69040511 C>T maps to NM_001007231.2 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:69053181 G>A maps to NM_001007231.2 K599K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:69049767 G>A maps to NM_001007231.2 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:69002467 C>T maps to NM_001007231.2 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr2:69034516 G>A maps to NM_001007231.2 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:69049812 G>A maps to NM_001007231.2 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:69002341 C>T maps to NM_001166276.1 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr2:68962367 C>T maps to NM_001007231.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr5:142586825 C>T maps to NM_015071.4 S684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:142437219 G>A maps to NM_015071.4 Q482Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:142393655 G>A maps to NM_015071.4 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:142435637 C>T maps to NM_015071.4 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:142513530 G>A did not map to a codon.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr5:142500670 C>T maps to NM_015071.4 Q553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:43473412 G>A maps to ENST00000428638 F774F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:43474070 G>A maps to ENST00000428638 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:43475368 C>T maps to ENST00000428638 S596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:43474303 C>T maps to ENST00000428638 E643E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:43480184 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr17:43473621 G>A maps to ENST00000428638 I734I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:43473423 G>A maps to ENST00000428638 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:6873689 G>A maps to ENST00000400091 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr18:6882233 C>T maps to ENST00000400091 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr18:6882257 C>T maps to ENST00000400091 F471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr18:6851121 C>T maps to ENST00000400091 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr18:6859865 G>A maps to ENST00000400091 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr18:6889984 C>T maps to ENST00000400091 F545F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:6882288 C>T maps to ENST00000400091 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:6890532 C>T maps to ENST00000400091 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:6908964 T>C maps to ENST00000419673 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr1:94652061 T>C maps to NM_004815.3 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:94668539 C>T maps to NM_004815.3 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:94674858 G>A maps to NM_004815.3 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:94650918 G>A maps to NM_004815.3 F633F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:94650951 C>T maps to NM_004815.3 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:94685904 G>A maps to NM_004815.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:94643686 G>A maps to NM_004815.3 S839S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:94668539 C>T maps to NM_004815.3 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:94650499 C>T maps to NM_004815.3 K679K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:94643671 C>T maps to NM_004815.3 V844V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:94643545 G>A maps to NM_004815.3 F886F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:94643671 C>T maps to NM_004815.3 V844V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr1:94643638 G>C maps to NM_004815.3 P855P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:94650951 C>T maps to NM_004815.3 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:94650957 G>A maps to NM_004815.3 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr1:94669545 C>T maps to NM_004815.3 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:161021227 C>T maps to NM_001025598.1 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:161018302 C>T maps to NM_001025598.1 K836K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:161017576 G>A maps to NM_001025598.1 P1078P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:161024187 G>A maps to NM_001025598.1 N168N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:161029453 C>T maps to NM_001025598.1 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr1:161022308 C>T maps to NM_001025598.1 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:161018296 C>T maps to NM_001025598.1 R838R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:161017844 C>T maps to NM_001025598.1 W989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:161018401 C>T maps to NM_001025598.1 R803R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:161018392 C>T maps to NM_001025598.1 G806G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:161018524 C>T maps to NM_001025598.1 Q762Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:161039387 C>T maps to NM_001025598.1 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:161019037 C>T maps to NM_001025598.1 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:161022293 G>A maps to NM_001025598.1 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:161022329 C>T maps to NM_001025598.1 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:119101168 C>T maps to NM_020754.2 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:119121008 C>T maps to NM_020754.2 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:119101180 C>T maps to NM_020754.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr3:119133526 C>T maps to NM_020754.2 P917P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:119128451 G>A maps to NM_020754.2 E585E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr3:119087270 C>T maps to NM_020754.2 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:119099806 C>T maps to NM_020754.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:119134261 C>T maps to NM_020754.2 P1162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr3:119134264 G>A maps to NM_020754.2 Q1163Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:119109764 C>T maps to NM_020754.2 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr3:119101162 C>T maps to NM_020754.2 H152H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr3:119101163 C>T maps to NM_020754.2 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:128851344 G>A maps to NM_001142685.1 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:128840322 C>T maps to NM_001142685.1 R1581R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:128842601 C>A maps to NM_001142685.1 E1253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:128850515 G>A maps to NM_001142685.1 I622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:128840352 G>A maps to NM_001142685.1 P1571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:128855914 G>A maps to NM_001142685.1 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr11:128842437 G>A maps to NM_001142685.1 P1307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:128851779 G>A maps to NM_001142685.1 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr19:36269472 C>T maps to ENST00000007510 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr19:36273349 C>T maps to ENST00000007510 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr19:36278215 C>T maps to ENST00000007510 Q917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:36279051 C>T maps to ENST00000007510 S1195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:36278421 C>T maps to ENST00000007510 P985P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:36278904 C>T maps to ENST00000007510 P1146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:36279315 C>T maps to ENST00000007510 T1283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr19:36278097 C>T maps to ENST00000007510 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr19:36278331 C>T maps to ENST00000007510 S955S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:36273298 C>T maps to ENST00000007510 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:36278136 C>T maps to ENST00000007510 P890P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q9-06A-11D-A19A-08 chr23:130218328 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:130215692 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr23:130215655 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr23:130215655 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:130218615 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:130217163 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr23:130222604 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr23:130215846 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:130218267 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:130218337 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr23:130220376 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:130222719 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:130215883 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:130217854 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr23:130218371 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr23:130222696 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:130218371 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:130218371 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:130220397 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:130215767 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:130219888 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr23:130218227 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:130219007 G>A did not map to a codon.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr23:130218304 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:130219667 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr23:130222624 C>T did not map to a codon.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr23:130220391 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:130222753 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:130218273 C>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:130218304 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:130218615 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:130220635 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:130222676 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr23:130215791 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:130215812 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:130218267 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr8:145770885 G>A maps to NM_025251.1 D756D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr8:145780996 C>T maps to NM_025251.1 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:145756163 G>A maps to NM_025251.1 P1024P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:145781005 G>A maps to NM_025251.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:145772558 G>A maps to NM_025251.1 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:145773446 C>T maps to NM_025251.1 Q341Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr8:145770963 G>A maps to NM_025251.1 P730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:145758631 T>A maps to NM_025251.1 A922A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr8:145755805 C>A maps to NM_025251.1 *1115Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr8:145770924 G>A maps to NM_025251.1 A743A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr8:145770732 G>A maps to NM_025251.1 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:145770732 G>A maps to NM_025251.1 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:145770957 G>A maps to NM_025251.1 I732I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:145773398 G>A maps to NM_025251.1 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:153186110 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:153191629 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:153184722 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:153175711 T>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:153186549 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:153174588 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr14:32562337 C>T maps to NM_001030055.1 I821I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr14:32562319 C>T maps to NM_001030055.1 S815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr14:32615490 C>T maps to NM_001030055.1 Y1296Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:32561407 T>C maps to NM_001030055.1 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr14:32560525 A>G maps to NM_001030055.1 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr14:32561665 C>T maps to NM_001030055.1 N597N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:11204501 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:11682526 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:11160412 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:11682617 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:11197548 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:11160412 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:11174742 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:11204448 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:11187672 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:11272673 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr23:11174716 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:11197562 C>T did not map to a codon.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr23:11206985 A>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr22:45243919 C>T maps to ENST00000352766 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr22:45244821 G>A maps to ENST00000352766 V463V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr22:45218331 C>T maps to ENST00000352766 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:45258225 C>T maps to ENST00000352766 I561I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr22:45255632 C>T maps to ENST00000352766 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr22:45258222 G>A maps to ENST00000352766 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr22:45241178 C>T maps to ENST00000352766 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:45258222 G>A maps to ENST00000352766 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:57870158 G>A maps to ENST00000393797 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:57867828 G>A maps to ENST00000393797 A728A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:57872934 C>T maps to ENST00000393797 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:57871367 G>A maps to ENST00000393797 C281C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:57867864 C>A maps to ENST00000393797 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr17:79827106 G>A maps to NM_004309.4 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:79827767 C>T maps to NM_004309.4 Q13Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:15103628 T>C maps to NM_001175.4 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:332779 G>A maps to NM_001176.3 W215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:42396719 C>T maps to NM_199002.1 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr19:42398369 C>T maps to NM_199002.1 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr19:42396403 T>G maps to NM_199002.1 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:1874622 C>T maps to ENST00000398564 F922F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr8:1808153 C>T maps to ENST00000398564 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr8:1876648 C>T maps to ENST00000398564 S943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:1844593 C>T maps to ENST00000398564 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr8:1808198 C>T maps to ENST00000398564 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr8:1842671 C>T maps to ENST00000398564 I483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr8:1851496 G>A maps to ENST00000398564 Q592Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr1:17934435 C>T maps to NM_018125.3 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:18023652 G>A maps to NM_018125.3 E1206E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:18023685 C>T maps to NM_018125.3 P1217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:18023760 C>T maps to NM_018125.3 S1242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:18021671 C>A maps to NM_018125.3 V1068V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:17983151 C>T maps to NM_018125.3 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr1:17950949 C>T maps to NM_018125.3 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:18014196 C>T maps to NM_018125.3 L1047L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr1:17965055 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:156937780 G>A maps to NM_198236.1 Q321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:156931483 G>A maps to NM_198236.1 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr1:156955922 G>A maps to NM_198236.1 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:156939109 C>T maps to NM_198236.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:156948061 G>A maps to NM_198236.1 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:156928583 G>A maps to NM_198236.1 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:156930234 G>A maps to NM_198236.1 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr1:156914848 G>A maps to NM_198236.1 L985L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:156906635 G>A maps to NM_198236.1 S1534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:156926340 G>A maps to NM_198236.1 F514F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:156909559 G>A maps to NM_198236.1 S1292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:156917204 G>A maps to NM_198236.1 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:120336014 C>T maps to NM_015313.2 L895L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr11:120343835 G>A maps to NM_015313.2 R1011R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:120349039 C>T maps to NM_015313.2 I1236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr11:120348913 T>C maps to NM_015313.2 S1194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:120331435 C>T maps to NM_015313.2 I861I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:120310836 G>C did not map to a codon.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr17:8222093 G>A maps to NM_173728.3 R633R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:8215939 C>T maps to NM_173728.3 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr17:8216516 C>T maps to NM_173728.3 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:8218222 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:8216544 C>T maps to NM_173728.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr17:8215733 C>A maps to NM_173728.3 S126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:8218757 G>A maps to NM_173728.3 E429E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:8221757 G>A maps to NM_173728.3 K586K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr17:8215407 T>C maps to NM_173728.3 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:3397033 C>T maps to NM_014448.3 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:3395107 C>T maps to NM_014448.3 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:3389975 C>T maps to NM_014448.3 R399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:3396451 G>C maps to NM_014448.3 V655V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:3397099 G>A maps to NM_014448.3 V693V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr1:3389978 G>T maps to NM_014448.3 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:3386025 C>T maps to NM_014448.3 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:3391321 C>T maps to NM_014448.3 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:3395113 G>A maps to NM_014448.3 Q584Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr1:3391300 C>T maps to NM_014448.3 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:3395095 C>A maps to NM_014448.3 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:73068122 C>T maps to NM_014786.3 I1315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr11:73073651 C>T maps to NM_014786.3 L1623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:73070877 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:73073627 G>A maps to NM_014786.3 S1615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr11:73020360 G>A maps to NM_014786.3 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:73022670 C>T maps to NM_014786.3 P996P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr11:73064051 C>T maps to NM_014786.3 Q1150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:73075267 C>T maps to NM_014786.3 V1795V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:73067263 C>T maps to NM_014786.3 L1236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:73021158 G>A maps to NM_014786.3 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:73064047 C>T maps to NM_014786.3 L1148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:73078665 C>T maps to NM_014786.3 S2011S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:73073477 G>A maps to NM_014786.3 R1565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr11:73022652 C>T maps to NM_014786.3 F990F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:73066681 C>T maps to NM_014786.3 L1186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:73022163 C>T maps to NM_014786.3 S827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:7506649 A>G maps to NM_001130955.1 E218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr19:7518551 C>T maps to NM_001130955.1 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:7534916 T>C did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:7509204 C>T maps to NM_001130955.1 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr19:7523558 C>T maps to NM_001130955.1 I593I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr19:7518407 C>T maps to NM_001130955.1 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:7531994 G>A maps to NM_001130955.1 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr19:7518551 C>T maps to NM_001130955.1 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:7527155 C>T maps to NM_001130955.1 F669F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr19:7509309 C>T maps to NM_001130955.1 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr19:7535024 C>T maps to NM_001130955.1 P1121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:7509156 C>T maps to NM_001130955.1 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:7518540 C>T maps to NM_001130955.1 Q494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:7527132 C>T maps to NM_001130955.1 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:16525147 G>A maps to NM_153213.3 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:16535153 C>T maps to NM_153213.3 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:16534706 C>T maps to NM_153213.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:16528292 G>A maps to NM_153213.3 V710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:16532065 G>A maps to NM_153213.3 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:155920997 C>T maps to NM_001162383.1 E775E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:155932416 G>A maps to NM_001162383.1 Y356Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:155935489 G>A maps to NM_001162383.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:155920150 G>A maps to NM_001162383.1 D942D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:155920177 G>A maps to NM_001162383.1 P933P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:155920222 G>A maps to NM_001162383.1 V918V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr1:155920753 G>A maps to NM_001162383.1 R857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:155931554 G>A maps to NM_001162383.1 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:155922467 G>A maps to NM_001162383.1 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:56763336 A>T maps to NM_001128615.1 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:56807810 G>A maps to NM_001128615.1 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:56763333 G>A maps to NM_001128615.1 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:56789140 G>A maps to NM_001128615.1 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:56789059 G>A maps to NM_001128615.1 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:56779370 G>A maps to NM_001128615.1 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr3:56779337 G>A maps to NM_001128615.1 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr3:56763489 G>A maps to NM_001128615.1 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr7:143884381 C>T maps to NM_001003702.2 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr5:149003639 G>A maps to NM_001001669.2 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:149001408 G>A maps to NM_001001669.2 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:149001561 C>T maps to NM_001001669.2 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:106534591 C>T maps to ENST00000420470 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr2:131796598 C>T maps to NM_015320.2 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:131798975 G>A maps to NM_015320.2 K426K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:131688697 G>A maps to NM_015320.2 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr2:131688754 G>A maps to NM_015320.2 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:131797937 C>T maps to NM_015320.2 F343F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:131688535 C>T maps to NM_015320.2 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr7:144077104 C>T maps to NM_005435.3 R1584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr7:144062326 C>T maps to NM_005435.3 P855P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:144061192 G>A maps to NM_005435.3 K477K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:144077133 G>A maps to NM_005435.3 V1593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr7:144075891 C>T maps to NM_005435.3 P1523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr7:144075892 C>T maps to NM_005435.3 R1524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr7:144062335 C>T maps to NM_005435.3 S858S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:144062344 G>A maps to NM_005435.3 R861R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr23:135829723 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:135862952 A>C did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:135764996 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:135757222 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:135827494 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:135762890 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:135762905 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:135770134 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:135764125 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:135751661 G>C did not map to a codon.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr23:135770137 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:135758807 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr13:111953095 T>C maps to ENST00000218789 R614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr13:111896266 C>T maps to NM_001113511.1 Q291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr13:111926202 C>T maps to NM_001113511.1 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr13:111926202 C>T maps to NM_001113511.1 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr13:111857667 G>A maps to NM_001113511.1 Q116Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr13:111768019 C>T maps to NM_001113511.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:62875601 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr23:62875521 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:62917013 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr23:62885798 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:27088682 C>T maps to NM_006015.4 S764S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr1:27057923 C>T maps to NM_006015.4 H544H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr1:27100918 C>T maps to NM_006015.4 Q1401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr1:27106860 C>T maps to NM_006015.4 R2158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:27092736 C>T maps to NM_006015.4 Q920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr1:27056143 A>G maps to NM_006015.4 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr1:27099359 C>T maps to NM_006015.4 F1199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr1:27099360 C>T maps to NM_006015.4 Q1200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:27088784 C>T maps to NM_006015.4 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:27100349 C>T maps to NM_006015.4 F1354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:27058010 C>T maps to NM_006015.4 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr1:27089777 T>C did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:27106860 C>A maps to NM_006015.4 R2158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:27094348 G>A maps to NM_006015.4 E1019E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:27087519 C>T maps to NM_006015.4 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:27106251 C>T maps to NM_006015.4 L1955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:27087519 C>T maps to NM_006015.4 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:27101403 C>T maps to NM_006015.4 P1562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:157521928 C>T maps to ENST00000367148 Q1441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:157505553 C>T maps to ENST00000367148 Q1219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:157521969 G>A maps to ENST00000367148 P1454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:157522413 C>T maps to ENST00000367148 S1602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr6:157527626 C>T maps to ENST00000367148 F1824F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:157405920 C>T maps to ENST00000367148 S708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr6:157488197 C>T maps to ENST00000367148 N955N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:157505534 C>A maps to ENST00000367148 T1212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:157528032 G>T maps to ENST00000367148 E1960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr6:157469764 C>G maps to ENST00000367148 Y840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:157528791 C>T maps to ENST00000367148 Q2213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:157505553 C>T maps to ENST00000367148 Q1219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:157521849 C>T maps to ENST00000367148 R1414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr12:46230570 C>T maps to NM_152641.2 R274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr12:46244795 G>T maps to NM_152641.2 G964*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr12:46244585 C>T maps to NM_152641.2 Q894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr12:46244257 T>A maps to NM_152641.2 P784P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr12:46244857 C>T maps to NM_152641.2 V984V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr12:46243471 C>T maps to NM_152641.2 Q609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:46245026 C>T maps to NM_152641.2 Q1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:46245026 C>T maps to NM_152641.2 Q1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr12:46244296 A>T maps to NM_152641.2 P797P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr12:46244297 C>T maps to NM_152641.2 Q798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr12:46245485 C>T maps to NM_152641.2 Q1194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr12:46242661 C>T maps to NM_152641.2 R542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:46244078 C>T maps to NM_152641.2 Q725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr12:46205281 T>G maps to NM_152641.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:46246330 C>T maps to NM_152641.2 T1475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr12:46230612 C>T maps to NM_152641.2 Q288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr12:46246414 T>G maps to NM_152641.2 V1503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr12:46298732 G>T maps to NM_152641.2 E1794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr12:46285665 C>T maps to NM_152641.2 Q1676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr12:46243877 C>T maps to NM_152641.2 Q658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr12:46242661 C>T maps to NM_152641.2 R542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr12:46125097 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:46244714 C>T maps to NM_152641.2 Q937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:46244786 C>T maps to NM_152641.2 Q961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr12:46245842 C>T maps to NM_152641.2 Q1313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr12:46230570 C>T maps to NM_152641.2 R274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr12:46244786 C>T maps to NM_152641.2 Q961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:46243471 C>T maps to NM_152641.2 Q609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:46243822 C>T maps to NM_152641.2 I639I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:46246001 A>T maps to NM_152641.2 K1366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:929674 C>T maps to NM_005224.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr15:74887988 C>T maps to ENST00000395077 I520I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr15:74882179 C>T maps to ENST00000395077 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:74865501 G>A maps to ENST00000395077 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr15:74883677 C>T maps to ENST00000395077 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr9:34623473 G>A maps to NM_001017363.1 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:34627699 G>A maps to NM_001017363.1 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr14:58813763 A>G maps to NM_002892.3 Q367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:235336014 G>A maps to NM_016374.5 I1243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:235338550 G>A maps to NM_016374.5 L1204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:235377133 G>A maps to NM_016374.5 V597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:235335939 C>T maps to NM_016374.5 E1268E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:235338497 C>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr2:97213175 G>A maps to NM_212481.1 E14E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:97217344 G>A maps to NM_212481.1 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:97215194 G>A maps to NM_212481.1 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:97215089 G>A maps to NM_212481.1 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:97216948 C>T maps to NM_212481.1 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:97216892 G>T maps to NM_212481.1 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr10:63851034 C>T maps to NM_032199.2 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr10:63851333 C>T maps to NM_032199.2 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr10:63852710 C>T maps to NM_032199.2 Y1163Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:63759868 G>A maps to NM_032199.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr10:63852267 C>T maps to NM_032199.2 L1016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:63852710 C>T maps to NM_032199.2 Y1163Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:63851847 C>T maps to NM_032199.2 Q876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr3:49020676 C>T maps to NM_006321.2 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:49005997 C>T maps to NM_006321.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr3:49005997 C>T maps to NM_006321.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr3:49017012 C>T maps to NM_006321.2 Q354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr12:101794878 T>A maps to NM_001177.3 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr5:175793396 G>A maps to NM_173664.4 E66E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr13:50204831 C>T maps to NM_138450.5 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:100243249 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:100240690 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:100240788 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:100242502 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:100229164 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:160395298 A>G maps to NM_025047.2 E55E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr3:160395289 C>T maps to NM_025047.2 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:79650825 G>A maps to NM_001040025.1 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:79650828 C>T maps to NM_001040025.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr11:64786189 C>T maps to NM_001667.3 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr11:64786190 C>T maps to NM_001667.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr16:18806847 G>A maps to NM_015161.1 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr16:18810080 G>T maps to NM_015161.1 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:69151145 C>T maps to NM_006407.3 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr3:69153702 G>A maps to NM_006407.3 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:202107543 G>A maps to NM_138795.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr4:57389958 C>T maps to ENST00000360096 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:57377505 C>T maps to ENST00000360096 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:57389936 G>A maps to ENST00000360096 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:66539521 G>A maps to NM_018120.4 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:66517709 G>A maps to NM_018120.4 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:66516709 G>A maps to NM_018120.4 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:66534582 G>A maps to NM_018120.4 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr7:102738831 G>A maps to NM_031905.3 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:102738814 C>T maps to NM_031905.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:109233634 G>A maps to NM_032131.4 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:109233635 G>T maps to NM_032131.4 G409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:109274370 C>T maps to NM_032131.4 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:109286188 G>C maps to NM_032131.4 V764V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:109190151 C>T maps to NM_032131.4 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:109190067 C>T maps to NM_032131.4 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr10:23326305 G>A maps to NM_173081.3 G839G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr10:23319623 G>A maps to NM_173081.3 W715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr10:23250818 C>T maps to NM_173081.3 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr10:23270362 C>T maps to NM_173081.3 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:23321934 C>T maps to NM_173081.3 R798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr10:28225686 C>T maps to NM_018076.2 W740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr10:28224180 C>T maps to NM_018076.2 K751K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr10:28101488 G>A maps to NM_018076.2 S1029S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:28228900 G>A maps to NM_018076.2 I674I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:28225686 C>T maps to NM_018076.2 W740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr10:28151542 C>T maps to NM_018076.2 G873G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:28224105 C>T maps to NM_018076.2 V776V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:28233285 G>A maps to NM_018076.2 G536G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:28149568 C>T maps to NM_018076.2 E1002E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:28224135 T>G maps to NM_018076.2 T766T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:28228903 C>T maps to NM_018076.2 R673R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr10:28149604 G>A maps to NM_018076.2 L990L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:28224024 C>T maps to NM_018076.2 V803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:28233270 C>T maps to NM_018076.2 V541V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:28260125 C>T maps to NM_018076.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr10:28274108 G>A maps to NM_018076.2 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr10:28224035 G>A maps to NM_018076.2 Q800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr10:28260044 A>G maps to NM_018076.2 N378N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr10:28276345 C>T maps to NM_018076.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:28196666 G>A maps to NM_018076.2 S845S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:28283984 C>T maps to NM_018076.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:28284002 G>A maps to NM_018076.2 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr10:28196591 C>T maps to NM_018076.2 K870K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr10:28250508 C>T maps to NM_018076.2 V458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:28229560 C>T maps to NM_018076.2 R639R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:28272834 C>T maps to NM_018076.2 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:28273188 C>T maps to NM_018076.2 K202K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:28272884 G>A maps to NM_018076.2 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:28284053 C>T maps to NM_018076.2 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr16:31475729 C>T maps to ENST00000408912 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:31477588 C>T maps to ENST00000408912 D824D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr16:31471027 C>T maps to ENST00000408912 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:31471312 C>T maps to ENST00000408912 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr16:31476419 C>T maps to NM_024742.2 A692A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr16:31471180 C>T maps to ENST00000408912 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:31475942 C>T maps to ENST00000408912 S628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:31477645 C>T maps to ENST00000408912 P843P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr16:31473665 C>T maps to ENST00000408912 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr16:31473779 C>T maps to ENST00000408912 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr16:31477597 C>T maps to ENST00000408912 S827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr19:19168361 C>T maps to ENST00000392336 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr19:19162881 G>A maps to ENST00000392336 W244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr19:19162882 G>A maps to ENST00000392336 W244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:19166144 C>T maps to ENST00000392336 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:19165057 G>A maps to ENST00000392336 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:73125006 G>A maps to NM_024585.2 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:137956153 C>T maps to ENST00000469044 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:138003355 C>T maps to ENST00000469044 I603I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr2:232209754 C>T maps to ENST00000359743 P649P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:232143164 C>T maps to ENST00000359743 N515N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:232104717 C>T maps to ENST00000359743 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr2:232137677 C>T maps to ENST00000359743 Y407Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr2:232196542 C>T maps to ENST00000359743 D604D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr2:232141432 C>T maps to ENST00000359743 D473D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:232127032 C>T maps to ENST00000359743 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr2:232087526 A>G maps to ENST00000359743 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr23:100808227 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:100808373 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:100808123 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr23:100808468 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:100807960 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr23:100911031 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr23:100911640 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:100911565 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:100911707 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:100911448 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr23:100911364 G>A did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:100911286 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:100880947 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:100880197 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3CE-06A-11D-A19A-08 chr23:101857273 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:101857409 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:101858320 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:101858024 T>C did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:101858160 C>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr23:101858399 G>A did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr23:101857707 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr23:100871241 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:100871377 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:100871378 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:124214455 C>T maps to NM_001099667.1 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:150795776 G>A maps to NM_001668.3 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr1:150811928 G>A maps to NM_001668.3 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:150830870 G>A maps to NM_001668.3 Q31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:150804339 G>A maps to NM_001668.3 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:150795737 G>A maps to NM_001668.3 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:150784568 C>G maps to NM_001668.3 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:80743332 C>T maps to NM_014862.3 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:80845036 C>T maps to NM_014862.3 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr15:80872805 G>A maps to NM_014862.3 T556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr15:80845063 C>T maps to NM_014862.3 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr15:80873677 C>T maps to NM_014862.3 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:13393714 C>T maps to ENST00000403290 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:13399896 G>A maps to ENST00000403290 R476R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:27553488 C>T maps to NM_020183.3 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr12:27543167 G>A maps to NM_020183.3 K305K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr12:27553479 C>T maps to NM_020183.3 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr12:27554550 C>T maps to NM_020183.3 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr7:98941934 G>A maps to NM_006409.3 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr7:98985734 G>A maps to NM_005720.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:98983390 G>A maps to NM_005720.2 K18K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr7:98988584 C>T maps to NM_005720.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:219103463 T>C maps to NM_005731.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr2:219114118 C>T maps to NM_005731.2 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr2:219110153 A>G maps to NM_005731.2 E187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:9845660 C>T maps to ENST00000453882 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:183599702 G>A maps to ENST00000294742 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr3:169485996 G>A maps to NM_032487.4 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr15:52849386 T>C maps to NM_006628.4 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr3:35763276 G>A maps to ENST00000458225 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr3:35763133 C>T maps to ENST00000458225 R311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:35833952 G>A maps to ENST00000458225 V705V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:35770837 C>T maps to ENST00000458225 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr3:35763117 G>A maps to ENST00000458225 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:35835203 C>T maps to ENST00000458225 T732T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr3:35731617 C>T maps to ENST00000458225 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:35781070 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:35756947 A>G maps to ENST00000458225 E271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:35729358 C>T maps to ENST00000458225 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:35732378 C>T maps to ENST00000458225 Q190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr3:35835377 C>T maps to ENST00000458225 V790V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:35763095 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:35781029 C>T maps to ENST00000458225 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr3:35732407 C>T maps to ENST00000458225 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:69500628 G>A did not map to a codon.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr23:69489978 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:74979993 G>A maps to NM_004041.3 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:74988417 G>T maps to NM_004041.3 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr17:4624282 G>A maps to ENST00000412477 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr17:4621233 C>T maps to ENST00000412477 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:4621955 T>A maps to ENST00000412477 C273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:4623546 C>T maps to ENST00000412477 I339I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A3JD-06A-11D-A20D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:140509072 G>A maps to NM_152285.2 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:18119241 C>T maps to NM_015683.1 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:18119155 T>C maps to NM_015683.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:18120703 G>A maps to NM_015683.1 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr19:18120411 G>A maps to NM_015683.1 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:18121441 C>T maps to NM_015683.1 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:18121489 C>T maps to NM_015683.1 F374F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr15:98514362 T>G maps to NM_183376.2 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr15:98512491 A>G maps to NM_183376.2 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:98511248 T>C maps to NM_183376.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:98512548 C>T maps to NM_183376.2 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:98512566 C>T maps to NM_183376.2 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:4902816 G>A maps to NM_001080523.1 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr19:4891231 G>A maps to NM_001080523.1 D285D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:4902756 C>T maps to NM_001080523.1 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:4896784 G>A maps to NM_001080523.1 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:4891444 C>T maps to NM_001080523.1 Q214Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:4902702 C>T maps to NM_001080523.1 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A264-06A-11D-A196-08 chr19:4902819 C>T maps to NM_001080523.1 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr22:51065137 G>A maps to ENST00000395624 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr22:51065309 G>A maps to ENST00000395624 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr22:51064618 C>T maps to ENST00000395624 E314E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:51063800 G>A maps to ENST00000395624 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:51063590 G>A maps to ENST00000395624 C504C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr22:51065359 G>A maps to ENST00000395624 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:51065085 G>A maps to ENST00000395624 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr22:51063674 G>A maps to ENST00000395624 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr22:51065038 G>A maps to ENST00000395624 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr22:51064663 G>A maps to ENST00000395624 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr22:51063770 C>A maps to ENST00000395624 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr22:51064588 G>A maps to ENST00000395624 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr22:51065635 C>T maps to ENST00000395624 Q141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr5:78260238 C>T maps to NM_000046.3 K230K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr5:78077708 T>C maps to NM_000046.3 R434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr5:78251202 G>A maps to NM_000046.3 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr5:78076339 G>A maps to NM_000046.3 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:2825552 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:2838651 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:2838652 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:2825383 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr23:2828784 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:2827939 G>C did not map to a codon.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr23:2853150 A>C did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:2867428 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:2878426 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:2876405 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:2853177 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:2867670 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:2867671 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:2873469 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:3007546 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:3021847 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:3030309 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:3007611 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:3002574 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:3021879 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:3030405 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:3030423 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:3028240 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:3007546 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:3019249 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:3019199 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr23:3030305 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:3021831 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:3028289 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:3002411 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:3028280 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:3030284 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:3007669 G>A did not map to a codon.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr23:3021864 G>A did not map to a codon.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr23:3007668 G>A did not map to a codon.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr23:3030370 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:3021912 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:3030422 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr23:3002494 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr23:3019198 G>A did not map to a codon.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr23:3002494 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:2999053 G>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:3002494 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:3021865 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr23:3002527 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr23:3030249 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:3002617 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:3019164 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:3030523 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:3007568 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:66339816 C>T maps to NM_014960.3 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:66339801 C>T maps to NM_014960.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr17:66339771 C>T maps to NM_014960.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:66391312 C>T maps to NM_014960.3 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr23:2933365 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr23:2933377 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr23:2931197 C>A did not map to a codon.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr23:2933278 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:2931202 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:2933227 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:2931088 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:2942156 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:2951251 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:2945413 C>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:2951407 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr23:2933117 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:2945447 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:2933365 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:2942107 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:2936598 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:2947359 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:2947360 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:2951251 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:2951234 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:2928181 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:2931165 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:2933010 G>A did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr23:2951168 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr5:149677574 C>T maps to NM_001012301.2 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:149681696 C>T maps to NM_001012301.2 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:149676815 G>A maps to NM_001012301.2 F557F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:149676815 G>A maps to NM_001012301.2 F557F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:149681729 G>A maps to NM_001012301.2 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:114824236 C>T maps to NM_024590.3 Q331Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:114823681 C>T maps to NM_024590.3 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:114824392 G>A maps to NM_024590.3 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr4:114823684 G>A maps to NM_024590.3 I515I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr4:114824458 C>T maps to NM_024590.3 K257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr4:114824377 G>A maps to NM_024590.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr4:114824377 G>A maps to NM_024590.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr5:94918712 C>T maps to NM_198150.2 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr11:3681005 G>A maps to NM_004314.2 W86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr11:3681024 G>A maps to NM_004314.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:3681453 C>T maps to NM_004314.2 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:3682614 G>A maps to NM_004314.2 K286K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:3681444 C>T maps to NM_004314.2 Y232Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr4:77003600 C>T maps to NM_001130016.1 Q232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr4:77003158 C>T maps to NM_001130016.1 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:14993628 G>A maps to NM_021071.2 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr12:14994060 G>A maps to NM_021071.2 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:14993592 C>T maps to NM_021071.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr12:14982346 G>A maps to NM_021071.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:3660958 T>A maps to NM_001079536.1 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:3661289 G>A maps to NM_001079536.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:3661514 C>T maps to NM_001079536.1 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:25031087 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:25033673 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:25033750 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr10:104629930 G>T maps to NM_020682.3 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr10:52008286 G>A maps to NM_019893.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:52008325 G>A maps to NM_019893.2 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr10:52008331 C>T maps to NM_019893.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:52008331 C>T maps to NM_019893.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:52003003 G>A maps to NM_019893.2 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:52003093 G>A maps to NM_019893.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:52502753 C>T maps to NM_001079516.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr11:122955363 G>A maps to NM_024769.2 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:122968637 C>T maps to NM_024769.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr11:122953835 G>A maps to NM_024769.2 N212N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr11:122955358 C>T maps to NM_024769.2 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:122968514 C>T maps to NM_024769.2 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr8:131124415 G>A maps to NM_018482.2 F775F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:131104326 G>A maps to NM_018482.2 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:9490986 C>T maps to NM_003887.2 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:9474911 C>T maps to NM_003887.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:9541479 G>A maps to NM_003887.2 E967E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:9528532 G>A maps to NM_003887.2 K747K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:9543449 T>C maps to NM_003887.2 A1005A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:9528614 C>T maps to NM_003887.2 Q775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:23758186 A>G did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:23763932 C>A maps to NM_017707.3 E379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:23779234 G>A maps to NM_017707.3 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:23768716 G>A maps to NM_017707.3 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr1:23758190 G>A maps to NM_017707.3 F848F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:23763957 C>T maps to NM_017707.3 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:23768692 G>A maps to NM_017707.3 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:23769056 G>A maps to NM_017707.3 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:23767936 C>T maps to NM_017707.3 Q259Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:23782433 G>A maps to NM_017707.3 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:23760145 C>T maps to NM_017707.3 K664K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:239342321 G>A maps to NM_001040445.1 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:150878478 G>A maps to ENST00000422024 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr7:150873297 G>A maps to ENST00000422024 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr7:150873315 G>A maps to ENST00000422024 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:150878459 G>T maps to ENST00000422024 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150878190 G>A maps to ENST00000422024 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:15332574 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:15311434 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:15311435 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:15307706 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:15311352 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:63444797 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:63444869 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:63444317 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:63445468 A>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:63445415 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:63444797 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:63444920 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:5683847 G>A maps to NM_024701.3 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:5690984 G>A maps to NM_024701.3 H155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:57312512 C>T maps to ENST00000295941 L2811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:123257650 G>A maps to NM_080928.3 W104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:123264836 C>T maps to NM_080928.3 H222H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:123277007 C>T maps to NM_080928.3 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr7:123254627 C>T maps to NM_080928.3 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr7:123256544 G>A maps to NM_080928.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr7:123264797 T>C maps to NM_080928.3 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:123264746 C>T maps to NM_080928.3 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:42255002 T>G maps to NM_080863.4 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr17:42248183 C>T maps to NM_080863.4 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:42249504 C>T maps to NM_080863.4 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:42249663 G>A maps to NM_080863.4 T184T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-ER-A42L-06A-11D-A24R-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:76397910 G>A maps to NM_080868.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:76397715 G>A maps to NM_080868.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:237103553 C>T maps to NM_212556.2 Q454Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:94404143 G>A maps to ENST00000434324 I557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr2:53977992 G>A maps to NM_001164165.1 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr2:53927520 G>A maps to NM_001164165.1 N413N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr7:95115432 C>T maps to NM_016116.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr4:177146477 G>A maps to NM_080874.3 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:177142700 G>A maps to NM_080874.3 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr4:177143535 G>A maps to NM_080874.3 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr4:177142360 G>A maps to NM_080874.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:132402972 G>A maps to NM_017873.2 R48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:101188568 C>T maps to NM_198243.2 R287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr23:15268624 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:15266922 G>A did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr10:73887914 C>T maps to NM_001198800.1 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:73892919 G>A maps to NM_001198800.1 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:73956618 G>A maps to NM_001198800.1 Q147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:30209462 G>A maps to NM_032204.3 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr22:30185010 G>A maps to NM_032204.3 I755I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:30197996 G>A maps to NM_032204.3 D518D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:30186468 G>A maps to NM_032204.3 L697L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:30202520 G>A maps to NM_032204.3 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q3-06A-11D-A196-08 chr6:101127553 A>G maps to NM_006828.2 C742C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:100957859 G>A maps to NM_006828.2 R2137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr6:101166118 G>A maps to NM_006828.2 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:101090561 G>A maps to NM_006828.2 Q1266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr6:101166000 G>A maps to NM_006828.2 R677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr6:101090550 G>A maps to NM_006828.2 I1269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:103352345 T>C maps to NM_004316.3 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:8959237 C>T maps to NM_020646.1 K157K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:8959624 G>A maps to NM_020646.1 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr11:8959255 A>G maps to NM_020646.1 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:14231321 G>A maps to NM_018154.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:14231336 G>A maps to NM_018154.2 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:14231300 G>A maps to NM_018154.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:7081840 C>T maps to NM_001671.3 E14E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:7012103 C>T maps to NM_080912.2 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr17:7010399 G>A maps to NM_080912.2 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:7012126 G>A maps to NM_080912.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:155449606 G>A maps to ENST00000368346 L1018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:155449606 G>A maps to ENST00000368346 L1018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr1:155316191 G>A maps to ENST00000368346 D2629D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr1:155313128 A>G maps to ENST00000368346 L2762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:155429668 T>A maps to ENST00000368346 K1669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:155448031 G>A maps to ENST00000368346 L1543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:155429660 G>A maps to ENST00000368346 S1671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:155348103 G>A maps to ENST00000368346 T2105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr1:155330169 G>A maps to ENST00000368346 L2244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr1:155448751 G>A maps to ENST00000368346 I1303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:155340394 G>A maps to ENST00000368346 L2201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr1:155340629 G>A maps to ENST00000368346 P2164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:155450032 G>A maps to ENST00000368346 S876S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:155313165 G>A maps to ENST00000368346 I2749I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:155448283 G>A maps to ENST00000368346 P1459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:155448166 G>A maps to ENST00000368346 P1498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr8:37986354 C>T maps to NM_004674.3 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:37967968 C>T maps to NM_004674.3 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr7:65547371 C>T maps to NM_000048.3 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr7:65553801 C>T maps to NM_000048.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:65546833 C>T maps to NM_000048.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr7:65553884 C>T maps to NM_000048.3 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:65551586 C>T maps to NM_000048.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr7:65552755 C>T maps to NM_000048.3 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:1755427 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:1755365 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:1761767 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:1742106 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:1742136 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:1761855 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:1742085 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:1761771 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:1742159 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:1761793 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZU-06A-12D-A196-08 chr23:1746652 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:1734099 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:1734131 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:1742180 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:1743170 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:1553922 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr23:1536943 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:1546839 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:1551203 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:1531635 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:1540609 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:1540610 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr23:1546779 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr23:1522330 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr23:1546835 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr23:1546836 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:1540588 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:1561105 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr19:12856464 G>A maps to NM_004317.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:12858872 C>T maps to NM_004317.2 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:12848456 T>G maps to NM_004317.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr19:12858339 C>T maps to NM_004317.2 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr7:97482506 G>A maps to NM_183356.3 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr7:97487703 G>A maps to NM_183356.3 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:190530902 C>T maps to NM_019048.2 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:190535412 C>T maps to NM_019048.2 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:51015408 G>A maps to NM_001114598.1 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr14:104571005 G>A maps to NM_001080464.1 E328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr14:104561947 C>T maps to NM_001080464.1 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:104571708 G>A maps to NM_001080464.1 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr14:104570684 G>A maps to NM_001080464.1 E266E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr14:104570978 C>T maps to NM_001080464.1 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr14:104570990 C>T maps to NM_001080464.1 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr8:62566151 G>A maps to NM_004318.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr8:62479729 G>A maps to NM_004318.3 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr8:62479787 A>G maps to NM_004318.3 D413D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:62593566 A>C maps to NM_004318.3 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr8:62416019 G>A maps to NM_004318.3 H725H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:62489366 G>A maps to NM_004318.3 Y371Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr8:62479784 G>A maps to NM_004318.3 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr8:62550914 A>T maps to NM_004318.3 Y266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr16:29912569 G>A maps to NM_181718.3 W93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr16:29912570 G>A maps to NM_181718.3 W93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr16:29912594 A>G maps to NM_181718.3 Q101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr16:29912767 G>A maps to NM_181718.3 W159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:29912864 C>T maps to NM_181718.3 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr22:26830174 C>T maps to NM_020437.4 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr22:26830120 C>T maps to NM_020437.4 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr22:26829736 C>T maps to NM_020437.4 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr22:26829982 C>T maps to NM_020437.4 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:26830117 C>T maps to NM_020437.4 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr22:26829805 T>C maps to NM_020437.4 C75C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q9-06A-11D-A19A-08 chr1:197115395 C>A maps to NM_018136.4 G58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr1:197073832 G>A maps to NM_018136.4 T1516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:197072539 G>A maps to NM_018136.4 L1947L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:197091050 G>A maps to NM_018136.4 R1288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:197086954 C>T maps to NM_018136.4 L1343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:197061161 G>A maps to NM_018136.4 R3107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr1:197112159 G>A maps to NM_018136.4 Q408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:197098367 G>A maps to NM_018136.4 S903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:197071056 G>A maps to NM_018136.4 R2442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:197071056 G>A maps to NM_018136.4 R2442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:197072847 G>A maps to NM_018136.4 Q1845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:197071093 G>A maps to NM_018136.4 S2429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr1:197071456 G>A maps to NM_018136.4 F2308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr1:197097756 G>A maps to NM_018136.4 F933F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:197073648 G>A maps to NM_018136.4 R1578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:197073619 G>A maps to NM_018136.4 I1587I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:95228676 C>T maps to NM_017680.4 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:70188628 C>T maps to NM_152792.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr2:70188780 G>A maps to NM_152792.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr2:70188298 G>A maps to NM_152792.2 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:70188220 C>T maps to NM_152792.2 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:70188514 G>A maps to NM_152792.2 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:70187830 C>T maps to NM_152792.2 E330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:70188487 G>A maps to NM_152792.2 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr17:79974727 C>T maps to ENST00000306729 A580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:79941489 T>C maps to ENST00000306729 N73N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:79954352 A>G maps to ENST00000306729 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr17:79968739 G>A maps to ENST00000306729 E411E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr11:62124473 C>T maps to NM_025080.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:62159692 C>T maps to NM_025080.3 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:133355801 C>T maps to NM_000050.4 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:133370260 G>A maps to NM_000050.4 W326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:133333810 G>A maps to NM_000050.4 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:133333933 G>A maps to NM_000050.4 Q107Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:133346887 C>T maps to NM_000050.4 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:133333957 C>T maps to NM_000050.4 S115S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A180-06A-11D-A21A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:130743961 G>A maps to ENST00000514044 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:130744045 A>C maps to ENST00000514044 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:96789942 C>T maps to NM_001002036.3 E314E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:96798414 G>A maps to NM_001002036.3 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr2:96799702 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:96789834 G>A maps to NM_001002036.3 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:96798393 C>T maps to NM_001002036.3 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:96795637 G>A maps to NM_001002036.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:96789921 C>T maps to NM_001002036.3 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr1:176863805 G>A maps to ENST00000281881 P952P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr1:176915159 C>T maps to ENST00000281881 E725E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:176833437 C>T maps to ENST00000281881 G1297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:176833425 C>T maps to ENST00000281881 E1301E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:176838011 G>A maps to ENST00000281881 F1213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr1:176903417 C>T maps to ENST00000281881 A855A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:176845697 G>A maps to ENST00000281881 P1154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:176927485 C>T maps to ENST00000281881 E585E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:177001814 C>T maps to ENST00000281881 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:176833485 C>T maps to ENST00000281881 R1281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:177001936 G>A maps to ENST00000281881 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:177001937 G>A maps to ENST00000281881 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:176863775 G>A maps to ENST00000281881 T962T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:176833455 G>A maps to ENST00000281881 I1291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:176992576 G>A maps to ENST00000281881 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:176905402 C>T maps to ENST00000281881 Q835Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:176863759 G>A maps to ENST00000281881 L968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:176833425 C>T maps to ENST00000281881 E1301E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:176927614 G>A maps to ENST00000281881 F542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:176993845 C>T maps to ENST00000281881 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:176838077 C>T maps to ENST00000281881 L1191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:176905450 G>A maps to ENST00000281881 V819V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:176852014 C>T maps to ENST00000281881 L1122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr1:176833599 G>A maps to ENST00000281881 L1243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr1:176853523 G>A maps to ENST00000281881 L1067L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:176934336 G>A maps to ENST00000281881 D528D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:176927614 G>A maps to ENST00000281881 F542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:176845760 C>T maps to ENST00000281881 W1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr1:176833656 C>T maps to ENST00000281881 R1224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr1:176984009 C>T maps to ENST00000281881 G488G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr1:176905441 C>T maps to ENST00000281881 V822V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr1:176838038 G>A maps to ENST00000281881 N1204N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr1:176915228 C>T maps to ENST00000281881 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr1:176915075 C>G maps to ENST00000281881 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr1:176992575 G>A maps to ENST00000281881 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:176998788 C>T maps to ENST00000281881 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:177001814 C>T maps to ENST00000281881 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr1:176853550 G>A maps to ENST00000281881 I1058I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:176833425 C>T maps to ENST00000281881 E1301E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:176853514 C>T maps to ENST00000281881 E1070E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:176992705 C>T maps to ENST00000281881 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:176905400 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:176915201 C>T maps to ENST00000281881 T711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:176853577 C>T maps to ENST00000281881 L1049L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr9:119204828 G>A maps to ENST00000313400 F1167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr9:119976640 C>T maps to ENST00000313400 K337K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr9:119976643 C>T maps to ENST00000313400 E336E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr9:119188210 G>A maps to ENST00000313400 I1313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr9:120053706 G>A maps to ENST00000313400 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:119188291 G>A maps to ENST00000313400 I1286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr9:119976925 C>T maps to ENST00000313400 K242K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:120053607 C>T maps to ENST00000313400 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:120053706 G>T maps to ENST00000313400 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:120053792 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr9:119202919 G>A maps to ENST00000313400 F1250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr9:119976661 T>C maps to ENST00000313400 E330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:119626012 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr9:119567999 G>A maps to ENST00000313400 F769F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:119567938 G>A maps to ENST00000313400 Q790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:120053706 G>A maps to ENST00000313400 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr9:119976886 G>A maps to ENST00000313400 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr9:119568092 C>T maps to ENST00000313400 V738V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr9:119188177 C>T maps to ENST00000313400 K1324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr9:119188350 G>A maps to ENST00000313400 L1267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr9:119858419 G>A maps to ENST00000313400 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr9:119188356 G>A maps to ENST00000313400 L1265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:119770440 G>A maps to ENST00000313400 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr20:31024546 C>T maps to ENST00000375687 S1344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr20:31021578 C>T maps to ENST00000375687 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr20:31024357 C>T maps to ENST00000375687 S1281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:31024660 C>T maps to ENST00000375687 A1382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr20:31024036 G>A maps to ENST00000375687 K1174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:31023913 C>T maps to ENST00000375687 S1133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:25973191 G>A maps to NM_018263.4 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr2:25990458 G>C maps to NM_018263.4 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:25973191 G>A maps to NM_018263.4 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:25967138 G>A maps to NM_018263.4 T689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:25966190 C>T maps to NM_018263.4 E1005E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr2:25976475 G>A maps to NM_018263.4 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:25965599 G>A maps to NM_018263.4 S1202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:25976475 G>A maps to NM_018263.4 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr18:31323471 C>T maps to NM_030632.1 T1220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr18:31320100 G>A maps to NM_030632.1 V911V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr18:31323747 C>T maps to NM_030632.1 S1312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr18:31323762 C>T maps to NM_030632.1 S1317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:31320001 T>G maps to NM_030632.1 P878P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:31323099 G>A maps to NM_030632.1 T1096T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr18:31319167 A>G maps to NM_030632.1 E600E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr18:31322973 C>T maps to NM_030632.1 L1054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:31324047 C>G maps to NM_030632.1 T1412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:31263381 G>A maps to NM_030632.1 W243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr18:31324347 G>A maps to NM_030632.1 Q1512Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr18:31320289 C>T maps to NM_030632.1 I974I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr18:31320205 C>T maps to NM_030632.1 S946S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr18:31325068 T>C maps to NM_030632.1 L1753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr18:31325439 A>G maps to NM_030632.1 Q1876Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr18:31323828 C>T maps to NM_030632.1 T1339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr18:31324785 G>A maps to NM_030632.1 R1658R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr18:31325946 C>T maps to NM_030632.1 L2045L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr18:31322973 C>T maps to NM_030632.1 L1054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr18:31323667 C>T maps to NM_030632.1 Q1286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr18:31323342 G>A maps to NM_030632.1 E1177E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:31325158 C>T maps to NM_030632.1 Q1783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr18:31326096 A>G maps to NM_030632.1 E2095E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr18:31325109 G>A maps to NM_030632.1 Q1766Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr18:31319240 C>T maps to NM_030632.1 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:117023161 G>A maps to NM_130768.2 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr7:117025763 C>T maps to NM_130768.2 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:117021075 C>A maps to NM_130768.2 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr7:117008755 G>A maps to NM_130768.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr10:89527455 G>A maps to NM_032810.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:124384031 G>A maps to NM_014109.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr8:124358363 C>A maps to NM_014109.3 G832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr8:124335306 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:124408488 T>G maps to NM_014109.3 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr8:124359339 A>T maps to NM_014109.3 L735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:124371872 G>A maps to NM_014109.3 R404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:124371872 G>A maps to NM_014109.3 R404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr2:24107742 C>A maps to NM_017552.1 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:24090766 G>T maps to NM_017552.1 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:1463113 C>T maps to NM_018188.3 F507F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:1417677 C>A maps to NM_031921.4 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:1421569 C>T maps to NM_031921.4 I348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:1417620 C>T maps to NM_031921.4 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:1389810 G>A maps to NM_001039211.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:1391199 C>T maps to NM_001039211.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:1403780 C>T maps to NM_001039211.2 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:1396177 C>T maps to NM_001039211.2 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:1389840 C>T maps to NM_001039211.2 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:1391168 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:1396132 C>T maps to NM_001039211.2 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:1396195 C>T maps to NM_001039211.2 D293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr1:1387780 C>T maps to NM_001039211.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr1:1387774 C>T maps to NM_001039211.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr17:29162876 C>G maps to NM_024857.3 S593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr17:29171040 C>T maps to NM_024857.3 S784S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:29219748 C>T maps to NM_024857.3 T1461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:29162097 C>T maps to NM_024857.3 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr17:29220571 G>A maps to NM_024857.3 K1567K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr17:29161413 C>T maps to NM_024857.3 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:3905498 C>T maps to NM_033064.4 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:3905627 G>A maps to NM_033064.4 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:3907801 G>A maps to NM_033064.4 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:3910881 C>T maps to NM_033064.4 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:3907801 G>A maps to NM_033064.4 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:3905603 G>A maps to NM_033064.4 E103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:3907852 G>A maps to NM_033064.4 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr19:3907813 C>T maps to NM_033064.4 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:123600676 G>A maps to NM_001001976.1 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:123629550 G>A maps to NM_001001976.1 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:175945430 T>C maps to NM_001880.2 K416K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr22:39917599 C>T maps to NM_182810.1 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:39918129 G>A maps to NM_182810.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr22:39918063 C>A maps to NM_182810.1 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:50436306 C>T maps to NM_001193646.1 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:161928360 C>T maps to NM_007348.2 Q644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:161928371 C>T maps to NM_007348.2 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:161761235 C>T maps to NM_007348.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr1:161736197 C>T maps to NM_007348.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:161761241 C>T maps to NM_007348.2 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:161753802 C>T maps to NM_007348.2 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr1:161816268 C>T maps to NM_007348.2 N406N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:32083536 G>A maps to NM_004381.4 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr6:32087645 G>A maps to NM_004381.4 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr6:32083620 C>T maps to NM_004381.4 Q669Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr6:32086586 G>A maps to NM_004381.4 F403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:32084284 G>A maps to NM_004381.4 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:32085143 G>A maps to NM_004381.4 Q524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:32087713 G>A maps to NM_004381.4 Q285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:32087714 G>A maps to NM_004381.4 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr6:32085697 G>A maps to NM_004381.4 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:53925562 G>A maps to NM_001130059.1 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:53931282 G>A maps to NM_001130059.1 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr12:14577478 C>T maps to NM_018179.3 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr12:14578045 A>G maps to NM_018179.3 E399E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:14631254 C>T maps to NM_018179.3 P982P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr12:14578075 G>A maps to NM_018179.3 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr12:14578321 C>T maps to NM_018179.3 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr12:14613435 A>G maps to NM_018179.3 S722S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:14613921 C>T maps to NM_018179.3 A884A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:10532043 G>A maps to NM_024997.2 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr16:10525282 G>A maps to NM_024997.2 W269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:10524918 C>T maps to NM_024997.2 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:10525052 G>A maps to NM_024997.2 K192K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:10534238 C>T maps to NM_024997.2 Q372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:10524803 G>A maps to NM_024997.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:115177141 A>C maps to ENST00000274459 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:234178647 G>A maps to ENST00000392018 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:234200863 C>T maps to ENST00000392018 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:72538326 C>T maps to NM_033388.1 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr11:72539460 C>T maps to NM_033388.1 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr11:64663932 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:64680845 C>T maps to ENST00000421419 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr11:64664942 G>A maps to ENST00000421419 I1699I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:64678104 G>A maps to ENST00000421419 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:64662857 G>A maps to ENST00000421419 S1830S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:64678736 G>A maps to ENST00000421419 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:64681834 G>A maps to ENST00000421419 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:64669436 G>A maps to ENST00000421419 I1374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:64668366 G>A maps to ENST00000421419 H1441H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr11:64677577 G>A maps to ENST00000421419 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr11:64676580 C>T maps to ENST00000421419 W749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:64678344 G>A maps to ENST00000421419 H516H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:64669577 G>A maps to ENST00000421419 P1327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:64673042 G>A maps to ENST00000421419 F1152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr11:64673910 T>C maps to ENST00000421419 E1026E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr11:64684505 G>A maps to ENST00000421419 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:64675084 G>A maps to ENST00000421419 P853P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:64681878 G>A maps to ENST00000421419 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:64663969 G>A maps to ENST00000421419 A1799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:64684436 C>T maps to ENST00000421419 W57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr11:64662525 G>A maps to ENST00000421419 L1914L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64662881 G>A maps to ENST00000421419 S1822S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64663999 G>A maps to ENST00000421419 A1789A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64669637 G>A maps to ENST00000421419 L1307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64675260 G>A maps to ENST00000421419 I822I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr11:64677516 G>A maps to ENST00000421419 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr11:64677517 G>A maps to ENST00000421419 G619G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:64673804 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr14:96761442 C>T maps to NM_018036.5 K1760K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr14:96792070 G>A maps to NM_018036.5 F784F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr14:96772122 G>A maps to NM_018036.5 I1512I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr14:96773200 G>A maps to NM_018036.5 F1452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr14:96775865 T>C maps to NM_018036.5 L1409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:96800165 G>A maps to NM_018036.5 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:96813606 G>A maps to NM_018036.5 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr14:96756091 G>A maps to NM_018036.5 I1969I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr14:96800142 C>T maps to NM_018036.5 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:96788537 G>A maps to NM_018036.5 I930I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:96768430 G>A maps to NM_018036.5 A1684A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr14:96795091 G>A maps to NM_018036.5 F631F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:112251590 G>A maps to NM_022488.3 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3BZ-06A-12D-A196-08 chr23:107381180 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:107377368 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:107381364 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:107381054 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:107393512 C>T did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:107395031 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr2:242598520 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:242590434 C>T maps to ENST00000337606 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr1:63307134 C>T maps to NM_032852.2 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:63299787 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:63299788 T>C did not map to a codon.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr19:10655729 C>T maps to NM_032885.4 D139D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr19:10662724 C>T maps to NM_032885.4 D350D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:10663559 G>A did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:10662727 C>T maps to NM_032885.4 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr3:11356815 A>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:11389370 C>T maps to NM_006395.2 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr3:11389358 C>T maps to NM_006395.2 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr3:11406183 C>T maps to NM_006395.2 T617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:11389499 C>T maps to NM_006395.2 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:220090284 G>A maps to NM_024085.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:220089207 G>A maps to NM_024085.3 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:220090284 G>A maps to NM_024085.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:220089006 G>A maps to NM_024085.3 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:220089165 G>A maps to NM_024085.3 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:220088623 C>T maps to NM_024085.3 R462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr7:150715840 G>A maps to NM_173681.5 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:150720252 G>A maps to NM_173681.5 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:150715446 C>T maps to NM_173681.5 E602E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:150721146 G>A maps to NM_173681.5 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr7:150718280 G>A maps to NM_173681.5 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:150718295 C>T maps to NM_173681.5 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:150720280 G>A maps to NM_173681.5 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr7:150713832 G>A maps to NM_173681.5 Q789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150714258 C>T maps to NM_173681.5 W718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150715527 G>A maps to NM_173681.5 F575F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150715858 G>A maps to NM_173681.5 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr11:293410 C>T maps to ENST00000409479 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:292007 C>T maps to ENST00000409479 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:294568 C>T maps to ENST00000409479 S705S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:216214333 G>T maps to NM_004044.6 G579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr14:51079994 C>T maps to ENST00000358385 R217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:51094843 G>A maps to ENST00000358385 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr11:63396853 G>A maps to NM_015459.3 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:63426316 G>A maps to NM_015459.3 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:108164092 C>T maps to NM_000051.3 L1555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:108139248 C>T maps to NM_000051.3 S917S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:108155010 G>A maps to NM_000051.3 V1268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:108124633 C>T maps to NM_000051.3 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:108175547 C>T maps to NM_000051.3 S1881S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:108236210 C>T maps to NM_000051.3 F3049F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr11:108199954 C>T maps to NM_000051.3 Q2433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:108224517 C>T maps to NM_000051.3 I2899I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:108138013 C>T maps to NM_000051.3 Y861Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:108202274 C>T maps to NM_000051.3 V2540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr11:108225535 A>G did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:108159736 T>C maps to NM_000051.3 F1381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:108163384 C>T maps to NM_000051.3 S1492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:108214073 C>T maps to NM_000051.3 A2798A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr16:81078292 C>T maps to NM_015251.2 S730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr16:81077593 G>A maps to NM_015251.2 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr12:7048060 C>T maps to NM_001940.3 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr12:7050043 C>T maps to NM_001940.3 A1072A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:7047861 C>T maps to NM_001940.3 D912D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr4:94751093 G>A maps to NM_005172.1 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr4:94750832 C>T maps to NM_005172.1 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr4:94750610 C>T maps to NM_005172.1 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr10:69991053 C>T maps to NM_145178.2 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr15:25924934 G>A maps to NM_024490.3 S1351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr15:26107817 G>A maps to NM_024490.3 H142H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr15:25958938 G>A maps to NM_024490.3 F742F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr15:25936909 G>A maps to NM_024490.3 I1039I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr15:25924898 G>A maps to NM_024490.3 S1363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr15:26026219 C>T maps to NM_024490.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:25925989 G>A maps to NM_024490.3 F1215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr15:26107964 G>A maps to NM_024490.3 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr15:25966938 G>A maps to NM_024490.3 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr15:25966939 G>A maps to NM_024490.3 C409C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:25936879 G>T maps to NM_024490.3 S1049S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:25961909 G>A maps to NM_024490.3 V581V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr15:25958929 G>A maps to NM_024490.3 V745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr5:160039885 C>T maps to NM_025153.2 T900T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:160029661 C>T maps to NM_025153.2 K1095K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr5:160039921 C>T maps to NM_025153.2 G888G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:160039885 C>T maps to NM_025153.2 T900T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr5:160018074 G>A maps to NM_025153.2 I1212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:159996681 G>A maps to NM_025153.2 F1253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:160049460 G>A maps to NM_025153.2 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:160063272 G>A maps to NM_025153.2 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:160115066 C>T maps to NM_025153.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr5:160025932 G>A maps to NM_025153.2 F1136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:160047948 G>A maps to NM_025153.2 I607I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:160059351 C>T maps to NM_025153.2 K468K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr5:160067516 G>A maps to NM_025153.2 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr5:160097640 C>T maps to NM_025153.2 K168K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr5:160067534 C>T maps to NM_025153.2 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:160039885 C>T maps to NM_025153.2 T900T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:160049499 C>T maps to NM_025153.2 K571K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:160113174 G>A maps to NM_025153.2 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:160114868 G>A maps to NM_025153.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr4:47538833 C>T maps to NM_020453.3 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr4:47556759 A>G maps to NM_020453.3 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:47582431 C>T maps to NM_020453.3 T1195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:47538909 C>T maps to NM_020453.3 R451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:47514829 A>G maps to NM_020453.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:47571047 C>T maps to NM_020453.3 F1016F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:47593256 T>C maps to NM_020453.3 S1380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:47517561 G>A maps to NM_020453.3 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:47527653 C>T maps to NM_020453.3 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:47559742 C>T maps to NM_020453.3 F629F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:47560240 G>A maps to NM_020453.3 T795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:47561042 G>A maps to NM_020453.3 K846K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr4:47556870 C>T maps to NM_020453.3 F588F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr4:47578884 C>A maps to NM_020453.3 L1154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr13:113536356 C>T maps to NM_032189.3 S1185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr13:113470452 C>T maps to NM_032189.3 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr13:113487280 C>T maps to NM_032189.3 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr13:113485771 C>T maps to NM_032189.3 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:113512582 C>T maps to NM_032189.3 L882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr13:113479872 G>A maps to NM_032189.3 E334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr3:182545993 T>A maps to NM_014616.1 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr3:182591615 C>T maps to NM_014616.1 R689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:182584160 C>T maps to NM_014616.1 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr23:138878605 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:138878600 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:138901536 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:138823169 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:138869361 C>G did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:138870378 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:138864888 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:138864758 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:138878600 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr23:138827913 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:138878533 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:138820207 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:138828015 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:138840014 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:138857015 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr13:25272953 C>T maps to NM_001185085.1 Y563Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr13:25280558 C>T maps to NM_001185085.1 S715S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr13:25281468 G>A maps to NM_001185085.1 K803K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr13:25274960 G>A maps to NM_001185085.1 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr13:25264589 C>T maps to NM_001185085.1 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr13:25284611 G>A maps to NM_001185085.1 R932R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr13:25262536 G>A maps to NM_001185085.1 E103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr13:25255746 C>T maps to NM_001185085.1 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr13:25281495 G>A maps to NM_001185085.1 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr13:25284953 C>T maps to NM_001185085.1 I980I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr13:25281309 C>T maps to NM_001185085.1 I779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:25264839 T>A maps to NM_001185085.1 Y260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:25281300 C>T maps to NM_001185085.1 F776F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:25283503 C>T maps to NM_001185085.1 I838I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr13:25265186 C>T maps to NM_001185085.1 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr13:25284644 C>T maps to NM_001185085.1 F943F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr13:25275032 C>T maps to NM_001185085.1 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:19757946 G>A maps to NM_020410.2 S1032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr19:19766130 T>A maps to NM_020410.2 K510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:19760600 G>A maps to NM_020410.2 L828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr19:19766391 G>A maps to NM_020410.2 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr19:19757946 G>A maps to NM_020410.2 S1032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:19766713 G>A maps to NM_020410.2 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19758334 G>A maps to NM_020410.2 D932D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19760573 G>A maps to NM_020410.2 F837F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19760618 G>A maps to NM_020410.2 T822T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19765373 G>A maps to NM_020410.2 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19766140 G>A maps to NM_020410.2 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19766364 G>A maps to NM_020410.2 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr1:17331976 G>A maps to NM_022089.2 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr1:17316750 G>A maps to NM_022089.2 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr1:17322553 G>A maps to NM_022089.2 R487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:17313447 G>A maps to NM_022089.2 F1029F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:17316660 G>A maps to NM_022089.2 F791F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr1:17327005 G>A maps to NM_022089.2 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:17318747 G>A maps to NM_022089.2 N665N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr1:17326972 G>A maps to NM_022089.2 D254D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:17322554 G>A maps to NM_022089.2 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr3:194158091 G>A maps to NM_024524.3 A649A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:194134538 T>A maps to NM_024524.3 V1144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr3:194177884 A>T maps to NM_024524.3 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:193209120 C>T maps to NM_032279.2 K200K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr3:193176920 C>T maps to NM_032279.2 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr3:193210748 G>A maps to NM_032279.2 Q164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr3:193188720 C>T maps to NM_032279.2 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:193185216 C>T maps to NM_032279.2 W334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:193156316 G>A maps to NM_032279.2 A873A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:193182887 G>A maps to NM_032279.2 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:193177019 G>A maps to NM_032279.2 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:193120602 G>A maps to NM_032279.2 F1143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:193180585 C>T maps to NM_032279.2 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr3:193158417 G>A maps to NM_032279.2 I816I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:193153514 G>A maps to NM_032279.2 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr3:193125149 G>A maps to NM_032279.2 S1110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:193175221 G>A maps to NM_032279.2 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:193188693 G>T maps to NM_032279.2 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:193210710 C>T maps to NM_032279.2 E176E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr3:193207524 G>A maps to NM_032279.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr3:193158408 G>A maps to NM_032279.2 T819T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:193120443 G>A maps to NM_032279.2 L1196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:193201770 G>A maps to NM_032279.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:193160187 C>T maps to NM_032279.2 G770G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:193132531 C>T maps to NM_032279.2 L950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:193185207 C>T maps to NM_032279.2 Q337Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:193068879 G>A maps to NM_198505.2 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr3:193039581 G>A maps to NM_198505.2 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr3:193042769 C>T maps to NM_198505.2 Q519Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr3:193031914 C>T maps to NM_198505.2 V742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:193023394 A>C maps to NM_198505.2 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr3:193019020 G>A maps to NM_198505.2 I918I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:193040354 T>C maps to NM_198505.2 E561E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:193031932 G>A maps to NM_198505.2 I736I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr3:193051604 G>A maps to NM_198505.2 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr3:193023421 T>A maps to NM_198505.2 S868S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:193031839 C>T maps to NM_198505.2 E767E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:193061824 G>A maps to NM_198505.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:193032885 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:193051658 G>A maps to NM_198505.2 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:193007717 G>A maps to NM_198505.2 L993L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:193071933 C>T maps to NM_198505.2 W196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr3:193028434 C>T maps to NM_198505.2 Q839Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:193029615 A>G maps to NM_198505.2 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:193081081 G>A maps to NM_198505.2 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:193036847 G>A maps to NM_198505.2 F655F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:193042757 C>T maps to NM_198505.2 W523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr3:193036883 G>A maps to NM_198505.2 F643F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:193019068 G>A maps to NM_198505.2 S902S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr3:193007753 G>A maps to NM_198505.2 S981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr3:193081162 A>G maps to NM_198505.2 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr3:193061833 C>T maps to NM_198505.2 E275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr3:192997196 G>A maps to NM_198505.2 F1091F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr3:193042715 G>A maps to NM_198505.2 I537I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:193080174 C>T maps to NM_198505.2 E177E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:193028502 G>A maps to NM_198505.2 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:193052802 C>T maps to NM_198505.2 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:193036814 C>T maps to NM_198505.2 K666K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr3:193080388 C>T maps to NM_198505.2 W141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:193048986 C>T maps to NM_198505.2 K462K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr3:193049022 C>T maps to NM_198505.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:116932208 C>T maps to NM_000701.7 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:116941600 C>T maps to NM_000701.7 T781T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr1:116931558 C>T maps to NM_000701.7 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:116943868 C>T maps to NM_000701.7 Q946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:116935537 T>C maps to NM_000701.7 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:160105689 C>T maps to NM_000702.3 P782P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:160106420 C>T maps to NM_000702.3 F875F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A6L9-06A-11D-A32N-08 chr1:160104347 T>C maps to NM_000702.3 G634G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:160098869 C>T maps to NM_000702.3 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:160109444 T>A maps to NM_000702.3 I952I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:160105279 G>A maps to NM_000702.3 K724K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:160105659 C>T maps to NM_000702.3 S772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:160090787 G>A maps to NM_000702.3 K35K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:160093109 C>T maps to NM_000702.3 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:160106360 G>A maps to NM_000702.3 G855G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:160091023 C>T maps to NM_000702.3 Q54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:160111090 G>A maps to NM_000702.3 V1014V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:160105252 G>A maps to NM_000702.3 G715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:160109727 C>T maps to NM_000702.3 F996F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:160109742 C>T maps to NM_000702.3 V1001V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:160109743 C>T maps to NM_000702.3 R1002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:42489288 G>A maps to ENST00000441343 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:42489288 G>A maps to ENST00000441343 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr19:42492160 C>T maps to ENST00000441343 W95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:42492156 G>A maps to ENST00000441343 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr19:42490288 G>A maps to ENST00000441343 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr19:42489162 G>A maps to ENST00000441343 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr19:42482128 G>A maps to ENST00000441343 I634I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:42489189 G>A maps to ENST00000441343 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:42489219 G>A maps to ENST00000441343 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:42489538 G>A maps to ENST00000441343 Q215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:42474557 G>A maps to ENST00000441343 I800I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr19:42489560 G>A maps to ENST00000441343 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:42479940 A>T maps to ENST00000441343 I701I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:42489188 G>A maps to ENST00000441343 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:42490330 G>A maps to ENST00000441343 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:42482806 G>A maps to ENST00000441343 A527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:42485933 G>A maps to ENST00000441343 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:42489108 G>A maps to ENST00000441343 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr19:42482944 G>A maps to ENST00000441343 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr19:42471467 G>A maps to ENST00000441343 F982F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:42490033 G>A maps to ENST00000441343 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:42479799 G>A maps to ENST00000441343 I748I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr19:42480591 G>A maps to ENST00000441343 I690I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:42479895 C>T maps to ENST00000441343 K716K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr1:160151514 G>A maps to NM_144699.3 T926T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:160129279 C>A maps to NM_144699.3 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:160156080 C>T maps to NM_144699.3 L995L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:160143375 C>T maps to NM_144699.3 I620I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:160125917 C>T maps to NM_144699.3 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:160156064 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:160156125 C>T maps to NM_144699.3 I1010I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:160124953 C>T maps to NM_144699.3 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:160128844 G>A maps to NM_144699.3 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:160124974 C>T maps to NM_144699.3 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:160136851 C>T maps to NM_144699.3 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:160151743 C>T maps to NM_144699.3 I964I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:160143990 C>T maps to NM_144699.3 I694I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:160141070 C>T maps to NM_144699.3 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:169094120 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr17:7554889 G>A maps to NM_001678.3 K18K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:7556716 T>G maps to NM_001678.3 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:7558867 C>T maps to NM_001678.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:119500505 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:119500514 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:119510246 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:119504678 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:119513343 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr23:119496049 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:119500468 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:119500592 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:119510246 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr16:28913329 G>A maps to NM_173201.3 E749E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:28898813 G>A maps to NM_173201.3 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:28892243 C>T maps to NM_173201.3 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:28912173 G>A maps to NM_173201.3 V679V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:28906195 C>T maps to NM_173201.3 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:28906196 C>T maps to NM_173201.3 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:110778513 C>T maps to NM_170665.3 I604I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr12:110782766 C>T maps to NM_170665.3 F866F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:110783853 C>T maps to NM_170665.3 I930I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr12:110719707 C>A maps to NM_170665.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr12:110784070 C>T maps to NM_170665.3 P975P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:110781219 C>T maps to NM_170665.3 F834F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr12:110778624 C>T maps to NM_170665.3 F641F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:110782763 C>T maps to NM_170665.3 S865S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr17:3839603 G>A maps to NM_174953.1 A827A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr17:3854587 G>A maps to NM_174953.1 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:3839720 G>A maps to NM_174953.1 I788I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:3844588 G>A maps to NM_174953.1 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr17:3831526 G>A maps to NM_174953.1 A1025A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:3846786 C>T maps to NM_174953.1 E439E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:3851089 C>T maps to NM_174953.1 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:3853996 G>A maps to NM_174953.1 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr17:3856721 C>T maps to NM_174953.1 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:3839693 C>G maps to NM_174953.1 L797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr17:3844927 G>A maps to NM_174953.1 I522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:3831550 C>T maps to NM_174953.1 W1017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:3844783 G>A maps to NM_174953.1 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:3850756 G>A maps to NM_174953.1 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr17:3833719 G>A maps to NM_174953.1 F873F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr17:3851044 C>T maps to NM_174953.1 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr12:89984763 G>C maps to ENST00000428670 L1249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:89998000 G>A maps to ENST00000428670 F855F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:89992998 A>C maps to ENST00000428670 P1082P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:90018043 G>A maps to ENST00000428670 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr12:90036049 G>A maps to ENST00000428670 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr12:90005119 C>T maps to ENST00000428670 R699R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:90018082 C>T maps to ENST00000428670 E407E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:89998000 G>A maps to ENST00000428670 F855F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:90010761 G>A maps to ENST00000428670 D628D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr12:89998000 G>A maps to ENST00000428670 F855F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:10442634 A>C did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr3:10400473 G>A maps to NM_001001331.2 F679F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:10387100 C>T maps to NM_001001331.2 V890V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:10443911 C>T maps to NM_001001331.2 W173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:10430006 G>A maps to NM_001001331.2 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:10428191 C>T maps to NM_001001331.2 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:10370569 C>T maps to NM_001001331.2 T1220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr3:10430030 G>A maps to NM_001001331.2 N279N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:10401738 G>A maps to NM_001001331.2 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:10430057 C>T maps to NM_001001331.2 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:10428191 C>T maps to NM_001001331.2 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:10400473 G>A maps to NM_001001331.2 F679F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:10413713 G>A maps to NM_001001331.2 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:10452326 G>A maps to NM_001001331.2 Y124Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:10420053 G>A maps to NM_001001331.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:10442696 G>A maps to NM_001001331.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:10452413 G>A maps to NM_001001331.2 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:10391802 C>T maps to NM_001001331.2 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr3:10400596 G>A maps to NM_001001331.2 I638I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:10384468 G>A maps to NM_001001331.2 Q962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:10442733 G>A maps to NM_001001331.2 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:10379964 C>T maps to NM_001001331.2 P1105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:10384493 C>T maps to NM_001001331.2 K953K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:10387187 G>A maps to NM_001001331.2 I861I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:10392111 G>A maps to NM_001001331.2 F762F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:10420094 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:10420945 C>T maps to NM_001001331.2 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:10452332 G>A maps to NM_001001331.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:10419993 C>T maps to NM_001001331.2 K381K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr3:10384604 G>A maps to NM_001001331.2 I916I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr23:152807133 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr23:152815567 C>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:152835062 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:152835063 G>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:152801761 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:152815136 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr23:152818589 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:152835064 A>T did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:152815106 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:152821605 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:152830488 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:152826320 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:152818530 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr23:152815550 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr23:152835129 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:152818564 G>A did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:152845446 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:152815719 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr23:152845622 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:152818520 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:152818549 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:152825334 T>A did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:152826143 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:203689717 C>T maps to NM_001001396.1 I816I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:203696696 C>T maps to NM_001001396.1 Q1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:203668663 T>C maps to NM_001001396.1 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:203668765 C>T maps to NM_001001396.1 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:203680016 C>T maps to NM_001001396.1 I604I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:203696662 C>T maps to NM_001001396.1 I1091I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:203678658 C>T maps to NM_001001396.1 I596I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr1:203708741 C>T maps to NM_001684.3 S1126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:203667415 C>T maps to NM_001001396.1 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:203676167 C>T maps to NM_001001396.1 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:203680139 C>T maps to NM_001001396.1 F645F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:203681212 C>T maps to NM_001001396.1 F719F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:130653539 C>T maps to NM_001001486.1 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:130659529 C>T maps to NM_001001486.1 C139C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:130714934 C>T maps to NM_001001486.1 F702F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr16:84442069 G>A maps to ENST00000416219 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr16:84456105 C>T maps to ENST00000416219 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:84444323 G>A maps to ENST00000416219 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:84472843 G>A maps to ENST00000416219 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:84486807 G>A maps to ENST00000416219 V632V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr16:84456093 C>T maps to ENST00000416219 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr16:84456269 C>T maps to ENST00000416219 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr16:84482185 C>T maps to ENST00000416219 I517I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:84459395 G>A maps to ENST00000416219 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:84456105 C>T maps to ENST00000416219 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr16:84494307 G>A maps to ENST00000416219 R823R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:84456239 C>T maps to ENST00000416219 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:84472807 C>T maps to ENST00000416219 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:84456111 C>T maps to ENST00000416219 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr16:84482158 C>T maps to ENST00000416219 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr19:36050054 C>T maps to NM_000704.2 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr19:36046379 G>A maps to NM_000704.2 Q707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr19:36051442 C>T maps to NM_000704.2 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:36050757 G>A maps to NM_000704.2 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr13:114307749 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr18:43667372 G>A maps to NM_001001937.1 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr12:57037237 G>A maps to NM_001686.3 Y247Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:57032175 G>A maps to NM_001686.3 F507F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:57032928 G>A maps to NM_001686.3 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr10:7841004 C>T maps to NM_001001973.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:54069841 C>T maps to NM_005176.5 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr12:54062945 G>A maps to NM_005176.5 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:54063086 T>A maps to NM_005176.5 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:176043861 A>C maps to NM_001689.4 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:667113 C>T maps to NM_007100.3 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr21:27097614 G>A maps to NM_001003701.1 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr7:99057784 G>A maps to NM_001198879.1 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:118277724 C>T maps to NM_006476.4 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr21:35281509 G>A maps to ENST00000429238 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr21:35275892 A>T maps to NM_001697.2 Y193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr14:50789411 C>T maps to NM_001003803.2 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:41944211 G>A maps to ENST00000417807 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr19:41939226 G>A maps to ENST00000417807 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:153664095 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:153664161 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:153662767 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:153664092 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:153657474 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:153657424 G>A did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr5:81608651 C>T maps to NM_001017971.1 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:40456804 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:40456824 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:40456557 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:40450600 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:40653288 C>T maps to NM_001130020.1 V664V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr17:40639345 C>T maps to NM_001130020.1 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:40618524 C>T maps to NM_001130020.1 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr17:40665946 C>T maps to NM_001130020.1 S734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr12:124228430 C>T maps to NM_012463.3 Q380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44Q-06A-11D-A25O-08 chr12:124229191 C>T maps to NM_012463.3 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:124221680 C>T maps to NM_012463.3 Q301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:124229289 C>T maps to NM_012463.3 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:124239058 C>T maps to NM_012463.3 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr12:124232227 C>T maps to NM_012463.3 I560I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr7:138418933 G>A maps to NM_130840.2 I546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:138418994 C>T maps to NM_130840.2 W526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:138447680 C>T maps to NM_130840.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:138453966 C>T maps to NM_130840.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:138394417 G>A maps to NM_130840.2 L794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:138406743 A>G maps to NM_130840.2 D679D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:138447752 C>T maps to NM_130840.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:138455976 G>A maps to NM_130840.2 R6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:138429968 G>A maps to NM_130840.2 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:138418921 G>A maps to NM_130840.2 V550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:138444532 G>A maps to NM_130840.2 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:138444499 C>T maps to NM_130840.2 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:138453617 A>T maps to NM_130840.2 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr7:138430020 C>T maps to NM_130840.2 W442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr7:138437390 C>T maps to NM_130840.2 K336K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr7:138437471 C>T maps to NM_130840.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr7:138394391 G>A maps to NM_130840.2 F802F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:138394382 G>A maps to NM_130840.2 A805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:138417780 G>A maps to NM_130840.2 I583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:138447770 C>T did not map to a codon.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr7:138453984 A>G maps to NM_130840.2 N43N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr16:2569309 C>T maps to NM_001694.3 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr16:2569324 T>C maps to NM_001694.3 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:2569619 G>A maps to NM_001694.3 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:67472454 G>A maps to NM_004691.4 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr16:67473035 G>A maps to NM_004691.4 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr16:67487502 G>A maps to NM_004691.4 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr16:67478593 G>A maps to NM_004691.4 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr8:87162441 C>T maps to NM_152565.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr8:87165115 G>A maps to NM_152565.1 K321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:87151709 G>A maps to NM_152565.1 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr5:172447303 C>T maps to NM_003945.3 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:113528255 C>T maps to NM_001690.3 F612F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:113508622 G>A maps to NM_001690.3 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr2:71187171 C>T maps to NM_001692.3 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:71187171 C>T maps to NM_001692.3 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr2:71191933 C>T maps to NM_001692.3 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:71163194 C>T maps to NM_001692.3 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:20075710 C>T maps to NM_001693.3 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:20069206 C>T maps to NM_001693.3 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:20072456 T>C maps to NM_001693.3 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:20077861 C>T maps to NM_001693.3 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr8:104054584 C>T maps to NM_001695.4 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:10912036 C>T maps to NM_001039362.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:10912725 C>A maps to NM_001039362.1 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:10866671 G>T maps to NM_001039362.1 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:10911967 G>A maps to NM_001039362.1 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr2:10918749 G>A maps to NM_001039362.1 W339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr14:67812507 G>A maps to NM_015994.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:46739706 G>A maps to NM_080653.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:46739427 G>A maps to NM_080653.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:46739391 G>A maps to NM_080653.3 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:46739709 T>C maps to NM_080653.3 Q47Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr7:128505544 C>T maps to ENST00000492758 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr6:31513936 C>T maps to NM_130463.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:198509743 G>A maps to ENST00000489986 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:198498222 T>C maps to ENST00000489986 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:198498227 G>A maps to ENST00000489986 R62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr8:54684652 C>T maps to NM_015941.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr8:54723721 A>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:77243746 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr23:77254171 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:77244167 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:77258648 G>A did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:77301935 A>G did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:77245369 A>C did not map to a codon.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr23:77244062 A>G did not map to a codon.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr23:77245338 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:77245350 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:77296149 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:77276521 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:77298180 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr23:77243949 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr23:77245140 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:77298913 G>T did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:77264756 T>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:77300980 A>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:77244103 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:77301984 T>A did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr23:77271292 C>T did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr23:77301834 G>A did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:77244960 C>T did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:77301832 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr13:52539037 G>A maps to NM_000053.2 I613I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr13:52518244 C>T maps to NM_000053.2 E1081E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:52548508 G>A maps to NM_000053.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr13:52542600 G>A maps to NM_000053.2 S562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr13:52549277 G>A maps to NM_000053.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr13:52520509 G>A maps to NM_000053.2 A990A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr13:52548410 G>A maps to NM_000053.2 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr13:52544778 C>T maps to NM_000053.2 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr13:52523878 G>A maps to NM_000053.2 I928I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr13:52539166 G>A maps to NM_000053.2 I570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr13:52548296 C>T maps to NM_000053.2 Q353Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr13:52531656 G>A maps to NM_000053.2 I814I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr13:52534367 G>A maps to NM_000053.2 H679H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr13:52542666 G>A maps to NM_000053.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr13:52516651 G>A maps to NM_000053.2 F1094F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr13:52548992 G>A maps to NM_000053.2 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:52548896 G>A maps to NM_000053.2 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr13:52516636 G>A maps to NM_000053.2 G1099G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr13:52511698 G>A maps to NM_000053.2 S1272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr13:52549112 G>A maps to NM_000053.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr13:52542732 G>T maps to NM_000053.2 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr13:52515322 G>A maps to NM_000053.2 N1150N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr13:52523878 G>A maps to NM_000053.2 I928I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr4:42414995 G>A maps to NM_006095.2 I1144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr4:42509060 C>T maps to NM_006095.2 G686G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr4:42583714 G>A maps to NM_006095.2 R253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:42467089 A>T maps to NM_006095.2 V776V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr4:42424885 G>C maps to NM_006095.2 V1081V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr4:42509069 G>A maps to NM_006095.2 I683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:42445674 C>T maps to NM_006095.2 A1010A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:42457418 A>T maps to NM_006095.2 P904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr4:42524176 C>T maps to NM_006095.2 K649K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:42580306 C>T maps to NM_006095.2 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:42414995 G>A maps to NM_006095.2 I1144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:42592856 G>A maps to NM_006095.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr4:42467035 G>A maps to NM_006095.2 V794V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr4:42466709 G>A maps to NM_006095.2 I872I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:42414956 C>T maps to NM_006095.2 T1157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:42509144 G>A maps to NM_006095.2 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr4:42414956 C>T maps to NM_006095.2 T1157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr13:26116178 G>A maps to NM_016529.4 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr13:26402263 C>T maps to NM_016529.4 F896F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr13:26129184 C>T maps to NM_016529.4 N414N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr13:26138144 G>T maps to NM_016529.4 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr13:26402290 G>A maps to NM_016529.4 Q905Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr13:26402290 G>A maps to NM_016529.4 Q905Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:26112151 C>T maps to NM_016529.4 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:26128027 G>A maps to NM_016529.4 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:26163833 G>A maps to NM_016529.4 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr18:55352330 G>A maps to NM_005603.4 A482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr18:55399012 C>A maps to NM_005603.4 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr18:55361812 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr18:55334334 C>T maps to NM_005603.4 G758G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr18:55368545 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:55336669 C>T maps to NM_005603.4 K659K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:55352345 C>T maps to NM_005603.4 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:154309861 C>T maps to NM_020452.3 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr1:154300325 C>A maps to NM_020452.3 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:154315294 C>T maps to NM_020452.3 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:154315294 C>T maps to NM_020452.3 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:154309993 C>A maps to NM_020452.3 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:154315360 C>T maps to NM_020452.3 I492I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:154309856 C>T maps to NM_020452.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:154314974 G>C maps to NM_020452.3 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:154320905 C>T maps to NM_020452.3 A1095A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:154317529 C>T maps to NM_020452.3 T823T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:154321392 C>T maps to NM_020452.3 S1157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr19:1789021 G>A maps to NM_138813.2 L981L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:1791839 G>A maps to NM_138813.2 I737I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:1784934 G>A maps to NM_138813.2 L1181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:1785506 G>A maps to NM_138813.2 V1118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:1808277 C>A maps to NM_138813.2 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:1808280 G>A maps to NM_138813.2 N152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr19:1783185 G>A maps to NM_138813.2 R1248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr19:1785533 G>A maps to NM_138813.2 S1109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:1785173 C>T maps to NM_138813.2 T1172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:1811606 G>A maps to NM_138813.2 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr19:1785584 G>C maps to NM_138813.2 V1092V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr15:50152463 C>T maps to NM_024837.2 W1169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr15:50158606 G>A maps to NM_024837.2 S1034S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr15:50212511 C>T maps to NM_024837.2 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr15:50212556 C>T maps to NM_024837.2 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr15:50209162 C>T maps to NM_024837.2 G703G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr15:50336868 G>A maps to NM_024837.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr15:50168585 G>A maps to NM_024837.2 I972I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:50158636 G>A maps to NM_024837.2 F1024F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:50339640 C>T maps to NM_024837.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr15:50223483 G>A maps to NM_024837.2 Q492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr15:50215659 A>G maps to NM_024837.2 Y558Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr15:50209219 G>A maps to NM_024837.2 I684I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:50215688 G>A maps to NM_024837.2 R549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:50226265 G>A maps to NM_024837.2 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:50190412 G>A maps to NM_024837.2 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:50264848 G>A maps to NM_024837.2 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr15:50288949 C>T maps to NM_024837.2 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr15:50168576 C>T maps to NM_024837.2 G975G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:50152612 C>T maps to NM_024837.2 R1119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:50158627 C>T maps to NM_024837.2 G1027G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr15:50211111 C>T maps to NM_024837.2 Q653Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr15:50171590 G>A maps to NM_024837.2 A921A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:50264893 C>T maps to NM_024837.2 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:50279642 C>T maps to NM_024837.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:50168633 G>A maps to NM_024837.2 F956F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr20:50286610 G>A maps to NM_006045.1 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr20:50241844 C>T maps to NM_006045.1 T634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:50226647 G>A maps to NM_006045.1 L876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr20:50230307 A>G maps to NM_006045.1 L827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr20:50346414 G>A maps to NM_006045.1 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:50235498 G>A maps to NM_006045.1 S733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:50230307 A>G maps to NM_006045.1 L827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr20:50290723 G>A maps to NM_006045.1 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:50235246 G>A maps to NM_006045.1 I768I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr20:50286537 G>A maps to NM_006045.1 Q431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr20:50342429 G>A maps to NM_006045.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr20:50273533 C>T maps to NM_006045.1 E483E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr20:50235534 C>T maps to NM_006045.1 R721R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:50221425 G>A maps to NM_006045.1 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr20:50238708 A>G maps to NM_006045.1 V673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:50217818 G>A maps to NM_006045.1 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr18:77119462 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr18:77104306 C>T maps to NM_198531.3 R809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr18:77105507 C>T maps to NM_198531.3 P851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr18:77013535 C>A maps to NM_198531.3 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr18:76870472 C>T maps to NM_198531.3 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:77104306 C>T maps to NM_198531.3 R809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:47130936 C>A maps to NM_022745.3 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:47131011 G>A maps to NM_022745.3 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:47101461 G>A maps to NM_022745.3 Q325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:17921863 C>A maps to NM_145691.3 *290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr17:17921913 G>A maps to NM_145691.3 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr15:35830579 G>A maps to NM_080650.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr3:142172026 T>C maps to NM_001184.3 P2568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr3:142234332 G>A maps to NM_001184.3 T1469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:142254970 G>A maps to NM_001184.3 A1266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:142280212 G>A maps to NM_001184.3 I407I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:142217460 G>A maps to NM_001184.3 R1846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:142274761 G>A maps to NM_001184.3 F766F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:142281766 G>A maps to NM_001184.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr3:142215205 G>A maps to NM_001184.3 S1965S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr3:142215244 G>A maps to NM_001184.3 L1952L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr3:142280121 G>A maps to NM_001184.3 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:142281946 G>A maps to NM_001184.3 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:142180805 G>A maps to NM_001184.3 L2390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr3:48506018 C>T maps to NM_130384.1 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:48506282 G>A maps to NM_130384.1 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:48501577 G>A maps to NM_130384.1 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr20:3543972 C>T maps to NM_139321.2 A583A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr20:3540070 C>T maps to NM_139321.2 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr20:3520921 G>A maps to NM_139321.2 W183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr20:3559286 T>C maps to NM_139321.2 T804T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZG-06A-11D-A197-08 chr20:3515899 A>G maps to NM_139321.2 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr10:117027874 G>A maps to NM_207303.2 W685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr10:116931015 T>C maps to NM_207303.2 Y438Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr10:117001392 C>T maps to NM_207303.2 Y522Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:117309039 G>A maps to NM_207303.2 R1263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:117061530 G>A maps to NM_207303.2 E932E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr10:117278771 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:117075214 G>A maps to NM_207303.2 K1002K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr10:117027809 T>C maps to NM_207303.2 S663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr10:117308988 G>C maps to NM_207303.2 L1246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:116975542 G>A maps to NM_207303.2 K479K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:117278828 C>T maps to NM_207303.2 F1237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:117704251 C>T maps to NM_207303.2 R1368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:116919961 C>T maps to NM_207303.2 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:117308973 C>T maps to NM_207303.2 F1241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:76938475 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:76939390 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:76939416 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:76939746 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:76920201 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:76931740 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:76907701 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:76845342 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:76939722 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:76855028 T>C did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:76937973 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr23:76938143 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:76937732 C>G did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:76938830 C>G did not map to a codon.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr23:76776954 C>T did not map to a codon.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr23:76931727 C>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr23:76937756 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr23:76814186 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:76777848 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:76939020 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:76939416 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:76952145 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:16327059 G>A maps to NM_000332.3 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:16328528 G>A maps to NM_000332.3 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:16327104 G>A maps to NM_000332.3 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:16328277 G>A maps to NM_000332.3 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:16328445 G>A maps to NM_000332.3 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr6:16327572 G>A maps to NM_000332.3 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:16328097 G>A maps to NM_000332.3 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr6:16327797 G>A maps to NM_000332.3 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr6:16326975 G>A maps to NM_000332.3 F522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr22:46134705 G>A maps to NM_013236.3 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:111990156 C>T maps to NM_002973.3 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:111908032 G>A maps to NM_002973.3 V1065V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:111948321 G>A maps to NM_002973.3 T701T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr12:111990745 A>G maps to NM_002973.3 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr12:111951326 G>A maps to NM_002973.3 S624S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D3-A5GO-06A-12D-A27K-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EB-A5KH-06A-11D-A27K-08 chr16:28845875 G>A maps to NM_148414.1 P765P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:28841343 G>A maps to NM_148414.1 Q333Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:28844624 C>T maps to NM_148414.1 P635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr16:28847423 C>T maps to NM_148414.1 P1022P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr16:28847567 G>T maps to NM_007245.2 R1070R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr16:28845420 C>T maps to NM_148414.1 P687P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:28841283 C>T maps to NM_148414.1 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:28848075 C>T maps to NM_145714.1 P1048P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:13337351 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:13337191 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:13337901 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:13338044 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr3:63973763 C>T maps to NM_001177387.1 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:63973943 C>T maps to NM_001177387.1 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:63973880 G>A maps to NM_001177387.1 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:63981438 C>T maps to NM_001177387.1 S647S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:63981840 C>T maps to NM_001177387.1 T781T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr3:63968663 C>T maps to NM_001177387.1 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr3:63973961 A>T maps to NM_001177387.1 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:63981489 C>T maps to NM_001177387.1 S664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr3:63981492 C>T maps to NM_001177387.1 S665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr1:110030388 G>A maps to NM_153340.4 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:110033816 C>T maps to NM_153340.4 S544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr1:110033909 C>T maps to NM_153340.4 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:110026686 C>T maps to NM_153340.4 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:110031605 C>T maps to NM_153340.4 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr1:110026625 G>A maps to NM_153340.4 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:110033549 C>T maps to NM_153340.4 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:110030319 C>T maps to NM_153340.4 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr1:110033882 G>A maps to NM_153340.4 E566E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:110029764 C>T maps to NM_153340.4 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:110032728 C>T maps to NM_153340.4 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr17:42274729 C>T maps to NM_020218.1 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr17:42272038 G>A maps to NM_020218.1 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:94123927 G>A maps to NM_001698.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:54961499 A>C maps to NM_198437.1 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:1309549 C>A maps to NM_001127230.1 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr17:8110588 G>A maps to NM_004217.2 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:57743451 G>A maps to NM_001015878.1 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:57743538 G>A maps to NM_001015878.1 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:57743921 C>T maps to NM_001015878.1 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr19:57743496 C>T maps to NM_001015878.1 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:57746709 C>T maps to NM_001015878.1 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr7:70229863 C>T maps to NM_015570.2 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:70246731 C>T maps to NM_015570.2 F712F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr7:70236593 C>T maps to NM_015570.2 G598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:70255390 C>T maps to NM_015570.2 Y1063Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:70255636 G>A maps to NM_015570.2 R1145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr7:70246653 C>T maps to NM_015570.2 F686F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr7:70228045 G>A maps to NM_015570.2 T311T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A2A2-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:70250941 G>A maps to NM_015570.2 E742E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:70227928 G>T maps to NM_015570.2 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:70255384 C>T maps to NM_015570.2 F1061F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:70231109 C>T maps to NM_015570.2 I493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr7:70255186 G>A maps to NM_015570.2 E995E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:70229977 G>A maps to NM_015570.2 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:70255708 C>T maps to NM_015570.2 S1169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr7:70254742 C>T maps to NM_015570.2 V847V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr7:70255399 C>T maps to NM_015570.2 F1066F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr15:34295319 G>A maps to NM_020371.2 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr15:34159948 G>A maps to NM_020371.2 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:34159737 G>A maps to NM_020371.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:34159738 G>A maps to NM_020371.2 D310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:34158855 G>C maps to NM_020371.2 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr12:58197440 C>T maps to NM_006576.3 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44Q-06A-11D-A25O-08 chr12:58197149 G>T maps to NM_006576.3 V614V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:58197419 C>T maps to NM_006576.3 K568K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:58204324 G>A maps to NM_006576.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:58201164 C>A maps to NM_006576.3 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:58197164 C>T maps to NM_006576.3 Q609Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:58204900 C>T maps to NM_006576.3 Q116Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr20:3065239 C>T maps to NM_000490.4 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr20:3065269 G>A maps to NM_000490.4 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:206224958 C>T maps to NM_000707.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:206224805 C>T maps to NM_000707.3 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:206230970 C>T maps to NM_000707.3 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:206224673 G>A maps to NM_000707.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:206225063 C>T maps to NM_000707.3 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:206230979 C>T maps to NM_000707.3 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr1:206225009 C>T maps to NM_000707.3 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr1:206225312 C>T maps to NM_000707.3 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:206224523 C>T maps to NM_000707.3 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr1:206225075 G>A maps to NM_000707.3 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:153171268 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:69460014 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:69459606 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:69458122 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:69455943 G>A did not map to a codon.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr23:69458153 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:69459766 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:69262221 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr23:69261692 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:69263352 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:69263028 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:69262175 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr16:338189 G>A maps to NM_003502.3 R841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr16:396884 C>T maps to NM_003502.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr16:354393 G>A maps to NM_003502.3 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr16:338171 G>A maps to NM_003502.3 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:339519 G>A maps to NM_003502.3 I794I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:343564 G>A maps to NM_003502.3 P703P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:343591 G>A maps to NM_003502.3 T694T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:63533653 G>A maps to NM_004655.3 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:41754461 G>A maps to NM_021913.3 R527R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:41759577 A>G maps to NM_021913.3 R667R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr19:41727077 G>A maps to NM_021913.3 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:41748902 G>A maps to NM_021913.3 K476K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:41727797 C>T maps to NM_021913.3 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:41727059 C>T maps to NM_021913.3 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr19:41736917 G>A maps to NM_021913.3 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr19:41743949 G>A maps to NM_021913.3 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:41758838 C>T maps to NM_021913.3 F631F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr19:41744417 G>A maps to NM_021913.3 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr19:41765670 G>A maps to NM_021913.3 K849K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr19:41749595 G>A maps to NM_021913.3 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr19:41744429 C>T maps to NM_021913.3 F350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:41758872 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:41743985 C>T maps to NM_021913.3 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:99565826 C>T maps to NM_001185.3 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr7:99565808 C>T maps to NM_001185.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr7:99565925 G>A maps to NM_001185.3 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:99564685 G>A maps to NM_001185.3 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr7:99564730 G>A maps to NM_001185.3 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:79181017 G>A maps to ENST00000269392 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr17:79168727 G>A maps to ENST00000269392 A690A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:79193715 G>A maps to ENST00000269392 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr17:79166326 G>A maps to ENST00000269392 A835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:79193781 G>A maps to ENST00000269392 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:79181017 G>A maps to ENST00000269392 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr8:103842066 G>C maps to NM_148174.2 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:831867 G>A maps to NM_001700.3 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:828239 C>T maps to NM_001700.3 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:830877 G>A maps to NM_001700.3 E177E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:828353 C>T maps to NM_001700.3 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr15:45003811 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:45007678 C>T maps to NM_004048.2 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr3:160803732 G>A maps to NM_033168.2 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr3:160804146 G>A maps to NM_033168.2 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:160804295 G>A maps to NM_033168.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:235617518 C>T maps to ENST00000366599 K461K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:168725896 C>T maps to NM_020981.3 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr2:168726176 G>T maps to NM_020981.3 G210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:168725992 C>T maps to NM_020981.3 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:168726365 C>T maps to NM_020981.3 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:168725714 C>T maps to NM_020981.3 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:168725896 C>T maps to NM_020981.3 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr1:193149576 C>T maps to NM_003783.3 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:33246056 C>T maps to NM_003782.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr21:41033307 C>T maps to NM_033172.1 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:41033055 C>T maps to NM_033172.1 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr21:41032743 G>A maps to NM_033172.1 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:41032494 C>T maps to NM_033172.1 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:41033271 C>T maps to NM_033172.1 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:41033328 C>T maps to NM_033172.1 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr1:1168026 C>T maps to NM_080605.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr13:31903732 C>T maps to NM_194318.3 F475F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr13:31848689 C>T maps to NM_194318.3 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr13:31843356 C>T maps to NM_194318.3 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:134257514 G>A maps to NM_054025.2 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:134251914 G>A maps to NM_054025.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:134253615 G>A maps to NM_054025.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:134257505 G>A maps to NM_054025.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:134253615 G>A maps to NM_054025.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr6:71603951 G>A maps to NM_080742.2 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:62389380 G>A maps to NM_012200.2 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:66114101 G>A maps to NM_006876.2 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:62450311 G>C maps to NM_006577.5 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr19:17919149 C>T maps to NM_014256.3 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:17918753 C>T maps to NM_014256.3 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:17918741 G>A maps to NM_014256.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:17922426 C>T maps to NM_014256.3 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:17922645 C>T maps to NM_014256.3 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr19:17919050 C>T maps to NM_014256.3 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:17922822 C>T maps to NM_014256.3 Y337Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr19:17922507 C>T maps to NM_014256.3 H232H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:17922513 C>T maps to NM_014256.3 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:122690863 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr12:122691325 G>A maps to NM_030765.2 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr12:122691280 G>T maps to NM_030765.2 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:76750726 G>A maps to ENST00000354301 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:76751272 C>T maps to ENST00000354301 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:232263083 G>A maps to NM_145236.2 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:232263128 C>T maps to NM_145236.2 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:232263128 C>T maps to NM_145236.2 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr16:67183497 G>A maps to NM_033309.2 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr17:80915339 G>A maps to NM_001009905.1 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CC-06A-11D-A19A-08 chr12:58022612 G>C maps to NM_001478.3 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr12:58025074 G>A maps to NM_001478.3 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr12:58022918 G>A maps to NM_001478.3 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:58020667 C>T maps to NM_001478.3 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:47219492 G>A maps to NM_153446.2 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:47218647 C>T maps to NM_153446.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:47246125 G>A maps to NM_153446.2 R453R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr17:47246906 G>A maps to NM_153446.2 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr17:47247030 C>A maps to NM_153446.2 R548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:47247026 C>T maps to NM_153446.2 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr17:47246972 C>T maps to NM_153446.2 D528D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:47236520 C>T maps to NM_153446.2 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:47241495 C>T maps to NM_153446.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:47247065 G>A maps to NM_153446.2 K559K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:47247087 T>C maps to NM_153446.2 *567Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr12:667717 C>T maps to NM_173593.3 F884F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr12:665886 C>T maps to NM_173593.3 V745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:662825 G>A maps to NM_173593.3 R579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:659061 G>A maps to NM_173593.3 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:662504 C>T maps to NM_173593.3 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr12:670544 C>T maps to NM_173593.3 S975S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A2MR-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr12:662546 G>A maps to NM_173593.3 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:670580 A>C maps to NM_173593.3 R987R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr12:662561 C>T maps to NM_173593.3 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ES-06A-11D-A20D-08 chr12:659074 C>T maps to NM_173593.3 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:657216 C>T maps to NM_173593.3 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:662561 C>T maps to NM_173593.3 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:666021 C>T maps to NM_173593.3 F790F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:670559 C>T maps to NM_173593.3 F980F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr12:662523 C>T maps to NM_173593.3 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:376087 C>T maps to NM_178537.4 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:373081 C>T maps to NM_178537.4 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:379483 C>T maps to NM_178537.4 F757F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr11:376072 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:381764 G>A maps to NM_178537.4 R1031R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:379693 C>T maps to NM_178537.4 I827I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:379965 C>T maps to NM_178537.4 F863F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:380831 G>A maps to NM_178537.4 W959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:372901 C>T maps to NM_178537.4 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr11:372916 G>A maps to NM_178537.4 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:376688 C>T maps to NM_178537.4 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr9:33167143 C>T maps to NM_001497.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr9:33166891 G>A maps to NM_001497.3 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:44451269 G>A maps to ENST00000309519 K344K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:44447571 C>T maps to ENST00000309519 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:44451236 C>T maps to ENST00000309519 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:44447080 C>T maps to ENST00000309519 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U9-06A-11D-A32N-08 chr1:44447427 C>T maps to ENST00000309519 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:161141692 G>A maps to NM_003779.3 F365F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D3-A2JO-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:118935163 G>A maps to NM_212543.1 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:118948831 G>A maps to NM_212543.1 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr20:48273210 G>T maps to NM_004776.3 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:29237966 G>A maps to NM_004775.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr18:29206972 G>A maps to NM_004775.3 D296D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:177031344 C>T maps to NM_007255.2 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:41863859 C>T maps to NM_030578.3 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:104240215 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr9:104133440 C>T maps to NM_001701.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr9:104125006 G>A maps to NM_001701.3 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:104125006 G>A maps to NM_001701.3 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:104125000 G>A maps to NM_001701.3 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr9:104133227 G>A maps to NM_001701.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr9:104125006 G>A maps to NM_001701.3 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:104125000 G>A maps to NM_001701.3 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr11:117163892 A>G maps to NM_012104.3 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr11:117167626 G>A maps to NM_012104.3 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr21:42540502 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr21:42647391 C>T maps to NM_012105.3 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr21:30698861 C>T maps to NM_206866.1 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr21:30693684 G>A maps to NM_206866.1 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr21:30693750 C>T maps to NM_206866.1 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr21:30693735 C>T maps to NM_206866.1 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr21:30693777 C>T maps to NM_206866.1 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr6:90661122 G>A maps to NM_001170794.1 Y234Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr6:90661506 G>A maps to NM_001170794.1 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:90647973 T>C maps to NM_001170794.1 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr6:90642342 C>T maps to NM_001170794.1 L770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:90648039 G>A maps to NM_001170794.1 I622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr6:90661200 G>A maps to NM_001170794.1 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr6:90660234 C>T maps to NM_001170794.1 E530E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr6:90660780 C>T maps to NM_001170794.1 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:57048590 T>G maps to NM_004282.3 L80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:121432050 C>T maps to NM_004281.3 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr10:121429449 C>T maps to NM_004281.3 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr8:38067590 C>T maps to NM_004874.2 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr8:38065148 C>T maps to NM_004874.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr14:104026187 G>A maps to NM_001015049.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr21:11097568 C>T maps to NM_182482.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr21:11058217 C>T maps to NM_182482.2 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr21:11058196 G>A maps to NM_182482.2 C81C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:11058253 G>A maps to NM_182482.2 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr21:11058277 C>T maps to NM_182482.2 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr21:11058274 C>T maps to NM_182482.2 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr17:79428153 C>T maps to ENST00000436173 A2155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr17:79428192 C>T maps to ENST00000436173 F2168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr17:79414270 G>T maps to ENST00000436173 E1125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:79418856 C>T maps to ENST00000436173 I1380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20I-06A-11D-A196-08 chr17:79409031 C>T maps to ENST00000436173 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:79411763 C>T maps to ENST00000436173 P861P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:79414170 G>A maps to ENST00000436173 P1091P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:79405438 C>T maps to ENST00000436173 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:79408917 C>T maps to ENST00000436173 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr17:79429065 C>T maps to ENST00000436173 P2459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr17:79410079 C>T maps to ENST00000436173 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:79428192 C>T maps to ENST00000436173 F2168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr15:40758310 C>T maps to NM_014952.3 I775I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr15:40758202 C>T maps to NM_014952.3 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr15:40757535 C>T maps to NM_014952.3 P685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr8:143623500 C>T maps to NM_001702.2 F1302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr8:143570441 G>A maps to NM_001702.2 R833R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr8:143563056 C>T maps to NM_001702.2 T705T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr8:143570777 C>T maps to NM_001702.2 I870I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr8:143562693 C>T maps to NM_001702.2 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr8:143623662 G>A maps to NM_001702.2 R1356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr8:143602234 C>T maps to NM_001702.2 I991I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr8:143562622 C>T maps to NM_001702.2 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr8:143605607 C>T maps to NM_001702.2 L1085L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:143545879 C>T maps to NM_001702.2 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr8:143562942 G>A maps to NM_001702.2 Q667Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr8:143599603 T>G did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr8:143623446 C>T maps to NM_001702.2 S1284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:143560783 C>T maps to NM_001702.2 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr8:143559618 C>T maps to NM_001702.2 R487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:143603399 C>T maps to NM_001702.2 A1033A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:32205231 G>A maps to NM_001703.2 I724I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr1:32221986 G>A maps to NM_001703.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr1:32196406 G>A maps to NM_001703.2 S1458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:32196484 G>A maps to NM_001703.2 A1432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:32205770 G>A maps to NM_001703.2 F666F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr1:32207321 G>A maps to NM_001703.2 F530F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:32207057 G>A maps to NM_001703.2 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:32196634 G>A maps to NM_001703.2 P1382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:32193866 G>A maps to NM_001703.2 T1477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:32221699 G>A maps to NM_001703.2 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:32207542 C>T maps to NM_001703.2 W481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:32221939 G>A maps to NM_001703.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:32204489 G>A maps to NM_001703.2 P848P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:32198638 G>A maps to NM_001703.2 L1186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr6:70049368 C>T maps to NM_001704.2 V1144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr6:70070770 G>A maps to NM_001704.2 K1202K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr6:69703820 G>A maps to NM_001704.2 R632R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr6:70049387 C>A maps to NM_001704.2 R1151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr6:70034816 C>T maps to NM_001704.2 F956F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:70049356 C>T maps to NM_001704.2 G1140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:69349059 C>T maps to NM_001704.2 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr6:70071211 C>T maps to NM_001704.2 F1349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:69348920 C>T maps to NM_001704.2 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:69666579 C>T maps to NM_001704.2 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:69703790 C>T maps to NM_001704.2 I622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:69348980 C>T maps to NM_001704.2 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr6:69944925 C>T maps to NM_001704.2 I870I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:69684751 C>A maps to NM_001704.2 A541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr6:70042882 G>A maps to NM_001704.2 K1057K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr6:70049223 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:69943247 G>A maps to NM_001704.2 T849T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:70071331 C>T maps to NM_001704.2 A1389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr6:70092802 G>A maps to NM_001704.2 R1452R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr6:69772900 G>A maps to NM_001704.2 L803L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr6:70070959 T>G maps to NM_001704.2 L1265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:69348920 C>T maps to NM_001704.2 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:69949066 C>T maps to NM_001704.2 I921I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:70049356 C>T maps to NM_001704.2 G1140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:70098768 C>T maps to NM_001704.2 Q1519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:70048810 G>A maps to NM_001704.2 Q1064Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr6:70098692 G>A maps to NM_001704.2 K1493K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:79058641 C>T maps to NM_017451.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr17:79060260 C>T maps to NM_017451.2 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr17:79077447 C>T maps to NM_017451.2 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:79078371 C>T maps to NM_017451.2 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr17:79077423 C>T maps to NM_017451.2 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr17:79031756 C>T maps to NM_017451.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr17:79078503 G>A maps to NM_017451.2 E419E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:97935800 C>T maps to NM_018842.4 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr22:38494423 G>A maps to NM_025045.4 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr22:38483272 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr22:38494447 C>T maps to NM_025045.4 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr22:38503918 C>T maps to NM_025045.4 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr16:1392256 C>T maps to NM_003933.4 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr16:1392721 G>A maps to NM_003933.4 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:1389507 C>T maps to NM_003933.4 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:1395327 G>A maps to NM_003933.4 R708R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:1396268 G>A maps to NM_003933.4 G835G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr16:1392256 C>T maps to NM_003933.4 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:33541630 C>T maps to ENST00000360661 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr11:65770750 C>T maps to NM_003860.3 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr11:65771194 C>T maps to NM_003860.3 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:17716332 C>T maps to NM_001159495.1 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:17705762 C>T maps to NM_001159495.1 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:17716332 C>T maps to NM_001159495.1 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr4:102951267 G>A maps to NM_017935.4 E582E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr4:102783699 C>T maps to NM_017935.4 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr4:102791788 G>A maps to NM_017935.4 E297E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr4:102951363 C>T maps to NM_017935.4 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:102751319 A>G maps to NM_017935.4 E142E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr4:102839333 C>T maps to NM_017935.4 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:102965000 C>T maps to NM_017935.4 Q636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr4:102965041 C>T maps to NM_017935.4 F649F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr3:52441476 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr3:52442558 G>A maps to NM_004656.2 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:52439272 G>A maps to NM_004656.2 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr3:52442570 G>A maps to NM_004656.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:91180110 G>A maps to NM_020063.1 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:91177970 C>T maps to NM_020063.1 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr11:129306736 C>T maps to NM_003658.4 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:129306718 C>T maps to NM_003658.4 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:129306850 G>A maps to NM_003658.4 K131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr11:129306862 G>A maps to NM_003658.4 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:129306736 C>T maps to NM_003658.4 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr11:129306655 C>T maps to NM_003658.4 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:129321089 C>T maps to NM_003658.4 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr6:31500583 G>A maps to ENST00000417556 D295D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr6:31508158 G>A maps to ENST00000417556 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:31503197 G>A maps to ENST00000417556 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:31503224 G>A maps to ENST00000417556 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr6:31593277 G>T maps to NM_080686.2 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr6:31593914 C>T maps to NM_080686.2 Q320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr6:31604378 C>T maps to NM_080686.2 A1976A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:31600169 C>T maps to NM_080686.2 P1240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr6:31603423 C>T maps to NM_080686.2 S1813S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:31594923 C>T maps to NM_080686.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:31603423 C>T maps to NM_080686.2 S1813S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr6:31597008 C>T maps to NM_080686.2 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:31593892 C>A maps to NM_080686.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr6:31597473 C>T maps to NM_080686.2 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:31595633 C>T maps to NM_080686.2 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr6:31595822 C>T maps to NM_080686.2 V524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:31600049 C>T maps to NM_080686.2 G1200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr6:31594905 C>T maps to NM_080686.2 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr6:31604045 A>G maps to NM_080686.2 L1895L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:31604520 C>G maps to NM_080686.2 P1982P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr6:31601242 C>T maps to NM_080686.2 I1469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:31594582 C>T maps to NM_080686.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:31593600 C>T maps to NM_080686.2 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:31599461 C>T maps to NM_080686.2 S1004S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr6:31603360 C>T maps to NM_080686.2 A1792A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:31601197 C>T maps to NM_080686.2 P1454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:31600106 C>T maps to NM_080686.2 S1219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr9:134323084 C>T maps to NM_013318.3 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:134350746 T>G maps to NM_013318.3 R1077R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr9:134353999 C>T maps to NM_013318.3 A1584A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr9:134350719 C>T maps to NM_013318.3 G1068G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr9:134321956 C>T maps to NM_013318.3 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr9:134321957 C>T maps to NM_013318.3 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:134321977 C>T maps to NM_013318.3 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr9:134350602 C>T maps to NM_013318.3 A1029A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:134342989 C>T maps to NM_013318.3 F587F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr1:171510669 G>A maps to ENST00000392078 R1355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr1:171504723 C>T maps to ENST00000392078 F677F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr1:171501963 A>G maps to ENST00000392078 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:171509754 A>T maps to ENST00000392078 V1050V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:171557583 C>T maps to ENST00000392078 F2713F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr1:171553298 C>T maps to ENST00000392078 S2538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:171486925 C>T maps to ENST00000392078 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:171486847 C>T maps to ENST00000392078 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:31608041 C>T maps to ENST00000404765 R1060R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:31607999 A>G maps to ENST00000404765 S1074S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr6:31613318 C>A maps to ENST00000404765 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:31612873 G>A maps to ENST00000404765 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr6:31609611 G>A maps to ENST00000404765 R816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:31608607 G>A maps to ENST00000404765 A965A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr6:31607321 G>A maps to ENST00000404765 S1116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr6:31610668 G>C maps to ENST00000404765 P660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr6:31614290 G>A maps to ENST00000404765 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:31630285 G>A maps to NM_033177.3 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr6:31631877 C>T maps to NM_033177.3 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:31655431 G>A maps to ENST00000375842 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:31656840 G>A maps to ENST00000375842 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:31656822 G>A maps to ENST00000375842 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr6:31659676 G>A maps to ENST00000375842 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr6:31659451 A>G maps to ENST00000375842 N292N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr6:31656528 G>A maps to ENST00000375842 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:64757230 G>A maps to NM_138456.3 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:64756798 G>A maps to NM_138456.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:212870374 C>T maps to NM_018664.2 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:212860306 C>T maps to NM_018664.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr1:212860168 G>A maps to NM_018664.2 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:49464236 C>T maps to NM_004324.3 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:49464237 C>T maps to NM_004324.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:49464299 C>T maps to NM_004324.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr14:35224117 G>A maps to NM_013448.2 V1463V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr14:35272176 C>T maps to NM_013448.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:35253104 G>A maps to NM_013448.2 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:72891687 A>C maps to NM_032408.3 V701V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:72861603 A>G maps to NM_032408.3 A1278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:72863879 G>A maps to NM_032408.3 S1240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:72892704 A>G maps to NM_032408.3 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:72861687 A>T maps to NM_032408.3 A1250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:72903595 G>A maps to NM_032408.3 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr12:57003921 G>A maps to NM_013449.3 F621F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr12:57007848 G>A maps to NM_013449.3 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr12:56994810 G>A maps to NM_013449.3 R1458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:57000470 C>T maps to NM_013449.3 K715K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr12:56992443 G>A maps to NM_013449.3 S1892S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:57003917 C>A maps to NM_013449.3 E623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:56998580 G>A maps to NM_013449.3 S919S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:160206704 G>A maps to NM_013450.2 F1459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr2:160303330 G>A maps to NM_013450.2 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr2:160289424 G>A maps to NM_013450.2 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:160194129 G>A maps to NM_013450.2 L1870L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:160194130 G>A maps to NM_013450.2 P1869P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:160269053 T>C maps to NM_013450.2 G823G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:160269008 G>A maps to NM_013450.2 I838I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr2:160240121 G>A maps to NM_013450.2 L1252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:160289874 C>A did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:160257129 G>A maps to NM_013450.2 R960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:47725011 G>A maps to NM_001127240.1 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:27077074 G>A maps to NM_003986.2 W33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr11:27078785 C>T maps to NM_003986.2 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:27077076 T>C maps to NM_003986.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:27078758 A>C maps to NM_003986.2 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr11:66283163 G>A maps to NM_024649.4 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr11:66283031 C>T maps to NM_024649.4 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr11:66283385 C>T maps to NM_024649.4 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr11:66287152 G>A maps to NM_024649.4 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:76740303 T>C maps to NM_024685.3 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr4:123663376 C>T maps to NM_152618.2 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:123663613 T>G maps to NM_152618.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr4:123663112 C>T maps to NM_152618.2 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:123664510 C>T maps to NM_152618.2 I488I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:123664558 C>T maps to NM_152618.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr4:123664081 G>A maps to NM_152618.2 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr4:122774170 G>A maps to NM_176824.1 D263D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr4:122749833 G>A maps to NM_176824.1 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:33397503 C>T maps to NM_198428.2 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:33296885 C>T maps to NM_198428.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:33312752 C>T maps to NM_198428.2 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:33195255 C>T maps to NM_198428.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:33313497 C>T maps to NM_198428.2 Q316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr3:107491929 G>A maps to NM_001142568.1 K454K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:107492196 C>T maps to NM_001142568.1 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:107524288 C>T maps to NM_001142568.1 S937S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr3:107491623 G>A maps to NM_001142568.1 K352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:107524237 C>T maps to NM_001142568.1 L920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:107517424 C>T maps to NM_001142568.1 I803I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr19:45317958 G>A maps to NM_005581.3 E340E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:45322846 C>T maps to NM_005581.3 Q543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:45321854 C>T maps to NM_005581.3 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:45316555 G>A maps to NM_005581.3 W185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:45315789 G>A maps to NM_005581.3 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr19:45322739 C>T maps to NM_005581.3 F537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:45322050 C>T maps to NM_005581.3 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:45316827 G>A maps to NM_005581.3 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:156621323 C>T maps to NM_021948.3 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:156616704 C>T maps to NM_021948.3 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:156621281 C>A maps to NM_021948.3 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:156622514 C>T maps to NM_021948.3 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:156617345 C>T maps to NM_021948.3 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:156626808 G>A maps to NM_021948.3 E710E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:156621398 C>T maps to NM_021948.3 I405I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:156626125 G>A maps to NM_021948.3 E665E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:156617414 C>A maps to NM_021948.3 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr7:107253874 C>T maps to NM_001008405.2 Q230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr7:107240939 G>A maps to NM_001008405.2 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:152981132 C>T did not map to a codon.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr23:152981106 C>T did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr23:152981045 G>A did not map to a codon.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr16:75268984 G>T maps to NM_001170714.1 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:75263822 T>G maps to NM_001170714.1 T779T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:75269070 G>A maps to NM_001170714.1 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr16:75263555 G>A maps to NM_001170714.1 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr16:75268867 G>A maps to NM_001170714.1 F689F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:94057854 G>A maps to NM_003567.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:94049647 G>A maps to NM_003567.2 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr1:94027809 C>T maps to NM_003567.2 Q822Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:94057827 G>A maps to NM_003567.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:94033369 G>A maps to NM_003567.2 H671H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:94032908 G>A maps to NM_003567.2 N742N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr20:52601879 G>A maps to NM_003657.2 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr20:52570033 C>T maps to NM_003657.2 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr20:52601927 C>T maps to NM_003657.2 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr20:52644981 C>T maps to NM_003657.2 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:52591930 C>T maps to NM_003657.2 E393E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr20:52611549 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr20:52645134 G>A maps to NM_003657.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr20:52601966 G>A maps to NM_003657.2 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:52591936 C>T maps to NM_003657.2 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:52601975 G>A maps to NM_003657.2 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:52645296 C>T maps to NM_003657.2 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr17:59067405 C>T maps to ENST00000407086 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr17:59445710 C>T maps to ENST00000407086 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:59161839 C>T maps to ENST00000407086 V810V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:58980028 C>T maps to ENST00000407086 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr17:58952088 C>T maps to ENST00000407086 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:59093110 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr20:49434749 G>A maps to NM_198799.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:49434758 G>A maps to NM_198799.2 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr20:49458307 C>T maps to NM_198799.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr20:49446838 C>T maps to NM_198799.2 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:49458421 C>T maps to NM_198799.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:49458427 C>T maps to NM_198799.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:25034320 G>A maps to NM_001178093.1 R114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr12:24985743 G>A maps to NM_001178093.1 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:24989495 G>A maps to NM_001178093.1 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr19:49302951 G>A maps to NM_001190.3 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:49309779 G>A maps to NM_001190.3 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr10:127520113 C>T maps to NM_016567.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr10:127520012 C>T maps to NM_016567.3 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr10:127520149 C>T maps to NM_016567.3 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr12:50232165 G>A maps to NM_181708.2 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr12:50232546 G>A maps to NM_181708.2 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr12:50232711 G>A maps to NM_181708.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:50232486 G>A maps to NM_181708.2 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:165503966 C>T maps to NM_000055.2 W550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:165503967 C>T maps to NM_000055.2 W550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:41928177 C>T maps to NM_000709.3 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr19:41925133 C>T maps to NM_000709.3 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:41928207 C>T maps to NM_000709.3 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:41925148 G>A maps to NM_000709.3 K198K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr6:80877512 C>T maps to NM_183050.2 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr6:80838929 C>T maps to NM_183050.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:60773127 G>A maps to NM_022893.3 C121C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr2:60688027 G>A maps to NM_022893.3 F673F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr2:60688588 C>T maps to NM_022893.3 E486E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:60688198 G>A maps to NM_022893.3 G616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:60689272 G>A maps to NM_022893.3 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:60688588 C>T maps to NM_022893.3 E486E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr2:60687570 G>A maps to NM_022893.3 R826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:60688870 C>T maps to NM_022893.3 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:60688312 G>A maps to NM_022893.3 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:60773202 G>A maps to NM_022893.3 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:60687931 C>T maps to NM_022893.3 E705E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:60688732 G>A maps to NM_022893.3 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:60688273 G>A maps to NM_022893.3 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:60688614 G>A maps to NM_022893.3 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr2:60688843 G>A maps to NM_022893.3 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:60688456 C>T maps to NM_022893.3 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:60773265 G>A maps to NM_022893.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:60773232 G>A maps to NM_022893.3 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr2:60695963 T>C maps to NM_022893.3 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr14:99640619 C>T maps to NM_138576.2 K851K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr14:99641879 G>A maps to NM_138576.2 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr14:99724039 G>A maps to NM_138576.2 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr14:99641843 G>A maps to NM_138576.2 I443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:99641456 C>T maps to NM_138576.2 G572G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr14:99640493 C>T maps to NM_138576.2 R893R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:99697790 G>A maps to NM_138576.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:99723973 G>A maps to NM_138576.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr14:99723934 G>A maps to NM_138576.2 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr14:99640586 G>A maps to NM_138576.2 P862P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:99640763 C>T maps to NM_138576.2 K803K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:99640961 G>A maps to NM_138576.2 F737F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:99724147 G>A maps to NM_138576.2 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:60985611 G>A maps to NM_000633.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr15:80263401 G>A maps to NM_004049.3 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr15:80253444 G>A maps to NM_004049.3 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:30309748 C>T maps to NM_138578.1 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr15:52404570 C>T maps to NM_020396.2 W118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr2:111907669 C>T maps to NM_138621.3 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr19:50172186 C>T maps to NM_138639.1 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr19:50173528 C>T maps to NM_138639.1 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr19:50173528 C>T maps to NM_138639.1 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:50169103 C>T maps to NM_138639.1 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr19:50169130 C>T maps to NM_138639.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:50169130 C>T maps to NM_138639.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:50169109 C>T maps to NM_138639.1 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:50169130 C>T maps to NM_138639.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:50169130 C>T maps to NM_138639.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:50169103 C>T maps to NM_138639.1 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:50169098 C>T maps to NM_138639.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr19:50169130 C>T maps to NM_138639.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:50169130 C>T maps to NM_138639.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:50169130 C>T maps to NM_138639.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr19:50169103 C>T maps to NM_138639.1 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:50169130 C>T maps to NM_138639.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:50169130 C>T maps to NM_138639.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:50169103 C>T maps to NM_138639.1 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:18171782 T>G maps to NM_015367.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:12247623 C>A maps to NM_138722.1 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:114424415 G>A maps to NM_001010922.2 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:23777110 C>T maps to NM_004050.4 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr19:45254541 C>T maps to NM_005178.4 N105N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr19:45262000 G>T maps to NM_005178.4 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:187444627 G>A maps to NM_001706.4 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:187444561 G>A maps to NM_001706.4 F555F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:187442764 G>A maps to NM_001706.4 S647S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:187442794 G>A maps to NM_001706.4 T637T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:187447571 G>A maps to NM_001706.4 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:187449585 C>T maps to NM_001706.4 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:6930105 G>A maps to NM_181844.3 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr17:6927947 G>A maps to NM_181844.3 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:6930093 C>T maps to NM_181844.3 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr17:6930931 G>A maps to NM_181844.3 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:6930396 G>A maps to NM_181844.3 K438K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:122496995 A>G did not map to a codon.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr7:72954260 G>A maps to NM_001707.3 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:72966520 C>T maps to NM_001707.3 W48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:72954227 G>A maps to NM_001707.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:147092681 C>T maps to NM_004326.2 S907S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:147096102 G>A maps to NM_004326.2 G1208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:147091874 G>A maps to NM_004326.2 E638E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:147096627 C>T maps to NM_004326.2 S1383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr1:147091184 C>T maps to NM_004326.2 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:147095668 C>T maps to NM_004326.2 R1064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:147094132 C>T maps to NM_004326.2 P988P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr11:118771496 G>A maps to NM_182557.2 V985V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:118771895 G>A maps to NM_182557.2 G852G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:118772713 G>A maps to NM_182557.2 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:118769573 G>A maps to NM_182557.2 P1350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr11:118771388 G>A maps to NM_182557.2 S1021S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:118773326 G>A maps to NM_182557.2 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:118773749 G>A maps to NM_182557.2 D261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:118770887 G>A maps to NM_182557.2 G1048G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:118779084 G>A maps to NM_182557.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:118769795 G>A maps to NM_182557.2 P1276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:118771388 G>A maps to NM_182557.2 S1021S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr6:136599699 G>A maps to NM_014739.2 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:136599036 G>A maps to NM_014739.2 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:136599466 C>T maps to NM_014739.2 Q184Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr6:136599067 G>A maps to NM_014739.2 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr6:136599058 C>T maps to NM_014739.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr6:136589406 G>A maps to NM_014739.2 R764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:136597444 C>T maps to NM_014739.2 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:136594271 G>A maps to NM_014739.2 Q636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:136597060 C>T maps to NM_014739.2 R534R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:136597444 C>T maps to NM_014739.2 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr6:136597141 G>A maps to NM_014739.2 D507D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:136597483 C>T maps to NM_014739.2 K393K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr6:136599499 G>A maps to NM_014739.2 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr6:136593186 C>T maps to NM_014739.2 R663R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr16:81295789 C>T maps to NM_017429.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:81303876 C>T maps to NM_017429.2 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr16:81298333 C>T maps to NM_017429.2 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:81303924 C>T maps to NM_017429.2 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:81320997 G>A maps to NM_017429.2 K467K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr16:81303969 C>T maps to NM_017429.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr16:81323951 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr16:81295857 C>T maps to NM_017429.2 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr16:81279167 C>T maps to NM_017429.2 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:112070434 G>A maps to NM_031938.4 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr11:112088572 C>T maps to NM_031938.4 F572F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr11:112064217 G>A maps to NM_031938.4 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr11:112088572 C>T maps to NM_031938.4 F572F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:112085528 G>A maps to NM_031938.4 K459K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:112084481 G>A maps to NM_031938.4 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr23:39923808 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr23:39930224 C>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:39934345 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:39933536 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr23:39933021 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:39930939 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:39932228 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:39933509 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr23:39923688 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:39923789 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:39923790 A>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:39933480 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr23:39932521 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:39933239 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:39923708 G>A did not map to a codon.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr23:39932211 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:39933056 T>C did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:39932368 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr23:39923818 G>A did not map to a codon.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr23:39932642 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:129148254 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:129149215 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:129147348 G>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:129189887 T>C did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:129159107 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:129147483 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:129190018 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:129148754 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:129147269 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:129147376 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:129149394 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:129149395 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:129173183 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr23:129149265 T>C did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:129149194 G>C did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:129150006 G>C did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:129148819 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:129162697 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:129147902 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:129148438 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:129149927 C>T did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr23:129147714 C>T did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr23:129156902 C>T did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr23:129149232 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:129189885 G>A did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:129173250 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr22:23656239 C>T maps to NM_004327.3 F1181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr22:23652512 C>T maps to NM_004327.3 I1025I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr22:23657639 C>T maps to NM_004327.3 F1249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr22:23653910 C>T maps to NM_004327.3 I1070I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:23523164 C>T maps to NM_004327.3 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:23596139 C>T maps to NM_004327.3 V478V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr22:23524070 C>T maps to NM_004327.3 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr22:23654021 C>T maps to NM_004327.3 V1107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr22:23653934 C>T maps to NM_004327.3 I1078I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:23653976 C>T maps to NM_004327.3 S1092S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:23657639 C>T maps to NM_004327.3 F1249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr22:23615825 G>A maps to NM_004327.3 L660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr22:23610669 C>T maps to NM_004327.3 Q610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr22:23630294 C>T maps to NM_004327.3 F846F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:23603603 C>T maps to NM_004327.3 I543I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr2:219527663 G>A maps to NM_004328.4 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:219525913 C>T maps to NM_004328.4 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:197238996 G>A maps to NM_203315.2 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr3:197238876 G>A maps to NM_203315.2 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:104012419 G>A maps to NM_020139.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr14:96730312 G>A maps to NM_000710.2 W98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr14:96730345 C>T maps to NM_000710.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr14:96731047 G>A maps to NM_000710.2 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr14:96730841 T>C maps to NM_000710.2 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr14:96731068 C>T maps to NM_000710.2 F350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr14:96730171 C>T maps to NM_000710.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:96731068 C>T maps to NM_000710.2 F350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr14:96730651 C>T maps to NM_000710.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:96730072 C>T maps to NM_000710.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:96730672 C>T maps to NM_000710.2 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:96707063 G>A maps to NM_000623.3 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr14:96707828 G>A maps to NM_000623.3 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr14:96707204 G>A maps to NM_000623.3 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:96707156 C>T maps to NM_000623.3 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:96707828 G>A maps to NM_000623.3 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr14:96706805 C>T maps to NM_000623.3 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr14:96703494 C>T maps to NM_000623.3 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:96706868 C>T maps to NM_000623.3 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:96706955 G>A maps to NM_000623.3 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr14:96706841 C>T maps to NM_000623.3 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:96707225 C>T maps to NM_000623.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:96706853 C>T maps to NM_000623.3 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:96707363 C>T maps to NM_000623.3 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:96706853 C>T maps to NM_000623.3 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:27679709 G>A maps to NM_001143810.1 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr11:27679988 C>T maps to NM_001143810.1 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr5:70782428 C>T maps to NM_018429.2 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr5:70845307 G>A maps to NM_018429.2 L2290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr5:70805912 C>T maps to NM_018429.2 G998G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:70820116 T>G maps to NM_018429.2 P1913P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:70819987 T>C maps to NM_018429.2 A1870A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr5:70805732 C>T maps to NM_018429.2 S938S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr5:70819936 C>T maps to NM_018429.2 T1853T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr5:70806887 A>G maps to NM_018429.2 L1323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IB-06A-11D-A196-08 chr14:101004686 G>C maps to NM_020836.3 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr14:101004368 G>A maps to NM_020836.3 G573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr14:101012896 C>T maps to NM_020836.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:101005160 C>T maps to NM_020836.3 E309E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:18221932 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:18234685 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr23:18220054 G>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:18213512 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:18230703 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:18213555 T>C did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:18234811 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr23:18195770 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr23:18189143 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:18221653 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:18195711 G>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:18221835 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:18221932 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr23:18183154 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:18230760 G>C did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:18192211 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:18209204 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:18219950 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:18192170 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:18192216 A>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:18192217 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:18221902 G>A did not map to a codon.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr6:107391194 G>A maps to NM_001080450.2 F400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:107390645 G>A maps to NM_001080450.2 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr6:107391440 C>T maps to NM_001080450.2 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:107391812 G>A maps to NM_001080450.2 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:107390734 G>A maps to NM_001080450.2 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr4:42122104 G>A maps to NM_207406.3 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr4:42119600 C>T maps to NM_207406.3 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:42119642 C>T maps to NM_207406.3 A499A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:42145654 G>A maps to NM_207406.3 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:42119747 G>A maps to NM_207406.3 F464F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr4:42119597 G>A maps to NM_207406.3 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr4:42122146 C>T maps to NM_207406.3 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr4:42122269 C>T maps to NM_207406.3 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:49224836 G>A maps to NM_024603.2 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:56846670 G>A maps to NM_152731.2 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:56857309 G>A maps to NM_152731.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:56879997 G>A maps to NM_152731.2 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr10:13489311 G>A maps to ENST00000396900 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:13541952 C>T maps to ENST00000396900 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr10:13541975 G>A maps to ENST00000396900 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr10:13523064 A>G maps to ENST00000396900 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:61727034 C>T maps to NM_001139443.1 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr19:12865694 T>C maps to NM_017682.2 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:70091476 C>T maps to NM_032735.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:70070719 G>A maps to NM_032735.2 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:70070980 C>T maps to NM_032735.2 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:70049394 C>T maps to NM_032735.2 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:70049223 C>T maps to NM_032735.2 V490V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:70087517 G>A maps to NM_032735.2 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr12:70049364 G>A maps to NM_032735.2 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:70049037 G>A maps to NM_032735.2 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:45251748 C>T maps to NM_153274.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:205490 G>A maps to NM_016526.4 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:102317847 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:102318004 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:101409139 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:101409139 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:101409098 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:14755849 C>T maps to NM_016561.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr16:14761503 G>A maps to NM_016561.2 Q391Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:14738442 C>T maps to NM_016561.2 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr20:17495446 G>A maps to NM_001195.3 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr20:17475600 C>T maps to NM_001195.3 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr20:17479504 G>A maps to NM_001195.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr20:17475273 G>A maps to NM_001195.3 D481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr20:17489584 G>A maps to NM_001195.3 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:133191376 C>T maps to NM_003571.2 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:133166237 A>G maps to NM_003571.2 K189K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr3:133167447 C>T maps to NM_003571.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:133119160 C>T maps to NM_003571.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr3:133191245 C>T maps to NM_003571.2 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:156212552 C>T maps to ENST00000368276 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr23:152773841 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr23:152773822 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:152771448 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:152772361 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:152772343 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:152770095 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:152770722 C>T did not map to a codon.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr23:152770228 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:102004754 A>G did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr23:102004790 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:102005055 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:102004335 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr23:102004255 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:102004553 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr8:65494420 C>T maps to NM_152414.3 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr8:65493400 C>T maps to NM_152414.3 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:65493763 C>T maps to NM_152414.3 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:5023177 C>T maps to NM_003670.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:5023178 C>T maps to NM_003670.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:78426764 G>A maps to NM_001713.2 K349K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:78379595 G>A maps to NM_017614.4 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:78384390 C>T maps to NM_017614.4 D362D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:78379595 G>A maps to NM_017614.4 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr10:60549602 C>T maps to NM_001080512.1 H319H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:60380642 G>A maps to NM_001080512.1 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:60560788 G>A maps to NM_001080512.1 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr10:60273022 C>T maps to NM_001080512.1 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:60549101 T>C maps to NM_001080512.1 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr12:32481284 C>T maps to NM_001714.2 I632I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:32481425 C>T maps to NM_001714.2 S679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:32481426 C>T maps to NM_001714.2 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr12:32481452 C>T maps to NM_001714.2 I688I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr9:95481033 G>A maps to NM_001003800.1 I631I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr9:95481453 G>A maps to NM_001003800.1 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:95482668 G>A maps to NM_001003800.1 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr9:95480125 C>T maps to NM_001003800.1 K737K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:95481687 C>T maps to NM_001003800.1 E413E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr9:95483034 C>T maps to NM_001003800.1 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:95480898 G>A maps to NM_001003800.1 I676I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr22:18220989 C>T maps to NM_197966.1 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr22:18232882 G>A maps to NM_197966.1 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:127828158 G>A maps to NM_139343.1 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:127808400 G>A maps to NM_139343.1 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:127808386 G>A maps to NM_139343.1 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:127821519 G>A maps to NM_139343.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr12:51685767 C>T maps to NM_016293.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:51685530 C>T maps to NM_016293.2 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr12:51685416 G>A maps to NM_016293.2 N491N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr12:51695881 C>T maps to NM_016293.2 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr12:51686090 G>A maps to NM_016293.2 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:51696469 C>T maps to NM_016293.2 W104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:51690899 C>T maps to NM_016293.2 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr12:51686090 G>A maps to NM_016293.2 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr12:51717847 G>A maps to NM_016293.2 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:51693414 C>T maps to NM_016293.2 K164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:51696895 C>T maps to NM_016293.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:51675281 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:22481736 G>A maps to NM_018688.4 Q160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr11:102221099 C>A maps to NM_001166.3 S172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr11:102196010 C>T maps to NM_182962.1 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:102201751 A>G maps to NM_182962.1 E368E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:102198821 C>T maps to NM_182962.1 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:76212780 C>T maps to NM_001012271.1 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:32824894 C>T maps to NM_016252.3 P4640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr2:32754815 A>T maps to NM_016252.3 K4007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr2:32640293 C>T maps to NM_016252.3 I645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:32768345 G>A maps to NM_016252.3 K4110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr2:32655963 C>T maps to NM_016252.3 T1018T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:32738122 T>A maps to NM_016252.3 S3490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:32768571 C>T maps to NM_016252.3 R4186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:32710713 G>A maps to NM_016252.3 L2567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:32715117 T>C maps to NM_016252.3 T2702T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr2:32800256 G>A maps to NM_016252.3 R4393R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr2:32738065 G>A maps to NM_016252.3 R3471R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:32724760 T>C maps to NM_016252.3 T2872T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:32724763 C>T maps to NM_016252.3 C2873C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:32724802 C>T maps to NM_016252.3 S2886S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr2:32640218 T>G maps to NM_016252.3 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr2:32828134 C>A maps to NM_016252.3 T4685T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr20:61869964 C>T maps to NM_139317.1 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr20:61870827 G>A maps to NM_139317.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr20:61870911 C>T maps to NM_139317.1 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr20:61870953 C>T maps to NM_139317.1 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr19:53793218 G>A maps to NM_033341.3 Q137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:103492121 C>T maps to NM_017693.3 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:36147522 G>A maps to NM_006698.3 N18N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr8:11400849 G>C maps to ENST00000427279 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr8:11415548 T>C did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:11412913 G>A maps to ENST00000427279 Q231Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr8:11400813 G>A maps to ENST00000427279 K27K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr8:11420486 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:11406604 C>T maps to ENST00000427279 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:11406605 C>T maps to ENST00000427279 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:11412922 G>A maps to ENST00000427279 W234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr8:11418821 G>A maps to ENST00000427279 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:11400786 G>A maps to ENST00000427279 K18K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr15:91298166 C>T maps to NM_000057.2 D362D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr15:91346769 C>T maps to NM_000057.2 I1126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr15:91295038 T>C maps to NM_000057.2 N274N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:91308553 C>T maps to NM_000057.2 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr15:91354459 C>T maps to NM_000057.2 S1300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr15:91292830 C>T maps to NM_000057.2 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr17:28613903 G>A maps to NM_000386.2 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr10:97969610 G>A maps to NM_013314.3 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr10:97983739 G>A maps to NM_013314.3 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr10:97987286 G>A maps to NM_013314.3 D80D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:97990570 C>T maps to NM_013314.3 E61E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:97956792 G>A maps to NM_013314.3 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:98002503 C>T maps to NM_013314.3 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr10:102039908 G>T maps to NM_173809.2 Y123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:45683138 G>A maps to NM_212550.3 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:43827615 C>T maps to NM_000712.3 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:43843288 G>T maps to NM_000712.3 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:43846777 C>T maps to NM_000712.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:169346024 C>T maps to NM_003666.2 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:169346075 C>T maps to NM_003666.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:40398106 G>A maps to NM_001003940.1 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:22033797 C>T maps to NM_006129.4 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:22058682 C>T maps to NM_001199.3 F720F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:22033821 C>T maps to NM_006129.4 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr8:22051976 G>A maps to NM_006129.4 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr8:22052091 C>T maps to NM_006129.4 Q478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:22049629 C>T maps to NM_006129.4 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:22051670 C>T maps to NM_006129.4 F427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:22059406 C>T maps to NM_006129.4 F733F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr2:69098178 G>A maps to NM_014482.1 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:69093647 G>A maps to NM_014482.1 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:69093152 C>T maps to NM_014482.1 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr2:69098190 G>A maps to NM_014482.1 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:69093239 C>T maps to NM_014482.1 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr23:50658932 G>A did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:50659042 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:50659176 C>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:50659392 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr23:50659472 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:50659190 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr23:50659303 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:50653836 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:50659176 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr20:6750865 G>A maps to NM_001200.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr20:6759177 C>T maps to NM_001200.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr20:6759102 C>T maps to NM_001200.2 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:6750865 G>A maps to NM_001200.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:6750958 C>T maps to NM_001200.2 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:6759298 C>T maps to NM_001200.2 Q252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:6759654 G>A maps to NM_001200.2 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:6759681 G>A maps to NM_001200.2 K379K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:6758995 C>T maps to NM_001200.2 Q151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr4:79786767 G>A maps to NM_198892.1 K375K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:79786836 C>T maps to NM_198892.1 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr4:81966919 C>T maps to NM_001201.2 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr4:81952626 C>T maps to NM_001201.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:81966961 T>A maps to NM_001201.2 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:81967121 C>T maps to NM_001201.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:81967642 G>A maps to NM_001201.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:81966988 G>A maps to NM_001201.2 E138E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr4:81967121 C>T maps to NM_001201.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr4:81974563 G>A maps to NM_001201.2 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr4:81967606 G>A maps to NM_001201.2 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr4:81967315 C>T maps to NM_001201.2 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:54418877 C>T maps to NM_130850.2 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:55684472 G>A maps to NM_021073.2 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr6:55638952 C>T maps to NM_021073.2 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr6:55638994 T>C maps to NM_021073.2 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr6:55684472 G>A maps to NM_021073.2 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:55638865 G>A maps to NM_021073.2 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr6:55739531 C>T maps to NM_021073.2 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:55739255 G>A maps to NM_021073.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr6:55739278 A>G maps to NM_021073.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:55659191 C>T maps to NM_021073.2 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr6:55739426 G>T maps to NM_021073.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:55638936 G>A maps to NM_021073.2 R313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:55739228 G>A maps to NM_021073.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr6:55625296 C>T maps to NM_021073.2 K354K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr6:55620381 G>A maps to NM_021073.2 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:7861758 G>A maps to NM_001718.4 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr6:7862699 C>T maps to NM_001718.4 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr6:7862546 C>T maps to NM_001718.4 H340H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:7880318 G>A maps to NM_001718.4 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:55777657 G>A maps to NM_001719.2 L211L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A2GS-06A-12D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr20:55777678 C>T maps to ENST00000371291 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:55758907 G>A maps to NM_001719.2 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:55758883 C>T maps to NM_001719.2 T284T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A29M-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:34125404 A>G maps to NM_133468.3 E482E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:34192881 G>A maps to NM_133468.3 R685R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr7:34118709 G>A maps to NM_133468.3 W440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr7:34125515 G>A maps to NM_133468.3 V519V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:34094911 C>T maps to NM_133468.3 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:34014389 C>T maps to NM_133468.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:34091494 C>T maps to NM_133468.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr7:34118706 C>T maps to NM_133468.3 R439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr7:34118751 C>T maps to NM_133468.3 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr7:34094806 C>T maps to NM_133468.3 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:34118536 C>T maps to NM_133468.3 Q383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:34125656 G>A maps to NM_133468.3 W566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:34091494 C>T maps to NM_133468.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr7:34125557 C>T maps to NM_133468.3 F533F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr10:88683458 C>T maps to NM_004329.2 Q528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr4:96046262 C>T maps to ENST00000440890 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:96070057 G>A maps to ENST00000440890 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:203420343 C>T maps to NM_001204.6 T652T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:43279929 C>T maps to NM_014753.3 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr10:43316000 C>T maps to NM_014753.3 R939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr10:43318678 C>T maps to NM_014753.3 F1082F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:43287154 T>C maps to NM_014753.3 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:43287193 T>G maps to NM_014753.3 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:43285836 C>T maps to NM_014753.3 Q172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr23:15544164 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr23:15554479 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr23:15540667 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr23:15555304 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr23:15560223 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:15534346 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:15540482 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:15540483 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr23:15540573 C>G did not map to a codon.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr23:15555256 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:15549482 G>A did not map to a codon.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr23:15568069 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr15:83932595 G>A maps to NM_001717.3 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr15:83935761 G>A maps to NM_001717.3 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr15:83926841 C>T maps to NM_001717.3 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr15:83926631 G>A maps to NM_001717.3 P849P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:83936883 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr15:83932099 C>A maps to NM_001717.3 E635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:83926502 C>T maps to NM_001717.3 G892G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr15:83932988 G>A maps to NM_001717.3 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:83932502 C>T maps to NM_001717.3 E500E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:83935803 G>A maps to NM_001717.3 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr15:83933263 G>A maps to NM_001717.3 Q247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:83933156 C>T maps to NM_001717.3 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr15:83932472 G>A maps to NM_001717.3 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:16552728 G>A maps to NM_017637.5 H156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:16436259 C>T maps to NM_017637.5 K644K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr9:16552545 G>A maps to NM_017637.5 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr5:172585809 A>G maps to NM_013979.2 K154K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr15:59961533 G>A maps to NM_004330.2 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:59964888 G>A maps to NM_004330.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:151015540 C>T maps to NM_138278.3 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:151015541 C>T maps to NM_138278.3 R182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:151015475 G>T maps to NM_138278.3 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:151016194 G>A maps to NM_138278.3 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:151018316 G>A maps to NM_138278.3 W299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr3:113002393 G>C maps to ENST00000273395 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:112991350 C>T maps to ENST00000273395 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:113002450 C>T maps to ENST00000273395 F876F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr4:13606584 C>A maps to NM_148894.2 E647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:13604872 G>A maps to NM_148894.2 N1217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr4:13604734 T>C maps to NM_148894.2 E1263E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr4:13615285 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:242509594 G>A maps to NM_032515.3 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:149871953 G>A maps to NM_016074.3 W114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:74362660 G>A maps to NM_001035505.1 I98I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A2GU-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:198640446 A>G maps to NM_197970.2 Y110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr7:134346735 G>A maps to NM_001724.4 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr7:134346747 G>A maps to NM_001724.4 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:134346484 C>T maps to NM_001724.4 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr6:3140659 C>T maps to NM_004332.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:3129331 C>T maps to NM_004332.2 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:3137650 C>T maps to NM_004332.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr6:3137608 T>A maps to NM_004332.2 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr20:36954767 C>T maps to NM_001725.2 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:36954782 C>T maps to NM_001725.2 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr20:36964042 C>T maps to NM_001725.2 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:36937433 G>A maps to NM_001725.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr20:36937391 C>T maps to NM_001725.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr20:36953196 C>T maps to NM_001725.2 R323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:36932651 G>A maps to NM_001725.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr20:36932729 G>A maps to NM_001725.2 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:36940285 C>T maps to NM_001725.2 Q187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:36940318 C>T maps to NM_001725.2 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:36954815 C>T maps to NM_001725.2 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr20:31607504 C>T maps to NM_025227.1 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr20:31608183 G>A maps to NM_025227.1 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr20:31607531 C>T maps to NM_025227.1 F352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:31598912 C>T maps to NM_025227.1 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:31607459 C>T maps to NM_025227.1 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr20:31606510 G>A maps to NM_025227.1 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr20:31606441 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:31606531 C>T maps to NM_025227.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:31606474 C>T maps to NM_025227.1 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:31606074 C>T maps to NM_025227.1 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:31606600 C>T maps to NM_025227.1 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:31611187 G>A maps to NM_025227.1 *459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:31607531 C>T maps to NM_025227.1 F352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr20:31598887 C>T maps to NM_025227.1 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr22:32833811 G>A maps to NM_174932.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr22:32811928 G>A maps to NM_174932.2 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr22:32828359 G>A maps to NM_174932.2 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:32827379 G>A maps to NM_174932.2 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:32829740 G>A maps to NM_174932.2 Q315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr22:32843212 G>A maps to NM_174932.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr22:32843302 A>G maps to NM_174932.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr22:32853334 G>A maps to NM_174932.2 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr22:32827389 G>A maps to NM_174932.2 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr22:32828467 G>A maps to NM_174932.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr22:32853349 G>A maps to NM_174932.2 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr22:32849443 C>T maps to NM_174932.2 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr20:31623452 G>A maps to NM_174897.2 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr20:31624267 C>T maps to NM_174897.2 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:31622589 G>A maps to NM_174897.2 E108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:31621994 G>A maps to NM_174897.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:31627274 C>T maps to NM_174897.2 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr20:31624249 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:220247341 C>T maps to NM_006085.4 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr17:65890258 C>T maps to ENST00000321892 R967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:65905701 A>G maps to ENST00000321892 K1065K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr17:65850418 G>A maps to ENST00000321892 W326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr17:65914853 C>T maps to ENST00000321892 S1902S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:65909117 A>G maps to ENST00000321892 P1832P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:65907641 C>T maps to ENST00000321892 F1340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:65914839 C>T maps to ENST00000321892 Q1898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:65909210 C>T maps to ENST00000321892 I1863I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:65909211 C>T maps to ENST00000321892 R1864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr17:65907492 C>T maps to ENST00000321892 R1291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr17:65909183 A>G maps to ENST00000321892 L1854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr17:65890230 T>C maps to ENST00000321892 V957V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:140477853 A>T maps to NM_004333.4 L485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr7:140453137 T>G maps to NM_004333.4 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr7:140453134 C>T maps to NM_004333.4 V600V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr7:140494230 G>A maps to NM_004333.4 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr7:140453134 C>T maps to NM_004333.4 V600V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:140494158 G>A maps to NM_004333.4 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr17:41223244 A>G maps to ENST00000471181 P1584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:41244175 G>A maps to ENST00000471181 F1124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:41247928 G>A maps to ENST00000471181 Q202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:41246106 G>A maps to ENST00000471181 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr13:32914692 C>T maps to NM_000059.3 S2067S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr13:32911140 C>T maps to NM_000059.3 F883F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:32913501 T>G maps to NM_000059.3 A1670A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr13:32915325 C>T maps to NM_000059.3 I2278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:32914044 C>T maps to NM_000059.3 I1851I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr13:32945212 C>T maps to NM_000059.3 Q2870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr13:32893343 A>G maps to NM_000059.3 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr13:32918761 C>T maps to NM_000059.3 S2303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr13:32915028 T>G maps to NM_000059.3 V2179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr13:32929058 C>T maps to NM_000059.3 L2357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr13:32912841 T>C maps to NM_000059.3 F1450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr13:32914707 C>T maps to NM_000059.3 S2072S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:32913744 C>T maps to NM_000059.3 Y1751Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:154348416 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:154300607 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr22:50191450 A>G did not map to a codon.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr22:50217212 G>A maps to ENST00000342989 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr22:50217209 G>A maps to ENST00000342989 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr22:50171393 G>A maps to ENST00000342989 A975A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr22:50167904 G>A maps to ENST00000342989 T1182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr22:50169267 G>A maps to ENST00000342989 L1119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:50169712 G>A maps to ENST00000342989 P1072P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr22:50187787 G>A maps to ENST00000342989 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:32947751 C>T maps to ENST00000395289 G698G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:32944030 C>T maps to ENST00000395289 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr6:32948437 C>T maps to ENST00000395289 S818S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CF-06A-11D-A196-08 chr9:136918455 C>T maps to NM_007371.3 K48K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:136913318 G>A maps to NM_007371.3 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:136901262 G>A maps to NM_007371.3 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:136916765 C>T maps to NM_007371.3 Q139Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr9:136915576 G>A maps to NM_007371.3 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr9:136915684 G>A maps to NM_007371.3 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr19:15376314 G>A maps to NM_058243.2 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:15366369 G>A maps to NM_058243.2 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:15349757 G>A maps to NM_058243.2 A1272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr19:15350485 G>A maps to NM_058243.2 P1143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr19:15349229 G>A maps to NM_058243.2 F1349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:15367915 G>A maps to NM_058243.2 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:15366210 G>A maps to NM_058243.2 N648N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr19:15350006 G>A maps to NM_058243.2 S1215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:15355556 T>C maps to NM_058243.2 S725S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:15366242 G>A maps to NM_058243.2 Q638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:15378341 T>C maps to NM_058243.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr19:15350536 G>A maps to NM_058243.2 S1126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr19:15350807 C>G maps to NM_058243.2 P1065P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr19:15376338 G>A maps to NM_058243.2 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15364969 G>A maps to NM_058243.2 S717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15375520 G>A maps to NM_058243.2 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:15354212 G>A maps to NM_058243.2 A889A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q9-06A-11D-A19A-08 chr16:50357601 C>A maps to NM_001173984.2 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr16:50388811 G>A maps to NM_001173984.2 R94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:50402111 G>A maps to NM_001173984.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr5:137485336 G>A maps to NM_139199.1 S1090S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:137481494 C>T maps to NM_139199.1 K1117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr5:137500714 G>A maps to NM_139199.1 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:137476507 T>C maps to NM_139199.1 Q1167Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:137497482 A>C did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:137481566 C>T maps to NM_139199.1 L1093L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr5:137502285 T>C maps to NM_139199.1 Q306Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr5:137486556 C>T maps to NM_139199.1 E999E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr5:876233 C>T maps to NM_001009877.2 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:876269 G>A maps to NM_001009877.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:865592 G>A maps to NM_001009877.2 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr5:865655 C>T maps to NM_001009877.2 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr5:884139 A>G maps to NM_001009877.2 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr5:876257 G>A maps to NM_001009877.2 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr5:878588 G>A maps to NM_001009877.2 S331S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-RP-A693-06A-13D-A30X-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:92446542 C>T maps to ENST00000347608 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:92470104 G>A maps to ENST00000347608 R853R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr1:92446852 A>G maps to ENST00000347608 E605E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:92459695 C>T maps to ENST00000347608 T736T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr1:92446460 G>A maps to ENST00000347608 R504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:92442775 G>A maps to ENST00000347608 K277K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:92469969 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr2:28210912 G>T maps to NM_004899.3 G87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:28550224 C>A maps to NM_004899.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr14:105693012 G>A maps to NM_001519.2 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr14:105677570 C>T maps to NM_001519.2 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr14:105752681 G>A maps to NM_001519.2 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr8:37704430 G>T maps to NM_018310.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr8:37702228 G>A maps to NM_018310.3 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr8:37702334 G>A maps to NM_018310.3 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:125509681 C>T maps to NM_080626.5 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:125509699 C>T maps to NM_080626.5 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:125509588 C>T maps to NM_080626.5 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:125509699 C>T maps to NM_080626.5 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr17:59886055 C>T maps to NM_032043.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr17:59926561 G>A maps to NM_032043.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr17:59858248 C>T maps to NM_032043.2 Q582Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:59857759 G>A maps to NM_032043.2 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:59770873 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:59853805 G>A maps to NM_032043.2 Q685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:66108722 G>A maps to NM_001024957.1 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr11:66109080 C>T maps to NM_001024957.1 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr11:66108329 C>T maps to NM_001024957.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:167889260 G>A maps to NM_001143674.1 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr1:167887566 G>A maps to NM_001143674.1 H126H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:9784839 C>T maps to NM_001003694.1 A738A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:9789030 T>C maps to NM_001003694.1 *1221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:9787361 C>T maps to NM_001003694.1 S1058S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr3:9781054 C>T maps to NM_001003694.1 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr3:9785335 C>T maps to NM_001003694.1 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr3:9785986 G>A maps to NM_001003694.1 P905P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:9786133 C>T maps to NM_001003694.1 P954P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr6:36178150 C>T maps to NM_015695.2 F675F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr6:36169208 C>T maps to NM_015695.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:36179134 C>T maps to NM_015695.2 S760S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr6:36196800 C>T maps to NM_015695.2 F1134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr6:36168368 C>T maps to NM_015695.2 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr6:36172573 C>T maps to NM_015695.2 Q530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:36172536 C>T maps to NM_015695.2 V517V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:36198361 C>T maps to NM_015695.2 S1198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:135570656 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr23:135570355 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr23:135572628 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:135570516 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:135574323 C>T did not map to a codon.
Sequencing variant TCGA-ER-A197-06A-32D-A197-08 chr23:135574442 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:135574321 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:55805450 C>T maps to NM_032430.1 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:55805462 C>T maps to NM_032430.1 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:55817699 C>T maps to NM_032430.1 F657F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:55820096 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:55816923 C>T maps to NM_032430.1 I620I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:55798595 C>T maps to NM_032430.1 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:55816890 C>T maps to NM_032430.1 F609F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:55815080 G>A maps to NM_032430.1 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:1459552 G>A maps to NM_003957.2 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:1459552 G>A maps to NM_003957.2 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr11:1467077 G>A maps to NM_003957.2 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:1466553 G>A maps to NM_003957.2 Q281Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr11:1471926 C>T maps to NM_003957.2 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr21:40642346 G>A maps to NM_018963.3 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr21:40581928 T>G maps to NM_018963.3 R1397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr21:40574326 A>G maps to NM_018963.3 G1503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:40590105 G>A maps to NM_018963.3 R1211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr23:79936923 A>G did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:79937547 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:79936965 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr23:79947402 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:79942375 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:79943580 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:79964983 A>T did not map to a codon.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr23:79978133 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr23:79945478 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:79932598 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:79932654 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:79960304 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr23:79985493 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:79948454 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:79973139 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:79973140 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:79932527 T>C did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:79945340 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr23:79947390 A>C did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:79942452 C>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:79932387 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:79978252 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:79947369 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:79980523 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:79939558 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:79939654 G>A did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:79984277 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr23:79980481 A>T did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:79947381 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:62458829 G>A maps to NM_001130702.1 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:62474645 G>A maps to NM_001130702.1 Q8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:62474646 G>A maps to NM_001130702.1 D7D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:62458111 T>C maps to NM_001130702.1 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:32842310 T>A maps to NM_001143888.1 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr1:32849429 C>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:32843854 G>A maps to NM_001143888.1 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:32842334 G>A maps to NM_001143888.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:32842271 G>A maps to NM_001143888.1 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:32834068 G>A maps to NM_001143888.1 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr19:582304 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:577990 C>T maps to NM_001728.2 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:578035 C>T maps to NM_001728.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr3:49693942 C>T maps to NM_003458.3 A2318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr3:49692712 C>T maps to NM_003458.3 P1908P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr3:49700786 C>T maps to NM_003458.3 P3732P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:49695235 C>T maps to NM_003458.3 I2749I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:49662815 G>A maps to NM_003458.3 Q211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:49662816 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:49690915 C>T maps to NM_003458.3 T1309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:49691890 C>T maps to NM_003458.3 A1634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:49690792 C>T maps to NM_003458.3 V1268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:49692991 C>T maps to NM_003458.3 I2001I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:49698343 C>T maps to NM_003458.3 L3022L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:49690462 C>T maps to NM_003458.3 F1158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr3:49699810 G>A maps to NM_003458.3 L3511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:49695088 C>T maps to NM_003458.3 I2700I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr3:49688502 G>A maps to NM_003458.3 G659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:49662416 G>A maps to NM_003458.3 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:49694788 G>A maps to NM_003458.3 R2600R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:49699630 G>A maps to NM_003458.3 G3451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:49688109 G>A maps to NM_003458.3 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr3:49689784 G>A maps to NM_003458.3 K932K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:49688995 C>T maps to NM_003458.3 Y669Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:49694050 C>T maps to NM_003458.3 F2354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr3:49689106 A>G maps to NM_003458.3 E706E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr3:49695058 C>T maps to NM_003458.3 I2690I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:49680224 C>T maps to NM_003458.3 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr3:49688292 G>A maps to NM_003458.3 Q589Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr3:49692022 C>T maps to NM_003458.3 I1678I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:49699003 G>A maps to NM_003458.3 K3242K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:49688097 C>T maps to NM_003458.3 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr3:49698187 G>A maps to NM_003458.3 K2970K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr3:49692304 C>T maps to NM_003458.3 A1772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr3:49689298 C>T maps to NM_003458.3 A770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr3:49692340 C>T maps to NM_003458.3 A1784A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:49662656 C>T maps to NM_003458.3 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr3:49689772 C>T maps to NM_003458.3 L928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:49662671 C>T maps to NM_003458.3 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:49688112 C>T maps to NM_003458.3 T529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:49690102 G>A maps to NM_003458.3 E1038E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:49700327 G>A maps to NM_003458.3 E3579E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr3:49689991 C>T maps to NM_003458.3 S1001S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:55464879 C>T maps to NM_057176.2 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr1:55474255 C>T maps to NM_057176.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr1:55474159 G>A maps to NM_057176.2 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:55472813 G>A maps to NM_057176.2 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:55474207 G>A maps to NM_057176.2 K290K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:55470744 G>A maps to NM_057176.2 K76K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr9:116131914 C>T maps to NM_017688.2 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:116131974 C>T maps to NM_017688.2 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr9:116132412 C>T maps to NM_017688.2 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr9:116116602 G>A maps to NM_017688.2 K95K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr9:116132361 C>T maps to NM_017688.2 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:116132055 C>T maps to NM_017688.2 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:116132181 C>T maps to NM_017688.2 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:17516153 G>A maps to NM_004335.2 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:122850163 C>T maps to NM_001098169.1 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr10:93723838 C>T maps to NM_003972.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:93741919 C>T maps to NM_003972.2 T662T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr10:93753465 C>T maps to NM_003972.2 L1021L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr10:93773458 C>T maps to NM_003972.2 F1449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:93773518 A>C maps to NM_003972.2 I1469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:93751879 C>A maps to NM_003972.2 S953S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr10:93767975 T>C maps to NM_003972.2 L1253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:93742421 C>T maps to NM_003972.2 S709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr15:83718903 A>G maps to NM_025238.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:13435173 G>A maps to NM_032320.5 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr12:108035865 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr12:108013892 C>T maps to NM_001018072.1 L861L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:108045515 G>A maps to NM_001018072.1 A1019A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:107937823 C>T maps to NM_001018072.1 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr12:108011997 G>A maps to NM_001018072.1 E765E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr12:107914402 C>T maps to NM_001018072.1 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:108013934 G>A maps to NM_001018072.1 A875A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:108029147 G>A maps to NM_001018072.1 R906R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:108045515 G>A maps to NM_001018072.1 A1019A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr12:107713181 C>A maps to NM_001018072.1 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:108034181 C>T maps to NM_001018072.1 A944A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:108035945 C>T maps to NM_001018072.1 Q974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:108013805 C>T maps to NM_001018072.1 I832I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:108051453 C>T maps to NM_001018072.1 Q1092*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:107914327 G>A maps to NM_001018072.1 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:107914336 C>T maps to NM_001018072.1 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:108006600 G>A maps to NM_001018072.1 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:108010939 C>T maps to NM_001018072.1 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:108013805 C>T maps to NM_001018072.1 I832I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:108013934 G>A maps to NM_001018072.1 A875A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:108051461 C>T maps to NM_001018072.1 I1094I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:108011985 C>T maps to NM_001018072.1 I761I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:108034133 G>A maps to NM_001018072.1 L928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr16:3632684 G>A maps to NM_032444.2 S1721S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr16:3633494 G>A maps to NM_032444.2 L1586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr16:3640455 G>A maps to NM_032444.2 S1061S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr16:3644579 A>C maps to NM_032444.2 V678V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr16:3639231 G>A maps to NM_032444.2 S1469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr16:3641184 G>A maps to NM_032444.2 L818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:3658899 G>A maps to NM_032444.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:3640461 G>A maps to NM_032444.2 P1059P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:3639789 G>A maps to NM_032444.2 A1283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:3645677 G>A maps to NM_032444.2 P647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr10:124043404 T>C maps to ENST00000368994 N70N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr10:124096112 C>T maps to ENST00000368994 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr10:124096113 C>T maps to ENST00000368994 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr10:124090760 C>T maps to ENST00000368994 N359N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr10:124066712 C>T maps to ENST00000368994 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr10:124097542 C>T maps to ENST00000368994 I489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr10:124050682 C>T maps to ENST00000368994 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:124045675 C>T maps to ENST00000368994 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:124049454 C>T maps to ENST00000368994 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:124094425 C>T maps to ENST00000368994 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:124050610 G>A maps to ENST00000368994 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:124045734 C>T maps to ENST00000368994 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr10:124036317 C>T maps to ENST00000368994 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr10:124034613 G>C maps to ENST00000368994 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr10:124036364 A>G maps to ENST00000368994 K27K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:124045711 C>T maps to ENST00000368994 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:124045737 G>C maps to ENST00000368994 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:124050682 C>T maps to ENST00000368994 I189I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A2GO-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:72356379 C>T maps to NM_001080466.1 Q30Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr19:1997392 C>T maps to NM_017797.3 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:11903449 C>T maps to NM_014962.2 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr20:11903872 C>T maps to NM_014962.2 H376H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:11903563 C>T maps to NM_014962.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:11903962 C>T maps to NM_014962.2 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr14:93728005 G>A maps to NM_001002860.2 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr14:93760500 G>A maps to NM_001002860.2 R289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:93709395 G>A maps to NM_001002860.2 I874I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr14:93755012 A>G maps to NM_018167.3 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:92554329 C>T maps to NM_183242.3 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:92613242 G>A maps to NM_183242.3 W341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr1:92612819 C>A maps to NM_183242.3 C338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:92573482 T>A maps to NM_183242.3 L196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:92595246 C>T maps to NM_183242.3 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:92568188 G>A maps to NM_183242.3 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:92606762 C>T maps to NM_183242.3 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:92568083 G>A maps to NM_183242.3 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr6:38160294 C>T maps to NM_052893.1 E547E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:38561814 A>C maps to NM_052893.1 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr6:38545386 G>A maps to NM_052893.1 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:38560549 A>G maps to NM_052893.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:38160327 G>A maps to NM_052893.1 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr6:38565686 G>A maps to NM_052893.1 R62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr6:38560555 G>A maps to NM_052893.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr4:75681109 C>T maps to NM_001729.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:75675847 C>T maps to NM_001729.2 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:75695355 G>A maps to NM_001729.2 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr3:15686328 C>T maps to NM_000060.2 Y322Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr3:15643375 C>T maps to NM_000060.2 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:92537990 G>A maps to NM_001731.2 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:100617209 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr23:100613677 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:100609664 C>A did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:100625024 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:100626635 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:100608962 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:100630260 C>T did not map to a codon.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr23:100615595 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:100625004 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr23:100608314 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:100608323 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:100611928 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:100612547 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:100625054 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr23:100615120 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:100625005 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:100611057 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:100626667 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:112218145 G>A maps to NM_181780.3 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr6:26505363 G>A maps to NM_001732.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr6:26506937 G>A maps to NM_001732.2 W246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:26502022 G>A maps to NM_001732.2 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:26509299 G>A maps to NM_001732.2 K493K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr6:26509209 G>A maps to NM_001732.2 W463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr6:26506929 G>A maps to NM_001732.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr6:26509341 G>A maps to NM_001732.2 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:26505393 C>T maps to NM_001732.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr6:26508828 G>A maps to NM_001732.2 E336E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:26509197 C>T maps to NM_001732.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr6:26508765 C>T maps to NM_001732.2 H315H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr6:26509290 C>T maps to NM_001732.2 D490D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr6:26460003 C>T maps to NM_007049.3 Y126Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr6:26460006 C>T maps to NM_007049.3 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr6:26392816 C>T maps to NM_001197237.1 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:26392646 C>T maps to NM_001197237.1 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr6:26413832 C>T maps to NM_007048.5 F485F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr6:26413718 C>T maps to NM_007048.5 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr6:26407990 C>T maps to NM_007048.5 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:26408019 G>A maps to NM_007048.5 E185E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr6:26407968 C>T maps to NM_007048.5 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr6:26409899 G>A maps to NM_007048.5 K285K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:26452275 C>T maps to NM_006994.4 F464F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr6:26452035 C>T maps to NM_006994.4 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:26452455 T>C maps to NM_006994.4 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr6:26444500 C>T maps to NM_006994.4 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr6:32362723 C>T maps to ENST00000468270 W386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:32362677 C>T maps to ENST00000468270 T401T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:32370910 G>A maps to ENST00000468270 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr6:32369580 C>T maps to ENST00000468270 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:32372983 G>A maps to ENST00000468270 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr5:180420074 C>T maps to NM_197975.2 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:180432701 C>T maps to NM_197975.2 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:180424351 C>T maps to NM_197975.2 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:180432607 C>T maps to NM_197975.2 V379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr5:180377474 C>T maps to NM_001040462.2 I478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:180377459 A>G maps to NM_001040462.2 Q473Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr5:180374620 C>T maps to NM_001040462.2 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr5:180335628 G>A maps to NM_001040462.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr5:180374695 C>T maps to NM_024850.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr5:180326348 G>A maps to NM_001040462.2 K13K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr5:180335685 C>T maps to NM_001040462.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:180338606 G>A maps to NM_001040462.2 Q222Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:180377042 G>A maps to NM_001040462.2 Q334Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:180335652 C>T maps to NM_001040462.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr5:180377219 C>T maps to NM_001040462.2 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr5:180374515 C>T maps to NM_001040462.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr5:180374720 C>T maps to NM_024850.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr5:180374510 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr5:180374695 C>T maps to NM_024850.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:180335745 G>A maps to NM_001040462.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:180338435 G>A maps to NM_001040462.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:180374515 C>T maps to NM_001040462.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr5:180475173 G>A maps to NM_152547.4 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr5:180486780 G>A maps to NM_152547.4 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:180477328 C>T maps to NM_152547.4 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:103292171 C>T maps to NM_033637.2 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:103310562 C>T maps to NM_033637.2 A588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:103292776 C>T maps to NM_033637.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:103292777 C>T maps to NM_033637.2 Q350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr10:103310574 C>T maps to NM_033637.2 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr10:103298055 T>A maps to NM_033637.2 I528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:111419205 G>A maps to NM_004336.3 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:40462854 T>C maps to ENST00000412359 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:40468866 C>T maps to ENST00000412359 Q206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:40494624 C>T maps to ENST00000412359 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr10:124917344 G>A maps to NM_004725.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:116633302 G>A maps to NM_032725.3 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:116631588 T>G maps to NM_032725.3 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:116633923 A>T maps to NM_032725.3 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:116633461 G>C maps to NM_032725.3 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:116633572 G>A maps to NM_032725.3 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr11:116633302 G>A maps to NM_032725.3 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:105572424 G>A maps to NM_007073.4 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:105577304 G>A maps to NM_007073.4 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr6:41889368 C>T maps to NM_004053.3 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:41889368 C>T maps to NM_004053.3 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr6:41899485 G>T maps to NM_004053.3 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr17:56403074 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr17:56382451 C>T maps to NM_004758.2 R1838R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:56382927 C>T maps to NM_004758.2 Q1778Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:56386569 G>A maps to NM_004758.2 R1355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:56386213 G>A maps to NM_004758.2 S1473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr17:56387342 C>T maps to NM_004758.2 R1292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:56386732 G>A maps to NM_004758.2 P1300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:56382490 G>A maps to NM_004758.2 F1825F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:56388553 G>A maps to NM_004758.2 P1034P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:56384173 G>A maps to NM_004758.2 L1713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr17:56389436 G>A maps to NM_004758.2 L915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr17:56403731 C>T maps to NM_004758.2 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr17:56387371 G>A maps to NM_004758.2 Q1283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr17:56386308 G>A maps to NM_004758.2 R1442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:56386726 G>A maps to NM_004758.2 P1302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:56387437 G>A maps to NM_004758.2 Q1261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:56387941 G>A maps to NM_004758.2 A1210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:56388019 G>A maps to NM_004758.2 P1184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:56403665 C>T maps to NM_004758.2 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr7:16734622 C>T maps to NM_014038.2 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:16725627 C>T maps to NM_014038.2 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:16737779 C>T maps to NM_014038.2 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:16714052 C>T maps to NM_014038.2 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:63450375 T>G maps to NM_173554.2 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr10:77818528 G>T maps to NM_032024.3 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr10:15138496 C>T maps to NM_153244.1 Q109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr10:21414811 G>A maps to NM_001010896.2 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr10:21414909 G>A maps to NM_001010896.2 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:21435361 G>A maps to NM_001010896.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr10:21414811 G>A maps to NM_001010896.2 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:21414811 G>A maps to NM_001010896.2 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:21414769 C>T maps to NM_001010896.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:21414829 C>T maps to NM_001010896.2 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:21414931 G>A maps to NM_001010896.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:115895957 G>A maps to NM_018017.2 V458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr10:115885776 C>G maps to NM_018017.2 R827R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr10:121619308 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr10:121612601 G>A maps to NM_024834.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:98742448 C>T maps to NM_015652.2 D434D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:98742643 C>T maps to NM_015652.2 F499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:98744593 C>T maps to NM_015652.2 I1149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr10:124459183 C>T maps to NM_001010912.1 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr10:124457673 G>A maps to NM_001010912.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:124458928 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr10:124457575 C>T maps to NM_001010912.1 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:124458882 C>T maps to NM_001010912.1 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:124457713 C>T maps to NM_001010912.1 Q181Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr10:124457746 C>T maps to NM_001010912.1 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr10:124457770 C>T maps to NM_001010912.1 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr10:124459258 C>T maps to NM_001010912.1 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:124459228 C>T maps to NM_001010912.1 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:124459231 C>T maps to NM_001010912.1 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:124459273 C>T maps to NM_001010912.1 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr10:124457482 G>A maps to NM_001010912.1 Y258Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:124457515 G>A maps to NM_001010912.1 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr10:50396345 G>A maps to ENST00000374148 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:50396354 C>T maps to ENST00000374148 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:96971650 C>T maps to NM_207321.2 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:96971739 C>T maps to NM_207321.2 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:96967004 G>A maps to NM_207321.2 K148K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:96970535 C>T maps to NM_207321.2 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:96971649 C>T maps to NM_207321.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:96971769 C>T maps to NM_207321.2 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:127438009 C>T maps to ENST00000356792 H1051H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr10:127412502 C>T maps to ENST00000356792 Q170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q1-06A-21D-A196-08 chr10:5788338 C>T maps to NM_017782.4 G985G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr10:5789304 G>A maps to NM_017782.4 E1307E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr10:5791321 C>T maps to NM_017782.4 L1980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr10:102749611 C>T maps to NM_021830.4 F485F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:102748845 C>T maps to NM_021830.4 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:102748998 G>A maps to NM_021830.4 E344E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr10:102748875 G>A maps to NM_021830.4 R303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr10:102750628 C>T maps to NM_021830.4 I532I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:102748839 C>T maps to NM_021830.4 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:45495837 G>T maps to NM_001039380.2 C119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr10:104572877 C>T maps to NM_001083913.1 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:104572833 C>A maps to NM_001083913.1 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:104572538 C>T maps to NM_001083913.1 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:72541686 G>A maps to NM_152710.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr10:72533990 C>A maps to NM_152710.2 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr10:72541686 G>A maps to NM_152710.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr10:72536919 G>A maps to NM_152710.2 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:72538357 G>A maps to NM_152710.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:72539487 C>T maps to NM_152710.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:72534975 G>A maps to NM_152710.2 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:99968041 C>T maps to ENST00000314594 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:99968075 C>T maps to ENST00000314594 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:99968551 C>T maps to ENST00000314594 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:104620123 G>A maps to NM_001136200.1 Q59Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:120450807 G>A maps to NM_153810.4 Q332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:11911717 G>A maps to NM_153256.3 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr10:50901851 C>T maps to NM_182554.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:50901910 C>T maps to NM_182554.2 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:50902646 G>A maps to NM_001042427.1 *94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:50902646 G>A maps to NM_001042427.1 *94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:50916661 G>A maps to NM_182554.2 *158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr10:73511466 G>A maps to NM_022153.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:73511434 G>A maps to NM_022153.1 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:73511581 G>A maps to NM_022153.1 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr10:73512751 C>T maps to NM_022153.1 Q228Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:75671463 G>A maps to NM_001001791.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:82185749 C>T maps to NM_032333.4 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr10:82187230 C>T maps to NM_032333.4 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr10:82185722 C>T maps to NM_032333.4 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:82187230 C>T maps to NM_032333.4 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr10:99349866 C>T maps to NM_001009997.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr10:99350160 G>A maps to NM_001009997.2 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:99349980 C>T maps to NM_001009997.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr10:33018275 C>T maps to ENST00000375025 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr10:33140831 C>T maps to ENST00000375025 H639H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr10:33094021 C>T maps to ENST00000375025 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:33136831 A>C maps to ENST00000375025 R562R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr10:32983861 A>G maps to ENST00000375025 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr10:33140759 C>T maps to ENST00000375025 P615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr10:50532584 C>T maps to NM_001135196.1 T665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr10:50530733 C>T maps to NM_001135196.1 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:50531939 C>T maps to NM_001135196.1 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:50532596 G>A maps to NM_001135196.1 E669E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:50531555 C>T maps to NM_001135196.1 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:50531453 G>A maps to NM_001135196.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr10:50531294 C>T maps to NM_001135196.1 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr10:50530820 G>A maps to NM_001135196.1 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr10:50531117 C>T maps to NM_001135196.1 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:50531804 C>T maps to NM_001135196.1 N405N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr10:50532236 G>A maps to NM_001135196.1 E549E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr10:50532572 G>A maps to NM_001135196.1 E661E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr10:50531639 G>A maps to NM_001135196.1 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:50531927 C>T maps to NM_001135196.1 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:50530607 G>A maps to NM_001135196.1 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:50531099 G>A maps to NM_001135196.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:50531153 C>T maps to NM_001135196.1 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:50531462 G>A maps to NM_001135196.1 K291K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:50531645 G>A maps to NM_001135196.1 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:50531706 C>T maps to NM_001135196.1 Q373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:50531759 G>A maps to NM_001135196.1 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr10:50532071 C>A maps to NM_001135196.1 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:50227718 G>A maps to NM_001031746.3 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:50315831 C>T maps to NM_001031746.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr10:50255026 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr10:50255027 C>T maps to NM_001031746.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:50315831 C>T maps to NM_001031746.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr10:50255060 C>T maps to NM_001031746.3 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr10:50315831 C>T maps to NM_001031746.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:50315670 C>T maps to NM_001031746.3 W142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:50315891 G>A maps to NM_001031746.3 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:50255038 T>A maps to NM_001031746.3 K276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr10:105938825 C>T maps to ENST00000389588 R808R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr10:105893467 C>T maps to ENST00000389588 W1503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr10:105906092 T>C maps to ENST00000389588 E1262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr10:105974129 C>T maps to ENST00000389588 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr10:105903396 C>T maps to ENST00000389588 R1316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:105926467 C>T maps to ENST00000389588 K940K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr10:105942239 G>A maps to ENST00000389588 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr10:105953667 G>A maps to ENST00000389588 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:105923958 G>A maps to ENST00000389588 R1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:115533987 G>A maps to NM_182601.1 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:115526240 C>T maps to NM_182601.1 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:115526405 G>A maps to NM_182601.1 K45K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:115529649 C>T maps to NM_182601.1 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr10:124697642 C>G maps to NM_024942.3 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:124711493 G>A maps to NM_024942.3 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:124692118 G>A maps to NM_024942.3 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:128192631 G>A maps to NM_001004298.2 N379N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:128147756 G>A maps to NM_001004298.2 F583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr10:128114453 G>A maps to NM_001004298.2 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:128114580 G>A maps to NM_001004298.2 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:134754509 C>A maps to ENST00000368586 G121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:134755112 C>T maps to ENST00000368586 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:134755112 C>T maps to ENST00000368586 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr10:118084884 C>T maps to NM_198515.2 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr10:85936234 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:111754510 T>A maps to NM_022761.2 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:8942928 C>T maps to NM_020643.2 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:8948715 C>T maps to NM_020643.2 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:8947544 C>T maps to NM_020643.2 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:8947544 C>T maps to NM_020643.2 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:8933050 C>T maps to NM_020642.3 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:64875962 C>T maps to NM_013265.2 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:64878953 C>T maps to NM_013265.2 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr11:64875962 C>T maps to NM_013265.2 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr11:64876823 C>T maps to NM_013265.2 Q506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64876879 C>T maps to NM_013265.2 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr11:64876942 C>A maps to NM_013265.2 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:64070987 G>A maps to NM_001039496.1 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr11:68029169 C>T maps to NM_022338.3 K431K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:68029328 G>A maps to NM_022338.3 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:68029159 G>A maps to NM_022338.3 Q435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:68029430 C>T maps to NM_022338.3 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:76255613 C>T maps to ENST00000393457 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:76255614 C>T maps to ENST00000393457 Q1009*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:76207325 C>T maps to ENST00000393457 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:76183642 C>T maps to ENST00000393457 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:76257160 G>A maps to ENST00000393457 A1199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr11:76255448 G>A maps to ENST00000393457 Q953Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:57509640 C>T maps to NM_170746.2 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr11:557448 G>A maps to NM_173573.2 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:558869 G>A maps to NM_173573.2 C48C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:4598978 C>T maps to NM_144663.1 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:4598921 G>A maps to NM_144663.1 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:33564059 T>C maps to ENST00000389726 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:33628310 C>T maps to ENST00000389726 P1377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:33564528 C>T maps to ENST00000389726 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:33682472 C>T maps to ENST00000389726 F1733F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:33565385 C>T maps to ENST00000389726 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:33569340 C>T maps to ENST00000389726 I848I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:33581440 G>A maps to ENST00000389726 P1043P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:33628244 C>T maps to ENST00000389726 A1355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:33564017 C>T maps to ENST00000389726 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:6231684 C>T maps to NM_173525.2 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr11:6231372 G>A maps to NM_173525.2 K122K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr11:6231300 G>A maps to NM_173525.2 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr11:128774430 G>A maps to NM_145013.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr11:128773323 T>C maps to NM_145013.1 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:128774389 G>A maps to NM_145013.1 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:111796862 G>A maps to NM_080659.2 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:111156715 C>T maps to NM_198498.1 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr11:111156451 C>T maps to NM_198498.1 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:111156655 C>T maps to NM_198498.1 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:111154972 C>T maps to NM_198498.1 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr11:111156715 C>T maps to NM_198498.1 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr11:16774375 C>T maps to NM_014267.5 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr11:16760351 G>A maps to NM_014267.5 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:124637767 G>A maps to ENST00000374979 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:122775004 C>T maps to NM_024806.2 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:122805453 C>T maps to NM_024806.2 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:122756682 C>T maps to NM_024806.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:122817289 A>G maps to NM_024806.2 Q573Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:122774734 G>A maps to NM_024806.2 E149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:122795645 G>A maps to NM_024806.2 Q302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:122805571 C>T maps to NM_024806.2 Q475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:108332208 G>A maps to NM_152587.3 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:108332208 G>A maps to NM_152587.3 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:108264075 G>T maps to NM_152587.3 S197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:108256662 A>G maps to NM_152587.3 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:61253370 C>T maps to NM_145017.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:61250165 G>A maps to NM_145017.2 Q89Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:61249307 C>T maps to NM_145017.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:101946666 C>T maps to NM_032930.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:101951949 C>T maps to NM_032930.2 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr11:101929618 C>T maps to NM_032930.2 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:36669620 C>T maps to NM_138787.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr11:36631724 C>T maps to NM_138787.2 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:93212343 G>A maps to NM_020179.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:93212283 C>T maps to NM_020179.2 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:66563828 C>T maps to ENST00000360962 H237H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:66571645 G>A maps to ENST00000360962 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:82644812 C>T maps to NM_145018.3 F811F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:82642922 C>T maps to NM_145018.3 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:82625825 C>T maps to NM_145018.3 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:82643114 C>T maps to NM_145018.3 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:82625884 C>T maps to NM_145018.3 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:82644404 C>T maps to NM_145018.3 A675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:82644812 C>T maps to NM_145018.3 F811F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:63585826 C>T maps to NM_138471.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr11:61543556 C>T maps to NM_001127392.1 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:61541528 C>T maps to NM_001127392.1 F402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:61539184 G>A maps to NM_001127392.1 Q318Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:61543820 G>A maps to NM_001127392.1 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr11:61550976 C>T maps to NM_001127392.1 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr11:61539202 G>A maps to NM_001127392.1 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:61533561 C>T maps to NM_001127392.1 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:61533564 C>T maps to NM_001127392.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:61533630 G>A maps to NM_001127392.1 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr11:61533510 C>T maps to NM_001127392.1 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr12:53700516 G>A maps to NM_021640.3 K273K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z4-06A-11D-A197-08 chr12:53696977 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr12:27078747 G>A maps to NM_018164.2 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:27081175 C>T maps to NM_018164.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr12:91347805 G>A maps to NM_152638.2 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr12:91348401 G>A maps to NM_152638.2 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr12:91347580 C>T maps to NM_152638.2 E313E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:91348213 G>A maps to NM_152638.2 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr12:91347589 C>T maps to NM_152638.2 E310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:91348333 G>A maps to NM_152638.2 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:91348264 C>T maps to NM_152638.2 W85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr12:91348039 C>T maps to NM_152638.2 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:91347553 G>A maps to NM_152638.2 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:91348351 G>A maps to NM_152638.2 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:82870467 C>T maps to NM_032230.2 R540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:82796877 C>T maps to NM_032230.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr12:82871079 C>T maps to NM_032230.2 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:32137576 C>T maps to NM_018169.3 Q1230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr12:13526306 C>T maps to ENST00000318426 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:13526359 C>T maps to ENST00000318426 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr12:13529164 G>A maps to ENST00000318426 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:13526286 G>A maps to ENST00000318426 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:13529185 G>A maps to ENST00000318426 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:13526230 C>T maps to ENST00000318426 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:13526359 C>T maps to ENST00000318426 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr12:13526306 C>T maps to ENST00000318426 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr12:4626314 G>A maps to NM_020374.2 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:4609423 C>T maps to NM_020374.2 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr12:4609465 G>A maps to NM_020374.2 I426I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr12:40040149 C>T maps to NM_001031748.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:40114656 G>A maps to NM_001031748.2 K521K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:40114939 C>T maps to NM_001031748.2 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:40115043 G>A maps to NM_001031748.2 K650K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr12:40020149 C>T maps to NM_001031748.2 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:40076667 G>A maps to NM_001031748.2 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:40114686 G>A maps to NM_001031748.2 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr12:49061512 G>T maps to NM_017822.3 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:103700001 G>A maps to NM_001099336.1 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr12:103700109 C>T maps to NM_001099336.1 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:103699881 C>T maps to NM_001099336.1 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:103696002 G>A maps to NM_001099336.1 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr12:103699956 C>T maps to NM_001099336.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr12:121442012 G>A maps to NM_022895.1 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:121454214 C>T maps to NM_022895.1 E21E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:121442888 G>A maps to NM_022895.1 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr12:52470967 C>T maps to NM_021934.4 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:52470667 C>T maps to NM_021934.4 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:105388386 C>T maps to NM_152318.2 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:102569431 C>T maps to NM_017915.3 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:117155665 G>A maps to NM_024738.1 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr12:88376889 C>T maps to NM_152589.1 K403K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr12:88390262 C>T maps to NM_152589.1 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr12:88379717 G>A maps to NM_152589.1 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:88379642 T>C maps to NM_152589.1 K370K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:88391962 G>A maps to NM_152589.1 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:88383122 C>T maps to NM_152589.1 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr12:88379684 C>T maps to NM_152589.1 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:88376913 T>C maps to NM_152589.1 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:88391962 G>A maps to NM_152589.1 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:88379809 G>A maps to NM_152589.1 Q315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:88381735 C>T maps to NM_152589.1 K236K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:88420334 C>T maps to NM_152589.1 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr12:112631296 C>T maps to NM_001109662.2 T2805T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr12:112632752 G>A maps to NM_001109662.2 I2723I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr12:112672930 G>A maps to NM_001109662.2 I1783I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:112608236 C>T maps to NM_001109662.2 T3812T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:112707632 G>A maps to NM_001109662.2 F550F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:112650371 G>A maps to NM_001109662.2 F2344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr12:112684753 G>A maps to NM_001109662.2 A1316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr12:112608217 G>A maps to NM_001109662.2 R3819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr12:112667564 G>A maps to NM_001109662.2 A1980A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:112622557 G>A maps to NM_001109662.2 I3232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:112648044 G>A maps to NM_001109662.2 T2375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr12:112673401 G>A maps to NM_001109662.2 V1705V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr12:112645750 G>A maps to NM_001109662.2 T2514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr12:112699193 G>A maps to NM_001109662.2 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:112686219 G>A maps to NM_001109662.2 F1177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:112743999 G>A maps to NM_001109662.2 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr12:112676997 G>A maps to NM_001109662.2 L1544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr12:112622377 G>A maps to NM_001109662.2 P3292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr12:112622398 G>A maps to NM_001109662.2 P3285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr12:112654695 G>A maps to NM_001109662.2 I2250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:112622518 G>A maps to NM_001109662.2 I3245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:112645735 G>A maps to NM_001109662.2 F2519F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr12:112669438 G>A maps to NM_001109662.2 I1854I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:113629231 C>T maps to NM_032848.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:113629414 C>T maps to NM_032848.1 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr12:6806657 G>A maps to NM_153685.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr12:48884615 C>T maps to NM_152319.3 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr12:48880501 G>A maps to NM_152319.3 W43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:48884611 G>A maps to NM_152319.3 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr12:64668752 T>A maps to NM_001170633.1 G504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:64668680 G>A maps to NM_001170633.1 I528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:64668704 G>A maps to NM_001170633.1 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:64746712 G>A maps to NM_001170633.1 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr12:10342588 C>T maps to NM_153022.2 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr12:14976270 G>A maps to NM_175874.3 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:14976468 C>T maps to NM_175874.3 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr12:14976117 G>A maps to NM_175874.3 K83K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr12:14976312 C>T maps to NM_175874.3 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr12:97043780 G>A maps to ENST00000342887 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:97102501 G>A maps to ENST00000342887 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:97078947 G>A maps to ENST00000342887 E407E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:97078498 C>T maps to ENST00000342887 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr12:97114191 C>T maps to ENST00000342887 L697L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr12:97082753 C>T maps to ENST00000342887 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:97137618 G>A maps to ENST00000342887 K921K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:97150266 G>A maps to ENST00000342887 E1049E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:97084956 C>T maps to ENST00000342887 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr12:97045529 C>T maps to ENST00000342887 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:97052042 T>C maps to ENST00000342887 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:97158895 G>A maps to ENST00000342887 K1152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:97147569 C>T maps to ENST00000342887 P1003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr12:97078896 C>T maps to ENST00000342887 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr12:97078995 C>T maps to ENST00000342887 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:97043780 G>A maps to ENST00000342887 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:97045401 C>T maps to ENST00000342887 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr12:97098519 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr12:97147662 C>T maps to ENST00000342887 I1034I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr12:97137676 C>T maps to ENST00000342887 L941L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:97073462 C>T maps to ENST00000342887 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:97045390 G>A maps to ENST00000342887 W58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:97078438 C>T maps to ENST00000342887 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr12:80704413 T>A maps to NM_173591.3 I1110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr12:80714335 C>T maps to NM_173591.3 Q1304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr12:80764420 G>A maps to NM_173591.3 L2220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr12:80655844 G>A maps to NM_173591.3 V653V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:80750683 C>T maps to NM_173591.3 S1994S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:80770954 G>A maps to NM_173591.3 R2269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr12:80764354 G>A maps to NM_173591.3 G2198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr12:80623120 C>T maps to NM_173591.3 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr12:80672877 C>T maps to NM_173591.3 R945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:80729861 C>T maps to NM_173591.3 F1505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:80746106 G>A maps to NM_173591.3 W1757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr12:80729753 T>C maps to NM_173591.3 F1469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr12:80729894 C>T maps to NM_173591.3 I1516I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr12:80665536 C>T maps to NM_173591.3 N867N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:80729819 C>T maps to NM_173591.3 S1491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:80729900 C>T maps to NM_173591.3 C1518C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr12:80765830 C>T maps to NM_173591.3 G2247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr12:80735866 G>A maps to NM_173591.3 R1721R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:80717527 G>A maps to NM_173591.3 R1360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr12:80647327 A>C maps to NM_173591.3 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:80730322 T>C maps to NM_173591.3 C1568C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr12:80704455 G>A maps to NM_173591.3 K1124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr12:80735761 G>A maps to NM_173591.3 R1686R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:80615937 C>T maps to NM_173591.3 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:80623120 C>T maps to NM_173591.3 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:80750644 C>T maps to NM_173591.3 F1981F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:80770936 C>T maps to NM_173591.3 I2263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:80761441 C>T maps to NM_173591.3 L2136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:80714205 A>G maps to NM_173591.3 L1260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr12:64588116 C>T maps to ENST00000311915 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:64588125 G>A maps to ENST00000311915 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:48578048 A>G maps to NM_001013635.3 K48K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:48578414 G>A maps to NM_001013635.3 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:14958948 G>A maps to NM_001013698.2 H222H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr12:14959304 C>A maps to NM_001013698.2 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr12:27234244 G>A maps to ENST00000398815 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr12:31815174 C>T maps to NM_001135864.1 Y96Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr12:93100481 G>A maps to NM_001037671.3 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:93100508 C>T maps to NM_001037671.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr12:93100878 C>T maps to NM_001037671.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:110495058 G>A maps to NM_207435.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:50505151 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:42041040 C>T maps to NM_014059.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr13:111995207 G>A maps to NM_152324.1 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr13:111992267 C>T maps to NM_152324.1 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr13:111996451 C>G maps to NM_152324.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:111992258 C>T maps to NM_152324.1 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr13:111980602 C>A maps to NM_152324.1 C44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr13:46917567 G>A maps to NM_025113.2 I647I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr13:46917579 C>T maps to NM_025113.2 R643R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:46942906 G>A maps to NM_025113.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr13:39587681 C>T maps to NM_025138.3 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr13:39602368 C>A maps to NM_025138.3 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr13:39611364 G>A maps to NM_025138.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr13:31540397 G>A maps to NM_152325.1 W170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr13:31531167 T>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr13:113086756 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr13:113052391 C>T maps to NM_145248.4 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr13:44464256 C>T maps to NM_153218.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:44464387 C>T maps to NM_153218.2 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr13:31495936 C>T maps to NM_032849.3 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:31495963 G>A maps to NM_032849.3 K256K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr13:73305504 T>A maps to ENST00000377815 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:37269293 C>T maps to NM_203451.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr13:37269358 C>T maps to NM_203451.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr13:37269358 C>T maps to NM_203451.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr13:103338769 G>A maps to NM_001010977.1 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr14:57114103 C>T maps to NM_017799.3 F671F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr14:57082682 G>A maps to NM_017799.3 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr14:90770341 A>G maps to NM_017970.2 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:90755258 G>A maps to NM_017970.2 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr14:90745471 G>A maps to NM_017970.2 S1101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:90755408 G>A maps to NM_017970.2 L770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:90784407 G>A maps to NM_017970.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:90754979 G>A maps to NM_017970.2 F913F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr14:90769097 G>A maps to NM_017970.2 H459H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:90770545 G>A maps to NM_017970.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:90755486 G>A maps to NM_017970.2 V744V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr14:57938120 G>A maps to NM_018168.2 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr14:57960230 C>T maps to NM_018168.2 W68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:57947409 C>T maps to NM_018168.2 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:57938250 C>T maps to NM_018168.2 W238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr14:45687483 C>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:45712030 G>A maps to NM_018353.4 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr14:74825331 C>T maps to NM_018228.2 Q616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr14:74824784 G>A maps to NM_018228.2 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr14:74825171 C>T maps to NM_018228.2 V562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:74825219 G>A maps to NM_018228.2 K578K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr14:74823911 C>T maps to NM_018228.2 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:74823752 G>A maps to NM_018228.2 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr14:74824769 C>T maps to NM_018228.2 F428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr14:74825030 C>T maps to NM_018228.2 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr14:74825432 G>A maps to NM_018228.2 T649T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:74824490 C>T maps to NM_018228.2 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:74824988 G>A maps to NM_018228.2 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr14:74824457 C>T maps to NM_018228.2 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:74824909 G>A maps to NM_018228.2 W475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr14:74824244 C>T maps to NM_018228.2 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr14:74823701 G>A maps to NM_018228.2 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr14:74825516 C>T maps to NM_018228.2 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:74824430 C>T maps to NM_018228.2 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:74824583 G>A maps to NM_018228.2 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:74825432 G>A maps to NM_018228.2 T649T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:74824814 C>T maps to NM_018228.2 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:76647108 C>T maps to NM_017926.2 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:96848751 C>T maps to NM_016472.3 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:60592361 C>T maps to ENST00000404681 L1030L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr14:50583132 G>A maps to NM_024558.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:90397919 G>A maps to NM_145231.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:90420995 G>A maps to NM_145231.2 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr14:81304582 G>A maps to NM_152446.3 Q297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr14:81227855 G>A maps to NM_152446.3 S826S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr14:81251541 G>A maps to NM_152446.3 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr14:81297573 G>A maps to NM_152446.3 F374F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr14:81251577 G>A maps to NM_152446.3 A624A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:81251697 G>A maps to NM_152446.3 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:81304582 G>A maps to NM_152446.3 Q297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr14:81382803 G>A maps to NM_152446.3 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr14:77861084 G>A maps to NM_001113475.1 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51K-06A-11D-A25O-08 chr14:77873091 T>C maps to NM_001113475.1 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:77889127 G>A maps to NM_001113475.1 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:77861021 G>A maps to NM_001113475.1 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr14:59939745 C>G maps to NM_144581.1 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr14:104056553 C>T maps to NM_032374.3 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr14:91681795 C>T maps to NM_001102368.1 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr14:91662737 C>T maps to NM_001102368.1 I405I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:91636448 C>T maps to NM_001102368.1 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr14:91642290 C>T maps to NM_001102368.1 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:52458056 C>T maps to NM_016039.2 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:52460466 C>T maps to NM_016039.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr14:77294697 C>T maps to NM_194287.2 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:77304258 C>T maps to NM_194287.2 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr14:77332333 C>T maps to NM_194287.2 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:77318762 G>A maps to NM_194287.2 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:77333739 G>A maps to NM_194287.2 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr14:77844381 G>A maps to NM_001010860.1 E207E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr14:99182644 G>A maps to NM_182560.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:99182644 G>A maps to NM_182560.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:76549580 C>T maps to NM_052873.2 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:76488725 G>A maps to NM_052873.2 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr14:76488734 G>A maps to NM_052873.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr14:69262644 G>T maps to NM_207442.2 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr14:69262882 C>T maps to NM_207442.2 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr14:50472358 G>A maps to NM_001012706.1 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr14:24771297 C>T maps to NM_174913.1 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr14:24774193 C>T maps to NM_174913.1 R602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:24769387 C>T maps to NM_174913.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:24774213 C>T maps to NM_174913.1 T608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr14:24769900 C>T maps to NM_174913.1 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:24771527 C>T maps to NM_174913.1 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr14:58563464 C>T maps to ENST00000438670 W707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:58604993 C>T maps to ENST00000438670 E379E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr14:58605023 C>T maps to ENST00000438670 E369E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr14:58605692 G>C maps to ENST00000438670 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:58563490 G>A maps to ENST00000438670 T698T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:58606037 G>A maps to ENST00000438670 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr14:60928260 C>T maps to NM_174978.2 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:60928078 C>T maps to NM_174978.2 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:60928117 T>G maps to NM_174978.2 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr14:60928269 T>G maps to NM_174978.2 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr14:60938166 G>A maps to NM_174978.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr14:77493061 G>A maps to NM_024496.2 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:77492581 G>A maps to NM_024496.2 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr14:74188197 G>A maps to NM_001043318.1 F913F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr14:74206072 G>A maps to NM_001043318.1 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr14:74206624 G>A maps to NM_001043318.1 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr14:74205721 G>A maps to NM_001043318.1 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr14:74196553 G>A maps to NM_001043318.1 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr14:74206605 G>A maps to NM_001043318.1 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:74203778 G>A maps to NM_001043318.1 N557N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr14:74188088 G>A maps to NM_001043318.1 Q950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr14:74188089 G>A maps to NM_001043318.1 I949I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr14:74486180 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:74500849 C>T maps to NM_025057.2 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:74500774 C>T maps to NM_025057.2 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr14:74500774 C>T maps to NM_025057.2 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr14:95903213 G>A maps to NM_152592.3 I827I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr14:95932474 G>A maps to NM_152592.3 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:95906268 G>A maps to NM_152592.3 S685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:95912269 G>A maps to NM_152592.3 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:95923555 C>T maps to NM_152592.3 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr14:95932342 G>A maps to NM_152592.3 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:95921883 G>A maps to NM_152592.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:95932531 G>A maps to NM_152592.3 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr14:65035144 G>A maps to NM_172365.1 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:65032074 G>A maps to NM_172365.1 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr14:65054820 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr14:65053937 G>A maps to NM_172365.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:65053925 C>T maps to NM_172365.1 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr14:100795124 G>A maps to NM_207117.2 Q130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:100795882 G>A maps to NM_207117.2 K276K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:100793622 C>T maps to NM_207117.2 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr14:100795882 G>A maps to NM_207117.2 K276K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr14:100795310 C>T maps to NM_207117.2 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr14:103566801 C>T maps to NM_001077594.1 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr14:103573826 A>T maps to NM_001077594.1 K550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr14:103566813 C>T maps to NM_001077594.1 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr14:103568548 G>A maps to NM_001077594.1 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr14:103574809 C>T maps to NM_001077594.1 I644I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr14:103574810 C>T maps to NM_001077594.1 Q645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr14:103574819 C>T maps to NM_001077594.1 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:103566712 C>T maps to NM_001077594.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:103566795 C>T maps to NM_001077594.1 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:103568560 C>T maps to NM_001077594.1 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr14:103566801 C>T maps to NM_001077594.1 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr14:105960204 C>T maps to ENST00000392523 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr14:23468223 G>A maps to NM_021944.2 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:75195109 C>A maps to NM_020447.3 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr15:24922084 C>T maps to NM_018958.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr15:24922006 G>A maps to NM_018958.2 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr15:24922216 C>T maps to NM_018958.2 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr15:24921468 G>A maps to NM_018958.2 W152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr15:24922597 C>T maps to NM_018958.2 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr15:24923710 C>T maps to NM_018958.2 S899S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr15:24921892 G>A maps to NM_018958.2 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr15:24921997 G>A maps to NM_018958.2 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr15:24921352 C>T maps to NM_018958.2 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:24921346 C>T maps to NM_018958.2 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:24922327 C>T maps to NM_018958.2 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr15:24924403 G>A maps to NM_018958.2 E1130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:24923761 G>A maps to NM_018958.2 L916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:24922117 C>T maps to NM_018958.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:24922624 C>T maps to NM_018958.2 S537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr15:24921295 C>T maps to NM_018958.2 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr15:24924371 C>T maps to NM_018958.2 Q1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr15:24923206 G>A maps to NM_018958.2 G731G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:24921161 C>T maps to NM_018958.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:24923014 C>T maps to NM_018958.2 F667F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr15:24922822 C>T maps to NM_018958.2 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:24922678 C>T maps to NM_018958.2 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:24921298 G>A maps to NM_018958.2 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr15:24921412 G>A maps to NM_018958.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr15:24922091 C>T maps to NM_018958.2 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr15:24921148 C>T maps to NM_018958.2 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr15:24921997 G>A maps to NM_018958.2 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr15:24921454 G>A maps to NM_018958.2 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr15:24922055 C>T maps to NM_018958.2 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:24922291 C>T maps to NM_018958.2 I426I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:24923206 G>A maps to NM_018958.2 G731G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr15:24923947 G>A maps to NM_018958.2 K978K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:24921998 A>T maps to NM_018958.2 K329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr15:24922024 G>A maps to NM_018958.2 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr15:24921403 A>C maps to NM_018958.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:24921322 G>A maps to NM_018958.2 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr15:24924034 G>A maps to NM_018958.2 V1007V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr15:24924145 G>A maps to NM_018958.2 G1044G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:24922780 C>T maps to NM_018958.2 F589F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr15:24921389 C>T maps to NM_018958.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr15:24921454 G>A maps to NM_018958.2 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr15:24921835 G>A maps to NM_018958.2 Q274Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr15:24922387 C>T maps to NM_018958.2 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr15:24924008 G>T maps to NM_018958.2 G999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr15:24922387 C>T maps to NM_018958.2 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr15:24921208 C>T maps to NM_018958.2 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr15:24921997 G>A maps to NM_018958.2 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr15:24923341 C>T maps to NM_018958.2 A776A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:24921208 C>T maps to NM_018958.2 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:24921214 C>T maps to NM_018958.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:24921235 C>T maps to NM_018958.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:24921361 C>T maps to NM_018958.2 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:24921424 C>T maps to NM_018958.2 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:24922291 C>T maps to NM_018958.2 I426I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:24922360 A>G maps to NM_018958.2 K449K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:24922678 C>T maps to NM_018958.2 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:24922861 G>A maps to NM_018958.2 K616K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:24923059 G>A maps to NM_018958.2 V682V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:24924371 C>T maps to NM_018958.2 Q1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:24923614 C>T maps to NM_018958.2 A867A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:24921257 C>T maps to NM_018958.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr15:24924169 C>T maps to NM_018958.2 F1052F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U9-06A-11D-A32N-08 chr15:24922990 T>G maps to NM_018958.2 A659A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr15:40675131 G>A maps to NM_033286.3 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr15:40675131 G>A maps to NM_033286.3 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:40684199 C>A maps to NM_033286.3 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr15:40675138 C>T maps to NM_033286.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr15:81426720 G>A maps to ENST00000458088 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:81427636 G>A maps to ENST00000458088 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr15:76452493 C>T maps to NM_152335.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr15:76430210 C>T maps to NM_152335.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:76430137 G>A maps to NM_152335.2 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr15:76430110 C>T maps to NM_152335.2 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr15:76494549 G>A maps to NM_152335.2 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:93043628 G>A maps to NM_153040.2 *179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr15:49860461 G>A maps to NM_152647.2 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr15:49800545 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:49659778 C>T maps to NM_152647.2 E379E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:49869030 G>A maps to NM_152647.2 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr15:49663591 G>A maps to NM_152647.2 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr15:49867219 G>A maps to NM_152647.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:49663591 G>A maps to NM_152647.2 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:90447117 G>A maps to ENST00000398333 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:90446516 G>A maps to ENST00000398333 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:90451590 G>A maps to ENST00000398333 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr15:75499696 C>T maps to NM_015492.4 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr15:75498826 G>C maps to NM_015492.4 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:75498754 C>T maps to NM_015492.4 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr15:83680266 C>T maps to NM_144597.2 K31K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr15:37100596 C>T maps to NM_001130010.1 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr15:90168916 C>T maps to NM_152259.3 D1792D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr15:90144982 C>T maps to NM_152259.3 I781I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:90128991 C>T maps to NM_152259.3 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr15:90118963 C>T maps to NM_152259.3 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:90152079 C>T maps to NM_152259.3 S923S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr15:90170218 G>T maps to NM_152259.3 E1879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr15:90137729 G>A maps to NM_152259.3 Q542Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:90129102 C>T maps to NM_152259.3 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:45270717 C>T maps to NM_152448.1 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr15:45270687 T>G maps to NM_152448.1 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:45248980 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:45249109 G>A maps to NM_152448.1 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr15:65890677 G>A maps to ENST00000420799 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr15:65890673 T>A maps to ENST00000420799 K281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr15:65883975 G>A maps to ENST00000420799 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr15:65892153 G>A maps to ENST00000420799 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr15:45723005 C>T maps to NM_197955.1 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:45724269 C>T maps to NM_197955.1 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr15:40632144 G>A maps to NM_207380.2 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr15:40629625 C>T maps to NM_207380.2 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:38990406 G>A maps to NM_207444.2 W67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr15:39544530 C>T maps to NM_207445.2 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:39544721 G>A maps to NM_207445.2 W129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr15:34649343 C>T maps to ENST00000438749 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr15:34649448 C>T maps to ENST00000438749 S1070S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr15:34640674 C>T maps to ENST00000438749 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:34648431 G>A maps to ENST00000438749 R731R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr15:34648548 A>G maps to ENST00000438749 V770V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:34640840 C>T maps to ENST00000438749 Q248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:34647954 G>A maps to ENST00000438749 G572G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:34649427 T>C maps to ENST00000438749 G1063G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr15:34640773 C>T maps to ENST00000438749 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr15:34642949 G>A maps to ENST00000438749 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:90784214 C>T maps to NM_001013657.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr15:90784904 C>T maps to NM_001013657.2 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:90784904 C>T maps to NM_001013657.2 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:74032632 G>A maps to NM_001039614.1 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr15:73852091 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr15:44093370 A>G maps to NM_016400.3 K76K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr16:615118 C>T maps to ENST00000293874 Q510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr16:613647 C>T maps to ENST00000293874 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr16:1400943 G>A maps to NM_001001410.2 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:1400073 G>A maps to NM_001001410.2 Q230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:1400074 G>A maps to NM_001001410.2 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr16:1400958 G>A maps to NM_001001410.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr16:15609186 G>A maps to NM_033201.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:15661857 C>T maps to NM_033201.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr16:15677011 G>A did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr16:15677012 G>A maps to NM_033201.2 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:15528611 G>A maps to NM_033201.2 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr16:15675128 C>T maps to NM_033201.2 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr16:81094906 G>A maps to NM_152337.2 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:81095011 G>A maps to NM_152337.2 D314D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:81095311 C>T maps to NM_152337.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:81097434 A>C maps to NM_152337.2 Y42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr16:81095626 G>A maps to NM_152337.2 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr16:67698987 G>T maps to NM_032140.1 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:67699045 C>T maps to NM_032140.1 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:67697081 G>A maps to NM_032140.1 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr16:4564077 C>T maps to ENST00000359075 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:58043977 C>T maps to NM_024598.3 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:58044007 C>T maps to NM_024598.3 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:31508265 G>A maps to NM_022744.2 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr16:31510691 G>A maps to NM_022744.2 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr16:2512221 C>T maps to NM_025108.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:2514158 C>T maps to NM_025108.2 Q362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:2511003 A>G maps to NM_025108.2 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:2512233 G>A maps to NM_025108.2 Q248Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:2514085 C>T maps to NM_025108.2 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr16:19628036 G>A maps to NM_020314.5 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr16:19711758 G>A maps to NM_020314.5 T1040T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:19648959 C>T maps to NM_020314.5 F649F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:19641093 C>A maps to NM_020314.5 Y591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:19592972 C>T maps to NM_020314.5 Q302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr16:19580813 C>T maps to NM_020314.5 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr16:19628024 C>T maps to NM_020314.5 V462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr16:19628025 C>T maps to NM_020314.5 Q463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:19580864 C>T maps to NM_020314.5 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:19644484 C>T maps to NM_020314.5 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:19641138 C>T maps to NM_020314.5 F606F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr16:8729066 C>T maps to NM_024109.2 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr16:8732969 C>T maps to NM_024109.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr16:89777063 G>A maps to NM_004913.2 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr16:89777093 G>A maps to NM_004913.2 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr16:89777110 C>A maps to NM_004913.2 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr16:67168100 C>T maps to NM_025187.3 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:67168356 C>T maps to NM_025187.3 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr16:4790200 G>A maps to NM_139170.2 Q108Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:4787832 C>T maps to NM_139170.2 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr16:4790200 G>A maps to NM_139170.2 Q108Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:9196898 A>G maps to NM_014117.2 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:9197093 C>T maps to NM_014117.2 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr16:11444532 C>T maps to NM_152308.1 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:49412445 G>A maps to NM_144602.2 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr16:49407909 G>A maps to NM_144602.2 W20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:49407897 G>A maps to NM_144602.2 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:49411640 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:49411661 G>C maps to NM_144602.2 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:49433080 C>T maps to NM_144602.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr16:19725553 T>C maps to NM_001012991.2 K268K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:19725859 G>A maps to NM_001012991.2 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:19718264 C>T maps to NM_001012991.2 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr16:19726324 C>T maps to NM_001012991.2 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr16:5106111 G>A maps to ENST00000350219 N273N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:5115948 C>T maps to ENST00000350219 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:5110324 C>T maps to ENST00000350219 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:5115761 G>A maps to ENST00000350219 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr16:5108553 C>T maps to ENST00000350219 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:1476274 C>T maps to NM_001010878.1 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr16:1476322 G>A maps to NM_001010878.1 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:30035348 C>T maps to NM_001109660.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:30035535 G>A maps to NM_001109660.1 Q129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr16:30035186 C>T maps to NM_001109660.1 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:30035189 C>T maps to NM_001109660.1 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr16:30768805 C>T maps to NM_001014979.2 K329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr17:80361887 G>T maps to NM_175902.4 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:80373319 G>A maps to NM_175902.4 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:80373337 G>A maps to NM_175902.4 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:80373277 G>A maps to NM_175902.4 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr17:80352402 C>T maps to NM_175902.4 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr17:32906107 G>A maps to NM_207454.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:42745072 G>A maps to NM_001145080.2 G598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr17:42744142 C>T maps to NM_001145080.2 Y288Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:72950431 G>A maps to NM_030630.2 I555I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:72952019 C>T maps to NM_030630.2 V501V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:72954852 G>A maps to NM_030630.2 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr17:72954514 C>T maps to NM_030630.2 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:72954843 G>A maps to NM_030630.2 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr17:72956159 C>T maps to NM_030630.2 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:72952046 G>A maps to NM_030630.2 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr17:72954843 G>A maps to NM_030630.2 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr17:72959142 G>A maps to NM_030630.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:17965253 C>A maps to NM_024052.4 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr17:17957493 C>T maps to NM_024052.4 H184H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr17:29231455 C>T maps to NM_024683.3 K41K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr17:29226321 G>A maps to NM_024683.3 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr17:43332771 G>A maps to NM_152343.2 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr17:56619993 G>A maps to NM_001038704.1 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:56619999 A>C maps to NM_001038704.1 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:56621403 A>C maps to NM_001038704.1 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:56620266 C>T maps to NM_001038704.1 W427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:10608566 G>A maps to NM_020233.4 W108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:42232018 C>T maps to NM_024032.3 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:42226382 C>T maps to NM_024032.3 I404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:42226383 C>T maps to NM_024032.3 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:42230108 C>T maps to NM_024032.3 F471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr17:42225821 C>T maps to NM_024032.3 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr17:79205474 G>A maps to NM_144679.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:79210863 G>A maps to NM_144679.2 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr17:79205747 G>A maps to NM_144679.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr17:79202911 C>T maps to NM_144679.2 W465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr17:45479562 T>C maps to NM_152347.4 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:45451970 G>A maps to NM_152347.4 K337K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:45452297 T>A maps to NM_152347.4 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr17:45419398 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:45412650 C>T maps to NM_152347.4 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:45473266 G>A maps to NM_152347.4 W623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:8092540 G>A maps to NM_017622.2 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:62462586 C>T maps to NM_001085423.1 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:34183755 C>T maps to NM_152781.2 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr17:34192238 C>T maps to NM_152781.2 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr17:54893237 A>C maps to NM_001085430.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr17:8132658 G>A maps to NM_025099.5 L1039L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr17:8141407 G>A maps to NM_025099.5 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr17:8141745 G>A maps to NM_025099.5 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr17:8138477 G>A maps to NM_025099.5 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:8139498 C>T maps to NM_025099.5 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr17:8135758 G>A maps to NM_025099.5 I660I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:8146430 G>A maps to NM_025099.5 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr17:79514094 G>A maps to NM_025161.5 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr17:79517322 C>T maps to NM_025161.5 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:79512819 G>A maps to NM_025161.5 I754I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:79517370 G>A maps to NM_025161.5 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:79517433 G>A maps to NM_025161.5 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr17:79517271 A>G did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:79517358 C>G maps to NM_025161.5 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:79517940 G>A maps to NM_025161.5 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr17:57287819 C>T maps to NM_018149.6 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:57288416 C>T maps to NM_018149.6 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:57288608 C>T maps to NM_018149.6 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:57287426 G>A maps to NM_018149.6 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:57290127 C>T maps to NM_018149.6 I648I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:57288905 C>T maps to NM_018149.6 N498N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:57292290 C>T maps to NM_018149.6 F968F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:57288299 C>T maps to NM_018149.6 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:57288584 C>G maps to NM_018149.6 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr17:7330089 C>T maps to NM_175734.4 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr17:7329630 C>T maps to NM_175734.4 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:7329868 G>T maps to NM_175734.4 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr17:7329696 C>T maps to NM_175734.4 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:7330551 G>A maps to NM_175734.4 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr17:7330296 C>T maps to NM_175734.4 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:7329880 C>T maps to NM_175734.4 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr17:7329714 C>T maps to NM_175734.4 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:30658841 G>A maps to NM_022344.2 A377A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A185-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:72588509 A>T maps to NM_152460.2 K109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:72588715 G>A maps to NM_152460.2 K177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:72588685 G>A maps to NM_152460.2 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:72588856 C>T maps to NM_152460.2 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr17:35745680 C>A maps to NM_173625.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr17:35743031 G>A maps to NM_173625.3 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:30179857 A>G maps to NM_018405.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:71232070 A>G maps to NM_017941.4 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:71232941 C>T maps to NM_017941.4 Q441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr17:7156240 G>T maps to NM_203414.1 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:79632341 G>A maps to NM_001039842.1 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:79633586 G>A maps to NM_001039842.1 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr17:36997591 C>T maps to NM_001080465.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr18:13621233 G>A maps to NM_181481.3 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr18:13645127 C>A maps to NM_181481.3 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr18:13387739 C>T maps to NM_181481.3 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr18:13681926 G>A maps to NM_152352.3 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr18:43842987 G>A maps to NM_145055.3 W373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr18:43820094 G>A maps to NM_145055.3 Q280Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:43796274 C>T maps to NM_145055.3 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:43796275 C>T maps to NM_145055.3 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:43796349 C>T maps to NM_145055.3 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr18:52265111 G>A maps to NM_173629.1 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr18:52262276 G>A maps to NM_173629.1 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:52265099 C>T maps to NM_173629.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr18:52265187 C>T maps to NM_173629.1 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr18:52258482 G>A maps to NM_173629.1 W16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr18:52262288 C>T maps to NM_173629.1 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr18:52265078 G>A maps to NM_173629.1 W112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr18:52258569 G>C maps to NM_173629.1 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr18:52262288 C>T maps to NM_173629.1 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr18:30873194 C>T maps to NM_001105528.1 K368K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr18:30950151 C>T maps to NM_001105528.1 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr18:30992028 G>A maps to NM_001105528.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr18:30913284 A>G maps to NM_001105528.1 H244H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr18:30926193 G>A maps to NM_001105528.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr18:30806792 G>A maps to NM_001105528.1 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr18:30873200 C>T maps to NM_001105528.1 E366E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr18:30672826 C>T maps to NM_001105528.1 E762E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:30803093 G>A maps to NM_001105528.1 T636T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:30926322 G>A maps to NM_001105528.1 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr18:30913172 G>A maps to NM_001105528.1 Q282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:30928857 C>T maps to NM_001105528.1 K151K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr18:20936595 G>A maps to NM_032933.4 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr18:20889666 G>A maps to NM_032933.4 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr18:51889213 C>T maps to ENST00000382911 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr18:51888049 C>T maps to ENST00000382911 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:51904573 C>T maps to ENST00000382911 D520D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr18:71816126 C>T maps to NM_014177.2 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr18:71816058 C>T maps to NM_014177.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr18:73130763 T>C maps to NM_001037331.2 K79K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr18:73130744 G>A maps to NM_001037331.2 R86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:73130766 C>T maps to NM_001037331.2 W78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr18:21110197 T>A maps to NM_013326.3 C535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr18:21109177 C>T maps to NM_013326.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:58472861 C>T maps to NM_152474.4 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr19:58485502 A>G maps to NM_152474.4 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr19:757878 G>A maps to NM_173481.2 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr19:763511 C>T maps to NM_173481.2 A654A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:758447 G>A maps to NM_173481.2 W501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr19:757080 G>A maps to NM_173481.2 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:763502 C>T maps to NM_173481.2 V651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:761644 G>A maps to NM_173481.2 S644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:758706 G>A maps to NM_173481.2 R587R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr19:758343 C>T maps to NM_173481.2 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:757302 G>A maps to NM_173481.2 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr19:758337 G>A maps to NM_173481.2 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:899632 G>A maps to NM_138774.3 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr19:900087 G>A maps to NM_138774.3 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr19:1230930 T>C maps to NM_152769.2 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr19:3542862 G>A maps to NM_021731.2 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:3547938 C>T maps to NM_021731.2 E248E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:3557245 G>A maps to NM_021731.2 A52A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A29X-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:3623988 G>A maps to NM_021231.1 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:3620797 G>A maps to NM_021231.1 A215A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A2MC-06A-12D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:2278609 C>T maps to NM_198532.2 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr19:2276360 C>T maps to NM_198532.2 W247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:11486271 C>T maps to NM_175871.3 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr19:50657867 G>A maps to NM_152358.2 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:7573213 G>A maps to NM_198534.2 E472E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:7566163 C>T maps to NM_198534.2 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr19:7570314 G>A maps to NM_198534.2 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr19:7573219 C>T maps to NM_198534.2 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr19:18679425 G>A maps to NM_024069.3 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:18672910 C>T maps to NM_024069.3 I15I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr19:55670813 G>A maps to ENST00000301249 Y481Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr19:55671283 G>A maps to ENST00000301249 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:55670923 C>T maps to ENST00000301249 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:55677911 G>A maps to ENST00000301249 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:55670968 G>A maps to ENST00000301249 V457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:41250077 G>A maps to NM_198476.3 Q181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr19:36255777 C>T maps to NM_001039887.2 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr19:36256039 C>T maps to NM_001039887.2 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr19:36256066 C>T maps to NM_001039887.2 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr19:36250880 C>T maps to NM_001039887.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:36255777 C>T maps to NM_001039887.2 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:14006279 C>T maps to ENST00000454313 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:14001202 G>A maps to ENST00000454313 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:14000018 G>A maps to ENST00000454313 F550F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:14000669 G>A maps to ENST00000454313 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:13993680 G>A maps to ENST00000454313 P647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:14000426 G>A maps to ENST00000454313 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:14001206 G>A maps to ENST00000454313 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:14001202 G>A maps to ENST00000454313 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:7742583 G>A maps to NM_174918.2 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:7743113 C>T maps to NM_174918.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr19:1013312 C>A maps to NM_001033026.1 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:1011890 G>A maps to NM_001033026.1 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:1014469 G>A maps to NM_001033026.1 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:1013324 G>A maps to NM_001033026.1 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr19:44242348 G>A maps to NM_019108.2 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:44254779 C>T maps to NM_019108.2 E38E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:17387375 C>T maps to NM_014173.2 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:17382413 C>T maps to NM_014173.2 C98C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:50984007 C>T maps to ENST00000376920 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:50983405 C>T maps to ENST00000376920 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:50984164 G>A maps to ENST00000376920 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:5679656 G>A maps to NM_205767.1 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:51768742 G>A maps to NM_173635.1 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:51770776 G>A maps to NM_173635.1 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:51770683 G>A maps to NM_173635.1 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:51768856 G>A maps to NM_173635.1 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:51770668 G>A maps to NM_173635.1 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:51770653 G>A maps to NM_173635.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:51769073 C>T maps to NM_173635.1 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:51769091 G>C maps to NM_173635.1 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:51770656 G>A maps to NM_173635.1 K147K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr2:68274370 G>C maps to ENST00000407324 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:7278222 C>A maps to NM_020156.3 Y186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:7278204 G>A maps to NM_020156.3 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr7:7283231 C>T maps to NM_020156.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:119760873 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:119760552 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:119760716 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr23:119760910 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:22965755 C>T maps to NM_015991.2 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:22965711 C>T maps to NM_015991.2 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:22987851 C>T maps to NM_000491.3 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:22987482 C>T maps to NM_000491.3 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:22987515 C>T maps to NM_000491.3 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:22987383 C>T maps to NM_000491.3 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:22987443 C>T maps to NM_000491.3 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr1:22973792 G>A maps to NM_172369.3 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:22974023 C>T maps to NM_172369.3 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr1:22973879 C>G maps to NM_172369.3 Y114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr1:22973792 G>A maps to NM_172369.3 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:119915314 G>A maps to NM_182528.3 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr2:119915314 G>A maps to NM_182528.3 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:16562763 G>A maps to NM_001010908.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr12:49726989 G>A maps to NM_001008223.1 D188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr17:77040133 C>T maps to ENST00000392445 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr17:77043689 G>A maps to ENST00000392445 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:77043938 G>A maps to ENST00000392445 K215K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:77043683 G>A maps to ENST00000392445 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr17:77043824 C>T maps to ENST00000392445 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr5:159776678 C>T maps to NM_031908.4 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr5:159776483 G>A maps to NM_031908.4 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:159776621 G>A maps to NM_031908.4 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr5:159776540 C>T maps to NM_031908.4 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:159776450 G>A maps to NM_031908.4 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr5:159782012 G>A maps to NM_031908.4 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr5:34020708 G>A maps to NM_181435.4 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:34043182 G>A maps to NM_181435.4 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:34033476 G>A maps to NM_181435.4 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:47612179 G>A maps to NM_031909.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr22:37581423 G>A maps to NM_182486.1 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr22:37581437 G>A maps to NM_182486.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:37578761 G>A maps to NM_182486.1 D101D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:15443837 G>A maps to NM_001135170.1 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:15444101 G>A maps to NM_001135170.1 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr4:15444215 C>T maps to NM_001135170.1 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr4:15437501 C>T maps to NM_001135170.1 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr4:15444107 C>T maps to NM_001135170.1 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr4:15444101 G>A maps to NM_001135170.1 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:15444101 G>A maps to NM_001135170.1 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr16:1144727 G>A maps to NM_207419.3 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr16:1144727 G>A maps to NM_207419.3 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:1144760 C>T maps to NM_207419.3 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr13:24895884 C>T maps to NM_178540.3 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr13:24895822 G>T maps to NM_178540.3 G307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr13:24895620 G>A maps to NM_178540.3 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr13:24895677 C>T maps to NM_178540.3 F258F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D3-A2JF-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr13:24465535 C>T maps to NM_001007537.1 G298G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D3-A5GO-06A-12D-A27K-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr13:24466078 C>T maps to NM_001007537.1 E117E. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A20C-06A-11D-A196-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-FW-A3R5-06A-11D-A23B-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:24465964 G>A maps to NM_001135816.1 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr12:7242712 G>A maps to ENST00000290575 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:7188162 C>T maps to ENST00000290575 G611G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr12:7242712 G>A maps to ENST00000290575 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:7187928 G>A maps to ENST00000290575 S689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:7244122 C>T maps to ENST00000290575 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr12:7187919 G>T maps to ENST00000290575 I692I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:7188459 G>A maps to ENST00000290575 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:7242034 G>A maps to ENST00000290575 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:7249508 C>T maps to NM_016546.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr12:7249397 C>A maps to NM_016546.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:7249424 G>A maps to NM_016546.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:7254674 G>A maps to NM_016546.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:7252511 G>A maps to NM_016546.2 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr12:7169847 C>T maps to NM_001734.3 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:7170303 G>A maps to NM_001734.3 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:7169928 C>T maps to NM_001734.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:7173834 T>G maps to NM_001734.3 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:7173251 G>A maps to NM_001734.3 W283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:7172536 C>T maps to NM_001734.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:7171667 C>T maps to NM_001734.3 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:7172503 C>T maps to NM_001734.3 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:7175787 C>T maps to NM_001734.3 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr12:7171655 C>T maps to NM_001734.3 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:7173933 G>A maps to NM_001734.3 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:7170371 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:7173260 C>T maps to NM_001734.3 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr12:7177234 C>T maps to NM_001734.3 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:7170351 T>A maps to NM_001734.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:244756720 G>A maps to NM_001130957.1 S738S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:244627249 A>T maps to NM_001130957.1 R36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:244724442 C>T maps to NM_001130957.1 F501F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:244756720 G>A maps to NM_001130957.1 S738S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:244798793 C>T maps to NM_001130957.1 F884F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr1:111490766 C>T maps to NM_018372.3 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:111494200 A>T maps to NM_018372.3 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:111492640 A>G maps to NM_018372.3 D567D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:111490994 T>A maps to NM_018372.3 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr1:111493992 G>A maps to NM_018372.3 Q505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:111494238 G>A maps to NM_018372.3 Q423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr1:111490691 T>A maps to NM_018372.3 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr1:111494239 G>A maps to NM_018372.3 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:111490703 G>A maps to NM_018372.3 F729F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr1:172425559 G>A maps to NM_139240.3 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:172425577 C>T maps to NM_139240.3 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:172417668 A>T maps to NM_139240.3 K66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr1:172434463 C>T maps to NM_139240.3 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:172425562 G>A maps to NM_139240.3 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q3-06A-11D-A196-08 chr1:200869293 T>A maps to NM_018265.2 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr1:200877984 C>T maps to NM_018265.2 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr1:200880952 C>T maps to NM_018265.2 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:200880598 G>A maps to NM_018265.2 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:200869302 G>A maps to NM_018265.2 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:200878056 G>A maps to NM_018265.2 W343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:200867495 C>T maps to NM_018265.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:200869305 C>T maps to NM_018265.2 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:200877897 C>T maps to NM_018265.2 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr1:200880916 C>T maps to NM_018265.2 F517F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:200880877 C>T maps to NM_018265.2 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr1:210016906 C>T maps to NM_014388.6 F631F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:210014264 T>C maps to NM_014388.6 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr1:38155519 C>T maps to NM_017850.1 Q11Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:38155297 C>T maps to NM_017850.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr1:162343955 C>T maps to NM_182581.3 W223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:162344317 G>A maps to NM_182581.3 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:162344299 C>T maps to NM_182581.3 E108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:162345158 G>A maps to NM_182581.3 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr1:169798452 G>T maps to NM_018186.2 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:169772407 C>T maps to NM_018186.2 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr1:169796269 A>G maps to NM_018186.2 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:36785871 C>T maps to NM_001162530.1 P536P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:169391296 C>T maps to ENST00000367806 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:169388304 G>A maps to ENST00000367806 V387V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:169390656 G>A maps to ENST00000367806 R338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:169388370 C>T maps to ENST00000367806 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:169388370 C>T maps to ENST00000367806 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:220870012 C>T maps to NM_024709.4 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:220869964 G>A maps to NM_024709.4 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:207195308 C>T maps to NM_023938.5 K600K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:207195953 G>A maps to NM_023938.5 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:207196694 G>A maps to NM_023938.5 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr1:207196811 C>T maps to NM_023938.5 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z4-06A-11D-A197-08 chr1:207195688 G>A maps to NM_023938.5 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:207196052 C>T maps to NM_023938.5 E352E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:207196514 G>A maps to NM_023938.5 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr1:53684128 G>A maps to NM_017887.1 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:231475562 C>T maps to NM_032018.4 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:179494552 C>T maps to NM_144696.4 Q861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr1:179460759 C>T maps to NM_144696.4 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:179354458 C>T maps to NM_144696.4 D276D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:179347891 G>A maps to NM_144696.4 K165K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:179497463 A>G maps to NM_144696.4 Q871Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr1:179503927 T>C maps to NM_144696.4 H954H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr1:179354410 C>T maps to NM_144696.4 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr1:179363151 C>T maps to NM_144696.4 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:179504006 C>T maps to NM_144696.4 Q981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr1:11008793 G>A maps to NM_001170754.1 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr1:11008295 G>A maps to NM_001170754.1 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr1:11008738 C>A maps to NM_001170754.1 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr1:11008739 C>T maps to NM_001170754.1 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:11008778 C>T maps to NM_001170754.1 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:11009731 C>T maps to NM_001170754.1 Q413Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:11015048 G>A maps to NM_001170754.1 Q325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:11008427 G>A maps to NM_001170754.1 F588F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:11008507 G>A maps to NM_001170754.1 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:11007823 G>A maps to NM_001170754.1 Q790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:11007824 G>A maps to NM_001170754.1 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr1:11017746 C>A maps to NM_001170754.1 G207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:170961316 G>A maps to NM_001163629.1 Q347Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:170959003 G>A maps to NM_001163629.1 K296K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:170961427 G>A maps to NM_001163629.1 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:170967539 G>A maps to NM_025063.2 *574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:170916684 C>T maps to NM_001163629.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:170941013 G>A maps to NM_001163629.1 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:170967483 C>T maps to NM_025063.2 F555F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:170961427 G>A maps to NM_001163629.1 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:170931074 G>A maps to NM_001163629.1 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr1:170955809 C>T maps to NM_001163629.1 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:170961409 G>A maps to NM_001163629.1 E378E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:170941019 G>A maps to NM_001163629.1 Q204Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr1:170967453 C>T maps to NM_025063.2 F545F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:170964645 G>A maps to NM_001163629.1 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:170965662 C>T maps to NM_001163629.1 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:170964594 C>T maps to NM_001163629.1 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:24932123 G>A maps to NM_001010980.4 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:24932236 G>A maps to NM_001010980.4 *103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:231362768 C>A maps to ENST00000421623 G186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr1:231362502 C>T maps to ENST00000421623 K225K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr1:182873316 G>A maps to ENST00000287709 Q598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:182908375 C>T maps to ENST00000287709 W406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr1:182898871 G>A maps to ENST00000287709 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr1:182909648 T>G maps to ENST00000287709 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr1:67581047 T>C maps to NM_001013674.1 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:67559155 G>A maps to NM_001013674.1 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr1:16721553 C>T maps to NM_001114600.1 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr1:247737635 T>C maps to NM_145278.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr1:247737617 G>A maps to NM_145278.3 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:247737515 C>T maps to NM_145278.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:247737452 G>A maps to NM_145278.3 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:247712507 C>T maps to NM_145278.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:169761909 G>A maps to NM_033418.1 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:169762311 G>A maps to NM_033418.1 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:12815747 G>A maps to NM_152290.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:12815747 G>A maps to NM_152290.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:12806419 G>A maps to NM_152290.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr1:1019745 C>T maps to ENST00000448924 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:116663651 C>T maps to NM_152367.2 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:116670890 C>T maps to NM_152367.2 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:116670177 G>A maps to NM_152367.2 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:116666736 C>T maps to NM_152367.2 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:116675958 G>A maps to NM_152367.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:116666838 G>A maps to NM_152367.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:116670240 C>T maps to NM_152367.2 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr1:53153450 G>A maps to NM_023077.2 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:53153411 G>A maps to NM_023077.2 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:57258436 G>A maps to NM_001004303.4 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr1:57258314 G>A maps to NM_001004303.4 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:57185696 G>A maps to NM_001004303.4 F721F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr1:57185990 C>T maps to NM_001004303.4 E662E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:57257936 C>T maps to NM_001004303.4 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:57257915 T>C maps to NM_001004303.4 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:57221594 C>T maps to NM_001004303.4 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:57257888 G>A maps to NM_001004303.4 H199H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:57192232 C>T maps to NM_001004303.4 W606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:57257936 C>T maps to NM_001004303.4 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr1:57216786 G>A maps to NM_001004303.4 A439A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:57216842 G>A maps to NM_001004303.4 Q421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:57257936 C>T maps to NM_001004303.4 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:57185365 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:57254688 G>A maps to NM_001004303.4 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:57257936 C>T maps to NM_001004303.4 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:57257987 G>A maps to NM_001004303.4 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:57254703 G>A maps to NM_001004303.4 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:57257765 C>T maps to NM_001004303.4 Q240Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:57258329 C>T maps to NM_001004303.4 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:27277920 C>T maps to NM_152365.2 E317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:27278628 C>T maps to NM_152365.2 W81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:27277247 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:27278511 C>T maps to NM_152365.2 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:27278865 G>A maps to NM_152365.2 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr1:27278364 G>A maps to NM_152365.2 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr1:75038210 C>T maps to NM_001002912.4 R1061R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:75037856 C>T maps to NM_001002912.4 G1179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:75038498 C>T maps to NM_001002912.4 K965K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr1:75037409 C>T maps to NM_001002912.4 K1328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr1:75039115 G>A maps to NM_001002912.4 Q760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr1:75072543 C>T maps to NM_001002912.4 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:75072543 C>T maps to NM_001002912.4 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr1:75038180 C>T maps to NM_001002912.4 R1071R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr1:75072543 C>T maps to NM_001002912.4 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:75036899 T>C maps to NM_001002912.4 P1498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr1:75072543 C>T maps to NM_001002912.4 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:75038906 C>T maps to NM_001002912.4 R829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:75037328 C>T maps to NM_001002912.4 E1355E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr1:75038357 G>A maps to NM_001002912.4 S1012S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:75036971 G>A maps to NM_001002912.4 F1474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:75065430 C>T maps to NM_001002912.4 V558V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:75038378 C>T maps to NM_001002912.4 R1005R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:75072534 C>T maps to NM_001002912.4 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:75078434 G>A maps to NM_001002912.4 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:75039158 G>A maps to NM_001002912.4 F745F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:75037535 C>T maps to NM_001002912.4 R1286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:75078425 C>T maps to NM_001002912.4 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:75037469 C>T maps to NM_001002912.4 A1308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:75037505 C>T maps to NM_001002912.4 E1296E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:75038255 C>T maps to NM_001002912.4 R1046R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:75038411 C>T maps to NM_001002912.4 L994L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:75038900 G>A maps to NM_001002912.4 I831I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr1:75038843 C>T maps to NM_001002912.4 R850R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:75078434 G>A maps to NM_001002912.4 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:75037163 C>T maps to NM_001002912.4 R1410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr1:75107095 A>G maps to NM_001002912.4 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:75038627 C>T maps to NM_001002912.4 L922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr1:75055423 C>T maps to NM_001002912.4 G689G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:75086532 C>T maps to NM_001002912.4 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr1:75078371 G>A maps to NM_001002912.4 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr1:75097585 C>T maps to NM_001002912.4 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:75114935 C>T maps to NM_001002912.4 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:75038615 C>T maps to NM_001002912.4 A926A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:75086496 G>A maps to NM_001002912.4 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr1:75101969 G>A maps to NM_001002912.4 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:75036995 C>T maps to NM_001002912.4 Q1466Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:75036941 C>T maps to NM_001002912.4 R1484R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:75037469 C>T maps to NM_001002912.4 A1308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:75037934 C>T maps to NM_001002912.4 V1153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:75038255 C>T maps to NM_001002912.4 R1046R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:75038663 G>A maps to NM_001002912.4 A910A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:75038702 C>T maps to NM_001002912.4 Q897Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:75055528 C>T maps to NM_001002912.4 V654V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:75108722 G>A maps to NM_001002912.4 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:75108734 C>T maps to NM_001002912.4 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:75086532 C>T maps to NM_001002912.4 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:55118811 G>A maps to ENST00000454855 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:55148382 C>T maps to ENST00000454855 V841V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:55119555 C>T maps to ENST00000454855 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:55166874 G>A maps to ENST00000454855 G1084G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr1:55118646 G>A maps to ENST00000454855 K16K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:55167773 C>T maps to ENST00000454855 V1128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:55175712 C>T maps to ENST00000454855 S1304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:55145667 C>T maps to ENST00000454855 F806F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:55151983 G>A maps to ENST00000454855 V887V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:55119588 C>T maps to ENST00000454855 I330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr1:55172121 A>G maps to ENST00000454855 R1222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr1:55175736 G>A maps to ENST00000454855 W1312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:55166820 C>T maps to ENST00000454855 A1066A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:55152109 C>T maps to ENST00000454855 F929F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:55136553 C>T maps to ENST00000454855 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:55139792 C>T maps to ENST00000454855 I664I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:55145562 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:55145664 C>T maps to ENST00000454855 S805S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:55175706 G>A maps to ENST00000454855 Q1302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:55148451 C>T maps to ENST00000454855 S864S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:55152040 C>T maps to ENST00000454855 I906I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr1:55136210 C>T maps to ENST00000454855 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr1:55139375 C>T maps to ENST00000454855 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:55118631 C>T maps to ENST00000454855 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr1:55277522 G>A maps to NM_001110533.1 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:55272740 T>G maps to NM_001110533.1 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:55307315 A>G maps to NM_152607.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:55282695 G>A maps to NM_001110533.1 W362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:55279590 G>A maps to NM_001110533.1 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:55280654 C>T maps to NM_001110533.1 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:55280708 C>T maps to NM_001110533.1 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:55282742 C>T maps to NM_001110533.1 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:112269700 G>A maps to NM_019099.4 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:112270348 G>A maps to NM_019099.4 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:206243249 T>C maps to NM_001007544.1 E4E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr1:206239498 C>T maps to NM_001007544.1 E133E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:206241533 C>T maps to NM_001007544.1 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:206241557 G>A maps to NM_001007544.1 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:206243201 G>A maps to NM_001007544.1 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:11766525 C>T maps to NM_198545.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:11766353 C>T maps to NM_198545.3 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:46685846 C>T maps to NM_001013615.2 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:46685579 C>T maps to NM_001013615.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr1:161335339 C>T maps to NM_001013625.2 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr1:109649633 G>T maps to NM_001122961.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:109650609 C>T maps to NM_001122961.1 W32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:230979282 G>A maps to NM_032800.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:24696300 C>T maps to ENST00000374409 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:43748509 C>T maps to NM_001164829.1 Q96Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:43748569 G>A maps to NM_001164829.1 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:23697669 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:36181916 G>A maps to NM_152374.1 F2F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:162353001 G>A maps to NM_001135240.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr1:162351846 G>A maps to NM_001135240.1 K95K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr1:162351852 G>A maps to NM_001135240.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr1:213009386 C>T maps to NM_001024601.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:213009266 C>T maps to NM_001024601.2 W75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:185153438 C>T maps to NM_001105518.1 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr1:185175758 C>T maps to NM_001105518.1 I612I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:185143737 T>C maps to NM_001105518.1 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr1:185143998 C>T maps to NM_001105518.1 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:185175887 C>T maps to NM_001105518.1 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:185240488 G>T maps to NM_001105518.1 E826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr1:186375272 C>T maps to NM_017847.5 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr1:28209070 G>A maps to NM_001105556.1 E412E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:28206197 G>A maps to NM_001105556.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:178483875 C>T maps to NM_032126.4 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr1:178489984 C>T maps to NM_032126.4 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:178491475 G>A maps to NM_032126.4 E201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:150259170 C>T maps to NM_144697.2 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:150257075 C>T maps to NM_144697.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:150256267 G>A maps to NM_144697.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:150259284 C>T maps to NM_144697.2 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:150257024 C>T maps to NM_144697.2 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:150255958 G>A maps to NM_144697.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:150259113 C>T maps to NM_144697.2 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:226183063 G>A maps to NM_152608.3 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:226176045 C>A maps to NM_152608.3 E229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr1:226180686 G>A maps to NM_152608.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:226175878 G>A maps to NM_152608.3 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:226183024 G>A maps to NM_152608.3 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr1:226179047 G>A maps to NM_152608.3 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr1:151020994 G>A maps to NM_017860.3 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:233092128 T>C maps to NM_032324.1 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:222892361 C>A maps to NM_144695.2 S66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr1:222906052 C>T maps to NM_144695.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr1:109191349 G>A maps to ENST00000370031 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:109198283 T>G maps to ENST00000370031 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:109191188 C>T maps to ENST00000370031 *425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:156376943 G>A maps to ENST00000357975 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:25569091 C>T maps to NM_020317.3 W287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:16332612 G>A maps to NM_178840.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr1:223568232 C>T maps to NM_152610.2 R472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr1:223567299 C>T maps to NM_152610.2 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:223568256 G>A maps to NM_152610.2 K480K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:223568256 G>A maps to NM_152610.2 K480K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:223567443 C>T maps to NM_152610.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:223568460 G>A maps to NM_152610.2 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr1:223568217 G>A maps to NM_152610.2 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:223567888 C>T maps to NM_152610.2 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr1:223568658 C>T maps to NM_152610.2 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:223567854 G>A maps to NM_152610.2 W346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:223567677 G>A maps to NM_152610.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr1:223568019 G>A maps to NM_152610.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr1:223567299 C>T maps to NM_152610.2 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:223568220 G>A maps to NM_152610.2 K468K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:156703212 G>T maps to NM_015997.3 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr1:156702138 C>T maps to NM_015997.3 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:156703863 C>T maps to NM_015997.3 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:228353813 C>T maps to NM_001010867.2 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:228363207 C>T maps to NM_001010867.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr1:228362563 G>A maps to NM_001010867.2 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:228363072 C>T maps to NM_001010867.2 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:228362886 C>T maps to NM_001010867.2 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:209956301 A>G maps to NM_152485.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:209956582 G>A maps to NM_152485.2 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:153614877 C>T maps to NM_015607.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr1:156264704 G>A maps to NM_144580.1 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr1:156262906 G>A maps to NM_144580.1 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:156264761 G>A maps to NM_144580.1 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr1:2125232 G>A maps to ENST00000359030 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:60506692 C>T maps to NM_152377.2 Q151Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr1:60463301 G>A maps to NM_152377.2 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr1:60463302 G>A maps to NM_152377.2 Y486Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:60456401 G>A maps to NM_152377.2 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:60456473 G>A maps to NM_152377.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:60505797 G>A maps to NM_152377.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:60505798 G>A maps to NM_152377.2 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr1:60538225 G>A maps to NM_152377.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:60456422 G>A maps to NM_152377.2 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr1:60505723 G>A maps to NM_152377.2 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr1:60505759 G>A maps to NM_152377.2 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:60463380 C>T maps to NM_152377.2 V460V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:60503776 C>T maps to NM_152377.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:111889589 C>T maps to NM_181643.4 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:172525082 C>T maps to ENST00000367723 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:172544682 C>T maps to ENST00000367723 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr1:172526542 C>T maps to ENST00000367723 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:32682471 C>T maps to NM_019118.3 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:156902312 G>A maps to NM_144702.2 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:2520011 G>A maps to NM_001195736.1 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:34667733 G>A maps to NM_001134734.1 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:34663305 G>A maps to NM_001134734.1 K267K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr1:34666391 G>A maps to NM_001134734.1 K343K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:34667857 C>T maps to NM_001134734.1 Q482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr1:34663239 G>A maps to NM_001134734.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:34663233 C>T maps to NM_001134734.1 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:34667829 C>T maps to NM_001134734.1 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:34663167 G>A maps to NM_001134734.1 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:34677851 C>T maps to NM_001134734.1 F522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:34667805 G>A maps to NM_001134734.1 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:34666596 C>T maps to NM_001134734.1 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:34663233 C>T maps to NM_001134734.1 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:34663233 C>T maps to NM_001134734.1 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:34677894 C>T maps to NM_001134734.1 Q537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:34663470 C>T maps to NM_001134734.1 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:226784623 C>T maps to ENST00000366788 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:226784509 C>T maps to ENST00000366788 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr6:31912778 C>T maps to NM_000063.4 F684F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr6:31895858 C>T maps to ENST00000437789 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr6:31901647 C>T maps to ENST00000437789 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:31911086 C>A maps to ENST00000437789 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:31901495 G>A maps to ENST00000437789 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr6:31911215 G>A maps to ENST00000437789 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:31901480 G>A maps to ENST00000437789 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:31912778 C>T maps to NM_000063.4 F684F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:31896605 G>A maps to ENST00000477310 E118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:31911490 C>T maps to ENST00000437789 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr6:31903827 C>T maps to NM_000063.4 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:31911515 C>T maps to ENST00000437789 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:31895858 C>T maps to ENST00000437789 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:31907062 C>T maps to ENST00000437789 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:9496651 C>T maps to NM_012261.3 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:9510289 G>A maps to NM_012261.3 E222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr20:9510385 G>A maps to NM_012261.3 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:9496669 C>T maps to NM_012261.3 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:9510430 C>T maps to NM_012261.3 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:9510313 G>A maps to NM_012261.3 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr20:9496747 C>G maps to NM_012261.3 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:9510421 G>A maps to NM_012261.3 Q266Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr20:9496115 C>T maps to NM_012261.3 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr20:55111277 G>A maps to NM_001013646.2 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr20:55111284 C>T maps to NM_001013646.2 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr20:55108453 C>T maps to NM_001013646.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:54941147 C>T maps to NM_080821.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr20:54940141 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr20:61574342 C>T maps to NM_017896.2 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:61572943 C>T maps to NM_017896.2 N30N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:61574860 C>T maps to NM_017896.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr20:42826003 G>A maps to NM_016470.6 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:42825912 G>A maps to NM_016470.6 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr20:31041378 G>A maps to NM_080616.3 N191N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr20:31894786 G>A maps to NM_033197.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:31894753 G>A maps to NM_033197.2 K452K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr20:31889047 T>C maps to NM_033197.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:31878789 C>T maps to NM_033197.2 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:31878780 C>T maps to NM_033197.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:31890759 C>T maps to NM_033197.2 I340I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr20:35444104 G>A maps to NM_080627.2 I580I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr20:35443639 G>A maps to NM_080627.2 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr20:35443717 G>A maps to NM_080627.2 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr20:35467643 G>A maps to NM_080627.2 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr20:35444326 C>T maps to NM_080627.2 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr20:35422878 G>A maps to NM_080627.2 S1202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr20:35467682 G>A maps to NM_080627.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr20:35507530 C>T maps to NM_080628.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr20:35507472 C>T maps to NM_080628.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:35504606 G>A maps to NM_080628.1 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr20:18374411 G>A maps to NM_001099407.1 I584I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr20:18396033 G>T maps to NM_001099407.1 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr20:18370463 G>A maps to NM_001099407.1 D633D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr20:35776281 G>A maps to ENST00000343811 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr20:35743677 C>T maps to ENST00000343811 K837K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:35738758 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr20:35742545 C>T maps to ENST00000343811 V872V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr20:35740804 C>T maps to ENST00000343811 W938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr20:35769576 G>A maps to ENST00000343811 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr20:35766334 G>A maps to ENST00000343811 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:35749411 G>A maps to ENST00000343811 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr20:2795835 C>T maps to NM_080739.2 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:32251357 C>T maps to NM_080825.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr20:32251363 G>A maps to NM_080825.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr20:60987793 G>A maps to NM_080833.2 Q588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr20:60986023 C>T maps to NM_080833.2 R635R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:60990934 G>A maps to NM_080833.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr20:60991861 C>T maps to NM_080833.2 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr20:60985999 G>A maps to NM_080833.2 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr20:60986023 C>T maps to NM_080833.2 R635R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr20:60989554 C>T maps to NM_080833.2 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr20:60989119 C>T maps to NM_080833.2 E429E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr20:34571960 C>T maps to ENST00000373973 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr20:34618320 G>A maps to ENST00000373973 W494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr20:34568454 C>T maps to ENST00000373973 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr20:34611586 C>T maps to ENST00000373973 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr20:34571960 C>T maps to ENST00000373973 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr20:34611615 G>A maps to ENST00000373973 K454K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:34571960 C>T maps to ENST00000373973 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:30610509 C>T maps to ENST00000300415 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr20:30602798 G>A maps to ENST00000300415 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr20:44515314 C>T maps to NM_080608.3 E175E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr20:44515308 C>T maps to NM_080608.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr20:44515164 G>A maps to NM_080608.3 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr20:61167715 C>T maps to NM_178463.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:58519432 C>T maps to NM_022106.2 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr20:58519432 C>T maps to NM_022106.2 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:58519432 C>T maps to NM_022106.2 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:31659973 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr20:31657761 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr20:31643345 C>T maps to NM_182658.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr20:31643288 A>G maps to NM_182658.1 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:31652320 C>T maps to NM_182658.1 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:31652476 C>T maps to NM_182658.1 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr20:31647189 G>A maps to NM_182658.1 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr20:31671389 A>G maps to NM_182519.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:31672796 G>A maps to NM_182519.2 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:31671440 G>A maps to NM_182519.2 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:31692662 C>T maps to NM_182519.2 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr20:31680352 C>T maps to NM_182519.2 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr20:31672706 C>T maps to NM_182519.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr20:31685473 C>T maps to NM_182519.2 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr20:31680451 C>T maps to NM_182519.2 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr20:31692638 G>A maps to NM_182519.2 V568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr20:3277505 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr20:3297411 G>A maps to NM_001009984.1 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr20:3240667 T>C maps to NM_001009984.1 E960E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:5843757 G>A maps to NM_152504.2 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr20:58645094 G>A maps to NM_173644.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr20:35240541 C>T maps to NM_199483.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr20:20177254 C>T maps to ENST00000389655 F547F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr20:20278859 G>A maps to ENST00000389655 G1087G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr20:20232361 C>T maps to ENST00000389655 I764I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr20:20144803 C>T maps to ENST00000389655 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr20:20232322 C>T maps to ENST00000389655 D751D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr20:20257921 C>T maps to ENST00000389655 S875S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:20269272 G>A maps to ENST00000389655 E942E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:20232361 C>T maps to ENST00000389655 I764I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A3AC-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr20:20037438 C>T maps to ENST00000494029 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr20:20209000 C>T maps to ENST00000389655 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:20150029 C>T maps to ENST00000389655 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:20172020 T>C maps to ENST00000389655 V519V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr20:20232323 C>T maps to ENST00000389655 R752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr20:20341037 G>A maps to ENST00000389655 W1236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr20:20051575 C>T maps to ENST00000389655 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:20226841 G>A maps to ENST00000389655 R717R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:20054962 C>T maps to ENST00000389655 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:20150047 C>T maps to ENST00000389655 F446F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:20150059 C>T maps to ENST00000389655 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:20168603 G>A maps to ENST00000389655 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:20258008 G>A maps to ENST00000389655 A904A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr20:20150032 G>A maps to ENST00000389655 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr20:20037428 C>T maps to ENST00000389655 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:3736161 G>A maps to NM_001039140.1 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr20:24959505 G>A maps to NM_020531.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr20:5090007 G>A maps to NM_001009923.1 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr20:5081502 G>A maps to NM_001009923.1 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr20:34832829 C>T maps to NM_015511.3 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr20:1161791 C>T maps to NM_018354.1 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr20:744299 G>A maps to NM_033409.3 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr20:742386 G>A maps to NM_033409.3 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:742356 C>T maps to NM_033409.3 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:744542 G>A maps to NM_033409.3 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr20:744235 G>A maps to NM_033409.3 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr20:13769243 C>T maps to NM_024120.4 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:13773845 C>T maps to NM_024120.4 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr20:13782283 C>T maps to NM_024120.4 D224D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr20:31760843 C>T maps to NM_080574.2 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:31760768 A>G maps to NM_080574.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr20:31761932 C>T maps to NM_080574.2 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr20:31763248 C>T maps to NM_080574.2 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr20:31767456 C>T maps to NM_080574.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:31757082 T>C maps to NM_080574.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:31763299 G>A maps to NM_080574.2 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:31761974 G>A maps to NM_080574.2 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:31763242 A>G maps to NM_080574.2 K147K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:31761911 G>A maps to NM_080574.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr20:31805384 C>T maps to NM_178466.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr20:31814247 C>T maps to NM_178466.3 N191N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr20:31814776 G>A maps to NM_178466.3 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr20:31805432 C>T maps to NM_178466.3 Q31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr20:31814776 G>A maps to NM_178466.3 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr20:31811761 G>A maps to NM_178466.3 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:18794488 G>A maps to NM_178483.2 K10K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr20:18794860 C>T maps to NM_178483.2 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:18794524 C>T maps to NM_178483.2 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr20:56735718 C>T maps to NM_178456.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:56735760 C>T maps to NM_178456.2 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr20:10603429 T>C maps to NM_001009608.1 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr20:10541454 C>G maps to NM_001009608.1 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr20:10602038 C>T maps to NM_001009608.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr20:10603435 C>T maps to NM_001009608.1 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:10603748 C>T maps to NM_001009608.1 R317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr20:10603511 C>T maps to NM_001009608.1 Q238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr20:10602047 T>C maps to NM_001009608.1 N164N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr20:259839 G>A maps to NM_153269.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr20:257908 G>T maps to NM_153269.1 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr21:45929218 G>A maps to ENST00000443468 F543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr21:45987854 G>A maps to ENST00000443468 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr21:45947240 G>A maps to ENST00000443468 F363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr21:45949807 C>T maps to ENST00000443468 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr21:45945704 A>G maps to ENST00000443468 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr21:45947297 C>T maps to ENST00000443468 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr21:45941993 G>T maps to ENST00000443468 G450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr21:45953806 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr21:45949735 G>A maps to ENST00000443468 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr21:45929239 G>A maps to ENST00000443468 F536F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr21:45929161 G>A maps to ENST00000443468 S562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr21:45941921 G>A maps to ENST00000443468 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:45929263 G>A maps to ENST00000443468 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:45947201 G>A maps to ENST00000443468 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:45949717 C>T maps to ENST00000443468 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr21:45987758 G>A maps to ENST00000443468 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr21:47716086 C>T maps to NM_058181.1 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr21:47742622 G>A maps to NM_058180.3 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr21:47731393 G>A maps to NM_058180.3 Q233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr21:33982301 T>C maps to NM_021254.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr21:33974256 G>A maps to NM_021254.2 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr21:33887341 C>T maps to NM_058187.3 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr21:30532350 G>A maps to NM_020152.2 K174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:38349105 C>T maps to NM_032561.3 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:32333917 G>A maps to NM_015372.1 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:20049179 C>T maps to NM_152906.4 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:32804214 G>A maps to NM_014306.4 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:32804215 G>A maps to NM_014306.4 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr22:32804820 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:19839541 G>A maps to NM_024627.5 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr22:19839295 G>A maps to NM_024627.5 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:19839241 G>A maps to NM_024627.5 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr22:32108220 G>A maps to NM_173566.2 S1868S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:29454858 C>T maps to NM_015370.1 W248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:29454859 C>T maps to NM_015370.1 W248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:42477981 C>T maps to NM_033318.3 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:37398036 T>A maps to NM_001163857.1 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr22:37398060 C>T maps to NM_001163857.1 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:37397961 C>T maps to NM_001163857.1 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:24982038 G>A maps to NM_207644.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr22:24982252 C>G maps to NM_207644.2 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr22:32550252 C>T maps to NM_001010859.1 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:32548081 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr22:32554992 C>T maps to NM_001010859.1 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr22:23968224 C>T maps to NM_016449.3 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:23974156 C>T maps to NM_016449.3 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:45598996 A>G maps to NM_001009880.1 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr22:45599723 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr22:45595850 G>A maps to NM_001009880.1 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr22:45593790 G>A maps to NM_001009880.1 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr22:45593791 G>A maps to NM_001009880.1 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:43339045 C>T maps to NM_015500.1 K172K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr21:43321858 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr21:43342115 G>A maps to NM_015500.1 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr21:43338964 C>T maps to NM_015500.1 E199E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr21:43327227 G>A maps to NM_015500.1 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr21:43309289 G>A maps to NM_015500.1 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr21:43338985 G>A maps to NM_015500.1 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:43327113 G>A maps to NM_015500.1 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:43332481 C>T maps to NM_015500.1 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:43332496 G>A maps to NM_015500.1 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr21:43332481 C>T maps to NM_015500.1 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:118986926 C>T maps to NM_014807.3 S695S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:118986956 C>T maps to NM_014807.3 P705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr11:73748583 C>A maps to ENST00000334126 G1940G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr11:73804913 G>A maps to ENST00000334126 F1097F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:73879530 G>A maps to ENST00000334126 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr11:73849825 C>T maps to ENST00000334126 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr11:73785331 G>A maps to ENST00000334126 I1639I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr11:73829376 G>A maps to ENST00000334126 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:73834125 G>A maps to ENST00000334126 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr11:73748720 G>A maps to ENST00000334126 Q1895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr15:62359859 G>A maps to NM_207322.2 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:99767018 C>T maps to NM_144706.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr2:27801613 G>A maps to NM_032266.3 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:27802153 G>A maps to NM_032266.3 R905R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:27800176 G>A maps to NM_032266.3 K246K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr2:27802108 C>T maps to NM_032266.3 S890S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr2:27803476 A>G maps to NM_032266.3 Q1346Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr2:27800746 C>T maps to NM_032266.3 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:27804280 C>T maps to NM_032266.3 H1614H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:27802153 G>A maps to NM_032266.3 R905R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr2:27801409 G>A maps to NM_032266.3 V657V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:27801022 G>A maps to NM_032266.3 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:27799492 T>C maps to NM_032266.3 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:27800585 C>T maps to NM_032266.3 Q383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:27804461 C>T maps to NM_032266.3 Q1675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr2:27802108 C>T maps to NM_032266.3 S890S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:27800116 G>A maps to NM_032266.3 E226E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr2:27804223 G>A maps to NM_032266.3 R1595R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:27800630 C>T maps to NM_032266.3 Q398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:27802501 G>A maps to NM_032266.3 G1021G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr2:27803713 G>A maps to NM_032266.3 E1425E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:27001360 C>T maps to NM_017877.3 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr2:220039718 C>G maps to NM_015680.4 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:220037364 A>G maps to NM_015680.4 C392C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:220037322 G>A maps to NM_015680.4 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:220038092 G>A maps to NM_015680.4 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:220037700 G>A maps to NM_015680.4 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr2:27438359 C>T maps to NM_080592.3 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr2:27439734 C>T maps to NM_080592.3 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:101874355 G>A maps to NM_017546.4 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:101883185 C>T maps to NM_017546.4 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr2:75929486 G>A maps to NM_003203.4 Q153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr2:75923423 A>T maps to NM_003203.4 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:75929357 G>A maps to NM_003203.4 Q196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:75929445 G>A maps to NM_003203.4 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:44617385 T>C maps to NM_024766.3 N106N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:26672862 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:26667733 G>A maps to NM_145038.2 W438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:26676318 G>A maps to NM_145038.2 K607K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:26677514 G>A maps to NM_145038.2 R640R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr2:106694259 C>T maps to NM_032411.2 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:106690396 C>T maps to NM_032411.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr2:106694292 C>T maps to NM_032411.2 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr2:106694330 G>A maps to NM_032411.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:106694259 C>T maps to NM_032411.2 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr2:106690396 C>T maps to NM_032411.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:70387888 G>A maps to NM_017880.1 Q462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:70392744 G>A maps to NM_017880.1 F389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:70387901 G>A maps to NM_017880.1 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:70402844 G>A maps to NM_017880.1 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:24261391 T>A maps to NM_025203.2 K325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:24253871 G>T maps to NM_025203.2 V699V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr2:200824583 C>T maps to NM_024520.2 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:10350491 C>T maps to NM_182626.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr2:105959565 C>T maps to NM_024093.1 D176D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:11280647 G>A maps to NM_182500.2 W90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:88828841 C>T maps to NM_152670.2 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr2:88828805 C>T maps to NM_152670.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:88825179 C>T maps to NM_152670.2 Y6Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:88828853 C>T maps to NM_152670.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr2:27361020 G>A maps to NM_178553.3 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr2:27360597 C>T maps to NM_178553.3 K200K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:27360390 C>T maps to NM_178553.3 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:27360042 G>A maps to NM_178553.3 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:27360639 G>A maps to NM_178553.3 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:27360858 G>T maps to NM_178553.3 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:241831025 G>A maps to NM_001085437.1 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:241830989 C>T maps to NM_001085437.1 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:241826525 G>A maps to NM_001085437.1 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:241831073 C>T maps to NM_001085437.1 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:241831097 G>A maps to NM_001085437.1 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:241829508 C>T maps to NM_001085437.1 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr2:99439604 G>A maps to NM_207362.2 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:99439517 G>A maps to NM_207362.2 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:99448965 G>A maps to NM_207362.2 Q129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:99438728 G>A maps to NM_207362.2 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:99448864 C>T maps to NM_207362.2 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:99438710 C>T maps to NM_207362.2 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:99438728 G>A maps to NM_207362.2 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:99448864 C>T maps to NM_207362.2 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr2:37471079 G>A maps to NM_144736.4 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr2:200801131 T>C maps to NM_001039693.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:200800762 T>C maps to NM_001039693.2 K194K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr2:219229427 G>A maps to NM_198559.1 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr2:219229428 G>T maps to NM_198559.1 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr2:219232509 C>T maps to NM_198559.1 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:219232204 G>A maps to NM_198559.1 E295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:99220615 G>A maps to NM_001008215.1 Y46Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr2:74834229 G>A maps to NM_138804.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr2:74834278 G>A maps to NM_138804.3 D166D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:74867171 G>A maps to NM_138804.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr2:74842096 G>A maps to NM_138804.3 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:74834278 G>A maps to NM_138804.3 D166D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:74803644 G>A maps to NM_138804.3 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:74842117 C>T maps to NM_138804.3 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:74803659 G>A maps to NM_138804.3 D285D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:74787385 G>A maps to NM_138804.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr2:197672277 G>A maps to NM_213608.1 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:197673971 C>T maps to NM_213608.1 W47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:211018910 G>A maps to NM_152519.2 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr2:210940449 G>A maps to NM_152519.2 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr2:26802209 C>T maps to NM_001105519.1 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr2:29296578 G>A maps to NM_001029883.1 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr2:29296512 G>A maps to NM_001029883.1 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:29295897 C>T maps to NM_001029883.1 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:29293656 C>T maps to NM_001029883.1 G1157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:29294310 C>T maps to NM_001029883.1 G939G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr2:29294355 C>A maps to NM_001029883.1 L924L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:29294235 G>A maps to NM_001029883.1 G964G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:29296692 C>T maps to NM_001029883.1 W145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr2:29295009 G>A maps to NM_001029883.1 I706I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:29293944 G>A maps to NM_001029883.1 P1061P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr2:29294547 C>T maps to NM_001029883.1 K860K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:29294505 C>T maps to NM_001029883.1 R874R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr2:29295717 G>A maps to NM_001029883.1 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:170502524 T>C maps to NM_001085447.1 K495K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:170518912 C>T maps to NM_001085447.1 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:170505778 A>G maps to NM_001085447.1 D410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:170518801 C>T maps to NM_001085447.1 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:170506913 C>T maps to NM_001085447.1 W359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr2:74044049 G>A maps to NM_001080474.1 G900G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:74041327 A>G maps to NM_001080474.1 Q274Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:74042631 C>T maps to NM_001080474.1 Q428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:74042726 C>T maps to NM_001080474.1 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:74043122 G>A maps to NM_001080474.1 G591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr2:74044064 C>T maps to NM_001080474.1 F905F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:74042345 G>A maps to NM_001080474.1 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:74042708 C>T maps to NM_001080474.1 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr2:25016003 C>T maps to NM_001013663.1 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:25016000 G>A maps to NM_001013663.1 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:25016030 G>A maps to NM_001013663.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:209046028 C>T maps to NM_001099334.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:228476241 G>A maps to NM_020161.3 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:228476115 C>T maps to NM_020161.3 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr2:228476229 G>A maps to NM_020161.3 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:242814228 G>A maps to NM_173821.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:242814396 C>T maps to NM_173821.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr2:242814327 C>T maps to NM_173821.2 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:242812009 G>A maps to NM_173821.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:242814636 C>T maps to NM_173821.2 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:242815134 C>T maps to NM_173821.2 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr2:63665008 C>T maps to NM_001042692.1 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:63660905 G>A maps to NM_015910.4 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:63720062 G>A maps to NM_015910.4 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr2:63631765 C>T maps to NM_015910.4 W284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:85051267 G>A maps to ENST00000409520 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:85097362 A>G maps to ENST00000409520 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:85049121 G>A maps to ENST00000409520 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:85051083 C>A maps to ENST00000409520 E443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:85097369 C>T maps to ENST00000409520 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:85059213 C>T maps to ENST00000409520 E349E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr2:85051282 G>A maps to ENST00000409520 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:85051078 C>T maps to ENST00000409520 E444E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:85097393 C>T maps to ENST00000409520 K208K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:6694442 C>T maps to NM_000064.2 K1051K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:6710853 G>A maps to NM_000064.2 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:6707096 G>A maps to NM_000064.2 G745G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:6712405 C>T maps to NM_000064.2 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:6707831 G>A maps to NM_000064.2 Q652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:6684607 G>A maps to NM_000064.2 F1361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:6702582 C>T maps to NM_000064.2 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:6707507 G>A maps to NM_000064.2 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:6679430 G>A maps to NM_000064.2 C1511C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:6694502 C>T maps to NM_000064.2 T1031T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:6679181 G>A maps to NM_000064.2 T1528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:6681978 C>T maps to NM_000064.2 R1441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:6707817 C>T maps to NM_000064.2 Q656Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:6690726 C>T maps to NM_000064.2 R1134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr19:6693000 G>A maps to NM_000064.2 I1108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:6697805 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:6693045 G>A maps to NM_000064.2 I1093I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:6709730 G>A maps to NM_000064.2 F603F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:6694598 C>T maps to NM_000064.2 R999R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:6707814 C>T maps to NM_000064.2 R657R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr19:6711044 G>A maps to NM_000064.2 R478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:6678293 C>T maps to NM_000064.2 S1573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:6694440 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:6709693 C>T did not map to a codon.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr19:6702495 C>T maps to NM_000064.2 E780E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr19:6685029 C>T maps to NM_000064.2 W1313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:6711044 G>A maps to NM_000064.2 R478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:6714367 G>A maps to NM_000064.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:6678260 G>A maps to NM_000064.2 F1584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:6678410 G>A maps to NM_000064.2 I1562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:6702213 C>T maps to NM_000064.2 T788T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:6711048 G>A maps to NM_000064.2 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:6711195 C>T maps to NM_000064.2 K427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr19:6682194 G>A maps to NM_000064.2 S1406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:6697420 C>T maps to NM_000064.2 V910V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr3:119219647 A>T maps to NM_016589.3 K101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:119236138 C>T maps to NM_016589.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:10157501 C>T maps to NM_018462.4 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:119462886 C>T maps to NM_033364.3 F582F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:119452209 G>A did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr3:119451184 T>C maps to NM_033364.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:119466062 G>A maps to NM_033364.3 E668E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr3:119422019 G>A maps to NM_033364.3 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:119466663 C>T maps to NM_033364.3 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:119469923 C>T maps to NM_033364.3 Q762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr3:119458133 C>T maps to NM_033364.3 Y498Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr3:119445027 C>T maps to NM_033364.3 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr3:119426291 C>T maps to NM_033364.3 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr3:119426348 C>T maps to NM_033364.3 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:112729988 G>A maps to NM_015412.3 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:112732174 A>C maps to NM_015412.3 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:112738392 G>A maps to NM_015412.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr3:14696015 A>G maps to NM_016474.4 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:14724303 C>T maps to NM_032137.4 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:14803053 G>A maps to NM_032137.4 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:14801435 G>A maps to NM_032137.4 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:14814315 G>A maps to NM_032137.4 V883V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr3:14724231 C>T maps to NM_032137.4 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:14746041 C>T maps to NM_032137.4 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr3:14725881 G>A maps to NM_032137.4 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:14755603 C>T maps to NM_032137.4 F417F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:14756822 G>A maps to NM_032137.4 E447E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:14802993 G>A maps to NM_032137.4 G789G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:14799049 C>T maps to NM_032137.4 R705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:194947471 G>A maps to NM_152531.4 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:194877305 G>A maps to NM_152531.4 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr3:194790593 G>A maps to NM_152531.4 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:126268751 G>A maps to NM_152533.1 Q129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:126270844 G>A maps to NM_152533.1 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:126270913 G>A maps to NM_152533.1 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:44408952 C>T maps to NM_173826.3 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:44408952 C>T maps to NM_173826.3 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:10146350 G>T maps to NM_001164839.1 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:128292265 G>A maps to NM_007354.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:118870138 G>A maps to NM_152539.2 *537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr3:118865230 C>T maps to NM_152539.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:118866238 C>T maps to NM_152539.2 D401D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr3:118865836 G>A maps to NM_152539.2 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:118865197 G>A maps to NM_152539.2 Q54Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:11885595 G>A maps to ENST00000444133 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr3:11885562 G>A maps to ENST00000444133 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr3:11887978 C>T maps to ENST00000444133 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:8675567 G>A maps to NM_015931.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:8667945 G>A maps to NM_015931.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:8675489 G>A maps to NM_015931.1 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:8675453 G>A maps to NM_015931.1 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr3:8672580 G>A maps to NM_015931.1 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr3:133647197 C>T maps to NM_025041.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:43121552 G>A maps to NM_032806.4 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr3:43122215 G>A maps to NM_032806.4 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:43122022 G>A maps to NM_032806.4 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:43122587 G>A maps to NM_032806.4 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:43121647 G>A maps to NM_032806.4 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr3:192517383 G>A maps to NM_178496.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr3:192517329 G>A maps to NM_178496.3 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr3:192516936 C>T maps to NM_178496.3 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:49314044 C>T maps to NM_198562.2 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr3:69047161 G>T maps to ENST00000383701 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:69047176 G>A maps to ENST00000383701 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:69053542 G>A maps to ENST00000383701 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:58853582 C>T maps to ENST00000482387 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr3:58855129 G>A maps to ENST00000482387 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:58870301 G>A maps to ENST00000482387 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr3:58899554 G>A maps to ENST00000482387 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr3:48956273 C>T maps to NM_001123040.1 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr3:138668405 C>T maps to NM_001040061.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:47551688 G>A maps to NM_001031703.2 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr6:31962438 C>T maps to NM_007293.2 F919F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:31996261 G>A maps to ENST00000425700 K1061K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:31962465 C>T maps to NM_007293.2 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr6:31994893 C>T maps to NM_001002029.3 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr6:31997550 C>T maps to ENST00000425700 F1295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:31996294 G>A maps to ENST00000425700 R1072R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:31997535 C>T maps to ENST00000425700 T1290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:31997526 C>T maps to ENST00000425700 A1287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:31997550 C>T maps to ENST00000425700 F1295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J6-06A-11D-A19A-08 chr1:207287556 C>T maps to NM_000715.3 Y85Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:207297305 C>T maps to NM_000715.3 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:207317944 C>T maps to NM_000715.3 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:207297684 G>A maps to NM_000715.3 W227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr1:207307800 G>A maps to NM_000715.3 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:207273142 C>T maps to NM_001017367.1 Q210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:207273195 G>A maps to NM_001017367.1 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:207273195 G>A maps to NM_001017367.1 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr4:57842671 C>T maps to NM_032313.2 E360E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr4:100460492 C>T maps to NM_032149.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr4:100434268 C>T maps to NM_032149.2 Q11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:100434255 G>A maps to NM_032149.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr4:100463202 G>A maps to NM_032149.2 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr4:113539801 C>A maps to NM_018392.4 G466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:113510952 G>A maps to NM_018392.4 F1018F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:113538640 G>A maps to NM_018392.4 Q853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:113540839 G>A maps to NM_018392.4 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr4:81283939 A>G maps to ENST00000508675 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr4:81866047 T>A maps to ENST00000508675 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr4:8469882 C>T maps to NM_152544.2 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr4:8467170 C>T maps to NM_152544.2 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr4:8469648 C>T maps to NM_152544.2 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr4:76489603 C>T maps to NM_178497.2 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr4:76489649 G>A maps to ENST00000435974 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr4:170663150 G>T maps to NM_017867.2 S202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr4:170663203 G>A maps to NM_017867.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr4:170671849 G>A maps to NM_017867.2 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr4:170650818 A>G maps to NM_017867.2 Y317Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr4:121957862 C>T maps to NM_024574.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr4:121958510 C>T maps to NM_024574.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr4:121957439 C>T maps to NM_024574.3 V562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr4:121958588 G>A maps to NM_024574.3 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:121958054 C>T maps to NM_024574.3 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:121966959 G>A maps to NM_024574.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:113108006 C>T maps to NM_152400.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:130023818 C>T maps to NM_001099783.1 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:39606741 G>A maps to NM_174921.1 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr4:71201232 C>T maps to NM_033122.3 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:71201724 C>T maps to NM_033122.3 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:71201034 G>A maps to NM_033122.3 Q93Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr4:71201871 G>A maps to NM_033122.3 K372K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:71201256 G>A maps to NM_033122.3 K167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr4:98633936 C>T maps to NM_174952.2 R411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr4:98902376 C>T maps to NM_174952.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr4:99030456 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:98480256 C>T maps to NM_174952.2 E444E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr4:98893471 G>A maps to NM_174952.2 Q298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr4:98633936 C>T maps to NM_174952.2 R411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr4:98762038 C>T maps to NM_174952.2 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr4:98633936 C>T maps to NM_174952.2 R411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:71024601 T>C maps to NM_214711.3 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr4:71024220 C>T maps to NM_214711.3 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:71024316 G>A maps to NM_214711.3 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:71024289 G>A maps to NM_214711.3 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr4:71024154 C>T maps to NM_214711.3 Y62Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:184615118 A>G maps to NM_021942.4 T812T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:184598668 C>T maps to NM_021942.4 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:184585043 C>T maps to NM_021942.4 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr4:184607855 A>T maps to NM_021942.4 P616P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr4:184595962 C>T maps to NM_021942.4 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr4:3255158 C>T maps to NM_001042690.1 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr4:3251110 C>T maps to NM_001042690.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr4:159590800 C>T maps to NM_001008393.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:140187968 C>T maps to ENST00000260011 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:5975405 G>A maps to ENST00000324058 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:5975478 C>T maps to ENST00000324058 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr4:5961112 A>G maps to ENST00000324058 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:5961200 G>A maps to ENST00000324058 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr4:5966753 C>T maps to ENST00000324058 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:5961232 G>A maps to ENST00000324058 Q234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr4:5961200 G>A maps to ENST00000324058 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr4:5990072 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:5961341 G>A maps to ENST00000324058 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr4:146651098 G>A maps to NM_001080531.1 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:146601510 C>T maps to NM_001080531.1 Y52Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr4:146653645 T>C maps to NM_001080531.1 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:146651098 G>A maps to NM_001080531.1 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:146601489 G>A maps to NM_001080531.1 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr9:123744130 G>A maps to NM_001735.2 C1159C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr9:123780001 G>A maps to NM_001735.2 I545I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:123725048 G>A maps to NM_001735.2 P1468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr9:123751987 G>A maps to NM_001735.2 P1004P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:123779750 G>A maps to NM_001735.2 G585G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr9:123812482 C>T maps to NM_001735.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:47823762 G>A maps to ENST00000355085 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:47823498 C>T maps to ENST00000355085 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:47823153 C>T maps to ENST00000355085 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:47823663 C>T maps to ENST00000355085 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr19:47823987 C>T maps to ENST00000355085 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:47823180 G>A maps to ENST00000355085 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:47823883 C>T maps to ENST00000355085 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:47823708 C>T maps to ENST00000355085 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr19:47823555 C>T maps to ENST00000355085 Y174Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:47823645 C>T maps to ENST00000355085 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:47823171 C>T maps to ENST00000355085 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:47823709 C>T maps to ENST00000355085 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr5:111066668 C>T maps to NM_001142475.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:111071186 G>A maps to NM_001142475.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr5:111066638 G>A maps to NM_001142475.1 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:111066647 G>A maps to NM_001142475.1 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr5:134782468 C>T maps to NM_130848.2 Q110Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr5:134782084 C>T maps to NM_130848.2 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:134782264 C>T maps to NM_130848.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:31541449 C>T maps to NM_018356.2 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr5:32789518 C>T maps to NM_024563.3 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr5:32789635 G>A maps to NM_024563.3 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:175772342 C>T maps to ENST00000443967 V838V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:175772234 G>A maps to ENST00000443967 R802R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:175772291 G>A maps to ENST00000443967 Q821Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:175772321 G>A maps to ENST00000443967 Q831Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr5:43446578 A>G maps to NM_022483.4 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr5:43446464 T>A maps to NM_022483.4 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr5:102612105 G>A maps to NM_033211.2 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:102611670 C>T maps to NM_033211.2 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr5:36225642 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:43508740 G>A maps to NM_198566.2 R75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr5:93859643 G>A maps to ENST00000513200 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:2752786 C>T maps to NM_178569.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr5:2752551 G>A maps to NM_178569.2 W58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:43040010 C>T maps to NM_001014279.2 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr5:156770373 C>T maps to NM_001001343.3 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:156770004 C>T maps to NM_001001343.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:156770010 G>A maps to NM_001001343.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr5:156770373 C>T maps to NM_001001343.3 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:172550205 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:172517805 T>C maps to NM_153607.2 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:37183115 G>A maps to NM_023073.3 Q1723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:37201713 G>A maps to NM_023073.3 P1162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:37170385 G>A maps to NM_023073.3 S2073S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr5:37167294 G>A maps to NM_023073.3 I2418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:37154075 G>A maps to NM_023073.3 F2659F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:37167249 T>C maps to NM_023073.3 L2433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:37185169 C>A maps to NM_023073.3 E1401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:37164387 G>A maps to NM_023073.3 F2525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr5:37186481 G>A maps to NM_023073.3 F1365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr5:64954238 C>G maps to NM_001093755.1 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:64957926 C>T maps to NM_001093755.1 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr5:179268956 G>T maps to NM_016175.3 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr5:147286009 G>A maps to NM_206966.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:125971752 C>T maps to NM_207408.1 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr5:159822449 G>A maps to NM_022090.3 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:159821390 C>T maps to NM_022090.3 E369E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr5:159821051 G>A maps to NM_022090.3 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr5:41158778 G>A maps to NM_001115131.1 I655I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr5:41161961 C>T did not map to a codon.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr5:41181508 G>A maps to NM_001115131.1 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr5:41142988 C>A maps to NM_001115131.1 G915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr5:41172414 C>T maps to NM_001115131.1 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:41172438 C>T maps to NM_001115131.1 E393E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr5:41160403 C>T maps to NM_001115131.1 R508R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr5:41203236 C>T maps to NM_001115131.1 W32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr5:41203237 C>T maps to NM_001115131.1 W32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:41203289 G>A maps to NM_001115131.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:41181562 C>T maps to NM_001115131.1 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr5:41181508 G>A maps to NM_001115131.1 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:41153960 C>T maps to NM_001115131.1 Q747Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr5:41159245 C>T maps to NM_001115131.1 G598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr5:41195919 G>A maps to NM_001115131.1 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:41176763 C>T maps to NM_001115131.1 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:41176727 C>T maps to NM_001115131.1 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:41203263 G>A maps to NM_001115131.1 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:41149418 C>T maps to NM_001115131.1 R849R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:41143049 T>C maps to NM_001115131.1 Q894Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr5:41161947 C>T maps to NM_001115131.1 Q435Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:41159245 C>T maps to NM_001115131.1 G598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:41176646 G>A maps to NM_001115131.1 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:41159224 C>T maps to NM_001115131.1 K605K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr5:41176814 A>G maps to NM_001115131.1 D310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:41160457 G>A maps to NM_001115131.1 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr5:41203302 G>A maps to NM_001115131.1 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:41154098 C>T maps to NM_001115131.1 R701R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr5:41154020 G>A maps to NM_001115131.1 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr5:41158844 G>A maps to NM_001115131.1 V633V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr5:41160457 G>A maps to NM_001115131.1 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr5:41149355 C>T maps to NM_001115131.1 W870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr5:41160403 C>T maps to NM_001115131.1 R508R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr5:41203246 C>T maps to NM_001115131.1 W29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:41143070 C>T maps to NM_001115131.1 Q887Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:41153948 C>T maps to NM_001115131.1 W751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:41161794 C>T maps to NM_001115131.1 E486E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:41161947 C>T maps to NM_001115131.1 Q435Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:41181550 G>A maps to NM_001115131.1 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:41203237 C>T maps to NM_001115131.1 W32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:41186299 G>A maps to NM_001115131.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr5:41153957 C>T maps to NM_001115131.1 G748G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr6:32261008 G>A maps to ENST00000447241 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:32260976 C>T maps to ENST00000447241 E491E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:32261669 C>T maps to ENST00000447241 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr6:32261072 C>T maps to ENST00000447241 K459K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:11723583 C>T maps to NM_001143948.1 W237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr6:11735907 G>A maps to NM_001143948.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr6:43193825 C>T maps to ENST00000509253 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr6:165703449 C>T maps to NM_144980.3 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:165715407 G>A maps to NM_144980.3 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:165715408 G>A maps to NM_144980.3 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr6:165715234 G>A maps to NM_144980.3 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr6:165715372 G>A maps to NM_144980.3 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:165712931 C>T maps to NM_144980.3 E312E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr6:165715345 C>T maps to NM_144980.3 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:165715312 C>T maps to NM_144980.3 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:165715585 C>T maps to NM_144980.3 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:165715372 G>A maps to NM_144980.3 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr6:165715498 C>T maps to NM_144980.3 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:165715372 G>A maps to NM_144980.3 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr6:165713882 C>T maps to NM_144980.3 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:165715546 C>T maps to NM_144980.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr6:165715585 C>T maps to NM_144980.3 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:33669179 G>A maps to NM_032340.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr6:35747190 G>A maps to NM_207409.2 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr6:35754863 G>A maps to NM_001010886.3 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr6:35755648 C>T maps to NM_001010886.3 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr6:35754897 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:35755681 G>A maps to NM_001010886.3 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:37452895 C>T maps to NM_138493.2 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr6:37450985 G>A maps to NM_138493.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr6:30617571 C>T maps to NM_001161376.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr6:47846803 G>A maps to NM_001013732.3 I592I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr6:47976639 G>A maps to NM_001013732.3 Q213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:47846656 G>A maps to NM_001013732.3 I641I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:48036001 C>T maps to NM_001013732.3 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr6:47847232 G>A maps to NM_001013732.3 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:47846656 G>A maps to NM_001013732.3 I641I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr6:47846458 G>A maps to NM_001013732.3 N707N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr6:48036237 G>A maps to NM_001013732.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:47846377 G>A maps to NM_001013732.3 F734F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:47846644 G>A maps to NM_001013732.3 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:47976805 C>T maps to NM_001013732.3 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:47847265 C>T maps to NM_001013732.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:54095636 C>T maps to ENST00000502396 P948P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr6:53989509 G>A maps to ENST00000502396 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:53986345 C>T maps to ENST00000502396 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr6:54095646 C>T maps to ENST00000502396 L952L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:53989329 G>A maps to ENST00000502396 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr6:53989383 C>T maps to ENST00000502396 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:54025202 G>A maps to ENST00000502396 K776K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr6:54095549 T>A maps to ENST00000502396 P919P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr6:53986274 C>T maps to ENST00000502396 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:53989329 G>A maps to ENST00000502396 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr6:54013894 C>T maps to ENST00000502396 I753I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr6:3727858 G>A maps to NM_183373.3 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr6:4069898 C>T maps to NM_173563.1 W186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:4070063 A>G maps to NM_173563.1 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:4069784 C>T maps to NM_173563.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:4069784 C>T maps to NM_173563.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr6:31079718 G>A maps to NM_014070.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:31079436 T>G maps to NM_014070.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr6:74155278 G>A maps to NM_138441.2 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr6:42996893 G>A maps to NM_033112.2 E236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr6:42992841 C>T maps to NM_033112.2 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr6:88046793 C>A maps to NM_020425.4 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr6:88173826 G>A maps to NM_001031743.2 K576K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:88170798 G>A maps to NM_001031743.2 Q518Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:88123610 G>A maps to NM_001031743.2 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:99739583 G>A maps to NM_032511.2 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:99797050 G>A maps to NM_032511.2 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:121613283 G>A maps to ENST00000275159 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:121600265 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:121412004 G>A maps to ENST00000275159 F1257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr6:121560233 A>G maps to ENST00000275159 I782I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr6:121560296 A>G maps to ENST00000275159 N761N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr6:121560299 G>C maps to ENST00000275159 S760S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:127797246 G>A maps to NM_001012279.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr6:127797361 C>T maps to NM_001012279.2 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:127797246 G>A maps to NM_001012279.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:127837546 C>T maps to NM_001012279.2 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:127796710 C>T maps to NM_001012279.2 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:127796944 C>T maps to NM_001012279.2 L742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:127796869 C>T maps to NM_001012279.2 R767R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:127797355 G>A maps to NM_001012279.2 I605I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:110644064 C>T maps to NM_001123364.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:2623786 G>A maps to NM_152554.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:2623696 C>T maps to NM_152554.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:4099399 G>A maps to NM_001085401.1 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr6:4099345 C>T maps to NM_001085401.1 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:4087874 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:4087911 C>T maps to NM_001085401.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:4099315 G>A maps to NM_001085401.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr6:118790463 G>A maps to NM_001042475.2 N675N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr6:118801627 G>A maps to NM_001042475.2 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:118887279 G>A maps to NM_001042475.2 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:118791735 T>C maps to NM_001042475.2 E662E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr6:74072879 C>T maps to NM_001017361.2 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:74073510 C>T maps to NM_001017361.2 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:74073306 C>T maps to NM_001017361.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr6:74073477 C>T maps to NM_001017361.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:74073402 T>C maps to NM_001017361.2 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:36293090 C>T maps to NM_001010903.4 E379E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr6:36287270 G>A maps to NM_001010903.4 N595N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:36288991 C>T maps to NM_001010903.4 E536E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:36298395 G>A maps to NM_001010903.4 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr6:36287321 C>T maps to NM_001010903.4 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr6:36291298 G>A maps to NM_001010903.4 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:36298146 G>A maps to NM_001010903.4 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:36298164 C>T maps to NM_001010903.4 K101K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr6:36298314 C>T maps to NM_001010903.4 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZU-06A-12D-A196-08 chr6:36288967 T>G maps to NM_001010903.4 A544A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:36287141 C>T maps to NM_001010903.4 E638E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr6:36287210 G>A maps to NM_001010903.4 N615N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:43968436 G>A maps to NM_153246.4 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:31692760 G>A maps to NM_138272.1 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr6:31691440 C>T maps to NM_138272.1 D29D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:31691455 C>T maps to NM_138272.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:31691593 C>T maps to NM_138272.1 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:31691204 C>T maps to NM_138272.1 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr6:31744325 G>A maps to NM_025258.2 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr6:31743953 G>A maps to NM_025258.2 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:31735471 C>T maps to NM_025258.2 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr6:31734071 G>A maps to NM_025258.2 D758D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:31741212 C>T maps to NM_025258.2 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr6:31743738 A>T did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr6:31733505 G>A maps to NM_025258.2 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:31734131 C>A maps to NM_025258.2 P738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:31734952 G>A maps to NM_025258.2 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:157743826 G>A maps to NM_018452.4 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr6:31807419 G>T maps to NM_001040438.1 G70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr6:127911456 G>A maps to NM_001010905.1 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:127898427 G>A maps to NM_001010905.1 W33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr6:127898533 G>A maps to NM_001010905.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:39073312 C>T maps to NM_018322.1 K149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:170155473 G>T maps to NM_018341.1 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr6:170156843 C>A maps to NM_018341.1 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:149901025 C>T maps to NM_138785.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:35716364 C>T maps to NM_145028.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr6:35715111 C>T maps to NM_145028.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr6:35715078 G>A maps to NM_145028.3 W189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr6:35715184 C>T maps to NM_145028.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:35705834 G>A maps to NM_145028.3 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr6:35704965 G>A maps to NM_145028.3 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr6:35715183 C>T maps to NM_145028.3 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr6:36887379 C>T maps to NM_152734.3 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr6:36887379 C>T maps to NM_152734.3 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:36882160 C>T maps to NM_152734.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr6:151865751 G>A maps to ENST00000367290 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr6:151914297 C>T maps to ENST00000367290 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr6:151894589 T>A maps to ENST00000367290 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr6:151936724 G>T maps to ENST00000367290 E627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr6:151936660 G>A maps to ENST00000367290 E605E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:151894334 A>G maps to ENST00000367290 K267K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:151894409 G>A maps to ENST00000367290 K292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:151859283 C>A maps to ENST00000367290 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:151869467 C>T maps to ENST00000367290 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:151907043 C>T maps to ENST00000367290 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:151939179 G>A maps to ENST00000367290 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr6:151939131 C>A maps to ENST00000367290 T673T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr6:151894439 T>A maps to ENST00000367290 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr6:151939192 C>T maps to ENST00000367290 Q694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:151917609 G>A maps to ENST00000367290 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr6:151894514 G>A maps to ENST00000367290 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:151869542 G>A maps to ENST00000367290 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:151865705 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr5:40945457 C>T maps to NM_000587.2 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr5:40936530 G>A maps to NM_000587.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr5:40958181 G>A maps to NM_000587.2 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr5:40936473 G>A maps to NM_000587.2 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:40947795 G>A maps to NM_000587.2 W277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr5:40947852 C>T maps to NM_000587.2 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr5:40958181 G>A maps to NM_000587.2 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:40958352 G>A maps to NM_000587.2 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:40955570 G>A maps to NM_000587.2 E392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr5:40972529 G>A maps to NM_000587.2 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:40958352 G>A maps to NM_000587.2 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr5:40972544 G>A maps to NM_000587.2 Q641Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:40962187 T>C maps to NM_000587.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:40964868 G>A maps to NM_000587.2 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr5:40945391 G>A maps to NM_000587.2 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr5:40981662 G>A maps to NM_000587.2 A840A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr5:40981530 G>A maps to NM_000587.2 E796E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr5:40947852 C>T maps to NM_000587.2 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr5:40981584 G>A maps to NM_000587.2 T814T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:40947777 A>G maps to NM_000587.2 Q271Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:40964868 G>A maps to NM_000587.2 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr5:40958352 G>A maps to NM_000587.2 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:40979841 A>G maps to NM_000587.2 V727V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr7:31735235 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:31735227 C>T maps to NM_006658.4 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:31735137 G>A maps to NM_006658.4 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:86827292 G>A maps to NM_024315.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr7:6639598 C>T maps to NM_024067.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr7:6647683 G>A maps to NM_024067.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:2577996 G>A maps to NM_152743.3 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:2579447 G>A maps to NM_152743.3 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:2582845 G>A maps to NM_152743.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:2583264 G>A maps to NM_152743.3 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr7:2581423 G>A maps to NM_152743.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:2578365 G>A maps to NM_152743.3 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:2578380 G>A maps to NM_152743.3 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr7:2583261 G>T maps to NM_152743.3 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr7:150027559 C>T maps to NM_138434.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:150027717 C>T maps to NM_138434.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr7:150027646 T>C maps to NM_138434.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:150027987 G>A maps to NM_138434.2 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:150027531 G>A maps to NM_138434.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:23339024 G>A maps to NM_138446.1 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:25176354 G>A maps to NM_138811.3 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:25176355 G>A maps to NM_138811.3 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:25176400 G>A maps to NM_138811.3 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:25175866 G>A maps to NM_138811.3 F499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:25181931 G>A maps to NM_138811.3 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr7:25175608 G>A maps to NM_138811.3 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr7:148311285 C>T maps to NM_145304.2 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr7:142637484 G>A maps to NM_178829.4 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:142637499 G>A maps to NM_178829.4 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr7:142636822 G>A maps to NM_178829.4 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:39610211 C>T maps to NM_020192.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:39611995 C>T maps to NM_020192.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr7:66406953 C>T maps to NM_017994.4 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:66410096 C>T maps to NM_017994.4 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:66418262 C>T maps to NM_017994.4 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:99755310 C>T maps to NM_018275.3 Q194Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr7:129856132 G>A maps to NM_145268.3 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:129856018 G>A maps to NM_145268.3 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:129856264 G>A maps to NM_145268.3 E230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr7:23729010 C>T maps to NM_199136.3 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr7:23731109 C>T maps to NM_199136.3 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:100086604 G>T maps to ENST00000423930 E421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr7:100085958 C>T maps to ENST00000423930 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:100086609 G>A maps to ENST00000423930 R422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr7:100086447 C>T maps to ENST00000423930 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:100086273 G>A maps to ENST00000423930 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:100085871 C>T maps to ENST00000423930 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr7:100091297 C>T maps to ENST00000423930 P767P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:100087111 C>T maps to ENST00000423930 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr7:100086078 C>T maps to ENST00000423930 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr7:100085943 C>T maps to ENST00000423930 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:100086624 C>T maps to ENST00000423930 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:100086690 C>T maps to ENST00000423930 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr7:100086054 C>T maps to ENST00000423930 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:100086312 C>T maps to ENST00000423930 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:100086435 G>A maps to ENST00000423930 K364K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:100815611 G>A maps to NM_198571.2 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:100817803 C>T maps to NM_198571.2 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr7:112129971 C>T maps to NM_182597.2 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr7:112129955 C>T maps to NM_182597.2 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:48092410 G>A maps to ENST00000430738 K285K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr7:48089490 C>T maps to ENST00000430738 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr7:120906862 G>T did not map to a codon.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr7:120935498 G>A maps to NM_024913.4 V958V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr7:120906283 C>T maps to NM_024913.4 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:120629734 G>A maps to NM_024913.4 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr7:120876766 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr7:120767262 C>T maps to NM_024913.4 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr7:120907286 C>T maps to NM_024913.4 I884I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:120782128 C>T maps to NM_024913.4 T663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:120906826 C>T maps to NM_024913.4 S866S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr7:120935616 C>T maps to NM_024913.4 R998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:120884391 G>A maps to NM_024913.4 K770K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:120935616 C>T maps to NM_024913.4 R998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr7:120767142 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:120911336 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:120906770 C>T maps to NM_024913.4 L848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:120740015 C>T maps to NM_024913.4 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr7:120884388 G>A maps to NM_024913.4 R769R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:112461938 G>A maps to NM_152556.2 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr7:112535636 C>A maps to NM_152556.2 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:112461984 G>A maps to NM_152556.2 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr7:112462246 C>T maps to NM_152556.2 W257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr7:100054485 G>A maps to ENST00000426357 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:89929368 C>A maps to NM_001039706.2 I682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:89891299 C>T maps to NM_001039706.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:89884765 T>C maps to NM_001039706.2 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr7:89912290 C>T maps to NM_001039706.2 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:92164169 C>T maps to NM_032120.2 N301N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr7:92158879 T>C maps to NM_032120.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr7:92161849 T>C maps to NM_032120.2 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr7:47694917 C>T maps to NM_001123065.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr7:47698747 G>A maps to NM_001123065.1 W126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr7:128097399 C>T maps to NM_001098786.1 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:6370347 G>A maps to NM_001037163.1 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:6370173 C>T maps to NM_001037163.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:57347217 C>T maps to NM_000562.2 R189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr1:57349353 G>A maps to NM_000562.2 K285K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:57347217 C>T maps to NM_000562.2 R189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:57347273 G>A maps to NM_000562.2 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr1:57378167 G>A maps to NM_000562.2 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:57347273 G>A maps to NM_000562.2 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:57347207 G>A maps to NM_000562.2 W185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:57351604 C>T maps to NM_000562.2 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr1:57347207 G>A maps to NM_000562.2 W185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:57333375 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:57347147 G>A maps to NM_000562.2 Q165Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:57406656 C>T maps to NM_000066.2 E421E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:57411608 G>A maps to NM_000066.2 Y330Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:57399071 G>A maps to NM_000066.2 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr1:57417852 C>T maps to NM_000066.2 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:57409438 G>A maps to NM_000066.2 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:57422538 T>C maps to NM_000066.2 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr1:57417852 C>T maps to NM_000066.2 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:57431582 C>T maps to NM_000066.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:57411682 G>A maps to NM_000066.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr1:57411524 G>A maps to NM_000066.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:57422541 C>T maps to NM_000066.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:57425764 G>A maps to NM_000066.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:57411605 C>T maps to NM_000066.2 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr1:57397492 G>A maps to NM_000066.2 S537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:57417762 C>T maps to NM_000066.2 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:57417738 C>T maps to NM_000066.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:57417840 G>A maps to NM_000066.2 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:57417762 C>T maps to NM_000066.2 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:57406575 C>T maps to NM_000066.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:57417738 C>T maps to NM_000066.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:57422541 C>T maps to NM_000066.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:57425698 C>T maps to NM_000066.2 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr8:49985431 C>T maps to NM_001007176.3 Q15*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A20C-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr8:49985419 C>T maps to NM_001007176.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr8:49985397 C>T maps to NM_001007176.3 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr8:144130624 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr8:144124456 G>A maps to NM_173687.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:144126223 G>A maps to NM_173687.2 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr8:69621255 G>A maps to NM_052958.2 R423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr8:69728119 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr8:69434060 C>T maps to NM_052958.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr8:69621312 C>T maps to NM_052958.2 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:69400279 C>T maps to NM_052958.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr8:69688665 G>A maps to NM_052958.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr8:69434032 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:69351777 C>T maps to NM_052958.2 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr8:69621312 C>T maps to NM_052958.2 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:69445292 C>T maps to NM_052958.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:40011116 C>T maps to NM_020130.3 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr8:40011330 C>T maps to NM_020130.3 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr8:40011116 C>T maps to NM_020130.3 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr8:33369705 G>A maps to NM_001102401.1 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:33367356 C>T maps to NM_001102401.1 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:33367347 G>A maps to NM_001102401.1 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:442448 G>A maps to NM_175075.3 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr8:67803269 C>A maps to NM_173518.4 S415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr8:67786586 C>T maps to NM_173518.4 R41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:67808487 C>T maps to NM_173518.4 Q455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr8:67791146 C>T maps to NM_173518.4 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr8:67428238 G>A maps to NM_152765.3 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr8:99102036 G>A maps to NM_173549.2 E264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:99101745 G>A maps to NM_173549.2 K167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr8:22459809 C>T maps to ENST00000450780 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:10555208 C>T maps to NM_001040032.1 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:10555178 C>T maps to NM_001040032.1 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:10555277 G>A maps to NM_001040032.1 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr8:10555382 G>A maps to NM_001040032.1 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr8:10557878 C>T maps to NM_001040032.1 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr8:10557854 G>A maps to NM_001040032.1 Q253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr8:10557905 C>T maps to NM_001040032.1 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:10557839 G>A maps to NM_001040032.1 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:10555133 G>A maps to NM_001040032.1 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr8:124250036 C>A did not map to a codon.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr8:124250169 C>T maps to NM_032847.1 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:124243745 G>A maps to NM_032847.1 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:27880860 C>T maps to ENST00000341513 K788K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr8:27880920 C>T maps to ENST00000341513 A768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr8:27880869 G>A maps to ENST00000341513 S785S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:27903172 G>A maps to ENST00000341513 I439I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr8:27925066 G>A maps to ENST00000341513 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:27931883 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:27888771 G>A maps to ENST00000341513 F632F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr8:27888813 C>T maps to ENST00000341513 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:27886809 C>T maps to ENST00000341513 R709R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:27917998 C>T maps to ENST00000341513 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr8:27888831 C>T maps to ENST00000341513 E612E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:27925192 C>T maps to ENST00000341513 E183E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr8:73993371 C>T maps to NM_153225.3 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:73982116 C>T maps to NM_153225.3 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:73993428 C>T maps to NM_153225.3 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr8:117954885 G>A maps to NM_001025357.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:117954903 C>T maps to NM_001025357.2 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:117954927 G>A maps to NM_001025357.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:38370084 G>A maps to NM_207412.1 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr5:39331857 C>A maps to NM_001737.3 G179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr5:39308392 T>C maps to NM_001737.3 E393E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr5:39315966 G>A maps to NM_001737.3 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr9:98643253 A>T maps to NM_001010895.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:98643394 A>G maps to NM_001010895.2 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:98728845 A>G maps to NM_001010895.2 Q661Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr9:86256506 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr9:27291061 C>T did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr9:27284921 C>T maps to NM_020641.2 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr9:130475121 G>A maps to NM_001012502.2 Q424Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr9:130471739 G>A maps to NM_001012502.2 K67K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr9:130473570 G>A maps to NM_001012502.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr9:131038441 G>A maps to NM_001040011.1 Q6Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr9:104238207 C>T maps to NM_032342.1 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr9:104239062 G>A maps to NM_032342.1 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr9:104238585 C>T maps to NM_032342.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr9:104238336 C>T maps to NM_032342.1 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:104238678 G>A maps to NM_032342.1 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:104238222 G>A maps to NM_032342.1 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:104238435 G>A maps to NM_032342.1 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:104238591 C>T maps to NM_032342.1 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:104239032 G>A maps to NM_032342.1 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:104238323 G>A maps to NM_032342.1 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr9:35819947 C>T maps to NM_001012446.2 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr9:35819899 G>A maps to NM_001012446.2 H280H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr9:35826008 C>T maps to NM_001012446.2 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:96097714 G>A maps to NM_001098808.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:35044974 G>A maps to NM_203299.2 W783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr9:35044893 G>A maps to NM_203299.2 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:35045535 G>A maps to NM_203299.2 G970G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr9:35043983 G>A maps to NM_203299.2 W453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr9:35045502 G>A maps to NM_203299.2 G959G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:35043897 G>A maps to NM_203299.2 W424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:35044527 A>G maps to NM_203299.2 E634E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr9:72521021 C>T maps to NM_001010940.1 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr9:72435857 C>T maps to NM_001010940.1 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr9:72501752 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr9:72471544 G>A maps to NM_001010940.1 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:139929106 C>G maps to NM_207511.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr9:139960000 G>A maps to NM_178448.3 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr9:139887630 C>T maps to NM_183241.1 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:12821461 G>A maps to NM_203403.1 W130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr9:112963359 G>A maps to NM_001012993.2 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr9:112963391 G>A maps to NM_001012993.2 Q186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr9:112969769 G>A maps to NM_001012993.2 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr9:112969849 A>G maps to NM_001012993.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr9:112969736 G>A maps to NM_001012993.2 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:112963359 G>A maps to NM_001012993.2 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:112963671 T>C maps to NM_001012993.2 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:88844512 G>A maps to NM_001010907.1 F2F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr9:139379478 C>T maps to NM_152571.2 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr9:140174064 G>A maps to NM_017723.2 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:89763692 C>T maps to NM_001001709.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:135357734 T>G maps to NM_207417.1 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr9:135374978 C>T maps to NM_207417.1 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:135374954 C>T maps to NM_207417.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:135413077 G>A maps to NM_207417.1 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr9:139741098 C>T maps to NM_001080482.2 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:139741098 C>T maps to NM_001080482.2 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr9:139739777 C>T maps to NM_001080482.2 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:140146306 G>A maps to ENST00000388931 Q76Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr9:99408251 C>T maps to NM_153698.1 W159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr9:99413952 G>A maps to NM_153698.1 Y101Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr9:34610830 G>A maps to NM_148179.1 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr9:34610831 G>A maps to NM_148179.1 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:34611257 G>A maps to NM_148179.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr9:34379724 A>T maps to NM_032596.3 C236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:34397523 G>A maps to NM_032596.3 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr9:34401681 G>A maps to NM_001184940.1 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:97730048 C>T maps to NM_001193329.1 Q628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr9:103204519 C>T maps to NM_001198812.1 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:103204552 C>T maps to NM_001198812.1 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr9:103213196 C>T maps to NM_001198805.1 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr9:77563004 G>A maps to NM_017998.2 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:116176159 C>A maps to ENST00000451722 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr9:5361159 G>A maps to NM_018465.2 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:5361158 G>A maps to NM_018465.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:5361159 G>A maps to NM_018465.2 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr9:91606092 G>A maps to NM_001001938.3 E61E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr9:111812951 G>A maps to NM_032012.3 I625I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr9:111798546 A>G maps to NM_032012.3 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr9:111812630 G>A maps to NM_032012.3 S685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:111812951 G>A maps to NM_032012.3 I625I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr9:86571376 G>A maps to NM_032307.3 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr9:86571208 G>A maps to NM_032307.3 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:4622492 G>A maps to ENST00000454239 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr9:71155628 G>A maps to NM_153237.1 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr9:132595787 G>A maps to NM_016520.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr9:90499836 G>A maps to NM_178828.4 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr9:90502617 C>A maps to NM_178828.4 T1072T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr9:90500778 G>A maps to NM_178828.4 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr9:90501426 C>T maps to NM_178828.4 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr9:90499971 C>T maps to NM_178828.4 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr9:90502478 G>A maps to NM_178828.4 W1026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:90500388 G>A maps to NM_178828.4 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:90497823 C>T maps to NM_178828.4 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr9:90501864 C>T maps to NM_178828.4 S821S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:90500730 C>T maps to NM_178828.4 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:90501771 C>T maps to NM_178828.4 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:90502083 C>T maps to NM_178828.4 F894F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:90503025 G>A maps to NM_178828.4 R1208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:90499515 C>T maps to NM_178828.4 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr9:90499935 G>A maps to NM_178828.4 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr9:90500766 C>T maps to NM_178828.4 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:26842532 G>C maps to NM_024828.3 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr9:26842532 G>A maps to NM_024828.3 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr9:114518603 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:114464452 C>T maps to NM_173521.3 L943L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:114490224 C>A maps to NM_173521.3 E444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr9:114462260 C>T maps to NM_173521.3 G988G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr9:139734636 G>A maps to NM_001173988.1 K655K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr9:139722972 T>G maps to NM_001173988.1 L114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr9:139733721 G>A maps to NM_001173988.1 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:139718064 C>T maps to NM_001173988.1 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr9:95872947 C>T maps to NM_032310.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:135759459 C>T maps to ENST00000372136 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:15745558 C>T maps to NM_173550.2 L867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr9:15591487 C>T maps to NM_173550.2 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:15744359 C>T maps to NM_173550.2 F713F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr9:77684848 G>A maps to NM_017881.2 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr9:136260749 G>A maps to NM_153710.3 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:136265580 G>A maps to NM_153710.3 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:136268833 G>A maps to NM_153710.3 V495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:135702304 G>A maps to NM_152572.2 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:135698622 G>A maps to NM_152572.2 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr8:86244769 G>A maps to NM_001738.3 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:86253847 C>T maps to NM_001738.3 W6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:86240893 G>A maps to NM_001738.3 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr8:86250532 G>A maps to NM_001738.3 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:86249250 G>A maps to NM_001738.3 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr17:50008458 C>T maps to NM_001082534.1 W57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr17:49708944 C>A maps to NM_001082534.1 *329Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:49710990 G>A maps to NM_001082534.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr17:49825169 C>T maps to NM_001082534.1 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr17:50008439 C>T maps to NM_001082534.1 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr17:49710962 G>A maps to NM_001082534.1 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr17:50008394 G>A maps to NM_001082534.1 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:49710966 G>A maps to NM_001082534.1 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:49825031 C>T maps to NM_001082534.1 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:50008439 C>T maps to NM_001082534.1 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:49143140 C>T did not map to a codon.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr15:63631024 G>A maps to NM_001218.3 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr1:150236067 G>A maps to NM_012113.1 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:150235699 G>T maps to NM_012113.1 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr1:150235483 C>T maps to NM_012113.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:150234997 T>G maps to NM_012113.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr8:86392999 C>T maps to NM_000067.2 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:86393017 A>G maps to NM_000067.2 *261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44Q-06A-11D-A25O-08 chr8:86393016 A>G maps to NM_000067.2 *261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr8:86386593 G>A maps to NM_000067.2 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:86389389 C>T maps to NM_000067.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZH-06A-11D-A197-08 chr8:86386611 T>C maps to NM_000067.2 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:86392930 G>A maps to NM_000067.2 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr8:86357410 G>A maps to NM_005181.3 Q157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr8:86351965 C>T maps to NM_005181.3 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:86358414 C>T maps to NM_005181.3 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J6-06A-11D-A19A-08 chr17:58235085 G>A maps to NM_000717.3 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr17:58227436 G>A maps to NM_000717.3 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:58234890 G>A maps to NM_000717.3 K124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr16:87960435 G>A maps to NM_001739.1 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:15794941 T>A did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:15794967 A>G did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:9031029 C>T maps to ENST00000413627 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:9027772 C>T maps to ENST00000413627 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr1:9009403 G>A maps to ENST00000413627 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr1:9019054 C>T maps to ENST00000413627 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:9034705 G>A maps to ENST00000413627 Q294Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:9019054 C>T maps to ENST00000413627 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:9017340 C>T maps to ENST00000413627 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr1:9009478 C>T maps to ENST00000413627 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:66887391 C>T maps to NM_005182.2 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr8:61121412 C>T maps to NM_004056.4 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:61192323 T>C maps to NM_004056.4 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr9:35675788 C>T maps to NM_001216.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr9:35675828 C>T maps to NM_001216.2 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr9:35676142 G>A maps to NM_001216.2 W229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr9:35675827 C>T maps to NM_001216.2 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr9:35680798 C>T maps to NM_001216.2 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:231663608 C>T maps to NM_001130850.1 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:231683274 C>T maps to NM_001130850.1 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:231663563 C>T maps to NM_001130850.1 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr13:49924969 G>A maps to NM_001079670.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr13:49951210 T>G maps to NM_001079670.1 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr13:49951176 G>A maps to NM_001079670.1 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr13:49906097 G>A maps to NM_001079670.1 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20I-06A-11D-A196-08 chr13:49906227 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr13:49885071 G>A maps to NM_001079670.1 Q298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr22:24463102 G>T maps to NM_012295.3 E735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr22:24563274 C>T maps to NM_012295.3 I1892I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr22:24456408 C>T maps to NM_012295.3 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr22:24487736 C>T maps to NM_012295.3 A1242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr22:24563145 C>T maps to NM_012295.3 L1849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr22:24439439 C>T maps to NM_012295.3 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr22:24447307 T>A maps to NM_012295.3 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr22:24451467 C>T maps to NM_012295.3 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr22:24573577 C>T maps to NM_012295.3 P2104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:24451495 C>T maps to NM_012295.3 Q323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:24515547 G>A maps to NM_012295.3 R1505R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr22:24472148 C>T maps to NM_012295.3 S888S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:24561587 C>T maps to NM_012295.3 L1667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr18:20832949 C>T maps to NM_001100619.2 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr18:20837243 C>T maps to NM_001100619.2 F605F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr12:121093969 C>T maps to ENST00000453000 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr12:121099005 C>T maps to NM_001033677.1 R358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:121093969 C>T maps to ENST00000453000 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr12:121098113 C>T maps to NM_001033677.1 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:121098585 C>T maps to NM_001033677.1 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:67287408 G>A maps to NM_016366.2 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:67287309 G>A maps to NM_016366.2 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:67287267 G>A maps to NM_016366.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr11:67287291 G>A maps to NM_016366.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr11:67223181 C>T maps to NM_145200.3 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:67226102 G>A maps to NM_145200.3 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:67223037 C>T maps to NM_145200.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:67222956 C>T maps to NM_145200.3 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr11:67223827 G>A maps to NM_145200.3 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:48547170 G>A maps to NM_019855.3 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr22:30123666 C>T maps to NM_182527.2 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr22:30123649 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr18:21740033 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:21739706 G>A maps to NM_138644.1 Q271Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:21736151 G>A maps to NM_012189.2 K229K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr18:21735698 G>A maps to NM_138644.1 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:65099752 C>G maps to ENST00000371073 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr1:65145290 C>T maps to ENST00000371073 I1086I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:65139131 C>T maps to ENST00000371073 F904F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:65130323 C>T maps to ENST00000371073 S746S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:65099821 G>A maps to ENST00000371073 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:65145411 C>T maps to ENST00000371073 Q1127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:65124443 G>A maps to ENST00000371073 V613V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:65141094 G>A maps to ENST00000371073 T913T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:65113661 C>T maps to ENST00000371073 N445N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr19:13445288 C>T maps to NM_023035.2 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:13410147 G>A maps to NM_023035.2 Q771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:13365962 G>A maps to NM_023035.2 F1571F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:13418658 G>A maps to NM_023035.2 F642F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:13397440 G>A maps to NM_023035.2 S1147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr19:13427929 G>A maps to NM_023035.2 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr19:13419007 G>A maps to NM_023035.2 I614I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:13418658 G>A maps to NM_023035.2 F642F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:13323212 G>A maps to NM_023035.2 S2062S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:13446681 G>A maps to NM_023035.2 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:13428094 C>T maps to NM_023035.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:13409728 C>T maps to NM_023035.2 R910R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr19:13563691 C>T maps to NM_023035.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:13476164 T>C maps to NM_023035.2 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:13346507 G>A maps to NM_023035.2 R1667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:13346508 G>A maps to NM_023035.2 F1666F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:13325356 G>A maps to NM_023035.2 L1937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:13365995 G>A maps to NM_023035.2 Y1560Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:13418658 G>A maps to NM_023035.2 F642F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr19:13325351 G>A maps to NM_023035.2 S1938S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:13409668 C>T maps to NM_023035.2 G930G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:13418658 G>A maps to NM_023035.2 F642F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:13365980 G>A maps to NM_023035.2 F1565F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:13418631 G>A maps to NM_023035.2 F651F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:13338322 C>T maps to NM_023035.2 L1853L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:13476227 G>A maps to NM_023035.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:13565989 C>T maps to NM_023035.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:13397780 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:13423557 G>A maps to NM_023035.2 S532S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:13445273 G>A maps to NM_023035.2 N372N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:13476260 C>T maps to NM_023035.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:13563790 G>A maps to NM_023035.2 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:13414614 G>A maps to NM_023035.2 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr19:13365980 G>A maps to NM_023035.2 F1565F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr19:13340939 C>T maps to NM_023035.2 L1832L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr19:13428133 A>G maps to NM_023035.2 G450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:13443704 C>T maps to NM_023035.2 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:13446672 G>A maps to NM_023035.2 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:13322931 G>A maps to NM_023035.2 L2100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:13366055 G>A maps to NM_023035.2 F1540F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:13386682 G>A maps to NM_023035.2 L1328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:13397554 G>A maps to NM_023035.2 P1109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:13397764 G>T maps to NM_023035.2 S1039S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:13418658 G>A maps to NM_023035.2 F642F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:13423581 G>A maps to NM_023035.2 F524F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:13563772 G>A maps to NM_023035.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr19:13397434 G>A maps to NM_023035.2 I1149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr19:13445222 G>A maps to NM_023035.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:13409890 C>T maps to NM_023035.2 Q856Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr19:13386716 C>T maps to NM_023035.2 W1316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr19:13386717 C>T maps to NM_023035.2 W1316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:13414695 G>A maps to NM_023035.2 I664I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr9:140846796 C>T maps to ENST00000277549 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr9:140953127 C>T maps to ENST00000277549 P1473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr9:141008851 G>A maps to ENST00000277549 K1854K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr9:140952614 C>T maps to ENST00000277549 F1408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr9:140991039 G>A maps to ENST00000277549 W1734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:140850221 C>T maps to ENST00000277549 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:140991054 G>A maps to ENST00000277549 P1739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr9:140953580 C>T maps to ENST00000277549 I1509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:140881233 G>A maps to ENST00000277549 Q635Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:140941379 C>T maps to ENST00000277549 I1147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:141010017 C>T maps to ENST00000277549 S1889S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr9:140777323 C>T maps to ENST00000277549 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr9:140967989 G>A maps to ENST00000277549 L1576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr9:140991031 C>A maps to ENST00000277549 R1732R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr9:140941903 G>A maps to ENST00000277549 V1200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr9:141016069 C>T maps to ENST00000277549 F2214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr9:140851250 G>A maps to ENST00000277549 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:140953055 C>T maps to ENST00000277549 P1449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:140968470 C>T maps to ENST00000277549 L1605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr9:140948323 C>T maps to ENST00000277549 S1279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:141012424 G>A maps to ENST00000277549 E1936E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:140938286 G>A maps to ENST00000277549 V1117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:141016328 C>T maps to ENST00000277549 L2301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr9:141016150 G>A maps to ENST00000277549 Q2241Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr9:140901301 C>T maps to ENST00000277549 S687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr9:140952240 G>A maps to ENST00000277549 K1343K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr9:140878645 C>T maps to ENST00000277549 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr9:140952578 C>T maps to ENST00000277549 F1396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr9:140946618 C>T maps to ENST00000277549 I1263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr9:140946555 G>A maps to ENST00000277549 G1242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:141012396 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:140907669 G>A maps to ENST00000277549 A751A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:140952614 C>T maps to ENST00000277549 F1408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:140953565 G>A maps to ENST00000277549 L1504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:140953625 C>T maps to ENST00000277549 I1524I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:140953628 C>T maps to ENST00000277549 A1525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:140991027 C>T maps to ENST00000277549 F1730F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:140777317 C>T maps to ENST00000277549 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:140953601 C>T maps to ENST00000277549 S1516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:141010044 G>A maps to ENST00000277549 L1898L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr9:140850161 G>A maps to ENST00000277549 K361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr12:2774772 C>T maps to NM_199460.2 I1523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:2705075 G>A maps to NM_199460.2 T900T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:2794988 C>T maps to NM_199460.2 F1970F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr12:2224600 G>A maps to NM_199460.2 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr12:2676816 C>T maps to NM_199460.2 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr12:2676816 C>T maps to NM_199460.2 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr12:2566814 A>T maps to NM_199460.2 K234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr12:2705048 C>T maps to NM_199460.2 L891L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr12:2716176 G>A maps to NM_199460.2 G1099G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:2702412 C>T maps to NM_199460.2 V855V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:2800217 C>T maps to NM_199460.2 P2173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:2676849 C>T maps to NM_199460.2 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr12:2714267 G>A maps to NM_199460.2 V1014V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:2690857 C>T maps to NM_199460.2 S666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:2693742 A>T maps to NM_199460.2 K767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr12:2693693 C>T maps to NM_199460.2 A750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr12:2797803 C>T maps to NM_199460.2 C2075C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:2690824 C>T maps to NM_199460.2 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr12:2774811 C>T maps to NM_199460.2 I1536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr12:2613672 C>T maps to ENST00000399634 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr12:2666140 C>T maps to NM_199460.2 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr12:2788893 G>A maps to NM_199460.2 E1840E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:2706433 C>T maps to NM_199460.2 F944F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:2717742 G>A maps to NM_199460.2 E1161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:2764356 G>A maps to NM_199460.2 R1443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:2786381 C>T maps to NM_199460.2 L1699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:2621980 G>A maps to NM_199460.2 E407E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr12:2721142 G>A maps to NM_199460.2 V1284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:2788662 G>A maps to NM_199460.2 R1763R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:2224707 G>A maps to NM_199460.2 W123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr12:2717802 C>T maps to NM_199460.2 F1181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr12:2690875 C>T maps to NM_199460.2 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:2714933 C>T maps to NM_199460.2 I1066I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:2797630 C>T maps to NM_199460.2 L2018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:2676816 C>T maps to NM_199460.2 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:2714933 C>T maps to NM_199460.2 I1066I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr12:2693744 G>A maps to NM_199460.2 K767K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:2693714 T>A maps to NM_199460.2 A757A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr12:2224707 G>A maps to NM_199460.2 W123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr12:2705038 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr12:2566792 G>A maps to NM_199460.2 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr12:2788690 C>T maps to NM_199460.2 Q1773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:2676816 C>T maps to NM_199460.2 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:2595387 G>A maps to NM_199460.2 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr12:2719801 C>T maps to NM_199460.2 S1238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr12:2705075 G>A maps to NM_199460.2 T900T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr12:2613672 C>T maps to ENST00000399634 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr12:2224480 G>A maps to NM_199460.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:2224555 C>T maps to NM_199460.2 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr12:2706445 T>C maps to NM_199460.2 I948I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr12:2690857 C>T maps to NM_199460.2 S666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:2595294 C>T maps to NM_199460.2 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:2614039 G>A maps to NM_199460.2 W382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:2690851 C>T maps to NM_199460.2 I664I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:2714297 G>A maps to NM_199460.2 R1024R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:2716281 C>T maps to NM_199460.2 F1134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:2717814 C>T maps to NM_199460.2 V1185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:2778187 G>A maps to NM_199460.2 R1619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:2786311 C>T maps to NM_199460.2 Y1675Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:2786978 G>A maps to NM_199460.2 L1727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:2705075 G>A maps to NM_199460.2 T900T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:2711108 C>T maps to NM_199460.2 L1001L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:2705123 C>T maps to NM_199460.2 S916S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr12:2788827 C>T maps to NM_199460.2 A1818A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:53845397 C>T maps to NM_001128840.1 L2151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:53774332 C>T maps to NM_001128840.1 F926F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr3:53785795 C>T maps to NM_001128840.1 A1179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr3:53694300 C>T maps to NM_001128840.1 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:53809999 G>A maps to NM_001128840.1 G1430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr3:53707810 C>T maps to NM_000720.2 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:53787612 C>T maps to NM_001128840.1 S1230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr3:53842754 C>T maps to NM_001128840.1 F1943F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:53769520 C>T maps to NM_001128840.1 F914F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:53707789 G>A maps to NM_000720.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:53778781 C>T maps to NM_001128840.1 S978S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr3:53779703 C>T maps to NM_001128840.1 I1020I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr3:53814127 C>T maps to NM_001128840.1 R1555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:53757635 G>A maps to NM_001128840.1 G614G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:53757542 C>T maps to NM_001128840.1 F583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr3:53699765 C>T maps to NM_001128840.1 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:53845297 G>A maps to NM_001128840.1 G2117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:53736790 C>T maps to NM_001128840.1 I448I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:53757998 C>T maps to NM_001128840.1 F691F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr3:53845309 C>T maps to NM_001128840.1 P2121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:53760924 G>A maps to NM_001128840.1 W707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:53845342 C>T maps to NM_001128840.1 D2132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:53757980 G>A maps to NM_001128840.1 R685R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr3:53781412 C>T maps to NM_001128840.1 F1084F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:53783435 C>T maps to NM_001128840.1 I1152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:53844186 C>T maps to NM_001128840.1 S2018S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:53694249 C>T maps to NM_001128840.1 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:181726162 C>T maps to ENST00000357570 F1410F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr1:181689359 G>A maps to ENST00000357570 R590R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr1:181724449 C>T maps to ENST00000357570 I1302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr1:181732606 G>A maps to ENST00000357570 K1585K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:181727952 C>T maps to ENST00000357570 T1518T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:181705549 C>T maps to ENST00000357570 F1134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr1:181741228 G>A maps to ENST00000357570 E1667E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr1:181740454 G>A maps to ENST00000357570 E1636E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:181706659 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:181706660 G>A maps to ENST00000357570 P1141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:181724440 C>T maps to ENST00000357570 F1299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:181701834 G>A maps to ENST00000357570 R871R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:181735722 C>T maps to ENST00000357570 F1619F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr1:181701795 G>A maps to ENST00000357570 G858G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:181726165 C>G maps to ENST00000357570 P1411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr1:181708320 C>T maps to ENST00000357570 Y1217Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:181726183 C>T maps to ENST00000357570 I1417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:181549869 C>T maps to ENST00000357570 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr1:181702638 C>T maps to ENST00000357570 P1005P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:181689960 C>T maps to ENST00000357570 T642T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:181727216 C>T maps to ENST00000357570 I1488I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:181767825 C>T maps to ENST00000357570 I2266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:181479681 T>A maps to ENST00000357570 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:181480508 G>A maps to ENST00000357570 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:181702758 C>T maps to ENST00000357570 V1045V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:181727982 G>A maps to ENST00000357570 K1528K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:181745295 C>T maps to ENST00000357570 S1733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:181754865 C>T maps to ENST00000357570 F1899F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:181767714 C>T maps to ENST00000357570 S2229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr1:181726162 C>T maps to ENST00000357570 F1410F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:181549845 C>T maps to ENST00000357570 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:181726090 G>A maps to ENST00000357570 E1386E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:181687204 C>T maps to ENST00000357570 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:181702149 G>A maps to ENST00000357570 E976E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:181732645 G>A maps to ENST00000357570 W1598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:181727102 C>T maps to ENST00000357570 A1450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:181741225 G>A maps to ENST00000357570 Q1666Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:181767741 C>T maps to ENST00000357570 D2238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:181480568 C>T maps to ENST00000357570 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:181701969 G>A maps to ENST00000357570 Q916Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:181745301 C>T maps to ENST00000357570 I1735I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:181767549 C>T maps to ENST00000357570 S2174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:181689431 C>T maps to ENST00000357570 I614I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr1:181767810 C>T maps to ENST00000357570 G2261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:181705456 G>A maps to ENST00000357570 E1103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:181741342 C>T maps to ENST00000357570 S1705S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:181754920 C>T maps to ENST00000357570 L1918L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:181726162 C>T maps to ENST00000357570 F1410F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:181690985 C>T maps to ENST00000357570 F683F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:181686316 C>T maps to ENST00000357570 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:181754460 C>T maps to ENST00000357570 D1862D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:181767783 C>T maps to ENST00000357570 F2252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:181759673 C>T maps to ENST00000357570 F1960F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:181620514 C>T maps to ENST00000357570 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:181725181 G>A maps to ENST00000357570 W1360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:181725112 G>A maps to ENST00000357570 E1337E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:181767744 C>T maps to ENST00000357570 S2239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:181727964 C>T maps to ENST00000357570 S1522S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr1:181767711 C>T maps to ENST00000357570 I2228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr1:181701871 C>T maps to ENST00000357570 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr1:181706659 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr1:181765864 G>A maps to ENST00000357570 K2090K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:181705456 G>A maps to ENST00000357570 E1103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr1:181684486 C>T maps to ENST00000357570 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:181480565 G>A maps to ENST00000357570 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:181546988 C>T maps to ENST00000357570 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:181620504 G>A maps to ENST00000357570 W328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:181689428 C>T maps to ENST00000357570 F613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:181702137 G>A maps to ENST00000357570 T972T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:181708303 C>T maps to ENST00000357570 L1212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:181726162 C>T maps to ENST00000357570 F1410F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:181732561 C>T maps to ENST00000357570 F1570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:181745298 C>T maps to ENST00000357570 S1734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:181752864 C>T maps to ENST00000357570 F1805F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:181701792 G>A maps to ENST00000357570 K857K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:181707531 G>A maps to ENST00000357570 T1194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:181726084 G>A maps to ENST00000357570 V1384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:181767783 C>T maps to ENST00000357570 F2252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr1:181740487 G>A maps to ENST00000357570 R1647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:181695217 A>G maps to ENST00000357570 E720E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:181754847 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr1:181754943 C>T maps to ENST00000357570 P1925P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:181700322 G>A maps to ENST00000357570 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:181767534 C>T maps to ENST00000357570 L2169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr23:49062996 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:49081430 A>G did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:49063310 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:49071631 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:49074212 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:49079201 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:49069182 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:49088166 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:49063014 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:49072915 A>C did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:49089750 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:49071938 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:49071939 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr23:49061614 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:49063531 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:49061644 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:49061645 A>T did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:49061779 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:49072961 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:49068735 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr23:49072879 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:49070636 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:49081360 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:49066809 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:49069132 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:49068392 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:49075367 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr23:49066206 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:49071987 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:49079546 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:49071669 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:49087450 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr23:49063546 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:49061739 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:49062077 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:49067927 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:49081360 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr23:49063568 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr17:48696107 C>T maps to NM_018896.3 F1840F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr17:48678420 C>T maps to NM_018896.3 L1267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr17:48678421 C>T maps to NM_018896.3 L1268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr17:48683416 G>A maps to NM_198397.1 V1485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr17:48669189 C>T maps to NM_018896.3 L910L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr17:48696257 C>T maps to NM_018896.3 F1890F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:48683299 C>T maps to NM_018896.3 T1446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:48703970 C>T maps to NM_018896.3 L2331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:48701284 G>A maps to NM_018896.3 T2026T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:48646308 C>T maps to NM_018896.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:48678453 C>T maps to NM_018896.3 F1278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:48696262 G>A maps to NM_018896.3 W1892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr17:48696107 C>T maps to NM_018896.3 F1840F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:48701350 C>T maps to NM_018896.3 P2048P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr17:48652935 G>A maps to NM_018896.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:48678462 G>A maps to NM_018896.3 V1281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:48680200 C>T maps to NM_018896.3 L1312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:48678507 G>A maps to NM_018896.3 E1296E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:48703397 C>T maps to NM_018896.3 S2140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:48694933 T>C did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:48701832 C>T maps to NM_018896.3 I2114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr17:48667890 C>T maps to NM_018896.3 A787A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr17:48695410 G>A maps to NM_018896.3 V1743V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:48683278 C>T maps to NM_018896.3 F1439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:48652917 C>T maps to NM_018896.3 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:48678420 C>T maps to NM_018896.3 L1267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:48678421 C>T maps to NM_018896.3 L1268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:48668807 C>T maps to NM_018896.3 I822I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:48695652 C>T maps to NM_018896.3 F1792F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:48646257 C>T maps to NM_018896.3 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:48649320 C>T maps to NM_018896.3 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:48678465 C>T maps to NM_018896.3 V1282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:48697079 C>T maps to NM_018896.3 Q1940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr17:48646647 C>T maps to NM_018896.3 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr16:1261269 C>T maps to NM_021098.2 I1442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:1265069 C>T maps to NM_021098.2 F1676F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr16:1270405 G>A maps to NM_021098.2 A2158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:1268385 G>A maps to NM_021098.2 A1874A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr16:1254292 G>A maps to NM_021098.2 R762R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr16:1255220 C>T maps to NM_021098.2 I853I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:1261965 C>T maps to NM_021098.2 P1529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr16:1250534 C>T maps to NM_021098.2 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr16:1261717 C>T maps to NM_021098.2 A1493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr16:1254208 C>T maps to NM_021098.2 V734V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:1258082 C>T maps to NM_021098.2 P1075P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:1265265 C>T maps to NM_021098.2 I1688I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:1270843 A>G maps to NM_021098.2 E2304E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:1270243 C>T maps to NM_021098.2 I2104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:1256115 C>T maps to NM_021098.2 I872I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr16:1260872 C>T maps to NM_021098.2 S1375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:1268000 C>T maps to NM_021098.2 F1802F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:1270150 C>T maps to NM_021098.2 T2073T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:1260920 C>T maps to NM_021098.2 I1391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:1246000 C>T maps to NM_021098.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:1250393 C>T maps to NM_021098.2 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:1245496 G>A maps to NM_021098.2 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr16:1260629 C>T maps to NM_021098.2 F1339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr16:1261269 C>T maps to NM_021098.2 I1442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:1254327 G>A maps to NM_021098.2 W774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:1254328 G>A maps to NM_021098.2 W774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr16:1261530 C>T maps to NM_021098.2 I1467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:1248753 C>T maps to NM_021098.2 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:1254124 C>T maps to NM_021098.2 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:1258014 C>T maps to NM_021098.2 L1053L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:1260590 C>T maps to NM_021098.2 V1326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:1262100 G>A maps to NM_021098.2 E1574E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:1270552 C>T maps to NM_021098.2 S2207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr16:1250534 C>T maps to NM_021098.2 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr16:1250321 C>A maps to NM_021098.2 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr16:1261263 C>T maps to NM_021098.2 F1440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr16:1260794 C>T maps to NM_021098.2 A1349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr22:39966858 C>T maps to NM_021096.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:40064307 C>T maps to NM_021096.3 S1372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr22:40057216 C>T maps to NM_021096.3 R935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr22:40073354 C>T maps to NM_021096.3 L1622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:40015313 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:40064361 G>A maps to NM_021096.3 L1390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:40075812 C>T maps to NM_021096.3 S1827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:40078598 C>T maps to NM_021096.3 F1921F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:40036907 G>A maps to NM_021096.3 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr22:39996601 G>A maps to NM_021096.3 K142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr22:40045902 C>T maps to NM_021096.3 V655V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr22:40064310 C>T maps to NM_021096.3 L1373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr22:40030691 C>T maps to NM_021096.3 L235L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A2MC-06A-12D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:40059776 C>T maps to NM_021096.3 V1176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr22:40066865 C>T maps to NM_021096.3 S1482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr22:40030576 G>A maps to NM_021096.3 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr22:40076987 C>T maps to NM_021096.3 S1865S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr22:40061887 C>T maps to NM_021096.3 L1327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:39966936 C>T maps to NM_021096.3 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:40061577 C>T maps to NM_021096.3 I1309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr22:39966825 G>A maps to NM_021096.3 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr22:40073344 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr22:40060862 C>G maps to NM_021096.3 A1262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr22:40055853 G>A maps to NM_021096.3 A867A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr22:40056381 C>T maps to NM_021096.3 Q880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr22:40069004 C>T maps to NM_021096.3 T1567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:39966858 C>T maps to NM_021096.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:40037087 G>A maps to NM_021096.3 W319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:40045875 C>T maps to NM_021096.3 I646I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:40061890 C>T maps to NM_021096.3 F1328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr22:40037159 C>T maps to NM_021096.3 I343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr1:201063041 C>T maps to NM_000069.2 W122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr1:201047232 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:201030571 G>A maps to NM_000069.2 S1026S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:201009204 C>T maps to NM_000069.2 L1792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr1:201046164 G>A maps to NM_000069.2 I570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:201031121 G>A maps to NM_000069.2 L1001L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr1:201028412 C>T maps to NM_000069.2 S1143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr1:201046173 G>A maps to NM_000069.2 F567F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:201017722 C>T maps to NM_000069.2 K1476K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:201054597 C>T maps to NM_000069.2 Q372Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:201060903 C>T maps to NM_000069.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:201063032 C>T maps to NM_000069.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:201039455 C>T maps to NM_000069.2 E768E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:201063146 C>T maps to NM_000069.2 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:201043665 C>T maps to NM_000069.2 K677K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:201013572 C>T maps to NM_000069.2 R1560R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:201031214 G>A maps to NM_000069.2 G970G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:201030529 C>T maps to NM_000069.2 E1040E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:201028334 G>A maps to NM_000069.2 L1169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:201028417 G>A maps to NM_000069.2 Q1142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:201042676 C>T maps to NM_000069.2 K719K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:201035025 G>A maps to NM_000069.2 I931I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:201030529 C>T maps to NM_000069.2 E1040E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:201008963 G>A maps to NM_000069.2 L1873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:201038276 C>T maps to NM_000069.2 E846E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:201046155 G>A maps to NM_000069.2 F573F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:201012515 G>A maps to NM_000069.2 F1647F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:201039491 G>A maps to NM_000069.2 P756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:201043644 C>T maps to NM_000069.2 R684R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:201035037 G>A maps to NM_000069.2 T927T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:201047152 G>A maps to NM_000069.2 Y491Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:201081344 C>T maps to NM_000069.2 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:201009481 G>A maps to NM_000069.2 S1749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:201047095 C>T maps to NM_000069.2 E510E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:201052398 G>A maps to NM_000069.2 I428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:201028385 G>A maps to NM_000069.2 I1152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr1:201052413 C>T maps to NM_000069.2 W423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:201030460 G>A maps to NM_000069.2 F1063F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:201010695 G>A maps to NM_000069.2 F1690F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:201016710 C>T maps to NM_000069.2 K1495K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:201023683 G>A maps to NM_000069.2 F1205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:201063041 C>T maps to NM_000069.2 W122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:201081318 C>T maps to NM_000069.2 W50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:201035007 G>A maps to NM_000069.2 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:201046155 G>A maps to NM_000069.2 F573F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr1:201009791 C>T maps to NM_000069.2 Q1728Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:201035067 C>T maps to NM_000069.2 V917V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:81579767 G>A maps to NM_000722.2 I1072I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:81598212 A>C maps to NM_000722.2 L795L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr7:81591789 G>A maps to NM_000722.2 L934L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:81600001 A>C maps to NM_000722.2 V731V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:81579778 G>A maps to NM_000722.2 L1069L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:81599242 C>T maps to NM_000722.2 R754R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr7:81746401 G>A maps to NM_000722.2 Q162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr3:50403275 G>A maps to ENST00000435965 F967F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:50416521 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:50413308 G>A maps to ENST00000435965 I592I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr3:50402201 G>A maps to ENST00000435965 F1119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:50413429 G>A maps to ENST00000435965 F579F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:50413428 G>A maps to ENST00000435965 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:50513578 C>T maps to ENST00000435965 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:50416865 C>T maps to ENST00000435965 Q383Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:50421648 G>A maps to ENST00000435965 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr3:50414963 C>T maps to ENST00000435965 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:50413308 G>A maps to ENST00000435965 I592I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr3:50425040 C>T maps to ENST00000435965 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:54913094 G>A maps to NM_018398.2 V587V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr3:54676165 G>A maps to NM_018398.2 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr3:54930826 C>T maps to NM_018398.2 F766F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:54676195 C>T maps to NM_018398.2 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr3:54930799 G>A maps to NM_018398.2 K757K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:54537681 G>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:54676262 C>T maps to NM_018398.2 R388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:55052248 G>A maps to NM_018398.2 Q964Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr3:54913091 G>A maps to NM_018398.2 E586E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr3:54919609 C>T maps to NM_018398.2 Q685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr3:54914840 C>T maps to NM_018398.2 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr3:55052248 G>A maps to NM_018398.2 Q964Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr3:54798352 G>A maps to NM_018398.2 W452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:55052317 G>A maps to NM_018398.2 G987G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:55002513 G>A maps to NM_018398.2 R829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:55052317 G>A maps to NM_018398.2 G987G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:54919306 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:54604067 G>A maps to NM_018398.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:54661842 C>T maps to NM_018398.2 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr3:55052299 C>T maps to NM_018398.2 T981T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr3:54919338 C>T maps to NM_018398.2 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr3:54537565 G>A maps to NM_018398.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:54604010 C>T maps to NM_018398.2 D256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:54604064 C>T maps to NM_018398.2 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:54913435 C>T maps to NM_018398.2 F614F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:54925475 C>T maps to NM_018398.2 Q749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr3:55107558 C>T maps to NM_018398.2 I1025I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr3:54537586 G>A maps to NM_018398.2 K150K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:54420800 G>A maps to NM_018398.2 Q127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:54604067 G>A maps to NM_018398.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:54661818 C>T maps to NM_018398.2 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:54798329 C>T maps to NM_018398.2 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:54798335 G>A maps to NM_018398.2 Q446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:54914861 C>T maps to NM_018398.2 F628F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:54922001 C>T maps to NM_018398.2 I691I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:55002507 C>T maps to NM_018398.2 F827F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:55108197 C>T maps to NM_018398.2 L1081L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr3:55052305 G>A maps to NM_018398.2 K983K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr3:55043453 C>T maps to NM_018398.2 S953S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr3:54604067 G>A maps to NM_018398.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr3:54661842 C>T maps to NM_018398.2 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr12:2019086 G>A maps to NM_172364.4 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:1965211 G>A maps to NM_172364.4 I706I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr12:1965395 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr12:1953598 G>A maps to NM_172364.4 F813F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:1995403 G>A maps to NM_172364.4 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:2016687 G>A maps to NM_172364.4 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:2027549 G>T maps to NM_172364.4 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr12:1983817 C>T maps to NM_172364.4 R610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:1963202 C>T maps to NM_172364.4 E720E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:2027447 G>A maps to NM_172364.4 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr12:1995502 C>T maps to NM_172364.4 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:1965395 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr12:1995502 C>T maps to NM_172364.4 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr12:1967791 G>A maps to NM_172364.4 S653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr12:1983829 G>A maps to NM_172364.4 A606A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr12:1983817 C>T maps to NM_172364.4 R610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:1953643 G>A maps to NM_172364.4 F798F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:1953694 C>T maps to NM_172364.4 R781R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:1994035 G>A maps to NM_172364.4 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:1996225 C>T maps to NM_172364.4 W264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:2017125 G>A maps to NM_172364.4 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:2022194 C>T maps to NM_172364.4 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr12:1994044 G>A maps to NM_172364.4 F387F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:37331556 G>A maps to NM_000723.3 N562N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:37340359 G>A maps to NM_000723.3 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:18803288 C>T maps to NM_201596.2 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr10:18828607 G>A maps to NM_201596.2 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:18789874 C>T maps to NM_201596.2 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr10:18803446 G>A maps to NM_201593.2 Q226Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:18828562 G>A maps to NM_201596.2 K631K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:18823029 G>A maps to NM_201596.2 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:18828607 G>A maps to NM_201596.2 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:49221399 G>A maps to NM_000725.2 E391E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:152739781 G>A maps to NM_000726.3 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr2:152695706 G>A maps to NM_000726.3 Q497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr2:152695707 G>A maps to NM_000726.3 Y496Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:152698470 C>T maps to NM_000726.3 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr2:152737313 C>T maps to NM_000726.3 E130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:152729005 T>A maps to NM_000726.3 K175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:152739782 G>A maps to NM_000726.3 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:152698470 C>T maps to NM_000726.3 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:152695832 G>A maps to NM_000726.3 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:65040976 G>A maps to NM_000727.3 K67K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr22:36983515 G>A maps to NM_006078.3 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr22:37098495 G>A maps to NM_006078.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr22:36960622 G>A maps to NM_006078.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr22:36960715 G>A maps to NM_006078.3 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr22:36962538 C>T maps to NM_006078.3 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr22:37098430 C>T maps to NM_006078.3 W64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:36983515 G>A maps to NM_006078.3 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr22:36960481 G>A maps to NM_006078.3 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:36960532 C>T maps to NM_006078.3 K279K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr16:24373081 C>T maps to NM_006539.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr16:24268230 G>A maps to NM_006539.3 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr16:24358115 G>A maps to NM_006539.3 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr16:24372985 C>T maps to NM_006539.3 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr16:24366208 C>T maps to NM_006539.3 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:24372880 C>T maps to NM_006539.3 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:24372923 C>T maps to NM_006539.3 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:24372901 C>T maps to NM_006539.3 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:24373006 C>T maps to NM_006539.3 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:24373006 C>T maps to NM_006539.3 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:24372778 C>T maps to NM_006539.3 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr16:24268164 G>A maps to NM_006539.3 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr16:24373177 C>T maps to NM_006539.3 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:24358082 C>T maps to NM_006539.3 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr16:24358082 C>T maps to NM_006539.3 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:24358082 C>T maps to NM_006539.3 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr16:24358082 C>T maps to NM_006539.3 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:24366208 C>T maps to NM_006539.3 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:24268269 G>A maps to NM_006539.3 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr16:24373117 C>T maps to NM_006539.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr17:65026930 C>T maps to NM_014405.3 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr17:65021057 G>A maps to NM_014405.3 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr17:65020988 C>T maps to NM_014405.3 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr17:65021057 G>A maps to NM_014405.3 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr17:65026606 C>T maps to NM_014405.3 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:64880765 C>T maps to NM_014404.1 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:64880762 C>T maps to NM_014404.1 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:64880636 C>T maps to NM_014404.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:64873458 C>T maps to NM_014404.1 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:64881221 C>T maps to NM_145811.2 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:64875093 G>A maps to NM_014404.1 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:64880906 C>T maps to NM_014404.1 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:64873548 G>A maps to NM_014404.1 W33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:64880831 G>A maps to NM_014404.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:64880990 C>T maps to NM_014404.1 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr17:64881024 C>T maps to NM_014404.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr17:64880684 G>A maps to NM_014404.1 E159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr19:54501562 G>A maps to NM_145814.1 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr19:54515286 G>A maps to NM_145814.1 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr19:54445411 C>T maps to NM_031896.4 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:54445474 C>T maps to NM_031896.4 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:54418664 C>T maps to NM_031896.4 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:54417817 G>A maps to NM_031896.4 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:54483245 C>T maps to NM_031895.5 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:54466542 C>T maps to NM_031895.5 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54466656 C>T maps to NM_031895.5 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr2:27462329 C>T maps to NM_004341.3 I1795I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:27457492 C>T maps to NM_004341.3 I1242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:27446838 C>T maps to NM_004341.3 F350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:27465618 C>T maps to NM_004341.3 F2118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr2:27457438 C>T maps to NM_004341.3 P1224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:27457093 G>A maps to NM_004341.3 K1206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr2:27444201 C>T maps to NM_004341.3 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr2:27445436 C>T maps to NM_004341.3 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr2:27456997 C>T maps to NM_004341.3 I1174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:27456982 C>T maps to NM_004341.3 T1169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:27461300 C>T maps to NM_004341.3 I1621I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:27456397 C>T maps to NM_004341.3 D1070D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:27455059 C>T maps to NM_004341.3 F871F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:27444207 C>T maps to NM_004341.3 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:27458129 C>T maps to NM_004341.3 F1268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:27458231 C>T maps to NM_004341.3 A1302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:27465589 C>T maps to NM_004341.3 L2109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:27465618 C>T maps to NM_004341.3 F2118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:115099881 G>A maps to NM_014333.3 H224H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:115102180 G>A maps to NM_014333.3 Q152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:115080360 G>A maps to NM_014333.3 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:85961619 G>T maps to NM_153184.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:85961589 C>T maps to NM_153184.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:86010690 G>A maps to NM_153184.3 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:85961583 G>A maps to NM_153184.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:86010708 C>T maps to NM_153184.3 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:86010786 C>T maps to NM_153184.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:86114834 C>T maps to NM_153184.3 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:159166698 G>A maps to NM_021189.3 W301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:159170696 G>A maps to NM_021189.3 K428K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:159163702 C>T maps to NM_021189.3 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:159169544 C>T maps to NM_021189.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:159169595 C>T maps to NM_021189.3 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:159141569 C>T maps to NM_021189.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:159163753 G>A maps to NM_021189.3 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:159166836 C>T maps to NM_021189.3 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:159170684 G>A maps to NM_021189.3 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:159170711 G>A maps to NM_021189.3 *433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:159163738 G>A maps to NM_021189.3 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:44128287 G>A maps to NM_145296.1 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:44131341 G>A maps to NM_145296.1 Q114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr19:44130961 C>T maps to NM_145296.1 W158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr19:44131904 C>T maps to NM_145296.1 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr19:44130996 G>A maps to NM_145296.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr3:62477974 G>A maps to ENST00000383709 L958L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:62423847 G>A maps to ENST00000383709 F1241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:62501818 C>T maps to ENST00000383709 E832E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:62535632 T>C maps to ENST00000383709 K637K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:62518604 G>A maps to ENST00000383709 I744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr3:62522182 G>A maps to ENST00000383709 S680S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:62499337 G>A maps to NM_183394.2 A875A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:62751563 A>C maps to ENST00000383709 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr3:62518604 G>A maps to ENST00000383709 I744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr3:62631467 G>A maps to ENST00000383709 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:62543092 G>A maps to ENST00000383709 T580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:62451122 G>A maps to ENST00000383709 F1190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr7:122078449 G>A maps to NM_001167940.1 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:122261756 G>A maps to NM_001167940.1 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:121960380 C>T maps to NM_001167940.1 R1247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:122114437 G>A maps to NM_001167940.1 C665C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:122111484 G>A maps to NM_001167940.1 D710D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:122377020 C>T maps to NM_001167940.1 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:122194650 G>A maps to NM_001167940.1 I476I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:122091456 G>A maps to NM_001167940.1 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr7:122131378 G>A maps to NM_001167940.1 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:122047606 G>A maps to NM_001167940.1 F915F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:121960386 G>A maps to NM_001167940.1 T1245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:122019442 G>A maps to NM_001167940.1 I1126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:121960373 G>A maps to NM_001167940.1 R1250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:122377071 G>A maps to NM_001167940.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr7:122091462 G>A maps to NM_001167940.1 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:122033544 G>A maps to NM_001167940.1 I950I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr6:7355290 G>A maps to NM_001170692.1 S784S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr6:7379052 T>A maps to NM_001170692.1 K162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:7373626 C>T maps to NM_001170692.1 R475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:7373614 G>A maps to NM_001170692.1 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:7373577 G>A maps to NM_001170692.1 Q492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:7374328 C>T maps to NM_001170692.1 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:7355323 G>A maps to NM_001170692.1 I773I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:91081393 C>T maps to NM_004929.2 E101E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:91094892 G>A maps to NM_004929.2 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr8:91081276 C>T maps to NM_004929.2 W107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:91075653 C>T maps to NM_004929.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr16:71411601 C>T maps to NM_001740.4 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr16:71418717 G>A maps to NM_001740.4 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr16:71411568 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:71423650 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr16:71411589 C>T maps to NM_001740.4 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr16:71418265 C>T maps to NM_001740.4 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr16:71408688 C>T maps to NM_001740.4 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:71423698 C>T maps to NM_001740.4 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:71417913 C>T maps to NM_001740.4 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:71423713 G>A maps to NM_001740.4 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr11:14992729 G>A maps to NM_001741.2 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:15098930 C>T maps to NM_000728.3 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr11:15098930 C>T maps to NM_000728.3 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr12:54117526 G>A maps to NM_020898.2 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:54109720 G>A maps to NM_020898.2 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:54107532 G>A maps to NM_020898.2 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:54107573 G>A maps to NM_020898.2 R568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr17:46926727 C>T maps to ENST00000448105 Q202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:46925442 C>T maps to ENST00000448105 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:93073038 G>A maps to NM_001164737.1 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:93098037 G>A maps to NM_001164737.1 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:93065371 G>A maps to NM_001164737.1 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:93106957 C>T maps to NM_001164737.1 W94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:93090201 C>T maps to NM_001164737.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr7:93101799 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:93055754 C>T maps to NM_001164737.1 E480E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr7:93067371 C>T maps to NM_001164737.1 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:93090138 C>T maps to NM_001164737.1 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:93098046 C>T maps to NM_001164737.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:93098091 A>G maps to NM_001164737.1 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:93106912 G>A maps to NM_001164737.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:93098043 C>T maps to NM_001164737.1 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr7:93065371 G>A maps to NM_001164737.1 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:188225439 C>T maps to NM_005795.4 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:188216658 G>A maps to NM_005795.4 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:188228120 G>A maps to NM_005795.4 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:188225385 G>A maps to NM_005795.4 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:188225373 G>A maps to NM_005795.4 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:188216917 G>A maps to NM_005795.4 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:188216843 G>A maps to NM_005795.4 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:188247996 C>T maps to NM_005795.4 E29E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:188216984 G>A maps to NM_005795.4 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr7:134625905 C>T maps to NM_033138.3 R484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:134613621 C>T maps to NM_033138.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr7:134625949 C>T maps to NM_033138.3 F498F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:134617987 C>T maps to NM_033138.3 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:134617988 C>T maps to NM_033138.3 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr10:105218493 G>A maps to NM_001001412.3 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:105215173 G>A maps to NM_001001412.3 Q296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr10:105215177 C>T maps to NM_001001412.3 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:105218355 G>A maps to NM_001001412.3 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:105215116 G>A maps to NM_001001412.3 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:90870296 C>T maps to NM_006888.4 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:5567392 G>A maps to NM_005185.2 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr10:5567294 G>T maps to NM_005185.2 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:5567255 C>T maps to NM_005185.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr10:5567350 C>T maps to NM_005185.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr10:5541193 G>A maps to NM_017422.4 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:5541146 G>A maps to NM_017422.4 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr10:5541194 G>A maps to NM_017422.4 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:1848628 G>A maps to NM_138705.2 Q181Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:71275405 C>T maps to NM_031468.3 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:71275405 C>T maps to NM_031468.3 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:71275384 G>A maps to NM_031468.3 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:71743779 G>A maps to NM_031468.3 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr7:71252846 C>T maps to NM_031468.3 K233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr7:71275405 C>T maps to NM_031468.3 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:71743779 G>A maps to NM_031468.3 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:71252858 G>A maps to NM_031468.3 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr19:16590073 C>T maps to NM_145046.3 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr19:16601310 C>T maps to NM_145046.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr7:128409142 C>T maps to ENST00000342367 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:128409142 C>T maps to ENST00000342367 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:128409142 C>T maps to ENST00000342367 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:135140381 C>T maps to NM_015722.3 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:9804896 C>T maps to NM_003656.3 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:9804606 C>T maps to NM_003656.3 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:9802388 C>T maps to NM_003656.3 K232K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:9799446 C>T maps to NM_003656.3 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr3:9799437 C>T maps to NM_003656.3 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:9799446 C>T maps to NM_003656.3 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:12595298 G>A maps to NM_153498.2 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr10:12708734 G>A maps to NM_153498.2 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr10:12858326 G>A maps to NM_153498.2 W278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:12858258 C>T maps to NM_153498.2 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr10:12595229 C>T maps to NM_153498.2 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:12866546 G>A maps to NM_153498.2 W306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr1:209776594 C>T maps to NM_020439.2 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:209785201 G>A maps to NM_020439.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:209782327 C>T maps to NM_020439.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:209773326 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:209785559 C>T maps to NM_020439.2 Q447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:209768396 C>T maps to NM_020439.2 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:209786147 C>T maps to NM_020439.2 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:209782414 C>T maps to NM_020439.2 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:209778983 C>T maps to NM_020439.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr5:149602589 G>A maps to NM_015981.3 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr5:149652700 T>C maps to NM_015981.3 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:149631318 G>A maps to NM_015981.3 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:149627350 G>A maps to NM_015981.3 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr5:149602637 C>T maps to NM_015981.3 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:44259810 G>A maps to NM_001220.4 I617I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:44283054 G>A maps to NM_001220.4 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:44282235 G>A maps to NM_001220.4 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:44286757 G>A maps to NM_001220.4 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:44323760 C>T maps to NM_001220.4 K43K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr7:44302604 G>A maps to NM_001220.4 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr7:44294151 C>T maps to NM_001220.4 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr7:44302631 G>A maps to NM_001220.4 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr4:114378552 G>A maps to ENST00000515496 R468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:114438808 G>A maps to ENST00000515496 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:114378624 C>T maps to ENST00000515496 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr10:75608801 G>A maps to ENST00000423381 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr10:75574907 G>A maps to ENST00000423381 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr10:75607050 G>A maps to ENST00000423381 Q251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:75607823 G>A maps to ENST00000423381 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr10:75634171 G>A maps to ENST00000423381 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr10:75576874 C>T maps to ENST00000423381 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:75634153 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:110820145 G>A maps to NM_001744.4 V468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr5:110710561 C>T maps to NM_001744.4 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr5:110820040 G>A maps to NM_001744.4 E433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:110782472 C>T maps to NM_001744.4 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:110710561 C>T maps to NM_001744.4 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:110809048 G>A maps to NM_001744.4 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:110710561 C>T maps to NM_001744.4 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr5:110820013 G>A maps to NM_001744.4 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr5:110784842 T>C maps to NM_001744.4 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:110730465 C>T maps to NM_001744.4 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:110819734 G>A maps to NM_001744.4 K331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr5:110710561 C>T maps to NM_001744.4 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr17:3773124 G>T maps to ENST00000381771 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:3773148 G>A maps to ENST00000381771 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr17:3788758 G>A maps to ENST00000381771 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr12:121712109 G>A maps to NM_006549.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:121691198 G>A maps to NM_006549.3 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:121691198 G>A maps to NM_006549.3 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr12:121711954 G>A maps to NM_006549.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr12:121711906 G>A maps to NM_006549.3 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:121683010 G>A maps to NM_006549.3 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:121682390 G>A maps to NM_006549.3 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr3:49898611 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:49898694 C>T maps to NM_024046.3 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:49897932 G>A maps to NM_024046.3 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:49898377 G>A maps to NM_024046.3 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:49897116 G>A maps to NM_024046.3 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr3:49899545 C>T maps to NM_024046.3 K53K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:49898257 C>T maps to NM_024046.3 E222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr5:134086594 C>T maps to NM_001745.2 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr9:138719359 G>A maps to ENST00000409386 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:138712876 G>A maps to ENST00000409386 S1221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:138714532 G>A maps to ENST00000409386 F669F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:138714337 G>A maps to ENST00000409386 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr9:138742012 G>A maps to ENST00000409386 Q350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:138713008 G>A maps to ENST00000409386 F1177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr9:138719413 G>A maps to ENST00000409386 H365H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr9:138714454 G>A maps to ENST00000409386 A695A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:138713689 G>A maps to ENST00000409386 Y950Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:138713956 G>A maps to ENST00000409386 A861A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:138714532 G>A maps to ENST00000409386 F669F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:200818530 A>G maps to ENST00000236925 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr1:200826531 C>T maps to ENST00000236925 Q1382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr1:200826982 C>A maps to ENST00000236925 I1422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:7724070 C>T maps to NM_015215.2 F488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr1:7723932 C>T maps to NM_015215.2 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr1:7724487 C>T maps to NM_015215.2 V627V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:7725051 C>T maps to NM_015215.2 T815T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:7724487 C>T maps to NM_015215.2 V627V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:7796525 C>T maps to NM_015215.2 F1063F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:7723464 C>T maps to NM_015215.2 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:7724910 C>T maps to NM_015215.2 S768S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:7724952 C>T maps to NM_015215.2 S782S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:7700578 G>A maps to NM_015215.2 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:7700578 G>A maps to NM_015215.2 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:7725009 G>A maps to NM_015215.2 T801T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr1:7724385 G>A maps to NM_015215.2 K593K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:7724445 C>T maps to NM_015215.2 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:6880264 G>T maps to NM_015215.2 G24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:7805041 C>T maps to NM_015215.2 L1444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr1:7798517 C>T maps to NM_015215.2 C1386C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:7700488 G>A maps to NM_015215.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:7723932 C>T maps to NM_015215.2 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:7700569 G>A maps to NM_015215.2 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:7724070 C>T maps to NM_015215.2 F488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:7724481 C>T maps to NM_015215.2 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr17:4889565 G>A maps to NM_001171168.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:4883401 G>A maps to NM_015099.3 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr17:4880473 C>T maps to NM_015099.3 G593G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr17:4883053 G>A maps to NM_015099.3 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr17:4875598 G>A maps to NM_015099.3 A912A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr17:4872114 C>T did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr12:67691612 C>T maps to NM_018448.3 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:67696295 C>T maps to NM_018448.3 Y398Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr12:67699409 C>T maps to NM_018448.3 I654I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:67691228 C>T maps to NM_018448.3 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:12854888 T>C did not map to a codon.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr3:12859142 C>T maps to NM_001162499.1 I904I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:12856862 G>A maps to NM_001162499.1 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:12869057 C>T maps to NM_001162499.1 F1110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:12859028 C>T maps to NM_001162499.1 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:12858845 C>T maps to NM_001162499.1 A805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:76993388 G>A maps to NM_138793.3 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:76993602 G>A maps to NM_138793.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr17:76993521 G>A maps to NM_138793.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:76993103 G>A maps to NM_138793.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr5:179150758 C>T maps to ENST00000415618 I534I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr1:40529909 C>T maps to NM_001105530.1 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr6:17463249 C>T maps to NM_006366.2 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:17426905 G>A maps to NM_006366.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr6:17551750 C>T maps to NM_006366.2 Y422Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr6:17539603 C>T maps to NM_006366.2 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr6:17541253 C>A maps to NM_006366.2 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:17543307 C>T maps to NM_006366.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr6:17463267 C>T maps to NM_006366.2 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:64956140 C>T maps to NM_005186.3 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr2:241533416 C>T maps to NM_023083.3 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:241537804 C>T maps to NM_023083.3 F660F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr2:241535932 C>T maps to NM_023083.3 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:241537804 C>T maps to NM_023083.3 F660F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:241537804 C>T maps to NM_023083.3 F660F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:241535875 C>T maps to NM_023083.3 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:241537767 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:241528842 C>T maps to NM_023083.3 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:241535812 C>T maps to NM_023083.3 D452D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:241555869 C>T maps to ENST00000270364 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:241535899 C>T maps to NM_023083.3 F481F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr6:44151445 C>T maps to NM_007058.3 F713F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr6:44148368 C>T maps to NM_007058.3 F572F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:44137168 C>T maps to NM_007058.3 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr6:44147819 C>T maps to NM_007058.3 I520I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:44141074 C>T maps to NM_007058.3 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:44137192 A>G maps to NM_007058.3 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:44149023 C>T maps to NM_007058.3 F635F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:44141110 T>C maps to NM_007058.3 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:44144730 C>T maps to NM_007058.3 H411H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:44145009 C>T maps to NM_007058.3 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:44141080 G>A maps to NM_007058.3 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr6:44147810 G>A maps to NM_007058.3 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:44144036 C>T maps to NM_007058.3 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:44149034 G>A maps to NM_007058.3 W639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:44137168 C>T maps to NM_007058.3 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr6:44144383 G>A maps to NM_007058.3 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:39232475 G>A maps to NM_144691.3 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:39234586 C>T maps to NM_144691.3 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:39228259 G>A maps to NM_144691.3 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:39230711 G>A maps to NM_144691.3 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:39234685 C>T maps to NM_144691.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:39233679 C>T maps to NM_144691.3 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:39234775 G>A maps to NM_144691.3 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:39229231 G>A maps to NM_144691.3 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr2:30976030 G>A maps to ENST00000295055 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr2:30961108 G>A maps to ENST00000295055 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr2:30966448 G>A maps to ENST00000404918 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr2:30955418 C>T maps to ENST00000295055 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:30975937 C>T maps to ENST00000295055 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:30980932 C>T maps to ENST00000295055 W282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:31010143 G>A maps to ENST00000295055 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:30966358 G>A maps to ENST00000295055 F445F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:30955418 C>T maps to ENST00000295055 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:30966433 C>T maps to ENST00000295055 E420E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr2:30954248 G>A maps to ENST00000295055 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:30998845 G>A maps to ENST00000295055 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:30998846 G>A maps to ENST00000295055 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:30993195 C>T maps to ENST00000295055 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:30987149 G>A maps to ENST00000295055 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:30954257 G>A maps to ENST00000295055 F645F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:30973980 G>A maps to ENST00000295055 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:30976045 G>A maps to ENST00000295055 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:31010116 C>T maps to ENST00000295055 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:30966370 G>A maps to ENST00000295055 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:223943207 C>T maps to NM_001748.4 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:223940530 C>T maps to NM_001748.4 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:42703482 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:42684883 C>T maps to NM_000070.2 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:76796027 C>T maps to ENST00000360841 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:76833640 C>T maps to ENST00000360841 I581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:76830113 G>T maps to ENST00000360841 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:76826569 T>C maps to ENST00000360841 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:110491824 T>C did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:110494809 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:110496410 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr23:110496371 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr23:110494266 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:110490609 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:110491988 T>C did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:110494209 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr23:110496398 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:110494856 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr23:110496371 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:110496294 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:110497614 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:110507122 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:110491198 G>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:110497533 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:110489987 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:110494918 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:110495666 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:15265033 C>T maps to NM_014296.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:15265020 C>T maps to NM_014296.2 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr1:230883403 C>T maps to NM_006615.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr1:230898472 C>T maps to NM_006615.2 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:230898472 C>T maps to NM_006615.2 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:230883313 C>T maps to NM_006615.2 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:230916266 C>T maps to NM_006615.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:230928654 G>A maps to NM_006615.2 R617R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:36636933 C>T maps to NM_001749.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr19:36637135 C>T maps to NM_001749.2 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr16:55600988 C>T maps to NM_032330.1 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:34097852 T>G maps to NM_005898.4 L146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr11:34118215 C>T maps to NM_005898.4 F632F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:34104503 T>G maps to NM_005898.4 Y294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:34113511 A>G maps to NM_005898.4 Q538Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr11:34097952 C>T maps to NM_005898.4 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:34093289 C>T maps to NM_005898.4 Y78Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr12:30867932 T>C maps to NM_001002259.1 R870R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:75698649 G>A maps to NM_032606.3 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr12:75685566 G>A maps to NM_032606.3 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:35921186 C>T maps to NM_144647.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:35904679 G>A maps to NM_144647.3 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:35910560 G>A maps to NM_144647.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:35910099 T>A maps to NM_144647.3 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr5:35910005 G>A maps to NM_144647.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr5:35910178 T>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:35910526 T>G maps to NM_144647.3 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:35910012 C>T maps to NM_144647.3 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr5:35921134 G>A maps to NM_144647.3 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr12:18891722 G>A maps to NM_033328.2 W174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr12:18891722 G>A maps to NM_033328.2 W174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr12:18891910 C>T maps to NM_033328.2 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr12:18891238 A>T maps to NM_033328.2 R13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:18891711 G>A maps to NM_033328.2 W170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:18891276 G>A maps to NM_033328.2 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:18891276 G>A maps to NM_033328.2 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:18891711 G>A maps to NM_033328.2 W170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:18891225 G>A maps to NM_033328.2 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:18891711 G>A maps to NM_033328.2 W170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:18891711 G>A maps to NM_033328.2 W170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:18891534 G>A maps to NM_033328.2 Q111Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:18891528 C>T maps to NM_033328.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr12:18891565 C>T maps to NM_033328.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr12:18891540 G>A maps to NM_033328.2 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr12:18891366 C>T maps to NM_033328.2 H55H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:18891564 T>A maps to NM_033328.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr12:18891975 G>A maps to NM_033328.2 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr12:18891276 G>A maps to NM_033328.2 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr12:18891528 C>T maps to NM_033328.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:18891225 G>A maps to NM_033328.2 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:18891729 C>T maps to NM_033328.2 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr22:37892010 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:37887775 A>G maps to NM_014550.3 N950N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr22:37892454 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr22:37906368 C>T maps to NM_014550.3 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:37900713 G>A maps to NM_014550.3 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr22:37891783 G>A maps to NM_014550.3 T762T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:37903939 G>A maps to NM_014550.3 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr7:2959007 G>A maps to NM_032415.4 S836S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:2962834 G>A maps to NM_032415.4 F691F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr7:2985561 C>T maps to NM_032415.4 K83K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr7:2951925 G>A maps to NM_032415.4 I1008I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:2977621 C>T maps to NM_032415.4 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:2979559 G>A maps to NM_032415.4 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:2953032 G>A maps to NM_032415.4 F969F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:2954958 C>T maps to NM_032415.4 E917E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr7:2979484 C>T maps to NM_032415.4 K254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:2959016 G>A maps to NM_032415.4 P833P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:2959205 G>A maps to NM_032415.4 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:2985572 G>A maps to NM_032415.4 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:2985561 C>T maps to NM_032415.4 K83K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr7:2946451 C>T maps to NM_032415.4 T1095T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:2969706 G>A maps to NM_032415.4 A524A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:2949715 G>A maps to NM_032415.4 I1076I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:2979457 C>T maps to NM_032415.4 K263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr7:2949685 G>A maps to NM_032415.4 F1086F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:2946451 C>T maps to NM_032415.4 T1095T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:2963961 G>A maps to NM_032415.4 S615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:2959072 G>A maps to NM_032415.4 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:2976697 G>A maps to NM_032415.4 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr17:78156503 C>T maps to NM_024110.2 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:78166351 G>A maps to NM_024110.2 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:78175583 G>A maps to NM_024110.2 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr17:78165119 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:78162231 G>A maps to NM_024110.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:78162279 G>C maps to NM_024110.2 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:104912354 C>T maps to NM_001017534.1 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:104971441 G>C maps to NM_001007232.1 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr11:105009722 T>C maps to NM_021571.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr5:40852465 C>T maps to NM_032587.3 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr5:40852420 C>T maps to NM_032587.3 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:40853615 C>T maps to NM_032587.3 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:40853623 C>T maps to NM_032587.3 N730N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:40841642 C>T maps to NM_032587.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:40843437 G>A maps to NM_032587.3 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr5:40852465 C>A maps to NM_032587.3 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr5:40854127 C>T maps to NM_032587.3 S898S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr5:40852456 G>A maps to NM_032587.3 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:40852888 C>T maps to NM_032587.3 I485I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:40853443 C>T maps to NM_032587.3 S670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:40854283 C>T maps to NM_032587.3 S950S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr5:40853290 G>A maps to NM_032587.3 R619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:48733883 G>A maps to NM_001184900.1 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:48733793 G>A maps to NM_001184900.1 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr19:48733814 G>A maps to NM_001184900.1 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:139259613 C>T maps to NM_052813.4 E471E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr9:139262130 C>T maps to NM_052813.4 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr9:139265102 C>T maps to NM_052813.4 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr13:111289542 C>T maps to NM_018210.2 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZY-06A-11D-A197-08 chr13:111289536 G>A maps to NM_018210.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:111277610 C>T maps to NM_018210.2 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:11018787 G>A maps to NM_199141.1 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:11018817 C>T maps to NM_199141.1 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr19:11031726 G>A maps to NM_199141.1 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr19:11022909 C>T maps to NM_199141.1 A203A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A20C-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:67191318 G>A maps to NM_001166222.1 R700R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A3JE-06A-11D-A20D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr11:67187008 C>T maps to NM_001166222.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr11:3041482 G>A maps to NM_001014437.2 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:3028115 G>A maps to NM_001014437.2 D714D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:3062235 G>A maps to ENST00000397114 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr11:3050295 A>G maps to NM_001014437.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:3040464 G>A maps to NM_001014437.2 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr13:111329418 G>A maps to NM_024537.2 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr5:71016375 G>A maps to NM_004291.3 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:25267736 G>A maps to NM_018272.3 F488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr12:25302632 G>A maps to NM_018272.3 Q172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:25261709 G>A maps to NM_018272.3 A647A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:25267778 G>A maps to NM_018272.3 I474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:25261757 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr12:25311444 C>T maps to NM_018272.3 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr12:25311483 C>T maps to NM_018272.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:25311435 C>T maps to NM_018272.3 E56E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:38325686 C>T maps to NM_007359.4 P692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr17:38319958 C>T maps to NM_007359.4 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:38319977 A>T maps to NM_007359.4 K344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:38320156 C>T maps to NM_007359.4 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr15:44581413 C>T maps to NM_138423.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:44705553 C>T maps to NM_138423.3 Q421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr15:40943752 G>A maps to NM_170589.3 E2125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr15:40917184 C>T maps to NM_170589.3 Q1601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr15:40901049 C>T maps to NM_170589.3 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr15:40942524 A>T maps to NM_170589.3 K2067*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr15:40942523 G>A maps to NM_170589.3 E2066E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr15:40913691 C>T maps to NM_170589.3 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr15:40921490 A>T maps to NM_170589.3 I1894I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr15:40901080 C>T maps to NM_170589.3 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:40913355 C>T maps to NM_170589.3 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:40916995 C>T maps to NM_170589.3 Q1538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:94174936 C>A maps to NM_022900.4 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:94164786 C>T maps to NM_022900.4 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q3-06A-11D-A196-08 chr23:41646526 C>G did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:41437745 T>G did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:41646435 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:41437615 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:41414860 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:41390396 G>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:41416310 G>A did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:41524604 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr16:2231001 C>T maps to NM_020764.3 Q789Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:2235404 G>A maps to NM_020764.3 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:2239521 C>T maps to NM_020764.3 E96E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:2231003 G>A maps to NM_020764.3 Q789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:2231247 C>T maps to NM_020764.3 Q707Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr16:2239440 G>A maps to NM_020764.3 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:73500745 C>T maps to NM_020753.3 E407E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:104900533 C>T maps to NM_033292.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr11:104896996 G>A maps to NM_033292.2 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:202093787 G>A maps to NM_032974.3 R516R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr2:202074177 C>T maps to NM_032977.3 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:202074096 C>T maps to NM_032977.3 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:202052437 C>T maps to NM_032977.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr2:202073797 C>T maps to NM_032977.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:202093739 C>T maps to NM_032974.3 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:202073922 C>T maps to NM_032977.3 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:202050820 C>T maps to NM_032977.3 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:202073874 C>T maps to NM_032977.3 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr2:202074267 G>A maps to NM_032977.3 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:202072835 C>T maps to NM_032977.3 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:15166845 G>A maps to NM_012114.2 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:15166854 C>T maps to NM_012114.2 N228N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:15164442 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:15164635 G>A maps to NM_012114.2 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr19:15164548 C>T maps to NM_012114.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15166851 G>A maps to NM_012114.2 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr19:15166307 G>A maps to NM_012114.2 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr4:185550458 G>T maps to NM_032991.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:185550602 A>G maps to NM_032991.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A197-06A-32D-A197-08 chr4:185552245 C>T maps to NM_032991.2 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr11:104825695 A>G maps to NM_001225.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr11:104825615 C>T maps to NM_001225.3 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr11:104825687 G>A maps to NM_001225.3 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:104820330 G>A maps to NM_001225.3 N240N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr11:104877830 G>A maps to NM_001136112.1 Q151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:110617578 G>C maps to NM_001226.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:202150029 C>T maps to NM_001080125.1 R491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr6:90576843 C>T maps to NM_012115.3 Q1279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr6:90572224 T>A maps to NM_012115.3 L266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr6:90578513 G>A maps to NM_012115.3 K1835K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:15819452 G>A maps to NM_001229.3 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr1:15819470 G>A maps to NM_001229.3 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:160167370 G>A maps to NM_001231.4 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:160160768 G>A maps to NM_001231.4 E76E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:160165263 C>T maps to NM_001231.4 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:160165305 C>T maps to NM_001231.4 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:116311087 G>A maps to NM_001232.3 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:116310979 A>G maps to NM_001232.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:116311117 G>A maps to NM_001232.3 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:121980880 C>T maps to NM_001178065.1 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:122002824 G>A maps to NM_001178065.1 W685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr3:121981093 C>T maps to NM_001178065.1 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr3:121981093 C>T maps to NM_001178065.1 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:121976191 C>T maps to NM_001178065.1 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr3:121994741 G>A maps to NM_001178065.1 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr3:122003125 C>T maps to NM_001178065.1 F785F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr3:121980434 C>T maps to NM_001178065.1 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:122002975 C>T maps to NM_001178065.1 F735F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr3:121976029 G>A maps to NM_001178065.1 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr3:121980874 G>A maps to NM_001178065.1 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:121980559 C>T maps to NM_001178065.1 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:122002864 C>T maps to NM_001178065.1 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:121980862 C>T maps to NM_001178065.1 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr3:121980682 C>T maps to NM_001178065.1 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr3:121980841 C>T maps to NM_001178065.1 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:121980727 G>A maps to NM_001178065.1 E282E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr3:122002864 C>T maps to NM_001178065.1 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr3:121975999 C>T maps to NM_001178065.1 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr3:121980880 C>T maps to NM_001178065.1 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:121994864 C>T maps to NM_001178065.1 I528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:122002900 C>T maps to NM_001178065.1 N710N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:122003539 C>T maps to NM_001178065.1 S923S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:122003080 C>T maps to NM_001178065.1 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:122002630 G>A maps to NM_001178065.1 E620E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr3:121994789 C>T maps to NM_001178065.1 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr3:121980841 C>T maps to NM_001178065.1 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:121980559 C>T maps to NM_001178065.1 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:121981225 C>T maps to NM_001178065.1 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:122002603 G>A maps to NM_001178065.1 K611K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:122003080 C>T maps to NM_001178065.1 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr3:121980841 C>T maps to NM_001178065.1 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:121976155 G>A maps to NM_001178065.1 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:122002642 C>T maps to NM_001178065.1 I624I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:121980580 G>A maps to NM_001178065.1 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:122002762 C>T maps to NM_001178065.1 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:122002999 C>T maps to NM_001178065.1 F743F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:121980901 G>A maps to NM_001178065.1 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:122003590 G>A maps to NM_001178065.1 Q940Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:122003186 A>T maps to NM_001178065.1 K806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr3:122002711 C>T maps to NM_001178065.1 F647F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:122002642 C>T maps to NM_001178065.1 I624I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:121980498 G>A maps to NM_001178065.1 W206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:122002675 C>T maps to NM_001178065.1 F635F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:122002609 C>T maps to NM_001178065.1 I613I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr3:122002675 C>T maps to NM_001178065.1 F635F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:122002960 G>A maps to NM_001178065.1 G730G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr3:121980880 C>T maps to NM_001178065.1 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:122001063 G>A maps to NM_001178065.1 G581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:122002627 G>A maps to NM_001178065.1 T619T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:122003482 C>T maps to NM_001178065.1 V904V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:122003722 C>T maps to NM_001178065.1 T984T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:122003770 G>A maps to NM_001178065.1 R1000R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:122003932 G>A maps to NM_001178065.1 V1054V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:121973134 C>T maps to NM_001178065.1 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:121994789 C>T maps to NM_001178065.1 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:122003248 C>T maps to NM_001178065.1 I826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr3:122003272 C>T maps to NM_001178065.1 A834A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:122003443 C>T maps to NM_001178065.1 F891F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr3:121980430 C>T maps to NM_001178065.1 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr3:122003770 G>A maps to NM_001178065.1 R1000R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:122003791 C>T maps to NM_001178065.1 S1007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr3:121976059 G>A maps to NM_001178065.1 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr3:122003770 G>A maps to NM_001178065.1 R1000R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr20:55033748 G>A maps to NM_020356.3 A769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr20:55012332 T>C maps to NM_020356.3 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr20:55026927 C>T maps to NM_020356.3 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr20:55028127 G>A maps to NM_020356.3 R632R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr20:55027731 C>T maps to NM_020356.3 V500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:55012584 C>T maps to NM_020356.3 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr20:55033748 G>A maps to NM_020356.3 A769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:55027536 G>A maps to NM_020356.3 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr20:55033445 G>A maps to NM_020356.3 R668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr20:55012398 G>A maps to NM_020356.3 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:55012398 G>A maps to NM_020356.3 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:55027341 G>A maps to NM_020356.3 K370K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:55012581 C>T maps to NM_020356.3 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:55027386 C>T maps to NM_020356.3 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:55012392 C>T maps to NM_020356.3 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr5:96073566 T>G maps to ENST00000508830 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:10705064 G>A maps to NM_001079843.1 L1259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr1:10720282 G>A maps to NM_001079843.1 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:10708135 G>A maps to NM_001079843.1 A1073A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:10725203 C>T maps to NM_001079843.1 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr1:10707916 C>T maps to NM_001079843.1 T1146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:10708003 G>A maps to NM_001079843.1 L1117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:10713647 A>C maps to NM_001079843.1 G822G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:10719844 G>A maps to NM_001079843.1 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:10725380 G>A maps to NM_001079843.1 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:10720039 C>T maps to NM_001079843.1 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr1:10719964 G>A maps to NM_001079843.1 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:10720327 G>A maps to NM_001079843.1 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:10713854 G>A maps to NM_001079843.1 A753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:34470872 G>A maps to NM_001752.3 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:65793106 G>A maps to NM_053054.3 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:65793415 C>T maps to NM_053054.3 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:65792908 G>A maps to NM_053054.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:65793163 G>A maps to NM_053054.3 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr11:65793307 G>A maps to NM_053054.3 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:65792698 C>T maps to NM_053054.3 Q384Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:65790383 G>A maps to NM_053054.3 F455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:65793565 G>A maps to NM_053054.3 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr11:65793310 G>A maps to NM_053054.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr11:65788039 G>A maps to NM_053054.3 F662F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr11:65793526 G>A maps to NM_053054.3 H108H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:65793331 G>A maps to NM_053054.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:65788285 G>A maps to NM_053054.3 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:65789010 C>T maps to NM_053054.3 K549K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:65789246 C>T maps to NM_053054.3 W511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:65788968 G>A maps to NM_053054.3 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr11:65790425 C>T maps to NM_053054.3 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr11:65793073 C>T maps to NM_053054.3 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:43924469 G>T maps to NM_172095.1 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:43939269 C>T maps to NM_172095.1 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr15:43924525 G>A maps to NM_172095.1 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr15:43924972 G>A maps to NM_172095.1 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:134344643 C>T maps to NM_178019.2 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:134347234 C>T maps to NM_178019.2 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:134332078 C>T maps to NM_178019.2 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:134343723 C>A maps to NM_178019.2 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr5:134343807 C>T maps to NM_178019.2 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:134343726 C>T maps to NM_178019.2 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:26524814 C>T maps to NM_198137.1 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr1:26526462 C>T maps to NM_198137.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:26524814 C>T maps to NM_198137.1 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:26517321 G>A maps to NM_198137.1 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:26524814 C>T maps to NM_198137.1 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:26526467 C>T maps to NM_198137.1 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr14:92174487 G>A maps to NM_024764.2 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr14:92139225 G>A maps to NM_024764.2 Y371Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:92084074 G>A maps to NM_024764.2 R756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr14:92091308 C>T maps to NM_024764.2 T595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr14:92091188 G>A maps to NM_024764.2 V635V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:92102860 G>A maps to NM_024764.2 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:92055885 C>T maps to NM_024764.2 W983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:92140528 G>A maps to NM_024764.2 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:92159532 G>A maps to NM_024764.2 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:92088078 C>T maps to NM_024764.2 W711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:92055941 G>A maps to NM_024764.2 V964V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr14:92174545 G>A maps to NM_024764.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:92105547 G>A maps to NM_024764.2 F493F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:92157893 G>A maps to NM_024764.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:92185774 G>A maps to NM_024764.2 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:92189533 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr14:92088093 C>T maps to NM_024764.2 R706R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr14:92126199 C>T maps to NM_024764.2 K471K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:92189527 G>A maps to NM_024764.2 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:92076823 C>T maps to NM_024764.2 P866P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:92189437 G>A maps to NM_024764.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr14:92102821 C>T maps to NM_024764.2 T563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr14:92058241 C>T maps to NM_024764.2 R938R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr14:92159565 C>T maps to NM_024764.2 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr14:92189527 G>A maps to NM_024764.2 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr14:92076892 G>A maps to NM_024764.2 I843I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr14:92174529 G>A maps to NM_024764.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:92102890 G>A maps to NM_024764.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:92150275 C>T maps to NM_024764.2 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:92191471 G>A maps to NM_024764.2 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:92136310 C>T maps to NM_024764.2 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr14:92088078 C>T maps to NM_024764.2 W711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:38860888 C>T maps to NM_021185.4 F1068F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:38860891 C>T maps to NM_021185.4 I1069I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr19:38858705 G>A maps to NM_021185.4 W983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:38852893 G>A maps to NM_021185.4 A713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr19:38857941 C>T maps to NM_021185.4 L920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:38850214 G>A maps to NM_021185.4 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:38860891 C>T maps to NM_021185.4 I1069I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:38847157 G>A maps to NM_021185.4 Q390Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:116199328 G>A maps to NM_001753.4 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:8787420 G>A maps to NM_001234.3 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr20:32194822 C>T maps to NM_005093.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr20:32232205 C>T maps to NM_005093.3 I523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr20:32232247 G>A maps to NM_005093.3 E537E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr16:88958654 C>T maps to NM_005187.5 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr16:88958774 G>A maps to NM_005187.5 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:88958294 G>A maps to NM_005187.5 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr16:88947894 G>A maps to NM_005187.5 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr16:88952472 G>A maps to NM_005187.5 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr16:88968043 T>A maps to NM_005187.5 K58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:119170442 C>T maps to NM_005188.2 I891I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:119142543 T>C maps to NM_005188.2 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr11:119103162 G>A maps to NM_005188.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr11:119149278 C>T maps to NM_005188.2 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:119156008 C>T maps to NM_005188.2 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr11:119145645 C>T maps to NM_005188.2 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr3:105422975 G>A maps to NM_170662.3 S483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:105400332 G>A maps to NM_170662.3 I806I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:105378047 G>A maps to NM_170662.3 P905P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:105421144 T>C maps to NM_170662.3 R584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:105438890 C>T maps to NM_170662.3 K469K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr3:105422933 G>C maps to NM_170662.3 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr3:105421147 G>A maps to NM_170662.3 S583S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:105377927 G>A maps to NM_170662.3 A945A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:105421074 G>A maps to NM_170662.3 R608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr19:45293284 C>T maps to NM_012116.3 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:45303657 C>T maps to NM_012116.3 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr19:45284595 C>T maps to NM_012116.3 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr19:45284595 C>T maps to NM_012116.3 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:45297531 G>A maps to NM_012116.3 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:45281353 C>T maps to NM_012116.3 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr19:45285646 G>A maps to NM_012116.3 K226K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr19:45303657 C>T maps to NM_012116.3 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr19:45281418 G>A maps to NM_012116.3 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:45281205 C>T maps to NM_012116.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:45284583 C>T maps to NM_012116.3 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:107399437 C>T maps to NM_024814.2 Q431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr16:49315256 G>A maps to NM_004352.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr18:70209152 G>A maps to NM_182511.3 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr18:70205950 C>T maps to NM_182511.3 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr18:70205503 C>T maps to NM_182511.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr18:70205503 C>T maps to NM_182511.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr18:70205893 G>A maps to NM_182511.3 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:70205890 G>A maps to NM_182511.3 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr18:70205415 G>A maps to NM_182511.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr20:54573645 G>A maps to NM_080617.4 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:54573732 C>T maps to NM_080617.4 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr20:54575900 G>A maps to NM_080617.4 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr20:54575885 A>G maps to NM_080617.4 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:54578951 G>A maps to NM_080617.4 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:54573723 G>A maps to NM_080617.4 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:54579089 C>T maps to NM_080617.4 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr21:44488691 C>T maps to ENST00000398168 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr21:44492179 G>A maps to ENST00000398168 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr21:44492175 C>T maps to ENST00000398168 W43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr21:44483155 G>A maps to ENST00000398168 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr21:44485499 G>A maps to ENST00000398168 D221D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr21:44478319 G>A maps to ENST00000398168 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr21:44478305 C>T maps to ENST00000398168 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr17:77755737 G>A maps to NM_032647.3 Q142Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr17:77755761 C>A maps to NM_032647.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:77808567 G>A maps to NM_003655.2 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr17:77809476 T>G maps to NM_003655.2 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:77808069 G>A maps to NM_003655.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr17:77811687 C>A maps to NM_003655.2 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr12:54651413 C>T maps to NM_012117.2 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr22:39262794 G>A maps to NM_014292.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:39263047 G>A maps to NM_014292.3 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr22:39262627 G>A maps to NM_014292.3 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr22:39262273 C>T maps to NM_014292.3 K393K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr22:39263083 G>A maps to NM_014292.3 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr22:39534664 C>T maps to NM_175709.3 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr22:39530535 G>A maps to NM_175709.3 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr22:39530027 G>A maps to NM_175709.3 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr22:39534693 G>T maps to NM_175709.3 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr17:77768994 G>A maps to NM_020649.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr17:77768487 G>A maps to NM_020649.2 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:77770083 G>A maps to NM_020649.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:14037991 C>T maps to NM_017721.4 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr19:14034564 C>T maps to NM_017721.4 F627F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr19:14037522 C>T maps to NM_017721.4 F686F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:14034381 C>T maps to NM_017721.4 Q596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:14031570 C>T maps to NM_017721.4 Q493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:14038818 C>T maps to NM_017721.4 D810D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:14020718 C>T maps to NM_017721.4 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr19:14038818 C>T maps to NM_017721.4 D810D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr19:14024386 G>A maps to NM_017721.4 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:14038071 C>T maps to NM_017721.4 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:52824026 G>A maps to NM_032449.2 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr1:52825462 G>A maps to NM_032449.2 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr1:52825463 G>A maps to NM_032449.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:15538612 T>C maps to NM_001080522.2 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:15518297 C>T maps to NM_001080522.2 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr10:97779024 C>A maps to NM_001159747.1 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:97772323 G>A maps to NM_001159747.1 Q52Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr10:70520835 C>T maps to NM_018237.2 R665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:70515273 C>T maps to NM_018237.2 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:70502257 C>T maps to NM_018237.2 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr10:70547712 C>T maps to NM_018237.2 L970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr10:70502218 C>T maps to NM_018237.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr10:70547682 G>C did not map to a codon.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr18:57106962 G>A maps to NM_133459.3 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr18:57147470 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr18:57136738 C>T maps to NM_133459.3 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:57115290 G>A maps to NM_133459.3 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr18:57103256 G>A maps to NM_133459.3 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr18:57103349 G>A maps to NM_133459.3 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:57103256 G>A maps to NM_133459.3 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:57107001 G>A maps to NM_133459.3 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr18:57103355 G>A maps to NM_133459.3 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:131598111 C>T maps to NM_004059.4 K267K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr9:131598134 G>A maps to NM_004059.4 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr9:131598135 G>A maps to NM_004059.4 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr9:131600338 G>A maps to NM_004059.4 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr3:42906332 G>A maps to NM_001296.4 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:42906431 C>T maps to NM_001296.4 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr3:42906653 C>T maps to NM_001296.4 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:42906686 C>T maps to NM_001296.4 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:42906137 C>T maps to NM_001296.4 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr3:42906431 C>T maps to NM_001296.4 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:42906413 G>A maps to NM_001296.4 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:42906677 C>T maps to NM_001296.4 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:42906395 C>T maps to NM_001296.4 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:42906851 C>T maps to NM_001296.4 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr16:28592444 C>T maps to NM_138414.2 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:28602159 C>T maps to NM_138414.2 D223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr16:28600456 C>T maps to NM_138414.2 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:57552138 C>T maps to NM_033212.3 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:57555045 C>T maps to NM_033212.3 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr16:57546745 C>T maps to NM_033212.3 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr16:57552090 C>T maps to NM_033212.3 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:57552560 C>T maps to NM_033212.3 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr18:66564556 C>T maps to NM_024781.2 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr18:66506046 G>A maps to NM_024781.2 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr18:66564553 G>A maps to NM_024781.2 K384K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr18:66564556 C>T maps to NM_024781.2 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr18:66721280 G>A maps to NM_024781.2 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr18:66721289 C>T maps to NM_024781.2 I486I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr18:66504047 C>T maps to NM_024781.2 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr18:66678185 C>T maps to NM_024781.2 Q427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:66506046 G>A maps to NM_024781.2 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr18:66678263 C>T maps to NM_024781.2 Q453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr18:66678259 G>A maps to NM_024781.2 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:42979993 C>T maps to NM_213607.1 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:55749277 G>A maps to ENST00000339012 E77E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:15132264 G>A maps to NM_173482.2 Q325Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:15132480 G>A maps to NM_173482.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr19:15132168 C>T maps to NM_173482.2 C293C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr19:15132480 G>A maps to NM_173482.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:15132204 C>T maps to NM_173482.2 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:15132480 G>A maps to NM_173482.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:56163841 C>G maps to NM_013301.2 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:219903228 G>A maps to NM_194302.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr2:219875559 C>T maps to NM_194302.2 W1372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:219874666 C>T maps to NM_194302.2 G1483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:219888009 G>A maps to NM_194302.2 F913F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:219903207 C>T maps to NM_194302.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr2:219888017 G>A maps to NM_194302.2 L911L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:219873831 C>T maps to NM_194302.2 Q1537Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:219903153 G>A maps to NM_194302.2 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr2:219874735 G>A maps to NM_194302.2 L1460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:219875354 G>A maps to NM_194302.2 P1407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:219878240 C>T maps to NM_194302.2 L1282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:219888009 G>A maps to NM_194302.2 F913F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr2:219870226 G>A maps to NM_194302.2 S1660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:219887961 G>A maps to NM_194302.2 P929P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:219875568 C>T maps to NM_194302.2 R1369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:219886907 G>A maps to NM_194302.2 L988L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr2:219878242 G>A maps to NM_194302.2 L1282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr2:219894277 G>A maps to NM_194302.2 F499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:219900218 G>T maps to NM_194302.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr2:219896317 C>T maps to NM_194302.2 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr2:219894795 A>G maps to NM_194302.2 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:219870226 G>A maps to NM_194302.2 S1660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:219875363 G>A maps to NM_194302.2 G1404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:219884424 C>T maps to NM_194302.2 E1092E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:219888003 C>T maps to NM_194302.2 W915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:219894229 G>A maps to NM_194302.2 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:219896314 G>A maps to NM_194302.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:219892668 G>A maps to NM_194302.2 F638F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr10:74644031 T>A maps to NM_138357.1 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:74620223 C>T maps to NM_138357.1 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:74619010 C>T maps to NM_138357.1 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:110605796 C>T maps to NM_017918.4 R271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr18:47753834 G>A maps to NM_145020.3 V487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr18:47769284 G>A maps to NM_145020.3 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr18:47778002 G>A maps to NM_145020.3 R209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr18:47777162 A>G maps to NM_145020.3 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr18:47769278 G>A maps to NM_145020.3 Q402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:47777886 C>T maps to NM_145020.3 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr18:47778093 C>T maps to NM_145020.3 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:186380585 G>A maps to NM_152775.3 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:186380140 A>G maps to NM_152775.3 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr4:186379978 A>G maps to NM_152775.3 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:185606817 C>T maps to NM_152683.2 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:58288048 C>T maps to NM_014157.3 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:58287927 C>T maps to NM_014157.3 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:58312480 C>T maps to NM_014157.3 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:48800454 G>A maps to NM_144577.3 G597G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:48801291 C>T maps to NM_144577.3 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:48800331 C>T maps to NM_144577.3 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:48800736 C>T maps to NM_144577.3 K503K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr2:131099641 C>T maps to NM_032357.2 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr2:131099445 G>A maps to NM_032357.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr22:21988811 C>T maps to NM_152612.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr22:21989369 T>C maps to NM_152612.2 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:46964838 G>A maps to NM_144716.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:48921476 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:48920023 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:27850324 C>T maps to ENST00000435516 K278K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr19:33372864 C>A maps to NM_032816.3 E674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:33417176 C>T maps to NM_032816.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:33414370 C>T maps to NM_032816.3 K414K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:33406352 C>T maps to NM_032816.3 E485E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:33390816 G>A maps to NM_032816.3 N607N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr7:23682704 A>T maps to NM_138771.3 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr5:205918 G>A maps to NM_145265.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr5:205857 A>G maps to NM_145265.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:31611730 T>C maps to NM_194300.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr7:31682627 T>C maps to NM_194300.2 H548H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:31617666 G>A maps to NM_194300.2 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:31692349 G>A maps to NM_194300.2 R1014R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:31617951 G>A maps to NM_194300.2 K358K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr7:31692214 G>A maps to NM_194300.2 Q969Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr7:31683098 C>A maps to NM_194300.2 S705S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr3:42774990 G>T maps to NM_144719.3 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:42781284 C>T maps to NM_144719.3 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:42750533 G>A maps to NM_144719.3 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:42784474 G>A maps to NM_144719.3 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:42750510 G>A maps to NM_144719.3 F703F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:42754798 C>T maps to NM_144719.3 E576E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:42754804 C>T maps to NM_144719.3 V574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:13873689 C>T maps to NM_030818.2 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:13873195 C>T maps to NM_030818.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr7:92978049 C>T maps to NM_017667.2 F745F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:92983056 C>T maps to NM_017667.2 R857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:92978029 T>C maps to NM_017667.2 L739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr7:92905652 C>T maps to NM_024553.2 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr7:92978049 C>T maps to NM_017667.2 F745F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:92953004 C>T maps to NM_017667.2 Y646Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:42204929 C>T maps to NM_024821.2 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr16:57738843 G>A maps to NM_032269.5 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:57752308 G>A maps to NM_032269.5 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:57756643 G>A maps to NM_032269.5 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:57761236 G>A maps to NM_032269.5 E704E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr16:57760122 C>T maps to NM_032269.5 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr16:57756700 C>T maps to NM_032269.5 Y452Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:57752292 G>A maps to NM_032269.5 W371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr16:57734061 C>T maps to NM_032269.5 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:57735981 G>A maps to NM_032269.5 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:57761236 G>A maps to NM_032269.5 E704E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:57761269 C>T maps to NM_032269.5 S715S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:57762303 G>A maps to NM_032269.5 E733E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr16:57738924 G>A maps to NM_032269.5 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:57738867 G>A maps to NM_032269.5 Q260Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:128455870 G>A maps to NM_022742.3 E1083E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:128450281 G>A maps to NM_022742.3 Q630Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:128452781 G>A maps to NM_022742.3 V854V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr7:128441253 C>T maps to NM_022742.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr17:79637483 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr17:79639160 C>T maps to NM_199287.2 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr2:109489922 C>T maps to NM_144978.1 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:109421373 C>T maps to NM_144978.1 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:109411017 C>T maps to NM_144978.1 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:123633734 G>T maps to NM_022757.4 S877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:123634300 G>C maps to NM_022757.4 S688S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:123665923 A>G maps to NM_022757.4 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:123633916 G>A maps to NM_022757.4 L816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr2:223169004 C>T maps to NM_153038.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:223168962 C>T maps to NM_153038.1 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr2:179742822 G>A maps to NM_173648.3 I589I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr2:179732779 G>A maps to NM_173648.3 V849V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr2:179733900 G>A maps to NM_173648.3 I779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr2:179720082 C>T maps to NM_173648.3 V1017V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr2:179702222 G>A maps to NM_173648.3 S1241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr2:179730553 C>T maps to NM_173648.3 E888E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:179710427 G>A maps to NM_173648.3 F1133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr2:179720256 C>T maps to NM_173648.3 R959R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:179733899 G>A maps to NM_173648.3 Q780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:179701822 G>A maps to NM_173648.3 Q1375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:179702183 C>T maps to NM_173648.3 G1254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:179710451 C>T maps to NM_173648.3 K1125K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:179730619 C>T maps to NM_173648.3 K866K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:179720118 C>T maps to NM_173648.3 K1005K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:179732806 G>A maps to NM_173648.3 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr2:179720181 C>T maps to NM_173648.3 L984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:179702426 C>T maps to NM_173648.3 G1173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr2:179718294 G>A maps to NM_173648.3 S1039S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:179730619 C>T maps to NM_173648.3 K866K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:179720256 C>T maps to NM_173648.3 R959R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:179733924 G>A maps to NM_173648.3 F771F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:179702222 G>A maps to NM_173648.3 S1241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:179732788 G>A maps to NM_173648.3 S846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr2:179701958 C>T maps to NM_173648.3 E1329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr2:179702042 G>A maps to NM_173648.3 T1301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179737039 C>T did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr2:179742708 G>A maps to NM_173648.3 F627F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr2:179710442 C>T maps to NM_173648.3 P1128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:179702222 G>A maps to NM_173648.3 S1241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:179732821 G>A maps to NM_173648.3 A835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:179702063 G>A maps to NM_173648.3 F1294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr2:179702012 G>A maps to NM_173648.3 A1311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr2:74709730 G>A maps to ENST00000393965 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:74707919 G>A maps to ENST00000393965 I493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr17:16664986 G>A maps to NM_014695.1 R1207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:16593941 C>T maps to NM_014695.1 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:16593785 G>A maps to NM_014695.1 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr17:16593800 C>T maps to NM_014695.1 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:16638369 C>T maps to NM_014695.1 Q929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:20799261 C>T maps to NM_001004306.1 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:20796747 C>T maps to NM_001004306.1 K124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:76889521 A>C maps to NM_020879.2 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr7:76909907 C>T maps to NM_020879.2 I619I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:76924179 C>T maps to NM_020879.2 I955I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:76885816 C>T maps to NM_020879.2 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr7:76903048 G>A maps to NM_020879.2 E404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr10:106214248 G>A maps to NM_001008723.1 G860G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:106124611 C>T maps to NM_001008723.1 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:106128209 C>T maps to NM_001008723.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr10:106128219 C>T maps to NM_001008723.1 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:106160634 G>A maps to NM_001008723.1 R671R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:106153214 G>A maps to NM_001008723.1 K552K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:106130762 C>T maps to NM_001008723.1 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:106163485 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr10:106121863 G>A maps to NM_001008723.1 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:159107316 C>T maps to NM_138803.3 K406K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:159201737 C>T maps to NM_138803.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:159035450 G>A maps to NM_138803.3 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr2:159028744 G>A maps to NM_138803.3 F552F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:24836585 G>A maps to NM_001130726.2 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:24833216 G>A maps to NM_001130726.2 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:124857468 C>T maps to NM_025004.2 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:124873824 T>A maps to NM_025004.2 S759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:124857469 C>T maps to NM_025004.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:197584354 G>A maps to NM_001080539.1 R710R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:197586254 C>T maps to NM_001080539.1 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:197590772 C>T maps to NM_001080539.1 Q836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr2:197540895 T>C maps to NM_001080539.1 F389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr2:197521390 C>T maps to NM_001080539.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:197540973 C>T maps to NM_001080539.1 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr19:11541754 A>G maps to NM_145045.4 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:11541766 G>A maps to NM_145045.4 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr19:11537854 C>T maps to NM_145045.4 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr11:119061484 G>A maps to NM_001145018.1 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:49912524 C>T maps to NM_144688.4 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:49918252 G>A maps to NM_144688.4 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr19:49910141 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr22:30762174 T>G maps to NM_001017437.2 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr22:30770063 C>G maps to NM_001017437.2 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:30765588 C>T maps to NM_001017437.2 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr22:30766436 C>T maps to NM_001017437.2 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr22:30766799 G>C maps to NM_001017437.2 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr22:30771579 A>G maps to NM_001017437.2 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr22:30766446 C>T maps to NM_001017437.2 Q185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr4:77288455 C>T maps to NM_001042784.1 K607K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr4:77288719 G>A maps to NM_001042784.1 I519I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr4:77247091 T>C maps to NM_001042784.1 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:77247025 T>A maps to NM_001042784.1 S1047S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:77247082 T>C maps to NM_001042784.1 S1028S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr4:77250089 C>T maps to NM_001042784.1 R987R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr4:77247049 A>G maps to NM_001042784.1 Y1039Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr4:77247154 C>T maps to NM_001042784.1 V1004V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr4:77288692 C>T maps to NM_001042784.1 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:77283312 C>T maps to NM_001042784.1 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:77290689 G>A maps to NM_001042784.1 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:77290749 C>T maps to NM_001042784.1 E392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr4:77317508 G>A maps to NM_001042784.1 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr4:77244458 G>A maps to NM_001042784.1 N1087N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:11460798 C>T maps to ENST00000427879 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:11462647 C>T maps to ENST00000427879 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:133379604 C>T did not map to a codon.
Sequencing variant TCGA-EE-A17Z-06A-11D-A196-08 chr23:133379085 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:133378857 G>A did not map to a codon.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr23:133379593 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:93646170 G>A maps to NM_206886.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr1:159858153 C>T maps to NM_012337.2 K135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:159846394 G>A maps to NM_012337.2 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:159842753 C>T maps to NM_012337.2 R519R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:159842768 G>A maps to NM_012337.2 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:159847180 C>T maps to NM_012337.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:159847189 G>A maps to NM_012337.2 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr1:159847207 C>T maps to NM_012337.2 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:159847248 G>A maps to NM_012337.2 R350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:159860370 G>A maps to NM_012337.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:159860289 C>T maps to NM_012337.2 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr1:26603072 G>A maps to NM_022778.2 Q650Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:49099886 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:49099918 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:49105170 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:44461750 G>A maps to NM_152499.1 W281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:44459600 C>T maps to NM_152499.1 N154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr1:44461724 C>T maps to NM_152499.1 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:44459630 C>T maps to NM_152499.1 H164H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:44459631 C>T maps to NM_152499.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:3673303 C>T maps to NM_152492.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:3670773 C>T maps to NM_152492.2 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:3686405 C>T maps to NM_152492.2 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:3672096 C>T maps to NM_152492.2 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr1:3677843 G>A did not map to a codon.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr1:3669218 G>A maps to NM_152492.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr6:139094903 C>T maps to NM_015439.2 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr6:139094903 C>T maps to NM_015439.2 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr6:139094903 C>T maps to NM_015439.2 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr6:139094903 C>T maps to NM_015439.2 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr10:12940426 G>A maps to NM_031455.3 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:12940553 C>T maps to NM_031455.3 K225K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:12940598 C>T maps to NM_031455.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:13040469 G>A maps to NM_031455.3 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:12940442 G>A maps to NM_031455.3 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr10:12940583 C>T maps to NM_031455.3 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:43021892 A>C maps to NM_001080850.2 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr1:43108259 G>A maps to NM_001080850.2 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:43011223 C>T maps to NM_001080850.2 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr1:43055040 T>C maps to NM_001080850.2 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:43108202 G>A maps to NM_001080850.2 R566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:43119575 G>A maps to NM_001080850.2 K743K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:43047116 A>G maps to NM_001080850.2 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr15:74610968 G>A maps to NM_182791.2 K13K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr15:74627404 G>A maps to ENST00000321288 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr15:74573042 C>T maps to ENST00000321288 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:74622633 C>T maps to ENST00000321288 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr15:74622552 C>T maps to ENST00000321288 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr15:74623055 G>A maps to ENST00000321288 R706R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr15:74623061 G>A maps to ENST00000321288 R708R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:74560741 C>T maps to ENST00000321288 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:74623377 C>A maps to ENST00000321288 A737A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr15:74627458 G>A maps to NM_182791.2 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:74625563 G>A maps to ENST00000321288 V850V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr15:74588150 C>T maps to ENST00000321288 P587P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr15:74560798 G>A maps to ENST00000321288 E385E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr15:74623548 C>T maps to ENST00000321288 I764I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:74625023 C>T maps to ENST00000321288 F795F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr15:74625131 G>A maps to ENST00000321288 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr11:27362300 C>T maps to NM_030771.1 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:27360393 C>A maps to NM_030771.1 G366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:49274000 G>A maps to NM_178173.3 W26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:49274046 C>T maps to NM_178173.3 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr3:49293769 C>T maps to NM_178173.3 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:126137304 G>A maps to ENST00000505024 K142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr3:126142182 C>A maps to ENST00000505024 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr3:126138653 G>A maps to ENST00000505024 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr3:126142433 G>A maps to ENST00000505024 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:126137365 C>T maps to ENST00000505024 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr3:126155216 G>A maps to ENST00000505024 E603E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr3:126137581 G>A maps to ENST00000505024 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:126138985 G>A maps to ENST00000505024 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:96292214 G>A maps to NM_182496.2 Q188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:96272008 C>A maps to NM_182496.2 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:96273483 G>T maps to NM_182496.2 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:180372714 C>T maps to NM_181426.1 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr3:180334459 G>A maps to NM_181426.1 I810I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:180378434 A>G maps to NM_181426.1 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr3:180372714 C>T maps to NM_181426.1 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:180359901 G>A maps to NM_181426.1 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr3:180366005 A>G maps to NM_181426.1 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:180365994 C>T maps to NM_181426.1 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:180372696 C>T maps to NM_181426.1 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:78022532 C>T maps to NM_017950.2 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:78058621 A>C maps to NM_017950.2 A690A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:78073400 C>T maps to NM_017950.2 L1086L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:78073552 C>T maps to NM_017950.2 L1136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:78023897 G>A maps to NM_017950.2 Q325Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:78069180 G>A maps to NM_017950.2 K984K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:78071108 C>T maps to NM_017950.2 S1029S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:78073339 C>T maps to NM_017950.2 I1065I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:78013837 C>T maps to NM_017950.2 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr17:8638461 C>T maps to NM_144681.2 K275K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr17:8647888 C>T maps to NM_144681.2 E13E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:8638437 C>T maps to NM_144681.2 E283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:8644971 C>T maps to NM_144681.2 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:42759459 G>A maps to NM_144609.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:63822404 G>A maps to NM_001037325.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:63633276 G>A maps to NM_145036.3 I943I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:64171217 C>T maps to NM_145036.3 W138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:128757681 G>A maps to NM_024768.2 S533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:191075886 C>T maps to NM_178335.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:191075886 C>T maps to NM_178335.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:191093010 C>T maps to NM_178335.2 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr3:48474297 C>A maps to NM_024661.3 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr3:113176006 A>G maps to NM_144718.3 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:113218402 C>T maps to NM_144718.3 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:107096541 G>A maps to NM_032600.2 K36K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:107096457 G>A maps to NM_032600.2 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:107097109 C>T maps to NM_032600.2 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:107097123 G>A maps to NM_032600.2 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:28505102 C>T maps to NM_032141.2 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:28511668 C>T maps to NM_032141.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr17:80059668 C>T maps to ENST00000445854 K880K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:80085757 G>A maps to ENST00000445854 T792T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr17:80151901 G>A maps to ENST00000445854 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr17:80146168 G>A maps to ENST00000445854 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr17:80159681 G>A maps to ENST00000445854 Q47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr17:80153204 C>T maps to ENST00000445854 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr10:61566765 C>T maps to ENST00000395341 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr12:119968802 C>T maps to NM_178499.3 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr12:119968747 G>A maps to NM_178499.3 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:119968741 C>T maps to NM_178499.3 I475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:119978480 G>A maps to NM_178499.3 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr12:119909918 C>T maps to NM_178499.3 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:119942884 C>T maps to NM_178499.3 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:119968741 C>T maps to NM_178499.3 I475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:119909855 G>A maps to NM_178499.3 E76E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:119957997 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr12:119960773 C>T maps to NM_178499.3 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr12:119942878 G>A maps to NM_178499.3 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:119909886 C>T maps to NM_178499.3 Q87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr12:119968747 G>A maps to NM_178499.3 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr12:119968747 G>A maps to NM_178499.3 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:119926575 C>T maps to NM_178499.3 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:119942977 G>A maps to NM_178499.3 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:119943025 G>A maps to NM_178499.3 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:119961496 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:119966477 C>T maps to NM_178499.3 Q430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr12:119961554 G>A maps to NM_178499.3 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr12:119916955 C>T maps to NM_178499.3 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr19:46498700 C>T maps to NM_001080402.1 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:123307950 C>T maps to NM_201435.3 T680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:123273345 T>A maps to NM_201435.3 C180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:123285919 C>T maps to NM_201435.3 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr12:123265709 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:123285916 C>T maps to NM_201435.3 N408N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr12:111330917 C>T maps to NM_152591.1 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr12:111311716 C>T maps to NM_152591.1 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:111321969 G>A maps to NM_152591.1 E330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr12:111317775 C>T maps to NM_152591.1 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr12:111336816 G>A maps to NM_152591.1 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:111318963 G>A maps to NM_152591.1 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr12:111342455 G>A maps to NM_152591.1 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:111336894 G>A maps to NM_152591.1 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr12:111345144 C>T maps to NM_152591.1 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:111311668 C>T maps to NM_152591.1 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:111342545 C>T maps to NM_152591.1 V499V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr12:111317744 T>C maps to NM_152591.1 N175N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr12:111342455 G>A maps to NM_152591.1 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:111291279 G>A maps to NM_152591.1 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr12:120499590 C>T maps to NM_207311.2 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:120502556 G>A maps to NM_207311.2 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr12:120436383 G>A maps to NM_207311.2 W163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:49315120 G>A maps to NM_033124.4 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:49314976 G>A maps to NM_033124.4 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:56627592 C>T maps to NM_001141947.1 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr3:56649274 T>C maps to NM_001141947.1 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr3:56605221 T>C maps to NM_001141947.1 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:56627977 C>T maps to NM_001141947.1 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:93170755 C>T maps to NM_181645.3 F562F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:93170755 C>T maps to NM_181645.3 F562F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr11:93103286 C>T maps to NM_181645.3 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:93088702 C>T maps to NM_181645.3 Q66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:93122227 G>A maps to NM_181645.3 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:93148276 A>T maps to NM_181645.3 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:93104331 C>T maps to NM_181645.3 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:93148219 G>A maps to NM_181645.3 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:93170761 G>A maps to NM_181645.3 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:93088614 G>A maps to NM_181645.3 W36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:93148219 G>A maps to NM_181645.3 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr18:52608310 G>A maps to NM_025214.2 R41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr18:52586521 G>A maps to NM_025214.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr18:52608287 C>T maps to NM_025214.2 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:52605226 G>A maps to NM_025214.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr18:52605226 G>A maps to NM_025214.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:150563996 C>T maps to NM_015621.2 E207E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:150578588 G>A maps to NM_015621.2 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr5:150563911 G>A maps to NM_015621.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr10:32860821 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:32742279 C>T maps to NM_001026383.1 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:32740821 C>T maps to NM_001026383.1 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr13:52439627 G>A maps to NM_031290.2 Q38Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:52439537 G>A maps to NM_031290.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:52439630 G>A maps to NM_031290.2 K39K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:52439798 A>G maps to NM_031290.2 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr3:49200966 G>A maps to NM_022903.3 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr3:49200990 C>T maps to NM_022903.3 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr3:49200300 G>A maps to NM_022903.3 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:49200240 G>A maps to NM_022903.3 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr11:32635934 C>T maps to NM_001008391.2 Q643Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:32637594 A>C maps to NM_001008391.2 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:32781684 C>T maps to NM_001008391.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:32674767 G>A maps to NM_001008391.2 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:32635807 G>A maps to NM_001008391.2 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:32636354 C>T maps to NM_001008391.2 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr11:32635091 C>T maps to NM_001008391.2 S924S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr11:32636408 G>A maps to NM_001008391.2 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr2:132290453 C>T maps to NM_138770.1 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:132290260 C>T maps to NM_138770.1 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr2:132290507 C>T maps to NM_138770.1 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:132288233 G>A maps to NM_138770.1 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:132290606 C>T maps to NM_138770.1 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:132289279 A>G maps to NM_138770.1 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr2:130897891 G>A maps to NM_207310.1 Q246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:130897226 G>A maps to NM_207310.1 I348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr2:130897651 G>A maps to NM_207310.1 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr2:130897756 G>A maps to NM_207310.1 Q291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr12:539841 C>T maps to NM_032358.3 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr12:542407 C>T maps to NM_032358.3 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr12:542443 T>C maps to NM_032358.3 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr12:527769 C>T maps to NM_032358.3 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:549865 C>T maps to NM_032358.3 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:550075 C>T maps to NM_032358.3 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr16:775517 G>A maps to NM_001031737.2 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr16:775577 G>A maps to NM_001031737.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr19:46914504 C>T maps to NM_032040.3 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:46914894 C>T maps to NM_032040.3 Q391Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:46914909 C>T maps to NM_032040.3 E386E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:46916019 C>T maps to NM_032040.3 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:46916049 C>T maps to NM_032040.3 E6E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:112357147 C>T maps to ENST00000447230 K546K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:112357417 G>A maps to ENST00000447230 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr3:112358254 G>A maps to ENST00000447230 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr3:112357285 C>T maps to ENST00000447230 K500K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:112358110 C>T maps to ENST00000447230 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:86123496 C>T maps to NM_001156474.1 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:86131095 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:86123496 C>T maps to NM_001156474.1 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:86098631 C>T maps to NM_001156474.1 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19T-06A-11D-A19A-08 chr11:86131053 G>A maps to NM_001156474.1 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:86126187 C>T maps to NM_001156474.1 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr11:86123499 G>A maps to NM_001156474.1 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:96104239 G>A maps to NM_024725.3 N382N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr11:96098254 G>A maps to NM_024725.3 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr11:85606408 G>A maps to NM_173556.3 K195K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:85610022 C>T maps to NM_173556.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:85597390 G>A maps to NM_173556.3 E164E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr11:85576198 T>C maps to NM_173556.3 D11D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr11:85606417 G>A maps to NM_173556.3 W198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:118881944 C>T maps to NM_198489.1 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:118869781 A>T maps to NM_198489.1 K116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:56419694 G>A maps to NM_001080433.1 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:56419871 C>T maps to NM_001080433.1 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr2:56419667 C>T maps to NM_001080433.1 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:56420021 G>A maps to NM_001080433.1 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:60609701 C>T maps to NM_024098.3 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr11:66359835 G>A maps to NM_018219.2 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:66359061 G>A maps to NM_018219.2 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:66358740 G>A maps to NM_018219.2 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:66358131 G>A maps to NM_018219.2 S785S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr11:66358271 C>A maps to NM_018219.2 E739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:66359694 G>A maps to NM_018219.2 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:66358089 G>A maps to NM_018219.2 I799I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr11:66357990 G>A maps to NM_018219.2 A832A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:66358662 G>A maps to NM_018219.2 F608F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:66359169 G>A maps to NM_018219.2 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:66358170 G>A maps to NM_018219.2 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:55566638 G>A maps to ENST00000436346 I493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr2:55543248 G>A maps to ENST00000436346 L1250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr2:55555444 G>A maps to ENST00000436346 R994R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:55566616 G>A maps to ENST00000436346 Q501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr2:55566692 G>A maps to ENST00000436346 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:64119690 C>T maps to NM_032251.5 S1063S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:64111791 C>T maps to NM_032251.5 G593G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:64108110 G>A maps to NM_032251.5 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:64111764 G>A maps to NM_032251.5 E584E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:64112199 C>T maps to NM_032251.5 A729A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:64112034 G>A maps to NM_032251.5 T674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr11:64112076 G>A maps to NM_032251.5 G688G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:64108451 C>T maps to NM_032251.5 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:64111695 C>T maps to NM_032251.5 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64116834 G>A maps to NM_032251.5 E883E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64117070 G>A maps to NM_032251.5 A931A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:64122705 C>T maps to NM_032251.5 S1380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr14:91755455 C>T maps to NM_001080414.2 V1478V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr14:91780200 G>A maps to NM_001080414.2 S653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr14:91779783 C>T maps to NM_001080414.2 L792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr14:91772234 C>T maps to NM_001080414.2 K1077K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:91770157 C>T maps to NM_001080414.2 L1174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:91738998 C>T maps to NM_001080414.2 Q2019Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr14:91760533 C>T maps to NM_001080414.2 E1365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr14:91780332 C>T maps to NM_001080414.2 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:91763743 G>A maps to NM_001080414.2 L1291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:91749676 G>A maps to NM_001080414.2 T1542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr14:91766380 C>T maps to NM_001080414.2 L1223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:91755548 G>A maps to NM_001080414.2 A1447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:91755686 C>T maps to NM_001080414.2 K1401K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr14:91773465 C>T maps to NM_001080414.2 G1037G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr14:91779426 C>T maps to NM_001080414.2 R911R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr14:91766302 G>A maps to NM_001080414.2 G1249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr14:91747816 G>A maps to NM_001080414.2 P1561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr14:91779804 C>T maps to NM_001080414.2 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:91739115 C>T maps to NM_001080414.2 K1980K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:91744421 G>A maps to NM_001080414.2 P1634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:91779642 C>T maps to NM_001080414.2 K839K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:91779836 G>A maps to NM_001080414.2 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:91805698 G>A maps to NM_001080414.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:91760554 C>T maps to NM_001080414.2 E1358E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:91804372 C>T maps to NM_001080414.2 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr14:91804390 C>T maps to NM_001080414.2 K336K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr11:85397040 G>A maps to NM_152723.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:85396578 G>A maps to NM_152723.1 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:85396714 C>T maps to NM_152723.1 E153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:85396405 G>A maps to NM_152723.1 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:47773840 C>T maps to NM_015603.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:47774721 C>T maps to NM_015603.2 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr6:13801537 G>A maps to NM_001031713.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr11:82991201 G>A maps to NM_021825.3 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr11:82985698 G>A maps to NM_021825.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr12:28459757 C>T maps to NM_018318.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:28605448 C>T maps to NM_018318.3 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:118688701 T>A maps to NM_019044.4 K585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:118766197 A>G maps to NM_019044.4 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:118753066 G>A maps to NM_019044.4 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:118698860 G>A maps to NM_019044.4 R476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:118753045 G>A maps to NM_019044.4 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr2:118715982 G>A maps to NM_019044.4 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr2:118698860 G>A maps to NM_019044.4 R476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:118753066 G>A maps to NM_019044.4 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:4254405 C>T maps to NM_018074.4 Q109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:4268648 C>T maps to NM_018074.4 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:41822724 C>T maps to NM_052848.1 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:169026117 C>T maps to NM_017785.4 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:169028326 C>T maps to NM_017785.4 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr5:169028326 C>T maps to NM_017785.4 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:169021291 C>T maps to NM_017785.4 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:31122524 G>A maps to NM_001105564.1 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr9:36170242 C>T maps to NM_005893.2 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:36170050 C>T maps to NM_005893.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr9:36170566 C>T maps to NM_005893.2 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:36169513 C>T maps to NM_005893.2 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:36170359 G>A maps to NM_005893.2 Q287Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:36170722 G>A maps to NM_005893.2 K408K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:42299703 G>A maps to NM_000729.4 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr3:42304945 G>A maps to NM_000729.4 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr4:26483700 G>A maps to NM_000730.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr4:26487353 G>A maps to NM_000730.2 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr4:26491811 C>T maps to NM_000730.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:26483655 C>T maps to NM_000730.2 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:26487488 C>T maps to NM_000730.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:26483309 G>A maps to NM_000730.2 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:26483787 C>T maps to NM_000730.2 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:26483439 G>A maps to NM_000730.2 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr4:26483481 G>A maps to NM_000730.2 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr4:26483643 G>A maps to NM_000730.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:26484790 C>T maps to NM_000730.2 K247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr11:6292679 C>T maps to NM_176875.2 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr11:6292679 C>A maps to NM_176875.2 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:6290974 C>T maps to NM_176875.2 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:6281241 C>T maps to NM_176875.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:6292265 C>T maps to NM_176875.2 C279C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:32687585 T>A maps to NM_002981.1 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:32614653 G>A maps to NM_002986.2 W80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr17:32614163 C>T maps to NM_002986.2 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:32612838 C>T maps to NM_002986.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:34324840 G>A maps to NM_032965.4 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:34308408 G>A maps to NM_004590.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:32583286 G>A maps to NM_002982.3 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr2:228681021 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:228680195 G>T maps to NM_004591.2 G35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr9:34709555 C>T maps to NM_002989.2 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:34340242 C>T maps to NM_005064.3 K136K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:34340866 G>A maps to NM_005064.3 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:34340845 G>A maps to NM_005064.3 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr17:34344886 G>A maps to NM_005064.3 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:34340941 C>T maps to NM_005064.3 W48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr19:8121276 G>A maps to NM_005624.2 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:8122781 C>T maps to NM_005624.2 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:8122724 C>T maps to NM_005624.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr7:75401321 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:75399064 C>T maps to NM_006072.4 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:75399048 T>A maps to NM_006072.4 K83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr5:43388546 C>T maps to NM_148672.2 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:34539887 C>T maps to NM_207007.2 Q66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:34199380 C>T maps to NM_002985.2 *92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:32598742 C>T maps to ENST00000378569 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:32597385 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:32647871 G>A maps to ENST00000394620 W92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr17:32647333 G>A maps to ENST00000394620 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:45104201 C>T maps to NM_001029835.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:45104171 G>A maps to NM_001029835.2 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:45104162 C>T maps to NM_001029835.2 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr7:45113981 G>A maps to NM_001029835.2 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr7:45115433 C>T maps to NM_001029835.2 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr13:37007294 C>T maps to NM_003914.3 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr13:37011824 G>A maps to NM_003914.3 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr13:37011992 C>T maps to NM_003914.3 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr13:37011824 G>A maps to NM_003914.3 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr4:122741863 A>G maps to NM_001237.3 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr14:20779822 C>A maps to NM_182849.1 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr15:59416998 C>T maps to NM_004701.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr15:59406710 C>T maps to NM_004701.2 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr23:50051655 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3BZ-06A-12D-A196-08 chr23:50094672 G>C did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:50054017 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:50052770 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:50031824 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:50052922 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:50054032 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:50089708 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:50094242 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:50085298 C>A did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr23:50053943 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr23:50053614 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:50052214 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:50051651 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:50094251 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:50052003 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr23:50085298 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:50053950 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:50052109 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:50094289 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr23:50053236 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr23:50053046 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:50052721 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:50053999 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr23:50054482 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:50052424 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:50053240 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:50051623 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr23:50052936 G>A did not map to a codon.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr23:50053594 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr23:50051947 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:50094634 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:50031799 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr23:50089665 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:50053841 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:50054461 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:50052707 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:50094242 C>T did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr23:50089727 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:50053070 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:50053604 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:50052149 C>T did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:50089775 C>T did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:50094365 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr11:69457860 C>G maps to NM_053056.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:69456257 C>T maps to NM_053056.2 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:4409165 C>T maps to NM_001759.3 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr12:4409051 G>A maps to NM_001759.3 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:4385250 G>A maps to NM_001759.3 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:4398041 C>T maps to NM_001759.3 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:4383337 C>T maps to NM_001759.3 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:4387924 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr15:43483810 G>A maps to NM_012142.3 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr15:43478430 G>A maps to NM_012142.3 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr15:43478431 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr19:30314584 C>T maps to NM_001238.1 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr8:95894422 A>G maps to NM_057749.1 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr8:95897702 G>T maps to NM_057749.1 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr16:2485843 C>T maps to NM_001761.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr16:2488084 C>T maps to NM_001761.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:2495513 C>T maps to NM_001761.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr16:2493717 C>T maps to NM_001761.2 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:78081962 T>C maps to NM_004354.2 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr4:78082695 C>T maps to NM_004354.2 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:86708572 G>A maps to NM_001239.3 F13F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A182-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:132087725 C>T maps to NM_001039780.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:159686485 G>A maps to NM_024565.5 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:159682680 G>A maps to NM_024565.5 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr5:159686746 G>A maps to NM_024565.5 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr5:159680612 G>A maps to NM_024565.5 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:159680612 G>T maps to NM_024565.5 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:159680708 G>A maps to NM_024565.5 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:159686608 G>A maps to NM_024565.5 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:99961965 G>A maps to ENST00000437596 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:99959862 C>T maps to ENST00000437596 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr14:99969074 G>A maps to ENST00000437596 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:156867341 G>A maps to NM_020307.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr3:156868169 C>T maps to NM_020307.2 W225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr3:156868170 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:1334430 G>A maps to NM_030937.4 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:1333982 G>A maps to NM_030937.4 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:1322765 G>A maps to NM_030937.4 R470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:1325679 G>A maps to NM_030937.4 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:54528359 G>A maps to NM_021147.3 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:49087484 T>C maps to NM_001240.2 R504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr12:49087187 G>A maps to NM_001240.2 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:49087348 G>A maps to NM_001240.2 Q550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:49087124 G>A maps to NM_001240.2 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:49087538 G>A maps to NM_001240.2 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr12:49110386 G>A maps to NM_001240.2 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr2:135711819 C>T maps to NM_058241.2 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:135676477 G>A maps to NM_058241.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:35819113 C>T maps to NM_145012.4 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr10:35857995 C>T maps to NM_145012.4 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:35819113 C>T maps to NM_145012.4 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr10:35819161 C>T maps to NM_145012.4 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr15:55652368 T>C maps to ENST00000442196 R534R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr15:55652854 C>T maps to ENST00000442196 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:55664174 G>A maps to ENST00000442196 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:55664195 G>A maps to ENST00000442196 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:46245003 G>A maps to NM_001295.2 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:46245711 G>A maps to NM_001295.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:46244742 C>T maps to NM_001295.2 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:46244937 G>A maps to NM_001295.2 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:46245531 G>A maps to NM_001295.2 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:46245420 C>T maps to NM_001295.2 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:46245705 C>T maps to NM_001295.2 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:46244763 C>T maps to NM_001295.2 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:46244895 G>A maps to NM_001295.2 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:46245219 C>T maps to NM_001295.2 W195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr3:46245396 G>A maps to NM_001295.2 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:46399758 C>T maps to NM_001123041.2 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:46399785 G>A maps to NM_001123041.2 W256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:46399701 C>T maps to NM_001123041.2 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr3:46399425 C>T maps to NM_001123041.2 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:46401275 C>T maps to NM_001123041.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr3:46399344 G>A maps to NM_001123041.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:46401236 G>A maps to NM_001123041.2 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:46399476 G>A maps to NM_001123041.2 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:46399938 C>T maps to NM_001123041.2 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:46307395 C>T maps to NM_178328.1 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:46307674 C>T maps to NM_178328.1 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr3:46306897 C>T maps to NM_178328.1 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:46307075 C>T maps to NM_178328.1 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:46307395 C>T maps to NM_178328.1 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr3:46306837 G>A maps to NM_178328.1 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr3:46307035 C>T maps to NM_178328.1 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:46306775 C>T maps to NM_178328.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:46307395 C>T maps to NM_178328.1 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:46307638 C>T maps to NM_178328.1 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:32995186 C>T maps to NM_005508.4 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:32995867 C>T maps to NM_005508.4 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr3:32995531 C>T maps to NM_005508.4 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F4-06A-12D-A25O-08 chr3:32994925 G>A maps to NM_005508.4 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:46414443 G>A maps to NM_001100168.1 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr3:46414752 C>T maps to NM_001100168.1 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr3:46414782 C>T maps to NM_001100168.1 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:46414629 C>T maps to NM_001100168.1 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:46414629 C>T maps to NM_001100168.1 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr3:46415076 G>A maps to NM_001100168.1 K228K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:46415025 C>T maps to NM_001100168.1 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr3:46414965 G>A maps to NM_001100168.1 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:46415188 C>T maps to NM_001100168.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr6:167549876 C>T maps to NM_004367.5 Y53Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:167550830 C>T maps to NM_004367.5 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:167549828 C>T maps to NM_004367.5 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr6:167550186 C>T maps to NM_004367.5 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:167550191 C>T maps to NM_004367.5 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:167550635 C>T maps to NM_004367.5 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr17:38711074 G>T maps to NM_001838.3 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr17:38712013 C>T maps to NM_001838.3 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr3:39373989 C>T maps to NM_005201.3 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr3:39374496 G>A maps to NM_005201.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:39374841 C>T maps to NM_005201.3 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr3:39374259 G>A maps to NM_005201.3 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:39374817 G>A maps to NM_005201.3 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:39374733 G>A maps to NM_005201.3 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:45942729 G>A maps to NM_031200.2 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:45943266 G>A maps to NM_031200.2 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:45943257 G>A maps to NM_031200.2 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr3:45942762 G>A maps to NM_031200.2 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:132319396 C>T maps to NM_178445.1 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr3:46449596 G>A maps to NM_001130910.1 E21E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:46450310 C>T maps to NM_001130910.1 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr3:46450310 C>T maps to NM_001130910.1 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr4:139965949 C>T maps to NM_012118.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:66373036 C>T maps to NM_005125.1 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:66366650 C>T maps to NM_005125.1 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:69983282 C>T maps to NM_006431.2 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr1:156303398 G>A maps to NM_005998.4 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:156280935 G>A maps to NM_005998.4 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:156279061 G>A maps to NM_005998.4 I522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:156294848 G>A maps to NM_005998.4 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:10261700 C>T maps to NM_012073.3 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr7:56122096 G>A maps to NM_001762.3 K79K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:56126105 C>T maps to NM_001762.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr2:73474895 C>T maps to NM_006429.3 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr2:73477003 C>T maps to NM_006429.3 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:73476201 C>T maps to NM_006429.3 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr2:73466832 G>T maps to NM_006429.3 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr21:30434538 G>T maps to NM_006585.2 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr22:17072807 C>T maps to NM_014406.4 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr22:17072480 C>T maps to NM_014406.4 W320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr22:17073026 C>T maps to NM_014406.4 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr22:17073302 G>A maps to NM_014406.4 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr22:17073119 G>A maps to NM_014406.4 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr22:17072927 G>A maps to NM_014406.4 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr22:17073041 C>A maps to NM_014406.4 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr22:17072522 C>T maps to NM_014406.4 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr22:17072011 G>A maps to NM_014406.4 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr22:17073080 C>T maps to NM_014406.4 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:17072849 G>A maps to NM_014406.4 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:17073119 G>A maps to NM_014406.4 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr22:17073302 G>A maps to NM_014406.4 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr22:17071880 G>A maps to NM_014406.4 I520I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:17071817 C>T maps to NM_014406.4 K541K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:17072198 G>A maps to NM_014406.4 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:17072450 C>T maps to NM_014406.4 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:17072666 C>T maps to NM_014406.4 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:17072762 C>T maps to NM_014406.4 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:17073119 G>A maps to NM_014406.4 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr22:17071988 C>T maps to NM_014406.4 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:17072846 G>A maps to NM_014406.4 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr22:17072012 G>A maps to NM_014406.4 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr1:117568356 C>T maps to NM_004258.3 Y885Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr1:117556280 C>T maps to NM_004258.3 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr1:117564358 C>T maps to NM_004258.3 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr1:117560847 C>T maps to NM_004258.3 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:117552637 C>T maps to NM_004258.3 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:117552760 C>T maps to NM_004258.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:117576596 G>A maps to NM_004258.3 K980K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:117560944 C>T maps to NM_004258.3 R594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:117554457 G>A maps to NM_004258.3 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr6:74472163 C>T maps to NM_133493.3 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:74440164 G>A maps to NM_133493.3 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:74519806 C>T maps to NM_133493.3 H1152H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:74481164 G>A maps to NM_133493.3 W563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:74481165 G>A maps to NM_133493.3 W563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:74516593 C>T maps to NM_133493.3 F996F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr5:140011895 G>A maps to NM_001174105.1 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:140012652 C>T did not map to a codon.
Sequencing variant TCGA-EB-A44R-06A-41D-A25O-08 chr5:140011716 C>T maps to NM_001174105.1 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr5:140012421 G>A maps to NM_001174105.1 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140011713 G>A maps to NM_001174105.1 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:145699063 A>G maps to NM_007053.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:145699067 C>T maps to NM_007053.2 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr12:7651770 C>T maps to NM_004244.4 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:7640234 G>A maps to NM_004244.4 T590T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr12:7637851 C>T maps to NM_004244.4 G873G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D3-A3MR-06A-11D-A21A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr12:7651746 C>T maps to NM_004244.4 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr12:7640468 G>A maps to NM_004244.4 F545F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:7635335 G>A maps to NM_004244.4 S1050S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr12:7651746 C>T maps to NM_004244.4 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr12:7635290 G>A maps to NM_004244.4 F1065F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:7635317 G>A maps to NM_004244.4 I1056I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:7651760 G>A maps to NM_004244.4 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:7653825 C>T maps to NM_004244.4 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr12:7635290 G>A maps to NM_004244.4 F1065F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr12:7637762 C>T maps to NM_004244.4 W903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr12:7651719 G>A maps to NM_004244.4 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr12:7635275 G>A maps to NM_004244.4 F1070F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:7636224 C>T maps to NM_004244.4 V942V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr12:7635290 G>A maps to NM_004244.4 F1065F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:7647787 G>A maps to NM_004244.4 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:7639970 G>A maps to NM_004244.4 A678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr12:7640468 G>A maps to NM_004244.4 F545F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:7633790 C>T maps to NM_004244.4 L1103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:7635320 C>T maps to NM_004244.4 G1055G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:7649412 A>G maps to NM_004244.4 C365C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:7651485 C>T maps to NM_004244.4 E252E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr12:7636158 C>T maps to NM_004244.4 Q964Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr12:7639559 G>A maps to NM_004244.4 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:7636080 C>T maps to NM_004244.4 P990P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:7649691 G>A maps to NM_004244.4 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr12:7635290 G>A maps to NM_004244.4 F1065F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr12:7635290 G>A maps to NM_004244.4 F1065F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr12:7635320 C>T maps to NM_004244.4 G1055G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr12:7639215 C>T maps to NM_004244.4 G779G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:7637845 G>A maps to NM_004244.4 I875I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr12:7653915 C>T maps to NM_004244.4 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:7637815 G>A maps to NM_004244.4 S885S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:7632466 A>T maps to NM_004244.4 *1157K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:7639173 G>A maps to NM_004244.4 S793S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:7639260 C>T maps to NM_004244.4 E764E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:7649457 C>T maps to NM_004244.4 W350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:7651533 C>T maps to NM_004244.4 W236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr12:7519913 C>T maps to ENST00000416109 R1409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr12:7585261 G>A maps to ENST00000416109 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:7527137 C>T maps to ENST00000416109 L1113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:7551064 C>T maps to ENST00000416109 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr12:7559383 C>T maps to ENST00000416109 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr12:7531820 C>T maps to ENST00000416109 Q718Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr12:7526033 G>A maps to ENST00000416109 F1214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr12:7550881 C>T maps to ENST00000416109 E579E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr12:7548982 C>A maps to ENST00000416109 V596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:7510082 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:7585082 C>T maps to ENST00000416109 W242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:7531709 G>A maps to ENST00000416109 F755F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:7586210 C>T maps to ENST00000416109 Q68Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr12:7586231 C>T maps to ENST00000416109 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr12:7556242 C>T maps to ENST00000416109 W442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:7527892 G>A maps to ENST00000416109 V1005V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:7520752 A>G maps to ENST00000416109 L1381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:7527907 G>A maps to ENST00000416109 I1000I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:7531616 C>T maps to ENST00000416109 Q786Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:7527913 G>A maps to ENST00000416109 P998P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:7531733 G>A maps to ENST00000416109 I747I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:7531670 G>A maps to ENST00000416109 G768G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:7559218 G>A maps to ENST00000416109 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:7586218 G>A maps to ENST00000416109 Q66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:7559342 C>T maps to ENST00000416109 W301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:7528302 G>A maps to ENST00000416109 V903V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr12:7550930 C>T maps to ENST00000416109 W563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr12:7526033 G>A maps to ENST00000416109 F1214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr12:7531622 C>T maps to ENST00000416109 W784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr12:7528551 C>T maps to ENST00000416109 V820V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr12:7551064 C>T maps to ENST00000416109 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:7510074 G>A maps to ENST00000416109 T1439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:7526060 G>A maps to ENST00000416109 A1205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:7528296 G>A maps to ENST00000416109 S905S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr12:7586231 C>T maps to ENST00000416109 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:7551074 C>T maps to ENST00000416109 W515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr6:109690178 G>A maps to NM_006016.4 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:109690058 G>A maps to NM_006016.4 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:27706566 C>T maps to NM_207397.2 K164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:27706629 G>A maps to NM_207397.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr19:43857895 G>A maps to NM_020406.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:43859873 A>C maps to NM_020406.2 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr19:43866410 G>A maps to NM_020406.2 W418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:43859891 G>A maps to NM_020406.2 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:43857889 C>T maps to NM_020406.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:43864435 G>A maps to NM_020406.2 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr19:43865723 C>T maps to NM_020406.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:43858076 G>A maps to NM_020406.2 W42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:43858485 G>A maps to NM_020406.2 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:43865642 C>T maps to NM_020406.2 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:43866321 G>A maps to NM_020406.2 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:66479787 G>A maps to NM_005582.2 Q295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr5:66480082 C>T maps to NM_005582.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:66478765 G>A maps to NM_005582.2 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:66479839 C>T maps to NM_005582.2 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:66479209 C>T maps to NM_005582.2 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:66479638 G>A maps to NM_005582.2 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr16:28946798 G>A maps to NM_001178098.1 W290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:28944295 C>T maps to NM_001178098.1 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:28944639 C>T maps to NM_001178098.1 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:158224895 C>T maps to NM_001763.2 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:158227292 G>A maps to NM_001763.2 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr1:158225030 G>A maps to NM_001763.2 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr1:158226855 T>C did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:158225006 C>T maps to NM_001763.2 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:158225873 C>T maps to NM_001763.2 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr1:158224916 C>T maps to NM_001763.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr1:158226831 C>T maps to NM_001763.2 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr1:158226832 C>T maps to NM_001763.2 Q288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:158224934 G>A maps to NM_001763.2 W40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158224973 G>A maps to NM_001763.2 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158226025 C>T maps to NM_001763.2 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158226031 G>A maps to NM_001763.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158226732 C>T maps to NM_001763.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:158299750 G>A maps to NM_001764.2 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:158300712 G>A maps to NM_001764.2 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:158298745 A>C maps to NM_001764.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:158300628 G>A maps to NM_001764.2 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:158299693 G>A maps to NM_001764.2 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:158299202 C>T maps to NM_001764.2 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158299229 C>T maps to NM_001764.2 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr1:158299160 C>T maps to NM_001764.2 W295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr1:158299161 C>T maps to NM_001764.2 W295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:158300775 G>A maps to NM_001764.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:158260951 C>T maps to NM_001765.2 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:158261901 C>T maps to NM_001765.2 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:158262419 C>T maps to NM_001765.2 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:158262102 C>T maps to NM_001765.2 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:158259880 A>G maps to NM_001765.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:158259857 C>T maps to NM_001765.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:158263251 C>T maps to NM_001765.2 Q330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:158261164 C>T maps to NM_001765.2 D101D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr1:158262022 C>T maps to NM_001765.2 Q160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr1:158263022 G>A maps to NM_001765.2 W304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158259857 C>T maps to NM_001765.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158262542 T>C maps to NM_001765.2 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:158262018 G>A maps to NM_001765.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:158152893 C>T maps to NM_001766.3 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IB-06A-11D-A196-08 chr1:158151870 C>T maps to NM_001766.3 N126N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr1:158151901 C>T maps to NM_001766.3 Q137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:158152902 G>A maps to NM_001766.3 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:158152077 G>A maps to NM_001766.3 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:158151328 G>A maps to NM_001766.3 W49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:158151828 G>A maps to NM_001766.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:158151885 C>T maps to NM_001766.3 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158151915 C>T maps to NM_001766.3 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:158325809 G>A maps to NM_030893.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:158325797 C>T maps to NM_030893.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr1:158326605 C>T maps to NM_030893.3 Q363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr1:158323822 G>A maps to NM_030893.3 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:158325884 C>T maps to NM_030893.3 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr1:158323822 G>A maps to NM_030893.3 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr1:158323801 C>T maps to NM_030893.3 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:158325174 C>T maps to NM_030893.3 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:158324389 G>A maps to NM_030893.3 Q94Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:158325229 C>T maps to NM_030893.3 Q166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:158325174 C>T maps to NM_030893.3 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:158325183 C>T maps to NM_030893.3 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:158323801 C>T maps to NM_030893.3 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:158324308 G>A maps to NM_030893.3 W67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr1:158325756 C>T maps to NM_030893.3 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:158324215 C>T maps to NM_030893.3 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158323822 G>A maps to NM_030893.3 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158326658 G>A maps to NM_030893.3 W380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:158325884 C>T maps to NM_030893.3 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:158323801 C>T maps to NM_030893.3 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:158325321 G>A maps to NM_030893.3 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:117307202 G>A maps to NM_001767.3 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr1:117297113 G>A did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:117303228 C>T maps to NM_001767.3 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:117307202 G>A maps to NM_001767.3 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:117311261 C>T maps to NM_001767.3 Q305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:117311312 C>T maps to NM_001767.3 Q322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr1:117311170 G>A maps to NM_001767.3 Q274Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:117311131 G>A maps to NM_001767.3 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:117297464 C>T maps to NM_001767.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:112064088 C>T maps to NM_001004196.2 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr3:112054803 A>G maps to NM_001004196.2 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:112066666 C>T maps to NM_001004196.2 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr3:112647744 C>T maps to NM_138806.3 W229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:112648220 C>T maps to NM_138806.3 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:112538668 G>A maps to NM_001008784.2 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:112546325 C>T maps to NM_001008784.2 Q106Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr3:112546212 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:112546002 G>A maps to NM_001008784.2 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:112546247 C>T maps to NM_001008784.2 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr3:112545960 G>A maps to NM_001008784.2 Y186Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:112545992 C>A maps to NM_001008784.2 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:71060972 G>A maps to NM_015717.3 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr2:71060132 G>A maps to NM_015717.3 N205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:71058881 C>T maps to NM_015717.3 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:71060791 A>G maps to NM_015717.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:71061151 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr2:71058195 G>A maps to NM_015717.3 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:71060969 C>T maps to NM_015717.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:71062643 G>A maps to NM_015717.3 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr2:71060879 G>A maps to NM_015717.3 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:7810953 G>A maps to NM_021155.3 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:7809952 C>T maps to NM_021155.3 W258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:7809953 C>T maps to NM_021155.3 W258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:7809886 G>A maps to NM_021155.3 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:7810923 C>T maps to NM_021155.3 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:7812350 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:7810694 G>A maps to NM_021155.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:7808048 C>T maps to NM_021155.3 W364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:35835989 G>A maps to NM_001771.3 E723E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:35827095 G>A maps to NM_001771.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:35827110 C>A maps to NM_001771.3 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:35832662 G>A maps to NM_001771.3 K610K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:35832743 C>T maps to NM_001771.3 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr19:35827095 G>A maps to NM_001771.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:35832028 C>T maps to NM_001771.3 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:35835956 G>A maps to NM_001771.3 W712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:35827095 G>A maps to NM_001771.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr19:35832285 T>A maps to NM_001771.3 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:35823537 G>A maps to NM_001771.3 W41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:35829245 C>T maps to NM_001771.3 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:35832297 C>T maps to NM_001771.3 H520H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:35832672 C>T maps to NM_001771.3 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr18:67614036 G>A maps to NM_006566.2 Y105Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr18:67563102 G>A maps to NM_006566.2 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr18:67614096 C>T maps to NM_006566.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr18:67531569 T>G maps to NM_006566.2 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:67540456 G>A maps to NM_006566.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr1:160832413 C>T maps to NM_001166663.1 Q18Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:160808807 G>A maps to NM_001166663.1 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:160811108 C>T maps to NM_001166663.1 E187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:160811240 C>T maps to NM_001166663.1 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:167407877 G>A maps to NM_198053.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:167409912 G>A maps to NM_198053.2 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:167487663 C>T maps to NM_198053.2 Q13Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:66082535 A>G maps to NM_020404.2 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:66083109 G>A maps to NM_020404.2 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr11:66083115 A>T maps to NM_020404.2 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:66082656 G>A maps to NM_020404.2 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:6559705 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6554698 G>A maps to NM_001242.4 E82E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:5463089 G>A maps to NM_014143.3 E217E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr9:5466800 C>T maps to NM_014143.3 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:5457415 C>T maps to NM_014143.3 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr9:5463113 C>T maps to NM_014143.3 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:73994884 C>T maps to NM_001024736.1 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr15:73996204 C>T maps to NM_001024736.1 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:73996075 C>T maps to NM_001024736.1 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr15:73994902 C>T maps to NM_001024736.1 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:73996201 C>T maps to NM_001024736.1 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:204591368 G>A maps to NM_006139.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:204591683 G>A maps to NM_006139.2 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr6:47576932 C>T maps to NM_012120.2 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr6:47575685 C>T maps to NM_012120.2 I518I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:47547125 T>C maps to NM_012120.2 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr6:47541891 C>T maps to NM_012120.2 R212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr6:47541941 G>A maps to NM_012120.2 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:47576990 C>T maps to NM_012120.2 Q589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr16:30364854 G>A maps to NM_006110.2 N214N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr16:30365329 G>A maps to NM_006110.2 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr16:30364907 G>A maps to NM_006110.2 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr16:30365004 G>A maps to NM_006110.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr17:72470794 G>A maps to NM_007261.2 Q168Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr17:72469801 C>T maps to NM_007261.2 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr17:72469801 C>T maps to NM_007261.2 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr17:72469867 G>A maps to NM_007261.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr17:72469891 C>T maps to NM_007261.2 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:72469981 C>T maps to NM_007261.2 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:72477887 C>T maps to NM_007261.2 H230H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr17:72469846 G>A maps to NM_007261.2 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:72473586 C>T maps to NM_007261.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:72473660 G>A maps to NM_007261.2 W207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:72469861 C>T maps to NM_007261.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:72540919 C>T maps to NM_006678.3 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:72539091 G>A maps to NM_006678.3 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:72540763 C>T maps to NM_006678.3 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:72540778 G>A maps to NM_006678.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:72540994 G>A maps to NM_006678.3 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr17:72610155 C>T maps to ENST00000426295 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr17:72613535 G>A maps to ENST00000426295 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr17:72608887 G>A maps to ENST00000426295 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:72608824 C>T maps to ENST00000426295 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:72522043 C>T maps to NM_174892.2 E108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:72522184 C>T maps to NM_174892.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr17:72576215 G>A maps to NM_001115152.1 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:72584677 C>T maps to NM_001115152.1 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:72584938 C>T maps to NM_001115152.1 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:72584796 G>A maps to NM_001115152.1 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr17:72584872 C>T maps to NM_001115152.1 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr17:72699181 C>T maps to ENST00000412086 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr17:72700932 G>A maps to ENST00000412086 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr17:41939260 G>A maps to NM_145273.3 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:41939260 G>A maps to NM_145273.3 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr17:41926190 G>A maps to NM_145273.3 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr17:41926250 C>T maps to NM_145273.3 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr17:41926250 C>T maps to NM_145273.3 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:160637468 A>C maps to NM_001198759.1 A1714A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:8367349 G>A maps to NM_016579.3 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:8367826 G>A maps to NM_016579.3 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:8367400 C>T maps to NM_016579.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:51729592 C>T maps to NM_001772.3 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:51729188 C>T maps to NM_001772.3 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr19:51742798 T>C maps to NM_001772.3 H317H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr19:51729248 C>T maps to NM_001772.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr19:51738906 C>T maps to NM_001772.3 H300H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:51729164 G>A maps to NM_001772.3 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:51738412 G>A maps to NM_001772.3 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:51738505 C>T maps to NM_001772.3 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:51729137 C>T maps to NM_001772.3 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr19:51729167 C>T maps to NM_001772.3 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:51738424 C>T maps to NM_001772.3 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr19:51729080 C>T maps to NM_001772.3 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:51729080 C>T maps to NM_001772.3 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:51729086 C>T maps to NM_001772.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:51729287 C>T maps to NM_001772.3 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:51742771 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:208061247 C>T maps to NM_001025109.1 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr7:80302685 G>A maps to NM_001127444.1 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:80303447 G>A maps to NM_001127444.1 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:80276160 G>A maps to NM_001127444.1 Q35Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr7:80303372 G>A maps to NM_001127444.1 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:49841244 G>T maps to NM_001774.2 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr19:49843548 G>T maps to NM_001774.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:15780090 C>T maps to NM_001775.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:15835867 G>A maps to NM_001775.2 W176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:15826514 G>A maps to NM_001775.2 W125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:15826535 C>T maps to NM_001775.2 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:15826514 G>A maps to NM_001775.2 W125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr11:118211282 C>T maps to NM_000732.4 E27E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:118209929 G>A maps to NM_000732.4 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:118211306 C>T maps to NM_000732.4 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr11:118184536 G>A maps to NM_000733.3 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:118183552 G>A maps to NM_000733.3 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:118183552 G>A maps to NM_000733.3 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:45912177 C>T maps to ENST00000423698 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr12:6909590 C>T maps to NM_000616.4 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:6923953 C>T maps to NM_000616.4 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:6927707 G>A maps to NM_000616.4 R426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:6928050 C>T maps to NM_000616.4 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr12:6909309 C>T maps to NM_000616.4 N2N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6924072 G>A maps to NM_000616.4 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6924123 G>A maps to NM_000616.4 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6925288 C>T maps to NM_000616.4 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6925420 C>T maps to NM_000616.4 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6926365 G>A maps to NM_000616.4 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr20:44750537 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:44750950 C>T maps to NM_001250.4 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:135730412 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr23:135732471 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:135732491 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:107777217 G>A maps to NM_001777.3 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr3:107779598 G>A maps to NM_001777.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:160648918 G>T maps to NM_001778.2 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:160681538 A>G maps to NM_001778.2 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:160654866 C>T maps to NM_001778.2 K65K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:160648919 G>A maps to NM_001778.2 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:160654854 C>T maps to NM_001778.2 W69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:160648855 G>A maps to NM_001778.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr11:60885710 G>A maps to NM_014207.3 K53K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:60889212 G>A maps to NM_014207.3 W312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr11:60885659 G>A maps to NM_014207.3 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr11:60886997 G>A maps to NM_014207.3 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:60892555 C>T maps to NM_014207.3 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr1:111437610 C>A maps to NM_000560.3 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr1:111441774 G>A maps to NM_000560.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:111440429 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:111435034 C>T maps to NM_000560.3 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr1:111441772 C>T maps to NM_000560.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:207499048 C>T maps to NM_001114752.1 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:207495858 C>A maps to NM_001114752.1 S78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:207510104 A>G maps to NM_001114752.1 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr1:117064555 A>T maps to NM_001779.2 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:157805727 G>A maps to NM_005894.2 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr1:157805892 C>T maps to NM_005894.2 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:157804521 G>A maps to NM_005894.2 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:157803288 C>T maps to NM_005894.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:157809177 G>A maps to NM_005894.2 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr11:60785270 C>T maps to NM_006725.3 N541N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr11:60777107 C>T maps to NM_006725.3 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:60783188 C>T maps to NM_006725.3 F464F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:60776165 C>T maps to NM_006725.3 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:60785797 C>T maps to NM_006725.3 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:60777152 G>A maps to NM_006725.3 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr12:56120528 C>T maps to NM_001780.4 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr12:56120543 C>T maps to NM_001780.4 Q122Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr12:56120576 C>T maps to NM_001780.4 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr12:56120712 C>T maps to NM_001780.4 E97E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr12:56120748 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:56121018 G>A maps to NM_001780.4 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:80274551 G>A maps to NM_006137.6 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr17:80274552 G>A maps to NM_006137.6 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr17:80274810 G>A maps to NM_006137.6 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:80274705 G>A maps to NM_006137.6 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:6586120 C>T maps to NM_001252.3 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:6590920 C>T maps to NM_001252.3 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26D-06A-11D-A19A-08 chr19:6586402 G>A maps to NM_001252.3 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:35612967 C>T maps to NM_001782.2 W237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr9:35611856 C>T maps to NM_001782.2 W298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr9:35611857 C>T maps to NM_001782.2 W298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr5:149786756 G>A maps to NM_001025159.1 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:149784692 C>T maps to NM_001025159.1 E164E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr19:42381430 C>T maps to NM_001783.3 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr19:42381430 C>T maps to NM_001783.3 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:62007707 G>A maps to NM_001039933.1 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:119256206 C>T maps to NM_005191.3 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr3:119263714 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:119263604 C>T maps to NM_005191.3 K70K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:160520778 C>T maps to NM_001184879.1 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:160518105 C>T maps to NM_001184879.1 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:160535311 C>T maps to NM_001184879.1 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr1:160523805 T>C maps to NM_001184879.1 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:160523162 C>T maps to NM_001184879.1 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:160549206 C>T maps to NM_001184879.1 W7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:160523162 C>T maps to NM_001184879.1 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:160535239 C>T maps to NM_001184879.1 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:160523209 G>A maps to NM_001184879.1 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:160519727 G>A maps to NM_001184879.1 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:160520778 C>T maps to NM_001184879.1 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:160535503 G>A maps to NM_001184879.1 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:160523700 G>A maps to NM_001184879.1 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:121822512 G>A maps to NM_175862.3 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:121825156 T>A maps to NM_175862.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr3:121828151 G>A maps to NM_175862.3 W248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:121828193 T>A maps to NM_175862.3 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:121825204 G>A maps to NM_175862.3 Q187Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:121828151 G>A maps to NM_175862.3 W248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:121825276 G>A maps to NM_175862.3 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr3:121828110 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr3:121822571 G>A maps to NM_175862.3 W93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:87013054 C>T maps to ENST00000456996 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:87016530 G>A maps to ENST00000456996 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:87017742 C>T maps to ENST00000456996 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr2:87085198 C>T maps to NM_172213.3 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:87085510 C>T maps to NM_172213.3 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr2:87042741 G>A maps to NM_172213.3 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:87085228 G>A maps to NM_172213.3 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr20:23065071 G>A maps to NM_012072.3 I586I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr20:23066295 G>A maps to NM_012072.3 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:23065317 C>T maps to NM_012072.3 R504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:23065773 G>A maps to NM_012072.3 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr20:23065182 G>A maps to NM_012072.3 I549I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:23066319 G>A maps to NM_012072.3 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:23066250 C>T maps to NM_012072.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr20:23065860 C>T maps to NM_012072.3 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr20:23065356 C>T maps to NM_012072.3 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:23064978 C>T maps to NM_012072.3 K617K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr20:23065194 C>T maps to NM_012072.3 R545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr20:23065308 C>T maps to NM_012072.3 E507E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr20:23064996 C>T maps to NM_012072.3 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:23065368 T>C maps to NM_012072.3 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr20:23066583 C>T maps to NM_012072.3 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr20:23066213 G>A maps to NM_012072.3 Q206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:23065575 G>A maps to NM_012072.3 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:23066016 G>T maps to NM_012072.3 C271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:23066115 G>A maps to NM_012072.3 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr20:23065209 G>A maps to NM_012072.3 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:23064990 C>T maps to NM_012072.3 R613R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:111304182 C>T maps to NM_198196.2 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:111296347 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:111304209 G>A maps to NM_198196.2 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:111343189 C>T maps to NM_198196.2 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:14512301 T>C maps to NM_078481.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:14512302 G>T maps to NM_078481.2 E335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr23:2609463 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:2632472 C>T did not map to a codon.
Sequencing variant TCGA-GN-A26D-06A-11D-A19A-08 chr23:2640666 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:149937519 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:149999714 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:149945928 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr23:149983390 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr1:20931526 C>T maps to NM_001785.2 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:20915648 C>T maps to NM_001785.2 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:20915651 G>A maps to NM_001785.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:20915771 C>T maps to NM_001785.2 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:20931478 C>T maps to NM_001785.2 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:43019896 G>A maps to NM_138477.2 A1006A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr15:43021261 G>A maps to NM_138477.2 F868F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr15:43018510 G>A maps to NM_138477.2 R1067R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr10:12279141 G>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:12279227 C>T maps to NM_006023.2 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr1:100856300 C>G maps to NM_033312.2 S77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr1:100964758 C>T maps to NM_033312.2 R566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr9:99381651 C>T maps to NM_033331.2 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr9:99296256 G>A maps to NM_033331.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:99296773 G>A maps to NM_033331.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:99285999 A>T maps to NM_033331.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:43825754 C>T maps to NM_001255.2 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:43825481 T>C maps to NM_001255.2 N139N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:43825721 C>T maps to NM_001255.2 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr1:43825261 C>T maps to NM_001255.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:54439466 G>A maps to NM_001170402.1 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:54416285 C>T maps to NM_001170402.1 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:137537131 G>A maps to NM_004661.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr3:48219436 G>A maps to NM_001789.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:48215914 G>A maps to NM_001789.2 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:48219373 G>A maps to NM_001789.2 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr20:3779074 C>T maps to NM_021873.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr5:137665314 G>A maps to NM_001790.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr5:137621476 A>G maps to NM_001790.3 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr17:45234748 A>C maps to NM_001114091.1 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr17:45201272 G>A maps to NM_001114091.1 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr17:45234394 A>T maps to NM_001114091.1 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NF-06A-11D-A19A-08 chr17:45234322 T>C maps to NM_001114091.1 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr17:45199824 G>A maps to NM_001114091.1 Q799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr17:45266511 C>T maps to NM_001114091.1 Q9Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:535889 C>T maps to NM_004359.1 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:536310 A>G maps to NM_004359.1 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:532077 C>T maps to NM_004359.1 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr19:10506831 C>T maps to NM_007065.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr9:4697102 G>A maps to NM_017913.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr9:4701868 G>A maps to NM_017913.2 E251E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr1:227192752 G>A maps to ENST00000366766 I1639I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:227221058 C>T maps to ENST00000366766 R1178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:227400878 G>A maps to ENST00000366766 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr14:103416168 G>A maps to NM_006035.3 L1128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr14:103465992 C>A maps to NM_006035.3 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr14:103442120 C>T maps to NM_006035.3 Q469Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:103440373 C>T maps to NM_006035.3 Q540Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr14:103470285 G>A maps to NM_006035.3 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr14:103404696 G>A maps to NM_006035.3 L1627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr14:103433412 C>T maps to NM_006035.3 W814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:103410324 G>A maps to NM_006035.3 Y1437Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:103442132 G>A maps to NM_006035.3 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr14:103410645 G>A maps to NM_006035.3 L1330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr14:103412808 G>A maps to NM_006035.3 I1248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:64593977 G>A maps to NM_017525.2 P1521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr11:64607731 C>T maps to NM_017525.2 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr11:64594560 G>A maps to NM_017525.2 G1450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:64597252 G>A maps to NM_017525.2 I1219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr11:64597719 G>A maps to NM_017525.2 R1105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:64594784 G>A maps to NM_017525.2 F1412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:64594814 G>A maps to NM_017525.2 F1402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:64604418 C>T maps to NM_017525.2 K426K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:64595226 G>A maps to NM_017525.2 F1332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:64603242 G>A maps to NM_017525.2 S583S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:64604451 C>T maps to NM_017525.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:64599959 G>A maps to NM_017525.2 T1009T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:64595014 G>A maps to NM_017525.2 L1378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64591998 G>A maps to NM_017525.2 V1534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64594814 G>A maps to NM_017525.2 F1402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64603063 C>T maps to NM_017525.2 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:64597719 G>A maps to NM_017525.2 R1105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:37964151 C>T maps to NM_152243.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr22:37962529 C>T maps to NM_152243.2 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr22:37962598 C>T maps to NM_152243.2 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr22:37964253 C>T maps to NM_152243.2 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:37962532 G>A maps to NM_152243.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:37964700 C>T maps to NM_152243.2 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:65088539 C>T maps to NM_006779.2 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:65088614 C>T maps to NM_006779.2 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:65088863 G>A maps to NM_006779.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr2:37873215 C>T maps to NM_006449.3 W172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:71281976 G>A maps to NM_012121.4 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr17:71281991 G>A maps to NM_012121.4 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr5:130721234 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr22:19504096 C>T maps to NM_001178010.1 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:19494938 C>T maps to NM_001178010.1 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr22:19486668 C>T maps to NM_001178010.1 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:19495025 C>T maps to NM_001178010.1 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:44392178 C>T maps to NM_001253.2 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:44413591 C>T maps to NM_001253.2 P764P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:44392178 C>T maps to NM_001253.2 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:44371579 C>T maps to NM_001253.2 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:44387331 C>T maps to NM_001253.2 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr6:44374128 A>G maps to NM_001253.2 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:44371557 C>T maps to NM_001253.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr6:44413472 C>T maps to NM_001253.2 Q725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:44387217 G>A maps to NM_001253.2 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr17:38457847 C>T maps to NM_001254.3 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:91977195 G>A maps to NM_001134420.1 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:91977432 C>T maps to NM_001134420.1 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:91979527 C>T maps to NM_001134420.1 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:91989596 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:193181589 C>T maps to NM_024529.4 D379D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:193205436 T>C maps to NM_024529.4 G456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr8:25337598 C>T maps to ENST00000434814 L332L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A180-06A-11D-A21A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr8:25340940 T>C maps to ENST00000434814 D354D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr8:25361031 C>T maps to ENST00000434814 S606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr8:25341638 C>T maps to ENST00000434814 F427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr8:25323824 C>T maps to ENST00000434814 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr8:25346121 C>T maps to ENST00000434814 Q531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr8:25343303 T>C maps to ENST00000434814 F466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q1-06A-21D-A196-08 chr12:6958753 C>T maps to NM_031299.4 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr14:105477975 G>A maps to NM_145701.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:64847067 G>A maps to ENST00000404147 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr11:64850833 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:21946200 G>A maps to NM_018719.4 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:21948001 G>A maps to NM_018719.4 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr1:38168922 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:38172708 G>A maps to NM_018101.2 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:38173995 C>T maps to NM_018101.2 N267N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr3:45127558 C>T maps to NM_022842.3 K694K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:45127447 G>A maps to NM_022842.3 S731S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:45127228 T>C maps to NM_022842.3 E804E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:45153629 C>T maps to NM_022842.3 W200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:45153630 C>T maps to NM_022842.3 W200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:45135120 C>T maps to NM_022842.3 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr3:45136971 G>A maps to NM_022842.3 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:45136995 G>A maps to NM_022842.3 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:45134814 C>T maps to NM_022842.3 E527E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:45134823 G>A maps to NM_022842.3 F524F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:45152067 C>T maps to NM_022842.3 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr3:45127318 G>A maps to NM_022842.3 P774P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:45127459 C>T maps to NM_022842.3 K727K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr3:45153716 C>A maps to NM_022842.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr1:54610220 G>A maps to NM_201546.2 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:54610286 C>T maps to NM_201546.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:54605662 G>A maps to NM_201546.2 Q294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:54610385 G>A maps to NM_201546.2 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:54605582 C>T maps to NM_201546.2 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:54610385 G>A maps to NM_201546.2 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:54610310 G>A maps to NM_201546.2 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:54605384 C>T maps to NM_201546.2 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:54605438 C>T maps to NM_201546.2 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:54610382 C>T maps to NM_201546.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:68844209 C>T maps to NM_004360.3 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:68835618 C>T maps to NM_004360.3 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:68856024 C>T maps to NM_004360.3 V611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr5:24488005 C>T maps to NM_006727.3 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr5:24487987 C>T maps to NM_006727.3 R717R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:24593539 G>A maps to NM_006727.3 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr5:24491859 C>T maps to NM_006727.3 V567V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:24492983 C>T maps to NM_006727.3 Q522Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:24593568 G>A maps to NM_006727.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:24491694 G>A maps to NM_006727.3 I622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:24593470 C>T maps to NM_006727.3 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr5:24535335 G>A maps to NM_006727.3 Y233Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr5:24491715 G>A maps to NM_006727.3 I615I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:24488232 T>G maps to NM_006727.3 R636R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:24509769 G>A maps to NM_006727.3 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:24487835 C>T maps to NM_006727.3 W768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr5:24488110 C>T maps to NM_006727.3 R676R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr16:64981595 C>T maps to NM_001797.2 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:65006921 A>G maps to NM_001797.2 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr16:64981856 G>A maps to NM_001797.2 T680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:65032558 C>T maps to NM_001797.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:64981795 G>A maps to NM_001797.2 Q701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:64981871 G>A maps to NM_001797.2 A675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:65016087 G>A maps to NM_001797.2 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:65006822 G>A maps to NM_001797.2 V458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:64984672 G>A maps to NM_001797.2 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:65006807 G>A maps to NM_001797.2 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr16:64984700 G>A maps to NM_001797.2 I621I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:65005941 G>A maps to NM_001797.2 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr16:64984766 C>A maps to NM_001797.2 G599G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZH-06A-11D-A197-08 chr16:64984721 G>T maps to NM_001797.2 G614G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:64981736 G>A maps to NM_001797.2 F720F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:65016087 G>A maps to NM_001797.2 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:65022164 T>C maps to NM_001797.2 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr16:65032666 T>G maps to NM_001797.2 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr5:22078745 G>A maps to NM_004061.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr5:21975287 G>A maps to NM_004061.3 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr5:21975458 C>T maps to NM_004061.3 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:21975485 G>A maps to NM_004061.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr5:21817064 T>A maps to NM_004061.3 K331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:21854884 G>A maps to NM_004061.3 Q181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:21842363 C>T maps to NM_004061.3 K240K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:22078590 T>C maps to NM_004061.3 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr5:21842281 G>A maps to NM_004061.3 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:21842281 G>A maps to NM_004061.3 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:21755883 G>A maps to NM_004061.3 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr5:21760697 G>A maps to NM_004061.3 I534I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr16:83636114 G>A maps to ENST00000268613 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:83520157 C>T maps to ENST00000268613 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:83378477 G>A maps to ENST00000268613 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr16:83520202 C>T maps to ENST00000268613 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:83636147 G>A maps to ENST00000268613 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:83781739 T>C maps to ENST00000268613 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr16:83816952 G>A maps to ENST00000268613 T670T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr16:83704402 C>T maps to ENST00000268613 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:83636147 G>A maps to ENST00000268613 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr16:83711853 C>T maps to ENST00000268613 I442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:83781745 G>A maps to ENST00000268613 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr16:83712033 G>A maps to ENST00000268613 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr16:83781838 C>T maps to ENST00000268613 F555F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr16:83636109 G>T maps to ENST00000268613 G338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr16:82660705 G>A maps to NM_001257.3 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr16:83704456 G>A maps to ENST00000268613 K388K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:83711928 T>G maps to ENST00000268613 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:83711967 C>T maps to ENST00000268613 D480D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:83817024 C>T maps to ENST00000268613 A694A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr16:89256853 G>A maps to NM_004933.2 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr16:89254572 G>A maps to NM_004933.2 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:89254617 G>A maps to NM_004933.2 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr16:89245979 C>T maps to NM_004933.2 Q67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr16:89245927 C>T maps to NM_004933.2 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr16:89246690 C>T maps to NM_004933.2 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:89251665 G>A maps to NM_004933.2 Q196Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:89256746 C>T maps to NM_004933.2 Q359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:89256787 C>T maps to NM_004933.2 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr16:89256814 G>A maps to NM_004933.2 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr16:66943996 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr16:66948289 C>T maps to NM_004062.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr16:66944361 G>A maps to NM_004062.2 F656F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr16:66945812 G>A maps to NM_004062.2 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr16:66944274 G>A maps to NM_004062.2 I685I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr16:66946333 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr16:66949201 C>T maps to NM_004062.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:66948283 C>T maps to NM_004062.2 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr16:66944307 G>T maps to NM_004062.2 Y674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr16:66943215 C>T maps to NM_004062.2 T782T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr16:66944274 G>A maps to NM_004062.2 I685I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr16:66949186 G>A maps to NM_004062.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr16:66946010 C>T maps to NM_004062.2 E527E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr16:66948193 C>T maps to NM_004062.2 E235E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:66947100 C>T maps to NM_004062.2 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr8:95183150 G>A maps to NM_001144663.1 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr8:95186177 C>T maps to NM_001144663.1 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:95172246 C>T maps to NM_001144663.1 G501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:95189877 C>T maps to NM_001144663.1 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr8:95178001 C>T maps to NM_001144663.1 E423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr8:95143164 G>A maps to NM_001144663.1 V741V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:95177986 A>G did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr8:95186483 C>T maps to NM_001144663.1 K143K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr8:95178081 G>A maps to NM_001144663.1 Q397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr8:95182691 A>T maps to NM_001144663.1 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr8:95164178 G>A maps to NM_001144663.1 F571F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:95172198 C>T maps to NM_001144663.1 K517K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr8:95178007 C>T maps to NM_001144663.1 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr8:95183180 G>A maps to NM_001144663.1 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:95201489 C>T maps to NM_001144663.1 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr8:95186441 G>A maps to NM_001144663.1 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr8:95186165 C>T maps to NM_001144663.1 K214K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr5:19473772 G>A maps to NM_004934.3 I645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr5:19544044 C>T maps to NM_004934.3 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr5:19483590 G>T maps to NM_004934.3 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr5:19483643 G>A maps to NM_004934.3 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr5:19571824 G>A maps to NM_004934.3 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:19520867 G>A maps to NM_004934.3 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:19838954 G>A maps to NM_004934.3 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr5:19544035 C>T maps to NM_004934.3 K444K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr5:19721468 G>A maps to NM_004934.3 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:19591300 C>T maps to NM_004934.3 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr5:19520764 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:19483413 G>A maps to NM_004934.3 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:19721471 G>A maps to NM_004934.3 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:19747138 G>A maps to NM_004934.3 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:19473501 G>A maps to NM_004934.3 Q736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:19483536 G>A maps to NM_004934.3 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr5:19473534 G>A maps to NM_004934.3 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr5:19483632 C>T maps to NM_004934.3 R553R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr5:19483629 C>T maps to NM_004934.3 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:19483608 C>T maps to NM_004934.3 Q561Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr5:19571830 C>T maps to NM_004934.3 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:19483476 G>A maps to NM_004934.3 F605F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr18:64235911 G>A maps to NM_021153.2 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:25589752 G>A maps to NM_001792.3 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr18:25593739 G>A maps to NM_001792.3 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr18:25572696 G>A maps to NM_001792.3 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr18:25570082 G>A maps to NM_001792.3 R526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr18:25570242 C>T maps to NM_001792.3 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr18:25543452 G>A maps to NM_001792.3 D794D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:25543329 G>A maps to NM_001792.3 F835F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:25572669 G>A maps to NM_001792.3 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr18:59212366 G>A maps to NM_031891.2 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr18:59221765 T>A maps to NM_031891.2 Y748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr18:59206329 C>T maps to NM_031891.2 F494F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr18:59157986 C>T maps to NM_031891.2 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr18:59157791 G>A maps to NM_031891.2 W2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr18:59166486 C>T maps to NM_031891.2 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr18:59157869 T>A maps to NM_031891.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr18:59221747 C>T maps to NM_031891.2 F742F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr18:59221636 C>T maps to NM_031891.2 I705I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr18:59157986 C>T maps to NM_031891.2 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:59157821 C>T maps to NM_031891.2 N12N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:59157986 C>T maps to NM_031891.2 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:59221603 C>T maps to NM_031891.2 A694A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr18:59221636 C>T maps to NM_031891.2 I705I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr18:59221465 A>G maps to NM_031891.2 Q648Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr18:59174648 C>T maps to NM_031891.2 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr18:59174789 G>A maps to NM_031891.2 K338K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:59166534 G>A maps to NM_031891.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:59166624 C>T maps to NM_031891.2 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:59221645 C>G maps to NM_031891.2 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr18:59170315 C>T maps to NM_031891.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr20:44815245 G>A maps to NM_021248.1 F548F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr20:44828152 G>A maps to NM_021248.1 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr20:44841651 G>A maps to NM_021248.1 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:44869683 G>A maps to NM_021248.1 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr20:44839106 G>A maps to NM_021248.1 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:44815245 G>A maps to NM_021248.1 F548F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr20:44806774 G>A maps to NM_021248.1 F575F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:44839136 C>T maps to NM_021248.1 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr20:44815476 G>A maps to NM_021248.1 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr20:44845507 G>A maps to NM_021248.1 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr20:44869686 G>A maps to NM_021248.1 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:44815230 G>A maps to NM_021248.1 I553I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:44845618 C>T maps to NM_021248.1 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr20:44815548 G>A maps to NM_021248.1 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr20:44845477 G>A maps to NM_021248.1 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:44869821 G>A maps to NM_021248.1 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr10:73494025 C>T maps to ENST00000398860 D1383D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr10:73537627 C>T maps to ENST00000398860 I1684I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr10:73567158 C>T maps to ENST00000398860 I2773I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr10:73377122 C>T maps to ENST00000398860 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:73501548 G>A maps to ENST00000398860 K1577K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:73453961 C>T maps to ENST00000398860 I750I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr10:73447447 C>T maps to ENST00000398860 F682F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:73545395 C>T maps to ENST00000398860 I1912I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:73544155 G>A maps to ENST00000398860 G1832G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:73556879 C>T maps to ENST00000398860 S2249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr10:73447447 C>T maps to ENST00000398860 F682F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:73544844 C>T maps to ENST00000398860 F1905F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr10:73461879 C>T maps to ENST00000398860 I838I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr10:73468966 C>T maps to ENST00000398860 I1078I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:73270724 C>T maps to ENST00000398860 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:73453961 C>T maps to ENST00000398860 I750I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:73551084 C>T maps to ENST00000398860 C2087C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr10:73439178 C>T maps to ENST00000398860 I601I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:73447423 C>T maps to ENST00000398860 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr10:73377128 C>T maps to ENST00000398860 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr10:73567294 C>T maps to ENST00000398860 F2782F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr10:73494025 C>T maps to ENST00000398860 D1383D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr10:73455257 C>T maps to ENST00000398860 T796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:73553032 C>T maps to ENST00000398860 F2121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr10:73437211 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:73437275 C>T maps to ENST00000398860 I531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:73447447 C>T maps to ENST00000398860 F682F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:73462315 C>T maps to ENST00000398860 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:73464771 G>A maps to ENST00000398860 V951V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:73464825 G>A maps to ENST00000398860 R969R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:73464831 G>A maps to ENST00000398860 V971V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:73490350 C>T maps to ENST00000398860 D1240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:73545473 G>A maps to ENST00000398860 E1938E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:73558988 C>T maps to ENST00000398860 I2397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr10:73377104 C>T maps to ENST00000398860 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:73464753 C>T maps to ENST00000398860 I945I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr10:73326626 C>T maps to ENST00000398860 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:73558934 C>T maps to ENST00000398860 A2379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr14:23518845 C>T maps to NM_022478.3 Q567Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr14:23523424 C>T maps to NM_022478.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr14:23524556 G>A maps to NM_022478.3 H69H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr14:23517671 G>A maps to NM_022478.3 F659F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:23524544 G>A maps to NM_022478.3 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:23524310 G>A maps to NM_022478.3 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr14:23523811 G>A maps to NM_022478.3 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:23517686 G>A maps to NM_022478.3 A654A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr14:23524289 G>A maps to NM_022478.3 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:58570990 C>T maps to NM_177980.2 V590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr20:58587586 C>T maps to NM_177980.2 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr20:58564174 C>T maps to NM_177980.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr20:58559805 C>T maps to NM_177980.2 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:58564128 C>T maps to NM_177980.2 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr20:58567441 G>A maps to NM_177980.2 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr20:58567483 C>T maps to NM_177980.2 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:58567465 C>T maps to NM_177980.2 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr16:68714893 C>T maps to NM_001793.4 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr16:68712429 C>A maps to NM_001793.4 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr16:68721502 C>T maps to NM_001793.4 I553I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:68732149 G>T maps to NM_001793.4 V779V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr20:60348123 G>A maps to NM_001794.2 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr20:60448955 G>A maps to NM_001794.2 E350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr20:60498606 G>A maps to NM_001794.2 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr20:60448859 C>T maps to NM_001794.2 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr20:60485587 C>T maps to NM_001794.2 I433I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:60485527 C>T maps to NM_001794.2 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:60503446 C>T maps to NM_001794.2 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr20:60498507 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr20:60448841 G>A maps to NM_001794.2 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:60448829 C>T maps to NM_001794.2 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr20:60503269 C>T maps to NM_001794.2 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr20:60498654 C>T maps to NM_001794.2 F507F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:60419755 C>T maps to NM_001794.2 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr16:66436843 C>T maps to NM_001795.3 I709I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:66436748 C>T maps to NM_001795.3 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr16:66434764 G>A maps to NM_001795.3 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr16:66431972 C>T maps to NM_001795.3 Y483Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:66423279 G>A maps to NM_001795.3 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:66426076 C>T maps to NM_001795.3 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:66436969 C>T maps to NM_001795.3 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:66423411 C>T maps to NM_001795.3 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:31267738 G>A maps to NM_004932.2 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr5:31305297 G>A maps to NM_004932.2 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr5:31323186 C>T maps to NM_004932.2 F715F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr5:31316358 C>T maps to NM_004932.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:31297447 G>A maps to NM_004932.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:31313487 G>A maps to NM_004932.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:31318020 G>A maps to NM_004932.2 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr5:31323135 C>T maps to NM_004932.2 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:31267600 C>T maps to NM_004932.2 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:31267717 T>C maps to NM_004932.2 N46N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr5:31323135 C>T maps to NM_004932.2 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:31322979 C>T maps to NM_004932.2 I646I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr5:31302389 T>C maps to NM_004932.2 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:31322997 C>T maps to NM_004932.2 I652I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr5:31299718 C>T maps to NM_004932.2 N264N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:31299679 C>T maps to NM_004932.2 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:31313512 C>T maps to NM_004932.2 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:31317549 G>A maps to NM_004932.2 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr5:31323177 C>T maps to NM_004932.2 V712V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:31305294 A>G maps to NM_004932.2 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr5:31323075 G>A maps to NM_004932.2 R678R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:31317546 C>T maps to NM_004932.2 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr5:31313487 G>A maps to NM_004932.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:31302254 G>A maps to NM_004932.2 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:31302377 C>T maps to NM_004932.2 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:31317933 G>A maps to NM_004932.2 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:31317954 G>A maps to NM_004932.2 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr5:31323186 C>T maps to NM_004932.2 F715F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr18:63511244 G>A maps to NM_004361.2 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr18:63489461 T>C maps to NM_004361.2 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr18:63430131 C>T maps to NM_004361.2 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr18:63548087 C>G maps to NM_004361.2 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr18:63477089 C>T maps to NM_004361.2 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr18:63477229 C>T maps to NM_004361.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr18:63489410 A>T maps to NM_004361.2 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr18:63481719 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr18:63477013 C>T maps to NM_004361.2 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr18:63547652 C>T maps to NM_004361.2 I627I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr18:63477013 C>T maps to NM_004361.2 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr18:63477151 C>A maps to NM_004361.2 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr18:63430209 G>A maps to NM_004361.2 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:63525114 C>T maps to NM_004361.2 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:63548114 G>A maps to NM_004361.2 E781E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr18:63430182 G>A maps to NM_004361.2 K35K. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D3-A1Q6-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr16:61761117 C>T maps to NM_001796.2 R472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr16:61935341 G>A maps to NM_001796.2 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:61935301 G>A maps to NM_001796.2 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr16:61858916 C>T maps to NM_001796.2 Q278Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44R-06A-41D-A25O-08 chr16:61761039 G>A maps to NM_001796.2 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr16:61823265 G>A maps to NM_001796.2 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:61747793 G>A maps to NM_001796.2 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr16:61689413 G>A maps to NM_001796.2 G622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr16:61935301 G>A maps to NM_001796.2 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:61747769 C>T maps to NM_001796.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr16:61859018 G>A maps to NM_001796.2 I244I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A29M-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:61761117 C>T maps to NM_001796.2 R472R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A29M-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr16:61851399 G>A maps to NM_001796.2 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:61854961 C>T maps to NM_001796.2 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:61851435 G>A maps to NM_001796.2 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr16:61851399 G>T maps to NM_001796.2 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr16:61935341 G>A maps to NM_001796.2 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:61687628 G>A maps to NM_001796.2 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr16:61935353 C>T maps to NM_001796.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr16:61935081 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr16:61747754 C>T maps to NM_001796.2 K548K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr16:61761045 G>A maps to NM_001796.2 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr16:62055070 C>T maps to NM_001796.2 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:61851630 C>T maps to NM_001796.2 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr5:26903763 C>G maps to NM_016279.3 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:26886186 A>G maps to NM_016279.3 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr5:26881658 G>A maps to NM_016279.3 V652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr5:26902838 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr5:26902839 T>A did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr5:26903763 C>T maps to NM_016279.3 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:26915837 C>T maps to NM_016279.3 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr10:85972144 G>A maps to NM_033100.2 G588G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr10:85973995 C>T maps to NM_033100.2 V733V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:85960388 C>T maps to NM_033100.2 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:85970860 C>T maps to NM_033100.2 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:85971426 C>T maps to NM_033100.2 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:85962833 C>T maps to NM_033100.2 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:85970857 C>T maps to NM_033100.2 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:85972965 C>T maps to NM_033100.2 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:85970857 C>T maps to NM_033100.2 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:85971438 G>A maps to NM_033100.2 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:85973845 C>T maps to NM_033100.2 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:85974124 G>A maps to NM_033100.2 E776E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:85961660 C>T maps to NM_033100.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:85973022 C>T maps to NM_033100.2 S653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr10:85967973 C>T maps to NM_033100.2 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr5:176008549 C>T maps to NM_001171976.1 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr5:176016345 C>T maps to NM_001171976.1 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr5:176004636 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr5:176002197 G>A maps to NM_001171976.1 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:176002427 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:175995790 G>A maps to NM_001171976.1 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:176017434 G>A maps to NM_001171976.1 R1121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:176001112 C>T maps to NM_001171976.1 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:176011609 G>A maps to NM_001171976.1 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:176016390 G>A maps to NM_001171976.1 R1023R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:176002511 C>T maps to NM_001171976.1 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:176003065 C>T maps to NM_001171976.1 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:176011702 C>T maps to NM_001171976.1 T807T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:176011703 C>T maps to NM_001171976.1 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr5:175998269 C>T maps to NM_001171976.1 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:176004675 C>T maps to NM_001171976.1 V463V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:176008477 G>A maps to NM_001171976.1 E651E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:176011642 G>A maps to NM_001171976.1 G787G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:176016168 C>T maps to NM_001171976.1 F998F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr5:176008462 G>A maps to NM_001171976.1 G646G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr7:105662800 G>A maps to NM_152750.4 R661R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:105635201 C>T maps to NM_152750.4 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr7:105656439 C>T maps to NM_152750.4 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr7:105667133 G>A maps to NM_152750.4 K755K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:105624728 C>T maps to NM_152750.4 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:105662884 G>A maps to NM_152750.4 T689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr7:105645016 C>T maps to NM_152750.4 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr7:105644978 C>T maps to NM_152750.4 R300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:105636704 C>T maps to NM_152750.4 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr3:49836760 C>T maps to NM_001007540.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:49836760 C>T maps to NM_001007540.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:49836293 G>A maps to NM_001007540.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:617548 C>T maps to NM_021924.4 K780K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:618055 G>A maps to NM_021924.4 G672G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:619079 C>T maps to NM_021924.4 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:618097 C>T maps to NM_021924.4 S658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr11:619079 C>T maps to NM_021924.4 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:62545508 C>T maps to NM_001786.4 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr10:62553726 G>A maps to NM_001786.4 K296K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr16:89759816 C>T maps to NM_052988.4 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr16:89761463 C>T maps to NM_052988.4 Y306Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr16:89758291 T>A maps to NM_052988.4 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr1:1635334 G>A maps to NM_024011.2 F613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:1573192 G>A maps to ENST00000401097 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:1572085 G>A maps to ENST00000401097 F623F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr17:37618600 C>T maps to NM_016507.2 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:37672044 C>T maps to NM_016507.2 Q944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr17:37687013 C>T maps to NM_016507.2 S1306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:40085495 C>T maps to NM_003718.4 G805G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:40041553 T>C maps to NM_003718.4 L759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:90741856 G>A maps to NM_012395.2 K367K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:90492553 G>A maps to NM_012395.2 K185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:90585030 C>T maps to NM_012395.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:90741916 G>A maps to NM_012395.2 K387K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:90741916 G>A maps to NM_012395.2 K387K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr2:202687610 C>T maps to ENST00000450471 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:47085786 A>C did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:47083084 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:96728503 C>T maps to NM_002595.4 K37K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr12:96674609 G>A maps to NM_002595.4 R504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:205499446 C>T maps to NM_212503.2 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:205492423 G>A maps to NM_212503.2 E43E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:205496926 C>T maps to NM_212503.2 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:205496941 C>T maps to NM_212503.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:205499795 G>A maps to NM_212503.2 K481K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr1:205500478 G>A maps to NM_212503.2 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:205494283 G>A maps to NM_212503.2 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:205497007 C>T maps to NM_212503.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr1:205497010 C>T maps to NM_212503.2 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:205498688 C>T maps to NM_212503.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:205497215 C>T maps to NM_212503.2 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:205494283 G>A maps to NM_212503.2 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:205494284 A>T maps to NM_212503.2 K170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:110959893 G>A maps to NM_015076.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr9:90586094 G>A maps to NM_001039803.2 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:90584725 G>A maps to NM_001039803.2 N224N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr9:90584716 G>A maps to NM_001039803.2 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:90586061 C>T maps to NM_001039803.2 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:67274938 G>A maps to NM_005851.3 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:73998611 C>G maps to NM_001258.2 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:73998026 C>T maps to NM_001258.2 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:73998029 C>T maps to NM_001258.2 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:73998207 C>T maps to NM_001258.2 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr12:58143033 G>A maps to NM_000075.2 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:150752424 G>A maps to NM_004935.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:150754173 C>T maps to NM_004935.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr2:219825519 G>A maps to NM_003936.3 K326K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr20:31975169 G>A maps to ENST00000357886 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr20:31967343 G>A maps to ENST00000357886 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:31958388 C>A maps to ENST00000357886 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr9:123216102 G>A maps to NM_018249.4 F808F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr9:123199717 G>A maps to NM_018249.4 S1270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr9:123215997 G>A maps to NM_018249.4 S843S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:123182165 G>A maps to NM_018249.4 L1359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:123202103 G>A maps to NM_018249.4 Q1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:123215754 G>A maps to NM_018249.4 S924S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr9:123163154 G>A maps to NM_018249.4 H1772H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:123301372 C>T maps to NM_018249.4 K151K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:123308023 G>A maps to NM_018249.4 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:123215751 G>A maps to NM_018249.4 L925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr9:123165122 T>C maps to NM_018249.4 Q1756Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr9:123334273 G>A maps to NM_018249.4 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:46057966 C>T maps to NM_176096.1 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr17:46058646 C>T maps to NM_176096.1 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:46052591 C>T maps to NM_176096.1 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr17:46054121 T>C maps to NM_176096.1 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:26975748 C>T maps to NM_001260.1 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:26974630 C>T maps to NM_001260.1 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:130550268 C>T maps to ENST00000373265 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr9:130551704 C>T maps to ENST00000373265 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:130550647 C>T maps to ENST00000373265 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:20739776 C>T maps to NM_017774.3 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr6:21000534 A>G maps to NM_017774.3 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:20781394 G>T maps to NM_017774.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:21231230 G>T maps to NM_017774.3 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr14:50796863 G>A maps to NM_004196.3 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:50862429 G>A maps to ENST00000356146 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr14:50807786 C>T maps to ENST00000356146 S878S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A197-06A-32D-A197-08 chr14:50805721 T>C maps to ENST00000356146 Q899Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr4:76529087 A>C maps to ENST00000307465 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr4:76529006 T>C maps to ENST00000307465 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:133634401 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:39406414 G>A maps to ENST00000395035 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:39406386 G>A maps to ENST00000395035 Q290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr23:18646511 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:18646506 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr23:18616668 C>T did not map to a codon.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr23:18643337 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:18613498 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:18606209 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:18626970 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:18627626 C>T did not map to a codon.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr23:18622216 G>T did not map to a codon.
Sequencing variant TCGA-FS-A4F4-06A-12D-A25O-08 chr23:18627600 A>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:18643340 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:18646616 C>T did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:18622844 C>T did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:18622845 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr6:36652069 C>T maps to ENST00000448526 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr6:36652071 G>A maps to ENST00000448526 W99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr6:36653555 C>T maps to ENST00000448526 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr12:12870979 C>T maps to NM_004064.3 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:2906617 G>A maps to NM_000076.2 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr9:21971027 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr9:21971028 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr9:21971120 G>A maps to NM_001195132.1 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr9:21971208 T>C did not map to a codon.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr9:21971096 C>T maps to NM_001195132.1 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr9:21971028 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr9:21971208 T>A did not map to a codon.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr9:21971207 C>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:21974678 G>A maps to NM_001195132.1 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr9:21974678 G>A maps to NM_001195132.1 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr9:21974679 G>A maps to NM_001195132.1 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:21974678 G>A maps to NM_001195132.1 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:21974679 G>T maps to NM_001195132.1 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr9:21971186 G>A maps to NM_001195132.1 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr9:21971186 G>A maps to NM_001195132.1 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr9:21971207 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr9:21968241 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr9:21971207 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr9:21974678 G>A maps to NM_001195132.1 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr9:21971152 C>A maps to NM_001195132.1 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:184366210 C>T maps to NM_017632.2 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr14:54884626 C>T maps to NM_005192.3 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:115151998 C>T maps to NM_001801.2 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:115146918 G>A maps to NM_001801.2 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:115152028 G>A maps to NM_001801.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr11:125893355 C>A maps to ENST00000392693 G6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr11:125830839 G>A maps to ENST00000392693 T1287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:125889517 G>A maps to ENST00000392693 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:125859625 G>A maps to ENST00000392693 H893H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:139866216 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr23:139865885 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr23:139865914 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr23:139866321 C>A did not map to a codon.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr23:139866303 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:139865894 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr23:139865808 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:139866500 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:139866341 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:139866446 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr23:139866497 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:139866503 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:139865905 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:139866473 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr23:139866083 T>A did not map to a codon.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr23:139866312 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:139866046 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:139866203 C>T did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:139866348 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:22360637 G>A maps to NM_001802.1 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr16:22385599 C>A maps to NM_001802.1 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr17:15518998 G>A maps to ENST00000455584 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:15522745 C>T maps to ENST00000261644 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:15517240 A>T maps to ENST00000455584 V583V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:15492461 G>A maps to ENST00000261644 Q726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr17:15522498 A>G maps to ENST00000261644 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr4:85569814 C>T maps to NM_001263.3 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr4:85530638 C>T maps to NM_001263.3 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:85562058 C>T maps to NM_001263.3 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:85564199 C>T maps to NM_001263.3 F352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr4:85530641 G>A maps to NM_001263.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:85555011 C>T maps to NM_001263.3 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr4:85562136 G>A maps to NM_001263.3 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:85525460 T>C maps to NM_001263.3 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:85540642 C>T maps to NM_001263.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr20:5165587 C>T maps to NM_003818.2 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr20:5170840 C>T maps to NM_003818.2 I433I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:31084283 G>A maps to NM_001264.4 Q370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:31084227 C>T maps to NM_001264.4 K388K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr6:31084719 G>A maps to NM_001264.4 D224D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:31083858 G>A maps to NM_001264.4 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:31084446 C>T maps to NM_001264.4 K315K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr6:31083846 G>A maps to NM_001264.4 D515D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr6:31084212 G>A maps to NM_001264.4 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:31084977 G>A maps to NM_001264.4 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr6:31083966 G>A maps to NM_001264.4 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr6:31084134 G>A maps to NM_001264.4 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr16:88873511 C>T maps to NM_030928.3 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:88873060 C>T maps to NM_030928.3 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr5:149562427 C>T maps to NM_001804.2 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:149563194 C>T maps to NM_001804.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr5:149563089 G>A maps to NM_001804.2 K215K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr13:28539057 G>A maps to NM_001265.3 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr13:28543050 G>A maps to NM_001265.3 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr13:28539093 C>T maps to NM_001265.3 E200E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:72673378 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr23:72667220 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:72667274 G>A did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:72674247 G>A did not map to a codon.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr23:72674275 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:72667296 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:72667297 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:72667220 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr23:72667170 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:72667220 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr23:72667311 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:72674276 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:72673411 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:72667172 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:72667347 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:72673352 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:4943785 C>T maps to ENST00000328908 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:80654829 G>A maps to NM_152342.2 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:80646537 G>A maps to NM_152342.2 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:80718435 G>A maps to NM_152342.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:80667065 C>T maps to NM_152342.2 K228K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:80646657 A>C maps to NM_152342.2 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:80718714 G>A maps to NM_152342.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr16:80646711 G>A maps to NM_152342.2 I343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:80718714 G>C maps to NM_152342.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr16:80638392 C>T maps to NM_152342.2 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:80718591 C>T maps to NM_152342.2 Q153Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr19:43026334 G>A maps to NM_001712.4 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr19:43031324 G>A maps to NM_001712.4 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:43026157 C>T maps to NM_001712.4 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:43023313 C>T maps to NM_001712.4 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:43026202 C>T maps to NM_001712.4 Q192Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:43023387 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr19:45211154 C>T maps to ENST00000396750 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:45211154 C>T maps to ENST00000396750 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:45211154 C>T maps to ENST00000396750 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:45209007 C>T maps to ENST00000396750 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr19:45208945 C>T maps to ENST00000396750 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:45207390 C>T maps to ENST00000396750 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:45208884 C>T maps to ENST00000396750 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:45206700 C>T maps to ENST00000396750 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:45211364 G>A maps to ENST00000396750 Q456Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr19:45206901 C>T maps to ENST00000396750 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr19:51983605 G>A maps to NM_001080405.1 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:51986343 C>T maps to NM_001080405.1 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:51983806 G>A maps to NM_001080405.1 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:51984695 G>A maps to NM_001080405.1 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr19:51984692 G>A maps to NM_001080405.1 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr19:51984671 C>T maps to NM_001080405.1 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:51983930 C>T maps to NM_001080405.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr19:51983635 C>T maps to NM_001080405.1 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:51986532 G>A maps to NM_001080405.1 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:51984797 C>T maps to NM_001080405.1 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:51986416 C>T maps to NM_001080405.1 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:51986373 C>T maps to NM_001080405.1 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr19:51986532 G>A maps to NM_001080405.1 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr19:51986514 C>T maps to NM_001080405.1 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:51981923 C>T maps to NM_001080405.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:51984887 G>A maps to NM_001080405.1 Q275Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr19:51986373 C>T maps to NM_001080405.1 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:51981871 C>T maps to NM_001080405.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:51986445 C>T maps to NM_001080405.1 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:51986461 G>T maps to NM_001080405.1 E350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:45182157 C>T maps to NM_020219.3 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr19:45179591 C>T maps to NM_020219.3 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr19:45184547 C>T maps to NM_020219.3 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:45179669 G>A maps to NM_020219.3 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr19:45175223 C>T maps to NM_020219.3 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:45015210 C>T maps to NM_001102597.1 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr19:45028022 C>T maps to NM_001102597.1 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr19:45021285 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr19:45026918 G>A maps to NM_001102597.1 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:45017002 C>T maps to NM_001102597.1 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:45015210 C>T maps to NM_001102597.1 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:45024658 G>A maps to NM_001102597.1 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:45024607 G>A maps to NM_001102597.1 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:45015213 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:45021273 G>A maps to NM_001102597.1 Q348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:45028294 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:45015146 G>A maps to NM_001102597.1 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr19:45028046 C>T maps to NM_001102597.1 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr19:45016927 G>A maps to NM_001102597.1 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:45017002 C>T maps to NM_001102597.1 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr19:45016927 G>A maps to NM_001102597.1 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr19:45021112 C>T maps to NM_001102597.1 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:45015120 G>A maps to NM_001102597.1 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:45024568 G>A maps to NM_001102597.1 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:45028280 G>A maps to NM_001102597.1 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:42085742 C>T maps to NM_001098506.1 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:42083814 C>T maps to NM_001098506.1 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:42085766 G>A maps to NM_001098506.1 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr19:42083708 G>A maps to NM_001098506.1 E74E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:42085861 G>A maps to NM_001098506.1 W194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:42090778 C>T maps to NM_001098506.1 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:42083876 G>A maps to NM_001098506.1 Q130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr19:42314868 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr19:42301773 C>T maps to NM_001815.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:42301774 C>T maps to NM_001815.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr19:42301620 C>T maps to NM_001815.2 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr19:42133271 G>A maps to NM_001817.2 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:42125768 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:42128034 G>A maps to NM_001817.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:42125729 G>A maps to NM_001817.2 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr19:42231193 C>T maps to NM_004363.2 V689V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:42219035 C>T maps to NM_004363.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:42223918 C>T maps to NM_004363.2 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:42222156 C>T maps to NM_004363.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr19:42218935 G>A maps to NM_004363.2 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr19:42221641 G>A maps to NM_004363.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:42224023 C>T maps to NM_004363.2 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr19:42223903 G>A maps to NM_004363.2 K516K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:42223948 C>T maps to NM_004363.2 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:42218944 G>A maps to NM_004363.2 K160K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:42221650 C>T maps to NM_004363.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:42231184 G>A maps to NM_004363.2 G686G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr19:42224884 C>T maps to NM_004363.2 Y605Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:42260748 C>T maps to NM_002483.4 Y102Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:42266030 C>T maps to NM_002483.4 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr19:42270133 G>A maps to NM_002483.4 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr19:42265352 G>A maps to NM_002483.4 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:42187797 C>T maps to NM_006890.3 K208K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr19:42190894 G>A maps to NM_006890.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr19:42190895 G>A maps to NM_006890.3 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:42187818 G>A maps to NM_006890.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:42187863 G>A maps to NM_006890.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:43093612 G>A maps to NM_001816.3 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:43097972 C>T maps to NM_001816.3 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:43092990 G>A maps to NM_001816.3 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:43093017 C>T maps to NM_001816.3 K292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:43097972 C>T maps to NM_001816.3 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr19:43093795 C>T maps to NM_001816.3 Q172Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:43097906 C>T maps to NM_001816.3 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr14:23587925 C>T maps to NM_001805.2 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr14:23588105 C>T maps to NM_001805.2 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:37455198 T>C maps to NM_005760.2 E379E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr22:17688088 G>A maps to NM_017424.2 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:17684653 C>T maps to NM_017424.2 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr22:17684452 C>T maps to NM_017424.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:17688073 G>A maps to NM_017424.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr22:17688079 C>T maps to NM_017424.2 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr22:17690465 C>T maps to NM_017424.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr22:17688076 C>T maps to NM_017424.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr22:17688073 G>A maps to NM_017424.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr22:17690306 G>A maps to NM_017424.2 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:18020473 C>T maps to ENST00000400579 P602P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr22:18028130 C>T maps to ENST00000400579 L1031L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:17983972 C>T maps to ENST00000400579 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr22:18022174 G>A maps to ENST00000400579 T760T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr22:17976560 C>T maps to ENST00000400579 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:17990867 G>A maps to ENST00000400579 K257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:18020356 C>T maps to ENST00000400579 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr22:17622111 G>A maps to NM_033070.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr22:17600967 C>T maps to NM_031890.3 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr22:17600952 G>A maps to NM_031890.3 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr9:135942010 C>T maps to NM_001807.3 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:135945961 C>T maps to NM_001807.3 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr9:135945895 C>T maps to NM_001807.3 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:135946023 G>A maps to NM_001807.3 W491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:15793990 C>T maps to ENST00000375924 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr1:15792602 C>T maps to ENST00000375924 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:15789233 C>T maps to ENST00000375924 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:15789949 C>T maps to ENST00000375924 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:15794026 C>T maps to ENST00000375924 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr1:15808870 C>T maps to ENST00000442979 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:15808768 G>A maps to ENST00000442979 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:22336292 C>T maps to NM_005747.4 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:22332202 G>A maps to NM_005747.4 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:22333382 C>T maps to NM_005747.4 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:22329550 G>A maps to NM_005747.4 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:22332004 C>T maps to NM_005747.4 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:22310195 C>T maps to NM_007352.2 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:22303558 C>T maps to NM_007352.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:22313148 C>T maps to NM_007352.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr11:47496920 G>A maps to NM_001172639.1 Q412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:47504245 C>A did not map to a codon.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr11:47505052 G>A maps to NM_001172639.1 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:11047404 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:11367871 C>T maps to NM_006561.3 F456F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:11363308 C>T maps to NM_006561.3 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:151681497 G>A maps to NM_007185.4 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr18:34850767 C>T maps to NM_020180.3 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr18:34853054 G>A maps to NM_020180.3 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr18:34850818 C>T maps to NM_020180.3 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr18:34854306 G>A maps to NM_020180.3 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr19:3224880 C>T maps to NM_021938.3 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:3281300 C>T maps to NM_021938.3 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:3290301 C>T maps to NM_021938.3 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr19:3282251 C>T maps to NM_021938.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:3293398 C>T maps to NM_021938.3 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr15:72580712 G>A maps to NM_052840.4 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr15:72582466 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr22:46835150 G>A maps to NM_014246.1 F1447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr22:46795742 G>A maps to NM_014246.1 S1761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr22:46795747 C>A maps to NM_014246.1 E1760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr22:46794534 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr22:46859637 G>A maps to NM_014246.1 G1383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr22:46835147 C>T maps to NM_014246.1 P1448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:46859930 G>A maps to NM_014246.1 L1286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr22:46776757 G>A maps to NM_014246.1 L2395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr22:46780572 G>A maps to NM_014246.1 V2250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr22:46765588 G>A maps to NM_014246.1 I2624I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr22:46860108 G>A maps to NM_014246.1 L1226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr22:46765660 G>A maps to NM_014246.1 P2600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:46790095 G>A maps to NM_014246.1 A1969A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:46792578 G>T maps to NM_014246.1 C1922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:46931915 G>A maps to NM_014246.1 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr22:46932281 G>A maps to NM_014246.1 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr22:46930582 G>A maps to NM_014246.1 Q829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr22:46792593 C>T maps to NM_014246.1 E1917E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr22:46805045 G>A maps to NM_014246.1 P1691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr22:46795688 G>A maps to NM_014246.1 I1779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr22:46761266 G>A maps to NM_014246.1 S2805S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr22:46860044 G>A maps to NM_014246.1 Q1248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:46782320 G>A maps to NM_014246.1 F2239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr22:46859772 G>A maps to NM_014246.1 F1338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr22:46930319 G>A maps to NM_014246.1 A916A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:109795544 C>T maps to NM_001408.2 P948P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:109814028 C>T maps to NM_001408.2 F2566F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:109816200 C>A maps to NM_001408.2 R2885R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:109793972 G>T maps to NM_001408.2 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:109803662 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:109801228 C>T maps to NM_001408.2 D1162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:109815911 G>A maps to NM_001408.2 E2821E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:109794275 C>T maps to NM_001408.2 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:109795157 C>T maps to NM_001408.2 S819S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:109804457 C>T maps to NM_001408.2 F1442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:109792761 T>C maps to NM_001408.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:109792764 C>T maps to NM_001408.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr1:109793468 C>T maps to NM_001408.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr1:109814010 G>T maps to NM_001408.2 S2560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:48691416 G>A maps to NM_001407.2 H1724H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:48696749 G>A maps to NM_001407.2 I1106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:48696569 G>A maps to NM_001407.2 S1166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr3:48683240 G>A maps to NM_001407.2 S2508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr3:48680280 C>A maps to NM_001407.2 E2815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:48690560 G>A maps to NM_001407.2 L1836L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:48697010 G>A maps to NM_001407.2 V1019V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:48677414 C>T maps to NM_001407.2 R3201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:48691866 G>A maps to NM_001407.2 G1669G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr3:48697367 G>A maps to NM_001407.2 N900N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:48687945 G>A maps to NM_001407.2 L2147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:48688502 G>A maps to NM_001407.2 F2064F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:48694668 G>A maps to NM_001407.2 F1287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:48698245 G>A maps to NM_001407.2 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:48696440 G>A maps to NM_001407.2 S1209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:48685348 G>A maps to NM_001407.2 R2352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:48698360 G>A maps to NM_001407.2 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:48696449 G>A maps to NM_001407.2 L1206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr3:48677498 G>A maps to NM_001407.2 P3173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:48696908 G>A maps to NM_001407.2 I1053I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr3:48677984 C>T maps to NM_001407.2 L3011L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:48697580 C>G maps to NM_001407.2 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr3:48677264 G>A maps to NM_001407.2 A3251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:48699998 G>A maps to NM_001407.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:48682555 G>A maps to NM_001407.2 Y2628Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:48691117 C>T maps to NM_001407.2 R1794R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr3:48679410 G>A maps to NM_001407.2 S2899S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr3:48696374 G>A maps to NM_001407.2 S1231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:48684205 G>A maps to NM_001407.2 R2429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:48684206 G>A maps to NM_001407.2 R2428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:48685382 G>A maps to NM_001407.2 A2340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:48698261 G>A maps to NM_001407.2 I602I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:48699764 G>A maps to NM_001407.2 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:48698849 C>T maps to NM_001407.2 Q406Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:48677423 C>T maps to NM_001407.2 S3198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:48699812 G>A maps to NM_001407.2 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr20:3766205 G>A maps to NM_001810.5 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr20:3765729 G>A maps to NM_001810.5 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr4:104081838 G>A maps to NM_001813.2 V743V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr4:104080164 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr4:104068602 G>A maps to NM_001813.2 T1348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr1:214814356 T>C maps to NM_016343.3 T892T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:214813532 C>T maps to NM_016343.3 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:214816471 C>T maps to NM_016343.3 C1597C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:214818957 C>T maps to NM_016343.3 L2015L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr1:214818198 C>T maps to NM_016343.3 F1762F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:214818204 G>A maps to NM_016343.3 G1764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr1:214826298 T>C maps to NM_016343.3 T2763T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr1:214830531 T>C maps to NM_016343.3 P2914P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr1:214815370 G>A maps to NM_016343.3 E1230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr1:214819326 C>T maps to NM_016343.3 I2138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:214813330 C>T maps to NM_016343.3 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:68504125 C>T maps to NM_022909.3 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:100387403 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:100375737 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:100387213 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr23:100417918 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:100403132 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:100402951 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr23:100381741 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:100382642 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:100402755 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr13:25487115 G>A maps to NM_018451.3 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr13:25478178 G>A maps to NM_018451.3 Q904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr13:25478179 G>A maps to NM_018451.3 S903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr13:25487157 G>A maps to NM_018451.3 F2F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr13:25458129 G>A maps to NM_018451.3 F1265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr13:25479568 G>A maps to NM_018451.3 F869F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr13:25457365 C>T maps to NM_018451.3 R1322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr13:25484174 T>A maps to NM_018451.3 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr13:25486138 G>A maps to NM_018451.3 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:64814355 G>A maps to NM_022145.3 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:173772406 G>C maps to NM_001127181.2 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr22:42335113 C>T maps to NM_024053.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr9:95099877 A>G maps to NM_001012267.1 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr6:49448693 C>T maps to NM_018132.3 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr16:67865768 G>A maps to NM_025082.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr16:67865212 C>T maps to NM_025082.3 Q203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr16:67865710 G>A maps to NM_025082.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:16256434 G>A maps to NM_181716.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr9:123921206 C>T maps to NM_007018.4 L1613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr9:123919770 C>T maps to NM_007018.4 F1463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr9:123912694 C>A maps to NM_007018.4 P1299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr9:123904443 C>T maps to NM_007018.4 L923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr9:123924521 G>A maps to NM_007018.4 W1799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:123932069 G>A maps to NM_007018.4 R2084R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:122758677 G>A maps to NM_153223.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr5:122727022 G>A maps to NM_153223.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:56878145 C>T maps to NM_025009.3 Q933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:56837482 C>T maps to NM_025009.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr15:49031357 G>T maps to NM_001194998.1 C1407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr11:117279655 C>T maps to NM_014956.4 T1220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:117279709 C>T maps to NM_014956.4 S1238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:117251343 G>A maps to NM_014956.4 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr11:117261549 G>A maps to NM_014956.4 E664E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:117280346 G>T maps to NM_014956.4 P1254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr11:117252449 C>T maps to NM_014956.4 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:117222541 C>T maps to NM_014956.4 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:243328039 C>T maps to NM_014812.2 T1074T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr1:243364123 G>A maps to NM_014812.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:243328063 G>A maps to NM_014812.2 S1066S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr18:13056096 C>T maps to NM_032142.3 L1170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr18:13056569 C>T maps to NM_032142.3 S1327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr18:13096207 C>T maps to NM_032142.3 F2153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr18:13049186 C>T maps to NM_032142.3 N799N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr18:13068115 C>T maps to NM_032142.3 F1546F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr18:13055828 C>T maps to NM_032142.3 A1080A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:34091456 C>T maps to NM_007186.3 Q1754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr20:34091512 C>T maps to NM_007186.3 L1772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:34050231 C>T maps to NM_007186.3 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:34091198 C>T maps to NM_007186.3 Q1668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr20:34091908 G>A maps to NM_007186.3 L1904L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr20:34067171 G>A maps to NM_007186.3 E737E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr20:34095952 C>T maps to NM_007186.3 A2280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr20:34091155 C>T maps to NM_007186.3 L1653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr20:34090781 C>T maps to NM_007186.3 L1529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr20:34091155 C>T maps to NM_007186.3 L1653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:34096009 C>T maps to NM_007186.3 T2299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:34055264 C>T maps to NM_007186.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:88482979 G>A maps to NM_025114.3 F1286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr12:88508883 G>A maps to NM_025114.3 Q634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr12:88472895 G>A maps to NM_025114.3 I1779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:88472895 G>A maps to NM_025114.3 I1779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:180031444 C>T maps to NM_014810.4 R1785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr1:180068002 C>T maps to NM_014810.4 F3024F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr1:180006153 C>G maps to NM_014810.4 S1347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:180063582 C>T maps to NM_014810.4 I2781I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:180056804 C>T maps to NM_014810.4 S2126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:179983357 C>T maps to NM_014810.4 H590H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr1:180062820 C>T maps to NM_014810.4 A2527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:180064815 G>A maps to NM_014810.4 K2890K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:95262875 C>T maps to NM_018131.4 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr10:95259876 C>A maps to NM_018131.4 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:95552019 C>T maps to NM_014679.3 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:134256001 C>T maps to NM_025180.3 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr2:65298832 C>T maps to NM_015147.2 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:65299153 A>G maps to NM_015147.2 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:65299154 C>T maps to NM_015147.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:65296934 G>A maps to NM_015147.2 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:138251410 A>G maps to NM_024491.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:138219579 T>C maps to NM_024491.2 E455E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr5:620263 C>T maps to NM_018140.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr5:647959 G>A maps to NM_018140.3 V569V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:637770 G>A maps to NM_018140.3 Q348Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:637791 G>A maps to NM_018140.3 E355E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr18:12699098 A>G maps to NM_024899.2 C133C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr18:12691398 G>A maps to NM_024899.2 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:80881578 C>T maps to NM_001098802.1 S690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr9:80879233 T>G did not map to a codon.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr3:101484341 C>T maps to ENST00000327230 Q875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:101483989 C>T maps to ENST00000327230 S757S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:101476029 C>T maps to ENST00000327230 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr3:101476916 A>T maps to ENST00000327230 I489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr9:14722532 G>A maps to NM_005454.2 N46N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr9:14722165 G>A maps to NM_005454.2 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:14722657 A>G maps to NM_005454.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr9:14722325 C>T maps to NM_005454.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr9:14722162 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:14722226 G>A maps to NM_005454.2 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr9:14722496 G>A maps to NM_005454.2 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr9:131198099 C>T maps to NM_016174.4 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr9:131196509 T>C did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr9:131185508 C>T maps to NM_016174.4 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:131186487 G>A maps to NM_016174.4 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr9:131198141 C>T maps to NM_016174.4 S582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:47116006 G>A maps to NM_022766.5 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:182521721 C>T maps to NM_001030311.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:182403988 G>A maps to NM_001030311.2 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:182468672 G>A maps to NM_001030311.2 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:182468741 C>T maps to NM_001030311.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:182403826 G>A maps to NM_001030311.2 V536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:182468747 G>A maps to NM_001030311.2 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:182430227 C>T maps to NM_001030311.2 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:182521565 C>T maps to NM_001030311.2 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:182468675 G>A maps to NM_001030311.2 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr2:182414388 C>T maps to NM_001030311.2 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:182412546 A>G did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:55862743 C>T maps to NM_001025195.1 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr16:55857492 G>A maps to NM_001025195.1 Q170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:55853479 C>T maps to NM_001025195.1 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:55862791 G>A maps to NM_001025195.1 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:55855408 C>T maps to NM_001025195.1 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr16:55844492 G>A maps to NM_001025195.1 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:66975530 C>T maps to NM_003869.5 F410F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:66969504 C>T maps to NM_003869.5 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:66976688 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr16:66974522 C>T maps to NM_003869.5 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr16:67000145 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:66997450 G>A maps to NM_024922.5 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr16:67006382 C>T maps to NM_024922.5 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr16:66997462 C>T maps to NM_024922.5 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:66997829 C>T maps to NM_024922.5 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr16:67006789 C>T maps to NM_024922.5 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:66998584 C>T maps to NM_024922.5 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:55886804 G>A maps to NM_001143685.1 R421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:55905640 G>A maps to NM_001143685.1 Q105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:55893497 G>A maps to NM_001143685.1 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:55886867 G>A maps to NM_001143685.1 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:55886880 G>A maps to NM_001143685.1 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr16:55886934 G>A maps to NM_001143685.1 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:55907803 C>T maps to NM_001143685.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr16:55880741 C>T maps to NM_001143685.1 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr16:67029621 C>T maps to ENST00000326686 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr16:67037199 G>A maps to ENST00000326686 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr16:67038036 C>T maps to ENST00000326686 D330D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:67038102 G>A maps to ENST00000326686 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr18:580551 C>T maps to NM_004066.1 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr18:580611 G>A maps to NM_004066.1 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr18:580809 G>A maps to NM_004066.1 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:580497 G>A maps to NM_004066.1 K30K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:580893 C>T maps to NM_004066.1 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:151997133 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:151997144 G>A did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:151998260 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:57003318 C>T maps to NM_000078.2 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:57005246 C>T maps to NM_000078.2 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:57009056 C>T maps to NM_000078.2 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:57003405 G>A maps to NM_000078.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:57012109 G>A maps to NM_000078.2 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr16:57007292 C>T maps to NM_000078.2 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:56996001 C>T maps to NM_000078.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:57003537 G>A maps to NM_000078.2 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:57009029 G>A maps to NM_000078.2 W316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:57004977 C>T maps to NM_000078.2 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr6:31914339 G>A maps to ENST00000437789 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr6:31915740 G>A maps to ENST00000437789 K762K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:31915257 G>A maps to ENST00000437789 Q708Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:31918678 C>T maps to ENST00000437789 R1107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:31915743 C>T maps to ENST00000437789 I763I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr6:31917270 G>T maps to ENST00000437789 E951*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:31918459 G>A maps to ENST00000437789 G1065G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr6:31915830 A>G maps to ENST00000437789 K792K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr6:31915257 G>A maps to ENST00000437789 Q708Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr6:31919250 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:31915561 C>T maps to ENST00000437789 F736F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:31918169 G>A maps to ENST00000437789 K1040K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:31915570 C>T maps to ENST00000437789 S739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr6:31915743 C>T maps to ENST00000437789 I763I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr2:131356272 C>T maps to NM_032545.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:196646615 T>C maps to NM_000186.3 C146C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr1:196716256 C>T maps to NM_000186.3 S1170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:196695936 G>A maps to NM_000186.3 W701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr1:196682901 G>A maps to NM_000186.3 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr1:196694338 C>T maps to NM_000186.3 F595F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr1:196716409 G>A maps to NM_000186.3 G1221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr1:196705993 C>T maps to NM_000186.3 P818P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:196716295 G>A maps to NM_000186.3 W1183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:196695903 C>T maps to NM_000186.3 T690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:196642282 G>A maps to NM_000186.3 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:196715004 C>T maps to NM_000186.3 F1123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:196654240 T>C maps to NM_000186.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:196694309 C>T maps to NM_000186.3 Q586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:196695739 C>T maps to NM_000186.3 Q672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:196642282 G>A maps to NM_000186.3 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:196714989 G>A maps to NM_000186.3 G1118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr1:196711157 G>A maps to NM_000186.3 W1037*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:196683012 G>A maps to NM_000186.3 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:196646780 G>A maps to NM_000186.3 E201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:196716442 G>A maps to NM_000186.3 *1232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:196801095 G>A maps to NM_002113.2 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr1:196796105 G>A maps to NM_002113.2 W134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:196794622 T>C maps to NM_002113.2 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:196801089 G>A maps to NM_002113.2 W318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:196799768 A>C maps to NM_002113.2 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:196928156 C>T maps to ENST00000367421 R254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr1:196927144 G>A maps to ENST00000367421 E185E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:196918591 C>T maps to ENST00000367421 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:196920048 T>C maps to ENST00000367421 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:196918755 G>A maps to ENST00000367421 W77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr1:196928176 G>A maps to ENST00000367421 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:196928209 G>A maps to ENST00000367421 *271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:196748928 A>T maps to NM_021023.5 K86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr1:196759337 G>A maps to NM_021023.5 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:196757490 T>C maps to NM_021023.5 C192C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:196762595 C>T maps to NM_021023.5 Q316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr1:196749095 C>T maps to NM_021023.5 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:196762595 C>T maps to NM_021023.5 Q316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3BZ-06A-12D-A196-08 chr1:196884212 T>A maps to NM_006684.2 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:196857300 C>T maps to NM_006684.2 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr1:196883787 C>T maps to NM_006684.2 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:196883700 G>A maps to NM_006684.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr1:196887502 G>A maps to NM_006684.2 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:196883688 C>T maps to NM_006684.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr1:196883754 C>T maps to NM_006684.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:196887466 G>A maps to NM_006684.2 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:196967405 G>A maps to ENST00000367414 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:196971687 G>A maps to ENST00000367414 Q432Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:196953237 G>A maps to ENST00000367414 W158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:196967405 G>A maps to ENST00000367414 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:196973902 C>T maps to ENST00000367414 F505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:196963357 G>A maps to ENST00000367414 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:196964875 C>T maps to ENST00000367414 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr1:196971795 T>C did not map to a codon.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:196953112 G>A maps to ENST00000367414 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr1:196964937 G>A maps to ENST00000367414 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:196964898 G>A maps to ENST00000367414 K244K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:196952084 C>T maps to ENST00000367414 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:196963289 T>C maps to ENST00000367414 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:196965308 G>A maps to ENST00000367414 W340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr4:110687841 G>A maps to ENST00000394635 Q66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr4:110662120 G>A maps to ENST00000394635 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:110682670 A>C did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:110687911 G>A maps to ENST00000394635 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr4:110662236 T>A maps to ENST00000394635 K530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr4:110681754 C>T maps to ENST00000394635 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:110663746 G>A maps to ENST00000394635 N486N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:110687869 C>T maps to ENST00000394635 E56E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:110667516 G>A maps to ENST00000394635 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr4:110687914 G>A maps to ENST00000394635 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr4:110682703 G>A maps to ENST00000394635 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:110662231 C>T maps to ENST00000394635 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:110670405 G>A maps to ENST00000394635 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:110667402 G>A maps to ENST00000394635 I476I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr11:65622827 G>A maps to NM_005507.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr2:202025476 C>T maps to NM_001127183.1 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:202025548 C>T maps to NM_001127183.1 H396H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:202028671 G>A maps to NM_001127183.1 K473K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:47487634 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:47487667 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:47487622 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:47485868 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:47485899 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr7:117175351 C>T maps to NM_000492.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr7:117175330 C>T maps to NM_000492.3 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr7:117175354 C>T maps to NM_000492.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:117282490 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:117282637 G>A maps to NM_000492.3 V1288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr7:117243606 G>A maps to NM_000492.3 G893G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:117199642 C>T maps to NM_000492.3 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:117199534 G>A maps to NM_000492.3 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:117176664 C>T maps to NM_000492.3 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:117171038 G>A maps to NM_000492.3 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:117175430 C>T maps to NM_000492.3 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:117180228 C>T maps to NM_000492.3 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:117304797 G>A maps to NM_000492.3 V1340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr7:117232392 C>T maps to NM_000492.3 I724I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:117175408 C>T maps to NM_000492.3 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr7:117171038 G>A maps to NM_000492.3 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:117175321 C>T maps to NM_000492.3 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:117242900 C>T maps to NM_000492.3 L881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:117175321 C>T maps to NM_000492.3 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:117232710 G>A maps to NM_000492.3 K830K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr7:117232287 G>A maps to NM_000492.3 Q689Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:117246731 G>A maps to NM_000492.3 G971G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:117174388 C>T maps to NM_000492.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:117246788 C>T maps to NM_000492.3 T990T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:117232020 G>A maps to NM_000492.3 R600R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:117175411 G>A maps to NM_000492.3 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:117175423 C>T maps to NM_000492.3 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:117199611 G>A maps to NM_000492.3 W496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:117149195 G>A maps to NM_000492.3 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr7:117174388 C>T maps to NM_000492.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:117175430 C>T maps to NM_000492.3 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:117120198 C>T maps to NM_000492.3 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:117171168 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr7:117149105 G>T maps to NM_000492.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:117243595 C>T maps to NM_000492.3 Q890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:117250682 C>T maps to NM_000492.3 F1033F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr7:117175430 C>T maps to NM_000492.3 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:117182158 G>A maps to NM_000492.3 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr7:117232674 G>A maps to NM_000492.3 L818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr7:117180228 C>T maps to NM_000492.3 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:117232119 C>T maps to NM_000492.3 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:117232170 C>T maps to NM_000492.3 F650F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:117235006 G>A maps to NM_000492.3 E838E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:117250682 C>T maps to NM_000492.3 F1033F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr7:117199594 C>T maps to NM_000492.3 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:117243762 G>A maps to NM_000492.3 S945S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr7:117282566 G>T maps to NM_000492.3 G1265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:87796036 C>T maps to NM_000735.2 K68K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:49526154 G>A maps to ENST00000448402 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:49538905 G>A maps to ENST00000391869 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:49539515 T>G maps to ENST00000391869 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr3:88104855 G>A maps to NM_001195308.1 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr3:88104978 G>A maps to NM_001195308.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr1:151509820 A>T maps to NM_020770.2 *1204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:151499555 T>C maps to NM_020770.2 D623D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr1:151495981 C>T maps to NM_020770.2 R405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:151506471 C>T maps to NM_020770.2 L922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:151502584 G>A maps to NM_020770.2 R769R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:151495950 G>A maps to NM_020770.2 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr15:57730211 C>T maps to NM_032866.3 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:57730547 G>A maps to NM_032866.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:57731423 G>A maps to NM_032866.3 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr15:57731084 C>T maps to NM_032866.3 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:57835964 C>T maps to NM_032866.3 S1121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:57731588 G>A maps to NM_032866.3 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr15:57730913 C>T maps to NM_032866.3 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr15:57838368 G>A maps to NM_032866.3 E1235E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr15:57744448 G>A maps to NM_032866.3 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:57809018 A>G maps to NM_032866.3 Q815Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr15:57753910 C>T maps to NM_032866.3 L742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr15:57731075 C>T maps to NM_032866.3 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:57839672 C>T maps to NM_032866.3 V1298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr15:57838287 G>A maps to NM_032866.3 L1208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr15:57730862 G>A maps to NM_032866.3 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:57730874 C>T maps to NM_032866.3 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr15:57744418 G>A maps to NM_032866.3 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:57731225 G>A maps to NM_032866.3 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr15:57734654 G>A maps to NM_032866.3 G594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr15:57809129 C>T maps to NM_032866.3 I852I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:57730673 G>A maps to NM_032866.3 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:57745892 G>A maps to NM_032866.3 V689V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:57809129 C>T maps to NM_032866.3 I852I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:57815730 G>A maps to NM_032866.3 E920E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:57730484 G>A maps to NM_032866.3 E96E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:27325066 G>A maps to ENST00000404694 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:27324159 C>T maps to ENST00000404694 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:90966299 G>A maps to NM_003956.3 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr15:41247708 C>T maps to NM_024111.3 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:41247758 C>A maps to NM_024111.3 Y194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr17:48545402 T>A maps to NM_001267.2 K258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr17:48546021 C>T maps to NM_001267.2 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:48545817 G>A maps to NM_001267.2 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr19:4442294 G>A maps to NM_005483.2 E909E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:4428806 C>T maps to NM_005483.2 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:4418030 C>T maps to NM_005483.2 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:4409288 C>T maps to NM_005483.2 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:4429772 C>T maps to NM_005483.2 S614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:4433241 C>T maps to NM_005483.2 P793P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:4432133 C>T maps to NM_005483.2 F711F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:4432134 C>T maps to NM_005483.2 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:4433533 C>T maps to NM_005483.2 Q891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:4422786 C>T maps to NM_005483.2 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr21:37785271 G>A maps to NM_005441.2 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr10:50854659 C>T maps to NM_020549.4 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr10:50856614 C>T maps to NM_020549.4 I448I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr10:50835826 G>A maps to NM_020549.4 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:50870725 G>A maps to NM_020549.4 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr10:50828602 C>T maps to NM_020549.4 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr10:50854650 A>C maps to NM_020549.4 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr10:50828587 C>T maps to NM_020549.4 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr10:50835823 C>T maps to NM_020549.4 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr10:50835802 G>A maps to NM_020549.4 W361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr10:50835718 G>A maps to NM_020549.4 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr10:50859977 G>A maps to NM_020549.4 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr10:50835682 C>T maps to NM_020549.4 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:75541844 C>T maps to NM_203298.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr22:24109662 T>A maps to ENST00000401675 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr22:24108363 G>A maps to ENST00000401675 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:56174058 G>A maps to NM_016139.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:113343824 C>T maps to ENST00000409719 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr8:57128949 C>T maps to NM_001011667.1 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr5:98228320 G>A maps to NM_001270.2 R696R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:98212151 C>T maps to NM_001270.2 R1116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr5:98206456 G>A maps to NM_001270.2 T1304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:98236985 G>T maps to NM_001270.2 S164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr15:93521461 A>G did not map to a codon.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr15:93492256 C>T maps to NM_001271.3 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr15:93522379 T>C maps to NM_001271.3 L915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr15:93543788 G>T maps to NM_001271.3 V1352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr15:93567670 C>T maps to NM_001271.3 F1741F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr15:93567671 C>T maps to NM_001271.3 R1742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr15:93499744 G>A maps to NM_001271.3 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr15:93492256 C>T maps to NM_001271.3 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr15:93528898 C>T maps to NM_001271.3 R1137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:93518141 A>T maps to NM_001271.3 K847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:93528870 C>T maps to NM_001271.3 L1127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr15:93567916 G>A maps to NM_001271.3 W1823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:7806312 C>T maps to NM_001005271.2 I1202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr17:7793965 C>A maps to NM_001005271.2 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr17:7803627 T>C maps to NM_001005271.2 G960G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:7798688 C>T maps to NM_001005271.2 I571I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:7808466 C>T maps to NM_001005271.2 F1433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:7808466 C>T maps to NM_001005271.2 F1433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:7806291 C>T maps to NM_001005271.2 T1195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr17:7803929 C>T maps to NM_001005271.2 I1012I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr17:7802713 C>T maps to NM_001005271.2 N858N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr17:7806014 C>T maps to NM_001005271.2 L1173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr17:7808416 G>A did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr17:7809172 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr12:6705211 G>A maps to ENST00000309577 Q662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr12:6705278 G>A maps to ENST00000309577 H639H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:6702264 G>A maps to ENST00000309577 Q882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:6702773 G>A maps to ENST00000309577 S774S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr12:6701682 G>A maps to ENST00000309577 Q942*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr12:6701683 G>A maps to ENST00000309577 D941D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:6687653 G>A maps to ENST00000309577 P1708P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:6709742 G>A maps to ENST00000309577 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:6700683 G>A maps to ENST00000309577 I1096I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:6705269 G>A maps to ENST00000309577 I642I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:6702614 G>A maps to ENST00000309577 A827A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:6700949 G>A maps to ENST00000309577 A1044A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:6697064 G>A maps to ENST00000309577 Y1172Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:6690228 A>G maps to ENST00000309577 P1658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:6690902 G>A maps to ENST00000309577 S1559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:6710656 G>T maps to ENST00000309577 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:6709723 G>A maps to ENST00000309577 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr12:6691338 A>G maps to ENST00000309577 L1521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr12:6691437 G>A maps to ENST00000309577 V1488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:6228337 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:6189051 C>T maps to NM_015557.2 E1155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr1:6204139 G>A maps to NM_015557.2 I626I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr1:6181562 C>T maps to NM_015557.2 L1590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr1:6228296 G>A maps to NM_015557.2 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr1:6215777 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:6184140 C>T maps to NM_015557.2 G1522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:6214930 C>T maps to NM_015557.2 K178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr1:6209356 C>T maps to NM_015557.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:6184110 C>T maps to NM_015557.2 E1532E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:6228296 G>A maps to NM_015557.2 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:6172242 C>T maps to NM_015557.2 G1699G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:6202250 C>T maps to NM_015557.2 R791R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:6203990 C>T maps to NM_015557.2 R645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr1:6206309 C>T maps to NM_015557.2 K588K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr1:6206301 C>T maps to NM_015557.2 W591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:6169885 C>T maps to NM_015557.2 G1849G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:6214774 G>A maps to NM_015557.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:6206354 G>A maps to NM_015557.2 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:6195420 C>T maps to NM_015557.2 K913K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:6194186 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:6185910 C>T maps to NM_015557.2 Q1362Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:6219500 G>A maps to NM_015557.2 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:6181207 C>T maps to NM_015557.2 E1623E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr1:6194870 G>A maps to NM_015557.2 S973S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:6214780 G>A maps to NM_015557.2 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:6181213 C>T maps to NM_015557.2 R1621R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:6188267 C>T maps to NM_015557.2 K1247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:6204139 G>A maps to NM_015557.2 I626I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:6173029 G>A maps to NM_015557.2 I1647I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:6166482 G>A maps to NM_015557.2 N1943N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:6184140 C>T maps to NM_015557.2 G1522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:6184609 G>A maps to NM_015557.2 T1502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:6189093 C>T maps to NM_015557.2 K1141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:6228308 G>A maps to NM_015557.2 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:6202196 G>A maps to NM_015557.2 F809F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:6204139 G>A maps to NM_015557.2 I626I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:6214927 G>A maps to NM_015557.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:6228296 G>A maps to NM_015557.2 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr1:6195312 C>T maps to NM_015557.2 R949R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr20:40033910 G>A maps to NM_032221.3 I2490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:40033757 G>A maps to NM_032221.3 P2541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:40034030 G>A maps to NM_032221.3 L2450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:40080652 C>T maps to NM_032221.3 W1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr20:40120435 C>T maps to NM_032221.3 W446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr20:40120436 C>T maps to NM_032221.3 W446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:40081462 C>T maps to NM_032221.3 T1080T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:40044086 G>A maps to NM_032221.3 S2226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr20:40102056 G>A maps to NM_032221.3 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr8:61735190 C>T maps to NM_017780.2 P1029P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:61749450 T>C maps to NM_017780.2 P1355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr8:61748830 C>T maps to NM_017780.2 L1326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr8:61766931 C>T maps to NM_017780.2 V2262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:61757560 C>T maps to NM_017780.2 F1663F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr8:61773533 C>A maps to NM_017780.2 P2560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr8:61743012 C>T maps to NM_017780.2 R1219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr8:61768562 C>T maps to NM_017780.2 N2322N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:61742997 C>T maps to NM_017780.2 Q1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:61769329 C>A maps to NM_017780.2 L2497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr14:21883940 G>A maps to NM_001170629.1 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr14:21861910 G>A maps to NM_001170629.1 Q2015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr14:21896139 C>A maps to NM_001170629.1 E497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:21871793 G>A maps to NM_001170629.1 F1112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr14:21870114 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr14:21871804 G>A maps to NM_001170629.1 L1109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr16:53279685 A>T maps to ENST00000219084 G1126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr16:53358666 C>T maps to ENST00000219084 Q2852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:53191227 C>T maps to ENST00000219084 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:53340207 C>T maps to ENST00000219084 Q2227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:53857355 C>T maps to NM_018397.4 W227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:53853614 G>A maps to NM_018397.4 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:53851899 G>A maps to NM_018397.4 I563I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:53852985 G>A maps to NM_018397.4 Q449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:53857355 C>T maps to NM_018397.4 W227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:29121233 G>A maps to NM_001005735.1 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:16634033 A>G maps to NM_006387.5 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:16643866 G>A maps to NM_006387.5 N159N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr19:16632417 G>A maps to NM_006387.5 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr19:16643488 C>T maps to NM_006387.5 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr12:133430056 G>A maps to NM_001161344.1 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr12:133448934 C>T maps to NM_001161344.1 Q93Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:133434030 G>A maps to NM_001161344.1 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:133434018 G>A maps to NM_001161344.1 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:133438074 G>A maps to NM_001161344.1 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:133433142 G>T maps to NM_001161344.1 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr14:93393934 G>A maps to NM_001275.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:93390580 G>A maps to NM_001275.3 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:93398964 G>A maps to NM_001275.3 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr20:5904143 C>T maps to NM_001819.2 Q452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr20:5903201 C>T maps to NM_001819.2 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr20:5903555 C>T maps to NM_001819.2 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A6L9-06A-11D-A32N-08 chr20:5902990 C>T maps to NM_001819.2 D67D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:5904100 G>A maps to NM_001819.2 E437E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr20:5904293 C>T maps to NM_001819.2 Q502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr20:5903701 G>A maps to NM_001819.2 K304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr20:5897563 G>A maps to NM_001819.2 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:5897494 C>T maps to NM_001819.2 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:5904346 G>A maps to NM_001819.2 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr20:5903561 C>T maps to NM_001819.2 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr20:5897512 G>A maps to NM_001819.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr20:5904517 C>T maps to NM_001819.2 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr20:5896999 G>A maps to NM_001819.2 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:5903152 G>A maps to NM_001819.2 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:5903941 G>A maps to NM_001819.2 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr20:5903092 G>A maps to NM_001819.2 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr1:203150400 G>A maps to NM_001276.2 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:203148993 G>A maps to NM_001276.2 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:203152893 G>A maps to NM_001276.2 Q114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:203152894 G>A maps to NM_001276.2 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:111783989 G>A maps to NM_004000.2 Q320Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:111781454 C>T maps to NM_004000.2 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr1:111862064 G>A maps to NM_201653.2 K384K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:111854317 C>T maps to NM_201653.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:111861113 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:111861281 G>A maps to NM_201653.2 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr1:111854905 C>T maps to NM_201653.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:111857954 C>T maps to NM_201653.2 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:111854893 C>T maps to NM_201653.2 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr1:111857954 C>T maps to NM_201653.2 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr23:72797280 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr4:54876272 G>A maps to NM_012110.2 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr1:203188414 G>A maps to NM_003465.2 Q320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr1:203188446 C>T maps to NM_003465.2 W309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:203194879 G>A maps to NM_003465.2 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:203186115 C>T maps to NM_003465.2 R434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:203191392 C>A maps to NM_003465.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr1:203188412 C>T maps to NM_003465.2 Q320Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:203194879 G>A maps to NM_003465.2 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:203197679 G>A maps to NM_003465.2 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:203194945 C>T maps to NM_003465.2 Q36Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:67832065 G>A maps to NM_001277.2 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr11:67821481 G>A maps to NM_001277.2 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:67829479 G>A maps to NM_001277.2 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr22:51020180 G>A maps to NM_005198.4 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr22:51018250 A>G maps to NM_005198.4 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:51017914 G>A maps to NM_005198.4 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr3:423919 G>A maps to NM_006614.2 R645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr3:382567 C>T maps to NM_006614.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr3:407798 G>T did not map to a codon.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr3:403448 C>T maps to NM_006614.2 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr3:447381 C>T maps to NM_006614.2 P1221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:369966 G>A maps to NM_006614.2 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:423910 G>A maps to NM_006614.2 R642R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:425547 G>A maps to NM_006614.2 K742K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr3:369885 C>T maps to NM_006614.2 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:430939 G>A maps to NM_006614.2 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:361521 C>T maps to NM_006614.2 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:402000 G>A maps to NM_006614.2 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr3:383721 G>A maps to NM_006614.2 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:85212874 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:85218956 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:85218957 G>C did not map to a codon.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr23:85119750 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr16:89712396 G>A maps to NM_001083314.1 C216C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q3-06A-11D-A196-08 chr18:11852106 G>A maps to NM_020412.4 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr3:87294926 C>T maps to NM_014043.3 Q64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:24682687 G>A maps to NM_014169.3 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr14:24682668 C>A maps to NM_014169.3 G36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr20:32436417 C>T maps to NM_176812.4 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr8:82645022 C>T maps to NM_152284.3 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:82667691 G>A maps to NM_152284.3 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:82665377 G>A maps to NM_152284.3 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:82667640 C>A maps to NM_152284.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:82670727 G>A maps to NM_152284.3 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:33276470 A>G maps to NM_016410.5 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr17:78972194 C>T maps to NM_024591.4 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr8:23113986 C>T maps to NM_152272.3 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:23106782 C>T maps to NM_152272.3 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr2:175742626 G>A maps to NM_001822.4 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:175779841 C>T maps to NM_001822.4 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:175677154 C>T maps to NM_001822.4 K256K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:175677169 G>A maps to NM_001822.4 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:29519971 G>A maps to NM_004067.2 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:29546895 C>T maps to NM_004067.2 I348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr21:19629390 G>A maps to NM_024944.2 W165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr21:19628952 C>T maps to NM_024944.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr21:19628896 C>T maps to NM_024944.2 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr21:19629403 G>A maps to NM_024944.2 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr21:19629024 G>A maps to NM_024944.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr21:19628995 T>C maps to NM_024944.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr15:41555046 C>T maps to NM_007236.4 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr15:41571572 C>T maps to NM_007236.4 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr16:23768610 G>A maps to NM_022097.2 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr16:23767467 C>T maps to NM_022097.2 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr2:220408028 C>A maps to NM_024536.5 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr7:150935418 G>A maps to NM_019015.1 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:150932642 G>A maps to NM_019015.1 W258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:150931225 C>T maps to NM_019015.1 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr7:150932235 T>C maps to NM_019015.1 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:150934797 G>A maps to NM_019015.1 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:150934933 C>T maps to NM_019015.1 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr8:141525237 G>A maps to NM_017444.4 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:184103937 C>T maps to NM_003741.2 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr3:184106423 G>A maps to NM_003741.2 G868G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:184100174 A>C did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:184106375 G>A maps to NM_003741.2 V852V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr3:184100506 G>A maps to NM_003741.2 E309E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:184103931 G>A maps to NM_003741.2 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:184102389 C>T maps to NM_003741.2 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:184099747 C>T maps to NM_003741.2 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:184104543 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:184106375 G>A maps to NM_003741.2 V852V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr3:184100833 C>T maps to NM_003741.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr3:184100937 G>A maps to NM_003741.2 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr23:109931893 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr23:109924752 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:109931905 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:109931859 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr23:109963151 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:109931859 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:109964647 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr23:109964647 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:109931982 G>C did not map to a codon.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr23:109922645 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:109943930 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:109924793 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:109922605 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr23:109931887 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:74413907 G>A maps to NM_015424.3 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr11:74415555 G>A maps to NM_015424.3 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr11:74414497 G>A maps to NM_015424.3 H266H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:74414479 G>A maps to NM_015424.3 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:74424494 G>A maps to NM_015424.3 H75H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr11:74415648 C>T maps to NM_015424.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:74414460 G>A maps to NM_015424.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr15:30659727 G>A maps to NM_139320.1 Q205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:62677551 G>A maps to NM_000738.2 Q341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:62678023 G>A maps to NM_000738.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:62677321 G>A maps to NM_000738.2 C417C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr7:136700665 C>T maps to NM_001006628.1 Q352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr7:136700133 G>A maps to NM_001006628.1 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:136700736 G>A maps to NM_001006628.1 K375K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr7:136700127 G>A maps to NM_001006628.1 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr7:136700445 G>A maps to NM_001006628.1 E278E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:136700490 C>T maps to NM_001006628.1 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:136700259 G>A maps to NM_001006628.1 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr7:136700760 G>A maps to NM_001006628.1 K383K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr7:136700445 G>A maps to NM_001006628.1 E278E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr7:136699959 C>T maps to NM_001006628.1 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:136700712 G>A maps to NM_001006628.1 K367K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr7:136700964 T>C maps to NM_001006628.1 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr7:136699737 C>T maps to NM_001006628.1 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:136700835 C>T maps to NM_001006628.1 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr1:240071147 C>T maps to NM_000740.2 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:240071542 G>A maps to NM_000740.2 E264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:240072451 G>A maps to NM_000740.2 K567K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:240071506 G>A maps to NM_000740.2 W252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:240071959 G>A maps to NM_000740.2 R403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr1:240071053 G>A maps to NM_000740.2 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:240071953 G>A maps to NM_000740.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:240072235 G>A maps to NM_000740.2 A495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:240071509 G>A maps to NM_000740.2 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:240071704 G>A maps to NM_000740.2 K318K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:240071161 G>A maps to NM_000740.2 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:240071791 G>A maps to NM_000740.2 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:240071425 C>T maps to NM_000740.2 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:240071161 G>A maps to NM_000740.2 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:240071797 C>T maps to NM_000740.2 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr1:240070798 C>T maps to NM_000740.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:46408062 G>T maps to NM_000741.2 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:46407528 T>C maps to NM_000741.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:46406976 G>A maps to NM_000741.2 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:46406895 G>T maps to NM_000741.2 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:46407939 G>A maps to NM_000741.2 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr11:46406904 C>T maps to NM_000741.2 T401T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:46406976 G>A maps to NM_000741.2 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr15:34355397 C>T maps to NM_012125.3 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr15:34356465 G>A maps to NM_012125.3 K516K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:34356318 C>T maps to NM_012125.3 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:34356375 C>T maps to NM_012125.3 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:34356342 C>T maps to NM_012125.3 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:34356393 C>T maps to NM_012125.3 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:175622397 C>T maps to NM_001039523.2 W105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:175614847 G>A maps to NM_001039523.2 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr2:175624214 C>T did not map to a codon.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr11:3690439 G>A maps to NM_020402.2 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr8:27321464 G>A maps to NM_000742.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:27321122 G>A maps to NM_000742.3 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:27321383 G>A maps to NM_000742.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr8:27319174 G>A maps to NM_000742.3 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr15:78889059 C>T maps to NM_000743.4 W468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr15:78909363 A>T did not map to a codon.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr15:78888993 C>T maps to NM_000743.4 G490G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-ER-A19A-06A-21D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr15:78894515 C>T maps to NM_000743.4 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:78888957 C>T maps to NM_000743.4 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:78894011 G>A maps to NM_000743.4 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr20:61981799 G>A maps to NM_000744.5 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:61981007 G>A maps to NM_000744.5 F585F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr20:61978119 G>A maps to NM_000744.5 F618F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr20:61981640 G>A maps to NM_000744.5 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:61981793 G>A maps to NM_000744.5 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr20:61982009 G>A maps to NM_000744.5 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr20:61981532 G>A maps to NM_000744.5 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr20:61982225 G>A maps to NM_000744.5 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:61981982 G>A maps to NM_000744.5 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:61982225 G>A maps to NM_000744.5 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:61981796 G>A maps to NM_000744.5 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:61981877 G>A maps to NM_000744.5 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:61982369 C>T maps to NM_000744.5 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:61990995 G>A maps to NM_000744.5 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:61981718 G>A maps to NM_000744.5 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr15:78882971 C>T maps to NM_000745.3 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr15:78873237 T>A maps to NM_000745.3 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:78882341 G>A maps to NM_000745.3 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr15:78882617 C>T maps to NM_000745.3 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:42611870 G>A maps to NM_004198.3 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:42611855 G>A maps to NM_004198.3 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:42612174 C>T maps to NM_004198.3 W90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr8:42611522 C>T maps to NM_004198.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:32450619 C>T maps to NM_001190455.1 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr15:32460295 G>A maps to NM_001190455.1 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr4:40356374 G>A maps to NM_017581.2 R426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:40351379 C>T maps to NM_017581.2 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr4:40351123 C>T maps to NM_017581.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr4:40356122 G>A maps to NM_017581.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr4:40356149 C>T maps to NM_017581.2 V351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr4:40351399 C>T maps to NM_017581.2 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:40350961 C>T maps to NM_017581.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:40356371 G>A maps to NM_017581.2 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr4:40356479 G>A maps to NM_017581.2 W461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:40337519 G>A maps to NM_017581.2 W12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:40351264 C>T maps to NM_017581.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:40356209 G>A maps to NM_017581.2 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:40351358 C>T maps to NM_017581.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:40351255 C>T maps to NM_017581.2 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr4:40351270 C>T maps to NM_017581.2 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:40337483 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:40351264 C>T maps to NM_017581.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:40356488 C>T maps to NM_017581.2 F464F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr4:40339307 C>T maps to NM_017581.2 Q98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr17:7358760 C>T maps to NM_000747.2 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:7358730 C>T maps to NM_000747.2 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:7350370 G>A maps to NM_000747.2 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:7350469 G>A maps to NM_000747.2 Q154Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:7352033 G>T maps to NM_000747.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:154542296 T>C maps to NM_000748.2 N80N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:154543766 G>A maps to NM_000748.2 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:154544018 C>T maps to NM_000748.2 N240N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:154543970 C>T maps to NM_000748.2 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:42587196 C>T maps to NM_000749.3 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:42587334 C>T maps to NM_000749.3 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:42586953 C>T maps to NM_000749.3 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr8:42587283 C>T maps to NM_000749.3 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:42587061 G>A maps to NM_000749.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr8:42586887 C>T maps to NM_000749.3 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr8:42591760 G>A maps to NM_000749.3 *459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:42587467 C>T maps to NM_000749.3 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr8:42586851 C>T maps to NM_000749.3 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:42586908 C>A maps to NM_000749.3 C153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:42587082 G>A maps to NM_000749.3 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:42587643 C>T maps to NM_000749.3 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr15:78921815 G>A maps to NM_000750.3 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr15:78921470 G>A maps to NM_000750.3 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr15:78927801 G>A maps to NM_000750.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr15:78922160 G>A maps to NM_000750.3 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr15:78923469 G>A maps to NM_000750.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr15:78923470 G>A maps to NM_000750.3 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr15:78921794 G>A maps to NM_000750.3 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:78923521 C>T maps to NM_000750.3 W85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr15:78922178 C>T maps to NM_000750.3 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:78921782 G>A maps to NM_000750.3 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:78922031 G>A maps to NM_000750.3 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr15:78921494 C>T maps to NM_000750.3 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:233396071 G>A maps to NM_000751.1 K277K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr2:233398648 G>A maps to NM_000751.1 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:233393057 C>T maps to NM_000751.1 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:233394805 C>T maps to NM_000751.1 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:233393643 C>T maps to NM_000751.1 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:233399003 G>A maps to NM_000751.1 G441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:233398735 G>C maps to NM_000751.1 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:233394685 G>A maps to NM_000751.1 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:4804297 G>A maps to NM_000080.3 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr17:4805555 G>A maps to NM_000080.3 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:233407616 C>T maps to NM_005199.4 H210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:233407617 C>T maps to NM_005199.4 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr2:233409159 G>A maps to NM_005199.4 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr2:233409126 G>A maps to NM_005199.4 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:233410254 G>A maps to NM_005199.4 G461G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr2:233409491 G>A maps to NM_005199.4 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:233410374 G>A maps to NM_005199.4 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr11:45671936 C>T maps to NM_003654.4 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:45671369 G>A maps to NM_003654.4 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:45671921 C>T maps to NM_003654.4 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:45671858 G>A maps to NM_003654.4 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:45672208 G>A maps to NM_003654.4 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:45672071 G>A maps to NM_003654.4 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr11:45672404 G>A maps to NM_003654.4 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:45671525 G>A maps to NM_003654.4 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:101014571 G>A maps to NM_004854.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:101010057 G>A maps to NM_004854.3 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:101012050 G>A maps to NM_004854.3 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:105151001 C>T maps to NM_018413.5 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr7:2473416 C>T maps to NM_018641.3 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr7:2473050 C>T maps to NM_018641.3 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr7:2473032 C>T maps to NM_018641.3 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:2472339 C>T maps to NM_018641.3 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:2472615 C>T maps to NM_018641.3 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr7:2472822 C>T maps to NM_018641.3 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:2473017 C>T maps to NM_018641.3 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:2473275 C>T maps to NM_018641.3 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:2473275 C>T maps to NM_018641.3 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:2472339 C>T maps to NM_018641.3 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr7:2472429 C>T maps to NM_018641.3 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:126261258 C>T maps to NM_152889.1 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:126255180 C>T maps to NM_152889.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:126261246 C>T maps to NM_152889.1 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:40764479 C>T maps to NM_130468.3 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:40764368 C>T maps to NM_130468.3 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:40764369 C>T maps to NM_130468.3 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr15:40764479 C>T maps to NM_130468.3 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr10:125801958 G>A maps to NM_015892.3 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:125801901 G>A maps to NM_015892.3 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:125805242 C>T maps to NM_015892.3 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr10:125771986 G>A maps to NM_015892.3 Q453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:125805437 G>A maps to NM_015892.3 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr10:125805482 G>A maps to NM_015892.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr10:125798076 G>A maps to NM_015892.3 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:125805233 G>A maps to NM_015892.3 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:142840668 G>T maps to NM_004267.3 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:142840920 G>A maps to NM_004267.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr10:73765671 C>A maps to NM_004273.4 Y24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:73768063 C>T maps to NM_004273.4 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr10:73767601 C>T maps to NM_004273.4 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr10:73766957 C>T maps to NM_004273.4 Q57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr16:71571650 G>T maps to NM_001166395.1 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr16:71571479 C>T maps to NM_001166395.1 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr16:71571179 C>T maps to NM_001166395.1 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr16:71571467 G>A maps to NM_001166395.1 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr16:71571179 C>T maps to NM_001166395.1 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:71571107 C>T maps to NM_001166395.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:71571068 G>A maps to NM_001166395.1 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:71571296 G>A maps to NM_001166395.1 E239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr16:71570948 C>T maps to NM_001166395.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr16:71571017 C>T maps to NM_001166395.1 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr16:71571179 C>T maps to NM_001166395.1 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr16:75563643 G>A maps to NM_024533.3 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:75563460 G>A maps to NM_024533.3 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:75563244 C>T maps to NM_024533.3 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:75563853 G>A maps to NM_024533.3 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:75563427 G>A maps to NM_024533.3 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr16:75513663 G>A maps to NM_021615.4 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr16:75513561 G>A maps to NM_021615.4 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr16:75512970 G>A maps to NM_021615.4 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:46433871 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:46434746 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:46433602 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr23:46433814 A>T did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:34263724 C>T maps to NM_022467.3 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:34180173 C>T maps to NM_022467.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:34263247 C>T maps to NM_022467.3 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:34263247 C>T maps to NM_022467.3 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:34263625 C>T maps to NM_022467.3 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:34263583 G>A maps to NM_022467.3 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:34263238 C>T maps to NM_022467.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr18:24496450 C>T maps to NM_031422.4 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:24496386 G>A maps to NM_031422.4 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr18:24496435 C>T maps to NM_031422.4 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:24628465 C>T maps to NM_031422.4 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr18:24496639 G>A maps to NM_031422.4 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr15:101718144 G>A maps to NM_014918.4 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr15:101718621 C>T maps to NM_014918.4 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr15:101717754 G>A maps to NM_014918.4 V749V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:101718570 G>A maps to NM_014918.4 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr15:101718471 G>A maps to NM_014918.4 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:129520868 G>A maps to NM_175856.4 Q678Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:129521354 T>C maps to NM_175856.4 P840P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr5:129521408 C>T maps to NM_175856.4 F858F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr16:844143 A>G maps to ENST00000317063 R840R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:843211 G>A maps to ENST00000317063 K770K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:846794 C>T maps to ENST00000317063 A1054A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr16:846740 C>T maps to ENST00000317063 F1036F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr16:839606 C>T maps to ENST00000317063 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr16:69154546 G>A maps to NM_001039690.3 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr16:69155018 G>A maps to NM_001039690.3 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr10:101980383 T>C maps to NM_001278.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:101977835 G>A maps to NM_001278.3 D283D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:65390782 T>C maps to ENST00000448390 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr14:65390803 C>T maps to ENST00000448390 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr2:96936906 C>T maps to NM_004804.2 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:78403551 G>A maps to NM_006383.2 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr15:78403581 G>A maps to NM_006383.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr15:78403590 G>A maps to NM_006383.2 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:16280479 C>T maps to NM_054113.2 K53K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:16275692 C>T maps to NM_054113.2 W126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:16280539 G>C maps to NM_054113.2 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:16275560 C>T maps to NM_054113.2 Q170Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:16280506 G>A maps to NM_054113.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:26818095 G>A maps to NM_001029881.1 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr2:26864149 C>T maps to NM_001029881.1 W11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:26806662 C>T maps to NM_001029881.1 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:26806662 C>T maps to NM_001029881.1 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:26863422 G>A maps to NM_001029881.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:42795610 C>T maps to NM_015125.3 P897P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:42796862 C>T maps to NM_015125.3 P1107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr19:42793553 C>T maps to NM_015125.3 V452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:42797225 C>T maps to NM_015125.3 A1196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:42798194 C>T maps to NM_015125.3 P1383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:42794644 C>T maps to NM_015125.3 P575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:42796862 C>T maps to NM_015125.3 P1107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:42796997 C>T maps to NM_015125.3 F1152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:42797177 G>A maps to NM_015125.3 V1180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:42798204 C>T maps to NM_015125.3 L1387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:42798876 C>T maps to NM_015125.3 F1483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr18:12264319 C>T maps to ENST00000342845 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr18:12277223 G>A maps to ENST00000342845 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:12277268 G>A maps to ENST00000342845 *254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:24775313 C>T maps to NM_014430.2 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr14:24776627 C>T maps to NM_014430.2 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr16:11000963 C>T maps to NM_000246.3 R539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr16:11012338 C>T maps to NM_000246.3 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr16:10997684 C>T maps to NM_000246.3 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr16:11001445 G>C maps to NM_000246.3 P699P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr16:10995380 G>A maps to NM_000246.3 E149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr16:11001700 G>A maps to NM_000246.3 R784R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:10996524 C>T maps to NM_000246.3 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr16:11000824 C>T maps to NM_000246.3 D492D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr16:11001283 G>T maps to NM_000246.3 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:10995406 G>A maps to NM_000246.3 W158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:10996551 C>T maps to NM_000246.3 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr16:10996614 C>T maps to NM_000246.3 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:11001472 C>T maps to NM_000246.3 F708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:10997603 C>T maps to NM_000246.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:11000809 C>T maps to NM_000246.3 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:11004047 G>A maps to NM_000246.3 T940T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr15:65496852 G>A maps to NM_003613.3 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr15:65490865 G>A maps to NM_003613.3 I586I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr15:65495734 C>T maps to NM_003613.3 K331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:65490745 G>A maps to NM_003613.3 F626F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr15:65499216 G>A maps to NM_003613.3 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr15:65499222 C>T maps to NM_003613.3 Q107Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr15:65490649 G>A maps to NM_003613.3 G658G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:65495725 C>T maps to NM_003613.3 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:65490097 G>A maps to NM_003613.3 F842F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:65490763 C>T maps to NM_003613.3 V620V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:65489926 G>A maps to NM_003613.3 L899L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr15:65490535 C>T maps to NM_003613.3 V696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr15:65489677 C>T maps to NM_003613.3 G982G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr15:65489677 C>T maps to NM_003613.3 G982G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr15:65490736 G>A maps to NM_003613.3 P629P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr15:65490952 G>A maps to NM_003613.3 F557F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr15:65489553 G>A maps to NM_003613.3 L1024L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:65489536 G>A maps to NM_003613.3 P1029P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:65500010 C>T maps to NM_003613.3 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr15:65490352 C>T maps to NM_003613.3 R757R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:65490892 G>A maps to NM_003613.3 I577I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr15:65502059 G>A maps to NM_003613.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:19656008 G>A maps to NM_153221.2 R885R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:19653721 C>T maps to NM_153221.2 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:19654547 G>A maps to NM_153221.2 E398E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:19655066 C>T maps to NM_153221.2 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr19:19656503 C>T maps to NM_153221.2 A1050A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:19655345 G>A maps to NM_153221.2 R664R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:19655942 C>T maps to NM_153221.2 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:19654823 C>T maps to NM_153221.2 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:19655942 C>T maps to NM_153221.2 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:19655234 C>T maps to NM_153221.2 F627F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:19654631 C>T maps to NM_153221.2 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:19656740 C>T maps to NM_153221.2 I1129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:19655066 C>T maps to NM_153221.2 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:19654535 C>T maps to NM_153221.2 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:19654541 C>T maps to NM_153221.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19655180 C>T maps to NM_153221.2 F609F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19655780 C>T maps to NM_153221.2 V809V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19656464 G>A maps to NM_153221.2 P1037P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19656740 C>T maps to NM_153221.2 I1129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:19655534 C>T maps to NM_153221.2 F727F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr2:175260317 C>T maps to NM_004882.3 K11K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:175213482 G>A maps to NM_004882.3 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:69194307 G>A maps to NM_032830.2 W498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:69184789 A>T maps to NM_032830.2 K329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr16:69184785 C>T maps to NM_032830.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr16:69184786 C>T maps to NM_032830.2 R328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr4:103806371 G>C did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr3:50645400 G>A maps to NM_013324.5 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr12:120156161 C>T maps to ENST00000392521 A1352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr12:120241140 A>G maps to ENST00000392521 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:120173009 G>A maps to ENST00000392521 R1037R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:120288022 G>A maps to ENST00000392521 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:120306861 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:120139552 G>A maps to ENST00000392521 F1806F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:120166408 G>A maps to ENST00000392521 L1163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:120204946 G>A maps to ENST00000392521 Q750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:120241179 G>A maps to ENST00000392521 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:120128033 G>A maps to ENST00000392521 P2036P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr12:120196498 G>A maps to ENST00000392521 I809I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:120221810 C>T maps to ENST00000392521 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr12:120195222 G>A maps to ENST00000392521 D886D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr12:120260702 G>A maps to ENST00000392521 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:120148154 G>A maps to ENST00000392521 L1658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:120150414 G>A maps to ENST00000392521 L1555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:120172083 G>A maps to ENST00000392521 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr23:71521586 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:71522678 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:71522094 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr6:139695072 G>A maps to NM_006079.3 D3D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr9:130941630 G>A maps to NM_012127.2 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr13:53035977 C>G maps to NM_001098525.1 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:113509849 G>A maps to NM_152515.3 I532I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr2:113514356 C>T maps to NM_152515.3 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:113509900 G>A maps to NM_152515.3 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:113514356 C>T maps to NM_152515.3 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:113513651 C>T maps to NM_152515.3 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr2:113496483 T>C maps to NM_152515.3 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr12:106633539 G>A maps to NM_006825.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr12:106633845 G>A maps to NM_006825.3 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:106633344 G>A maps to NM_006825.3 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr12:106633302 G>A maps to NM_006825.3 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr11:46801773 G>A maps to ENST00000415402 L801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr11:46799754 G>A maps to ENST00000415402 I894I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr11:46812067 C>T maps to ENST00000415402 K572K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:46772098 G>A maps to ENST00000415402 G1848G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:46771898 G>A maps to ENST00000415402 Q1884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr11:46797834 G>A maps to ENST00000415402 L987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr11:46832645 G>A maps to ENST00000415402 R181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:66592127 C>T maps to NM_016951.2 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr16:66599829 G>A maps to NM_016951.2 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:66599832 C>T maps to NM_016951.2 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr19:45810755 C>T maps to NM_001824.3 E310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr19:45815062 G>A maps to NM_001824.3 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:45822866 G>A maps to NM_001824.3 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:43991268 C>T maps to ENST00000424065 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr15:43990945 C>T maps to ENST00000424065 D404D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr15:43891434 C>T maps to ENST00000413657 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr15:43890395 G>A maps to ENST00000413657 E325E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:80555015 G>A maps to NM_001825.2 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr5:80547041 C>T maps to NM_001825.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:154950477 C>A maps to NM_001826.2 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr2:122202527 G>A maps to NM_001142273.1 T641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:122217647 G>A maps to NM_015282.2 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:122125380 G>A maps to NM_015282.2 S1223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:122104658 G>A maps to NM_015282.2 I1495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:122285421 G>A maps to NM_015282.2 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:122217647 G>A maps to NM_015282.2 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr3:33558657 G>A maps to ENST00000359576 L1275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr3:33576728 A>C maps to ENST00000359576 P1270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:33644588 G>A maps to ENST00000359576 S594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:40222068 C>T maps to NM_001828.4 W127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr19:40222124 G>A maps to NM_001828.4 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr19:40222085 C>T maps to NM_001828.4 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:40222085 C>T maps to NM_001828.4 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:86965349 C>T maps to NM_001285.3 I789I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:86959979 G>A maps to NM_001285.3 T597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:86951180 C>T maps to NM_001285.3 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:86959194 C>T maps to NM_001285.3 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr1:86964336 C>T maps to NM_001285.3 S732S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:86959979 G>A maps to NM_001285.3 T597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:86957011 C>T maps to NM_001285.3 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:86916402 T>C maps to NM_006536.5 G714G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr1:86905983 C>T maps to NM_006536.5 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:86898133 A>T maps to NM_006536.5 K223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:86896590 C>T maps to NM_006536.5 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:86921096 T>C maps to NM_006536.5 L907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:87040389 G>A maps to ENST00000263723 V545V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:87045721 G>A maps to ENST00000263723 K819K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:87025892 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:87040383 C>T maps to ENST00000263723 F543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:87012828 C>T maps to ENST00000263723 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:87026000 C>T maps to ENST00000263723 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:87040293 G>A maps to ENST00000263723 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:87040428 A>T maps to ENST00000263723 G558G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:87040245 G>A maps to ENST00000263723 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:109486496 G>A maps to NM_001048210.1 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:67134990 C>T maps to NM_013246.2 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:143028680 C>T maps to NM_000083.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:143048770 C>T maps to NM_000083.2 R894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr7:143039049 C>T maps to NM_000083.2 S537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr7:143027918 G>A maps to NM_000083.2 W303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:143029875 G>A maps to NM_000083.2 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:143047568 G>A maps to NM_000083.2 K836K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:143048976 G>A maps to NM_000083.2 L962L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:143018931 G>A maps to NM_000083.2 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:143043243 C>T maps to NM_000083.2 S728S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr7:143028367 C>T maps to NM_000083.2 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:143017763 C>T maps to NM_000083.2 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:143018563 C>T maps to NM_000083.2 H180H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:143016846 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr7:143013371 C>T maps to NM_000083.2 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr7:143048850 G>A maps to NM_000083.2 G920G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:143047535 C>T maps to NM_000083.2 P825P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:143018506 C>T maps to NM_000083.2 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:143021571 G>T maps to NM_000083.2 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:143048913 C>T maps to NM_000083.2 S941S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr7:143016939 G>A maps to NM_000083.2 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr7:143028643 G>A maps to NM_000083.2 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:143013382 C>T maps to NM_000083.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:143027959 C>T maps to NM_000083.2 R317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr7:143028642 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:143020463 C>T maps to NM_000083.2 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:143048916 G>A maps to NM_000083.2 L942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:143028355 C>T maps to NM_000083.2 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:143049048 G>A maps to NM_000083.2 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:143036676 C>T maps to NM_000083.2 I515I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr3:184070899 C>T maps to NM_004366.4 R688R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:184076901 A>G maps to NM_004366.4 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:184069833 G>A maps to NM_004366.4 P794P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr3:184075584 G>A maps to NM_004366.4 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:184075881 G>A maps to NM_004366.4 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr3:184073218 G>A maps to NM_004366.4 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:170618773 C>T maps to NM_173872.2 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr4:170618536 C>T maps to NM_173872.2 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:10181782 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:10176550 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:10181844 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:10176169 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:10176398 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr23:10182111 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:10174570 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:10181892 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:10176260 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:10181825 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:10182059 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:10181892 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:10176099 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:10176239 C>T did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:10188759 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr23:49854957 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr23:49855112 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:49855126 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:49855486 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:49855481 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr23:49845366 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr23:49853374 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:49855003 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:49855004 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:49856859 C>T did not map to a codon.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr23:49846335 T>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:49855098 C>T did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr23:49851136 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:11897453 C>T maps to ENST00000376496 T731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:11883831 C>T maps to ENST00000376496 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:11898650 C>T maps to ENST00000376496 S821S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:11889375 C>T maps to ENST00000376496 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr16:1499017 G>A maps to ENST00000382745 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:1498400 G>A maps to ENST00000382745 S656S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr16:1503866 G>A maps to ENST00000382745 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr16:1505731 G>A maps to ENST00000382745 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:1505731 G>A maps to ENST00000382745 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr16:1504439 G>A maps to ENST00000382745 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:16352729 C>T maps to NM_004070.3 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr1:16356499 C>T maps to NM_004070.3 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr1:16358707 C>T maps to NM_004070.3 I589I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:16355733 G>A maps to NM_004070.3 W389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr1:16354560 C>T maps to NM_004070.3 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:16352729 C>T maps to NM_004070.3 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr1:16352684 G>A maps to NM_004070.3 K147K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:16359690 C>T maps to NM_004070.3 N652N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:16351294 C>T maps to NM_004070.3 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:16353029 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:16355339 G>A maps to NM_004070.3 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr1:16381936 G>A maps to NM_000085.3 Q588Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:16378903 C>T maps to NM_000085.3 I540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:16374526 C>T maps to NM_000085.3 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:16378295 A>C maps to NM_000085.3 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr1:16378295 A>C maps to NM_000085.3 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:16372083 C>T maps to NM_000085.3 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:16378203 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:16374433 G>A maps to NM_000085.3 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:16373105 C>T maps to NM_000085.3 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U9-06A-11D-A32N-08 chr1:16378295 A>C maps to NM_000085.3 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:190039947 C>T maps to NM_021101.4 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:190026080 C>T maps to NM_021101.4 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr3:190030676 C>T maps to NM_021101.4 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:190030808 G>A maps to NM_021101.4 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr3:190027971 G>A maps to NM_021101.4 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:190039812 C>T maps to NM_021101.4 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:190039866 G>A maps to NM_021101.4 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr3:190026140 G>A maps to NM_021101.4 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr13:96086219 C>T maps to NM_182848.3 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr13:96229503 C>T maps to NM_182848.3 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr3:170150444 C>T maps to NM_005602.5 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:170150513 C>T maps to NM_005602.5 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:170140969 C>T maps to NM_005602.5 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:90042625 C>T maps to NM_001185072.2 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:90042412 C>T maps to NM_001185072.2 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr21:37833399 G>A maps to NM_001146077.1 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr21:37833795 G>A maps to NM_001146077.1 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr21:37833618 G>A maps to NM_001146077.1 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:37833959 G>A maps to NM_001146077.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr21:37833621 G>A maps to NM_001146077.1 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:100880829 G>A maps to NM_014343.2 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr7:100876136 G>A maps to NM_014343.2 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:190122641 G>A maps to NM_006580.3 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:190106189 C>T maps to NM_006580.3 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr21:31538557 G>A maps to NM_012131.2 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr21:31538539 G>A maps to NM_012131.2 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr21:31538578 C>T maps to NM_012131.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr21:31538539 G>A maps to NM_012131.2 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr21:31538548 C>G maps to NM_012131.2 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr21:31538770 G>A maps to NM_012131.2 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr3:137717796 G>A maps to NM_001002026.2 Q29Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr3:137717742 C>T maps to NM_001002026.2 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr3:137742644 G>A maps to NM_016369.3 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr3:137743455 T>C maps to NM_016369.3 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:137717826 C>T maps to NM_001002026.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:137717742 C>T maps to NM_001002026.2 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr3:137729135 G>A maps to NM_016369.3 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:43204143 G>A maps to NM_148960.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:106171925 G>T did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:106171883 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr23:106171613 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:106171842 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:106171785 G>A did not map to a codon.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr23:106171618 G>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:106171925 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr8:8560415 C>T maps to NM_194284.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr8:8560184 C>T maps to NM_194284.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:8560000 G>A maps to NM_194284.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:113651041 C>T maps to NM_001101389.1 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:113650777 C>T maps to NM_001101389.1 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr11:113651137 C>T maps to NM_001101389.1 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:113650663 G>A maps to NM_001101389.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:113650813 C>T maps to NM_001101389.1 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr7:73184199 C>T maps to NM_001306.3 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:73184325 C>T maps to NM_001306.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr7:73245887 C>T maps to NM_001305.3 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr7:73245959 C>T maps to NM_001305.3 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr16:3065767 G>A maps to NM_021195.4 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:3065566 C>T maps to NM_021195.4 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr16:3065692 C>T maps to NM_021195.4 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr16:3065464 G>A maps to NM_021195.4 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr21:31587916 C>T maps to NM_199328.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr21:31588123 G>A maps to NM_199328.2 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:31588018 C>T maps to NM_199328.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr16:3063851 C>T maps to NM_020982.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:3063627 C>T maps to NM_020982.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:3063920 C>T maps to NM_020982.3 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:3063713 C>T maps to NM_020982.3 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr3:98240106 G>A maps to NM_001040182.1 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr17:6979058 C>T maps to NM_182906.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:6980103 C>T maps to NM_182906.2 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:6980214 G>A maps to NM_182906.2 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:6979058 C>T maps to NM_182906.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr12:10124233 G>A maps to ENST00000355690 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr14:38723922 C>T maps to NM_175060.1 K435K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr14:38724357 C>T maps to NM_175060.1 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr14:38724522 C>T maps to NM_175060.1 W235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr14:38724534 G>A maps to NM_175060.1 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr14:38724756 C>T maps to NM_175060.1 W157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:38724261 C>T maps to NM_175060.1 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:11114053 C>T maps to ENST00000409790 I436I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr16:11272444 C>T maps to ENST00000409790 S1020S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:11038591 G>A maps to ENST00000409790 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:11063147 C>T maps to ENST00000409790 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:11114065 C>T maps to ENST00000409790 I440I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:11097025 G>A maps to ENST00000409790 K389K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr16:11272438 C>T maps to ENST00000409790 L1018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:11051707 C>A maps to ENST00000409790 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr16:11272357 T>A maps to ENST00000409790 I991I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:11154775 C>T maps to ENST00000409790 F671F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:14710879 C>T maps to ENST00000417570 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr19:14707811 G>A maps to ENST00000417570 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:14706127 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr16:74452088 C>T maps to NM_001011880.2 W108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:74443539 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:74447493 G>A maps to NM_001011880.2 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:74447544 G>A maps to NM_001011880.2 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:74452063 A>G maps to NM_001011880.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:74455096 G>A maps to NM_001011880.2 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr16:74443493 C>T maps to NM_001011880.2 W428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr16:74447025 G>T maps to NM_001011880.2 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:74447034 C>T maps to NM_001011880.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:74455129 G>A maps to NM_001011880.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr16:74446933 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:70211331 C>T maps to NM_173619.2 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:70219786 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr12:10224057 G>A maps to NM_016511.2 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr12:10224048 C>T maps to NM_016511.2 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr12:10007019 G>A maps to NM_005127.2 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr12:10010224 G>A maps to NM_005127.2 R29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:10007083 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:10010182 G>A maps to NM_005127.2 Q43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:139226792 G>A maps to NM_001080511.2 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:139226836 G>A maps to NM_001080511.2 W168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:139225184 C>T maps to NM_001080511.2 C128C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:139229057 C>T maps to NM_001080511.2 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:78064407 C>T maps to NM_005752.3 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr16:78064446 C>T maps to NM_005752.3 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr16:78062058 C>T maps to NM_005752.3 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:78056612 G>A maps to NM_005752.3 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr16:78064398 G>A maps to NM_005752.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:78056579 G>A maps to NM_005752.3 Q19Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:78064728 C>T maps to NM_005752.3 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr16:78056531 G>A maps to NM_005752.3 K3K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:78064554 G>A maps to NM_005752.3 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr16:78064648 C>T maps to NM_005752.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:45077103 C>T maps to NM_003278.2 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr3:45067940 G>A maps to NM_003278.2 K29K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:45077053 C>T maps to NM_003278.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr12:7894076 G>A maps to NM_130441.2 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr12:7882200 G>A maps to NM_130441.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:7883483 T>G maps to NM_130441.2 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr12:7890134 G>A maps to NM_130441.2 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:7890162 G>A maps to NM_130441.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr12:7882227 C>T maps to NM_130441.2 Q202Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:8673833 G>A maps to NM_080387.4 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:8671756 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:8671611 C>T maps to NM_080387.4 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:8671719 G>A maps to NM_080387.4 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:8673860 G>A maps to NM_080387.4 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:8670787 G>A maps to NM_080387.4 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr12:8691860 G>A maps to NM_014358.2 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:8693355 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:8687389 C>T maps to NM_014358.2 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:8692526 A>G maps to NM_014358.2 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr12:8692541 C>T maps to NM_014358.2 E13E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:8687401 G>A maps to NM_014358.2 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr12:8687401 G>A maps to NM_014358.2 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:71039587 C>T maps to NM_173535.2 K510K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:71043180 G>A maps to NM_173535.2 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:71044170 G>A maps to NM_173535.2 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:71039587 C>T maps to NM_173535.2 K510K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:71036468 C>T maps to NM_173535.2 V568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr2:71036426 G>A maps to NM_173535.2 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:71043969 C>T maps to NM_173535.2 Q181Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:71043999 A>G maps to NM_173535.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:71044107 G>A maps to NM_173535.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:71046973 G>A maps to NM_173535.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:71046973 G>A maps to NM_173535.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:7794807 C>T maps to NM_198492.3 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr19:7796640 C>T maps to NM_198492.3 W24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:7794919 C>T maps to NM_198492.3 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:7796583 G>A maps to NM_198492.3 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr19:7830629 C>T maps to NM_014257.4 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr19:7830104 C>A maps to NM_014257.4 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:7832467 C>T maps to NM_014257.4 Q335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:7831540 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr19:7830143 C>T maps to NM_014257.4 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:7828325 C>T maps to NM_014257.4 Q32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:7830656 G>A maps to NM_014257.4 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:7828163 C>T maps to NM_014257.4 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:7830110 C>T maps to NM_014257.4 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:7828362 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:141643714 G>A maps to NM_013252.2 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:141629927 C>T maps to NM_013252.2 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr7:141643747 C>T maps to NM_013252.2 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:141629993 G>A maps to NM_013252.2 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:141631542 G>A maps to NM_013252.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:141631587 A>G maps to NM_013252.2 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr7:141635670 C>T maps to NM_013252.2 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:141635723 G>A maps to NM_013252.2 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:141631616 G>A maps to NM_013252.2 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr7:141629993 G>A maps to NM_013252.2 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:141629999 C>T maps to NM_013252.2 Q157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:141629990 G>A maps to NM_013252.2 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:8630023 G>A maps to NM_001007033.1 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr12:8618203 G>C maps to NM_001007033.1 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:8628732 C>T maps to NM_001007033.1 Q128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr12:8612271 C>T maps to NM_001007033.1 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:9885740 C>T maps to NM_172004.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:9885731 C>T maps to NM_172004.2 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:141317006 C>T maps to NM_004362.2 W372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:141323144 C>T maps to NM_004362.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:141317280 A>G maps to NM_004362.2 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr6:31698735 G>A maps to NM_001288.4 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr6:31699999 T>A maps to NM_001288.4 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:31700062 C>T maps to NM_001288.4 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:154508604 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:154528437 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:154507334 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:154508513 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:154507272 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr6:45870869 G>A maps to NM_001114086.1 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr6:45922903 G>A maps to NM_001114086.1 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:45882123 C>T maps to NM_001114086.1 K302K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr21:36079600 C>T maps to ENST00000360731 I484I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr21:36081685 G>A maps to ENST00000360731 R601R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr21:36081766 G>A maps to ENST00000360731 R628R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:36081685 G>A maps to ENST00000360731 R601R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr5:157240098 G>A maps to NM_001195555.1 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr5:157232930 C>T maps to NM_001195555.1 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:122825461 T>C maps to ENST00000302528 T763T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr12:122825944 G>A maps to ENST00000302528 N602N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:73800894 T>C maps to NM_003388.4 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:73790453 C>T maps to NM_003388.4 Q575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:73790812 G>A maps to NM_003388.4 E694E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr7:73814774 C>T maps to NM_003388.4 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:73790983 C>T maps to NM_003388.4 F751F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:73768220 G>A maps to NM_003388.4 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:73768316 G>A maps to NM_003388.4 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:73790983 C>T maps to NM_003388.4 F751F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:73752880 C>T maps to NM_003388.4 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:73731908 C>T maps to NM_003388.4 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:73731902 C>T maps to NM_003388.4 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr7:73791002 C>T maps to NM_003388.4 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:73770738 G>A did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr7:73811451 C>T maps to NM_003388.4 S923S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:36517545 C>T maps to NM_015526.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:36509890 C>T maps to NM_015526.2 V364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:36517887 G>A maps to NM_015526.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:29356671 G>A maps to ENST00000379543 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:29366723 C>T maps to ENST00000379543 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:29356662 G>A maps to ENST00000379543 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:201718043 C>T maps to NM_001162407.1 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:201718716 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:201722763 G>A maps to NM_001162407.1 Y241Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:201724938 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:201726167 A>T maps to NM_001162407.1 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:155236604 G>A maps to ENST00000368361 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:155233149 G>A maps to ENST00000368361 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:155239407 G>A maps to ENST00000368361 Y90Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:155234487 G>A maps to ENST00000368361 H337H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr15:74922067 C>T maps to NM_001130028.1 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:92818596 G>A maps to NM_001025233.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr12:92814812 C>T maps to NM_001025232.1 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:92814812 C>T maps to NM_001025232.1 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr14:95679659 G>A maps to NM_024734.3 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:95670707 G>A maps to NM_024734.3 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:95670764 G>A maps to NM_024734.3 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr16:28497789 G>A maps to NM_000086.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:28498849 G>A maps to NM_000086.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr16:28493842 G>A maps to NM_000086.2 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:28499932 G>A maps to NM_000086.2 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr16:28497720 G>A maps to NM_000086.2 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr16:28489123 G>A maps to NM_000086.2 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr15:68500586 C>T maps to NM_017882.2 W276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr15:68500615 G>A maps to NM_017882.2 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:68502090 G>A maps to NM_017882.2 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr4:10599618 G>A maps to NM_052964.2 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:10599660 C>T maps to NM_052964.2 K8K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:77330735 C>T maps to NM_001293.2 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr4:56308642 G>T maps to NM_004898.2 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr4:56304484 C>T maps to NM_004898.2 Q775Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:56342131 C>A maps to NM_004898.2 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr11:57428554 C>T maps to NM_006831.2 R309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:57428448 T>C maps to NM_006831.2 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:57426974 G>A maps to NM_006831.2 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr11:57427469 C>A maps to NM_006831.2 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:57427178 C>T maps to NM_006831.2 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr11:72084002 C>T maps to NM_030813.3 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:72084026 G>A maps to NM_030813.3 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr11:72005077 G>A maps to NM_030813.3 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:72005443 G>A maps to NM_030813.3 I565I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:72004416 G>A maps to NM_030813.3 T706T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:72005443 G>A maps to NM_030813.3 I565I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr19:6366266 A>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:35764996 C>T maps to NM_001832.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr6:35765053 G>A maps to NM_001832.2 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:35764996 C>T maps to NM_001832.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:45490629 C>T maps to NM_001294.2 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:45493791 C>T maps to NM_001294.2 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:45490614 G>A maps to NM_001294.2 K324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:45495626 C>T maps to NM_001294.2 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr19:45494146 C>T maps to NM_001294.2 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr19:45476416 G>T maps to NM_001294.2 G87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:45495626 C>G maps to NM_001294.2 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr19:45476361 C>T maps to NM_001294.2 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr5:1339042 G>A maps to NM_030782.3 N177N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:1339086 G>A maps to NM_030782.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:1338078 G>A maps to NM_030782.3 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr15:65443232 G>A maps to NM_006660.3 S610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr15:65456424 G>A maps to NM_006660.3 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr3:150645782 G>A maps to NM_001195794.1 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:17528482 G>A maps to NM_001079827.2 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:17528500 G>A maps to NM_001079827.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:17528534 C>T maps to NM_001079827.2 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr4:17517086 C>T maps to NM_001079827.2 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:17528620 G>A maps to NM_001079827.2 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:129682032 G>A maps to NM_152311.3 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:129676499 G>A maps to NM_152311.3 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:36209112 C>T maps to NM_022111.3 E995E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:36226354 G>A maps to NM_022111.3 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:36215301 G>A maps to NM_022111.3 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:36202571 G>A maps to NM_022111.3 V1284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:9795219 C>T maps to NM_001009566.1 E632E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:9793577 C>A maps to NM_001009566.1 E770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:9795568 G>A maps to NM_001009566.1 F613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:140185515 G>A maps to NM_022131.2 K429K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:140277682 G>A maps to NM_022131.2 G675G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:140167427 G>A maps to NM_022131.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:140282887 G>A maps to NM_022131.2 R856R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:140167508 G>A maps to NM_022131.2 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:140281651 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:140178396 C>T maps to NM_022131.2 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr3:140123432 C>T maps to NM_022131.2 N154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:139894810 G>A maps to NM_022131.2 W43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr3:140178486 C>T maps to NM_022131.2 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr3:140123408 C>T maps to NM_022131.2 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:140123537 C>T maps to NM_022131.2 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:140167493 G>A maps to NM_022131.2 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:140277661 C>T maps to NM_022131.2 F668F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:139894844 G>A maps to NM_022131.2 E54E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr12:7289519 C>T maps to NM_014718.3 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:7289620 C>T maps to NM_014718.3 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr12:7289560 C>T maps to NM_014718.3 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:7293875 C>T maps to NM_014718.3 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr12:7290644 C>T maps to NM_014718.3 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:7288862 C>T maps to NM_014718.3 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:7288817 C>T maps to NM_014718.3 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:7289617 C>T maps to NM_014718.3 F374F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:7288817 C>T maps to NM_014718.3 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr12:7301720 C>T maps to NM_014718.3 F667F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr12:7295772 C>T maps to NM_014718.3 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr12:7288853 C>T maps to NM_014718.3 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr12:7303612 G>A maps to NM_014718.3 P827P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:7287994 G>A maps to NM_014718.3 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:7289620 C>T maps to NM_014718.3 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:7310145 C>T maps to NM_014718.3 V863V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:7288817 C>T maps to NM_014718.3 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr12:7288060 C>T maps to NM_014718.3 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:175843196 C>T maps to NM_007097.2 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:57741222 G>A maps to NM_004859.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:57758364 C>T maps to NM_004859.3 L1004L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:57738835 G>A maps to NM_004859.3 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr22:19223299 G>A maps to NM_007098.3 N296N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr22:19170971 G>T maps to NM_007098.3 A1586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr22:19196486 G>A maps to NM_007098.3 I1129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:19178916 G>A maps to NM_007098.3 L1408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:19226875 T>A maps to NM_007098.3 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr22:19184074 G>A maps to NM_007098.3 I1322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr22:19221046 G>A maps to NM_007098.3 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr22:19197868 G>A maps to NM_007098.3 F1072F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr22:19230399 G>A maps to NM_007098.3 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr22:19211482 G>A maps to NM_007098.3 I741I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr22:19197919 G>A maps to NM_007098.3 I1055I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr22:19220998 C>T maps to NM_007098.3 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:19178916 G>A maps to NM_007098.3 L1408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr22:19197880 G>A maps to NM_007098.3 A1068A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:19197877 G>A maps to NM_007098.3 F1069F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr8:27457479 G>A maps to NM_001831.2 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:27456143 G>A maps to NM_001831.2 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:27462696 G>A maps to NM_001831.2 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr8:27462447 G>A maps to NM_001831.2 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr8:27462837 C>T maps to NM_001831.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:27455996 C>T maps to NM_001831.2 Q492Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:27456008 C>T maps to NM_001831.2 E488E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:27456059 G>A maps to NM_001831.2 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr8:27457500 C>T maps to NM_001831.2 Q372Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:3562381 G>A did not map to a codon.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr16:3562478 G>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:618099 C>T maps to NM_199167.1 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr18:618074 G>A maps to NM_199167.1 K25K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr18:624989 T>A maps to NM_199167.1 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:641369 G>A maps to NM_199167.1 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr8:62366803 G>A maps to NM_173519.2 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:62371062 G>A maps to NM_173519.2 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:62212613 C>T maps to NM_173519.2 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr8:62289310 C>T maps to NM_173519.2 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:62289181 C>T maps to NM_173519.2 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr8:62212698 C>T maps to NM_173519.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:62212397 C>T maps to NM_173519.2 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:62212799 G>A maps to NM_173519.2 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:62371062 G>A maps to NM_173519.2 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:62412055 G>A maps to NM_173519.2 E340E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr8:62212826 T>C maps to NM_173519.2 N147N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr8:62212397 C>T maps to NM_173519.2 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:62212751 G>A maps to NM_173519.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:62212799 G>A maps to NM_173519.2 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr8:62212754 C>T maps to NM_173519.2 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr8:62289310 C>T maps to NM_173519.2 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr8:62212823 C>T maps to NM_173519.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr6:123376970 C>T maps to NM_001010852.2 N232N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:123377162 C>T maps to NM_001010852.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:123384873 G>T maps to NM_001010852.2 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:123369852 C>T maps to NM_001010852.2 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:123369870 G>A maps to NM_001010852.2 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr6:123369855 G>A maps to NM_001010852.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr6:123319269 G>A maps to NM_001010852.2 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr6:123319254 G>A maps to NM_001010852.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:123369774 C>T maps to NM_001010852.2 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr13:100425194 G>A maps to NM_206808.2 K60K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr13:100517152 C>T maps to NM_206808.2 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr13:100517130 C>T maps to NM_206808.2 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr13:100511123 C>T maps to NM_206808.2 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr14:24976698 C>T maps to NM_001836.2 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr14:24975719 T>C maps to NM_001836.2 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:24975305 G>A maps to NM_001836.2 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr14:24974802 C>T maps to NM_001836.2 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:24975482 C>T maps to NM_001836.2 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:22215237 C>T maps to NM_018686.3 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr12:22215348 G>A maps to NM_018686.3 W365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:10282389 C>T maps to NM_138809.3 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr16:81730265 C>T maps to NM_198390.2 A544A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr16:81735266 C>T maps to NM_198390.2 I586I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:81725422 C>T maps to NM_198390.2 Q478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:108685853 G>A maps to NM_001142344.1 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:108686310 G>A maps to NM_001142344.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr12:108686388 G>A maps to NM_001142344.1 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr12:108686388 G>A maps to NM_001142344.1 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr12:108686457 G>A maps to NM_001142344.1 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:108686625 C>T maps to NM_001142344.1 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr12:108686184 C>T maps to NM_001142344.1 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr2:6991690 G>A maps to NM_207315.2 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:7003697 A>G maps to NM_207315.2 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:6991666 C>T maps to NM_207315.2 E380E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr16:66612744 C>T maps to NM_052999.3 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:66603927 C>T maps to NM_052999.3 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr16:66612855 G>A maps to NM_052999.3 K271K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3BZ-06A-12D-A196-08 chr16:66613632 G>A maps to NM_144673.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr16:66657375 G>A maps to NM_178818.2 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:23846555 C>T maps to ENST00000339180 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr3:32529465 G>A maps to NM_017801.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:32490977 C>T maps to NM_138410.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr3:32490965 C>T maps to NM_138410.2 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:32409428 C>T maps to NM_178868.3 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:79024848 C>T maps to NM_153610.3 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:79030767 G>A maps to NM_153610.3 V2060V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:79034730 G>A maps to NM_153610.3 E3381E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr5:79027155 C>T maps to NM_153610.3 F856F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr5:79027101 G>A maps to NM_153610.3 K838K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:79034796 C>T maps to NM_153610.3 V3403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:79034937 C>T maps to NM_153610.3 V3450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr5:79026636 G>A maps to NM_153610.3 E683E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:79032756 C>T maps to NM_153610.3 F2723F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:79034205 G>A maps to NM_153610.3 K3206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:79034202 G>A maps to NM_153610.3 K3205K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:79030980 A>G maps to NM_153610.3 Q2131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr5:79089358 C>T maps to NM_153610.3 S3963S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr5:79034730 G>A maps to NM_153610.3 E3381E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:79033164 C>T maps to NM_153610.3 S2859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:79089292 C>T maps to NM_153610.3 S3941S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:79027332 G>A maps to NM_153610.3 E915E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr5:79032217 C>T maps to NM_153610.3 Q2544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:79030491 C>T maps to NM_153610.3 S1968S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:79028079 C>T maps to NM_153610.3 T1164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr5:79031657 G>A maps to NM_153610.3 W2357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr5:79025949 C>T maps to NM_153610.3 D454D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:79026978 G>A maps to NM_153610.3 L797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:79030212 G>C maps to NM_153610.3 A1875A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:79033516 T>C maps to NM_153610.3 L2977L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr5:79026252 G>A maps to NM_153610.3 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:79030038 C>T maps to NM_153610.3 L1817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:79033080 G>A maps to NM_153610.3 V2831V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:79032309 C>T maps to NM_153610.3 I2574I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:79033449 G>A maps to NM_153610.3 L2954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr5:79031121 C>T maps to NM_153610.3 F2178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr5:79095399 C>T maps to NM_153610.3 H4057H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr8:88365901 G>A maps to NM_173538.2 K397K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr8:88365928 C>T maps to NM_173538.2 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:88249291 C>T maps to NM_173538.2 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr8:88249249 C>T maps to NM_173538.2 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr8:88365892 G>A maps to NM_173538.2 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:87917372 C>T maps to NM_173538.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:88365872 C>T maps to NM_173538.2 Q388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:128889944 G>A maps to NM_001127192.1 D133D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr18:72234658 C>T maps to NM_032649.5 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr18:72228143 G>A maps to NM_032649.5 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr18:72238422 G>C maps to NM_032649.5 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr18:72228155 G>A maps to NM_032649.5 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr18:72234658 C>T maps to NM_032649.5 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr18:72180827 C>T maps to NM_018235.2 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr18:72180890 C>T maps to NM_018235.2 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr18:72173109 C>T maps to NM_018235.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:72178142 C>T maps to NM_018235.2 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr18:72186304 C>T maps to NM_018235.2 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr4:47939759 G>A maps to NM_001142564.1 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr4:47942866 G>A maps to NM_001142564.1 Q262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:47939363 G>A maps to NM_001142564.1 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:47942804 G>A maps to NM_001142564.1 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr4:47939214 C>T maps to NM_001142564.1 K501K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:47939240 G>A maps to NM_001142564.1 R493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr4:47939334 G>A maps to NM_001142564.1 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr4:47944164 C>T maps to NM_001142564.1 E219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr23:150911704 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr23:150912779 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr23:150912080 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr23:150912207 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:150911041 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr23:150912013 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:150908138 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:150911611 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr23:150912075 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:150912137 A>C did not map to a codon.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr23:150906988 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr23:150906989 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr23:150912025 C>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:150906983 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:150908124 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:150911718 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:150911751 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:150912179 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr23:150907031 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:150912754 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr23:150906978 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr23:150906981 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:150912080 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:150909265 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:150912096 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:150912515 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:150911102 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:150912736 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr23:150911671 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr23:150908111 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:150912690 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:150912369 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:150909282 T>C did not map to a codon.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr23:150908150 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:150912577 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr23:150912736 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr23:150911806 C>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:150907030 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:150909265 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:150912753 G>A did not map to a codon.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr23:150912706 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:99013315 G>A maps to NM_001298.2 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr2:99013543 G>A maps to NM_001298.2 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr2:99012790 G>A maps to NM_001298.2 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:99013246 C>T maps to NM_001298.2 F538F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:99013036 C>T maps to NM_001298.2 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:99012538 G>A maps to NM_001298.2 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:99013441 G>A maps to NM_001298.2 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:99013660 C>T maps to NM_001298.2 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:99013054 G>C maps to NM_001298.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr11:6260613 G>A maps to NM_001037329.2 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:6261569 G>A maps to NM_001037329.2 W182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:6265408 C>T maps to NM_001037329.2 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:6260613 G>A maps to NM_001037329.2 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:6260703 C>T maps to NM_001037329.2 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:6261361 G>A maps to NM_001037329.2 W113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:6265191 G>A maps to NM_001037329.2 G427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr16:57918085 C>T maps to NM_001297.4 R1246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr16:57931787 G>A maps to NM_001297.4 Q1003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr16:57921905 G>A maps to NM_001297.4 T1105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:57992358 C>T maps to NM_001297.4 E264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:57931766 A>G maps to NM_001297.4 L1010L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr16:57931788 G>A maps to NM_001297.4 I1002I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:57965771 C>T maps to NM_001297.4 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:57931749 C>T maps to NM_001297.4 G1015G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:58001094 C>T maps to NM_001297.4 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:57951297 G>A maps to NM_001297.4 F680F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr16:57918211 G>A maps to NM_001297.4 S1204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr16:57931767 G>A maps to NM_001297.4 V1009V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr8:87679329 G>A maps to NM_019098.4 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr8:87680322 C>T maps to NM_019098.4 W189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr8:87680366 C>A maps to NM_019098.4 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr8:87680385 C>T maps to NM_019098.4 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:87591015 C>T maps to NM_019098.4 P668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr8:87666269 C>T maps to NM_019098.4 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr8:87738831 G>A maps to NM_019098.4 Q89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr8:87679278 G>A maps to NM_019098.4 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:87616322 G>A maps to NM_019098.4 I593I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:87683196 G>A maps to NM_019098.4 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:87641294 C>T maps to NM_019098.4 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:87591015 C>T maps to NM_019098.4 P668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:87683208 C>T maps to NM_019098.4 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:87679271 G>A maps to NM_019098.4 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr8:87591091 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:87641240 G>A maps to NM_019098.4 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr8:87680391 C>T maps to NM_019098.4 K166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr8:87666241 G>A maps to NM_019098.4 Q301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr8:87623851 G>A maps to NM_019098.4 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr8:87588163 T>C maps to NM_019098.4 E766E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:87679346 G>A maps to NM_019098.4 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:87679347 G>A maps to NM_019098.4 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:87679358 G>A maps to NM_019098.4 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:87683256 C>T maps to NM_019098.4 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr8:87680299 A>C maps to NM_019098.4 L197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr8:87679188 C>T maps to NM_019098.4 Q272Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr8:87755798 C>T maps to NM_019098.4 E19E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr11:66050609 C>T maps to NM_182553.1 H101H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:224868707 C>T maps to NM_152495.1 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:224868682 G>A maps to NM_152495.1 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:224804899 C>T maps to NM_152495.1 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:224872499 G>A maps to NM_152495.1 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:26514778 C>T maps to ENST00000374253 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:26507008 C>T maps to ENST00000374253 Q40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:26514757 G>A maps to ENST00000374253 K503K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:26515324 C>T maps to ENST00000374253 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:26508984 T>A maps to ENST00000374253 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:26514781 C>T maps to ENST00000374253 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:26515861 G>A maps to ENST00000374253 R662R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:26510621 C>T maps to ENST00000374253 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:26514726 G>A maps to ENST00000374253 W493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:21508619 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:21627557 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:21609149 A>G did not map to a codon.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr23:21613507 G>A did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:21627524 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr23:21581384 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:21627232 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr23:21624973 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:21627397 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr23:21450847 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr23:21667099 G>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:21549989 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:21627570 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:21444709 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:21624964 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr23:21627552 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:21627647 G>A did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:21627599 T>C did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:21534730 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:11658685 G>A maps to NM_001299.4 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:11657666 C>T maps to NM_001299.4 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:11651946 G>A maps to NM_001299.4 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:1032429 C>T maps to NM_004368.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:95367311 A>G maps to NM_001839.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr10:101122014 G>A maps to NM_020348.2 S630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr10:101124758 C>T maps to NM_020348.2 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr10:104679595 C>G maps to NM_017649.3 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:104678308 T>G maps to NM_017649.3 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr10:104679625 C>T maps to NM_017649.3 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:104679799 C>T maps to NM_017649.3 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:104835966 C>T maps to NM_017649.3 L786L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:104679673 C>T maps to NM_017649.3 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:97490891 C>T maps to NM_017623.4 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:97494388 T>G maps to NM_017623.4 Y624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr2:97464957 C>T maps to NM_020184.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr2:97464924 C>T maps to NM_020184.3 R605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:97462803 C>T maps to NM_020184.3 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:97427863 C>T maps to NM_020184.3 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:97464957 C>T maps to NM_020184.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:97426936 C>T maps to NM_020184.3 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:97464924 C>T maps to NM_020184.3 R605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr16:58580318 C>T maps to NM_016284.3 K1304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr16:58620521 G>A maps to NM_016284.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:58559988 A>G maps to NM_016284.3 T2169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr16:58570931 G>A maps to NM_016284.3 G1869G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr16:58583758 C>T maps to NM_016284.3 W1129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr16:58589734 G>A maps to NM_016284.3 Q853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr16:58617061 G>A maps to NM_016284.3 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr16:58622708 G>A maps to NM_016284.3 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr16:58576340 T>C maps to NM_016284.3 R1522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr16:58621103 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr3:32776306 G>A maps to NM_015442.1 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr3:32757800 C>T maps to NM_015442.1 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr12:70724189 G>A maps to NM_014515.5 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:54656726 C>T maps to NM_014516.3 Y676Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:54649503 C>T maps to NM_014516.3 D218D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:54652019 C>T maps to NM_014516.3 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:54647225 C>T maps to NM_014516.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:135047786 G>A maps to NM_001190850.1 I664I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:135098320 C>T maps to NM_001190850.1 K201K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:135073605 G>A maps to NM_001190848.1 T556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:135078814 C>T maps to NM_001190850.1 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr7:135079072 G>A maps to NM_001190850.1 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:135078868 G>A maps to NM_001190850.1 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:179996263 C>T maps to NM_015455.3 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr5:179956362 C>T maps to NM_015455.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:78697485 G>A maps to ENST00000512485 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:78650092 G>A maps to ENST00000512485 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:78641626 G>A maps to ENST00000512485 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:154254879 A>T maps to NM_004779.4 K254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:56708935 C>T maps to NM_014255.5 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr6:42903378 G>T maps to NM_006586.3 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr6:88854231 G>A maps to NM_016083.4 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:88854231 G>A maps to NM_016083.4 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:88854369 G>A maps to NM_016083.4 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:88854381 C>T maps to NM_016083.4 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:88853865 C>T maps to NM_016083.4 K376K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:88854039 G>A maps to NM_016083.4 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:88854819 G>A maps to NM_016083.4 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr6:88853934 G>A maps to NM_016083.4 I353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:88854123 G>A maps to NM_016083.4 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:88854819 G>A maps to NM_016083.4 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr6:88853949 G>A maps to NM_016083.4 I348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr6:88854924 C>T maps to NM_016083.4 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:88853871 G>A maps to NM_016083.4 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:88853988 G>A maps to NM_016083.4 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr6:88854654 G>A maps to NM_016083.4 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr1:24201330 G>A maps to NM_001841.2 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:24201849 G>A maps to NM_001841.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:24201873 C>T maps to NM_001841.2 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:24201075 C>T maps to NM_001841.2 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr1:24201504 G>A maps to NM_001841.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:24201315 G>A maps to NM_001841.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr2:68520993 T>A maps to NM_015463.2 *165C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr2:68520994 C>T maps to NM_015463.2 *165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:68546483 G>A maps to NM_015463.2 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr1:246810636 C>T maps to NM_152609.2 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:246797224 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:246811000 C>T maps to NM_152609.2 Q500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr17:40956323 G>A maps to NM_173478.2 W109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr17:40951249 C>T maps to NM_173478.2 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr17:40955690 C>T maps to NM_173478.2 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr17:40958722 G>A maps to NM_173478.2 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:40732302 C>T maps to NM_024877.3 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr19:40732317 T>C maps to NM_024877.3 E77E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr11:58391964 C>T maps to NM_000614.3 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr9:34552751 C>T maps to NM_147164.1 W290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr9:34556384 G>A maps to NM_147164.1 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:34556354 C>T maps to NM_147164.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:17502559 C>T maps to NM_017738.2 A1377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr9:17135128 C>T maps to NM_017738.2 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:17466873 C>T maps to NM_017738.2 F1280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr9:17457622 C>T maps to NM_017738.2 S1072S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr9:17409437 G>A maps to NM_017738.2 Q921Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:17332634 C>T maps to NM_017738.2 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:17464555 C>T maps to NM_017738.2 R1156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr12:41333179 C>T maps to NM_001843.2 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr12:41421716 C>T maps to NM_001843.2 I923I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr12:41410718 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr12:41330594 G>A maps to NM_001843.2 W333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:41463806 C>T maps to NM_001843.2 A1009A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:41410656 C>T maps to NM_001843.2 A786A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:41323781 C>T maps to NM_001843.2 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:41419076 C>T maps to NM_001843.2 A883A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:41386973 C>T maps to NM_001843.2 I672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:41374852 G>A maps to NM_001843.2 W649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr12:41318410 G>C maps to NM_001843.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr12:41337962 G>A maps to NM_001843.2 R558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:41463833 C>T maps to NM_001843.2 F1018F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr12:41337962 G>A maps to NM_001843.2 R558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:41316120 C>T maps to NM_001843.2 N97N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:41318428 C>T maps to NM_001843.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:41327597 G>A maps to NM_001843.2 Q301Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:41419022 G>A maps to NM_001843.2 S865S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr12:41410482 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr12:41352929 G>A maps to NM_001843.2 G566G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:41410560 G>A maps to NM_001843.2 W754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:205034330 C>T maps to NM_005076.3 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr1:205033864 C>T maps to NM_005076.3 I502I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr1:205033865 C>T maps to NM_005076.3 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:205027169 G>A maps to NM_005076.3 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:205033516 C>T maps to NM_005076.3 I436I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr1:205031686 A>G maps to NM_005076.3 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:205042350 C>T maps to NM_005076.3 I1000I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:205041640 G>A maps to NM_005076.3 W921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:205027461 G>A maps to NM_005076.3 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:205042350 C>T maps to NM_005076.3 I1000I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr3:74347204 G>A maps to NM_020872.1 I768I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:74315713 C>T maps to NM_020872.1 E968E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:74347204 G>A maps to NM_020872.1 I768I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:74350678 C>T maps to NM_020872.1 G655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:74419074 A>T maps to NM_020872.1 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr3:74350816 A>G maps to NM_020872.1 G642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:74344348 G>A maps to NM_020872.1 L814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:74383906 A>C maps to NM_020872.1 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:74351883 C>A maps to NM_020872.1 T581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:74350889 C>T maps to NM_020872.1 W618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr3:74334516 A>C maps to NM_020872.1 A881A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:74347204 G>A maps to NM_020872.1 I768I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:74414830 G>A maps to NM_020872.1 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:74383951 G>A maps to NM_020872.1 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:2908472 C>T maps to NM_175607.1 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:2928873 G>A maps to NM_175607.1 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:3067885 C>T maps to NM_175607.1 I529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr3:2908550 G>A maps to NM_175607.1 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr3:3085305 G>A maps to NM_175607.1 W910*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr3:2967439 G>A maps to NM_175607.1 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr3:3076355 C>T maps to NM_175607.1 I608I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:3095504 G>A maps to NM_175607.1 W942*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr3:3067885 C>T maps to NM_175607.1 I529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr3:3030097 C>T maps to NM_175607.1 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:2928873 G>A maps to NM_175607.1 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:3030151 G>A maps to NM_175607.1 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:3085291 C>T maps to NM_175607.1 P905P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr3:3084743 G>A maps to NM_175607.1 T865T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr3:2787268 G>A maps to NM_175607.1 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr3:3081845 G>A maps to NM_175607.1 R763R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:3072564 C>T maps to NM_175607.1 I563I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr3:3085300 C>T maps to NM_175607.1 I908I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:2908472 C>A maps to NM_175607.1 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:2928831 G>A maps to NM_175607.1 E288E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:3080683 G>A maps to NM_175607.1 W720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr3:2967439 G>A maps to NM_175607.1 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:2928801 A>G maps to NM_175607.1 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:2613200 G>A maps to NM_175607.1 W5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:2613201 G>A maps to NM_175607.1 W5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:3085321 C>T maps to NM_175607.1 S915S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:2928813 C>T maps to NM_175607.1 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:3084743 G>A maps to NM_175607.1 T865T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:100211855 G>A maps to NM_014361.2 W983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:99690431 G>A maps to NM_014361.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:99827604 C>T maps to NM_014361.2 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:100211307 C>T maps to NM_014361.2 F948F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:99827574 C>T maps to NM_014361.2 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:100061890 C>T maps to NM_014361.2 I538I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:100126510 G>A maps to NM_014361.2 G675G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:100170009 C>T maps to NM_014361.2 F834F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr11:100141824 C>T maps to NM_014361.2 V722V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr11:99872784 G>A maps to NM_014361.2 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:99690323 A>G maps to NM_014361.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:100170009 C>T maps to NM_014361.2 F834F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:99827574 C>T maps to NM_014361.2 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:99786864 T>G maps to NM_014361.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:100179156 G>A maps to NM_014361.2 W896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:100126490 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:100126510 G>A maps to NM_014361.2 G675G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-ER-A3ET-06A-11D-A20D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr11:99690275 G>A maps to NM_014361.2 E19E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr11:100211268 C>T maps to NM_014361.2 V935V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr11:100226920 G>A maps to NM_014361.2 L1091L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:100170009 C>T maps to NM_014361.2 F834F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:100141897 C>T maps to NM_014361.2 R747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:100226908 C>G maps to NM_014361.2 V1087V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:99944897 G>A maps to NM_014361.2 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:1443210 T>G maps to NM_014461.2 S933S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr3:1369178 G>A maps to NM_014461.2 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:1444000 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr3:1337435 G>A maps to NM_014461.2 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr3:1414547 G>A maps to NM_014461.2 R565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr3:1418755 G>A maps to NM_014461.2 W721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:1418759 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:1363426 G>A maps to NM_014461.2 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:1367634 G>A maps to NM_014461.2 E361E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:1424774 T>G maps to NM_014461.2 S772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:1414148 G>A maps to NM_014461.2 R553R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr3:1367619 A>G maps to NM_014461.2 E356E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr3:1269595 C>T maps to NM_014461.2 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NF-06A-11D-A19A-08 chr3:1414547 G>A maps to NM_014461.2 R565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:1444012 G>A maps to NM_014461.2 R943R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr3:1424654 G>A maps to NM_014461.2 E732E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:1189697 G>A maps to NM_014461.2 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:1415400 C>T maps to NM_014461.2 Q634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:1418758 G>A maps to NM_014461.2 E722E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:1427377 G>A maps to NM_014461.2 T867T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:1414073 C>T maps to NM_014461.2 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr17:40844535 C>T maps to NM_003632.2 F850F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr17:40850804 C>T maps to NM_003632.2 T1344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr17:40836075 G>A maps to NM_003632.2 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr17:40837319 C>T maps to NM_003632.2 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr17:40837274 C>T maps to NM_003632.2 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr17:40837253 C>T maps to NM_003632.2 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr17:40837993 A>T maps to NM_003632.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:40837271 C>A maps to NM_003632.2 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr17:40840997 C>T maps to NM_003632.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:40839961 C>T maps to NM_003632.2 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:40844652 C>T maps to NM_003632.2 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:40844653 C>T maps to NM_003632.2 R890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr17:40839805 C>T maps to NM_003632.2 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:40837121 C>T maps to NM_003632.2 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:146818227 G>A maps to NM_014141.5 E304E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:146805362 C>T maps to NM_014141.5 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:148080840 C>T maps to NM_014141.5 A1192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr7:146471396 C>T maps to NM_014141.5 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr7:147600753 C>T maps to NM_014141.5 I732I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:146536849 C>T maps to NM_014141.5 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr7:146997272 C>T maps to NM_014141.5 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr7:146471423 C>T maps to NM_014141.5 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:146536840 C>T maps to NM_014141.5 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:147926840 C>T maps to NM_014141.5 I1117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr7:146997239 G>A maps to NM_014141.5 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:148112590 C>T maps to NM_014141.5 Y1293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr7:148080825 C>T maps to NM_014141.5 I1187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr7:148112555 C>T maps to NM_014141.5 L1282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr7:147914404 G>A maps to NM_014141.5 G1012G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:147844631 G>A maps to NM_014141.5 E868E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:147914404 G>A maps to NM_014141.5 G1012G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr7:147092833 C>T maps to NM_014141.5 F544F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:147926771 C>T maps to NM_014141.5 T1094T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:147092818 G>A maps to NM_014141.5 R539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:148112665 C>T maps to NM_014141.5 F1318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:148080747 G>A maps to NM_014141.5 G1161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr7:146829449 C>T maps to NM_014141.5 F399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr7:147964198 C>T maps to NM_014141.5 L1152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr7:147600732 C>T maps to NM_014141.5 I725I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:146997272 C>T maps to NM_014141.5 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:147336288 C>T maps to NM_014141.5 L663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr7:147926751 C>T maps to NM_014141.5 R1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr7:148112692 G>A maps to NM_014141.5 K1327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr7:147674959 G>A maps to NM_014141.5 K754K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:147914560 C>T maps to NM_014141.5 L1064L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:146825843 C>T maps to NM_014141.5 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:147336209 G>A maps to NM_014141.5 W637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:146741092 G>A maps to NM_014141.5 W166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:147092833 C>T maps to NM_014141.5 F544F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:147844742 C>T maps to NM_014141.5 I905I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr7:147815210 G>A maps to NM_014141.5 R795R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr7:148080747 G>A maps to NM_014141.5 G1161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr7:147092833 C>T maps to NM_014141.5 F544F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr7:146829449 C>T maps to NM_014141.5 F399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr7:147926819 A>G maps to NM_014141.5 G1110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr7:148080747 G>A maps to NM_014141.5 G1161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr7:146471444 C>T maps to NM_014141.5 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:146825864 C>T maps to NM_014141.5 I340I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:147926751 C>T maps to NM_014141.5 R1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:148112692 G>A maps to NM_014141.5 K1327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr7:147092786 C>T maps to NM_014141.5 Q529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr7:147844691 G>A maps to NM_014141.5 E888E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr7:147092833 C>T maps to NM_014141.5 F544F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr7:147815210 G>A maps to NM_014141.5 R795R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr9:39171441 G>A maps to NM_033655.3 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr9:39171441 G>A maps to NM_033655.3 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:39171503 G>A maps to NM_033655.3 R399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:39109156 G>A maps to NM_033655.3 Q789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr9:39171461 G>A maps to NM_033655.3 R413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr9:39171441 G>A maps to NM_033655.3 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr9:39171398 G>A maps to NM_033655.3 Q434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr9:39109232 C>T maps to NM_033655.3 Q763Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:39109265 G>A maps to NM_033655.3 V752V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:39085751 G>A maps to NM_033655.3 L1141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr9:39140594 C>T maps to NM_033655.3 G599G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr9:39177401 G>A maps to NM_033655.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr9:39171399 G>A maps to NM_033655.3 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr9:39103849 G>A maps to NM_033655.3 F809F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr9:39171435 G>A maps to NM_033655.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:39109232 C>T maps to NM_033655.3 Q763Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:39178268 A>T maps to NM_033655.3 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:39109259 G>A maps to NM_033655.3 S754S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr16:76569508 C>T maps to NM_033401.3 T940T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr16:76513373 C>T maps to NM_033401.3 Y606Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:76486595 C>T maps to NM_033401.3 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:76573628 C>T maps to NM_033401.3 I1077I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr16:76572237 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:76481969 C>T maps to NM_033401.3 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:76483655 C>T maps to NM_033401.3 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:76482005 C>T maps to NM_033401.3 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:76592520 A>T maps to NM_033401.3 K1289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr16:76532462 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr16:76461482 C>T maps to NM_033401.3 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:76461443 G>A maps to NM_033401.3 W161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:76486466 G>A maps to NM_033401.3 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:76572046 G>A maps to NM_033401.3 V1009V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr16:76555130 T>C maps to NM_033401.3 F819F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr16:76482752 C>T maps to NM_033401.3 Q277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:76481970 C>T maps to NM_033401.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:76486499 G>A maps to NM_033401.3 E388E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr16:76461442 G>A maps to NM_033401.3 W161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr16:76573628 C>T maps to NM_033401.3 I1077I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr16:76482814 G>A maps to NM_033401.3 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr16:76569604 G>A maps to NM_033401.3 G972G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr16:76574679 G>A maps to NM_033401.3 R1144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:76482829 C>T maps to NM_033401.3 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:76573650 C>T maps to NM_033401.3 Q1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr16:76556122 C>T maps to NM_033401.3 V907V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr16:76501375 G>A maps to NM_033401.3 G536G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr16:76532517 C>T maps to NM_033401.3 I763I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr16:76501375 G>A maps to NM_033401.3 G536G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:125261994 C>T maps to NM_130773.2 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr2:125261927 C>T maps to NM_130773.2 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr2:125204363 C>T maps to NM_130773.2 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr2:125262125 C>T maps to NM_130773.2 I439I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:125192256 C>T maps to NM_130773.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:125555886 C>T maps to NM_130773.2 L1068L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr2:125504851 C>T maps to NM_130773.2 H707H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr2:125175120 C>A maps to NM_130773.2 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:125192187 C>T maps to NM_130773.2 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:125204408 G>A maps to NM_130773.2 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr2:125192238 G>A maps to NM_130773.2 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr2:125261994 C>T maps to NM_130773.2 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:125261994 C>T maps to NM_130773.2 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:125192115 G>A maps to NM_130773.2 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:125555859 T>A maps to NM_130773.2 S1059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:125192187 C>T maps to NM_130773.2 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:125284988 G>A maps to NM_130773.2 G534G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:125521677 C>T maps to NM_130773.2 F828F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:125530563 C>T maps to NM_130773.2 R907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr2:125530529 G>A maps to NM_130773.2 R895R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr2:125367417 G>A maps to NM_130773.2 G598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr2:125261994 C>T maps to NM_130773.2 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:125175030 A>G maps to NM_130773.2 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:125192247 C>T maps to NM_130773.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:125284947 C>T maps to NM_130773.2 Q521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:125530385 G>A maps to NM_130773.2 E847E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr2:125192200 C>T maps to NM_130773.2 Q224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:124999969 G>A maps to NM_130773.2 W127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr17:7852462 C>T maps to NM_001037144.4 I880I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:7839763 C>T maps to NM_001037144.4 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr17:7846732 C>T maps to NM_001037144.4 Q446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr17:40717007 C>T maps to NM_001042532.2 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr17:40714960 C>T maps to NM_001042532.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:40716743 C>T maps to NM_001042532.2 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr17:40714458 C>T maps to NM_001042532.2 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr17:40714459 C>T maps to NM_001042532.2 R11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:51092901 G>A maps to ENST00000395542 S1306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:51111249 G>A maps to ENST00000395542 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr7:51111351 C>T maps to ENST00000395542 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr7:51096200 G>A maps to ENST00000395542 S946S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:51111156 G>A maps to ENST00000395542 D525D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:51096980 G>A maps to ENST00000395542 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr7:51097007 C>T maps to ENST00000395542 E677E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:51096437 C>T maps to ENST00000395542 E867E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:51097238 G>A maps to ENST00000395542 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr7:51096085 G>A maps to ENST00000395542 L985L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:51092838 G>A maps to ENST00000395542 I1327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr7:51111162 G>A maps to ENST00000395542 D523D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:51287565 G>A maps to ENST00000395542 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr7:51287472 A>G maps to ENST00000395542 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:51096503 G>A maps to ENST00000395542 P845P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:165551015 C>T maps to ENST00000392717 Q1038Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:165551321 G>A maps to ENST00000392717 A936A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr2:165584551 C>T maps to ENST00000392717 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:140157634 G>A maps to NM_015456.3 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr9:140161466 G>A maps to NM_015456.3 V389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr9:140151502 C>T maps to NM_015456.3 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr9:140161695 C>T maps to NM_015456.3 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr14:31344158 G>A maps to NM_004086.2 W5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:31355240 G>A maps to NM_004086.2 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr17:71189273 C>T maps to NM_018714.2 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:230807341 C>T maps to NM_007357.2 H285H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr13:46067544 T>G maps to NM_031431.2 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr16:70514999 C>T maps to NM_015386.2 T761T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:70543247 G>A maps to NM_015386.2 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:70534927 G>A maps to NM_015386.2 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr16:70546162 G>A maps to NM_015386.2 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr16:70546201 G>A maps to NM_015386.2 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr7:107013043 C>T maps to NM_006348.3 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:106964933 C>T maps to NM_006348.3 W384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr13:40268835 C>T maps to ENST00000255468 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:23444940 G>A maps to NM_153603.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:23444871 A>G maps to NM_153603.3 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr16:23415115 G>A maps to NM_153603.3 R568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr16:23445989 G>C maps to NM_153603.3 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:23409420 G>A maps to NM_153603.3 T611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:23428364 G>A maps to NM_153603.3 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr16:23436219 G>A maps to NM_153603.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr16:69364885 C>T maps to NM_032382.4 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:55027861 G>A maps to NM_004645.2 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:55027767 A>G maps to NM_004645.2 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:55027330 G>A maps to NM_004645.2 S424S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DA-A1HY-06A-11D-A19A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr6:116442960 C>T maps to ENST00000430695 F114F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DA-A1I0-06A-11D-A20D-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-DA-A1I7-06A-22D-A197-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-EE-A29M-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr6:116442621 C>T maps to NM_000493.3 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr6:116442255 C>T maps to NM_000493.3 G341G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-FS-A1ZA-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr1:103405960 C>T maps to NM_080629.2 G1114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:103428301 C>T maps to NM_080629.2 E989E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr1:103544215 C>T maps to NM_080629.2 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:103343610 G>A maps to NM_080629.2 F1807F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:103356005 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:103444976 G>A maps to NM_080629.2 F869F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:103461553 C>T maps to NM_080629.2 R774R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:103388894 G>A maps to NM_080629.2 P1229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:103343685 G>A maps to NM_080629.2 I1782I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:103427791 C>T maps to NM_080629.2 G1030G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:103488486 C>T maps to NM_080629.2 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:103487307 T>A maps to NM_080629.2 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:103488486 C>T maps to NM_080629.2 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr1:103356018 G>A maps to NM_080629.2 S1460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:103491496 G>A maps to NM_080629.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr1:103345353 C>T maps to NM_080629.2 W1732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:103491502 C>T maps to NM_080629.2 K262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:103471817 C>T maps to NM_080629.2 R591R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:103352590 G>A maps to NM_080629.2 Q1556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:103354171 C>T maps to NM_080629.2 Q1535Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:103355094 C>T maps to NM_080629.2 L1472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:103488467 G>A maps to NM_080629.2 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:103491484 C>T maps to NM_080629.2 K268K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:103352474 G>A maps to NM_080629.2 S1594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:103467998 C>T maps to NM_080629.2 G706G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr1:103352588 C>T maps to NM_080629.2 Q1556Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:103471392 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:103343646 G>A maps to NM_080629.2 V1795V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:103400010 A>T maps to NM_080629.2 G1210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:103427791 C>T maps to NM_080629.2 G1030G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:103467998 C>T maps to NM_080629.2 G706G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:103471420 C>T maps to NM_080629.2 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:103573704 C>T maps to NM_080629.2 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:33132169 G>A maps to NM_080680.2 H1648H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:33146699 C>T maps to NM_080680.2 V554V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr6:33156165 G>A maps to NM_080680.2 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr6:33137225 C>T maps to NM_080680.2 Q1244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr6:33132136 G>A maps to NM_080680.2 A1659A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:33138616 G>A maps to NM_080680.2 F1148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr6:33138363 C>T maps to NM_080680.2 E1166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:33133413 G>A maps to NM_080680.2 I1554I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:33141828 G>A maps to NM_080680.2 L830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:33157100 G>A maps to NM_080680.2 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr6:33144518 G>A maps to NM_080680.2 P698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr6:33133740 T>C maps to NM_080680.2 G1483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:33133761 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:33146223 C>T maps to NM_080680.2 E587E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr6:33137243 C>T maps to NM_080680.2 E1238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:33135605 G>A maps to NM_080680.2 S1328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr6:33139582 T>C maps to NM_080680.2 E1019E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:33134888 C>T maps to NM_080680.2 G1396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:33156921 G>A maps to NM_080680.2 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:33135052 G>A maps to NM_080680.2 P1388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr6:33139880 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:33154558 G>A maps to NM_080680.2 Q215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr6:33156783 G>A maps to NM_080680.2 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr6:33156870 G>A maps to NM_080680.2 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:33140080 G>A maps to NM_080680.2 G991G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:33152023 G>A maps to NM_080680.2 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:33148109 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:33132115 G>A maps to NM_080680.2 L1666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr6:33139492 G>A maps to NM_080680.2 V1049V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr6:33135090 G>A maps to NM_080680.2 Q1376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr6:75899095 C>T maps to ENST00000322507 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr6:75843693 C>T maps to ENST00000322507 R1848R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:75884835 C>T maps to ENST00000322507 G876G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:75801229 C>T maps to ENST00000322507 G2887G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:75884928 G>A maps to ENST00000322507 L845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:75828861 C>T maps to ENST00000322507 W2417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr6:75823423 C>T maps to ENST00000322507 T2578T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr6:75799850 C>T maps to ENST00000322507 G2972G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:75893708 C>T maps to ENST00000322507 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr6:75893012 G>A maps to ENST00000322507 I548I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:75899008 C>T maps to ENST00000322507 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr6:75899337 C>T maps to ENST00000322507 Q196Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:75858112 C>T maps to ENST00000322507 K1416K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr6:75893174 C>T maps to ENST00000322507 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:75831062 G>A maps to ENST00000322507 F2347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr6:75853080 G>A maps to ENST00000322507 L1572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr6:75887457 C>T maps to ENST00000322507 T786T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr6:75799829 T>C maps to ENST00000322507 E2979E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr10:71665556 C>T maps to ENST00000356340 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr10:71690232 G>A maps to ENST00000356340 V525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr10:71690274 G>A maps to ENST00000356340 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:71690232 G>A maps to ENST00000356340 V525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:71681678 C>T maps to ENST00000356340 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr10:71655328 C>T maps to ENST00000356340 H218H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr10:71640272 C>T maps to ENST00000356340 D150D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:71657229 G>A did not map to a codon.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr10:71707088 G>A maps to ENST00000356340 K672K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:71634885 G>A maps to ENST00000356340 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:71705446 G>A maps to ENST00000356340 G652G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:71707097 G>C maps to ENST00000356340 R675R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:121220503 T>C maps to NM_021110.1 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:121379408 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr8:121298142 G>A maps to NM_021110.1 G1337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:121215984 C>T maps to NM_021110.1 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:121220505 G>A maps to NM_021110.1 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:121237403 C>T maps to NM_021110.1 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:121381647 G>A maps to NM_021110.1 G1745G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:121174683 G>A maps to NM_021110.1 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:121228713 G>A maps to NM_021110.1 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr8:121210140 C>T maps to NM_021110.1 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr8:121293298 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr8:121293265 C>T maps to NM_021110.1 L1264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:121379422 C>T maps to NM_021110.1 I1697I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:121357668 C>T maps to NM_021110.1 S1648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr8:121282289 G>A maps to NM_021110.1 K1030K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:121298181 G>A maps to NM_021110.1 R1350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:121326181 C>T maps to NM_021110.1 G1489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr8:121301972 C>T maps to NM_021110.1 R1402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr8:121237400 C>T maps to NM_021110.1 F604F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr8:121243856 G>A maps to NM_021110.1 T783T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:121290693 C>T maps to NM_021110.1 R1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr8:121309793 C>T maps to NM_021110.1 A1427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr8:121256206 G>C maps to NM_021110.1 T813T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr8:121322262 C>T maps to NM_021110.1 R1473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr8:121238908 G>A maps to NM_021110.1 T636T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:121290797 C>T maps to NM_021110.1 S1154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:121301911 G>A maps to NM_021110.1 K1381K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:121381701 A>C maps to NM_021110.1 S1763S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr8:121328220 C>T maps to NM_021110.1 G1548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:121211695 G>A maps to NM_021110.1 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:121209075 C>T maps to NM_021110.1 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr8:121209081 C>T maps to NM_021110.1 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr8:121238864 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr9:101797333 G>A maps to NM_001855.3 G706G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr9:101818676 C>T maps to NM_001855.3 L1110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr9:101806875 C>T maps to NM_001855.3 I867I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:101748018 C>T maps to NM_001855.3 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr9:101787265 T>G maps to NM_001855.3 G655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr9:101748249 C>T maps to NM_001855.3 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr9:101829169 T>C maps to NM_001855.3 L1220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr9:101797333 G>A maps to NM_001855.3 G706G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr9:101767301 C>T maps to NM_001855.3 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:101777697 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:101748165 G>A maps to NM_001855.3 E140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr9:101817608 C>T maps to NM_001855.3 F1049F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:101818678 G>A maps to NM_001855.3 L1110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr9:101748012 G>A maps to NM_001855.3 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr9:101797333 G>A maps to NM_001855.3 G706G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:101767274 C>T maps to NM_001855.3 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:101778391 G>A maps to NM_001855.3 W546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr9:101767250 G>A maps to NM_001855.3 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr9:101765775 C>T maps to NM_001855.3 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr1:32151371 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr1:32122012 A>G maps to NM_001856.3 P1363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:32157059 G>T maps to NM_001856.3 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:32134408 C>T maps to NM_001856.3 G1081G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:32163541 G>A maps to NM_001856.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:32118302 C>T maps to NM_001856.3 P1588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr10:105815128 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr10:105815687 C>T maps to NM_000494.3 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr10:105819931 G>A maps to NM_000494.3 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr10:105800168 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:105800154 G>A maps to NM_000494.3 S905S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:105815714 C>T maps to NM_000494.3 R504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:105798212 G>A maps to NM_000494.3 I1007I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:105803262 G>A maps to NM_000494.3 A837A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:105831819 G>A maps to NM_000494.3 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:105833948 C>T maps to NM_000494.3 K124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:105819913 C>T maps to NM_000494.3 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:105798284 C>T maps to NM_000494.3 G983G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:105836091 T>G maps to NM_000494.3 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr21:46901890 T>A maps to ENST00000359759 P957P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr21:46900419 C>T maps to ENST00000359759 L895L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr21:46912602 C>T maps to ENST00000359759 G1145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr21:46888516 C>G maps to ENST00000359759 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr21:46888696 C>T maps to ENST00000359759 F631F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr21:46916433 A>C maps to ENST00000359759 G1258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr21:46900639 C>T maps to ENST00000359759 P908P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:46888189 C>T maps to ENST00000359759 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr21:46901893 G>A maps to ENST00000359759 P958P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr21:46893816 C>T maps to ENST00000359759 I635I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr6:70672761 G>A maps to NM_001858.4 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:70897924 C>T maps to NM_001858.4 G1001G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:70637923 G>A maps to NM_001858.4 Q130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:70646762 G>A maps to NM_001858.4 K278K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:70744135 G>A did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr6:70897936 C>T maps to NM_001858.4 I1005I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr6:70647928 G>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:70812071 G>A maps to NM_001858.4 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:70916888 C>T maps to NM_001858.4 Q1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:70897789 G>A maps to NM_001858.4 G956G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:70850850 G>A maps to NM_001858.4 E484E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr6:70778319 C>T maps to NM_001858.4 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr6:70856588 G>A maps to NM_001858.4 G603G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr6:70637888 C>T maps to NM_001858.4 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr6:70778325 G>A maps to NM_001858.4 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:70916953 C>T maps to NM_001858.4 A1135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:70866041 C>T maps to NM_001858.4 A701A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:48271375 G>A maps to NM_000088.3 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr17:48264037 G>A maps to NM_000088.3 C1259C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr17:48263698 C>T maps to NM_000088.3 E1328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr17:48266830 C>T maps to NM_000088.3 E912E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:48263866 T>C maps to NM_000088.3 G1272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:48266764 T>C maps to NM_000088.3 K934K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:48269835 C>T maps to NM_000088.3 Q661Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:48267364 G>A maps to NM_000088.3 P852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr17:48277308 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr17:48274391 G>A maps to NM_000088.3 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr17:48271393 G>A maps to NM_000088.3 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:48271375 G>A maps to NM_000088.3 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:48262925 G>A maps to NM_000088.3 P1444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr17:48271808 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr17:48266758 G>A maps to NM_000088.3 S936S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:48275351 G>A maps to NM_000088.3 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:48264055 C>T maps to NM_000088.3 K1253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr17:48263848 G>A maps to NM_000088.3 P1278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:94044560 C>T maps to NM_000089.3 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr7:94039090 C>T maps to NM_000089.3 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr7:94024396 C>T maps to NM_000089.3 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:94038683 C>T maps to NM_000089.3 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:94054920 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr7:94040250 C>T maps to NM_000089.3 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr7:94054460 T>C maps to NM_000089.3 P902P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr7:94053706 C>T maps to NM_000089.3 L875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:94028395 G>A maps to NM_000089.3 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:94039066 C>T maps to NM_000089.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:94041909 C>T maps to NM_000089.3 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr20:61929331 G>A maps to ENST00000326996 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr20:61937371 C>T maps to ENST00000326996 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr20:61939900 C>T maps to ENST00000326996 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr20:61936862 C>T maps to ENST00000326996 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:61946783 C>T maps to ENST00000326996 S846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:61937320 G>A maps to ENST00000326996 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:61929358 G>A maps to ENST00000326996 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:61943026 G>A maps to ENST00000326996 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:61941815 C>T maps to ENST00000326996 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr20:61941758 C>T maps to ENST00000326996 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr20:61939413 C>T maps to ENST00000326996 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:61940041 G>A maps to ENST00000326996 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:61947986 C>T maps to ENST00000326996 F876F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:61945237 A>T maps to ENST00000326996 K792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:61959770 C>T maps to ENST00000326996 P1279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr6:55924002 C>T maps to NM_030820.3 G882G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr6:55925772 C>T maps to NM_030820.3 V756V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr6:55989060 G>A maps to NM_030820.3 G560G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr6:55989072 C>T maps to NM_030820.3 K556K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:55942326 C>T maps to NM_030820.3 K619K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr6:56044433 C>T maps to NM_030820.3 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:55939080 A>T maps to NM_030820.3 G638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:56021726 C>T maps to NM_030820.3 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:56044655 G>A maps to NM_030820.3 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:56033059 G>A maps to NM_030820.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:56044664 C>T maps to NM_030820.3 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:55989069 C>T maps to NM_030820.3 G557G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:56044777 G>A maps to NM_030820.3 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr6:55925688 G>A maps to NM_030820.3 P784P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:55925700 C>T maps to NM_030820.3 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:55929416 G>A maps to NM_030820.3 Q711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr8:139833558 C>T maps to NM_152888.1 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr8:139703117 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr8:139712375 G>A maps to NM_152888.1 F857F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr8:139839023 C>T maps to NM_152888.1 E282E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr8:139611072 G>A maps to NM_152888.1 I1418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:139838969 C>T maps to NM_152888.1 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr8:139712352 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr8:139642949 G>A maps to NM_152888.1 I1217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr8:139838921 G>A maps to NM_152888.1 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:139638483 C>T maps to NM_152888.1 G1222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:139890032 G>A maps to NM_152888.1 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr8:139701183 C>T maps to NM_152888.1 G946G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:139603679 G>A maps to NM_152888.1 P1560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:139833473 G>A maps to NM_152888.1 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr8:139895406 G>A maps to NM_152888.1 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr8:139729103 A>G maps to NM_152888.1 I788I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:139601551 G>A maps to NM_152888.1 Q1609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:139629192 C>T maps to NM_152888.1 K1278K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr8:139856363 G>A maps to NM_152888.1 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr5:177676174 C>T maps to ENST00000390654 E364E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:177694307 C>T maps to ENST00000390654 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NF-06A-11D-A19A-08 chr5:177683869 C>T maps to ENST00000390654 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:177683399 T>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:177675234 C>T maps to ENST00000390654 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:177686748 C>T did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:177690241 C>T maps to ENST00000390654 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:86591736 G>A maps to NM_152890.5 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr1:86515854 A>G maps to NM_152890.5 F619F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:86590674 C>T maps to NM_152890.5 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:86315040 T>A maps to NM_152890.5 K1117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:86590794 G>A maps to NM_152890.5 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:86591025 C>T maps to NM_152890.5 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:86200454 T>A maps to NM_152890.5 K1659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:86249816 G>A maps to NM_152890.5 F1400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr1:86200548 C>T maps to NM_152890.5 R1627R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:86210382 T>C maps to NM_152890.5 K1546K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr4:109895522 C>T maps to ENST00000333642 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:109783698 C>T maps to ENST00000333642 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:109780826 G>A maps to ENST00000333642 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr4:109971324 C>T maps to ENST00000333642 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:109895687 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:109745365 C>T maps to ENST00000333642 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr4:109861727 C>T maps to ENST00000333642 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:109765722 G>A maps to ENST00000333642 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:110222986 G>A maps to ENST00000333642 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:110222992 C>T maps to ENST00000333642 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:117063374 C>T maps to NM_032888.2 P1575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:116931442 C>T maps to NM_032888.2 P536P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr9:117051535 C>T maps to NM_032888.2 P1389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr9:116931601 C>T maps to NM_032888.2 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr9:117072863 C>T maps to NM_032888.2 T1824T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr9:117071541 C>T maps to NM_032888.2 V1740V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:116930317 C>T maps to NM_032888.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:116931268 C>T maps to NM_032888.2 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:117072881 C>T maps to NM_032888.2 P1830P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr9:116930425 C>T maps to NM_032888.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr7:7413016 G>A maps to NM_001037763.2 I840I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:7484054 C>T maps to NM_001037763.2 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr7:7571503 G>A maps to NM_001037763.2 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:7571421 G>A maps to NM_001037763.2 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr7:7571503 G>A maps to NM_001037763.2 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr7:7420475 C>T maps to NM_001037763.2 R741R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:7529088 C>A did not map to a codon.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr7:7483254 G>A maps to NM_001037763.2 G537G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:7572485 G>A maps to NM_001037763.2 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:48383064 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr12:48387815 G>A maps to NM_001844.4 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr12:48391394 A>G maps to NM_001844.4 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:48393852 C>T maps to NM_001844.4 W47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:48378798 G>A maps to NM_001844.4 F604F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:48393714 G>A maps to NM_001844.4 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr12:48369115 G>A maps to NM_001844.4 H1290H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:48375123 A>C did not map to a codon.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr12:48368635 C>T maps to NM_001844.4 W1299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:48393853 C>T maps to NM_001844.4 W47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:48380959 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:48374375 G>A maps to NM_001844.4 A862A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr12:48376368 G>A maps to NM_001844.4 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:48391403 G>A maps to NM_001844.4 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr12:48367871 C>T maps to NM_001844.4 T1439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:189871090 C>T maps to NM_000090.3 G1038G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr2:189875616 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr2:189850504 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr2:189875408 C>T maps to NM_000090.3 V1349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr2:189868748 G>A maps to NM_000090.3 K901K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr2:189875502 C>T maps to NM_000090.3 Q1381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:189869011 G>A maps to NM_000090.3 G951G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:189872239 A>C maps to NM_000090.3 P1090P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:189875510 T>C maps to NM_000090.3 S1383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:189849943 C>T maps to NM_000090.3 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:189869026 G>A maps to NM_000090.3 R956R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr2:189859280 G>A maps to NM_000090.3 K436K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:189870086 G>A maps to NM_000090.3 G981G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:189872819 C>T maps to NM_000090.3 P1159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr2:189861889 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:189867064 C>T maps to NM_000090.3 F811F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:189873780 T>A maps to NM_000090.3 Y1219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:189875060 G>A maps to NM_000090.3 W1327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr2:189850416 T>C maps to NM_000090.3 N120N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:189855064 C>T maps to NM_000090.3 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:189872636 C>T maps to NM_000090.3 I1130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:189875433 C>T maps to NM_000090.3 R1358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:189875433 C>T maps to NM_000090.3 R1358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr2:189854120 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr13:110850835 G>A maps to NM_001845.4 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr13:110813567 C>T maps to NM_001845.4 T1537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr13:110835394 C>T maps to NM_001845.4 E680E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr13:110838730 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr13:110827618 C>T maps to NM_001845.4 E1048E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr13:110828849 A>C maps to NM_001845.4 G993G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr13:110857735 G>A maps to NM_001845.4 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr13:110827027 G>A maps to NM_001845.4 I1089I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr13:110823080 T>C did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr13:110835382 C>T maps to NM_001845.4 V684V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr13:110827603 G>A maps to NM_001845.4 G1053G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr13:110807628 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr13:110822957 G>A maps to NM_001845.4 S1226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr13:110814730 G>A maps to NM_001845.4 P1436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:110829373 G>A maps to NM_001845.4 G909G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:110830537 G>A maps to NM_001845.4 F833F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:110831645 G>A maps to NM_001845.4 I772I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:110857885 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr13:110827672 G>A maps to NM_001845.4 I1030I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr13:111164315 A>C maps to NM_001846.2 S1639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr13:111090368 G>A maps to NM_001846.2 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr13:111141853 C>T maps to NM_001846.2 F1090F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr13:111114709 C>T maps to NM_001846.2 F585F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr13:111138125 C>T maps to NM_001846.2 F1050F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr13:111109729 C>T maps to NM_001846.2 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr13:111098180 C>T maps to NM_001846.2 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr13:111111223 G>A maps to NM_001846.2 R513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr13:111114658 C>A maps to NM_001846.2 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr13:111111268 C>T maps to NM_001846.2 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZU-06A-12D-A196-08 chr13:111137366 C>T maps to NM_001846.2 G1006G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:111109729 C>T maps to NM_001846.2 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:111141853 C>T maps to NM_001846.2 F1090F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:111143687 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:111156290 C>T maps to NM_001846.2 P1412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:111164363 C>T maps to NM_001846.2 F1655F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:228167821 G>A maps to NM_000091.4 V1317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:228131217 G>A maps to NM_000091.4 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:228148570 G>A maps to NM_000091.4 R915R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:228102733 G>A maps to NM_000091.4 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr2:228149035 G>A maps to NM_000091.4 G952G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:228135598 G>A maps to NM_000091.4 G563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:228155602 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:74695191 G>A maps to NM_001130105.1 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:227896978 C>T maps to ENST00000396625 V1197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr2:227922197 C>T maps to ENST00000396625 G834G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:227946858 C>T maps to ENST00000396625 K556K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr2:227912265 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr2:227907858 G>A maps to ENST00000396625 Q1111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:227872751 G>A maps to ENST00000396625 I1597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:227964389 G>A maps to ENST00000396625 R349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:227953464 C>T maps to ENST00000396625 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:227946829 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr2:227875215 C>T maps to ENST00000396625 G1445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:227914841 C>T maps to ENST00000396625 E1052E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:227917033 G>A maps to ENST00000396625 F985F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:227920745 C>T maps to ENST00000396625 R877R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:227945197 C>T maps to ENST00000396625 R588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:227963491 G>A maps to ENST00000396625 F374F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:227973563 C>T maps to ENST00000396625 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr2:227958859 C>T maps to ENST00000396625 Q450Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:227922197 C>T maps to ENST00000396625 G834G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr2:227915857 G>T maps to ENST00000396625 P995P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr2:227892725 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:227924163 C>T maps to ENST00000396625 G780G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:227924927 G>A maps to ENST00000396625 A696A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:227946861 C>T maps to ENST00000396625 A555A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:227967504 C>T maps to ENST00000396625 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:227983444 T>C maps to ENST00000396625 K135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:227954671 C>T maps to ENST00000396625 V457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr23:107911598 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:107938100 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr23:107924159 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr23:107858226 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:107938069 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:107802371 C>T did not map to a codon.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr23:107783034 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr23:107802339 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:107911652 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr23:107815041 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:107846279 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr23:107829911 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr23:107923940 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr23:107866028 G>A did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:107807132 C>T did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:107814675 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr23:107865091 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:107821573 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:107863561 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:107911652 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:107814642 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:107869004 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr23:107819141 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:107938565 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr23:107814657 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:107863517 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:107826128 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr23:107829887 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr23:107815063 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:107911599 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:107829937 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr23:107840643 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr23:107821308 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:107842026 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:107865085 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr23:107816836 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:107811989 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:107814657 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:107834829 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr23:107821327 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr23:107824249 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:107811877 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:107869488 A>C did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:107865031 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:107865992 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:107935982 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr23:107850055 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:107924161 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr23:107925059 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr23:107925060 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:107829882 A>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:107840635 C>T did not map to a codon.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr23:107939565 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:107850080 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:107850121 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:107850122 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:107834828 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:107849981 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr23:107841969 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:107936107 G>T did not map to a codon.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr23:107863575 G>T did not map to a codon.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr23:107815041 G>A did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:107924161 G>A did not map to a codon.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr23:107840790 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr23:107925059 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:107814657 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:107846275 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:107811989 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:107844632 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:107858194 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:107865086 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:107868958 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:107923950 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:107938510 G>A did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr23:107838824 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:107815054 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:107840616 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:107841956 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:107911613 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:107911628 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:107930849 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:107840643 G>A did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:107911734 G>A did not map to a codon.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr23:107869517 A>T did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:107840691 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:107422625 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr23:107417780 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr23:107464509 A>G did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:107417841 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:107417842 C>A did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:107412741 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:107431883 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:107419008 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr23:107431169 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:107402884 T>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:107422580 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:107431773 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:107464576 C>T did not map to a codon.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr23:107430340 G>A did not map to a codon.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr23:107430341 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:107414670 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr23:107417829 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr23:107431208 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:107412784 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:107430381 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:107418429 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:107418433 T>G did not map to a codon.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr23:107554041 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr23:107408126 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr23:107408127 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:107418928 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:107447582 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:107418388 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:107415743 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:107433708 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:107436861 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:107415710 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:107424152 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:107413903 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:107436888 A>T did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:107437779 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr23:107407868 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr23:107422662 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:107431127 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr23:107420086 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr23:107417841 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:107407871 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:107417674 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:107413864 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:107408187 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:107430420 C>T did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:107415698 C>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:107431789 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:107438345 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:107438354 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr9:137623469 G>T maps to NM_000093.3 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr9:137717716 G>A maps to NM_000093.3 S1678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:137671946 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr9:137734037 C>T maps to NM_000093.3 I1802I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr9:137644475 G>A maps to NM_000093.3 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr9:137620553 C>T maps to NM_000093.3 Y275Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr9:137671961 C>T maps to NM_000093.3 I800I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr9:137702117 G>T maps to NM_000093.3 P1164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:137676935 G>A maps to NM_000093.3 G862G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr9:137702114 G>A maps to NM_000093.3 E1163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:137630653 G>A maps to NM_000093.3 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr9:137642407 C>T maps to NM_000093.3 G505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr9:137620601 C>T maps to NM_000093.3 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:137660266 G>A maps to NM_000093.3 G748G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:137630330 C>T maps to NM_000093.3 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:137717650 C>T maps to NM_000093.3 V1656V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:137620646 C>T maps to NM_000093.3 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:137623451 C>T maps to NM_000093.3 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:137707429 G>A maps to NM_000093.3 V1341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr9:137593136 C>T maps to NM_000093.3 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr9:137674559 T>G maps to NM_000093.3 G826G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr9:137693828 C>T maps to NM_000093.3 G994G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr9:137676836 G>A maps to NM_000093.3 G829G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr9:137734004 C>T maps to NM_000093.3 T1791T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr9:137659199 G>A maps to NM_000093.3 K744K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr9:137591824 G>A maps to NM_000093.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr9:137650102 C>T maps to NM_000093.3 F632F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr9:137716701 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr9:137688743 C>T maps to NM_000093.3 P965P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr9:137650105 C>T maps to NM_000093.3 D633D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:137593094 C>T maps to NM_000093.3 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:137623484 G>A maps to NM_000093.3 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:137712029 C>T maps to NM_000093.3 L1505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:137716507 C>T maps to NM_000093.3 I1587I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:137642637 C>T maps to NM_000093.3 F524F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:137619120 C>T maps to NM_000093.3 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:137702111 G>A maps to NM_000093.3 G1162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:189899662 G>A maps to NM_000393.3 I1444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:189901341 C>T maps to NM_000393.3 Q1371Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:189904058 C>T maps to NM_000393.3 S1288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:189901515 A>G maps to NM_000393.3 I1313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:189927734 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr2:189957034 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:189904208 C>T maps to NM_000393.3 G1238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:189912955 C>T maps to NM_000393.3 R1060R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:10097267 G>A maps to NM_015719.3 F735F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:10089285 C>T maps to NM_015719.3 K994K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr19:10089816 C>T maps to NM_015719.3 E955E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:10077064 C>T maps to NM_015719.3 R1569R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr19:10088148 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr19:10091338 C>T maps to NM_015719.3 G863G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:10080328 C>G maps to NM_015719.3 G1340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:10084244 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:10116263 C>T maps to NM_015719.3 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:10081683 C>T maps to NM_015719.3 G1283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:10085068 G>A maps to NM_015719.3 Q1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:10112452 C>T maps to NM_015719.3 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:10114306 C>T maps to NM_015719.3 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr19:10071164 C>T maps to NM_015719.3 W1720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:10108067 G>A maps to NM_015719.3 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:10092761 G>T maps to NM_015719.3 P813P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:10088085 C>A maps to NM_015719.3 L1063L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:10112452 C>T maps to NM_015719.3 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr19:10079153 C>T maps to NM_015719.3 L1407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr19:10085075 G>A maps to NM_015719.3 D1117D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:10073500 C>T maps to NM_015719.3 G1615G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:10077377 G>A maps to NM_015719.3 F1501F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:10084864 G>A maps to NM_015719.3 V1162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:10088272 G>A maps to NM_015719.3 S1041S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:10089653 C>T maps to NM_015719.3 G959G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:10106263 T>A maps to NM_015719.3 G521G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:10080283 C>T maps to NM_015719.3 G1355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:10087931 C>T maps to NM_015719.3 K1087K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:47423851 C>T maps to NM_001848.2 F1004F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr21:47423518 C>T maps to NM_001848.2 F893F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr21:47412100 C>T maps to NM_001848.2 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr21:47409529 C>G maps to NM_001848.2 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr21:47531995 C>T maps to NM_001849.3 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr21:47546095 C>T maps to NM_001849.3 F789F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr21:47545921 G>A maps to NM_001849.3 T731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:47549146 C>T maps to NM_058174.2 F833F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr21:47542841 A>G maps to NM_001849.3 K554K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr21:47545415 C>T maps to NM_001849.3 F618F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr21:47549317 G>A maps to NM_058174.2 Q890Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr21:47545523 C>T maps to NM_001849.3 S654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr21:47552186 C>G maps to NM_001849.3 A927A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr21:47532367 G>A maps to NM_001849.3 K197K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr21:47542441 C>T maps to NM_001849.3 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:47532340 C>T maps to NM_001849.3 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:47545984 C>A maps to NM_001849.3 V752V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:238274598 G>A maps to NM_004369.3 S1860S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr2:238249665 G>A maps to NM_004369.3 T2631T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr2:238285802 C>T maps to NM_004369.3 Q894Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:238290071 G>A maps to NM_004369.3 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr2:238274678 C>T did not map to a codon.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr2:238249692 G>A maps to NM_004369.3 F2622F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:238249692 G>A maps to NM_004369.3 F2622F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:238285526 G>A maps to NM_004369.3 I986I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:238274451 C>T maps to NM_004369.3 E1909E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:238245120 C>T maps to NM_004369.3 T2874T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:238269787 G>A maps to NM_004369.3 G2062G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:238280963 C>T maps to NM_004369.3 R1232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr2:238253406 G>A maps to NM_004369.3 F2418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr2:238270417 C>T maps to NM_004369.3 R2040R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:238249664 G>A maps to NM_004369.3 L2632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:238277428 G>A maps to NM_004369.3 F1559F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:238272036 G>A maps to NM_004369.3 V1974V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:238266501 C>T maps to NM_004369.3 Q2165Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:238280756 C>T maps to NM_004369.3 R1301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:238290008 G>A maps to NM_004369.3 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr2:238280588 C>T maps to NM_004369.3 V1357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:238243404 G>A maps to NM_004369.3 S3031S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:238296321 G>A maps to NM_004369.3 F405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:238277278 G>A maps to NM_004369.3 I1609I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:238244916 C>T maps to NM_004369.3 A2942A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr2:238285736 C>A maps to NM_004369.3 L916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr2:238275438 G>A maps to NM_004369.3 F1797F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr2:238267683 T>A maps to NM_004369.3 G2134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:238245120 C>T maps to NM_004369.3 T2874T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:238285571 G>A maps to NM_004369.3 F971F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:238253034 G>A maps to NM_004369.3 F2542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:238296684 G>A maps to NM_004369.3 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:238296651 G>A maps to NM_004369.3 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:238296528 C>T maps to NM_004369.3 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:238283529 G>A maps to NM_004369.3 A1068A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:238283547 C>T maps to NM_004369.3 Q1062Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr2:238283352 C>T maps to NM_004369.3 R1127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr2:238243355 G>A maps to NM_004369.3 L3048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr2:238280783 C>T maps to NM_004369.3 K1292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:238247692 G>A maps to NM_004369.3 P2844P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr2:238275612 C>T maps to NM_004369.3 L1739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F4-06A-12D-A25O-08 chr2:238245159 G>A maps to NM_004369.3 N2861N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:238249230 C>T maps to NM_004369.3 R2776R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:238270462 G>A maps to NM_004369.3 A2025A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:238277482 G>A maps to NM_004369.3 P1541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:238277715 G>A maps to NM_004369.3 R1464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:238303251 C>T maps to NM_004369.3 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr2:238277428 G>A maps to NM_004369.3 F1559F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:238285985 C>T maps to NM_004369.3 E833E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:130095497 G>A maps to ENST00000312481 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr3:130162393 C>T maps to ENST00000312481 Q2188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:130095497 G>A maps to ENST00000312481 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr3:130187918 G>A maps to ENST00000312481 L2357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:130095497 G>A maps to ENST00000312481 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr3:130162386 G>A maps to ENST00000312481 E2185E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:130162344 G>A maps to ENST00000312481 P2171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:130187703 C>T maps to ENST00000312481 Q2286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:130187861 C>T maps to ENST00000312481 V2338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr3:130095626 C>T maps to ENST00000312481 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr3:130095149 C>T maps to ENST00000312481 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr3:130284111 C>T maps to NM_001102608.1 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr3:130284199 C>T maps to NM_001102608.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:130293211 C>T maps to NM_001102608.1 I1130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:130353468 G>A maps to NM_001102608.1 K1676K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr3:130282242 C>T maps to NM_001102608.1 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:130282257 C>T maps to NM_001102608.1 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr3:130318650 G>A maps to NM_001102608.1 K1550K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:130285981 G>A maps to NM_001102608.1 K573K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:130283889 C>T maps to NM_001102608.1 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr3:130289767 G>A maps to NM_001102608.1 V836V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr3:130284117 G>A maps to NM_001102608.1 K314K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:130285618 C>T maps to NM_001102608.1 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr3:130368261 G>A maps to NM_001102608.1 T1863T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:130345327 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr3:130300723 G>A maps to NM_001102608.1 Q1289Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr3:130285720 G>A maps to NM_001102608.1 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr3:130300459 G>A maps to NM_001102608.1 Q1201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr3:130284163 C>T maps to NM_001102608.1 Q330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:130285585 C>T maps to NM_001102608.1 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr3:130318623 C>T maps to NM_001102608.1 P1541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:130282323 G>A maps to NM_001102608.1 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr3:130368180 C>T maps to NM_001102608.1 S1836S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:130284069 C>T maps to NM_001102608.1 N298N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:130285591 C>T maps to NM_001102608.1 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:130287236 G>A maps to NM_001102608.1 T730T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:130292830 C>T maps to NM_001102608.1 F1003F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:130292923 C>T maps to NM_001102608.1 L1034L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:130308019 G>A maps to NM_001102608.1 G1404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr3:130285909 C>T maps to NM_001102608.1 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:48616710 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr3:48613166 C>T maps to NM_000094.3 R1957R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:48619144 C>T maps to NM_000094.3 G1572G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr3:48605967 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr3:48626195 G>A maps to NM_000094.3 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr3:48622172 C>T maps to NM_000094.3 G1347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr3:48616930 C>T maps to NM_000094.3 R1751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr3:48622169 C>T maps to NM_000094.3 E1348E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:48623786 G>A maps to NM_000094.3 P1176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:48615933 G>A maps to NM_000094.3 L1813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:48607063 G>A maps to NM_000094.3 I2525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr3:48605294 G>A maps to NM_000094.3 G2635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr3:48614162 G>A maps to NM_000094.3 I1882I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr3:48628249 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr3:48631023 G>A maps to NM_000094.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:48605946 C>T maps to NM_000094.3 G2593G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:48619946 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr3:48630556 A>G maps to NM_000094.3 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:48624917 C>T maps to NM_000094.3 W976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:48614334 T>C maps to NM_000094.3 S1862S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr3:48613091 C>T maps to NM_000094.3 G1982G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr3:48613142 C>T maps to NM_000094.3 E1965E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:48609815 C>T maps to NM_000094.3 E2325E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:48613160 G>A maps to NM_000094.3 I1959I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:48626889 G>A maps to NM_000094.3 S728S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:48628969 C>G maps to NM_000094.3 G521G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:48621766 G>A maps to NM_000094.3 P1387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:48623515 G>A maps to NM_000094.3 F1238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:48629343 C>T maps to NM_000094.3 W448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr3:48605069 C>T did not map to a codon.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr3:48624931 C>T maps to NM_000094.3 S971S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:99513869 G>A maps to ENST00000429802 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:99513593 G>A maps to ENST00000429802 Q284Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr3:99514643 G>A maps to ENST00000429802 V634V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr3:99513710 G>A maps to ENST00000429802 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:99509612 C>T maps to ENST00000429802 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:99513659 G>A maps to ENST00000429802 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:99514946 C>T maps to ENST00000429802 S735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:99513110 C>T maps to ENST00000429802 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:99513677 G>A maps to ENST00000429802 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:36564375 C>T maps to NM_005202.2 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:36564630 C>T maps to NM_005202.2 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:70944502 G>C maps to NM_001851.4 G751G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr6:71004229 G>A maps to NM_001851.4 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr6:71009876 C>T maps to NM_001851.4 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:70935695 C>T maps to NM_001851.4 K840K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:70961997 C>T maps to NM_001851.4 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:71010048 G>A maps to NM_001851.4 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:71011743 G>A maps to NM_001851.4 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:71004055 C>T maps to NM_001851.4 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:70991122 G>A maps to NM_001851.4 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:70944263 C>T maps to NM_001851.4 Q764Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:40775781 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr1:40777384 C>T maps to NM_001852.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:40767561 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:40767048 G>T maps to NM_001852.3 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:40773887 C>T maps to NM_001852.3 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:40771392 C>T maps to NM_001852.3 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr20:61471990 G>A maps to NM_001853.3 G654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:61468540 C>T maps to NM_001853.3 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:61452567 G>A maps to NM_001853.3 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr20:61453959 C>T maps to NM_001853.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:61468559 C>T maps to NM_001853.3 R577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:120118180 C>T maps to NM_006438.3 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:120118156 G>A maps to NM_006438.3 K187K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr8:120114596 G>A maps to NM_006438.3 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr8:120118180 C>T maps to NM_006438.3 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:120118297 G>A maps to NM_006438.3 W234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr18:346918 G>A maps to NM_130386.2 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:333030 A>T maps to NM_130386.2 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr18:346954 G>A maps to NM_130386.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr18:346918 G>A maps to NM_130386.2 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:347135 G>A maps to NM_130386.2 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:346891 G>A maps to NM_130386.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:480749 G>A maps to NM_130386.2 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:15493156 G>A maps to NM_005677.3 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr3:15498040 G>A maps to NM_005677.3 Q334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr3:15498004 G>A maps to NM_005677.3 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr3:15495346 G>A maps to NM_005677.3 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr3:15495391 C>T maps to NM_005677.3 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr2:62228056 C>T maps to NM_152516.2 H134H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:62132962 C>T maps to NM_152516.2 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:115469812 C>T maps to NM_016144.2 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr10:22608918 C>T maps to NM_012071.2 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr10:22607904 C>T maps to NM_012071.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr15:75632212 C>T maps to NM_017828.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr15:75632324 C>T maps to NM_017828.3 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr13:76101960 G>A maps to NM_203497.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:36302278 G>A maps to NM_014186.3 Q54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr19:18895134 C>T maps to NM_000095.2 R651R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:18895711 T>C maps to NM_000095.2 Q636Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:18895056 C>T maps to NM_000095.2 K677K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:18897383 C>T maps to NM_000095.2 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:18900091 G>C maps to NM_000095.2 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr22:19950225 C>T maps to NM_001135162.1 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr22:19951784 G>A maps to NM_001135162.1 W193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q1-06A-21D-A196-08 chr1:160281718 G>T maps to NM_001098398.1 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:160275484 G>C maps to NM_001098398.1 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:160276186 G>A maps to NM_001098398.1 R467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:160280026 G>A maps to NM_001098398.1 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr1:160262335 G>A maps to NM_001098398.1 G975G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr1:160260464 G>A maps to NM_001098398.1 I1153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:160282957 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:160260463 G>A maps to NM_001098398.1 L1154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:160261984 C>T maps to NM_001098398.1 K997K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:160265559 G>A maps to NM_001098398.1 S823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:160261861 G>A maps to NM_001098398.1 F1038F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:160261900 G>A maps to NM_001098398.1 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr3:128987353 C>T maps to NM_016128.3 I555I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr3:128990614 T>C maps to NM_016128.3 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:128979212 C>T maps to NM_016128.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr3:128971792 C>T maps to NM_016128.3 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr3:128976653 C>T maps to NM_016128.3 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:128987835 C>T maps to NM_016128.3 I612I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr7:130295861 G>A maps to NM_012133.4 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr15:49426225 A>C maps to NM_001143887.1 Y272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:49436469 C>T maps to NM_001143887.1 W67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr15:49423005 G>A maps to NM_001143887.1 Q326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:49420923 A>G maps to NM_001143887.1 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:49437167 G>A maps to NM_001143887.1 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:17165340 A>T maps to NM_003653.3 L234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr17:17179479 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:83970439 C>T maps to ENST00000503682 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:67969656 G>A maps to NM_006837.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:67968839 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:67958054 T>C maps to NM_006837.2 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:99687269 C>A maps to NM_006833.4 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr12:6840168 C>T maps to NM_001164093.1 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:6839854 C>T maps to NM_001164093.1 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:232660829 C>T maps to NM_022730.1 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:232656504 C>T maps to NM_022730.1 Y75Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr2:232672282 C>T maps to NM_022730.1 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:232660850 G>A maps to NM_022730.1 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:232660845 C>T maps to NM_022730.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:232672237 C>T maps to NM_022730.1 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:54743417 C>T maps to NM_016057.1 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr12:54741789 C>T maps to NM_016057.1 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr17:46110609 G>A maps to NM_016429.2 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:46110609 G>A maps to NM_016429.2 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:46110609 G>A maps to NM_016429.2 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:46109535 C>T maps to NM_016429.2 E158E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr12:56662921 C>T maps to NM_144576.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr4:84185423 G>A maps to NM_015697.7 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr4:84194713 G>A maps to NM_015697.7 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr9:131094457 C>T maps to NM_016035.3 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr9:131088141 C>T maps to NM_016035.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr12:120942759 C>A maps to NM_032314.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr14:74428157 G>A maps to NM_182476.1 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr14:74422196 C>T maps to NM_182476.1 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:19083403 G>A maps to NM_016138.4 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr4:47597788 G>A maps to NM_006587.2 F1026F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr4:47605540 G>A maps to NM_006587.2 I895I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr4:47644046 C>T maps to NM_006587.2 V696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:47597917 A>G maps to NM_006587.2 G983G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:47695044 C>T maps to NM_006587.2 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:47663827 C>T maps to NM_006587.2 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:47625724 C>T maps to NM_006587.2 R801R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:47647107 C>T maps to NM_006587.2 E649E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr4:47605663 C>T maps to NM_006587.2 W854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr4:47746512 C>T maps to NM_006587.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:47605683 T>G maps to NM_006587.2 R848R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:47663776 C>T maps to NM_006587.2 E562E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:47746590 G>A maps to NM_006587.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:47765424 G>A maps to NM_006587.2 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:47809028 G>A maps to NM_006587.2 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr4:47808953 G>A maps to NM_006587.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr4:47605498 C>T maps to NM_006587.2 R909R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr16:30199303 C>T maps to NM_007074.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr16:30196586 C>A maps to NM_007074.3 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:30198141 G>A maps to NM_007074.3 W109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr16:30199815 G>A maps to NM_007074.3 K400K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:30199824 G>A maps to NM_007074.3 E403E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:30199683 G>A maps to NM_007074.3 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:67210078 G>A maps to NM_020441.2 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:67207677 G>A maps to NM_020441.2 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr12:109046187 G>A maps to ENST00000420959 D340D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr12:109041220 A>G maps to ENST00000420959 R514R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr12:109046151 G>A maps to ENST00000420959 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:109051151 G>A maps to ENST00000420959 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr12:109042614 G>A maps to ENST00000420959 F410F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr9:100897141 C>T maps to NM_052820.3 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:100890912 G>A maps to NM_052820.3 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr9:100897225 C>T maps to NM_052820.3 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr9:100890918 G>A maps to NM_052820.3 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:100890473 C>T maps to NM_052820.3 E383E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr9:100892097 G>A maps to NM_052820.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:100899902 C>T maps to NM_052820.3 W90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr15:68987558 C>T maps to NM_006091.3 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr15:68987585 G>A maps to NM_006091.3 E108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr15:69007646 C>T maps to NM_006091.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr15:69011842 C>T maps to NM_006091.3 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr15:69006962 C>T maps to NM_006091.3 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:27943745 C>T maps to ENST00000345068 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:4411247 A>G maps to NM_024535.3 A563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:4409335 G>A maps to NM_024535.3 F767F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr16:4463324 G>A maps to NM_024535.3 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr16:4412724 G>A maps to NM_024535.3 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr16:4409353 G>A maps to NM_024535.3 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr16:84600516 C>T maps to NM_021149.2 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:84623782 G>A maps to NM_021149.2 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:14110256 C>T maps to NM_001303.3 C353C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr17:13980197 T>A maps to NM_001303.3 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A264-06A-11D-A196-08 chr17:53045938 C>A maps to NM_004375.3 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr10:101486874 G>A maps to NM_078470.4 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr4:73923971 G>A maps to NM_173827.2 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:85840353 C>T maps to NM_001861.2 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr20:30226840 G>A maps to NM_032609.2 W7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr16:85814034 G>A maps to NM_006067.4 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:85813388 G>A maps to NM_006067.4 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr2:98264519 C>T maps to NM_001862.2 C113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:55865856 C>T maps to NM_144613.4 K11K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q9-06A-11D-A19A-08 chr6:75950900 T>C maps to NM_001865.3 K65K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:75950053 G>A maps to NM_001865.3 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr6:75953459 T>C maps to NM_001865.3 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr2:42578481 G>A maps to NM_004718.2 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:77155056 C>T did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr4:46737014 C>T maps to NM_130902.2 W65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr3:148939459 C>T maps to NM_000096.3 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:148925384 A>G maps to NM_000096.3 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:148925148 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr3:148904370 C>T maps to NM_000096.3 R671R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:148924064 G>A maps to NM_000096.3 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:148927952 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:148930247 C>T maps to NM_000096.3 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:19547458 T>A maps to NM_014711.4 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:19539301 C>T maps to NM_014711.4 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:19548406 A>G maps to NM_014711.4 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:19554063 C>T maps to NM_014711.4 A783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr16:19547896 C>T maps to NM_014711.4 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:19548853 C>T maps to NM_014711.4 Y621Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr7:130027770 C>T maps to NM_001868.2 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr7:130027800 G>C maps to NM_001868.2 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:130023568 C>T maps to NM_001868.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:130023287 C>T maps to NM_001868.2 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr7:130027836 G>A maps to NM_001868.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:130021676 C>T maps to NM_001868.2 N118N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:130021484 G>A maps to NM_001868.2 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:129909540 G>A maps to NM_001869.2 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:129909540 G>A maps to NM_001869.2 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:129909543 G>A maps to NM_001869.2 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr7:129916532 C>T maps to NM_001869.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:129922005 G>A maps to NM_001869.2 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr3:148614367 C>T maps to NM_001870.2 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr3:148596480 C>T maps to NM_001870.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:148601523 C>T maps to NM_001870.2 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr3:148614334 G>A maps to NM_001870.2 W365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:148583259 G>A maps to NM_001870.2 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:129962491 G>A maps to NM_016352.3 E414E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr7:129951960 C>T maps to NM_016352.3 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr7:129951876 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:129986367 C>T maps to NM_080385.4 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:130007339 C>T maps to NM_080385.4 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:129986406 C>T maps to NM_080385.4 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr7:130002795 C>T maps to NM_080385.4 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:130002768 G>A maps to NM_080385.4 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:129986367 C>T maps to NM_080385.4 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:130008365 C>T maps to NM_080385.4 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr8:68419058 C>T maps to NM_020361.4 W200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr8:68423886 G>A maps to NM_020361.4 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:68419058 C>T maps to NM_020361.4 W200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr8:68423853 C>T maps to NM_020361.4 K118K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr8:68334777 C>T maps to NM_020361.4 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr8:68396081 C>T maps to NM_020361.4 W253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:68423835 G>A maps to NM_020361.4 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:68346386 G>A maps to NM_020361.4 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr8:68536416 T>C maps to NM_020361.4 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr8:68396958 G>A maps to NM_020361.4 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:68396089 G>A maps to NM_020361.4 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:68396093 C>T did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr8:68346382 G>A maps to NM_020361.4 R311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr8:68658322 G>A maps to NM_020361.4 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr19:17122507 C>T maps to ENST00000443236 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr19:17025598 G>A maps to ENST00000443236 S1275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr19:17007075 C>T maps to ENST00000443236 P1836P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:17056388 C>T maps to ENST00000443236 V978V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr19:17017783 G>A maps to ENST00000443236 L1392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr19:17013546 G>T maps to ENST00000443236 R1590R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr19:17085951 G>A maps to ENST00000443236 F732F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:17100581 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:17088252 G>C maps to ENST00000443236 V618V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:17091441 G>A maps to ENST00000443236 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:17017846 G>A maps to ENST00000443236 A1371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr19:17038951 G>T maps to ENST00000443236 T1136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr19:17088186 G>A maps to ENST00000443236 F640F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:17081753 G>A maps to ENST00000443236 F777F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:17115152 C>T maps to ENST00000443236 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:17068706 C>T maps to ENST00000443236 R801R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:17013604 C>T maps to ENST00000443236 Q1570Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr19:17088186 G>A maps to ENST00000443236 F640F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:17038873 C>T maps to ENST00000443236 L1162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:17100464 G>A maps to ENST00000443236 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr19:17088324 C>T maps to ENST00000443236 E594E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:17120124 T>C maps to ENST00000443236 E221E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:17108001 G>A maps to ENST00000443236 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr19:17132981 C>T maps to ENST00000443236 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:17007099 C>T maps to ENST00000443236 G1828G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:17010354 G>A maps to ENST00000443236 L1650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:17012085 G>A maps to ENST00000443236 S1626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:17013508 C>T maps to ENST00000443236 A1602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:17017873 G>A maps to ENST00000443236 P1362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:17038903 C>T maps to ENST00000443236 V1152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:17088209 G>A maps to ENST00000443236 Q633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:17104306 G>A maps to ENST00000443236 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:17107959 C>T maps to ENST00000443236 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:17122441 G>A maps to ENST00000443236 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:17108133 C>T maps to ENST00000443236 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:17038954 G>A maps to ENST00000443236 S1135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:17120112 C>T maps to ENST00000443236 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr3:148577629 G>A maps to NM_001871.2 W365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:148559659 C>T maps to NM_001871.2 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:148559644 C>T maps to NM_001871.2 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr3:148563298 C>T maps to NM_001871.2 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr17:28789001 T>G maps to NM_001304.4 G1246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr17:28750030 C>T maps to NM_001304.4 V549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr17:28770827 G>A maps to NM_001304.4 Q794Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:28750596 C>T maps to NM_001304.4 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:28712021 A>G maps to NM_001304.4 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr17:28791721 G>T maps to NM_001304.4 E1345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:28788250 C>T maps to NM_001304.4 C1184C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr4:166388934 G>A maps to NM_001873.2 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:166388869 C>T maps to NM_001873.2 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr4:166385566 G>A maps to NM_001873.2 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:166405616 C>T maps to NM_001873.2 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr4:166416767 C>G maps to NM_001873.2 S424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:166388880 C>T maps to NM_001873.2 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr15:83222286 G>A maps to ENST00000261723 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:83218213 G>A maps to ENST00000261723 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:83224839 G>A maps to ENST00000261723 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr15:83224662 G>A maps to ENST00000261723 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr15:83221279 G>A maps to ENST00000261723 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr15:83226580 G>A maps to ENST00000261723 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr4:15005679 C>T maps to NM_001177382.1 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:15063815 C>T maps to NM_001177382.1 Q937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr10:93851680 G>A maps to NM_014912.4 N531N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:93902867 G>A maps to NM_014912.4 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr5:173317641 C>G maps to NM_030627.2 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:175306945 C>T maps to NM_001008220.1 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr15:75122641 C>T maps to NM_001030005.2 Q142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:75122493 C>T maps to NM_001030005.2 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:75122544 C>T maps to NM_001030005.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr18:56985685 G>A maps to NM_181654.3 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr12:69265723 C>A maps to NM_001874.4 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:69265631 G>A maps to NM_001874.4 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:69265694 G>A maps to NM_001874.4 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:69264139 G>A maps to NM_001874.4 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:69264142 G>A maps to NM_001874.4 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:69265640 C>T maps to NM_001874.4 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr10:101835838 C>T maps to NM_001308.2 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:101829479 C>T maps to NM_001308.2 W189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:101835745 G>A maps to NM_001308.2 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:194062183 C>T maps to NM_001080513.2 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:194062012 C>T maps to NM_001080513.2 Q473Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr3:194062894 G>A maps to NM_001080513.2 N179N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:194062954 G>A maps to NM_001080513.2 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr3:194063008 G>A maps to NM_001080513.2 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:194062170 G>A maps to NM_001080513.2 Q421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr3:194062945 C>T maps to NM_001080513.2 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:194063278 C>T maps to NM_001080513.2 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:194063425 G>A maps to NM_001080513.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:194063008 G>A maps to NM_001080513.2 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:194063278 C>T maps to NM_001080513.2 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr3:194063398 G>A maps to NM_001080513.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr3:194062353 G>A maps to NM_001080513.2 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:194062984 G>A maps to NM_001080513.2 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:194062945 C>T maps to NM_001080513.2 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr20:34220241 C>G maps to NM_003915.5 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr20:34219678 G>A maps to NM_003915.5 N191N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr20:34219455 G>A maps to NM_003915.5 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr20:34218406 C>T maps to NM_003915.5 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr16:57171133 C>T maps to NM_152727.5 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:87568536 C>T maps to NM_003909.3 Q488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:87570628 G>A maps to NM_003909.3 Q535Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19T-06A-11D-A19A-08 chr8:87563303 C>T maps to NM_003909.3 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:87557008 C>T maps to NM_003909.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr3:131418767 C>T maps to ENST00000502818 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr3:131261424 G>A maps to ENST00000502818 F523F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr3:131624236 G>A maps to ENST00000502818 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:131442364 G>A maps to ENST00000502818 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr3:131261628 G>A maps to ENST00000502818 F455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:131624107 C>T maps to ENST00000502818 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:131274339 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr3:131306333 C>T maps to ENST00000502818 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr3:131261451 C>T maps to ENST00000502818 E514E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:131271332 G>A maps to ENST00000502818 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr6:36724063 C>T maps to NM_020939.1 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr6:36724044 T>A maps to NM_020939.1 K296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:36742781 A>C maps to NM_020939.1 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr6:36762371 G>A maps to NM_020939.1 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:36759833 G>A maps to NM_020939.1 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr6:36710089 G>A maps to NM_020939.1 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr6:36759866 G>A maps to NM_020939.1 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:36716034 G>A maps to NM_020939.1 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:36767802 G>A maps to NM_020939.1 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr6:36767802 G>A maps to NM_020939.1 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr6:36714265 G>A maps to NM_020939.1 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr6:36746698 C>T maps to NM_020939.1 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr6:36730753 C>T maps to NM_020939.1 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:36716040 G>A maps to NM_020939.1 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:36766012 G>A maps to NM_020939.1 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr14:24542790 G>A maps to NM_006032.2 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:24546583 C>T maps to NM_006032.2 F507F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:24543813 G>A maps to NM_006032.2 W191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:24546361 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr16:89662950 G>A maps to NM_014427.4 E608E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr16:89661986 C>T maps to NM_014427.4 F580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:89662896 C>T maps to NM_014427.4 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr16:89657538 C>T maps to NM_014427.4 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:89650479 C>T maps to NM_014427.4 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:89653509 C>T maps to NM_014427.4 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:39223218 G>A maps to NM_153634.2 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:39064596 G>A maps to NM_153634.2 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr3:9757671 C>T maps to ENST00000383832 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr3:9771351 G>A maps to ENST00000383832 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr3:9757668 C>A maps to ENST00000383832 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:9754727 C>T maps to ENST00000383832 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr3:9754248 G>A maps to ENST00000383832 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:9756993 C>T maps to ENST00000383832 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr2:207814427 C>T maps to NM_173077.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:98300345 T>C maps to NM_000097.5 E394E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:98312018 G>A maps to NM_000097.5 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr16:12798720 G>A maps to NM_018340.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:12758943 G>A maps to NM_018340.2 Y248Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:12758852 G>A maps to NM_018340.2 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:12798700 G>A maps to NM_018340.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:12798715 G>A maps to NM_018340.2 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:211455618 C>A maps to NM_001122633.1 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:211541729 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:211523351 G>A maps to NM_001122633.1 K1238K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:211457631 C>T maps to NM_001122633.1 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:211459281 C>T maps to NM_001122633.1 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr2:211473189 G>A maps to NM_001122633.1 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:211540555 C>T maps to NM_001122633.1 S1428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:211438074 C>T maps to NM_001122633.1 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:211473171 C>T maps to NM_001122633.1 A766A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:145619978 G>A maps to NM_013291.2 P1149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr8:145619713 C>T maps to NM_013291.2 T1208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:1247736 C>T maps to NM_017871.4 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:1256441 G>A maps to NM_017871.4 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:69651632 G>T maps to ENST00000266679 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr12:69656227 C>T maps to ENST00000266679 D552D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:69652865 C>T maps to ENST00000266679 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:61188021 G>A maps to NM_024811.3 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:61183596 G>A maps to NM_024811.3 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr11:68548116 G>A maps to NM_001876.3 H483H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:68529011 G>A maps to NM_001876.3 F673F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:68525120 G>A maps to NM_001876.3 S771S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:68552353 C>T maps to NM_001876.3 Q364Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:68548125 G>A maps to NM_001876.3 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:68527090 C>G maps to NM_001876.3 V727V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:68552314 C>T maps to NM_001876.3 E377E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:68552398 A>G maps to NM_001876.3 H349H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr22:51011431 G>A maps to NM_152245.2 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr22:51012927 G>A maps to NM_152245.2 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr22:51007789 G>A maps to NM_152245.2 Q766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr22:51007790 G>A maps to NM_152245.2 F765F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr19:50200689 G>A maps to NM_152359.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr19:50200632 C>T maps to NM_152359.2 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:50209262 C>T maps to NM_152359.2 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr19:50212080 G>A maps to NM_152359.2 W517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:50212044 G>A maps to NM_152359.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:50216831 C>T maps to NM_152359.2 S794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:50214098 G>A maps to NM_152359.2 E617E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr19:50209289 G>A maps to NM_152359.2 Q363Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:50203939 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:50208316 C>T maps to NM_152359.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:50208332 C>T maps to NM_152359.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:50209535 G>A maps to NM_152359.2 E403E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:50213656 C>T maps to NM_152359.2 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:50208262 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:50209532 G>A maps to NM_152359.2 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:53679098 C>T maps to NM_000098.2 A603A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:53679048 C>T maps to NM_000098.2 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr7:29105638 C>T maps to NM_031311.3 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr7:29135785 C>A maps to NM_031311.3 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:88008523 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:88009101 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:88008985 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:88008631 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr23:88008943 T>C did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:88008616 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr23:88009214 T>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:88008758 G>A did not map to a codon.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr23:88009058 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr20:2775246 G>A maps to NM_019609.4 D633D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr20:2779093 G>A maps to NM_019609.4 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr20:2776302 C>T maps to NM_019609.4 Q554Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:2776458 G>A maps to NM_019609.4 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr20:2774946 G>A maps to NM_019609.4 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:2774946 G>A maps to NM_019609.4 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr20:2775009 G>A maps to NM_019609.4 G677G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr10:125516743 G>A maps to NM_198148.2 I634I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr10:125528185 G>A maps to NM_198148.2 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:125528155 G>A maps to NM_198148.2 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:125557534 C>T maps to NM_198148.2 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr10:125516743 G>A maps to NM_198148.2 I634I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:125650902 C>T maps to NM_198148.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:125530444 C>T maps to NM_198148.2 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:125528155 G>A maps to NM_198148.2 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:125516743 G>A maps to NM_198148.2 I634I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr10:125530480 C>T maps to NM_198148.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr4:8602949 G>A maps to NM_001014447.2 E74E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:8616137 G>A maps to NM_001014447.2 E472E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr4:8620163 G>A maps to NM_001014447.2 R504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr4:8609121 G>A maps to NM_001014447.2 E399E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:8602877 C>T maps to NM_001014447.2 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr4:8603045 C>T maps to NM_001014447.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:8616155 C>T maps to NM_001014447.2 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr4:8602913 C>A maps to NM_001014447.2 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr4:8621151 G>A maps to NM_001014447.2 K589K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr4:8621280 C>T maps to NM_001014447.2 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr4:8621298 C>T maps to NM_001014447.2 F638F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:8602907 C>T maps to NM_001014447.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:8621298 C>T maps to NM_001014447.2 F638F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr4:8608531 C>T maps to NM_001014447.2 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:207680089 G>A maps to NM_000651.4 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr1:207803915 A>C maps to NM_000651.4 G2469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:207751264 G>A maps to NM_000651.4 G1551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr1:207700143 G>A maps to NM_000651.4 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr1:207790105 G>A maps to NM_000651.4 W2283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:207796353 G>A maps to NM_000651.4 T2431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:207680089 G>A maps to NM_000651.4 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:207793384 C>T maps to NM_000651.4 D2409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:207789918 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr1:207787807 G>A maps to NM_000651.4 W2212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr1:207787808 G>A maps to NM_000651.4 W2212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:207753666 C>T maps to NM_000651.4 F1673F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:207796380 C>T maps to NM_000651.4 F2440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr1:207785062 C>T maps to NM_000651.4 L2113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:207787769 T>C maps to NM_000651.4 S2199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:207751180 C>T maps to NM_000651.4 A1523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:207751210 G>A maps to NM_000651.4 E1533E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:207751309 C>T maps to NM_000651.4 T1566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:207760773 G>A maps to NM_000651.4 T1858T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr1:207741238 C>T maps to NM_000651.4 P1341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:207785043 C>T maps to NM_000651.4 I2106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:207782821 G>A maps to NM_000651.4 W2028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:207890917 A>T maps to NM_175710.1 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:207867872 A>G maps to NM_175710.1 Q213Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:207851591 G>A maps to NM_175710.1 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:207867857 C>T maps to NM_175710.1 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:207850749 G>A maps to NM_175710.1 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:207851609 C>T maps to NM_175710.1 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:207881564 G>A maps to NM_175710.1 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:207641875 C>T maps to NM_001006658.2 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr1:207644139 C>T maps to NM_001006658.2 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr1:207647634 G>T maps to NM_001006658.2 G764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:207641905 C>T maps to NM_001006658.2 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:207627816 C>T maps to NM_001006658.2 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:207640066 C>T maps to NM_001006658.2 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr1:207643211 G>A maps to NM_001006658.2 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr1:207640228 G>A maps to NM_001006658.2 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:207643226 G>A maps to NM_001006658.2 W335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:207653368 C>T maps to NM_001006658.2 T1053T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr1:207646441 T>C maps to NM_001006658.2 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr1:207651287 G>A maps to NM_001006658.2 R987R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:207644766 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:207643160 G>A maps to NM_001006658.2 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr1:207641905 C>T maps to NM_001006658.2 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:207644817 G>A maps to NM_001006658.2 W515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr1:207640118 A>C maps to NM_001006658.2 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:207646947 C>T maps to NM_001006658.2 F679F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:207639871 G>A maps to NM_001006658.2 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:207640180 C>T maps to NM_001006658.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:207643160 G>A maps to NM_001006658.2 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:207644766 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:207649737 G>A maps to NM_001006658.2 W959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr15:78633400 G>A maps to NM_004378.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr12:94243946 G>A maps to NM_003805.3 W167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr12:94243947 G>A maps to NM_003805.3 W167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr16:1716086 C>T maps to NM_020825.3 F922F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr16:1719011 C>T maps to NM_020825.3 V1115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:1716429 C>T maps to NM_020825.3 I955I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:131860835 G>A maps to NM_000755.3 I393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:131870245 G>A maps to NM_000755.3 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:131857786 C>T maps to NM_000755.3 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:131858389 G>A maps to NM_000755.3 R518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr9:131860613 G>A maps to NM_000755.3 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr9:131864771 G>A maps to NM_000755.3 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr1:197396719 G>A maps to NM_201253.2 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:197404340 C>T maps to NM_201253.2 F1116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:197396683 C>T maps to NM_201253.2 V743V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:197446813 C>T maps to NM_201253.2 S1342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:197396623 T>G maps to NM_201253.2 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:197390637 C>T maps to NM_201253.2 H560H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:197396629 C>T maps to NM_201253.2 V725V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr1:197396932 G>A maps to NM_201253.2 K826K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:197390496 G>A maps to NM_201253.2 R513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:197398613 C>T maps to NM_201253.2 S904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:197390664 C>T maps to NM_201253.2 F569F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:197390610 G>A maps to NM_201253.2 Q551Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:197396998 C>T maps to NM_201253.2 F848F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr1:197396582 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:197390664 C>T maps to NM_201253.2 F569F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr1:197411331 G>T maps to NM_201253.2 P1305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:197407715 G>A maps to NM_201253.2 K1263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:197390733 C>T maps to NM_201253.2 I592I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:197390664 C>T maps to NM_201253.2 F569F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr1:197390976 G>A maps to NM_201253.2 K673K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:197298035 G>A maps to NM_201253.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr1:197390436 C>T maps to NM_201253.2 F493F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr1:197407691 C>T maps to NM_201253.2 P1255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:197390596 C>T maps to NM_201253.2 Q547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:197390706 C>T maps to NM_201253.2 I583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:197446913 C>T maps to NM_201253.2 Q1376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:197313471 T>G maps to NM_201253.2 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:197390623 C>T maps to NM_201253.2 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:197390880 C>T maps to NM_201253.2 G641G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:197396919 G>A maps to NM_201253.2 W822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:197390616 G>A maps to NM_201253.2 K553K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr1:197398658 G>A maps to NM_201253.2 G919G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr1:197396827 A>T maps to NM_201253.2 G791G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr1:197313432 T>C maps to NM_201253.2 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr1:197390532 C>T maps to NM_201253.2 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:197411415 G>A maps to NM_201253.2 E1333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:197446822 C>T maps to NM_201253.2 F1345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:197446858 G>A maps to NM_201253.2 L1357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:197390391 C>T maps to NM_201253.2 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:197404269 C>T maps to NM_201253.2 L1093L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr1:197398613 C>T maps to NM_201253.2 S904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:197326021 C>T maps to NM_201253.2 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:197390628 C>T maps to NM_201253.2 F557F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:197404043 C>T maps to NM_201253.2 S1017S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:126134535 G>A maps to NM_173689.5 G839G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:126128260 C>T maps to NM_173689.5 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:126132957 C>T maps to NM_173689.5 A542A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:126133696 G>A maps to NM_173689.5 W759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:126133131 C>T maps to NM_173689.5 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:126133132 C>T maps to NM_173689.5 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:126139193 C>T maps to NM_173689.5 L1237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:126132825 G>A maps to NM_173689.5 W498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:126133595 C>T maps to NM_173689.5 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr9:126128625 C>T maps to NM_173689.5 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr9:126133212 C>T maps to NM_173689.5 F627F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:126132588 C>T maps to NM_173689.5 V419V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:6465616 C>T maps to NM_174881.2 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:152487945 C>T maps to NM_019060.2 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:208440041 C>A maps to NM_134442.3 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr2:208440041 C>T maps to NM_134442.3 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr9:35733136 C>T maps to NM_006368.4 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:35735336 C>T maps to NM_006368.4 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:46334009 G>A maps to ENST00000288400 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:46334006 G>A maps to ENST00000288400 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:137590525 A>T maps to NM_194071.2 Y279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19T-06A-11D-A19A-08 chr7:137612995 C>T maps to NM_194071.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:4171731 C>T maps to NM_032607.1 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:4171732 C>T maps to NM_032607.1 R385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:4154993 G>A maps to NM_032607.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:4159754 C>T maps to NM_032607.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr19:4159754 C>T maps to NM_032607.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr19:4171722 C>T maps to NM_032607.1 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr19:4171689 C>T maps to NM_032607.1 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:4168352 G>A maps to NM_032607.1 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr7:28857704 G>A maps to NM_182898.2 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr7:28609990 G>A maps to NM_182898.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr7:28758480 C>T maps to NM_182898.2 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:28534528 C>T maps to NM_182898.2 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:28763870 C>T maps to NM_182898.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:28858880 G>A maps to NM_182898.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:28547261 G>A maps to NM_182898.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:28547321 C>T maps to NM_182898.2 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr7:28610107 G>A maps to NM_182898.2 Q139Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr7:28848901 C>T maps to NM_182898.2 D375D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:28857792 C>T maps to NM_182898.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr16:3828060 C>T maps to NM_004380.2 P688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr16:3777766 G>A maps to NM_004380.2 V2427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:3794897 T>A maps to NM_004380.2 K1327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:3778042 G>A maps to NM_004380.2 I2335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr16:3860726 T>A maps to NM_004380.2 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr16:3900837 T>A maps to NM_004380.2 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr16:3828033 C>T maps to NM_004380.2 Q697Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:3900297 C>T maps to NM_004380.2 K266K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:3777961 G>A maps to NM_004380.2 S2362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr16:3827649 G>A maps to NM_004380.2 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:3790454 G>A maps to NM_004380.2 R1360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:3795351 G>A maps to NM_004380.2 F1280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr16:3777724 G>A maps to NM_004380.2 G2441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:12788820 C>T maps to NM_001310.2 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:12788821 C>T maps to NM_001310.2 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr11:85375615 G>A maps to NM_001039618.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr11:85375615 G>A maps to NM_001039618.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:85375598 C>T maps to NM_001039618.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:167515372 G>A maps to NM_003851.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:167515372 G>A maps to NM_003851.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:9984767 C>T maps to NM_001077415.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr3:9979723 C>T maps to NM_001077415.2 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:9984503 T>C maps to NM_001077415.2 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:9985700 C>T maps to NM_001031717.3 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:9982705 T>C maps to NM_001077415.2 C211C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr22:50313428 C>T maps to NM_001135101.1 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr22:50315945 C>T maps to NM_001135101.1 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr22:50313863 C>T maps to NM_001135101.1 C128C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr10:35495853 C>T maps to ENST00000429130 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr10:35437403 C>T maps to ENST00000429130 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:67089148 C>T maps to NM_000756.2 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr5:76251506 G>A maps to NM_001882.3 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:76249003 C>T maps to NM_001882.3 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:43906642 C>T maps to NM_001145146.1 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr17:43911172 G>A maps to NM_001145146.1 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr17:43908261 C>T maps to NM_001145146.1 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr17:43893931 C>T maps to NM_001145146.1 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr17:43912007 A>T maps to NM_001145146.1 K405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:43911181 C>T maps to NM_001145146.1 F373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr17:43910563 C>T maps to NM_001145146.1 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr17:43911142 C>T maps to NM_001145146.1 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr17:43907877 C>T maps to NM_001145146.1 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr17:43898778 C>T maps to NM_001145146.1 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:43907534 C>T maps to NM_001145146.1 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr17:43911151 C>T maps to NM_001145146.1 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr7:30693177 C>T maps to ENST00000348438 Q405Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:30693198 C>T maps to ENST00000348438 R398R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr7:30695559 G>A maps to ENST00000348438 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:30702319 G>A maps to ENST00000348438 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr7:30721618 G>A maps to ENST00000348438 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:36740727 C>T maps to NM_016441.2 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:36740747 C>T maps to NM_016441.2 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:36623930 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr6:43276121 C>T maps to ENST00000449267 K23K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:1388823 A>G maps to NM_175918.3 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr4:1389529 C>T maps to NM_175918.3 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr4:1388637 A>G maps to NM_175918.3 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:1389324 C>T maps to NM_175918.3 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr6:49803097 C>T maps to NM_001131.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:49808678 G>A maps to NM_001131.2 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr6:49806192 G>A maps to NM_001131.2 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr6:49819839 C>T maps to NM_001131.2 K23K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:49668449 C>T maps to ENST00000211238 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:49660563 C>T maps to ENST00000211238 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:49676845 T>A maps to ENST00000211238 K22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:49667580 C>T maps to ENST00000211238 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:49668449 C>T maps to ENST00000211238 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr6:49696523 C>T maps to NM_001190986.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr6:49701442 G>T maps to NM_001190986.1 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:49701544 C>T maps to NM_001190986.1 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:49704163 C>T maps to NM_001190986.1 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:49703225 G>A maps to NM_001190986.1 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr6:49703298 C>T maps to NM_001190986.1 W88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr6:49700981 G>A maps to NM_001190986.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr16:84902463 C>T maps to NM_031476.3 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr16:84906695 G>A maps to NM_031476.3 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:84906635 C>T maps to NM_031476.3 I340I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr16:84922915 G>T maps to NM_031476.3 V462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:84900626 C>T maps to NM_031476.3 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:84888358 C>T maps to NM_031476.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:84911068 C>T maps to NM_031476.3 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr17:1340234 G>C maps to NM_016823.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr19:18707558 G>A maps to NM_004750.4 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:18709598 G>A maps to NM_004750.4 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:18707710 C>T maps to NM_004750.4 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:18707839 G>A maps to NM_004750.4 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:18710615 G>A maps to NM_004750.4 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr19:18709613 G>A maps to NM_004750.4 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:1317421 G>A did not map to a codon.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr23:1321286 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:1317571 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:1327757 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:1314896 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:1321286 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:1317434 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:1325439 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:1317530 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:1321371 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:1321316 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:1325380 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:1325381 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:1331457 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:5857876 C>T maps to NM_001014809.1 Q271Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr4:5853182 G>A maps to NM_001014809.1 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:5868471 G>A maps to NM_001014809.1 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:5851178 G>A maps to NM_001014809.1 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:5843134 G>A maps to NM_001014809.1 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:5837731 C>T maps to NM_001014809.1 R511R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr4:5841405 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr4:5837687 C>T maps to NM_001014809.1 W526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr4:5843033 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:5868477 G>A maps to NM_001014809.1 D129D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr4:5868432 G>A maps to NM_001014809.1 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr20:20033085 G>A maps to NM_016652.4 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr20:20026059 A>G maps to NM_016652.4 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:20033085 G>A maps to NM_016652.4 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:20033114 G>A maps to NM_016652.4 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:20033115 G>A maps to NM_016652.4 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr20:20033133 C>T maps to NM_016652.4 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr1:152383100 G>A maps to NM_016190.2 Q153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:152383386 G>A maps to NM_016190.2 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:152382336 C>T maps to NM_016190.2 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr1:152382651 C>T maps to NM_016190.2 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:152382912 C>T maps to NM_016190.2 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:152382810 C>T maps to NM_016190.2 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:152382906 C>T maps to NM_016190.2 Q217Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr1:152382618 G>A maps to NM_016190.2 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:152382993 C>T maps to NM_016190.2 Q188Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:152382957 C>T maps to NM_016190.2 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:152382404 G>A maps to NM_016190.2 Q385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:152384616 C>T maps to NM_016190.2 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:152383100 G>A maps to NM_016190.2 Q153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr1:152382957 C>T maps to NM_016190.2 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:152382198 G>A maps to NM_016190.2 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:152383233 C>T maps to NM_016190.2 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr1:152383100 G>A maps to NM_016190.2 Q153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr1:152382093 G>A maps to NM_016190.2 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr1:17274869 C>T maps to NM_014675.3 A853A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:17263329 G>A maps to NM_014675.3 Q385Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr1:17256818 C>T maps to NM_014675.3 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr1:17279835 C>T maps to NM_014675.3 L1016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr1:17257787 C>T maps to NM_014675.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:17272815 C>T maps to NM_014675.3 S733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr1:17292502 C>A maps to NM_014675.3 R1529R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:87021006 C>T maps to NM_001143935.1 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:87005029 C>T maps to NM_001143935.1 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:159683617 G>A maps to NM_000567.2 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:159683854 C>T maps to NM_000567.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr1:159683928 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:159683503 C>T maps to NM_000567.2 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:159683617 G>A maps to NM_000567.2 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:159683512 G>A maps to NM_000567.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:159683764 C>T maps to NM_000567.2 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr1:159683617 G>A maps to NM_000567.2 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:159684230 A>G maps to NM_000567.2 H15H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr10:99661390 G>A maps to NM_018058.4 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr10:99771024 C>A maps to NM_018058.4 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:99770905 G>A maps to NM_018058.4 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr10:99696020 G>A maps to NM_018058.4 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:99770961 G>A maps to NM_018058.4 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:99625471 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:99695990 G>A maps to NM_018058.4 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:122742082 C>T maps to NM_019604.2 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:122720887 C>T maps to NM_019604.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:122738186 C>T maps to NM_019604.2 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr19:18885744 G>A maps to NM_001098482.1 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:18888005 C>T maps to NM_001098482.1 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:18853835 G>A maps to NM_001098482.1 Q81Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr19:18886506 G>T maps to NM_001098482.1 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr1:153921593 C>T maps to NM_181715.2 G557G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:153924113 G>A maps to NM_181715.2 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:153924599 G>A maps to NM_181715.2 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:153923984 G>A maps to NM_181715.2 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:91181685 C>A maps to NM_022769.3 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr15:91172682 T>C maps to NM_022769.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr15:91136932 C>T maps to NM_022769.3 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:91169121 C>T maps to NM_022769.3 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:91172589 C>T maps to NM_022769.3 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:48342935 C>T maps to NM_000554.4 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:48343157 C>T maps to NM_000554.4 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:48343112 C>T maps to NM_000554.4 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:48342935 C>T maps to NM_000554.4 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:48342686 G>A maps to NM_000554.4 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:48343181 G>A maps to NM_000554.4 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:48342764 C>T maps to NM_000554.4 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:48343034 C>T maps to NM_000554.4 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44R-06A-41D-A25O-08 chr12:107386773 G>A maps to NM_004075.3 G542G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:107398998 C>A maps to NM_004075.3 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:45883614 C>T maps to NM_021117.3 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:45868998 C>T maps to NM_021117.3 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr11:45869046 G>A maps to NM_021117.3 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:45891259 C>T maps to NM_021117.3 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:45868995 C>T maps to NM_021117.3 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr11:45882452 C>T maps to NM_021117.3 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr11:45891259 C>T maps to NM_021117.3 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:45868989 C>T maps to NM_021117.3 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr11:45882539 G>A maps to NM_021117.3 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:45891907 C>T maps to NM_021117.3 F479F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr21:44590649 C>T maps to NM_000394.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr21:44592344 C>T maps to NM_000394.2 I159I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A20C-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:111779559 G>A maps to ENST00000403628 E7E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:27581345 G>A maps to NM_005208.4 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr17:27581267 G>A maps to NM_005208.4 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr2:219855671 G>A maps to NM_057094.1 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr2:219856823 C>T maps to NM_057094.1 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr2:219857883 G>A maps to NM_057094.1 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr22:27024385 C>T maps to NM_001886.2 H145H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr22:27019280 C>T maps to NM_001886.2 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:27026441 C>T maps to NM_001886.2 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr22:27019244 C>T maps to NM_001886.2 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:27019207 G>A maps to NM_001886.2 W17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr22:27026390 G>A maps to NM_001886.2 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr22:27021579 C>T maps to NM_001886.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr22:27012112 C>T maps to NM_001887.3 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr22:27003981 C>T maps to NM_001887.3 W101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:27003942 G>A maps to NM_001887.3 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr22:27003978 G>A maps to NM_001887.3 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr22:26997874 G>A maps to NM_001887.3 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr22:25623924 C>T maps to NM_000496.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr22:25625497 C>T maps to NM_000496.2 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr22:25623891 G>A maps to NM_000496.2 W82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr22:25597419 C>T maps to NM_004076.3 D19D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:97596262 C>T maps to ENST00000182096 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:97596130 T>G maps to ENST00000182096 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:97596781 C>T maps to ENST00000182096 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:97596412 C>T maps to ENST00000182096 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:209025689 G>A maps to NM_014617.3 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:209028142 G>A maps to NM_014617.3 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:209025545 C>T maps to NM_014617.3 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr2:209010707 G>A maps to NM_005210.3 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr2:209010521 G>A maps to NM_005210.3 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:209007463 C>T maps to NM_005210.3 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:208994170 G>A maps to NM_020989.3 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:208986435 G>A maps to NM_006891.3 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:208986441 C>T maps to NM_006891.3 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:151133345 G>A maps to NM_144727.1 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:151135225 G>A maps to NM_144727.1 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr7:151133375 A>G maps to NM_144727.1 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:151133363 C>T maps to NM_144727.1 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:151127229 G>A maps to NM_144727.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr13:21006378 G>A maps to NM_015974.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr13:21013860 C>T maps to NM_015974.2 K103K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:75190469 T>C maps to NM_001889.3 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:75184933 G>A maps to NM_001889.3 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:56676658 G>A maps to NM_004077.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:56666954 C>T maps to NM_004077.2 W438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:56679768 C>T maps to NM_004077.2 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr12:53552462 G>A maps to NM_015989.4 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr23:151908846 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:151908874 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr23:151909158 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:151908888 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:151909176 A>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr12:10862626 C>T maps to NM_003651.4 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:10856654 G>A maps to NM_003651.4 Y291Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr22:41968136 C>T maps to NM_014460.3 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:115272905 G>A maps to NM_001130523.1 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:115276669 C>T maps to NM_001130523.1 K232K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:115266542 G>A maps to NM_001130523.1 Q627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr20:47706112 C>T maps to NM_001316.2 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr20:47705914 C>T maps to NM_001316.2 I651I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr20:47695140 T>C maps to NM_001316.2 I488I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr20:47675075 C>A maps to NM_001316.2 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:110460043 C>T maps to NM_000757.4 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:110466436 G>A maps to NM_000757.4 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:110465857 C>T maps to NM_000757.4 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:110464542 G>A maps to NM_000757.4 K157K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:110466381 G>A maps to NM_000757.4 W380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:110465833 C>T maps to NM_000757.4 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr5:149452976 G>A maps to NM_005211.3 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:149441313 C>T maps to NM_005211.3 W575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:149435820 C>T maps to NM_005211.3 R801R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:149453024 C>T maps to NM_005211.3 Q307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:149457737 G>A maps to NM_005211.3 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:149457737 G>A maps to NM_005211.3 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:149459765 G>A maps to NM_005211.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:149456917 G>A maps to NM_005211.3 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:149457752 C>T maps to NM_005211.3 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:149449833 G>A maps to NM_005211.3 F410F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:149453009 C>T maps to NM_005211.3 E312E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:149460540 C>T maps to NM_005211.3 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:149449565 C>T maps to NM_005211.3 Q460Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr5:149439321 C>T maps to NM_005211.3 Q691Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:131409650 G>A maps to NM_000758.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:1413231 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr23:1401650 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:1407771 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:1409342 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:1407733 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:1419393 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:1404761 C>A did not map to a codon.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr23:1407512 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:1407759 T>A did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:1407760 T>A did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr23:1428419 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:1407430 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:1407441 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr23:1407723 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:1401666 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:1428397 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr23:1407688 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:1404809 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:1424357 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:1424364 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:1401669 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:1428360 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:1407502 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:1404724 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:1404800 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:1428424 G>A did not map to a codon.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr23:1409324 A>G did not map to a codon.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr23:1428360 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr23:1401655 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:1422827 G>C did not map to a codon.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr23:1407771 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:1422864 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:1409239 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:1407739 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:1428302 G>A did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:1407658 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:1428347 C>T did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:1424417 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr22:37333556 C>T maps to ENST00000262825 P575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr22:37334333 G>A maps to ENST00000262825 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr22:37325506 G>A maps to ENST00000262825 W152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr22:37328825 C>T maps to ENST00000262825 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr22:37334021 G>A maps to ENST00000262825 G730G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr22:37326801 G>A maps to ENST00000262825 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr22:37326417 G>A maps to ENST00000262825 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr22:37334372 C>T maps to ENST00000262825 S847S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr22:37329989 G>A maps to ENST00000262825 G429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr22:37334240 G>A maps to ENST00000262825 G803G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr22:37334429 C>T maps to ENST00000262825 P866P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:37319367 C>T maps to ENST00000262825 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:37319368 C>T maps to ENST00000262825 Q54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:37325462 G>A maps to ENST00000262825 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:37333916 G>A maps to ENST00000262825 K695K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:37334447 C>T maps to ENST00000262825 P872P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr22:37334144 C>T maps to ENST00000262825 G771G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr17:38173118 C>T maps to NM_000759.3 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:38173073 C>T maps to NM_000759.3 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:38172547 C>T maps to NM_000759.3 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr1:36932011 G>A maps to NM_156039.3 F846F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:36945037 G>A maps to NM_156039.3 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:36941239 G>A maps to NM_156039.3 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:36941029 C>T maps to NM_156039.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr1:36938261 C>T maps to NM_156039.3 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:36945040 G>A maps to NM_156039.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:19266160 C>T maps to NM_018371.4 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:19362976 G>A maps to NM_018371.4 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:19362865 C>T maps to NM_018371.4 E160E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:43654271 C>A maps to NM_018590.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:43650773 C>T maps to NM_018590.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:43651085 C>T maps to NM_018590.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr10:43659460 C>T maps to NM_018590.3 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:43678848 C>T maps to NM_018590.3 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:43659415 C>T maps to NM_018590.3 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:61972438 G>A maps to NM_001317.3 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:61949950 G>A maps to NM_020991.3 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:61949533 G>A maps to NM_020991.3 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr17:61949557 C>T maps to NM_020991.3 K194K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr17:61949647 G>A maps to NM_020991.3 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:61949960 C>T maps to NM_020991.3 E144E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr17:61987860 G>A maps to NM_022579.1 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr17:61987859 G>A maps to NM_022579.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:61988170 G>A maps to NM_022579.1 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:61987554 C>T maps to NM_022579.1 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:61988213 G>A maps to NM_022579.1 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr15:75094688 C>T maps to NM_004383.2 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr15:75094396 C>T maps to NM_004383.2 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr8:2910110 G>A maps to NM_033225.5 F2511F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr8:3165260 G>A maps to NM_033225.5 L1302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr8:3611458 C>T maps to NM_033225.5 Q308Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr8:2820756 G>A maps to NM_033225.5 I3147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr8:3000146 G>A maps to NM_033225.5 F2027F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr8:3224755 G>A maps to NM_033225.5 I971I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr8:2976017 G>A maps to NM_033225.5 F2111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr8:2876007 G>A maps to NM_033225.5 R2674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr8:3226872 G>A maps to NM_033225.5 I934I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:2815272 C>T maps to NM_033225.5 T3253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr8:3045436 G>A maps to NM_033225.5 I1858I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr8:3224644 G>A maps to NM_033225.5 I1008I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr8:3081371 G>A maps to NM_033225.5 L1455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr8:3000080 G>A maps to NM_033225.5 L2049L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:3165972 C>T maps to NM_033225.5 R1228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr8:2832060 G>A maps to NM_033225.5 S2884S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr8:2855629 C>T maps to NM_033225.5 V2760V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr8:3008994 G>A maps to NM_033225.5 I1985I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr8:3200905 G>A maps to NM_033225.5 L1181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:3432541 G>A maps to NM_033225.5 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:2855557 C>T maps to NM_033225.5 W2784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:3141788 G>A maps to NM_033225.5 L1344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:3245067 G>A maps to NM_033225.5 P910P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:2813222 G>A maps to NM_033225.5 F3294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:2949062 C>T maps to NM_033225.5 K2420K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:2855632 G>A maps to NM_033225.5 V2759V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr8:2965278 G>A maps to NM_033225.5 Q2266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr8:3008940 C>T maps to NM_033225.5 R2003R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr8:3047536 G>A maps to NM_033225.5 F1765F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:3224728 G>A maps to NM_033225.5 S980S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:2807755 A>T maps to NM_033225.5 G3437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:3224590 G>A maps to NM_033225.5 F1026F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:3226851 G>A maps to NM_033225.5 V941V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:3889439 A>T maps to NM_033225.5 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr8:3045478 C>T maps to NM_033225.5 V1844V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr8:3046513 G>A maps to NM_033225.5 F1806F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr8:3265454 G>A maps to NM_033225.5 S679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:3200885 G>A maps to NM_033225.5 S1187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:2818668 G>A maps to NM_033225.5 G3232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:2830729 G>A maps to NM_033225.5 F2944F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr8:3046513 G>A maps to NM_033225.5 F1806F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:3224647 C>T maps to NM_033225.5 T1007T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:3009021 C>T maps to NM_033225.5 G1976G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr8:2813222 G>A maps to NM_033225.5 F3294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr8:2813183 G>A maps to NM_033225.5 F3307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr8:3432490 G>A maps to NM_033225.5 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr8:2886914 A>T maps to NM_033225.5 L2594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:3165993 G>T maps to NM_033225.5 G1221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr8:2831997 C>T maps to NM_033225.5 W2905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr8:2813183 G>A maps to NM_033225.5 F3307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr8:2855629 C>T maps to NM_033225.5 V2760V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:2820858 G>A maps to NM_033225.5 F3113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:3081375 C>T maps to NM_033225.5 G1453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr8:2855665 G>A maps to NM_033225.5 F2748F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr8:3245064 G>A maps to NM_033225.5 L911L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr8:2818683 C>T maps to NM_033225.5 Q3227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr8:3265736 G>A maps to NM_033225.5 F585F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr8:2824185 G>T maps to NM_033225.5 I3002I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr8:2824192 G>T maps to NM_033225.5 S3000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr8:2976068 C>T maps to NM_033225.5 Q2094Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr8:2976070 G>A maps to NM_033225.5 Q2094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr8:2813136 C>T maps to NM_033225.5 W3323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr8:3253833 G>A maps to NM_033225.5 I825I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr8:2815308 G>A maps to NM_033225.5 F3241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr8:3008917 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr8:3141780 C>T maps to NM_033225.5 K1346K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr8:2813183 G>A maps to NM_033225.5 F3307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZU-06A-12D-A196-08 chr8:3081267 G>A maps to NM_033225.5 I1489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:2823396 G>A maps to NM_033225.5 S3060S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:3141825 G>A maps to NM_033225.5 I1331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:3889559 C>T maps to NM_033225.5 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:2808777 G>A maps to NM_033225.5 F3353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:2813222 G>A maps to NM_033225.5 F3294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:2820135 G>A maps to NM_033225.5 I3160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:2855542 G>A maps to NM_033225.5 P2789P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:2886877 C>T maps to NM_033225.5 G2606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:2910071 G>A maps to NM_033225.5 G2524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:2967780 C>T maps to NM_033225.5 L2169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:3046492 G>A maps to NM_033225.5 I1813I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:3087636 G>A maps to NM_033225.5 Q1424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:3200900 G>A maps to NM_033225.5 I1182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:3265541 G>A maps to NM_033225.5 V650V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:3351176 C>T maps to NM_033225.5 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:3855570 G>A maps to NM_033225.5 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr8:2857627 C>T maps to NM_033225.5 P2685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:3081261 C>T maps to NM_033225.5 L1491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:3081267 G>A maps to NM_033225.5 I1489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:3141813 C>T maps to NM_033225.5 W1335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:3165890 G>A maps to NM_033225.5 L1256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:3566011 C>T maps to NM_033225.5 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr8:2830744 C>T maps to NM_033225.5 K2939K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr8:3200830 G>A maps to NM_033225.5 Q1206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr8:3081375 C>T maps to NM_033225.5 G1453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr8:3256959 C>T maps to NM_033225.5 W786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr8:2818683 C>T maps to NM_033225.5 Q3227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr8:2966270 C>T did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr8:2967723 G>A maps to NM_033225.5 F2188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr1:34101974 G>T maps to ENST00000373381 R1612R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr1:34087803 G>A maps to ENST00000373381 I1890I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:34190204 G>A maps to ENST00000373381 S892S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:34276406 G>A maps to ENST00000373381 F421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr1:34006260 C>T maps to ENST00000373381 G3125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:34049278 G>A maps to ENST00000373381 L2361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:34209040 G>A maps to ENST00000373381 F631F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr1:34276406 G>A maps to ENST00000373381 F421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:34082531 C>T maps to ENST00000373381 W1957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:34083125 G>A maps to ENST00000373381 F1933F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:34090196 G>A maps to ENST00000373381 S1809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr1:34285416 G>A maps to ENST00000373381 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr1:34087803 G>A maps to ENST00000373381 I1890I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:34066540 C>T maps to ENST00000373381 Q2220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:34189892 G>A maps to ENST00000373381 Q929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:34209108 G>A maps to ENST00000373381 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:33990613 G>A maps to ENST00000373381 L3382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr1:34049347 G>A maps to ENST00000373381 F2338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr1:34238206 C>T maps to ENST00000373381 K563K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:34276421 G>A maps to ENST00000373381 I416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:34182075 G>A maps to ENST00000373381 F969F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:34002636 A>G maps to ENST00000373381 N3248N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:34209028 C>T maps to ENST00000373381 K635K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:34006185 C>T maps to ENST00000373381 L3150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:34090145 G>A maps to ENST00000373381 I1826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:34038289 A>T maps to ENST00000373381 A2486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:34180193 C>T maps to ENST00000373381 R1093R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:34066480 G>A maps to ENST00000373381 F2240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:34090117 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:34100925 G>A maps to ENST00000373381 P1618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:34035067 G>A maps to ENST00000373381 I2639I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:34401394 G>A maps to ENST00000373381 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr1:34042908 G>A maps to ENST00000373381 I2481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:34182042 G>A maps to ENST00000373381 I980I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:34208908 C>T maps to ENST00000373381 G675G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:34174811 G>A maps to ENST00000373381 S1111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:34258121 G>A maps to ENST00000373381 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:34080164 G>A maps to ENST00000373381 F1984F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:34192203 G>A maps to ENST00000373381 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:34209000 G>A maps to ENST00000373381 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:34191034 G>A maps to ENST00000373381 F830F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:34238195 C>T maps to ENST00000373381 W567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:34312590 G>A maps to ENST00000373381 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:34080128 C>T maps to ENST00000373381 W1996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr1:34038106 G>A maps to ENST00000373381 V2547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:34015942 G>A maps to ENST00000373381 S2877S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:33987126 G>A maps to ENST00000373381 A3471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:34035052 G>A maps to ENST00000373381 S2644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:34285383 G>A maps to ENST00000373381 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr1:33998707 G>A maps to ENST00000373381 S3331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:33985458 G>A maps to ENST00000373381 F3523F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:33985518 G>A maps to ENST00000373381 S3503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:34008416 G>A maps to ENST00000373381 I3020I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:34015870 C>T maps to ENST00000373381 R2901R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:34015942 G>A maps to ENST00000373381 S2877S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:34070912 C>T maps to ENST00000373381 R2127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:34090196 G>A maps to ENST00000373381 S1809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:34112368 G>A maps to ENST00000373381 L1511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:34158555 G>A maps to ENST00000373381 I1302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:34182036 C>T maps to ENST00000373381 E982E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:34066528 G>A maps to ENST00000373381 N2224N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:34090702 G>A maps to ENST00000373381 L1776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:34180319 C>T maps to ENST00000373381 K1051K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:34080128 C>T maps to ENST00000373381 W1996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:34286137 G>A maps to ENST00000373381 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:34080129 C>T maps to ENST00000373381 W1996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:34174709 G>A maps to ENST00000373381 L1145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:34089036 C>T maps to ENST00000373381 Q1845Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:34006260 C>T maps to ENST00000373381 G3125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:33999492 G>A maps to ENST00000373381 V3258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:34401379 G>A maps to ENST00000373381 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr1:34102011 G>A maps to ENST00000373381 I1599I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:34038121 G>A maps to ENST00000373381 V2542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:34092083 A>T did not map to a codon.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:34189827 G>A maps to ENST00000373381 C950C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr1:34006188 G>A maps to ENST00000373381 S3149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr1:33985536 C>T maps to ENST00000373381 L3497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr1:34238289 G>T maps to ENST00000373381 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:34554591 C>T maps to ENST00000373381 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z4-06A-11D-A197-08 chr1:34276406 G>A maps to ENST00000373381 F421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr1:34008416 G>A maps to ENST00000373381 I3020I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr1:34038259 C>T maps to ENST00000373381 K2496K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr1:34117981 C>T maps to ENST00000373381 K1469K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:34192242 G>A maps to ENST00000373381 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr1:34038142 G>A maps to ENST00000373381 G2535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:34090133 T>C maps to ENST00000373381 E1830E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr1:34209040 G>A maps to ENST00000373381 F631F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr1:34180291 A>G maps to ENST00000373381 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:33985437 G>A maps to ENST00000373381 G3530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:33998704 C>T maps to ENST00000373381 E3332E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:33998740 G>A maps to ENST00000373381 S3320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:34002690 C>T maps to ENST00000373381 P3230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:34003129 G>A maps to ENST00000373381 S3197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:34006239 G>A maps to ENST00000373381 F3132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:34087765 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:34090711 G>A maps to ENST00000373381 I1773I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:34123546 G>A maps to ENST00000373381 I1442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:34158555 G>A maps to ENST00000373381 I1302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:34164422 C>T maps to ENST00000373381 R1245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:34174757 C>T maps to ENST00000373381 Q1129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:34181934 G>A maps to ENST00000373381 F1016F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:34182084 G>A maps to ENST00000373381 F966F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr1:34189857 G>A maps to ENST00000373381 F940F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr1:34080129 C>T maps to ENST00000373381 W1996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr1:34401532 C>T maps to ENST00000373381 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:34033265 G>A maps to ENST00000373381 F2729F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:34052158 C>T maps to ENST00000373381 L2292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:34076689 G>A maps to ENST00000373381 F2058F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:34087803 G>A maps to ENST00000373381 I1890I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:34204929 G>A maps to ENST00000373381 R687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:34401547 G>A maps to ENST00000373381 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:34008416 G>A maps to ENST00000373381 I3020I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:34189908 G>A maps to ENST00000373381 L923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:34401487 G>A maps to ENST00000373381 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr1:34037261 C>T maps to ENST00000373381 E2569E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:34182069 C>T maps to ENST00000373381 L971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:34285416 G>A maps to ENST00000373381 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:34006850 G>A maps to ENST00000373381 F3072F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr8:114031298 G>A maps to NM_198123.1 Q343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr8:113348945 C>T maps to NM_198123.1 G2318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr8:113275982 G>A maps to NM_198123.1 F3249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr8:113363429 C>T maps to NM_198123.1 W2100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:114111073 C>T maps to NM_198123.1 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr8:113246680 G>T maps to NM_198123.1 R3551R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr8:113275982 G>A maps to NM_198123.1 F3249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:113657363 C>T maps to NM_198123.1 W1095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr8:113275982 G>A maps to NM_198123.1 F3249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr8:113529290 G>A maps to NM_198123.1 F1576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr8:113323216 A>T maps to NM_198123.1 P2625P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:113267573 G>A maps to NM_198123.1 F3315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:113326281 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:113326805 T>G maps to NM_198123.1 G2467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr8:113266483 G>A maps to NM_198123.1 Q3370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr8:113277715 C>T maps to NM_198123.1 T3204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr8:113308068 G>A maps to NM_198123.1 S2869S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:114186059 G>A maps to NM_198123.1 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr8:113318267 C>T maps to NM_198123.1 W2680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr8:113318248 G>A maps to NM_198123.1 T2686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr8:114185975 C>T maps to NM_198123.1 W228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:113585886 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:113326685 C>T maps to NM_198123.1 K2507K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:113841919 G>A maps to NM_198123.1 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr8:113323315 G>A maps to NM_198123.1 V2592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr8:113960106 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr8:113420568 C>T maps to NM_198123.1 K1861K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:113326249 G>A maps to NM_198123.1 S2527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:113267555 G>A maps to NM_198123.1 F3321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:113318319 G>A maps to NM_198123.1 R2663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr8:113323257 T>A maps to NM_198123.1 K2612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr8:113649118 C>T maps to NM_198123.1 L1214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr8:113518936 G>A maps to NM_198123.1 I1626I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:113308068 G>A maps to NM_198123.1 S2869S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:113363429 C>T maps to NM_198123.1 W2100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:114326878 G>A maps to NM_198123.1 Q108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr8:113841985 C>T maps to NM_198123.1 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr8:114111079 C>T maps to NM_198123.1 E274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr8:113668565 G>A maps to NM_198123.1 Q941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr8:113246629 C>T maps to NM_198123.1 K3568K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr8:113275866 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:113364644 C>T maps to NM_198123.1 Q2085Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:113599462 A>C maps to NM_198123.1 A1239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr8:113504730 C>T maps to NM_198123.1 L1755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr8:113316975 C>T maps to NM_198123.1 W2747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:113275931 G>A maps to NM_198123.1 S3266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:113421177 G>A maps to NM_198123.1 L1827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:113519002 G>A maps to NM_198123.1 F1604F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:114111042 G>A maps to NM_198123.1 Q287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr8:113697682 G>A maps to NM_198123.1 Q812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:113418822 G>A maps to NM_198123.1 S1913S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr8:114326960 A>G maps to NM_198123.1 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:113518963 A>T maps to NM_198123.1 T1617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:113585730 G>A maps to NM_198123.1 T1347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:113871493 C>T maps to NM_198123.1 V545V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr8:114031325 G>A maps to NM_198123.1 R334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr8:113988231 C>T maps to NM_198123.1 E392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr8:113301618 C>T maps to NM_198123.1 W3041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr4:70823219 C>T maps to NM_001891.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:70823159 C>T maps to NM_001891.2 W169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:70823294 G>A maps to NM_001891.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:70823170 G>A maps to NM_001891.2 Q166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr4:71114746 G>A maps to NM_005212.2 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:148891413 T>C maps to NM_001025105.1 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr5:148891413 T>C maps to NM_001025105.1 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr5:148930446 G>A maps to NM_001025105.1 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr13:37678625 G>A maps to NM_145203.5 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr13:37679360 G>A maps to NM_145203.5 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:37679312 G>A maps to NM_145203.5 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr13:37679198 C>T maps to NM_145203.5 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr13:37679105 G>A maps to NM_145203.5 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:37679360 G>A maps to NM_145203.5 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:80209308 G>A maps to NM_001893.3 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:80210337 G>A maps to NM_001893.3 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:80213451 C>T maps to NM_001893.3 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr17:80213334 G>A maps to NM_001893.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:80209290 G>A maps to NM_001893.3 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr15:64495288 G>A maps to NM_022048.3 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr15:64508804 G>A maps to NM_022048.3 R134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr19:1969908 C>T maps to NM_001319.6 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:1979045 G>A maps to NM_001319.6 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr19:1979364 C>T maps to NM_001319.6 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr20:470459 C>T maps to NM_177559.2 K229K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr20:472936 G>A maps to NM_177559.2 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:31636403 C>T maps to ENST00000375885 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr15:75982508 G>A maps to NM_001897.4 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr15:75985518 G>A maps to NM_001897.4 D48D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr15:75981197 C>A maps to NM_001897.4 V736V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr15:75974675 C>T maps to NM_001897.4 Q1636Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr15:75983117 C>T maps to NM_001897.4 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:75968883 C>T maps to NM_001897.4 V1992V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:75983030 G>A maps to NM_001897.4 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr15:75983078 G>A maps to NM_001897.4 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr3:47604200 C>T maps to ENST00000383738 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr3:47618693 G>A maps to ENST00000383738 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:68007874 C>T maps to ENST00000389042 D321D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:68007875 C>T maps to ENST00000389042 Q322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr8:68007695 C>T maps to ENST00000389042 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:68007773 C>T maps to ENST00000389042 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:39184701 G>A maps to NM_033027.3 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:39184650 G>A maps to NM_033027.3 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:39185385 C>T maps to NM_033027.3 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:39185301 G>A maps to NM_033027.3 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:39186736 G>A maps to NM_033027.3 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:39184920 G>A maps to NM_033027.3 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr3:39185750 G>A maps to NM_033027.3 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:51458119 G>T maps to NM_030809.1 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:51457690 G>A maps to NM_030809.1 N490N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:166451661 C>T maps to ENST00000409420 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:166514529 G>A maps to ENST00000409420 K168K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr2:166535620 G>A maps to ENST00000409420 E404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr2:166533018 C>T maps to ENST00000409420 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr2:166533019 C>T maps to ENST00000409420 R235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:77254061 A>T did not map to a codon.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr20:18131466 C>A maps to NM_020536.4 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:18142488 C>T maps to NM_020536.4 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr20:18163820 C>T maps to NM_020536.4 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr20:18167943 G>A maps to NM_020536.4 K730K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr20:18142719 C>T maps to NM_020536.4 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:18123477 C>T maps to NM_020536.4 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:18165324 C>T maps to NM_020536.4 G688G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:19206522 T>A maps to NM_003476.3 K162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:19204264 C>T maps to NM_003476.3 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:19209753 C>T maps to NM_003476.3 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:19207762 C>T maps to NM_003476.3 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr20:23728482 G>A maps to NM_001898.2 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr20:23731431 C>T maps to NM_001898.2 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr20:23729757 C>T maps to NM_001898.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr20:23731353 G>A maps to NM_001898.2 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:23729754 C>T maps to NM_001898.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:23731353 G>A maps to NM_001898.2 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:23433415 G>A maps to NM_130794.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:23432485 C>T maps to NM_130794.1 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:23432485 C>T maps to NM_130794.1 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:23614576 C>T maps to NM_000099.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr20:23669471 C>T maps to NM_001899.2 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:23667727 C>T maps to NM_001899.2 Q113Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:23669435 C>T maps to NM_001899.2 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:23667823 C>T maps to NM_001899.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr20:23858219 C>T maps to NM_001900.4 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr20:24937983 C>A maps to ENST00000376835 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr20:23472381 G>A maps to NM_005492.2 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr20:23472501 C>T maps to NM_005492.2 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:23472402 G>A maps to NM_005492.2 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr20:23472366 G>A maps to NM_005492.2 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:23472381 G>A maps to NM_005492.2 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr20:23472435 C>T maps to NM_005492.2 N44N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr20:23584340 G>A maps to NM_001008693.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:23584152 C>T maps to NM_001008693.2 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr20:23545668 G>A maps to NM_080610.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr20:23549012 C>T maps to NM_080610.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:54972518 C>T maps to NM_001033522.1 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr20:54972860 C>T maps to NM_001033522.1 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr23:100077325 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr23:100077326 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:100088233 T>C did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:100078282 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:100087727 A>T did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:100092351 A>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr10:53458235 G>A maps to NM_015235.2 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr11:33121204 A>C maps to NM_001326.2 Y295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:33163454 C>T maps to NM_001326.2 W35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr20:23421108 C>T maps to NM_138283.1 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:134947927 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:134947977 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:134948037 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr23:134947908 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:134947908 C>T did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:134948155 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3CF-06A-11D-A196-08 chr23:120007817 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:120008800 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:120007814 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:120009247 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:120008778 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:120009366 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:120008881 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr23:120008797 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:120008990 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:120008991 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr23:120008961 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:120008839 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:120009404 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr23:120007781 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:120009408 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:120008957 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr23:120009252 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr23:120009362 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr23:120007787 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:120007814 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:120009332 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:120009152 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr15:71403675 C>T maps to NM_001102658.1 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:153880488 G>A did not map to a codon.
Sequencing variant TCGA-EB-A44Q-06A-11D-A25O-08 chr23:153880425 C>G did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:153880776 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:153880850 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:153880689 C>T did not map to a codon.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr23:153880703 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:153880691 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:153880895 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:153881734 C>T did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:153880761 C>A did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr18:19995557 G>A maps to NM_172241.2 F739F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr18:19996084 G>A maps to NM_172241.2 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr18:19995557 G>A maps to NM_172241.2 F739F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr18:19996519 G>A maps to NM_172241.2 Q419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr18:19997483 C>T maps to NM_172241.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr18:19995557 G>A maps to NM_172241.2 F739F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr18:19995710 G>A maps to NM_172241.2 F688F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr18:19995557 G>A maps to NM_172241.2 F739F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr18:19997690 G>A maps to NM_172241.2 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr18:19995557 G>A maps to NM_172241.2 F739F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr18:19996502 G>A maps to NM_172241.2 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr18:19997663 C>T maps to NM_172241.2 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr18:19995557 G>A maps to NM_172241.2 F739F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:19997228 C>T maps to NM_172241.2 W182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:19997480 C>T maps to NM_172241.2 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:143882719 G>A maps to NM_198495.2 V708V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr14:39818152 C>T maps to ENST00000396158 F745F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr7:143453509 C>T maps to NM_178561.4 E414E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:143453551 C>T maps to NM_178561.4 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:143453536 C>T maps to NM_178561.4 E405E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr4:1208228 G>A maps to NM_001328.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:126715605 G>A maps to NM_022802.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:126714999 G>A maps to NM_022802.2 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:126715322 G>A maps to NM_022802.2 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr10:126678260 C>T maps to NM_022802.2 P928P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr10:126716207 G>A maps to NM_022802.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:126715449 G>A maps to NM_022802.2 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr1:85029074 G>A maps to NM_004388.2 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr16:67644818 C>T maps to NM_006565.3 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:67650747 C>T maps to NM_006565.3 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:67650693 C>T maps to NM_006565.3 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:67662403 C>T maps to NM_006565.3 F550F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr20:56090865 G>A maps to ENST00000423479 R362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:56078573 C>T maps to ENST00000423479 K586K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr20:56094314 C>T maps to ENST00000423479 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:56098751 C>A maps to ENST00000423479 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr20:56078531 C>T maps to ENST00000423479 K600K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:56098187 T>C maps to ENST00000423479 Q230Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:56083793 G>A maps to ENST00000423479 F514F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr20:56078501 C>T maps to ENST00000423479 A610A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr18:77477836 C>T maps to NM_004715.3 D746D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr18:77475253 C>T maps to NM_004715.3 V598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr18:77474842 C>T maps to NM_004715.3 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:77475382 C>T maps to NM_004715.3 F641F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:58221361 G>A maps to NM_005730.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr3:38012932 C>T maps to NM_001008392.1 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr15:44811378 C>T maps to NM_016396.2 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr8:104394719 A>G maps to NM_138455.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr8:104388111 G>A maps to NM_138455.2 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:204735490 C>T maps to NM_005214.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr2:204735603 C>T maps to NM_005214.3 Y135Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr5:138260978 C>T maps to ENST00000355078 A594A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr5:138163295 C>T maps to ENST00000355078 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:80874813 C>T maps to ENST00000402739 V893V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:80101284 C>T maps to ENST00000402739 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr2:79878711 G>A maps to ENST00000402739 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:80835430 C>T maps to ENST00000402739 L806L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr2:80646704 G>A maps to ENST00000402739 E423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:80772162 G>A maps to ENST00000402739 R449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:80085235 C>T maps to ENST00000402739 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:80782935 C>T maps to ENST00000402739 I553I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr2:80874934 C>T maps to ENST00000402739 Q934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr2:79971574 G>A maps to ENST00000402739 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:80782860 C>T maps to ENST00000402739 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:80874909 C>T maps to ENST00000402739 F925F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:79971565 G>A maps to ENST00000402739 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:80874885 G>A maps to ENST00000402739 V917V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:80874852 G>A maps to ENST00000402739 W906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr10:67748449 C>T maps to NM_013266.2 Q755Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr10:69366765 C>T maps to NM_013266.2 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr10:68940197 G>A maps to NM_013266.2 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr10:67829076 T>G maps to NM_013266.2 T716T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr10:68979532 A>G maps to NM_013266.2 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr10:68940119 G>A maps to NM_013266.2 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:68280387 G>A maps to NM_013266.2 F506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:67726405 C>T maps to NM_013266.2 E788E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr10:68940134 G>A maps to NM_013266.2 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:67748509 C>T maps to NM_013266.2 A735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:67829091 G>A maps to NM_013266.2 I711I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:68979460 G>A maps to NM_013266.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:68526054 C>T maps to NM_013266.2 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:67862956 G>A maps to NM_013266.2 V645V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:69366777 G>A maps to NM_013266.2 N43N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:67829184 G>A maps to NM_013266.2 F680F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:67862926 C>T maps to NM_013266.2 G655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:67726432 C>T maps to NM_013266.2 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:68526135 G>A maps to NM_013266.2 F389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr10:67829091 G>A maps to NM_013266.2 I711I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr10:69281710 C>T maps to NM_013266.2 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:68280417 G>A maps to NM_013266.2 A496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:68940103 G>A maps to NM_013266.2 Q340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:68940197 G>A maps to NM_013266.2 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:69281667 G>A maps to NM_013266.2 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:67862968 C>T maps to NM_013266.2 E641E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:67862926 C>T maps to NM_013266.2 G655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr10:69407238 G>A maps to NM_013266.2 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr9:111714529 C>T maps to NM_003798.2 R598R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr9:111727723 C>A maps to NM_003798.2 E509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:41266076 G>A maps to NM_001904.3 W25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:41275737 C>T maps to NM_001904.3 Q545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr1:9931302 G>A maps to ENST00000361853 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr20:36407714 C>T maps to NM_030877.3 Q337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr20:36468528 C>T maps to NM_030877.3 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr20:36500336 G>A maps to NM_030877.3 E538E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:57575929 T>C maps to NM_001085458.1 T720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:57577602 C>T maps to NM_001085458.1 R820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr11:57564317 G>A maps to NM_001085458.1 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr5:11098695 C>T maps to NM_001332.2 G876G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr5:11117597 G>A maps to NM_001332.2 I747I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr5:11023011 C>T maps to NM_001332.2 S956S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr5:11082808 G>A maps to NM_001332.2 I929I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:10973729 G>A maps to NM_001332.2 F1171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:11565152 T>G maps to NM_001332.2 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:10973600 C>T maps to NM_001332.2 T1214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:11110999 C>T maps to NM_001332.2 K811K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:11364853 C>T maps to NM_001332.2 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:10981884 C>T maps to NM_001332.2 Q1139Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr5:10992669 G>A maps to NM_001332.2 N1068N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:10988307 C>T maps to NM_001332.2 R1086R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr5:11346713 G>A maps to NM_001332.2 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:11364891 G>A maps to NM_001332.2 Q430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:11159782 G>A maps to NM_001332.2 I688I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr5:11565149 G>A maps to NM_001332.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:10992744 G>A maps to NM_001332.2 I1043I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr5:10973717 C>T maps to NM_001332.2 Q1175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr5:11732265 G>A maps to NM_001332.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:11022918 G>A maps to NM_001332.2 I987I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:11732343 C>T maps to NM_001332.2 E26E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:11022918 G>A maps to NM_001332.2 I987I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:11082892 G>A maps to NM_001332.2 L901L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:11199604 A>G maps to NM_001332.2 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr5:10973693 G>A maps to NM_001332.2 S1183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:11023080 G>A maps to NM_001332.2 A933A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr5:11364994 G>T maps to NM_001332.2 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr5:11082930 G>A maps to NM_001332.2 R889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr5:11117570 G>A maps to NM_001332.2 I756I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr5:11565168 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:11397205 G>T maps to NM_001332.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr5:11732301 C>T maps to NM_001332.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:11022969 C>T maps to NM_001332.2 V970V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:11117597 G>A maps to NM_001332.2 I747I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:11236894 G>A maps to NM_001332.2 Q557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:11384819 C>T maps to NM_001332.2 E378E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:10973660 G>A maps to NM_001332.2 T1194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:11082806 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:11110999 C>T maps to NM_001332.2 K811K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:11565117 G>A maps to NM_001332.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr5:11565117 G>A maps to NM_001332.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:11117570 G>A maps to NM_001332.2 I756I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr1:41454276 C>T maps to NM_001905.2 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:41450607 C>T maps to NM_001905.2 Y94Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:41466747 C>G maps to NM_001905.2 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:41450631 G>C maps to NM_001905.2 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:16688705 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:16720908 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr23:16720903 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:16608949 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:16688710 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:16720939 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr11:10783501 C>T maps to NM_014633.3 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:10797123 A>C maps to NM_014633.3 I1013I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:10773004 G>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:10785931 C>A maps to NM_014633.3 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr11:10786219 C>T maps to NM_014633.3 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:75238127 G>A maps to NM_001025200.3 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:15772135 C>T maps to NM_007272.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:15767059 C>T maps to NM_007272.2 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:15771197 G>A maps to NM_007272.2 K197K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:15770003 C>T maps to NM_007272.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr20:44520572 G>A maps to NM_000308.2 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr20:44521929 C>T maps to NM_000308.2 Y242Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr20:44520617 C>T maps to NM_000308.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr20:44521077 C>T maps to NM_000308.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr20:44523488 G>A maps to NM_000308.2 Q317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr8:11710135 C>T maps to NM_147783.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:88033706 G>A maps to NM_001814.4 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:88033707 A>C maps to NM_001814.4 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:88033706 G>A maps to NM_001814.4 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:88027353 A>G maps to NM_001814.4 N404N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:88027629 T>C maps to NM_001814.4 Q312Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:1775298 G>A maps to NM_001909.3 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:1775231 G>A maps to NM_001909.3 Q322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:206331148 G>A maps to ENST00000361052 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:206325395 G>A maps to ENST00000361052 Q212Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr1:206331019 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:206320264 C>T maps to ENST00000361052 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:206331106 G>A maps to ENST00000361052 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:206319207 C>T maps to ENST00000361052 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr11:66333314 G>A maps to NM_003793.3 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr11:66332101 G>A maps to NM_003793.3 I416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:66334759 C>T maps to NM_003793.3 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:66335114 G>A maps to NM_003793.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr14:25042851 G>A maps to NM_001911.2 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr14:25043690 G>A maps to NM_001911.2 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:25044535 C>T maps to NM_001911.2 Q46Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr14:25042968 G>A maps to NM_001911.2 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr14:25043609 G>A maps to NM_001911.2 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr14:25042968 G>A maps to NM_001911.2 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr14:25043013 C>T maps to NM_001911.2 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr14:25043013 C>T maps to NM_001911.2 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr14:25043946 C>T maps to NM_001911.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr14:25043007 G>A maps to NM_001911.2 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZU-06A-12D-A196-08 chr14:25043624 C>T maps to NM_001911.2 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:25042866 C>T maps to NM_001911.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:79227364 C>A maps to NM_004390.3 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:150769330 G>A maps to NM_000396.3 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:150772119 G>T maps to NM_000396.3 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:90343256 C>T maps to NM_145918.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr9:90343220 G>A maps to NM_145918.2 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr9:99799643 G>A maps to NM_001333.2 R96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr9:99798969 G>A maps to NM_001333.2 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr9:99795231 C>T maps to NM_001333.2 *335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:99800310 G>A maps to NM_001333.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:99799643 G>A maps to NM_001333.2 R96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr4:156864340 G>A maps to NM_001334.2 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:150727593 G>A maps to NM_004079.4 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:150724268 G>A maps to NM_004079.4 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:150724442 G>A maps to NM_004079.4 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:150722494 G>A maps to NM_004079.4 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:57581452 G>C maps to NM_001336.3 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:70275244 G>A maps to NM_001184740.1 E335E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr11:70265885 C>T maps to NM_001184740.1 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:70260709 C>T maps to NM_001184740.1 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:117424494 G>A maps to NM_033427.2 S694S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:117351749 A>G maps to NM_033427.2 S1611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:117450994 G>A maps to NM_033427.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:117450995 A>G maps to NM_033427.2 N79N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:117431892 G>A maps to NM_033427.2 Q453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:117432244 G>A maps to NM_033427.2 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr7:117431533 G>A maps to NM_033427.2 A572A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:117364745 G>A maps to NM_033427.2 F1434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr7:117364736 G>A maps to NM_033427.2 S1437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:117400741 C>T maps to NM_033427.2 R973R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr7:117432736 G>A maps to NM_033427.2 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:112999512 C>T maps to NM_018704.2 Q467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr1:112999050 C>T maps to NM_018704.2 Q313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:112999064 T>C maps to NM_018704.2 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr1:112998720 C>T maps to NM_018704.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:112958819 C>T maps to NM_018704.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:51602352 G>A maps to NM_145232.3 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr16:88780098 C>T maps to ENST00000378384 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr5:126993359 C>T maps to NM_001048252.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:126993428 G>A maps to NM_001048252.2 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr10:16960671 G>A maps to NM_001081.3 R2317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr10:17026169 G>A maps to NM_001081.3 R1487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr10:17142112 G>A maps to NM_001081.3 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:17083112 T>G maps to NM_001081.3 A1312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr10:17088026 G>T maps to NM_001081.3 I1132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:17088023 G>A maps to NM_001081.3 I1133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:17157511 G>A maps to NM_001081.3 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:17083064 T>C maps to NM_001081.3 E1328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr10:16932472 C>T maps to NM_001081.3 G2884G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr10:17087008 C>T maps to NM_001081.3 L1223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:16955965 A>T maps to NM_001081.3 S2459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:16967671 G>A maps to NM_001081.3 Q2125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr10:16877087 C>T maps to NM_001081.3 Q3429Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:16948207 G>A maps to NM_001081.3 R2636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:17061852 G>A maps to NM_001081.3 Q1383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr17:55943870 G>A maps to NM_017949.1 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:55950090 G>A maps to NM_017949.1 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:55950090 G>A maps to NM_017949.1 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:55962751 G>A maps to NM_017949.1 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr17:55962835 G>A maps to NM_017949.1 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr10:104183553 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:148427273 C>T maps to NM_003592.2 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:148484199 C>T maps to NM_003592.2 I489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:35333705 G>A maps to NM_001198778.1 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:35328006 G>A maps to NM_001198778.1 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr10:35343418 G>A maps to NM_001198778.1 D141D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:225360605 G>A maps to NM_003590.3 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:225365135 G>A maps to NM_003590.3 A518A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr13:113909008 G>T maps to NM_001008895.1 G585G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr13:113899311 C>T maps to NM_001008895.1 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr13:113909297 C>T maps to NM_001008895.1 S630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:113909297 C>T maps to NM_001008895.1 S630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:119708440 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:119664109 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:119694131 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:119680415 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:119672014 C>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:119675485 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:119675557 C>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:119708452 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:119678366 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:119674286 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr11:107965644 A>T maps to NM_003478.3 V558V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr11:107920792 G>A maps to NM_003478.3 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr11:107965614 T>A maps to NM_003478.3 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:107920787 C>T maps to NM_003478.3 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:43019203 G>A maps to NM_001168370.1 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:43014733 T>A maps to NM_001168370.1 K845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr6:43013086 C>A maps to NM_001168370.1 T1056T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:43016082 G>A maps to NM_001168370.1 L768L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:43014821 G>A maps to NM_001168370.1 F815F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:43019451 C>T maps to NM_001168370.1 E294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:43018888 G>T maps to NM_001168370.1 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:43008414 G>A maps to NM_001168370.1 I1376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr6:43153910 C>T maps to ENST00000354495 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr6:43170917 G>A maps to ENST00000354495 Q1275Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:43188297 C>T maps to ENST00000354495 F2128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:43155680 C>T maps to ENST00000354495 F604F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:43168530 C>T maps to ENST00000354495 S1202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr6:43164421 C>T maps to ENST00000354495 N875N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:43167690 C>T maps to ENST00000354495 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr6:43171672 G>A maps to ENST00000354495 K1369K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr6:43153715 C>T maps to ENST00000354495 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:43184063 T>A maps to ENST00000354495 A2035A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:43172999 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr6:43181574 C>T maps to ENST00000354495 L1871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:43154030 C>T maps to ENST00000354495 F363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:43173927 C>T maps to ENST00000354495 F1659F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:43156450 G>A maps to ENST00000354495 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:43173765 C>T maps to ENST00000354495 L1605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr6:43164397 G>A maps to ENST00000354495 A867A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr6:43163916 C>T maps to ENST00000354495 A833A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:101926379 T>C maps to NM_001913.2 *679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr7:101847762 C>T maps to ENST00000360264 I1011I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr7:101840248 C>T maps to ENST00000360264 Q531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr7:101840358 C>T maps to ENST00000360264 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:101840328 C>T maps to ENST00000360264 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr7:101870821 C>A maps to ENST00000360264 P1113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr7:101877386 C>T maps to ENST00000360264 D1174D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr7:101892183 C>T maps to ENST00000360264 F1471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr7:101882852 C>T maps to ENST00000360264 F1303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:101918602 C>T maps to NM_001913.2 F512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:101840437 C>T maps to ENST00000360264 Q594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:101845318 C>T maps to ENST00000360264 S925S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:101844694 C>T maps to ENST00000360264 I717I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:101671376 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:101740677 C>T maps to ENST00000360264 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:101892267 C>T maps to ENST00000360264 I1499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:101870864 C>T maps to ENST00000360264 Q1128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr7:101847805 C>T maps to ENST00000360264 L1026L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr7:101844908 C>T maps to ENST00000360264 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr7:101844964 C>T maps to ENST00000360264 P807P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:101671416 C>T maps to ENST00000360264 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:101844952 C>T maps to ENST00000360264 P803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:101845423 C>T maps to ENST00000360264 T960T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:101892273 C>T maps to ENST00000360264 R1501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr7:101847706 C>T maps to ENST00000360264 L993L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr7:101892297 G>A maps to ENST00000360264 E1509E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr7:101821822 G>A maps to ENST00000360264 Q312Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr12:111749988 C>T maps to NM_015267.3 I662I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:111776114 C>T maps to NM_015267.3 I1074I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr12:111744810 G>A maps to NM_015267.3 K315K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:111758422 C>T maps to NM_015267.3 A870A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr12:111729273 C>T maps to NM_015267.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:111746304 G>A maps to NM_015267.3 E411E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:111749955 C>T maps to NM_015267.3 I651I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:111786113 G>A maps to NM_015267.3 L1482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:111772374 C>T maps to NM_015267.3 S1019S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:111744858 C>A maps to NM_015267.3 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:111785930 C>T maps to NM_015267.3 S1421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:111785405 C>T maps to NM_015267.3 I1246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr12:111772437 C>T maps to NM_015267.3 I1040I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:111785459 G>A maps to NM_015267.3 E1264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:111785471 G>A maps to NM_015267.3 Q1268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr12:111748274 G>A maps to NM_015267.3 K563K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:111785549 C>T maps to NM_015267.3 A1294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr12:111779806 C>T maps to NM_015267.3 F1203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:111772338 G>A maps to NM_015267.3 E1007E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:111785345 G>A maps to NM_015267.3 E1226E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr10:124598676 G>A maps to NM_022034.4 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:124593227 G>A maps to NM_022034.4 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:124597014 G>A maps to NM_022034.4 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:124594229 G>A maps to NM_022034.4 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:124596416 T>G maps to NM_022034.4 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr10:124591856 G>A maps to NM_022034.4 I587I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:124591826 T>C maps to NM_022034.4 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:124596524 G>A maps to NM_022034.4 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:124597035 C>T maps to NM_022034.4 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr2:180810260 A>G maps to NM_020943.2 G774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:180810044 G>A maps to NM_020943.2 F846F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:180846609 G>A maps to NM_020943.2 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:36962602 G>A maps to NM_017748.3 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr17:36958425 G>A maps to NM_017748.3 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr5:64079667 A>G maps to NM_005869.2 E86E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:64084835 C>T maps to NM_005869.2 R220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:64273000 C>T maps to NM_005869.2 Q398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr10:101993103 G>A maps to NM_018294.4 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr10:102013296 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:107299649 C>G maps to NM_152434.2 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:107260882 G>A maps to NM_152434.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr4:49046861 C>T maps to NM_025087.2 I621I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr4:49009218 G>A maps to NM_025087.2 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr4:49052779 C>T maps to NM_025087.2 I645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:49032927 T>C maps to NM_025087.2 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr4:48996663 G>A maps to NM_025087.2 K180K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:49009249 C>T maps to NM_025087.2 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:48990611 C>T maps to NM_025087.2 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr4:49063905 G>A maps to NM_025087.2 *700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr4:48990671 G>A maps to NM_025087.2 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:49005818 C>T maps to NM_025087.2 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr4:49019272 G>A maps to NM_025087.2 W398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:48990632 G>A maps to NM_025087.2 W61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr4:49046861 C>T maps to NM_025087.2 I621I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr4:49052842 T>C maps to NM_025087.2 S666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr4:49040061 C>T maps to NM_025087.2 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr4:49040100 G>A maps to NM_025087.2 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr4:49005893 C>T maps to NM_025087.2 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:49019267 C>T maps to NM_025087.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:49040067 G>A maps to NM_025087.2 R558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr4:49030719 A>G maps to NM_025087.2 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr4:49034654 C>T maps to NM_025087.2 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr16:57416934 G>A maps to NM_002996.3 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr16:57416259 C>T maps to NM_002996.3 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr16:57416898 C>T maps to NM_002996.3 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:39307670 G>A maps to NM_001171174.1 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:39307169 C>T maps to NM_001171174.1 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:39307286 G>A maps to NM_001171174.1 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:39307742 G>A maps to NM_001171174.1 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:39307400 G>A maps to NM_001171174.1 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:39307820 C>T maps to NM_001171174.1 K92K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:39307646 G>A maps to NM_001171174.1 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:39307001 C>T maps to NM_001171174.1 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:39307673 G>A maps to NM_001171174.1 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:39307286 G>A maps to NM_001171174.1 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr3:39307073 C>T maps to NM_001171174.1 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:39307607 G>A maps to NM_001171174.1 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr3:39307277 G>A maps to NM_001171174.1 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr3:39307643 G>A maps to NM_001171174.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr3:39307589 G>A maps to NM_001171174.1 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr21:18937937 C>T maps to NM_001338.3 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr21:18931354 G>A maps to NM_001338.3 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr21:18937814 C>T maps to NM_001338.3 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr21:18933053 C>T maps to NM_001338.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr21:18933731 C>T maps to NM_001338.3 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr4:76943917 T>C maps to NM_001565.2 Q38Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr10:44880420 G>A maps to NM_001178134.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr10:44871455 C>T maps to NM_001033886.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr10:44873214 G>A maps to NM_001178134.1 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:44871445 T>A maps to NM_001033886.2 K101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:44871422 C>T maps to NM_001033886.2 Q108Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:44873328 C>T maps to NM_001178134.1 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr10:44876284 G>A maps to NM_001178134.1 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr4:76924822 C>T maps to NM_002416.1 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:76928578 G>A maps to NM_002416.1 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:76928578 G>A maps to NM_002416.1 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr2:219029127 C>T maps to NM_000634.2 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:219029805 G>A maps to NM_000634.2 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5KH-06A-11D-A27K-08 chr2:219029814 A>C maps to NM_000634.2 Y40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:219029298 G>A maps to NM_000634.2 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:219029808 C>T maps to NM_000634.2 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:219029418 G>A maps to NM_000634.2 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:219029046 G>A maps to NM_000634.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:219029055 C>T maps to NM_000634.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:219029118 C>T maps to NM_000634.2 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:219028986 G>A maps to NM_000634.2 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr2:219029412 G>A maps to NM_000634.2 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:219028986 G>A maps to NM_000634.2 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:219029523 C>T maps to NM_000634.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:219029609 G>A maps to NM_000634.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:219000147 G>A maps to NM_001168298.1 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:218999901 G>A maps to NM_001168298.1 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:219000201 C>T maps to NM_001168298.1 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:219000399 C>T maps to NM_001168298.1 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:219000423 G>A maps to NM_001168298.1 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:219000366 G>A maps to NM_001168298.1 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:219000174 C>T maps to NM_001168298.1 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:70836738 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:70836808 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:70836565 C>T did not map to a codon.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr23:70836524 A>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:70837016 A>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:70836293 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr2:136873377 G>A maps to NM_001008540.1 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:136872777 G>A maps to NM_001008540.1 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:136875621 C>T maps to NM_003467.2 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:136872630 G>A maps to NM_001008540.1 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:136872831 G>A maps to NM_001008540.1 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:136872834 A>T maps to NM_001008540.1 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:136872762 G>A maps to NM_001008540.1 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr2:136872603 G>A maps to NM_001008540.1 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:118764768 C>T maps to NM_001716.3 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:118754685 G>A maps to NM_001716.3 E12E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:45988185 G>A maps to NM_006564.1 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr3:45988746 G>A maps to NM_006564.1 W258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:45988647 G>A maps to NM_006564.1 Q225Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr2:237489143 G>A maps to NM_020311.2 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:237489791 C>T maps to NM_020311.2 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr2:237489158 C>T maps to NM_020311.2 I17I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:237489866 C>T maps to NM_020311.2 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:237489137 G>A maps to NM_020311.2 E10E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr2:237489737 C>T maps to NM_020311.2 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:237489272 C>T maps to NM_020311.2 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:237490195 G>A maps to NM_020311.2 *363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:237489785 C>T maps to NM_020311.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:237489410 G>A maps to NM_020311.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:237489659 G>A maps to NM_020311.2 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:237489755 C>T maps to NM_020311.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:237489956 C>T maps to NM_020311.2 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:237490145 C>T maps to NM_020311.2 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:237489254 C>T maps to NM_020311.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:237489272 C>T maps to NM_020311.2 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr18:47810872 G>A maps to NM_001101654.1 H364H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr18:47811703 G>A maps to NM_001101654.1 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZG-06A-11D-A197-08 chr18:47812186 T>A maps to NM_001101654.1 K191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:105412203 G>A maps to NM_025212.1 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr4:105393493 G>A maps to NM_025212.1 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr5:139060872 C>T maps to NM_016463.7 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:139060857 C>T maps to NM_016463.7 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr5:139060347 C>T maps to NM_016463.7 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr5:139060329 C>T maps to NM_016463.7 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:139060311 C>T maps to NM_016463.7 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr23:144909377 T>A did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:144909530 A>G did not map to a codon.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr23:30577914 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr23:30577766 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr23:30578039 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr23:30577861 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:30578106 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:30578125 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:30578349 A>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:30578384 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:30577570 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:30578039 G>A did not map to a codon.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr23:30578045 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:35993849 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr23:35959407 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:35974298 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr23:35985896 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:35993911 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr23:35969445 C>T did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:36007507 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:35974254 A>T did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr23:35969373 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:35971753 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:35974280 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr23:35974125 C>T did not map to a codon.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr23:35989767 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:35993307 A>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:35993311 C>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:35974118 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:35974119 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr23:35993924 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:35971788 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:35985767 A>C did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:35974177 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr23:35971730 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:35988924 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:35993900 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:35988948 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:36007617 G>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:35984827 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:35985751 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:35969475 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:35944283 G>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:35974139 T>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:35944274 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:35974252 A>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr23:35994001 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr23:35993820 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:35974079 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:35974125 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:35974177 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:35988893 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:35993898 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:36007456 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:35993911 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:35944274 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr23:35944205 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr23:35993385 C>T did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:35985752 C>G did not map to a codon.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr23:19983591 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr23:19983690 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:19968922 G>A did not map to a codon.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr23:19984421 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:19984627 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:19983445 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:19983591 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:75397605 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:37850444 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:37850231 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:37850184 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:45010907 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:45013410 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr23:45059937 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:45011043 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:45011046 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr23:45051053 T>A did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr23:45011043 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr23:45013380 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:45059963 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:45013352 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr23:45010965 C>A did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr23:45059861 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr23:45051206 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr23:40496278 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr23:148627266 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr23:149100869 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:106456204 G>A did not map to a codon.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr23:106482178 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:106465999 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:106466000 T>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:106482182 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr23:106482196 G>A did not map to a codon.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr23:134292129 C>T did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr23:134303675 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:118676540 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:118676490 C>T did not map to a codon.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr23:118699268 C>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:105912432 C>G did not map to a codon.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr23:105905472 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:105876213 T>C did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:105875871 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:105876181 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:105905301 G>C did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr23:105881013 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:105876358 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:105891582 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:105891583 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:105855708 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:105855709 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr23:23953460 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:23934379 C>T did not map to a codon.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr23:23945390 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:23953393 C>T did not map to a codon.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr23:23933855 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:23929947 T>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:23956694 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:23928429 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:36156081 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr23:36103546 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr23:36091332 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:36083859 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:36162768 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr23:36117967 G>A did not map to a codon.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr23:36162700 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:36116913 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:36156122 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:36091443 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:36091477 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:36162876 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:36162701 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr23:36117930 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:36103546 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:36091362 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:36091373 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:36122791 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:36156554 G>A did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr23:36162747 C>T did not map to a codon.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr23:36083832 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:36089965 C>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:36090073 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr23:115592966 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:115593145 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:115593161 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:115593013 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr23:115593953 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:70325896 G>T did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:70325934 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:139047613 T>A did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:139038682 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:139038646 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:139038470 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:139038683 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:139038112 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:139038337 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:139047571 A>C did not map to a codon.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr23:139038311 T>C did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:139038759 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:139038209 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:139040375 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr1:110038844 C>T maps to NM_001134400.1 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:7688982 C>T maps to NM_016229.3 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:43015822 G>A maps to NM_001171660.1 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:43032819 G>A maps to NM_001171660.1 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr6:84574019 A>T maps to NM_016230.3 K68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:84669578 C>T maps to NM_016230.3 I516I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr6:84669578 C>T maps to NM_016230.3 I516I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr6:84573932 C>T maps to NM_016230.3 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:54644968 G>A maps to NM_001031672.2 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr1:54645013 G>A maps to NM_001031672.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:54640384 G>A maps to NM_001031672.2 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:54644875 G>A maps to NM_001031672.2 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:54640375 G>A maps to NM_001031672.2 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CF-06A-11D-A196-08 chr16:88713221 C>A maps to NM_000101.2 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:61121387 G>A maps to NM_001161454.1 H104H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr23:37670054 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr23:37641394 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:37642817 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:37641430 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:37664341 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:37664342 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr23:37664329 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:37668881 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:37658287 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:37663302 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr23:37652980 C>T did not map to a codon.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr23:37652937 C>T did not map to a codon.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr23:37665728 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:172379234 C>T maps to NM_024843.3 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:172398101 C>T maps to NM_024843.3 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr8:145151056 G>A maps to NM_001916.3 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr8:145151982 C>T maps to NM_001916.3 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr15:22969284 G>A maps to NM_014608.2 G837G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr15:22960807 C>T maps to NM_014608.2 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:22993142 C>T maps to NM_014608.2 I1010I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr15:22960865 C>T maps to NM_014608.2 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:22933830 G>A maps to NM_014608.2 E250E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr15:22999478 G>A maps to NM_014608.2 G1117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr15:22933599 C>T maps to NM_014608.2 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr15:22940811 C>T maps to NM_014608.2 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:22928506 C>T maps to NM_014608.2 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:22969326 C>T maps to NM_014608.2 F851F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:22999451 C>T maps to NM_014608.2 I1108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr15:22990187 C>T maps to NM_014608.2 V936V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:22945068 C>T maps to NM_014608.2 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr5:156816384 C>T maps to ENST00000442283 A1157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr5:156816258 C>T maps to ENST00000442283 S1115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:156742035 C>T maps to ENST00000442283 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:156741410 C>T maps to ENST00000442283 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:156816273 C>T maps to ENST00000442283 I1120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr5:156736807 A>T maps to ENST00000442283 K320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr5:156788476 G>A maps to ENST00000442283 G995G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr5:156817537 C>T maps to ENST00000442283 F1177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr5:156723779 C>T maps to ENST00000442283 Q129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:156734866 C>T maps to ENST00000442283 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr5:156731367 C>T maps to ENST00000442283 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:156752574 C>T maps to ENST00000442283 F662F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:156786095 C>T maps to ENST00000442283 L944L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:156817609 C>T maps to ENST00000442283 F1201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:156741359 G>A maps to ENST00000442283 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:156816270 C>T maps to ENST00000442283 V1119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr5:156746840 G>A maps to ENST00000442283 R476R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:156757854 C>T maps to ENST00000442283 V779V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr5:156786156 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:156727805 C>T maps to ENST00000442283 Y157Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:156742095 C>T maps to ENST00000442283 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:156747678 C>T maps to ENST00000442283 R514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:156787339 C>T maps to ENST00000442283 P981P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:156816274 C>T maps to ENST00000442283 L1121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr5:156760447 C>T maps to ENST00000442283 S818S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr23:83129107 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr23:83126512 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:83128805 A>C did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:83129492 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr23:83128140 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:83128073 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:83128366 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr23:83129298 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:83128245 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:83128354 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:83128739 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr23:83126561 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:83128091 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:83129299 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:83128068 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:83128011 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:83128721 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr23:83128354 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr23:83129137 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:83126556 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:83129106 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr23:83129237 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:83129492 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:83126512 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr23:83129185 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr23:83129178 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:83128217 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:83129178 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:83128038 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:83129237 G>A did not map to a codon.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr23:83128265 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr23:83129492 G>A did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:83128759 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr23:83128412 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr23:83128979 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:83128139 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:83128431 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:83129337 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:83129492 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr23:83128909 G>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:83129565 C>T did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:83129149 G>A did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:83129216 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr9:105767287 G>A maps to NM_001340.3 K125K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:105767743 C>T maps to NM_001340.3 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr9:105767356 G>A maps to NM_001340.3 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr9:105767023 G>A maps to NM_001340.3 W76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZG-06A-11D-A197-08 chr9:105765475 T>C maps to NM_001340.3 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr9:105767022 G>A maps to NM_001340.3 W76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:105767872 G>A maps to NM_001340.3 K320K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:50783722 C>T maps to ENST00000311559 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr15:74636267 G>A maps to NM_000781.2 Q231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr15:74630381 G>A maps to NM_000781.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:74659851 C>T maps to NM_000781.2 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr15:74659680 G>A maps to NM_000781.2 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr15:74636193 G>A maps to NM_000781.2 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr15:74630947 C>T maps to NM_000781.2 R466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:74630351 G>A maps to NM_000781.2 F509F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr15:74659854 C>T maps to NM_000781.2 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr15:74630920 G>A maps to NM_000781.2 F475F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr15:74640302 G>A maps to NM_000781.2 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:74631995 G>A maps to NM_000781.2 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:74635413 G>A maps to NM_000781.2 Y298Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:74640335 G>A maps to NM_000781.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:74659800 G>A maps to NM_000781.2 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:74637391 G>A maps to NM_000781.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr8:143957219 C>T maps to ENST00000377675 E414E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr8:143956420 G>A maps to ENST00000377675 C521C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:143958227 G>A maps to ENST00000377675 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr8:143961103 G>A maps to ENST00000377675 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr8:143960497 G>A maps to ENST00000377675 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:143961163 C>T maps to ENST00000377675 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:143957195 G>A maps to ENST00000377675 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:143996193 C>T maps to NM_000498.3 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr8:143996220 G>A maps to NM_000498.3 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr8:143998578 C>T maps to NM_000498.3 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:143993404 C>T maps to NM_000498.3 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr8:143994723 C>T maps to NM_000498.3 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:143994728 G>A maps to NM_000498.3 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:143999043 G>A maps to NM_000498.3 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:143999037 C>T maps to NM_000498.3 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:143999136 G>A maps to NM_000498.3 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr8:143995793 G>A maps to NM_000498.3 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:143999085 C>T maps to NM_000498.3 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:143993425 G>A maps to NM_000498.3 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:143996537 C>T maps to NM_000498.3 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:143999048 G>A maps to NM_000498.3 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr8:143996127 G>A maps to NM_000498.3 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:104597061 C>T maps to NM_000102.3 K19K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr10:104597025 G>A maps to NM_000102.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:104596854 C>T maps to NM_000102.3 K88K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr15:51514602 G>A maps to NM_031226.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr15:51507962 C>T maps to NM_031226.2 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr15:51519993 G>A maps to NM_031226.2 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr15:51510799 G>A maps to NM_031226.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:51504558 G>A maps to NM_031226.2 F407F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:51514558 C>T maps to NM_031226.2 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr15:51507375 C>T maps to NM_031226.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr15:51514564 G>A maps to NM_031226.2 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:51507372 G>A maps to NM_031226.2 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr15:51535061 G>A maps to NM_031226.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr15:75012979 G>T maps to NM_000499.3 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr15:75012957 G>A maps to NM_000499.3 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr15:75013589 G>A maps to NM_000499.3 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:75014994 G>A maps to NM_000499.3 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:75014040 G>A maps to NM_000499.3 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr15:75015003 G>A maps to NM_000499.3 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr15:75015173 G>A maps to NM_000499.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr15:75015174 G>A maps to NM_000499.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr15:75014709 T>G maps to NM_000499.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr15:75042882 C>T maps to NM_000761.3 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr15:75044175 G>A maps to NM_000761.3 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr15:75047290 C>T maps to NM_000761.3 F471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr15:75042123 C>T maps to NM_000761.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr15:75042124 C>T maps to NM_000761.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr15:75044514 C>T maps to NM_000761.3 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:75042858 C>T maps to NM_000761.3 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:75044175 G>A maps to NM_000761.3 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:75042852 G>A maps to NM_000761.3 Q258Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:75047275 G>A maps to NM_000761.3 W466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:75044489 G>A maps to NM_000761.3 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:75044546 C>T maps to NM_000761.3 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr15:75044175 G>A maps to NM_000761.3 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr15:75042579 G>A maps to NM_000761.3 K167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:75042351 G>A maps to NM_000761.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:75042756 C>T maps to NM_000761.3 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:75047366 C>T maps to NM_000761.3 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:38298035 C>T maps to NM_000104.3 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:204116693 C>T maps to ENST00000429815 D98D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F4-06A-12D-A25O-08 chr2:204154578 C>T maps to ENST00000429815 R363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr6:32008220 G>A maps to NM_000500.5 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr6:32007572 G>A maps to NM_000500.5 K233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr6:32006366 C>T maps to NM_000500.5 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:32007584 C>T maps to NM_000500.5 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr6:31975462 T>C maps to NM_000500.5 *316Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:32006997 G>A maps to NM_000500.5 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr20:52774094 C>T maps to NM_000782.4 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:52790076 G>A maps to NM_000782.4 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr20:52789587 G>A maps to NM_000782.4 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:94836736 G>A maps to NM_000783.3 K390K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:94837051 G>A maps to NM_000783.3 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr10:94837051 G>A maps to NM_000783.3 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr10:94836371 G>C maps to NM_000783.3 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr2:72362023 G>A maps to NM_019885.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr2:72359358 G>A maps to NM_019885.2 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:72361997 G>A maps to NM_019885.2 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:94822676 G>A maps to NM_183374.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr10:94824256 G>A maps to NM_183374.2 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr10:94828204 C>T maps to NM_183374.2 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:219679734 C>T maps to NM_000784.3 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:219677347 C>T maps to NM_000784.3 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:219676953 C>T maps to NM_000784.3 H152H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr2:219679734 C>T maps to NM_000784.3 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:127950675 C>T maps to NM_001001665.3 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr2:127961020 G>A maps to NM_001001665.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr2:127956996 C>T maps to NM_001001665.3 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:127958728 G>A maps to NM_001001665.3 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:41600949 C>T maps to NM_000766.3 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:41600252 C>T maps to NM_000766.3 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:41596459 C>T maps to NM_000766.3 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr19:41600330 C>T maps to NM_000766.3 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:41600318 G>A maps to NM_000766.3 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:41594480 G>A maps to NM_000766.3 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr19:41597770 C>T maps to NM_000766.3 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr19:41599626 C>T maps to NM_000766.3 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:41594835 C>T maps to NM_000766.3 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:41594886 C>T maps to NM_000766.3 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr19:41600877 C>T maps to NM_000766.3 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:41355867 G>A maps to NM_000762.5 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:41349778 C>T maps to NM_000762.5 K469K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:41349793 G>A maps to NM_000762.5 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr19:41386105 G>A maps to NM_000764.2 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:41386417 C>T maps to NM_000764.2 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:41383127 C>T maps to NM_000764.2 K376K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr19:41383127 C>T maps to NM_000764.2 K376K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:41387626 G>A maps to NM_000764.2 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr19:41383103 G>A maps to NM_000764.2 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:41497263 C>T maps to NM_000767.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:41522720 C>T maps to NM_000767.4 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:41522596 C>T maps to NM_000767.4 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:41522638 C>T maps to NM_000767.4 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:41510223 C>T maps to NM_000767.4 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr19:41518706 C>T maps to NM_000767.4 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr19:41518326 C>T maps to NM_000767.4 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:41497233 C>T maps to NM_000767.4 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:41510232 G>A maps to NM_000767.4 K122K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:41515242 C>T maps to NM_000767.4 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:41510036 C>T maps to NM_000767.4 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:41518613 C>T maps to NM_000767.4 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:41512909 C>T maps to NM_000767.4 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr10:96480238 G>A maps to NM_000772.2 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr10:96454740 C>T maps to NM_000772.2 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:96466554 C>T maps to NM_000772.2 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:96484283 C>T maps to NM_000772.2 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:96493118 G>A maps to NM_000772.2 E405E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:96454809 G>A maps to NM_000772.2 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:96443701 C>T maps to NM_000772.2 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:96493178 C>T maps to NM_000772.2 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr10:96480238 G>A maps to NM_000772.2 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:96495026 G>A maps to NM_000772.2 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr10:96447940 C>T maps to NM_000772.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:96466662 G>A maps to NM_000772.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:96480248 C>T maps to NM_000772.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:96454695 C>T maps to NM_000772.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr10:96447960 G>A maps to NM_000772.2 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:96448008 G>A maps to NM_000772.2 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr10:96443701 C>T maps to NM_000772.2 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr10:96466554 C>T maps to NM_000772.2 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr10:96495101 G>A maps to NM_000772.2 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr10:96480224 G>T maps to NM_000772.2 G298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr10:96454813 C>T maps to NM_000772.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:96447568 C>T maps to NM_000772.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:96484113 G>T maps to NM_000772.2 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr10:96540304 G>A maps to NM_000769.1 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr10:96522593 G>A maps to NM_000769.1 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr10:96541741 C>T maps to NM_000769.1 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr10:96602717 C>T maps to NM_000769.1 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:96535150 C>T maps to NM_000769.1 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:96540334 C>T maps to NM_000769.1 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr10:96540391 G>A maps to NM_000769.1 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr10:96540286 C>T maps to NM_000769.1 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:96535250 C>T maps to NM_000769.1 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:96580386 G>A maps to NM_000769.1 E318E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:96535267 C>T maps to NM_000769.1 C151C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr10:96612559 G>A maps to NM_000769.1 Q454Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr10:96540334 C>T maps to NM_000769.1 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr10:96602759 C>T maps to NM_000769.1 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr10:96602609 G>A maps to NM_000769.1 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr10:96609706 C>T maps to NM_000769.1 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:96540304 G>A maps to NM_000769.1 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:96612634 C>T maps to NM_000769.1 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr10:96612669 G>A maps to NM_000769.1 *491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:96535261 C>T maps to NM_000769.1 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr10:96522587 C>T maps to NM_000769.1 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr10:96535210 G>A maps to NM_000769.1 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:96540376 G>A maps to NM_000769.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:96541741 C>T maps to NM_000769.1 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr10:96534945 C>T maps to NM_000769.1 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr10:96535147 A>G maps to NM_000769.1 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:96602717 C>T maps to NM_000769.1 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:96602759 C>T maps to NM_000769.1 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:96612496 G>A maps to NM_000769.1 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr10:96522587 C>T maps to NM_000769.1 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:96522548 C>T maps to NM_000769.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr10:96541600 C>T maps to NM_000769.1 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr10:96829084 C>T maps to NM_000770.3 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr10:96827109 G>A maps to NM_000770.3 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:96827076 G>A maps to NM_000770.3 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:96826963 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:96824556 C>T maps to NM_000770.3 Q214Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:96824694 G>A maps to NM_000770.3 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:96802709 G>A maps to NM_000770.3 V362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:96802817 C>T maps to NM_000770.3 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr10:96829084 C>T maps to NM_000770.3 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr10:96824690 G>A maps to NM_000770.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:96827086 C>T maps to NM_000770.3 W120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:96827109 G>A maps to NM_000770.3 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr10:96829126 G>A maps to NM_000770.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr10:96796893 G>A maps to NM_000770.3 I488I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr10:96748692 C>T maps to NM_000771.3 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr10:96741117 C>T maps to NM_000771.3 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr10:96748783 G>A maps to NM_000771.3 *491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr10:96741124 A>T maps to NM_000771.3 K383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:96745899 G>A maps to NM_000771.3 K420K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:96702027 G>A maps to NM_000771.3 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr10:96707584 G>A maps to NM_000771.3 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr10:96748772 C>T maps to NM_000771.3 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:96707560 C>T maps to NM_000771.3 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:96698565 C>T maps to NM_000771.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:96701947 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr10:96701640 C>T maps to NM_000771.3 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr10:96698564 C>T maps to NM_000771.3 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:96698525 C>T maps to NM_000771.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:96701997 C>T maps to NM_000771.3 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:96701745 C>T maps to NM_000771.3 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr10:96708998 C>T maps to NM_000771.3 N259N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:96740947 C>T maps to NM_000771.3 Q324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr10:96708899 C>T maps to NM_000771.3 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:96731976 C>T maps to NM_000771.3 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:96740982 G>A maps to NM_000771.3 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr10:96707542 C>T maps to NM_000771.3 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr10:96745845 C>T maps to NM_000771.3 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr10:96731970 C>T maps to NM_000771.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr10:96748664 C>T maps to NM_000771.3 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr10:96741003 G>A maps to NM_000771.3 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:96698453 G>A maps to NM_000771.3 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:96698513 G>A maps to NM_000771.3 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:96702057 G>A maps to NM_000771.3 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:96698486 C>T maps to NM_000771.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:96731865 G>A maps to NM_000771.3 K275K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:42525763 G>A maps to NM_000106.4 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:42525764 G>A maps to NM_000106.4 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr22:42525764 G>A maps to NM_000106.4 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:135345655 C>T maps to NM_000773.3 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr10:135351391 C>T maps to NM_000773.3 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:135340949 C>T maps to NM_000773.3 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr10:135350624 G>A maps to NM_000773.3 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:135345209 C>T maps to NM_000773.3 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:135347378 C>T maps to NM_000773.3 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:135350687 C>T maps to NM_000773.3 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr19:41622454 G>A maps to NM_000774.3 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:41628752 C>T maps to NM_000774.3 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr19:41626255 C>T maps to NM_000774.3 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:41626321 C>T maps to NM_000774.3 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr19:41627420 C>T maps to NM_000774.3 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:41622409 G>A maps to NM_000774.3 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:41626274 C>T maps to NM_000774.3 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr19:41622409 G>A maps to NM_000774.3 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:60392340 G>A maps to NM_000775.2 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:60375599 G>A maps to NM_000775.2 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:60377918 C>T maps to NM_000775.2 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:60377396 G>A maps to NM_000775.2 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr1:60366724 C>T maps to NM_000775.2 E414E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:60377918 C>T maps to NM_000775.2 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr1:60373473 G>A maps to NM_000775.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:60377417 G>A maps to NM_000775.2 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:60366655 G>A maps to NM_000775.2 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:60375620 G>A maps to NM_000775.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:60377840 C>T maps to NM_000775.2 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:14902177 A>T maps to NM_024514.4 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr11:14901712 A>G maps to NM_024514.4 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:14913745 C>T maps to NM_024514.4 W2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:14913746 C>T maps to NM_024514.4 W2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:41711861 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:41704645 C>T maps to ENST00000301173 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:41700522 G>A maps to ENST00000301173 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr19:41707227 C>T maps to ENST00000301173 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:41704514 C>T maps to ENST00000301173 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:41712263 C>T maps to ENST00000301173 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr4:108866409 C>T maps to NM_183075.2 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:1024667 G>A maps to NM_017781.2 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr6:46609918 T>C maps to NM_016593.3 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:46604199 T>A maps to NM_016593.3 K220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr6:46593236 A>G maps to NM_016593.3 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:99367480 T>G did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:99367467 G>A maps to NM_017460.3 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:99355842 C>T maps to NM_017460.3 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr7:99364063 G>A maps to NM_017460.3 H267H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:99361516 C>T maps to NM_017460.3 Q329Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr7:99445172 G>A maps to NM_022820.3 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr7:99454469 C>T maps to NM_022820.3 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:99453256 C>T maps to NM_022820.3 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:99445220 G>A maps to NM_022820.3 K143K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:99436750 G>A maps to NM_022820.3 W58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:99436795 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:99459390 G>A maps to NM_022820.3 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:99264685 A>G maps to NM_000777.3 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:99273831 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:99273832 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr7:99270253 C>T maps to NM_000777.3 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr7:99272199 C>T maps to NM_000777.3 W58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:99247855 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:99270201 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr7:99328744 C>T maps to ENST00000292414 K34K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr7:99306665 G>A maps to ENST00000292414 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:99317938 C>T maps to ENST00000292414 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:99305458 G>A maps to ENST00000292414 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:99313379 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr7:99306851 C>T maps to ENST00000292414 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr7:99332659 C>T maps to ENST00000292414 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:99315202 C>T maps to ENST00000292414 W126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr14:100182516 C>T maps to NM_006668.1 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr14:100157477 C>T maps to NM_006668.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr14:100182480 G>A maps to NM_006668.1 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:100187629 G>A maps to NM_006668.1 E345E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:100182516 C>T maps to NM_006668.1 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr14:100173996 C>T maps to NM_006668.1 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr14:100184454 C>T maps to NM_006668.1 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:100182516 C>T maps to NM_006668.1 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:100192535 C>T maps to NM_006668.1 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:47403794 C>T maps to ENST00000371904 Q70Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:47400172 G>A maps to ENST00000371904 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr1:47403679 G>A maps to ENST00000371904 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:47399660 G>A maps to ENST00000371904 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:47402383 G>A maps to ENST00000371904 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr1:47400181 C>T maps to ENST00000371904 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:47400825 C>T maps to ENST00000371904 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:47406925 G>A maps to ENST00000371904 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:47400738 G>A maps to ENST00000371904 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr1:47399642 G>A maps to ENST00000371904 F400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr1:47407006 C>T maps to ENST00000371904 K33K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:47399642 G>A maps to ENST00000371904 F400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:47402382 G>A maps to ENST00000371904 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr1:47401202 C>T maps to ENST00000371904 Q209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:47398708 G>A maps to ENST00000371904 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:47402413 C>T maps to ENST00000371904 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:47402422 C>T maps to ENST00000371904 Q141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:47395933 C>T maps to ENST00000371904 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:47398482 C>G maps to ENST00000371904 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr1:47400026 C>T maps to ENST00000371904 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:47402362 G>A maps to ENST00000371904 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:47400204 G>A maps to ENST00000371904 Q274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:47400211 C>T maps to ENST00000371904 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:47401262 G>C maps to ENST00000371904 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:47403771 C>T maps to ENST00000371904 W78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:47395894 G>A maps to ENST00000371904 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:47603210 C>T maps to NM_001010969.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:47609011 G>A maps to NM_001010969.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:47603345 C>T maps to NM_001010969.2 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:47610065 G>A maps to NM_001010969.2 K276K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:47610256 C>T maps to NM_001010969.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr1:47606477 G>A maps to NM_001010969.2 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:47614402 C>T maps to NM_001010969.2 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr1:47610238 C>T maps to NM_001010969.2 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr1:47610322 C>T maps to NM_001010969.2 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:47610322 C>T maps to NM_001010969.2 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:47603271 C>T maps to NM_001010969.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:47610047 G>A maps to NM_001010969.2 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:47610065 G>A maps to NM_001010969.2 K276K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr1:47610232 G>A maps to NM_001010969.2 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:47607786 C>T maps to NM_001010969.2 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:47608978 G>A maps to NM_001010969.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:47610047 G>A maps to NM_001010969.2 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:47603165 C>T maps to NM_001010969.2 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr1:47276850 G>A maps to NM_001099772.1 W121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:47276529 C>T maps to NM_001099772.1 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:47279879 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:47284395 G>A maps to NM_001099772.1 R483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr1:47283858 C>T maps to NM_001099772.1 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:47276553 C>T maps to NM_001099772.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:47279583 G>A maps to NM_001099772.1 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:47279700 C>T maps to NM_001099772.1 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr1:47279727 C>T maps to NM_001099772.1 D256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:47283643 G>A maps to NM_001099772.1 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:47264902 C>T maps to NM_001099772.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:47282749 C>T maps to NM_001099772.1 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:47284434 G>A maps to NM_001099772.1 K496K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:47279700 C>T maps to NM_001099772.1 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:47280909 C>T maps to NM_001099772.1 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr1:47283673 G>A maps to NM_001099772.1 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:47264839 C>T maps to NM_001099772.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:47278192 G>A maps to NM_001099772.1 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:47279209 G>A maps to NM_001099772.1 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:47279167 G>A maps to NM_001099772.1 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:47280900 C>A maps to NM_001099772.1 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr1:47276490 G>A maps to NM_001099772.1 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:16038264 G>A maps to NM_021187.3 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:16034825 C>T maps to NM_021187.3 Q238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr19:16024697 G>A maps to NM_021187.3 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:16032950 G>A maps to NM_021187.3 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:16038276 C>T maps to NM_021187.3 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:16024622 G>A maps to NM_021187.3 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:16024553 C>T maps to NM_021187.3 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:16032846 C>T maps to NM_021187.3 W372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr19:16034681 G>A maps to NM_021187.3 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:16024571 C>T maps to NM_021187.3 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:16024709 G>A maps to NM_021187.3 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:16038252 C>T maps to NM_021187.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:16025447 C>T maps to NM_021187.3 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:16045047 C>T maps to NM_021187.3 Q57Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:16024616 C>T maps to NM_021187.3 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:16034837 C>T maps to NM_021187.3 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:16034681 G>A maps to NM_021187.3 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:16025617 A>G maps to NM_021187.3 C401C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr19:16034660 G>A maps to NM_021187.3 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:16045047 C>T maps to NM_021187.3 Q57Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr19:16045092 A>G maps to NM_021187.3 Y42Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:16025447 C>T maps to NM_021187.3 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr19:16034810 C>T maps to NM_021187.3 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr19:16024553 C>T maps to NM_021187.3 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:16025626 G>A maps to NM_021187.3 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:16034645 G>A maps to NM_021187.3 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:16035626 G>A maps to NM_021187.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr19:16034681 G>A maps to NM_021187.3 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr19:15794561 C>T maps to NM_023944.2 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr19:15791298 G>A maps to NM_023944.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:15806808 C>T maps to NM_023944.2 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr19:15791259 G>A maps to NM_023944.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:15791298 G>A maps to NM_023944.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr19:15795920 C>T maps to NM_023944.2 N343N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr19:15784509 G>A maps to NM_023944.2 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:15806745 G>A maps to NM_023944.2 W372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:15791298 G>A maps to NM_023944.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr19:15806986 C>T maps to NM_023944.2 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:15794302 G>A maps to NM_023944.2 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:15807285 C>A maps to NM_023944.2 S454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:15789168 C>T maps to NM_023944.2 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr19:15795941 C>T maps to NM_023944.2 Y350Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:15794548 C>T maps to NM_023944.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr19:15794548 C>T maps to NM_023944.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:15784424 G>A maps to NM_023944.2 W29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:15794317 T>A maps to NM_023944.2 Y221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:15807819 G>A maps to NM_023944.2 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:15794390 C>T maps to NM_023944.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:15791298 G>A maps to NM_023944.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15793284 G>A maps to NM_023944.2 Q204Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15806998 G>A maps to NM_023944.2 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15807280 G>A maps to NM_023944.2 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr19:15807290 C>T maps to NM_023944.2 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr19:15784416 G>A maps to NM_023944.2 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:15793263 C>T maps to NM_023944.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:15807819 G>A maps to NM_023944.2 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:15789168 C>T maps to NM_023944.2 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:15794542 G>A maps to NM_023944.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr19:15989631 C>T maps to NM_001082.3 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:16006400 C>T maps to NM_001082.3 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr19:16000403 G>A maps to NM_001082.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr19:15989694 C>G maps to NM_001082.3 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:16003244 C>T maps to NM_001082.3 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:16000292 G>A maps to NM_001082.3 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr19:16000502 C>T maps to NM_001082.3 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr19:15989715 C>T maps to NM_001082.3 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr19:16000309 G>A maps to NM_001082.3 Q281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr19:16006319 G>A maps to NM_001082.3 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:16006376 G>A maps to NM_001082.3 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr19:15997106 C>T maps to NM_001082.3 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr19:16003244 C>T maps to NM_001082.3 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr19:16006367 G>A maps to NM_001082.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15989592 C>T maps to NM_001082.3 E517E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15990196 C>T maps to NM_001082.3 E452E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15990682 G>A maps to NM_001082.3 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15996759 C>T maps to NM_001082.3 K363K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:16000415 G>A maps to NM_001082.3 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:16008340 G>A maps to NM_001082.3 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr19:16003235 G>A maps to NM_001082.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr19:15655082 C>T maps to NM_173483.3 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:15640605 C>T maps to NM_173483.3 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:15651488 G>A maps to NM_173483.3 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr19:15654825 A>G maps to NM_173483.3 E328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:15651426 C>T maps to NM_173483.3 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr19:15640641 C>T maps to NM_173483.3 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:15648425 C>T maps to NM_173483.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:15636215 G>A maps to NM_173483.3 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr19:15636249 C>T maps to NM_173483.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15636351 C>T maps to NM_173483.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15651287 C>T maps to NM_173483.3 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15654991 G>A maps to NM_173483.3 W346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15655018 G>A maps to NM_173483.3 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr19:15651518 C>T maps to NM_173483.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:15655084 G>A maps to NM_173483.3 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:15752389 G>A maps to NM_000896.2 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:15756623 C>T maps to NM_000896.2 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:15770029 G>A maps to NM_000896.2 R466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:15770131 G>A maps to NM_000896.2 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:15752254 C>T maps to NM_000896.2 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr19:15763657 C>T maps to NM_000896.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:15760809 C>T maps to NM_000896.2 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:15769553 C>T maps to NM_000896.2 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:15760824 C>T maps to NM_000896.2 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:15756644 C>T maps to NM_000896.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr19:15752389 G>A maps to NM_000896.2 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:15752224 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:15758115 G>A maps to NM_000896.2 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:15757898 C>T maps to NM_000896.2 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:15760722 G>A maps to NM_000896.2 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr19:15770038 C>T maps to NM_000896.2 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15756581 C>T maps to NM_000896.2 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15756623 C>T maps to NM_000896.2 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15770050 C>T maps to NM_000896.2 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:15728896 C>T maps to NM_007253.3 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:15740023 C>T maps to NM_007253.3 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr19:15728887 G>A maps to NM_007253.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:15740023 C>T maps to NM_007253.3 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:15728929 C>T maps to NM_007253.3 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr19:15739365 C>T maps to NM_007253.3 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:15730455 C>T maps to NM_007253.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:15730325 C>T maps to NM_007253.3 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:15739141 C>T maps to NM_007253.3 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:15739156 G>A maps to NM_007253.3 E386E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr19:15730446 G>A maps to NM_007253.3 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr19:15728896 C>T maps to NM_007253.3 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:15730512 C>T maps to NM_007253.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15739638 C>T maps to NM_007253.3 F460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:15740002 G>A maps to NM_007253.3 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:15733938 G>A maps to NM_007253.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:187118750 T>G maps to NM_207352.3 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr1:47505114 C>T maps to NM_178033.1 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:47515117 C>T maps to NM_178033.1 Q433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:47515704 G>A maps to NM_178033.1 E463E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:47514288 G>A maps to NM_178033.1 W420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:47515670 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:47514237 G>A maps to NM_178033.1 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:47504341 C>T maps to NM_178033.1 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:47515791 C>T maps to NM_178033.1 I492I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:47501542 G>A maps to NM_178033.1 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:47515791 C>T maps to NM_178033.1 I492I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:47515809 G>A maps to NM_178033.1 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:47515725 G>A maps to NM_178033.1 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:47514288 G>A maps to NM_178033.1 W420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:47515776 C>T maps to NM_178033.1 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:47515122 G>A maps to NM_178033.1 E434E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:47489497 C>T maps to NM_178033.1 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:47514237 G>A maps to NM_178033.1 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:47514288 G>A maps to NM_178033.1 W420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:47515776 C>T maps to NM_178033.1 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:47489650 C>T maps to NM_178033.1 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:47564785 C>T maps to NM_178134.2 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:47548096 C>T maps to NM_178134.2 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:47564866 C>T maps to NM_178134.2 I326I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:47534358 C>T maps to NM_178134.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:47548114 G>A maps to NM_178134.2 E158E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr1:47533323 C>T maps to NM_178134.2 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:47548007 C>T maps to NM_178134.2 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:47560259 G>A maps to NM_178134.2 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:47571799 G>A maps to NM_178134.2 W356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:47533215 C>T maps to NM_178134.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:47560331 G>A maps to NM_178134.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:47571889 C>T maps to NM_178134.2 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:59405028 A>T maps to NM_000780.3 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr8:59409674 G>A maps to NM_000780.3 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr8:59410910 A>T maps to NM_000780.3 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr8:59409270 A>T maps to NM_000780.3 L267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:59409674 G>A maps to NM_000780.3 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr8:65528318 C>T maps to NM_004820.3 W260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:65528647 C>T maps to NM_004820.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:65528445 T>A maps to NM_004820.3 K218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:65528559 G>A maps to NM_004820.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr8:65527589 G>A maps to NM_004820.3 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:65527616 G>A maps to NM_004820.3 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:65527670 G>A maps to NM_004820.3 D323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr8:65537044 C>T maps to NM_004820.3 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr8:65509423 C>T maps to NM_004820.3 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr3:42916669 G>A maps to NM_004391.2 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:42916048 G>A maps to NM_004391.2 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:42916466 C>T maps to NM_004391.2 W281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:42916030 G>A maps to NM_004391.2 I426I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:42915958 C>T maps to NM_004391.2 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:42916456 C>T maps to NM_004391.2 Q284Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:42916519 C>T maps to NM_004391.2 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:42916741 C>T maps to NM_004391.2 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:42917071 G>A maps to NM_004391.2 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:42916030 G>A maps to NM_004391.2 I426I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:42916477 G>A maps to NM_004391.2 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:86046708 C>T maps to NM_001554.4 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:86047911 G>A maps to NM_001554.4 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:77528441 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:77528274 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr23:77528800 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:77529009 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:77529032 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:77528538 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:77528606 T>G did not map to a codon.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr23:77528598 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:77528251 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:77528718 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr13:49281732 C>T maps to NM_020377.2 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr13:49281441 G>A maps to NM_020377.2 W163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:49281282 C>T maps to NM_020377.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:49281891 G>A maps to NM_020377.2 K313K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:48977535 C>T maps to NM_017457.4 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A6L9-06A-11D-A32N-08 chr19:48976635 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr19:48977502 C>T maps to NM_017457.4 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr7:6210175 G>A maps to ENST00000396741 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:6213338 G>A maps to ENST00000396741 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:6210258 T>A maps to ENST00000396741 K244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr22:37707062 C>T maps to NM_013385.3 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr22:37688668 G>A maps to NM_013385.3 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr22:37708068 G>A maps to NM_013385.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:37690747 C>T maps to NM_013385.3 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:37707062 C>T maps to NM_013385.3 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:37709491 C>T maps to NM_013385.3 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr2:158272368 C>T maps to NM_004288.4 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr2:158283931 C>T maps to NM_004288.4 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:158272365 C>T maps to NM_004288.4 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr2:158283903 G>A maps to NM_004288.4 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr2:158272553 G>A maps to NM_004288.4 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:158287453 C>T maps to NM_004288.4 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:158272239 T>C maps to NM_004288.4 K343K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr2:158300433 G>A maps to NM_004288.4 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:158272365 C>T maps to NM_004288.4 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:158283903 G>A maps to NM_004288.4 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:158272404 C>T maps to NM_004288.4 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr2:158272434 C>T maps to NM_004288.4 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:158283901 C>T maps to NM_004288.4 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr2:158272401 C>T maps to NM_004288.4 E289E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:5021055 G>A maps to NM_018659.2 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:20149277 T>C maps to NM_001033553.1 A797A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr17:20013849 G>A maps to NM_001033553.1 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:20149271 C>T maps to NM_001033553.1 V795V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr21:27945214 C>T maps to ENST00000435845 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr21:27852612 G>A maps to ENST00000435845 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr21:27840825 C>T maps to ENST00000435845 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr2:242684182 C>T maps to NM_152783.3 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr2:242684287 C>T maps to NM_152783.3 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:242689686 C>T maps to NM_152783.3 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr2:242689686 C>T maps to NM_152783.3 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:242684290 C>T maps to NM_152783.3 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:4389469 C>T maps to NM_001040101.1 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:4411406 C>T maps to NM_001040101.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr14:59835522 C>T maps to NM_014992.1 T1061T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:59820638 G>A maps to NM_014992.1 K781K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:39846279 G>A maps to ENST00000398904 K487K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:39832258 C>T maps to ENST00000398904 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:39864651 C>T maps to ENST00000398904 I802I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:39856455 T>C maps to ENST00000398904 L688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:39847147 C>T maps to ENST00000398904 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr6:39867947 C>T maps to ENST00000398904 S925S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:57756639 C>T maps to ENST00000371231 K21K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:57480811 G>A maps to ENST00000371231 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:57480637 C>T maps to ENST00000371231 Q487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:57756690 C>T maps to ENST00000371231 E4E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:57535065 G>A maps to ENST00000371231 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:57480649 G>A maps to ENST00000371231 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:57536725 C>T maps to ENST00000371231 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr1:57535062 A>T maps to ENST00000371231 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:57602290 G>A maps to ENST00000371231 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:57489282 G>A maps to ENST00000371231 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr1:57602245 T>A maps to ENST00000371231 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:57481072 G>A maps to ENST00000371231 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr1:57611076 C>T maps to ENST00000371231 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:57476448 C>T maps to ENST00000371231 Q562Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:57611082 G>A maps to ENST00000371231 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:57481072 G>T maps to ENST00000371231 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:57476370 G>A maps to ENST00000371231 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:57476828 C>A maps to ENST00000371231 E554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:57476409 C>T maps to ENST00000371231 G575G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:57476415 G>A maps to ENST00000371231 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:57602218 T>C maps to ENST00000371231 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:57480744 G>A maps to ENST00000371231 Q452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:57480640 T>G maps to ENST00000371231 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr5:39381616 G>C maps to NM_001343.2 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr5:39383358 G>A maps to NM_001343.2 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:39382767 G>A maps to NM_001343.2 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:39382833 C>T maps to NM_001343.2 Q409Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:39376176 G>A maps to NM_001343.2 S723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr5:39377256 G>A maps to NM_001343.2 V544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:39376947 C>T maps to NM_001343.2 E647E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:39381673 G>A maps to NM_001343.2 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:124534922 G>T maps to ENST00000408936 E706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:124535734 G>A maps to ENST00000408936 G976G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:124522693 C>T maps to ENST00000408936 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr9:124535047 C>T maps to ENST00000408936 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr9:124533000 C>T maps to ENST00000408936 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:124535060 C>T maps to ENST00000408936 Q752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr13:72440118 C>T maps to ENST00000359684 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr13:72255942 C>T maps to ENST00000359684 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:72256014 C>T maps to ENST00000359684 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr13:72204732 G>A maps to ENST00000359684 Q363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr13:72147040 G>A maps to ENST00000359684 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr13:72440847 G>A maps to ENST00000359684 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:72049907 C>T maps to ENST00000359684 T702T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:72049967 C>T maps to ENST00000359684 K682K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr13:72255990 C>T maps to ENST00000359684 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:85906119 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:85950043 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:85906112 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:85969582 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:86069748 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:86067879 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:85769310 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:85969710 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:86068205 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:85906066 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:85950140 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:86068205 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:85404080 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:85403979 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr14:59113794 C>T maps to NM_016651.5 L818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr14:59113602 C>T maps to NM_016651.5 F754F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr14:59113376 G>A maps to NM_016651.5 W679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:59113691 G>A maps to NM_016651.5 W784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:59113692 G>A maps to NM_016651.5 W784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr14:59112402 G>A maps to NM_016651.5 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr14:59113644 G>A maps to NM_016651.5 G768G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:59113077 G>A maps to NM_016651.5 V579V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:59113755 C>T maps to NM_016651.5 P805P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:47151936 G>A maps to NM_145056.2 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:47151903 C>T maps to NM_145056.2 W575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:49548071 C>T maps to NM_004393.4 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:49568969 C>T maps to NM_004393.4 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:49569060 C>T maps to NM_004393.4 R373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr3:49569035 G>A maps to NM_004393.4 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr3:49568306 C>T maps to NM_004393.4 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:49569671 C>T maps to NM_004393.4 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr11:61503209 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr11:61511331 C>T maps to NM_006133.2 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:61488333 C>T maps to NM_006133.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr11:61503049 C>T maps to NM_006133.2 F382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:61504697 C>T maps to NM_006133.2 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:61505675 C>T maps to NM_006133.2 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:61487707 C>T maps to NM_006133.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr11:61511195 C>T maps to NM_006133.2 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:61507964 T>C maps to NM_006133.2 F628F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr11:61511135 G>A maps to NM_006133.2 A768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr11:61504775 C>T maps to NM_006133.2 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr11:61511888 C>T maps to NM_006133.2 I1019I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:61511582 C>T maps to NM_006133.2 I917I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr7:6476164 C>T did not map to a codon.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr7:6449867 C>T maps to NM_139179.3 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:6465684 G>A maps to NM_139179.3 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr7:6465717 G>A maps to NM_139179.3 D319D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:6476069 C>T maps to NM_139179.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:6476060 G>A maps to NM_139179.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr11:61113372 G>A maps to NM_015533.3 K510K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr11:61105546 G>A maps to NM_015533.3 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:61106611 C>T maps to NM_015533.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:61110895 C>T maps to NM_015533.3 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:61106810 C>T maps to NM_015533.3 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr3:49053041 G>A maps to NM_001009996.1 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:49055844 G>A maps to NM_001009996.1 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:49055202 G>A maps to NM_001009996.1 S187S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A3JI-06A-11D-A21A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:49053942 G>A maps to NM_001009996.1 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr19:13084348 C>T maps to NM_152654.2 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:13080479 C>T maps to NM_152654.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:13084207 C>T maps to NM_152654.2 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:13084384 C>T maps to NM_152654.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:109292554 C>T maps to NM_001917.4 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr12:109278889 G>T maps to NM_001917.4 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:109283258 G>A maps to NM_001917.4 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr13:106119400 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr13:106124923 G>A maps to NM_172370.3 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr13:106124923 G>A maps to NM_172370.3 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:10683670 G>A maps to NM_004394.2 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:155695217 C>T maps to NM_004632.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr1:155691322 C>T maps to NM_004632.3 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:155697498 C>T maps to NM_004632.3 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:90312084 C>T maps to NM_004938.2 F859F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:90219967 G>A maps to NM_004938.2 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:90321519 C>T maps to NM_004938.2 N1178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr9:90322083 C>T maps to NM_004938.2 T1366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr9:90321405 C>T maps to NM_004938.2 F1140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr9:90321630 G>A maps to NM_004938.2 V1215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:90321117 C>T maps to NM_004938.2 V1044V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr9:90322044 C>T maps to NM_004938.2 F1353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr15:64263738 G>A maps to NM_014326.3 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr15:64218269 G>A maps to NM_014326.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:64275841 C>T maps to NM_014326.3 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr15:64275880 C>T maps to NM_014326.3 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr15:64275880 C>T maps to NM_014326.3 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr15:64332400 C>T maps to NM_014326.3 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:64275847 C>T maps to NM_014326.3 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:3964703 G>A maps to NM_001348.1 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:3964922 G>A maps to NM_001348.1 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr2:159663564 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:159672312 C>T maps to NM_001017920.2 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr4:100787271 G>A maps to NM_014395.2 W256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr4:100738096 G>A maps to NM_014395.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:100787271 G>A maps to NM_014395.2 W256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:159176191 C>T maps to NM_001122951.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:159175619 C>T maps to NM_001122951.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:159175915 G>A maps to NM_001122951.2 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:159176101 C>T maps to NM_001122951.2 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:159176191 C>T maps to NM_001122951.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr1:159175261 C>T maps to NM_001122951.2 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr1:159175963 C>T maps to NM_001122951.2 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:159174754 G>A maps to NM_002036.3 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:159175741 G>A maps to NM_001122951.2 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:136700968 G>A maps to NM_001349.2 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr1:173799874 C>T maps to NM_018122.4 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:33287362 G>T maps to NM_001350.4 T578T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:33288174 G>A maps to NM_001350.4 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:33289561 G>A maps to NM_001350.4 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr6:33289050 G>A maps to NM_001350.4 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr6:33286917 C>T maps to NM_001350.4 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr6:33288198 G>A maps to NM_001350.4 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:1430314 C>T maps to NM_018959.2 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:1434802 C>A maps to NM_018959.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr12:51634701 C>T maps to NM_014764.3 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:16636057 C>T maps to NM_001190811.1 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr3:16633646 C>T maps to NM_001190811.1 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr9:121929642 G>A maps to NM_014618.2 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr9:121930444 C>T maps to NM_014618.2 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr9:121929508 C>T maps to NM_014618.2 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr9:121976230 A>G maps to NM_014618.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr9:121929508 C>T maps to NM_014618.2 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr9:121929508 C>G maps to NM_014618.2 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr9:121971175 G>A maps to NM_014618.2 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr9:121929508 C>T maps to NM_014618.2 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr9:121929906 C>A maps to NM_014618.2 E581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr9:121930072 G>A maps to NM_014618.2 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr9:121929508 C>T maps to NM_014618.2 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr9:121976380 G>A maps to NM_014618.2 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr9:121929940 C>T maps to NM_014618.2 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:121930183 C>T maps to NM_014618.2 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:121929823 C>T maps to NM_014618.2 W608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:121929406 C>T maps to NM_014618.2 T747T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:121930198 G>A maps to NM_014618.2 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr9:121929736 G>A maps to NM_014618.2 P637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr9:121930501 C>T maps to NM_014618.2 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr9:122011342 G>A maps to NM_014618.2 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr9:121976368 G>A maps to NM_014618.2 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:121929811 G>A maps to NM_014618.2 F612F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr9:121929508 C>T maps to NM_014618.2 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:121929508 C>T maps to NM_014618.2 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:121929823 C>T maps to NM_014618.2 W608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:121976368 G>A maps to NM_014618.2 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr9:122075564 G>A maps to NM_014618.2 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr9:121929766 G>A maps to NM_014618.2 T627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr9:122075600 G>A maps to NM_014618.2 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:121929477 G>A maps to NM_014618.2 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:121929811 G>A maps to NM_014618.2 F612F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:121971091 C>T maps to NM_014618.2 E350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:121976335 C>T maps to NM_014618.2 Q261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:122075600 G>A maps to NM_014618.2 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:122075624 C>T maps to NM_014618.2 W3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr9:121929877 G>A maps to NM_014618.2 I590I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:121971124 C>T maps to NM_014618.2 Q339Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr9:121929508 C>T maps to NM_014618.2 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr9:122004447 C>T maps to NM_014618.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr7:87537202 C>T maps to NM_006716.3 R584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:87537441 C>T maps to NM_006716.3 F663F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:42828218 C>T maps to NM_145663.2 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:42828062 C>T maps to NM_145663.2 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:42828063 C>T maps to NM_145663.2 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr17:42818718 C>T maps to NM_145663.2 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr17:42828617 T>C maps to NM_145663.2 G615G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr17:42828497 C>T maps to NM_145663.2 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr9:136516865 G>A maps to NM_000787.3 V434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:136516835 G>A maps to NM_000787.3 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:136523444 G>A maps to NM_000787.3 W577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:136501714 C>T maps to NM_000787.3 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr9:136505041 G>A maps to NM_000787.3 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:136505107 C>T maps to NM_000787.3 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr9:136516772 G>A maps to NM_000787.3 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr9:136505098 G>A maps to NM_000787.3 K157K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr9:136501804 G>A maps to NM_000787.3 W104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr9:136516841 G>A maps to NM_000787.3 R426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr9:136501645 C>T maps to NM_000787.3 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr5:176885601 G>A maps to ENST00000393565 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:176894000 G>A maps to ENST00000393565 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr5:176885601 G>A maps to ENST00000393565 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:90076440 C>T maps to NM_024043.2 W5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:90072784 G>A maps to ENST00000392973 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr20:44037232 C>T maps to NM_001048225.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr7:44100394 C>T maps to NM_001122956.1 S400S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-ER-A3EV-06A-11D-A20D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:100715331 C>T maps to NM_001918.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr11:20178200 G>A maps to ENST00000227256 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:20178179 G>A maps to ENST00000227256 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:20178600 C>T maps to ENST00000227256 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr11:20178609 C>T maps to ENST00000227256 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:20180803 G>A maps to ENST00000227256 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:20181576 G>A maps to ENST00000227256 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr12:45410179 G>A maps to NM_001004329.2 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr12:45410266 A>T maps to NM_001004329.2 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:45410242 G>A maps to NM_001004329.2 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr12:45410374 C>T maps to NM_001004329.2 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr12:45410385 G>A maps to NM_001004329.2 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:45410272 G>A maps to NM_001004329.2 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr14:24587347 C>T maps to NM_025230.4 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr14:24586911 C>T maps to NM_025230.4 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr14:24590117 C>T maps to NM_025230.4 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr14:24587636 C>T maps to NM_025230.4 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:24590592 C>T maps to NM_025230.4 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr14:24590045 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:125686228 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr23:125685885 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:125685445 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr23:125685241 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr23:125686564 C>G did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:125685551 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:125685874 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:125686404 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:125685273 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:125685343 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:125685856 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:125686003 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:125685896 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:125685745 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr23:125686140 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr23:125686525 G>C did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:125685551 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:125686155 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr23:125685447 A>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:125685671 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:125299162 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr23:125299166 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:125298626 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr23:125299643 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:125298806 G>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:125298561 G>A did not map to a codon.
Sequencing variant TCGA-EB-A44Q-06A-11D-A25O-08 chr23:125299815 G>C did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:125298601 A>G did not map to a codon.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr23:125299289 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr23:125298682 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:125299074 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:125299238 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:125299402 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:125299436 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:125299508 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:125298918 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:125298728 G>A did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:125299826 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:104427481 A>G maps to NM_015420.6 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:104427556 C>T maps to NM_015420.6 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr8:104427607 G>A maps to NM_015420.6 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr19:14070064 C>T maps to NM_138353.2 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:14071303 G>A maps to NM_138353.2 K553K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:172333453 C>T maps to NM_025000.3 N392N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr14:73404716 C>T maps to NM_015604.3 R11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr14:73425458 G>A maps to NM_015604.3 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr14:73409707 C>T maps to NM_015604.3 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:73409797 C>T maps to NM_015604.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr14:73406970 C>T maps to NM_015604.3 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr4:41984760 C>T maps to NM_001029955.3 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr4:41984144 C>T maps to NM_001029955.3 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:41984414 A>G maps to NM_001029955.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr4:41984771 T>C maps to NM_001029955.3 H321H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:41984084 C>T maps to NM_001029955.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr4:41984912 C>T maps to NM_001029955.3 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr4:41984424 C>T maps to NM_001029955.3 Q206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:41984912 C>T maps to NM_001029955.3 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr8:88885086 G>A maps to NM_152418.3 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:88885875 C>T maps to NM_152418.3 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:88885041 C>T maps to NM_152418.3 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr8:88886031 C>T maps to NM_152418.3 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:88885041 C>T maps to NM_152418.3 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:88885074 G>A maps to NM_152418.3 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr8:88885998 G>A maps to NM_152418.3 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:88885779 G>A maps to NM_152418.3 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:88885347 G>A maps to NM_152418.3 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr8:88885263 C>T maps to NM_152418.3 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:88885824 C>T maps to NM_152418.3 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr8:88885233 C>G maps to NM_152418.3 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr8:88886021 G>A maps to NM_152418.3 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr8:88886022 G>A maps to NM_152418.3 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr8:88885170 G>A maps to NM_152418.3 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr8:88886082 G>A maps to NM_152418.3 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:88885215 G>A maps to NM_152418.3 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:69529121 A>G maps to NM_003861.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:69520768 G>A maps to NM_003861.2 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:69521725 G>A maps to NM_003861.2 S559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr14:69522034 G>A maps to NM_003861.2 Y456Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr14:69521268 G>A maps to NM_003861.2 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:69558596 G>A maps to NM_003861.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:168007708 G>A maps to ENST00000367840 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:168014417 C>T maps to ENST00000367840 D737D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:168032873 C>T maps to ENST00000367840 A772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:168014466 T>C did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:168014195 C>T maps to ENST00000367840 D663D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:61657258 C>T maps to NM_005828.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr17:61666410 C>T maps to NM_005828.3 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:160194882 G>A maps to NM_015726.3 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr1:160209929 G>A maps to NM_015726.3 R94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:160209837 G>A maps to NM_015726.3 N124N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr23:27998062 G>C did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:27999378 C>G did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:27999267 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:27998736 C>T did not map to a codon.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr23:27998032 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:27997683 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:27998320 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr23:27999213 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:27997671 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:27999003 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:27998065 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr23:27999037 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr23:27999213 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:27998980 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:27999213 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr23:27999111 C>T did not map to a codon.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr23:27999146 T>C did not map to a codon.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr23:27999148 C>T did not map to a codon.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr23:27999152 C>A did not map to a codon.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr23:27999378 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:27998892 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:27998710 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:27999122 T>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:27997755 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:27997848 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:27998537 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:27999222 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:27999274 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:27998042 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:27999285 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr23:27998304 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:27766187 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:27766202 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:27766702 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:27766202 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:27766904 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:27766043 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:27766244 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr23:27766202 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr23:27766553 T>C did not map to a codon.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr23:27766573 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:27766496 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr23:27765057 A>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:27766567 T>A did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr23:27766344 G>A did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:27766046 C>T did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:27766344 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr6:117825083 C>T maps to ENST00000338728 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr6:117858353 C>T maps to ENST00000338728 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr3:98520450 G>A maps to ENST00000326857 D571D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr3:98600534 G>A maps to ENST00000326857 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr18:51025777 C>T maps to NM_005215.3 R1337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr18:50734089 G>A maps to NM_005215.3 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr18:50705413 C>T maps to NM_005215.3 R501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr18:50832016 C>T maps to NM_005215.3 R661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr18:50432607 C>T maps to NM_005215.3 Q203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr18:50936946 C>T maps to NM_005215.3 R1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr18:50705382 A>T maps to NM_005215.3 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr18:50985643 G>A maps to NM_005215.3 Q1145Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr18:50734114 C>T maps to NM_005215.3 R597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr18:51025845 G>A maps to NM_005215.3 P1359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr18:50985601 G>A maps to NM_005215.3 K1131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr18:50432426 C>T maps to NM_005215.3 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr18:50985601 G>A maps to NM_005215.3 K1131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr18:50918175 C>T maps to NM_005215.3 V869V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr18:51025845 G>A maps to NM_005215.3 P1359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:50912422 C>T maps to NM_005215.3 S790S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:50976942 C>T maps to NM_005215.3 I1101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr18:50278508 C>T maps to NM_005215.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr18:50866119 G>A maps to NM_005215.3 V734V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr18:50450105 C>T maps to NM_005215.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr18:50705391 G>A maps to NM_005215.3 K493K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr18:50937011 G>A maps to NM_005215.3 L1042L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr18:50683828 G>A maps to NM_005215.3 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr18:51025777 C>T maps to NM_005215.3 R1337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr18:50985601 G>A maps to NM_005215.3 K1131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr18:50278517 C>T maps to NM_005215.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:50731718 C>T maps to NM_005215.3 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr18:50866257 T>A maps to NM_005215.3 Y780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr18:50929216 C>T maps to NM_005215.3 V963V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr18:50278478 C>T maps to NM_005215.3 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr18:50866128 G>A maps to NM_005215.3 Q737Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr18:50705413 C>T maps to NM_005215.3 R501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr18:51013170 C>T maps to NM_005215.3 V1247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr18:50976954 C>T maps to NM_005215.3 T1105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:50734080 G>A maps to NM_005215.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:51053023 C>T maps to NM_005215.3 S1383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr18:50278623 C>T maps to NM_005215.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr18:50936946 C>T maps to NM_005215.3 R1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr18:50936946 C>T maps to NM_005215.3 R1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr18:50705337 A>G maps to NM_005215.3 R475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr18:51025845 G>A maps to NM_005215.3 P1359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr18:50278517 C>T maps to NM_005215.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:50278457 C>T maps to NM_005215.3 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:50683828 G>A maps to NM_005215.3 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:50731718 C>T maps to NM_005215.3 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:50976921 G>A maps to NM_005215.3 K1094K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:51053095 G>A maps to NM_005215.3 E1407E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr18:50592469 C>T maps to NM_005215.3 Q399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr18:50705413 C>T maps to NM_005215.3 R501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr18:50683780 G>A maps to NM_005215.3 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:50278676 C>T maps to NM_005215.3 Y115Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr18:50936946 C>T maps to NM_005215.3 R1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr12:55038514 G>A maps to NM_053283.2 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:55038535 G>A maps to NM_053283.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:31312268 G>A maps to NM_181807.2 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:31312261 G>A maps to NM_181807.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:31312207 C>A maps to NM_181807.2 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr11:31329439 G>A maps to NM_181807.2 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr11:31349770 G>A maps to NM_181807.2 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr6:24357737 G>A maps to NM_016356.3 Q81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr6:24178683 G>A maps to NM_016356.3 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:24289097 G>A maps to NM_016356.3 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:24278289 G>A maps to NM_016356.3 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:24302257 G>A maps to NM_016356.3 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:32678135 G>A maps to NM_001099434.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr11:6651131 G>A maps to NM_003737.2 S1602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:6662607 G>A maps to NM_003737.2 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:6650990 G>A maps to NM_003737.2 F1649F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:6646551 C>T maps to NM_003737.2 Q2341Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:6655411 G>A maps to NM_003737.2 T641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:6643348 G>A maps to NM_003737.2 L3186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr11:6648376 G>A maps to NM_003737.2 L1965L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:6661490 G>A maps to NM_003737.2 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:6661491 T>A maps to NM_003737.2 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr11:6648740 C>T maps to NM_003737.2 V1843V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:6655519 C>T maps to NM_003737.2 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr4:155219057 C>T maps to NM_017639.3 K1681K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:155219179 G>A maps to NM_017639.3 Q1641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr4:155219726 C>T maps to NM_017639.3 R1458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr4:155295098 C>T maps to NM_017639.3 Q145Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr4:155312344 C>T maps to NM_017639.3 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr4:155253657 T>C maps to NM_017639.3 G735G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:155157595 G>A maps to NM_017639.3 F2281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr4:155155885 C>T maps to NM_017639.3 P2851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:155155969 G>A maps to NM_017639.3 P2823P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:155156308 C>T maps to NM_017639.3 G2710G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr4:155156815 G>A maps to NM_017639.3 I2541I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:155242368 G>A maps to NM_017639.3 I939I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:155157246 G>A maps to NM_017639.3 Q2398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr4:155157700 G>A maps to NM_017639.3 I2246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:155256131 G>A maps to NM_017639.3 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr4:155156590 C>T maps to NM_017639.3 W2616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:155252750 G>A maps to NM_017639.3 F783F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr4:155312326 C>T maps to NM_017639.3 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr4:155157163 G>A maps to NM_017639.3 F2425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr4:155156833 G>A maps to NM_017639.3 F2535F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr4:155156137 C>T maps to NM_017639.3 T2767T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:155156134 G>A maps to NM_017639.3 T2768T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:155156833 G>A maps to NM_017639.3 F2535F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:155254413 G>A maps to NM_017639.3 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:155287467 G>A maps to NM_017639.3 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:155287560 C>T maps to NM_017639.3 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:155256161 G>A maps to NM_017639.3 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:2294496 G>A maps to NM_001919.3 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr16:2290029 G>A maps to NM_001919.3 Q287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr13:36401879 G>A maps to NM_004734.4 I433I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr13:36382423 C>T maps to NM_004734.4 Q600Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr13:36700118 G>A maps to NM_004734.4 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:36348817 C>T maps to NM_004734.4 R717R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:36402444 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:151023714 C>T maps to NM_001040261.4 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr4:151153562 G>A maps to NM_001040261.4 E475E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr3:36759614 G>A maps to NM_033403.1 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:36779343 C>T maps to NM_033403.1 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr3:36779907 C>T maps to NM_033403.1 E81E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr3:36763054 G>A maps to NM_033403.1 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr3:36763054 G>A maps to NM_033403.1 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:36779043 G>A maps to NM_033403.1 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:36779220 C>T maps to NM_033403.1 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:36779856 C>T maps to NM_033403.1 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:36759551 G>A maps to NM_033403.1 Q568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:36759552 G>A maps to NM_033403.1 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:36779526 C>T maps to NM_033403.1 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:36778776 G>A maps to NM_033403.1 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:36778827 G>A maps to NM_033403.1 D441D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr3:36779025 G>A maps to NM_033403.1 H375H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:36779910 G>A maps to NM_033403.1 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:36779646 C>T maps to NM_033403.1 K168K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:36759618 G>A maps to NM_033403.1 I545I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr3:36779919 C>T maps to NM_033403.1 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:36778803 G>A maps to NM_033403.1 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr10:115612743 G>A maps to NM_014881.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:115607038 G>A maps to NM_014881.3 A727A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:114454750 C>T maps to NM_022836.3 Q513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:114448321 G>A maps to NM_022836.3 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr1:114454473 G>A maps to NM_022836.3 K420K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr1:114454683 C>T maps to NM_022836.3 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:14965056 G>A maps to NM_001033855.1 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr10:14977505 C>T maps to NM_001033855.1 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr12:91539911 G>A maps to NM_133503.2 Q335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:91552087 G>A maps to NM_133503.2 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:91552124 G>A maps to NM_133503.2 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:91572191 G>A maps to NM_133503.2 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:91539903 C>T maps to NM_133503.2 W337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr12:91546919 G>A maps to NM_133503.2 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr12:91552219 A>G maps to NM_133503.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:53326728 C>T maps to ENST00000480258 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:53326710 G>A maps to ENST00000480258 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:2064597 C>T maps to NM_152640.3 Q217Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:2062037 G>A maps to NM_152640.3 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:126176517 G>A maps to NM_014026.3 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr1:155011915 C>T maps to NM_152494.3 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:155014006 G>A maps to NM_152494.3 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:155014087 C>T maps to NM_152494.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:155015274 C>T maps to NM_152494.3 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:155013988 G>A maps to NM_152494.3 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3BZ-06A-12D-A196-08 chr1:155004048 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:155005954 G>A maps to NM_144622.2 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:155005176 G>A maps to NM_144622.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:155005657 G>A maps to NM_144622.2 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:155002969 G>A maps to NM_144622.2 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:155003687 G>A maps to NM_144622.2 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:155005648 G>A maps to NM_144622.2 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:155004050 G>A maps to NM_144622.2 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:155005934 G>A maps to NM_144622.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:154997066 G>A maps to NM_144622.2 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:155003669 G>A maps to NM_144622.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr13:95092304 C>T maps to NM_001129889.1 W502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr13:95131434 G>A maps to NM_001129889.1 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr13:95092198 G>A maps to NM_001129889.1 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr13:95092199 G>A maps to NM_001129889.1 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr13:95118853 G>A maps to NM_001129889.1 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr4:183814197 G>A maps to NM_001012732.1 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr4:183812629 C>T maps to NM_001012732.1 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr2:74598269 G>A maps to NM_004082.4 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr2:74598270 G>A maps to NM_004082.4 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:74593971 G>A maps to NM_004082.4 R802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:74593972 G>A maps to NM_004082.4 I801I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr2:74593063 G>A maps to NM_004082.4 R948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:74592676 C>T maps to NM_004082.4 L998L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:74595935 G>A maps to NM_004082.4 F591F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr12:57929323 G>A maps to ENST00000434715 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr9:34616096 G>A maps to NM_007234.3 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:34614059 G>A maps to NM_007234.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:150095182 A>G maps to NM_001135643.1 D378D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:150102494 G>A maps to NM_001135643.1 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr5:150112929 C>T maps to NM_001135643.1 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr5:150090911 G>A maps to NM_001135643.1 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr5:150133176 G>A maps to NM_001135643.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr16:23677032 C>A maps to NM_032486.3 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr16:23672550 C>T maps to NM_032486.3 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:182662917 G>A maps to NM_020640.2 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:20871501 G>A maps to NM_173475.2 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:20873617 G>A maps to NM_173475.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr23:110644526 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:110653285 C>T did not map to a codon.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr23:110654045 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:110644400 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr23:110544955 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:110574169 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:110544970 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:110574250 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:110644343 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:110644319 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:110644261 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:110654097 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:110544925 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:110574160 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:110653521 A>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:110574140 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:110574131 C>G did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:110654010 C>A did not map to a codon.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr23:110653557 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr23:110654118 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr23:110654119 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:110576365 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr23:110576360 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:17426786 C>T maps to NM_024050.5 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:85817206 G>A maps to NM_012137.3 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:85816136 G>A maps to NM_012137.3 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:31696230 G>A maps to NM_013974.1 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr6:31696663 C>T maps to NM_013974.1 W92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:61070582 G>A maps to NM_001923.3 I959I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:61070606 G>A maps to NM_001923.3 P951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:61096996 C>T maps to NM_001923.3 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr11:61083813 G>A maps to NM_001923.3 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:47256141 G>C maps to NM_000107.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:50611690 A>G maps to NM_000790.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr7:50597006 G>A maps to NM_000790.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:50607687 G>A maps to NM_000790.3 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr7:50571700 G>A maps to NM_000790.3 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr7:50611612 G>A maps to NM_000790.3 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:50537851 C>T maps to NM_000790.3 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:50596995 C>T maps to NM_000790.3 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:50531039 A>G maps to NM_000790.3 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:50605623 C>T maps to NM_000790.3 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:50607615 G>A maps to NM_000790.3 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:50611660 C>T maps to NM_000790.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:50605572 C>T maps to NM_000790.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr7:50566848 C>T maps to NM_000790.3 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:50537851 C>T maps to NM_000790.3 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:50611657 G>A maps to NM_000790.3 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:50611759 C>T maps to NM_000790.3 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:50607696 G>A maps to NM_000790.3 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:50611639 C>T maps to NM_000790.3 Q48Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:50605602 C>T maps to NM_000790.3 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:50596938 G>A maps to NM_000790.3 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr14:53529881 G>A maps to NM_001160148.1 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:53560138 G>A maps to NM_001160148.1 R346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:53560127 C>A maps to NM_001160148.1 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:53513665 C>T maps to NM_001160148.1 V841V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:53522576 G>A maps to NM_001160148.1 V682V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr14:53513521 G>A maps to NM_001160148.1 H889H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr14:53539313 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr14:53558540 C>T maps to NM_001160148.1 Q417Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:53560055 G>A maps to NM_001160148.1 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr14:53539338 A>G maps to NM_001160148.1 Y493Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr8:38099837 G>A maps to NM_001164232.1 Q261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:38109455 T>A maps to NM_001164232.1 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr11:103908173 G>A maps to NM_001001711.2 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:103907684 C>T maps to NM_001001711.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr11:103907690 C>T maps to NM_001001711.2 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:103908104 G>A maps to NM_001001711.2 E185E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:103907978 C>T maps to NM_001001711.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:103908167 G>A maps to NM_001001711.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr11:103908032 G>A maps to NM_001001711.2 K161K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:15978205 C>T maps to NM_032341.4 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A264-06A-11D-A196-08 chr12:57911174 T>G maps to NM_001195056.1 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr10:74034733 C>T maps to NM_019058.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr4:101109105 G>A maps to NM_145244.3 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr4:101109085 C>T maps to NM_145244.3 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr4:101108908 G>A maps to NM_145244.3 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:49390945 T>C maps to NM_015086.1 Q571Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr12:49392427 G>A maps to NM_015086.1 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr12:49390534 C>T maps to NM_015086.1 R708R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:49390678 G>T maps to NM_015086.1 P660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr12:49391191 G>A maps to NM_015086.1 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr12:49390573 G>A maps to NM_015086.1 F695F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:110729534 A>G did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:110734569 G>A maps to NM_003649.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr6:110726085 G>A maps to NM_003649.2 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:110714133 G>A maps to NM_003649.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:110714217 C>T maps to NM_003649.2 E290E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:110714538 C>T maps to NM_003649.2 K183K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr6:110726050 G>A maps to NM_003649.2 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:110714214 G>A maps to NM_003649.2 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:110714265 C>T maps to NM_003649.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr6:110714418 C>T maps to NM_003649.2 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:20980209 C>T maps to NM_005216.4 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr6:30864587 C>T maps to NM_013994.2 F605F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:30863262 C>T maps to NM_013994.2 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr6:30865344 C>T maps to NM_013994.2 D735D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:30857131 C>T maps to NM_013994.2 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr6:30866002 C>T maps to NM_013994.2 N796N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:30864867 T>A maps to NM_013994.2 P649P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:30860212 C>T maps to NM_013994.2 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr6:30862329 C>T maps to NM_013994.2 V465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr6:30860239 C>T maps to NM_013994.2 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:30865182 C>T maps to NM_013994.2 I681I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:30860293 C>T maps to NM_013994.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:30864449 C>T maps to NM_013994.2 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr1:162740135 C>T maps to NM_006182.2 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:162743359 C>A maps to NM_006182.2 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr1:162731114 C>T maps to NM_006182.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:162724980 C>T maps to NM_006182.2 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:162746106 C>T maps to NM_006182.2 Q744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:15763585 C>T maps to NM_004939.1 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:15769733 C>T maps to NM_004939.1 Y628Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:15770984 C>T maps to NM_004939.1 F726F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr2:15763626 G>A maps to NM_004939.1 K505K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr2:15735287 G>A maps to NM_004939.1 E12E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:108562652 C>T maps to NM_004398.2 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:108544192 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:108712143 C>T maps to NM_004398.2 Q730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:108559731 C>T maps to NM_004398.2 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:108709292 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19T-06A-11D-A19A-08 chr11:108712204 T>C did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:31236829 C>T maps to NM_030653.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr12:31249910 C>T maps to NM_030653.3 I583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:31236787 C>T maps to NM_030653.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:31244759 C>T maps to NM_030653.3 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:31254894 C>T maps to NM_030653.3 G727G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr12:31255458 C>T maps to NM_030653.3 G790G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:31256286 C>T maps to NM_030653.3 L832L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr22:38884114 C>A maps to NM_001098504.1 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr22:38890738 G>A maps to NM_001098504.1 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:38891909 G>A maps to NM_001098504.1 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr22:38902170 C>T maps to NM_001098504.1 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr22:38891815 G>A maps to NM_001098504.1 R289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr2:118583060 C>T maps to NM_006773.3 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr16:70404176 C>T maps to NM_018332.3 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr16:70363884 C>T maps to NM_007242.4 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr16:70351452 G>A maps to NM_007242.4 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr1:112308794 C>A maps to NM_007204.4 I583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:112309274 C>T maps to NM_007204.4 S743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr1:112309443 C>T maps to NM_007204.4 Q800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZH-06A-11D-A197-08 chr1:112308357 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:70742363 A>T maps to NM_004728.2 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:70730012 C>T maps to NM_004728.2 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr10:70719938 T>C maps to NM_004728.2 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr12:49231348 G>A maps to NM_004818.2 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:49237772 T>G maps to NM_004818.2 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:49228129 C>T maps to NM_004818.2 Q511Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:49237774 G>T maps to NM_004818.2 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:49233688 G>A maps to NM_004818.2 Q140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr12:49225072 T>A maps to NM_004818.2 G697G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr12:49230028 A>G maps to NM_004818.2 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:49228276 G>A maps to NM_004818.2 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr14:94526550 G>A maps to NM_020414.3 R602R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr14:94528938 G>A maps to NM_020414.3 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr14:94521400 T>A maps to NM_020414.3 K707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr14:94526796 G>A maps to NM_020414.3 I520I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr14:94519364 G>A maps to NM_020414.3 L763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:94545434 G>A maps to NM_020414.3 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr14:94526553 T>C maps to NM_020414.3 K601K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr14:94527377 G>A maps to NM_020414.3 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr11:125787136 C>T maps to NM_013264.3 I343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:125787073 G>A maps to NM_013264.3 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:125787043 C>T maps to NM_013264.3 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:134706879 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr23:134683698 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:134711292 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:134714074 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr23:134690139 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr23:134706943 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr23:134706944 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr23:134706810 G>A did not map to a codon.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr23:134714071 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr20:47850196 C>T maps to NM_017895.7 F439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr20:47845303 C>T maps to NM_017895.7 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr20:47852895 C>T maps to NM_017895.7 T543T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A3J7-06A-11D-A20D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:47859198 C>T maps to NM_017895.7 L760L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-FW-A3TU-06A-11D-A23B-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:68056769 C>G maps to NM_018380.3 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:68056961 C>T maps to NM_018380.3 Q48Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr16:68055779 G>A maps to NM_018380.3 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr16:68056396 G>A maps to NM_018380.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr9:135534099 G>A maps to NM_022779.7 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:135487631 G>A maps to NM_022779.7 S717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr9:135521431 G>A maps to NM_022779.7 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:14520411 G>A maps to ENST00000451994 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:14523404 G>A maps to ENST00000451994 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr23:41204720 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:41202523 A>C did not map to a codon.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr23:41204553 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:41203557 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr23:41205504 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:41203369 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr23:41202596 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr23:41202597 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr23:41198306 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:41196685 C>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:41205588 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:41203368 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:41203369 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:41205844 A>C did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:41205853 A>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:41204720 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:41202554 T>C did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:41198332 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr24:15027837 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr24:15025719 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr5:55110938 C>T maps to NM_024415.2 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:55088500 G>A maps to NM_024415.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr5:55075796 C>T maps to NM_024415.2 R134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr5:55088553 T>A maps to NM_024415.2 L463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr5:55081647 C>G maps to NM_024415.2 Y271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:176943307 G>A maps to NM_016222.2 H93H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:176941706 G>A maps to NM_016222.2 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr5:176943934 C>T maps to NM_016222.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:176939112 G>A maps to NM_016222.2 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr5:176940757 G>C maps to NM_016222.2 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:61886221 C>T maps to NM_203499.1 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr17:61894225 A>G did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:74123752 A>C maps to NM_018665.2 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:74104736 C>T maps to NM_018665.2 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:74110015 G>A maps to NM_018665.2 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:74117748 C>T maps to NM_018665.2 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr6:74115537 C>T maps to NM_018665.2 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:74117796 C>T maps to NM_018665.2 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr6:74116199 A>G maps to NM_018665.2 Q307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr5:134126190 T>G maps to ENST00000452510 Y525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr5:134154611 C>T maps to ENST00000452510 A965A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:134120157 C>T maps to ENST00000452510 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:134102612 C>T maps to ENST00000452510 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:134121251 C>G maps to ENST00000452510 Y480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:134121242 C>T maps to ENST00000452510 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr5:134118746 C>T maps to ENST00000452510 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr19:19032526 C>T maps to NM_019070.4 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr19:19035780 C>T maps to NM_019070.4 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:62496324 G>A maps to NM_004396.3 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:62496325 G>A maps to NM_004396.3 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr10:70679598 C>T maps to NM_024045.1 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:70670971 A>G maps to NM_024045.1 Q203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:132624298 G>A maps to NM_175066.3 R619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr12:132626120 G>A maps to NM_175066.3 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:132625405 C>T maps to NM_175066.3 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr17:35992204 G>A maps to NM_007010.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:35993377 T>C maps to NM_007010.3 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:36002294 G>A maps to NM_007010.3 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr17:35986128 T>A maps to NM_007010.3 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:23018312 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:23018768 G>A did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:23018311 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:23019766 T>G did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:23018476 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:23018583 A>T did not map to a codon.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr23:23019217 C>T did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:23018471 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr23:23019337 C>T did not map to a codon.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr23:23019374 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr23:23018496 C>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr23:23018474 A>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:23018891 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr23:23018768 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:23019032 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:23019756 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:23020049 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:23018228 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:113617046 G>A maps to NM_001111322.1 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:113603607 G>A maps to NM_001111322.1 F548F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:124093274 G>A maps to NM_020936.1 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr12:124090488 C>T maps to NM_020936.1 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:124091995 C>T maps to NM_020936.1 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:124094581 C>T maps to NM_020936.1 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr9:32500833 G>A maps to NM_014314.3 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:32493802 G>A maps to NM_014314.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:32500833 G>A maps to NM_014314.3 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:200635235 A>T maps to NM_001031725.4 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr11:118626209 G>A maps to NM_004397.4 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:118656855 G>C maps to NM_004397.4 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr4:169229234 G>A maps to NM_017631.5 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr4:169204659 G>A maps to NM_017631.5 I553I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr4:169194504 C>T maps to NM_017631.5 T833T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr4:169176902 T>C maps to NM_017631.5 K1172K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:169204671 G>A maps to NM_017631.5 V549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr4:169196630 C>T maps to NM_017631.5 V723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr4:169190006 G>T maps to NM_017631.5 T928T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:169188837 G>A maps to NM_017631.5 L978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr4:169176881 G>A maps to NM_017631.5 S1179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:169206649 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr4:169197321 C>T maps to NM_017631.5 T663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:169176898 G>A maps to NM_017631.5 R1174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:169142906 G>A maps to NM_017631.5 S1650S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:169195105 G>A maps to NM_017631.5 V811V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr4:169204703 G>A maps to NM_017631.5 Q539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr4:169227532 C>T maps to NM_017631.5 W201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr4:169227533 C>T maps to NM_017631.5 W201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr4:169201584 A>G maps to NM_017631.5 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:169158565 G>A maps to NM_017631.5 Q1428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:169138131 G>A maps to NM_017631.5 A1697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr4:169204757 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:169158937 T>G maps to NM_017631.5 S1391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr4:169176920 G>A maps to NM_017631.5 A1166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr4:169172185 C>T maps to NM_017631.5 R1259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr4:169374305 C>T maps to NM_001012967.1 W322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:169362490 G>A maps to NM_001012967.1 Q431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:169305891 G>A maps to NM_001012967.1 P1329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:169374298 C>T maps to NM_001012967.1 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:169292857 C>T maps to NM_001012967.1 W1611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr4:169374346 G>A maps to NM_001012967.1 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:169321984 C>T maps to NM_001012967.1 Q1161Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:169344860 C>T maps to NM_001012967.1 E665E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:169351757 G>A maps to NM_001012967.1 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:169300897 G>A maps to NM_001012967.1 S1400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr4:169305792 C>T maps to NM_001012967.1 K1362K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:169279420 G>A maps to NM_001012967.1 S1666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:169340493 G>A maps to NM_001012967.1 Q857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr4:169351661 C>T maps to NM_001012967.1 E548E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr4:169340515 G>A maps to NM_001012967.1 I849I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr11:688031 C>T maps to NM_021008.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr11:654045 G>A maps to NM_021008.2 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:687962 G>A maps to NM_021008.2 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr11:674754 G>A maps to NM_021008.2 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr9:118162655 G>A maps to NM_017418.2 W11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr9:118163566 G>A maps to NM_017418.2 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr8:91029410 C>T maps to NM_001359.1 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr8:91029365 G>A maps to NM_001359.1 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr8:91029431 G>A maps to NM_001359.1 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:91057135 T>A maps to NM_001359.1 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:457471 C>T maps to NM_020664.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:461397 C>T maps to NM_020664.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr16:461433 C>T maps to NM_020664.3 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:461032 C>T maps to NM_020664.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr1:161092179 G>C maps to ENST00000368005 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr1:161092131 G>A maps to ENST00000368005 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:42703976 G>A maps to NM_133328.2 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr19:42713915 G>A maps to NM_133328.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr6:35280206 C>T maps to NM_022047.3 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr6:35280207 C>T maps to NM_022047.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:35289108 C>T maps to NM_022047.3 S606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:35280080 G>A maps to NM_022047.3 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr16:90025447 C>T maps to NM_207514.1 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr16:90023926 C>T maps to NM_207514.1 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr8:6873613 C>T maps to NM_004084.3 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr8:6873621 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:6794400 G>A maps to NM_001925.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr8:6794286 G>A maps to NM_001925.1 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr8:6782348 G>A maps to NM_001926.3 C98C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr8:6782432 G>A maps to NM_001926.3 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:6783524 G>A maps to NM_001926.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:6782384 C>T maps to NM_001926.3 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr8:6782432 G>A maps to NM_001926.3 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:6782351 G>A maps to NM_001926.3 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:50011319 G>A maps to NM_001037498.1 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr6:50011341 G>A maps to NM_001037498.1 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:49936572 C>T maps to NM_001037729.1 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr20:29847268 G>A maps to NM_001037730.1 W34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr20:29847305 G>A maps to NM_001037730.1 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr20:29847380 G>A maps to NM_001037730.1 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:29847305 G>A maps to NM_001037730.1 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr20:29891092 A>G maps to NM_001037731.1 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr20:29956461 C>T maps to NM_054112.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:29960754 C>T maps to NM_054112.2 R52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:29966156 G>A maps to NM_173460.1 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr20:29977000 A>G maps to NM_153323.3 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr20:29993946 G>A maps to NM_001011878.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr20:30060795 G>A maps to NM_001037500.1 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr20:30053464 C>T maps to NM_001037500.1 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr20:76659 C>T maps to NM_153325.2 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr20:76673 G>A maps to NM_153325.2 K29K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:138196 C>T maps to NM_139074.2 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr20:139424 A>G maps to NM_139074.2 Q20Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr20:138223 G>A maps to NM_139074.2 Q13Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr20:168661 C>T maps to NM_001037732.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr20:209997 G>A maps to NM_080831.3 Q46Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr8:7752251 C>T maps to NM_004942.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr14:100615478 G>A maps to NM_206918.2 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:100615478 G>A maps to NM_206918.2 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr14:100615376 C>T maps to NM_206918.2 W251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:100615442 G>A maps to NM_206918.2 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr14:100613235 C>T maps to NM_206918.2 K278K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:100615377 C>T maps to NM_206918.2 W251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:40980290 C>T maps to NM_022774.1 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:40980365 C>T maps to NM_022774.1 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:40980260 A>G maps to NM_022774.1 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr9:126520022 G>A maps to NM_020946.1 C87C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr9:126520031 G>A maps to NM_020946.1 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr9:126202650 G>A maps to NM_020946.1 V492V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:126214554 G>A maps to NM_020946.1 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:126219701 G>A maps to NM_020946.1 R371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:126144300 G>A maps to NM_020946.1 Q814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr9:126371732 G>A maps to NM_020946.1 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:126439052 G>A maps to NM_020946.1 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr9:126319881 G>A maps to NM_020946.1 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:126144640 G>A maps to NM_020946.1 P700P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:126531809 G>A maps to NM_020946.1 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:197564451 C>T maps to NM_001195215.1 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:197522229 G>A maps to NM_001195215.1 R388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:6479030 G>A maps to NM_024898.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:6467967 G>A maps to NM_024898.2 V651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:6468069 G>A maps to NM_024898.2 P617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:6468913 G>T maps to NM_024898.2 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr19:6479051 G>A maps to NM_024898.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:6479878 G>A maps to NM_024898.2 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:6480022 C>G maps to NM_024898.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:6475320 G>A maps to NM_024898.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr19:6467910 G>A maps to NM_024898.2 P670P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:6468112 C>T maps to NM_024898.2 W603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:6479869 C>T maps to NM_024898.2 Q42Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26D-06A-11D-A19A-08 chr19:6477463 G>C maps to NM_024898.2 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr7:140273658 G>A maps to NM_015689.3 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:140301492 C>T maps to NM_015689.3 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr7:140301537 C>T maps to NM_015689.3 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr7:140301516 G>A maps to NM_015689.3 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr7:140301948 C>T maps to NM_015689.3 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr7:140301462 C>T maps to NM_015689.3 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:140266981 C>T maps to NM_015689.3 E561E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:140223202 G>A maps to NM_015689.3 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr7:140246634 G>A maps to NM_015689.3 I714I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr7:140301798 C>T maps to NM_015689.3 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:140223158 C>T maps to NM_015689.3 Q871Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr7:140301360 C>T maps to NM_015689.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:140285409 G>A maps to NM_015689.3 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr1:115161025 C>T maps to ENST00000393274 K435K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:115147607 A>G maps to ENST00000393274 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:115130439 G>A maps to ENST00000393274 S855S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr1:115167888 T>C maps to ENST00000393274 E239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:115142865 G>A maps to ENST00000393274 L688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr1:115144802 G>A maps to ENST00000393274 S560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr1:115137162 G>A maps to ENST00000393274 Q788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:115147571 C>T maps to ENST00000393274 K546K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:115130448 G>A maps to ENST00000393274 F852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:115141951 G>A maps to ENST00000393274 F742F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:115166152 C>T maps to ENST00000393274 E306E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:111741361 C>T maps to NM_024901.3 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr8:142178403 C>T maps to NM_014957.2 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr8:142176348 G>A maps to NM_014957.2 K458K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:142154306 C>T maps to NM_014957.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr8:142202547 G>A maps to NM_014957.2 E1086E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:142160971 C>T maps to NM_014957.2 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:142161839 C>T maps to NM_014957.2 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:142176315 G>A maps to NM_014957.2 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:142151411 C>T maps to NM_014957.2 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr8:142188235 C>A maps to NM_014957.2 S846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr8:142199113 G>A maps to NM_014957.2 Q958Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:142146753 C>T maps to NM_014957.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr8:142161758 C>T maps to NM_014957.2 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr15:66021916 G>A maps to ENST00000443035 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr15:66048611 G>A maps to ENST00000443035 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr15:65994201 G>A maps to ENST00000443035 L819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr15:66021534 C>T maps to ENST00000443035 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr15:65988767 G>A maps to ENST00000443035 S1006S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr15:65962214 G>A maps to ENST00000443035 S1563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr15:65957040 G>A maps to ENST00000443035 V1793V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:153909203 C>T maps to NM_014856.2 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:153906755 G>A maps to NM_014856.2 S932S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:153912184 G>A maps to NM_014856.2 Q567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:153906739 G>A maps to NM_014856.2 Q938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:153906614 G>A maps to NM_014856.2 A979A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:153913882 G>A maps to NM_014856.2 F363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:153907326 C>T maps to NM_014856.2 R894R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:19316413 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr9:19361849 C>T maps to NM_017925.4 L1520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:19350782 C>T maps to NM_017925.4 I1182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr11:9171740 G>A maps to NM_015213.2 I874I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:9168651 C>A maps to NM_015213.2 E928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:9202334 T>C maps to NM_015213.2 R478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:9161241 G>A maps to NM_015213.2 S1280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr11:9225654 G>A maps to NM_015213.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:9164350 A>T maps to NM_015213.2 L1143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:9172243 G>A maps to NM_015213.2 S863S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:9187422 C>T maps to NM_015213.2 W748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr12:31577540 C>T maps to NM_144973.3 E773E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr12:31552615 T>G maps to NM_144973.3 R1014R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr12:31552616 G>A maps to NM_144973.3 V1013V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr12:31540607 G>A maps to NM_144973.3 R1252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr12:123238314 T>C maps to ENST00000455982 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr1:68947230 A>T maps to NM_001114120.1 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr1:68960117 G>A maps to NM_001114120.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr1:68943574 A>G maps to NM_001114120.1 D731D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:68947831 G>A maps to NM_001114120.1 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:100660800 C>T maps to ENST00000422147 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:100660749 G>A maps to ENST00000422147 N35N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:100649876 G>A maps to ENST00000422147 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr22:32200847 C>T maps to NM_001136029.1 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr22:32275613 C>T maps to NM_001136029.1 L1294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr22:32194571 C>T maps to NM_001136029.1 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr22:32233066 C>T maps to NM_001136029.1 F751F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr22:32193654 C>T maps to NM_001136029.1 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:32275562 C>T maps to NM_001136029.1 F1277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:32275640 C>T maps to NM_001136029.1 L1303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:32302431 G>A maps to NM_001136029.1 L1578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr22:32202146 C>T maps to NM_001136029.1 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr22:32215149 C>A maps to NM_001136029.1 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr22:32302356 C>T maps to NM_001136029.1 A1553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:32233120 T>G maps to NM_001136029.1 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:32239699 C>T maps to NM_001136029.1 F892F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:32272247 C>T maps to NM_001136029.1 R1259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:32289577 C>T maps to NM_001136029.1 V1339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:32215146 T>A maps to NM_001136029.1 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr22:32218714 C>T maps to NM_001136029.1 S681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr8:121061852 C>T maps to NM_022783.2 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:121013893 C>T maps to NM_022783.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr11:33053930 G>A maps to NM_001077242.1 K348K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:33053942 C>T maps to NM_001077242.1 F352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr12:16111240 C>T maps to NM_015954.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:16109924 G>A maps to NM_015954.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr12:16111228 C>T maps to NM_015954.2 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr8:124054284 G>A maps to NM_024295.4 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr8:124031496 G>A maps to NM_024295.4 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:124033697 G>A maps to NM_024295.4 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:124034950 T>A maps to NM_024295.4 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:5378036 G>A maps to NM_016041.3 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr17:5388503 G>A maps to NM_016041.3 Y42Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:5383829 G>A maps to NM_016041.3 R134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:5383830 G>A maps to NM_016041.3 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr2:220286117 C>T maps to NM_001927.3 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:220285374 G>A maps to NM_001927.3 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:220284877 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:89056205 G>A maps to NM_017996.3 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr15:89074605 G>A maps to NM_017996.3 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr15:89074576 G>A maps to NM_017996.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:10521635 A>G maps to NM_004401.2 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:3800161 C>T maps to ENST00000430539 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr1:3786329 C>T maps to ENST00000430539 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:3786215 C>T maps to ENST00000430539 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr7:24747814 C>T maps to NM_001127453.1 Q307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr7:24789246 G>T maps to NM_001127453.1 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:24742399 G>A maps to NM_001127453.1 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:24758683 G>A maps to NM_001127453.1 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr7:24747847 G>A maps to NM_001127453.1 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr9:117186685 C>T maps to NM_015404.3 E448E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:117168926 G>A maps to NM_015404.3 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr9:117240937 G>A maps to NM_015404.3 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr9:117185659 G>A maps to NM_015404.3 V520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:117169088 G>A maps to NM_015404.3 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr9:117168911 G>A maps to NM_015404.3 S653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr9:117228673 T>A did not map to a codon.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr9:117168830 G>A maps to NM_015404.3 F680F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZH-06A-11D-A197-08 chr9:117266601 C>T maps to NM_015404.3 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:117188501 C>T maps to NM_015404.3 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:179325826 C>T maps to NM_001042702.3 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr2:179318186 G>A maps to NM_001042702.3 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:145540342 A>G maps to NM_012079.4 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:145540554 T>A maps to NM_012079.4 R424R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr8:145542016 G>A maps to NM_012079.4 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:75501755 C>T maps to NM_032564.3 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:75508275 C>T maps to NM_032564.3 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr11:75509400 C>T maps to NM_032564.3 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:75495678 C>T maps to NM_032564.3 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:75501773 C>T maps to NM_032564.3 Q143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:75509331 C>T maps to NM_032564.3 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr23:69420274 G>A did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:69424329 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr23:69424191 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:69420264 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:69419701 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:69424822 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:69421837 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:69424320 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr23:69419695 C>T did not map to a codon.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr23:69424191 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:69424275 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:69419660 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:69420298 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5KH-06A-11D-A27K-08 chr22:19125791 C>G maps to NM_022719.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:19130257 G>A maps to NM_022719.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr22:19125788 G>A maps to NM_022719.2 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr22:19124868 G>A maps to NM_022719.2 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr22:19127224 G>A maps to NM_022719.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr22:19127495 G>A maps to NM_022719.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr22:19035968 G>A maps to NM_005137.2 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr22:19055730 G>C maps to NM_005137.2 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr22:19036103 G>A maps to NM_005137.2 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr22:19052575 G>A maps to NM_005137.2 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:19076955 G>A maps to NM_005137.2 Q43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr22:19035968 G>A maps to NM_005137.2 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:18897763 G>A maps to NM_005675.4 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr22:20096480 C>T maps to NM_022720.6 I731I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:20079123 T>C maps to NM_022720.6 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:20073938 C>T maps to NM_022720.6 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:20074196 C>T maps to NM_022720.6 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr22:20074157 C>T maps to NM_022720.6 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr22:20077222 C>G maps to NM_022720.6 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr12:56334204 G>A maps to NM_201554.1 W302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:56346938 C>T maps to NM_201554.1 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:56346857 G>A maps to NM_201554.1 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:56334724 C>T maps to NM_201554.1 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:56345461 G>A maps to NM_201554.1 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:56347172 C>T maps to NM_201554.1 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr7:14613938 G>A maps to NM_004080.2 I557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:14378230 C>T maps to NM_004080.2 K678K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:14613938 G>A maps to NM_004080.2 I557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr7:14613890 C>T maps to NM_004080.2 E573E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:14647117 G>A maps to NM_004080.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:14613860 G>A maps to NM_004080.2 I583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:14613938 G>A maps to NM_004080.2 I557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:14620485 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr7:14613967 G>A maps to NM_004080.2 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:14613938 G>A maps to NM_004080.2 I557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr7:14517793 G>A maps to NM_004080.2 F610F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:234367000 C>T maps to NM_152879.2 A884A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:234355426 C>T maps to NM_152879.2 F468F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:234360640 C>T maps to NM_152879.2 P733P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A2GH-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr2:234360704 C>T maps to ENST00000430834 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr2:234367007 C>T maps to NM_152879.2 R887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:234356785 C>T maps to NM_152879.2 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:234368862 C>T maps to NM_152879.2 S951S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:234357777 C>T maps to NM_152879.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr2:234344551 C>T maps to NM_152879.2 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr17:54940013 G>A maps to NM_003647.2 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr17:54939585 C>T maps to NM_003647.2 R500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:54912182 G>C maps to NM_003647.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:54923091 C>T maps to NM_003647.2 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr17:54940013 G>A maps to NM_003647.2 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:54925354 C>T maps to NM_003647.2 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:54925374 G>A maps to NM_003647.2 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:185997654 C>T maps to NM_001346.2 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr3:185993420 G>A maps to NM_001346.2 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:186015886 C>T maps to NM_001346.2 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:185867923 C>T maps to NM_001346.2 K777K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:185975697 G>A maps to NM_001346.2 F485F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:185983041 G>A maps to NM_001346.2 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:186038224 G>A maps to NM_001346.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr3:186006598 G>A maps to NM_001346.2 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:185997693 G>A maps to NM_001346.2 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr13:42783483 C>T maps to NM_178009.2 I911I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr13:42763383 C>T maps to NM_178009.2 I617I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr13:42733441 A>T maps to NM_178009.2 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr13:42729876 C>T maps to NM_178009.2 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr13:42763257 C>T maps to NM_178009.2 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr13:42752275 G>A maps to NM_178009.2 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:137304590 G>A maps to NM_004717.2 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:137255923 A>G maps to NM_004717.2 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:137080406 C>A maps to NM_004717.2 R1006R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:137263038 G>A maps to NM_004717.2 R559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr7:137237206 C>T maps to NM_004717.2 R685R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:137284622 C>T maps to NM_004717.2 W399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr7:137237233 G>A maps to NM_004717.2 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr7:137263038 G>A maps to NM_004717.2 R559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:137080382 C>T maps to NM_004717.2 L1014L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr7:137271944 G>A maps to NM_004717.2 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr7:137339506 G>A maps to NM_004717.2 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr7:137237173 C>T maps to NM_004717.2 R696R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr7:137271862 G>A maps to NM_004717.2 R469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:137304578 C>T maps to NM_004717.2 K328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:137374654 C>T maps to NM_004717.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr7:137263038 G>A maps to NM_004717.2 R559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr7:137304632 G>A maps to NM_004717.2 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:50129461 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:50121157 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:50119761 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:50127734 T>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:50131543 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:50134556 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:50119820 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr23:50163488 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:50133403 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:50167290 A>G did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:50111970 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr23:50119859 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:50119874 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:50131543 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:50134467 C>A did not map to a codon.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr23:50129462 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:50146128 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:50127722 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr23:50111994 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:50136220 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:50146155 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr23:50163488 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:50114814 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:50130632 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr23:50163468 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:50144127 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:50147110 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:50163488 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr23:50121161 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:50119068 T>C did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:50129458 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr4:959281 G>A maps to NM_001347.2 Q539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr4:961363 G>A maps to NM_001347.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr4:960962 G>A maps to NM_001347.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr4:954931 G>A maps to NM_001347.2 R878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr11:46392867 C>T maps to NM_001105540.1 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:46400028 C>T maps to NM_001105540.1 A987A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:46397924 C>T maps to NM_001105540.1 S901S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr11:46395973 C>T maps to NM_001105540.1 S665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr11:46393074 C>T maps to NM_001105540.1 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:74177717 C>T maps to NM_080916.1 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:74185844 C>T maps to NM_080916.1 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:55340858 G>A maps to NM_014762.3 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr11:71152463 G>A maps to NM_001360.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:71155080 C>T maps to NM_001360.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:71150110 G>A maps to NM_001360.2 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:71146477 C>T maps to NM_001360.2 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:71152364 G>A maps to NM_001360.2 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr11:71146729 C>T maps to NM_001360.2 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:71153327 C>T maps to NM_001360.2 E131E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr11:71152364 G>A maps to NM_001360.2 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr1:26769250 C>T maps to NM_024887.2 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr1:26769251 C>T maps to NM_024887.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:49442758 C>T maps to NM_014475.3 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr10:99359852 G>A maps to NM_138413.3 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr10:99359855 C>T maps to NM_138413.3 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr3:93780184 G>A maps to NM_001195643.1 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr3:93780295 G>A maps to NM_001195643.1 N20N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:49484962 G>A maps to NM_021044.2 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:49483722 G>A maps to NM_021044.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:72057475 C>T maps to NM_001361.3 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr19:12790529 G>A maps to NM_001930.2 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr19:12791115 C>T maps to NM_001930.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr17:34956104 C>T maps to NM_024308.3 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr17:34956602 C>T maps to NM_024308.3 Q252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr17:34951504 C>T maps to NM_024308.3 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr13:52373719 C>A maps to NM_001031719.1 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr17:27225770 G>A maps to NM_144683.3 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:27228607 G>A maps to NM_144683.3 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr14:24109097 G>A maps to NM_182908.4 W138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr14:24108420 G>A maps to NM_182908.4 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:24108412 C>T maps to NM_182908.4 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:24114077 C>T maps to NM_182908.4 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:24108540 G>A maps to NM_182908.4 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:12628377 C>T maps to NM_004753.4 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:12639419 C>T maps to NM_004753.4 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr1:12639359 G>A maps to NM_004753.4 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:12628404 G>C maps to NM_004753.4 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12638969 G>A maps to NM_004753.4 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12677179 G>A maps to NM_004753.4 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:12639389 C>T maps to NM_004753.4 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:12639398 G>A maps to NM_004753.4 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:24424252 C>T maps to NM_021004.2 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr14:24517981 C>T maps to NM_001082488.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:60620751 A>G maps to NM_016029.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:21086926 C>T maps to NM_015510.3 Y110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:21094339 G>A maps to NM_015510.3 K284K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr17:9676087 C>T maps to ENST00000330255 W242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr17:9675002 C>T maps to ENST00000330255 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:9674858 G>A maps to ENST00000330255 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr17:9680537 C>T maps to ENST00000330255 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr17:9683184 C>T maps to ENST00000330255 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr17:9694526 C>T maps to ENST00000330255 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:9680576 C>T maps to ENST00000330255 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:2343328 A>C did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:2343329 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:2139169 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:2209607 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:2184887 C>A did not map to a codon.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr23:2343290 A>C did not map to a codon.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr23:2139244 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:12129676 C>T maps to NM_018706.5 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:12162787 C>T maps to NM_018706.5 L887L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:12139836 C>T maps to NM_018706.5 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:12143137 C>T maps to NM_018706.5 I618I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr10:12149947 C>T maps to NM_018706.5 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr10:12142223 C>G maps to NM_018706.5 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr10:12160759 C>T maps to NM_018706.5 L805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:24534618 G>C maps to NM_001358.2 S656S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:24543555 A>G maps to NM_001358.2 R475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr6:30627937 G>A maps to NM_003587.4 F542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr6:30632958 G>A maps to NM_003587.4 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr6:30632943 G>A maps to NM_003587.4 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr6:30630408 A>G maps to NM_003587.4 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr6:30627338 G>A maps to NM_003587.4 I639I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:30633411 G>A maps to NM_003587.4 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr5:54593124 G>A maps to NM_019030.2 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr5:54566424 G>A maps to NM_019030.2 R992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr5:54552318 G>A maps to NM_019030.2 N1369N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:54577319 G>A maps to NM_019030.2 I663I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr5:54577306 G>A maps to NM_019030.2 R668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:54579185 G>A maps to NM_019030.2 Q604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr3:47882443 C>T maps to NM_138615.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:47887899 C>T maps to NM_138615.2 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:47887311 C>T maps to NM_138615.2 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:47887830 G>C maps to NM_138615.2 R423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr10:127548266 G>A maps to NM_018180.2 Q252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr17:5347749 G>A maps to ENST00000457531 A692A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:5359379 G>A maps to ENST00000457531 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:5364306 C>T maps to ENST00000457531 Q326Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:5353684 G>A maps to ENST00000457531 I581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:5353594 G>A maps to ENST00000457531 F611F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:47880399 C>T maps to NM_014681.5 F881F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr19:47879314 C>T maps to NM_014681.5 V814V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:47885321 C>T maps to NM_014681.5 F1128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:47856916 C>T maps to NM_014681.5 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:47856688 C>T maps to NM_014681.5 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:47865835 C>T maps to NM_014681.5 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:47885321 C>T maps to NM_014681.5 F1128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr19:47856775 C>T maps to NM_014681.5 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr19:47858351 C>T maps to NM_014681.5 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr20:37634886 C>A maps to NM_021931.3 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr20:37632433 C>T maps to NM_021931.3 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:37653907 C>T maps to NM_021931.3 F569F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr20:37631465 C>T maps to NM_021931.3 H269H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr20:37653907 C>T maps to NM_021931.3 F569F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr20:37650493 C>T maps to NM_021931.3 G503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:37634982 T>C maps to NM_021931.3 C402C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr3:154027597 T>C maps to NM_020865.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:154042036 G>A maps to NM_020865.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr12:125457054 G>A maps to NM_032656.3 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr12:125465047 G>A maps to NM_032656.3 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr12:125438542 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:125461958 G>A maps to NM_032656.3 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr12:125460022 G>A maps to NM_032656.3 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr12:125453414 T>A maps to NM_032656.3 K431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr12:125432362 G>C maps to NM_032656.3 P1153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:72132921 C>T maps to NM_014003.3 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:72142232 C>T maps to NM_014003.3 S1024S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:57650550 C>T maps to NM_024612.4 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:57676817 C>T maps to NM_024612.4 R594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr17:57665344 C>T maps to NM_024612.4 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr17:57644042 G>A maps to NM_024612.4 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:57650524 C>T maps to NM_024612.4 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:57682818 G>T maps to NM_024612.4 E662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:57679905 C>T maps to NM_024612.4 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr2:39046274 C>T maps to NM_198963.1 W1101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr2:39055482 G>A maps to NM_198963.1 R880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:39088660 T>C maps to NM_198963.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:39082212 A>G maps to NM_198963.1 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:39090549 T>C maps to NM_198963.1 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:39033709 C>T maps to NM_198963.1 V1269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:39053683 G>A maps to NM_198963.1 I929I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:39029994 G>A maps to NM_198963.1 F1293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:39085889 C>T maps to NM_198963.1 K500K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:39088945 G>A maps to NM_198963.1 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:39033766 A>T maps to NM_198963.1 A1250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr2:39088479 G>A maps to NM_198963.1 R358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:39050236 G>T maps to NM_198963.1 P1063P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:39085813 G>A maps to NM_198963.1 R526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:39050182 C>T maps to NM_198963.1 L1081L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:40255813 G>A maps to NM_024119.2 I522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr17:41599483 C>T maps to NM_004941.1 F1111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:41569585 G>A maps to NM_004941.1 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:41599555 C>T maps to NM_004941.1 I1135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:41585812 C>T maps to NM_004941.1 I809I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:182847206 C>T maps to NM_001357.4 T750T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:182845261 A>G maps to NM_001357.4 E631E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:182853891 C>T maps to NM_001357.4 I1135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:182856421 C>T maps to NM_001357.4 S1222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:182845606 C>T maps to NM_001357.4 P685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:182852337 C>T maps to NM_001357.4 S993S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr12:122693122 G>A maps to NM_019887.4 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:122702926 G>A maps to NM_019887.4 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr5:140909189 G>A maps to ENST00000398557 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:140903737 T>C maps to ENST00000398557 A1211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:140896444 G>A maps to ENST00000398557 A1264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr5:140954565 G>A maps to ENST00000398557 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:140951529 G>A maps to ENST00000398557 F812F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:140908357 G>A maps to ENST00000398557 L977L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:140908358 G>A maps to ENST00000398557 L976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:96212902 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:96369744 A>G did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:96192234 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:96354748 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:96212845 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:96213035 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:96185812 C>G did not map to a codon.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr23:96213114 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr23:96136644 C>T did not map to a codon.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr23:96369878 A>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:96502836 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:96213025 C>T did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:96724731 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr13:60240756 G>A maps to NM_001042517.1 P1181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:60548484 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr13:60240801 C>T maps to NM_001042517.1 K1166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr13:60566233 G>A maps to NM_001042517.1 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr13:60582690 G>T maps to NM_001042517.1 S334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr14:95582789 C>T maps to NM_177438.2 K584K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:95570393 G>A maps to NM_177438.2 S1113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:95596408 G>A maps to NM_177438.2 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr14:95573952 G>A maps to NM_177438.2 I932I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr14:95593074 G>A maps to NM_177438.2 Q249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr14:95583016 G>A maps to NM_177438.2 R509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr14:95584027 A>G maps to NM_177438.2 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr14:95556875 G>A maps to NM_177438.2 R1910*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:95570177 G>A maps to NM_177438.2 A1185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr14:95570078 G>A maps to NM_177438.2 S1218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr20:61537179 G>A maps to NM_022105.4 I549I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:61542876 G>A maps to NM_033081.2 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr20:61513263 G>A maps to NM_033081.2 T1348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr20:61542876 G>A maps to NM_033081.2 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr20:61537179 G>A maps to NM_022105.4 I549I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:61511757 C>T maps to NM_033081.2 G1850G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:61512324 G>A maps to NM_033081.2 P1661P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:61542778 C>T maps to NM_033081.2 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:61542307 G>A maps to NM_033081.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr20:61512939 G>A maps to NM_033081.2 S1456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:61511763 G>A maps to NM_033081.2 P1848P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:61525226 G>A maps to NM_033081.2 S964S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:61511406 G>A maps to NM_033081.2 F1967F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:61511322 G>A maps to NM_033081.2 S1995S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr20:61528166 G>A maps to NM_033081.2 F590F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr20:61513425 C>G maps to NM_033081.2 A1294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr20:61528271 G>A maps to NM_033081.2 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr20:61528238 G>A maps to NM_033081.2 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:61513218 G>A maps to NM_033081.2 I1363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:54360101 C>T maps to NM_000792.5 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:54360020 G>A maps to NM_000792.5 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:54370351 G>A maps to NM_000792.5 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr14:80669067 G>A maps to NM_001007023.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:80669139 A>G maps to NM_001007023.2 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:80669340 C>T maps to NM_001007023.2 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr14:80669400 G>A maps to NM_001007023.2 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:80669427 G>A maps to NM_001007023.2 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr14:80669067 G>A maps to NM_001007023.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr14:102028735 C>T maps to NM_001362.3 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr14:102028606 C>T maps to NM_001362.3 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:102027847 C>T maps to NM_001362.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:102028225 G>A maps to NM_001362.3 E131E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:102028018 C>T maps to NM_001362.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr21:47971643 C>T maps to ENST00000318711 D980D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr21:47918537 C>T maps to ENST00000318711 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr21:47961708 C>T maps to ENST00000318711 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr21:47969773 C>T maps to ENST00000318711 F872F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr21:47959799 C>T maps to ENST00000318711 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr21:47977513 C>T maps to ENST00000318711 Q1217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr21:47985696 C>T maps to ENST00000318711 D1413D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr21:47971610 C>T maps to ENST00000318711 S969S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr21:47969774 C>T maps to ENST00000318711 Q873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr12:51079695 A>G maps to NM_173602.2 K466K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:51086730 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr12:51069146 C>T maps to NM_173602.2 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr12:51130859 C>T maps to NM_173602.2 T1381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr12:51128912 G>A maps to NM_173602.2 K1367K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr12:51126159 C>T maps to NM_173602.2 I1274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr12:51108323 C>T maps to NM_173602.2 L932L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:51100334 C>T maps to NM_173602.2 F807F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:51122404 C>T maps to NM_173602.2 I1195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:329245 G>A maps to NM_014974.2 F1420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr10:409148 G>A maps to NM_014974.2 S860S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:408427 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:409159 G>A maps to NM_014974.2 Q857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:465053 G>A maps to NM_014974.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:395334 G>C maps to NM_014974.2 A1015A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:409159 G>A maps to NM_014974.2 Q857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr10:486817 G>A maps to NM_014974.2 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr10:735476 C>T maps to NM_014974.2 E14E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:409208 G>A maps to NM_014974.2 I840I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:410450 G>A maps to NM_014974.2 F780F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr10:436311 A>G maps to NM_014974.2 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr19:2717366 G>A maps to NM_145173.3 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr19:2717723 G>A maps to NM_145173.3 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:2717324 G>A maps to NM_145173.3 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:2717668 G>A maps to NM_145173.3 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr9:93375782 C>T maps to NM_017594.3 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:93375884 G>A maps to NM_017594.3 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr9:93375668 G>A maps to NM_017594.3 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr9:93375575 G>A maps to NM_017594.3 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:93375782 C>T maps to NM_017594.3 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr9:93375545 C>T maps to NM_017594.3 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:68512857 C>T maps to NM_004675.2 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:68512701 C>T maps to NM_004675.2 K93K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:68512383 C>T maps to NM_004675.2 K199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:68512781 G>A maps to NM_004675.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:68512545 G>A maps to NM_004675.2 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:68512953 C>T maps to NM_004675.2 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:189599362 C>T maps to NM_052952.2 W95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr3:122598218 C>A maps to NM_032839.2 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:122591289 G>C maps to NM_032839.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:122525734 C>T maps to NM_032839.2 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr13:73334726 G>A maps to NM_014953.3 I911I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr13:73335650 G>A maps to NM_014953.3 F840F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr2:233194675 C>T maps to NM_152383.4 P631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr2:232952408 C>T maps to NM_152383.4 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr2:233001211 C>T maps to NM_152383.4 R245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:233198569 G>A maps to NM_152383.4 S677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr2:233001423 C>T maps to NM_152383.4 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:233201318 C>T maps to NM_152383.4 P879P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:233201319 G>T maps to NM_152383.4 E880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:233028321 C>T maps to NM_152383.4 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr1:231830097 C>T maps to NM_001164537.1 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:231906691 C>T maps to NM_001164537.1 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:231906696 C>T maps to NM_001164537.1 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:231954090 G>A maps to NM_001164537.1 T635T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr1:223116275 C>A maps to NM_032890.2 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:223175965 C>T maps to NM_032890.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr1:223176193 C>T maps to NM_032890.2 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:223178083 C>T maps to NM_032890.2 I1115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr1:223177153 G>A maps to NM_032890.2 K805K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:223177378 C>T maps to NM_032890.2 P880P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr1:223178734 C>T maps to NM_032890.2 I1332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:223177294 C>T maps to NM_032890.2 F852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:223178530 C>T maps to NM_032890.2 F1264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:223168256 C>A maps to NM_032890.2 S307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr1:223177255 C>T maps to NM_032890.2 F839F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr1:223176829 C>T maps to NM_032890.2 A697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr15:40657470 C>T maps to NM_033510.1 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr15:40655876 C>T maps to NM_033510.1 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:40661288 C>T maps to NM_033510.1 S992S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr15:40659788 C>T maps to NM_033510.1 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr15:40661933 C>T maps to NM_033510.1 P1207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:40660823 C>T maps to NM_033510.1 F837F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr15:40657832 G>A maps to NM_033510.1 K284K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:40662158 C>T maps to NM_033510.1 F1282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr15:40662090 C>T maps to NM_033510.1 L1260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:111863712 C>T maps to NM_001037954.2 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:111887484 G>A maps to NM_001037954.2 R608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:111889717 G>A maps to NM_001037954.2 G669G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:154001511 T>G did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:153995641 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:153995568 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:153997501 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr11:65546385 C>T maps to NM_138368.3 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:65545599 G>A maps to NM_138368.3 S731S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr11:65547164 G>A maps to NM_138368.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:54074331 C>T maps to NM_012242.2 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:107845206 G>A maps to NM_014421.2 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr4:107845813 G>A maps to NM_014421.2 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:107845206 G>A maps to NM_014421.2 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr4:107846994 G>A maps to NM_014421.2 R112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:107845188 C>T maps to NM_014421.2 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:107845750 C>T maps to NM_014421.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:107845143 G>A maps to NM_014421.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr4:107845782 G>A maps to NM_014421.2 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:12029958 C>T maps to ENST00000450094 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:11987474 C>T maps to ENST00000450094 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr8:42231803 C>T maps to NM_014420.2 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr8:42234551 G>A maps to NM_014420.2 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:49878086 G>A maps to NM_014419.3 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr19:49867984 C>T maps to NM_014419.3 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr19:49878173 G>A maps to NM_014419.3 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:111914232 T>C maps to NM_001931.4 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:111915932 C>T maps to NM_001931.4 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr11:111896989 G>A maps to NM_001931.4 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:111896273 G>A maps to NM_001931.4 Q26Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr8:12957028 C>T maps to NM_182643.2 S939S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr8:13162804 G>A maps to NM_182643.2 Q441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr8:12957133 G>A maps to NM_182643.2 P904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr8:13357559 C>T maps to NM_182643.2 K7K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr8:12973119 G>A maps to NM_182643.2 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr8:12958027 G>A maps to NM_182643.2 H606H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr3:38158037 G>A maps to NM_007335.2 R1317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr3:38103859 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:38104269 C>T maps to NM_007335.2 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr3:38149957 C>T maps to NM_007335.2 G1027G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:38141856 C>T maps to NM_007335.2 A935A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr3:38135150 G>A maps to NM_007335.2 Q604Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:38149936 C>T maps to NM_007335.2 S1020S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr3:38158037 G>A maps to NM_007335.2 R1317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr3:38087059 G>A maps to NM_007335.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:38157947 C>T maps to NM_007335.2 I1287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr3:38101311 C>A maps to NM_007335.2 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38103774 C>T maps to NM_007335.2 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38141866 C>T maps to NM_007335.2 Q939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:38149907 C>T maps to NM_007335.2 Q1011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:38134315 G>A maps to NM_007335.2 E567E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr13:51417401 C>T maps to ENST00000504404 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr3:197009612 G>A maps to NM_004087.2 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr3:196921403 G>A maps to NM_004087.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr11:83243756 C>T maps to NM_001142699.1 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:83195190 C>T maps to NM_001142699.1 Q758Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr11:84996409 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:84245708 T>C maps to NM_001142699.1 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:83497757 C>T maps to NM_001142699.1 T600T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:83497757 C>T maps to NM_001142699.1 T600T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:83182696 G>A maps to NM_001142699.1 F806F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr11:83810090 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:84996305 G>A maps to NM_001142699.1 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr11:83497757 C>T maps to NM_001142699.1 T600T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:84634156 G>A maps to NM_001364.3 F2F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr23:69719868 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr23:69674134 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:69669257 A>C did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:69665392 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:69669617 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:69722077 T>C did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:69669254 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:69669637 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:69699101 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:69718371 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:69719812 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr17:7096425 C>T maps to NM_001365.3 R611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:7095231 G>A maps to NM_001365.3 P695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:7095249 G>A maps to NM_001365.3 I689I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:7107048 G>A maps to NM_001365.3 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:7100081 G>A maps to NM_001365.3 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr17:7097292 A>C maps to NM_001365.3 L545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:7095249 G>A maps to NM_001365.3 I689I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr17:7111498 G>A maps to NM_001365.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr10:79566600 G>A maps to NM_004747.3 Q1628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr10:79565429 G>A maps to NM_004747.3 L1719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:79572008 G>A maps to NM_004747.3 H1384H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:79570961 G>A maps to NM_004747.3 S1451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:79590510 G>A maps to NM_004747.3 F623F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:79603325 G>A maps to NM_004747.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr10:79581145 G>C maps to NM_004747.3 S1032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:79566544 G>A maps to NM_004747.3 I1646I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:79571761 G>A maps to NM_004747.3 I1414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:79579740 G>A maps to NM_004747.3 S1146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:79565591 G>A maps to NM_004747.3 L1665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:79570913 G>A maps to NM_004747.3 I1467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:79589263 G>A maps to NM_004747.3 I678I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:79572068 G>A maps to NM_004747.3 I1364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:79579212 G>A maps to NM_004747.3 P1179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:79554635 G>A maps to NM_004747.3 F1839F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr18:3581881 G>A maps to NM_004746.2 I652I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr18:3729133 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr18:3879492 C>T maps to NM_004746.2 K192K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr18:3879231 C>T maps to NM_004746.2 W279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr18:3879232 C>T maps to NM_004746.2 W279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr18:3534282 G>A maps to NM_004746.2 F796F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr18:3814213 G>A maps to NM_004746.2 C339C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr18:3742508 G>A maps to NM_004746.2 I392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:3581926 C>T maps to NM_004746.2 E637E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:3879423 G>A maps to NM_004746.2 Y215Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:3879861 G>A maps to NM_004746.2 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr8:1626556 G>A maps to ENST00000357934 R764R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr8:1581003 G>A maps to ENST00000357934 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr8:1624769 G>A maps to ENST00000357934 V700V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr8:1624743 G>T maps to ENST00000357934 E692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr8:1639758 C>T maps to ENST00000357934 F863F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:1497491 C>T maps to ENST00000357934 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr8:1649496 C>T maps to ENST00000357934 S973S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:1497107 G>A maps to ENST00000357934 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:1616561 G>A maps to ENST00000357934 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:1626439 G>A maps to ENST00000357934 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:1497182 C>T maps to ENST00000357934 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr8:1649496 C>T maps to ENST00000357934 S973S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr8:1581130 C>T maps to ENST00000357934 Q519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZU-06A-12D-A196-08 chr8:1624757 C>T maps to ENST00000357934 V696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZY-06A-11D-A197-08 chr8:1497674 G>A maps to ENST00000357934 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:1497305 C>T maps to ENST00000357934 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:1513856 G>A maps to ENST00000357934 Q355Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr8:1616834 C>T maps to ENST00000357934 I659I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr1:35365832 C>T maps to NM_001080418.1 K383K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:35351345 C>T maps to NM_001080418.1 Q549Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:35334368 C>T maps to NM_001080418.1 W774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:35365326 G>A maps to NM_001080418.1 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:35351750 G>A maps to NM_001080418.1 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:35351751 G>A maps to NM_001080418.1 I507I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:35334584 G>A maps to NM_001080418.1 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:35370261 C>T maps to NM_001080418.1 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:35331758 G>A maps to NM_001080418.1 S955S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:35333168 G>A maps to NM_001080418.1 Q849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:35370291 G>A maps to NM_001080418.1 H231H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:35370480 G>A maps to NM_001080418.1 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:35332720 G>A maps to NM_001080418.1 I883I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:35331758 G>A maps to NM_001080418.1 S955S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr20:35155349 G>A maps to ENST00000339266 R965R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:35128790 C>T maps to ENST00000339266 S763S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr20:35060251 C>T maps to ENST00000339266 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:35061004 C>T maps to ENST00000339266 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr20:35060740 C>T maps to ENST00000339266 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr20:35060257 C>T maps to ENST00000339266 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr20:35060380 C>T maps to ENST00000339266 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr14:55637459 G>A maps to NM_014750.4 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr14:55637495 G>A maps to NM_014750.4 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:101201151 G>A maps to NM_003836.5 E357E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:101200536 C>T maps to NM_003836.5 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr14:101201187 C>T maps to NM_003836.5 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr6:43418789 C>T maps to NM_206539.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr6:43418615 C>T maps to NM_206539.1 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:43418633 C>T maps to NM_206539.1 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr6:170592530 G>A maps to NM_005618.3 I612I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:39994873 C>T maps to NM_016941.3 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44R-06A-41D-A25O-08 chr19:39994709 G>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr19:39998571 C>T maps to NM_016941.3 F592F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:39994873 C>T maps to NM_016941.3 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr15:41229023 G>A maps to NM_019074.3 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:41228856 C>T maps to NM_019074.3 R558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr15:41228900 G>A maps to NM_019074.3 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:41228588 C>T maps to NM_019074.3 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:41223734 C>T maps to NM_019074.3 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:41229657 G>A maps to NM_019074.3 R662R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr15:41227211 G>A maps to NM_019074.3 E379E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr15:41222068 C>T maps to NM_019074.3 Q31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr14:75357820 G>C maps to NM_001933.4 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr14:75365132 C>T maps to NM_001933.4 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:172952912 C>T maps to NM_178120.4 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr2:172966255 C>T maps to NM_004405.3 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:172966261 G>A maps to NM_004405.3 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:48072064 C>A maps to NM_005220.2 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:48050404 C>T maps to NM_001934.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:48050470 C>T maps to NM_138281.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr7:96651667 G>A maps to NM_005221.5 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:96637040 C>T maps to NM_005222.3 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:96639301 T>G maps to NM_005222.3 Y275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr7:96635339 C>T maps to NM_005222.3 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr10:124402871 C>T maps to ENST00000368915 I2529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr10:124350196 G>A maps to ENST00000368915 S708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr10:124339121 G>A maps to ENST00000368915 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr10:124392773 G>A maps to ENST00000368915 G2155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr10:124395579 C>T maps to ENST00000368915 R2208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr10:124350190 C>T maps to ENST00000368915 S706S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr10:124395626 C>T maps to ENST00000368915 F2223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:124399729 C>T maps to ENST00000368915 Q2373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:124339143 C>T maps to ENST00000368915 R244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr10:124399761 C>T maps to ENST00000368915 D2383D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr10:124399587 C>T maps to ENST00000368915 F2325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:124402817 G>A maps to ENST00000368915 S2511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr10:124358537 C>T maps to ENST00000368915 L1069L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:124399740 A>G maps to ENST00000368915 E2376E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:124358449 C>T maps to ENST00000368915 A1039A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:124345822 C>T maps to ENST00000368915 Y569Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:124345823 T>C maps to ENST00000368915 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:124395545 C>T maps to ENST00000368915 F2196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr10:124395545 C>T maps to ENST00000368915 F2196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:124335981 C>T maps to ENST00000368915 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:124335982 C>T maps to ENST00000368915 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:124390642 C>T maps to ENST00000368915 A2064A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:124395545 C>T maps to ENST00000368915 F2196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:124389354 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:124390786 C>T maps to ENST00000368915 V2112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:124390603 G>A maps to ENST00000368915 V2051V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:124351992 C>T maps to ENST00000368915 P794P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr10:124390685 C>T maps to ENST00000368915 L2079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr10:124399764 G>A maps to ENST00000368915 V2384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr10:124402886 C>T maps to ENST00000368915 P2534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr10:124348526 C>T maps to ENST00000368915 V617V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr10:124380646 C>T maps to ENST00000368915 R1787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:124358542 G>A maps to ENST00000368915 W1070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:124389488 C>T maps to ENST00000368915 N1934N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr10:124380646 C>T maps to ENST00000368915 R1787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:124358398 G>A maps to ENST00000368915 W1022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:124377614 C>T maps to ENST00000368915 S1658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:124380825 G>A maps to ENST00000368915 W1846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr10:124390708 G>A maps to ENST00000368915 G2086G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:124361460 C>T maps to ENST00000368915 G1164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr10:124380663 C>G maps to ENST00000368915 T1792T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr10:124399743 C>T maps to ENST00000368915 V2377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr10:124358341 G>A maps to ENST00000368915 Q1003Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:124345585 C>T maps to ENST00000368915 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:124345684 G>A maps to ENST00000368915 W523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:124358350 G>A maps to ENST00000368915 V1006V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:124390561 G>A maps to ENST00000368915 G2037G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:124402856 C>T maps to ENST00000368915 V2524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:124402703 C>T maps to ENST00000368915 F2473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:124348469 C>T maps to ENST00000368915 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr10:124399827 G>A maps to ENST00000368915 V2405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:46977892 C>T maps to NM_147192.2 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:46978055 C>T maps to NM_147192.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:46976226 C>T maps to NM_147192.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:46976782 C>T maps to NM_147192.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr1:46976686 G>A maps to NM_147192.2 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:46976323 C>T maps to NM_147192.2 Q116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:46976843 C>T maps to NM_147192.2 Q196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr22:38934314 G>A maps to NM_007068.2 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr22:38934375 G>A maps to NM_007068.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr22:38934543 C>T maps to NM_007068.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr22:38917728 G>A maps to NM_007068.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr22:38934386 G>A maps to NM_007068.2 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:38962606 C>T maps to NM_007068.2 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:32834584 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:31227663 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:31227664 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:31893358 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:32364151 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:32404488 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:31947832 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:32235168 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:32328380 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr23:31514963 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:31792177 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:31697515 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr23:31462693 A>G did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr23:31462744 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:32382751 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:31152235 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:32563280 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:32472781 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:32536165 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:32867891 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:32407791 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:32632559 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:32519903 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:32834594 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:31341754 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:32472946 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:31222095 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:32328308 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:32380964 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:32305679 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:31227663 G>T did not map to a codon.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr23:32472870 C>T did not map to a codon.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr23:32509576 G>A did not map to a codon.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr23:32408204 G>A did not map to a codon.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr23:31196836 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr23:32429958 T>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:31462649 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:32662368 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZG-06A-11D-A197-08 chr23:32486763 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr23:31196840 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:31165472 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:31190523 T>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:31645816 T>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:31645818 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:31201000 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:31645924 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:31697608 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:32366634 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:32466745 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:32486706 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:32716074 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:32407760 G>A did not map to a codon.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr23:31200999 C>T did not map to a codon.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr23:31187622 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr5:78338221 C>T maps to NM_013391.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr5:78359495 C>T maps to NM_013391.2 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:78350117 C>T maps to NM_013391.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:78325773 C>T maps to NM_013391.2 G589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:78329200 C>T maps to NM_013391.2 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:78322273 C>T maps to NM_013391.2 E721E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:78328592 C>T maps to NM_013391.2 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr5:78326664 G>A maps to NM_013391.2 V558V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:36002315 G>A maps to NM_033317.4 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:36003653 A>G maps to NM_033317.4 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:36001154 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:88583343 G>A maps to NM_004407.3 E138E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr4:88583724 G>A maps to NM_004407.3 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr4:88583736 G>A maps to NM_004407.3 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:88584105 C>T maps to NM_004407.3 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr4:88584096 G>A maps to NM_004407.3 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:88584063 G>A maps to NM_004407.3 Q378Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr4:88584264 G>A maps to NM_004407.3 E445E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:46282617 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:46280936 G>A maps to NM_004409.3 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:46281005 G>A maps to NM_004409.3 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:46280716 G>A maps to NM_004409.3 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:46282605 G>A maps to NM_004409.3 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr19:46280656 G>A maps to NM_004409.3 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:46280936 G>A maps to NM_004409.3 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:46275919 C>T maps to NM_004409.3 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr9:894119 G>A maps to NM_021951.2 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:1057089 G>A maps to NM_181872.4 K501K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr9:1056912 G>A maps to NM_181872.4 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:990185 G>A maps to NM_021240.2 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:990287 C>T maps to NM_021240.2 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:990518 G>A maps to NM_021240.2 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:990275 C>T maps to NM_021240.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr9:990878 A>G maps to NM_021240.2 E431E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:990671 C>T maps to NM_021240.2 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:990473 G>A maps to NM_021240.2 E296E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr9:22451456 G>A maps to NM_022160.2 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr9:22451439 C>T maps to NM_022160.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr9:22447216 C>A maps to NM_022160.2 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:22451123 C>T maps to NM_022160.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:50885197 G>A maps to NM_032110.1 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr1:53925161 G>A maps to NM_033067.1 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr1:53927248 C>T maps to NM_033067.1 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:53927153 C>T maps to NM_033067.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:53930377 C>T maps to NM_033067.1 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:53925584 G>A maps to NM_033067.1 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:42353035 C>T maps to ENST00000427618 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:42351873 C>T maps to ENST00000427618 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:86820319 C>T maps to NM_021145.3 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:86817409 T>C maps to NM_021145.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr19:46289184 G>A maps to NM_004943.1 F523F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:46289451 C>T maps to NM_004943.1 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:46289280 G>A maps to NM_004943.1 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:46288920 G>A maps to NM_004943.1 F611F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:46289987 G>A maps to NM_004943.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr19:46288929 G>A maps to NM_004943.1 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:118500927 T>A maps to NM_005509.4 I1641I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:118484797 C>T maps to NM_005509.4 V1092V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr5:118513856 A>G maps to NM_005509.4 L2351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:118533520 C>T maps to NM_005509.4 R2539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr5:118450178 C>T maps to NM_005509.4 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr5:118450179 C>T maps to NM_005509.4 Q170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:118506065 C>T maps to NM_005509.4 T1860T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:118487696 C>T maps to NM_005509.4 S1556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr5:118485076 C>T maps to NM_005509.4 L1185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr15:51837932 T>A maps to NM_001174116.1 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr15:51783791 G>T maps to NM_001174116.1 R1646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr15:51829947 G>A maps to NM_001174116.1 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr15:51830431 A>G maps to NM_001174116.1 G441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr15:51757790 G>A maps to NM_001174116.1 F2526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr15:51791363 A>G maps to NM_001174116.1 L1353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr15:51773611 G>A maps to NM_001174116.1 C1897C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr15:51742484 G>A maps to NM_001174116.1 L2915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr15:51857295 C>T maps to NM_001174116.1 W118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:51830439 C>A maps to NM_001174116.1 E439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:51791009 G>A maps to NM_001174116.1 L1471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:51792132 A>T maps to NM_001174116.1 V1096V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:51773524 G>A maps to NM_001174116.1 F1926F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:51741365 G>A maps to NM_001174116.1 L2977L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr15:51772993 G>A maps to NM_001174116.1 S2103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr15:51763563 G>A maps to NM_001174116.1 H2416H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr15:51749619 G>A maps to NM_001174116.1 Q2727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr15:51790821 G>A maps to NM_001174116.1 F1533F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr15:51757772 C>T maps to NM_001174116.1 L2532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:51839475 G>A maps to NM_001174116.1 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr10:70225554 G>A maps to NM_001080449.1 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr10:70229751 G>A maps to NM_001080449.1 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr10:70178910 G>A maps to NM_001080449.1 I1035I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:70182599 G>A maps to NM_001080449.1 S838S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr10:70192194 G>A maps to NM_001080449.1 T659T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr3:52380753 C>T maps to ENST00000273600 V641V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:52403857 C>T maps to ENST00000273600 F1987F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr3:52404563 C>T maps to ENST00000273600 S2110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:52427425 C>T maps to ENST00000273600 L3581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr3:52417986 C>T maps to ENST00000273600 A2754A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr3:52433700 G>A maps to ENST00000273600 E4258E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:52422242 C>T maps to ENST00000273600 Q3022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr3:52422546 C>T maps to ENST00000273600 Y3095Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:52429346 C>T maps to ENST00000273600 F3728F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:52404798 T>C maps to ENST00000273600 S2161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr3:52366278 G>A maps to ENST00000273600 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr3:52412750 C>T maps to ENST00000273600 S2444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:52425238 C>T maps to ENST00000273600 D3326D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:52403980 C>T maps to ENST00000273600 P2028P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr3:52433083 G>A maps to ENST00000273600 W4167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:52407020 T>C maps to ENST00000273600 L2313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:52383327 C>T maps to ENST00000273600 F806F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr3:52394356 C>T maps to ENST00000273600 I1534I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr3:52428617 C>T maps to ENST00000273600 S3652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:52394074 C>T maps to ENST00000273600 F1517F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr3:52426492 C>T maps to ENST00000273600 Q3420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr3:52365206 C>T maps to ENST00000273600 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:52365243 C>T maps to ENST00000273600 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:52390703 C>T maps to ENST00000273600 I1256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:52395697 C>T maps to ENST00000273600 F1632F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:52384039 C>T maps to ENST00000273600 I854I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:52394377 C>T maps to ENST00000273600 F1541F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:52381848 G>A maps to ENST00000273600 K655K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr3:52422286 C>T maps to ENST00000273600 I3036I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:52398928 C>T maps to ENST00000273600 I1804I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:52422226 C>T maps to ENST00000273600 I3016I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr3:52416371 G>A maps to ENST00000273600 K2614K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:52433000 G>A maps to ENST00000273600 W4139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr3:52395224 T>C maps to ENST00000273600 G1577G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:52404139 C>T maps to ENST00000273600 F2051F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:52384570 C>T maps to ENST00000273600 F898F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:52387453 C>T maps to ENST00000273600 I1095I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:52382950 C>T maps to ENST00000273600 S718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:52395326 C>T maps to ENST00000273600 L1611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:52400879 G>A maps to ENST00000273600 E1914E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:52420784 C>T maps to ENST00000273600 T2973T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:52425319 C>T maps to ENST00000273600 A3353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr3:52402786 G>A maps to ENST00000273600 R1932R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr3:52416419 C>T maps to ENST00000273600 L2630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:52429460 C>T maps to ENST00000273600 A3766A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr12:124268612 C>T maps to NM_207437.3 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr12:124350536 C>T maps to NM_207437.3 R2244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr12:124358151 C>T maps to NM_207437.3 I2493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr12:124325996 G>A maps to NM_207437.3 V1637V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr12:124419270 C>T maps to NM_207437.3 I4409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr12:124419271 C>T maps to NM_207437.3 L4410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr12:124330278 G>A maps to NM_207437.3 R1713R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr12:124293343 G>A maps to NM_207437.3 K878K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr12:124332539 C>T maps to NM_207437.3 A1831A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:124323031 G>A maps to NM_207437.3 V1526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr12:124330679 G>A maps to NM_207437.3 R1813R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:124252198 T>C maps to NM_207437.3 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:124317791 T>G maps to NM_207437.3 T1441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:124298404 C>T maps to NM_207437.3 L1124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr12:124332554 C>T maps to NM_207437.3 T1836T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr12:124330287 C>T maps to NM_207437.3 H1716H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:124274640 G>A maps to NM_207437.3 V535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:124399055 C>T maps to NM_207437.3 F3393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:124267766 C>T maps to NM_207437.3 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr12:124289470 G>A maps to NM_207437.3 L839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:124297748 C>T maps to NM_207437.3 C943C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:124315152 C>T maps to NM_207437.3 T1366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:124352568 G>A maps to NM_207437.3 E2356E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:124270402 G>A maps to NM_207437.3 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:124298162 C>T maps to NM_207437.3 L1081L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:124363813 C>T maps to NM_207437.3 F2674F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:124415043 C>T maps to NM_207437.3 F4118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:124399400 G>A maps to NM_207437.3 W3408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr12:124317686 G>A maps to NM_207437.3 W1406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:124341781 C>T maps to NM_207437.3 V2088V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr12:124341692 C>T maps to NM_207437.3 L2059L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:124350588 G>A maps to NM_207437.3 W2261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:124285947 G>A maps to NM_207437.3 S743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:124305289 C>T maps to NM_207437.3 L1270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:124330206 G>A maps to NM_207437.3 W1689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:124350520 C>T maps to NM_207437.3 S2238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:124298347 C>T maps to NM_207437.3 L1105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:124257472 C>T maps to NM_207437.3 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:124330317 C>T maps to NM_207437.3 I1726I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:124377954 C>T maps to NM_207437.3 T2939T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:124411259 C>T maps to NM_207437.3 L3882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr12:124265688 T>G maps to NM_207437.3 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr12:124330296 C>T maps to NM_207437.3 I1719I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:124311421 G>A maps to NM_207437.3 L1338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:124333347 C>T maps to NM_207437.3 I1889I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:124341760 G>A maps to NM_207437.3 L2081L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:124383314 C>T maps to NM_207437.3 A3080A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr12:124323031 G>A maps to NM_207437.3 V1526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr12:124272419 C>T maps to NM_207437.3 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr12:124323232 C>T maps to NM_207437.3 I1593I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr12:124268492 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:124256170 G>T maps to NM_207437.3 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr12:124401077 C>T maps to NM_207437.3 F3481F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:124284800 G>A maps to NM_207437.3 R658R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr12:124268666 C>T maps to NM_207437.3 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:124323163 C>T maps to NM_207437.3 F1570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:124311370 G>A maps to NM_207437.3 L1321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:124333365 C>T maps to NM_207437.3 S1895S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:124345681 G>A maps to NM_207437.3 R2173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:124355018 C>T maps to NM_207437.3 F2424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:124360019 C>T maps to NM_207437.3 I2609I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:124371783 G>A maps to NM_207437.3 A2855A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr12:124272494 C>T maps to NM_207437.3 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:124364269 C>T maps to NM_207437.3 F2734F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:124387579 C>T maps to NM_207437.3 T3127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr12:124335559 C>T maps to NM_207437.3 I1958I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr12:124350589 G>A maps to NM_207437.3 W2261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:124323034 C>T maps to NM_207437.3 I1527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr12:124416201 C>T maps to NM_207437.3 I4194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr7:21920342 G>A maps to NM_003777.3 K4080K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr7:21789944 G>A maps to NM_003777.3 W2975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr7:21628921 G>A maps to NM_003777.3 W690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:21847522 C>T maps to NM_003777.3 S3403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr7:21892164 G>A maps to NM_003777.3 A3666A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:21727061 C>T maps to NM_003777.3 F1954F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr7:21940838 T>G maps to NM_003777.3 V4513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr7:21646281 C>T maps to NM_003777.3 F1261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr7:21912938 T>C maps to NM_003777.3 L4012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr7:21695475 C>T maps to NM_003777.3 F1662F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:21882167 C>T maps to NM_003777.3 I3573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:21654752 T>C maps to NM_003777.3 L1292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:21857903 G>A maps to NM_003777.3 T3553T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr7:21781627 C>T maps to NM_003777.3 F2673F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr7:21894069 G>A maps to NM_003777.3 L3740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:21641175 G>A maps to NM_003777.3 T1196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:21856131 G>A maps to NM_003777.3 T3467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr7:21856293 G>A maps to NM_003777.3 L3521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:21847501 G>A maps to NM_003777.3 K3396K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:21788348 C>T maps to NM_003777.3 Q2895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:21924012 C>T maps to NM_003777.3 F4171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:21598583 G>A maps to NM_003777.3 K220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:21695475 C>T maps to NM_003777.3 F1662F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:21775301 C>T maps to NM_003777.3 F2502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:21655873 G>T maps to NM_003777.3 V1353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:21906165 G>T maps to NM_003777.3 E3866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr7:21721169 C>T maps to NM_003777.3 Q1784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr7:21908506 C>T maps to NM_003777.3 D3962D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr7:21658815 G>A maps to NM_003777.3 A1456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:21737788 C>T maps to NM_003777.3 F2053F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr7:21934242 T>A maps to NM_003777.3 V4258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:21631029 G>A maps to NM_003777.3 V834V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:21631158 C>T maps to NM_003777.3 I877I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:21721261 C>T maps to NM_003777.3 A1814A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:21747440 G>A maps to NM_003777.3 W2231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:21789342 C>T maps to NM_003777.3 P2914P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:21789387 C>T maps to NM_003777.3 F2929F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr7:21658839 G>A maps to NM_003777.3 K1464K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:21640764 T>C maps to NM_003777.3 F1131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr7:21646060 G>A maps to NM_003777.3 W1222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr3:57488086 C>T maps to NM_178504.4 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:57488119 C>T maps to NM_178504.4 W391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:57494214 G>A maps to NM_178504.4 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr17:76457745 G>A maps to ENST00000389840 L3059L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr17:76511014 C>T maps to ENST00000389840 K1314K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr17:76430277 C>T maps to ENST00000389840 K4013K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr17:76472764 G>A maps to ENST00000389840 V2667V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:76503746 C>T maps to ENST00000389840 L1455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:76548869 C>T maps to ENST00000389840 K732K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr17:76503638 G>A maps to ENST00000389840 T1491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:76482353 G>A maps to ENST00000389840 F2337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr17:76455199 G>A maps to ENST00000389840 I3234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr17:76458970 C>T maps to ENST00000389840 E3029E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr17:76440867 C>T maps to ENST00000389840 E3768E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:76482446 C>T maps to ENST00000389840 T2306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr17:76497832 G>A maps to ENST00000389840 I1760I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:76455097 G>T maps to ENST00000389840 I3268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr17:76450747 G>A maps to ENST00000389840 L3390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr17:76490698 C>T maps to ENST00000389840 R2068R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:76525586 C>T maps to ENST00000389840 E1158E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr17:76455103 G>A maps to ENST00000389840 S3266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr17:76528650 C>T maps to ENST00000389840 G1009G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:76492063 G>A maps to ENST00000389840 F1918F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr17:76535914 C>T maps to ENST00000389840 K860K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:76533466 G>A maps to ENST00000389840 L925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:76456267 C>T maps to ENST00000389840 Q3123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:76482353 G>A maps to ENST00000389840 F2337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:76491046 C>T maps to ENST00000389840 S1998S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:76528618 C>T maps to ENST00000389840 W1020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:76567697 G>A maps to ENST00000389840 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:76471855 C>T maps to ENST00000389840 G2724G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:76526585 G>A maps to ENST00000389840 S1041S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:76566442 G>A maps to ENST00000389840 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:76503578 C>T maps to ENST00000389840 G1511G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:76528662 G>A maps to ENST00000389840 F1005F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:76464941 T>A maps to ENST00000389840 I2831I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:76437247 G>A maps to ENST00000389840 F3840F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr17:76525709 C>T maps to ENST00000389840 G1117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr17:76570812 C>T maps to ENST00000389840 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr17:76506585 C>T maps to ENST00000389840 V1368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr17:76548856 G>A maps to ENST00000389840 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:76475109 G>A maps to ENST00000389840 F2649F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:76506585 C>T maps to ENST00000389840 V1368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:76571058 C>T maps to ENST00000389840 W27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:76455199 G>A maps to ENST00000389840 I3234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:76455253 G>A maps to ENST00000389840 F3216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:76471437 G>A maps to ENST00000389840 S2797S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:76482353 G>A maps to ENST00000389840 F2337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:76511065 C>T maps to ENST00000389840 W1297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:76511083 G>A maps to ENST00000389840 D1291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:76525571 C>T maps to ENST00000389840 E1163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:76525745 G>A maps to ENST00000389840 V1105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:76570809 G>A maps to ENST00000389840 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:76491082 G>A maps to ENST00000389840 F1986F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:76498985 G>A maps to ENST00000389840 I1684I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr17:76568963 G>A maps to ENST00000389840 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:76548881 C>T maps to ENST00000389840 K728K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:76455265 G>A maps to ENST00000389840 F3212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr17:76557813 C>T maps to ENST00000389840 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:76481749 C>T maps to ENST00000389840 G2441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:76567791 G>A maps to ENST00000389840 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr17:76437280 C>T maps to ENST00000389840 K3829K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr17:76506498 C>T maps to ENST00000389840 V1397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:76462805 G>A maps to ENST00000389840 F2943F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:76498997 C>T maps to ENST00000389840 R1680R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:76525568 G>A maps to ENST00000389840 I1164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:76570935 G>A maps to ENST00000389840 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:76455163 G>T maps to ENST00000389840 P3246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:76510951 G>C maps to ENST00000389840 T1335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:76571088 G>C maps to ENST00000389840 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr17:76491046 C>T maps to ENST00000389840 S1998S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr17:76455870 G>A maps to ENST00000389840 A3202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:76498989 C>T maps to ENST00000389840 W1683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr17:76525715 C>T maps to ENST00000389840 K1115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:76457736 C>T maps to ENST00000389840 K3062K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:76450700 G>A maps to ENST00000389840 L3405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:76451896 C>T maps to ENST00000389840 S3319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:76455286 G>A maps to ENST00000389840 P3205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:76464929 C>T maps to ENST00000389840 V2835V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:76471398 C>T maps to ENST00000389840 Q2810Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:76491046 C>T maps to ENST00000389840 S1998S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:76521135 G>A maps to ENST00000389840 H1269H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:76565477 C>T maps to ENST00000389840 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr17:76490156 G>A maps to ENST00000389840 S2109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr17:76503718 G>A maps to ENST00000389840 L1465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:76482380 G>A maps to ENST00000389840 S2328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr17:76502849 G>A maps to ENST00000389840 S1581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr17:7699861 G>A maps to NM_020877.2 G2585G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr17:7710495 C>T maps to NM_020877.2 I3157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr17:7720943 C>T maps to NM_020877.2 T3362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr17:7646341 C>T maps to NM_020877.2 R596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:7630450 C>T maps to NM_020877.2 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr17:7696091 G>A maps to NM_020877.2 G2421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr17:7668872 C>T maps to NM_020877.2 F1167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr17:7724582 G>T maps to NM_020877.2 E3680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr17:7701963 C>T maps to NM_020877.2 F2829F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr17:7669790 C>T maps to NM_020877.2 L1223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5KH-06A-11D-A27K-08 chr17:7623090 C>G maps to NM_020877.2 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr17:7681645 C>T maps to NM_020877.2 S1800S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:7680801 G>A maps to NM_020877.2 G1699G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:7727909 G>A maps to NM_020877.2 L3906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:7667199 C>T maps to NM_020877.2 I1010I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:7689895 T>C maps to NM_020877.2 P2119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:7695607 G>A maps to NM_020877.2 R2364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:7710627 G>A maps to NM_020877.2 R3201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr17:7661812 G>A maps to NM_020877.2 R684R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr17:7697627 C>T maps to NM_020877.2 S2542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:7695640 G>A maps to NM_020877.2 K2375K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr17:7683946 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:7727470 C>T maps to NM_020877.2 L3837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr17:7663239 C>T maps to NM_020877.2 P923P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:7689557 C>T maps to NM_020877.2 I2082I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:7691315 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:7701559 C>T maps to NM_020877.2 A2772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:7664187 C>T maps to NM_020877.2 S972S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr17:7708668 C>T maps to NM_020877.2 R3134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:7630450 C>T maps to NM_020877.2 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:7662897 G>A maps to NM_020877.2 L869L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:7681414 C>T maps to NM_020877.2 I1756I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:7721109 G>A maps to NM_020877.2 W3391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:7644282 C>T maps to NM_020877.2 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:7701532 C>T maps to NM_020877.2 I2763I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:7678167 C>T maps to NM_020877.2 F1531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr17:7721971 C>T maps to NM_020877.2 A3516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:7671249 C>T maps to NM_020877.2 I1236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:7691233 C>T maps to NM_020877.2 S2220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:7707603 G>A maps to NM_020877.2 L3001L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:7720014 T>C maps to NM_020877.2 L3286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:7678083 G>A maps to NM_020877.2 L1503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:7696447 C>T maps to NM_020877.2 P2498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:7702554 C>T maps to NM_020877.2 P2898P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:7679358 G>A maps to NM_020877.2 V1613V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:7644255 C>A maps to NM_020877.2 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:7674160 G>A maps to NM_020877.2 K1424K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:7673711 C>T maps to NM_020877.2 L1362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr17:7679379 C>T maps to NM_020877.2 T1620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr17:7724581 C>T maps to NM_020877.2 F3679F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:7637887 C>T maps to NM_020877.2 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:7673915 C>T maps to NM_020877.2 L1380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:7678626 C>T maps to NM_020877.2 F1596F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:7691432 C>T maps to NM_020877.2 F2257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:7700762 C>T maps to NM_020877.2 F2665F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:7701592 C>T maps to NM_020877.2 T2783T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:7673915 C>T maps to NM_020877.2 L1380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:7736236 T>G maps to NM_020877.2 Y4323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr17:7671297 C>T maps to NM_020877.2 F1252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:7695362 G>A maps to NM_020877.2 E2343E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr17:7727272 C>T maps to NM_020877.2 I3817I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:7707642 C>T maps to NM_020877.2 I3014I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr16:20976238 C>T maps to NM_017539.1 G2989G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr16:20996809 C>T maps to NM_017539.1 R2418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr16:21136651 C>T maps to NM_017539.1 K416K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr16:21011621 G>A maps to NM_017539.1 I2115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr16:21051235 G>A maps to NM_017539.1 V1556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr16:21042417 C>T maps to NM_017539.1 V1796V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr16:21071677 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr16:21147681 C>T maps to NM_017539.1 K283K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr16:21042505 C>T maps to NM_017539.1 W1767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr16:20952788 A>T maps to NM_017539.1 L3863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr16:21031018 G>A maps to NM_017539.1 I1983I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr16:21078704 C>T maps to NM_017539.1 Q1139Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr16:20974844 C>T maps to NM_017539.1 W3454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr16:20975020 G>A maps to NM_017539.1 F3395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr16:20946801 C>T maps to NM_017539.1 W3955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr16:21147747 C>T maps to NM_017539.1 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr16:20946802 C>T maps to NM_017539.1 W3955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr16:21078643 G>A maps to NM_017539.1 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr16:20970594 A>G maps to NM_017539.1 L3578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr16:20944553 G>A maps to NM_017539.1 S4091S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr16:20996485 G>A maps to NM_017539.1 I2526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr16:20990797 G>A maps to NM_017539.1 R2644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr16:21014452 C>T maps to NM_017539.1 E2033E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:21078706 G>A maps to NM_017539.1 Q1139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr16:21042504 C>T maps to NM_017539.1 W1767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr16:20976175 G>A maps to NM_017539.1 G3010G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:21031050 T>A maps to NM_017539.1 K1973*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:21080783 C>T maps to NM_017539.1 R1111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:20975263 G>A maps to NM_017539.1 I3314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:20975446 G>A maps to NM_017539.1 I3253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:21063004 G>A maps to NM_017539.1 T1408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:21049163 C>T maps to NM_017539.1 E1623E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr16:20994191 C>T maps to NM_017539.1 G2570G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr16:20963830 C>T maps to NM_017539.1 R3704R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr16:20975581 G>A maps to NM_017539.1 I3208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr16:21092964 G>A maps to NM_017539.1 F987F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr16:20959849 G>A maps to NM_017539.1 L3766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:21011567 C>T maps to NM_017539.1 G2133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:21157304 C>T maps to NM_017539.1 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr16:21156556 T>C maps to NM_017539.1 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:21061242 G>A maps to NM_017539.1 A1445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:20974680 G>A maps to NM_017539.1 Q3509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr16:20976118 C>T maps to NM_017539.1 K3029K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:21011705 G>A maps to NM_017539.1 F2087F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr16:20996727 G>A maps to NM_017539.1 L2446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:21115823 C>T maps to NM_017539.1 K778K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr16:20955865 G>A maps to NM_017539.1 V3821V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:20999289 C>T maps to NM_017539.1 G2233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:21053492 G>A maps to NM_017539.1 I1498I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:20975917 C>T maps to NM_017539.1 E3096E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:20976490 C>T maps to NM_017539.1 R2905R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:20998677 G>A maps to NM_017539.1 F2325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:21060982 G>A maps to NM_017539.1 S1456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:21078725 C>T maps to NM_017539.1 R1132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr16:20996485 G>A maps to NM_017539.1 I2526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr16:20974996 C>T maps to NM_017539.1 L3403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:21008665 G>A maps to NM_017539.1 I2180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:20966156 C>T maps to NM_017539.1 E3683E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr16:20974660 G>A maps to NM_017539.1 S3515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr16:20999053 C>T maps to NM_017539.1 V2281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr16:20976138 G>A maps to NM_017539.1 Q3023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:20975995 G>A maps to NM_017539.1 I3070I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr16:20970676 C>T maps to NM_017539.1 Q3550Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr16:20999068 C>T maps to NM_017539.1 R2276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr16:20999095 C>T maps to NM_017539.1 S2267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr16:20999053 C>T maps to NM_017539.1 V2281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr16:21063042 G>A maps to NM_017539.1 L1396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr16:21033335 G>A maps to NM_017539.1 I1911I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:20975683 G>A maps to NM_017539.1 T3174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr16:21136654 C>T maps to NM_017539.1 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr16:21063073 G>A maps to NM_017539.1 I1385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr16:21038410 G>A maps to NM_017539.1 S1826S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr16:21053351 G>A maps to NM_017539.1 L1545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:20955879 G>A maps to NM_017539.1 L3817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:20966147 G>A maps to NM_017539.1 N3686N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:20974807 G>A maps to NM_017539.1 F3466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:20975410 G>A maps to NM_017539.1 S3265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:20975911 C>T maps to NM_017539.1 A3098A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:20976097 G>A maps to NM_017539.1 F3036F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:20996623 G>A maps to NM_017539.1 V2480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:20999044 C>T maps to NM_017539.1 G2284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:21035983 C>T maps to NM_017539.1 W1860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:21042516 C>T maps to NM_017539.1 V1763V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:21063132 G>A maps to NM_017539.1 Q1366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:21122983 G>A maps to NM_017539.1 Q688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:21145599 C>T maps to NM_017539.1 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr16:21065750 G>A maps to NM_017539.1 I1343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr16:21073826 C>T maps to NM_017539.1 Q1232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:20966231 G>A maps to NM_017539.1 F3658F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:20994179 C>T maps to NM_017539.1 R2574R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:20996644 A>G maps to NM_017539.1 L2473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:21042582 C>T maps to NM_017539.1 V1741V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:21045350 G>A maps to NM_017539.1 G1714G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:20996677 C>T maps to NM_017539.1 K2462K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:21073849 T>A maps to NM_017539.1 K1225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr16:21042383 G>A maps to NM_017539.1 L1808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr16:21063132 G>A maps to NM_017539.1 Q1366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr16:21122989 G>A maps to NM_017539.1 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr5:13792186 G>A maps to NM_001369.2 F2788F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr5:13829666 C>T maps to NM_001369.2 R2132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr5:13700911 C>T maps to NM_001369.2 W4520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr5:13824349 C>T maps to NM_001369.2 T2179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr5:13911556 G>A maps to NM_001369.2 Q528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr5:13714629 G>A maps to NM_001369.2 L4337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr5:13814898 G>A maps to NM_001369.2 L2349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr5:13692244 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:13770868 G>A maps to NM_001369.2 T3198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:13792273 C>T maps to NM_001369.2 V2759V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:13876801 G>A maps to NM_001369.2 S1129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr5:13850768 G>A maps to NM_001369.2 S1702S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr5:13841968 C>T maps to NM_001369.2 T1772T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr5:13769651 C>T maps to NM_001369.2 A3226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr5:13780987 C>T maps to NM_001369.2 R2967R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr5:13736030 C>T maps to NM_001369.2 R3822R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr5:13859614 C>T maps to NM_001369.2 W1632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr5:13841134 G>A maps to NM_001369.2 F1863F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr5:13814812 G>A maps to NM_001369.2 F2377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr5:13923484 G>A maps to NM_001369.2 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr5:13737547 C>T maps to NM_001369.2 R3756R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr5:13919442 G>A maps to NM_001369.2 Q273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr5:13769651 C>T maps to NM_001369.2 A3226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr5:13914634 C>T maps to NM_001369.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr5:13830226 G>A maps to NM_001369.2 L2053L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr5:13719165 G>A maps to NM_001369.2 F4108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr5:13729619 C>T maps to NM_001369.2 W3937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr5:13766132 C>T maps to NM_001369.2 Q3351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr5:13793675 G>A maps to NM_001369.2 F2724F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr5:13864592 G>A maps to NM_001369.2 T1503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr5:13864595 G>A maps to NM_001369.2 L1502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr5:13923484 G>A maps to NM_001369.2 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr5:13850768 G>A maps to NM_001369.2 S1702S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:13788936 C>T maps to NM_001369.2 K2845K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:13886117 T>A maps to NM_001369.2 K900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr5:13901543 G>A maps to NM_001369.2 I623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr5:13777444 G>A maps to NM_001369.2 L2991L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr5:13762881 C>T maps to NM_001369.2 T3410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr5:13717575 G>A maps to NM_001369.2 L4185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:13701464 G>A maps to NM_001369.2 F4473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:13727621 G>A maps to NM_001369.2 I4009I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:13727741 C>T maps to NM_001369.2 W3969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:13737583 A>T maps to NM_001369.2 T3744T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:13770901 G>A maps to NM_001369.2 F3187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:13871681 G>A maps to NM_001369.2 L1197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr5:13793756 G>A maps to NM_001369.2 I2697I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr5:13931260 C>T maps to NM_001369.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:13735982 C>T maps to NM_001369.2 E3838E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:13864544 G>A maps to NM_001369.2 I1519I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr5:13721276 C>T maps to NM_001369.2 E4037E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr5:13871742 G>A maps to NM_001369.2 F1176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr5:13823392 C>T maps to NM_001369.2 L2222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr5:13766132 C>T maps to NM_001369.2 Q3351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr5:13794092 A>G maps to NM_001369.2 V2654V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr5:13823470 C>T maps to NM_001369.2 E2196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr5:13911563 G>A maps to NM_001369.2 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:13735384 G>A maps to NM_001369.2 I3872I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:13850879 G>A maps to NM_001369.2 I1665I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:13900362 G>A maps to NM_001369.2 S737S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:13923484 G>A maps to NM_001369.2 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr5:13824411 G>A maps to NM_001369.2 L2159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr5:13780995 G>A maps to NM_001369.2 L2965L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr5:13727714 C>T maps to NM_001369.2 P3978P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr5:13864607 C>T maps to NM_001369.2 R1498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:13917338 G>A maps to NM_001369.2 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:13944538 C>T maps to NM_001369.2 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:13862835 C>T maps to NM_001369.2 V1539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr5:13766188 T>A maps to NM_001369.2 K3333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr5:13766288 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:13729619 C>T maps to NM_001369.2 W3937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:13867896 G>A maps to NM_001369.2 L1347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr5:13721111 C>T maps to NM_001369.2 A4092A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr5:13752395 G>A maps to NM_001369.2 I3625I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr5:13901522 G>A maps to NM_001369.2 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:13721195 C>T maps to NM_001369.2 K4064K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:13737595 C>T maps to NM_001369.2 E3740E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:13753569 C>T maps to NM_001369.2 K3548K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:13769651 C>T maps to NM_001369.2 A3226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:13776740 G>A maps to NM_001369.2 F3060F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:13830772 C>T maps to NM_001369.2 G1998G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:13729616 G>A maps to NM_001369.2 I3938I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:13911581 C>T maps to NM_001369.2 K519K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:13914691 G>A maps to NM_001369.2 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:13923484 G>A maps to NM_001369.2 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr5:13859659 G>A maps to NM_001369.2 N1617N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:13727615 C>T maps to NM_001369.2 Q4011Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:13701464 G>A maps to NM_001369.2 F4473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:13721243 G>A maps to NM_001369.2 L4048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:13727711 C>T maps to NM_001369.2 E3979E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:13781068 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:13845059 G>A maps to NM_001369.2 F1719F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:13871742 G>A maps to NM_001369.2 F1176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr5:13751221 G>A maps to NM_001369.2 Q3726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr5:13824397 C>T maps to NM_001369.2 R2163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr5:13735348 G>A maps to NM_001369.2 A3884A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr5:13794104 C>T maps to NM_001369.2 K2650K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr5:13753554 C>T maps to NM_001369.2 R3553R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr5:13829654 C>T maps to NM_001369.2 T2136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:13735321 G>A maps to NM_001369.2 F3893F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:13788873 T>C maps to NM_001369.2 G2866G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:13811767 C>T maps to NM_001369.2 L2465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:13820479 G>A maps to NM_001369.2 I2272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr5:13776578 G>A maps to NM_001369.2 F3114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:13786368 G>A maps to NM_001369.2 F2913F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:13824358 C>T maps to NM_001369.2 T2176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr5:13737547 C>T maps to NM_001369.2 R3756R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:13752266 G>A maps to NM_001369.2 F3668F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr5:13770901 G>A maps to NM_001369.2 F3187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr5:13762983 T>C maps to NM_001369.2 E3376E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr5:13913968 G>A maps to NM_001369.2 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr5:13766228 G>A maps to NM_001369.2 I3319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:13777417 G>A maps to NM_001369.2 R3000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:13781028 G>A maps to NM_001369.2 L2954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:13841133 G>A maps to NM_001369.2 L1864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr5:13727741 C>T maps to NM_001369.2 W3969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr5:13841026 G>A maps to NM_001369.2 I1899I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr5:13883120 G>A maps to NM_001369.2 V1022V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:13717511 C>T maps to NM_001369.2 W4206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr5:13864532 A>C maps to NM_001369.2 P1523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:13729598 C>T maps to NM_001369.2 L3944L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:13751221 G>A maps to NM_001369.2 Q3726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr5:13885251 C>T maps to NM_001369.2 R943R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:13721222 G>A maps to NM_001369.2 P4055P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:13729598 C>T maps to NM_001369.2 L3944L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:13766174 C>T maps to NM_001369.2 V3337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:13829789 C>T maps to NM_001369.2 Q2091Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:13766174 C>T maps to NM_001369.2 V3337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:13823446 C>T maps to NM_001369.2 L2204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:13829759 G>A maps to NM_001369.2 F2101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr5:13766105 C>T maps to NM_001369.2 G3360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr5:13820500 C>T maps to NM_001369.2 G2265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr5:13864607 C>T maps to NM_001369.2 R1498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:13900440 G>A maps to NM_001369.2 D711D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:13901543 G>A maps to NM_001369.2 I623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr5:13721243 G>A maps to NM_001369.2 L4048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr5:13919389 C>T maps to NM_001369.2 W290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:13717603 C>T maps to NM_001369.2 V4175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:13763004 G>A maps to NM_001369.2 F3369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:13901534 C>T maps to NM_001369.2 K626K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:13901504 C>T maps to NM_001369.2 R636R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:13781029 G>A maps to NM_001369.2 L2953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr5:13901399 C>T maps to NM_001369.2 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:13824439 A>C maps to NM_001369.2 V2149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr5:13708339 G>A maps to NM_001369.2 T4410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr5:13824343 G>A maps to NM_001369.2 V2181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr5:13883156 G>A maps to NM_001369.2 F1010F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:13770901 G>A maps to NM_001369.2 F3187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr5:13817804 T>G did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:13776634 G>A maps to NM_001369.2 R3096*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:13788855 C>T maps to NM_001369.2 V2872V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:13830772 C>T maps to NM_001369.2 G1998G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:13841809 G>A maps to NM_001369.2 F1825F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:13862706 G>A maps to NM_001369.2 I1582I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr5:13708294 G>A maps to NM_001369.2 S4425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:13735384 G>A maps to NM_001369.2 I3872I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:13876921 G>A maps to NM_001369.2 T1089T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:13920672 C>T maps to NM_001369.2 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr5:13823434 G>A maps to NM_001369.2 L2208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr5:13763004 G>A maps to NM_001369.2 F3369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:13700896 A>T maps to NM_001369.2 I4525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:13736002 C>A maps to NM_001369.2 E3832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr5:13766228 G>A maps to NM_001369.2 I3319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr5:13862670 G>A maps to NM_001369.2 S1594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:13752395 G>A maps to NM_001369.2 I3625I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr5:13719165 G>A maps to NM_001369.2 F4108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr5:13920607 C>T maps to NM_001369.2 W260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr5:13717504 G>A maps to NM_001369.2 I4208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr5:13727621 G>A maps to NM_001369.2 I4009I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr5:13776796 G>A maps to NM_001369.2 R3042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z4-06A-11D-A197-08 chr5:13864595 G>A maps to NM_001369.2 L1502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:13829720 G>A maps to NM_001369.2 I2114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:13830772 C>T maps to NM_001369.2 G1998G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:13841875 C>T maps to NM_001369.2 V1803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:13876828 A>T maps to NM_001369.2 V1120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr5:13692193 G>A maps to NM_001369.2 R4592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr5:13876807 G>A maps to NM_001369.2 I1127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr5:13700767 C>T maps to NM_001369.2 R4568R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:13716661 G>A maps to NM_001369.2 F4281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:13766174 C>T maps to NM_001369.2 V3337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:13841098 C>T maps to NM_001369.2 T1875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:13841968 C>T maps to NM_001369.2 T1772T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:13901543 G>A maps to NM_001369.2 I623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr5:13809158 C>T maps to NM_001369.2 Q2582Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr5:13793756 G>A maps to NM_001369.2 I2697I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr5:13839595 C>T maps to NM_001369.2 L1917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr5:13901534 C>T maps to NM_001369.2 K626K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr5:13737547 C>T maps to NM_001369.2 R3756R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr5:13727711 C>T maps to NM_001369.2 E3979E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr5:13885215 G>A maps to NM_001369.2 A955A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr5:13920624 C>T maps to NM_001369.2 E254E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:13692203 C>T maps to NM_001369.2 K4588K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:13700827 C>T maps to NM_001369.2 R4548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:13717552 G>A maps to NM_001369.2 H4192H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:13735243 A>G maps to NM_001369.2 I3919I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:13735279 C>T maps to NM_001369.2 R3907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:13735321 G>A maps to NM_001369.2 F3893F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:13737472 G>A maps to NM_001369.2 L3781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:13752395 G>A maps to NM_001369.2 I3625I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:13762863 G>A maps to NM_001369.2 F3416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:13770901 G>A maps to NM_001369.2 F3187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:13792150 G>A maps to NM_001369.2 V2800V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:13793684 C>T maps to NM_001369.2 K2721K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:13793831 C>T maps to NM_001369.2 T2672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:13794062 G>A maps to NM_001369.2 I2664I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:13841133 G>A maps to NM_001369.2 L1864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:13841809 G>A maps to NM_001369.2 F1825F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:13870917 C>T maps to NM_001369.2 R1264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:13870919 T>G maps to NM_001369.2 R1264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:13870965 C>T maps to NM_001369.2 K1248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:13870992 G>A maps to NM_001369.2 F1239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:13882839 G>A maps to NM_001369.2 Q1087*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:13901375 C>T maps to NM_001369.2 R679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:13920607 C>T maps to NM_001369.2 W260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:13922278 G>A maps to NM_001369.2 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr5:13841032 C>T maps to NM_001369.2 R1897R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:13766194 G>A maps to NM_001369.2 Q3331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:13793756 G>A maps to NM_001369.2 I2697I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:13830772 C>T maps to NM_001369.2 G1998G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr5:13781029 G>A maps to NM_001369.2 L2953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:13719030 A>T maps to NM_001369.2 P4153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:13762881 C>T maps to NM_001369.2 T3410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:13793771 C>T maps to NM_001369.2 G2692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:13793831 C>T maps to NM_001369.2 T2672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:13817699 C>T maps to NM_001369.2 G2315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:13841983 A>T maps to NM_001369.2 S1767S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr5:13911563 G>A maps to NM_001369.2 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr5:13769245 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr5:13920607 C>T maps to NM_001369.2 W260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr5:13762881 C>T maps to NM_001369.2 T3410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr5:13913896 T>C maps to NM_001369.2 Q497Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:13762830 C>T maps to NM_001369.2 K3427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:13867921 G>A maps to NM_001369.2 F1338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:13944520 G>A maps to NM_001369.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr5:13820556 G>A maps to NM_001369.2 Q2247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr5:13864559 A>G maps to NM_001369.2 F1514F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr5:13864685 G>A maps to NM_001369.2 I1472I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:84780119 C>T maps to NM_001370.1 Q522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:84780040 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:84811169 G>A maps to NM_001370.1 K759K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:84800701 C>T maps to NM_001370.1 Q639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr2:196729429 G>A maps to NM_018897.2 R2317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr2:196619142 C>T maps to NM_018897.2 R3894R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr2:196651812 C>T maps to NM_018897.2 W3600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr2:196774798 G>A maps to NM_018897.2 F1352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr2:196729520 G>A maps to NM_018897.2 I2286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr2:196825162 C>T maps to NM_018897.2 A904A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr2:196753693 C>T maps to NM_018897.2 R1686R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:196834803 C>T maps to NM_018897.2 R691R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr2:196651859 G>A maps to NM_018897.2 F3584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:196620889 C>T maps to NM_018897.2 V3851V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:196681593 A>C maps to NM_018897.2 S3173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:196722273 C>T maps to NM_018897.2 R2747R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr2:196837172 C>T maps to NM_018897.2 V617V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:196722309 G>A maps to NM_018897.2 F2735F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:196723311 C>T maps to NM_018897.2 A2651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:196723506 C>T maps to NM_018897.2 K2586K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr2:196801381 G>A maps to NM_018897.2 F1071F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr2:196729223 C>T maps to NM_018897.2 R2385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr2:196726448 C>T maps to NM_018897.2 K2576K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr2:196636560 G>A maps to NM_018897.2 V3752V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44R-06A-41D-A25O-08 chr2:196621000 T>G maps to NM_018897.2 A3814A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:196738409 G>A maps to NM_018897.2 R2099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:196883958 C>T maps to NM_018897.2 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:196922840 C>T maps to ENST00000312446 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:196728871 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:196728874 G>A maps to NM_018897.2 Q2502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:196774855 C>T maps to NM_018897.2 G1333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr2:196723506 C>T maps to NM_018897.2 K2586K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr2:196636524 G>A maps to NM_018897.2 F3764F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:196673455 T>A maps to NM_018897.2 R3345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:196729520 G>A maps to NM_018897.2 I2286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:196602737 C>T maps to NM_018897.2 T3994T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:196746635 G>A maps to NM_018897.2 I1948I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:196681527 C>T maps to NM_018897.2 K3195K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:196788417 C>T maps to NM_018897.2 L1242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:196722213 G>A maps to NM_018897.2 I2767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:196749421 G>A maps to NM_018897.2 R1884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr2:196837010 C>T maps to NM_018897.2 R671R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:196602737 C>T maps to NM_018897.2 T3994T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr2:196709844 G>A maps to NM_018897.2 I2942I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:196746620 C>T maps to NM_018897.2 L1953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:196749451 G>A maps to NM_018897.2 R1874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:196822161 C>T maps to NM_018897.2 E967E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr2:196602644 T>G maps to NM_018897.2 *4025Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr2:196602737 C>T maps to NM_018897.2 T3994T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:196837180 G>A maps to NM_018897.2 Q615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:196722389 C>A maps to NM_018897.2 E2709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:196729520 G>A maps to NM_018897.2 I2286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr2:196746716 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr2:196737150 G>A maps to NM_018897.2 I2152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:196605555 G>A maps to NM_018897.2 S3934S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:196620935 C>T maps to NM_018897.2 W3836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:196753606 C>T maps to NM_018897.2 L1715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr2:196749356 G>A maps to NM_018897.2 V1905V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:196681569 C>T maps to NM_018897.2 E3181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr2:196640650 G>A maps to NM_018897.2 I3707I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:196602809 C>T maps to NM_018897.2 R3970R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:196659082 G>A maps to NM_018897.2 F3565F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:196801390 G>A maps to NM_018897.2 F1068F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:196866569 T>C maps to NM_018897.2 E334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:196759828 G>A maps to NM_018897.2 S1589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:196822152 G>A maps to NM_018897.2 L970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr2:196651832 C>T maps to NM_018897.2 R3593R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr2:196659166 C>T maps to NM_018897.2 V3537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:196602737 C>T maps to NM_018897.2 T3994T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:196749451 G>A maps to NM_018897.2 R1874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:196673491 G>A maps to NM_018897.2 R3333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:196636422 G>A maps to NM_018897.2 T3798T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:196749421 G>A maps to NM_018897.2 R1884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:196659100 C>T maps to NM_018897.2 P3559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr2:196722213 G>A maps to NM_018897.2 I2767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr2:196620889 C>T maps to NM_018897.2 V3851V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:196651832 C>T maps to NM_018897.2 R3593R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr2:196620880 G>A maps to NM_018897.2 F3854F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:196636428 C>T maps to NM_018897.2 L3796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:196664076 G>A maps to NM_018897.2 F3432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr2:196913018 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:196746610 G>A maps to NM_018897.2 R1957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:196718246 G>A maps to NM_018897.2 D2867D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:196837010 C>T maps to NM_018897.2 R671R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:196642612 G>A maps to NM_018897.2 L3659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:196659120 G>A maps to NM_018897.2 R3553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:196659193 G>A maps to NM_018897.2 F3528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:196659214 C>T maps to NM_018897.2 T3521T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:196722402 G>T maps to NM_018897.2 V2704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:196729429 G>A maps to NM_018897.2 R2317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:196749451 G>A maps to NM_018897.2 R1874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:196771385 C>T maps to NM_018897.2 L1444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:196799398 C>T maps to NM_018897.2 E1129E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:196801381 G>A maps to NM_018897.2 F1071F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:196852767 G>A maps to NM_018897.2 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:196621009 C>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:196722327 C>T maps to NM_018897.2 G2729G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:196759921 C>A maps to NM_018897.2 G1558G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:196659082 G>A maps to NM_018897.2 F3565F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:196681401 A>G maps to NM_018897.2 L3237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:196659124 G>A maps to NM_018897.2 I3551I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:196837004 G>A maps to NM_018897.2 I673I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:38825466 C>T maps to ENST00000327475 F1957F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr6:38950196 C>T maps to ENST00000327475 Q4292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr6:38843575 C>T maps to ENST00000327475 T2598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr6:38885852 C>T maps to ENST00000327475 L3475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr6:38951991 G>A maps to ENST00000327475 W4309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:38831832 G>A maps to ENST00000327475 T2153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr6:38891765 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:38867667 G>A maps to ENST00000327475 Q3048Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr6:38885837 G>A maps to ENST00000327475 G3470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr6:38899762 G>A maps to ENST00000327475 E3805E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr6:38840745 C>T maps to ENST00000327475 S2422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44R-06A-41D-A25O-08 chr6:38879297 T>C maps to ENST00000327475 G3253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr6:38758066 G>A maps to ENST00000327475 V877V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:38899588 G>A maps to ENST00000327475 V3747V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:38840388 G>A maps to ENST00000327475 T2344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:38997990 C>T maps to ENST00000327475 L4637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr6:38942248 T>C maps to ENST00000327475 L4248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:38759332 C>T maps to ENST00000327475 I916I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:38834546 C>T maps to ENST00000327475 I2184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:38941543 G>A maps to ENST00000327475 W4199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:38980314 G>A maps to ENST00000327475 W4527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr6:38881673 G>A maps to ENST00000327475 Q3291Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr6:38899615 C>T maps to ENST00000327475 I3756I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:38770970 G>A maps to ENST00000327475 W961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:38877409 C>T maps to ENST00000327475 F3198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:38749133 C>T maps to ENST00000327475 P736P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:38891880 G>A maps to ENST00000327475 R3623R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:38919198 G>A maps to ENST00000327475 W4106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr6:38754580 G>A maps to ENST00000327475 G800G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:38917292 C>T maps to ENST00000327475 I4053I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr6:38840745 C>T maps to ENST00000327475 S2422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:38862524 C>T maps to ENST00000327475 R2866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:38805725 C>T maps to ENST00000327475 F1446F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:38702322 G>A maps to ENST00000327475 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:38875790 G>A maps to ENST00000327475 V3124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr6:38890916 C>T maps to ENST00000327475 I3570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr6:38917250 G>A maps to ENST00000327475 W4039*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr6:38891858 G>A maps to ENST00000327475 W3616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:38813485 C>A maps to ENST00000327475 S1649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr6:38980369 G>A maps to ENST00000327475 G4545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr6:38899615 C>A maps to ENST00000327475 I3756I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:38743636 T>C maps to ENST00000327475 V612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:38976595 G>A maps to ENST00000327475 Q4395Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:38976649 G>A maps to ENST00000327475 E4413E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:38877409 C>T maps to ENST00000327475 F3198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr6:38998092 G>T maps to ENST00000327475 V4671V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr6:38854602 G>T maps to ENST00000327475 E2754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr6:38867566 C>T maps to ENST00000327475 R3015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr6:38879330 C>T maps to ENST00000327475 F3264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr6:38879242 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:38802383 C>G maps to ENST00000327475 P1432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr6:38813384 C>T maps to ENST00000327475 I1615I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr6:38874113 C>T maps to ENST00000327475 I3081I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:38877313 C>T maps to ENST00000327475 A3166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr6:38738262 G>A maps to ENST00000327475 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:38791385 C>T maps to ENST00000327475 L1245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr6:38897411 G>A maps to ENST00000327475 K3736K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr6:38743714 C>T maps to ENST00000327475 I638I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:38743714 C>T maps to ENST00000327475 I638I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:38750778 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:38750844 C>T maps to ENST00000327475 S763S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:38783392 G>A maps to ENST00000327475 V1149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:38793987 C>T maps to ENST00000327475 R1290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:38805725 C>T maps to ENST00000327475 F1446F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:38830178 C>T maps to ENST00000327475 V2073V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:38877409 C>T maps to ENST00000327475 F3198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:38885837 G>A maps to ENST00000327475 G3470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:38903381 G>A maps to ENST00000327475 E3812E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:38917343 C>T maps to ENST00000327475 I4070I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:38957886 C>T maps to ENST00000327475 Q4373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:38997933 G>A maps to ENST00000327475 R4618R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:38877322 G>A maps to ENST00000327475 L3169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:38976649 G>A maps to ENST00000327475 E4413E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr6:38905945 C>T maps to ENST00000327475 I3908I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr6:38862524 C>T maps to ENST00000327475 R2866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:38997969 C>A maps to ENST00000327475 L4630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr6:38877372 G>A maps to ENST00000327475 W3186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr6:38749041 C>T maps to ENST00000327475 Q706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr17:11865374 G>A maps to NM_001372.3 W4345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr17:11593107 C>A maps to NM_001372.3 P1323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr17:11687792 C>T maps to NM_001372.3 F2666F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr17:11666768 C>T maps to NM_001372.3 I2336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr17:11554399 G>A maps to NM_001372.3 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:11725837 C>T maps to NM_001372.3 I2978I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:11672467 C>T maps to NM_001372.3 I2458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:11687792 C>T maps to NM_001372.3 F2666F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr17:11659917 C>T maps to NM_001372.3 L2258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:11604563 G>A maps to NM_001372.3 Q1717Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:11666861 G>A maps to NM_001372.3 K2367K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr17:11650883 G>A maps to NM_001372.3 L2137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:11592933 C>T maps to NM_001372.3 I1265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:11666906 C>T maps to NM_001372.3 F2382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:11774973 G>A maps to NM_001372.3 Q3371Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:11535902 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:11726308 G>A maps to NM_001372.3 R3068R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr17:11687807 C>T maps to NM_001372.3 I2671I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr17:11686983 C>T maps to NM_001372.3 S2580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr17:11687642 C>T maps to NM_001372.3 S2616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:11593452 G>A maps to NM_001372.3 K1438K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr17:11696951 C>T maps to NM_001372.3 Q2732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:11603115 G>A maps to NM_001372.3 G1647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr17:11603200 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:11572943 C>T maps to NM_001372.3 I1062I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:11738139 G>A maps to NM_001372.3 K3144K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:11631208 C>T maps to NM_001372.3 S1928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr17:11659919 G>A maps to NM_001372.3 L2258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:11666783 G>A maps to NM_001372.3 E2341E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:11872807 G>A maps to NM_001372.3 W4475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:11775033 C>T maps to NM_001372.3 G3391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:11666755 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr17:11622764 C>T maps to NM_001372.3 I1889I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr17:11523064 G>A maps to NM_001372.3 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:11778369 C>T maps to NM_001372.3 S3449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:11778372 G>A maps to NM_001372.3 V3450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:11648244 G>A maps to NM_001372.3 K2081K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr17:11556318 G>A maps to NM_001372.3 Q865Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:11520839 C>T maps to NM_001372.3 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:11572836 C>T maps to NM_001372.3 Q1027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:11726146 C>T maps to NM_001372.3 F3014F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr17:11687852 C>T maps to NM_001372.3 F2686F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr17:11648355 G>A maps to NM_001372.3 A2118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr17:11584056 G>A maps to NM_001372.3 W1198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr17:11642240 C>T maps to NM_001372.3 F1953F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr17:11642246 C>T maps to NM_001372.3 F1955F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr17:11835359 G>A maps to NM_001372.3 T4045T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:11651074 G>A maps to NM_001372.3 W2201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:11597736 C>T maps to NM_001372.3 I1615I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr17:11726146 C>T maps to NM_001372.3 F3014F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr17:11711057 C>T maps to NM_001372.3 I2810I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr17:11687825 C>T maps to NM_001372.3 F2677F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:11593582 C>T maps to NM_001372.3 L1482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr17:11659887 C>T maps to NM_001372.3 L2248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr17:11622779 C>T maps to NM_001372.3 F1894F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:11671864 C>T maps to NM_001372.3 I2422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:11784660 G>A maps to NM_001372.3 R3579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:11532846 G>A maps to NM_001372.3 E488E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:11648271 C>T maps to NM_001372.3 F2090F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:11666768 C>T maps to NM_001372.3 I2336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:11684401 C>T maps to NM_001372.3 F2543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:11700963 C>T maps to NM_001372.3 H2758H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:11725333 G>A maps to NM_001372.3 E2935E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:11725816 C>T maps to NM_001372.3 A2971A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:11738215 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr17:11584152 C>T maps to NM_001372.3 F1230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr17:11687660 C>T maps to NM_001372.3 A2622A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:11583116 T>C maps to NM_001372.3 L1133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:11584086 G>A maps to NM_001372.3 V1208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:11592948 C>T maps to NM_001372.3 S1270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:11666922 C>T maps to NM_001372.3 Q2388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr17:11784564 C>A maps to NM_001372.3 P3547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr17:11797734 C>T maps to NM_001372.3 F3776F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26D-06A-11D-A19A-08 chr17:11572799 G>A maps to NM_001372.3 S1014S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr17:11648316 G>A maps to NM_001372.3 R2105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr17:11550484 G>A maps to NM_001372.3 T689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr17:11795110 C>T maps to NM_001372.3 F3710F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr17:11550484 G>A maps to NM_001372.3 T689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr17:11593191 G>A maps to NM_001372.3 R1351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr17:11711081 G>A maps to NM_001372.3 R2818R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr9:34506685 C>T maps to NM_012144.2 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:34485216 C>T maps to NM_012144.2 D53D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr9:34491551 G>A maps to NM_012144.2 Q227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:34500828 C>T maps to NM_012144.2 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr9:34497150 C>T maps to NM_012144.2 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:34506727 C>T maps to NM_012144.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:34517350 G>A maps to NM_012144.2 K629K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:72281236 G>A maps to NM_023036.4 W81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr17:72305514 C>T maps to NM_023036.4 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:72278109 C>T maps to NM_023036.4 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:72301377 G>A maps to NM_023036.4 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:33038720 A>G maps to NM_001539.2 K338K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr16:47001494 G>A maps to NM_005880.3 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:47001557 G>A maps to NM_005880.3 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:47001556 G>A maps to NM_005880.3 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:4492303 G>A maps to NM_005147.4 K222K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr16:4476019 C>T maps to NM_005147.4 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:4491431 C>T maps to NM_005147.4 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr15:78567972 C>T maps to NM_018602.3 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr19:14627706 C>T maps to NM_006145.1 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:186299258 C>T maps to NM_016306.4 Q186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr3:186303136 C>T maps to NM_016306.4 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:186300544 C>T maps to NM_016306.4 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr10:74100815 G>A maps to NM_017626.4 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:73676055 C>A maps to NM_153614.2 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:73676028 C>T maps to NM_153614.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:73681101 C>T maps to NM_153614.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr11:73676007 C>T maps to NM_153614.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:73679475 C>T maps to NM_153614.2 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr2:220146739 C>T maps to NM_006736.5 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr9:34996328 C>T maps to NM_001135005.1 D165D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr9:34996724 C>T maps to NM_001135005.1 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr9:34993367 G>A maps to NM_001135005.1 K118K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr7:157159235 A>G maps to NM_058246.3 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr22:41257101 C>T maps to NM_145174.1 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:41257812 C>T maps to NM_145174.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr22:41257770 A>G maps to NM_145174.1 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:128182007 G>A maps to NM_153330.2 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr3:128182016 G>A maps to NM_153330.2 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:128181419 C>T maps to NM_153330.2 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:183605027 T>C maps to NM_018981.1 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:183623941 C>T maps to NM_018981.1 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:183601004 C>T maps to NM_018981.1 D293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:183640122 C>T maps to NM_018981.1 L782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:183601061 T>C maps to NM_018981.1 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr2:183616502 C>T maps to NM_018981.1 F475F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:6705992 G>A maps to NM_018198.3 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:6711617 G>T maps to NM_018198.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:69571260 C>T maps to NM_201262.1 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr3:132165330 C>T maps to NM_015268.3 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr3:132218015 T>G maps to NM_015268.3 T1401T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:132196697 G>A maps to NM_015268.3 E837E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:132222071 C>T maps to NM_015268.3 S1577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr12:56221259 G>A maps to NM_032364.5 Q395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr12:56215835 C>T maps to NM_032364.5 K678K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr1:15870912 C>T maps to NM_015291.2 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr1:15890474 C>T maps to NM_015291.2 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr1:15892467 C>T maps to NM_015291.2 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:15892437 C>T maps to NM_015291.2 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:15888702 C>T maps to NM_015291.2 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr15:41068487 G>A maps to NM_018163.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr15:41068814 G>A maps to NM_018163.2 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:138764371 C>T maps to NM_152686.3 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr5:138773083 C>T maps to NM_152686.3 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:102956220 T>C maps to NM_014377.1 E542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr7:102967027 G>A maps to NM_014377.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr5:34937618 C>T maps to NM_194283.3 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:49745266 C>T maps to NM_024902.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr12:49742681 T>C maps to NM_024902.2 Y9Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:114411978 C>T maps to NM_001015882.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr9:114411965 C>T maps to NM_001015882.2 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr9:114409478 C>T maps to NM_001015882.2 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr13:96412326 C>T maps to NM_006260.4 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr20:62560692 A>T maps to NM_025219.2 K46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr8:66992625 C>T maps to NM_033105.4 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:66989092 G>A maps to NM_033105.4 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr8:66988912 C>T maps to NM_033105.4 H46H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr8:66989087 C>T maps to NM_033105.4 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr8:67012242 C>T maps to NM_033105.4 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr8:66992640 G>A maps to NM_033105.4 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:27499703 C>T maps to NM_173650.1 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr1:65858516 C>T maps to ENST00000371069 T624T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:65851392 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:65849956 C>T maps to ENST00000371069 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:65845149 G>A maps to ENST00000371069 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr17:40169386 C>T maps to NM_003315.3 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:28527821 C>T maps to NM_014280.2 K233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr14:74125554 G>A maps to NM_031427.2 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr22:39175482 G>A maps to NM_005740.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr22:39178679 G>A maps to NM_005740.2 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:38027680 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:38023280 C>T maps to NM_003462.3 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:38027302 G>A maps to NM_003462.3 Q203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:38027254 G>A maps to NM_003462.3 Q187Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr23:153633862 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:153633215 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:153633209 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr16:2286834 T>A maps to NM_001374.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:2287544 G>A maps to NM_001374.2 Q162Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:58178530 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:58183699 G>A maps to NM_004944.2 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:58178428 C>T maps to NM_004944.2 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:58179123 G>A maps to NM_004944.2 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:58196621 C>T maps to NM_004944.2 E4E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:58183699 G>A maps to NM_004944.2 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:58196576 C>T maps to NM_004944.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:58190532 C>T maps to NM_004944.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:84878171 C>T maps to NM_021233.2 Q230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:84880304 C>T maps to NM_021233.2 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:84880388 G>A maps to NM_021233.2 W308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:230411737 G>A maps to NM_139072.3 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:230282869 C>T maps to NM_139072.3 R521R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr2:230377580 C>T maps to NM_139072.3 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr2:230456370 C>T maps to NM_139072.3 Q170Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr2:230231824 C>T maps to NM_139072.3 W622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:230377580 C>T maps to NM_139072.3 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr2:230341925 G>A maps to NM_139072.3 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:230282863 G>A maps to NM_139072.3 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:230377607 G>A maps to NM_139072.3 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:230312224 C>T maps to NM_139072.3 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:230231824 C>T maps to NM_139072.3 W622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:230450636 G>A maps to NM_139072.3 Q262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:230231824 C>T maps to NM_139072.3 W622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr2:230456469 G>T maps to NM_139072.3 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr2:230456303 G>A maps to NM_139072.3 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:230231586 A>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:230253044 C>T maps to NM_139072.3 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:230453180 C>T maps to NM_139072.3 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:230231656 C>T maps to NM_139072.3 E678E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:230252981 G>A maps to NM_139072.3 I618I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:230272017 G>A maps to NM_139072.3 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:230456298 C>T maps to NM_139072.3 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:230312071 G>A maps to NM_139072.3 C482C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr11:6519579 C>T maps to NM_144666.2 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:6519924 C>T maps to NM_144666.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:6519549 C>T maps to NM_144666.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr11:6520101 C>T maps to NM_144666.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:6532653 C>T maps to NM_144666.2 R463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:130985127 C>T maps to ENST00000372923 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:130982547 C>T maps to ENST00000372923 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr9:130985085 G>A maps to ENST00000372923 E381E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr9:130984794 C>T maps to ENST00000372923 Q350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:130985127 C>T maps to ENST00000372923 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr9:130984862 C>T maps to ENST00000372923 F372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr9:131008773 G>A maps to ENST00000372923 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr9:130984862 C>T maps to ENST00000372923 F372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:130984528 G>A maps to ENST00000372923 Q301Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:32871634 C>T maps to ENST00000381000 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr19:10941010 C>A maps to NM_001005361.2 R834R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:10941039 C>T maps to NM_001005361.2 P843P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr19:10940943 C>T maps to NM_001005361.2 S811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr19:10934478 C>T maps to NM_001005361.2 D599D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr19:10893720 C>T maps to NM_001005361.2 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:10930699 C>T maps to NM_001005361.2 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr1:172002323 G>A maps to ENST00000359070 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr1:172007472 C>T maps to ENST00000359070 H288H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr1:172100388 C>G maps to ENST00000359070 V550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:171958196 G>A maps to ENST00000359070 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr1:171958193 G>A maps to ENST00000359070 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:172007499 G>A maps to ENST00000359070 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:172001621 C>T maps to ENST00000359070 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:172357742 G>A maps to ENST00000359070 R782R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr10:101646230 C>T maps to ENST00000342239 E1172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr10:101639993 G>A maps to ENST00000342239 F1398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr10:101654767 G>A maps to ENST00000342239 R1055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:101715237 G>A maps to ENST00000342239 R665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:101731859 G>A maps to ENST00000342239 R8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr10:101715157 G>A maps to ENST00000342239 C691C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:101646248 C>T maps to ENST00000342239 K1166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr10:101716581 G>A maps to ENST00000342239 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr10:101715816 G>A maps to ENST00000342239 Q472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:101715886 G>A maps to ENST00000342239 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:101731859 G>A maps to ENST00000342239 R8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr10:101646371 C>T maps to ENST00000342239 R1125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr10:101659800 C>T maps to ENST00000342239 R859R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr19:10251808 A>G maps to NM_001130823.1 P1122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:10250420 G>A maps to NM_001130823.1 S1293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:10247956 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr19:10265583 G>T maps to NM_001130823.1 I547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:10248602 G>A maps to NM_001130823.1 L1400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:10260593 G>A maps to NM_001130823.1 T772T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr19:10249160 G>A maps to NM_001130823.1 L1357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:10248570 G>A maps to NM_001130823.1 S1410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr19:10246814 G>A maps to NM_001130823.1 P1546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr19:10264998 G>A maps to NM_001130823.1 A663A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:10265055 G>A maps to NM_001130823.1 F644F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:25464475 C>G maps to NM_175629.1 G679G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr2:25457288 C>T maps to NM_175629.1 R866R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr2:25457289 C>T did not map to a codon.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr2:25467475 G>A maps to NM_175629.1 Q534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:25467047 G>A maps to NM_175629.1 F609F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:25462015 G>A maps to NM_175629.1 N797N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr2:25471034 G>A maps to NM_175629.1 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr20:31374369 C>T maps to NM_006892.3 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr20:31375127 G>A maps to NM_006892.3 E175E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr20:31374316 C>T maps to NM_006892.3 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:31395664 C>T maps to NM_006892.3 R840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr20:31387100 C>T maps to NM_006892.3 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr20:31374420 C>T maps to NM_006892.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:31374318 A>T maps to NM_006892.3 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:31386388 C>T maps to NM_006892.3 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr21:45678546 C>T maps to NM_013369.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr21:45666333 G>A maps to NM_013369.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr21:45679414 G>A maps to NM_013369.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr21:45666381 C>T maps to NM_013369.2 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:45670698 G>A maps to NM_013369.2 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:45671560 G>A maps to NM_013369.2 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:45678477 G>A maps to NM_013369.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:45681058 G>A maps to NM_013369.2 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:220239597 G>A maps to NM_012100.2 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:220246091 G>A maps to NM_012100.2 R402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:220239720 G>A maps to NM_012100.2 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:220239732 G>A maps to NM_012100.2 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr10:98092350 C>A maps to NM_004088.3 R453R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:98064427 G>A maps to NM_004088.3 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:98092299 C>T maps to NM_004088.3 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:98080481 C>T maps to NM_004088.3 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:98092339 G>A maps to NM_004088.3 W449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:98092169 G>A maps to NM_004088.3 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr10:98088480 G>A did not map to a codon.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr10:98087354 G>A maps to NM_004088.3 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr10:98079147 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:44420687 G>A maps to NM_052951.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:94337725 G>A maps to NM_014597.4 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:94342881 G>C maps to NM_014597.4 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr16:30018393 G>A maps to NM_003586.2 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:30021291 C>T maps to NM_003586.2 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:30018571 C>T maps to NM_003586.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:30020408 C>T maps to NM_003586.2 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr10:129237335 C>T maps to ENST00000398025 S1747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:129242484 C>T maps to ENST00000398025 S1830S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:129055603 C>T maps to ENST00000398025 F1030F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:129202693 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr10:129237476 C>T maps to ENST00000398025 I1794I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr10:128908529 C>T maps to ENST00000398025 F824F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr10:128830007 C>T maps to ENST00000398025 I552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr10:129224220 C>T maps to ENST00000398025 A1665A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr10:129179589 C>G maps to ENST00000398025 T1300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr2:225739008 G>A maps to NM_014689.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:225729786 C>A maps to NM_014689.2 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:225670000 G>A maps to NM_014689.2 R1325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr2:225739406 G>A maps to NM_014689.2 N331N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr2:225751241 T>C maps to NM_014689.2 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr2:225639826 G>A maps to NM_014689.2 N1936N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr2:225740794 G>A maps to NM_014689.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr2:225781459 T>A maps to NM_014689.2 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:225639751 G>A maps to NM_014689.2 I1961I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:225750836 G>A maps to NM_014689.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:117749609 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:117775214 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3CE-06A-11D-A19A-08 chr23:117752566 T>C did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:117706350 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr23:117727191 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:117788918 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:117814592 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr23:117744239 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:117739214 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr23:117695391 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr23:117724264 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:117815029 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:117788728 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:117680002 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:117731476 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:117786036 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:117676959 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:117714067 G>A did not map to a codon.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr23:117712601 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:117722242 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:117722243 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:117762187 C>G did not map to a codon.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr23:117727236 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:117762224 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:117744353 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr23:117805074 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr23:117758534 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:117788608 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr23:117744303 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:117727236 C>T did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:117700053 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:117718739 G>A did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:117707774 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr23:117676892 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr5:169454943 G>A maps to NM_004946.2 L1153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr5:169507174 G>A maps to NM_004946.2 R1725R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr5:169484666 G>A maps to NM_004946.2 S1488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:169494644 G>A maps to NM_004946.2 G1533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:169446039 C>T maps to NM_004946.2 L1103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:169494533 G>A maps to NM_004946.2 E1496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr5:169474611 C>T maps to NM_004946.2 F1355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr5:169141085 C>T maps to NM_004946.2 R572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr5:169423152 G>A maps to NM_004946.2 T1019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:169096331 G>A maps to NM_004946.2 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:169143222 C>T maps to NM_004946.2 Q650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:169186716 T>C maps to NM_004946.2 A795A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:169508870 C>T maps to NM_004946.2 I1771I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr5:169144386 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:169468062 C>T maps to NM_004946.2 L1224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:169125405 G>A maps to NM_004946.2 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr5:169423092 C>T maps to NM_004946.2 V999V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr5:169111327 C>T maps to NM_004946.2 Y245Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:169116291 C>T maps to NM_004946.2 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:169412860 C>T maps to NM_004946.2 F976F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:169081455 C>T maps to NM_004946.2 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:169454910 G>A maps to NM_004946.2 G1142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:169461456 C>T maps to NM_004946.2 F1174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:169477381 G>A maps to NM_004946.2 V1398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:51297693 C>T maps to NM_004947.4 F764F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:51297744 C>T maps to NM_004947.4 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:51370666 A>G maps to NM_004947.4 E1198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr3:51378680 C>T maps to NM_004947.4 T1260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:51263125 C>T maps to NM_004947.4 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr3:51263119 G>A maps to NM_004947.4 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr3:51395390 G>T did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr3:51264838 G>A maps to NM_004947.4 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:51378770 G>A maps to NM_004947.4 K1290K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:51352495 C>T maps to NM_004947.4 I1113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:51266195 C>T maps to NM_004947.4 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:51349989 G>A maps to NM_004947.4 R1059R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:51394463 C>T maps to NM_004947.4 I1525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:51284162 C>T maps to NM_004947.4 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:51418497 C>T maps to NM_004947.4 I1867I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr3:51263125 C>T maps to NM_004947.4 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:51393866 C>T maps to NM_004947.4 T1482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:51112816 G>A maps to NM_004947.4 K165K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:51264820 C>T maps to NM_004947.4 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:51352489 G>A maps to NM_004947.4 R1111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr3:51394409 G>A maps to NM_004947.4 L1507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr3:51352507 C>T maps to NM_004947.4 I1117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:51101925 A>G maps to NM_004947.4 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:51274928 C>T maps to NM_004947.4 I670I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:51308340 G>A maps to NM_004947.4 G817G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:51263086 C>T maps to NM_004947.4 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:51297628 C>T maps to NM_004947.4 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr3:51267024 G>A maps to NM_004947.4 G634G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:51378815 G>A maps to NM_004947.4 K1305K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:51387801 G>A maps to NM_004947.4 R1362R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:51370630 C>A maps to NM_004947.4 G1186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr3:51418833 C>T maps to NM_004947.4 H1979H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:51297627 C>T maps to NM_004947.4 I742I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:51349911 G>A maps to NM_004947.4 W1033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr3:50816190 T>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:51266124 C>T maps to NM_004947.4 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr3:51266973 C>T maps to NM_004947.4 A617A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:51370587 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:51387786 C>T maps to NM_004947.4 V1357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:51352507 C>T maps to NM_004947.4 I1117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:111368758 G>A maps to ENST00000428084 F1833F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:111430623 G>A maps to ENST00000428084 G1068G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:111448895 G>A maps to ENST00000428084 F1049F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:111430617 G>A maps to ENST00000428084 F1070F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr7:111503500 C>T maps to ENST00000428084 V800V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr7:111484898 G>A maps to ENST00000428084 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:111584864 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:111503491 G>A maps to ENST00000428084 S803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr7:111398778 C>T maps to ENST00000428084 P1410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:111509674 C>T maps to ENST00000428084 R688R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr7:111409608 G>A maps to ENST00000428084 I1268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr7:111381657 C>A maps to ENST00000428084 V1619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:111584887 G>A maps to ENST00000428084 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr8:25174577 G>A maps to NM_024940.6 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:25168013 C>T maps to NM_024940.6 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:25246713 T>G maps to NM_024940.6 P1413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:25209302 C>T maps to NM_024940.6 N937N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr19:11325237 G>A maps to ENST00000319867 I1398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:11326103 C>T maps to ENST00000319867 K1355K. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A181-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:11363580 G>A maps to ENST00000319867 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr19:11326521 G>A maps to ENST00000319867 L1326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:11333707 C>T maps to ENST00000319867 R1010R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-FS-A4FC-06A-11D-A24R-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:11319415 G>A maps to ENST00000319867 F1678F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr19:11319448 G>A maps to ENST00000319867 P1667P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr1:63005461 G>A maps to ENST00000371140 V1049V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr1:63099228 T>C maps to ENST00000371140 Q352Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:62979529 G>A maps to ENST00000371140 R1326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:63042953 A>G maps to ENST00000371140 A697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:63099246 T>A maps to ENST00000371140 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19T-06A-11D-A19A-08 chr1:62958386 A>T maps to ENST00000371140 A1783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:63024828 G>A maps to ENST00000371140 V754V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr9:418203 C>T maps to NM_203447.3 S1279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr9:406940 C>T maps to NM_203447.3 S1134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:406953 C>T maps to NM_203447.3 Q1139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr9:325673 C>T maps to NM_203447.3 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:406928 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr9:441915 C>T maps to NM_203447.3 F1799F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:463585 C>A maps to NM_203447.3 L2046L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr9:332408 C>T maps to NM_203447.3 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr9:399219 G>A maps to NM_203447.3 R1065R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:420555 C>T maps to NM_203447.3 F1332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr9:379849 C>T maps to NM_203447.3 D840D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr13:99567640 G>A maps to ENST00000428223 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr13:99535331 G>A maps to ENST00000428223 A841A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr13:99537974 G>A maps to ENST00000428223 V749V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr13:99515322 G>A maps to ENST00000428223 Q1177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr13:99538815 G>A maps to ENST00000428223 H702H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr13:99489771 A>G maps to ENST00000428223 L1407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:99515686 G>A maps to ENST00000428223 I1134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr13:99462527 G>A maps to ENST00000428223 L1716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr13:99483947 C>T maps to ENST00000428223 T1446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr13:99575588 G>A maps to ENST00000428223 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr13:99515290 G>A maps to ENST00000428223 F1187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:99582505 G>A maps to ENST00000428223 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:3496632 G>C maps to NM_001145165.1 Y60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:3496710 G>A maps to NM_001145165.1 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:3492320 G>A maps to NM_001145165.1 Y176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr2:74782573 C>T maps to NM_001381.3 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr2:74783859 C>T maps to NM_001381.3 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr2:74783057 C>T maps to NM_001381.3 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:21767051 G>A maps to NM_003974.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr8:21767094 A>T maps to NM_003974.2 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:21766992 G>A maps to NM_003974.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:21767127 C>A maps to NM_003974.2 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:21766992 G>A maps to NM_003974.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:176931105 G>A maps to NM_024872.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:176931914 C>T maps to NM_024872.2 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr5:176931355 G>A maps to NM_024872.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:57507917 G>A maps to NM_018110.3 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr20:53205047 C>T maps to NM_018431.3 N67N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:53205054 C>T maps to NM_018431.3 R70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:53266969 G>A maps to NM_018431.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr18:67231814 C>T maps to NM_152721.5 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr18:67345045 G>A maps to NM_152721.5 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr18:67365638 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr18:67231814 C>T maps to NM_152721.5 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr4:3495068 G>A maps to ENST00000389653 R452R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:3495005 C>T maps to ENST00000389653 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr4:3475241 C>T maps to ENST00000389653 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr4:3495008 G>A maps to ENST00000389653 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:131708607 G>A maps to NM_014908.3 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr9:131843439 C>T maps to NM_020438.4 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:131847309 C>T maps to NM_020438.4 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr9:131847366 G>A maps to NM_020438.4 Q81Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr21:34955848 G>A maps to NM_017613.2 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr6:83850122 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:83847745 C>T maps to NM_015018.2 L1329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr6:83877667 G>T maps to NM_015018.2 E2394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:83834471 C>T maps to NM_015018.2 D463D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:83810446 C>T maps to NM_015018.2 Y54Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:83810447 C>T maps to NM_015018.2 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr6:83839878 T>G maps to NM_015018.2 T793T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:83828677 G>A maps to NM_015018.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr21:37581027 C>T maps to NM_005128.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr21:37591676 A>G maps to NM_005128.2 Q379Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr21:37618855 C>T maps to NM_005128.2 S1526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr21:37591780 C>A maps to NM_005128.2 S414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:37603280 G>A maps to NM_005128.2 E733E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr21:37571507 C>T maps to NM_005128.2 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr21:37602938 G>A maps to NM_005128.2 K619K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr21:37636075 C>T maps to NM_005128.2 P1817P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr21:37605195 C>T maps to NM_005128.2 S815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr21:37665781 G>A maps to NM_005128.2 L2270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr21:37602854 C>T maps to NM_005128.2 I591I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr21:37660348 C>T maps to NM_005128.2 S2066S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr21:37618712 C>T maps to NM_005128.2 Q1479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr21:37597943 C>T maps to NM_005128.2 F484F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr21:37597944 C>T maps to NM_005128.2 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr21:37617406 C>G maps to NM_005128.2 P1043P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr21:37605228 C>T maps to NM_005128.2 S826S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr21:37597931 C>T maps to NM_005128.2 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:37650509 C>T maps to NM_005128.2 A1942A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr21:37571507 C>T maps to NM_005128.2 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr19:2216416 C>T maps to ENST00000221482 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:2222197 C>T maps to ENST00000221482 P1010P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:2226332 C>T maps to ENST00000221482 S1271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:2226941 C>T maps to ENST00000221482 F1474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:2222479 C>T maps to ENST00000221482 S1104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:2216324 C>T maps to ENST00000221482 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr19:2180749 C>T maps to ENST00000221482 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr19:2220135 C>T maps to ENST00000221482 P907P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:2217046 C>T maps to ENST00000221482 S834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:2217877 C>T maps to ENST00000221482 P884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr19:2211777 C>T maps to ENST00000221482 F498F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:118969131 C>A maps to NM_001382.3 G237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:118969168 G>A maps to NM_001382.3 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr11:118969159 G>A maps to NM_001382.3 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:118967875 G>A maps to NM_001382.3 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr6:30919831 C>T maps to NM_080870.3 T1197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr6:30920764 G>A maps to NM_080870.3 R1351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr16:89703004 C>T maps to NM_004413.3 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:89702701 C>T maps to NM_004413.3 Q90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:89704246 C>T maps to NM_004413.3 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr16:68021585 G>A maps to NM_022355.2 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:68024016 G>A maps to NM_022355.2 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr16:68021799 A>C maps to NM_022355.2 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr16:68024789 G>A maps to NM_022355.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:68009904 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr16:68010127 G>A maps to NM_022357.3 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr16:68011630 C>T maps to NM_022357.3 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr19:38706801 G>A maps to NM_001135155.1 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr19:38709272 G>A maps to NM_001135155.1 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:65119202 C>T maps to NM_006268.3 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:65107855 C>T maps to NM_006268.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr14:73137987 C>G maps to NM_012074.3 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:73138023 C>T maps to NM_012074.3 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr14:73190412 A>G maps to NM_012074.3 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:73190400 C>T maps to NM_012074.3 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:73159784 C>T maps to NM_012074.3 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr17:1943099 C>T maps to NM_001383.3 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:1943833 C>T maps to NM_001383.3 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:44437137 C>T maps to NM_001384.4 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:49551728 C>T maps to ENST00000449701 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:49575051 G>A maps to ENST00000449701 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:116447264 T>A maps to NM_020868.3 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:116535371 G>A maps to NM_020868.3 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:116066840 G>A maps to NM_020868.3 Q29Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:116503667 C>T maps to NM_020868.3 Q287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr2:116257131 G>A maps to NM_020868.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:116572407 C>T maps to NM_020868.3 F580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr2:116572407 C>T maps to NM_020868.3 F580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:116599798 G>T maps to NM_020868.3 E757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr2:116548735 C>T maps to NM_020868.3 I537I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr2:115200378 C>T maps to NM_020868.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr2:116538497 C>T maps to NM_020868.3 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:66249784 C>T maps to NM_005700.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:66272216 C>T maps to NM_005700.3 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:66260349 C>A maps to NM_005700.3 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:66258745 G>T maps to NM_005700.3 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:66254782 C>T maps to NM_005700.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr11:66254124 C>T maps to NM_005700.3 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:162849795 A>C maps to NM_001935.3 P766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:162873616 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:162881448 C>T maps to NM_001935.3 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:162873346 A>G maps to NM_001935.3 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:162873627 C>T maps to NM_001935.3 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr2:162875263 C>T maps to NM_001935.3 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr7:154143390 C>T maps to NM_130797.2 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr7:153584806 G>A maps to NM_001039350.1 Q13Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:154172102 C>T maps to NM_130797.2 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr7:154672627 G>A maps to NM_130797.2 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:154561130 G>A maps to NM_130797.2 E296E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:154684120 C>T maps to NM_130797.2 F843F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:154667732 C>T maps to NM_130797.2 F667F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr7:154593138 G>A maps to NM_130797.2 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr7:154595635 C>T maps to NM_130797.2 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:154667810 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:154684135 G>A maps to NM_130797.2 R848R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr9:140006200 T>G maps to NM_013379.2 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr15:65772706 C>T maps to NM_197960.2 Q399Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr19:4697660 G>A maps to ENST00000357909 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:4679939 G>A maps to ENST00000357909 I910I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:4683593 G>T maps to ENST00000357909 A821A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:4684698 G>A maps to ENST00000357909 F797F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:4682739 G>A maps to ENST00000357909 S893S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr3:109031533 G>A maps to NM_138815.3 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:109027926 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr3:109019281 C>T maps to NM_138815.3 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:109023323 C>T maps to NM_138815.3 K284K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19T-06A-11D-A19A-08 chr3:109033384 G>C maps to NM_138815.3 S2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr3:109023371 G>A maps to NM_138815.3 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr3:109031470 G>A maps to NM_138815.3 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:7868816 G>A maps to NM_199286.2 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:7867806 G>A maps to NM_199286.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:7867917 C>T maps to NM_199286.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:7867806 G>A maps to NM_199286.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:7869614 G>A maps to NM_199286.2 W141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:7867833 C>T maps to NM_199286.2 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:109047900 G>A maps to NM_018189.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:109050813 G>A maps to NM_018189.3 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:109047909 C>T maps to NM_018189.3 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr3:109049622 T>A maps to NM_018189.3 K143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:109049623 C>T maps to NM_018189.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:109046860 A>G maps to NM_018189.3 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:109049428 C>T maps to NM_018189.3 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr3:109049503 G>A maps to NM_018189.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:109050777 C>T maps to NM_018189.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:109049512 C>T maps to NM_018189.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr6:74063755 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr6:74063702 G>A maps to NM_001025290.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr6:74063663 G>A maps to NM_001025290.2 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:74063622 C>T maps to NM_001025290.2 W82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr19:54140070 C>T maps to NM_001012728.1 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:54140038 C>T maps to NM_001012728.1 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr19:54140082 C>T maps to NM_001012728.1 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54140038 C>T maps to NM_001012728.1 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:54140240 G>A maps to NM_001012728.1 *192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:54140038 C>T maps to NM_001012728.1 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:168698194 C>T maps to NM_001937.4 W73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:168670274 G>A maps to NM_001937.4 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:168698214 C>T maps to NM_001937.4 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr7:35009086 G>A maps to NM_015283.1 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr7:35013199 C>T maps to NM_015283.1 W207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr7:35051047 A>G maps to NM_015283.1 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr12:64061909 G>A maps to NM_173812.4 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:63974481 C>T maps to NM_173812.4 Q620Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:63963094 G>A maps to NM_173812.4 R679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr19:32954831 C>T maps to NM_001172774.1 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr19:32954295 G>C maps to NM_001172774.1 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:32949391 C>T maps to NM_001172774.1 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:32954810 C>T maps to NM_001172774.1 F494F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr19:32971432 C>T maps to NM_001172774.1 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:95777442 C>T maps to NM_181787.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:95778880 C>T maps to NM_181787.2 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr8:95778880 C>T maps to NM_181787.2 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:97915749 G>A maps to NM_000110.3 I590I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr1:97658660 C>T maps to NM_000110.3 G862G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:98165082 G>A maps to NM_000110.3 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:98039397 C>T maps to NM_000110.3 W419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr1:97547906 G>A maps to NM_000110.3 T962T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr1:97564143 G>A maps to NM_000110.3 I889I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:97981407 G>A maps to NM_000110.3 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:97700482 G>A maps to NM_000110.3 P789P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:98164964 G>A maps to NM_000110.3 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:97658666 C>T maps to NM_000110.3 Q860Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:97547927 G>A maps to NM_000110.3 N955N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:98165055 A>T maps to NM_000110.3 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:97564163 G>A maps to NM_000110.3 L883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:98058818 G>A maps to NM_000110.3 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr1:98164977 A>T maps to NM_000110.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr1:98187200 T>G maps to NM_000110.3 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr1:97981302 G>A maps to NM_000110.3 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr1:98165082 G>A maps to NM_000110.3 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:98058821 G>A maps to NM_000110.3 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:97915657 C>T maps to NM_000110.3 W621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:97839128 C>T maps to NM_000110.3 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr8:105405218 C>T maps to NM_001385.2 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr8:105405095 G>A maps to NM_001385.2 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr8:105393509 G>A maps to NM_001385.2 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:105440309 G>A maps to NM_001385.2 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr8:105440327 C>T maps to NM_001385.2 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:105456638 C>T maps to NM_001385.2 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:105405095 G>A maps to NM_001385.2 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr8:105393485 C>T maps to NM_001385.2 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr8:105405170 G>A maps to NM_001385.2 F428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr8:26505249 C>T maps to NM_001197293.1 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:26501042 C>T maps to NM_001197293.1 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr8:26505264 C>T maps to NM_001197293.1 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:26501099 C>T maps to NM_001197293.1 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:26435787 G>A maps to NM_001386.4 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:146775140 C>T maps to NM_001197294.1 Q649Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:146781107 C>G maps to NM_001197294.1 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:146780332 C>T maps to NM_001197294.1 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:146785233 G>A maps to NM_001197294.1 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr10:134012475 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:134013998 C>T maps to NM_006426.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:134016274 C>T maps to NM_006426.2 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:27147816 C>T maps to NM_020134.3 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr2:27147840 C>T maps to NM_020134.3 C116C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr2:27147841 C>T maps to NM_020134.3 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr2:27157446 G>A maps to NM_020134.3 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr2:27165449 C>T maps to NM_020134.3 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr2:27121456 C>T maps to NM_020134.3 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:27167570 C>T maps to NM_020134.3 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:27167591 G>A maps to NM_020134.3 G503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:27163024 C>T maps to NM_020134.3 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:27151148 G>A maps to NM_020134.3 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:27151187 G>A maps to NM_020134.3 E222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:27167663 C>T maps to NM_020134.3 D527D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:74750028 C>T maps to NM_133637.2 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:74751155 C>T maps to NM_133637.2 W237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:74751425 C>T maps to NM_133637.2 W147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:102302022 C>T maps to NM_018370.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:111667495 A>G maps to NM_178454.4 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr5:174869118 G>A maps to NM_000794.3 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:174868953 C>T maps to NM_000794.3 K383K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:174868800 C>T maps to NM_000794.3 K434K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr5:174868995 C>T maps to NM_000794.3 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:174869337 T>C maps to NM_000794.3 Q255Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr5:174869085 C>T maps to NM_000794.3 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:174869874 C>T maps to NM_000794.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr5:174868995 C>T maps to NM_000794.3 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr5:174868953 C>T maps to NM_000794.3 K383K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:174869919 G>A maps to NM_000794.3 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:113283332 C>T maps to ENST00000355319 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr11:113286190 G>A maps to ENST00000355319 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:113283383 C>T maps to ENST00000355319 Q346Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr11:113281475 C>T maps to ENST00000355319 K437K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:113286232 C>T maps to ENST00000355319 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:113287660 G>A maps to ENST00000355319 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:113281466 C>T maps to ENST00000355319 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr11:113286292 G>A maps to ENST00000355319 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr11:113281469 G>A maps to ENST00000355319 F439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr11:113288813 G>A maps to ENST00000355319 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:113283287 G>A maps to ENST00000355319 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:113283332 C>T maps to ENST00000355319 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:113288759 G>A maps to ENST00000355319 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:113295193 G>A maps to ENST00000355319 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:113283470 G>A maps to ENST00000355319 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr3:113847727 G>A maps to NM_000796.3 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr3:113890704 G>A maps to NM_000796.3 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr3:113890764 C>T maps to NM_000796.3 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr3:113878690 G>A maps to NM_000796.3 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:113890710 G>A maps to NM_000796.3 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:113890722 G>A maps to NM_000796.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr3:113890623 A>G maps to NM_000796.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:113890710 G>A maps to NM_000796.3 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr4:9784921 G>A maps to NM_000798.4 R423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr4:9784954 C>T maps to NM_000798.4 F434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:9785080 C>T maps to NM_000798.4 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr4:9784591 C>T maps to NM_000798.4 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr4:9784954 C>T maps to NM_000798.4 F434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:9784198 G>A maps to NM_000798.4 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr4:9784492 C>T maps to NM_000798.4 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr4:9784135 C>T maps to NM_000798.4 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:9785023 G>A maps to NM_000798.4 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr4:9783796 C>T maps to NM_000798.4 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr4:9784033 C>T maps to NM_000798.4 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr4:9783892 C>T maps to NM_000798.4 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr4:9784015 C>T maps to NM_000798.4 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:9784260 G>A maps to NM_000798.4 W203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:9783967 T>C maps to NM_000798.4 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr4:9784666 G>A maps to NM_000798.4 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr4:9784681 C>T maps to NM_000798.4 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:9784036 C>T maps to NM_000798.4 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:9784540 G>A maps to NM_000798.4 K296K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:9784684 C>T maps to NM_000798.4 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:9784984 C>T maps to NM_000798.4 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr22:31829902 G>A maps to NM_004147.3 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:31807017 C>T maps to NM_004147.3 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr17:18004831 C>T maps to NM_001388.3 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr17:18007133 C>T maps to NM_001388.3 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr17:18004858 C>T maps to NM_001388.3 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr10:50599296 G>T maps to NM_001080520.1 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr10:50594599 G>A maps to NM_001080520.1 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:50594775 G>A maps to NM_001080520.1 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr10:50594751 C>T maps to NM_001080520.1 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:50599892 G>A maps to NM_001080520.1 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:50594874 C>T maps to NM_001080520.1 W93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr23:100505940 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:100490967 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:100490864 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:100497447 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr23:100497921 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr23:100511120 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:100493978 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:100496793 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr23:100486726 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:100503575 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:100497446 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:100515074 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:100492725 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr18:28725675 C>T maps to NM_024421.2 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr18:28725699 T>C maps to NM_024421.2 E271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr18:28725603 G>A maps to NM_024421.2 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr18:28710795 G>A maps to NM_004948.3 S831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr18:28737417 C>T maps to NM_024421.2 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr18:28737417 C>T maps to NM_024421.2 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr18:28710545 C>T maps to NM_024421.2 E872E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr18:28720198 G>A maps to NM_024421.2 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr18:28742521 G>A maps to NM_024421.2 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr18:28737399 G>A maps to NM_024421.2 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:28712646 G>A maps to NM_024421.2 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr18:28719848 G>A maps to NM_024421.2 Q509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr18:28720072 G>A maps to NM_024421.2 F484F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr18:28711787 G>A maps to NM_024421.2 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr18:28714588 G>A maps to NM_024421.2 Q608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr18:28737399 G>A maps to NM_024421.2 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr18:28711670 G>A maps to NM_024421.2 S791S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr18:28737417 C>T maps to NM_024421.2 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr18:28714631 C>T maps to NM_024421.2 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr18:28722081 C>T maps to NM_024421.2 Q380Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:28710545 C>T maps to NM_024421.2 E872E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:28714583 G>A maps to NM_024421.2 F609F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:28722111 C>T maps to NM_024421.2 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:28725630 G>A maps to NM_024421.2 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr18:28739449 G>A maps to NM_024421.2 R36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr18:28648937 C>T maps to ENST00000438199 R823R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr18:28648979 G>A maps to ENST00000438199 S809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr18:28651783 G>A maps to ENST00000438199 Q651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr18:28659858 G>A maps to ENST00000438199 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr18:28670999 G>A maps to ENST00000438199 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr18:28666640 C>T maps to ENST00000438199 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr18:28659869 C>A maps to ENST00000438199 E549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr18:28669478 A>G maps to ENST00000438199 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr18:28650810 G>A maps to ENST00000438199 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:28647981 C>T maps to ENST00000438199 *915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:28650781 C>T maps to ENST00000438199 G733G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:28659861 C>T maps to ENST00000438199 E551E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr18:28667686 G>A maps to ENST00000438199 Y253Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr18:28602424 C>T maps to NM_001941.3 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr18:28609492 G>A maps to NM_001941.3 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr18:28609498 G>A maps to NM_001941.3 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:28584174 C>T maps to NM_001941.3 R682R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr18:28581685 T>C maps to NM_001941.3 V711V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr18:28574456 G>A maps to NM_024423.2 S833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr18:28609492 G>A maps to NM_001941.3 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr18:28611118 G>A maps to NM_001941.3 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr18:28576968 G>A maps to NM_001941.3 Q761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr18:28598156 C>T maps to NM_001941.3 K381K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr18:28609538 C>T maps to NM_001941.3 W137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr18:28602371 G>T maps to NM_001941.3 S291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr18:28598186 C>T maps to NM_001941.3 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr18:28588090 G>A maps to NM_001941.3 I518I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr21:42080488 G>A maps to NM_001389.3 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr21:41684098 G>T maps to NM_001389.3 S657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr21:41711283 C>T maps to NM_001389.3 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr21:41423966 C>T maps to NM_001389.3 T1701T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CC-06A-11D-A19A-08 chr21:41455871 A>C maps to NM_001389.3 S1398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr21:41414556 G>A maps to NM_001389.3 S1809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr21:41711172 C>T maps to NM_001389.3 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr21:41496160 G>A maps to NM_001389.3 I1219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr21:41539148 C>T maps to NM_001389.3 W1005*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr21:41496202 G>A maps to NM_001389.3 V1205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr21:41539144 C>T maps to NM_001389.3 K1006K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr21:41719804 G>A maps to NM_001389.3 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr21:42064799 G>A maps to NM_001389.3 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr21:41719783 C>T maps to NM_001389.3 E341E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr21:41424008 C>T maps to NM_001389.3 T1687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44Q-06A-11D-A25O-08 chr21:41710217 C>A maps to NM_001389.3 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr21:41447000 C>T maps to NM_001389.3 R1617R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr21:41457667 C>T maps to NM_001389.3 T1331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr21:41668000 G>A maps to NM_001389.3 I721I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr21:41668060 C>T maps to NM_001389.3 G701G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr21:41516577 G>A maps to NM_001389.3 F1033F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr21:41539165 C>T maps to NM_001389.3 Q999Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr21:41719771 G>A maps to NM_001389.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr21:41711181 C>T maps to NM_001389.3 Q457Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr21:41684188 C>T maps to NM_001389.3 T627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr21:41719714 C>T maps to NM_001389.3 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr21:41496238 C>T maps to NM_001389.3 A1193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr21:41559848 C>T maps to NM_001389.3 E873E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr21:41385158 C>T maps to NM_001389.3 P1947P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr21:41559875 G>A maps to NM_001389.3 S864S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr21:41711082 C>T maps to NM_001389.3 A490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr21:42064778 G>A maps to NM_001389.3 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr21:42080613 G>A maps to NM_001389.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr21:41450635 G>A maps to NM_001389.3 F1563F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr21:42080545 C>T maps to NM_001389.3 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr21:41414574 G>A maps to NM_001389.3 S1803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr21:42080677 G>A maps to NM_001389.3 H21H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr21:41559881 G>A maps to NM_001389.3 F862F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr21:42080488 G>A maps to NM_001389.3 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr21:41447140 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr21:41711233 C>T maps to NM_001389.3 W440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr21:41719711 G>A maps to NM_001389.3 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr21:41741059 C>T maps to NM_001389.3 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr21:41385203 C>T maps to NM_001389.3 Q1932Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr21:42080527 C>T maps to NM_001389.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr21:42064772 G>A maps to NM_001389.3 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr21:41711241 C>T maps to NM_001389.3 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr21:42080488 G>A maps to NM_001389.3 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr21:41648176 G>A maps to NM_001389.3 Q735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr21:41496136 G>A maps to NM_001389.3 S1227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr21:41725545 C>T maps to NM_001389.3 K260K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr21:41496208 G>A maps to NM_001389.3 S1203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr21:42064778 G>A maps to NM_001389.3 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr21:42080488 G>A maps to NM_001389.3 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A197-06A-32D-A197-08 chr21:41561097 G>A maps to NM_001389.3 S808S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr21:41385239 C>T maps to NM_001389.3 R1920R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr21:41725662 C>T maps to NM_001389.3 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr21:41711157 C>A maps to NM_001389.3 V465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr21:42080413 C>T maps to NM_001389.3 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr21:42080617 C>T maps to NM_001389.3 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr21:41719723 C>T maps to NM_001389.3 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr21:41465789 C>T maps to NM_001389.3 E1236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr21:41450722 G>A maps to NM_001389.3 I1534I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr21:41550860 G>A maps to NM_001389.3 D980D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr21:41711214 C>T maps to NM_001389.3 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:41385134 G>A maps to NM_001389.3 S1955S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:41416084 C>T maps to NM_001389.3 W1768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:41450712 G>A maps to NM_001389.3 L1538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:41496172 C>T maps to NM_001389.3 L1215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:41516649 C>T maps to NM_001389.3 K1009K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:41559881 G>A maps to NM_001389.3 F862F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:41710034 G>A maps to NM_001389.3 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:41711232 C>T maps to NM_001389.3 W440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:42080467 G>A maps to NM_001389.3 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr21:41668000 G>A maps to NM_001389.3 I721I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr21:42064802 G>A maps to NM_001389.3 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr21:41447045 G>A maps to NM_001389.3 I1602I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr21:41452103 G>A maps to NM_001389.3 I1465I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr21:41711316 G>T maps to NM_001389.3 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr21:41385212 C>T maps to NM_001389.3 L1929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr21:41711175 G>A maps to NM_001389.3 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr21:41450904 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr11:117302310 G>A maps to NM_020693.2 S1831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr11:117651307 G>A maps to NM_020693.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:117335832 G>A maps to NM_020693.2 S1090S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:117302340 G>A maps to NM_020693.2 T1821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr11:117335787 C>T maps to NM_020693.2 T1105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr11:117342656 G>A maps to NM_020693.2 I1020I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr11:117403166 G>A maps to NM_020693.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr11:117332271 G>A maps to NM_020693.2 I1162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:117329625 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:117374728 C>T maps to NM_020693.2 G790G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:117391857 G>A maps to NM_020693.2 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:117392001 C>T maps to NM_020693.2 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr11:117647623 C>T maps to NM_020693.2 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr11:117391914 G>A maps to NM_020693.2 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:117651427 C>T maps to NM_020693.2 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:117329476 C>T maps to NM_020693.2 K1247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:117335655 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr11:117376337 C>T maps to NM_020693.2 R691R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:117376406 G>A maps to NM_020693.2 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:117304179 C>T maps to NM_020693.2 K1688K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:117392040 C>T maps to NM_020693.2 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr11:117299430 G>A maps to NM_020693.2 P1985P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:117389346 G>A maps to NM_020693.2 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:117376436 C>T maps to NM_020693.2 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:117329476 C>T maps to NM_020693.2 K1247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:117299058 G>A maps to NM_020693.2 S2109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:117310546 C>T maps to NM_020693.2 W1383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:117352752 G>A maps to NM_020693.2 V888V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:117403124 G>A maps to NM_020693.2 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr11:117376190 C>T maps to NM_020693.2 R740R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:117352779 G>A maps to NM_020693.2 I879I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:117299163 C>T maps to NM_020693.2 G2074G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:117301630 G>A maps to NM_020693.2 I1891I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:120865424 T>C maps to NM_024094.2 Q71Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr21:39426999 C>T maps to NM_005867.2 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr21:39492468 G>A maps to ENST00000398948 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:39427005 G>A maps to NM_005867.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr21:38390458 C>T maps to NM_018962.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr21:38390413 G>A maps to NM_018962.2 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr21:38380459 C>T maps to NM_018962.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:116756872 C>T maps to NM_013352.2 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr6:116758424 C>T maps to NM_013352.2 Q932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:116756947 G>A maps to NM_013352.2 W439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:116757958 C>T maps to NM_013352.2 R776R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr6:116757310 C>T maps to NM_013352.2 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr6:116756872 C>T maps to NM_013352.2 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:116757788 C>T maps to NM_013352.2 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr6:116752270 C>T maps to NM_013352.2 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr6:116757796 C>T maps to NM_013352.2 D722D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:116720700 C>T maps to NM_013352.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:116757238 C>T maps to NM_013352.2 F536F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr6:116747781 C>T maps to NM_013352.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr18:65179112 G>A maps to NM_032160.2 I921I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:65181845 G>A maps to NM_032160.2 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr18:65179019 G>A maps to NM_032160.2 P952P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr18:65178608 G>A maps to NM_032160.2 F1089F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr18:65178425 C>T maps to NM_032160.2 R1150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr18:65180051 G>A maps to NM_032160.2 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr18:65178796 G>A maps to NM_032160.2 Q1027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr18:65180609 G>A maps to NM_032160.2 F422F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:65178593 C>T maps to NM_032160.2 L1094L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:65180987 G>A maps to NM_032160.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr18:28906968 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr18:28913664 C>T maps to NM_001942.2 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr18:28918417 G>A did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr18:28913664 C>T maps to NM_001942.2 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr18:28916318 C>T maps to NM_001942.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr18:28914044 G>A maps to NM_001942.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr18:28911670 G>A maps to NM_001942.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr18:28911800 C>T maps to NM_001942.2 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr18:28926125 C>T maps to NM_001942.2 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:28934681 C>T maps to NM_001942.2 Y841Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:28913664 C>T maps to NM_001942.2 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr18:28934828 G>A maps to NM_001942.2 S890S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr18:28935264 C>T maps to NM_001942.2 R1036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:28906922 C>T maps to NM_001942.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:28913994 C>T maps to NM_001942.2 Q279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:28918361 G>A maps to NM_001942.2 K450K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr18:28934849 G>A maps to NM_001942.2 R897R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr18:29104709 G>A maps to NM_001943.3 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr18:29126474 G>A maps to NM_001943.3 Q1042Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr18:29111071 G>A maps to NM_001943.3 V379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr18:29122619 G>A maps to NM_001943.3 E713E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr18:29116201 C>T maps to NM_001943.3 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr18:29116336 C>T maps to NM_001943.3 S532S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr18:29126390 C>T maps to NM_001943.3 V1014V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr18:29102103 G>A maps to NM_001943.3 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr18:29100903 C>T maps to NM_001943.3 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr18:29101159 C>T maps to NM_001943.3 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr18:29039066 G>A maps to NM_001944.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr18:29049073 C>T maps to NM_001944.2 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:29055970 C>T maps to NM_001944.2 V916V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr18:29039108 C>T maps to NM_001944.2 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr18:29052253 C>T maps to NM_001944.2 P635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr18:29046703 C>T maps to NM_001944.2 I541I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr18:29046628 G>A maps to NM_001944.2 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:29039817 G>A maps to NM_001944.2 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:29044153 C>T maps to NM_001944.2 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:29049289 C>T maps to NM_001944.2 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:29056048 C>T maps to NM_001944.2 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:29049229 G>A maps to NM_001944.2 G605G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr18:29040923 G>A maps to NM_001944.2 Q271Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr18:28986202 C>T maps to NM_001134453.1 A600A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr18:28971153 C>T maps to NM_001134453.1 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr18:28993143 G>A maps to NM_001134453.1 G922G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr18:28968392 C>T maps to NM_001134453.1 R94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr18:28971160 T>C maps to NM_001134453.1 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr18:28991326 G>A maps to NM_001134453.1 R776R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr18:28993438 C>T maps to NM_001134453.1 Q1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr18:28989706 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr18:28993510 C>T maps to NM_001134453.1 R1045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr18:28972275 C>T maps to NM_001134453.1 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:28971129 G>A maps to NM_001134453.1 K258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr18:28989457 G>A maps to NM_001134453.1 Q659Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr18:28989469 G>A maps to NM_001134453.1 L663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr18:28986335 T>C maps to NM_001134453.1 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr18:28968853 G>A maps to NM_001134453.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr18:28971153 C>T maps to NM_001134453.1 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr18:28966652 G>A maps to NM_001134453.1 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr18:28992957 G>A maps to NM_001134453.1 R860R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr18:28972251 C>T maps to NM_001134453.1 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr18:28986100 C>T maps to NM_001134453.1 I566I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:28966721 C>T maps to NM_001134453.1 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:28968349 G>A maps to NM_001134453.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:28968392 C>T maps to NM_001134453.1 R94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr18:28966760 G>C maps to NM_001134453.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr18:28993278 G>A maps to NM_001134453.1 G967G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:28968349 G>A maps to NM_001134453.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:28989757 G>A maps to NM_177986.3 R708R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr20:35396434 C>T maps to NM_001145315.1 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr20:35399429 G>A maps to NM_001145315.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr6:7583626 C>T maps to NM_004415.2 S2044S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr6:7568800 C>T maps to NM_004415.2 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr6:7584637 G>A maps to NM_004415.2 K2381K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr6:7585390 C>T maps to NM_004415.2 S2632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:7558353 G>A maps to NM_004415.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr6:7583533 G>A maps to NM_004415.2 R2013R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr6:7580937 G>A maps to NM_004415.2 A1505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:7581042 C>T maps to NM_004415.2 I1540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:7585957 G>A maps to NM_004415.2 S2821S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr6:7581252 C>T maps to NM_004415.2 I1610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:7567681 G>A maps to NM_004415.2 Q380Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:7579755 C>T maps to NM_004415.2 I1111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:7584061 G>A maps to NM_004415.2 R2189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr6:7570789 C>T maps to NM_004415.2 I565I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:7583090 C>T maps to NM_004415.2 Q1866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:7583626 C>T maps to NM_004415.2 S2044S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:7569516 C>T maps to NM_004415.2 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:7580161 C>T maps to NM_004415.2 R1247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:7581387 G>A maps to NM_004415.2 R1655R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:7569423 C>T maps to NM_004415.2 I475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:7580517 G>A maps to NM_004415.2 Q1365Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:7585672 C>T maps to NM_004415.2 F2726F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr6:7584253 C>T maps to NM_004415.2 F2253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr6:7576532 G>A maps to NM_004415.2 W879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:7580447 G>A maps to NM_004415.2 W1342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:7581438 G>A maps to NM_004415.2 Q1672Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:7583527 C>T maps to NM_004415.2 F2011F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:7583683 G>A maps to NM_004415.2 R2063R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:7568117 G>A maps to NM_004415.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:7568686 C>T maps to NM_004415.2 I428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr6:7580073 G>A maps to NM_004415.2 T1217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr6:7585852 G>A maps to NM_004415.2 K2786K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr6:7565653 C>T maps to NM_004415.2 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr6:7569543 G>A maps to NM_004415.2 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr6:7583977 C>T maps to NM_004415.2 S2161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr6:7584253 C>T maps to NM_004415.2 F2253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:7581405 C>T maps to NM_004415.2 V1661V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr6:7585570 G>A maps to NM_004415.2 Q2692Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:7579584 G>A maps to NM_004415.2 K1054K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr6:7583116 G>A maps to NM_004415.2 K1874K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr6:7575658 C>T maps to NM_004415.2 F856F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr6:7580073 G>A maps to NM_004415.2 T1217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr6:7585753 G>A maps to NM_004415.2 K2753K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr6:7565728 C>T maps to NM_004415.2 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr6:7584610 C>T maps to NM_004415.2 I2372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:7581100 C>T maps to NM_004415.2 Q1560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:7585915 C>T maps to NM_004415.2 S2807S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr6:7569417 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:7585489 G>A maps to NM_004415.2 T2665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:7565752 C>T maps to NM_004415.2 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:7571683 C>T maps to NM_004415.2 F590F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:7576562 G>A maps to NM_004415.2 R889R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:7581369 G>A maps to NM_004415.2 R1649R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:7581549 C>T maps to NM_004415.2 L1709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:7584535 C>T maps to NM_004415.2 I2347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:7585342 G>A maps to NM_004415.2 S2616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:7581783 C>T maps to NM_004415.2 F1787F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:7583077 G>A maps to NM_004415.2 Q1861Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:7583575 A>G maps to NM_004415.2 E2027E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:7579758 C>T maps to NM_004415.2 T1112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr6:7584184 G>A maps to NM_004415.2 P2230P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D9-A6EC-06A-11D-A30X-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:88533670 G>A maps to NM_014208.3 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr4:88533670 G>A maps to NM_014208.3 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr4:88533472 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr4:88535190 C>T maps to NM_014208.3 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr4:88533577 G>A maps to NM_014208.3 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr6:56422232 G>A maps to ENST00000361203 Q4631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:56496082 G>A maps to ENST00000361203 T1145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr6:56458571 G>T maps to ENST00000361203 A3994A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr6:56334925 C>T maps to ENST00000361203 E7254E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr6:56357835 G>A maps to ENST00000361203 Q6605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr6:56357836 G>A maps to ENST00000361203 L6604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr6:56391320 G>A maps to ENST00000361203 S5778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:56462756 G>A maps to ENST00000361203 N3781N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:56483899 T>C maps to ENST00000281662 R2208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:56374635 C>T maps to ENST00000361203 L6061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr6:56324943 G>A maps to ENST00000361203 R7452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:56483104 G>A maps to ENST00000281662 S2473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr6:56481112 G>A maps to ENST00000281662 S2948S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr6:56494202 G>A maps to ENST00000361203 F1229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:56479240 G>T maps to ENST00000361203 A1446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:56374635 C>T maps to ENST00000361203 L6061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:56324980 C>T maps to ENST00000361203 E7439E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:56483821 C>T maps to ENST00000281662 Q2234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr6:56462804 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr6:56418154 G>A maps to ENST00000361203 T4934T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr6:56496731 G>C maps to ENST00000361203 P1093P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr6:56504762 T>C maps to ENST00000361203 E650E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:56481388 G>A maps to ENST00000281662 F2856F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr6:56357848 G>A maps to ENST00000361203 F6600F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr1:205138810 G>A maps to NM_015375.2 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:205129294 G>A maps to NM_015375.2 V684V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:205116757 G>A maps to NM_015375.2 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:205126505 C>A maps to NM_015375.2 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:205138440 C>A maps to NM_015375.2 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr1:205138705 A>G maps to NM_015375.2 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:205132912 G>A maps to NM_015375.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:205133000 G>A maps to NM_015375.2 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44Q-06A-11D-A25O-08 chr20:18576793 C>T maps to NM_080820.4 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr20:18724886 G>A maps to NM_080820.4 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:212273636 G>A maps to NM_016448.2 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:212276200 C>T maps to NM_016448.2 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:212241643 C>T maps to NM_016448.2 Y264Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr18:32398131 C>T maps to NM_001390.4 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr18:32398221 G>A maps to NM_001390.4 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr18:32455318 C>T maps to NM_001390.4 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr18:32374193 C>T maps to NM_001390.4 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:32455267 C>T maps to NM_001390.4 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:25611083 C>T maps to NM_021907.3 E574E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr6:15533576 G>C maps to NM_032122.4 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:15627668 C>T maps to NM_032122.4 W87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:15651587 A>C maps to NM_032122.4 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:49924492 C>T maps to NM_001144955.1 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:118274913 G>A maps to NM_173666.2 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:118176689 T>G maps to NM_173666.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr5:118264252 G>A maps to NM_173666.2 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CE-06A-11D-A19A-08 chr12:113515256 C>T maps to NM_004416.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:113532691 C>T maps to NM_004416.2 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr12:113496248 G>A maps to NM_004416.2 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr12:113532724 C>T maps to NM_004416.2 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:113532926 C>T maps to NM_004416.2 F489F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr12:113534560 C>T maps to NM_004416.2 I560I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:113532914 G>A maps to NM_004416.2 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:113532956 C>T maps to NM_004416.2 F499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:113532971 C>T maps to NM_004416.2 T504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr7:76126702 C>T maps to NM_020892.2 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:76109951 C>T maps to NM_020892.2 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr7:76111876 C>T maps to NM_020892.2 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:76112062 C>T maps to NM_020892.2 C169C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:76112101 G>T maps to NM_020892.2 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:76111855 C>T maps to NM_020892.2 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:58001062 C>T maps to NM_178502.2 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:58001366 C>T maps to NM_178502.2 Q241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr12:58000658 C>T maps to NM_178502.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr12:58000786 C>T maps to NM_178502.2 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:58000756 G>A maps to NM_178502.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr12:58002892 G>A maps to NM_178502.2 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:122283299 C>T maps to NM_138287.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr15:45431688 C>T maps to NM_175940.1 G427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr15:45436414 C>T maps to NM_175940.1 I706I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr15:45454089 G>A maps to NM_175940.1 R1337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:45439719 G>A maps to NM_175940.1 R804R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:45426451 G>A maps to NM_175940.1 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:45428766 C>T maps to NM_175940.1 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:45433148 C>T maps to NM_175940.1 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr15:45424172 C>T maps to NM_175940.1 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:45426392 C>T maps to NM_175940.1 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:45454532 G>C maps to NM_175940.1 L1402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr15:45433597 C>T maps to NM_175940.1 V558V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr15:45433531 C>A maps to NM_175940.1 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr15:45401085 G>A maps to NM_014080.4 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr15:45396350 C>T maps to NM_014080.4 V849V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr15:45386799 G>A maps to NM_014080.4 F1495F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:45394075 C>T maps to NM_014080.4 E922E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:45389916 G>A maps to NM_014080.4 L1196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr15:45399579 G>A maps to NM_014080.4 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr15:45387729 A>G maps to NM_014080.4 L1382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:45398523 C>T maps to NM_014080.4 A649A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr15:45389835 G>A maps to NM_014080.4 H1223H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr15:45398381 G>A maps to NM_014080.4 L697L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:45392329 G>A maps to NM_014080.4 F1034F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:45398340 G>A maps to NM_014080.4 I710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr15:45389469 C>T maps to NM_014080.4 E1271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr15:45387154 G>A maps to NM_014080.4 F1458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr15:45397873 G>A maps to NM_014080.4 I767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr15:45387154 G>A maps to NM_014080.4 F1458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr15:45396413 G>A maps to NM_014080.4 F828F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:45387766 C>T maps to NM_014080.4 E1369E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:45402902 G>A maps to NM_014080.4 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:45404007 C>T maps to NM_014080.4 W157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:45389544 G>A maps to NM_014080.4 F1246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr15:45394108 C>T maps to NM_014080.4 S911S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr15:45413408 G>A maps to NM_144565.2 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr15:45415185 G>A maps to NM_144565.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:45409339 C>T maps to NM_207581.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:45410014 C>T maps to NM_207581.3 Q291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr15:45408346 C>T maps to NM_207581.3 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:76797701 C>T maps to NM_001003892.1 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr17:80022716 G>A maps to NM_022156.3 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:80018757 G>A maps to NM_022156.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:68109263 C>A maps to NM_017803.3 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr16:68112355 C>T maps to NM_017803.3 R393R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:68110571 C>T maps to NM_017803.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:68108046 C>T maps to NM_017803.3 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:5789330 G>A maps to NM_020175.2 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:5789331 G>A maps to NM_020175.2 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:5789613 G>A maps to NM_020175.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:5786500 A>G maps to NM_020175.2 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr5:172195794 C>T maps to NM_004417.3 Q358Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:172196656 G>A maps to NM_004417.3 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr5:172197250 G>A maps to NM_004417.3 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:221875828 G>A maps to NM_007207.3 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:221913006 A>C maps to NM_007207.3 L27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:221912311 G>A maps to NM_007207.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr10:76868834 G>A maps to NM_001007272.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr10:76855507 G>A maps to ENST00000356369 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:76861671 C>T maps to ENST00000356369 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:76857621 C>T maps to ENST00000356369 Q136Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr10:76854535 G>A maps to ENST00000356369 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr10:76854535 G>A maps to ENST00000356369 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:76857612 C>T maps to ENST00000356369 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:76867937 C>T maps to NM_001007271.1 W60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr10:76854559 C>T maps to ENST00000356369 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr20:30450448 G>A maps to NM_080611.3 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:12633224 G>A maps to NM_030640.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr22:31059612 G>A maps to NM_152511.3 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr22:31059546 C>T maps to NM_152511.3 W148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:183960157 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:44703828 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr23:44703446 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:44703566 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr23:44703828 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr6:348141 A>G maps to ENST00000457386 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:345883 C>T maps to ENST00000457386 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr6:348174 G>A maps to ENST00000457386 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:348267 C>T maps to ENST00000457386 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:348243 C>T maps to ENST00000457386 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr6:348138 C>T maps to ENST00000457386 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:33454891 A>G maps to NM_024025.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:33451265 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:167096536 C>T maps to NM_001080426.1 I723I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:167096287 C>T maps to NM_001080426.1 S640S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:167096524 C>T maps to NM_001080426.1 S719S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr1:167095138 G>A maps to NM_001080426.1 K257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr1:167095024 G>A maps to NM_001080426.1 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:167096098 G>A maps to NM_001080426.1 G577G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr1:167095468 G>A maps to NM_001080426.1 Q367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr1:167097625 G>A maps to NM_001080426.1 R1086R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:167095447 C>T maps to NM_001080426.1 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:167083000 C>T maps to NM_001080426.1 H55H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:167097832 G>A maps to NM_001080426.1 R1155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:167088674 C>T maps to NM_001080426.1 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:167097202 G>A maps to NM_001080426.1 E945E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:167088600 C>T maps to NM_001080426.1 Q185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:167097199 G>A maps to NM_001080426.1 T944T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr1:167097295 C>T maps to NM_001080426.1 S976S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr1:167097469 G>A maps to NM_001080426.1 E1034E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:167096041 G>A maps to NM_001080426.1 K558K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:167086742 G>A maps to NM_001080426.1 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr17:41852140 G>A maps to NM_004090.3 N97N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:41847126 G>A maps to NM_004090.3 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:29202953 G>A maps to NM_057158.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr8:29194635 G>A maps to NM_001394.5 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:29194911 G>A maps to NM_001394.5 C272C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr8:29194635 G>A maps to NM_001394.5 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:112266907 C>T maps to NM_004419.3 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr3:52088052 G>A maps to NM_001947.3 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr3:52088046 G>A maps to NM_001947.3 H287H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:52088019 G>A maps to NM_001947.3 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:1586954 G>A maps to NM_004420.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr11:1578617 G>A maps to NM_004420.2 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:152914835 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:152914785 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:152915589 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:48624483 C>T maps to NM_001025248.1 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q3-06A-11D-A196-08 chr19:57666737 A>T maps to NM_001012729.1 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr19:57666692 C>T maps to NM_001012729.1 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:57666633 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr19:57670571 C>T maps to NM_001012729.1 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:57666724 G>A maps to NM_001012729.1 R152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:57666740 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:57672124 G>A maps to NM_001012729.1 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:57666740 C>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:57666741 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:57666703 G>A maps to NM_001012729.1 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:57670544 C>T maps to NM_001012729.1 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:57665800 G>A maps to NM_001012729.1 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZH-06A-11D-A197-08 chr19:57666724 G>A maps to NM_001012729.1 R152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:57666644 C>T maps to NM_001012729.1 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:57670610 G>A maps to NM_001012729.1 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:57670610 G>A maps to NM_001012729.1 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:1275672 G>A maps to ENST00000378888 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:1275456 G>A maps to ENST00000378888 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:1275528 G>A maps to ENST00000378888 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:1275129 G>A maps to ENST00000378888 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:1271704 C>T maps to ENST00000378888 S635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:1273685 G>A maps to ENST00000378888 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr17:7134112 C>A maps to NM_004422.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:7132930 C>T maps to NM_004422.2 K241K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr3:183887839 C>T maps to NM_004423.3 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:183888308 C>T maps to NM_004423.3 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:183883229 C>T maps to NM_004423.3 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:183887884 C>T maps to NM_004423.3 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr3:183885815 C>T maps to NM_004423.3 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:183888434 C>T maps to NM_004423.3 A681A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:82126469 G>A maps to ENST00000372198 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr10:82122219 G>A maps to ENST00000372198 K21K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr10:82126484 C>T maps to ENST00000372198 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:82122264 G>A maps to ENST00000372198 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr18:46956725 T>C maps to NM_017653.3 K13K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr18:46784833 T>C maps to NM_017653.3 E427E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr18:46645157 G>A maps to NM_017653.3 R568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr18:46645262 G>A maps to NM_017653.3 R533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr18:46860171 G>A maps to NM_017653.3 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:46956740 G>A maps to NM_017653.3 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr14:102495967 C>T maps to NM_001376.4 F3187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr14:102483832 C>T maps to NM_001376.4 L2723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr14:102476378 C>T maps to NM_001376.4 F2059F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr14:102486384 C>T maps to NM_001376.4 F2833F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:102442085 C>T maps to NM_001376.4 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:102446266 C>T maps to NM_001376.4 Q244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr14:102509003 C>T maps to NM_001376.4 I4144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr14:102482416 C>T maps to NM_001376.4 Y2489Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:102481641 G>A maps to NM_001376.4 G2405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr14:102516133 C>T maps to NM_001376.4 S4533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:102472430 C>T maps to NM_001376.4 V1880V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr14:102449437 G>A maps to NM_001376.4 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr14:102442130 C>T maps to NM_001376.4 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr14:102508411 C>T maps to NM_001376.4 V4055V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:102460558 C>T maps to NM_001376.4 F1018F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:102476783 C>T maps to NM_001376.4 L2131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:102500765 C>T maps to NM_001376.4 A3577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:102516079 C>T maps to NM_001376.4 F4515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr14:102508357 C>T maps to NM_001376.4 P4037P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr14:102463511 G>A maps to NM_001376.4 Q1235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr14:102452743 C>T maps to NM_001376.4 R728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr14:102478656 C>T maps to NM_001376.4 I2288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr14:102505054 C>T maps to NM_001376.4 L3692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr14:102461080 C>A maps to NM_001376.4 L1076L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr14:102494083 C>T maps to NM_001376.4 I3059I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr14:102452895 C>T maps to NM_001376.4 A778A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:102469296 C>T maps to NM_001376.4 F1626F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:102470965 C>T maps to NM_001376.4 I1665I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:102477165 C>T maps to NM_001376.4 F2165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:102494352 C>T maps to NM_001376.4 L3115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:102478442 C>T maps to NM_001376.4 L2284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:102495922 C>T maps to NM_001376.4 T3172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:102516139 C>T maps to NM_001376.4 S4535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr14:102449924 C>T maps to NM_001376.4 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr7:95614187 C>T maps to NM_004411.4 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:95726820 G>A maps to NM_004411.4 W618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr7:95709712 C>T maps to NM_004411.4 A580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:95664989 C>T maps to NM_004411.4 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr7:95442562 A>T maps to NM_004411.4 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr3:32587395 C>T maps to NM_016141.3 K94K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr3:32570043 C>T maps to NM_016141.3 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr16:66770009 G>A maps to NM_006141.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr16:66768133 C>T maps to NM_006141.2 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr16:66770094 G>A maps to NM_006141.2 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr16:66783165 C>A maps to NM_006141.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr11:103194684 C>T maps to NM_001080463.1 I4009I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:103339405 C>T maps to NM_001080463.1 L4253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr11:103092761 C>T maps to NM_001080463.1 F3037F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr11:102995996 C>T maps to NM_001080463.1 F610F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:103025221 C>T maps to NM_001080463.1 S1115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:103039680 G>T maps to NM_001080463.1 E1654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:103173891 C>T maps to NM_001080463.1 P3729P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr11:103027442 C>T maps to NM_001080463.1 G1357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:103026061 C>T maps to NM_001080463.1 I1192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:103128386 C>T maps to NM_001080463.1 F3511F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:103048370 G>A maps to NM_001080463.1 T1987T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr11:103059314 A>T maps to NM_001080463.1 G2410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr11:103070114 T>C maps to NM_001080463.1 S2666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:103194684 C>T maps to NM_001080463.1 I4009I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:103124012 G>A did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr11:103070048 G>A maps to NM_001080463.1 L2644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr11:103026061 C>T maps to NM_001080463.1 I1192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:44016839 C>A maps to NM_001193464.1 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr2:44028837 C>T maps to NM_001193464.1 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:56166549 A>C maps to NM_080677.2 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr20:33122559 C>A maps to ENST00000374846 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr16:80584430 C>T maps to NM_130897.1 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr21:38862573 C>T maps to NM_001396.3 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:40316605 G>A maps to NM_004714.1 R547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:40320538 C>T maps to NM_004714.1 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:40318978 G>A maps to NM_004714.1 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:40319017 G>T maps to NM_004714.1 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:40319106 G>A maps to NM_004714.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr12:68051850 C>T maps to NM_006482.2 Y388Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:68052219 C>T maps to NM_006482.2 F511F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:68052204 C>T maps to NM_006482.2 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:68051931 C>T maps to NM_006482.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:68043583 T>A maps to NM_006482.2 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:206821164 C>T maps to NM_003582.2 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:206822099 C>T maps to NM_003582.2 H519H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr1:206821271 G>A maps to NM_003582.2 E243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:206820810 C>T maps to NM_003582.2 Q90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:206821850 C>T maps to NM_003582.2 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr12:4705787 C>T maps to NM_003845.1 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:4700453 G>A maps to NM_003845.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:4705364 G>A maps to NM_003845.1 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:4705766 G>A maps to NM_003845.1 Q144Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr2:71766326 C>T maps to NM_001130987.1 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:71795187 G>A maps to NM_001130987.1 G891G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:71894515 G>A maps to NM_001130987.1 R1776R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:71892429 G>A maps to NM_001130987.1 E1771E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr2:71762203 C>T maps to NM_001130987.1 I478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr2:71896265 G>A maps to NM_001130987.1 W1857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr2:71909665 C>T maps to NM_001130987.1 P2060P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:71839874 C>T maps to NM_001130987.1 S1442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:71906328 C>T maps to NM_001130987.1 P2009P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:71838412 G>A maps to NM_001130987.1 R1332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:71909779 C>T maps to NM_001130987.1 F2098F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:71708022 G>A maps to NM_001130987.1 K34K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:71783144 G>A maps to NM_001130987.1 T720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:71871174 G>A maps to NM_001130987.1 K1536K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:71895907 C>T maps to NM_001130987.1 L1828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr2:71766286 G>A maps to NM_001130987.1 W498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr2:71892300 G>A maps to NM_001130987.1 P1728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr2:71896827 C>T maps to NM_001130987.1 F1912F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:71825769 G>A maps to NM_001130987.1 W1217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr2:71909734 G>A maps to NM_001130987.1 R2083R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:71778789 G>A maps to NM_001130987.1 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:71780259 C>T maps to NM_001130987.1 F642F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:71886051 C>T maps to NM_001130987.1 P1600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:71797378 C>T maps to NM_001130987.1 P1000P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:71896815 G>A maps to NM_001130987.1 W1908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr2:71740984 G>A maps to NM_001130987.1 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:71825745 G>A maps to NM_001130987.1 V1209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr2:71730395 C>T maps to NM_001130987.1 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:71840530 C>T maps to NM_001130987.1 I1485I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:71840536 C>T maps to NM_001130987.1 I1487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:71894518 C>T maps to NM_001130987.1 I1777I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:71891487 C>T maps to NM_001130987.1 I1698I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:71894587 C>T maps to NM_001130987.1 V1800V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:71894599 G>A maps to NM_001130987.1 V1804V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:71791228 G>A maps to NM_001130987.1 Q817Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:71709085 G>A maps to NM_001130987.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:71825754 C>T maps to NM_001130987.1 T1212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:71781021 C>T maps to NM_001130987.1 I690I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:71827911 G>A maps to NM_001130987.1 T1279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr2:71871147 G>A maps to NM_001130987.1 R1527R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:71892336 C>T maps to NM_001130987.1 L1740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:71816793 C>G maps to NM_001130987.1 P1158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:71894638 C>T maps to NM_001130987.1 I1817I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr2:71730346 C>T maps to NM_001130987.1 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:71743371 G>A maps to NM_001130987.1 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:71709034 C>T maps to NM_001130987.1 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:71730342 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:71747976 G>A maps to NM_001130987.1 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:71778762 G>A maps to NM_001130987.1 R573R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:71795106 C>T maps to NM_001130987.1 A864A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:71871186 C>T maps to NM_001130987.1 T1540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:71887769 C>T maps to NM_001130987.1 P1664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:71891403 C>T maps to NM_001130987.1 F1670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:71906322 G>A maps to NM_001130987.1 W2007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:71909717 C>T maps to NM_001130987.1 L2078L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr2:71827914 G>A maps to NM_001130987.1 R1280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr2:71740913 C>T maps to NM_001130987.1 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:71747917 G>A did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:71740930 G>A maps to NM_001130987.1 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr2:207530662 C>T maps to NM_001093730.1 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:207572174 G>A maps to NM_001093730.1 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:207559597 G>A maps to NM_001093730.1 Y241Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr2:207557951 C>T maps to NM_001093730.1 Q309Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr2:207558008 G>A maps to NM_001093730.1 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:207530695 G>A maps to NM_001093730.1 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:207516586 G>A maps to NM_001093730.1 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:207530602 C>T maps to NM_001093730.1 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:207572057 G>A maps to NM_001093730.1 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr2:207527783 G>A maps to NM_001093730.1 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:55789928 C>T maps to NM_130810.2 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:55742461 G>A maps to NM_130810.2 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr15:55783386 T>C maps to NM_130810.2 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:55727240 C>T maps to NM_130810.2 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:96282323 G>A maps to NM_198968.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr13:96263711 G>A maps to NM_198968.2 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr13:96239871 C>T maps to NM_198968.2 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr13:96293734 G>A maps to NM_198968.2 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr13:96237062 C>T maps to NM_198968.2 A817A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr13:96277042 C>T maps to NM_198968.2 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr3:137811341 T>C maps to NM_173543.2 E251E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:137781669 G>A maps to NM_173543.2 V764V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:137790620 G>A maps to NM_173543.2 V493V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:137790599 C>T maps to NM_173543.2 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr3:137790620 G>A maps to NM_173543.2 V493V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr3:137787162 C>T maps to NM_173543.2 K554K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr3:137803019 G>A maps to NM_173543.2 Q380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:137783574 C>T maps to NM_173543.2 E679E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr3:108363191 C>T maps to NM_014648.3 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr3:108406915 C>T maps to NM_014648.3 S1081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:108330160 C>T maps to NM_014648.3 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr3:108380783 C>T maps to NM_014648.3 Q754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr3:108363542 C>T maps to NM_014648.3 I558I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr3:108363530 C>A maps to NM_014648.3 P554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19T-06A-11D-A19A-08 chr3:108363491 G>A maps to NM_014648.3 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr20:32268180 C>A maps to NM_005225.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr20:32267567 G>A maps to NM_005225.2 Q189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:32264548 G>A maps to NM_005225.2 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:32267679 G>A maps to NM_005225.2 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr20:32264636 G>A maps to NM_005225.2 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:23847472 G>A maps to NM_004091.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:23848335 G>A maps to NM_004091.3 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:23848336 G>A maps to NM_004091.3 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr6:20483064 C>T maps to NM_001949.3 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:20490567 C>T maps to NM_001949.3 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:20490514 C>T maps to NM_001949.3 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr16:67226216 C>T maps to NM_001950.3 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:67227418 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:86115412 G>A maps to ENST00000256117 K143K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:11593742 G>A maps to NM_198256.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:11593907 C>T maps to NM_198256.2 K60K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:11593742 G>A maps to NM_198256.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:77449687 C>A maps to NM_203394.2 G106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:77449679 G>A maps to NM_203394.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr11:19246914 G>A maps to NM_024680.2 I758I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:19246336 G>A maps to NM_024680.2 F824F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:19251063 G>A maps to NM_024680.2 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:19251087 T>C maps to NM_024680.2 R602R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:19253874 G>A maps to NM_024680.2 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:19256312 G>A maps to NM_024680.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:19246246 G>A maps to NM_024680.2 V854V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:19251333 G>A maps to NM_024680.2 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:19258859 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr16:2283183 G>A maps to NM_004424.3 E352E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:2285284 C>T maps to NM_004424.3 I689I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr16:2284184 C>T maps to NM_004424.3 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:121554155 A>T maps to NM_018456.4 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr3:121575913 G>A maps to NM_018456.4 W132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:121575902 A>G maps to NM_018456.4 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:121591510 C>T maps to NM_018456.4 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr14:35005438 G>A maps to NM_018453.3 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr14:35005308 G>A maps to NM_018453.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:110567013 C>T maps to ENST00000276658 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:158140143 C>T maps to NM_024007.3 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:158250196 A>C maps to NM_024007.3 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:158250199 G>A maps to NM_024007.3 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr5:158140086 T>C maps to NM_024007.3 Q420Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr5:158140038 C>T maps to NM_024007.3 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr5:158524053 G>A maps to NM_024007.3 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr5:158250325 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:158223376 G>A maps to NM_024007.3 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr5:158267039 G>A maps to NM_024007.3 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr8:25708155 G>A maps to NM_022659.2 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:25718676 G>A maps to NM_022659.2 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr8:25747343 C>T maps to NM_022659.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr8:25708164 C>T maps to NM_022659.2 R547R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:25708230 G>A maps to NM_022659.2 I525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr8:25766037 C>T maps to NM_022659.2 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr8:25899682 C>T maps to NM_022659.2 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr8:25766039 G>A maps to NM_022659.2 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:25715850 G>A maps to NM_022659.2 T504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:25890626 A>T maps to NM_022659.2 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:25747280 G>A maps to NM_022659.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:131755538 G>A maps to ENST00000355311 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:131671773 C>T maps to ENST00000355311 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:131666093 G>A maps to ENST00000355311 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:131641442 C>T maps to ENST00000355311 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr10:131671815 G>A maps to ENST00000355311 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr10:131640527 G>A maps to ENST00000355311 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:131640551 G>A maps to ENST00000355311 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr10:131640554 C>T maps to ENST00000355311 E399E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:131640551 G>A maps to ENST00000355311 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:4234772 G>A maps to NM_005755.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:4231287 C>T maps to NM_005755.2 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:4231305 C>T maps to NM_005755.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr13:50235108 G>A maps to NM_032565.3 Q206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:50235187 G>A maps to NM_032565.3 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:74894571 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:21546453 G>A maps to NM_001397.2 V769V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:21548329 G>A maps to NM_001397.2 Y682Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:21562381 G>A maps to NM_001397.2 F509F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:21563259 G>A maps to NM_001397.2 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:21562381 G>A maps to NM_001397.2 F509F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:21564647 G>A maps to NM_001397.2 F456F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:21605852 G>A maps to NM_001113347.1 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:184005662 G>A maps to NM_014693.3 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr3:184009944 C>T maps to NM_014693.3 S857S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr3:183967667 C>T maps to NM_014693.3 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:184009211 C>T maps to NM_014693.3 F820F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:184008849 G>A maps to NM_014693.3 G737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:183995168 G>A maps to NM_014693.3 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:184008616 C>T maps to NM_014693.3 G719G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr3:184008434 C>T maps to NM_014693.3 F700F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:183975447 C>T maps to NM_014693.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:184008978 G>A maps to NM_014693.3 E780E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr3:184009923 C>T maps to NM_014693.3 F850F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:183995964 G>A maps to NM_014693.3 W323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr3:183995785 G>A maps to NM_014693.3 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:183976273 C>T maps to NM_032331.3 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:183995768 C>T maps to NM_014693.3 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:184003361 C>T maps to NM_014693.3 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:184009977 C>T maps to NM_014693.3 C868C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr2:233347634 C>T maps to NM_004826.2 K537K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:233348800 C>G maps to NM_004826.2 R439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr2:233349716 G>A maps to NM_004826.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:233345514 C>T maps to NM_004826.2 Q688Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:233349186 G>A maps to NM_004826.2 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr2:233349192 G>A maps to NM_004826.2 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr2:233344934 C>T maps to NM_004826.2 E752E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:233346543 C>T maps to NM_004826.2 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr2:233349797 G>A maps to NM_004826.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:39308179 G>A maps to NM_001398.2 Q129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:39306637 G>A maps to NM_001398.2 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr19:39308096 G>A maps to NM_001398.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:53373570 G>A maps to ENST00000371522 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:135179549 G>A maps to NM_004092.3 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr10:135182472 C>T maps to NM_004092.3 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:150484120 C>T maps to ENST00000369049 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:150484886 C>T maps to ENST00000369049 H408H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:150483433 C>T maps to ENST00000369049 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:150482191 C>T maps to ENST00000369049 H59H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr9:95272207 G>A maps to NM_001393.3 Q427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr9:95277108 C>T maps to NM_001393.3 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr9:95285031 C>T maps to NM_001393.3 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr9:95277285 C>T maps to NM_001393.3 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:95263229 C>T maps to NM_001393.3 R570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr9:95277480 G>A maps to NM_001393.3 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:11624679 G>A maps to NM_016581.3 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:11624691 G>A maps to NM_016581.3 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:11624639 G>A maps to NM_016581.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:11624841 C>T maps to NM_016581.3 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:172537975 C>T maps to ENST00000392692 F898F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:172482201 C>T maps to ENST00000392692 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr3:172472442 T>A maps to ENST00000392692 Y41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr6:139222234 A>T maps to NM_001195037.2 I855I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr6:139164126 G>A maps to NM_001195037.2 W118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:139186241 C>T maps to NM_001195037.2 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:68836179 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:69255269 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:68836179 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:69255458 G>A did not map to a codon.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr23:69255254 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:65825018 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr23:65824905 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:65824339 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:65819654 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:109546614 C>T maps to ENST00000376651 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr2:109545721 G>A maps to ENST00000376651 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr2:109522809 C>T maps to ENST00000376651 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr2:109524405 G>A maps to ENST00000376651 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr2:109527451 G>A maps to ENST00000376651 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr2:109522809 C>T maps to ENST00000376651 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:109522809 C>T maps to ENST00000376651 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr2:109513596 C>T maps to ENST00000376651 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:109545658 G>A maps to ENST00000376651 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:109513554 C>T maps to ENST00000376651 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:109526962 C>T maps to ENST00000376651 K284K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:109513548 C>T maps to ENST00000376651 E419E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:236645579 C>T maps to NM_145861.2 D93D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:236645792 C>T maps to NM_145861.2 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:236645762 C>T maps to NM_145861.2 C154C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr15:74964045 G>A maps to NM_025083.3 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr15:74948194 G>A maps to NM_025083.3 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr15:74963886 G>A maps to NM_025083.3 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:67913598 C>T maps to NM_014329.3 F581F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:67912637 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr16:67914530 C>T maps to NM_014329.3 S723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr16:67911492 C>T maps to NM_014329.3 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:67913805 T>C maps to NM_014329.3 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr16:67915272 C>T maps to NM_014329.3 S914S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:67912441 C>T maps to NM_014329.3 V364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr14:21216050 G>A maps to NM_006683.4 E104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr14:21216122 C>T maps to NM_006683.4 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:21216086 G>A maps to NM_006683.4 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr14:21238599 G>A maps to NM_022360.4 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:5249906 C>T maps to NM_014674.2 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr3:5252852 C>T maps to NM_014674.2 D544D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:5229906 C>T maps to NM_014674.2 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:5241371 C>T maps to NM_014674.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr20:33722741 G>A maps to NM_018217.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr20:33703685 G>A maps to NM_018217.2 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:184663274 G>A maps to NM_025191.3 V907V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:184702000 G>A maps to NM_025191.3 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr9:139757823 G>A maps to NM_003792.2 H69H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:83402468 G>A maps to NM_005711.3 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr5:83362368 C>T maps to NM_005711.3 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr5:83356193 C>T maps to NM_005711.3 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:83549908 C>T maps to NM_005711.3 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr5:83356163 C>T maps to NM_005711.3 V364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr5:83360576 G>A maps to NM_005711.3 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr6:12294299 G>A maps to NM_001955.4 W120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr20:57876654 G>A maps to NM_207034.1 Q81Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr20:57876726 G>A maps to NM_207034.1 K105K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr20:57876761 G>A maps to NM_207034.1 W117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:57876711 C>T maps to NM_207034.1 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr20:57876514 C>T maps to NM_207034.1 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr20:57876603 G>A maps to NM_207034.1 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr20:57876597 C>T maps to NM_207034.1 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr4:148441109 C>T maps to NM_001957.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:148406859 C>T maps to NM_001957.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:148461042 C>T maps to NM_001957.3 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr4:148407087 G>A maps to NM_001957.3 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:148453711 A>T maps to NM_001957.3 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:148407108 C>T maps to NM_001957.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:148453753 C>T maps to NM_001957.3 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr4:148407108 C>T maps to NM_001957.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:148463634 C>T maps to NM_001957.3 C383C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr12:93209993 G>A maps to NM_003566.3 V637V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:93173036 G>A maps to NM_003566.3 Q1170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:93221821 G>A maps to NM_003566.3 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:93244931 G>A maps to NM_003566.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:85989561 C>T maps to ENST00000351625 R466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:74229628 T>A maps to NM_001402.5 K41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:62126155 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr20:62120337 C>T maps to NM_001958.2 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr20:62121948 G>C maps to NM_001958.2 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr20:62129044 C>G maps to NM_001958.2 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr20:62126160 G>A maps to NM_001958.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr20:62121831 C>T maps to NM_001958.2 Q343Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:62126322 C>T maps to NM_001958.2 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:62126343 C>T maps to NM_001958.2 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr2:207024726 C>T maps to NM_021121.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr8:144671342 G>A maps to NM_032378.4 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr8:144663477 G>A maps to NM_032378.4 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:144662885 G>A maps to NM_032378.4 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr8:144662304 C>T maps to NM_032378.4 W594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr6:8102718 C>T maps to NM_004280.4 K12K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:8097577 G>A maps to NM_004280.4 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:62339038 G>A maps to ENST00000378019 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr11:62327657 G>A maps to ENST00000378019 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:62327224 G>A maps to ENST00000378019 R464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr11:62327153 C>T maps to ENST00000378019 K487K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:62327778 G>A maps to ENST00000378019 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:3979425 G>A maps to NM_001961.3 I538I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:3977512 G>A maps to NM_001961.3 I721I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:3977563 G>A maps to NM_001961.3 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:3976653 G>A maps to NM_001961.3 F825F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:3981384 G>A maps to NM_001961.3 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr19:3982419 G>A maps to NM_001961.3 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr19:3978041 G>A maps to NM_001961.3 A614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr19:3982419 G>A maps to NM_001961.3 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:3980660 G>A maps to NM_001961.3 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr16:22278014 C>T maps to NM_013302.3 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr16:22268202 C>T maps to NM_013302.3 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr16:22268094 C>T maps to NM_013302.3 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:22269864 C>T maps to NM_013302.3 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:22269865 C>T maps to NM_013302.3 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:22269972 C>T maps to NM_013302.3 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:22255971 C>T maps to NM_013302.3 Q90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr16:22237193 G>A maps to NM_013302.3 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr16:22262006 C>T maps to NM_013302.3 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:22237184 C>T maps to NM_013302.3 D45D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr16:22278175 C>T maps to NM_013302.3 I581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:128060383 C>T maps to NM_021937.3 D365D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:127983488 G>A maps to NM_021937.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:127980973 C>T maps to NM_021937.3 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:128060521 G>A maps to NM_021937.3 W411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:127965787 C>T maps to NM_021937.3 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19T-06A-11D-A19A-08 chr3:127965853 C>A maps to NM_021937.3 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr3:128077181 C>T maps to NM_021937.3 F522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:128126936 G>A maps to NM_021937.3 K542K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr7:36194145 C>T maps to NM_030636.2 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr7:36194505 C>T maps to NM_030636.2 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr7:36194328 C>T maps to NM_030636.2 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr7:36278626 C>T maps to NM_030636.2 D304D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:245246774 C>T maps to ENST00000421886 R235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:60493449 G>A maps to NM_001144933.1 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:60484032 G>A maps to NM_001144933.1 K279K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:60493518 G>A maps to NM_001144933.1 W434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr17:60483846 C>T maps to NM_001144933.1 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:60493443 C>T maps to NM_001144933.1 I409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:828657 G>A maps to NM_173584.3 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:3763390 G>A maps to NM_001144958.1 Q345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr12:3805955 G>A maps to NM_001144958.1 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr12:3757712 G>A maps to NM_001144958.1 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:3782724 C>T maps to NM_001144958.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:3788205 G>A maps to NM_001144958.1 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:3806147 C>T maps to NM_001144958.1 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr17:28407115 G>A maps to NM_198529.3 K1018K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr17:28296355 G>A maps to NM_198529.3 K246K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr17:28408000 T>C did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr17:28378134 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:28405449 C>T maps to NM_198529.3 I985I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr22:43976448 C>T maps to NM_022785.3 K1041K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr22:44004440 G>A maps to NM_022785.3 R868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr22:43933266 G>A maps to NM_022785.3 S1346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr22:43985982 G>A maps to NM_022785.3 T1001T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr22:44107416 C>T maps to NM_022785.3 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr22:43930615 C>T maps to NM_022785.3 K1395K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:44063094 C>T maps to NM_022785.3 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr22:43976364 G>A maps to NM_022785.3 S1069S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr22:44074037 G>A maps to NM_022785.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:44063082 G>A maps to NM_022785.3 F628F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:44068143 G>A maps to NM_022785.3 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr22:43950817 C>T maps to NM_022785.3 T1193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr22:43972185 G>A maps to NM_022785.3 F1137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr22:44074028 C>T maps to NM_022785.3 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr22:43950762 G>A maps to NM_022785.3 L1212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr22:43950763 G>A maps to NM_022785.3 I1211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr22:44083390 A>G maps to NM_022785.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:43924810 G>A maps to NM_022785.3 F1476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:44079695 G>A maps to NM_022785.3 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr22:44067857 G>A maps to NM_022785.3 F545F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr22:43986063 G>T maps to NM_022785.3 T974T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:44168906 C>T maps to NM_022785.3 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr22:43972299 C>T maps to NM_022785.3 K1099K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr22:43996121 C>T maps to NM_022785.3 G901G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr22:43996103 T>C maps to NM_022785.3 E907E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr22:43926742 G>A maps to NM_022785.3 S1445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:43976493 G>A maps to NM_022785.3 F1026F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:44004473 G>A maps to NM_022785.3 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr22:44067857 G>A maps to NM_022785.3 F545F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr22:43930669 C>T maps to NM_022785.3 G1377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:64038152 G>A maps to NM_032437.2 W619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:64022863 G>T maps to NM_032437.2 E432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:56144908 G>A maps to NM_001039349.1 N136N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:56098003 G>A maps to NM_001039349.1 Q391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr2:56145088 C>T maps to NM_001039349.1 Q76Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:56149494 C>T maps to NM_001039349.1 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr2:56145186 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:56097944 G>A maps to NM_001039349.1 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr2:56149557 G>A maps to NM_001039349.1 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr2:56097971 T>A maps to NM_001039349.1 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:56108788 G>A maps to NM_001039349.1 Q200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:65635848 G>A maps to NM_016938.3 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:65637337 G>A maps to NM_016938.3 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr11:65634493 C>T maps to NM_016938.3 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:65637649 G>A maps to NM_016938.3 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:65638022 G>A maps to NM_016938.3 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:65638022 G>A maps to NM_016938.3 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:22095461 G>A maps to NM_152726.2 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr13:22113824 T>A maps to NM_152726.2 K121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr8:16962937 C>T maps to NM_181723.2 Q368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr8:16962000 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:16935308 C>T maps to NM_181723.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:19975237 G>A maps to NM_144715.3 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:19940268 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:52303323 C>T maps to NM_018100.3 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:52317557 C>T maps to NM_018100.3 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr6:52344579 A>C maps to NM_018100.3 A545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:52343839 C>T maps to NM_018100.3 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:44101480 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:44088966 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:44120371 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:44202801 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr23:44089002 A>C did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:233546296 C>T maps to NM_025202.3 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:233546297 C>T maps to NM_025202.3 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr1:15752486 C>T maps to NM_024329.5 D143D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:15752468 C>T maps to NM_024329.5 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:15752507 C>T maps to NM_024329.5 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:15752393 C>T maps to NM_024329.5 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr1:15752397 C>T maps to NM_024329.5 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:1299910 C>T maps to NM_001405.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr1:155039319 C>T maps to NM_182689.1 Y76Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:155039325 G>A maps to NM_182689.1 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr5:106723428 G>C maps to NM_001962.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:106762981 G>A maps to NM_001962.2 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr23:68060318 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:68059535 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:68060236 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:68060445 C>T did not map to a codon.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr23:68060376 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr13:107145726 G>A maps to NM_004093.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:107145750 G>A maps to NM_004093.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr13:107145429 C>T maps to NM_004093.2 E320E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr17:7612848 G>A maps to NM_001406.3 Q326Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr17:7608942 G>A maps to NM_001406.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:7611846 T>G did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:7611368 C>T maps to NM_001406.3 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:7611452 C>T maps to NM_001406.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A197-06A-32D-A197-08 chr17:7612699 C>T maps to NM_001406.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr17:7612674 C>T maps to NM_001406.3 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr8:132968065 T>A maps to NM_015137.3 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:133008665 T>G maps to NM_015137.3 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:133008660 C>T maps to NM_015137.3 R692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr8:133008660 C>T maps to NM_015137.3 R692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr14:23828855 C>T maps to NM_005864.2 Q277Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:23829916 G>A maps to NM_005864.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr15:82444124 G>A maps to NM_024580.5 V890V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr15:82456242 G>A maps to NM_024580.5 N611N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr15:82523260 T>C maps to NM_024580.5 E261E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr15:82450159 G>A maps to NM_024580.5 Q642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr15:82450160 G>A maps to NM_024580.5 N641N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:82532857 G>A maps to NM_024580.5 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:82444610 G>A maps to NM_024580.5 I728I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr15:82517552 G>A maps to NM_024580.5 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:82507160 G>A maps to NM_024580.5 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:82422899 G>A maps to NM_024580.5 I1059I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:42937401 G>A maps to NM_004247.3 F577F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr17:42934474 G>A maps to NM_004247.3 S671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr17:42936450 G>A maps to NM_004247.3 I653I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:42937814 G>A maps to NM_004247.3 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr17:42940268 G>A maps to NM_004247.3 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:42962667 G>A maps to NM_004247.3 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:42940082 G>A maps to NM_004247.3 A535A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:42953378 G>A maps to NM_004247.3 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CF-06A-11D-A196-08 chr4:110882135 C>T maps to NM_001963.4 R394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:110880474 A>G maps to NM_001963.4 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:110932358 G>A maps to NM_001963.4 G1124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:110932391 C>T maps to NM_001963.4 P1135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:110925678 G>A maps to NM_001963.4 S1064S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr4:110901980 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:13636086 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr23:13636017 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr23:13624583 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:13621441 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:13624617 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:13637344 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:13588039 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr23:13645195 T>G did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:13607757 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:13651118 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:13636122 A>T did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:13635871 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:13624617 G>A did not map to a codon.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr23:13624561 T>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr23:13624542 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:13613030 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:13621513 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr6:32135727 C>T maps to NM_030652.2 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:32135729 A>C maps to NM_030652.2 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr5:38406928 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr5:38409182 C>T maps to ENST00000354891 I442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:38425168 G>A maps to ENST00000354891 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:38427201 C>T maps to ENST00000354891 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr5:38412635 C>T maps to ENST00000354891 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr5:38427348 C>T maps to ENST00000354891 V683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:38370451 C>T maps to ENST00000354891 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:38407024 C>T maps to ENST00000354891 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:38418292 G>A maps to ENST00000354891 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr5:38370427 C>T maps to ENST00000354891 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr5:38407087 G>A maps to ENST00000354891 Q329Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr5:38427312 G>A maps to ENST00000354891 V671V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr5:38370406 C>T maps to ENST00000354891 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:38412653 C>T maps to ENST00000354891 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:38418301 G>A maps to ENST00000354891 R543R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:38463997 C>T maps to ENST00000354891 I988I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr5:38438423 C>G maps to ENST00000354891 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:38352427 C>T maps to ENST00000354891 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:38451521 C>T maps to ENST00000354891 F891F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr5:38370439 C>T maps to ENST00000354891 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr5:38427348 C>T maps to ENST00000354891 V683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:38352304 C>T maps to ENST00000354891 C139C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr5:38407207 C>T maps to ENST00000354891 C369C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:38407198 C>T maps to ENST00000354891 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:38412635 C>T maps to ENST00000354891 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:38418266 C>T maps to ENST00000354891 Q532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:38451467 G>A maps to ENST00000354891 K873K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:38406333 C>T maps to ENST00000354891 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:55249164 C>T maps to NM_005228.3 I821I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr7:55214302 C>T maps to NM_005228.3 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr7:55272964 C>A maps to NM_005228.3 S1096S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:55259446 C>T maps to NM_005228.3 H835H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:55259464 G>A maps to NM_005228.3 R841R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:55211104 C>T maps to NM_005228.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:55238900 G>A maps to NM_005228.3 T638T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:55249164 C>T maps to NM_005228.3 I821I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:55241648 C>A maps to NM_005228.3 P699P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:55268063 C>T maps to NM_005228.3 F968F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:55240813 G>A maps to NM_005228.3 R686R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:55269036 C>T maps to NM_005228.3 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr7:55240684 C>T maps to NM_005228.3 I643I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr7:55231515 G>A maps to NM_005228.3 R574R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:55266527 C>T maps to NM_005228.3 T940T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:55223556 C>T maps to NM_005228.3 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:55260514 G>A maps to NM_005228.3 Q894Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:55269011 C>T maps to NM_005228.3 S1026S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr7:55268924 C>T maps to NM_005228.3 F997F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr7:55268066 C>T maps to NM_005228.3 S969S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr7:55214413 C>T maps to NM_005228.3 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:55219017 G>A maps to NM_005228.3 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:55238215 C>T maps to NM_201284.1 I699I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:55268103 C>T maps to NM_005228.3 Q982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:55269447 C>T maps to NM_005228.3 S1045S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:55272964 C>T maps to NM_005228.3 S1096S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:55259425 G>A maps to NM_005228.3 L828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:55221762 C>T maps to NM_005228.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr1:231557538 G>T maps to NM_022051.2 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:231506357 G>A maps to NM_022051.2 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:41307068 C>T maps to NM_053046.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr14:34398385 C>T maps to NM_022073.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:34419856 G>A maps to NM_022073.3 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:137802971 G>A maps to NM_001964.2 E278E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:137802461 C>T maps to NM_001964.2 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:137803493 C>T maps to NM_001964.2 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:137802693 C>T maps to NM_001964.2 Q186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr5:137803562 C>T maps to NM_001964.2 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:137803292 C>T maps to NM_001964.2 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:137802596 C>T maps to NM_001964.2 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr10:64573152 G>A maps to NM_001136178.1 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr10:64573722 G>A maps to NM_001136178.1 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:73519394 C>T maps to NM_001965.3 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:63175537 C>T maps to NM_015252.3 V554V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:63215082 G>T maps to NM_015252.3 E911*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:65347679 T>C maps to NM_001099409.1 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr11:65347601 C>T maps to NM_001099409.1 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr11:65350740 C>T maps to NM_001099409.1 T866T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:65358036 C>T maps to NM_001099409.1 I1419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr11:65350677 G>A maps to NM_001099409.1 E845E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:65347939 C>T maps to NM_001099409.1 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:65359558 G>A maps to NM_001099409.1 R1490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr11:65343826 C>T maps to NM_001099409.1 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr11:64622931 G>A maps to NM_006795.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr11:64622296 G>A maps to NM_006795.2 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:64622203 G>A maps to NM_006795.2 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:64621903 C>A maps to NM_006795.2 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:64622143 G>A maps to NM_006795.2 F422F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr11:64622296 G>A maps to NM_006795.2 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:64622317 C>T maps to NM_006795.2 Q364Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:64645687 G>A maps to NM_006795.2 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64627776 G>A maps to NM_006795.2 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:64627464 G>A maps to NM_006795.2 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:48229099 C>T maps to NM_014601.3 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:48229069 C>T maps to NM_014601.3 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:48220222 G>A maps to NM_014601.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr19:48220192 C>T maps to NM_014601.3 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:48239705 C>T maps to NM_014601.3 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:48229099 C>T maps to NM_014601.3 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:48220033 C>T maps to NM_014601.3 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:48239741 G>A maps to NM_014601.3 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:31483664 C>T maps to NM_014600.2 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:31484536 C>T maps to NM_014600.2 H346H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr2:31472267 C>T maps to NM_014600.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr2:31483601 C>T maps to NM_014600.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:31489122 C>T maps to NM_014600.2 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:31489530 C>A maps to NM_014600.2 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:31483544 C>T maps to NM_014600.2 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:42245962 G>A maps to NM_139265.3 R138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr15:42193052 C>T maps to NM_139265.3 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:34664227 C>T maps to NM_012153.4 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:184966220 T>C maps to NM_001966.3 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr3:184910289 G>A maps to NM_001966.3 F632F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:184947265 G>C maps to NM_001966.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:184922294 G>A maps to NM_001966.3 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr9:140729341 C>T maps to NM_024757.4 A1278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr9:140674131 C>T maps to NM_024757.4 A746A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:140674128 C>T maps to NM_024757.4 S745S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:140729356 G>A maps to NM_024757.4 E1283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:140638379 C>T maps to NM_024757.4 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:140728940 C>T maps to NM_024757.4 F1227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr9:140728853 C>T maps to NM_024757.4 F1198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr9:140638523 G>A maps to NM_024757.4 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr9:140711971 C>T maps to NM_024757.4 V1152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:140708908 C>T maps to NM_024757.4 S1069S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr9:140710439 C>T maps to NM_024757.4 P1100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr6:31851633 C>T maps to ENST00000395728 E1012E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:31855987 A>T maps to ENST00000395728 S582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr6:31848610 G>A maps to ENST00000395728 Y1154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:31860663 G>A maps to ENST00000395728 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:31856800 G>A maps to ENST00000395728 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr6:31864149 G>A maps to ENST00000395728 Q215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr6:31864150 G>A maps to ENST00000395728 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr11:125449999 G>A maps to ENST00000278903 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:125446178 C>T maps to ENST00000278903 Q90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:125448110 C>T maps to ENST00000278903 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:40023289 G>A maps to NM_152361.1 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:104698384 T>C maps to NM_001008394.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr23:20156736 T>C did not map to a codon.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr23:20156722 T>C did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr23:20156728 T>C did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr24:22737760 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr3:40352420 C>T maps to NM_005875.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:150264609 C>T maps to NM_032025.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr7:6078275 G>A maps to NM_014413.3 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:6084288 G>A maps to NM_014413.3 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:6094293 G>A maps to NM_014413.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr2:37349785 T>C maps to NM_001135651.1 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr2:37353502 G>A maps to NM_001135651.1 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:37334418 A>G maps to NM_001135651.1 C551C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:37374037 G>A maps to NM_001135651.1 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr2:88882948 G>A maps to NM_004836.5 R588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:88885505 G>A maps to NM_004836.5 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:88874524 G>A maps to NM_004836.5 R826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr15:40295427 C>T maps to NM_001013703.2 P1090P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr15:40300311 C>G maps to NM_001013703.2 V1164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr15:40259717 C>T maps to NM_001013703.2 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr15:40247834 T>C maps to NM_001013703.2 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr15:40235621 C>G maps to NM_001013703.2 S99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr15:40293385 C>T maps to NM_001013703.2 S1040S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr15:40259840 C>T maps to NM_001013703.2 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:40301882 C>T maps to NM_001013703.2 I1215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:40259714 C>T maps to NM_001013703.2 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr12:124114967 G>A maps to NM_001414.3 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:124114979 G>A maps to NM_001414.3 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr12:124111661 G>A maps to NM_001414.3 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:124114823 G>A maps to NM_001414.3 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr12:124114955 G>A maps to NM_001414.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr14:75469737 C>T maps to NM_014239.3 I15I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:45363040 G>A maps to NM_020365.3 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:45363097 G>A maps to NM_020365.3 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:45316634 G>A maps to NM_020365.3 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr3:183858486 C>A maps to NM_003907.2 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:183859857 G>A maps to NM_003907.2 Q434Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr1:36379790 C>T maps to NM_012199.2 A583A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr1:36354142 C>T maps to NM_012199.2 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:36359680 C>T maps to NM_012199.2 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:36385145 C>T maps to NM_012199.2 Q838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:36379560 C>T maps to NM_012199.2 V567V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:36360794 C>T maps to NM_012199.2 N315N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:36384807 G>A maps to NM_012199.2 L806L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:36383198 C>T maps to NM_012199.2 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr1:36384664 C>T maps to NM_012199.2 R759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:36385144 C>T maps to NM_012199.2 P837P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr8:141559345 G>A maps to NM_012154.3 I485I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr8:141545599 G>A maps to NM_012154.3 F746F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:141572556 G>A maps to NM_012154.3 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr8:141595378 G>A maps to NM_012154.3 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:141554380 G>A maps to NM_012154.3 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr8:141583024 G>A maps to NM_012154.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr8:141542232 G>A maps to NM_012154.3 T830T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr8:141568588 G>A maps to NM_012154.3 H291H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:36411311 C>T maps to NM_024852.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:36509115 C>T maps to NM_024852.2 F747F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:36439062 C>T maps to NM_024852.2 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:36292379 G>A maps to NM_017629.2 Q264Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:24089793 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:24089794 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:24086118 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr10:120801506 T>C maps to NM_003750.2 P1175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:120817748 G>A maps to NM_003750.2 Q566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr7:2419113 C>T maps to ENST00000314800 P809P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:2412392 C>T maps to ENST00000314800 F591F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:2402288 C>T maps to ENST00000314800 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr22:36908514 G>A maps to NM_003753.3 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr22:36912527 G>A maps to NM_003753.3 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:109240512 G>A maps to NM_001568.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr8:109215672 A>T maps to NM_001568.2 L374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:8016889 G>A maps to ENST00000449102 E339E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:8013683 T>A maps to ENST00000449102 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:8014499 C>T maps to ENST00000449102 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:8016538 C>T maps to ENST00000449102 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:10227828 G>A maps to NM_003755.3 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:10226422 G>A maps to NM_003755.3 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr8:117658842 C>A did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:32688146 C>T maps to NM_003757.2 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr19:39125706 C>T maps to NM_013234.2 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:39123098 G>A maps to NM_013234.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr22:38271939 C>T maps to ENST00000262832 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr22:38273862 C>T maps to ENST00000262832 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr17:7479909 C>T maps to NM_001416.2 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z4-06A-11D-A197-08 chr17:7480011 T>A did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:7478545 C>T maps to NM_001416.2 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:186502262 C>T maps to ENST00000440191 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:186502860 T>C maps to ENST00000440191 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:78112042 G>A maps to NM_014740.3 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:53421853 G>A maps to ENST00000438209 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr4:99806185 A>G maps to NM_001130679.1 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:176072430 G>A maps to NM_001099408.1 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:233431624 C>T maps to NM_004846.2 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:233431624 C>T maps to NM_004846.2 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:37914671 G>A maps to NM_004095.3 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr22:31850258 G>A maps to NM_019843.3 H461H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:184041251 C>T maps to NM_001194947.1 I722I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:184035275 C>T maps to NM_001194947.1 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr3:184035254 C>T maps to NM_001194947.1 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:184045626 C>T maps to NM_001194947.1 Q1271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr3:184052516 C>T maps to NM_001194947.1 L1548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:184043639 C>T maps to NM_001194947.1 S1048S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:10820826 G>A maps to ENST00000429377 H896H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:21151664 C>T maps to NM_001198801.1 W1412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr1:21212836 G>A maps to NM_001198801.1 Q741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:21186887 C>T maps to NM_001198801.1 K1058K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:21151600 A>G maps to NM_001198801.1 L1434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:21212827 G>A maps to NM_001198801.1 Q744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:21306908 G>A maps to NM_001198801.1 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:21307660 G>A maps to NM_001198801.1 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr14:103802235 C>T maps to NM_183004.3 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:103802253 C>T maps to NM_183004.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:103804739 C>T maps to NM_183004.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:103805663 C>T maps to NM_183004.3 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr17:7212974 C>T maps to NM_001143760.1 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:7213001 C>T maps to NM_001143760.1 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:81272722 G>A maps to NM_001099692.1 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:81272746 C>T maps to NM_001099692.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:99977973 C>T maps to NM_015904.3 Q204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr2:99988137 G>A maps to NM_015904.3 E499E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr20:33867750 G>A maps to NM_002212.2 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr17:12921030 G>A maps to NM_018127.6 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:12899105 G>A maps to NM_018127.6 H574H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:12899063 G>A maps to NM_018127.6 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:12901799 G>A maps to NM_018127.6 I483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr17:12903526 G>A maps to NM_018127.6 Q457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:12896135 C>T maps to NM_018127.6 *827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:12903527 G>A maps to NM_018127.6 F456F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr19:855691 C>T maps to NM_001972.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr19:855769 G>A maps to NM_001972.2 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr19:856085 C>T maps to NM_001972.2 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr19:856085 C>T maps to NM_001972.2 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr9:23704928 G>A maps to ENST00000359598 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr9:23704973 C>T maps to ENST00000359598 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr9:23701405 T>C maps to ENST00000359598 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr9:23705063 G>A maps to ENST00000359598 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr9:23692807 C>T maps to ENST00000359598 W304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr9:23692761 G>A maps to ENST00000359598 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr9:23762052 C>T maps to ENST00000359598 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr9:23701588 A>G maps to ENST00000359598 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:23704985 C>T maps to ENST00000359598 K167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:11565409 C>T maps to NM_001420.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:11569321 G>A maps to NM_001420.3 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:11569054 C>T maps to NM_001420.3 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:11576998 C>T maps to NM_001420.3 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:11568979 C>T maps to NM_001420.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:11577594 G>A maps to NM_001420.3 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:11569354 G>A maps to NM_001420.3 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:50610819 G>A maps to NM_021952.3 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:50666630 C>T maps to NM_021952.3 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr1:50572065 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:50666516 C>T maps to NM_021952.3 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr13:41515130 A>T maps to NM_172373.3 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:139994656 G>A maps to ENST00000379550 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr4:140058810 A>G maps to ENST00000379550 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:139983200 G>A maps to ENST00000379550 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:139980138 A>C maps to ENST00000379550 *594E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr1:201980308 C>T maps to NM_004433.4 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:201982371 C>T maps to NM_004433.4 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:201981876 C>T maps to NM_004433.4 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:201983065 C>T maps to NM_004433.4 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:201981789 G>A maps to NM_004433.4 Q167Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:129200985 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:129203369 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:129203627 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:129201361 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:129200778 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:129200779 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:129205173 G>A did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:129201424 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:34501800 T>C maps to NM_198381.1 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr11:34533098 G>A maps to NM_198381.1 H6H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:34502435 C>T maps to NM_198381.1 W195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:34502434 C>T maps to NM_198381.1 W195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:37771253 G>A maps to NM_052906.3 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr22:37770176 G>T maps to NM_052906.3 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:37771274 C>T maps to NM_052906.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr22:37770743 G>A maps to NM_052906.3 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr22:37769186 G>A maps to NM_052906.3 V796V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr22:37769957 C>T maps to NM_052906.3 K539K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr22:37769771 G>A maps to NM_052906.3 F601F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:37769834 G>A maps to NM_052906.3 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr22:37769189 C>T maps to NM_052906.3 K795K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:37770344 G>A maps to NM_052906.3 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:47500832 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:47500671 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:47497357 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr23:47498704 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:96641178 C>A maps to NM_005230.2 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:96640770 C>T maps to NM_005230.2 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q3-06A-11D-A196-08 chr1:205588102 A>G maps to NM_001973.2 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:205589678 C>T maps to NM_001973.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:205588961 G>A maps to NM_021795.2 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:205589255 G>A maps to NM_001973.2 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:205592992 G>A maps to NM_001973.2 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr19:18557178 C>T maps to NM_006532.3 R548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:18557151 G>T maps to NM_006532.3 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:18572429 C>T maps to NM_006532.3 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:18572510 G>A maps to NM_006532.3 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr5:95236438 T>C maps to NM_012081.5 E304E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr5:95226814 C>A maps to NM_012081.5 E585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr7:36927267 C>T maps to NM_014800.9 K537K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr7:37298862 C>T maps to NM_014800.9 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:36917627 G>A maps to NM_014800.9 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:37283971 G>A maps to NM_014800.9 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:37382273 G>A maps to NM_014800.9 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:37172794 C>T maps to NM_014800.9 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:37252980 G>A maps to NM_014800.9 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:37264596 C>T maps to NM_014800.9 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr7:37382253 C>T maps to NM_014800.9 W14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr7:36895173 G>A maps to NM_014800.9 F722F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:36895317 C>T maps to NM_014800.9 G674G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:37251038 C>T maps to NM_014800.9 E346E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:37256297 C>T maps to NM_014800.9 E261E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:37262240 C>T maps to NM_014800.9 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:37354526 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr20:45003019 G>A maps to ENST00000439931 A422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:45004420 G>A maps to ENST00000439931 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr20:45022719 G>A maps to ENST00000439931 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr20:45012129 G>A maps to ENST00000439931 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:44999141 G>A maps to ENST00000439931 A620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr16:67236315 G>A maps to NM_024712.3 Q479Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr16:67233463 C>T maps to NM_024712.3 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr16:67236597 C>T maps to NM_024712.3 F542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr16:67233249 G>A maps to NM_024712.3 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr11:107501286 C>T maps to NM_018712.3 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr11:107501438 G>A maps to NM_018712.3 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:141471528 A>C maps to NM_153702.3 *294Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:85598229 C>T maps to NM_001135023.1 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:85590218 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:85598216 C>T maps to NM_001135023.1 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr7:73481101 C>T maps to ENST00000358929 F777F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:73483002 G>A maps to ENST00000358929 G784G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr7:73482999 G>T maps to ENST00000358929 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:73450915 T>G did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:73474219 A>G maps to ENST00000358929 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr7:73452040 G>T maps to ENST00000358929 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:73483002 G>A maps to ENST00000358929 G784G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr7:73462833 G>A maps to ENST00000358929 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:73462008 C>T maps to ENST00000358929 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:73474512 C>T maps to ENST00000358929 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr7:73474217 T>C maps to ENST00000358929 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr7:73471043 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr7:73456981 C>T maps to ENST00000358929 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:73462884 C>T maps to ENST00000358929 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:73477501 C>T maps to ENST00000358929 V670V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr7:73460542 C>T maps to ENST00000358929 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr7:73456956 C>T maps to ENST00000358929 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr1:43830934 C>T maps to NM_022821.2 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:43830676 G>A maps to NM_022821.2 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:43830264 G>A maps to NM_022821.2 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr1:43829640 G>A maps to NM_022821.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:10995378 G>A maps to NM_017770.3 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:10990061 G>A maps to NM_017770.3 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:11000334 C>T maps to NM_017770.3 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr6:10995336 C>T maps to NM_017770.3 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:10995327 C>T maps to NM_017770.3 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:10995348 G>A maps to NM_017770.3 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:103987394 C>T maps to NM_152310.1 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr10:103988323 C>T maps to NM_152310.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr6:80635909 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr6:80626596 G>A maps to NM_022726.3 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr6:80629180 G>A maps to NM_022726.3 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:110972565 G>A maps to NM_024090.2 Y242Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:110972697 G>A maps to NM_024090.2 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr5:60053374 C>T maps to NM_024930.2 K199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr5:60060117 G>A maps to NM_024930.2 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:60053413 G>A maps to NM_024930.2 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr5:60050594 C>T maps to NM_024930.2 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:60067762 G>A maps to NM_024930.2 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:60067863 G>A maps to NM_024930.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr18:33744541 C>T maps to ENST00000442325 F687F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:33718366 C>G maps to ENST00000442325 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr18:33713199 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr8:28017826 T>C maps to NM_018091.5 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr11:31669374 C>T maps to ENST00000395934 N338N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:31653927 C>T maps to ENST00000395934 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:48519291 G>A maps to NM_022142.4 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr19:48519296 G>A did not map to a codon.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr19:48523018 C>T maps to NM_022142.4 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:48519168 C>T maps to NM_022142.4 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr19:48511955 G>A maps to NM_022142.4 W11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:48511929 C>T maps to NM_022142.4 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:48523090 G>A maps to NM_022142.4 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:79385975 G>A maps to NM_022159.3 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr1:79470893 G>A maps to NM_022159.3 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:79470842 G>A maps to NM_022159.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:79357343 G>A maps to NM_022159.3 F625F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:79392695 G>A maps to NM_022159.3 Q320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:79357241 G>A maps to NM_022159.3 F659F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:79383581 G>A maps to NM_022159.3 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:79403546 C>T maps to NM_022159.3 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:79357241 G>A maps to NM_022159.3 F659F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr1:79387393 C>T maps to NM_022159.3 E387E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr1:79383603 C>T maps to NM_022159.3 K531K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:79357250 C>T maps to NM_022159.3 Q656Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:79387417 G>A maps to NM_022159.3 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:79392660 G>A maps to NM_022159.3 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:49707047 G>A maps to NM_198449.2 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:49698145 C>T maps to NM_198449.2 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:49699164 G>A maps to NM_198449.2 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:49706744 C>T maps to NM_198449.2 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:49706753 G>A maps to NM_198449.2 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:49699069 A>T maps to NM_198449.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:49699224 G>A maps to NM_198449.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:49724061 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:49707185 G>A maps to NM_198449.2 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:49701639 C>T maps to NM_198449.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:101401113 C>T maps to NM_016242.3 Q49Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:101396231 C>T maps to NM_016242.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:153609345 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr23:153608117 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:153609332 T>A did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:153608124 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr17:48452994 C>T maps to NM_001166131.1 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr12:7080097 C>T maps to ENST00000261406 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr22:29611578 G>A maps to NM_133455.2 W93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr22:29628257 C>T maps to NM_133455.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr7:101063356 G>A maps to ENST00000397927 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr7:101063374 C>T maps to ENST00000397927 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:101183235 G>A maps to ENST00000397927 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:101200734 C>T maps to ENST00000397927 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr7:101183319 G>A maps to ENST00000397927 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr2:27305086 G>A maps to NM_007046.3 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:27305021 C>T maps to NM_007046.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr2:27305119 G>C maps to NM_007046.3 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:27306761 C>T maps to NM_007046.3 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr18:2885024 G>A maps to NM_032048.2 W107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr18:2891763 C>T maps to NM_032048.2 Q547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:2891090 C>T maps to NM_032048.2 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr18:2884976 C>T maps to NM_032048.2 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:2891504 G>A maps to NM_032048.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr18:2890865 G>A maps to NM_032048.2 Q247Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:2891891 G>A maps to NM_032048.2 T589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr18:2892254 G>A maps to NM_032048.2 E710E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr20:39990078 C>T maps to NM_052846.1 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr20:39991689 C>T maps to NM_052846.1 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:39991482 C>T maps to NM_052846.1 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr20:39991017 G>A maps to NM_052846.1 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr20:39992395 G>A maps to NM_052846.1 H132H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr20:39991689 C>T maps to NM_052846.1 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:39991053 A>G maps to NM_052846.1 C385C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:39992362 C>T maps to NM_052846.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr20:39992501 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:39990858 C>T maps to NM_052846.1 R450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr14:100406370 C>T maps to NM_001008707.1 V809V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr14:100374015 C>T maps to NM_001008707.1 D369D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:100331890 C>T maps to NM_001008707.1 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr14:100344867 C>T maps to NM_001008707.1 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr14:100363550 C>T maps to NM_001008707.1 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr14:100374009 C>T maps to NM_001008707.1 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:100376661 C>T maps to NM_001008707.1 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:46133220 C>A maps to NM_001193268.1 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:62375206 G>A maps to ENST00000278845 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr11:62377143 G>A maps to ENST00000278845 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:62376025 G>A maps to ENST00000278845 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:62373636 G>A maps to ENST00000278845 F519F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:62376926 G>A maps to ENST00000278845 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:62376049 G>A maps to ENST00000278845 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr11:62373338 G>A maps to ENST00000278845 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:62372640 G>A maps to ENST00000278845 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:62373636 G>A maps to ENST00000278845 F519F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:62376528 G>A maps to ENST00000278845 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr2:42557082 A>G maps to NM_019063.3 Q894Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr2:42543111 C>T maps to NM_019063.3 L660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr14:89154728 C>T maps to ENST00000380664 E876E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr14:89206849 G>A maps to ENST00000380664 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr14:89206787 C>T maps to ENST00000380664 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr14:89220906 C>T maps to ENST00000380664 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr14:89148294 G>A maps to ENST00000380664 T1021T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:89083223 C>T did not map to a codon.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr14:89091323 T>A maps to ENST00000380664 K1630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:13366657 C>T maps to NM_001423.2 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr16:10631854 G>A maps to NM_001424.4 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr16:10641414 G>A maps to NM_001424.4 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr19:6913830 G>A maps to ENST00000381407 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr19:6937271 C>T maps to ENST00000381407 A802A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr19:6921866 C>T maps to ENST00000381407 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:6903929 G>A maps to ENST00000381407 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:6926552 G>A maps to ENST00000381407 P723P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:6928203 A>C maps to ENST00000381407 P759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:6897304 C>T maps to ENST00000381407 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:6937592 G>A maps to ENST00000381407 T865T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:6924759 C>T maps to ENST00000381407 I623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:6921749 C>T maps to ENST00000381407 I551I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:6903929 G>A maps to ENST00000381407 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:6904108 C>T maps to ENST00000381407 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:6928182 C>T maps to ENST00000381407 F752F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr19:6913830 G>A maps to ENST00000381407 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:6924811 C>T maps to ENST00000381407 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr19:6896499 C>T maps to ENST00000381407 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr19:6901964 C>T maps to ENST00000381407 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:6908773 T>A maps to ENST00000381407 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr19:6937403 C>T maps to ENST00000381407 H846H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr19:6937553 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:6897451 C>T maps to ENST00000381407 C136C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:6937592 G>A maps to ENST00000381407 T865T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:6926417 C>T maps to ENST00000381407 F678F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:6904113 C>T maps to ENST00000381407 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr19:6913719 C>T maps to ENST00000381407 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr19:14875263 G>A maps to NM_013447.2 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:14877889 G>A maps to NM_013447.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr19:14865890 G>A maps to NM_013447.2 Q489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:14854481 G>A maps to NM_013447.2 I766I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:14877185 A>G maps to NM_013447.2 N165N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:14752278 G>A maps to NM_032571.3 F400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr19:14740968 C>T maps to NM_032571.3 W565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:14765818 G>A maps to NM_032571.3 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:14749088 G>A maps to NM_032571.3 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:14755049 C>T maps to NM_032571.3 W307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:14774248 G>A maps to NM_032571.3 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:14744098 C>T maps to NM_032571.3 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:14769330 C>T maps to NM_032571.3 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:14740883 G>A maps to NM_032571.3 F593F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:14752244 G>A maps to NM_032571.3 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:14765809 G>A maps to NM_032571.3 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:14765860 C>T maps to NM_032571.3 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z4-06A-11D-A197-08 chr19:14748942 C>T maps to NM_032571.3 W486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:14754918 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:14749140 G>A maps to NM_032571.3 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:14765923 C>T maps to NM_032571.3 W149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:14740982 G>A maps to NM_032571.3 I560I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:119604386 C>T maps to NM_001426.3 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr2:119604320 C>G maps to NM_001426.3 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr7:155255076 C>T maps to NM_001427.3 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:225692709 G>A maps to NM_001008493.1 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:225700643 G>A maps to ENST00000284563 G678G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr4:71507922 G>A maps to NM_031889.2 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr4:71509503 G>A maps to NM_031889.2 W787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr4:71508129 T>G maps to NM_031889.2 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:71508741 T>G maps to NM_031889.2 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:71510226 C>T maps to NM_031889.2 S1028S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:71500251 A>G maps to NM_031889.2 Q146Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:71508069 G>A maps to NM_031889.2 W309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:71508453 G>A maps to NM_031889.2 K437K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:71508966 C>T maps to NM_031889.2 P608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:71508462 C>T maps to NM_031889.2 P440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:71500275 A>G maps to NM_031889.2 Q154Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:71501553 C>T maps to NM_031889.2 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr4:71509926 C>T maps to NM_031889.2 I928I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr4:71508042 G>A maps to NM_031889.2 Q300Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:71509610 G>A maps to NM_031889.2 W823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:71510535 G>A maps to NM_031889.2 Q1131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr5:73931416 G>A maps to NM_003633.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:73931020 G>A maps to NM_003633.2 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:73931359 G>A maps to NM_003633.2 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr5:73932232 G>A maps to NM_003633.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr5:73931416 G>A maps to NM_003633.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr5:73931665 A>G maps to NM_003633.2 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr5:73931056 G>A maps to NM_003633.2 D418D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr11:94862475 C>T maps to NM_015036.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:94862601 C>T maps to NM_015036.2 D454D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr9:130580443 G>A maps to NM_001114753.1 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr9:130588122 G>A maps to NM_001114753.1 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr17:77082172 C>T maps to NM_001042573.1 V658V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr17:77081743 C>T maps to NM_001042573.1 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr17:77081373 C>T maps to NM_001042573.1 A550A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:77079620 C>T maps to NM_001042573.1 F400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:77079886 C>T maps to NM_001042573.1 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:77079572 C>T maps to NM_001042573.1 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:77079620 C>T maps to NM_001042573.1 F400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:77082358 C>T maps to NM_001042573.1 V720V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:8925416 G>A maps to NM_001428.2 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:8924023 G>A maps to NM_001428.2 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr1:8927217 G>A maps to NM_001428.2 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:8926470 G>A maps to NM_001428.2 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr12:7026757 C>T maps to NM_001975.2 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:7026766 C>T maps to NM_001975.2 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:7028902 C>T maps to NM_001975.2 Q281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr17:4860302 C>T maps to NM_053013.3 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr17:4858533 T>C maps to NM_053013.3 D203D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr17:4859291 C>T maps to NM_053013.3 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:83375877 C>T maps to NM_021204.3 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr18:683326 G>A maps to ENST00000319815 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr18:677818 G>A maps to ENST00000319815 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr13:43788200 C>T maps to NM_001127615.1 Q619Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:43918694 A>G maps to NM_001127615.1 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr13:43918818 C>T maps to NM_001127615.1 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr13:43986163 C>T maps to NM_001127615.1 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr13:43872619 G>A maps to NM_001127615.1 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr13:43843641 G>A maps to NM_001127615.1 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:43788173 C>T maps to NM_001127615.1 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:43872642 G>A maps to NM_001127615.1 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:43918845 G>A maps to NM_001127615.1 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:43930229 C>T maps to NM_001127615.1 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:129771313 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:129804054 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr23:129813710 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:129804107 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr23:129804160 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:129813719 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr23:129771273 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:129790563 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr23:129771336 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr4:111397992 C>T maps to NM_001977.3 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr4:111409720 A>G maps to NM_001977.3 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr4:111474557 G>A maps to NM_001977.3 G863G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr4:111398145 C>T maps to NM_001977.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:111470886 C>T maps to NM_001977.3 L782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr4:111397935 C>T maps to NM_001977.3 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:111397857 C>T maps to NM_001977.3 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr4:111474531 C>T maps to NM_001977.3 R855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:111398064 G>A maps to NM_001977.3 K165K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr4:111474476 G>A maps to NM_001977.3 L836L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr4:111397747 C>T maps to NM_001977.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr4:111397746 C>T maps to NM_001977.3 H59H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:111436583 C>T maps to NM_001977.3 Q499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr4:111398145 C>T maps to NM_001977.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr4:111398052 C>T maps to NM_001977.3 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr4:111470995 C>T maps to NM_001977.3 L819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr4:111397938 C>T maps to NM_001977.3 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:111398052 C>T maps to NM_001977.3 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:111441411 C>T maps to NM_001977.3 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:111470889 G>A maps to NM_001977.3 R783R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr6:132201155 C>T maps to NM_006208.2 S694S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr6:132207716 C>T maps to NM_006208.2 I820I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:132204910 C>T maps to NM_006208.2 Q770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr6:132168965 G>A maps to NM_006208.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:132173318 G>A maps to NM_006208.2 E187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr8:120608146 C>T maps to NM_006209.3 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr8:120629430 G>A maps to NM_006209.3 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr8:120620199 G>A maps to NM_006209.3 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr8:120608181 T>A maps to NM_006209.3 K345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr6:132006567 C>T maps to NM_005021.3 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr6:131992442 C>T maps to NM_005021.3 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr6:132004285 C>T maps to NM_005021.3 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:132045205 G>A maps to NM_005021.3 Q591Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:131973690 G>A maps to NM_005021.3 W96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr6:46107657 G>A maps to NM_014936.4 W113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:46107841 G>A maps to NM_014936.4 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr6:46107691 G>A maps to NM_014936.4 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:46111148 G>A maps to NM_014936.4 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:46111019 C>T maps to NM_014936.4 D335D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr6:46135639 C>T maps to NM_021572.4 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:46135444 G>A maps to NM_021572.4 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:46129413 C>T maps to NM_021572.4 K361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:46129490 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:46133189 G>A maps to NM_021572.4 Q314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:46133189 G>A maps to NM_021572.4 Q314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:46135627 C>T maps to NM_021572.4 W124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr4:185074731 C>T maps to NM_153343.3 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr4:185138933 G>A maps to NM_153343.3 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:185138771 G>A maps to NM_153343.3 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:185038968 C>T maps to NM_153343.3 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:185038968 C>T maps to NM_153343.3 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr4:185039046 G>A maps to NM_153343.3 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr4:185033884 C>T maps to NM_153343.3 K311K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr4:185038026 G>A maps to NM_153343.3 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr4:185038146 C>T maps to NM_153343.3 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr17:77708876 G>A maps to NM_178543.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr17:77709026 C>T maps to NM_178543.3 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr17:77711003 C>T maps to NM_178543.3 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr17:77710967 C>T maps to NM_178543.3 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:77708957 G>A maps to NM_178543.3 W172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr17:77709386 C>T maps to NM_178543.3 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr17:77708918 A>G maps to NM_178543.3 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:77705075 C>T maps to NM_178543.3 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr17:77709191 G>A maps to NM_178543.3 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:150598176 G>A maps to NM_207042.1 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:40217100 C>T maps to NM_152512.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:40283623 C>T maps to NM_152512.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr22:40231963 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr22:40139866 G>A maps to NM_152512.3 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr22:40140133 G>A maps to NM_152512.3 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr22:40139854 A>G maps to NM_152512.3 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr22:40161537 G>A maps to NM_152512.3 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr22:40283632 G>A maps to NM_152512.3 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr22:40139788 A>G maps to NM_152512.3 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr22:40161378 G>A maps to NM_152512.3 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr10:97604313 T>C maps to NM_001098175.1 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:97605215 C>T maps to NM_001098175.1 Q233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:97599470 T>C maps to NM_001098175.1 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr9:139945548 C>T maps to NM_203468.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr9:139945548 C>T maps to NM_203468.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr9:139945978 C>T maps to NM_203468.1 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:139944957 G>A maps to NM_203468.1 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:139945764 G>T maps to NM_203468.1 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr3:40457368 G>A maps to NM_001248.2 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:40457328 A>T did not map to a codon.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr3:40442419 C>T maps to NM_001248.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:40457386 G>A maps to NM_001248.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:40464384 G>A maps to NM_001248.2 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:23290645 G>A maps to NM_004901.3 F548F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr8:23294536 G>A maps to NM_004901.3 F428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:23290576 G>A maps to NM_004901.3 F571F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:23305331 G>A maps to NM_004901.3 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr14:74439638 G>A maps to NM_001249.2 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr14:74433630 T>C maps to NM_001249.2 *429W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr14:74433631 C>T maps to NM_001249.2 *429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr14:74436805 G>A maps to NM_001249.2 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:74444065 G>A maps to NM_001249.2 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr20:25187899 C>T maps to NM_001247.2 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr20:25197350 C>T maps to NM_001247.2 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:25203576 C>T maps to NM_001247.2 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:25201907 C>T maps to NM_001247.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr10:101439503 T>C maps to NM_020354.3 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr10:101458473 C>T maps to NM_020354.3 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr9:140332641 G>A maps to NM_001033113.1 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr9:140332467 C>T maps to NM_001033113.1 K65K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr9:140331356 C>T maps to NM_001033113.1 W173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr9:140331428 G>A maps to NM_001033113.1 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:140332515 C>G maps to NM_001033113.1 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:140331431 C>T maps to NM_001033113.1 Q148Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:27761770 G>T maps to ENST00000449599 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:27761749 G>A maps to ENST00000449599 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:27762915 C>T maps to ENST00000449599 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr22:41572462 C>T maps to NM_001429.3 D1664D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:41553270 T>C maps to NM_001429.3 D1120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr22:41572330 C>T maps to NM_001429.3 P1620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr22:41537069 C>T maps to NM_001429.3 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr22:41551053 C>T maps to NM_001429.3 Y1066Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr22:41572388 G>T maps to NM_001429.3 E1640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr12:132547143 G>A maps to ENST00000333577 Q2780Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr12:132474603 C>T maps to ENST00000333577 A871A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:132466779 C>T maps to ENST00000333577 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:132510206 C>T maps to ENST00000333577 I1660I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr12:132551329 C>T maps to ENST00000333577 P2891P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:132529466 G>A maps to ENST00000333577 K2287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:132522319 C>T maps to ENST00000333577 S2051S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr12:132529391 C>T maps to ENST00000333577 L2262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:132474600 C>T maps to ENST00000333577 A870A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:132522281 C>T maps to ENST00000333577 L2039L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:132530312 C>T maps to ENST00000333577 I2392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr12:132490708 C>T maps to ENST00000333577 I1032I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:132547140 G>A maps to ENST00000333577 Q2779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr12:132551949 G>A maps to ENST00000333577 L2967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr12:132561999 C>T maps to ENST00000333577 Q3088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:132471240 C>T maps to ENST00000333577 S740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:132471078 C>T maps to ENST00000333577 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:132516577 C>T maps to ENST00000333577 N1981N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr12:132466716 G>C maps to ENST00000333577 G577G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr12:132498055 C>T maps to ENST00000333577 I1247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:46588100 C>T maps to NM_001430.4 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:46583359 G>A maps to NM_001430.4 E96E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:46607832 C>A maps to NM_001430.4 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr2:46611753 C>T maps to NM_001430.4 L856L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:46607817 C>T maps to NM_001430.4 P669P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:46609672 C>T maps to NM_001430.4 F799F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr1:29319972 C>T maps to NM_001166005.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:29391576 A>C maps to NM_001166005.1 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:29379655 T>C maps to NM_001166005.1 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:29379625 C>T maps to NM_001166005.1 V549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr20:34802334 C>T maps to NM_012156.2 I747I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr20:34775630 C>T maps to NM_012156.2 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr20:34765944 C>T maps to NM_012156.2 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr20:34763555 C>T maps to NM_012156.2 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr20:34806814 C>T maps to NM_012156.2 S762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:34807690 G>A maps to NM_012156.2 G788G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:34782227 G>A maps to NM_012156.2 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr20:34817258 C>T maps to NM_012156.2 S881S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:34797711 C>T maps to NM_012156.2 F657F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr20:34807690 G>A maps to NM_012156.2 G788G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr20:34776267 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr20:34782227 G>C maps to NM_012156.2 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr20:34806853 G>A maps to NM_012156.2 T775T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr20:34761872 A>G maps to NM_012156.2 E58E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr20:34810282 C>T maps to NM_012156.2 D868D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr20:34800279 C>T maps to NM_012156.2 S722S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:34785878 G>A maps to NM_012156.2 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr20:34778561 C>T maps to NM_012156.2 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr20:34778245 G>A maps to NM_012156.2 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:34773095 C>T maps to NM_012156.2 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr20:34778702 C>T maps to NM_012156.2 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr20:34797621 C>T maps to NM_012156.2 D627D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:34773071 C>T maps to NM_012156.2 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:34770215 C>T maps to NM_012156.2 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:34775645 G>A maps to NM_012156.2 K278K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:34778552 C>T maps to NM_012156.2 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:34810306 G>A maps to NM_012156.2 K876K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:131277394 G>A maps to NM_001431.3 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:131201288 A>G maps to NM_001431.3 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr6:131222106 G>A maps to NM_001431.3 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:131186708 G>A maps to NM_001431.3 S932S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:131186723 G>A maps to NM_001431.3 T927T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:131191230 C>T maps to NM_001431.3 K693K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:131220669 C>T maps to NM_001431.3 K399K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr18:5406802 G>A maps to NM_012307.2 P774P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr18:5433987 C>A maps to NM_012307.2 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr18:5423385 A>G maps to NM_012307.2 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr18:5416332 G>A maps to NM_012307.2 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr18:5410562 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr18:5423518 G>A maps to NM_012307.2 F399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:5396313 C>T maps to NM_012307.2 T953T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:5434068 G>A maps to NM_012307.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:5489038 G>A maps to NM_012307.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr18:5410588 G>A maps to NM_012307.2 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr18:5416089 G>C maps to NM_012307.2 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:111643178 C>T maps to NM_022140.3 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:111576447 C>T maps to NM_022140.3 W285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr5:111530275 T>C maps to NM_022140.3 K497K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:111540172 A>G maps to NM_022140.3 N425N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:111576444 C>T maps to NM_022140.3 K286K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:111595652 G>A maps to NM_022140.3 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr5:111643178 C>T maps to NM_022140.3 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:111595607 C>T maps to NM_022140.3 K237K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:111541185 C>T maps to NM_022140.3 K398K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr9:111979208 G>A maps to NM_019114.3 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr9:112018068 G>A maps to NM_019114.3 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:111979237 G>A maps to NM_019114.3 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:111965971 C>T maps to NM_019114.3 K639K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:112004082 G>A maps to NM_018424.2 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr9:112004016 G>A maps to NM_018424.2 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr9:111979346 G>A maps to NM_019114.3 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr9:112030708 C>T maps to NM_019114.3 W139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:111938889 C>T maps to NM_019114.3 E858E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:112018714 C>T maps to NM_019114.3 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:112029763 C>T maps to NM_019114.3 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr9:111970317 C>T maps to NM_019114.3 K588K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr9:112003967 G>A maps to NM_018424.2 R511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr9:112015766 C>T maps to NM_019114.3 R411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr9:111956661 G>A maps to NM_019114.3 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:120857837 G>A maps to NM_020909.3 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:120834849 C>T maps to NM_020909.3 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:120834607 C>T maps to NM_020909.3 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:120834607 C>T maps to NM_020909.3 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr2:120776752 A>T maps to NM_020909.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:120889254 C>T maps to NM_020909.3 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:120903845 C>T maps to NM_020909.3 Q592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:120922486 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr15:43508576 G>T maps to NM_000119.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:43500503 C>T maps to NM_000119.2 W363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr15:43500530 C>T maps to NM_000119.2 W354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:43500524 G>A maps to NM_000119.2 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr15:43494123 G>A maps to NM_000119.2 Q641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:43501607 C>T maps to NM_000119.2 Q262Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:43503702 G>A maps to NM_000119.2 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:43507419 G>A maps to NM_000119.2 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:43508586 G>A maps to NM_000119.2 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:21925111 C>T maps to ENST00000265800 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:21938631 C>T maps to ENST00000265800 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:32580219 G>T maps to NM_025209.2 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q1-06A-21D-A196-08 chr2:149528377 T>G maps to NM_015630.3 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr2:149519472 C>T maps to NM_015630.3 H263H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:149528936 C>G maps to NM_015630.3 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:149511696 C>T maps to NM_015630.3 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr7:37960618 C>T maps to NM_017549.3 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr7:37988585 C>T maps to NM_017549.3 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr7:143095437 G>A maps to NM_005232.4 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr7:143092273 T>A maps to NM_005232.4 R695R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr7:143095970 T>C maps to NM_005232.4 E353E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:143090819 C>T maps to NM_005232.4 L880L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:143097140 G>A maps to NM_005232.4 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:143095446 C>T maps to NM_005232.4 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:143092430 C>T maps to NM_005232.4 L688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr7:143098581 C>T maps to NM_005232.4 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:143096027 C>T maps to NM_005232.4 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:143098599 G>A maps to NM_005232.4 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr7:143095982 G>A maps to NM_005232.4 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:38227188 C>T maps to NM_001099439.1 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr1:38227362 G>A maps to NM_001099439.1 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:38227491 G>A maps to NM_001099439.1 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr1:38227620 G>A maps to NM_001099439.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:38227479 G>A maps to NM_001099439.1 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:38184466 G>A maps to NM_001099439.1 D926D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:38188737 G>A maps to NM_001099439.1 V645V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr1:38227563 G>A maps to NM_001099439.1 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr1:38227620 G>A maps to NM_001099439.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:38192814 G>A maps to NM_001099439.1 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:38187512 C>T maps to NM_001099439.1 R655R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:38187410 G>A maps to NM_001099439.1 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr1:38227461 G>A maps to NM_001099439.1 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr1:38197176 G>A maps to NM_001099439.1 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:38192814 G>A maps to NM_001099439.1 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:38227464 C>T maps to NM_001099439.1 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:38227470 G>A maps to NM_001099439.1 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:38185153 G>A maps to NM_001099439.1 I896I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:38227206 G>T maps to NM_001099439.1 C240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:38228489 G>A maps to NM_001099439.1 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:16475116 G>A maps to NM_004431.3 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:16475014 G>A maps to NM_004431.3 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:16458926 G>A maps to NM_004431.3 P687P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr1:16464803 C>T maps to NM_004431.3 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:16475410 G>A maps to NM_004431.3 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:16456035 G>A maps to NM_004431.3 F906F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:16475028 G>A maps to NM_004431.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:16475029 G>A maps to NM_004431.3 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:16461624 G>A maps to NM_004431.3 D496D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr3:89390207 C>T maps to NM_005233.5 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr3:89521622 C>T maps to NM_005233.5 N900N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr3:89445047 C>T maps to NM_005233.5 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:89391079 C>T maps to NM_005233.5 F382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:89480430 T>C maps to NM_005233.5 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:89498472 G>A maps to NM_005233.5 W815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr3:89480457 C>T maps to NM_005233.5 F765F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:89259261 C>T maps to NM_005233.5 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:89259506 C>G maps to NM_005233.5 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr3:89480403 C>T maps to NM_005233.5 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:89259261 C>T maps to NM_005233.5 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr3:89480403 C>T maps to NM_005233.5 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:89156912 C>T maps to NM_005233.5 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:89391131 C>T maps to NM_005233.5 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:89448643 C>T maps to NM_182644.2 F536F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:89456470 G>A maps to NM_005233.5 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr3:89259254 G>A maps to NM_005233.5 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr3:89480344 C>T maps to NM_005233.5 R728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:222428736 C>T maps to NM_004438.3 K179K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr2:222321351 C>T maps to NM_004438.3 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr2:222428598 G>A maps to NM_004438.3 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:222291221 A>G maps to NM_004438.3 G936G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr2:222320319 C>T maps to NM_004438.3 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:222307681 C>T maps to NM_004438.3 E647E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:222347180 G>A maps to NM_004438.3 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:222428585 G>A maps to NM_004438.3 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:222291233 G>A maps to NM_004438.3 F932F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:222428865 G>A maps to NM_004438.3 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:222347195 G>A maps to NM_004438.3 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:222294724 G>A maps to NM_004438.3 L881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:222291233 G>A maps to NM_004438.3 F932F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:222428682 G>A maps to NM_004438.3 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:222428585 G>A maps to NM_004438.3 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:222347189 G>A maps to NM_004438.3 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:222307621 G>A maps to NM_004438.3 F667F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:222436923 C>T maps to NM_004438.3 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:222428964 G>A maps to NM_004438.3 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:222321435 G>A maps to NM_004438.3 I500I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:222307702 G>A maps to NM_004438.3 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:222429003 G>A maps to NM_004438.3 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:222298921 G>A maps to NM_004438.3 I812I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:222365815 G>A maps to NM_004438.3 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr4:66535316 G>A maps to NM_004439.5 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr4:66280067 G>A maps to NM_004439.5 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr4:66280149 G>A maps to NM_004439.5 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:97311468 C>T maps to NM_001080448.2 A800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr3:96706604 C>T maps to NM_001080448.2 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr3:97251244 G>A maps to NM_001080448.2 G748G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr3:97167452 C>T maps to NM_001080448.2 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr3:96962973 C>T maps to NM_001080448.2 I483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr3:97356760 C>T maps to NM_001080448.2 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr3:96962850 T>A maps to NM_001080448.2 I442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr3:97124034 C>T maps to NM_001080448.2 Q550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:96706322 C>T maps to NM_001080448.2 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:96706445 G>A maps to NM_001080448.2 K241K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:97311570 G>A maps to NM_001080448.2 R834R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr3:97251217 C>T maps to NM_001080448.2 V739V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:96962853 G>A maps to NM_001080448.2 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:97311498 C>T maps to NM_001080448.2 F810F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:97466356 G>A maps to NM_001080448.2 K1073K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:96706569 C>T maps to NM_001080448.2 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr3:97439160 C>T maps to NM_001080448.2 F947F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr3:97124003 G>A maps to NM_001080448.2 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:96962973 C>T maps to NM_001080448.2 I483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr3:97329699 T>G did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:96706184 C>T maps to NM_001080448.2 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:97185261 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr3:96706247 A>G maps to NM_001080448.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr3:97194223 G>A maps to NM_001080448.2 Q641Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr3:97311498 C>T maps to NM_001080448.2 F810F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr3:96945225 C>T maps to NM_001080448.2 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:96533502 C>T maps to NM_001080448.2 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:96706529 G>A maps to NM_001080448.2 E269E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:97329688 C>T maps to NM_001080448.2 S855S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:97466365 C>T maps to NM_001080448.2 F1076F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr3:96963124 C>T maps to NM_001080448.2 Q534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr3:97124018 G>A maps to NM_001080448.2 R544R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr3:96962844 C>T maps to NM_001080448.2 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr6:94120516 G>A maps to NM_004440.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:93956610 C>T maps to NM_004440.3 K875K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:94066666 G>A maps to NM_004440.3 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr6:93955112 C>A maps to NM_004440.3 G929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:93974316 C>T maps to NM_004440.3 G579G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:93982048 G>A maps to NM_004440.3 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:93979288 G>A maps to NM_004440.3 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:94120759 C>T maps to NM_004440.3 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:94120783 C>T maps to NM_004440.3 W89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:93964436 C>T maps to NM_004440.3 W820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:93979363 C>T maps to NM_004440.3 R488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:93965743 C>T maps to NM_004440.3 G728G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:93967958 C>T maps to NM_004440.3 G656G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr6:93953209 G>A maps to NM_004440.3 I977I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr6:93967994 G>A maps to NM_004440.3 F644F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr6:93964397 T>A maps to NM_004440.3 G833G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:94120642 C>T maps to NM_004440.3 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:94129029 C>T maps to NM_004440.3 W10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:93967212 G>A maps to NM_004440.3 F713F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr6:93967239 C>T maps to NM_004440.3 G704G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr6:93968002 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:94066597 T>A maps to NM_004440.3 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr6:94120354 C>T maps to NM_004440.3 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr6:93965731 G>A maps to NM_004440.3 V732V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:94120738 G>A maps to NM_004440.3 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr6:94068037 G>A maps to NM_004440.3 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:93955131 G>A maps to NM_004440.3 F922F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr6:93979369 C>T maps to NM_004440.3 R486R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:94068087 G>A maps to NM_004440.3 Q292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:94120429 G>A maps to NM_004440.3 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:94120729 C>T maps to NM_004440.3 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr6:94120809 G>A maps to NM_004440.3 Q81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr6:93965617 G>A maps to NM_004440.3 L770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr1:22927227 G>T maps to NM_020526.3 V821V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:22902906 G>A maps to NM_020526.3 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:22923919 T>C maps to NM_020526.3 T627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr1:22923820 C>T maps to NM_020526.3 F594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:22895812 G>A maps to NM_020526.3 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:22920042 C>T maps to NM_020526.3 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:22915619 C>T maps to NM_020526.3 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr1:22902711 G>A maps to NM_020526.3 W54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr1:22927260 G>A maps to NM_020526.3 L832L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:22903155 G>A maps to NM_020526.3 K202K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:22915718 C>T maps to NM_001006943.1 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:22902819 C>T maps to NM_020526.3 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr1:22927915 C>T maps to NM_020526.3 F951F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:22927560 G>A maps to NM_020526.3 R903R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:22927861 C>T maps to NM_020526.3 L933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:22913000 C>T maps to NM_020526.3 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:22927885 C>T maps to NM_020526.3 S941S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr3:134898762 C>T maps to NM_004441.4 V607V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:134968303 C>T maps to NM_004441.4 S939S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:134670505 C>T maps to NM_004441.4 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr3:134851607 C>T maps to NM_004441.4 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:134911658 C>T maps to NM_004441.4 F708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:134960078 C>T maps to NM_004441.4 I812I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr3:134670460 G>A maps to NM_004441.4 K124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A197-06A-32D-A197-08 chr3:134670613 C>T maps to NM_004441.4 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:134920413 G>A maps to NM_004441.4 R743R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:134968303 C>T maps to NM_004441.4 S939S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:134968306 C>T maps to NM_004441.4 L940L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:134670754 G>A maps to NM_004441.4 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:134911574 C>T maps to NM_004441.4 I680I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:134920527 C>T maps to NM_004441.4 S781S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr3:134898711 G>A maps to NM_004441.4 G590G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr3:134960072 T>C maps to NM_004441.4 Y810Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:23219429 C>T maps to ENST00000400191 T494T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:23191388 G>A maps to ENST00000400191 Q329Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr1:23222924 T>C maps to ENST00000400191 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr1:23235525 C>T maps to ENST00000400191 I788I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr1:23189626 T>C maps to ENST00000400191 C303C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:23222019 C>T maps to ENST00000400191 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:23222930 G>A maps to ENST00000400191 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:23233344 C>T maps to ENST00000400191 F677F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr1:23111291 C>T maps to ENST00000400191 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:23234597 G>A maps to ENST00000400191 S763S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr1:23235513 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:23233371 G>A maps to ENST00000400191 E686E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:23236990 C>T maps to ENST00000400191 F873F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr1:23240061 G>A maps to NM_004442.6 *988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:23222939 G>A maps to ENST00000400191 T578T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:23235570 C>T maps to ENST00000400191 F803F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:23237023 C>T maps to ENST00000400191 I884I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:23111537 C>T maps to ENST00000400191 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:23191379 C>T maps to ENST00000400191 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:23235552 C>T maps to ENST00000400191 A797A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:23236933 C>T maps to ENST00000400191 A854A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:23236959 G>A maps to ENST00000400191 W863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:23236960 G>A maps to ENST00000400191 W863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr1:23191691 C>T maps to ENST00000400191 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:23238963 G>A maps to ENST00000400191 T908T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:23234567 C>T maps to ENST00000400191 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr1:23233359 C>T maps to ENST00000400191 V682V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:23233410 C>T maps to ENST00000400191 T699T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:184298380 C>T maps to NM_004443.3 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:184290678 C>T maps to NM_004443.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:184295755 C>T maps to NM_004443.3 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:184297595 G>A maps to NM_004443.3 E682E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr3:184295459 C>T maps to NM_004443.3 A498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:184295719 C>T maps to NM_004443.3 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr3:184290368 C>T maps to NM_004443.3 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:184293693 C>T maps to NM_004443.3 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:184298851 G>A maps to NM_004443.3 R877R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:184299058 G>A maps to NM_004443.3 L917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:100410419 G>A maps to NM_004444.4 V689V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:100417781 G>A maps to NM_004444.4 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr7:100405169 G>A maps to NM_004444.4 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr7:100417332 G>A maps to NM_004444.4 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:100411641 C>T maps to NM_004444.4 E530E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:142561797 C>T maps to NM_004445.3 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:142566872 G>A maps to NM_004445.3 K810K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr7:142566053 C>T maps to NM_004445.3 I658I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr7:142568055 G>A maps to NM_004445.3 Q899Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:142565435 C>T maps to NM_004445.3 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr7:142568294 C>T maps to NM_004445.3 A938A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:142564674 C>T maps to NM_004445.3 S533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:142562472 C>T maps to NM_004445.3 Y305Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr7:142562172 C>G maps to NM_004445.3 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:142566358 C>T maps to NM_004445.3 F716F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:142562190 G>A maps to NM_004445.3 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr7:142568094 G>A maps to NM_004445.3 V912V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:142565411 C>T maps to NM_004445.3 S599S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:142566815 C>T maps to NM_004445.3 F791F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:142561815 G>A maps to NM_004445.3 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:142564287 C>T maps to NM_004445.3 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:142566054 C>T maps to NM_004445.3 R659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:142563803 C>T maps to NM_004445.3 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:226019640 C>T maps to NM_001136018.2 H115H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:226026478 C>T maps to NM_001136018.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr1:226033023 C>T maps to NM_001136018.2 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr1:226019496 C>T maps to NM_001136018.2 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:226019505 C>T maps to NM_001136018.2 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:27401306 C>T maps to ENST00000458037 F514F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr8:27358511 G>A maps to ENST00000458037 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:27399007 C>T maps to ENST00000458037 Y483Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr8:27362506 G>T maps to ENST00000458037 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:15338586 G>A maps to NM_001142886.1 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr19:15338646 G>A maps to NM_001142886.1 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr19:15338472 C>T maps to NM_001142886.1 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr1:92528791 G>A maps to NM_173567.4 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:92511194 C>T maps to NM_173567.4 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr6:146007361 G>A maps to NM_005670.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:145948662 G>A maps to NM_005670.3 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:56206589 C>A maps to NM_001130071.1 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:56203241 C>T maps to NM_001130071.1 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:56204341 C>T maps to NM_001130071.1 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr17:19186623 G>A maps to NM_014964.4 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:19215450 G>A maps to NM_014964.4 K322K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:19237302 C>T maps to NM_014964.4 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:19186758 C>T maps to NM_014964.4 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:48616567 T>C maps to NM_017957.2 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr17:48614369 G>A maps to NM_017957.2 K151K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr17:48617660 C>T maps to NM_017957.2 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr17:48614414 G>A maps to NM_017957.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr7:100320291 G>A maps to NM_000799.2 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:100320645 C>T maps to NM_000799.2 R158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:100320390 C>A maps to NM_000799.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:100320614 C>T maps to NM_000799.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr19:11489123 G>A maps to NM_000121.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr19:11489124 G>A maps to NM_000121.3 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr8:144943374 C>T maps to NM_031308.1 Q1349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr8:144941964 G>A maps to NM_031308.1 A1819A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr8:144940740 C>T maps to NM_031308.1 A2227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr8:144940332 G>A maps to NM_031308.1 Y2363Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr8:144941697 C>T maps to NM_031308.1 R1908R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr8:144945153 G>A maps to NM_031308.1 I756I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr8:144940332 G>A maps to NM_031308.1 Y2363Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr8:144940608 G>A maps to NM_031308.1 F2271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:144940317 G>A maps to NM_031308.1 F2368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:144941601 G>A maps to NM_031308.1 L1940L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:144946352 G>A maps to NM_031308.1 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr8:144940719 C>T maps to NM_031308.1 K2234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr8:144943356 G>A maps to NM_031308.1 L1355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:144946005 G>T maps to NM_031308.1 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:144940527 C>T maps to NM_031308.1 E2298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:144941022 C>T maps to NM_031308.1 E2133E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:144941994 C>T maps to NM_031308.1 R1809R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:144942576 G>A maps to NM_031308.1 I1615I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:144946527 C>T maps to NM_031308.1 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:144943557 G>A maps to NM_031308.1 F1288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:144944645 G>A maps to NM_031308.1 L926L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:144945174 G>A maps to NM_031308.1 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr8:144941667 C>T maps to NM_031308.1 R1918R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr8:144940569 C>T maps to NM_031308.1 E2284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr8:144945156 C>T maps to NM_031308.1 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr8:144945249 G>A maps to NM_031308.1 I724I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr8:144942234 G>A maps to NM_031308.1 F1729F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:144945384 C>T maps to NM_031308.1 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:144946632 C>T maps to NM_031308.1 E263E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:144947142 G>A maps to NM_031308.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr8:144944040 C>T maps to NM_031308.1 Q1127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:144941946 C>T maps to NM_031308.1 E1825E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr8:144946533 G>A maps to NM_031308.1 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:144941145 G>A maps to NM_031308.1 S2092S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr8:144940455 G>A maps to NM_031308.1 F2322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr8:144942405 G>A maps to NM_031308.1 I1672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr8:144940533 G>A maps to NM_031308.1 I2296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:144940455 G>A maps to NM_031308.1 F2322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:144942906 G>A maps to NM_031308.1 V1505V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:144940302 G>A maps to NM_031308.1 N2373N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:144947004 C>T maps to NM_031308.1 K139K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr8:144945249 G>A maps to NM_031308.1 I724I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr8:144947160 G>A maps to NM_031308.1 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr8:144945044 G>A maps to NM_031308.1 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr8:144942030 C>T maps to NM_031308.1 W1797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:144942630 C>T maps to NM_031308.1 R1597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr8:144944880 C>T maps to NM_031308.1 R847R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:144944100 A>G maps to NM_031308.1 T1107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:144946491 G>A maps to NM_031308.1 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:144940785 C>T maps to NM_031308.1 E2212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr8:144940220 G>A maps to NM_031308.1 L2401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr8:144941931 G>A maps to NM_031308.1 I1830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:144942582 G>A maps to NM_031308.1 F1613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr8:144944109 C>T maps to NM_031308.1 R1104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr8:144945561 G>A maps to NM_031308.1 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr8:144945888 C>T maps to NM_031308.1 W511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr8:144947067 G>A maps to NM_031308.1 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:144946740 G>T maps to NM_031308.1 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr8:144940356 G>A maps to NM_031308.1 H2355H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr8:144945633 C>T maps to NM_031308.1 V596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:144940422 C>T maps to NM_031308.1 E2333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:144940458 G>A maps to NM_031308.1 L2321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:144940497 G>A maps to NM_031308.1 T2308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:144940608 G>A maps to NM_031308.1 F2271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:144941151 C>T maps to NM_031308.1 R2090R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:144942441 C>T maps to NM_031308.1 Q1660Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:144943767 G>A maps to NM_031308.1 T1218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:144944739 C>T maps to NM_031308.1 E894E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:144940830 G>A maps to NM_031308.1 L2197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:144944961 G>A maps to NM_031308.1 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr8:144943557 G>A maps to NM_031308.1 F1288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr8:144943092 G>A maps to NM_031308.1 D1443D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr8:144943077 C>T maps to NM_031308.1 V1448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:220178603 A>C maps to NM_004446.2 P683P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:220193454 C>T maps to NM_004446.2 W408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:220193455 C>T maps to NM_004446.2 W408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:220170330 G>A maps to NM_004446.2 S845S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr1:220170518 G>A maps to NM_004446.2 Q783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:220191808 G>A maps to NM_004446.2 I492I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:51929353 G>A maps to NM_001981.2 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr19:16528445 G>A maps to ENST00000455140 D370D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:16536009 G>A maps to ENST00000455140 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr19:16514714 T>C maps to ENST00000455140 Q485Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:16545262 G>A maps to ENST00000455140 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:16547762 G>A maps to ENST00000455140 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:16496007 A>G maps to ENST00000455140 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:16472742 G>A maps to ENST00000455140 P811P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:15813622 G>A maps to NM_004447.5 Q288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:55591170 G>A maps to NM_133180.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:55597331 C>T maps to NM_133180.2 D503D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr19:55589496 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:55597559 G>A maps to NM_133180.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:55591119 G>A maps to NM_133180.2 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr11:720117 C>T maps to NM_022772.3 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr11:722402 C>T maps to NM_022772.3 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:721582 C>T maps to NM_022772.3 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:723305 C>T maps to NM_022772.3 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr1:110294733 G>T maps to NM_139053.1 P440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:110294299 C>T maps to NM_139053.1 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:110304161 G>A maps to NM_139053.1 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:110299787 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:110302422 G>A maps to NM_139053.1 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:110301245 C>T maps to NM_139053.1 W168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:110293934 G>A maps to NM_139053.1 V535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:110294353 C>T maps to NM_139053.1 R496R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:110300620 G>C maps to NM_139053.1 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:110302389 G>A maps to NM_139053.1 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:110295780 G>A maps to NM_139053.1 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:43537393 C>T maps to NM_001002264.1 E162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:43463357 C>T maps to NM_001002264.1 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:26596325 T>C maps to NM_033505.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:26607904 C>T maps to NM_033505.2 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr17:56274325 G>A maps to NM_000502.4 K276K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:56276519 C>T maps to NM_000502.4 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr17:56272380 C>T maps to NM_000502.4 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:56271412 G>A maps to NM_000502.4 W185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:56272452 C>T maps to NM_000502.4 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:56270887 C>T maps to NM_000502.4 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:56271341 G>A maps to NM_000502.4 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:56271347 C>T maps to NM_000502.4 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:91363871 C>T maps to NM_004950.4 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:91366695 T>C maps to NM_004950.4 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr12:91363871 C>T maps to NM_004950.4 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr12:91365698 G>A maps to NM_004950.4 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:91363862 G>A maps to NM_004950.4 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr17:27185488 C>T maps to NM_005702.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr17:27185479 C>T maps to NM_005702.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:27183391 C>T maps to NM_005702.2 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr5:96098932 C>T did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr5:96139152 G>A maps to NM_016442.3 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr5:96124331 C>T maps to NM_016442.3 Q527Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr5:96237350 C>T maps to NM_001130140.1 Q572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr5:96253236 G>A maps to NM_001130140.1 T937T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr5:96251464 T>C maps to NM_001130140.1 L911L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:96224935 T>C maps to NM_001130140.1 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:96249153 C>T maps to NM_001130140.1 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr5:96253209 G>A maps to NM_001130140.1 L928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr5:96215913 C>T maps to NM_001130140.1 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:48688110 C>T did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:48687973 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr17:37881309 C>T maps to NM_004448.2 S834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:37882044 G>A maps to NM_004448.2 K937K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:37879847 C>T maps to NM_004448.2 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:37872082 C>T maps to NM_004448.2 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:37866369 C>T maps to NM_004448.2 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:37883081 C>T maps to NM_004448.2 G995G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:37865596 C>T maps to NM_004448.2 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:37871607 C>T maps to NM_004448.2 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:37864605 C>T maps to NM_004448.2 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:65319137 A>T maps to ENST00000506030 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:65349461 T>C maps to ENST00000506030 T772T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr5:65350367 C>T maps to ENST00000506030 I1074I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:65288686 C>T maps to ENST00000506030 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:65349980 G>A maps to ENST00000506030 K945K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:65350439 G>A maps to ENST00000506030 Q1098Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:56487189 C>T maps to NM_001982.2 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:56488218 C>T maps to NM_001982.2 R580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:56488260 C>T maps to NM_001982.2 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr12:56487287 G>A maps to NM_001982.2 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:56487293 G>A maps to NM_001982.2 E480E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr2:212568875 G>A maps to NM_005235.2 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr2:212522511 C>T maps to NM_005235.2 W638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr2:212576791 T>G maps to NM_005235.2 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:212578362 C>T maps to NM_005235.2 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:212587205 G>A maps to NM_005235.2 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr2:212589845 T>C maps to NM_005235.2 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr2:212251871 G>A maps to NM_005235.2 Q1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:212568914 G>A maps to NM_005235.2 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:212293131 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:212488679 G>A maps to NM_005235.2 V723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:212587180 G>A maps to NM_005235.2 Q274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr2:212587180 G>A maps to NM_005235.2 Q274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:212652843 G>A maps to NM_005235.2 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:212248411 G>A maps to NM_005235.2 L1285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr2:212248744 C>T maps to NM_005235.2 R1174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:212293153 G>A maps to NM_005235.2 Q900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:212488709 C>T maps to NM_005235.2 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:212495275 G>A maps to NM_005235.2 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:212652879 G>A maps to NM_005235.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:212587163 G>A maps to NM_005235.2 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:212587136 G>A maps to NM_005235.2 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr2:212295741 C>T maps to NM_005235.2 V857V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:212570073 C>T maps to NM_005235.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:212495234 C>T maps to NM_005235.2 R677R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:1553828 C>T maps to NM_178040.2 L1042L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr3:56330088 C>T maps to ENST00000460849 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr3:56330088 C>T maps to ENST00000460849 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:56468456 C>T maps to ENST00000460849 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:56468693 G>A maps to ENST00000460849 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:56468789 C>T maps to ENST00000460849 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:56330088 C>T maps to ENST00000460849 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:56468693 G>A maps to ENST00000460849 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr3:55922538 C>T maps to ENST00000460849 Q814Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:56207482 G>A maps to ENST00000460849 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:56330151 C>T maps to ENST00000460849 E323E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:56468380 G>A maps to ENST00000460849 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr3:56026137 C>T maps to ENST00000460849 K734K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:56468507 T>G maps to ENST00000460849 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:56468773 G>A maps to ENST00000460849 R88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:55984566 C>T maps to ENST00000460849 K763K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr3:56468981 G>A maps to ENST00000460849 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:56026251 C>T maps to ENST00000460849 R696R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:56468630 G>A maps to ENST00000460849 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:56468845 G>A maps to ENST00000460849 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr3:56468624 G>A maps to ENST00000460849 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr3:55922445 C>T maps to ENST00000460849 R845R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr3:56173548 G>A maps to ENST00000460849 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr3:56053049 A>G maps to ENST00000460849 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z4-06A-11D-A197-08 chr3:56207503 C>T maps to ENST00000460849 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:56183148 G>A maps to ENST00000460849 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:56044596 C>T maps to ENST00000460849 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:56026098 G>A maps to ENST00000460849 I747I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:56468777 T>A maps to ENST00000460849 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr19:45924636 G>A maps to NM_202001.2 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr19:45864785 G>A maps to NM_000400.3 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:45868161 G>A maps to NM_000400.3 N176N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:45855601 G>A maps to NM_000400.3 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr19:45860599 C>T maps to NM_000400.3 K469K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:45867733 G>A maps to NM_000400.3 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:45857993 A>C maps to NM_000400.3 Y553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:128047035 G>A maps to NM_000122.1 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:128028987 G>A maps to NM_000122.1 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:128047393 G>A maps to NM_000122.1 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr16:14029274 C>T maps to NM_005236.2 Q496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr16:14042071 C>T maps to NM_005236.2 I873I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:14042071 C>T maps to NM_005236.2 I873I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr16:14029556 C>T maps to NM_005236.2 Q590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:14029258 G>A maps to NM_005236.2 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr13:103510650 G>A maps to NM_000123.2 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr13:103515341 C>T maps to NM_000123.2 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr13:103514776 G>A maps to NM_000123.2 E426E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:103524667 C>T maps to NM_000123.2 A933A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr13:103525626 C>T maps to NM_000123.2 F966F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:103510681 C>T maps to NM_000123.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:50740989 G>A maps to ENST00000515869 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:50690900 G>A maps to NM_000124.2 T667T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr10:50691555 G>A maps to NM_000124.2 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:50682165 C>T maps to NM_000124.2 W835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr10:50666970 A>G maps to NM_000124.2 L1458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:50678837 G>A maps to NM_000124.2 F1056F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:50682237 G>A maps to NM_000124.2 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:50691549 G>A maps to NM_000124.2 R612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr10:50667244 G>A maps to NM_000124.2 V1366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:50684305 G>A maps to NM_000124.2 F779F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:50701194 G>A maps to NM_000124.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:50701287 A>G maps to NM_000124.2 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:71427527 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:71425189 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr23:71427377 A>G did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:71427198 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:71427392 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr23:71425173 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr23:71425174 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:71427069 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:71425869 T>C did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr23:71424979 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:71427431 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:71427356 C>T did not map to a codon.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr23:71428080 G>A did not map to a codon.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr23:71428081 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:71426009 A>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:75250453 C>T maps to NM_001432.2 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr4:75250500 G>A maps to NM_001432.2 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:75250453 C>T maps to NM_001432.2 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr4:75250500 G>A maps to NM_001432.2 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr19:42752970 C>T maps to NM_006494.2 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:42752988 G>A maps to NM_006494.2 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr21:39817370 G>A maps to NM_001136154.1 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr21:39817409 G>A maps to NM_001136154.1 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr21:39772547 G>A maps to NM_001136154.1 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr21:39755816 G>A maps to NM_001136154.1 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr21:39795449 G>A maps to NM_001136154.1 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr21:39817364 G>A maps to NM_001136154.1 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:39755816 G>A maps to NM_001136154.1 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr21:39795359 C>T maps to NM_001136154.1 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr5:172362240 C>T maps to NM_001031711.2 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:172324008 C>T maps to NM_001031711.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:172324023 C>T maps to NM_001031711.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr5:172336720 C>T maps to NM_001031711.2 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr20:34136411 C>T maps to ENST00000447986 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr20:34144809 C>T maps to ENST00000447986 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:34145015 C>T maps to ENST00000447986 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr20:34136574 C>T maps to ENST00000447986 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:69847311 C>T maps to NM_004450.2 W86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:8887318 C>T maps to NM_153332.3 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr8:8869060 G>A maps to NM_153332.3 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:8865529 C>T maps to NM_153332.3 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr16:20810647 G>A maps to NM_001142725.1 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:44820605 G>A maps to NM_024066.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr1:44804889 A>G maps to NM_024066.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:614674 G>A maps to NM_207332.1 D420D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:54024891 C>T maps to NM_015701.3 Y150Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr2:54014421 G>A maps to NM_015701.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:54040123 A>T maps to NM_015701.3 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:101911953 G>A maps to NM_001100626.1 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:101943536 G>A maps to NM_001100626.1 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:101912013 G>A maps to NM_001100626.1 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:37601890 C>T maps to NM_007175.6 Y85Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:37611016 C>A maps to NM_007175.6 Y263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr8:37611494 G>A maps to NM_007175.6 K294K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr1:43296562 C>T maps to NM_018538.3 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr1:43300730 C>T maps to NM_018538.3 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr2:158178150 G>A maps to NM_001009959.1 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:158178033 G>A maps to NM_001009959.1 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr2:158177965 C>T maps to NM_001009959.1 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:5832912 G>A maps to NM_024896.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:5805110 G>A maps to NM_024896.2 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:62130277 G>A maps to NM_001433.3 I705I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:62130145 C>T maps to NM_001433.3 E749E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:62133119 G>A maps to NM_001433.3 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:62144125 G>A maps to NM_001433.3 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:62132153 A>T maps to NM_001433.3 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:62125253 G>A maps to NM_001433.3 F831F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr16:23702488 C>T maps to NM_033266.3 G891G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:23712303 C>T maps to NM_033266.3 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr16:23716292 G>A maps to NM_033266.3 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:23722237 C>T maps to NM_033266.3 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr16:23712414 C>T maps to NM_033266.3 E456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr16:23716267 G>A maps to NM_033266.3 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr16:23702455 C>T maps to NM_033266.3 R902R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr16:23706523 C>T maps to NM_033266.3 Q647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr16:23703322 G>A maps to NM_033266.3 P827P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr16:23713502 C>T maps to NM_033266.3 E439E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:23716292 G>A maps to NM_033266.3 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:23716292 G>A maps to NM_033266.3 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:53149099 G>A maps to NM_014584.1 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr12:15067691 T>A maps to NM_152321.2 K267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr12:15091352 G>A maps to NM_152321.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:15090924 G>A maps to NM_152321.2 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr1:8073677 C>T maps to NM_018948.3 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:8073388 G>A maps to NM_018948.3 Q424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:8074055 G>A maps to NM_018948.3 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr7:64452372 G>A maps to NM_001007253.3 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:19140891 T>C maps to NM_052911.2 T627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr18:19153718 A>G maps to NM_052911.2 C362C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr18:19116056 G>A maps to NM_052911.2 F711F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:27634106 C>T maps to NM_001017420.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr8:27657107 G>A maps to NM_001017420.2 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:27660930 C>T maps to NM_001017420.2 F594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:13695709 G>A maps to NM_016649.3 I789I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:13695736 G>A maps to NM_016649.3 F780F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr20:13755844 G>A maps to NM_016649.3 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A264-06A-11D-A196-08 chr20:13695703 C>T maps to NM_016649.3 E791E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:54281072 A>G maps to NM_007036.4 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:54281312 G>A maps to NM_007036.4 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:54277897 C>T maps to NM_007036.4 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:54281333 G>A maps to NM_007036.4 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr12:53683350 C>T maps to NM_012291.4 Q1696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr12:53687092 C>T maps to NM_012291.4 D2066D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:53677304 G>A maps to NM_012291.4 K1020K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:53686160 C>T maps to NM_012291.4 R1966*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:53664582 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:53663154 G>A maps to NM_012291.4 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:53685835 C>T maps to NM_012291.4 S1920S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:53682884 C>T maps to NM_012291.4 L1574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:53662561 C>T maps to NM_012291.4 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:6511936 C>T maps to NM_031475.2 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:6505808 G>A maps to NM_031475.2 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:6505808 G>A maps to NM_031475.2 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:6488419 C>T maps to NM_031475.2 H143H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr1:6488371 C>T maps to NM_031475.2 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:6501055 G>A maps to NM_031475.2 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:6520097 G>A maps to NM_031475.2 R819R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:239010658 C>T maps to NM_194312.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:239039091 C>T maps to NM_194312.2 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:239025581 C>T maps to NM_194312.2 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:239040159 G>A maps to NM_194312.2 W935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:239040036 G>A maps to NM_194312.2 W894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr2:239040159 G>A maps to NM_194312.2 W935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:239016598 G>A maps to NM_194312.2 E280E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:239025620 G>A maps to NM_194312.2 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U9-06A-11D-A32N-08 chr2:239040198 C>T maps to NM_194312.2 L948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:152332923 G>A maps to NM_001122741.1 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr14:64723948 C>T maps to NM_001437.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr14:64724038 C>T maps to NM_001437.2 E332E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr14:64727428 C>T maps to NM_001437.2 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:64716294 G>A maps to NM_001437.2 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:64749411 G>A maps to NM_001437.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr8:95677407 C>T maps to NM_017697.3 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr8:95653668 C>T maps to NM_017697.3 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr8:95683689 C>T maps to NM_017697.3 R415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr8:95680312 G>A maps to NM_017697.3 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr8:95690596 C>A maps to NM_017697.3 P606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr8:95654215 G>A maps to NM_017697.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:95680195 C>T maps to NM_017697.3 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:95680210 G>A maps to NM_017697.3 K322K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:95683709 C>T maps to NM_017697.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:95680312 G>A maps to NM_017697.3 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr8:95653584 G>A maps to NM_017697.3 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:68268010 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr16:68267908 C>T maps to NM_024939.2 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:68266309 C>T maps to NM_024939.2 Q306Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64074764 C>T maps to NM_004451.3 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr14:76906079 G>A maps to NM_004452.3 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr14:76905875 C>T maps to NM_004452.3 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:76967054 C>T maps to NM_004452.3 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:76906016 G>A maps to NM_004452.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr14:76948947 G>A maps to NM_004452.3 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr14:76948977 G>T maps to NM_004452.3 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:76928969 C>T maps to NM_004452.3 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr14:76957850 C>T maps to NM_004452.3 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr1:216680420 G>A maps to NM_001438.2 R413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:216850544 C>T maps to NM_001438.2 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:216680388 G>A maps to NM_001438.2 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:216850619 G>A maps to NM_001438.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:216680313 T>C maps to NM_001438.2 K448K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:216850661 C>T maps to NM_001438.2 Q76Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:216737576 C>T maps to NM_001438.2 W282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:103499520 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:103495542 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:103499526 C>T did not map to a codon.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr23:103495483 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr23:103495236 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:103498963 C>T did not map to a codon.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr23:103499517 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr12:56528176 C>T maps to NM_001184796.1 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr12:56530607 C>T maps to NM_001184796.1 I581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:56524876 C>T maps to NM_001184796.1 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:56525337 C>T maps to NM_001184796.1 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:56531833 C>T maps to NM_001184796.1 V751V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:158531733 G>A maps to NM_020728.2 I776I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:158536336 C>T maps to NM_020728.2 G586G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:158590695 G>A maps to NM_020728.2 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr7:158528223 G>A maps to NM_020728.2 F852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr3:138178088 G>A maps to NM_031913.3 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr3:138174109 C>T maps to NM_031913.3 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr3:138179481 C>T maps to NM_031913.3 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr3:138181032 C>T maps to NM_031913.3 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:138192383 G>A maps to NM_031913.3 G748G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr3:138184245 G>A maps to NM_031913.3 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr2:67631259 G>A maps to NM_019002.3 E482E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:67631706 G>A maps to NM_019002.3 K631K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr5:137853288 A>G maps to NM_004730.2 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr5:137849281 G>A maps to NM_004730.2 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:51850296 G>A maps to NM_001014763.1 Q243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:44015616 A>C maps to NM_014297.3 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:44011003 A>G maps to NM_014297.3 *255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:22814071 G>C maps to NM_018638.4 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:22826573 C>T maps to NM_018638.4 Q398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:128332375 G>A maps to NM_001143820.1 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:128354877 G>A maps to NM_001143820.1 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr21:40191607 C>T maps to NM_005239.4 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr21:40191595 A>G maps to NM_005239.4 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr21:40191499 C>T maps to NM_005239.4 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr21:40191547 C>T maps to NM_005239.4 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr21:40191502 G>A maps to NM_005239.4 W296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:40191556 C>T maps to NM_005239.4 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr21:40191544 C>T maps to NM_005239.4 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr7:13935664 G>A maps to NM_004956.4 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr7:13949260 G>A maps to NM_004956.4 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:13975400 G>A maps to NM_004956.4 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr19:36133947 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:157105324 G>A maps to NM_001145312.1 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:157105387 G>A maps to NM_001145312.1 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:157068664 G>A maps to NM_001004341.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:157067776 G>A maps to NM_001004341.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:41610060 C>T maps to NM_001079675.1 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:41610700 G>A maps to NM_001079675.1 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:185823274 C>T maps to NM_004454.2 Q48Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:185783620 C>T maps to NM_004454.2 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:11905493 C>T maps to NM_001987.4 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr12:12022506 C>T maps to NM_001987.4 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:36336836 G>A maps to NM_016135.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr6:36339257 G>A maps to NM_016135.2 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:36343726 C>T maps to NM_016135.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr6:36336839 G>A maps to NM_016135.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:36334472 C>T maps to NM_016135.2 Q325Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr4:5731071 C>T maps to NM_153717.2 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr4:5785472 C>T maps to NM_153717.2 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr4:5747007 C>T maps to NM_153717.2 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:5812150 C>T maps to NM_153717.2 S956S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr4:5806559 C>T maps to NM_153717.2 V851V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr4:5798916 C>T maps to NM_153717.2 S685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr4:5743513 C>T maps to NM_153717.2 Y258Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr4:5785331 C>T maps to NM_153717.2 F539F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:5731071 C>T maps to NM_153717.2 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr4:5564587 A>T maps to NM_147127.4 L1305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr4:5624385 C>T maps to NM_147127.4 G793G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr4:5690977 G>A maps to NM_147127.4 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr4:5630350 G>A maps to NM_147127.4 T607T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr4:5624457 G>A maps to NM_147127.4 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr1:93201977 C>T maps to NM_005665.4 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:93091479 G>A maps to NM_005665.4 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:93170288 C>T maps to NM_005665.4 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:93170178 C>T maps to NM_005665.4 W135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr19:7914194 C>T maps to NM_001159944.1 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:7916577 C>T maps to NM_001159944.1 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:7913847 C>T maps to NM_001159944.1 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:7925472 C>T maps to NM_001159944.1 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:7912714 C>T maps to NM_001159944.1 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:7911464 C>T maps to NM_001159944.1 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:100551164 C>T maps to NM_016337.2 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr17:74005573 G>A maps to NM_001988.2 L1238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr17:74005598 C>T maps to NM_001988.2 K1229K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr17:74006207 G>A maps to NM_001988.2 P1026P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:74004104 G>A maps to NM_001988.2 T1727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:74004347 G>A maps to NM_001988.2 L1646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:74004662 C>T maps to NM_001988.2 E1541E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:74023228 G>A maps to NM_001988.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:74004334 G>A maps to NM_001988.2 Q1651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:74005103 G>A maps to NM_001988.2 S1394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:74006213 C>T maps to NM_001988.2 R1024R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr17:74004836 C>T maps to NM_001988.2 W1483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr17:74005370 C>T maps to NM_001988.2 R1305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:74003609 G>A maps to NM_001988.2 S1892S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:74015006 C>T maps to NM_001988.2 W424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:74010614 G>A maps to NM_001988.2 F755F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr17:74004281 C>T maps to NM_001988.2 R1668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:74019639 G>A maps to NM_001988.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:74005811 G>A maps to NM_001988.2 L1158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr17:74015719 G>C maps to NM_001988.2 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:74003693 G>A maps to NM_001988.2 A1864A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:74004844 G>A maps to NM_001988.2 L1481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:74005340 C>T maps to NM_001988.2 K1315K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:74006117 C>T maps to NM_001988.2 L1056L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:74015057 C>T maps to NM_001988.2 Q407Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr17:74004308 G>A maps to NM_001988.2 L1659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:74005880 G>A maps to NM_001988.2 I1135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:74007749 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr17:74020173 G>A maps to NM_001988.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:74003753 G>C maps to NM_001988.2 A1844A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr17:74003216 G>A maps to NM_001988.2 S2023S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr17:74004740 C>T maps to NM_001988.2 Q1515Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr17:74006471 C>T maps to NM_001988.2 Q938Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr17:74004824 C>T maps to NM_001988.2 Q1487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr17:74011655 C>T maps to NM_001988.2 K588K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:74004824 C>T maps to NM_001988.2 Q1487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:74005673 C>T maps to NM_001988.2 P1204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:74007900 G>A maps to NM_001988.2 A840A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:74011529 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:74013915 C>T maps to NM_001988.2 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:74013981 G>A maps to NM_001988.2 G516G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:74017760 G>A maps to NM_001988.2 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:74018547 G>A maps to NM_001988.2 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:74019402 G>A maps to NM_001988.2 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr17:74008110 G>A maps to NM_001988.2 S811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:18286822 G>A maps to NM_001145127.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:18284799 G>A maps to NM_001145127.1 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr7:27284923 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr7:27285647 C>T maps to NM_001989.3 H276H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:27282762 G>A maps to NM_001989.3 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:176948372 C>T maps to NM_001080458.1 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:176948120 G>A maps to NM_001080458.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:176946974 C>T maps to NM_001080458.1 E210E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr2:176944867 C>T maps to NM_001080458.1 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:29693827 C>T maps to NM_013986.3 Q441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr22:29695760 C>T maps to NM_013986.3 G622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr22:29694810 C>T maps to NM_013986.3 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F4-06A-12D-A25O-08 chr22:29688154 C>T maps to NM_013986.3 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr15:41476728 C>T maps to NM_152596.2 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr15:41483765 C>T maps to NM_152596.2 Q188Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr15:41482308 C>T maps to NM_152596.2 W236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:41482326 C>T maps to ENST00000458580 Q28Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr15:41476749 C>T maps to NM_152596.2 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr15:41482191 C>T maps to NM_152596.2 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr15:41488010 G>A maps to NM_152596.2 Q170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:41476197 G>A maps to NM_152596.2 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr14:69701575 C>T maps to NM_001193363.1 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:69702849 C>T maps to NM_001193363.1 Y379Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:140242630 G>A maps to NM_017820.3 F630F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr9:140218299 G>A maps to NM_017820.3 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:242020714 T>C maps to NM_006027.4 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:242042533 C>T maps to NM_006027.4 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:242016658 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:242042275 T>C maps to NM_006027.4 F580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr1:242016692 A>G maps to NM_006027.4 Q105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:242042458 C>T maps to NM_006027.4 T641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:56726625 C>T maps to NM_018261.3 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:56759716 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:549180 G>A maps to NM_018303.4 I744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:572624 G>A maps to NM_018303.4 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:486757 C>G maps to NM_018303.4 L896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:556007 G>A maps to NM_018303.4 F646F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr5:465365 C>T maps to ENST00000315013 F649F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr5:454109 C>T maps to ENST00000315013 D340D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr5:454110 C>T maps to ENST00000315013 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:464437 C>T maps to ENST00000315013 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:458136 C>T maps to ENST00000315013 F439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr16:67221660 C>T maps to NM_178516.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr16:67223039 C>T maps to NM_178516.3 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:67222705 C>T maps to NM_178516.3 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr16:67220461 C>T maps to NM_178516.3 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:67223018 G>A maps to NM_178516.3 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr19:45719416 G>A maps to NM_138568.3 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:45731473 G>A maps to NM_138568.3 H47H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:133041195 C>T maps to NM_021807.3 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr7:133059704 C>T maps to NM_021807.3 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:133002040 C>T maps to NM_021807.3 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:133622736 C>T maps to NM_021807.3 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr7:133502233 T>C maps to NM_021807.3 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr7:132990749 C>T maps to NM_021807.3 H197H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:133502260 C>T maps to NM_021807.3 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:132959760 C>T maps to NM_021807.3 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr14:57710978 G>T maps to ENST00000340918 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr10:94594494 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr10:94733880 T>A maps to NM_019053.4 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr10:94715366 C>T maps to NM_019053.4 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:94733940 C>T maps to NM_019053.4 D635D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr10:94712079 C>A maps to NM_019053.4 Y489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:94653168 C>T maps to NM_019053.4 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:94708029 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:72723612 T>C maps to NM_015189.1 Q471Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:72786607 G>A maps to NM_015189.1 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr2:72802652 G>A maps to NM_015189.1 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:72786583 G>A maps to NM_015189.1 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:72786607 G>A maps to NM_015189.1 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:74084898 G>A maps to NM_001145297.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:74084899 G>A maps to NM_001145297.2 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:74079830 C>T maps to NM_001145297.2 K702K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:74079831 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr17:74099764 G>A maps to NM_001145297.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:74090657 G>A maps to NM_001145297.2 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr17:74097429 C>A maps to NM_001145297.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:74093954 G>A maps to NM_001145297.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:231472953 C>A maps to NM_175876.3 G180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38565540 C>T maps to NM_005107.3 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:11158086 A>G maps to NM_001001998.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:11129706 G>A maps to NM_001001998.1 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:11151151 G>A maps to NM_001001998.1 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:11141285 G>A maps to NM_001001998.1 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr9:133578457 C>T maps to NM_014285.5 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:133576300 G>A maps to NM_014285.5 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr19:41898820 G>A maps to NM_020158.3 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:45046795 C>T maps to NM_015004.3 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr3:45052800 C>A maps to NM_015004.3 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:45038638 C>T maps to NM_015004.3 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr13:37581123 C>T maps to NM_181503.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:122722618 C>T maps to NM_001034194.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:108380662 G>A maps to NM_015065.2 S1857S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr11:108381478 C>T maps to NM_015065.2 G1585G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr11:108409811 G>A maps to NM_015065.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr11:108409812 G>A maps to NM_015065.2 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:108383908 C>T maps to NM_015065.2 R775R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr11:108381787 C>T maps to NM_015065.2 R1482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr11:108412424 T>C maps to NM_015065.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:108409797 C>T maps to NM_015065.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:108381694 T>A maps to NM_015065.2 A1513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr11:108381985 G>A maps to NM_015065.2 S1416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:108383401 C>T maps to NM_015065.2 E944E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:108409797 C>T maps to NM_015065.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr11:108381646 G>A maps to NM_015065.2 N1529N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:108380668 G>A maps to NM_015065.2 L1855L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:108382639 G>A maps to NM_015065.2 S1198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:108383740 C>T maps to NM_015065.2 Q831Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:108385507 G>A maps to NM_015065.2 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr11:108388965 G>A maps to NM_015065.2 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A690-06A-11D-A30X-08 chr11:108384831 G>A maps to NM_015065.2 R468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr8:118819583 G>A maps to NM_000127.2 F585F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr8:118831998 G>A maps to NM_000127.2 I484I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:118842549 G>A maps to NM_000127.2 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr8:119122643 C>T maps to NM_000127.2 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr8:118830694 G>A maps to NM_000127.2 V537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:118819607 G>A maps to NM_000127.2 F577F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:44146473 C>T maps to NM_000401.3 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr11:44193159 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:44255676 C>T maps to NM_000401.3 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr11:44129351 C>T maps to NM_000401.3 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:44148445 C>T maps to NM_000401.3 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr11:44130750 C>T maps to NM_000401.3 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr1:26360197 C>T maps to NM_004455.2 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:101339917 A>G maps to NM_001439.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr8:28595035 G>A maps to NM_001440.2 R759R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr8:28608235 C>T maps to NM_001440.2 S871S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:28575714 C>T maps to NM_001440.2 V713V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:28574277 C>T maps to NM_001440.2 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr8:28574874 C>T maps to NM_001440.2 I433I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:28573692 C>T maps to NM_001440.2 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:28575120 C>T maps to NM_001440.2 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr8:28574772 C>T maps to NM_001440.2 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr8:28573819 C>T maps to NM_001440.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr8:28574494 C>T maps to NM_001440.2 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr8:28574592 G>C maps to NM_001440.2 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:28575417 C>T maps to NM_001440.2 F614F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:28574865 C>T maps to NM_001440.2 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr8:28575526 C>T maps to NM_001440.2 Q651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:72211354 G>A maps to NM_000503.4 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr8:72128986 A>G maps to NM_000503.4 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:72267065 G>A maps to NM_000503.4 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:72127688 C>T maps to NM_000503.4 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:72127688 C>T maps to NM_000503.4 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr8:72229850 G>A maps to NM_000503.4 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr8:72229865 T>A maps to NM_000503.4 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:72111607 G>A maps to NM_000503.4 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:72129197 A>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:72184055 C>T maps to NM_000503.4 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr20:45717914 G>A maps to ENST00000360649 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr20:45702822 C>A maps to ENST00000360649 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr20:45702823 C>T maps to ENST00000360649 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:45808447 T>C maps to ENST00000360649 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr20:45618737 G>A maps to ENST00000360649 W35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr20:45618738 G>A maps to ENST00000360649 W35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr20:45717956 G>A maps to ENST00000360649 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr20:45801393 C>T maps to ENST00000360649 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:45717902 T>G maps to ENST00000360649 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr20:45702960 C>T maps to ENST00000360649 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr20:45725794 C>T maps to ENST00000360649 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr20:45717956 G>A maps to ENST00000360649 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr20:45630109 C>T maps to ENST00000360649 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr20:45725731 C>T maps to ENST00000360649 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr20:45808551 C>T maps to ENST00000360649 I440I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr20:45700822 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:45633598 C>T maps to ENST00000360649 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr20:45630082 C>T maps to ENST00000360649 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:133783825 G>A maps to ENST00000452339 Q216Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:133783816 C>T maps to ENST00000452339 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:133595932 G>A maps to ENST00000452339 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:133789846 C>T maps to ENST00000452339 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr6:133834096 G>A maps to ENST00000452339 G480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr6:66054026 G>A maps to ENST00000370616 F501F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr6:66204769 C>T maps to ENST00000370616 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr17:40864380 G>A maps to ENST00000264646 R446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:148508725 G>A maps to NM_004456.3 Y646Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:148524335 C>T maps to NM_004456.3 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr7:148523567 G>A maps to NM_004456.3 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr7:148514972 G>A maps to NM_004456.3 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr6:159188496 G>A maps to NM_001111077.1 H464H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:159188460 G>A maps to NM_001111077.1 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:159206567 G>A maps to NM_001111077.1 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:159206477 G>A maps to NM_001111077.1 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr6:159205709 G>A maps to NM_001111077.1 Q173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr13:113803659 C>T maps to NM_000504.3 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr13:113803758 C>T maps to NM_000504.3 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:113803278 G>A maps to NM_000504.3 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr13:113798180 G>A maps to NM_000504.3 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr13:113798366 C>T maps to NM_000504.3 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr13:113803236 G>A maps to NM_000504.3 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr13:113803659 C>T maps to NM_000504.3 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr13:113803737 C>T maps to NM_000504.3 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr4:187205273 C>T maps to NM_000128.3 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:187197490 C>T maps to NM_000128.3 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr4:187205273 C>T maps to NM_000128.3 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr4:187192919 C>T maps to NM_000128.3 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:187197403 C>T maps to NM_000128.3 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr4:187209624 C>T maps to NM_000128.3 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:187201177 C>T maps to NM_000128.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:187205267 C>T maps to NM_000128.3 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:187206876 C>T maps to NM_000128.3 Q464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr4:187197475 C>T maps to NM_000128.3 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:160970541 G>A maps to NM_016946.4 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:160970469 C>T maps to NM_016946.4 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:160970834 G>A maps to NM_016946.4 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:176831609 C>T maps to NM_000505.3 R230R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D3-A3MU-06A-11D-A21A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:6167711 G>A maps to NM_000129.3 T629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A6L9-06A-11D-A32N-08 chr6:6318795 G>A maps to NM_000129.3 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr6:6305713 C>T maps to NM_000129.3 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr6:6225051 C>T maps to NM_000129.3 W280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr6:6225015 G>A maps to NM_000129.3 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr6:6174882 G>A maps to NM_000129.3 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr6:6167789 C>T maps to NM_000129.3 A603A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:6197498 T>C maps to NM_000129.3 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:6174837 G>A maps to NM_000129.3 F574F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:6174882 G>A maps to NM_000129.3 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:6174984 C>T maps to NM_000129.3 V525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:6224993 G>A maps to NM_000129.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:197032161 C>T maps to NM_001994.2 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:197019883 C>A maps to NM_001994.2 G561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr1:197030983 C>T maps to NM_001994.2 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:197029642 C>A maps to NM_001994.2 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:197021830 G>A maps to NM_001994.2 T496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr1:197021896 C>T maps to NM_001994.2 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:197009743 A>G maps to NM_001994.2 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:197032119 G>A maps to NM_001994.2 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:197029610 G>A maps to NM_001994.2 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:197026242 C>T maps to NM_001994.2 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:197026194 C>T maps to NM_001994.2 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:197026251 A>G maps to NM_001994.2 Y354Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:197036338 G>A maps to NM_001994.2 N5N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:197009649 A>C did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr11:46750212 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:46760876 G>A maps to NM_000506.3 R596R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr11:46747430 G>A maps to NM_000506.3 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr11:46750980 G>A maps to NM_000506.3 K508K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:46748336 C>T maps to NM_000506.3 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:46749617 C>T maps to NM_000506.3 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:46747445 C>T maps to NM_000506.3 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr11:46750980 G>A maps to NM_000506.3 K508K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:46747499 G>A maps to NM_000506.3 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr11:46760857 G>A maps to NM_000506.3 W590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr11:46760924 G>A maps to NM_000506.3 W612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr5:76028216 G>A maps to NM_001992.3 W56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr5:76129239 C>T maps to NM_005242.4 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:76129487 G>A maps to NM_005242.4 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr5:76129229 C>T maps to NM_005242.4 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:76129574 G>A maps to NM_005242.4 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr5:76129574 G>A maps to NM_005242.4 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:76129185 C>T maps to NM_005242.4 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:76128962 C>T maps to NM_005242.4 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr5:76128662 C>T maps to NM_005242.4 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:76128662 C>T maps to NM_005242.4 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr5:75914171 G>A maps to NM_004101.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:75914363 C>T maps to NM_004101.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:75914291 C>T maps to NM_004101.2 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:17001317 G>A maps to NM_003950.2 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:17000948 C>T maps to NM_003950.2 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:17000831 C>T maps to NM_003950.2 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:17001308 C>T maps to NM_003950.2 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr1:94997945 G>T maps to NM_001993.4 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr1:95001605 G>A maps to NM_001993.4 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:94998771 C>T maps to NM_001993.4 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:94997928 C>T maps to NM_001993.4 K233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:169505800 T>C maps to ENST00000367796 E1643E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:169512206 C>T maps to ENST00000367796 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:169510676 G>A maps to ENST00000367796 L1222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:169484717 C>T maps to ENST00000367796 W2169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:169509983 G>A maps to ENST00000367796 L1453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:169529804 A>C maps to ENST00000367796 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:169525914 G>A maps to ENST00000367796 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:169524445 T>G maps to ENST00000367796 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:169510945 G>A maps to ENST00000367796 Q1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:169512079 C>A maps to ENST00000367796 E755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:169512095 C>T maps to ENST00000367796 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:169528508 C>T maps to ENST00000367796 Q204Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:169510043 G>A maps to ENST00000367796 S1433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr1:169510778 C>T maps to ENST00000367796 Q1188Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:169484696 G>A maps to ENST00000367796 S2176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:169515827 C>T maps to ENST00000367796 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:169509662 C>T maps to ENST00000367796 R1560R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:169511108 G>A maps to ENST00000367796 S1078S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:169525902 G>A maps to ENST00000367796 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:169492554 G>A maps to ENST00000367796 I1981I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr1:169526007 C>G maps to ENST00000367796 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:169511189 C>T maps to ENST00000367796 R1051R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr13:113760178 C>T maps to NM_000131.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr13:113768159 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr13:113771785 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr13:113772925 C>T maps to NM_000131.3 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr13:113770100 C>T maps to NM_000131.3 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr23:154197611 G>T did not map to a codon.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr23:154088761 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr23:154128147 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:154124377 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:154156855 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:154157026 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:154194289 T>C did not map to a codon.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr23:154215574 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:154157221 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr23:154176064 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:154134828 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:154189431 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:154157464 G>A did not map to a codon.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr23:154159697 G>C did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:154132798 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:154158549 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr23:154159775 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:154159921 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr23:154157676 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr23:154176014 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr23:154194286 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:154159615 G>C did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:154157567 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:154132586 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:154159289 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:154157411 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:154175985 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:154156897 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:154175985 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:154185238 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr23:154124373 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:154159545 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr23:154158046 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:154156960 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:154158766 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:154215553 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:154159077 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr23:154157317 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:154157482 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:154225333 T>G did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:154158604 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr23:154227795 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr23:154227796 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:154157817 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:154158172 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:154159084 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:154157305 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:154133155 T>C did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:154182200 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:154132187 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:154159352 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:154185422 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:154197699 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:154250707 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:154088745 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:154185345 C>G did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:154132638 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:154134722 A>G did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:154157961 G>C did not map to a codon.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr23:154194717 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr23:154157262 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr23:154157052 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:154157926 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:154157624 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr23:154159723 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:154159267 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:154124376 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:154158557 C>T did not map to a codon.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr23:154090035 G>A did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:154182264 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:154159405 C>T did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:154159038 A>G did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:154185318 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:138619206 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:138633288 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:138633333 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr23:138630640 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr23:138630613 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:138619173 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:138630544 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:138643951 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:138644071 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:138644167 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr23:138630644 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:138623298 C>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr23:138644028 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:138633288 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:138633242 T>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:138633390 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr23:138644104 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:138644167 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:74752906 G>A maps to NM_024306.4 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:74760213 G>A maps to NM_024306.4 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:74752921 G>A maps to NM_024306.4 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr1:46860091 G>A maps to NM_001441.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:46876081 C>T maps to NM_001441.2 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr1:46879240 A>G maps to NM_001441.2 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:46872006 C>T maps to NM_001441.2 D306D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:57475081 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:57358036 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr23:57515254 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:57515255 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:57407443 C>T did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:57337089 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:57318997 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:57405109 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:57458437 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:57458367 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:57473398 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:57405151 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr23:57405109 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr23:57358230 G>T did not map to a codon.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr23:57358231 G>T did not map to a codon.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr23:57458403 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:57473419 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr23:57407402 G>A did not map to a codon.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr23:57337072 C>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:57337128 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr23:57515238 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr23:57405105 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:57473466 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:57405125 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:57407425 C>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:57473360 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr23:57405109 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:57337089 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr2:88425736 C>T maps to NM_001443.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:88425811 G>A maps to NM_001443.1 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:88425769 C>T maps to NM_001443.1 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr8:82439278 C>T maps to NM_001105281.1 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:82439284 C>T maps to NM_001105281.1 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr8:82441670 A>C did not map to a codon.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr8:82441825 C>T maps to NM_001105281.1 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:82441729 G>A maps to NM_001105281.1 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:120241920 G>A maps to NM_000134.3 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:31840317 C>T maps to NM_004102.3 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:31840266 C>T maps to NM_004102.3 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr8:82195724 C>T maps to NM_001444.1 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr8:82195725 C>T maps to NM_001444.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr5:159661891 G>A maps to NM_001040442.1 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:159661849 G>A maps to NM_001040442.1 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr5:159659228 C>T maps to NM_001040442.1 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr6:123101436 C>A maps to NM_001446.3 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr8:82371552 C>T maps to NM_001080526.1 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:61631243 C>T maps to NM_004265.2 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:61631250 G>T maps to NM_004265.2 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:61596038 C>T maps to NM_004265.2 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:61646235 G>A maps to NM_021727.3 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:61646235 G>A maps to NM_021727.3 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:61645657 G>A maps to NM_021727.3 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:61643378 C>T maps to NM_021727.3 K410K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:61647529 G>A maps to NM_021727.3 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr17:72888727 C>T maps to ENST00000310226 K98K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:72878756 C>T maps to ENST00000310226 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr17:72877224 G>A maps to ENST00000310226 H238H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr17:72877248 G>A maps to ENST00000310226 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:72875692 G>A maps to ENST00000310226 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:72878705 G>A maps to ENST00000310226 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:51121200 C>T did not map to a codon.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr1:51323653 C>A maps to NM_007051.2 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr1:50941336 G>A maps to NM_007051.2 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:51061848 G>A maps to NM_007051.2 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:175921193 C>T maps to NM_014613.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:80452763 C>T maps to NM_000137.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr15:80460456 C>T maps to NM_000137.1 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:80467378 C>T maps to NM_000137.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr16:1877844 C>A maps to NM_001018104.2 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:96078439 C>T maps to NM_016044.2 Y270Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr2:97749750 C>T maps to NM_199336.1 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:97757236 G>A maps to NM_199336.1 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:138340341 G>A maps to NM_001033030.1 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:50291357 G>A maps to NM_012306.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:50284485 G>A maps to NM_012306.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr12:50295090 C>T maps to NM_012306.2 K11K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:50283262 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:50283910 C>A maps to NM_012306.2 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:50295081 C>T maps to NM_012306.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:207086367 T>C maps to NM_005449.4 E131E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:207095172 G>A maps to NM_005449.4 Y9Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:74266361 C>T maps to NM_182565.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:74261618 G>A maps to NM_182565.3 Q11Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:293167 C>T maps to NM_182705.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr9:130710455 G>A maps to NM_001035254.2 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:130710404 G>A maps to NM_001035254.2 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr9:130707122 G>A maps to NM_001035254.2 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr17:71228277 C>T maps to NM_001098832.1 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:71223333 G>A maps to NM_001098832.1 N97N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:55185589 G>C did not map to a codon.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr5:14601460 G>A maps to NM_019018.2 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:14601460 G>A maps to NM_019018.2 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:14607557 G>A maps to NM_019018.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr10:14816509 G>A maps to NM_031453.2 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr10:14816560 C>T maps to NM_031453.2 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:14709677 G>A maps to NM_031453.2 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:14816575 G>A maps to NM_031453.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:1881265 G>A maps to NM_031213.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr19:1881301 G>A maps to NM_031213.3 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr19:1881346 A>G maps to NM_031213.3 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr9:74481740 A>G maps to NM_016014.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:111801114 G>A maps to NM_001177996.1 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr20:826241 C>T maps to NM_031424.4 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr8:59059712 C>T maps to NM_147189.2 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr8:59059229 C>T maps to NM_147189.2 H147H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:45662 C>T maps to NM_001077710.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr2:46016 C>T maps to NM_001077710.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:46016 C>T maps to NM_001077710.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr11:58919258 C>T maps to NM_198847.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr11:58892631 C>T maps to NM_198947.3 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:58893162 C>T maps to NM_198947.3 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr11:58892778 G>A maps to NM_198947.3 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr20:2816131 G>A maps to NM_022760.3 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:2816918 G>A maps to NM_022760.3 Q295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:2816919 G>A maps to NM_022760.3 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr12:47629784 C>T maps to NM_138371.1 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr12:47629330 G>A maps to NM_138371.1 W162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr12:47629013 C>T maps to NM_138371.1 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr12:47630094 C>T maps to NM_138371.1 R417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr12:47629323 C>T maps to NM_138371.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr12:47629041 C>T maps to NM_138371.1 Q66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:47628851 C>T maps to NM_138371.1 I2I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:47629791 C>T maps to NM_138371.1 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:47629748 C>T maps to NM_138371.1 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:47629472 C>T maps to NM_138371.1 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:47629001 G>A maps to NM_138371.1 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr12:47628896 C>T maps to NM_138371.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:47629802 G>A maps to NM_138371.1 Q319Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:47628995 A>G maps to NM_138371.1 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:47629899 C>T maps to NM_138371.1 Q352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:47629082 C>T maps to NM_138371.1 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:47629322 C>T maps to NM_138371.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr12:47629949 C>T maps to NM_138371.1 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr12:47629853 T>A maps to NM_138371.1 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:47629523 C>T maps to NM_138371.1 H226H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:47629760 C>T maps to NM_138371.1 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:47628896 C>T maps to NM_138371.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:47630060 C>T maps to NM_138371.1 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:47629265 G>A maps to NM_138371.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:47629997 C>T maps to NM_138371.1 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr12:47629310 C>T maps to NM_138371.1 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:47629091 C>T maps to NM_138371.1 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr4:38907395 C>T maps to NM_138389.2 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr4:38937389 G>A maps to NM_138389.2 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:38907179 C>T maps to NM_138389.2 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:38937368 C>T maps to NM_138389.2 A498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr5:153414363 C>T maps to ENST00000442256 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr5:153406840 G>T maps to ENST00000442256 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:153372607 G>A maps to ENST00000442256 I489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:143573476 G>A maps to NM_014719.1 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr7:143573470 G>T maps to NM_014719.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:143421594 C>T maps to ENST00000441159 F770F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr7:143417117 C>T maps to ENST00000441159 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr7:143417118 C>T maps to ENST00000441159 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:143421618 C>T maps to ENST00000441159 T778T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:143421816 G>A maps to NM_001130025.1 R844R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr3:57616706 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:57649397 G>A maps to NM_152678.2 R160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z4-06A-11D-A197-08 chr3:57651847 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:50755727 G>A maps to NM_001001794.3 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr22:50750840 G>A maps to NM_001001794.3 I522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:50757411 G>A maps to NM_001001794.3 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr17:47788721 C>T maps to NM_030802.3 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr17:47788682 G>A maps to NM_030802.3 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:203630258 C>T maps to NM_173511.3 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr2:203589650 A>C maps to NM_173511.3 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:203622096 C>T maps to NM_173511.3 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:203621973 C>T maps to NM_173511.3 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:45719238 C>T maps to NM_017911.2 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:45723823 C>T maps to NM_017911.2 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:126110770 C>G maps to NM_024556.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr12:58174203 C>T maps to NM_015433.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr12:58174275 C>T maps to NM_015433.2 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:96261095 C>T maps to ENST00000333936 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:170700138 C>T maps to NM_032448.1 V843V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:54143143 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr23:54107878 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:54161360 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:54161967 T>G did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:54184189 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:54209043 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:54161360 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr23:54185882 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:54177716 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr23:54161464 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr23:54162930 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:54107814 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:54209099 C>G did not map to a codon.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr23:54162997 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:54159223 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:54184165 G>A did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:54209118 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr23:54117841 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr23:133922778 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:133941575 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:133948837 A>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:133948838 T>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:133981470 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr13:25744176 G>A maps to NM_152704.2 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr13:25743771 C>T maps to NM_152704.2 T662T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr13:25744446 C>T maps to NM_152704.2 Q437Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr23:63410333 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr23:63412220 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr23:63411347 C>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:63410326 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:63410655 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:63409813 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:63412487 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:63409896 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr23:63410309 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:63410057 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:63411496 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:63410354 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:63410231 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr23:63410945 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr23:63411266 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:63411266 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:63412415 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:63411446 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:63413105 G>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:63410325 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:63410326 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr23:63411446 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:63412502 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr23:63411311 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:63411575 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr23:63412631 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:131520775 C>T maps to NM_001105195.1 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:131521405 G>A maps to NM_001105195.1 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr2:131520646 G>A maps to NM_001105195.1 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:131520817 C>T maps to NM_001105195.1 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr2:131520520 G>A maps to NM_001105195.1 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:131520272 C>T maps to NM_001105195.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:131520727 C>T maps to NM_001105195.1 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr2:131519902 C>T maps to NM_001105195.1 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:131520712 G>A maps to NM_001105195.1 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:131521891 C>T maps to NM_001105195.1 V749V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr2:131520745 C>T maps to NM_001105195.1 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:131520247 C>T maps to NM_001105195.1 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:131520397 G>A maps to NM_001105195.1 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:131522170 C>T maps to NM_001105195.1 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:225266164 A>T maps to NM_001122779.1 C107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:225265793 C>T maps to NM_001122779.1 W231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr19:17531348 C>T maps to NM_138401.2 N64N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:17533259 C>T maps to NM_138401.2 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:17534588 C>T maps to NM_138401.2 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr9:129143401 C>T maps to NM_033446.1 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr9:129154429 C>T maps to NM_033446.1 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:22999934 G>A maps to NM_032581.3 R311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:201876141 G>A maps to NM_173822.3 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:134166495 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:134166496 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:134185922 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr23:134156472 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:134156297 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:184764938 C>T maps to NM_052966.2 E653E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr1:184787804 G>A maps to NM_052966.2 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr1:184767258 G>A maps to NM_052966.2 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:184764305 C>T maps to NM_052966.2 E864E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:184764971 G>A maps to NM_052966.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:184764695 C>T maps to NM_052966.2 T734T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:184801031 C>T maps to NM_052966.2 Q222Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:184764548 C>T maps to NM_052966.2 E783E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:184777333 G>A maps to NM_052966.2 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr1:184777222 C>T maps to NM_052966.2 Q440Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:184775091 G>A maps to NM_052966.2 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr1:184772733 C>T maps to NM_052966.2 A513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:184765084 G>A maps to NM_052966.2 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:184787891 C>T maps to NM_052966.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:184765070 C>T maps to NM_052966.2 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:184792439 C>T maps to NM_052966.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:184764239 G>A maps to NM_052966.2 A886A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:184764539 C>T maps to NM_052966.2 G786G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:184764623 G>A maps to NM_052966.2 I758I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr9:130271284 G>A maps to NM_022833.2 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:130279139 G>A maps to NM_022833.2 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:130279193 G>A maps to NM_022833.2 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr9:130270443 C>T maps to NM_022833.2 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:130286072 G>A maps to NM_022833.2 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:130287385 G>A maps to NM_022833.2 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr19:17660307 G>A maps to ENST00000335393 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:17654160 G>A maps to ENST00000335393 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr19:17648260 C>T maps to ENST00000335393 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:17653060 G>A maps to ENST00000335393 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:184060568 C>T maps to NM_144635.4 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr3:184062652 C>T maps to NM_144635.4 C332C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:143053711 C>T maps to NM_001031690.2 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr7:143053690 G>A maps to NM_001031690.2 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:143054115 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:143056115 C>T maps to NM_001031690.2 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:143055977 C>T maps to NM_001031690.2 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:143053834 T>A maps to NM_001031690.2 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr7:143057240 C>T maps to NM_001031690.2 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:16388594 C>T maps to NM_182623.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:1179871 G>A maps to NM_001014980.1 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:92965001 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr23:92964699 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:92964505 A>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:92964423 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:92964695 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr7:92207461 A>C did not map to a codon.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr2:220047131 C>T maps to NM_024293.4 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr2:220047113 C>T maps to NM_024293.4 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr17:40734028 G>A maps to NM_178126.3 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr6:71246049 C>T maps to NM_001162529.1 T1351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:71190693 C>T maps to NM_001162529.1 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr6:71235822 C>T maps to NM_001162529.1 I1012I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:71191789 C>T maps to NM_001162529.1 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr8:139263088 C>T maps to NM_015912.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr8:139144976 A>C maps to NM_015912.3 T1360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr8:139165195 G>A maps to NM_015912.3 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr8:139151313 C>T maps to NM_015912.3 K1272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr8:139158221 G>A maps to NM_015912.3 L1174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr8:139164167 C>T maps to NM_015912.3 G850G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr8:139155298 G>A maps to NM_015912.3 I1198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr8:139164683 T>C maps to NM_015912.3 R678R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:139153531 G>A maps to NM_015912.3 F1233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:139209795 G>A maps to NM_015912.3 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:139278019 A>G maps to NM_015912.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr8:139144922 G>A maps to NM_015912.3 I1378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr8:139164293 G>A maps to NM_015912.3 S808S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:139158293 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:139163459 C>T maps to NM_015912.3 E1086E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr8:139163732 G>A maps to NM_015912.3 S995S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr8:139164773 C>T maps to NM_015912.3 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:139160832 G>A maps to NM_015912.3 F1126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:139160921 G>A maps to NM_015912.3 Q1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:139165313 G>A maps to NM_015912.3 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:139323150 G>A maps to NM_015912.3 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr8:139158222 G>A maps to NM_015912.3 F1173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:139165085 C>T maps to NM_015912.3 E544E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:139149480 G>A maps to NM_015912.3 V1308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:139153501 G>A maps to NM_015912.3 F1243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:139190801 G>A maps to NM_015912.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:139144922 G>A maps to NM_015912.3 I1378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:139151307 G>A maps to NM_015912.3 S1274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:139163510 C>T maps to NM_015912.3 Q1069Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:139190782 G>A maps to NM_015912.3 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr8:139164740 C>T maps to NM_015912.3 K659K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr8:139207548 C>T maps to NM_015912.3 E275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr8:139323149 G>A maps to NM_015912.3 R31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr8:139144880 G>A maps to NM_015912.3 F1392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr8:139164395 G>A maps to NM_015912.3 P774P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr8:139158222 G>A maps to NM_015912.3 F1173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr8:139144922 G>A maps to NM_015912.3 I1378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr8:139163711 C>T maps to NM_015912.3 E1002E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr8:139380205 C>A maps to NM_015912.3 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr8:139158222 G>A maps to NM_015912.3 F1173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr8:139180255 C>T maps to NM_015912.3 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:139163756 G>A maps to NM_015912.3 P987P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:139164632 G>A maps to NM_015912.3 V695V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:139190909 G>A maps to NM_015912.3 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr8:139164488 G>A maps to NM_015912.3 I743I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:139158243 G>A maps to NM_015912.3 L1166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr8:139190843 G>A maps to NM_015912.3 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr4:89668817 C>T maps to NM_014883.2 E782E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr4:89670140 C>T maps to NM_014883.2 W708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr4:89670942 G>A maps to NM_014883.2 F686F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:89671017 C>T maps to NM_014883.2 E661E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr4:89772258 G>A maps to NM_014883.2 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr4:89658685 C>T maps to NM_014883.2 R861R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr5:137354779 A>C maps to NM_016603.2 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:61022397 C>T maps to ENST00000442566 K387K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:61028351 C>T maps to ENST00000442566 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr10:61112164 C>T maps to ENST00000442566 W85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:61023887 C>T maps to ENST00000442566 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:61028372 C>T maps to ENST00000442566 Q337Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:61112071 G>A maps to ENST00000442566 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:61112092 G>A maps to ENST00000442566 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr10:61028360 C>T maps to ENST00000442566 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:61023881 C>T maps to ENST00000442566 W372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:61029690 G>A maps to ENST00000442566 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:61022202 C>T maps to ENST00000442566 E452E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:61028351 C>T maps to ENST00000442566 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr4:187078776 C>T maps to ENST00000356371 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr8:53454955 G>A maps to NM_207413.3 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr8:53454997 G>A maps to NM_207413.3 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:55080521 C>T maps to NM_176782.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:55077408 C>T maps to NM_176782.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:55089041 C>T maps to NM_176782.2 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:55080512 C>T maps to NM_176782.2 K145K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:55080461 C>T maps to NM_176782.2 E162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:55080479 G>A maps to NM_176782.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:55081804 C>T maps to NM_176782.2 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr5:177163601 C>T maps to ENST00000425383 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr9:18941722 G>A maps to NM_153707.2 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr9:18928075 G>A maps to NM_153707.2 Q467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:18950913 G>A maps to NM_153707.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr9:18929006 C>A maps to NM_153707.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr13:107822873 G>A maps to NM_001080396.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:108518794 G>A maps to NM_001080396.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr23:68749552 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:68748925 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:68748967 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:68749602 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr23:68725706 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:53122567 G>A maps to NM_001042693.1 Q143Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:53122528 G>A maps to NM_001042693.1 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:6232842 A>G maps to NM_032127.3 L952L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:6235746 G>A maps to NM_032127.3 F831F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:6245695 G>A maps to NM_032127.3 H17H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:6239228 G>A maps to NM_032127.3 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr11:6239108 G>A maps to NM_032127.3 C583C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:116595297 T>A maps to NM_020940.3 C99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:116606029 C>T maps to NM_020940.3 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:116595896 C>T maps to NM_020940.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:116605951 C>T maps to NM_020940.3 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr10:116593055 G>C maps to NM_020940.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:116615041 C>T maps to NM_020940.3 F630F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:116605815 C>T maps to NM_020940.3 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:21958160 G>A maps to NM_022749.5 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr8:21958474 C>T maps to NM_022749.5 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr8:21959319 C>T maps to NM_022749.5 F603F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr8:21958468 C>T maps to NM_022749.5 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:21958474 C>T maps to NM_022749.5 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr8:21959687 A>G maps to NM_022749.5 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr8:21959319 C>T maps to NM_022749.5 F603F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr8:21959747 C>T maps to NM_022749.5 P638P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr2:62081061 G>A maps to ENST00000404929 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:62069261 A>G maps to ENST00000404929 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:62067597 G>A maps to ENST00000404929 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:62067000 G>A maps to ENST00000404929 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:62067637 G>A maps to ENST00000404929 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:62067373 G>A maps to ENST00000404929 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:62067292 G>A maps to ENST00000404929 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr14:74411479 G>A maps to NM_152445.1 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:74411284 G>A maps to NM_152445.1 Y226Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:122123195 C>T maps to NM_014367.3 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr6:117086374 G>A maps to NM_001085480.2 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr1:179783101 C>T maps to NM_173509.2 H94H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr8:79627471 C>T maps to NM_016010.2 R241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr8:79629649 C>T maps to NM_016010.2 C300C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr21:35757831 C>T maps to NM_058182.4 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr9:140139595 G>A maps to NM_001001710.1 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U9-06A-11D-A32N-08 chr9:140138223 G>T maps to NM_001001710.1 Y294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr9:35562961 C>T maps to NM_001164310.1 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr11:73141786 G>A maps to ENST00000064778 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:73130925 C>T maps to ENST00000064778 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:131812887 G>A maps to NM_001009993.2 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:74100323 C>T maps to NM_015566.1 Q302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr15:98995171 C>T maps to NM_182562.2 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:118968491 G>A maps to ENST00000420106 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr5:118970375 G>A maps to ENST00000420106 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr5:118969895 C>T maps to ENST00000420106 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr5:118970318 G>A maps to ENST00000420106 E292E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr5:118969689 C>T maps to ENST00000420106 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr5:118969985 C>T maps to ENST00000420106 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr5:118970009 G>A maps to ENST00000420106 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr5:118970426 G>A maps to ENST00000420106 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:118970426 G>A maps to ENST00000420106 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:118969871 G>A maps to ENST00000420106 W143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:118969928 C>T maps to ENST00000420106 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:118969874 G>A maps to ENST00000420106 E144E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:15255959 G>A maps to NM_001010924.1 R543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr10:15255090 C>T maps to NM_001010924.1 Q832Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr10:15255780 G>A maps to NM_001010924.1 V602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr10:15256416 C>T maps to NM_001010924.1 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:15256407 C>T maps to NM_001010924.1 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:15256467 G>A maps to NM_001010924.1 F373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr10:15290722 G>A maps to NM_001010924.1 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:15255222 G>A maps to NM_001010924.1 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:15256023 G>A maps to NM_001010924.1 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:15256416 C>T maps to NM_001010924.1 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr10:15296774 G>A maps to NM_001010924.1 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr10:15256350 G>A maps to NM_001010924.1 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:15255081 C>T maps to NM_001010924.1 T835T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:15256005 C>T maps to NM_001010924.1 E527E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:15290644 C>T maps to NM_001010924.1 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:15290704 G>A maps to NM_001010924.1 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:15326030 G>A maps to NM_001010924.1 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:15255222 G>A maps to NM_001010924.1 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr2:187626904 C>T maps to NM_177454.3 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr2:187627295 C>T maps to NM_177454.3 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:187627228 C>T maps to NM_177454.3 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr2:187626883 C>T maps to NM_177454.3 I605I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:187626569 C>T maps to NM_177454.3 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:187615975 G>A maps to NM_177454.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:187627381 C>T maps to NM_177454.3 I771I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr2:187627262 C>T maps to NM_177454.3 Q732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:187627273 C>T maps to NM_177454.3 I735I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:187627132 C>T maps to NM_177454.3 S688S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:93159892 G>A maps to NM_032042.5 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:93294640 A>G maps to NM_032042.5 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:93410360 G>C maps to NM_032042.5 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr5:10239294 G>A maps to NM_199133.2 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:10239211 G>A maps to NM_199133.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:126505148 C>T maps to NM_032182.3 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr10:126523137 G>A maps to NM_032182.3 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:75745191 G>A maps to NM_032181.2 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:75720526 C>T maps to NM_032181.2 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:75745251 G>A maps to NM_032181.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:75720658 C>T maps to NM_032181.2 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:222922891 G>A maps to NM_207468.2 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr1:222920391 G>A maps to NM_207468.2 W70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:222919964 C>T maps to NM_207468.2 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:222919937 C>T maps to NM_207468.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:102689754 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:102683837 C>T maps to NM_001136123.1 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:102676651 C>T maps to NM_001136123.1 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr2:29259495 C>T maps to NM_199280.2 L836L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:29246014 C>T maps to NM_199280.2 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:29259555 C>T maps to NM_199280.2 L856L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:29226425 G>A maps to NM_199280.2 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:29240745 G>A maps to NM_199280.2 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:29259492 C>T maps to NM_199280.2 P835P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:29259573 G>A maps to NM_199280.2 G862G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr2:29245102 G>A maps to NM_199280.2 K480K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:29247147 C>T maps to NM_199280.2 F587F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr2:29256360 C>T maps to NM_199280.2 P719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:29221099 C>T maps to NM_199280.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr2:29222194 C>T maps to NM_199280.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:29222071 C>T maps to NM_199280.2 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:29255913 G>A maps to NM_199280.2 Q709Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:29245120 G>A maps to NM_199280.2 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:45431791 C>T maps to ENST00000361462 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:45513921 C>T maps to ENST00000361462 Q1335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:45475274 C>T maps to ENST00000361462 S903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:45475275 C>A maps to ENST00000361462 R904R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:45478135 C>T maps to ENST00000361462 S975S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:135419001 G>A maps to NM_205855.3 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:135418854 C>T maps to NM_205855.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:135418971 G>A maps to NM_205855.3 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr14:94395002 G>A maps to NM_138344.3 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:94391688 G>A maps to NM_138344.3 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:94391700 G>A maps to NM_138344.3 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:94394933 G>A maps to NM_138344.3 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr14:94394705 G>A maps to NM_138344.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr14:94395278 C>T maps to NM_138344.3 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr14:94394882 C>T maps to NM_138344.3 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr14:94395152 G>A maps to NM_138344.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:94395107 C>T maps to NM_138344.3 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:43621917 G>A maps to NM_001101376.2 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:119327614 C>T maps to NM_024581.4 V604V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr6:119345371 G>A maps to NM_024581.4 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr6:119297153 C>T maps to NM_024581.4 R837R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr6:119324214 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:119338109 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:119345393 A>T maps to NM_024581.4 Y248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr6:119332541 G>A maps to NM_024581.4 Q529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:119345459 C>T maps to NM_024581.4 E226E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:49994666 C>T maps to NM_032130.2 K252K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:35719418 G>A maps to NM_152481.1 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:15828601 G>A maps to NM_024948.2 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:15858884 G>A maps to NM_024948.2 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr7:30880417 C>T maps to NM_032222.2 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:30830929 C>T maps to NM_032222.2 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:30931613 C>T maps to NM_032222.2 I756I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:30911860 C>T maps to ENST00000509504 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:30825436 C>T maps to NM_032222.2 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:30922584 C>T maps to ENST00000509504 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:71992359 C>T maps to NM_001127608.1 Y109Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:72000819 C>T maps to NM_001127608.1 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:155217665 G>A maps to ENST00000368370 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:155220457 G>A maps to ENST00000368370 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr1:155220898 G>A maps to ENST00000368370 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:10867217 C>T maps to NM_001079512.2 W135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:91549209 C>T maps to NM_001145065.1 Q587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr4:91549259 G>A maps to NM_001145065.1 A603A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr4:91229509 A>G maps to NM_001145065.1 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:91229611 G>C maps to NM_001145065.1 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr4:91229575 C>T maps to NM_001145065.1 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr4:91549209 C>T maps to NM_001145065.1 Q587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:91234062 G>A maps to NM_001145065.1 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:86131044 C>T maps to ENST00000372088 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:86131536 C>T maps to ENST00000372088 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr10:86131488 C>T maps to ENST00000372088 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:2661592 C>T maps to ENST00000324666 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr4:2701825 C>T maps to ENST00000324666 L1018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr4:2661598 C>T maps to ENST00000324666 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr4:2661598 C>T maps to ENST00000324666 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:2648483 C>A maps to ENST00000324666 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr4:2696693 C>T maps to ENST00000324666 H747H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr4:2698149 C>T maps to ENST00000324666 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr5:176951978 G>A maps to ENST00000442143 G581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr5:176965995 G>A maps to ENST00000442143 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:176952109 C>A maps to ENST00000442143 E538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:176958510 G>A maps to ENST00000442143 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr5:176958471 G>T maps to ENST00000442143 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:176966007 G>A maps to ENST00000442143 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr5:176963396 G>A maps to ENST00000442143 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:176958471 G>A maps to ENST00000442143 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:150404139 C>T maps to NM_152394.3 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr3:150403779 C>T maps to NM_152394.3 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr3:150404121 C>T maps to NM_152394.3 E191E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:150421571 C>T maps to NM_152394.3 E38E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:150404136 C>T maps to NM_152394.3 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr3:150384764 G>A maps to NM_152394.3 Q513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr3:150396228 G>A maps to NM_152394.3 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr3:150398318 C>T maps to NM_152394.3 Q349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr3:150377861 G>A maps to NM_152394.3 I603I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr3:150421556 C>T maps to NM_152394.3 E43E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:150387156 G>A maps to NM_152394.3 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:150396254 G>A maps to NM_152394.3 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr3:150400022 G>A maps to NM_152394.3 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr10:128973906 C>T maps to NM_001039762.2 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:128974284 C>T maps to NM_001039762.2 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:128973867 C>T maps to NM_001039762.2 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr10:128974536 C>T maps to NM_001039762.2 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:159092245 C>T maps to NM_001128424.1 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:103432938 T>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:103431287 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:103434386 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:103431142 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr3:68055809 G>A maps to NM_213609.2 W14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:68587910 C>T maps to NM_213609.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:68055861 C>T maps to NM_213609.2 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr3:68055809 G>A maps to NM_213609.2 W14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:68587993 G>A maps to NM_213609.2 W116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:68055846 C>T maps to NM_213609.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr12:62147423 C>T maps to NM_178539.3 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:62261131 C>T maps to NM_178539.3 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr12:62148788 C>T maps to NM_178539.3 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:62147423 C>T maps to NM_178539.3 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr12:62147516 C>T maps to NM_178539.3 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:68802050 C>T maps to NM_182522.3 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:68788228 C>T maps to NM_182522.3 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:68788333 C>T maps to NM_182522.3 Q101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:68788228 C>T maps to NM_182522.3 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr22:49042448 C>T maps to ENST00000336769 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr22:49103613 C>T maps to ENST00000336769 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:99145985 A>G maps to NM_145111.3 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr17:66551832 T>G maps to NM_017565.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr17:66538259 C>T maps to NM_017565.3 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr17:66538259 C>T maps to NM_017565.3 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:66533872 C>T maps to NM_017565.3 K457K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:179023748 C>T maps to NM_014864.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr7:195667 C>T maps to NM_020223.2 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr10:88994202 G>A maps to NM_001099338.1 W792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr10:88994203 G>A maps to NM_001099338.1 W792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:88988176 C>T maps to NM_001099338.1 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr9:97081944 A>G maps to NM_017561.1 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:97081903 G>A maps to NM_017561.1 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:97082624 C>T maps to NM_017561.1 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:124671194 C>T maps to NM_001029888.1 I15I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:124671176 G>A maps to NM_001029888.1 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:124671179 G>A maps to NM_001029888.1 K10K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr10:124610019 G>A maps to NM_152644.2 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:124609992 G>A maps to NM_152644.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:116879328 G>A maps to ENST00000368596 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:116836899 G>A maps to NM_153711.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:116836884 G>A maps to NM_153711.2 K221K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr6:116833182 G>A maps to NM_153711.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:116784567 G>A maps to NM_001010919.1 Q216Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr6:116784549 G>A maps to NM_001010919.1 W210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:116784810 G>A maps to NM_001010919.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:16301696 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:88917886 T>C maps to ENST00000298786 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr18:10691381 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr18:10671550 G>A maps to NM_022068.2 I2744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr18:10672700 G>A maps to NM_022068.2 F2664F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:10696163 C>T maps to NM_022068.2 R2253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr18:10696184 C>T maps to NM_022068.2 V2246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:10696235 G>A maps to NM_022068.2 V2229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr18:10681663 C>T maps to NM_022068.2 R2478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:10696118 G>A maps to NM_022068.2 F2268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr18:10671736 C>T maps to NM_022068.2 G2682G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr18:10680263 C>T maps to NM_022068.2 Q2515Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:10689790 G>A maps to NM_022068.2 L2340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:10696208 G>A maps to NM_022068.2 L2238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:153736901 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:153735628 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr21:42694868 C>T maps to ENST00000398652 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr3:58622929 G>A maps to NM_138805.2 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:58629398 G>A maps to NM_138805.2 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:58639462 C>T maps to NM_138805.2 W20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:58620086 C>T maps to NM_138805.2 K198K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:58639508 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:58635048 C>T maps to NM_138805.2 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:58631267 G>A maps to NM_138805.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:110581845 C>T maps to NM_033088.2 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:110596311 C>T maps to NM_033088.2 F764F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr7:129091562 C>T maps to ENST00000450266 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:129104485 C>T maps to ENST00000450266 I620I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:129103953 C>T maps to ENST00000450266 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr7:129104485 C>T maps to ENST00000450266 I620I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr7:129093095 C>T maps to ENST00000450266 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr7:129098201 C>T maps to ENST00000450266 D454D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:129095169 C>T maps to ENST00000450266 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:129122723 C>T maps to ENST00000450266 A756A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr10:120877126 C>T maps to NM_207009.2 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr6:82459714 G>A maps to ENST00000369756 N423N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr6:82459705 C>T maps to ENST00000369756 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:27333250 G>A maps to NM_052943.3 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:27332848 C>T maps to NM_052943.3 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:27333295 G>A maps to NM_052943.3 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr1:27332473 G>A maps to NM_052943.3 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:27333151 C>T maps to NM_052943.3 W187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:118166323 C>T maps to NM_017709.3 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:118166491 C>T maps to NM_017709.3 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:118165666 G>A maps to NM_017709.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr1:118166041 C>T maps to NM_017709.3 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr23:79698896 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:79698281 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:79698499 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:79698636 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:79699197 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:79698071 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:79698130 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:79699003 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:79698624 A>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:79698481 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:79698901 C>T did not map to a codon.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr23:79698281 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr23:34148192 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr23:34149183 G>T did not map to a codon.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr23:34149263 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr23:34150005 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr23:34150006 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:34148502 A>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:34148531 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:34149090 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:34149885 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr23:34148165 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:34148067 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:34148954 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:34149335 G>A did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:34148745 A>G did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:34149811 G>A did not map to a codon.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr23:34150049 C>T did not map to a codon.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr23:34150132 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:34149840 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr23:34148921 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:34148364 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:34150031 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:34148677 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:34148257 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:34148258 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:34150160 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr23:34149455 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:34148523 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:34148765 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:34150081 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:34149397 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:34148539 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:34149123 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:34149161 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:34148364 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:34150270 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:34148450 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:34148571 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:34149420 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:34149559 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:34149013 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:34148639 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:34150302 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:34148668 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:34150305 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr23:34149530 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr23:34148948 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:34148154 G>C did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:34148253 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:34150172 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr23:34150007 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:34149227 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:34149228 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:34150081 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:34149263 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:34149362 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:34149923 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:34148364 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:34150260 G>A did not map to a codon.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr23:34148219 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:34148280 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:34150244 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr23:34149263 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:34150188 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:34148805 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr23:34148474 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:34148257 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:34148668 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:34149045 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr23:34149820 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:34148981 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:34148246 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:34148677 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:34150388 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:34149068 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:34149782 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr23:34148571 G>A did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:34148364 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr23:34962606 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:34962877 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:34961322 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:34962682 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:34961616 C>T did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:34961494 C>T did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:34961617 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:34962064 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:34960954 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:34961494 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr23:34961862 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:34961359 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:34961229 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:34961418 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr23:34961103 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:34961076 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:34962640 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr23:34961229 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr23:34962048 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr23:34962049 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:34961467 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:34962618 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:34961602 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:34961627 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr23:34961289 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr23:34961077 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:34961802 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:34962222 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:34961674 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:34961753 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:34961845 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:34961962 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:34961967 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:34962327 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:34962774 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:34961412 C>T did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:34962807 T>G did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:34962817 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr23:34961289 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:37028257 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr23:37027833 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr23:37028774 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:37028485 C>G did not map to a codon.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr23:37029342 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:37028886 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:37029444 A>G did not map to a codon.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr23:37027437 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:37027035 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:37027207 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:37028725 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:37027081 C>A did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:37027535 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:37026572 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:37027069 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:37028053 C>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:37029437 C>T did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:37027431 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:37029225 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:37026572 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:37028480 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:37029029 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr23:37027899 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr23:37027985 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr23:37029242 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:37027309 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:37027310 G>C did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:37028252 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr23:37027407 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:37027797 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:37028774 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:37027925 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:37027257 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr23:37029028 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:37026871 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:37026887 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:37028489 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:37027701 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:37026575 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:37029038 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:37029437 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:37027272 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:37027789 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:37026647 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:37027155 C>G did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:37027199 A>C did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:37027130 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:37026696 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:37027581 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:37029309 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:37029325 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr23:37027155 C>G did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:37027684 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr23:37029044 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr23:37026708 T>A did not map to a codon.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr23:37027773 C>T did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:37026635 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:37028886 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:37026801 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:37028266 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:37028267 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:37029211 A>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr23:37026915 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:37028689 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr23:37028582 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:37027076 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:37027303 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:37027524 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:37027566 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:37027661 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:37028545 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:37028737 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:37028766 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:37029579 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:37026488 G>A did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr23:37026556 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:37027531 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:37028655 C>T did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:37028200 A>G did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:37027035 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:37027272 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr23:37028354 G>A did not map to a codon.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr23:37029245 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr13:37618229 G>A maps to NM_001014286.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr13:37583907 T>C maps to NM_001014286.2 A747A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr13:37619410 G>A maps to NM_001014286.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:16734263 G>A maps to NM_030797.3 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:16746991 G>A maps to NM_030797.3 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:16740730 G>A maps to NM_030797.3 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:16740730 G>A maps to NM_030797.3 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:16742505 G>A maps to NM_030797.3 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:16740757 C>T maps to NM_030797.3 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:16745362 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:16769357 C>T maps to NM_030797.3 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:16740832 C>T maps to NM_030797.3 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:130891647 G>A maps to NM_016623.3 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr8:130891647 G>A maps to NM_016623.3 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:153678614 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:153678615 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr23:153678386 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr6:3850384 A>T maps to NM_012135.1 K114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:3850848 C>T maps to NM_012135.1 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:3850989 C>T maps to NM_012135.1 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr6:3850488 G>A maps to NM_012135.1 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:3850680 C>T maps to NM_012135.1 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:3850650 G>A maps to NM_012135.1 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr4:1643070 G>A maps to NM_001174070.1 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr4:1656718 G>A maps to NM_001174070.1 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:126370430 G>A maps to NM_014661.3 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:126370408 G>A maps to NM_014661.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:137680656 C>T maps to NM_001135647.1 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:137681039 C>T maps to NM_001135647.1 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr5:137680895 C>T maps to NM_001135647.1 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:26156150 A>C maps to NM_001099626.1 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:26158411 G>A maps to NM_001099626.1 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr11:114401201 G>C maps to ENST00000424269 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:114393811 C>T maps to ENST00000424269 K299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:114393140 C>T maps to ENST00000424269 W398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:114393664 G>A maps to ENST00000424269 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr11:114569392 C>T maps to NM_182495.5 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:114568807 G>A maps to NM_182495.5 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr11:114569080 C>T maps to NM_182495.5 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:114569185 G>A maps to NM_182495.5 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:101535693 T>A maps to NM_145037.2 Y326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr3:101540500 G>A maps to NM_145037.2 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:101540557 C>T maps to NM_145037.2 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:114453518 A>T maps to NM_001077639.1 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:114453638 C>T maps to NM_001077639.1 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr11:114453572 G>A maps to NM_001077639.1 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:114453254 C>T maps to NM_001077639.1 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:114453575 G>A maps to NM_001077639.1 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:114442192 G>A maps to NM_001077639.1 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:114453476 C>T maps to NM_001077639.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr11:114442127 C>T maps to NM_001077639.1 R389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:114451013 G>A maps to NM_001077639.1 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:114441695 T>A maps to NM_001077639.1 G533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:114450893 C>T maps to NM_001077639.1 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5VV-06A-11D-A32N-08 chr17:641145 C>T maps to NM_024792.1 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr17:641229 C>T maps to NM_024792.1 N117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr16:30037137 C>T maps to NM_031478.4 W150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:30040820 G>A maps to NM_031478.4 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr16:30037048 G>A maps to NM_031478.4 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr23:152860030 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:152860003 C>G did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:152860003 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr23:152858168 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr18:29867641 G>A maps to ENST00000269209 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr18:29867602 G>A maps to ENST00000269209 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr18:29848121 G>A maps to ENST00000269209 Y781Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr18:29867098 G>A maps to ENST00000269209 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:29848133 G>A maps to ENST00000269209 F777F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:29867298 G>A maps to ENST00000269209 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:29867767 G>A maps to ENST00000269209 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr18:29847905 C>T maps to ENST00000269209 E853E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr18:29867614 T>A maps to ENST00000269209 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr18:29867419 G>A maps to ENST00000269209 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr18:29867530 G>A maps to ENST00000269209 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr1:177249715 C>T maps to NM_021165.2 H468H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr1:177242649 G>T maps to NM_021165.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr1:177247852 C>T maps to NM_021165.2 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr1:177226327 C>T maps to NM_021165.2 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:177226507 G>A maps to NM_021165.2 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:177250483 G>A maps to NM_021165.2 R724R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:177249619 C>T maps to NM_021165.2 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:177247804 G>A maps to NM_021165.2 Q373Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:177249595 G>A maps to NM_021165.2 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:177250384 C>T maps to NM_021165.2 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:177226423 G>A maps to NM_021165.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:177250268 C>T maps to NM_021165.2 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:177250225 C>T maps to NM_021165.2 F638F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:177250216 G>A maps to NM_021165.2 W635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:177247849 G>A maps to NM_021165.2 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:177250215 G>A maps to NM_021165.2 W635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:177225096 G>A maps to NM_021165.2 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:177199272 G>A maps to NM_021165.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:177245526 C>T maps to NM_021165.2 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:177249949 G>A maps to NM_021165.2 W546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:177250408 C>T maps to NM_021165.2 D699D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:177250447 C>T maps to NM_021165.2 S712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:177199086 G>T maps to NM_021165.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:177250588 C>T maps to NM_021165.2 I759I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:177249595 G>A maps to NM_021165.2 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:177250191 G>A maps to NM_021165.2 W627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:177247705 C>T maps to NM_021165.2 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr1:177250267 C>T maps to NM_021165.2 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:177250483 G>A maps to NM_021165.2 R724R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:177242625 C>T maps to NM_021165.2 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:177249595 G>A maps to NM_021165.2 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:177225144 G>A maps to NM_021165.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:177226447 C>T maps to NM_021165.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:177247705 C>T maps to NM_021165.2 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:177249619 C>T maps to NM_021165.2 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:177249814 C>T maps to NM_021165.2 N501N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:177250405 G>A maps to NM_021165.2 R698R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:177225234 C>T maps to NM_021165.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:177249565 G>A maps to NM_021165.2 W418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:177245529 G>A maps to NM_021165.2 Q324Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr1:190129814 G>A maps to NM_199051.1 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr1:190067594 C>T maps to NM_199051.1 W618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:190067903 G>A maps to NM_199051.1 I515I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:190234017 G>A maps to NM_199051.1 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:190423971 G>A maps to NM_199051.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:190250852 G>A maps to NM_199051.1 N88N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:190067642 G>A maps to NM_199051.1 D602D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr1:190067324 G>A maps to NM_199051.1 D708D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:190067594 C>T maps to NM_199051.1 W618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr1:190250795 G>A maps to NM_199051.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr1:190067225 C>T maps to NM_199051.1 R741R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:190250828 G>A maps to NM_199051.1 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:190129976 G>A maps to NM_199051.1 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr1:190068026 G>T maps to NM_199051.1 C474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:190067855 C>T maps to NM_199051.1 K531K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:190068134 G>A maps to NM_199051.1 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:190129847 G>A maps to NM_199051.1 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:190423888 G>A maps to NM_199051.1 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:190067225 C>T maps to NM_199051.1 R741R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr1:190250828 G>A maps to NM_199051.1 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:190067563 G>A maps to NM_199051.1 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr1:190130015 T>C maps to NM_199051.1 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr1:190203592 C>A maps to NM_199051.1 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:190067594 C>T maps to NM_199051.1 W618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:190068212 C>T maps to NM_199051.1 E412E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:190129976 G>A maps to NM_199051.1 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:190234048 C>T maps to NM_199051.1 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:190250828 G>A maps to NM_199051.1 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:190067618 C>T maps to NM_199051.1 W610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:190067594 C>T maps to NM_199051.1 W618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr12:31448265 A>G maps to NM_001135812.1 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:31451023 G>A maps to NM_001135812.1 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr1:150971966 G>A maps to NM_001163258.1 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:150971859 G>A maps to NM_001163258.1 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:150975030 G>A maps to NM_001163258.1 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:59063689 G>A maps to NM_001040450.1 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:6350796 C>T maps to NM_001195228.1 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr17:6350820 G>A maps to NM_001195228.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr16:67576105 C>T maps to NM_001193523.1 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr6:24873930 G>A maps to NM_014722.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:24875980 G>A maps to NM_014722.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:24848351 G>A maps to NM_014722.2 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr6:24848258 G>A maps to NM_014722.2 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:24848320 G>A maps to NM_014722.2 Q337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr20:49224936 C>T maps to NM_080829.2 E311E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr20:49225246 C>T maps to NM_080829.2 W234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:49224981 G>A maps to NM_080829.2 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:49225236 C>T maps to NM_080829.2 K237K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:49247282 C>T maps to NM_080829.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:49236545 G>A maps to NM_080829.2 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr20:49218806 G>A maps to NM_080829.2 S483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr20:49218974 G>A maps to NM_080829.2 F427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr20:49212699 G>A maps to NM_080829.2 Q627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:49218977 G>A maps to NM_080829.2 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:49219118 G>A maps to NM_080829.2 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:93312880 A>C maps to NM_001006605.3 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr9:139616458 C>T maps to NM_152421.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr18:72109237 A>G maps to NM_001044369.2 C330C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:119410841 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:119419544 T>C did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:119410864 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:119427888 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:119410841 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:119419519 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr13:114469086 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr13:114507928 C>T maps to NM_182614.2 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr13:114502316 G>A maps to NM_182614.2 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr13:114514836 C>T maps to NM_182614.2 Y314Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr13:114498131 G>A maps to NM_182614.2 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr13:114502331 G>A maps to NM_182614.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:114498179 C>T maps to NM_182614.2 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr1:212799718 G>A maps to NM_153606.3 K500K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:212799949 G>A maps to NM_153606.3 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:212799805 C>T maps to NM_153606.3 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:212799805 C>T maps to NM_153606.3 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:212798416 C>T maps to NM_153606.3 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:212798698 G>A maps to NM_153606.3 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:212799040 G>A maps to NM_153606.3 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:212799400 C>T maps to NM_153606.3 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:212799895 G>A maps to NM_153606.3 R559R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr5:156590261 T>A maps to NM_130899.2 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr5:156589595 G>A maps to NM_130899.2 I560I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:156589658 C>T maps to NM_130899.2 R539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr5:156590243 G>A maps to NM_130899.2 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:156589727 C>T maps to NM_130899.2 G516G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:156592957 G>A maps to NM_130899.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr5:156589973 C>T maps to NM_130899.2 K434K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr5:156589772 G>A maps to NM_130899.2 T501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:156589595 G>A maps to NM_130899.2 I560I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:156589604 C>T maps to NM_130899.2 E557E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:156590417 C>T maps to NM_130899.2 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:156590534 C>T maps to NM_130899.2 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:156592906 T>C maps to NM_130899.2 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:156590669 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:156589952 C>T maps to NM_130899.2 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr5:156589595 G>A maps to NM_130899.2 I560I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr5:156592657 G>A maps to NM_130899.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr14:67664892 C>T maps to NM_173526.3 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:67664955 G>A maps to NM_173526.3 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:50979170 G>A maps to ENST00000391816 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:50979489 G>A maps to ENST00000391816 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:128357011 G>A maps to NM_032599.2 W132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr7:128356880 G>A maps to NM_032599.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr7:128315742 G>A maps to NM_001012454.3 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:128317744 C>T maps to NM_001012454.3 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:206145495 C>T maps to NM_001123168.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr1:78249029 C>T maps to NM_198549.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:78309058 C>T maps to NM_198549.2 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:78309082 C>T maps to NM_198549.2 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:78309070 T>C maps to NM_198549.2 D325D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:78324726 C>T maps to NM_198549.2 Y367Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr9:131830144 C>T maps to NM_032809.2 R422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr9:131832548 G>A maps to NM_032809.2 R533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr9:39888155 C>G maps to ENST00000377642 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:39361103 G>A maps to ENST00000451313 R1128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:40702777 T>C maps to NM_001083124.1 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr9:40702792 C>T maps to NM_001083124.1 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:40704190 G>A maps to NM_001083124.1 R616R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:43626721 C>T maps to NM_001145196.1 V655V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:43627777 G>A maps to NM_001145196.1 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr9:43627000 C>T maps to NM_001145196.1 Q562Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr9:43627090 G>A maps to NM_001145196.1 S532S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr9:43627543 G>A maps to NM_001145196.1 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:43626726 T>A maps to NM_001145196.1 K654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:43625416 T>C maps to NM_001145196.1 Q1090Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:90535944 C>T maps to NM_001145124.1 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:90535307 C>T maps to NM_001145124.1 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:90534240 G>A maps to NM_001145124.1 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr9:90534219 G>A maps to NM_001145124.1 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr9:90535775 G>A maps to NM_001145124.1 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr9:90535427 C>T maps to NM_001145124.1 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:28075617 C>T maps to NM_001143912.1 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:28075617 C>T maps to NM_001143912.1 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:28081762 C>T maps to NM_001143912.1 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:166135290 G>A maps to NM_001017961.3 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:166039756 G>A maps to NM_001017961.3 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr15:59752221 C>T maps to NM_152450.2 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:59799516 G>A maps to NM_152450.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr5:94727107 C>T maps to NM_152548.2 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:94749761 C>T maps to NM_152548.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr5:94772523 G>A maps to NM_152548.2 K269K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr5:94764393 C>T maps to NM_152548.2 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:94772574 G>A maps to NM_152548.2 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr2:38178942 T>G maps to NM_144713.3 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:38179101 C>T maps to NM_144713.3 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr2:38216695 G>A maps to NM_144713.3 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr2:38224656 G>A maps to NM_144713.3 K526K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:38178624 C>T maps to NM_144713.3 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:38216752 C>T maps to NM_144713.3 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:38179101 C>T maps to NM_144713.3 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr15:41044185 G>A maps to NM_018145.1 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr15:41029488 G>A maps to NM_018145.1 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr8:124206316 G>A maps to NM_032899.4 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr8:124219444 C>T maps to NM_032899.4 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr8:124206262 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr8:124206334 C>T maps to NM_032899.4 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:124195458 G>A maps to NM_032899.4 W121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:124219537 C>T maps to NM_032899.4 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr8:124195161 C>T maps to NM_032899.4 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:54791182 G>A maps to NM_001010872.1 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:54805265 C>T maps to NM_001010872.1 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr6:54804968 C>T maps to NM_001010872.1 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr6:54806276 G>A maps to NM_001010872.1 S836S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr6:54804802 T>A maps to NM_001010872.1 L345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:54805728 C>T maps to NM_001010872.1 Q654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:54805638 T>C maps to NM_001010872.1 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44R-06A-41D-A25O-08 chr6:54735161 T>C maps to NM_001010872.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:54805943 C>T maps to NM_001010872.1 T725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:54806552 A>T maps to NM_001010872.1 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr6:54804614 C>T maps to NM_001010872.1 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr6:54735173 C>T maps to NM_001010872.1 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:54805015 G>A maps to NM_001010872.1 W416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr6:54735445 G>A maps to NM_001010872.1 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr6:54792311 C>T maps to NM_001010872.1 R206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:54805505 G>A maps to NM_001010872.1 E579E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr6:54804572 C>T maps to NM_001010872.1 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:54805517 C>T maps to NM_001010872.1 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr6:54735238 G>A maps to NM_001010872.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:54805190 C>T maps to NM_001010872.1 I474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:54805565 C>T maps to NM_001010872.1 I599I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr6:54735190 G>A maps to NM_001010872.1 Q49Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr6:54805145 G>A maps to NM_001010872.1 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:54804968 C>T maps to NM_001010872.1 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:54805523 G>A maps to NM_001010872.1 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr6:54804968 C>T maps to NM_001010872.1 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr6:54804969 C>T maps to NM_001010872.1 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:54805838 G>A maps to NM_001010872.1 R690R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr6:54806471 G>A maps to NM_001010872.1 E901E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr6:54805091 C>T maps to NM_001010872.1 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr6:54805092 C>T maps to NM_001010872.1 Q442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr6:54806757 C>T maps to NM_001010872.1 R997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:54805314 T>C maps to NM_001010872.1 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr20:33875156 C>T maps to NM_178468.4 E475E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr20:33876638 G>A maps to NM_178468.4 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr20:33879968 G>A maps to NM_178468.4 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr20:33879633 G>A maps to NM_178468.4 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr20:33874754 G>A maps to NM_178468.4 P609P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:33875402 G>A maps to NM_178468.4 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr20:33879594 C>T maps to NM_178468.4 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr20:33879630 C>T maps to NM_178468.4 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr20:33875225 G>A maps to NM_178468.4 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr20:33879674 G>A maps to NM_178468.4 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:33879666 C>T maps to NM_178468.4 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr20:33874910 G>A maps to NM_178468.4 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr20:33875197 G>A maps to NM_178468.4 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr20:33875228 G>A maps to NM_178468.4 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:37570693 C>T maps to NM_030919.2 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr20:37580265 C>T maps to NM_030919.2 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:37570693 C>T maps to NM_030919.2 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr20:37581057 G>A maps to NM_030919.2 R581R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr19:49104407 C>T maps to NM_017708.3 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:49104497 G>A maps to NM_017708.3 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:49104392 G>A maps to NM_017708.3 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:49106981 G>A maps to NM_017708.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:49107041 G>A maps to NM_017708.3 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr19:49106807 G>A maps to NM_017708.3 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:49116545 G>A maps to NM_017708.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:40417333 C>T maps to NM_138435.2 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr22:40417842 C>T maps to NM_138435.2 F443F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr22:40417710 G>A maps to NM_138435.2 K399K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr22:40417689 C>T maps to NM_138435.2 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:18907102 C>T maps to NM_001039999.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr17:18881397 C>T maps to NM_001039999.2 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr17:18881076 T>A maps to NM_001039999.2 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr17:18874995 T>A maps to NM_001039999.2 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr8:144808642 G>A maps to NM_198488.3 P996P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:144809115 G>A maps to NM_198488.3 Q839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr8:144810889 G>A maps to NM_198488.3 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr8:144808129 G>A maps to NM_198488.3 F1167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:144808843 G>A maps to NM_198488.3 P929P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr8:144810184 A>G maps to NM_198488.3 G482G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr8:144812587 G>A maps to NM_198488.3 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr8:144808444 G>A maps to NM_198488.3 P1062P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr8:144808129 G>A maps to NM_198488.3 F1167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr8:144810154 G>A maps to NM_198488.3 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr8:144812400 G>A maps to NM_198488.3 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:127569211 C>T maps to NM_174911.4 Q141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr16:5140542 G>A maps to NM_201400.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr16:5139113 C>A maps to NM_201400.2 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr16:5135647 C>G maps to NM_201400.2 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr16:5140226 A>G maps to NM_201400.2 N200N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:12042897 G>A maps to NM_001083537.1 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:12044026 C>T maps to NM_001083537.1 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:71507080 A>T maps to NM_018172.2 K94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:231155614 G>A maps to NM_198552.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr12:8376700 C>T maps to NM_018088.3 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr12:8374894 C>T maps to NM_018088.3 K306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:8374644 G>A maps to NM_018088.3 Q390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:8374675 G>A maps to NM_018088.3 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:8374906 C>T maps to NM_018088.3 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:8374816 T>C maps to NM_018088.3 Q332Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:8374534 C>T maps to NM_018088.3 Q426Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:8374825 C>T maps to NM_018088.3 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:8376721 C>T maps to NM_018088.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:8376068 G>A maps to NM_018088.3 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:8374540 G>A maps to NM_018088.3 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:8375250 T>A maps to NM_018088.3 K188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr8:124790921 C>T maps to NM_144963.2 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr8:124792265 C>T maps to NM_144963.2 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:124811842 C>T maps to NM_144963.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:124797889 C>T maps to NM_144963.2 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr8:124790912 G>A maps to NM_144963.2 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr8:124792283 C>T maps to NM_144963.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr8:124818422 C>T maps to NM_144963.2 S662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr16:85135861 G>A maps to ENST00000393246 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr16:85141472 T>G maps to ENST00000393246 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:33810710 G>A maps to ENST00000395190 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:38757491 C>T maps to NM_173611.2 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:38893810 G>A maps to NM_174905.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:8767067 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:8766515 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:8766189 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:8767045 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:8768136 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr23:8767099 T>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:8768128 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:8763147 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:8997362 T>A did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:9000382 C>T did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:9000488 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:8995991 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr23:13058953 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:13061896 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:13057998 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr23:13056598 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:89831326 G>A maps to NM_000135.2 R917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:89831327 G>A maps to NM_000135.2 F916F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr16:89809282 C>T maps to NM_000135.2 L1230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr16:89831399 G>A maps to NM_000135.2 S892S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:89831330 G>A maps to NM_000135.2 T915T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr16:89813021 C>T maps to NM_000135.2 T1161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:89805687 G>A maps to NM_000135.2 S1340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr16:89805561 C>T maps to NM_000135.2 R1382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:89858884 G>A maps to NM_000135.2 Y359Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:14868779 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:14863067 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr23:14871184 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:14861850 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:14862006 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:14868790 T>A did not map to a codon.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr23:14883217 C>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:14883543 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr9:98009752 A>G maps to NM_000136.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:10081488 C>T maps to NM_033084.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:10101994 G>A maps to NM_033084.3 V558V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr3:10106089 G>A maps to NM_033084.3 V666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr3:10128859 C>A maps to NM_033084.3 P1126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:10106107 G>A maps to NM_033084.3 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:10136909 C>T maps to NM_033084.3 T1330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:10142870 G>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr3:10136043 C>T maps to NM_033084.3 H1320H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:10081487 C>T maps to NM_033084.3 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:10088350 C>T maps to NM_033084.3 R408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr3:10084757 T>C maps to NM_033084.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:35425695 T>C maps to NM_021922.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr6:35423925 C>T maps to NM_021922.2 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:35428334 C>T maps to NM_021922.2 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr6:35434022 C>T maps to NM_021922.2 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:22646372 G>A maps to NM_022725.3 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr15:89820091 C>T maps to NM_001113378.1 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:89811690 C>T maps to NM_001113378.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr15:89837174 T>C maps to NM_001113378.1 S801S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr15:89848346 G>A maps to NM_001113378.1 E1020E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:58390195 C>T maps to NM_001114636.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr14:45645572 C>T maps to NM_020937.2 Q1206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr14:45645533 C>T maps to NM_020937.2 Q1193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:45618194 C>T maps to NM_020937.2 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:45618068 A>G maps to NM_020937.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr14:45628327 G>T maps to NM_020937.2 E476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr10:127693491 G>A maps to ENST00000368692 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr10:127677119 G>A maps to ENST00000368692 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr10:127697112 C>T maps to ENST00000368692 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr10:127686009 T>C maps to ENST00000368692 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:127668814 G>A maps to ENST00000368692 K33K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr2:163039978 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:163029329 G>A maps to NM_004460.2 F724F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:163070512 G>A maps to NM_004460.2 Q313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:163031386 C>T maps to NM_004460.2 W653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:163044758 A>C maps to NM_004460.2 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:163044740 G>A maps to NM_004460.2 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:163029329 G>A maps to NM_004460.2 F724F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:13736176 C>T maps to NM_032228.5 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:13729485 T>C maps to NM_032228.5 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:13749203 C>T maps to NM_032228.5 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr11:13736123 C>T maps to NM_032228.5 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr13:99042344 C>T maps to NM_005766.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr13:99047563 G>A maps to NM_005766.2 K416K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:99061619 C>T maps to NM_005766.2 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr13:99083331 C>T maps to NM_005766.2 A647A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr13:99047617 C>T maps to NM_005766.2 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr13:99037971 G>A maps to NM_005766.2 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr13:99037074 C>T maps to NM_005766.2 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr13:99042299 C>T maps to NM_005766.2 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:242396267 C>T maps to NM_014808.2 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:242373706 C>T maps to NM_014808.2 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr6:5613427 C>T maps to NM_006567.3 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr6:5545500 C>T maps to NM_006567.3 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr6:5404774 T>C maps to NM_006567.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:13035925 G>A maps to NM_004461.2 Q302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr19:13041107 C>T maps to NM_004461.2 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:13033638 G>A maps to NM_004461.2 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:13041247 G>A maps to NM_004461.2 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr2:223507585 G>A maps to NM_005687.3 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:90770294 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:90773984 C>T maps to NM_000043.3 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:90762814 C>T maps to NM_000043.3 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:90770528 G>A maps to NM_000043.3 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:172633472 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:172634973 C>T maps to NM_000639.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:172634990 G>A maps to NM_000639.1 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:172634991 A>T maps to NM_000639.1 K228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:172628556 G>A maps to NM_000639.1 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr1:172628635 C>T maps to NM_000639.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:172628355 C>T maps to NM_000639.1 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr17:80039492 G>A maps to NM_004104.4 A2130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:80047516 C>T maps to NM_004104.4 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:80053274 G>A maps to NM_004104.4 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:80039891 G>A maps to NM_004104.4 G2052G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:80038592 G>A maps to NM_004104.4 P2267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:80040271 G>A maps to NM_004104.4 L1980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr17:80041109 G>A maps to NM_004104.4 Q1845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:80041435 G>A maps to NM_004104.4 F1766F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:80046410 G>A maps to NM_004104.4 F816F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:80044324 G>A maps to NM_004104.4 P1179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:80048889 G>A maps to NM_004104.4 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr17:80045587 G>A maps to NM_004104.4 Q1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:170425746 G>A maps to NM_024622.3 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:170411656 C>T maps to NM_024622.3 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:170428487 G>A maps to NM_024622.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:207636625 C>T maps to NM_014929.3 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:207636625 C>T maps to NM_014929.3 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:207655358 C>T maps to NM_014929.3 F654F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr20:3128186 G>A maps to NM_021826.4 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:3129383 G>A maps to NM_021826.4 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:3127865 C>T maps to NM_021826.4 R617R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:3128798 G>A maps to NM_021826.4 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:3129116 G>A maps to NM_021826.4 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:187540263 G>A maps to ENST00000260147 F2495F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr4:187549869 A>T maps to ENST00000260147 S1457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:187521123 G>A maps to ENST00000260147 L4014L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:187628026 G>A maps to ENST00000260147 I985I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:187517877 G>A maps to ENST00000260147 S4275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr4:187524504 G>A maps to ENST00000260147 I3728I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:187534476 G>A maps to ENST00000260147 T3086T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr4:187509766 G>A maps to ENST00000260147 S4585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:187539950 G>A maps to ENST00000260147 R2600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:187521124 G>A maps to ENST00000260147 F4013F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:187531065 G>A maps to ENST00000260147 A3322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr4:187541982 G>A maps to ENST00000260147 T1922T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:187541874 G>A maps to ENST00000260147 S1958S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:187628026 G>A maps to ENST00000260147 I985I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr4:187629535 G>A maps to ENST00000260147 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr4:187535363 G>A maps to ENST00000260147 F3073F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr4:187541327 T>A maps to ENST00000260147 K2141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:187539894 G>A maps to ENST00000260147 V2618V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr4:187557861 G>A maps to ENST00000260147 P1283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr4:187535405 A>C maps to ENST00000260147 A3059A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:187554954 G>A maps to ENST00000260147 F1402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr4:187510312 G>A maps to ENST00000260147 F4403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr4:187524476 G>A maps to ENST00000260147 Q3738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr4:187524477 G>A maps to ENST00000260147 F3737F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:187509916 G>A maps to ENST00000260147 V4535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:187535465 G>A maps to ENST00000260147 V3039V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:187542684 G>A maps to ENST00000260147 F1688F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:187542888 G>A maps to ENST00000260147 G1620G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr4:187510252 G>A maps to ENST00000260147 I4423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:150914096 G>A maps to NM_001447.2 T3100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:150945465 G>A maps to NM_001447.2 A1009A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:150946443 G>A maps to NM_001447.2 I683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr5:150947934 G>A maps to NM_001447.2 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:150901481 G>A maps to NM_001447.2 R3558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:150901482 G>A maps to NM_001447.2 D3557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:150922865 A>G maps to NM_001447.2 L2608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:150924672 G>A maps to NM_001447.2 L2005L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:150946320 G>A maps to NM_001447.2 V724V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr5:150922488 C>T maps to NM_001447.2 E2733E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:150924777 C>T maps to NM_001447.2 Q1970Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:150945774 G>A maps to NM_001447.2 F906F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr5:150922724 G>A maps to NM_001447.2 Q2655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:150947742 G>A maps to NM_001447.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:150922196 G>A maps to NM_001447.2 Q2831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:150901329 G>A maps to NM_001447.2 T3608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:150946878 C>T maps to NM_001447.2 W538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:150923883 G>A maps to NM_001447.2 N2268N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:150935937 C>T maps to NM_001447.2 L1200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr5:150932927 C>A maps to NM_001447.2 G1322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr5:150885197 C>T maps to NM_001447.2 R4326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:150920163 G>A maps to NM_001447.2 V3001V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:150929030 G>A maps to NM_001447.2 F1538F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:150948209 G>A maps to NM_001447.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:150905409 G>A maps to NM_001447.2 F3475F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr11:92087983 G>A maps to ENST00000298047 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:92086159 G>A maps to ENST00000298047 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr11:92543180 C>T maps to ENST00000298047 V3140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr11:92086879 G>A maps to ENST00000298047 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:92600283 G>A maps to ENST00000298047 T4012T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:92523156 C>T maps to ENST00000298047 Q1462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:92615918 C>A maps to ENST00000298047 I4099I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:92495272 C>T maps to ENST00000298047 D1307D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr11:92616089 C>T maps to ENST00000298047 I4156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr11:92087932 C>T maps to ENST00000298047 I885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr11:92531998 C>T maps to ENST00000298047 T1940T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr11:92086819 G>A maps to ENST00000298047 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:92534137 C>T maps to ENST00000298047 I2653I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:92085898 C>T maps to ENST00000298047 H207H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:92599968 C>T maps to ENST00000298047 I3907I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:92600362 C>T maps to ENST00000298047 L4039L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:92613901 C>T maps to ENST00000298047 Q4045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr11:92531314 G>A maps to ENST00000298047 G1712G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr11:92087395 G>A maps to ENST00000298047 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:92534800 G>A maps to ENST00000298047 W2874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:92086694 C>T maps to ENST00000298047 Q473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:92523161 G>A maps to ENST00000298047 P1463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:92534971 G>A maps to ENST00000298047 G2931G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr11:92086159 G>A maps to ENST00000298047 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:92623990 C>T maps to ENST00000298047 L4494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr11:92258085 G>A maps to ENST00000298047 Q1193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr11:92087122 C>T maps to ENST00000298047 I615I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:92565151 G>A maps to ENST00000298047 G3282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr11:92086924 C>G maps to ENST00000298047 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:92577194 G>A maps to ENST00000298047 L3554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr11:92525956 C>T maps to ENST00000298047 R1546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr11:92085754 A>C maps to ENST00000298047 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:92257899 C>T maps to ENST00000298047 T1131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:92532832 C>T maps to ENST00000298047 I2218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:92534884 C>T maps to ENST00000298047 F2902F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:92087719 G>A maps to ENST00000298047 W814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr11:92531182 C>T maps to ENST00000298047 H1668H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr11:92532382 G>A maps to ENST00000298047 V2068V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr11:92086810 C>T maps to ENST00000298047 I511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:92533810 C>T maps to ENST00000298047 F2544F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:92543051 C>T maps to ENST00000298047 P3097P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr11:92564896 G>A maps to ENST00000298047 Q3197Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:92616260 C>T maps to ENST00000298047 R4213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:92532463 G>A maps to ENST00000298047 V2095V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:92532706 C>T maps to ENST00000298047 I2176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:92577104 G>A maps to ENST00000298047 K3524K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr11:92507291 C>T maps to ENST00000298047 S1427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:92085775 C>G maps to ENST00000298047 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:92577212 C>A maps to ENST00000298047 T3560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr11:92616152 G>A maps to ENST00000298047 K4177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr11:92623666 G>A maps to ENST00000298047 W4386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:92087641 C>T maps to ENST00000298047 P788P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr11:92531410 C>T maps to ENST00000298047 T1744T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr11:92088425 G>T maps to ENST00000298047 G1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr11:92600130 G>A maps to ENST00000298047 L3961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:92088436 G>A maps to ENST00000298047 K1053K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:92532484 G>A maps to ENST00000298047 L2102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:92086444 C>T maps to ENST00000298047 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:92087068 C>T maps to ENST00000298047 I597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:92087395 G>A maps to ENST00000298047 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:92088157 C>T maps to ENST00000298047 T960T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:92531164 C>T maps to ENST00000298047 T1662T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:92531887 G>A maps to ENST00000298047 L1903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:92564839 C>T maps to ENST00000298047 F3178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:92577686 G>A maps to ENST00000298047 L3718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:92600088 C>T maps to ENST00000298047 F3947F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:92600262 C>T maps to ENST00000298047 F4005F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:92616110 C>T maps to ENST00000298047 F4163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:92616311 C>T maps to ENST00000298047 V4230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:92623780 C>T maps to ENST00000298047 S4424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:92616290 G>A maps to ENST00000298047 Q4223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:92616344 C>T maps to ENST00000298047 F4241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr11:92533432 C>T maps to ENST00000298047 A2418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr11:92534371 G>A maps to ENST00000298047 R2731R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:92533039 C>T maps to ENST00000298047 F2287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:92523209 C>T maps to ENST00000298047 I1479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q3-06A-11D-A196-08 chr4:126371455 T>C maps to NM_024582.4 S3095S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr4:126237754 C>G maps to NM_024582.4 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr4:126328138 G>A maps to NM_024582.4 R1804R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr4:126371308 C>T maps to NM_024582.4 S3046S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr4:126411860 C>T maps to NM_024582.4 I4628I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:126328291 C>T maps to NM_024582.4 I1855I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr4:126240823 T>G maps to NM_024582.4 V1086V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr4:126371770 C>T maps to NM_024582.4 F3200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr4:126411725 C>T maps to NM_024582.4 I4583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr4:126329777 C>T maps to NM_024582.4 R1917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr4:126411725 C>T maps to NM_024582.4 I4583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr4:126408630 A>C maps to NM_024582.4 T4316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:126319955 G>A maps to NM_024582.4 Q1731Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:126242681 C>T maps to NM_024582.4 L1706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr4:126239234 C>T maps to NM_024582.4 Q557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr4:126372502 C>T maps to NM_024582.4 I3444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr4:126336327 C>T maps to NM_024582.4 F2070F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:126411404 G>A maps to NM_024582.4 G4476G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:126373564 G>A maps to NM_024582.4 V3798V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr4:126373735 G>A maps to NM_024582.4 A3855A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:126239486 T>C maps to NM_024582.4 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:126389872 A>T maps to NM_024582.4 R4036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:126412031 C>T maps to NM_024582.4 S4685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:126369769 A>G maps to NM_024582.4 E2533E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:126371902 C>T maps to NM_024582.4 D3244D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:126372883 G>A maps to NM_024582.4 E3571E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:126370700 C>T maps to NM_024582.4 R2844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:126372578 C>T maps to NM_024582.4 R3470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:126372844 C>T maps to NM_024582.4 F3558F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:126373645 C>T maps to NM_024582.4 S3825S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:126401003 G>A maps to NM_024582.4 G4194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:126329692 C>T maps to NM_024582.4 I1888I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:126411284 G>A maps to NM_024582.4 Q4436Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr4:126370045 A>G maps to NM_024582.4 Q2625Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr4:126373918 G>A maps to NM_024582.4 Q3916Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:126239213 C>T maps to NM_024582.4 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:126241933 C>T maps to NM_024582.4 S1456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:126411356 G>A maps to NM_024582.4 R4460R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr4:126369631 G>A maps to NM_024582.4 A2487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:126336807 G>A maps to NM_024582.4 Q2230Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:126411232 G>A maps to NM_024582.4 W4419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:126411536 C>T maps to NM_024582.4 V4520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:126389778 G>A maps to NM_024582.4 T4004T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr4:126367456 C>T maps to NM_024582.4 I2401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:126241798 G>A maps to NM_024582.4 R1411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr4:126239527 C>T maps to NM_024582.4 F654F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr4:126238441 G>A maps to NM_024582.4 E292E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr4:126412766 G>A maps to NM_024582.4 W4930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr4:126239461 C>T maps to NM_024582.4 F632F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:126242290 C>T maps to NM_024582.4 F1575F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr4:126371323 G>A maps to NM_024582.4 L3051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr4:126370108 C>T maps to NM_024582.4 F2646F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr4:126411605 G>A maps to NM_024582.4 P4543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr4:126371362 G>A maps to NM_024582.4 K3064K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr4:126372791 C>T maps to NM_024582.4 Q3541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr4:126369721 A>T maps to NM_024582.4 P2517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr4:126372958 C>T maps to NM_024582.4 S3596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:126411746 C>T maps to NM_024582.4 Y4590Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr4:126372220 G>A maps to NM_024582.4 K3350K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr4:126370909 C>T maps to NM_024582.4 S2913S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr4:126329749 A>G maps to NM_024582.4 E1907E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:126241006 G>A maps to NM_024582.4 E1147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:126242398 G>A maps to NM_024582.4 R1611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:126328048 C>T maps to NM_024582.4 L1774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:126328132 G>A maps to NM_024582.4 L1802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:126370369 G>A maps to NM_024582.4 R2733R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:126372172 C>T maps to NM_024582.4 H3334H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:126373564 G>A maps to NM_024582.4 V3798V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:126370108 C>T maps to NM_024582.4 F2646F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:126411608 G>A maps to NM_024582.4 K4544K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr4:126411404 G>A maps to NM_024582.4 G4476G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr4:126240610 C>T maps to NM_024582.4 F1015F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr4:126336846 C>T maps to NM_024582.4 S2243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr4:126371309 C>T maps to NM_024582.4 L3047L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:150889962 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr23:150889961 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr23:150889961 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:150885772 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr23:150889962 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:150889962 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:150885783 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:150889903 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:150891135 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:150891176 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr17:73913920 C>T maps to ENST00000389570 E785E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:73921465 G>A maps to ENST00000389570 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:73923613 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:73908302 C>T maps to ENST00000389570 R1097R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr17:73908359 A>G maps to ENST00000389570 R1078R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr17:73914147 G>A maps to ENST00000389570 S736S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:73924190 C>T maps to ENST00000389570 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:73916501 G>A maps to ENST00000389570 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr17:73919478 G>A maps to ENST00000389570 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:40331416 G>A maps to NM_001436.3 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:40328402 G>A maps to NM_001436.3 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:16101276 G>A maps to NM_017556.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:16091720 C>T maps to NM_017556.2 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:16095057 C>T maps to NM_017556.2 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:16091591 G>A maps to NM_017556.2 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:16103736 C>T maps to NM_017556.2 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr22:45929725 G>A maps to ENST00000348697 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr22:45996278 C>T maps to ENST00000348697 R689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr22:45923825 C>T maps to ENST00000348697 Q141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr22:45959037 C>T maps to ENST00000402984 V686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:45938071 G>A maps to ENST00000348697 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:45923762 C>T maps to ENST00000348697 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:45946459 C>T maps to ENST00000348697 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr3:13679061 G>A maps to NM_001165035.1 T1113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:13670697 C>T maps to NM_001165035.1 C916C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:13660509 C>T maps to NM_001165035.1 T682T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:13659747 C>T maps to NM_001165035.1 G634G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr3:13660446 G>A maps to NM_001165035.1 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr3:13679061 G>A maps to NM_001165035.1 T1113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr3:13679196 C>T maps to NM_001165035.1 A1158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:13678032 C>T maps to NM_001165035.1 F1101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr3:13663296 T>G maps to NM_001165035.1 G726G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr14:92336645 G>A maps to ENST00000267620 I520I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr14:92349319 C>T maps to ENST00000267620 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:92343866 G>A maps to ENST00000267620 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr14:92336627 G>A maps to ENST00000267620 I526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:92403440 G>A maps to ENST00000267620 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr14:92413554 A>T did not map to a codon.
Sequencing variant TCGA-ER-A3ES-06A-11D-A20D-08 chr14:92361348 G>A maps to ENST00000267620 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:92347739 C>T maps to ENST00000267620 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:92353615 G>A maps to ENST00000267620 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:92343974 G>A maps to ENST00000267620 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr2:112942829 C>T maps to NM_153214.2 C287C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:112944800 C>T maps to NM_153214.2 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr2:112944962 G>A maps to NM_153214.2 Q400Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:112940464 C>A maps to NM_153214.2 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:112922659 C>T maps to NM_153214.2 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:112944887 C>T maps to NM_153214.2 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr15:48766500 G>A maps to NM_000138.4 Y1387Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr15:48807692 G>A maps to NM_000138.4 C453C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:48704768 G>A maps to NM_000138.4 I2741I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:48703269 G>A maps to NM_000138.4 L2845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:48760185 G>A maps to NM_000138.4 L1566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:48738927 G>A maps to NM_000138.4 I1921I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr15:48756171 A>G maps to NM_000138.4 C1663C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr15:48788333 C>T maps to NM_000138.4 K794K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr15:48719794 G>A maps to NM_000138.4 P2391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:48744864 C>T maps to NM_000138.4 Q1813Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:48704768 G>A maps to NM_000138.4 I2741I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:48718056 G>A maps to NM_000138.4 I2403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr15:48713791 C>T maps to NM_000138.4 R2554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr15:48808425 G>A maps to NM_000138.4 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr15:48782255 G>A maps to NM_000138.4 C958C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr15:48807599 G>A maps to NM_000138.4 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:48718017 C>T maps to NM_000138.4 G2416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr15:48797303 C>T maps to NM_000138.4 G626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr15:48719890 G>T maps to NM_000138.4 T2359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:48764778 G>A maps to NM_000138.4 F1435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:48797261 G>A maps to NM_000138.4 F640F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:48782180 G>A maps to NM_000138.4 S983S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr5:127730893 C>T maps to NM_001999.3 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr5:127626457 C>T maps to NM_001999.3 G2137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr5:127654672 G>A maps to NM_001999.3 Q1498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr5:127730893 C>T maps to NM_001999.3 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:127730908 G>A maps to NM_001999.3 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr5:127599331 G>A maps to NM_001999.3 S2659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:127730908 G>A maps to NM_001999.3 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:127674733 A>T maps to NM_001999.3 I1121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:127686623 C>T maps to NM_001999.3 L916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:127674667 G>A maps to NM_001999.3 F1143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr5:127730851 G>A maps to NM_001999.3 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:127674736 C>T maps to NM_001999.3 R1120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:127681178 G>A maps to NM_001999.3 V1029V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:127595311 C>G maps to NM_001999.3 T2858T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:127613668 G>A maps to NM_001999.3 N2458N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:127622431 C>T maps to NM_001999.3 R2330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:127623021 C>T maps to NM_001999.3 R2286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:127855038 C>T maps to NM_001999.3 Q185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr19:8153022 C>T maps to NM_032447.3 G2139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr19:8176870 G>A maps to NM_032447.3 F1317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:8194178 G>A maps to NM_032447.3 Y705Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:8130904 C>T maps to NM_032447.3 E2776E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:8175828 C>T maps to NM_032447.3 G1411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:8154823 G>A maps to NM_032447.3 C2068C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr19:8193921 C>T maps to NM_032447.3 E762E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr19:8176005 G>A maps to NM_032447.3 P1382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:8152826 G>A maps to NM_032447.3 I2167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:8146338 G>A maps to NM_032447.3 P2413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:8188378 G>A maps to NM_032447.3 F1017F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:8176550 C>T maps to NM_032447.3 G1355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:8188869 G>A maps to NM_032447.3 F918F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr19:8188692 G>A maps to NM_032447.3 F977F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr19:8174213 G>A maps to NM_032447.3 S1505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:8176035 G>A maps to NM_032447.3 L1372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr19:8206851 G>A maps to NM_032447.3 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:8131009 G>A maps to NM_032447.3 I2741I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:8176654 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:8188892 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:8194187 C>T maps to NM_032447.3 R702R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:8154796 G>A maps to NM_032447.3 G2077G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:8131006 G>A maps to NM_032447.3 V2742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr19:8190869 G>A maps to NM_032447.3 V879V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:8137015 G>A maps to NM_032447.3 L2668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:8154838 G>A maps to NM_032447.3 A2063A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:8188378 G>A maps to NM_032447.3 F1017F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:8146320 G>A maps to NM_032447.3 L2419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:8176915 C>T maps to NM_032447.3 G1302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:8175972 A>G maps to NM_032447.3 F1393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:8175828 C>T maps to NM_032447.3 G1411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:8156382 G>A maps to NM_032447.3 G1999G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr19:8190878 G>A maps to NM_032447.3 F876F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:8156469 G>A maps to NM_032447.3 I1970I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:8130985 G>A maps to NM_032447.3 F2749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:8146260 C>T maps to NM_032447.3 E2439E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:8152009 G>A maps to NM_032447.3 V2235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:8176870 G>A maps to NM_032447.3 F1317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:8180456 G>A maps to NM_032447.3 S1260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:8181591 G>A maps to NM_032447.3 G1226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:8188818 C>T maps to NM_032447.3 R935R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:8200926 G>A maps to NM_032447.3 G503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:8206854 G>A maps to NM_032447.3 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr19:8181639 G>A maps to NM_032447.3 G1210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr19:8165821 C>T maps to NM_032447.3 P1708P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr19:8146296 G>A maps to NM_032447.3 F2427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr19:8194142 G>A maps to NM_032447.3 A717A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr9:97365737 C>T maps to NM_001127628.1 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr9:97382634 G>T maps to NM_001127628.1 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr9:97369102 G>A maps to NM_001127628.1 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr9:97365779 C>T maps to NM_001127628.1 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr9:97329557 G>A maps to NM_003837.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr9:97321384 C>T maps to NM_003837.2 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:97329620 C>T maps to NM_003837.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:97355968 G>A maps to NM_003837.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr16:30679962 C>T maps to ENST00000356166 F719F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:30676391 C>T maps to ENST00000356166 R534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:30680788 C>T maps to ENST00000356166 H922H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr16:30677846 C>T maps to ENST00000356166 F596F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:30680857 C>T maps to ENST00000356166 L945L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:9921727 G>A maps to NM_017703.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:9922060 G>A maps to NM_017703.1 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr7:102518845 C>T maps to NM_145032.3 R480R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr7:102665602 G>A maps to NM_145032.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:102604100 G>A maps to NM_145032.3 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:102495289 G>T maps to NM_145032.3 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:102669158 G>A maps to NM_145032.3 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr7:102667979 G>A maps to NM_145032.3 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:1675931 C>T maps to NM_152441.2 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr12:1675964 C>T maps to NM_152441.2 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr12:1702392 G>A maps to NM_152441.2 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:745560 C>T maps to NM_153350.3 K332K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:746787 C>T maps to NM_153350.3 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:747066 C>T maps to NM_153350.3 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:5540753 G>A maps to ENST00000312577 C382C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:5540960 G>A maps to ENST00000312577 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:5541074 C>T maps to ENST00000312577 E275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr7:5545150 G>A maps to ENST00000312577 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr7:5540381 G>A maps to ENST00000312577 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:5540285 G>A maps to ENST00000312577 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:5545194 G>A maps to ENST00000312577 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr7:5540213 G>A maps to ENST00000312577 S562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr16:30958425 C>T maps to NM_001099784.2 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr16:30958126 C>T maps to NM_001099784.2 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr16:30941554 G>A maps to NM_001099784.2 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr3:33400834 C>T maps to NM_012157.3 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr17:37441795 G>A maps to NM_032875.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr15:63893548 G>A maps to NM_203373.2 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr13:77581759 G>A maps to NM_012158.2 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr6:99374369 A>G maps to NM_012160.3 N165N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:99347335 G>A maps to NM_012160.3 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:15640310 G>A maps to NM_012161.3 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:15607371 G>A maps to NM_012161.3 R684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr8:145579874 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:145580113 G>A maps to NM_012162.1 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr5:15928107 C>T maps to NM_012304.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr5:15936667 C>T maps to NM_012304.3 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr5:15928473 C>T maps to NM_012304.3 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr5:15936880 C>T maps to NM_012304.3 Y354Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:15928221 C>T maps to NM_012304.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr5:15928185 C>T maps to NM_012304.3 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr5:15936847 G>A maps to NM_012304.3 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr5:15936871 C>T maps to NM_012304.3 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:15928545 C>T maps to NM_012304.3 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:15936778 G>A maps to NM_012304.3 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:15936889 C>T maps to NM_012304.3 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:15937162 C>T maps to NM_012304.3 I448I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr5:15936667 C>T maps to NM_012304.3 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr16:67197713 C>A maps to NM_018378.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr9:37537331 G>A maps to NM_012166.2 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr9:37515908 G>A maps to NM_012166.2 F896F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr9:37522953 G>A maps to NM_012166.2 Q600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr9:37537214 G>A maps to NM_012166.2 F437F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:37518343 C>T maps to NM_012166.2 Q764Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:37515998 G>A maps to NM_012166.2 I866I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr9:37521706 G>A maps to NM_012166.2 R687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:48066044 A>G maps to NM_001190274.1 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr2:48050433 A>G maps to NM_001190274.1 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:48036846 C>G did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr18:71797880 G>A maps to NM_001142958.1 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:71740869 G>C maps to NM_001142958.1 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr8:28309981 C>T maps to NM_172366.2 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr10:5948021 C>T maps to NM_032807.3 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr10:5937085 C>T maps to NM_032807.3 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr10:5950914 C>T maps to NM_032807.3 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr10:5953046 G>T maps to NM_032807.3 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:5963507 C>T maps to NM_032807.3 F817F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:5979146 C>T maps to NM_032807.3 F1063F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:5956153 C>T maps to NM_032807.3 Q491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr10:5979200 C>T maps to NM_032807.3 I1081I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:11709882 C>T maps to NM_012168.4 W190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:117612501 G>A maps to NM_033624.2 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr12:117595802 C>T maps to NM_033624.2 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr7:100189320 A>T maps to NM_012172.4 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:100187819 C>T maps to NM_012172.4 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:100187893 G>A maps to NM_012172.4 W117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:100187601 G>A maps to NM_012172.4 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr7:100198503 C>T maps to NM_012172.4 P613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr7:100198503 C>T maps to NM_012172.4 P613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:100198467 G>C maps to NM_012172.4 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:100198449 G>A maps to NM_012172.4 W595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:100189428 C>T maps to NM_012172.4 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:100189521 G>A maps to NM_012172.4 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:100190593 C>T maps to NM_012172.4 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:100197700 C>T maps to NM_012172.4 H456H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:385682 C>T maps to NM_183421.1 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr8:400072 C>T maps to NM_183421.1 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A6L9-06A-11D-A32N-08 chr8:401278 C>T maps to NM_183421.1 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr19:39517596 T>C maps to NM_178820.3 Q207Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr19:39516071 G>A maps to NM_178820.3 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr19:39517560 G>A maps to NM_178820.3 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:39516071 G>A maps to NM_178820.3 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr11:33777441 G>A maps to NM_012175.3 Q185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:33790445 G>A maps to NM_012175.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:33768801 T>C maps to NM_012175.3 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr11:33795989 G>A maps to NM_012175.3 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:146121322 G>T maps to NM_032145.4 I719I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:146127184 T>C maps to NM_032145.4 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr6:146127121 G>A maps to NM_032145.4 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr6:146127255 G>A maps to NM_032145.4 R96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr16:87367778 G>A maps to NM_024735.3 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr16:87367550 G>A maps to NM_024735.3 F446F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr16:87364905 G>A maps to NM_024735.3 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:124553242 G>A maps to NM_058229.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:124553146 G>A maps to NM_058229.2 D36D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr14:39870724 G>A maps to NM_203301.3 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:55818526 C>T maps to NM_152231.1 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr14:55818781 C>T maps to NM_152231.1 F558F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr2:230875488 G>A maps to NM_174899.4 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:230861575 C>T maps to NM_174899.4 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:230875579 C>T maps to NM_174899.4 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:147806818 C>T maps to NM_205836.1 S654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr5:147796733 C>T maps to NM_205836.1 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr5:147820745 C>T maps to NM_205836.1 R1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:147803582 C>T maps to NM_205836.1 I547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr17:6683580 C>T maps to NM_153230.2 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr17:6684089 C>T maps to NM_153230.2 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr17:6683756 G>A maps to NM_153230.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:6684059 G>A maps to NM_153230.2 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:6683894 C>T maps to NM_153230.2 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:6690202 C>T maps to NM_153230.2 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:6683990 C>T maps to NM_153230.2 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:6684050 C>T maps to NM_153230.2 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr17:6684107 G>A maps to NM_153230.2 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:6683601 C>T maps to NM_153230.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:6683531 C>T maps to NM_153230.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:41941381 G>T maps to NM_012176.2 *388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr5:41934070 C>T maps to NM_012176.2 Q224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr3:121342138 G>A maps to NM_016298.3 W621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr3:121340281 G>A maps to NM_016298.3 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr3:121340572 G>A maps to NM_016298.3 W99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr3:121340542 C>T maps to NM_016298.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr3:121341092 C>T maps to NM_016298.3 Q273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:121341139 C>T maps to NM_016298.3 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:121340368 C>T maps to NM_016298.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr3:121340281 G>A maps to NM_016298.3 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:121345645 G>A maps to NM_016298.3 E673E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:121340650 G>A maps to NM_016298.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr3:121345714 C>T maps to NM_016298.3 V696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:121340446 C>T maps to NM_016298.3 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:121341092 C>T maps to NM_016298.3 Q273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:121341814 C>T maps to NM_016298.3 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr3:121341739 C>T maps to NM_016298.3 F488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr2:73493767 C>T maps to ENST00000295133 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:73491468 G>A maps to ENST00000295133 F642F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:73490897 G>A maps to ENST00000295133 I722I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:16577614 G>A maps to NM_018994.1 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr8:101153269 G>A maps to NM_001029860.3 H404H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr8:101146505 C>T maps to NM_001029860.3 R587R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr8:101153890 A>G maps to NM_001029860.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr8:101153415 G>A maps to NM_001029860.3 Q356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:11716078 C>T maps to ENST00000376768 Q63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:11718435 C>T maps to NM_033182.5 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:196304364 C>T maps to NM_001105573.1 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:46215700 G>A maps to NM_001080469.1 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr19:46215196 C>T maps to NM_001080469.1 W519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr19:46215197 C>T maps to NM_001080469.1 W519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:37118295 C>T maps to NM_001008777.2 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr17:37101345 C>T maps to NM_001008777.2 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:68691400 G>A maps to NM_001024680.1 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr6:153296352 G>A maps to NM_012177.3 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr22:32887121 C>G maps to NM_012179.3 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:32889264 C>T maps to NM_012179.3 R381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr22:32894165 C>T maps to NM_012179.3 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr4:175184101 G>A maps to NM_012180.2 Q48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:175184039 G>A maps to NM_012180.2 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr17:18682421 G>A maps to ENST00000395665 V990V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr17:18675802 G>A maps to ENST00000395665 T695T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr17:18654335 G>A maps to ENST00000395665 V364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:18675802 G>A maps to ENST00000395665 T695T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:18668093 C>T maps to ENST00000395665 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:18671986 C>T maps to ENST00000395665 P615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:171337700 C>T maps to NM_012300.2 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:171299924 G>A maps to NM_012300.2 Q410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr5:171327048 A>G maps to NM_012300.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:48419919 G>A maps to NM_207102.2 W173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr3:48415088 G>A maps to NM_207102.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:48414337 G>A maps to NM_207102.2 Q27Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:48423241 G>A maps to NM_207102.2 W346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr9:123550194 C>T maps to NM_012164.3 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr10:103433372 G>A maps to ENST00000331272 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:103371485 G>A maps to ENST00000331272 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:103433354 G>A maps to ENST00000331272 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr10:103433354 G>A maps to ENST00000331272 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:103433320 G>A maps to ENST00000331272 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:103433354 G>A maps to ENST00000331272 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:139835911 G>A maps to NM_018998.2 Y416Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr9:139836503 G>A maps to NM_018998.2 Q364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr4:153332597 G>A maps to NM_033632.2 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr4:153332597 G>A maps to NM_033632.2 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr4:153247169 G>C maps to NM_033632.2 V544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U9-06A-11D-A32N-08 chr4:153253808 A>T maps to NM_033632.2 C308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:117462047 C>T maps to NM_153348.2 I488I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr12:117465252 G>A maps to NM_153348.2 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr12:117402561 C>T maps to NM_153348.2 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:117462068 C>A maps to NM_153348.2 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:117462069 C>T maps to NM_153348.2 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr12:117383326 C>T maps to NM_153348.2 N194N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr19:12800922 G>A maps to ENST00000380339 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:12800062 G>A maps to ENST00000380339 D478D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:12800360 G>A maps to ENST00000380339 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:12802013 G>A maps to ENST00000380339 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr1:207135759 C>T maps to NM_001170631.1 W150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:207131961 G>A maps to NM_001170631.1 Q545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:207133108 G>A maps to NM_001170631.1 T496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:207143430 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr19:55401051 C>T maps to NM_002000.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:55399689 C>T maps to NM_133279.2 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:55396830 C>T maps to NM_002000.2 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:55396926 G>A maps to NM_002000.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:55401078 C>T maps to NM_002000.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:55399440 C>T maps to NM_002000.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:55401048 G>A maps to NM_002000.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr19:55401097 C>T maps to NM_002000.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:55399626 C>T maps to NM_002000.2 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr19:55396920 G>A maps to NM_002000.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:55401168 G>A maps to NM_002000.2 W268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:159273742 G>A maps to ENST00000368115 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:159277547 G>A maps to ENST00000368115 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:159273775 G>A maps to ENST00000368115 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:159275793 G>A maps to ENST00000368115 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:159277646 C>T maps to ENST00000368115 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr1:159277547 G>A maps to ENST00000368115 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:159275791 C>T maps to ENST00000368115 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:159273799 G>A maps to ENST00000368115 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr1:159272174 C>T maps to ENST00000368115 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr1:159273753 G>A maps to ENST00000368115 W41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:159275793 G>A maps to ENST00000368115 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:159272207 C>T maps to ENST00000368115 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:159275787 C>T maps to ENST00000368115 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr1:159277709 C>T maps to ENST00000368115 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr19:7755381 G>A maps to NM_002002.4 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:7754150 C>T maps to NM_002002.4 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:7755309 G>A maps to NM_002002.4 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:7761753 C>T maps to NM_002002.4 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr19:7763657 C>T maps to NM_002002.4 W35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr14:75200789 C>T maps to NM_015962.4 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr14:75200808 C>A maps to NM_015962.4 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr14:75200843 A>G maps to NM_015962.4 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr19:40354370 C>T maps to NM_003890.2 G5366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr19:40408527 C>T maps to NM_003890.2 G1437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:40395961 G>A maps to NM_003890.2 L2479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr19:40430373 G>A maps to NM_003890.2 R523R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr19:40421208 C>T maps to NM_003890.2 R904R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr19:40405987 G>A maps to NM_003890.2 Q1620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:40354370 C>T maps to NM_003890.2 G5366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:40433641 G>A maps to NM_003890.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr19:40368657 G>A maps to NM_003890.2 F4230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:40384075 G>A maps to NM_003890.2 A3178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:40419768 G>A maps to NM_003890.2 F1075F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr19:40398384 G>A maps to NM_003890.2 F2194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr19:40424009 C>T maps to NM_003890.2 S731S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:40354137 T>C did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:40357469 G>A maps to NM_003890.2 V5281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr19:40433425 C>T maps to NM_003890.2 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr19:40433467 G>A maps to NM_003890.2 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:40368399 C>T maps to NM_003890.2 G4316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:40398330 C>T maps to NM_003890.2 G2212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:40420092 C>T maps to NM_003890.2 R967R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:40397973 G>A maps to NM_003890.2 D2331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:40433119 C>T maps to NM_003890.2 W383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr19:40384162 G>A maps to NM_003890.2 I3149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:40424300 C>T maps to NM_003890.2 V634V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr19:40395989 G>A maps to NM_003890.2 F2469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:40430451 C>T maps to NM_003890.2 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr19:40424417 C>T maps to NM_003890.2 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:40395812 C>T maps to NM_003890.2 W2528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:40364280 T>A maps to NM_003890.2 V4787V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:40368804 C>T maps to NM_003890.2 S4181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:40357523 G>A maps to NM_003890.2 S5263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr19:40364435 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:40368474 G>A maps to NM_003890.2 F4291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:40419942 C>T maps to NM_003890.2 R1017R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr19:40357496 G>A maps to NM_003890.2 I5272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr19:40362949 C>T maps to NM_003890.2 E5040E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr19:40398330 C>T maps to NM_003890.2 G2212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:40408553 G>A maps to NM_003890.2 L1429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:40408593 G>A maps to NM_003890.2 F1415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:40424150 G>A maps to NM_003890.2 F684F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:40424183 G>A maps to NM_003890.2 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:40399430 G>A maps to NM_003890.2 F2088F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr19:40421286 C>T maps to NM_003890.2 R878R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:40392520 G>A maps to NM_003890.2 F2661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr19:40398009 G>A maps to NM_003890.2 A2319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:40408082 G>A maps to NM_003890.2 S1546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:40434208 C>T maps to NM_003890.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr19:40408028 C>T maps to NM_003890.2 E1564E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:40384060 G>C maps to NM_003890.2 P3183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr19:40433353 G>A maps to NM_003890.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:40363204 C>T maps to NM_003890.2 Q4955Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr19:40397967 A>T maps to NM_003890.2 C2333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr19:40362889 G>A maps to NM_003890.2 F5060F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:40357748 G>A maps to NM_003890.2 S5188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:40362802 G>A maps to NM_003890.2 F5089F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:40362892 G>A maps to NM_003890.2 P5059P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:40363884 C>T maps to NM_003890.2 V4919V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:40364091 G>A maps to NM_003890.2 A4850A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:40368831 C>T maps to NM_003890.2 G4172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:40392511 G>A maps to NM_003890.2 L2664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:40412183 G>A maps to NM_003890.2 G1148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:40368657 G>A maps to NM_003890.2 F4230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:40411742 C>T maps to NM_003890.2 Q1295Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:40421496 G>A maps to NM_003890.2 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:120930273 G>A maps to NM_001017986.2 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr1:161476236 C>T maps to NM_001136219.1 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:161476157 C>T maps to NM_001136219.1 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:161476145 G>A maps to NM_001136219.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:161642804 G>A maps to NM_004001.4 E144E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:161518304 G>A maps to NM_000569.6 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:161514503 G>A maps to NM_000569.6 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr1:161514742 G>A maps to NM_000569.6 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:161518409 C>T maps to NM_000569.6 K76K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr1:161512966 T>A maps to NM_000569.6 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:161518460 G>A maps to NM_000569.6 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:161599661 G>A maps to ENST00000367964 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:161594379 G>A maps to ENST00000367964 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:161594379 G>A maps to ENST00000367964 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:161595947 G>A maps to ENST00000367964 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:50017666 C>T maps to NM_004107.4 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:17875219 G>A maps to NM_015122.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:17888969 G>A maps to NM_015122.2 E428E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr19:17881370 G>A maps to NM_015122.2 Q158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:17892524 C>T maps to NM_015122.2 V611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:17892611 C>T maps to NM_015122.2 F640F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr19:17895688 G>T maps to NM_015122.2 V794V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr19:17865972 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr5:72370606 C>T maps to NM_138782.2 Q540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:72348219 G>A maps to NM_138782.2 K353K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:72333012 C>T maps to NM_138782.2 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr5:72337117 G>A maps to NM_138782.2 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr5:141028736 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:141028538 C>T maps to ENST00000354789 Q188Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:141023973 G>A maps to ENST00000354789 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:141029032 G>A maps to ENST00000354789 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:72549865 C>T maps to ENST00000409314 K755K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:72579047 G>A maps to ENST00000409314 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:72695195 G>A maps to ENST00000409314 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:72560919 G>T maps to ENST00000409314 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr9:137808302 C>T maps to NM_002003.3 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:137806234 C>T maps to NM_002003.3 E101E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr9:137806246 C>T maps to NM_002003.3 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr9:137803075 C>T maps to NM_002003.3 E212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr9:137779164 G>A maps to NM_004108.2 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr9:137777098 A>T maps to NM_004108.2 K106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr9:137777100 G>A maps to NM_004108.2 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr9:137778322 C>T maps to NM_004108.2 Q203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr9:137774390 G>T maps to NM_004108.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:137779020 C>T maps to NM_004108.2 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr9:137779203 G>A maps to NM_004108.2 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:137777708 G>A maps to NM_004108.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:137772723 C>T maps to NM_004108.2 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr1:27700471 G>A maps to NM_003665.2 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:27697463 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr1:157765930 C>T maps to NM_052938.4 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:157789803 C>T maps to NM_052938.4 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:157771831 C>T maps to NM_052938.4 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr1:157771849 G>A maps to NM_052938.4 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:157773788 G>A maps to NM_052938.4 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:157789803 C>T maps to NM_052938.4 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr1:157772443 G>A maps to NM_052938.4 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:157773773 G>A maps to NM_052938.4 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:157773773 G>A maps to NM_052938.4 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:157766890 C>T maps to NM_052938.4 K406K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr1:157771746 G>A maps to NM_052938.4 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr1:157771747 G>A maps to NM_052938.4 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:157773722 C>T maps to NM_052938.4 W77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:157772380 G>A maps to NM_052938.4 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:157773656 C>T maps to NM_052938.4 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:157768002 G>A maps to NM_052938.4 F354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:157772374 G>A maps to NM_052938.4 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr1:157740250 T>C maps to NM_030764.3 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:157740217 T>A maps to NM_030764.3 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:157739826 G>A maps to NM_030764.3 Q142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:157667644 C>T maps to NM_052939.3 Q121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:157665917 C>T maps to NM_052939.3 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:157665296 G>A maps to NM_052939.3 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:157665254 C>T maps to NM_052939.3 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:157660297 G>A maps to NM_052939.3 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:157666085 G>A maps to NM_052939.3 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr1:157660219 C>T maps to NM_052939.3 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr1:157665254 C>T maps to NM_052939.3 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr1:157650537 C>T maps to NM_052939.3 P660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:157666951 C>T maps to NM_052939.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:157659642 G>A maps to NM_052939.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:157667106 G>A maps to NM_052939.3 Q223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:157667560 G>A maps to NM_052939.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:157667020 C>T maps to NM_052939.3 W251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:157548297 C>T maps to NM_031282.2 E465E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr1:157556183 C>T maps to NM_031282.2 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr1:157548608 G>A maps to NM_031282.2 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:157548632 G>A maps to NM_031282.2 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:157556240 G>A maps to NM_031282.2 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:157556093 C>T maps to NM_031282.2 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr1:157556084 A>C maps to NM_031282.2 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:157557225 G>A maps to NM_031282.2 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr1:157556141 C>T maps to NM_031282.2 G317G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-FS-A1ZS-06A-12D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr1:157557754 G>A maps to NM_031282.2 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:157557279 G>A maps to NM_031282.2 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:157497578 G>A maps to NM_031281.2 I596I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:157516943 G>A maps to NM_031281.2 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr1:157514166 C>T maps to NM_031281.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:157488243 G>A maps to NM_031281.2 I929I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:157514088 G>A maps to NM_031281.2 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr1:157504540 C>T maps to NM_031281.2 W515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:157504473 C>T maps to NM_031281.2 G537G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr1:157494240 G>A maps to NM_031281.2 I689I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:157494246 G>A maps to NM_031281.2 S687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:157494240 G>A maps to NM_031281.2 I689I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:157514283 C>T maps to NM_031281.2 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:157514298 G>A maps to NM_031281.2 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:157490867 G>A maps to NM_031281.2 S818S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr1:157514088 G>A maps to NM_031281.2 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:157514229 G>A maps to NM_031281.2 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:157514160 G>A maps to NM_031281.2 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr1:157514861 G>A maps to NM_031281.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:157485637 C>T maps to NM_031281.2 R946R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:157494321 G>A maps to NM_031281.2 T662T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:157497641 G>A maps to NM_031281.2 A575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:157497542 C>T maps to NM_031281.2 G608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:157516850 C>T maps to NM_031281.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:157516807 G>A maps to NM_031281.2 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:157516817 G>A maps to NM_031281.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:157516961 G>A maps to NM_031281.2 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:159778211 G>A maps to NM_001004310.2 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:159779411 C>T maps to NM_001004310.2 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:159778040 G>A maps to NM_001004310.2 W42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr1:159779288 C>T maps to NM_001004310.2 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr1:159785420 C>T maps to NM_001004310.2 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:159779366 C>T maps to NM_001004310.2 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:159777980 C>T maps to NM_001004310.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:159778039 G>A maps to NM_001004310.2 W42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:159779423 G>A maps to NM_001004310.2 E279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:159779288 C>T maps to NM_001004310.2 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:159778088 C>T maps to NM_001004310.2 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:159779372 C>T maps to NM_001004310.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:159778901 G>A maps to NM_001004310.2 Q157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:159778946 G>A maps to NM_001004310.2 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:159783291 C>T maps to NM_001004310.2 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:161681928 C>T maps to NM_001184866.1 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:161681103 C>T maps to NM_001184866.1 Y136Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:161681104 C>T maps to NM_001184866.1 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:161677098 C>T maps to NM_001184866.1 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:161683038 C>T maps to NM_001184866.1 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:161692489 C>T maps to NM_001002901.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:161697268 C>T maps to NM_001002901.2 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:161697269 C>T maps to NM_001002901.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr8:11683690 C>T maps to NM_004462.3 D223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:155279905 C>T maps to NM_001135821.1 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:110327750 G>C maps to NM_004109.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:10421287 G>A maps to NM_001031734.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:10426588 C>T maps to NM_001031734.2 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:111746466 G>A maps to NM_138378.1 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:111749798 G>A maps to ENST00000428306 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr17:72859025 G>A maps to ENST00000442102 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:72862339 G>A maps to ENST00000442102 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:72860066 G>A maps to ENST00000442102 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr17:72862250 A>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:72862288 G>A maps to ENST00000442102 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr18:55218047 G>A maps to NM_001012515.2 Q396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr18:55247339 G>A maps to NM_001012515.2 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr18:55230186 T>C maps to NM_001012515.2 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:4792819 C>T maps to NM_018708.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:4793788 C>T maps to NM_018708.2 C641C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:4793242 C>T maps to NM_018708.2 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:4793083 C>T maps to NM_018708.2 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:4793083 C>T maps to NM_018708.2 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr19:4793179 C>T maps to NM_018708.2 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:68582854 C>T maps to NM_015322.3 R387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:68582854 C>T maps to NM_015322.3 R387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr15:68583222 T>C maps to NM_015322.3 F509F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr5:114860481 T>C maps to NM_020177.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:61563657 C>T maps to NM_004111.4 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:61563516 C>T maps to NM_004111.4 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr5:108516558 G>A maps to NM_005246.2 K720K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:97363283 A>T maps to NM_001113382.1 K1396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr2:97364780 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr2:97370338 G>A maps to NM_001113382.1 K2064K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr2:97366108 G>A maps to NM_001113382.1 K1684K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:97363850 G>A maps to NM_001113382.1 Q1465Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr2:97361522 G>A maps to NM_001113382.1 K1340K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr2:97361639 A>G maps to NM_001113382.1 P1379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr8:125113391 C>T maps to NM_001039112.2 S1646S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr8:124988245 G>A maps to NM_001039112.2 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr8:125076648 C>T maps to NM_001039112.2 P1130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr8:124978496 G>A maps to NM_001039112.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr8:125094564 C>T maps to NM_001039112.2 S1419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr8:125082754 G>A maps to NM_001039112.2 W1294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr8:125058036 G>A maps to NM_001039112.2 W873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:124968291 C>T maps to NM_001039112.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:124998378 G>A maps to NM_001039112.2 K494K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr8:124982333 C>A maps to NM_001039112.2 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr8:124968252 G>A maps to NM_001039112.2 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:125076784 C>T maps to NM_001039112.2 Q1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr8:125025756 C>T maps to NM_001039112.2 F636F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:124989697 G>A maps to NM_001039112.2 W304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:124992756 G>A maps to NM_001039112.2 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:125103771 G>A maps to NM_001039112.2 Q1500Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr8:124989742 G>A maps to NM_001039112.2 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr8:125115441 C>T maps to NM_001039112.2 A1727A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr8:125072929 C>T maps to NM_001039112.2 Q1043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr8:124989727 C>T maps to NM_001039112.2 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr8:125061864 G>A maps to NM_001039112.2 L914L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr8:125074091 G>C did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:124978439 G>A maps to NM_001039112.2 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:124989727 C>T maps to NM_001039112.2 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:124992897 G>A maps to NM_001039112.2 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:125061926 T>A maps to NM_001039112.2 L935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZG-06A-11D-A197-08 chr8:125035703 C>T maps to NM_001039112.2 D718D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr8:125103756 C>T maps to NM_001039112.2 H1495H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr8:125131979 C>T maps to NM_001039112.2 F1841F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:124982285 C>T maps to NM_001039112.2 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:124988178 G>A maps to NM_001039112.2 W242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:125025714 G>A maps to NM_001039112.2 Q622Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:125081670 G>A maps to NM_001039112.2 K1263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:125083790 G>A maps to NM_001039112.2 E1337E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:125131979 C>T maps to NM_001039112.2 F1841F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr8:125072473 C>T maps to NM_001039112.2 T976T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:125061996 G>A maps to NM_001039112.2 Q958Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr8:125058036 G>A maps to NM_001039112.2 W873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr8:124988149 C>T maps to NM_001039112.2 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:19184937 G>A maps to NM_152898.2 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:19184565 G>A maps to NM_152898.2 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:19184937 G>A maps to NM_152898.2 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr20:6100138 G>T maps to NM_017671.4 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr20:6065811 C>T maps to NM_017671.4 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:6060172 C>T maps to NM_017671.4 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:6077560 C>T maps to NM_017671.4 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:6091072 G>A maps to NM_017671.4 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:6069690 G>A maps to NM_017671.4 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:6091072 G>A maps to NM_017671.4 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:6093214 C>T maps to NM_017671.4 K147K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:6096536 C>T maps to NM_017671.4 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr20:6091021 T>C maps to NM_017671.4 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr14:53347813 C>T maps to NM_001134999.1 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:53360116 G>A maps to NM_001134999.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:63978206 C>T maps to NM_178443.2 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr11:63987249 C>G maps to NM_178443.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr11:63978104 C>T maps to NM_178443.2 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:63979140 C>T maps to NM_178443.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr15:91433698 C>T maps to NM_002005.3 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr11:125359591 G>A maps to NM_005103.4 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr7:121944260 G>A maps to NM_001024613.2 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr7:121944266 G>A maps to NM_001024613.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr7:121943281 T>C maps to NM_001024613.2 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:121942287 C>T maps to NM_001024613.2 K397K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:121942230 C>T maps to NM_001024613.2 K416K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:62357300 G>A maps to NM_018008.3 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:35842699 C>T maps to NM_005303.2 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:35842699 C>T maps to NM_005303.2 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr19:35940954 C>T maps to NM_005306.2 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:35940699 C>T maps to NM_005306.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:35850523 C>T maps to NM_005304.3 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:35849866 C>T maps to NM_005304.3 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:35850310 C>T maps to NM_005304.3 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:35850302 C>T maps to NM_005304.3 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:35850641 C>T maps to NM_005304.3 Q284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr19:35850334 C>T maps to NM_005304.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:35849908 C>T maps to NM_005304.3 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:35849941 G>A maps to NM_005304.3 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr4:155507509 G>T maps to NM_000508.3 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr4:155508666 C>T maps to NM_000508.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr4:155506993 G>A maps to NM_000508.3 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr4:155506750 T>C maps to NM_000508.3 E610E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr4:155506870 G>A maps to NM_000508.3 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr4:155507776 C>T maps to NM_000508.3 E268E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr4:155507650 A>G maps to NM_000508.3 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:155506870 G>A maps to NM_000508.3 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:155506993 G>A maps to NM_000508.3 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:155507731 C>T maps to NM_000508.3 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr4:155487750 G>A maps to NM_005141.4 Q139Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:155486958 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr23:54492240 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:54496553 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:54496549 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:54497076 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:54492257 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:54497797 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr23:54481898 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr6:36983599 C>T maps to NM_173558.3 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr6:36978768 C>T maps to NM_173558.3 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr6:36995248 C>T maps to NM_173558.3 F550F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr6:36995236 G>A maps to NM_173558.3 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr6:36978765 C>T maps to NM_173558.3 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr6:36995937 G>A maps to NM_173558.3 *656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:36995830 C>T maps to NM_173558.3 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:36983599 C>T maps to NM_173558.3 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:36982747 C>T maps to NM_173558.3 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr6:36982813 G>A maps to NM_173558.3 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr6:36993605 G>A maps to NM_173558.3 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:36973613 G>A maps to NM_173558.3 E7E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:36995236 G>A maps to NM_173558.3 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:36979489 C>T maps to NM_173558.3 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr6:36981495 G>A maps to NM_173558.3 W213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:36979528 C>T maps to NM_173558.3 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:36982420 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:36982672 G>A maps to NM_173558.3 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:36995278 G>A maps to NM_173558.3 K560K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:36995323 C>T maps to NM_173558.3 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr9:95738972 G>A maps to NM_033086.2 K145K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr9:95780428 C>T maps to NM_033086.2 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr12:32786515 C>T maps to NM_139241.2 Q599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr12:32755163 T>A maps to NM_139241.2 Y302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr3:14964554 C>T maps to NM_152536.3 I1270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:14862278 G>A maps to NM_152536.3 E567E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr3:14862386 C>T maps to NM_152536.3 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:14861369 G>A maps to NM_152536.3 E264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:14861822 C>T maps to NM_152536.3 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:14939517 C>T maps to NM_152536.3 I994I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:14952405 G>A maps to NM_152536.3 G1125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr3:14964554 C>T maps to NM_152536.3 I1270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr3:14905766 G>A maps to NM_152536.3 K886K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:14939083 G>A maps to NM_152536.3 R939R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr3:14861870 G>A maps to NM_152536.3 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:14939526 C>T maps to NM_152536.3 F997F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:14861591 C>T maps to NM_152536.3 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr3:14862923 G>A maps to NM_152536.3 S782S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:14862950 C>G maps to NM_152536.3 P791P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:14958784 C>T maps to NM_152536.3 P1145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:14862326 C>T maps to NM_152536.3 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:14862572 G>A maps to NM_152536.3 T665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:95501341 G>A maps to NM_018351.3 F1110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:95488459 C>A maps to NM_018351.3 E1170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:95603961 C>T maps to NM_018351.3 Q366Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:95604834 G>A maps to NM_018351.3 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:95502185 G>A maps to NM_018351.3 Q1068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:95603934 C>T maps to NM_018351.3 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:95500771 C>T maps to NM_018351.3 G1125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:141974938 C>T maps to NM_001144935.1 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr5:141974977 C>T maps to NM_001144935.1 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr5:141993608 G>A maps to NM_001144935.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:141993536 C>T maps to NM_001144935.1 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr5:44305162 C>T maps to NM_004465.1 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr5:44305141 C>T maps to NM_004465.1 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr5:44305162 C>T maps to NM_004465.1 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr5:44310582 G>A maps to NM_004465.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr5:44305141 C>T maps to NM_004465.1 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:7345983 T>C maps to NM_004112.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:7345188 C>T maps to NM_004112.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr17:7345941 G>A maps to NM_004112.2 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:7345122 C>T maps to NM_004112.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:192078283 C>T maps to NM_021032.4 Q81Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:191888301 C>T maps to NM_021032.4 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:191888445 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:191861857 C>T maps to NM_021032.4 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:191888289 C>T maps to NM_021032.4 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr3:191861815 C>T maps to NM_021032.4 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr23:137715098 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr23:137785195 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:137717807 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:137785177 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:137715086 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:137717625 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:137717626 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:137715133 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:137715021 C>T did not map to a codon.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr13:102375279 C>T maps to NM_175929.2 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr13:102521125 C>T maps to NM_175929.2 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr23:76709695 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:76711905 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr23:76709677 G>C did not map to a codon.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr23:76711854 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:76711793 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:76711794 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:76711795 G>T did not map to a codon.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr23:76709691 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:21903802 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:21905468 C>T maps to NM_003867.2 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:170863197 C>T maps to NM_003862.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:170883571 C>T maps to NM_003862.2 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:170876211 G>A maps to NM_003862.2 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr11:69514185 G>A maps to NM_005117.2 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr11:69514185 G>A maps to NM_005117.2 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr8:16850655 A>G maps to NM_019851.2 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:16850715 C>T maps to NM_019851.2 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr19:49259615 G>A maps to NM_019113.2 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:49261308 G>A maps to NM_019113.2 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:49259612 C>T maps to NM_019113.2 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:49261308 G>A maps to NM_019113.2 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:49261257 C>T maps to NM_019113.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr12:4488628 G>A maps to NM_020638.2 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr12:4479733 G>A maps to NM_020638.2 H177H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr12:4479940 G>A maps to NM_020638.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:4479544 G>A maps to NM_020638.2 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:4479940 G>A maps to NM_020638.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:4479940 G>A maps to NM_020638.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr12:4479703 C>T maps to NM_020638.2 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:4479589 C>T maps to NM_020638.2 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:4479934 C>T maps to NM_020638.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr11:69631105 C>T maps to NM_005247.2 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr11:69631150 G>A maps to NM_005247.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr11:69588127 C>T maps to NM_002007.2 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr4:81207517 C>T maps to NM_004464.3 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:81188022 C>T maps to NM_004464.3 I15I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:81207612 C>T maps to NM_004464.3 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr4:81207633 G>A maps to NM_004464.3 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr4:81207507 G>A maps to NM_004464.3 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr4:81207664 C>T maps to NM_004464.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr4:81207777 G>A maps to NM_004464.3 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr4:81207687 G>A maps to NM_004464.3 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:81207504 C>T maps to NM_004464.3 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:4553334 G>A maps to NM_020996.1 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:4553334 G>A maps to NM_020996.1 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:4543547 G>A maps to NM_020996.1 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:4554709 G>A maps to NM_020996.1 I9I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:4554478 C>T maps to NM_020996.1 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr15:49775435 A>G maps to NM_002009.3 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr15:49716676 A>G maps to NM_002009.3 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr10:103530211 G>A maps to NM_033163.3 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr13:22275498 C>T maps to NM_002010.2 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr13:22275366 C>T maps to NM_002010.2 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr13:22275366 C>T maps to NM_002010.2 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr13:22246206 G>A maps to NM_002010.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr13:22275498 C>T maps to NM_002010.2 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:22275366 C>T maps to NM_002010.2 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr4:15937834 T>A maps to NM_005130.3 K141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:15937658 C>T maps to NM_005130.3 E199E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:15938218 G>A maps to NM_005130.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr4:15964236 C>A maps to NM_031950.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr4:15964407 G>A maps to NM_031950.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr4:15964131 C>T maps to NM_031950.3 W207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:93668633 C>T maps to NM_152429.4 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr8:38275783 C>T maps to NM_001174067.1 E495E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:38282137 G>A maps to NM_001174067.1 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr8:38282209 G>A maps to NM_001174067.1 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:38282037 G>A maps to NM_001174067.1 Q340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr8:38282032 G>A maps to NM_001174067.1 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr8:38277176 G>A maps to NM_001174067.1 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr8:38271319 C>T maps to NM_001174067.1 E796E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr6:167438347 C>T maps to NM_007045.2 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:123243277 G>A maps to ENST00000351936 S765S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr10:123239526 C>T maps to ENST00000351936 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr10:123278253 G>T maps to ENST00000351936 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr10:123256162 G>A maps to ENST00000351936 P602P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr10:123274774 G>A maps to ENST00000351936 Y401Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:123245003 C>T maps to ENST00000351936 G720G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:123324093 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr10:123276956 C>T maps to ENST00000357555 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:123298187 G>A maps to ENST00000351936 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr10:123276926 C>T maps to ENST00000357555 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:1807475 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:1803417 C>T maps to NM_000142.4 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:1806141 C>T maps to NM_000142.4 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr5:176519690 G>A maps to NM_213647.1 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr5:176517622 C>T maps to NM_213647.1 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr5:176522567 G>A maps to NM_213647.1 K555K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr5:176516671 G>A maps to NM_213647.1 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:176524652 C>T maps to NM_213647.1 P795P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr5:176522717 C>T maps to NM_213647.1 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr5:176522660 C>T maps to NM_213647.1 F586F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:176520540 C>T maps to NM_213647.1 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr5:176517622 C>T maps to NM_213647.1 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr5:176517571 C>T maps to NM_213647.1 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr4:1018762 C>T maps to NM_021923.3 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:1018753 C>T maps to NM_021923.3 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:1018174 C>T maps to NM_021923.3 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr4:1018888 C>T maps to NM_021923.3 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr4:155531291 C>T maps to ENST00000407946 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:155527971 G>A maps to ENST00000407946 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:155528081 G>A maps to ENST00000407946 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:155530859 T>C maps to ENST00000407946 K204K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:155528040 G>A maps to ENST00000407946 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:155533027 C>T maps to ENST00000407946 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:60073476 C>T maps to NM_001113411.1 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:59805662 C>T maps to NM_001113411.1 R79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:60139792 C>T maps to NM_001113411.1 F524F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr1:60107001 C>A maps to NM_001113411.1 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:59844488 G>A maps to NM_001113411.1 K178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:60228237 G>A maps to NM_001113411.1 A570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:17743009 C>T maps to NM_201552.1 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr8:17722260 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:17726124 C>T maps to NM_201552.1 W237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr7:76828951 C>T maps to NM_006682.2 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr7:76828888 C>T maps to NM_006682.2 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:76826195 A>C maps to NM_006682.2 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:76828969 C>T maps to NM_006682.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:76825643 G>A maps to NM_006682.2 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr1:27942077 C>T maps to NM_005248.2 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:27949653 C>T maps to NM_005248.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:27949629 G>A maps to NM_005248.2 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:27942116 C>T maps to NM_005248.2 W282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr1:27941431 A>G maps to NM_005248.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZH-06A-11D-A197-08 chr1:27939460 G>A maps to NM_005248.2 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:27941043 G>A maps to NM_005248.2 D382D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:27949644 C>T maps to NM_005248.2 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:241669300 A>C did not map to a codon.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr4:153895900 C>T maps to NM_033393.2 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr4:153896920 C>T maps to NM_033393.2 S826S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr4:153897235 C>T maps to NM_033393.2 P931P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:153884263 C>T maps to NM_033393.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:153897565 C>T maps to NM_033393.2 A1041A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr4:153896809 C>T maps to NM_033393.2 T789T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr4:153896275 C>T maps to NM_033393.2 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr3:59908128 G>A maps to NM_002012.2 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr3:60522611 C>T maps to NM_002012.2 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:135288747 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:135289324 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:135288738 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr23:135289971 A>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:135289977 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:106002912 G>A maps to ENST00000344213 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr1:38465045 G>A maps to NM_004468.3 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:38465024 G>A maps to NM_004468.3 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:38463359 G>A maps to NM_004468.3 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:38465045 G>A maps to NM_004468.3 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr6:97053778 T>C maps to NM_020482.4 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:97053871 C>T maps to NM_020482.4 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:97052717 G>A maps to NM_020482.4 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr6:97052705 T>C maps to NM_020482.4 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr6:97052624 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr6:97051539 G>A maps to NM_020482.4 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr16:67268018 G>A maps to NM_013241.2 I529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr16:67266055 G>A maps to NM_013241.2 D696D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:67264529 C>T maps to NM_013241.2 R944R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:67265198 C>T maps to NM_013241.2 T853T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:67264381 G>A maps to NM_013241.2 G962G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:67268165 G>A maps to NM_013241.2 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr18:34320692 C>T maps to NM_025135.2 I1042I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr18:34081943 C>T maps to NM_025135.2 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr18:34324131 C>T maps to NM_025135.2 I1164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr18:34335240 G>A maps to NM_025135.2 E1289E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr9:133787191 C>T maps to NM_001145106.1 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:133799744 C>T maps to NM_001145106.1 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:133799654 G>A maps to NM_001145106.1 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:133787239 G>A maps to NM_001145106.1 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:133799148 C>T maps to NM_001145106.1 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:133805016 C>T maps to NM_001145106.1 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:133805037 C>T maps to NM_001145106.1 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr11:27016609 C>T maps to NM_203371.1 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:27016165 G>A maps to NM_203371.1 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:27016435 G>A maps to NM_203371.1 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr11:27016324 C>T maps to NM_203371.1 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr11:27016324 C>T maps to NM_203371.1 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:27016342 G>A maps to NM_203371.1 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:27016390 C>T maps to NM_203371.1 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:65652609 G>A maps to NM_198897.1 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:65653046 G>A maps to NM_198897.1 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr6:110083359 C>T maps to NM_014845.5 F446F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:110036289 C>T maps to NM_014845.5 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr6:110098156 C>T maps to NM_014845.5 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr6:110098167 C>T maps to NM_014845.5 F598F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr6:110086271 G>A maps to NM_014845.5 Q497Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:110146338 C>T maps to NM_014845.5 P865P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:110098155 C>T maps to NM_014845.5 F594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr6:110146466 G>A maps to NM_014845.5 *908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr23:15365418 A>T did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:15364351 C>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:15373284 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:15373285 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:15376146 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:15376195 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr2:164466469 G>A maps to NM_018086.2 I624I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:164466982 G>A maps to NM_018086.2 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr2:164466640 G>A maps to NM_018086.2 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:164466910 G>A maps to NM_018086.2 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr2:164468317 T>C did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:50513287 G>A maps to NM_022116.3 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:50514457 G>A maps to NM_022116.3 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr7:50513368 G>A maps to NM_022116.3 I539I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:76124460 G>A maps to NM_015687.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr6:76024011 C>T maps to NM_015687.2 R512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr6:76022271 G>A maps to NM_015687.2 V1092V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr6:76023723 T>C maps to NM_015687.2 R608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr6:76023519 G>A maps to NM_015687.2 F676F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr6:76023072 C>T maps to NM_015687.2 R825R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:76023969 C>T maps to NM_015687.2 V526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:76022427 G>A maps to NM_015687.2 T1040T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:76022715 G>A maps to NM_015687.2 T944T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:76022778 C>T maps to NM_015687.2 A923A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:76024866 C>T maps to NM_015687.2 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:76022610 G>A maps to NM_015687.2 S979S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr6:76024878 G>A maps to NM_015687.2 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr6:76063409 C>T maps to NM_015687.2 Q158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:76022382 G>A maps to NM_015687.2 S1055S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr6:76023636 C>T maps to NM_015687.2 E637E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr6:76023210 G>A maps to NM_015687.2 S779S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:76023519 G>A maps to NM_015687.2 F676F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:76024323 C>T maps to NM_015687.2 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:76024397 G>A maps to NM_015687.2 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:76024623 C>T maps to NM_015687.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:76023411 C>T maps to NM_015687.2 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr3:99643114 C>T maps to NM_001042459.1 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:99567726 C>T maps to NM_001042459.1 T931T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr3:99567925 C>T maps to NM_001042459.1 W865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:99567804 C>T maps to NM_001042459.1 K905K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:54257598 C>A maps to NM_030917.3 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr4:54294255 C>T maps to NM_030917.3 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr4:54294255 C>T maps to NM_030917.3 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr7:100884134 C>A maps to NM_016068.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:24600933 C>T maps to NM_203402.2 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:56104193 G>A maps to NM_032836.2 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:39975474 C>T maps to NM_021939.3 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:39969291 C>T maps to NM_021939.3 F2F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:39974732 G>A maps to NM_021939.3 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:39975504 C>T maps to NM_021939.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:30058623 G>A maps to NM_017946.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr9:115930837 T>C did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:115931754 G>A maps to ENST00000446284 V1103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:115946643 G>A maps to ENST00000446284 S573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr9:115973808 G>A maps to ENST00000446284 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:115932876 G>A maps to ENST00000446284 S922S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr9:115947058 G>A maps to ENST00000446284 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr9:115946089 C>T maps to ENST00000446284 K609K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr9:115931682 G>A maps to ENST00000446284 P1127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:24285926 C>T maps to NM_054033.2 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64010706 C>T maps to NM_057092.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:45603623 C>T maps to NM_002013.3 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:2910422 C>T maps to NM_002014.3 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:35547917 C>T maps to NM_001145775.1 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:35544965 C>T maps to NM_001145775.1 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:35554773 C>T maps to NM_001145777.1 K262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:35547962 C>T maps to NM_001145775.1 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:35544968 C>T maps to NM_001145775.1 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:35547980 C>T maps to NM_001145775.1 Q286Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:35587929 C>T maps to NM_001145775.1 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:72744285 C>T maps to NM_003602.3 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:72744228 G>A maps to NM_003602.3 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:72745694 G>A maps to NM_003602.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr7:72745658 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr19:18648542 C>T maps to NM_012181.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:33035787 C>A maps to NM_007270.3 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr7:33014932 G>A maps to NM_007270.3 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr7:33014863 C>T maps to NM_007270.3 D146D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZG-06A-11D-A197-08 chr7:33042360 G>A maps to NM_007270.3 E482E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:32097092 A>C maps to NM_022110.3 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:32096837 G>A maps to NM_022110.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr19:47260077 C>T maps to NM_024301.4 F457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:47258814 C>T maps to NM_024301.4 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:47259900 C>T maps to NM_024301.4 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr9:108377611 G>A maps to NM_006731.2 K278K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:108370211 G>T maps to NM_006731.2 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr1:154961377 C>T maps to NM_001184892.1 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:154960576 C>T maps to ENST00000405236 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:154960577 C>T maps to ENST00000405236 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:154956338 C>T maps to NM_025207.4 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:154965399 G>T maps to NM_025207.4 E551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:154960589 C>T maps to NM_025207.4 Q128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr1:154960567 C>T maps to ENST00000405236 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr17:17118315 G>C maps to NM_144997.5 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr1:152279023 G>A maps to NM_002016.1 Q2780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr1:152285303 C>T maps to NM_002016.1 Q686Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr1:152281091 G>A maps to NM_002016.1 F2090F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:152275973 C>T maps to NM_002016.1 R3796R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr1:152281091 G>A maps to NM_002016.1 F2090F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:152279849 G>A maps to NM_002016.1 S2504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:152284088 C>T maps to NM_002016.1 Q1091Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr1:152282093 C>T maps to NM_002016.1 G1756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:152282111 G>A maps to NM_002016.1 S1750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:152276825 C>T maps to NM_002016.1 Q3512Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:152287815 C>T maps to NM_002016.1 K39K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:152283638 G>A maps to NM_002016.1 A1241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:152285531 C>T maps to NM_002016.1 G610G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:152279795 T>C maps to NM_002016.1 Q2522Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:152283350 G>A maps to NM_002016.1 S1337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:152283845 C>T maps to NM_002016.1 R1172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:152285777 C>T maps to NM_002016.1 Q528Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:152282039 C>T maps to NM_002016.1 Q1774Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:152275223 C>T maps to NM_002016.1 S4046S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:152284874 G>A maps to NM_002016.1 S829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:152275799 C>T maps to NM_002016.1 R3854R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:152286886 T>A maps to NM_002016.1 K159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr1:152283191 G>T maps to NM_002016.1 S1390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:152283695 C>T maps to NM_002016.1 K1222K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:152276531 C>T maps to NM_002016.1 Q3610Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:152285984 C>T maps to NM_002016.1 G459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:152283875 C>T maps to NM_002016.1 Q1162Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:152275655 G>A maps to NM_002016.1 P3902P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:152275784 C>T maps to NM_002016.1 Q3859Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:152281937 C>T maps to NM_002016.1 E1808E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:152283026 C>T maps to NM_002016.1 V1445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:152285990 C>T maps to NM_002016.1 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:152287815 C>T maps to NM_002016.1 K39K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:152276762 C>T maps to NM_002016.1 R3533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:152282636 C>T maps to NM_002016.1 Q1575Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:152276762 C>T maps to NM_002016.1 R3533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:152280547 G>A maps to NM_002016.1 Q2272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:152276738 C>T maps to NM_002016.1 Q3541Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:152280467 G>A maps to NM_002016.1 S2298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:152282066 G>A maps to NM_002016.1 F1765F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:152279638 C>A maps to NM_002016.1 G2575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:152280872 G>A maps to NM_002016.1 H2163H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:152277515 G>A maps to NM_002016.1 S3282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:152287135 G>A maps to NM_002016.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:152275649 G>A maps to NM_002016.1 S3904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:152286548 C>T maps to NM_002016.1 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:152286689 A>G maps to NM_002016.1 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:152284310 C>T maps to NM_002016.1 Q1017Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:152279678 C>T maps to NM_002016.1 R2561R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr1:152276188 C>A maps to NM_002016.1 G3725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:152281160 G>A maps to NM_002016.1 P2067P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:152329346 C>T maps to NM_001014342.2 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr1:152323958 C>T maps to NM_001014342.2 R2101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:152328760 G>A maps to NM_001014342.2 Q501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:152326070 C>T maps to NM_001014342.2 E1397E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr1:152327954 G>A maps to NM_001014342.2 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:152330123 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:152329729 G>A maps to NM_001014342.2 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:152324978 G>A maps to NM_001014342.2 S1761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:152328910 G>A maps to NM_001014342.2 Q451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr1:152323913 C>T maps to NM_001014342.2 G2116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:152326949 T>C maps to NM_001014342.2 Q1104Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:152329817 C>T maps to NM_001014342.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:152325725 C>T maps to NM_001014342.2 G1512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr1:152327261 G>A maps to NM_001014342.2 G1000G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:152329886 A>G maps to NM_001014342.2 H125H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:152326000 C>A maps to NM_001014342.2 G1421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:152326001 C>T maps to NM_001014342.2 R1420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:152327429 C>T maps to NM_001014342.2 Q944Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:152323256 C>T maps to NM_001014342.2 R2335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:152325416 C>T maps to NM_001014342.2 E1615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:152329729 G>A maps to NM_001014342.2 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:152327954 G>A maps to NM_001014342.2 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:152326310 C>T maps to NM_001014342.2 Q1317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:152329709 G>A maps to NM_001014342.2 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:152326847 G>A maps to NM_001014342.2 S1138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr11:128651877 C>A maps to NM_002017.3 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:128677123 G>A maps to NM_002017.3 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:128680642 G>A maps to NM_002017.3 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr17:18148562 G>A maps to NM_002018.2 S1233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:18150581 G>A maps to NM_002018.2 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr17:18150578 G>A maps to NM_002018.2 S860S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:18160273 G>A maps to NM_002018.2 N41N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr17:18149955 G>A maps to NM_002018.2 T1001T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:18156661 G>A maps to NM_002018.2 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:18156697 G>A maps to NM_002018.2 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr17:18154328 G>A maps to NM_002018.2 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:21543584 C>T maps to NM_018071.3 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr14:21553045 G>A maps to NM_018071.3 G1308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr14:21550558 C>T maps to NM_018071.3 F1136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr14:21542560 C>T maps to NM_018071.3 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:21544720 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr14:21542539 T>G maps to NM_018071.3 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:60982869 G>A maps to NM_173667.2 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr8:142488819 G>A maps to NM_207414.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:142487887 G>A maps to NM_207414.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:142486222 C>T maps to NM_207414.2 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr8:142458047 G>T maps to NM_207414.2 P926P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr8:142498692 G>A maps to NM_207414.2 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr8:142476519 G>A maps to NM_207414.2 I822I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A2GO-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:142488718 C>T maps to NM_207414.2 W414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:142500262 G>A maps to NM_207414.2 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:142458067 G>A maps to NM_207414.2 L920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr8:142490440 C>T maps to NM_207414.2 K286K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr8:142487551 G>A maps to NM_207414.2 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:142486024 C>T maps to NM_207414.2 Q556Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:142505527 C>T maps to NM_207414.2 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr8:142504957 C>T maps to NM_207414.2 W163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr8:142487552 A>G maps to NM_207414.2 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr8:142476633 G>A maps to NM_207414.2 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr8:142506591 G>A maps to NM_207414.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr8:142445268 C>T maps to NM_207414.2 W1212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:142458110 G>A maps to NM_207414.2 F905F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:142500311 C>T maps to NM_207414.2 W201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr8:142486216 C>T maps to NM_207414.2 R492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:142476600 C>T maps to NM_207414.2 K795K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr9:84605377 G>A maps to NM_001001670.2 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr9:84606041 C>T maps to NM_001001670.2 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:84606146 G>A maps to NM_001001670.2 E254E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr9:84607622 G>A maps to NM_001001670.2 K746K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:84604718 G>A maps to NM_001001670.2 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:84606248 C>T maps to NM_001001670.2 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:84607562 G>A maps to NM_001001670.2 E726E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr9:84606345 T>C maps to NM_001001670.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr9:84607769 G>A maps to NM_001001670.2 K795K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr9:84608237 C>T maps to NM_001001670.2 I951I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr9:84606659 C>T maps to NM_001001670.2 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr9:84605861 G>A maps to NM_001001670.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr9:84605855 C>T maps to NM_001001670.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr9:84609947 G>A maps to NM_001001670.2 R1521R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr9:84607124 C>T maps to NM_001001670.2 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:84605984 C>T maps to NM_001001670.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:84606557 G>A maps to NM_001001670.2 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:84607826 G>A maps to NM_001001670.2 G814G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr9:84607226 G>C maps to NM_001001670.2 R614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr9:84609947 G>A maps to NM_001001670.2 R1521R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:84608516 C>T maps to NM_001001670.2 P1044P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:153588525 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:153589683 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr23:153595893 T>C did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr23:153585863 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:153577217 C>A did not map to a codon.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr23:153580734 T>C did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:153593318 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:153590642 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:153594952 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:153588742 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:153582085 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:153583355 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:153579320 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:153586927 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:153577853 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:153577875 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:153592646 G>C did not map to a codon.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr23:153594956 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:153594724 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:153585855 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:153588909 G>A did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr23:153594929 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:153581487 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:153594968 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr23:153578162 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr23:153578163 G>A did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:153594421 G>A did not map to a codon.
Sequencing variant TCGA-RP-A690-06A-11D-A30X-08 chr23:153583051 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:58095012 C>T maps to NM_001164317.1 V721V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr3:58135709 C>T maps to NM_001164317.1 F2106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:58118607 G>A maps to NM_001164317.1 E1519E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr3:58087984 C>T maps to NM_001164317.1 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr3:58155359 C>T maps to NM_001164317.1 S2518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:58139105 C>T maps to NM_001164317.1 I2155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr3:58095322 C>T maps to NM_001164317.1 S740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:58155359 C>T maps to NM_001164317.1 S2518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr3:58084468 G>A maps to NM_001164317.1 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr3:58094261 G>A maps to NM_001164317.1 K673K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:58095018 A>G maps to NM_001164317.1 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:58131714 C>T maps to NM_001164317.1 L1862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:58135685 G>A maps to NM_001164317.1 G2098G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr3:58139288 G>A maps to NM_001164317.1 V2216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr3:58067483 A>G maps to NM_001164317.1 K256K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:58141799 C>T maps to NM_001164317.1 Q2327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:58124078 G>A maps to NM_001164317.1 G1675G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr3:58154353 C>T maps to NM_001164317.1 I2493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:58134454 C>T maps to NM_001164317.1 P2020P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr3:58134493 C>T maps to NM_001164317.1 A2033A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr3:58111338 C>T maps to NM_001164317.1 D1310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr3:58084615 C>T maps to NM_001164317.1 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:58067415 C>T maps to NM_001164317.1 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:58107028 G>A maps to NM_001164317.1 G975G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:58111347 C>T maps to NM_001164317.1 I1313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr7:128480650 C>T maps to NM_001458.4 F533F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr7:128494536 C>T maps to NM_001458.4 I2266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:128477556 C>T maps to NM_001458.4 R269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr7:128485028 C>T maps to NM_001458.4 V1170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr7:128480650 C>T maps to NM_001458.4 F533F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr7:128489436 G>A maps to NM_001458.4 V1668V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr7:128487820 G>A maps to NM_001458.4 L1453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr7:128487775 G>A maps to NM_001458.4 K1438K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr7:128487760 C>T maps to NM_001458.4 F1433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:128493529 G>A maps to NM_001458.4 G2072G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:128497187 C>T maps to NM_001458.4 F2526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:128491635 C>T maps to NM_001458.4 F1932F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:128475584 G>A maps to NM_001458.4 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:128494133 G>A maps to NM_001458.4 R2197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:128481302 G>A maps to NM_001458.4 W631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:128494220 G>A maps to NM_001458.4 L2226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr7:128478741 T>C maps to NM_001458.4 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr7:128489397 C>T maps to NM_001458.4 G1655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr7:128484133 G>A maps to NM_001458.4 R1002R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:128488635 C>T maps to NM_001458.4 L1534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:128490511 C>T maps to NM_001458.4 F1791F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr7:128494181 C>T maps to NM_001458.4 V2213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:128483516 G>A maps to NM_001458.4 K899K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr7:128490100 C>T maps to NM_001458.4 P1757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:128477265 C>T maps to NM_001458.4 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:128478687 C>T maps to NM_001458.4 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:128487751 G>A maps to NM_001458.4 G1430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:128488719 C>T maps to NM_001458.4 F1562F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr7:128489577 C>T maps to NM_001458.4 V1715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:128477588 C>T maps to NM_001458.4 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:128478852 G>A maps to NM_001458.4 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:128482971 G>A maps to NM_001458.4 A838A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:128491626 C>T maps to NM_001458.4 I1929I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:128491635 C>T maps to NM_001458.4 F1932F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:128498131 C>T maps to NM_001458.4 S2617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr7:128489238 C>T maps to NM_001458.4 S1644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr7:128494172 C>T maps to NM_001458.4 S2210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr7:128480206 G>A maps to NM_001458.4 K514K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr7:128484917 C>T maps to NM_001458.4 I1133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:30708042 A>G maps to NM_005803.2 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:30709056 G>A maps to NM_005803.2 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:30708087 C>T did not map to a codon.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr17:27210165 G>A maps to ENST00000394906 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:27209605 G>A maps to ENST00000394906 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:63884923 G>A maps to NM_013280.4 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr11:63885559 G>A maps to NM_013280.4 K607K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr11:63884758 G>A maps to NM_013280.4 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:63884857 C>T maps to NM_013280.4 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:63884170 G>A maps to NM_013280.4 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr11:63884923 G>A maps to NM_013280.4 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:63883876 G>A maps to NM_013280.4 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:63885181 G>A maps to NM_013280.4 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:63884314 C>T maps to NM_013280.4 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr14:86088637 G>A maps to NM_013231.4 Q260Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr14:86087926 C>T maps to NM_013231.4 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:86089657 G>A maps to NM_013231.4 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr14:86088319 C>T maps to NM_013231.4 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:86088140 C>T maps to NM_013231.4 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:86089313 C>T maps to NM_013231.4 R486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:86088166 C>T maps to NM_013231.4 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:86089054 T>G maps to NM_013231.4 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:86087875 A>C maps to NM_013231.4 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:86088739 G>A maps to NM_013231.4 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr14:86088458 C>T maps to NM_013231.4 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr14:86089474 C>A maps to NM_013231.4 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr14:86089780 C>T maps to NM_013231.4 I641I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr14:86087962 C>T maps to NM_013231.4 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr14:86089129 G>A maps to NM_013231.4 R424R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr14:86089609 G>A maps to NM_013231.4 R584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:86088043 G>A maps to NM_013231.4 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:86089438 C>T maps to NM_013231.4 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr14:86087989 G>A maps to NM_013231.4 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr20:14306598 C>T maps to NM_198391.2 E518E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr20:14306244 G>T maps to NM_198391.2 Y636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr20:14306628 G>A maps to NM_198391.2 N508N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:14306802 T>C maps to NM_198391.2 G450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:14306613 G>A maps to NM_198391.2 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr20:14306934 G>A maps to NM_198391.2 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr13:29012393 C>T maps to NM_002019.4 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr13:28895677 C>T maps to NM_002019.4 E1032E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr13:28963984 C>T maps to NM_002019.4 R639R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr13:29005399 G>A maps to NM_002019.4 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr13:28896932 C>A maps to NM_002019.4 E983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr13:28877372 C>T maps to NM_002019.4 R1316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr13:28971100 G>A maps to NM_002019.4 I552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr13:29041079 C>T maps to NM_002019.4 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr13:28893575 C>T maps to NM_002019.4 W1090*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr13:28877366 G>A maps to NM_002019.4 I1318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr13:28877372 C>T maps to NM_002019.4 R1316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr13:29001961 C>T maps to NM_002019.4 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr13:28919656 G>A maps to NM_002019.4 I760I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr13:29008291 G>A maps to NM_002019.4 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr13:28908227 G>A maps to NM_002019.4 Q843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr13:28963960 G>A maps to NM_002019.4 I647I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr13:28893658 G>A maps to NM_002019.4 L1063L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr13:29012444 G>A maps to NM_002019.4 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr13:29041172 G>C maps to NM_002019.4 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr13:28919595 G>A maps to NM_002019.4 R781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:28895626 C>T maps to NM_002019.4 K1049K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:29002036 C>T maps to NM_002019.4 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:29005438 C>T maps to NM_002019.4 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:29007988 C>T maps to NM_002019.4 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:29008200 G>A maps to NM_002019.4 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:29012408 G>A maps to NM_002019.4 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr13:28610178 C>T maps to NM_004119.2 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr13:28631574 C>T maps to NM_004119.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr13:28597537 A>G maps to NM_004119.2 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr13:28597564 C>T maps to NM_004119.2 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr13:28609647 G>A maps to NM_004119.2 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr13:28623771 C>T maps to NM_004119.2 E294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr13:28602360 T>A maps to NM_004119.2 G669G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr13:28626772 T>A maps to NM_004119.2 K175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr13:28578205 G>A maps to NM_004119.2 Q989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr13:28588639 G>A maps to NM_004119.2 F936F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:28610178 C>T maps to NM_004119.2 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:49982275 C>T maps to NM_001459.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:49979048 C>T maps to NM_001459.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:49983819 C>T maps to NM_001459.2 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:49983633 C>T maps to NM_001459.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr5:180056355 G>A maps to NM_182925.4 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr5:180058776 G>C maps to NM_182925.4 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:180049770 C>T maps to NM_182925.4 K539K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr5:180057579 G>A maps to NM_182925.4 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr5:180041131 C>T maps to NM_182925.4 K1089K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:180043411 A>T maps to NM_182925.4 L1058L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:180056958 G>A maps to NM_182925.4 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:180051015 C>T maps to NM_182925.4 W489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:180056295 G>A maps to NM_182925.4 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:180043462 C>T maps to NM_182925.4 R1041R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr5:180056973 G>A maps to NM_182925.4 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:180055957 G>A maps to NM_182925.4 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:180056391 G>A maps to NM_182925.4 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:180047290 G>A maps to NM_182925.4 I808I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:180048671 C>T maps to NM_182925.4 G630G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:180057042 G>A maps to NM_182925.4 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:180039511 G>C maps to NM_182925.4 G1177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:180048899 G>A maps to NM_182925.4 I554I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr5:180057594 G>A maps to NM_182925.4 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:180041159 C>T maps to NM_182925.4 W1080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:180048703 G>A maps to NM_182925.4 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:180057014 G>A maps to NM_182925.4 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr5:180041159 C>T maps to NM_182925.4 W1080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr5:180043914 G>A maps to NM_182925.4 F1027F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr5:180053174 G>A maps to NM_182925.4 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:213046069 C>T maps to NM_014053.2 Q312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr1:213037185 A>G maps to NM_014053.2 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:213046095 C>T maps to NM_014053.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:76045917 C>T maps to NM_017791.2 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:76105704 C>T maps to NM_017791.2 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr14:76045383 G>A maps to NM_017791.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr16:2979712 G>A maps to ENST00000399667 Q9Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:2987336 C>T maps to ENST00000399667 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:2988350 C>T maps to ENST00000399667 H697H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr16:2946569 C>T maps to NM_138439.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:33359008 C>T maps to NM_001103184.2 K359K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:240351538 A>T maps to ENST00000406993 K798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:240286554 G>A maps to ENST00000406993 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:240286557 C>T maps to ENST00000406993 I708I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:240286641 T>C maps to ENST00000406993 F736F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:240341309 C>T maps to ENST00000406993 S767S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:240371411 C>T maps to ENST00000406993 P1243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:240370841 C>T maps to ENST00000406993 P1053P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr1:240371444 C>T maps to ENST00000406993 P1254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20I-06A-11D-A196-08 chr1:240255957 C>A maps to ENST00000406993 I326I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:240256758 C>T maps to ENST00000406993 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:240497239 T>C maps to ENST00000406993 F1689F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:240601477 G>A maps to ENST00000406993 W1819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr1:240370322 G>A maps to ENST00000406993 R880R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:240341339 G>A maps to ENST00000406993 E777E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:240601432 C>T maps to ENST00000406993 F1804F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:240286539 G>A maps to ENST00000406993 E702E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:240255933 C>T maps to ENST00000406993 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:240256866 G>A maps to ENST00000406993 T629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:240370907 C>T maps to ENST00000406993 L1075L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:240371642 C>T maps to ENST00000406993 P1320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:240286551 C>T maps to ENST00000406993 S706S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:240555832 G>A maps to ENST00000406993 E1770E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:240255645 G>A maps to ENST00000406993 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:240492662 C>T maps to ENST00000406993 I1587I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:240286503 C>T maps to ENST00000406993 F690F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:240458173 C>T maps to ENST00000406993 L1545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr1:240341255 A>G maps to ENST00000406993 Q749Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:240371477 C>T maps to ENST00000406993 P1265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:240371123 C>T maps to ENST00000406993 P1147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr1:240371807 C>T maps to ENST00000406993 I1375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:240256101 G>A maps to ENST00000406993 E374E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:240256737 C>T maps to ENST00000406993 I586I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:240286575 C>T maps to ENST00000406993 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:240370121 G>A maps to ENST00000406993 E813E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:240371006 C>T maps to ENST00000406993 P1108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:240371657 G>A maps to ENST00000406993 V1325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:240374522 G>A maps to ENST00000406993 T1494T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:240493994 G>A maps to ENST00000406993 Q1653Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:240497464 G>A maps to ENST00000406993 Q1710Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:240635689 G>A maps to ENST00000406993 E1836E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:240371072 C>T maps to ENST00000406993 P1130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Z-06A-11D-A196-08 chr17:43309816 G>A maps to NM_005892.3 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr17:43321187 C>T maps to NM_005892.3 F748F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:43321208 C>T maps to NM_005892.3 F755F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr17:43309831 G>A maps to NM_005892.3 W104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:43314975 C>T maps to NM_005892.3 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:43319819 G>A maps to NM_005892.3 E666E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:43321364 C>T maps to NM_005892.3 F807F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr2:153484860 G>C maps to NM_052905.3 R738R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:153475481 G>A maps to NM_052905.3 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:153481955 G>A maps to NM_052905.3 V614V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:153417456 G>A maps to NM_052905.3 W168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:153484971 C>T maps to NM_052905.3 I775I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:153431697 G>T maps to NM_052905.3 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr12:50050216 G>A maps to NM_175736.4 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:50045893 G>A maps to NM_175736.4 V475V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:50045806 G>A maps to NM_175736.4 D504D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr12:50062307 G>A maps to NM_175736.4 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr12:50045848 G>A maps to NM_175736.4 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:171248009 G>A maps to NM_002021.1 K209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:171254676 C>T maps to NM_002021.1 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr1:171251293 C>T maps to NM_002021.1 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:171251359 C>T maps to NM_002021.1 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:171254339 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:171244612 T>A maps to NM_002021.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:171251293 C>T maps to NM_002021.1 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:171251242 G>A maps to NM_002021.1 K318K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:171174705 C>T maps to NM_001460.2 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:171174594 T>C maps to NM_001460.2 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:171165930 C>T maps to NM_001460.2 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr1:171162616 G>A maps to NM_001460.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:171174720 C>T maps to NM_001460.2 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:171168518 C>T maps to NM_001460.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:171154905 G>A maps to NM_001460.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:171168626 G>A maps to NM_001460.2 Q209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:171174687 C>T maps to NM_001460.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:171178037 C>T maps to NM_001460.2 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:171154962 T>C maps to NM_001460.2 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:171168548 G>A maps to NM_001460.2 E183E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:171086451 G>A maps to NM_006894.5 W490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:171072936 G>A maps to NM_006894.5 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:171086467 A>G maps to NM_006894.5 K495K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:171080039 C>T maps to NM_006894.5 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:171079946 C>T maps to NM_006894.5 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:171080036 C>T maps to NM_006894.5 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:171083440 C>T maps to NM_006894.5 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:171079970 G>A maps to NM_006894.5 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:171076867 G>A maps to NM_006894.5 W125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:171079952 C>T maps to NM_006894.5 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr1:171076867 G>A maps to NM_006894.5 W125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:171086446 C>T maps to NM_006894.5 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr1:171073095 G>A maps to NM_006894.5 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:171080015 C>T maps to NM_006894.5 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:171076823 A>G maps to NM_006894.5 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:171083155 G>A maps to NM_006894.5 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr1:171289011 C>T maps to NM_002022.1 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:171310798 C>T maps to NM_002022.1 R500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:171293296 G>A maps to NM_002022.1 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:146672833 C>T maps to NM_001461.2 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr1:146658592 C>T maps to NM_001461.2 R496R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:146672875 T>C maps to NM_001461.2 K347K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:146684031 T>G maps to NM_001461.2 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr1:203316899 G>A maps to NM_002023.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:203317362 G>A maps to NM_002023.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:203316945 G>A maps to NM_002023.3 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:203316738 C>T maps to NM_002023.3 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:203316867 G>A maps to NM_002023.3 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:203317140 G>A maps to NM_002023.3 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:203317371 C>T maps to NM_002023.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr23:147019004 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:147019651 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr23:147022102 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:147024746 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:147026415 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:147090222 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:147106385 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:147088234 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:147088274 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:147062950 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:147084829 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:216239935 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:216248206 C>A did not map to a codon.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr2:216289994 G>A maps to NM_212482.1 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:216271099 C>T maps to NM_212482.1 E949E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr2:216262451 C>T maps to NM_212482.1 L1156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:216264012 G>A maps to NM_212482.1 I1105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:216293029 G>A maps to NM_212482.1 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:216251559 G>A maps to NM_212482.1 F1488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr2:216253024 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr2:216271879 G>A maps to NM_212482.1 Q895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:216288193 G>A maps to NM_212482.1 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr2:216262424 T>C maps to NM_212482.1 P1165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:216296643 G>A maps to NM_212482.1 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:216251617 C>T maps to NM_212482.1 W1469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:216230321 C>T maps to NM_212482.1 K2350K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:80684935 C>T maps to NM_024619.3 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:80684890 C>T maps to NM_024619.3 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:132658144 G>A maps to NM_015033.2 V606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr9:132662283 G>A maps to NM_015033.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:94014864 C>T maps to ENST00000370253 N506N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:93996313 C>T maps to ENST00000370253 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:47755677 G>A maps to NM_015308.2 Q529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:47744677 A>T maps to NM_015308.2 A885A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr11:47776088 G>A maps to NM_015308.2 N147N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:47746310 G>A maps to NM_015308.2 S676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:47776085 G>A maps to NM_015308.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:47767640 G>A maps to NM_015308.2 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr11:47754102 G>A maps to NM_015308.2 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr11:47774549 G>A maps to NM_015308.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr6:159687131 G>A maps to NM_032532.2 W1767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:159687215 C>T maps to NM_032532.2 F1795F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr6:159650964 C>T maps to NM_032532.2 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:159653262 C>T maps to NM_032532.2 G573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:159644599 G>A maps to NM_032532.2 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:159677660 G>A maps to NM_032532.2 T1724T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:159672448 G>A maps to NM_032532.2 K1650K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr6:159653193 G>A maps to NM_032532.2 E550E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:159644572 G>A maps to NM_032532.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr6:159650964 C>T maps to NM_032532.2 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:159654315 C>T maps to NM_032532.2 P924P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr6:159687215 C>T maps to NM_032532.2 F1795F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr6:159653325 G>A maps to NM_032532.2 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:159618523 C>T maps to NM_032532.2 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:159646590 G>A maps to NM_032532.2 E303E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:159654375 C>T maps to NM_032532.2 S944S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:159677660 G>A maps to NM_032532.2 T1724T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr13:49705415 A>T maps to NM_001079673.1 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr13:49772338 C>T maps to NM_001079673.1 S904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr13:49765343 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:172052738 T>A maps to NM_022763.3 T549T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr3:171965528 C>T maps to NM_022763.3 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr3:172061987 C>T maps to NM_022763.3 V730V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr3:172080539 T>C maps to NM_022763.3 P971P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr3:171965444 C>T maps to NM_022763.3 H129H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:172013286 A>G maps to NM_022763.3 K328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr2:27715589 C>T maps to NM_022823.2 K204K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:27715583 C>T maps to NM_022823.2 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:33333417 C>T maps to ENST00000291421 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:109271473 G>A maps to NM_001144937.1 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:109268396 G>A maps to NM_001144937.1 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:109275945 C>T maps to NM_001144937.1 I644I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:109265206 G>A maps to NM_001144937.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr1:109268612 C>T maps to NM_001144937.1 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:109270445 T>C maps to NM_001144937.1 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr17:33454267 C>G maps to NM_017559.2 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr17:33456447 G>A maps to NM_017559.2 W198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr5:131054746 A>G maps to NM_133372.2 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr5:131008069 T>C maps to NM_133372.2 V689V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:131006311 G>T maps to NM_133372.2 I984I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:159812770 C>T maps to ENST00000379346 L1064L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:159782869 C>T maps to ENST00000379346 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr4:159790118 C>T maps to ENST00000379346 C800C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr8:42932450 C>T maps to NM_002027.2 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr8:42940406 A>T maps to NM_002027.2 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr14:65470995 C>T maps to ENST00000448390 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr14:65499384 C>T maps to ENST00000448390 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr14:65494183 C>T maps to ENST00000448390 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:49208240 C>T maps to NM_004476.1 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr11:49208267 T>C maps to NM_004476.1 E189E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:49175807 C>T maps to NM_004476.1 Q620Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:49178312 G>A maps to NM_004476.1 R527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr11:49214395 A>T maps to NM_004476.1 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr11:49227622 A>G maps to NM_004476.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:49190807 C>T maps to NM_004476.1 E437E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr11:49196492 C>T maps to NM_004476.1 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:49207394 G>A maps to NM_004476.1 Q218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:49229943 G>A maps to NM_004476.1 H6H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr11:49195013 G>A maps to NM_004476.1 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:89421764 G>T maps to NM_153696.2 G208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr11:89424675 C>T maps to NM_153696.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:89424675 C>T maps to NM_153696.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr11:89405091 G>A maps to NM_153696.2 W73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:89431628 C>T maps to NM_153696.2 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:71906445 C>T maps to NM_016729.2 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr11:71907091 C>T maps to NM_016729.2 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr11:71907151 G>A maps to NM_016729.2 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:71907163 G>A maps to NM_016729.2 W239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:71907115 G>A maps to NM_016729.2 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:71907124 G>A maps to NM_016729.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:71907034 C>T maps to NM_016729.2 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr11:71932096 C>T maps to NM_001113536.1 Q112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:94039752 C>T maps to NM_001080486.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr11:94040623 C>T maps to NM_001080486.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:94040782 C>T maps to NM_001080486.1 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr11:94040457 G>A maps to NM_001080486.1 W152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:94039821 C>T maps to NM_001080486.1 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr11:94039809 C>T maps to NM_001080486.1 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:75747345 G>A maps to NM_005252.3 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr14:75747342 G>A maps to NM_005252.3 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr14:75747712 C>T maps to NM_005252.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:45975996 G>A maps to NM_006732.2 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NF-06A-11D-A19A-08 chr19:45974074 C>T maps to NM_006732.2 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr2:28635176 C>T maps to NM_005253.3 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:28627158 C>T maps to NM_005253.3 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:28635173 C>T maps to NM_005253.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:28634949 C>T maps to NM_005253.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr2:28627122 C>T maps to NM_005253.3 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr2:28635284 C>T maps to NM_005253.3 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr20:22563675 G>A maps to NM_021784.4 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr20:22563276 G>A maps to NM_021784.4 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:22562577 C>T maps to NM_021784.4 T434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:46375988 C>T maps to NM_004497.2 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr19:46376132 G>A maps to NM_004497.2 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:46375568 G>A maps to NM_004497.2 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:46375568 G>A maps to NM_004497.2 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:46376126 C>T maps to NM_004497.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:79635163 C>T maps to NM_001013735.1 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr16:86602437 G>A maps to NM_005251.2 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr16:86601501 C>T maps to NM_005251.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:86602380 C>T maps to NM_005251.2 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr9:117900 G>A maps to NM_207305.3 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr9:117693 G>A maps to NM_207305.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:117519 G>A maps to NM_207305.3 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:117474 G>A maps to NM_207305.3 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:117807 C>T maps to NM_207305.3 K104K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:117681 G>A maps to NM_207305.3 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:116865 C>T maps to NM_207305.3 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:114257522 C>T maps to NM_012184.4 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:114257054 C>T maps to NM_012184.4 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:114257126 C>T maps to NM_012184.4 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:114257369 C>T maps to NM_012184.4 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:114257231 C>T maps to NM_012184.4 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr9:70177137 C>T maps to NM_001126334.1 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr9:100616456 C>T maps to NM_004473.3 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:47882373 C>T maps to NM_012186.2 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr16:86544357 C>T maps to NM_001451.2 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr16:86546576 G>A maps to NM_001451.2 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z4-06A-11D-A197-08 chr6:1394973 C>T maps to NM_001452.1 D405D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr6:1394940 C>T maps to NM_001452.1 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr14:29237738 C>T maps to NM_005249.3 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr14:29237834 C>T maps to NM_005249.3 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:29237429 C>T maps to NM_005249.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr14:29237248 G>A maps to NM_005249.3 W255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:29237399 C>T maps to NM_005249.3 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr8:145700629 G>A maps to NM_003923.2 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr5:169532972 C>T maps to NM_012188.4 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr5:169535125 G>A maps to NM_012188.4 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr5:169535119 G>A maps to NM_012188.4 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:169532972 C>T maps to NM_012188.4 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:169535305 T>G maps to NM_012188.4 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr5:169535320 C>T maps to NM_012188.4 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:169533035 C>T maps to NM_012188.4 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr5:169533104 C>T maps to NM_012188.4 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:169533503 C>T maps to NM_012188.4 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr5:169535098 C>T maps to NM_012188.4 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr5:169533455 C>G maps to NM_012188.4 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:169535233 G>A maps to NM_012188.4 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr5:169533059 G>A maps to NM_012188.4 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:169535587 C>T maps to NM_012188.4 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:169535377 C>T maps to NM_012188.4 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr5:169535146 C>T maps to NM_012188.4 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:129537219 C>T maps to NM_207426.2 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:129536802 C>T maps to NM_207426.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:129537087 C>T maps to NM_207426.2 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr17:74133667 C>T maps to NM_001454.3 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:74133826 G>A maps to NM_001454.3 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr17:74134114 C>T maps to NM_001454.3 W195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:74133577 C>T maps to NM_001454.3 E374E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:74134003 G>A maps to NM_001454.3 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:74134102 G>A maps to NM_001454.3 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:8200491 C>T maps to NM_018416.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr12:8202048 C>T maps to NM_018416.2 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:8197487 C>T maps to NM_018416.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:8192619 C>T maps to NM_018416.2 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:8196617 C>T maps to NM_018416.2 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr12:8192440 C>T maps to NM_018416.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:4794140 C>T maps to ENST00000450194 Y244Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:4798969 C>T maps to ENST00000450194 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:80559179 C>T maps to NM_004514.3 A596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:80540673 C>T maps to NM_004514.3 Q323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:80543813 C>A maps to NM_004514.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr17:80543957 C>G maps to NM_004514.3 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:80543888 C>T maps to NM_004514.3 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:80541915 G>C maps to NM_004514.3 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:80540786 C>T maps to NM_004514.3 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr17:80521331 C>T maps to NM_004514.3 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:86612502 C>T maps to NM_005250.2 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:86613327 C>T maps to NM_005250.2 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:86612424 C>T maps to NM_005250.2 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr12:2968799 A>G maps to NM_202002.1 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:2983233 G>A maps to NM_202002.1 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr12:2975600 G>A maps to NM_202002.1 H311H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:2983281 G>A maps to NM_202002.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr17:26864393 G>A maps to NM_003593.2 T629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:26851654 C>T maps to NM_003593.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:26856215 C>T maps to NM_003593.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr17:26861509 G>A maps to NM_003593.2 W363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr17:26862088 C>T maps to NM_003593.2 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr17:26851061 G>A maps to NM_003593.2 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr2:48602500 C>T maps to NM_002158.3 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:48589799 C>T maps to NM_002158.3 H219H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr14:89628892 G>T maps to NM_001085471.1 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:89629012 C>T maps to NM_001085471.1 K406K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr14:89878538 G>A maps to NM_001085471.1 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:109717604 G>A maps to NM_213596.2 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:109719440 G>A maps to NM_213596.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:109717724 C>T maps to NM_213596.2 W435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:109723223 G>A maps to NM_213596.2 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr13:41134637 G>A maps to NM_002015.3 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr13:41134547 G>A maps to NM_002015.3 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr13:41134157 C>T maps to NM_002015.3 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr13:41133722 C>T maps to NM_002015.3 V635V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:108984917 C>T maps to NM_001455.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr23:70321290 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:70316610 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:70321416 C>T did not map to a codon.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr3:71247406 C>T maps to NM_032682.4 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:71021713 C>T maps to NM_032682.4 K548K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:71247352 C>T maps to NM_032682.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:71161710 C>T maps to NM_032682.4 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr3:71096117 G>A maps to NM_032682.4 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:71247487 G>T maps to NM_032682.4 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:114282579 C>T maps to NM_148898.3 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr7:114282576 C>T maps to NM_148898.3 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:114329979 G>A maps to NM_148898.3 *741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr7:114270029 G>A maps to NM_148898.3 Q214Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:114268723 C>T maps to NM_148898.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:114292281 G>A maps to NM_148898.3 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:114298149 G>A maps to NM_148898.3 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U9-06A-11D-A32N-08 chr7:114270014 A>G maps to NM_148898.3 Q209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr7:114284781 C>T maps to NM_148898.3 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr7:114282633 C>T maps to NM_148898.3 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr23:49113390 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr6:41558048 C>T maps to NM_001012426.1 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:41558078 C>T maps to NM_001012426.1 I476I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:41565544 C>T maps to NM_001012426.1 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:41555130 C>T maps to NM_001012426.1 D251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:41552568 C>T maps to NM_001012426.1 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr11:118849898 C>T maps to NM_181721.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:118851202 G>A maps to NM_181721.2 K205K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:55650609 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:55650821 C>T did not map to a codon.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr23:55650513 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:55650561 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:55650544 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:55650331 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:55650278 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:55650561 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:55650473 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:55650948 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr23:55650468 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:55650709 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:55650143 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:55650495 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:55650864 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr11:126141522 C>T maps to NM_017547.3 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:126147009 C>T maps to NM_017547.3 F382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:126143268 C>T maps to NM_017547.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:36902048 G>A maps to NM_001102371.1 Q141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr22:36892218 G>A maps to NM_001102371.1 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr20:30433273 G>A maps to NM_004118.3 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr20:30432475 G>A maps to NM_004118.3 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:30432526 G>A maps to NM_004118.3 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:30433000 G>A maps to NM_004118.3 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:30433255 G>A maps to NM_004118.3 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr9:130575600 C>T maps to NM_004957.4 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr1:74670195 C>T maps to NM_003838.3 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:52250220 C>T maps to NM_002029.3 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr19:52249629 G>A maps to NM_002029.3 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr19:52249635 G>A maps to NM_002029.3 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr19:52249845 C>T maps to NM_002029.3 Q134Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr19:52249599 G>A maps to NM_002029.3 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:52249677 C>T maps to NM_002029.3 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:52249992 C>T maps to NM_002029.3 K85K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:52249995 C>T maps to NM_002029.3 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:52250019 G>A maps to NM_002029.3 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:52249974 C>T maps to NM_002029.3 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:52272087 C>T maps to NM_001005738.1 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:52272906 T>G maps to NM_001005738.1 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:52271983 C>T maps to NM_001005738.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:52272264 C>T maps to NM_001005738.1 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr19:52272051 G>A maps to NM_001005738.1 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:52272348 C>T maps to NM_001005738.1 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:52272678 C>T maps to NM_001005738.1 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:52272747 C>T maps to NM_001005738.1 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr19:52272359 G>A maps to NM_001005738.1 W150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:52272198 C>T maps to NM_001005738.1 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr19:52272894 C>T maps to NM_001005738.1 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:52272348 C>T maps to NM_001005738.1 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:52272264 C>T maps to NM_001005738.1 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr19:52272867 C>T maps to NM_001005738.1 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:52272051 G>A maps to NM_001005738.1 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:52272393 C>T maps to NM_001005738.1 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:52272639 C>T maps to NM_001005738.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q9-06A-11D-A19A-08 chr19:52327144 C>A maps to NM_002030.3 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:52327441 G>A maps to NM_002030.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr19:52327435 G>A maps to NM_002030.3 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr19:52327426 C>A maps to NM_002030.3 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:52327435 G>A maps to NM_002030.3 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:52327321 C>T maps to NM_002030.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr19:52327093 A>G maps to NM_002030.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr19:52327534 C>T maps to NM_002030.3 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr19:52327382 C>T maps to NM_002030.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:52327123 C>T maps to NM_002030.3 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:52327382 C>T maps to NM_002030.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr10:95454673 G>A maps to NM_145246.4 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr10:95452437 G>A maps to NM_145246.4 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:95443820 G>A maps to NM_145246.4 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:95454690 G>A maps to NM_145246.4 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr4:79429940 G>A maps to NM_025074.6 K3187K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr4:79236829 G>A maps to NM_025074.6 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr4:79284703 C>T maps to NM_025074.6 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr4:79199861 G>A maps to NM_025074.6 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr4:79429997 C>T maps to NM_025074.6 F3206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr4:79430111 C>T maps to NM_025074.6 P3244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr4:79373449 G>A maps to NM_025074.6 L2235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:79410209 G>A maps to NM_025074.6 R2978R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:79367948 G>A maps to NM_025074.6 V1975V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:79308839 G>A maps to NM_025074.6 V1320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:79429916 A>G maps to NM_025074.6 E3179E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:79387519 G>A maps to NM_025074.6 K2396K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr4:79173605 C>T maps to NM_025074.6 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr4:79360139 G>T maps to NM_025074.6 L1817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:79205702 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:79308707 C>T maps to NM_025074.6 I1276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:79366898 C>T maps to NM_001166133.1 P1963P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:79369339 C>T maps to NM_025074.6 V2048V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr4:79442681 C>T maps to NM_025074.6 Q3516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr4:79440573 C>T maps to NM_025074.6 S3493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:79360133 C>T maps to NM_025074.6 N1815N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:79369462 C>T maps to NM_025074.6 L2089L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:79462121 G>A maps to NM_025074.6 R3961R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:79373338 C>T maps to NM_025074.6 S2198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:79369303 G>A maps to NM_025074.6 G2036G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr4:79254486 G>A maps to NM_025074.6 G733G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr4:79328973 G>A maps to NM_025074.6 Q1429Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr4:79396645 G>A maps to NM_025074.6 G2579G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr4:79432513 C>T maps to NM_025074.6 P3289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:79308608 C>T maps to NM_025074.6 I1243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:79301096 G>A maps to NM_025074.6 W1170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:79258882 C>T maps to NM_025074.6 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:79334178 G>A maps to NM_025074.6 A1455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr4:79371305 G>A maps to NM_025074.6 G2092G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr4:79400699 T>C maps to NM_025074.6 L2757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:79295331 C>T maps to NM_025074.6 L1026L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:79369264 C>T maps to NM_025074.6 V2023V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:79369265 C>T maps to NM_025074.6 Q2024*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr4:79373404 C>T maps to NM_025074.6 T2220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:79343149 C>T maps to NM_025074.6 F1558F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:79387438 C>T maps to NM_025074.6 F2369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:79399105 G>A maps to NM_025074.6 A2663A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:79418032 C>T maps to NM_025074.6 G3011G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:79429946 C>T maps to NM_025074.6 S3189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:79440570 C>T maps to NM_025074.6 A3492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:79458175 G>A maps to NM_025074.6 W3707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr4:79321902 C>T maps to NM_025074.6 Q1331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr9:14859388 C>T maps to ENST00000380880 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr9:14824882 C>T maps to ENST00000380880 K666K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr9:14857658 G>A maps to ENST00000380880 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr9:14775891 C>T maps to ENST00000380880 G1587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr9:14775953 G>A maps to ENST00000380880 Q1567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr9:14859444 G>A maps to ENST00000380880 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr9:14846006 G>A maps to ENST00000380880 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:14842401 C>T maps to ENST00000380880 V553V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr9:14750146 C>T maps to ENST00000380880 V1848V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr9:14806682 T>A maps to ENST00000380880 K1087*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:14750161 C>T maps to ENST00000380880 K1843K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:14823286 G>A maps to ENST00000380880 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:14737435 C>T maps to ENST00000380880 R2169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:14746950 G>A maps to ENST00000380880 I2039I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:14859409 G>A maps to ENST00000380880 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:14748410 C>T maps to ENST00000380880 G1931G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:14776176 C>T maps to ENST00000380880 R1492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr9:14770702 G>A maps to ENST00000380880 S1656S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr9:14859207 G>A maps to ENST00000380880 Q202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr9:14748455 G>A maps to ENST00000380880 G1916G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr9:14851398 C>T maps to ENST00000380880 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr9:14859352 C>T maps to ENST00000380880 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:14848670 C>T maps to ENST00000380880 W421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:14789049 C>T maps to ENST00000380880 L1351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:14851329 G>A maps to ENST00000380880 I371I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr9:14737459 C>T maps to ENST00000380880 G2161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:14823313 G>A maps to ENST00000380880 N730N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr9:14851344 G>A maps to ENST00000380880 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr9:14824924 C>T maps to ENST00000380880 R652R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr9:14740156 G>A maps to ENST00000380880 S2113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr9:14746953 C>T maps to ENST00000380880 G2038G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr9:14805028 G>A maps to ENST00000380880 S1135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr9:14857628 C>T maps to ENST00000380880 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr9:14859409 G>A maps to ENST00000380880 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr9:14801677 G>A maps to ENST00000380880 H1225H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr9:14805141 G>A maps to ENST00000380880 Q1098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr9:14868834 C>T maps to ENST00000380880 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:14747288 G>A maps to ENST00000380880 S1997S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:14748568 G>A maps to ENST00000380880 L1879L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:14775942 G>A maps to ENST00000380880 F1570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:14812855 G>A maps to ENST00000380880 F952F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:14819257 C>T maps to ENST00000380880 W843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:14823175 C>T maps to ENST00000380880 V776V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:14859436 G>A maps to ENST00000380880 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr9:14859436 G>A maps to ENST00000380880 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:14842638 G>A maps to ENST00000380880 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:14746466 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:14841567 G>A maps to ENST00000380880 F589F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:14842656 C>T maps to ENST00000380880 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr9:14769801 T>A maps to ENST00000380880 I1711I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr9:14859207 G>A maps to ENST00000380880 Q202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr13:39263137 T>C maps to NM_207361.4 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr13:39453035 G>A maps to NM_207361.4 V2976V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr13:39433566 G>A maps to NM_207361.4 V2453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr13:39358913 T>C maps to NM_207361.4 A1996A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr13:39263706 G>C maps to NM_207361.4 V742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr13:39264486 G>A maps to NM_207361.4 E1002E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr13:39452976 C>T maps to NM_207361.4 Q2957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr13:39263886 C>T maps to NM_207361.4 F802F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr13:39454665 G>A maps to NM_207361.4 K3084K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr13:39453101 A>G maps to NM_207361.4 T2998T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr13:39265017 C>T maps to NM_207361.4 F1179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr13:39265029 C>T maps to NM_207361.4 I1183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr13:39266419 C>T maps to NM_207361.4 Q1647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr13:39448700 C>T maps to NM_207361.4 G2753G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:39263122 C>T maps to NM_207361.4 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:39451348 C>T maps to NM_207361.4 F2880F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr13:39452382 C>A maps to NM_207361.4 P2928P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr13:39454854 G>A maps to NM_207361.4 P3147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr13:39343823 G>A maps to NM_207361.4 R1840R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr13:39358925 C>T maps to NM_207361.4 I2000I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr13:39454683 G>A maps to NM_207361.4 G3090G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr13:39343796 C>T maps to NM_207361.4 G1831G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr13:39263502 C>T maps to NM_207361.4 V674V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:39265900 C>T maps to NM_207361.4 Q1474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:39425937 C>T maps to NM_207361.4 S2286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:39452308 C>T maps to NM_207361.4 Q2904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr13:39343904 C>T maps to NM_207361.4 F1867F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr4:190876287 G>A maps to NM_004477.2 W138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr10:135438845 G>A maps to ENST00000443774 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:135440204 G>A maps to ENST00000443774 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:135440216 G>A maps to ENST00000443774 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:116277702 G>A maps to NM_002031.2 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:116289863 T>G maps to NM_002031.2 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:116325088 G>A maps to NM_002031.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr6:116289876 G>A maps to NM_002031.2 H164H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr6:116264246 G>A maps to NM_002031.2 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:116277726 C>T maps to NM_002031.2 K282K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:168467475 G>A maps to NM_024919.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr6:168464328 C>T maps to NM_024919.3 E252E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:168467484 G>A maps to NM_024919.3 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:168465604 C>T maps to NM_024919.3 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:168475946 G>A maps to NM_024919.3 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:168465649 G>A maps to NM_024919.3 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr6:168467457 G>A maps to NM_024919.3 Y146Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:168479714 G>A maps to NM_024919.3 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr9:85964640 C>T maps to NM_174938.4 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:85905578 T>C maps to NM_174938.4 E378E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:85926815 G>A maps to NM_174938.4 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:85928662 C>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr9:85863228 G>A maps to NM_174938.4 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:85863063 C>T maps to NM_174938.4 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:85926836 G>A maps to NM_174938.4 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:13698878 G>A maps to NM_018027.3 L904L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q9-06A-11D-A19A-08 chr3:69221131 T>C maps to NM_015123.1 R995R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr3:69231776 G>T maps to NM_015123.1 R671R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr3:69247889 G>A maps to NM_015123.1 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:69230587 A>T maps to NM_015123.1 V771V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:69360498 G>A maps to NM_015123.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:44166469 C>T maps to NM_032892.3 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr15:44211675 G>A maps to NM_032892.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr15:44181069 C>T maps to NM_032892.3 W243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr23:131218543 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr23:131212839 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:131218611 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:131212553 A>C did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:131216438 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:131212234 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:131212787 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:131214288 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:131220008 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:131228138 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:131216397 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:131212786 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr23:131212559 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:131212471 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:131212600 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:131234670 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:131212012 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr23:131231324 C>G did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:131212336 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr23:131212864 C>T did not map to a codon.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr23:131212600 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:131212946 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:131212171 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:131231364 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:131234713 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:131212907 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:131219667 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr11:65161521 C>T maps to NM_031904.3 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:65172501 G>A maps to NM_031904.3 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:37708486 C>T maps to NM_014907.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr9:37740120 G>A maps to NM_014907.2 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr9:37719094 G>A maps to NM_014907.2 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr9:37740765 C>T maps to NM_014907.2 P747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr9:37729759 C>T maps to NM_014907.2 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:37729768 C>T maps to NM_014907.2 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:37744536 G>A maps to NM_014907.2 R836R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:37746726 C>T maps to NM_014907.2 F1566F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:37729768 C>T maps to NM_014907.2 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr9:37737190 C>T maps to NM_014907.2 F500F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr9:37707445 G>A maps to NM_014907.2 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:37746219 C>T maps to NM_014907.2 S1397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:37707487 G>A maps to NM_014907.2 K59K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr9:37740552 G>A maps to NM_014907.2 E676E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr9:37708478 C>T maps to NM_014907.2 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr9:37707466 C>T maps to NM_014907.2 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:37707445 G>A maps to NM_014907.2 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:37724313 G>A maps to NM_014907.2 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:37744552 C>T maps to NM_014907.2 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:37692688 A>C maps to NM_014907.2 I17I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr9:37744557 G>A maps to NM_014907.2 Q843Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:49448472 C>T maps to NM_001018071.3 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr10:49420143 C>T maps to NM_001018071.3 E488E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr10:49409373 G>A maps to NM_001018071.3 V617V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:49482595 C>T maps to NM_001018071.3 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:49395277 G>A maps to NM_001018071.3 T741T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr10:49392705 C>T maps to NM_001018071.3 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:49386155 G>A maps to NM_001018071.3 I943I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr10:49420095 G>A maps to NM_001018071.3 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr10:49431252 C>T maps to NM_001018071.3 W410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr10:49448472 C>T maps to NM_001018071.3 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr10:49430445 G>A maps to NM_001018071.3 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr10:49386155 G>A maps to NM_001018071.3 I943I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr10:49400817 G>A maps to NM_001018071.3 Q692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr10:49444536 C>T maps to NM_001018071.3 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr10:49440320 C>T maps to NM_001018071.3 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:49440320 C>T maps to NM_001018071.3 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:49446129 C>T maps to NM_001018071.3 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:49459654 G>A maps to NM_001018071.3 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:12734765 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:12734766 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr23:12712556 A>C did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:12516830 C>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:12735227 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:12736260 G>A did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:12712544 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:12734463 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr23:12734280 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr23:12728641 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:12736795 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:12708396 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:12734738 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:12734931 C>T did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:12712496 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:12736324 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr23:12736018 G>C did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:12627909 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:12735935 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:12735961 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:12735779 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:12735780 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr23:12736280 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:12736222 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:12722488 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:12734244 A>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:12736726 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:12516909 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr23:12627934 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:12735173 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr23:12734874 A>G did not map to a codon.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr23:12728627 C>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:12734425 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:12735168 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr23:12734514 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:12735961 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:12734463 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:12736280 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:12632948 A>T did not map to a codon.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr23:12736774 A>T did not map to a codon.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr1:100207778 G>A maps to NM_001013660.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:100183019 G>A maps to NM_001013660.2 F394F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr1:100195220 A>G maps to NM_001013660.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:69967819 A>G maps to NM_006654.3 E204E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:69965065 C>T maps to NM_006654.3 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:69965946 C>T maps to NM_006654.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr12:69968584 C>T maps to NM_006654.3 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:41738517 G>A maps to NM_006653.3 Q440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr13:32745228 G>A maps to NM_023037.2 W658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr13:32808804 C>T maps to NM_023037.2 F1874F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr13:32711036 C>T maps to NM_023037.2 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr13:32753924 C>T maps to NM_023037.2 S995S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr13:32835892 C>G maps to NM_023037.2 S2519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr13:32760499 G>A maps to NM_023037.2 L1141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr13:32798486 C>T maps to NM_023037.2 L1627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr13:32813461 G>A maps to NM_023037.2 K2164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr13:32836467 C>T maps to NM_023037.2 P2545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr13:32776605 C>T maps to NM_023037.2 A1320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr13:32776086 C>T maps to NM_023037.2 P1252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr13:32776494 C>T maps to NM_023037.2 I1283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr13:32811633 C>A maps to NM_023037.2 R1977R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr13:32836500 C>T maps to NM_023037.2 T2556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr13:32802674 C>T maps to NM_023037.2 I1763I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr13:32811723 C>T maps to NM_023037.2 Q2007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:32735335 C>T maps to NM_023037.2 R614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:32841336 C>T maps to NM_023037.2 P2659P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr13:32745226 T>C maps to NM_023037.2 D657D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr13:32811686 C>T maps to NM_023037.2 S1994S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr13:32776086 C>T maps to NM_023037.2 P1252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr13:32835911 G>T maps to NM_023037.2 E2526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr13:32836600 G>T maps to NM_023037.2 E2590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:32698943 C>T maps to NM_023037.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:32705811 C>T maps to NM_023037.2 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:32792918 C>T maps to NM_023037.2 L1572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:32811800 C>T maps to NM_023037.2 S2032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:32812097 C>T maps to NM_023037.2 S2131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:32818261 C>T maps to NM_023037.2 V2257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:32868614 C>T maps to NM_023037.2 T2897T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr13:32798441 G>A maps to NM_023037.2 P1612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:48584555 C>T maps to NM_015030.1 W648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:48555247 G>A maps to NM_015030.1 I1473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr4:48525100 G>A maps to NM_015030.1 F2446F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr4:48545928 G>A maps to NM_015030.1 S1829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:48525001 G>A maps to NM_015030.1 N2479N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:48552674 G>T maps to NM_015030.1 R1523R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:48581195 A>T maps to NM_015030.1 S774S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr4:48566104 G>A maps to NM_015030.1 G1152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr4:48503668 G>A maps to NM_015030.1 Q2855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr4:48503669 G>A maps to NM_015030.1 N2854N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr4:48517229 T>G maps to NM_015030.1 I2584I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr2:183707233 C>T maps to NM_001463.3 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:183731064 G>A maps to NM_001463.3 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:44975512 G>A maps to NM_032135.3 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:44975395 G>A maps to NM_032135.3 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr14:44974375 C>T maps to NM_032135.3 E605E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:44974300 G>A maps to NM_032135.3 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:44975116 G>A maps to NM_032135.3 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:5642948 C>T maps to ENST00000340250 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:5633103 C>T maps to ENST00000340250 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:5643509 C>T maps to ENST00000340250 F382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:79495958 C>T maps to NM_001077182.2 H134H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:79503603 G>A maps to NM_001077182.2 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:127238523 C>T maps to NM_020369.2 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:127235622 G>A maps to NM_020369.2 W136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:127235365 G>A maps to NM_020369.2 W50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:127236430 C>T maps to NM_020369.2 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr19:4323567 G>A maps to NM_024333.2 Q473Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr19:4311968 C>T maps to NM_024333.2 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:4307943 G>A maps to NM_024333.2 Q103Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr19:4311956 G>A maps to NM_024333.2 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr19:4318403 C>T maps to NM_024333.2 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:4323543 C>T maps to NM_024333.2 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr15:83455797 C>T maps to NM_001007122.2 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:83447560 G>A maps to NM_001007122.2 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:83456025 C>T maps to NM_001007122.2 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr15:83456037 G>A maps to NM_001007122.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:83437732 C>T maps to NM_001007122.2 E484E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr15:83440852 C>T maps to NM_001007122.2 Q413Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr15:83447551 C>T maps to NM_001007122.2 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr15:83451552 G>A maps to NM_001007122.2 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:83456103 C>T maps to NM_001007122.2 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr11:30255154 G>A maps to NM_001018080.1 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:30255172 G>A maps to NM_001018080.1 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:30255247 C>T maps to NM_001018080.1 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:49190249 G>A maps to NM_000145.3 I570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:49189955 C>T maps to NM_000145.3 R668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr2:49190570 G>A maps to NM_000145.3 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:49190006 G>A maps to NM_000145.3 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:49216168 G>A maps to NM_000145.3 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr2:49191041 C>T maps to NM_000145.3 Q306Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:49190510 G>A maps to NM_000145.3 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:49190006 G>A maps to NM_000145.3 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:49190867 G>A maps to NM_000145.3 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:49244650 C>T maps to NM_000145.3 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:49189898 G>A maps to NM_000145.3 V687V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:49217772 T>C maps to NM_000145.3 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:49295371 C>T maps to NM_000145.3 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr2:49190126 C>T maps to NM_000145.3 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr2:49190045 G>A maps to NM_000145.3 F638F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr2:49190801 G>A maps to NM_000145.3 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr2:49190276 G>A maps to NM_000145.3 I561I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:49210259 G>A maps to NM_000145.3 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:49244650 C>T maps to NM_000145.3 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:49295429 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:49210282 G>A maps to NM_000145.3 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:49190762 G>A maps to NM_000145.3 F399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:39910026 G>A maps to NM_152597.4 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr15:40057915 T>C maps to NM_152597.4 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr15:39910329 C>T maps to NM_152597.4 E435E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr15:40068662 G>A maps to NM_152597.4 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:40034004 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:186678720 G>A maps to NM_173651.2 T6848T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:186672119 C>T maps to NM_173651.2 S6118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr2:186673304 C>T maps to NM_173651.2 S6513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:186672380 C>T maps to NM_173651.2 N6205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:186672203 A>C maps to NM_173651.2 T6146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:186672248 C>T maps to NM_173651.2 T6161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:186669972 A>T maps to NM_173651.2 K5403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:186672479 C>T maps to NM_173651.2 I6238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:186671201 G>A maps to NM_173651.2 R5812R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:186669989 G>A maps to NM_173651.2 L5408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:186669995 G>A maps to NM_173651.2 R5410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:186672368 C>T maps to NM_173651.2 I6201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:186671597 C>T maps to NM_173651.2 F5944F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr5:52781516 G>A maps to NM_006350.2 *318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr3:120121691 G>A maps to NM_007085.4 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:120123743 G>A maps to NM_007085.4 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:120128465 G>A maps to NM_007085.4 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:120122200 C>T maps to NM_007085.4 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr5:132556460 C>T maps to NM_015082.1 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:132535014 G>A maps to NM_015082.1 S767S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr5:132648405 G>A maps to NM_015082.1 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:132534887 G>A maps to NM_015082.1 R810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr5:132535167 G>A maps to NM_015082.1 I716I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:132552947 G>A maps to NM_015082.1 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:132552995 G>A maps to NM_015082.1 N511N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:132652231 C>T maps to NM_015082.1 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:132736598 C>T maps to NM_015082.1 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:132939626 G>A maps to NM_015082.1 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr5:132552947 G>A maps to NM_015082.1 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:132939620 C>T maps to NM_015082.1 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr5:132535089 G>A maps to NM_015082.1 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:132560845 C>T maps to NM_015082.1 K436K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:132736523 C>T maps to NM_015082.1 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:132939659 G>A maps to NM_015082.1 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr4:162577571 G>A maps to NM_020116.3 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr4:162459387 G>A maps to NM_020116.3 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr4:162508616 G>A maps to NM_020116.3 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr4:162421233 C>T maps to NM_020116.3 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:162402297 C>T maps to NM_020116.3 E494E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:162841790 C>T maps to NM_020116.3 Q58Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:162307360 C>T maps to NM_020116.3 T694T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:162459345 A>T maps to NM_020116.3 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:162402207 G>A maps to NM_020116.3 V524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr4:162402240 G>A maps to NM_020116.3 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr4:162508676 G>A maps to NM_020116.3 H315H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr4:162421169 G>A maps to NM_020116.3 Q486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr21:47574147 G>A maps to ENST00000397748 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr21:47574102 G>A maps to ENST00000397748 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr21:47566214 G>A maps to ENST00000397748 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr21:47558816 C>T maps to ENST00000397748 K427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr21:47558457 G>A maps to ENST00000397748 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:61732863 G>A maps to NM_002032.2 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:31089733 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:31090061 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:31089886 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr23:31089817 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:31089886 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:31089920 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:31089817 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:31089934 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:121188115 G>A maps to NM_177478.1 W153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr5:121187735 C>T maps to NM_177478.1 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:121188308 G>A maps to NM_177478.1 K217K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:121188020 G>A maps to NM_177478.1 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:48336903 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:48340018 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:48341134 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr7:2275011 G>A maps to NM_013393.1 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr7:2279182 G>A maps to NM_013393.1 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:2274924 G>A maps to NM_013393.1 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:61902689 C>T maps to NM_017647.3 W169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr17:61902914 G>A maps to NM_017647.3 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:61902518 G>A maps to NM_017647.3 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:61903469 A>G maps to NM_017647.3 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:61897242 G>A maps to NM_017647.3 F821F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr16:71319193 G>A maps to NM_018348.5 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:71319423 G>A maps to NM_018348.5 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr6:37414176 C>T maps to NM_015050.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr6:37446926 C>T maps to NM_015050.2 P757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr6:37420893 C>T maps to NM_015050.2 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr6:37443125 C>T maps to NM_015050.2 I658I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:37429774 C>T maps to NM_015050.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:37442304 C>T maps to NM_015050.2 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:37411832 T>G maps to NM_015050.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:37426560 C>T maps to NM_015050.2 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr6:37438795 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr1:78433884 G>A maps to ENST00000436586 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr1:78430857 G>A maps to ENST00000436586 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:78432424 G>A maps to ENST00000436586 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr9:133507358 C>T maps to NM_003934.1 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:133498141 G>A maps to NM_003934.1 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr1:24181002 G>A maps to NM_000147.4 H272H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr1:24172602 G>C maps to NM_000147.4 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:24175136 A>C did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:70508744 G>A maps to NM_145059.2 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr16:70497569 C>T maps to NM_145059.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:70506487 C>T maps to NM_145059.2 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:70497631 C>T maps to NM_145059.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:154282916 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:154282916 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:154282876 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:91419062 C>T maps to NM_002569.2 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:91424576 C>T maps to NM_002569.2 F618F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:91424897 C>T maps to NM_002569.2 I725I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr15:91424777 C>T maps to NM_002569.2 S685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr16:31195176 A>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr16:31202392 G>A maps to NM_004960.3 G501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:31202347 C>T maps to NM_004960.3 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:31198143 C>T maps to NM_004960.3 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr16:31195197 A>T maps to NM_004960.3 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr16:31195272 C>T maps to NM_004960.3 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:31200471 C>T maps to NM_004960.3 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:31201370 C>T maps to NM_004960.3 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr16:31200456 A>G maps to NM_004960.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr19:49254040 G>A maps to NM_000148.3 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:49253550 G>A maps to NM_000148.3 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:49254217 G>T maps to NM_000148.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:49254055 G>A maps to NM_000148.3 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:49254490 G>A maps to NM_000148.3 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr8:33318913 G>A maps to ENST00000380081 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr8:33230220 A>G maps to ENST00000380081 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:75533489 C>G maps to NM_173540.2 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr10:75532994 G>A maps to NM_173540.2 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:49206491 C>T maps to NM_001097638.2 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:49206782 C>T maps to NM_001097638.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:49206743 G>A maps to NM_001097638.2 E177E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:49206575 G>A maps to NM_001097638.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr19:49207160 C>T maps to NM_001097638.2 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:5843767 G>A maps to NM_001097641.1 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:5843806 G>A maps to NM_001097641.1 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:5844660 G>A maps to NM_001097641.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:5844391 G>A maps to NM_001097641.1 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:94278471 G>A maps to NM_002033.3 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:94277910 C>T maps to NM_002033.3 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:94278654 C>T maps to NM_002033.3 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr19:5867529 C>T maps to NM_002034.2 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:5867302 C>T maps to NM_002034.2 W145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:5867502 G>A maps to NM_002034.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr19:5867301 C>T maps to NM_002034.2 W145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:5867494 C>T maps to NM_002034.2 W81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:5831950 G>A maps to NM_001040701.1 Q210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:5832372 C>T maps to NM_001040701.1 W69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:139926118 G>A maps to NM_004479.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr14:66199957 T>C maps to NM_178155.1 N423N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr14:66082995 C>T maps to NM_178155.1 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A6L9-06A-11D-A32N-08 chr14:66135995 G>A maps to NM_178155.1 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:66200042 C>T maps to NM_178155.1 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr14:66028472 C>T maps to NM_178155.1 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:66209074 C>T maps to NM_178155.1 R559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:96651990 G>A maps to NM_006581.3 K320K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr6:96651294 C>T maps to NM_006581.3 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr6:96651999 T>C maps to NM_006581.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr6:96651675 C>T maps to NM_006581.3 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr6:96651294 C>T maps to NM_006581.3 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:96651085 C>T maps to NM_006581.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr6:96651189 C>T maps to NM_006581.3 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:96651273 C>T maps to NM_006581.3 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:50311712 G>A maps to NM_025129.4 R331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr11:6503273 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:71668064 T>C maps to NM_000144.4 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr17:7496150 C>T maps to NM_004860.3 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr17:7496404 G>A maps to NM_004860.3 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr17:7504809 G>A maps to NM_004860.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr19:35633399 G>A maps to NM_005031.3 E77E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:35614186 G>T maps to NM_021910.2 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr10:43871007 C>T maps to NM_173160.2 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:35642568 C>T maps to NM_022006.1 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:39202603 C>T maps to ENST00000263405 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr5:39203056 C>T maps to ENST00000263405 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr5:39202456 C>T maps to ENST00000263405 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr5:39202528 C>T maps to ENST00000263405 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr5:39134963 C>T maps to ENST00000263405 R565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:39153647 G>A maps to ENST00000263405 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr5:39202483 G>A maps to ENST00000263405 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr5:39202036 C>T maps to ENST00000263405 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr5:39202234 G>A maps to ENST00000263405 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr5:39202987 C>T maps to ENST00000263405 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:39202123 G>A maps to ENST00000263405 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr3:46009751 C>T maps to NM_024513.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:46014620 C>T maps to NM_024513.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr3:46008476 C>T maps to NM_024513.2 G783G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:46011171 G>A maps to NM_024513.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr3:46008745 G>A maps to NM_024513.2 Q694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:46009313 C>T maps to NM_024513.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:46008469 G>A maps to NM_024513.2 Q786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr3:46009379 G>A maps to NM_024513.2 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:46023067 G>A maps to NM_024513.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:112025282 G>A maps to NM_153047.1 R156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr7:90895682 C>T maps to NM_003505.1 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:90895445 C>T maps to NM_003505.1 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:90895664 C>T maps to NM_003505.1 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:90895664 C>T maps to NM_003505.1 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr12:130648491 C>T maps to NM_007197.3 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr12:130649205 C>T maps to NM_007197.3 I573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:130648035 G>A maps to NM_007197.3 K183K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:130649061 C>T maps to NM_007197.3 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr12:130648677 C>T maps to NM_007197.3 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr12:130648593 C>T maps to NM_007197.3 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:130648350 C>T maps to NM_007197.3 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:130648725 C>T maps to NM_007197.3 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:130648608 G>A maps to NM_007197.3 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:130648152 G>A maps to NM_007197.3 E222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:42636525 G>A maps to NM_001466.3 W490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr17:42636300 C>T maps to NM_001466.3 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr17:42636090 G>A maps to NM_001466.3 W345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:42636333 C>T maps to NM_001466.3 I426I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:42636135 G>A maps to NM_001466.3 W360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr17:42636369 C>T maps to NM_001466.3 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr17:42636174 C>T maps to NM_001466.3 H373H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr17:42636354 C>T maps to NM_001466.3 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:28420431 T>C maps to NM_017412.3 H635H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr8:28384778 G>T maps to NM_017412.3 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:86665986 G>A maps to NM_012193.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:86666028 C>T maps to NM_012193.2 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr2:208632176 G>A maps to NM_003468.3 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr8:104330891 C>T maps to NM_003506.3 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr8:104337155 C>T maps to NM_003506.3 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:104340521 G>A maps to NM_003506.3 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:202900791 C>T maps to NM_003507.1 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:202900182 C>T maps to NM_003507.1 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:202900659 C>T maps to NM_003507.1 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr10:35929460 G>A maps to NM_031866.2 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr10:35928512 G>A maps to NM_031866.2 S615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:35928827 G>A maps to NM_031866.2 I510I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:35929514 G>A maps to NM_031866.2 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr10:35928311 G>A maps to NM_031866.2 S682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:3527036 C>T maps to NM_001136198.1 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr19:3527748 C>A maps to NM_001136198.1 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:3523025 C>T maps to NM_001136198.1 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:3526982 C>T maps to NM_001136198.1 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:3527036 C>T maps to NM_001136198.1 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:3527685 C>T maps to NM_001136198.1 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr19:3527805 C>T maps to NM_001136198.1 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr19:3527703 C>T maps to NM_001136198.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr14:31085541 C>T maps to NM_017769.3 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:31084662 C>T maps to NM_017769.3 I594I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr14:31066624 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:151170505 C>T maps to NM_198395.1 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr17:41061428 C>T maps to NM_000151.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:41063430 G>A maps to NM_000151.2 K354K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:41063292 C>T maps to NM_000151.2 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:41063391 C>T maps to NM_000151.2 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:41063349 C>T maps to NM_000151.2 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J6-06A-11D-A19A-08 chr23:153774256 A>C did not map to a codon.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr23:153760418 G>A did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:153762622 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr23:153760654 T>A did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:153760405 C>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:153761271 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:78082399 C>T maps to NM_001079804.1 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:78092137 C>T maps to NM_001079804.1 V876V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr17:78084623 C>T maps to NM_001079804.1 F512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr17:78082286 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:78081397 C>T maps to NM_001079804.1 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:78084762 C>T maps to NM_001079804.1 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:78086481 C>T maps to NM_001079804.1 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr17:78078435 C>T maps to NM_001079804.1 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:78092029 C>T maps to NM_001079804.1 P840P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:78084545 C>T maps to NM_001079804.1 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr17:78083817 C>T maps to NM_001079804.1 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:78085842 C>T maps to NM_001079804.1 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr4:144361296 A>G maps to NM_207123.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:144381636 C>T maps to NM_207123.2 D630D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:77937787 C>T maps to NM_080491.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:77931433 C>T maps to NM_080491.2 K606K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:153908453 A>T did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:153925420 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr23:153925438 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:153944424 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr23:153908420 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr23:153944499 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:153928315 G>A did not map to a codon.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr23:153944400 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:153944591 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr22:17472952 C>T maps to NM_001037814.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr22:17447125 G>A maps to NM_001037814.1 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr22:17445655 C>T maps to NM_001037814.1 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:17468992 G>A maps to NM_001037814.1 C181C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:17445658 G>A maps to NM_001037814.1 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:7144738 G>A maps to NM_007278.1 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr16:75601933 G>C did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr6:29581118 G>A maps to NM_001470.2 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:29572396 G>A maps to NM_001470.2 T862T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:29572282 C>T maps to NM_001470.2 K900K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr6:29581097 C>T maps to NM_001470.2 E496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:29595316 G>A maps to NM_001470.2 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr6:29572297 G>A maps to NM_001470.2 N895N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:29571448 C>T maps to NM_001470.2 R919R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:101258771 G>A maps to NM_005458.7 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:101156520 C>T maps to NM_005458.7 K438K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr9:101133788 C>T maps to NM_005458.7 W576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr9:101061632 C>T maps to NM_005458.7 L805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:101056137 C>T maps to NM_005458.7 Q863Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr21:27141392 T>A maps to NM_002040.3 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr21:27121431 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:50593566 T>C did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr15:50596162 C>T maps to NM_005254.5 K92K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr15:50570923 G>A maps to NM_005254.5 R365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:151079543 C>T maps to NM_144618.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:151062911 C>T maps to NM_144618.2 Q47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr1:151076050 C>T maps to NM_144618.2 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr1:151070437 C>T maps to NM_144618.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:151062928 C>T maps to NM_144618.2 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr1:151079642 C>T maps to NM_144618.2 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:151090539 C>T maps to NM_144618.2 Y385Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr5:161281226 G>A maps to NM_001127648.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr5:161309652 C>T maps to NM_001127648.1 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr5:161324262 C>T maps to NM_001127648.1 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr5:161292769 C>T maps to NM_001127648.1 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:161281226 G>A maps to NM_001127648.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:161277863 C>T maps to NM_001127648.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr5:161292769 C>T maps to NM_001127648.1 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:161300262 G>A maps to NM_001127648.1 K132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:46334682 G>A maps to ENST00000507069 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr4:46252456 C>T maps to ENST00000507069 K468K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr4:46314595 C>T maps to ENST00000507069 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:46312247 T>C maps to ENST00000507069 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:46314658 G>A maps to ENST00000507069 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:46252528 G>A maps to ENST00000507069 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:46307624 C>T maps to ENST00000507069 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:46388187 G>A maps to ENST00000507069 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:46305600 G>A maps to ENST00000507069 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr4:46314708 G>A maps to ENST00000507069 R94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:46263976 C>T maps to ENST00000507069 W342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:46312190 G>A maps to ENST00000507069 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:46307612 G>A maps to ENST00000507069 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr4:46252588 G>A maps to ENST00000507069 N424N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr4:46314595 C>T maps to ENST00000507069 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:151358361 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr23:151376472 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:151424281 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:151336925 T>G did not map to a codon.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr23:151514132 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr23:151453207 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:151358361 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:151424445 G>A did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:151336802 G>A did not map to a codon.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr23:151376544 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:151424267 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:151532951 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:151366214 T>A did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:151336984 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:151424270 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:151358361 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:151336951 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:151336711 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:151532988 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:151393273 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:151532973 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr23:151453190 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:151336912 G>T did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:151514066 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:151376556 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:151424445 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:151514097 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:151336937 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:151376573 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:151376574 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:151336774 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:151393282 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:151393283 C>T did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:151336723 G>A did not map to a codon.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr23:151514097 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr4:46973211 C>T maps to NM_000809.2 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr4:46994905 G>A maps to NM_000809.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr4:46930340 G>A maps to NM_000809.2 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr4:46979123 C>T maps to NM_000809.2 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:46930754 C>T maps to NM_000809.2 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr15:27159994 G>A maps to NM_000810.3 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr15:27128355 C>T maps to NM_000810.3 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr15:27193268 C>T maps to NM_000810.3 D426D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr15:27185162 G>A maps to NM_000810.3 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr15:27128373 G>A maps to NM_000810.3 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr5:161117306 C>T maps to NM_000811.2 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr5:161116136 C>T maps to NM_000811.2 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr5:161128526 G>A maps to NM_000811.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr5:161113343 G>A maps to NM_000811.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr5:161119160 G>A maps to NM_000811.2 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr5:161116328 C>T maps to NM_000811.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr5:161116663 C>T maps to NM_000811.2 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:161117249 G>A maps to NM_000811.2 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:161113234 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:161119130 G>A maps to NM_000811.2 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:161116025 G>A maps to NM_000811.2 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr5:161119130 G>A maps to NM_000811.2 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr5:161117246 G>A maps to NM_000811.2 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:161118947 G>A maps to NM_000811.2 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr5:161116046 G>A maps to NM_000811.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr5:161119082 C>T maps to NM_000811.2 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:161115986 C>T maps to NM_000811.2 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:161116025 G>A maps to NM_000811.2 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:47408762 C>T maps to NM_000812.3 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr4:47408912 G>A maps to NM_000812.3 E350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr4:47408891 A>G maps to NM_000812.3 K343K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr4:47405720 C>T maps to NM_000812.3 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr4:47405407 C>T maps to NM_000812.3 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:47428007 C>T maps to NM_000812.3 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:47408898 C>T maps to NM_000812.3 Q346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr4:47408823 C>T maps to NM_000812.3 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:47427917 C>T maps to NM_000812.3 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:47427929 C>T maps to NM_000812.3 I440I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:47427764 G>A maps to NM_000812.3 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:47408879 G>A maps to NM_000812.3 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr4:47427764 G>A maps to NM_000812.3 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr4:47163299 G>A maps to NM_000812.3 W92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:47405690 G>A maps to NM_000812.3 W266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr4:47427947 G>A maps to NM_000812.3 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr5:160761828 G>A maps to NM_021911.2 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:160758021 G>A maps to NM_021911.2 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:160758021 G>A maps to NM_021911.2 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:160757910 C>T maps to NM_021911.2 K352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr5:160757948 T>A maps to NM_021911.2 K340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:160757960 G>A maps to NM_021911.2 Q336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:160757961 G>A maps to NM_021911.2 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:160763708 C>T maps to NM_021911.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:160721204 C>T maps to NM_021911.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr5:160761780 A>C maps to NM_021911.2 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:160838059 G>A maps to NM_021911.2 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:160753373 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:160761765 C>T maps to NM_021911.2 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:160721435 C>A did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr5:160721204 C>T maps to NM_021911.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr5:160758015 G>A maps to NM_021911.2 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr5:160721114 G>A maps to NM_021911.2 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr5:160721144 G>A maps to NM_021911.2 F494F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr5:160757970 C>T maps to NM_021911.2 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr5:160721237 C>T maps to NM_021911.2 K463K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr15:26792987 G>A maps to NM_021912.4 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr15:26792967 A>C maps to NM_021912.4 L465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:26792999 G>A maps to NM_021912.4 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr15:26825532 C>T maps to NM_021912.4 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr15:26792999 G>A maps to NM_021912.4 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:26806165 G>A maps to NM_021912.4 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:26806323 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:26793152 C>T maps to NM_021912.4 R403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:26825603 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:26793216 G>C maps to NM_021912.4 S382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr15:26792999 G>A maps to NM_021912.4 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr15:26825472 G>A maps to NM_021912.4 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr15:26825472 G>A maps to NM_021912.4 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr15:26806141 C>T maps to NM_021912.4 Q339Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:26825472 G>A maps to NM_021912.4 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:26825569 C>T maps to NM_021912.4 W193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:1956994 G>A maps to NM_000815.4 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:1961504 C>T maps to NM_000815.4 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:1961050 G>A maps to NM_000815.4 R303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr23:151124223 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:151123950 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:151123220 A>T did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:151124191 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:151124192 G>A did not map to a codon.
Sequencing variant TCGA-EB-A44R-06A-41D-A25O-08 chr23:151128425 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:151130983 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:151131031 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:151138773 C>T did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:151138794 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr23:151128444 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:151128444 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr23:151124258 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:151123887 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:151123217 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:151123932 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr23:151123983 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:151124223 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:151123443 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:151123444 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:151131054 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:151128323 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:151128325 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:151138708 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:151138707 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:151123309 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:151124194 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:151124223 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr23:151123420 C>T did not map to a codon.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr23:151124306 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1YX-06A-11D-A197-08 chr23:151128358 C>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr23:151123983 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:151123208 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr23:151123252 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:151130953 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:151124223 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:151123528 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:151123529 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:151128378 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:151138713 G>A did not map to a codon.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr23:151123231 A>C did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr4:46066509 C>T maps to NM_173536.3 Q191Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:46043061 G>A maps to NM_173536.3 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:46060538 C>T maps to NM_173536.3 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:46043061 G>A maps to NM_173536.3 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:46060330 G>A maps to NM_173536.3 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:46043157 G>A maps to NM_173536.3 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr4:46060532 C>T maps to NM_173536.3 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr4:46066479 G>A maps to NM_173536.3 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:46067417 G>A maps to NM_173536.3 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:46060604 C>T maps to NM_173536.3 W220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr4:46067379 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:46060384 C>T maps to NM_173536.3 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:46125900 G>A maps to NM_173536.3 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr5:161569284 G>A maps to NM_198903.2 W335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:161524651 T>C maps to NM_198903.2 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:161580160 T>C maps to NM_198903.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr5:161580137 C>T maps to NM_198903.2 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr5:161580115 C>T maps to NM_198903.2 I430I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:161576177 C>T maps to NM_198903.2 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:161524744 G>A maps to NM_198903.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:161576277 C>A maps to NM_198903.2 R403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:161524819 G>A maps to NM_198903.2 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:27772726 C>T maps to NM_033223.4 N338N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr15:27572083 C>T maps to NM_033223.4 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr15:27574021 G>A maps to NM_033223.4 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr15:27572134 C>T maps to NM_033223.4 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:27725916 C>T maps to NM_033223.4 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:27777960 G>A maps to NM_033223.4 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr15:27572068 C>T maps to NM_033223.4 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr15:27772759 G>A maps to NM_033223.4 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr15:27572161 C>T maps to NM_033223.4 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr15:27772684 C>T maps to NM_033223.4 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr15:27572011 C>T maps to NM_033223.4 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr15:27778020 T>A maps to NM_033223.4 Y466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:27571982 C>T maps to NM_033223.4 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr15:27777912 G>A maps to NM_033223.4 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr5:170239060 C>T maps to NM_014211.2 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:170222291 G>A maps to NM_014211.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:170239210 G>A maps to NM_014211.2 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:170222312 C>T maps to NM_014211.2 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr5:170232825 C>T maps to NM_014211.2 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr5:170239141 G>A maps to NM_014211.2 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:170235688 C>T maps to NM_014211.2 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr5:170222423 C>T maps to NM_014211.2 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr5:170222402 C>T maps to NM_014211.2 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:170236608 C>T maps to NM_014211.2 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:170222289 C>T maps to NM_014211.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:170235727 C>T maps to NM_014211.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:151818906 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr23:151820051 T>A did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:151821086 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:151821243 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:151821257 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:151821285 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:151820121 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:151820191 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:151821285 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr23:151821279 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:151821303 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:151821285 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:151821632 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:151821262 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr23:151818906 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:151821656 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:151806766 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:151818283 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:151815515 G>T did not map to a codon.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr23:151818303 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:151820082 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:151821279 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:151820004 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:151818292 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:151818226 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr6:89891672 C>T maps to NM_002042.3 W300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr6:89891673 C>T maps to NM_002042.3 W300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr6:89891702 G>A maps to NM_002042.3 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:89895080 G>A maps to NM_002042.3 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr6:89907953 C>A maps to NM_002042.3 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr6:89895098 C>T maps to NM_002042.3 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:89895098 C>A maps to NM_002042.3 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:89967664 G>A maps to NM_002043.2 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:89967510 G>A maps to NM_002043.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:89978947 G>A maps to NM_002043.2 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:89975400 G>A maps to NM_002043.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:97753801 G>A maps to NM_001105580.1 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr3:97711707 C>T maps to NM_001105580.1 K364K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr3:97744495 A>G maps to NM_001105580.1 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:97711710 G>A maps to NM_001105580.1 F363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:97731255 G>A maps to NM_001105580.1 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr2:171709221 A>T did not map to a codon.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr2:171687658 C>T maps to NM_000817.2 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:171716241 G>A maps to NM_000817.2 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr2:171705803 G>A maps to NM_000817.2 W376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:171686120 C>T maps to NM_000817.2 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:171702043 C>T maps to NM_000817.2 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr10:26589853 G>A maps to NM_001134366.1 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:26508015 C>T maps to NM_001134366.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:26575314 C>T maps to NM_001134366.1 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr10:26508002 C>A maps to NM_001134366.1 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:26513566 G>A maps to NM_001134366.1 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:26589850 C>T maps to NM_001134366.1 F573F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:26518624 C>T maps to NM_001134366.1 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:26575278 G>A maps to NM_001134366.1 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:26513536 C>T maps to NM_001134366.1 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr10:26513470 C>T maps to NM_001134366.1 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr10:26508080 G>A maps to NM_001134366.1 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:26589850 C>T maps to NM_001134366.1 F573F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr19:2477114 C>T maps to NM_015675.3 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr19:2477182 C>T maps to NM_015675.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr3:30875356 C>T maps to NM_207359.2 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr3:30842484 G>A maps to NM_207359.2 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:30885919 C>T maps to NM_207359.2 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:30819688 G>A maps to NM_207359.2 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr23:49173730 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:49161357 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr23:49173755 G>A did not map to a codon.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr23:49161351 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:49161410 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:49161357 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:49355892 C>G did not map to a codon.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr23:49236843 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:49355800 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr4:887206 G>A maps to NM_005255.2 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr4:860792 G>A maps to NM_005255.2 A941A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:853510 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:860807 G>A maps to NM_005255.2 L936L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr4:887662 G>A maps to NM_005255.2 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr4:845553 G>A maps to NM_005255.2 V1164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr4:887677 G>A maps to NM_005255.2 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr22:30951491 C>T maps to NM_004861.1 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr22:30953355 G>A maps to NM_004861.1 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr22:30951053 G>A maps to NM_004861.1 H386H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr22:30951122 C>T maps to NM_004861.1 Q363Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:30951701 G>A maps to NM_004861.1 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr22:30951446 G>A maps to NM_004861.1 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr22:30950951 G>A maps to NM_004861.1 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:30951848 G>A maps to NM_004861.1 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr22:30950969 C>T maps to NM_004861.1 W414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:30951446 G>A maps to NM_004861.1 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr22:30951821 C>T maps to NM_004861.1 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr2:242716378 C>T maps to NM_022134.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:242742833 C>T maps to NM_022134.2 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr2:242742800 C>T maps to NM_022134.2 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:242741357 C>T maps to NM_022134.2 Y94Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:242742893 C>T maps to NM_022134.2 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:242741285 C>T maps to NM_022134.2 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:65811069 G>A maps to NM_033036.2 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr11:65810673 G>A maps to NM_033036.2 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:65810823 G>A maps to NM_033036.2 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:65811141 G>A maps to NM_033036.2 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr11:65810580 C>T maps to NM_033036.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:65810760 G>A maps to NM_033036.2 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:65810928 G>A maps to NM_033036.2 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:65810958 G>A maps to NM_033036.2 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:88417020 A>G maps to NM_000153.2 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr14:88450794 G>A maps to NM_000153.2 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:88448554 A>T maps to NM_000153.2 Y205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:88448547 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:88414168 G>A maps to NM_000153.2 F464F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:88429745 G>A maps to NM_000153.2 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr14:88417023 G>A maps to NM_000153.2 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:24125209 G>A maps to NM_001008216.1 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:24124653 G>A maps to NM_001008216.1 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:24123213 C>T maps to NM_001008216.1 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr17:73758812 G>A maps to ENST00000437911 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:73760002 G>A maps to ENST00000437911 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:73759117 G>A maps to ENST00000437911 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:73758812 G>A maps to ENST00000437911 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr17:73754178 G>A maps to ENST00000437911 Y409Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:38958933 C>T maps to NM_138801.2 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:88901702 G>A maps to NM_000512.4 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:88923279 C>T maps to NM_000512.4 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:88902209 G>A maps to NM_000512.4 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr16:88909219 G>A maps to NM_000512.4 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:153755895 C>T maps to NM_198321.3 R210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr5:153765887 C>A maps to NM_198321.3 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr5:153755895 C>T maps to NM_198321.3 R210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:153765878 C>G maps to NM_198321.3 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:153765948 T>C maps to NM_198321.3 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr7:151815815 G>A maps to NM_022087.2 Q502Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr7:151791497 C>T maps to NM_022087.2 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:151797961 C>T maps to NM_022087.2 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr7:151818698 G>A maps to NM_022087.2 K588K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:151818042 G>A maps to NM_022087.2 W562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr9:101594158 C>T maps to NM_024642.3 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:101585546 G>A maps to NM_024642.3 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:101589064 T>A maps to NM_024642.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr2:155099271 T>A maps to NM_052917.2 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:155099232 G>A maps to NM_052917.2 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr2:155099232 G>A maps to NM_052917.2 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:155265591 C>T maps to NM_052917.2 Q465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr2:154801127 A>T maps to NM_052917.2 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:155102465 G>A maps to NM_052917.2 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:154801054 G>A maps to NM_052917.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:155307002 G>A maps to NM_052917.2 Q537Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr2:155099340 C>T maps to NM_052917.2 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr2:155102423 G>A maps to NM_052917.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:154996946 C>T maps to NM_052917.2 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:155099241 G>A maps to NM_052917.2 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:155265587 A>T maps to NM_052917.2 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:154801015 G>A maps to NM_052917.2 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr2:31135093 G>A maps to NM_024572.2 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr2:31168700 G>A maps to NM_024572.2 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr2:31135115 G>A maps to NM_024572.2 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:31133832 C>T maps to NM_024572.2 K531K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:31135208 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:31165109 C>T maps to NM_024572.2 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr2:31154986 G>A maps to NM_024572.2 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr2:31178564 C>T maps to NM_024572.2 Q191Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr2:31133920 C>T maps to NM_024572.2 W502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:31135151 G>A maps to NM_024572.2 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:31133826 G>A maps to NM_024572.2 I533I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:31152265 G>A maps to NM_024572.2 F382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:31152340 C>T maps to NM_024572.2 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:31155016 G>A maps to NM_024572.2 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:31215707 G>A maps to NM_024572.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr2:31178492 C>T maps to NM_024572.2 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr2:31181290 G>A maps to NM_024572.2 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:31147107 G>A maps to NM_024572.2 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:31133898 G>A maps to NM_024572.2 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:31133826 G>A maps to NM_024572.2 I533I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:31167798 C>T maps to NM_024572.2 W251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:31167797 C>T maps to NM_024572.2 W251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:230415146 G>A maps to NM_004481.3 E553E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:230400985 G>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:230381828 A>G maps to NM_004481.3 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:230338998 C>T maps to NM_004481.3 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:166606257 G>A maps to NM_004482.3 I591I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr2:166616015 G>A maps to NM_004482.3 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:166611211 A>G maps to NM_004482.3 C517C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:89917435 C>T maps to NM_003774.4 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:89917185 G>T maps to NM_003774.4 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:89917456 G>A maps to NM_003774.4 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr2:158115962 A>T maps to NM_014568.1 R457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:158115349 C>T maps to NM_014568.1 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:158152205 G>A maps to NM_014568.1 V591V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:158157216 C>T maps to NM_014568.1 I715I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:158157375 C>T maps to NM_014568.1 I768I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:158114749 G>A maps to NM_014568.1 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:158142596 G>A maps to NM_014568.1 E564E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr2:158142525 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:158114662 C>T maps to NM_014568.1 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr2:158165143 C>T maps to NM_014568.1 I862I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:51754528 C>T maps to NM_007210.3 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:51752918 T>C maps to NM_007210.3 Q455Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr12:51751231 G>A maps to NM_007210.3 I501I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:51751177 C>T maps to NM_007210.3 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:51754507 G>A maps to NM_007210.3 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:51754510 G>A maps to NM_007210.3 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:51753044 G>A maps to NM_007210.3 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr12:51748165 G>A maps to NM_007210.3 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:51752036 G>A maps to NM_007210.3 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:51757906 G>A maps to NM_007210.3 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:51758029 G>A maps to NM_007210.3 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:51759244 C>T maps to NM_007210.3 Q261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:174169414 C>T maps to NM_017423.2 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:4872537 C>T maps to NM_017417.1 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr12:4848449 C>T maps to NM_017417.1 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:4853788 C>T maps to NM_017417.1 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr12:4853770 G>A maps to NM_017417.1 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:4853836 G>A maps to NM_017417.1 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:4870256 G>A maps to NM_017417.1 W436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:4870182 G>A maps to NM_017417.1 E411E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:4829878 C>T maps to NM_017417.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:4835914 C>T maps to NM_017417.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:132683751 C>T maps to NM_001122636.1 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr14:69795191 G>A maps to NM_020692.2 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr14:69795227 G>A maps to NM_020692.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr14:69814700 C>T maps to NM_020692.2 N507N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr14:69787426 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:69805410 C>T maps to NM_020692.2 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr14:69800303 G>A maps to NM_020692.2 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr14:69805410 C>T maps to NM_020692.2 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr3:16216759 C>T maps to NM_054110.4 H34H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:16252732 C>T maps to NM_054110.4 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr3:16250048 G>A maps to NM_054110.4 W317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr3:16217017 C>T maps to NM_054110.4 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:16217065 G>C maps to NM_054110.4 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:16237353 G>A maps to NM_054110.4 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:16216933 G>A maps to NM_054110.4 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:16250069 C>T maps to NM_054110.4 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:16237311 C>T maps to NM_054110.4 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr3:16217065 G>A maps to NM_054110.4 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr3:16237389 C>T maps to NM_054110.4 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:16254141 C>T maps to NM_054110.4 Q422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:11348662 G>A maps to NM_198516.2 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:11400710 G>A maps to NM_198516.2 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:11314704 C>T maps to NM_198516.2 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:11400638 G>A maps to NM_198516.2 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:11354309 G>A maps to NM_198516.2 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:11400710 G>A maps to NM_198516.2 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr11:11394175 C>T maps to NM_198516.2 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr11:11394176 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr7:151716757 C>T maps to NM_145292.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr7:151664386 G>A maps to NM_145292.3 W19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:151700003 C>T maps to NM_145292.3 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr7:151716804 G>A maps to NM_145292.3 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:151716745 C>T maps to NM_145292.3 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr7:151711861 G>A maps to NM_145292.3 W387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:151668141 G>A maps to NM_145292.3 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr7:151716745 C>T maps to NM_145292.3 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr4:173734778 G>A maps to NM_001034845.2 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr4:173852373 G>A maps to NM_001034845.2 R368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:173269755 C>T maps to NM_001034845.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr4:173873270 C>T maps to NM_001034845.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:173852373 G>A maps to NM_001034845.2 R368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr4:173269811 C>T maps to NM_001034845.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:56694573 G>A maps to NM_033106.3 E96E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr19:56688491 C>T maps to NM_033106.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:56688528 C>T maps to NM_033106.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:56696611 C>T maps to NM_033106.3 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56696614 G>A maps to NM_033106.3 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr18:74963124 C>T maps to NM_001480.3 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:74980602 C>T maps to NM_001480.3 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr18:74980683 G>A maps to NM_001480.3 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr18:74963118 C>T maps to NM_001480.3 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr18:74963142 C>T maps to NM_001480.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr18:74968154 G>A maps to NM_001480.3 K236K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr18:74968115 C>T maps to NM_001480.3 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:74968154 G>A maps to NM_001480.3 K236K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr18:74968139 G>A maps to NM_001480.3 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:74071155 C>T maps to NM_003857.2 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr22:38221145 G>A maps to NM_003614.1 W259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr9:34647891 C>T maps to NM_000155.2 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr9:34647855 G>A maps to NM_000155.2 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:34647827 G>C did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:34649470 C>T maps to NM_000155.2 Y323Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr16:81411176 C>T maps to NM_022041.3 F590F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:62398279 G>A maps to NM_198335.2 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr15:42619582 C>T maps to NM_198141.2 F481F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:42643619 C>G maps to NM_198141.2 T875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr15:42631882 C>T maps to NM_198141.2 F620F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F4-06A-12D-A25O-08 chr15:42632948 C>T maps to NM_198141.2 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr3:115439674 C>T maps to NM_001130064.1 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr3:115395158 G>A maps to NM_001130064.1 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:6644006 G>A maps to NM_002046.3 K3K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:36035821 G>T maps to NM_014364.4 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr19:36033243 G>A maps to NM_014364.4 W158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr5:57790677 A>T maps to NM_152687.2 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:57790722 C>T maps to NM_152687.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:128069804 C>T maps to NM_015635.2 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr9:128088794 G>A maps to NM_015635.2 E653E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr9:128064777 C>T maps to NM_015635.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr9:128099779 C>T maps to NM_015635.2 L956L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr9:128111771 C>T maps to NM_015635.2 H1118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr4:110737532 C>T maps to NM_018983.3 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:110745160 C>T maps to NM_018983.3 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr9:130075765 C>T maps to NM_032293.4 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:130098438 C>T maps to NM_032293.4 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:130152977 C>T maps to NM_032293.4 P934P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr9:130111234 C>T maps to NM_032293.4 F488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr21:34876802 G>A maps to NM_001136006.1 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr21:34889365 G>A maps to NM_001136006.1 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:22707214 G>A maps to NM_005256.3 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:22777492 C>T maps to NM_005256.3 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:22747965 A>G maps to NM_005256.3 E132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:22747926 G>A maps to NM_005256.3 W119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr22:29704610 C>T maps to NM_152236.1 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr22:29704232 G>A maps to NM_152236.1 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr22:29704556 C>T maps to NM_152236.1 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr22:29704304 C>T maps to NM_152236.1 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:34073270 C>T maps to NM_139285.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:34072304 C>T maps to NM_139285.2 E737E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:34074222 C>T maps to NM_139285.2 Q299Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:34072433 C>T maps to NM_139285.2 G694G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:34071944 T>C maps to NM_139285.2 Q857Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:34073195 G>A maps to NM_139285.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr17:34072178 C>T maps to NM_139285.2 R779R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr17:34072046 C>T maps to NM_139285.2 K823K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr17:34072166 C>T maps to NM_139285.2 R783R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr17:34079560 G>A maps to NM_139285.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr17:34072331 C>T maps to NM_139285.2 S728S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:34072031 G>A maps to NM_139285.2 S828S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:34074267 G>A maps to NM_139285.2 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:101005899 C>T maps to NM_174942.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr12:101017575 A>T maps to NM_174942.1 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr13:114524979 G>T maps to ENST00000357389 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:114535376 G>A maps to ENST00000357389 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:9820630 G>A maps to NM_201433.1 R449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:9820658 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr17:9828802 G>A maps to NM_201433.1 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:9850237 G>A maps to NM_201433.1 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr17:9820592 G>A maps to NM_201433.1 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:9873044 G>A maps to NM_201433.1 H140H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:90104192 C>T maps to NM_001481.2 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:90097792 C>T maps to NM_001481.2 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:39872036 C>T maps to NM_000805.3 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:39872042 G>A maps to NM_000805.3 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:48652529 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:48650335 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:48649639 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:48652279 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:48652474 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:48651591 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:128200014 T>G maps to NM_032638.4 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:128204927 G>A maps to NM_032638.4 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr3:128199960 G>A maps to NM_032638.4 H448H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:128199903 G>A maps to NM_032638.4 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:128204927 G>A maps to NM_032638.4 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr3:128199921 G>A maps to NM_032638.4 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:128200679 G>A maps to NM_032638.4 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:128205203 C>T maps to NM_032638.4 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:128205211 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:8111503 G>A maps to NM_001002295.1 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:8115916 G>A maps to NM_001002295.1 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:8115859 C>T maps to NM_001002295.1 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr8:11607645 C>T maps to NM_002052.3 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:11612577 G>A maps to NM_002052.3 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:11612604 G>A maps to NM_002052.3 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:11615842 C>T maps to NM_002052.3 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr20:61048532 G>A maps to NM_080473.4 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr7:92080049 C>T maps to NM_021167.3 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:153791326 T>G maps to NM_020699.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr12:120884560 C>T maps to NM_176818.2 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr15:45660330 G>A maps to ENST00000432007 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:45657032 C>T maps to ENST00000432007 W388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr15:45668900 C>T maps to ENST00000432007 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:45656179 G>A maps to ENST00000432007 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr22:30681832 G>A maps to ENST00000434291 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr22:30683442 G>A maps to ENST00000434291 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:30683448 G>A maps to ENST00000434291 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:155206067 G>A maps to NM_001005742.2 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:155209782 G>A maps to NM_001005742.2 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr9:35739702 G>A maps to NM_020944.2 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr9:35738892 T>C maps to NM_020944.2 E601E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr4:22749268 C>T maps to NM_020973.3 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr4:22749498 C>T maps to NM_020973.3 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:22749268 C>T maps to NM_020973.3 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:22749696 A>G maps to NM_020973.3 K355K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:22820494 C>T maps to NM_020973.3 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr4:22749087 C>T maps to NM_020973.3 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr4:22820479 C>A maps to NM_020973.3 V448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:22737781 C>T maps to NM_020973.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr4:22820512 C>T maps to NM_020973.3 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:56051491 C>T maps to NM_001483.1 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:81698073 G>A maps to ENST00000264326 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr10:104140010 C>T maps to NM_004193.2 F1627F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr10:104122405 C>T maps to NM_004193.2 R620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr10:104135127 C>T maps to NM_004193.2 L1224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr10:104128019 G>A maps to NM_004193.2 R895R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:104142017 C>T maps to NM_004193.2 I1835I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr10:104126903 C>T maps to NM_004193.2 I831I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr10:104120831 C>T maps to NM_004193.2 F481F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr10:104120094 C>T maps to NM_004193.2 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZY-06A-11D-A197-08 chr10:104120106 C>T maps to NM_004193.2 T448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr10:104136510 C>T maps to NM_004193.2 L1413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr9:136029197 G>A maps to NM_021996.4 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr9:136029371 C>T maps to NM_021996.4 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:89520409 G>T maps to NM_002053.2 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:89528827 G>A maps to NM_002053.2 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:89523813 C>T maps to NM_002053.2 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr1:89522680 C>T maps to NM_002053.2 Q337Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr1:89582840 G>A maps to NM_004120.3 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr1:89586828 C>T maps to NM_004120.3 E105E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:89587523 C>T maps to NM_004120.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:89582870 G>A maps to NM_004120.3 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:89582837 G>A maps to NM_004120.3 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr1:89478910 G>A maps to NM_018284.2 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:89480309 G>A maps to NM_018284.2 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:89476670 C>T maps to NM_018284.2 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:89481011 G>A maps to NM_018284.2 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:89652710 G>A maps to NM_052941.4 A495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:89657031 G>A maps to NM_052941.4 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr1:89658996 C>T maps to NM_052941.4 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:89655735 G>A maps to NM_052941.4 F394F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:89661102 G>A maps to NM_052941.4 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:89655735 G>A maps to NM_052941.4 F394F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr1:89652761 G>A maps to NM_052941.4 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:89735112 C>T maps to NM_052942.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr1:89732655 G>A maps to NM_052942.3 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr1:89732245 G>A maps to NM_052942.3 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr1:89733187 G>A maps to NM_052942.3 Q114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:89730415 T>A maps to NM_052942.3 K368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr1:89846140 T>G maps to NM_198460.2 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr1:89851006 A>G maps to NM_198460.2 K627K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:89846119 T>C maps to NM_198460.2 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:89845981 G>A maps to NM_198460.2 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:89846008 A>G maps to NM_198460.2 K230K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:89844101 G>A maps to NM_198460.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:89618367 C>T maps to NM_207398.2 Q137Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:89613372 T>C maps to NM_207398.2 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:89614988 G>A maps to NM_207398.2 Q380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr1:89618020 C>T maps to NM_207398.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr1:89607328 T>G maps to NM_207398.2 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr2:237074898 G>A maps to NM_001485.2 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr4:72620796 A>G maps to ENST00000504199 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr4:72618249 A>T maps to ENST00000504199 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr2:163216049 C>T maps to NM_012198.3 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:163204218 C>T maps to NM_012198.3 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr22:38208988 C>T maps to NM_001171690.1 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:38211242 C>T maps to NM_001171690.1 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr22:38211287 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr22:38211685 G>A maps to NM_001171690.1 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr22:38212688 C>T maps to NM_001171690.1 F434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:38211195 C>T maps to NM_001171690.1 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr7:127223348 C>T maps to NM_024523.5 E349E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:127225113 G>T maps to NM_024523.5 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr7:127224624 C>T maps to NM_024523.5 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr7:127222361 C>T maps to NM_024523.5 E678E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr2:109087818 A>G maps to NM_181453.3 E678E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr2:109099570 G>A maps to NM_181453.3 K1133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:109092240 C>T maps to NM_181453.3 R999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr2:109087300 G>T maps to NM_181453.3 E506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:109104199 C>T maps to NM_181453.3 R1326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr19:13007021 C>T maps to NM_000159.2 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:13007225 C>T maps to NM_000159.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:13004357 G>A maps to NM_000159.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:13010514 C>T maps to NM_013976.2 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr3:111842514 C>T maps to NM_001190259.1 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:111845879 C>T maps to NM_001190259.1 W50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:34117201 G>A maps to NM_016631.3 D697D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr21:34131545 G>A maps to NM_016631.3 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:34123225 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:163002102 G>A maps to ENST00000233604 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr14:55310755 G>A maps to NM_001024024.1 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr15:41059480 G>A maps to NM_005258.2 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:44186117 G>C maps to NM_000162.3 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:44191959 C>T maps to NM_000162.3 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:44197674 G>A maps to NM_033508.1 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr7:44193017 C>T maps to NM_000162.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr7:44189362 G>A maps to NM_000162.3 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:44191932 G>A maps to NM_000162.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr7:44190560 G>A maps to NM_000162.3 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:44228525 C>T maps to NM_000162.3 E9E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:27720145 G>A maps to NM_001486.3 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:27731111 C>T maps to NM_001486.3 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:27741758 G>A maps to NM_001486.3 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:27720497 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:27745391 G>A maps to NM_001486.3 Q546Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:27741758 G>A maps to NM_001486.3 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:27745388 C>T maps to NM_001486.3 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:27731105 G>A maps to NM_001486.3 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:27726414 C>T maps to NM_001486.3 R227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:27731105 G>A maps to NM_001486.3 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:27746304 G>A maps to NM_001486.3 *626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr2:27729362 C>T maps to NM_001486.3 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr2:27721646 C>T maps to NM_001486.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr6:53387243 G>A maps to NM_001498.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:53364878 G>A maps to NM_001498.3 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:53379055 C>A maps to NM_001498.3 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:53372314 C>T maps to NM_001498.3 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:94354691 G>A maps to NM_002061.2 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr6:52993714 C>T maps to NM_003643.3 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:52993584 G>A maps to NM_003643.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr6:52993246 C>T maps to NM_003643.3 W356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:52993216 C>T maps to NM_003643.3 E366E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:10876689 C>T maps to NM_004752.3 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:10876689 C>T maps to NM_004752.3 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:10874605 G>A maps to NM_004752.3 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:10875067 A>T maps to NM_004752.3 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:10876134 G>A maps to NM_004752.3 R191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:10876689 C>T maps to NM_004752.3 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:10876689 C>T maps to NM_004752.3 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr12:120582577 G>A maps to NM_006836.1 I1739I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr12:120582577 G>A maps to NM_006836.1 I1739I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr12:120595817 G>A maps to NM_006836.1 S974S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr12:120580373 G>A maps to NM_006836.1 I1922I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44Q-06A-11D-A25O-08 chr12:120580427 G>T maps to NM_006836.1 S1904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44Q-06A-11D-A25O-08 chr12:120583077 G>A maps to NM_006836.1 D1668D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:120580352 G>A maps to NM_006836.1 L1929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr12:120615492 G>A maps to NM_006836.1 Y241Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:120578755 G>A maps to NM_006836.1 I1967I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr12:120587452 G>A maps to NM_006836.1 S1501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:120582577 G>A maps to NM_006836.1 I1739I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:120593412 G>A maps to NM_006836.1 I1141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:120582844 C>T maps to NM_006836.1 K1679K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:120582727 C>T maps to NM_006836.1 Q1718Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr12:120602262 G>A maps to NM_006836.1 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:120580451 G>A maps to NM_006836.1 T1896T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:120585059 G>A maps to NM_006836.1 L1581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr12:120574380 G>A maps to NM_006836.1 I2311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr12:120582537 G>A maps to NM_006836.1 R1753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr12:120575809 G>A maps to NM_006836.1 F2096F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:120575761 G>A maps to NM_006836.1 I2112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:120568515 G>A maps to NM_006836.1 L2535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:120582832 G>A maps to NM_006836.1 A1683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:120584893 G>A maps to NM_006836.1 Q1637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:120598019 G>A maps to NM_006836.1 L826L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr12:120600895 G>A maps to NM_006836.1 I672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr12:120586106 C>T maps to NM_006836.1 K1530K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:120576636 G>A maps to NM_006836.1 L2006L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:79118028 G>A maps to NM_001097636.1 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:79117395 G>A maps to NM_001097636.1 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:79118280 G>A maps to NM_001097636.1 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr9:79118079 C>T maps to NM_001097636.1 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr9:79117386 C>T maps to NM_001097636.1 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:79118199 G>A maps to NM_001097636.1 Q301Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr6:10557297 C>T maps to NM_001491.2 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr15:59910436 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr15:59910664 G>A maps to NM_004751.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr15:59911079 C>T maps to NM_004751.2 Q215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr15:59910964 C>T maps to NM_004751.2 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:59911231 G>A maps to NM_004751.2 W265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:59910706 G>A maps to NM_004751.2 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr15:59911183 G>A maps to NM_004751.2 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:59910952 C>T maps to NM_004751.2 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:59911342 C>T maps to NM_004751.2 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr5:74325412 G>A maps to NM_016591.2 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:74324902 G>A maps to NM_016591.2 I320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:74325202 C>T maps to NM_016591.2 W220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q3-06A-11D-A196-08 chr15:57913896 C>G maps to NM_001018090.3 S137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr15:57910262 G>A maps to NM_001018090.3 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:57918002 G>A maps to NM_001018090.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr15:57910262 G>A maps to NM_001018090.3 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr15:57921994 G>A maps to NM_001018090.3 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:57913874 C>T maps to NM_001018090.3 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:57925875 C>T maps to NM_001018090.3 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:57896504 G>A maps to NM_001018090.3 E38E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:58006750 C>T maps to NM_001018090.3 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr15:57910308 C>T maps to NM_001018090.3 Q81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:57910259 C>T maps to NM_001018090.3 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:57931688 C>T maps to NM_001018090.3 H355H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:57931718 G>A maps to NM_001018090.3 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr16:81121263 C>T maps to NM_004483.4 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr9:74828889 G>A maps to ENST00000238018 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:74856214 G>A did not map to a codon.
Alternatively spliced codon TCGA-EE-A2MM-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr9:74838088 G>A maps to ENST00000238018 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:74825628 C>T maps to ENST00000238018 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr8:75263657 G>A maps to NM_018972.2 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr8:75276226 C>T maps to NM_018972.2 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr8:75276227 C>T maps to NM_018972.2 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr8:75263639 G>A maps to NM_018972.2 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr8:75262743 G>A maps to NM_018972.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:42893191 G>A maps to NM_024034.3 E251E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:42891968 T>C did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr20:42891891 G>A maps to NM_024034.3 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:118426140 G>A maps to NM_017686.3 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr16:19522234 G>A maps to NM_016641.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr10:48429147 G>T maps to NM_004962.2 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr10:48429198 C>T maps to NM_004962.2 E229E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr10:48438485 G>A maps to NM_004962.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:48428862 C>T maps to NM_004962.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr10:48426626 C>T maps to NM_004962.2 R460R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:48428706 C>T maps to NM_004962.2 W393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:48429371 G>A maps to NM_004962.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr10:48428784 C>T maps to NM_004962.2 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:48426626 C>T maps to NM_004962.2 R460R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:48429243 G>A maps to NM_004962.2 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:48429195 C>T maps to NM_004962.2 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:48428730 G>A maps to NM_004962.2 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:48429348 C>T maps to NM_004962.2 Q179Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr10:48429460 C>T maps to NM_004962.2 W142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:48429258 G>A maps to NM_004962.2 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr10:48428967 C>T maps to NM_004962.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:18499351 C>T maps to NM_004864.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:18497276 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:18497265 C>T maps to NM_004864.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr10:48413874 G>A maps to NM_016204.1 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr10:48416645 C>T maps to NM_016204.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:48414275 G>A maps to NM_016204.1 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:48416651 G>A maps to NM_016204.1 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:48414411 G>A maps to NM_016204.1 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:48413835 C>T maps to NM_016204.1 W344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:48413859 G>A maps to NM_016204.1 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:48413859 G>A maps to NM_016204.1 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:48416419 G>A maps to NM_016204.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:48416537 G>C maps to NM_016204.1 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:48413754 C>T maps to NM_016204.1 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:48414000 C>T maps to NM_016204.1 K289K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:48413715 G>A maps to NM_016204.1 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:48413781 G>A maps to NM_016204.1 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:48414341 G>A maps to NM_016204.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:48416518 G>A maps to NM_016204.1 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:48416468 G>A maps to NM_016204.1 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q1-06A-21D-A196-08 chr12:7848183 C>T maps to NM_020634.1 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr12:7843021 G>A maps to NM_020634.1 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr12:7843135 G>A maps to NM_020634.1 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:7842959 C>T maps to NM_020634.1 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr12:7842821 C>T maps to NM_020634.1 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:7842920 A>G maps to NM_020634.1 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:7848099 C>T maps to NM_020634.1 E75E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:7843025 G>A maps to NM_020634.1 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:7842998 C>T maps to NM_020634.1 W190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:7848198 C>T maps to NM_020634.1 Q42Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:7843047 C>T maps to NM_020634.1 W174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:7848084 C>T maps to NM_020634.1 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr12:7848233 G>A maps to NM_020634.1 Q31*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DA-A1IC-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr20:34021880 C>T maps to NM_000557.2 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:34025150 C>T maps to NM_000557.2 K186K. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A29P-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr20:34022111 C>T maps to ENST00000374375 V52V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A2GE-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr20:34021880 C>T maps to NM_000557.2 T444T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A2GO-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:34022225 G>A maps to ENST00000374375 S90S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A2GS-06A-12D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr20:34025182 G>A maps to NM_000557.2 L176L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A2MR-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr20:34025486 G>A maps to NM_000557.2 A74A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-ER-A198-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:34021838 G>A maps to NM_000557.2 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:34021739 C>T maps to NM_000557.2 E491E. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-FW-A3R5-06A-11D-A23B-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:34022006 C>T maps to ENST00000374375 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:34025288 G>A maps to NM_000557.2 V140V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-GN-A265-06A-21D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr20:34022050 G>A maps to NM_000557.2 Q388*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-GN-A265-06A-21D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr20:34022051 G>A maps to ENST00000374375 W32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:34025276 G>A maps to NM_000557.2 F144F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-QB-A6FS-06A-11D-A30X-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr20:34021880 C>T maps to NM_000557.2 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:97172845 C>T maps to NM_001001557.2 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:97156931 G>A maps to NM_001001557.2 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:97157006 C>T maps to NM_001001557.2 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:20870929 G>A maps to NM_182828.2 W366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:132198243 G>A maps to NM_005260.3 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:132198078 A>G maps to NM_005260.3 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:132200042 G>A maps to NM_005260.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:132197784 A>C maps to NM_005260.3 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:153667182 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr23:153668319 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:153670590 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:153668800 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:69646804 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:69652227 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:69652228 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:69649816 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr23:69645639 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:69646511 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:69649857 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr16:30119698 C>T maps to NM_024307.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:76980027 G>A maps to ENST00000376217 Q189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:76980046 C>T maps to ENST00000376217 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:76969472 G>A maps to ENST00000376217 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr11:76982220 G>A maps to ENST00000376217 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr11:76990377 G>A maps to ENST00000376217 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:76969472 G>A maps to ENST00000376217 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:76944135 C>T maps to ENST00000376217 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr11:76940247 G>A maps to ENST00000376217 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:76980019 C>T maps to ENST00000376217 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:75152222 G>A maps to NM_030792.6 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr11:75146614 G>A maps to NM_030792.6 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr11:75160935 G>A maps to NM_030792.6 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:75152258 G>A maps to NM_030792.6 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:75153560 G>A maps to NM_030792.6 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr11:75160973 G>A maps to NM_030792.6 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr12:58009384 C>T maps to NM_001111270.1 R416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:58010181 G>A maps to NM_001111270.1 Q551Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:58009766 C>T maps to NM_001111270.1 Q502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr12:58010634 C>T maps to NM_001111270.1 P606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr12:58007139 C>T maps to NM_001111270.1 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr8:95265293 C>T maps to NM_181702.2 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr8:95262714 C>T maps to NM_181702.2 Q238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr8:95262810 C>T maps to NM_181702.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:95262777 G>A maps to NM_181702.2 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr8:95264275 A>C maps to NM_181702.2 L195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr8:95262654 C>T maps to NM_181702.2 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr17:648240 A>G maps to NM_015721.2 T1014T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:650805 G>A maps to NM_015721.2 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:649221 G>A maps to NM_015721.2 Y687Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr17:649016 G>A maps to NM_015721.2 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr17:649278 G>A maps to NM_015721.2 D668D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:154308187 C>T maps to NM_015465.3 K271K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr5:154282155 G>A maps to NM_015465.3 Q937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:154296621 G>A maps to NM_015465.3 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr5:154272025 G>A maps to NM_015465.3 L1227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr5:154311725 G>A maps to NM_015465.3 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:154311044 G>A maps to NM_015465.3 R252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr5:154267829 G>A maps to NM_015465.3 L1489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr5:154311711 C>T maps to NM_015465.3 W203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:154271116 G>A maps to NM_015465.3 Q1316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:39008703 C>G maps to NM_024775.9 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:45593554 C>T maps to NM_024707.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:14038219 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:14038279 A>C did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:14038613 G>A did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:17950003 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:927100 C>T maps to NM_015949.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:933448 C>T maps to NM_015949.2 N273N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr7:931926 A>G maps to NM_015949.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr17:42992740 G>A maps to NM_002055.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:42991116 G>A maps to NM_002055.3 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr17:42988734 C>T maps to NM_002055.3 E332E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:42988758 A>C maps to NM_002055.3 Y324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:92941723 G>A maps to NM_005263.3 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr1:92946640 C>T maps to NM_005263.3 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr9:135862154 C>T maps to NM_004188.4 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:135862080 C>T maps to NM_004188.4 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:135862085 G>A maps to NM_004188.4 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:135866328 C>T maps to NM_004188.4 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:135864539 C>T maps to NM_004188.4 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:158376775 C>T maps to ENST00000264263 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:158363443 T>C maps to ENST00000264263 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:74046475 G>A maps to NM_032380.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr5:74046439 A>C maps to NM_032380.3 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr6:13365151 G>A maps to NM_018988.2 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr6:13365763 G>A maps to NM_018988.2 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:13365589 G>A maps to NM_018988.2 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:13365763 G>A maps to NM_018988.2 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr6:13365622 G>A maps to NM_018988.2 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr6:13365562 G>A maps to NM_018988.2 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:13365136 G>A maps to NM_018988.2 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:13365805 G>A maps to NM_018988.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr16:67709903 G>A maps to NM_030819.3 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:67709603 G>A maps to NM_030819.3 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr2:69556547 T>A maps to ENST00000357308 K536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr2:69556548 A>T maps to ENST00000357308 I535I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:69575351 G>T maps to ENST00000357308 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:69555564 G>A maps to ENST00000357308 I577I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:69556864 G>A maps to ENST00000357308 S516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:179744023 G>A maps to NM_005110.2 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:179743353 G>A maps to NM_005110.2 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr5:179743969 G>A maps to NM_005110.2 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:179743855 G>A maps to NM_005110.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr5:179729449 G>A maps to NM_005110.2 F659F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:179745922 G>A maps to NM_005110.2 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr5:179728599 G>A maps to NM_005110.2 F671F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:179728596 G>A maps to NM_005110.2 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:179739454 G>A maps to NM_005110.2 I507I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:179745904 G>A maps to NM_005110.2 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr10:117825119 G>A maps to NM_005264.4 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:117849332 C>T maps to NM_005264.4 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr10:117884787 C>T maps to NM_005264.4 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr10:117853249 C>T maps to NM_005264.4 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr10:118029036 G>A maps to NM_005264.4 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:117884973 G>A maps to NM_005264.4 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:117885048 C>T maps to NM_005264.4 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:21562497 G>A maps to NM_001495.4 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr5:137600193 G>A maps to NM_001496.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr5:137593428 C>T maps to NM_001496.3 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:137600046 C>T maps to NM_001496.3 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:137593380 C>T maps to NM_001496.3 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr5:137593407 G>A maps to NM_001496.3 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr5:137589836 C>A maps to NM_001496.3 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:137593449 G>A maps to NM_001496.3 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:137600187 G>A maps to NM_001496.3 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr5:137600085 C>T maps to NM_001496.3 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr5:137589781 G>A maps to NM_001496.3 Q285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr5:137588737 G>A maps to NM_001496.3 N374N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr6:55266586 G>A did not map to a codon.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr6:55198716 T>G maps to NM_207410.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr6:55216066 G>A maps to NM_207410.2 W129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:55223890 T>C maps to NM_207410.2 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:55264216 C>T maps to NM_207410.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:55216069 C>T maps to NM_207410.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:55198659 C>T maps to NM_207410.2 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:55196519 G>A maps to NM_207410.2 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:55223766 C>T maps to NM_207410.2 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr6:55216235 T>C maps to NM_207410.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr6:55216205 C>T maps to NM_207410.2 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:55216049 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:55198608 G>A maps to NM_207410.2 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:55223685 G>A maps to NM_207410.2 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr6:55216330 C>T maps to NM_207410.2 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr22:38010227 C>T maps to ENST00000381756 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:38028515 C>T maps to ENST00000381756 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:38028042 C>T maps to ENST00000381756 F540F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr22:38028054 C>T maps to ENST00000381756 F544F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr22:38016336 C>T maps to ENST00000381756 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr16:23499998 C>T maps to NM_015044.4 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr16:23497446 G>A maps to NM_015044.4 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr16:23489717 G>A maps to NM_015044.4 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr2:85778938 G>A maps to NM_000821.4 F535F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:85788064 C>T maps to NM_000821.4 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:63948261 G>A maps to NM_003878.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr19:38877841 C>T maps to NM_152657.3 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:38877094 C>T maps to NM_152657.3 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:34937856 C>A maps to NM_024835.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr22:25011011 A>G maps to NM_005265.2 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr22:25019804 C>T maps to NM_005265.2 H314H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr22:25023935 C>T maps to NM_005265.2 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr22:25024078 G>A maps to NM_005265.2 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr22:25016460 C>T maps to NM_005265.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:25023490 C>T maps to NM_005265.2 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:25010853 C>T maps to NM_005265.2 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr22:25023484 C>T maps to NM_005265.2 Y369Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr22:25019810 C>T maps to NM_005265.2 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr22:24622607 C>T maps to NM_001099781.1 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr22:24616027 G>A maps to NM_001099781.1 F558F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr22:24622625 C>T maps to NM_001099781.1 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr22:24622694 C>T maps to NM_001099781.1 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr22:24621538 C>T maps to NM_001099781.1 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:4461978 C>T maps to ENST00000414312 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr17:4461723 C>T maps to ENST00000414312 V362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:33442401 G>A maps to NM_178026.2 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr20:33440319 G>A maps to NM_178026.2 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:33437842 G>A maps to NM_178026.2 T582T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:33440070 G>A maps to NM_178026.2 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr20:33451190 G>A maps to NM_178026.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:33440059 G>A maps to NM_178026.2 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr20:23965942 G>A maps to NM_178311.2 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr20:23966375 C>T maps to NM_178311.2 W153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr20:23966722 G>A maps to NM_178311.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr20:23966393 G>A maps to NM_178311.2 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:23966722 G>A maps to NM_178311.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:23966797 G>A maps to NM_178311.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr20:23966722 G>A maps to NM_178311.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:23966722 G>A maps to NM_178311.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr22:22989316 G>A maps to ENST00000215938 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr22:22989340 C>T maps to ENST00000215938 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:22989340 C>T maps to ENST00000215938 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr17:61995206 G>A maps to NM_000515.3 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:61995445 G>A maps to NM_000515.3 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:61995777 G>A maps to NM_000515.3 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr17:61995481 G>A maps to NM_000515.3 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:61994689 C>T maps to NM_000515.3 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr17:61994715 G>A maps to NM_000515.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr17:61958122 C>A maps to NM_022557.2 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr17:61958456 G>A maps to NM_002059.3 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:61957839 G>A maps to NM_002059.3 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:61958409 C>T maps to NM_002059.3 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:61957615 G>A maps to NM_022558.2 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:61957616 G>A maps to NM_022558.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr17:40343154 G>A maps to NM_032484.4 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr17:40343157 A>G maps to NM_032484.4 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:40343100 A>T maps to NM_032484.4 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr17:40343145 G>T maps to NM_032484.4 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:40344691 G>A maps to NM_032484.4 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:85909907 C>T maps to ENST00000436406 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr5:42719516 C>T maps to NM_000163.2 I636I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr5:42700096 G>A maps to NM_000163.2 W204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr5:42718721 G>A maps to NM_000163.2 E371E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:42719192 C>T maps to NM_000163.2 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:42718805 C>T maps to NM_000163.2 F399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:42718946 C>T maps to NM_000163.2 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:42719192 C>T maps to NM_000163.2 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr5:42719240 C>T maps to NM_000163.2 I544I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:42700046 G>A maps to NM_000163.2 W187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr5:42718877 C>T maps to NM_000163.2 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:42718805 C>T maps to NM_000163.2 F399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr5:42718153 G>A maps to NM_000163.2 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr5:42719192 C>T maps to NM_000163.2 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr5:42719291 C>T maps to NM_000163.2 N561N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr5:42629200 G>A maps to NM_000163.2 K44K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:42718223 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:42719312 C>T maps to NM_000163.2 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr20:35884813 G>A maps to NM_021081.4 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:35885232 G>A maps to NM_021081.4 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:31016058 G>A maps to NM_000823.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr7:31015393 G>A maps to NM_000823.3 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr7:31015393 G>A maps to NM_000823.3 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr7:31011631 C>T maps to NM_000823.3 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:31014621 G>A maps to NM_000823.3 W283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr7:31008514 C>T maps to NM_000823.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr7:31014609 C>T maps to NM_000823.3 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:31008744 C>T maps to NM_000823.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr7:31008692 G>A maps to NM_000823.3 W59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:31014597 G>A maps to NM_000823.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:31013634 C>T maps to NM_000823.3 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:172163169 G>A maps to NM_198407.2 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:172163184 G>A maps to NM_198407.2 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:172165672 G>A maps to NM_198407.2 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:172165939 G>A maps to NM_198407.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:172165666 G>A maps to NM_198407.2 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:172166041 G>A maps to NM_198407.2 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:172163025 G>A maps to NM_198407.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:59604767 C>T maps to NM_005142.2 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr11:59610056 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:59612875 C>T maps to NM_005142.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:59599223 G>A maps to NM_005142.2 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr11:59611433 C>T maps to NM_005142.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr11:59611397 C>T maps to NM_005142.2 K70K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr11:59610594 G>A maps to NM_005142.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:100285476 G>A maps to NM_022574.4 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr7:100281647 G>A maps to NM_022574.4 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:100283656 G>A maps to NM_022574.4 Q332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr7:100285684 G>A maps to NM_022574.4 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:100285672 G>A maps to NM_022574.4 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:233715037 C>T maps to ENST00000373566 Q1273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:233651923 A>C maps to ENST00000373566 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:233671354 C>T maps to ENST00000373566 P620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:233671240 G>A maps to ENST00000373566 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:233677176 C>T maps to ENST00000373566 Q717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr2:233680380 G>A maps to ENST00000373566 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:150417985 G>A maps to NM_130759.3 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr7:150417538 C>T maps to NM_130759.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:150417205 C>G maps to NM_130759.3 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:150417904 C>T maps to NM_130759.3 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:150416146 G>A maps to NM_130759.3 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr7:150417742 C>T maps to NM_130759.3 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:150417885 G>A maps to NM_130759.3 W265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:150417448 C>T maps to NM_130759.3 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr7:150417481 G>A maps to NM_130759.3 Q130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:150417508 C>T maps to NM_130759.3 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr7:150417520 C>T maps to NM_130759.3 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:150417928 C>T maps to NM_130759.3 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:150417661 C>T maps to NM_130759.3 N190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr7:150417169 C>T maps to NM_130759.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150416155 G>A maps to NM_130759.3 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150417463 C>T maps to NM_130759.3 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150417778 G>A maps to NM_130759.3 Q229Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:150417601 G>A maps to NM_130759.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:150389784 C>T maps to NM_015660.2 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:150390042 G>A maps to NM_015660.2 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:150389736 G>A maps to NM_015660.2 Q121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:150389991 G>A maps to NM_015660.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:150389904 G>A maps to NM_015660.2 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:150389490 G>A maps to NM_015660.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr7:150389631 C>T maps to NM_015660.2 D86D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr7:150389910 C>T maps to NM_015660.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:150389490 G>A maps to NM_015660.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr7:150269946 C>T maps to ENST00000430830 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr7:150269703 C>T maps to ENST00000430830 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr7:150270000 G>A maps to ENST00000430830 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:150269460 G>A maps to ENST00000430830 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:150269235 C>T maps to ENST00000430830 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:150269403 C>T maps to ENST00000430830 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr7:150269886 C>T maps to ENST00000430830 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:150269427 C>T maps to ENST00000430830 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:150269556 C>T maps to ENST00000430830 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr7:150270060 G>A maps to ENST00000430830 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr7:150269904 G>A maps to ENST00000430830 E263E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150266997 C>T maps to ENST00000430830 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150269484 G>A maps to ENST00000430830 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150269703 C>T maps to ENST00000430830 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150269997 G>A maps to ENST00000430830 E294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:150269685 A>G maps to ENST00000430830 Q190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr7:150439760 G>A maps to ENST00000447239 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:150439529 G>A maps to ENST00000447239 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:150439343 G>A maps to ENST00000447239 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr7:150439343 G>A maps to ENST00000447239 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:150439844 G>A maps to ENST00000447239 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:150439911 C>T maps to ENST00000447239 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:150439526 C>T maps to ENST00000447239 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr7:150439460 C>T maps to ENST00000447239 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:150440127 C>T maps to ENST00000447239 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr7:150439880 C>T maps to ENST00000447239 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr7:150439622 G>A maps to ENST00000447239 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150439391 C>T maps to ENST00000447239 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150439454 G>A maps to ENST00000447239 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150439637 C>T maps to ENST00000447239 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150440091 C>T maps to ENST00000447239 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:150439745 G>A maps to ENST00000447239 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:150325544 C>T maps to ENST00000438845 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr7:150325267 G>A maps to ENST00000438845 Q210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr7:150324854 C>T maps to ENST00000438845 K347K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:150325183 G>A maps to ENST00000438845 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:150325034 C>T maps to ENST00000438845 E287E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:150325427 C>T maps to ENST00000438845 W156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr7:150325585 C>A maps to ENST00000438845 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:150325592 C>T maps to ENST00000438845 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr7:150325487 G>A maps to ENST00000438845 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:150327160 G>A maps to ENST00000438845 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:150325207 G>A maps to ENST00000438845 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:150325562 C>T maps to ENST00000438845 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:150324821 C>T maps to ENST00000438845 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr7:150325055 G>A maps to ENST00000438845 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150325054 G>A maps to ENST00000438845 Q281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150325310 G>A maps to ENST00000438845 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150325337 G>A maps to ENST00000438845 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:150325190 C>T maps to ENST00000438845 K235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr7:150325190 C>T maps to ENST00000438845 K235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr7:150325544 C>T maps to ENST00000438845 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:150217106 G>A maps to NM_153236.3 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:150217394 C>T maps to NM_153236.3 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr7:150217106 G>A maps to NM_153236.3 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr7:150217903 G>A maps to NM_153236.3 W281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:150217094 C>T maps to NM_153236.3 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr7:150217496 C>T maps to NM_153236.3 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:150217235 C>T maps to NM_153236.3 D58D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr7:150217655 G>A maps to NM_153236.3 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr7:150217898 G>A maps to NM_153236.3 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr7:150217481 G>A maps to NM_153236.3 Q140Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:150217106 G>A maps to NM_153236.3 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:150217121 G>A maps to NM_153236.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:150174258 C>T maps to NM_175571.2 V463V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:150174693 G>A maps to NM_175571.2 Q608Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr7:150174549 G>A maps to NM_175571.2 A560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr7:150174219 G>A maps to NM_175571.2 G450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr7:150174384 G>A maps to NM_175571.2 K505K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:150171640 G>A maps to NM_175571.2 E408E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:150174465 C>T maps to NM_175571.2 F532F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr7:150174612 C>T maps to NM_175571.2 N581N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr7:150174549 G>A maps to NM_175571.2 A560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr7:150163899 C>T maps to NM_175571.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:150174301 C>T maps to NM_175571.2 Q478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:150164103 C>T maps to NM_175571.2 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:150164226 C>T maps to NM_175571.2 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:150174577 C>T maps to NM_175571.2 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:150174219 G>A maps to NM_175571.2 G450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:150164226 C>T maps to NM_175571.2 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr7:150174540 G>A maps to NM_175571.2 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:150174540 G>A maps to NM_175571.2 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr7:150174234 G>T maps to NM_175571.2 G455G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr7:150174697 C>T maps to NM_175571.2 Q610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150163995 C>T maps to NM_175571.2 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150163998 C>T maps to NM_175571.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150164370 G>A maps to NM_175571.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150171583 C>T maps to NM_175571.2 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr7:150164322 C>T maps to NM_175571.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr7:150164382 C>T maps to NM_175571.2 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr7:150171145 G>A maps to NM_175571.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr7:150174540 G>A maps to NM_175571.2 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:102440249 G>A maps to NM_017676.2 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:58438587 C>T maps to NM_001126129.1 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:41397210 C>T maps to NM_032336.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:41399593 C>T maps to NM_032336.2 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:41399594 C>T maps to NM_032336.2 Q221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr8:41387741 C>T maps to NM_032336.2 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr8:41387798 C>T maps to NM_032336.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr8:41399551 C>T maps to NM_032336.2 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:47044510 G>A maps to NM_004123.2 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:14591153 G>A maps to NM_202470.1 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr19:14589319 G>A maps to NM_202470.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr19:14593659 G>C maps to NM_202470.1 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:14591231 G>A maps to NM_202470.1 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr19:14591192 C>T maps to NM_202470.1 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:3590103 C>T maps to NM_133261.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:3586990 C>T maps to NM_133261.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:3590079 G>A maps to NM_133261.2 Q277Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:3589543 G>T maps to NM_133261.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:3589544 G>T maps to NM_133261.2 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:3589507 G>A maps to NM_133261.2 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr19:46177966 C>T maps to NM_000164.2 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:46176121 C>T maps to NM_000164.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:46180350 C>T maps to NM_000164.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:46181174 C>T maps to NM_000164.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:27909802 G>A maps to NM_001085454.1 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:27902102 G>A maps to NM_001085454.1 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:110399130 G>A maps to NM_057169.3 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:110418763 C>T maps to NM_057169.3 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:121768106 G>A maps to NM_000165.3 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:121768739 G>A maps to NM_000165.3 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:121768238 C>T maps to NM_000165.3 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr6:121768667 C>T maps to NM_000165.3 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:121768082 C>T maps to NM_000165.3 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:121768625 C>T maps to NM_000165.3 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr6:90605620 A>C maps to NM_032602.1 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:90604396 C>T maps to NM_032602.1 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:90604402 C>T maps to NM_032602.1 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:90604270 C>T maps to NM_032602.1 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:90604654 T>C maps to NM_032602.1 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:90604283 C>T maps to NM_032602.1 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:90604459 C>T maps to NM_032602.1 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr13:20716974 G>A maps to NM_021954.3 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr13:20716812 G>A maps to NM_021954.3 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr13:20716950 G>A maps to NM_021954.3 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:35259867 G>A maps to NM_002060.2 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:35260146 G>A maps to NM_002060.2 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:35259981 G>A maps to NM_002060.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:35260593 G>A maps to NM_002060.2 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:35260323 C>T maps to NM_002060.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:147230992 C>G maps to NM_005266.5 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:147230569 C>T maps to NM_005266.5 Q259Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:147231250 G>A maps to NM_005266.5 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr1:147231316 G>A maps to NM_005266.5 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:147230827 G>A maps to NM_005266.5 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:147230461 G>A maps to NM_005266.5 N295N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:147230686 G>A maps to NM_005266.5 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr1:147380210 C>T maps to NM_005267.4 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:147380612 C>T maps to NM_005267.4 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:147380210 C>T maps to NM_005267.4 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr1:147380717 G>C maps to NM_005267.4 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:147380099 C>T maps to NM_005267.4 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:147380092 G>A maps to NM_005267.4 W4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr1:147380903 C>T maps to NM_005267.4 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:147380327 C>T maps to NM_005267.4 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr1:147380189 C>T maps to NM_005267.4 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:147380210 C>T maps to NM_005267.4 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:147380918 C>T maps to NM_005267.4 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:147380189 C>T maps to NM_005267.4 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:147380327 C>T maps to NM_005267.4 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:147380210 C>T maps to NM_005267.4 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:147381081 G>T maps to NM_005267.4 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:147380579 C>T maps to NM_005267.4 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:147380612 C>T maps to NM_005267.4 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr1:147380981 C>T maps to NM_005267.4 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:147380735 C>T maps to NM_005267.4 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:147381125 G>A maps to NM_005267.4 E348E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:147380417 G>A maps to NM_005267.4 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:39341344 C>T maps to NM_030772.4 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:39340267 C>T maps to NM_030772.4 T501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:70443914 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr13:20763696 C>T maps to NM_004004.5 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr13:20763234 G>A maps to NM_004004.5 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr13:20763696 C>T maps to NM_004004.5 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr13:20763300 G>A maps to NM_004004.5 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr13:20763507 G>A maps to NM_004004.5 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:35250683 G>A maps to NM_001005752.1 Q107Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:35250782 C>T maps to NM_001005752.1 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:35227592 G>A maps to NM_153212.2 E246E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr1:35227277 G>A maps to NM_153212.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:35227259 C>T maps to NM_153212.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:35227421 C>T maps to NM_153212.2 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:35227175 G>A maps to NM_153212.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:35227547 C>T maps to NM_153212.2 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:35223137 C>T maps to NM_005268.2 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr1:35223536 C>T maps to NM_005268.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:35223302 G>A maps to NM_005268.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:35223449 G>A maps to NM_005268.2 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:35223368 C>T maps to NM_005268.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:35223284 G>A maps to NM_005268.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:35223200 C>T maps to NM_005268.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr13:20797124 C>T maps to NM_001110221.2 W165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr13:20797559 G>A maps to NM_001110221.2 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr13:20797187 G>A maps to NM_001110221.2 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr13:20797592 G>A maps to NM_001110221.2 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr13:20797109 C>T maps to NM_001110221.2 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr13:20797385 G>A maps to NM_001110221.2 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr6:87994565 C>T maps to NM_198568.2 W22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr17:42883110 G>A maps to NM_001080383.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr17:42882354 A>G maps to NM_001080383.1 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr17:42882795 C>T maps to NM_001080383.1 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr1:228345524 C>T maps to NM_020435.2 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr7:99521203 C>T maps to NM_181538.2 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr7:99521203 C>T maps to NM_181538.2 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:99526587 C>T maps to NM_181538.2 W219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr15:35045083 G>A maps to NM_020660.1 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:35045158 C>T maps to NM_020660.1 K162K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:35046623 G>A maps to NM_020660.1 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr15:35045211 A>G maps to NM_020660.1 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:35896617 G>A maps to NM_153368.2 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr10:35896518 C>T maps to NM_153368.2 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:30714752 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr23:30683658 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:30742288 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:30714761 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:30738985 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:30736684 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr23:30736684 C>T did not map to a codon.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr23:30745605 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr4:80328610 C>T maps to NM_033214.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:80328544 G>A maps to NM_033214.2 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:80329288 G>A maps to NM_033214.2 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr4:80327845 C>T maps to NM_033214.2 W503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr4:80327846 C>T maps to NM_033214.2 W503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:80329013 C>T maps to NM_033214.2 W114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:80328861 G>A maps to NM_033214.2 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr4:80328148 G>A maps to NM_033214.2 F402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr4:80328421 C>T maps to NM_033214.2 E311E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:80329055 C>T maps to NM_033214.2 W100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr4:80329276 C>T maps to NM_033214.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:141923586 A>G maps to NM_001039547.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:141884532 T>C maps to NM_001039547.2 E507E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:141944198 G>A maps to NM_001039547.2 C33C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr9:86383825 A>G maps to NM_025211.3 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr9:86357477 T>C maps to NM_025211.3 E314E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:86354622 G>A maps to NM_025211.3 Q364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:69207868 C>T maps to NM_019617.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr2:69204834 G>T maps to NM_019617.3 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:69172502 A>G maps to NM_182536.2 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:69173469 G>A maps to NM_182536.2 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:69174313 G>A maps to NM_182536.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr23:100656775 G>T did not map to a codon.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr23:100656650 A>C did not map to a codon.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr3:33065757 C>T maps to NM_000404.2 K376K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:33038575 G>A maps to NM_000404.2 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr3:33038623 G>A maps to NM_000404.2 T649T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:33093394 G>A maps to NM_000404.2 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:220103064 G>A maps to NM_024506.3 Y416Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:220103909 G>A maps to NM_024506.3 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr2:220104816 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:220108283 C>T maps to NM_024506.3 K4K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:220104314 C>T maps to NM_024506.3 E290E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:220107271 G>A maps to NM_024506.3 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:220108018 G>A maps to NM_024506.3 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:220107567 G>A maps to NM_024506.3 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:134217227 C>T maps to NM_138342.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:134214296 C>T maps to NM_138342.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:134241692 C>T maps to NM_138342.3 N492N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:134228964 C>T maps to NM_138342.3 D221D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:134241355 G>A maps to NM_138342.3 K466K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:134212722 C>T maps to NM_138342.3 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:134214954 C>T maps to NM_138342.3 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:134212752 C>T maps to NM_138342.3 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:134214954 C>T maps to NM_138342.3 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:134240214 T>A maps to NM_138342.3 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr11:134214954 C>T maps to NM_138342.3 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:134151286 C>T maps to NM_001080407.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:134151924 C>T maps to NM_001080407.2 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:134179595 C>T maps to NM_001080407.2 N346N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:134179544 C>T maps to NM_001080407.2 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr11:134151279 G>A maps to NM_001080407.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:134158753 G>A maps to NM_001080407.2 K233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:134163081 C>T maps to NM_001080407.2 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:134183895 G>A maps to NM_001080407.2 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr11:134151945 C>T maps to NM_001080407.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr7:8125849 C>T maps to NM_138426.2 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:8125930 C>T maps to NM_138426.2 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:8125882 C>T maps to NM_138426.2 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr7:8125960 C>T maps to NM_138426.2 N479N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr7:8125885 C>T maps to NM_138426.2 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:8126014 C>T maps to NM_138426.2 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:6556178 G>A maps to NM_000170.2 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:6565392 G>A maps to NM_000170.2 I629I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr9:6606656 C>T maps to NM_000170.2 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr9:6620206 C>T maps to NM_000170.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr9:6589235 G>A maps to NM_000170.2 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr9:6554673 G>A maps to NM_000170.2 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:6587205 G>A maps to NM_000170.2 F595F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:6589217 G>A maps to NM_000170.2 F519F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr15:51689706 C>T maps to NM_181789.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:51687032 G>A maps to NM_181789.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr15:51687122 G>A maps to NM_181789.2 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr15:51689712 C>T maps to NM_181789.2 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr9:131284952 C>T maps to NM_001003722.1 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr16:74508512 C>T maps to NM_012201.5 Q661Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr16:74530428 G>A maps to NM_012201.5 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr16:74496042 G>A maps to NM_012201.5 S995S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:74497347 G>A maps to NM_012201.5 T899T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:74516937 G>A maps to NM_012201.5 F552F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr16:74493681 G>A maps to NM_012201.5 S1014S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:74497266 G>A maps to NM_012201.5 I926I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr16:74525027 G>A maps to NM_012201.5 I440I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr16:74491787 G>A maps to NM_012201.5 T1083T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:74524978 G>A maps to NM_012201.5 R457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr12:57865814 G>T maps to NM_005269.2 E1098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:57865063 C>T maps to NM_005269.2 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:57865552 C>T maps to NM_005269.2 S1010S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr12:57865690 C>A maps to NM_005269.2 P1056P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:57865354 A>C maps to NM_005269.2 P944P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:57865163 C>T maps to NM_005269.2 L881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr12:57859602 G>A maps to NM_005269.2 E219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:57864712 G>A maps to NM_005269.2 L730L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr2:121746990 T>A maps to NM_005270.4 P1167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr2:121736036 G>T maps to NM_005270.4 E466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr2:121726458 T>C maps to NM_005270.4 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:121745958 C>T maps to NM_005270.4 S823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:121740330 C>T maps to NM_005270.4 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:121747776 C>T maps to NM_005270.4 P1429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:121748124 C>T maps to NM_005270.4 T1545T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr2:121748013 C>T maps to NM_005270.4 P1508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr2:121748184 C>T maps to NM_005270.4 V1565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr2:121747128 C>T maps to NM_005270.4 S1213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:121742240 G>A maps to NM_005270.4 E626E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:121728001 C>T maps to NM_005270.4 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr2:121726353 C>T maps to NM_005270.4 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:121744125 C>T maps to NM_005270.4 S743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr2:121746900 G>A maps to NM_005270.4 L1137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:121745925 G>A maps to NM_005270.4 T812T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:121747929 G>A maps to NM_005270.4 Q1480Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:121748157 C>T maps to NM_005270.4 I1556I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr2:121744158 G>A maps to NM_005270.4 R754R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:121743987 G>A maps to NM_005270.4 L697L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr7:42004781 G>A maps to NM_000168.5 L1297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr7:42004782 G>A maps to NM_000168.5 G1296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr7:42004227 G>A maps to NM_000168.5 S1481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr7:42004023 C>T maps to NM_000168.5 A1549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:42064976 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:42116430 G>A maps to NM_000168.5 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:42004029 G>A maps to NM_000168.5 F1547F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:42005139 G>A maps to NM_000168.5 L1177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr7:42065833 G>A maps to NM_000168.5 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:42004227 G>A maps to NM_000168.5 S1481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:42005076 G>A maps to NM_000168.5 V1198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:42003945 G>A maps to NM_000168.5 F1575F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr7:42004785 G>A maps to NM_000168.5 F1295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr7:42085040 G>A maps to NM_000168.5 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr8:144358682 C>T maps to NM_138465.3 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:144358574 C>A maps to NM_138465.3 C244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr12:75875633 C>T maps to NM_006851.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr12:75875726 G>A maps to NM_006851.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:75737647 G>A maps to ENST00000378695 W117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:53975558 G>A maps to NM_147193.2 F500F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:54060296 G>A maps to NM_147193.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:54060404 G>A maps to NM_147193.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr1:53975536 G>A maps to NM_147193.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:54060391 G>A maps to NM_147193.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:53980362 C>T maps to NM_147193.2 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:53972351 G>A maps to NM_147193.2 F601F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:54060278 G>A maps to NM_147193.2 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:54060476 G>A maps to NM_147193.2 T33T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D3-A51T-06A-11D-A25O-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-EE-A2A6-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:3937168 G>A maps to NM_001042413.1 A577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr9:4286121 G>A maps to NM_001042413.1 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr9:3932395 C>T maps to NM_001042413.1 K649K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:4118529 G>A maps to NM_001042413.1 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:92752118 C>T maps to NM_053274.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:92754649 C>T maps to NM_053274.2 W151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:92754650 C>T maps to NM_053274.2 W151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:92755791 G>A maps to NM_053274.2 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:92713504 G>A maps to NM_053274.2 F505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr23:48631746 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:39024226 C>T maps to NM_002062.3 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:39024170 A>C did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr6:39053728 C>T maps to NM_002062.3 H424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr6:39024186 C>T maps to NM_002062.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:39034052 C>T maps to NM_002062.3 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:39034007 C>T maps to NM_002062.3 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:39046895 C>T maps to NM_002062.3 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr6:39053785 G>A maps to NM_002062.3 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr6:39046750 C>T maps to NM_002062.3 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr6:39047369 C>T maps to NM_002062.3 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZG-06A-11D-A197-08 chr6:39041403 C>T maps to NM_002062.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr6:39040655 G>A maps to NM_002062.3 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr6:39046768 C>T maps to NM_002062.3 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:9765376 C>T maps to NM_004246.1 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:9760826 C>T maps to NM_004246.1 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr17:9783826 C>T maps to NM_004246.1 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr17:9760793 C>T maps to NM_004246.1 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr17:9774074 C>T maps to NM_004246.1 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr17:9783805 C>T maps to NM_004246.1 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr17:9765380 C>A maps to NM_004246.1 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr5:151239413 G>A maps to NM_001146040.1 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:151239434 G>A maps to NM_001146040.1 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:151234727 C>T maps to NM_001146040.1 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:151239534 C>T maps to NM_001146040.1 W96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:151231165 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:151234727 C>T maps to NM_001146040.1 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr5:151271932 G>A maps to NM_001146040.1 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr5:151266280 C>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr5:151239413 G>A maps to NM_001146040.1 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:151230974 G>A maps to NM_001146040.1 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:151304098 G>A maps to NM_001146040.1 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr5:151271998 G>A maps to NM_001146040.1 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:151202344 C>T maps to NM_001146040.1 K421K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:14708899 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr23:14625262 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:14548225 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:14627221 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:14748586 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:14748446 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr23:14748378 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:14622458 C>T did not map to a codon.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr23:14625274 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:14708920 C>T did not map to a codon.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr23:14625356 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr4:175649720 G>A maps to NM_006529.2 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:175688128 G>A maps to NM_006529.2 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr4:175565125 G>A maps to NM_006529.2 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:175598360 G>A maps to NM_006529.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr23:102979936 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:102978823 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:102974110 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:102974110 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:102979083 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:102962306 C>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:102974001 G>T did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:102962404 C>G did not map to a codon.
Sequencing variant TCGA-GN-A26D-06A-11D-A19A-08 chr23:102968472 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:158091609 T>G maps to NM_001166060.1 V408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr4:158057640 C>T maps to NM_001166060.1 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:158064986 C>T maps to NM_001166060.1 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:158057738 G>A maps to NM_001166060.1 W139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:158041794 G>A maps to NM_001166060.1 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr4:158091771 G>A maps to NM_001166060.1 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:157999188 T>C maps to NM_001166060.1 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:158091582 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:158057739 G>A maps to NM_001166060.1 W139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr4:158057739 G>A maps to NM_001166060.1 W139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:157999190 G>A maps to NM_001166060.1 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr4:158065067 C>T maps to NM_001166060.1 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:131959076 C>T maps to NM_006541.4 D98D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:131959077 C>T maps to NM_006541.4 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:191792204 C>T maps to NM_014905.3 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:56868869 C>T maps to NM_013267.2 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr12:56868854 G>A maps to NM_013267.2 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:56868894 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:129373193 C>T maps to ENST00000442111 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr12:129442121 G>A maps to ENST00000442111 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr12:129467574 G>A maps to ENST00000442111 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr12:129442127 C>T maps to ENST00000442111 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr12:129373188 C>T maps to ENST00000442111 R75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:17679496 C>T maps to NM_024656.2 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:17692108 C>T maps to NM_024656.2 V575V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr19:17692027 C>T maps to NM_024656.2 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr19:17690352 C>T maps to NM_024656.2 F443F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr1:183933101 G>A maps to NM_015101.2 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr9:138516047 G>A maps to NM_182974.2 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:138517988 G>A maps to NM_182974.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:138516218 C>T maps to NM_182974.2 E185E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:138516286 G>A maps to NM_182974.2 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:138516269 G>A maps to NM_182974.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr9:138516464 G>A maps to NM_182974.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr9:138516356 G>A maps to NM_182974.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr9:138518015 G>A maps to NM_182974.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:138516323 A>G maps to NM_182974.2 H150H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:138516119 G>A maps to NM_182974.2 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:138518015 G>A maps to NM_182974.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:138516047 G>A maps to NM_182974.2 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:52734290 C>T maps to NM_018446.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:104408854 G>A maps to NM_031302.3 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:104387194 G>A maps to NM_031302.3 N285N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr1:1262674 C>T maps to NM_001029885.1 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr1:1263010 C>T maps to NM_001029885.1 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr17:4692374 C>T maps to NM_001014985.2 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:48198218 C>T maps to NM_015711.3 S986S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr19:48201917 G>A maps to NM_015711.3 Q1092Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:48197742 C>T maps to NM_015711.3 S885S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr19:48183956 C>T maps to NM_015711.3 I510I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:48253489 C>T maps to NM_015710.4 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:48254251 C>T maps to NM_015710.4 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr10:88818904 A>C did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:88836408 G>A maps to NM_005271.3 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:88819995 G>A maps to NM_005271.3 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:88811609 G>A maps to NM_005271.3 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr23:120182575 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:120181777 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:120182568 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr23:120182674 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr23:120181872 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:120183213 A>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:120181965 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:182353818 G>A maps to NM_002065.5 H281H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:182357710 C>T maps to NM_002065.5 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr11:58491912 C>T maps to NM_201648.2 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr11:58477265 C>T maps to NM_201648.2 W288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr11:58478112 G>A maps to NM_201648.2 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:58480260 G>A maps to NM_201648.2 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:58477520 G>A maps to NM_201648.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:58477256 C>T maps to NM_201648.2 W291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:58477508 G>A maps to NM_201648.2 C207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr11:58491918 G>A maps to NM_201648.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:58723485 C>T maps to NM_080661.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:58722337 C>T maps to NM_080661.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:58722337 C>T maps to NM_080661.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr11:58722673 G>A maps to NM_080661.2 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:58711092 G>A maps to NM_080661.2 Q34Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:58722322 G>A maps to NM_080661.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:58723157 G>A maps to NM_080661.2 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:58723409 C>T maps to NM_080661.2 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:58723112 G>A maps to NM_080661.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:58607022 G>A maps to NM_145016.3 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:58602309 C>T maps to NM_145016.3 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:58601913 C>T maps to NM_145016.3 K291K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr11:58602123 A>G maps to NM_145016.3 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:58605775 G>A maps to NM_145016.3 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr11:58604591 C>T maps to NM_145016.3 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:58607013 G>A maps to NM_145016.3 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr11:58601913 C>T maps to NM_145016.3 K291K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr11:58602237 C>T maps to NM_145016.3 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr11:58605741 G>A maps to NM_145016.3 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:58602018 A>G maps to NM_145016.3 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:58601984 G>A maps to NM_145016.3 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr3:52325014 C>T maps to NM_145262.3 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:52324537 C>A maps to NM_145262.3 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:52324537 C>T maps to NM_145262.3 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr3:52326290 C>T maps to NM_145262.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr3:52325071 C>T maps to NM_145262.3 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:52326769 C>T maps to NM_145262.3 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr3:52324414 C>T maps to NM_145262.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr16:4867658 G>A maps to NM_032569.3 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr16:4867658 G>A maps to NM_032569.3 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:4861672 G>A maps to NM_032569.3 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr5:150646987 C>T maps to NM_000405.4 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:150646432 C>T maps to NM_000405.4 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:70096879 C>T maps to NM_178439.3 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:70096879 C>T maps to NM_178439.3 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr6:1742778 G>A maps to NM_001500.2 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:1742736 G>A maps to NM_001500.2 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr6:2116043 G>A maps to NM_001500.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr6:1624739 C>T maps to NM_001500.2 Q341Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:29028998 G>A maps to NM_006582.2 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:29030839 A>T maps to NM_006582.2 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:29041248 A>G maps to NM_006582.2 Q562Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:29028968 C>T maps to NM_006582.2 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:29023459 G>A maps to NM_006582.2 Q164Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr1:29040900 C>T maps to NM_006582.2 F446F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:29040708 C>T maps to NM_006582.2 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr20:62221684 G>A maps to NM_012384.3 D450D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:62223910 G>A maps to NM_012384.3 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:62229132 G>A maps to NM_012384.3 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:39823751 C>T maps to NM_004877.2 E55E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:39820262 G>A maps to NM_004877.2 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr19:19744890 G>A maps to NM_016573.2 I731I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:19746465 C>T maps to NM_016573.2 E464E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:19745419 G>A maps to NM_016573.2 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:19749273 C>T maps to NM_016573.2 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr19:19746292 C>T maps to NM_016573.2 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:19744833 G>A maps to NM_016573.2 I750I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19740990 G>A maps to NM_016573.2 T898T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19752826 G>A maps to NM_016573.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:19741116 G>A maps to NM_016573.2 L856L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr8:143922534 G>A maps to NM_002066.2 W25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:143927898 A>G maps to NM_002066.2 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr6:24781781 C>T maps to NM_015895.3 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr2:220366256 C>T maps to ENST00000373917 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:220370718 C>T maps to ENST00000373917 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr2:220366280 G>A maps to ENST00000373917 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr2:220370188 C>T maps to ENST00000373917 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr3:49759759 G>A maps to NM_013334.2 D224D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:49759663 C>T maps to NM_013334.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:49759378 G>A maps to NM_013334.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr6:16254962 T>C maps to NM_006877.3 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:24706338 C>T maps to ENST00000348719 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:155632256 A>T maps to NM_003875.2 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:3118966 C>T maps to NM_002067.2 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:3121119 C>T maps to NM_002067.2 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:3119227 C>T maps to NM_002067.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr19:3114974 G>A maps to NM_002067.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr7:2771219 G>A maps to NM_007353.2 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:2771242 G>A maps to NM_007353.2 Q240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr7:2771123 G>A maps to NM_007353.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:2770901 G>A maps to NM_007353.2 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr17:63049742 G>A maps to NM_006572.4 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr9:80039047 G>A maps to NM_004297.3 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr9:80049348 T>C maps to NM_004297.3 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr9:80144077 C>T maps to NM_004297.3 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:3155823 C>T maps to NM_002068.2 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:3155943 C>T maps to NM_002068.2 N246N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr19:3155862 G>A maps to NM_002068.2 W219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:3151734 G>A maps to NM_002068.2 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:3155832 C>T maps to NM_002068.2 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:3151806 C>T maps to NM_002068.2 C196C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:3155823 C>T maps to NM_002068.2 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:3157829 G>A maps to NM_002068.2 E283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr7:79818514 T>C maps to NM_002069.5 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:79818489 T>C maps to NM_002069.5 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:50294241 C>T maps to NM_002070.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:50295058 C>T maps to NM_002070.2 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:50293704 C>T maps to NM_002070.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr3:50290553 C>T maps to NM_002070.2 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:50293692 C>T maps to NM_002070.2 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr3:50294494 C>T maps to NM_002070.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr18:11868594 C>T maps to NM_182978.2 R322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr18:11872338 G>A maps to NM_182978.2 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr16:56374801 C>T maps to NM_138736.2 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:56370699 G>A maps to NM_020988.2 E217E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr9:80646120 G>A maps to NM_002072.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr20:57430164 C>T maps to NM_080425.2 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr20:57428697 G>A maps to NM_080425.2 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr20:57429141 C>T maps to NM_080425.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:57429084 C>T maps to NM_080425.2 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:57415766 G>A maps to NM_016592.2 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:57415169 G>A maps to NM_016592.2 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr20:57415481 C>T maps to NM_016592.2 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr20:57430050 C>T maps to NM_080425.2 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:57415742 C>T maps to NM_016592.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:57428859 G>A maps to NM_080425.2 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr20:57415682 C>T maps to NM_016592.2 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:57429084 C>T maps to NM_080425.2 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:50232076 G>A maps to NM_000172.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr3:50229239 C>T maps to NM_000172.3 R28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:110152748 G>A maps to NM_005272.3 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:110148693 G>T maps to NM_005272.3 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:80117910 G>A maps to NM_001102386.1 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:80117913 G>A maps to NM_001102386.1 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:23438256 G>A maps to NM_002073.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr22:23438160 C>T maps to NM_002073.2 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr22:23438262 C>T maps to NM_002073.2 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr22:23465353 C>T maps to NM_002073.2 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr22:23465354 C>T maps to NM_002073.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr22:23438160 C>T maps to NM_002073.2 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:1721866 G>A maps to NM_002074.2 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr22:19808194 A>T maps to NM_053004.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr22:19799822 C>T maps to NM_053004.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr22:19808830 G>A maps to NM_053004.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr22:19776447 G>A maps to NM_053004.2 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:100275173 C>T maps to NM_005273.3 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr5:180668524 C>T maps to NM_006098.4 W132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:180668593 C>T maps to NM_006098.4 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr5:180666102 G>A maps to NM_006098.4 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr12:6956007 C>T maps to NM_002075.2 D323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr3:179132721 C>T maps to NM_021629.3 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr15:52416675 G>A maps to NM_016194.3 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:52446244 G>A maps to NM_016194.3 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr9:36218284 A>G maps to NM_001128227.2 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr9:36227306 G>A maps to NM_001128227.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr9:36233982 G>A maps to NM_001128227.2 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr14:52433398 C>T maps to NM_053064.3 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:52433335 C>T maps to NM_053064.3 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:62476262 C>T maps to NM_012202.3 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:235747057 G>A maps to NM_004485.3 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:47137368 G>A maps to NM_033258.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr19:47137437 G>A maps to NM_033258.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr7:93540181 G>A maps to NM_021955.3 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:47284742 C>T maps to NM_001198754.1 E14E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr6:30520349 C>T maps to NM_005275.3 E331E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:38049512 G>A maps to NM_013285.2 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:38042067 C>T maps to NM_013285.2 K333K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr3:52721399 G>T did not map to a codon.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr23:54569417 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:54569417 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:54574664 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:54578015 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:54578135 C>T did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:54585022 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:85923142 C>T maps to NM_006433.3 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:85924771 G>A maps to NM_006433.3 E133E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:42930849 G>A maps to NM_018960.4 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr6:42931338 C>T maps to NM_018960.4 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr1:231402069 C>T maps to NM_014236.3 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr5:141384619 G>A maps to NM_005471.4 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:141391560 C>A maps to NM_005471.4 E14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr4:44724173 G>A maps to NM_138335.1 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr4:44712984 C>T maps to NM_138335.1 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:3025445 C>T maps to NM_001501.1 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:68610307 C>T maps to NM_000406.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr9:127684012 C>T maps to NM_002077.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:127650641 G>A maps to NM_002077.3 Q599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:127651724 G>A maps to NM_002077.3 Q530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:127651725 G>A maps to NM_002077.3 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:127683503 A>T maps to NM_002077.3 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:127651552 G>A maps to NM_002077.3 Q544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:131029751 G>A maps to NM_004486.4 N155N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr9:131021447 G>A maps to NM_004486.4 Q672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:131019732 G>A maps to NM_004486.4 F903F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr9:131019927 C>T maps to NM_004486.4 E863E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr12:133357461 G>A maps to NM_005895.3 R1168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:133353291 G>A maps to NM_005895.3 S1302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr12:133393300 G>A maps to NM_005895.3 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr12:133372443 G>A maps to NM_005895.3 S821S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr12:133381569 G>A maps to NM_005895.3 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:133381502 G>A maps to NM_005895.3 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:37367217 T>C maps to NM_001172713.1 L1303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr3:37367210 T>C maps to NM_001172713.1 L1300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:37366305 C>T maps to NM_001172713.1 Q999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:37369100 C>T maps to NM_001172713.1 S1930S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:37379167 A>T maps to NM_001172713.1 A2128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:37379168 C>T maps to NM_001172713.1 Q2129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr3:37366815 C>T maps to NM_001172713.1 L1169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr3:37368449 G>A maps to NM_001172713.1 L1713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr3:37340795 G>A maps to NM_001172713.1 E362E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr14:93264101 C>A maps to NM_005113.2 S107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr14:93276679 T>C maps to NM_005113.2 D358D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr14:93290920 C>T maps to NM_005113.2 R551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr15:74368302 G>A maps to NM_001038640.2 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr15:74365119 T>C maps to NM_001038640.2 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:74364603 C>T maps to NM_001038640.2 R516R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:74367328 G>A maps to NM_001038640.2 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr15:72953657 G>A maps to NM_018652.4 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:72954752 G>A maps to NM_018652.4 K336K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr15:72954764 G>A maps to NM_018652.4 Q340Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:72958207 G>A maps to NM_018652.4 Q594Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:72958219 G>A maps to NM_018652.4 E598E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr15:75562479 C>T maps to NM_001164404.1 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:41355057 C>T maps to NM_001002296.1 R48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr15:34673701 C>T maps to NM_181077.3 E574E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr3:121437282 G>A maps to ENST00000393667 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:121383331 G>A maps to ENST00000393667 L3269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr3:121409708 G>A maps to ENST00000393667 N2834N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:121438522 G>A maps to ENST00000393667 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr3:121416750 A>G maps to ENST00000393667 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr3:121416681 G>A maps to ENST00000393667 T896T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:121437282 G>A maps to ENST00000393667 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:121388157 G>A maps to ENST00000393667 L3074L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr3:121416834 C>T maps to ENST00000393667 L845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:121416025 A>T maps to ENST00000393667 L1115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:121410778 G>A maps to ENST00000393667 R2478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr3:121409693 A>G maps to ENST00000393667 F2839F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:167745584 T>G maps to NM_014498.3 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:167747026 G>A maps to NM_014498.3 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr9:88667463 G>A maps to ENST00000376023 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:88655716 G>T maps to ENST00000376023 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:150620961 G>A maps to ENST00000369003 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:150621113 G>A maps to ENST00000369003 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:150620934 G>A maps to ENST00000369003 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr12:21661378 C>T maps to NM_016072.4 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr12:21661378 C>T maps to NM_016072.4 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr12:21661379 C>T maps to NM_016072.4 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:21654862 C>T maps to NM_016072.4 I2I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:155796744 G>A maps to ENST00000368331 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:155735999 G>A maps to ENST00000368331 S1088S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:155747456 G>A maps to ENST00000368331 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:155735708 A>C maps to ENST00000368331 V1185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:155774904 G>A maps to ENST00000368331 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:155823529 G>A maps to ENST00000368331 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:155774884 G>A maps to ENST00000368331 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:117896401 G>A maps to NM_020399.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:117888029 G>A maps to NM_020399.3 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:170521291 T>C maps to NM_152281.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:170501357 C>A maps to NM_152281.2 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:171804873 C>T maps to NM_015530.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:171822504 C>T maps to NM_015530.3 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr2:171819347 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr17:28817160 C>T maps to NM_004871.2 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr10:101163499 G>A maps to NM_002079.2 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr10:101163499 G>A maps to NM_002079.2 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:101163311 G>A maps to NM_002079.2 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:37794818 G>A maps to NM_152413.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:37796274 G>A maps to NM_152413.2 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:37793364 C>T maps to NM_152413.2 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr16:58753134 C>A maps to NM_002080.2 G134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:58750624 G>A maps to NM_002080.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr16:20335567 G>A maps to NM_001007240.1 N35N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr16:20335498 G>A maps to NM_001007240.1 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:20335152 G>A maps to NM_001007240.1 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:20322598 G>A maps to NM_001007240.1 F520F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:20335309 C>T maps to NM_001007240.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:20335564 G>A maps to NM_001007240.1 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:20329514 G>A maps to NM_001007240.1 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr16:20330985 C>G maps to NM_001007240.1 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr16:20329727 C>T maps to NM_001007240.1 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:20328615 G>A maps to NM_001007240.1 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:20328686 G>A maps to NM_001007240.1 Q425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:20329571 C>T maps to NM_001007240.1 R399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:20337702 G>A maps to NM_001007240.1 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:20329727 C>A maps to NM_001007240.1 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:20328585 G>A maps to NM_001007240.1 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr16:20328585 G>A maps to NM_001007240.1 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr3:194118414 A>G maps to NM_004488.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr3:194118240 G>A maps to NM_004488.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:194118768 G>A maps to NM_004488.2 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:194118165 C>T maps to NM_004488.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:194118497 G>A maps to NM_004488.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:194117700 C>T maps to NM_004488.2 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:194118750 G>A maps to NM_004488.2 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:194118741 G>A maps to NM_004488.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr19:55526397 G>A maps to NM_001083899.1 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:55525973 G>A maps to NM_001083899.1 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:55526346 G>A maps to NM_001083899.1 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:55525593 C>T maps to NM_001083899.1 R573R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:128780668 G>A maps to NM_000174.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:167038167 A>G maps to NM_005814.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:167059495 C>T maps to NM_005814.1 W10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:167023579 G>A maps to NM_005814.1 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:167042665 G>A maps to NM_005814.1 R52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr1:167032861 C>T maps to NM_005814.1 K176K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:167042669 G>A maps to NM_005814.1 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr8:145138651 G>A maps to NM_003801.3 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr8:145139184 C>T maps to NM_003801.3 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr8:145138666 C>T maps to NM_003801.3 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr10:113928237 G>A maps to NM_020918.4 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr10:113928204 G>A maps to NM_020918.4 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:33617588 C>T maps to NM_018025.2 S905S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:33617589 C>T maps to NM_018025.2 Q906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:33587156 C>A maps to NM_018025.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:33600767 C>T maps to NM_018025.2 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr19:33608897 C>T maps to NM_018025.2 F788F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr19:33604796 C>T maps to NM_018025.2 R673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:33592449 C>T maps to NM_018025.2 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:217688183 G>A maps to NM_018040.2 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr1:217665070 G>A maps to NM_018040.2 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:217784255 G>A maps to NM_018040.2 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:217784271 A>C maps to NM_018040.2 L326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr1:27224142 C>T maps to NM_022078.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr1:27217644 G>A maps to NM_022078.2 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:156566270 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr17:42475679 G>A maps to NM_001002909.2 S1255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:42478253 G>A maps to NM_001002909.2 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:42476375 C>A maps to NM_001002909.2 R1023R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:42477635 G>A maps to NM_001002909.2 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:42476474 C>T maps to NM_001002909.2 R990R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:42475712 G>A maps to NM_001002909.2 L1244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr17:42478300 G>A maps to NM_001002909.2 R382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr17:42475517 G>A maps to NM_001002909.2 P1309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:42475589 G>T maps to NM_001002909.2 P1285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr17:42476849 G>A maps to NM_001002909.2 S865S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr5:56557063 C>T maps to NM_001127236.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:56527006 C>T maps to NM_001127236.2 Y97Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:46120895 A>T maps to NM_021639.4 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:241401947 C>T maps to NM_002081.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:99773254 G>A maps to NM_152742.1 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:99773367 A>G maps to NM_152742.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr7:99774680 G>A maps to NM_152742.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:99771473 G>A maps to NM_152742.1 D292D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr7:99773356 G>A maps to NM_152742.1 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr7:99769796 G>A maps to NM_152742.1 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:132833928 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:132887945 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:132730587 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:132730485 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:132887939 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:132888182 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:132670236 T>G did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:132826494 G>A did not map to a codon.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr23:132670162 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:132826486 A>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:132888042 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:133119349 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:132730509 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:132438839 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:132458543 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr23:132437218 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr23:132440124 A>C did not map to a codon.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr23:132445400 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:132439840 C>A did not map to a codon.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr23:132458249 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr23:132445422 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr23:132458256 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:132440113 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr23:132445397 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:132439916 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:132445386 C>G did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:132445317 C>T did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr23:132439894 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:132439913 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr23:132548900 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr13:93518534 G>A maps to NM_004466.4 W521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr13:93518535 G>A maps to NM_004466.4 W521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr13:92345654 C>T maps to NM_004466.4 N180N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr13:92345507 G>A maps to NM_004466.4 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:93518682 G>A maps to NM_004466.4 G570G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr13:92380914 A>C maps to NM_004466.4 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr13:92101084 G>A maps to NM_004466.4 Q78Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr13:92408649 G>A maps to NM_004466.4 W419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:92346065 G>A maps to NM_004466.4 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr13:92101145 C>T maps to NM_004466.4 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr13:94680005 C>T maps to NM_005708.3 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr13:95055278 C>T maps to NM_005708.3 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr13:95055326 G>A maps to NM_005708.3 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr13:94958286 C>T maps to NM_005708.3 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr13:94482701 G>A maps to NM_005708.3 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr13:94482599 G>A maps to NM_005708.3 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr13:95034771 G>A maps to NM_005708.3 E419E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:5545698 G>A maps to NM_019593.3 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr12:50498356 G>A maps to NM_005276.2 W14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:50501528 C>T maps to NM_005276.2 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:32181841 C>T maps to NM_015141.3 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:157414075 C>T maps to NM_000408.4 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:157425914 C>T maps to NM_000408.4 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:157425454 C>T maps to NM_000408.4 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr14:63784458 G>A maps to ENST00000314140 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr14:63784479 C>T maps to ENST00000314140 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr14:63784527 G>T maps to ENST00000314140 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr14:63784434 G>A maps to ENST00000314140 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr14:63784485 G>A maps to ENST00000314140 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr14:67589052 A>G maps to NM_020806.4 E569E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr14:67589067 G>A maps to NM_020806.4 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:67525456 C>T maps to NM_020806.4 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:67147885 C>T maps to NM_020806.4 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr14:67389391 C>T maps to NM_020806.4 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr14:67390966 C>T maps to NM_020806.4 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:34856260 C>T maps to NM_000175.3 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:34890116 C>T maps to NM_000175.3 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:34884841 C>T maps to NM_000175.3 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:34884842 C>T maps to NM_000175.3 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr19:34859580 C>T maps to NM_000175.3 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:144295163 C>T maps to NM_178172.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:48979933 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:48974082 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:48973500 G>T did not map to a codon.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr6:24448237 C>T maps to NM_001503.2 W515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:24448180 G>A maps to NM_001503.2 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:24475399 G>A maps to NM_001503.2 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:24480148 G>A maps to NM_001503.2 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr6:24448198 G>A maps to NM_001503.2 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr6:24460548 A>G maps to NM_001503.2 Y322Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:24447199 C>T maps to NM_001503.2 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:24454269 C>T maps to NM_001503.2 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr4:176556175 C>T maps to NM_005277.3 W239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:176594941 G>A maps to NM_005277.3 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr4:176622877 G>A maps to NM_005277.3 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:176556166 C>T maps to NM_005277.3 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:13801601 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:13834992 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr23:13803744 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr2:27851918 G>A maps to NM_007266.3 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr1:27212478 G>A maps to NM_018066.3 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:27215460 C>G maps to NM_018066.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:110891654 G>A maps to NM_001164373.1 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:110895367 G>A maps to NM_001164373.1 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr7:23293869 C>T maps to ENST00000435486 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr7:23293815 T>C maps to ENST00000435486 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr2:207041071 G>A maps to NM_005279.3 N300N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:207041959 C>T maps to NM_005279.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr23:136113173 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr23:136112392 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:136112389 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:136112600 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:136112407 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:136113377 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr23:136113014 C>T did not map to a codon.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr23:136112704 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr23:136112883 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:136112661 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:136112785 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:132890959 G>T maps to NM_001136557.1 T542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:132862931 C>T maps to NM_001136557.1 Q322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:6732082 G>A maps to NM_001080452.1 F403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:6733258 G>A maps to NM_001080452.1 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:6734245 G>A maps to NM_001080452.1 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:6733030 G>A maps to NM_001080452.1 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:6733303 G>A maps to NM_001080452.1 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:6732360 G>A maps to NM_001080452.1 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:6731104 G>A maps to NM_001080452.1 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:6733288 G>A maps to NM_001080452.1 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:123186912 G>A maps to NM_177551.3 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:123187410 G>A maps to NM_177551.3 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr12:123187119 G>A maps to NM_177551.3 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:123187023 G>A maps to NM_177551.3 Y269Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:123187332 C>T maps to NM_177551.3 K166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:123187617 C>T maps to NM_177551.3 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr12:123187422 C>T maps to NM_177551.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:123201116 G>A maps to NM_006018.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:123200396 G>A maps to NM_006018.2 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:123200606 G>A maps to NM_006018.2 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr6:46995452 C>T maps to ENST00000283297 K39K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:46996734 G>A maps to ENST00000283297 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:46979808 C>T maps to ENST00000283297 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr6:46979925 G>A maps to ENST00000283297 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr6:46979925 G>A maps to ENST00000283297 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr6:46977271 G>A maps to ENST00000283297 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:46988501 A>G maps to ENST00000283297 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:46976893 G>A maps to ENST00000283297 F760F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:46976938 G>A maps to ENST00000283297 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr6:47649917 C>T maps to NM_153839.6 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr6:47649531 C>T maps to NM_153839.6 Q345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr6:47649584 C>T maps to NM_153839.6 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:47650088 G>A maps to NM_153839.6 W530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:47649680 C>T maps to NM_153839.6 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:47649947 C>T maps to NM_153839.6 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr6:47650307 C>T maps to NM_153839.6 I603I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr6:47649086 C>T maps to NM_153839.6 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr6:47650361 G>A maps to NM_153839.6 Q621Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:47646749 C>T maps to NM_153839.6 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr6:47649086 C>T maps to NM_153839.6 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr6:47654738 C>T maps to NM_153839.6 I625I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:47650115 C>T maps to NM_153839.6 F539F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:47650328 C>T maps to NM_153839.6 F610F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:47649311 C>T maps to NM_153839.6 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr23:135431585 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr23:135430339 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr23:135427471 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:135430105 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:135431575 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr23:135428901 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:135429120 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:135427864 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:135427549 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:135430097 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:135431320 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:135429707 G>A did not map to a codon.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr23:135427955 C>T did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:135427811 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:135426615 A>G did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:135482132 A>G did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:135494460 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:135428724 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:135431703 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr23:135477633 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr23:135494508 A>C did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:135428078 T>A did not map to a codon.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr23:135426738 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:135431320 C>T did not map to a codon.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr23:135426718 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:135431815 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:135390974 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:135427096 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:135428071 T>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:135429447 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr23:135428481 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:135428273 A>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:135429840 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:135432444 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:135428481 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:135430784 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:135494423 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr23:135430024 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:135496358 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr23:135428105 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:135430316 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:135428774 C>A did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:135430316 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr23:135427217 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:135429625 T>G did not map to a codon.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr23:135431857 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:135430933 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:135482076 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:135482251 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr23:135427485 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:135432150 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:135432541 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:135453591 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:135429747 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:135405473 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr23:135453676 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:135405400 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:135427102 C>G did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:135427663 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:135429805 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:135455069 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:135428846 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr23:135427791 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr23:135469927 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:135428095 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr23:135430516 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr23:135469964 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:135429116 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:135469916 C>G did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:135429028 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:135480077 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:135480088 T>G did not map to a codon.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr23:135433682 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr23:135480113 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:135487866 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:135429842 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:135431694 G>A did not map to a codon.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr23:135426619 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:135432542 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:135431444 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:135469903 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr23:135430934 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:135431957 T>C did not map to a codon.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr23:135445669 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr23:135498644 C>T did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:135427353 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:135431594 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:135469993 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1YX-06A-11D-A197-08 chr23:135427554 T>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr23:135439872 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:135431966 A>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:135480047 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:135430443 A>G did not map to a codon.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr23:135431959 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:135429698 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:135429707 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:135427030 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:135427317 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:135427571 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:135428792 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:135428893 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:135429947 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:135430250 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:135430763 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:135431119 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:135431685 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:135441521 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:135480068 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:135482014 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:135485427 C>T did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr23:135445711 C>T did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr23:135431104 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:135405490 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:135429120 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:135429878 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:135431263 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:135433609 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:135480118 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:135496362 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:135496363 G>A did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:135430653 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:135428875 C>T did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:135428452 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr23:135431405 C>T did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:135430954 C>T did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:135430405 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:26534447 G>A maps to NM_001145168.1 V716V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:26533850 C>T maps to NM_001145168.1 G915G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:26537354 G>A maps to NM_001145168.1 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr2:26534300 C>T maps to NM_001145168.1 P765P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:26534180 G>A maps to NM_001145168.1 S805S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr2:26536364 G>A maps to NM_001145168.1 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr2:26534870 C>T maps to NM_001145168.1 R575R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:26534030 G>A maps to NM_001145168.1 T855T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr2:26533823 C>T maps to NM_001145168.1 G924G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:26537450 C>T maps to NM_001145168.1 W321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr6:47675988 G>A maps to NM_153838.3 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr6:47682220 C>T maps to NM_153838.3 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr6:47682747 T>C maps to NM_153838.3 I589I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr6:47682429 C>T maps to NM_153838.3 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:47680208 C>T maps to NM_153838.3 C139C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:47678597 C>T maps to NM_153838.3 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr6:47682090 C>T maps to NM_153838.3 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr6:47682498 C>T maps to NM_153838.3 F506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:47681823 G>A maps to NM_153838.3 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:47682213 C>T maps to NM_153838.3 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:47682165 G>A maps to NM_153838.3 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:47681689 G>T maps to NM_153838.3 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:47684582 G>A maps to NM_153838.3 K658K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr6:47680196 C>T maps to NM_153838.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr6:47675988 G>A maps to NM_153838.3 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr6:47682333 G>A maps to NM_153838.3 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr6:47682711 T>A maps to NM_153838.3 V577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr6:47680329 C>T maps to NM_153838.3 R180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:47680241 G>A maps to NM_153838.3 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:47681865 C>T maps to NM_153838.3 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr6:47682870 C>T maps to NM_153838.3 S630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:46826171 A>G maps to NM_015234.4 Y1156Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr6:46874484 C>T maps to NM_015234.4 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:46826915 G>A maps to NM_015234.4 I908I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr6:46825898 G>A maps to NM_015234.4 F1247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr6:46849210 G>A maps to NM_015234.4 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:46826048 G>A maps to NM_015234.4 I1197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:46851843 G>A maps to NM_015234.4 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:46846011 C>T maps to NM_015234.4 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:46874484 C>T maps to NM_015234.4 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr6:46826468 G>A maps to NM_015234.4 I1057I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr6:46874490 G>A maps to NM_015234.4 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:46826617 G>A maps to NM_015234.4 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:46826783 C>T maps to NM_015234.4 T952T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:46828585 G>A maps to NM_015234.4 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:46846122 C>T maps to NM_015234.4 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:46849838 C>T maps to NM_015234.4 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr6:46851898 G>A maps to NM_015234.4 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:46847630 C>T maps to NM_015234.4 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr6:46874425 C>T maps to NM_015234.4 W25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:46826783 C>T maps to NM_015234.4 T952T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:46826168 C>T maps to NM_015234.4 T1157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:46826468 G>A maps to NM_015234.4 I1057I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:46834689 G>A maps to NM_015234.4 F602F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:46847693 G>A maps to NM_015234.4 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr6:46830681 C>T maps to NM_015234.4 E714E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:46832787 G>A maps to NM_015234.4 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:46847630 C>T maps to NM_015234.4 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr6:46826900 G>A maps to NM_015234.4 I913I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr6:46828469 T>C maps to NM_015234.4 V787V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:46826468 G>A maps to NM_015234.4 I1057I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:46826216 G>A maps to NM_015234.4 A1141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr6:46851901 G>A maps to NM_015234.4 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr6:46826618 G>T maps to NM_015234.4 L1007L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr23:129519282 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:129518780 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:129518963 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:129518895 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr23:129518463 C>T did not map to a codon.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr23:129518562 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr13:27333040 G>A maps to NM_005288.3 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr13:27332998 G>A maps to NM_005288.3 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr13:27333417 G>A maps to NM_005288.3 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr10:95335921 G>A maps to NM_181745.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr10:95347053 G>A maps to NM_181745.3 Q274Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr10:95346993 G>A maps to NM_181745.3 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:95347350 G>A maps to NM_181745.3 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:95335846 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:95338947 C>T maps to NM_181745.3 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:95347002 C>T maps to NM_181745.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:134941913 C>T maps to ENST00000368577 F734F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr10:134912194 C>T maps to ENST00000368577 F602F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr10:134942979 C>T maps to ENST00000368577 R1090*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr10:134910572 G>A maps to ENST00000368577 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:134916262 G>A maps to ENST00000368577 R647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr8:37693121 C>T maps to NM_032777.9 S628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr8:37693274 C>T maps to NM_032777.9 I679I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr8:37691639 C>T maps to NM_032777.9 I534I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr8:37692834 C>T maps to NM_032777.9 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:37689060 C>T maps to NM_032777.9 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr8:37688325 C>T maps to NM_032777.9 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr4:22390766 G>A maps to NM_145290.2 C889C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:22414873 A>G maps to NM_145290.2 H721H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:22389747 G>A maps to NM_145290.2 S1182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:22389806 G>A maps to NM_145290.2 R1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:22390167 G>A maps to NM_145290.2 F1042F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr4:22404389 C>T maps to NM_145290.2 A755A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr6:142737022 G>A maps to NM_198569.2 W920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr6:142758583 C>T maps to NM_198569.2 F1111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr6:142737021 G>A maps to NM_198569.2 W920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr6:142737022 G>A maps to NM_198569.2 W920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr6:142711422 G>A maps to NM_198569.2 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr6:142729376 C>T maps to NM_198569.2 Q787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr6:142721670 C>T maps to NM_198569.2 I539I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:100354609 C>T maps to NM_032787.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr3:100354663 A>C maps to NM_032787.2 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:100368601 C>T maps to NM_032787.2 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr3:100352146 C>T maps to NM_032787.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:100373861 C>T maps to NM_032787.2 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr3:100373733 T>C maps to NM_032787.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:100378687 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:105517999 G>A maps to NM_013345.2 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:105517528 G>A maps to NM_013345.2 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr12:131487839 C>T maps to NM_198827.3 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr12:131498746 C>T maps to NM_198827.3 I445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:131471868 C>T maps to NM_198827.3 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr12:131569138 C>T maps to NM_198827.3 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:131620580 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:131471823 C>T maps to NM_198827.3 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:131487746 G>A maps to NM_198827.3 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:131471649 G>A maps to NM_198827.3 W167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:131471823 C>T maps to NM_198827.3 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr11:64055267 C>A maps to NM_001170726.1 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr11:64054477 C>T maps to NM_001170726.1 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64055333 C>T maps to NM_001170726.1 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr11:64055333 C>T maps to NM_001170726.1 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:64055574 C>T maps to NM_001170726.1 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr14:53066869 C>T maps to NM_001099652.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr14:53100345 C>T maps to NM_001099652.1 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr14:53066834 C>T maps to NM_001099652.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr16:20043680 C>T maps to NM_001002911.2 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:20043410 G>A maps to NM_001002911.2 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:20043734 G>A maps to NM_001002911.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:20084857 G>A maps to NM_001002911.2 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr16:20043674 G>A maps to NM_001002911.2 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:20043734 G>A maps to NM_001002911.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:20043425 G>A maps to NM_001002911.2 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:20043635 G>A maps to NM_001002911.2 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:20043242 G>A maps to NM_001002911.2 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:20043848 G>A maps to NM_001002911.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr16:20043689 G>A maps to NM_001002911.2 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr16:20043518 G>A maps to NM_001002911.2 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr16:20043446 C>T maps to NM_001002911.2 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:20043734 G>A maps to NM_001002911.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:20043911 G>A maps to NM_001002911.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:20043560 G>A maps to NM_001002911.2 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr16:20043848 G>A maps to NM_001002911.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr7:37780114 C>T maps to NM_181791.1 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:37780318 G>A maps to NM_181791.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:37780294 C>T maps to NM_181791.1 Y100Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr7:37780890 G>A maps to NM_181791.1 W299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr7:37780891 G>A maps to NM_181791.1 W299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr7:37780594 G>A maps to NM_181791.1 Q200Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr17:72367904 C>T maps to ENST00000440684 A1148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr17:72363680 C>T maps to NM_181790.1 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr17:72367874 C>T maps to ENST00000440684 L1138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:72363865 G>A maps to NM_181790.1 K74K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr17:72368513 G>A maps to ENST00000440684 R1351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:72368372 G>A maps to ENST00000440684 R1304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr17:72368060 G>A maps to ENST00000440684 L1200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr17:72368513 G>A maps to ENST00000440684 R1351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr17:72368423 C>T maps to ENST00000440684 I1321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:72363847 C>T maps to NM_181790.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:72367985 C>T maps to ENST00000440684 F1175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:9714139 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr23:9714169 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr23:9711603 C>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr23:9716650 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr7:1097585 G>A maps to NM_138445.2 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:1097780 C>T maps to NM_138445.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:1097762 C>T maps to NM_138445.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr2:131487206 C>T maps to NM_207364.2 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:131487350 C>T maps to NM_207364.2 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:131487308 G>A maps to NM_207364.2 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:131486882 C>T maps to NM_207364.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:131487743 C>T maps to NM_207364.2 H340H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:131487692 C>T maps to NM_207364.2 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr2:131487494 C>T maps to NM_207364.2 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:131487716 C>T maps to NM_207364.2 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:131486882 C>T maps to NM_207364.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:154055906 G>A maps to NM_001038705.1 R593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:154138959 T>G maps to NM_001038705.1 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:154147233 G>A maps to NM_001038705.1 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:154147350 C>T maps to NM_001038705.1 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:154056018 C>T maps to NM_001038705.1 Q555Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:154055946 C>T maps to NM_001038705.1 G579G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:154146579 G>A maps to NM_001038705.1 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:154146612 A>G maps to NM_001038705.1 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:154139226 C>T maps to NM_001038705.1 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:154147140 G>A maps to NM_001038705.1 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:98251935 G>A maps to NM_005290.1 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:98250981 C>T maps to NM_005290.1 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:98251248 C>T maps to NM_005290.1 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr5:145894713 C>T maps to NM_194251.2 W321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:145894734 C>T maps to NM_194251.2 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:67219721 C>T maps to NM_206997.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:67220039 C>T maps to NM_206997.1 W52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr11:67219373 C>T maps to NM_206997.1 W274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:67219346 C>T maps to NM_206997.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr11:67219613 C>T maps to NM_206997.1 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr11:67219601 G>A maps to NM_206997.1 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:67220114 G>A maps to NM_206997.1 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:6314055 G>A maps to NM_207370.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:6314056 G>A maps to NM_207370.2 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr1:6311560 G>A maps to NM_207370.2 D272D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:6314158 C>T maps to NM_207370.2 W135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:175333750 G>A maps to NM_152529.5 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:119911851 G>A maps to NM_153002.2 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:119962575 G>A maps to NM_153002.2 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr3:119962557 C>T maps to NM_153002.2 W54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr3:119962558 C>T maps to NM_153002.2 W54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr3:119886925 G>A maps to NM_153002.2 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:119892173 C>T maps to NM_153002.2 E359E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:9171505 C>T maps to NM_024980.4 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:9165601 G>A maps to NM_024980.4 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:9164480 G>A maps to NM_024980.4 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr10:25888038 C>T maps to NM_020752.2 Q1162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:25464843 G>A maps to NM_020752.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr10:25886954 G>A maps to NM_020752.2 G800G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr10:25684865 C>T maps to NM_020752.2 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:25886963 G>A maps to NM_020752.2 K803K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr10:25839975 T>C maps to NM_020752.2 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr10:25887845 G>A maps to NM_020752.2 E1097E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr10:25888088 C>A maps to NM_020752.2 T1178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:25886960 C>T maps to NM_020752.2 S802S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr10:25887245 G>A maps to NM_020752.2 S897S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr10:25701362 C>T maps to NM_020752.2 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr10:25861748 G>A maps to NM_020752.2 G562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr10:25684904 C>T maps to NM_020752.2 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr10:25755614 G>A maps to NM_020752.2 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr10:25886795 G>A maps to NM_020752.2 K747K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr10:25886960 C>T maps to NM_020752.2 S802S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr10:25886747 G>A maps to NM_020752.2 K731K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr10:25886747 G>A maps to NM_020752.2 K731K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr10:25886954 G>A maps to NM_020752.2 G800G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr10:25886858 G>A maps to NM_020752.2 Q768Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr10:25701266 C>T maps to NM_020752.2 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr10:25886855 G>C maps to NM_020752.2 R767R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr10:25885643 C>T maps to NM_020752.2 R691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:25684928 G>A maps to NM_020752.2 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:25886969 G>A maps to NM_020752.2 E805E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr10:25887446 G>A maps to NM_020752.2 A964A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr10:25464450 C>T maps to NM_020752.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr10:25701293 C>T maps to NM_020752.2 F409F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr10:25840014 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:168065880 G>A maps to NM_153832.1 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:168066366 G>A maps to NM_153832.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:168065815 C>T maps to NM_153832.1 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:168066389 C>T maps to NM_153832.1 W152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:168073893 G>A maps to NM_153832.1 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:168065881 G>A maps to NM_153832.1 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:6936218 C>T maps to NM_019858.1 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6933225 C>T maps to NM_019858.1 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr2:128408725 C>T maps to NM_005291.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr3:150917041 C>T maps to NM_013308.3 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:150916711 G>A maps to NM_013308.3 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:145583580 C>T maps to NM_024531.3 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr8:145584130 C>T maps to NM_024531.3 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr8:145583691 C>T maps to NM_024531.3 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr8:145584614 G>T maps to NM_024531.3 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:145583637 C>T maps to NM_024531.3 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:145583658 C>T maps to NM_024531.3 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr17:4937339 G>A maps to NM_017986.3 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr17:4936278 C>T maps to NM_017986.3 K440K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:4936278 C>T maps to NM_017986.3 K440K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:4936588 G>A maps to NM_017986.3 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr23:53106031 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr23:78426876 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:78427034 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:78426737 C>T did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:78426956 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:78427048 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:78427143 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr23:78427408 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr23:78427143 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:78426747 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:78426610 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:78427484 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:78427254 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:78426882 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:78427281 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:78427121 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:78426647 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr15:40093773 G>A maps to NM_007223.1 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:40094283 G>T maps to NM_007223.1 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr15:40094247 G>A maps to NM_007223.1 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:40093614 G>A maps to NM_007223.1 A422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr15:40099352 G>A maps to NM_007223.1 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr15:40093418 G>A maps to NM_007223.1 Q488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr15:40099226 G>A maps to NM_007223.1 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:40099394 G>A maps to NM_007223.1 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr17:36484408 C>T maps to ENST00000398597 V1682V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:36489277 G>A maps to ENST00000398597 F632F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr17:36490663 C>T maps to ENST00000398597 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:36486904 C>T maps to ENST00000398597 K850K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:36483547 G>A maps to ENST00000398597 S1969S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr17:36486525 G>A maps to ENST00000398597 L977L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr17:36483958 C>T maps to ENST00000398597 L1832L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr17:36498877 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:36485158 C>T maps to ENST00000398597 E1432E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr17:36486211 C>T maps to ENST00000398597 Q1081Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr17:36482779 C>T maps to ENST00000398597 W2225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:36486595 C>T maps to ENST00000398597 R953R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:36493588 C>T maps to ENST00000398597 E307E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr17:36495407 C>T maps to ENST00000398597 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr17:36483100 C>T maps to ENST00000398597 W2118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr17:36499252 C>T maps to ENST00000398597 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:36499483 G>A maps to ENST00000398597 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr13:99907670 C>T maps to NM_005292.3 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr13:95264594 C>T maps to NM_180989.4 N152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr12:57389214 G>A maps to NM_007264.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr13:99948258 C>T maps to NM_004951.4 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:12815264 G>A maps to NM_006143.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr12:12815019 G>A maps to NM_006143.2 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:142367831 G>A maps to NM_005293.2 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr8:142367270 G>A maps to NM_005293.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:142367015 G>A maps to NM_005293.2 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:125797420 C>T maps to NM_005294.1 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:125797633 C>T maps to NM_005294.1 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:200842324 C>T maps to NM_005298.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr10:125447528 C>T maps to NM_153442.3 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:125434402 C>T maps to NM_153442.3 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr10:125426024 G>A maps to NM_153442.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:125434414 C>T maps to NM_153442.3 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:125426513 G>A maps to NM_153442.3 K197K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:125447573 C>T maps to NM_153442.3 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr10:125434441 C>T maps to NM_153442.3 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr10:125434438 G>A maps to NM_153442.3 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr3:71804084 C>T maps to NM_018971.1 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:71804033 G>A maps to NM_018971.1 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:71804102 C>T maps to NM_018971.1 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:71803814 C>T maps to NM_018971.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:71804291 G>A maps to NM_018971.1 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:27720802 G>A maps to NM_005281.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:27720877 G>A maps to NM_005281.2 K192K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr1:27721039 T>C maps to NM_005281.2 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr6:167570977 G>A maps to NM_005299.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr6:167570908 G>A maps to NM_005299.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr6:167570452 G>A maps to NM_005299.2 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:167571070 G>A maps to NM_005299.2 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:167571112 G>A maps to NM_005299.2 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr6:167571112 G>A maps to NM_005299.2 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr6:167571229 C>T maps to NM_005299.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:167570884 G>A maps to NM_005299.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:167570662 C>T maps to NM_005299.2 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr19:51274519 C>T maps to NM_001506.1 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr19:51274354 G>A maps to NM_001506.1 W166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr19:51274657 C>T maps to NM_001506.1 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr19:51274066 C>T maps to NM_001506.1 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:51274294 C>T maps to NM_001506.1 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr19:51274003 C>T maps to NM_001506.1 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:51274810 C>T maps to NM_001506.1 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:51274747 C>T maps to NM_001506.1 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:51274921 G>A maps to NM_001506.1 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:51274867 G>A maps to NM_001506.1 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:51274810 C>T maps to NM_001506.1 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:41555681 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:41555475 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:41555493 T>G did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr2:241569698 C>T maps to NM_001195381.1 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:241569593 C>T maps to NM_001195381.1 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr2:241569854 C>T maps to NM_001195381.1 C193C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:241570127 G>A maps to NM_001195381.1 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:241569434 C>T maps to NM_001195381.1 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:241569725 G>A maps to NM_001195381.1 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:241569893 C>T maps to NM_001195381.1 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr7:124386988 G>A maps to NM_005302.2 R478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr7:124386788 G>A maps to NM_005302.2 V544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr7:124387043 G>A maps to NM_005302.2 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr7:124404607 G>A maps to NM_005302.2 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:124404307 C>T maps to NM_005302.2 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:124386995 G>A maps to NM_005302.2 A475A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:124386812 G>A maps to NM_005302.2 F536F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:202092430 C>T maps to NM_004767.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:202092104 G>A maps to NM_004767.3 W5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:133175109 G>A maps to NM_001508.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr2:133175310 C>T maps to NM_001508.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:133174902 G>A maps to NM_001508.2 W96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:133175079 G>A maps to NM_001508.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:133175289 C>T maps to NM_001508.2 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr2:133175433 G>A maps to NM_001508.2 E273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:133175421 C>G maps to NM_001508.2 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:133175157 G>A maps to NM_001508.2 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:133174767 C>T maps to NM_001508.2 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:133175433 G>A maps to NM_001508.2 E273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:133402743 A>G maps to NM_001508.2 K309K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:133175088 C>T maps to NM_001508.2 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:46094956 C>T maps to NM_005282.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr19:46094356 C>T maps to NM_005282.2 W256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr19:46094563 G>A maps to NM_005282.2 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:46094749 G>A maps to NM_005282.2 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:46094626 G>A maps to NM_005282.2 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr19:46094941 G>A maps to NM_005282.2 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:46094511 G>A maps to NM_005282.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:46094036 C>T maps to NM_005282.2 *363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:46094149 G>A maps to NM_005282.2 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:46094341 C>T maps to NM_005282.2 E261E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:105859055 G>A maps to NM_007227.3 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:105858314 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:105859316 C>T maps to NM_007227.3 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:105859070 G>A maps to NM_007227.3 Q252Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr23:150348249 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr23:150349132 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr23:150348763 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:150348411 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:150345357 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr23:150349668 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:150349223 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr23:150348645 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr23:150348516 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr23:150349282 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:150345309 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:150349894 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:150349147 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr23:150348808 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:150349587 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:150349104 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:150349594 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr23:150349229 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr23:150349429 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:150349132 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:150349696 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr23:150348274 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr23:150349340 C>T did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:150348630 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr23:150349594 G>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:150349342 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:150348463 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:150349679 C>T did not map to a codon.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr23:150348292 T>A did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:150348568 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:174418004 C>T maps to NM_005684.4 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:174417608 C>T maps to NM_005684.4 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:174417980 C>T maps to NM_005684.4 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:231775371 G>A maps to NM_005683.3 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr2:231775584 G>A maps to NM_005683.3 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:231774972 G>A maps to NM_005683.3 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr2:231775269 C>T maps to NM_005683.3 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:231775413 G>A maps to NM_005683.3 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:57693312 C>T maps to NM_005682.5 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr16:57685238 C>T maps to NM_005682.5 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:57685472 C>T maps to NM_005682.5 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:110300566 A>G maps to ENST00000414000 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:110300858 C>T maps to ENST00000414000 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr6:110300401 G>A maps to ENST00000414000 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:110301028 C>T maps to ENST00000414000 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:110301202 C>T maps to ENST00000414000 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:110085863 C>T maps to NM_031936.4 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:110085847 C>T maps to NM_031936.4 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:110085754 G>A maps to NM_031936.4 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr1:110086462 G>A maps to NM_031936.4 Q273Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:110085661 C>T maps to NM_031936.4 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:110086228 T>C maps to NM_031936.4 C195C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr6:97247112 C>T maps to NM_030784.2 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:97246509 C>T maps to NM_030784.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:97246359 C>T maps to NM_030784.2 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:97246356 C>T maps to NM_030784.2 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr6:97246998 C>T maps to NM_030784.2 W203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:97246839 C>T maps to NM_030784.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr6:97246953 G>A maps to NM_030784.2 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:97246851 G>A maps to NM_030784.2 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:97246842 G>A maps to NM_030784.2 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:19042050 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:19028763 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:19027874 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:19014269 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:19027766 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr23:19031930 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr14:88477400 G>A maps to NM_003608.3 W70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:88477853 G>A maps to NM_003608.3 K221K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:88477562 C>T maps to NM_003608.3 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr14:88477727 G>A maps to NM_003608.3 W179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:88477391 C>T maps to NM_003608.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr14:88477717 T>A maps to NM_003608.3 L176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:88477322 G>A maps to NM_003608.3 K44K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr14:91700824 G>A maps to ENST00000238699 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr14:91701061 G>A maps to ENST00000238699 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr2:54080989 G>A maps to NM_006794.2 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr2:54080990 G>A maps to NM_006794.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:54081074 C>T maps to NM_006794.2 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:54081275 G>A maps to NM_006794.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr2:54081854 G>C maps to NM_006794.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:54080837 G>A maps to NM_006794.2 F352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:47844799 C>T maps to NM_018485.1 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:47844844 C>T maps to NM_018485.1 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr19:47844172 C>T maps to NM_018485.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:47844142 G>A maps to NM_018485.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr19:47845018 G>A maps to NM_018485.1 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr4:8582879 G>A maps to NM_080819.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:8582717 C>T maps to NM_080819.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr4:8584275 C>T maps to NM_080819.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:8584314 G>A maps to NM_080819.2 K242K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr4:8588792 C>T maps to NM_080819.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:8588792 C>T maps to NM_080819.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:8588888 C>T maps to NM_080819.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:8583215 C>T maps to NM_080819.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr4:8584302 C>T maps to NM_080819.2 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr12:123214634 C>T maps to NM_032554.3 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:123213938 C>T maps to NM_032554.3 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr12:123214541 G>A maps to NM_032554.3 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:41586558 C>T did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:41586350 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:94113725 C>T maps to NM_016540.3 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:94113902 G>A maps to NM_016540.3 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr11:94129667 C>T maps to NM_016540.3 W137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:94113386 G>A maps to NM_016540.3 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:94113368 G>A maps to NM_016540.3 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:94134035 G>A maps to NM_016540.3 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:112724554 G>A maps to NM_018970.6 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:112724659 G>A maps to NM_018970.6 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr7:112724152 G>A maps to NM_018970.6 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:151012559 C>T maps to NM_023915.3 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr3:151012364 G>A maps to NM_023915.3 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr3:151012466 G>A maps to NM_023915.3 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:151012160 G>A maps to NM_023915.3 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:151012586 G>A maps to NM_023915.3 D149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:101004698 C>T maps to NM_022049.2 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:147400669 C>A maps to NM_016334.3 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr16:57719838 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr16:57718005 C>T maps to NM_170776.4 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr16:57718362 C>T maps to NM_170776.4 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr16:57719771 T>C maps to NM_170776.4 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr16:57707356 C>T maps to NM_170776.4 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:57702285 C>T maps to NM_170776.4 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:57702286 C>T maps to NM_170776.4 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:57707305 G>A maps to NM_170776.4 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr16:57717957 G>A maps to NM_170776.4 K332K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:57719661 G>A maps to NM_170776.4 W455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:57713103 C>T maps to NM_170776.4 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:57714213 G>A maps to NM_170776.4 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr5:90281228 C>T maps to NM_032119.3 F6014F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:90049473 G>A maps to NM_032119.3 V3735V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr5:89938476 G>A maps to NM_032119.3 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr5:90050854 T>C maps to NM_032119.3 D3811D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr5:90106985 C>T maps to NM_032119.3 F5303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr5:89923416 T>C maps to NM_032119.3 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr5:90001235 C>T maps to NM_032119.3 I2802I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr5:90046366 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:90020787 G>A maps to NM_032119.3 G3296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr5:89979728 C>T maps to NM_032119.3 I1997I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr5:90049425 C>T maps to NM_032119.3 I3719I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr5:89990390 G>A maps to NM_032119.3 V2606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr5:90074266 G>A maps to NM_032119.3 E4230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr5:89924432 G>A maps to NM_032119.3 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:89940641 C>T maps to NM_032119.3 Q952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:89949050 G>A maps to NM_032119.3 Q1220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr5:90074719 C>T maps to NM_032119.3 G4296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr5:89938698 C>T maps to NM_032119.3 I798I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr5:89979722 G>A maps to NM_032119.3 Q1995Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:89949104 C>T maps to NM_032119.3 P1238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:90004661 C>T maps to NM_032119.3 F2920F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:89986684 C>T maps to NM_032119.3 R2260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:90072345 C>T maps to NM_032119.3 I4160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:90086949 G>A maps to NM_032119.3 S4768S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr5:89940673 C>T maps to NM_032119.3 S962S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:90084057 C>T maps to NM_032119.3 F4608F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr5:89990241 C>T maps to NM_032119.3 Q2557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr5:89990342 C>T maps to NM_032119.3 S2590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr5:89925199 T>A maps to NM_032119.3 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr5:90124924 G>A maps to NM_032119.3 K5511K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr5:90136682 C>T maps to NM_032119.3 Q5634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr5:90059210 C>T maps to NM_032119.3 V4070V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr5:90136564 C>T maps to NM_032119.3 R5594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:90015893 G>A maps to NM_032119.3 T3159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:90106232 G>A maps to NM_032119.3 L5052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:89992898 C>T maps to NM_032119.3 A2697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr5:89924492 G>A maps to NM_032119.3 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:89948161 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr5:89992805 G>A maps to NM_032119.3 E2666E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr5:90459686 G>A maps to NM_032119.3 R6297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:89949581 C>T maps to NM_032119.3 S1397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr5:89990021 G>A maps to NM_032119.3 R2483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:90040907 G>A maps to NM_032119.3 W3532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr5:89986684 C>T maps to NM_032119.3 R2260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr5:89979668 G>A maps to NM_032119.3 G1977G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:90012353 C>T maps to NM_032119.3 F3085F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:90136682 C>T maps to NM_032119.3 Q5634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:89979590 C>T maps to NM_032119.3 V1951V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:89968361 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:90073769 G>A maps to NM_032119.3 R4192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:89992929 C>T maps to NM_032119.3 Q2708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:89924420 G>A maps to NM_032119.3 G427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr5:90012450 C>T maps to NM_032119.3 Q3118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr5:90041001 G>A maps to NM_032119.3 K3563K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr5:90046513 G>A maps to NM_032119.3 V3707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr5:89924432 G>A maps to NM_032119.3 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr5:90073775 C>T maps to NM_032119.3 F4194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:89931016 G>C maps to NM_032119.3 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr5:90084057 C>T maps to NM_032119.3 F4608F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:89925211 G>A maps to NM_032119.3 V565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:90079759 C>T maps to NM_032119.3 P4513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr5:89924537 A>G maps to NM_032119.3 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr5:89981777 G>A maps to NM_032119.3 V2152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:89924432 G>A maps to NM_032119.3 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:89948162 G>A maps to NM_032119.3 W1139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:89949434 G>A maps to NM_032119.3 R1348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:89953917 C>T maps to NM_032119.3 F1525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:89979992 G>A maps to NM_032119.3 A2085A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:89999522 C>T maps to NM_032119.3 R2733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:90008190 C>T maps to NM_032119.3 Q3044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:90016010 G>A maps to NM_032119.3 G3198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:90025463 C>T maps to NM_032119.3 Q3478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:90119262 C>T maps to NM_032119.3 V5406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:90281261 G>A maps to NM_032119.3 V6025V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:90398132 C>T maps to NM_032119.3 L6136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:90012537 C>T maps to NM_032119.3 R3147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr5:90074405 C>T maps to NM_032119.3 R4277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:90136462 G>A maps to NM_032119.3 V5560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:90449126 C>T maps to NM_032119.3 F6238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr5:89923387 C>T maps to NM_032119.3 Q345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr5:89949266 C>T maps to NM_032119.3 F1292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr5:90106259 G>A maps to NM_032119.3 G5061G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr5:89938512 G>A maps to NM_032119.3 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:90103461 C>T maps to NM_032119.3 F4960F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr5:90151561 T>C maps to NM_032119.3 L5867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr5:90261312 C>T maps to NM_032119.3 L5980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:101910183 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:101909675 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:101910755 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:101911789 T>C did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:101910586 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:101909134 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:101910616 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:101912112 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:101911117 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:101910899 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:101912383 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr23:101911015 G>A did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:101910947 A>G did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:101911621 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:101970946 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:101972233 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:101970442 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:101971511 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:101971488 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:101970301 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:101972233 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:101972233 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:101969867 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:101970346 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:101971113 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:13061548 C>T maps to NM_003979.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:13061551 C>T maps to NM_003979.3 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:13061500 C>T maps to NM_003979.3 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr12:13061494 C>T maps to NM_003979.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr12:13061857 G>T maps to NM_003979.3 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr12:13065067 C>T maps to NM_003979.3 Q325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:19883309 G>A maps to NM_016235.1 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:19883576 G>A maps to NM_016235.1 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr16:19883870 G>A maps to NM_016235.1 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr16:19883879 G>A maps to NM_016235.1 H96H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:19883978 G>A maps to NM_016235.1 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr16:19883786 G>A maps to NM_016235.1 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr16:19883615 G>A maps to NM_016235.1 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:19884065 G>A maps to NM_016235.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr16:19883960 G>A maps to NM_016235.1 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr16:19884065 G>A maps to NM_016235.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:72436586 C>T maps to NM_022036.2 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr17:72436694 C>T maps to NM_022036.2 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:72436805 C>T maps to NM_022036.2 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr17:72436124 C>T maps to NM_022036.2 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr17:72436925 C>T maps to NM_022036.2 F382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr17:72435914 G>A maps to NM_022036.2 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:72443164 T>G maps to NM_022036.2 *487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:72436787 C>T maps to NM_022036.2 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr12:13103120 G>A maps to NM_018654.1 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr6:117128081 C>T maps to NM_148963.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr6:117121791 G>A maps to NM_148963.2 F501F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr6:117114039 C>T maps to NM_148963.2 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr6:117114213 C>T maps to NM_148963.2 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:117127757 A>G maps to NM_148963.2 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:117113511 G>A maps to NM_148963.2 S858S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:117113718 G>A maps to NM_148963.2 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:117113610 G>A maps to NM_148963.2 I825I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:117113865 G>A maps to NM_148963.2 I740I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:117128138 C>T maps to NM_148963.2 E243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:117150140 C>T maps to NM_148963.2 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:117150068 G>A maps to NM_148963.2 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:117121794 G>A maps to NM_148963.2 V500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr6:117114282 G>A maps to NM_148963.2 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:117114300 G>A maps to NM_148963.2 I595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:117127874 C>T maps to NM_148963.2 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr6:117114180 C>T maps to NM_148963.2 V635V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr6:117127685 C>T maps to NM_148963.2 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr6:117127826 G>A maps to NM_148963.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:117113327 G>A maps to NM_148963.2 R920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr6:117130755 T>C maps to NM_148963.2 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr6:117127853 G>A maps to NM_148963.2 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr5:176025032 G>A maps to NM_052899.2 I601I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:176024765 G>A maps to NM_052899.2 S690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:176025272 G>A maps to NM_052899.2 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:176024765 G>A maps to NM_052899.2 S690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:176026790 C>T maps to NM_052899.2 K15K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr5:176026118 T>C maps to NM_052899.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr5:176026370 G>A maps to NM_052899.2 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr10:46999698 G>A maps to NM_014696.3 Q273Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:46999401 G>A maps to NM_014696.3 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr10:46999707 G>A maps to NM_014696.3 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:46998939 C>T maps to NM_014696.3 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:46999548 C>T maps to NM_014696.3 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:46999995 G>A maps to NM_014696.3 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr10:46998915 A>C maps to NM_014696.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:46999749 C>T maps to NM_014696.3 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr10:47000209 C>T maps to NM_014696.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr4:90169875 G>A maps to NM_198281.2 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr4:90169314 C>T maps to NM_198281.2 V649V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:90171111 G>A maps to NM_198281.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr4:90169803 C>T maps to NM_198281.2 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:90170277 G>A maps to NM_198281.2 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr4:90170493 G>A maps to NM_198281.2 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:80010325 G>A maps to NM_212492.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:7217804 A>G did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:7217665 G>A maps to NM_004489.4 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:139252506 A>G maps to NM_001145638.1 V621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr9:139252515 G>T maps to NM_001145638.1 R624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:139250995 G>A maps to NM_001145638.1 K605K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr9:139250281 C>T maps to NM_001145638.1 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:139232391 C>T maps to NM_001145638.1 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:109440159 G>T maps to NM_013296.4 G109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:109466652 G>C maps to NM_013296.4 T544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:32159542 G>A maps to NM_022107.1 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr6:32159177 C>A maps to NM_022107.1 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr16:46943702 C>T maps to NM_133443.2 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:46952657 C>T maps to NM_133443.2 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:46943651 C>T maps to NM_133443.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:46956279 C>T maps to NM_133443.2 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:49395099 G>A maps to NM_000581.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:150407675 G>A maps to NM_002084.3 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr6:28501835 C>T maps to NM_001509.2 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr6:28500096 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr6:28501820 G>A maps to NM_001509.2 W181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:28501754 C>T maps to NM_001509.2 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr6:28501835 C>T maps to NM_001509.2 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr6:28500197 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:28497334 C>T maps to NM_001509.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr6:28501814 C>T maps to NM_001509.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:28501787 C>T maps to NM_001509.2 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:28483436 C>T maps to NM_182701.1 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr6:28472260 C>T maps to NM_182701.1 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:28472175 G>A maps to NM_182701.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:28474201 C>T maps to NM_182701.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:28472260 C>T maps to NM_182701.1 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:28483478 G>A maps to NM_182701.1 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr6:28483505 G>A maps to NM_182701.1 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:28473542 G>A maps to NM_182701.1 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:28483514 G>A maps to NM_182701.1 F2F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr6:28472260 C>T maps to NM_182701.1 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr6:28483478 G>A maps to NM_182701.1 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr6:28473485 G>A maps to NM_182701.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr6:28483486 G>A maps to NM_182701.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr6:28473579 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:28472175 G>A maps to NM_182701.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr6:28472192 C>T maps to NM_182701.1 W181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZG-06A-11D-A197-08 chr1:53072381 C>T maps to NM_015696.4 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:53072486 C>T maps to NM_015696.4 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:35510182 C>T maps to NM_020895.3 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:35502382 C>T maps to NM_020895.3 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:35514220 C>T maps to NM_020895.3 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr11:123484181 G>A maps to ENST00000456860 T545T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr11:123484349 G>A maps to ENST00000456860 R601R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:123484268 C>T maps to ENST00000456860 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:123484286 C>T maps to ENST00000456860 V580V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr3:113658822 C>T maps to NM_017577.4 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:113658823 C>T maps to NM_017577.4 Q595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr3:113634686 T>C did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr15:72459430 C>T maps to NM_001012642.2 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr15:72455734 C>T maps to NM_001012642.2 K276K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:72455779 C>T maps to NM_001012642.2 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:125816167 C>T maps to NM_023927.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr5:125801180 C>T maps to NM_023927.2 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr22:47068738 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr22:47059986 C>T maps to NM_015124.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr22:47064587 C>T maps to NM_015124.2 N311N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:47062745 C>T maps to NM_015124.2 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:47071397 C>T maps to NM_015124.2 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:18927553 G>A maps to NM_006613.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr22:40356157 G>A maps to NM_004810.2 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:40367081 C>T maps to NM_004810.2 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:40351839 G>A maps to NM_004810.2 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:52408955 C>T maps to NM_181711.2 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr12:52408955 C>T maps to NM_181711.2 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr7:50682475 G>A maps to NM_005311.4 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:50685827 G>A maps to NM_005311.4 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr7:50680499 A>G maps to NM_005311.4 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:50671702 G>A maps to NM_005311.4 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:50682526 G>A maps to NM_005311.4 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr7:50737505 G>A maps to NM_005311.4 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:165353882 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:165404236 G>A maps to NM_004490.2 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:165476205 C>T maps to NM_004490.2 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:165383592 C>T maps to NM_004490.2 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr2:165365353 C>T maps to NM_004490.2 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:165383592 C>T maps to NM_004490.2 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr2:165353892 G>A maps to NM_004490.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:165404204 C>T maps to NM_004490.2 W149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:73317850 G>A maps to NM_002086.4 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:37899716 C>T maps to ENST00000445327 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr17:37898851 C>T maps to ENST00000445327 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr17:37898851 C>T maps to ENST00000445327 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:37903011 G>A maps to ENST00000445327 E510E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:37898920 C>T maps to ENST00000445327 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:37898851 C>T maps to ENST00000445327 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr17:37898595 G>A maps to ENST00000445327 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:37901700 G>A maps to ENST00000445327 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:37898851 C>T maps to ENST00000445327 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr17:37899505 C>T maps to ENST00000445327 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:37899206 T>A maps to ENST00000445327 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr17:37899514 G>A maps to ENST00000445327 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr17:37902190 C>T maps to ENST00000445327 F455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:11733175 G>A maps to NM_014668.3 K540K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:11716605 C>T maps to NM_014668.3 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:11770144 C>T maps to NM_014668.3 F1507F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:11758669 C>T maps to NM_014668.3 S1223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:11742593 C>T maps to NM_014668.3 T864T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:11773063 C>T maps to NM_014668.3 L1622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:11750945 G>A maps to NM_014668.3 Q933Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:11773138 C>T maps to NM_014668.3 S1647S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:11775491 C>T maps to NM_014668.3 I1769I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:11706630 G>A maps to NM_014668.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr2:11761041 A>G maps to NM_014668.3 T1352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:11702694 C>T maps to NM_014668.3 C88C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:11706748 T>C maps to NM_014668.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:11718522 G>A maps to NM_014668.3 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:11758699 G>A maps to NM_014668.3 V1233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr2:11758600 C>T maps to NM_014668.3 P1200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:11733241 C>T maps to NM_014668.3 I562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:33022968 G>A maps to NM_013372.6 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr1:240656511 C>T maps to NM_022469.3 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr1:240656376 C>T maps to NM_022469.3 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:240656346 G>A maps to NM_022469.3 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:240656744 G>A maps to NM_022469.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr2:10101264 C>T maps to NM_198182.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:10105479 C>T maps to NM_198182.2 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:10136027 G>A maps to NM_198182.2 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:10104168 C>T maps to NM_198182.2 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:10132198 C>T maps to NM_198182.2 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr2:10105487 G>A maps to NM_198182.2 W363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr8:102570757 G>A maps to NM_024915.3 E132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr8:102631909 G>A maps to NM_024915.3 K414K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:102678843 C>T maps to NM_024915.3 I597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr8:102611372 G>A maps to NM_024915.3 E364E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:102644467 T>C maps to NM_024915.3 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:102555576 C>T maps to NM_024915.3 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr8:102589724 G>A maps to NM_024915.3 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr8:102570808 C>T maps to NM_024915.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:102589724 G>A maps to NM_024915.3 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:102611375 G>A maps to NM_024915.3 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr8:102643863 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:102582565 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr1:24668747 G>A maps to NM_021180.3 K402K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr1:24662998 G>A maps to NM_021180.3 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:24663620 G>A maps to NM_021180.3 E227E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:24658071 G>A maps to NM_021180.3 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:24674031 C>T maps to NM_021180.3 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:37424931 C>T maps to ENST00000377824 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr5:153085396 C>T maps to NM_001114183.1 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr5:153149861 G>A maps to NM_001114183.1 E719E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:153181965 C>T maps to NM_001114183.1 I812I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr5:153149864 C>T maps to NM_001114183.1 S720S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:153029986 G>A maps to NM_001114183.1 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr5:153144011 C>T maps to NM_001114183.1 I614I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:153181971 C>T maps to NM_001114183.1 I814I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr5:153029899 C>T maps to NM_001114183.1 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr5:153174179 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr5:153054109 G>A maps to NM_001114183.1 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:153149813 G>A maps to NM_001114183.1 G703G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr5:153174179 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr5:153190622 C>T maps to NM_001114183.1 A853A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr5:153056645 G>A maps to NM_001114183.1 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr5:153054091 G>A maps to NM_001114183.1 K244K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr5:153077629 G>A maps to NM_001114183.1 K387K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:153026563 C>T maps to NM_001114183.1 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:153035404 C>T maps to NM_001114183.1 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:153085342 G>A maps to NM_001114183.1 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:153078449 G>A maps to NM_001114183.1 K423K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr5:153190640 C>T maps to NM_001114183.1 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr5:153085288 C>T maps to NM_001114183.1 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr5:153085390 C>T maps to NM_001114183.1 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:153030055 C>T maps to NM_001114183.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:153026599 G>A maps to NM_001114183.1 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:153054169 G>A maps to NM_001114183.1 W270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:153149828 G>A maps to NM_001114183.1 R708R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:153149856 C>T maps to NM_001114183.1 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:153190712 C>T maps to NM_001114183.1 F883F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:153190595 G>A maps to NM_001114183.1 L844L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:153190673 C>T maps to NM_001114183.1 G870G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:152873488 G>A maps to NM_001114183.1 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:153190775 G>A maps to NM_001114183.1 T904T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr5:153056654 G>A maps to NM_001114183.1 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr4:158242726 T>A maps to NM_000826.3 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr4:158234027 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr4:158284072 G>A maps to NM_000826.3 A843A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr4:158238850 C>T maps to NM_000826.3 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr4:158257857 C>T maps to NM_000826.3 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr4:158281184 C>T maps to NM_000826.3 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr4:158254053 C>T maps to NM_000826.3 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:158262475 C>T maps to NM_000826.3 S635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr4:158256914 C>T maps to NM_000826.3 I453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:158254080 G>C maps to NM_000826.3 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr4:158257614 G>A maps to NM_000826.3 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:158224907 G>A maps to NM_000826.3 W145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr4:158224908 G>A maps to NM_000826.3 W145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:158256914 C>T maps to NM_000826.3 I453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr4:158242619 C>T maps to NM_000826.3 Q251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:158242618 C>T maps to NM_000826.3 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr4:158254128 C>T maps to NM_000826.3 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr4:158254005 G>A maps to NM_000826.3 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:122538600 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3CE-06A-11D-A19A-08 chr23:122551411 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr23:122538698 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:122319726 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr23:122613937 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:122528858 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:122387390 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:122459948 G>A did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:122551546 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:122598945 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:122459932 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:122459933 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:122551516 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:122551444 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr23:122459948 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr23:122538613 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr23:122387390 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:122538604 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:122551350 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:122318471 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:122459973 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:122318443 C>A did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:122538686 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:122551580 G>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:122598808 C>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr23:122599573 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:122538604 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:122387214 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:122532571 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:122536927 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:122551356 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:122551489 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:122459895 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:122459986 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:122551294 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:122561842 C>T did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:122387350 T>A did not map to a codon.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr11:105782606 G>A maps to NM_001112812.1 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr11:105797559 G>A maps to NM_000829.3 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr11:105483099 T>C maps to NM_000829.3 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:105775925 C>T maps to NM_000829.3 R353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:105845059 G>A maps to NM_000829.3 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:105842676 G>A maps to NM_000829.3 E777E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:105789610 C>T maps to NM_000829.3 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr11:105623842 C>T maps to NM_000829.3 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr11:105623910 G>A maps to NM_000829.3 W151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:105769153 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr10:88123743 G>A maps to NM_017551.2 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr10:87898617 G>A maps to NM_017551.2 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr10:87487641 C>T maps to NM_017551.2 W501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:87484277 G>A maps to NM_017551.2 F563F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr10:87614357 G>A maps to NM_017551.2 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:87628829 C>T maps to NM_017551.2 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:87484310 G>A maps to NM_017551.2 I552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:87362268 G>A maps to NM_017551.2 L931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr10:88123842 G>A maps to NM_017551.2 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:87487689 G>A maps to NM_017551.2 Y485Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:87489365 C>T maps to NM_017551.2 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:87373163 C>T maps to NM_017551.2 E867E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr10:87487650 G>A maps to NM_017551.2 N498N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr10:87482860 G>A maps to NM_017551.2 I632I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr10:87628916 G>A maps to NM_017551.2 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr10:87966199 G>A maps to NM_017551.2 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:87362035 G>A maps to NM_017551.2 S1008S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:87373166 C>T maps to NM_017551.2 K866K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:87373271 G>A maps to NM_017551.2 F831F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:87487746 G>A maps to NM_017551.2 F466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:87487803 C>T maps to NM_017551.2 E447E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:87615821 C>T maps to NM_017551.2 W359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:87966145 G>A maps to NM_017551.2 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:88123743 G>A maps to NM_017551.2 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr10:87373169 G>A maps to NM_017551.2 P865P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr4:94138037 G>A maps to NM_001510.2 K313K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr4:94411886 C>T maps to NM_001510.2 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr4:94411886 C>T maps to NM_001510.2 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr4:94693337 C>T maps to NM_001510.2 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr4:94006284 G>A maps to NM_001510.2 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr4:94032085 C>A maps to NM_001510.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr4:94137896 C>T maps to NM_001510.2 N266N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:94137944 G>A maps to NM_001510.2 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr4:94128559 G>A maps to NM_001510.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr4:94006368 C>T maps to NM_001510.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:94436522 G>A maps to NM_001510.2 S718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:93225818 C>T maps to NM_001510.2 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr4:94377027 G>A maps to NM_001510.2 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:94690534 C>T maps to NM_001510.2 S845S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr4:94137944 G>A maps to NM_001510.2 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:94128595 C>T maps to NM_001510.2 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr4:94032104 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr4:94411793 G>A maps to NM_001510.2 G621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr4:94316859 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr4:94032038 C>T maps to NM_001510.2 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr4:94128595 C>T maps to NM_001510.2 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:93225884 C>T maps to NM_001510.2 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:94032058 G>A maps to NM_001510.2 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:94145922 G>A maps to NM_001510.2 K374K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:94316838 C>T maps to NM_001510.2 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:94006275 G>A maps to NM_001510.2 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr21:30961251 G>A maps to ENST00000327783 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr21:30934106 G>A maps to ENST00000327783 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr21:30971200 C>T maps to ENST00000327783 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr21:31027129 C>T maps to ENST00000327783 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr21:30926025 C>T did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr21:31023497 G>A maps to ENST00000327783 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr6:102307215 C>T maps to NM_021956.4 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:102307301 G>A maps to NM_021956.4 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:102307251 T>C maps to NM_021956.4 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:102516256 G>A maps to NM_021956.4 R866R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:101847167 C>T maps to NM_021956.4 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:102503253 G>A maps to NM_021956.4 E787E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr6:102307301 G>A maps to NM_021956.4 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr6:102134191 G>A maps to NM_021956.4 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr6:102247615 C>T maps to NM_021956.4 R349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:102337513 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:102124582 G>A maps to NM_021956.4 K209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr1:37267466 G>A maps to NM_000831.3 A915A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr1:37356551 G>A maps to NM_000831.3 H87H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:37307453 C>T maps to NM_000831.3 K471K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr1:37267568 C>T maps to NM_000831.3 Q881Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:37267466 G>A maps to NM_000831.3 A915A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:37270689 G>A maps to NM_000831.3 I821I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:37335350 G>A maps to NM_000831.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:37356631 G>A maps to NM_000831.3 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:37270689 G>A maps to NM_000831.3 I821I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr1:37356686 G>A maps to NM_000831.3 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:37270689 G>A maps to NM_000831.3 I821I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:37267466 G>A maps to NM_000831.3 A915A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:37270689 G>A maps to NM_000831.3 I821I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:37346269 C>T maps to NM_000831.3 W172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:37307390 C>T maps to NM_000831.3 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:37307486 G>A maps to NM_000831.3 D460D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:37346334 C>T maps to NM_000831.3 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:37356578 G>A maps to NM_000831.3 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:37282711 G>A maps to NM_000831.3 T680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr1:37282687 C>T maps to NM_000831.3 K688K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:37271918 C>T maps to NM_000831.3 K700K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:37282782 G>A maps to NM_000831.3 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:37324717 G>A maps to NM_000831.3 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:37346322 G>A maps to NM_000831.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:37307480 G>A maps to NM_000831.3 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:37270697 G>A maps to NM_000831.3 Q819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:37285335 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr11:120745846 G>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:120702606 G>A maps to NM_014619.2 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:120702666 G>A maps to NM_014619.2 E206E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:120856866 C>G maps to NM_014619.2 P923P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:120833373 G>A maps to NM_014619.2 G750G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:120745930 C>T maps to NM_014619.2 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:120702594 C>T maps to NM_014619.2 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:120852904 G>A maps to NM_014619.2 W829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr11:120776099 C>T maps to NM_014619.2 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:120690525 C>T maps to NM_014619.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:120702687 C>T maps to NM_014619.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:120707540 C>T maps to NM_014619.2 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr19:42507519 G>A maps to NM_002088.3 F826F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr19:42507570 G>A maps to NM_002088.3 I809I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:42566781 G>A maps to NM_002088.3 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:42558546 G>A maps to NM_002088.3 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr19:42563644 G>A maps to NM_002088.3 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:42546859 C>T maps to NM_002088.3 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:140058062 C>T maps to ENST00000371546 Q817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr9:140040182 C>T maps to ENST00000371546 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr9:140058346 G>A maps to ENST00000371546 K881K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:140034154 C>T maps to ENST00000371546 Q73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr9:140058343 G>A maps to ENST00000371546 R880R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:140043561 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr9:140057148 G>A maps to ENST00000371546 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr16:9892224 G>A maps to NM_000833.3 I755I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr16:10032354 C>T maps to NM_000833.3 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr16:9857656 G>A maps to NM_000833.3 I1248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr16:9858415 C>T maps to NM_000833.3 T995T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr16:9858084 G>A maps to NM_000833.3 L1106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr16:9858265 G>A maps to NM_000833.3 S1045S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:10274118 T>C maps to NM_000833.3 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:10274181 C>T maps to NM_000833.3 K29K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr16:9892321 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr16:9858628 G>A maps to NM_000833.3 F924F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:10274187 C>T maps to NM_000833.3 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr16:9858298 C>T maps to NM_000833.3 R1034R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr16:10031958 C>T maps to NM_000833.3 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr16:10273905 G>A maps to NM_000833.3 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr16:9857974 G>A maps to NM_000833.3 P1142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:9857461 G>A maps to NM_000833.3 L1313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:9857974 G>A maps to NM_000833.3 P1142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:9858382 C>T maps to NM_000833.3 A1006A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr16:10273952 G>A maps to NM_000833.3 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr16:9858427 G>A maps to NM_000833.3 S991S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr16:9858586 C>T maps to NM_000833.3 K938K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:9857185 C>T maps to NM_000833.3 L1405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:9857581 C>T maps to NM_000833.3 Q1273Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:9892320 C>T maps to NM_000833.3 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr16:9858709 G>A maps to NM_000833.3 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr16:9857521 A>G maps to NM_000833.3 D1293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr16:9857611 C>T maps to NM_000833.3 G1263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:9916247 G>A maps to NM_000833.3 R681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr16:9857020 G>A maps to NM_000833.3 I1460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:10032273 G>A maps to NM_000833.3 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:9858355 C>T maps to NM_000833.3 K1015K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:9858625 G>A maps to NM_000833.3 I925I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr16:9858382 C>T maps to NM_000833.3 A1006A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr16:10032213 C>T maps to NM_000833.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:10032312 G>A maps to NM_000833.3 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:9858741 G>A maps to NM_000833.3 L887L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:9923455 G>A maps to NM_000833.3 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr16:10032372 G>A maps to NM_000833.3 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr16:9857368 G>A maps to NM_000833.3 F1344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:9857545 C>T maps to NM_000833.3 R1285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr16:9857545 C>T maps to NM_000833.3 R1285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr16:9857386 C>T maps to NM_000833.3 G1338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:10032213 C>T maps to NM_000833.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:9857299 G>A maps to NM_000833.3 F1367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:9857959 G>A maps to NM_000833.3 F1147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:9943662 G>A maps to NM_000833.3 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr16:9862743 G>A maps to NM_000833.3 C853C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr16:9858799 G>T maps to NM_000833.3 I867I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr16:9862774 C>T maps to NM_000833.3 W843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr16:10032408 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:9892236 C>T maps to NM_000833.3 G751G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:10273995 G>A maps to NM_000833.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:9857824 G>A maps to NM_000833.3 T1192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:9857926 G>A maps to NM_000833.3 F1158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:9857959 G>A maps to NM_000833.3 F1147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:9858067 G>A maps to NM_000833.3 S1111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:9858355 C>T maps to NM_000833.3 K1015K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:9858499 C>T maps to NM_000833.3 V967V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:9934827 T>A maps to NM_000833.3 K488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:9943623 G>A maps to NM_000833.3 F439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr16:9857635 C>T maps to NM_000833.3 Q1255Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr16:10274088 C>T maps to NM_000833.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr16:9857491 G>A maps to NM_000833.3 D1303D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:10273905 G>A maps to NM_000833.3 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:10273905 G>A maps to NM_000833.3 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr16:10273956 C>T maps to NM_000833.3 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr16:9857845 T>C maps to NM_000833.3 K1185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr12:13761656 G>A maps to NM_000834.3 I630I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:13716247 C>T maps to NM_000834.3 V1308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:14018773 G>A maps to NM_000834.3 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr12:13715746 C>T maps to NM_000834.3 E1475E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr12:13716382 C>T maps to NM_000834.3 L1263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr12:13716007 G>A maps to NM_000834.3 I1388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr12:13906489 G>A maps to NM_000834.3 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr12:13715824 C>T maps to NM_000834.3 G1449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:13720141 C>T maps to NM_000834.3 K805K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:13761719 G>A maps to NM_000834.3 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:13828696 C>T maps to NM_000834.3 K369K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr12:13724871 G>A maps to NM_000834.3 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr12:13716186 G>A maps to NM_000834.3 R1329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr12:13769423 C>T maps to NM_000834.3 R431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr12:13717348 G>A maps to NM_000834.3 F941F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:13717312 G>A maps to NM_000834.3 P953P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:13761581 G>A maps to NM_000834.3 I655I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:13828690 C>T maps to NM_000834.3 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:14018772 G>A maps to NM_000834.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr12:13720054 G>A maps to NM_000834.3 I834I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr12:13906747 G>A maps to NM_000834.3 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:13716343 G>A maps to NM_000834.3 A1276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:13717003 G>A maps to NM_000834.3 I1056I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:13724781 G>A maps to NM_000834.3 F709F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:13761587 G>A maps to NM_000834.3 F653F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:13761665 G>A maps to NM_000834.3 T627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:13716751 C>T maps to NM_000834.3 K1140K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:13828762 C>T maps to NM_000834.3 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:13717042 G>A maps to NM_000834.3 S1043S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr12:13716760 G>A maps to NM_000834.3 F1137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr12:14018854 C>T maps to NM_000834.3 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:13715851 G>A maps to NM_000834.3 A1440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:13716964 G>A maps to NM_000834.3 T1069T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr12:13906477 C>T maps to NM_000834.3 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr12:13715833 G>A maps to NM_000834.3 I1446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZY-06A-11D-A197-08 chr12:13761662 G>A maps to NM_000834.3 S628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:13716550 C>T maps to NM_000834.3 E1207E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:13720096 C>T maps to NM_000834.3 G820G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:13764671 G>A maps to NM_000834.3 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:13716622 C>G maps to NM_000834.3 T1183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr12:13906732 G>A maps to NM_000834.3 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr12:13906828 G>A maps to NM_000834.3 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr12:13768456 G>A maps to NM_000834.3 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:13906489 G>A maps to NM_000834.3 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr17:72846774 G>A maps to NM_000835.3 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:72848612 C>T maps to NM_000835.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:48925100 C>T maps to NM_000836.2 S717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:48908343 C>T maps to NM_000836.2 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:48922857 C>T maps to NM_000836.2 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:48918288 G>A maps to NM_000836.2 E527E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:48908544 C>T maps to NM_000836.2 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr9:104499592 G>A maps to NM_133445.2 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr9:104449344 G>A maps to NM_133445.2 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr9:104340057 C>A maps to NM_133445.2 V1000V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr9:104432833 G>A maps to NM_133445.2 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr9:104432854 C>T maps to NM_133445.2 W613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:104432869 C>T maps to NM_133445.2 W608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:104448900 G>A maps to NM_133445.2 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr9:104432571 G>A maps to NM_133445.2 R708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr9:104432660 C>T maps to NM_133445.2 W678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr9:104340090 C>T maps to NM_133445.2 E989E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr9:104433232 T>C maps to NM_133445.2 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:104499743 C>T maps to NM_133445.2 W173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:104449251 G>A maps to NM_133445.2 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr9:104432908 G>A maps to NM_133445.2 F595F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:104432603 C>T maps to NM_133445.2 W697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr9:104432833 G>A maps to NM_133445.2 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:104432632 G>A maps to NM_133445.2 I687I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr9:104433260 C>T maps to NM_133445.2 W478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:104432377 C>T maps to NM_133445.2 K772K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:104433277 G>A maps to NM_133445.2 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr9:104449482 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr9:104375732 A>G maps to NM_133445.2 H897H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr9:104432779 C>T maps to NM_133445.2 R638R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr9:104432869 C>T maps to NM_133445.2 W608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:104433088 G>A maps to NM_133445.2 G535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:104449241 G>A maps to NM_133445.2 Q314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr9:104449254 G>A maps to NM_133445.2 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr9:104433301 G>A maps to NM_133445.2 F464F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:1005326 C>T maps to NM_138690.1 N609N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:1005143 C>T maps to NM_138690.1 F548F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:1005272 C>T maps to NM_138690.1 F591F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr8:145065396 C>T maps to NM_001009184.1 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:145065531 C>T maps to NM_001009184.1 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:145066417 C>T maps to NM_001009184.1 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:66765503 G>A maps to ENST00000359742 I994I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:66838418 G>A maps to ENST00000359742 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr12:66923613 G>A maps to ENST00000359742 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr12:66838421 G>A maps to ENST00000359742 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:66765698 G>A maps to ENST00000359742 I929I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:66771022 C>T maps to ENST00000359742 E888E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr12:66932939 G>A maps to ENST00000359742 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:14536359 C>T maps to ENST00000507975 R1085R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr3:14565999 C>T maps to ENST00000507975 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr3:14559292 C>T maps to ENST00000507975 Q479Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:14554360 G>A maps to ENST00000507975 S646S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:14549102 C>T maps to ENST00000507975 E826E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:14535313 C>T maps to ENST00000507975 R1095R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr3:14548330 G>A maps to ENST00000507975 T890T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:14565185 C>T maps to ENST00000507975 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr23:48840276 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:48839662 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:48847416 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:48847121 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZG-06A-11D-A197-08 chr23:48847415 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr13:114322261 G>A maps to NM_002929.2 E187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr13:114322063 C>T maps to NM_002929.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr13:114324051 C>T maps to NM_002929.2 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr13:114322231 G>A maps to NM_002929.2 W177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr13:114322096 G>A maps to NM_002929.2 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr13:114322123 C>A maps to NM_002929.2 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr13:114322078 G>A maps to NM_002929.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr4:3029657 C>T maps to NM_182982.2 D330D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr4:3040188 C>T maps to NM_182982.2 T544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:3015491 G>A maps to NM_182982.2 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:3037240 C>T maps to NM_182982.2 F466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:121182769 C>T maps to NM_005308.2 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr10:121203197 G>A maps to NM_005308.2 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:121189920 C>T maps to NM_005308.2 R190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr5:176860631 G>A maps to NM_002082.3 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:176859235 C>T maps to NM_002082.3 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr5:176863137 C>T maps to NM_002082.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr5:176860177 T>C maps to NM_002082.3 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:141497383 C>T maps to NM_139209.2 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:141499436 C>T maps to NM_139209.2 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:141499481 G>A maps to NM_139209.2 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr3:141497383 C>T maps to NM_139209.2 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr3:141535597 G>A maps to NM_139209.2 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr3:141497623 C>T maps to NM_139209.2 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:141499397 C>T maps to NM_139209.2 C265C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:141535597 G>A maps to NM_139209.2 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:141497485 G>A maps to NM_139209.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:141499572 C>T maps to NM_139209.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:47423617 C>A maps to NM_004491.4 C562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:47422256 C>T maps to NM_004491.4 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:47422231 T>A maps to NM_004491.4 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:47422256 C>T maps to NM_004491.4 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:47423266 C>T maps to NM_004491.4 F445F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:47422099 C>T maps to NM_004491.4 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr6:146625857 C>T maps to NM_000838.3 F354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr6:146678763 C>T maps to NM_000838.3 I512I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:146755484 G>A maps to NM_000838.3 P1046P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr6:146480484 G>A maps to NM_000838.3 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:146720091 C>T maps to NM_000838.3 F639F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr6:146351186 C>T maps to NM_000838.3 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:146673563 C>T maps to NM_000838.3 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr6:146720091 C>T maps to NM_000838.3 F639F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:146720175 C>T maps to NM_000838.3 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:146720076 C>T maps to NM_000838.3 I634I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:146708078 G>A maps to NM_000838.3 E552E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:146351222 C>T maps to NM_000838.3 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr3:51751696 C>T maps to NM_000839.3 S803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr3:51747198 C>T maps to NM_000839.3 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:51743181 C>T maps to NM_000839.3 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:51749973 T>C maps to NM_000839.3 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:51747030 C>T maps to NM_000839.3 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:51749228 G>A maps to NM_000839.3 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr3:51747030 C>T maps to NM_000839.3 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:51743020 C>T maps to NM_000839.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:51749297 C>T maps to NM_000839.3 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:51749831 C>T maps to NM_000839.3 A681A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:51749248 G>A maps to NM_000839.3 W487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:51747048 G>A maps to NM_000839.3 W337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:86468899 C>T maps to NM_000840.2 F690F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:86468464 C>T maps to NM_000840.2 T545T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:86468785 C>T maps to NM_000840.2 F652F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:86469068 C>T maps to NM_000840.2 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr7:86394511 G>A maps to NM_000840.2 K17K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr7:86493598 C>T maps to NM_000840.2 S856S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr7:86468875 C>T maps to NM_000840.2 F682F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr7:86415992 C>T maps to NM_000840.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr7:86394590 C>T maps to NM_000840.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr7:86415830 C>T maps to NM_000840.2 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr7:86394655 G>A maps to NM_000840.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:86415920 C>T maps to NM_000840.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:86468680 C>T maps to NM_000840.2 I617I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:86469046 C>T maps to NM_000840.2 I739I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:86479780 A>G maps to NM_000840.2 Q829Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr7:86468912 C>T maps to NM_000840.2 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:86415599 C>T maps to NM_000840.2 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr7:86416340 C>T maps to NM_000840.2 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:86394532 G>A maps to NM_000840.2 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:86415736 G>A maps to NM_000840.2 W210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:86468242 C>T maps to NM_000840.2 F471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:86415788 C>T maps to NM_000840.2 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:86394863 C>T maps to NM_000840.2 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:86479780 A>G maps to NM_000840.2 Q829Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr7:86416310 C>T maps to NM_000840.2 A401A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:86415779 G>A maps to NM_000840.2 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr7:86469139 C>T maps to NM_000840.2 F770F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:86394883 C>T maps to NM_000840.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F4-06A-12D-A25O-08 chr7:86416244 C>T maps to NM_000840.2 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:86415926 C>T maps to NM_000840.2 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:86415992 C>T maps to NM_000840.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:86416106 C>T maps to NM_000840.2 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:86416199 G>A maps to NM_000840.2 Q364Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:86416289 G>A maps to NM_000840.2 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:86493637 G>A maps to NM_000840.2 R869R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:86468416 G>A maps to NM_000840.2 W529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr7:86468434 A>G maps to NM_000840.2 E535E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr6:34101228 G>A maps to NM_000841.1 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr6:34008041 C>T maps to NM_000841.1 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:34026781 G>A maps to NM_000841.1 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:34004152 G>A maps to NM_000841.1 I578I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:34059807 G>A maps to NM_000841.1 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:34101213 G>A maps to NM_000841.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:34059747 G>A maps to NM_000841.1 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr6:34004035 G>A maps to NM_000841.1 I617I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:34101036 C>T maps to NM_000841.1 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:34003735 C>T maps to NM_000841.1 W717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:34003954 G>A maps to NM_000841.1 I644I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:34004284 C>T maps to NM_000841.1 K534K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:34026757 G>A maps to NM_000841.1 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr6:34059677 G>A maps to NM_000841.1 Q240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr6:34100928 G>A maps to NM_000841.1 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:34004267 C>T maps to NM_000841.1 W540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:88300257 G>A maps to NM_001143831.2 L865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr11:88780632 G>A maps to NM_001143831.2 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:88780833 C>T maps to NM_001143831.2 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:88780812 C>T maps to NM_001143831.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:88781022 G>A maps to NM_001143831.2 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:88780986 C>T maps to NM_001143831.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr11:88301125 C>T maps to NM_001143831.2 W575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:88241774 G>A maps to NM_001143831.2 S1208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:88300911 G>A maps to NM_001143831.2 Q647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:88583165 C>T maps to NM_001143831.2 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:88780704 G>A maps to NM_001143831.2 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:88780986 C>T maps to NM_001143831.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr5:178409973 G>A maps to NM_000843.3 T791T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr5:178418925 G>T maps to NM_000843.3 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:178418522 C>T maps to NM_000843.3 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr5:178417596 G>A maps to NM_000843.3 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr5:178413415 C>T maps to NM_000843.3 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:178419000 G>A maps to NM_000843.3 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:178413172 G>T maps to NM_000843.3 P694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr5:178413289 G>A maps to NM_000843.3 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr5:178418560 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:178418979 G>A maps to NM_000843.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:178419000 G>A maps to NM_000843.3 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr5:178417599 G>A maps to NM_000843.3 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:178413574 C>T maps to NM_000843.3 G560G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:178413136 G>A maps to NM_000843.3 S706S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr5:178413397 C>G maps to NM_000843.3 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:178409937 G>A maps to NM_000843.3 F803F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:178410063 G>A maps to NM_000843.3 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:178410186 G>A maps to NM_000843.3 P720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:178413679 C>T maps to NM_000843.3 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:178416044 G>A maps to NM_000843.3 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:178416278 G>A maps to NM_000843.3 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:178416281 G>A maps to NM_000843.3 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:178417659 G>A maps to NM_000843.3 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:178418885 G>A maps to NM_000843.3 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr5:178417616 G>A maps to NM_000843.3 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:178413358 G>A maps to NM_000843.3 F632F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:7456806 G>A maps to NM_181874.2 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:7620407 C>T maps to NM_181874.2 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:7340485 G>A maps to NM_181874.2 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr3:7620707 C>T maps to NM_181874.2 I705I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr3:7348307 C>T maps to NM_181874.2 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:7188287 C>T maps to NM_181874.2 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:7620395 G>A maps to NM_181874.2 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:7340485 G>A maps to NM_181874.2 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:7494381 C>T maps to NM_181874.2 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr3:7721863 G>A maps to NM_181874.2 K860K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:7620608 C>T maps to NM_181874.2 A672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:7188329 C>T maps to NM_181874.2 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:7721851 C>T maps to NM_181874.2 V856V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:7494348 C>T maps to NM_181874.2 F410F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr3:7620515 C>T maps to NM_181874.2 I641I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:7620746 C>T maps to NM_181874.2 F718F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr3:7620137 C>T maps to NM_181874.2 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr3:7340473 C>T maps to NM_181874.2 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:7620191 G>A maps to NM_181874.2 K533K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr3:7620938 G>A maps to NM_181874.2 E782E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:7620650 G>A maps to NM_181874.2 Q686Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr3:7503288 G>A maps to NM_181874.2 V465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:7494351 G>A maps to NM_181874.2 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:7620980 G>A maps to NM_181874.2 T796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:7620124 G>A maps to NM_181874.2 W511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr3:7620137 C>T maps to NM_181874.2 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:7456763 G>A maps to NM_181874.2 W363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr3:7721803 A>C maps to NM_181874.2 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr3:7494456 G>A maps to NM_181874.2 K446K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:6903177 C>T maps to NM_181874.2 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:6903239 C>T maps to NM_181874.2 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:7340401 C>T maps to NM_181874.2 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:7620137 C>T maps to NM_181874.2 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:7620854 C>T maps to NM_181874.2 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:6903389 C>T maps to NM_181874.2 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:7494462 G>A maps to NM_181874.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:126173041 G>A maps to NM_001127323.1 I798I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr7:126544705 G>A maps to NM_001127323.1 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:126173629 G>A maps to NM_001127323.1 I602I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:126173341 G>T maps to NM_001127323.1 I698I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr7:126249547 A>G maps to NM_001127323.1 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:126173431 G>A maps to NM_001127323.1 T668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:126173158 C>T maps to NM_001127323.1 L759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:126542626 C>T maps to NM_001127323.1 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:126173044 G>A maps to NM_001127323.1 F797F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:126746567 G>A maps to NM_001127323.1 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:126173077 G>A maps to NM_001127323.1 T786T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:126882982 G>A maps to NM_001127323.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:126882982 G>A maps to NM_001127323.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr7:126173890 G>A maps to NM_001127323.1 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:126544638 G>A maps to NM_001127323.1 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:126883141 G>A maps to NM_001127323.1 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr7:126173044 G>A maps to NM_001127323.1 F797F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:126544085 G>A maps to NM_001127323.1 Q320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:126173059 G>A maps to NM_001127323.1 I792I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:126173755 C>T maps to NM_001127323.1 Q560Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr7:126173314 G>A maps to NM_001127323.1 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:126173164 G>A maps to NM_001127323.1 I757I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:126173368 G>A maps to NM_001127323.1 F689F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:126173530 G>A maps to NM_001127323.1 I635I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr7:126173551 C>T maps to NM_001127323.1 G628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:126882949 G>A maps to NM_001127323.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr7:126173395 C>T maps to NM_001127323.1 G680G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:126079217 G>A maps to NM_000845.2 S894S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:126173188 G>A maps to NM_001127323.1 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:126882787 G>A maps to NM_001127323.1 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:126086141 C>T maps to NM_001127323.1 G905G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:126173044 G>A maps to NM_001127323.1 F797F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr7:126882994 C>T maps to NM_001127323.1 K88K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr7:126173839 G>A maps to NM_001127323.1 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr17:42427698 C>T maps to NM_002087.2 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr17:42427919 C>T maps to NM_002087.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:42426861 C>T maps to NM_002087.2 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:42429911 G>A maps to NM_002087.2 Q539Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:42429827 C>T maps to NM_002087.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr17:42427594 G>A did not map to a codon.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr17:42429872 C>T maps to NM_002087.2 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr17:42428478 C>T maps to NM_002087.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr4:7062906 C>T maps to NM_025196.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:148730805 C>T maps to NM_152407.3 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:16170556 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:16170692 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:16170693 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr23:16142205 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:16170678 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:16142261 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:16170503 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:16170385 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:16168604 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:16170510 C>T did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:16168608 T>A did not map to a codon.
Sequencing variant TCGA-GN-A4U9-06A-11D-A32N-08 chr4:71691019 G>A maps to NM_002092.3 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z4-06A-11D-A197-08 chr13:114009758 G>A maps to NM_024719.2 H73H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr13:113999238 T>G maps to NM_024719.2 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:48956005 C>T maps to NM_031485.3 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:48955987 C>T maps to NM_031485.3 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:48953956 C>T maps to NM_031485.3 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:48953983 C>T maps to NM_031485.3 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:48956278 C>A maps to NM_031485.3 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:42895468 G>A maps to NM_001080476.2 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr4:43032467 C>T maps to NM_001080476.2 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr4:43032541 G>A maps to NM_001080476.2 K286K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:43032467 C>T maps to NM_001080476.2 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:42895294 G>A maps to NM_001080476.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:43032467 C>T maps to NM_001080476.2 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:42965091 C>T maps to NM_001080476.2 R190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr4:42964943 G>A maps to NM_001080476.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:145252193 A>G did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:145252311 G>A maps to NM_001080516.1 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr5:145246198 C>T maps to NM_001080516.1 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:145246230 G>A maps to NM_001080516.1 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:145252279 C>T maps to NM_001080516.1 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:145252309 C>T maps to NM_001080516.1 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr5:145252486 T>C maps to NM_001080516.1 K15K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr17:38133118 C>T maps to NM_178171.4 F382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:38126759 C>T maps to NM_178171.4 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:38121960 C>T maps to NM_178171.4 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:38133079 G>A maps to NM_178171.4 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:38130526 G>A maps to NM_178171.4 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr17:38122528 G>A maps to NM_178171.4 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:38126809 G>A maps to NM_178171.4 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:38121984 A>G maps to NM_178171.4 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr17:38122029 C>T maps to NM_178171.4 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr17:38131250 C>T maps to NM_178171.4 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr17:38122576 G>A maps to NM_178171.4 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr17:38063220 G>A maps to NM_001165958.1 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr17:38068631 G>A maps to NM_001165958.1 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr17:38065229 G>A maps to NM_001165958.1 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr17:38066100 G>A maps to NM_001165958.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr17:38062459 G>A maps to NM_001165958.1 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr17:38068654 G>A maps to NM_001165958.1 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:130761727 C>T maps to NM_031415.2 E419E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:130761733 G>A maps to NM_031415.2 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:130789735 A>C maps to NM_031415.2 L33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr8:130789638 G>A maps to NM_031415.2 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:130789706 T>A maps to NM_031415.2 K43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr8:130789650 G>A maps to NM_031415.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:130760938 G>A maps to NM_031415.2 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:130761733 G>A maps to NM_031415.2 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr8:130762251 G>A maps to NM_031415.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:130788430 C>T maps to NM_031415.2 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:130789653 G>A maps to NM_031415.2 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:130789704 C>T maps to NM_031415.2 K43K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:130777903 C>T maps to NM_031415.2 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:13243455 C>T maps to NM_001080555.1 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Z-06A-11D-A196-08 chr16:27974489 C>T maps to NM_001109763.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr16:27856320 G>A maps to NM_001109763.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr16:27802768 C>T maps to NM_001109763.1 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:27895873 G>A maps to NM_001109763.1 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:3627553 C>T maps to NM_031965.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:3628185 C>T maps to NM_031965.2 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr3:119634958 C>T maps to NM_002093.3 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:119631641 G>A maps to NM_002093.3 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:119634958 C>T maps to NM_002093.3 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr3:119634982 G>A maps to NM_002093.3 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:124074639 C>T maps to NM_000177.4 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr9:124091551 C>T maps to NM_000177.4 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr16:11970008 G>A maps to NM_002094.3 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr16:11990493 G>A maps to NM_002094.3 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:51487253 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:51488234 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:51487843 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:51488323 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:51487586 C>T did not map to a codon.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr23:51488446 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr23:51486786 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:51486938 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:51487112 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr23:51488474 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:51487950 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:51487059 C>T did not map to a codon.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr23:51487451 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:30560631 G>A maps to NM_000637.3 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr8:30550506 C>T maps to NM_000637.3 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:30560721 G>A maps to NM_000637.3 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr8:30560739 G>A maps to NM_000637.3 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr20:33517322 G>A maps to NM_000178.2 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:33530421 G>A maps to NM_000178.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr20:33516754 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:52656670 C>T maps to NM_145740.3 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr6:52657656 C>T maps to NM_145740.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr6:52617666 G>A maps to NM_000846.4 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:52619769 G>A maps to NM_000846.4 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:52761660 C>T maps to NM_000847.4 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:52764806 T>A maps to NM_000847.4 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr6:52847503 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:52698974 C>T maps to NM_153699.1 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:52696654 G>A maps to NM_153699.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:52696663 C>T maps to NM_153699.1 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:52701056 C>T maps to NM_153699.1 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:106647956 A>G maps to NM_001031720.2 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr4:106640671 C>T maps to NM_001031720.2 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr4:106766629 C>T maps to NM_001031720.2 R600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr4:106755697 C>T maps to NM_001031720.2 C537C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr4:106755688 C>T maps to NM_001031720.2 F534F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr4:106640680 C>T maps to NM_001031720.2 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:142960653 C>T maps to NM_001143679.1 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr1:110217382 C>T maps to ENST00000369830 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr1:110217427 C>T maps to ENST00000369830 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:110282107 G>A maps to NM_000849.4 D44D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:110280149 G>A maps to NM_000849.4 Q170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:110257570 G>A maps to ENST00000369812 E140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:110255295 G>A maps to ENST00000369812 K31K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:67353864 C>T maps to NM_000852.3 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:67353921 C>T maps to NM_000852.3 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr22:24379450 C>T maps to NM_000853.2 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr22:24376533 C>T maps to NM_000853.2 E204E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr22:24323178 G>A maps to NM_000854.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:77791233 C>T maps to NM_145870.2 R13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:77795494 G>A maps to NM_145870.2 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr4:54968052 C>T maps to NM_133267.2 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr4:54966536 C>A maps to NM_133267.2 S9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:54968082 C>T maps to NM_133267.2 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:54967894 C>T maps to NM_133267.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:54967869 G>A maps to NM_133267.2 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:54966672 G>A maps to NM_133267.2 K54K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr4:54967818 G>A maps to NM_133267.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr2:48906502 C>T maps to NM_172311.2 F1157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr2:48873958 G>A maps to NM_172311.2 Q956Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:48869596 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:48873631 G>A maps to NM_172311.2 E847E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:48898788 G>A maps to NM_172311.2 T1137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr2:48898777 C>T maps to NM_172311.2 L1134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:48873823 G>A maps to NM_172311.2 R911R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr2:48873823 G>A maps to NM_172311.2 R911R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:89325690 G>A maps to NM_001514.5 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:89329675 G>T maps to NM_001514.5 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:120495419 C>T maps to NM_005513.2 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr8:30511064 A>T maps to NM_002095.4 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:30469913 G>A maps to NM_002095.4 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:30469914 G>A maps to NM_002095.4 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr8:30469830 G>A maps to NM_002095.4 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:6389648 C>T did not map to a codon.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr19:6387446 G>A maps to NM_002096.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:6387512 G>A maps to NM_002096.2 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr19:6380618 G>A maps to NM_002096.2 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:124123844 T>C maps to NM_001516.3 D16D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:124139514 C>T maps to NM_001516.3 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:30879242 C>T maps to NM_001517.4 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:30877807 C>T maps to NM_001517.4 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:158613179 C>T maps to NM_207118.2 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:74159268 C>T maps to NM_032999.2 F641F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:74159268 C>T maps to NM_032999.2 F641F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr7:74114634 C>T maps to NM_032999.2 D144D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:74159268 C>T maps to NM_032999.2 F641F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:74146889 T>A maps to NM_032999.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:73938416 C>T maps to NM_016328.2 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:73933882 C>T maps to NM_016328.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr7:73933934 C>T maps to NM_016328.2 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:73973311 C>T maps to NM_016328.2 F758F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:73932634 C>T maps to NM_016328.2 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:73922529 C>T maps to NM_016328.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr7:74004222 G>A maps to NM_016328.2 R803R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:73944175 C>T maps to NM_016328.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:73927254 C>T maps to NM_016328.2 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr7:73944160 C>T maps to NM_016328.2 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr7:73933933 C>T maps to NM_016328.2 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr7:73933882 C>T maps to NM_016328.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr7:73961559 C>T maps to NM_016328.2 I620I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr7:73961532 C>T maps to NM_016328.2 S611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:74005166 C>T maps to NM_016328.2 G819G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr7:73944208 C>T maps to NM_016328.2 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr7:74211426 G>A maps to NM_173537.2 T808T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:74212451 G>A maps to NM_173537.2 Q467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:74211372 G>A maps to NM_173537.2 I826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr16:27499674 C>T maps to NM_001520.3 W1191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:27523103 G>A maps to NM_001520.3 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:27506538 C>T maps to NM_001520.3 T875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:27483214 C>T maps to NM_001520.3 K1460K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr16:27506733 G>A maps to NM_001520.3 L810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:27476019 G>A maps to NM_001520.3 D1831D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:27475727 G>A maps to NM_001520.3 Q1929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:27503758 G>A maps to NM_001520.3 S1017S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:27556756 G>A maps to NM_001520.3 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:27475767 A>G maps to NM_001520.3 A1915A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr16:27549502 G>A maps to NM_001520.3 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr16:27499545 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr16:27487824 G>A maps to NM_001520.3 Q1434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:27549247 C>T maps to NM_001520.3 K203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr16:27506149 G>A maps to NM_001520.3 L904L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr16:27476015 G>A maps to NM_001520.3 Q1833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:27476004 G>A maps to NM_001520.3 P1836P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:27481568 G>A maps to NM_001520.3 A1558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr16:27503769 G>A maps to NM_001520.3 L1014L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:27517294 G>T maps to NM_001520.3 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr16:27506676 C>T maps to NM_001520.3 R829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr2:27552142 G>A maps to NM_001521.2 F628F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:27558792 G>A maps to NM_001521.2 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:27550130 G>A maps to NM_001521.2 L810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:27549688 G>T maps to NM_001521.2 I863I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:27551025 G>A maps to NM_001521.2 Q763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:197650230 G>A maps to NM_012086.2 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:197664272 G>A maps to NM_012086.2 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:197654647 G>A maps to NM_012086.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr9:135553440 C>T maps to NM_012204.2 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:135554172 C>T maps to NM_012204.2 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr9:135929309 C>T maps to NM_001122823.1 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr9:135919196 C>T maps to NM_001122823.1 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr9:135932206 G>A maps to NM_001122823.1 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:135919190 C>T maps to NM_001122823.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr22:39117757 T>C maps to NM_004286.4 N282N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr22:39123255 T>G maps to NM_004286.4 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr22:39122009 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr22:39122339 C>T maps to NM_004286.4 D432D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:39112740 C>T maps to NM_004286.4 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:90003661 C>T maps to NM_033107.3 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:89983813 C>T maps to NM_033107.3 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr6:43592392 G>A maps to NM_019096.3 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:43589865 G>A maps to NM_019096.3 I502I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:43591731 G>A maps to NM_019096.3 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr6:43593276 G>A maps to NM_019096.3 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:17452352 T>C maps to NM_133644.3 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:17448978 C>T maps to NM_133644.3 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:17449364 C>T maps to NM_133644.3 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:17452295 C>T maps to NM_133644.3 D453D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr10:1052981 C>T maps to NM_012341.2 R343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:1042120 C>T maps to NM_012341.2 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:1038575 C>T maps to NM_012341.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr20:60773898 C>T maps to NM_015666.3 H226H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr20:60775991 G>A maps to NM_015666.3 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr20:60768521 C>T maps to NM_015666.3 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:60775748 C>T maps to NM_015666.3 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr20:60772926 C>T maps to NM_015666.3 S124S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A2M6-06A-12D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr22:46708186 C>T maps to NM_016426.6 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:46704371 C>T maps to NM_016426.6 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:42355046 G>A maps to NM_176791.3 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr20:42354941 C>T maps to NM_176791.3 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr20:42355244 C>T maps to NM_176791.3 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:42355238 C>T maps to NM_176791.3 K32K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr20:42354905 G>A maps to NM_176791.3 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr6:42152630 C>T maps to NM_002098.5 W175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr6:42162357 C>T maps to NM_002098.5 K67K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:42156424 G>A maps to NM_002098.5 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:42156424 G>A maps to NM_002098.5 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:108626883 C>T maps to NM_005459.3 K205K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:108627030 G>A maps to NM_005459.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr3:108672597 G>T maps to NM_005459.3 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr3:108672411 C>T maps to NM_005459.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr3:108627000 C>T maps to NM_005459.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:108672603 C>T maps to NM_005459.3 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:42628606 G>A maps to NM_033553.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:42621239 G>A maps to NM_007102.2 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr11:106810340 G>A maps to ENST00000282249 R351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr11:106810257 G>A maps to ENST00000282249 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:106849447 C>T maps to ENST00000282249 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:106558457 G>A maps to ENST00000282249 F703F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr11:106558295 G>A maps to ENST00000282249 F757F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:106810350 C>T maps to ENST00000282249 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr11:106810344 C>T maps to ENST00000282249 Q349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:106680916 G>A maps to ENST00000282249 F498F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:106810340 G>A maps to ENST00000282249 R351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr11:106810422 G>A maps to ENST00000282249 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr4:156618030 G>A maps to NM_001130684.1 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr4:156632309 C>T maps to NM_001130684.1 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr4:156634437 G>A maps to NM_001130684.1 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr4:156631964 C>T maps to NM_001130684.1 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:156651205 C>T maps to NM_001130684.1 F632F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:156618072 C>T maps to NM_001130684.1 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr4:156631872 G>T maps to NM_001130684.1 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr4:156634458 G>A maps to NM_001130684.1 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:156618033 G>A maps to NM_001130684.1 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:156629386 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:156634494 G>A maps to NM_001130684.1 E444E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:156651214 C>T maps to NM_001130684.1 T635T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr4:156651325 G>A maps to NM_001130684.1 K672K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr4:156715050 T>G maps to ENST00000502959 L202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:156716566 G>A maps to ENST00000502959 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:156711038 C>T maps to ENST00000502959 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:156698721 C>T maps to ENST00000502959 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr4:156726368 T>C maps to ENST00000502959 N630N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr12:14766224 C>T maps to NM_004963.3 V1016V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr12:14773997 C>T maps to NM_004963.3 W918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr12:14796583 G>A maps to NM_004963.3 T618T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:14829846 G>A maps to NM_004963.3 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:14813982 C>T maps to NM_004963.3 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr12:14794031 G>A maps to NM_004963.3 S684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:14827636 G>A maps to NM_004963.3 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr12:14766068 C>T maps to NM_004963.3 K1068K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:14781587 C>T maps to NM_004963.3 K747K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr12:14794067 C>T maps to NM_004963.3 E672E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:14813931 G>A maps to NM_004963.3 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:14796604 G>A maps to NM_004963.3 V611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr12:14849244 G>A maps to NM_004963.3 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr12:14778781 G>A maps to NM_004963.3 R773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:14804438 G>A maps to NM_004963.3 Q538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr12:14792858 G>A maps to NM_004963.3 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:14839147 C>A maps to NM_004963.3 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:14798249 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:14792867 C>T maps to NM_004963.3 V695V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:14778728 C>T maps to NM_004963.3 R790R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr12:14839147 C>T maps to NM_004963.3 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr12:14774138 G>A maps to NM_004963.3 I871I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr12:14804922 G>A maps to NM_004963.3 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:14766125 C>T maps to NM_004963.3 R1049R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:14792843 G>A maps to NM_004963.3 P703P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:14834374 G>A maps to NM_004963.3 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:14781641 C>T maps to NM_004963.3 E729E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:14834332 C>T maps to NM_004963.3 K230K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:7915541 C>T maps to NM_000180.3 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:7907224 C>T maps to NM_000180.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr17:7916451 G>A maps to NM_000180.3 R715R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:7910812 C>T maps to NM_000180.3 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:7907263 C>T maps to NM_000180.3 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:7916508 C>T maps to NM_000180.3 I734I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:7909859 C>T maps to NM_000180.3 F402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr17:7915820 G>A maps to NM_000180.3 R670R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:7909970 G>A maps to NM_000180.3 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr17:7911259 G>A maps to NM_000180.3 G526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr23:108647690 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:108636169 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:108641796 C>T did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:108708564 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:108691314 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr23:108673534 C>T did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:108641813 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:108696841 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:108696927 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:108673540 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr23:108708448 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:108619171 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr23:108708564 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:108631793 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:108719108 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:108638691 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:108718801 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:108652301 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:108696821 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:108718991 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:108684588 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:108718987 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:108684588 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr23:108619380 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:108718807 C>T did not map to a codon.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr23:108619380 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr23:108684597 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:108631726 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:108684706 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:108697015 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:108697043 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:44684356 C>T maps to NM_021927.2 Q172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:228334615 C>T maps to ENST00000366720 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:189449113 T>C maps to NM_016315.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:65444844 C>T maps to NM_000181.3 E150E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr7:65444469 G>A maps to NM_000181.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr7:65435304 G>A maps to NM_000181.3 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr12:42512861 G>A maps to NM_173601.1 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr12:42499823 G>A maps to NM_173601.1 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:42491380 G>A maps to NM_173601.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:72971410 C>T maps to NM_001080393.1 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:73006468 G>A maps to NM_001080393.1 Q314Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr23:2772068 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:2795272 C>T did not map to a codon.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr23:2772117 G>A did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:2799121 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:45947833 G>A maps to NM_152312.3 W315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:45945704 G>A maps to NM_152312.3 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr11:45948961 C>T maps to NM_152312.3 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:45945704 G>A maps to NM_152312.3 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:45950284 C>T maps to NM_152312.3 C685C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:45949593 G>T maps to NM_152312.3 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr4:145035896 A>T maps to NM_002099.6 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:145038045 C>T maps to NM_002099.6 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr4:145038045 C>T maps to NM_002099.6 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:145032547 C>T maps to NM_002099.6 *151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr4:145038045 C>T maps to NM_002099.6 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr4:145038045 C>T maps to NM_002099.6 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:144918698 C>T maps to ENST00000283128 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:144922344 C>T maps to ENST00000283128 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:144922362 C>T maps to ENST00000283128 K37K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:144918731 C>T maps to ENST00000283128 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:127453564 C>T maps to NM_002101.3 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr2:127453654 C>T maps to NM_002101.3 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr4:144801562 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr4:144801624 C>T maps to NM_198682.2 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:144797982 C>T maps to NM_198682.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr19:49473832 G>A maps to NM_002103.4 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:49474230 G>A maps to NM_002103.4 G533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:49473058 G>A maps to NM_002103.4 F621F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:49490543 G>A maps to NM_002103.4 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:49490507 G>A maps to NM_002103.4 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:49489289 G>A maps to NM_002103.4 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr12:21716250 A>G maps to NM_021957.3 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:21695463 G>A maps to NM_021957.3 F537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:21727173 C>T maps to NM_021957.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:21727181 G>A maps to NM_021957.3 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:21712068 G>A maps to NM_021957.3 R422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr12:21715932 G>A maps to NM_021957.3 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr12:21712631 A>G maps to NM_021957.3 H394H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:21733317 A>C maps to NM_021957.3 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:21693415 G>A maps to NM_021957.3 R579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:21715851 C>T maps to NM_021957.3 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:21715878 G>A maps to NM_021957.3 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr20:23345625 G>A maps to NM_022482.3 K202K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:23346016 C>T maps to NM_022482.3 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:54403621 G>A maps to NM_006144.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:54403990 C>T maps to NM_006144.3 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr14:25100297 C>T maps to ENST00000382542 K275K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr14:25076889 G>A maps to NM_033423.3 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr14:25078795 C>T maps to NM_033423.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr14:25075949 C>T maps to NM_033423.3 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:25076910 C>T maps to NM_033423.3 Q82Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr5:54326315 G>A maps to NM_002104.2 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:54329612 G>A maps to NM_002104.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:54329642 C>T maps to NM_002104.2 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr19:549117 G>A maps to NM_005317.2 W182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr12:48723376 G>A maps to NM_181788.1 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:48723793 G>A maps to NM_181788.1 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr12:48723127 G>T maps to NM_181788.1 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr12:48723226 G>A maps to NM_181788.1 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:48723445 G>A maps to NM_181788.1 K124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr12:48723736 G>A maps to NM_181788.1 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:129267890 C>T maps to NM_153833.1 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:129267878 G>A maps to NM_153833.1 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:129034463 C>T maps to NM_006026.3 K94K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr12:14927697 G>A maps to NM_177925.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr12:14927469 G>A maps to NM_177925.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr10:71835479 C>T maps to NM_018649.2 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:71851670 G>A maps to NM_018649.2 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:71853600 G>A maps to NM_018649.2 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr10:71868921 G>A maps to NM_018649.2 K304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:103267862 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr23:103267876 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr23:103268041 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:103268124 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:103267898 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr23:103268041 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:103267932 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:103268163 C>T did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:103268114 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr17:73775222 G>A maps to NM_005324.3 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr12:31944878 G>A maps to NM_001013699.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:31944878 G>A maps to NM_001013699.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr12:31944911 C>T maps to NM_001013699.2 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:31944955 G>A maps to NM_001013699.2 R49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr1:9324114 C>T maps to NM_004285.3 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:9324816 C>T maps to NM_004285.3 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr1:9322190 C>T maps to NM_004285.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:9307128 C>T maps to NM_004285.3 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:9305247 C>T maps to NM_004285.3 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:9305601 C>T maps to NM_004285.3 D203D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:9324504 C>T maps to NM_004285.3 I651I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:9324772 A>T maps to NM_004285.3 K741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr10:115335689 G>A maps to NM_004132.3 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr10:115327255 G>A maps to NM_004132.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:115343019 G>A maps to NM_004132.3 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr10:115343961 G>A maps to NM_004132.3 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:115335716 C>T maps to NM_004132.3 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:115341722 G>A maps to NM_004132.3 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:115341821 C>T maps to NM_004132.3 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:105192054 G>A maps to NM_020771.3 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:105198314 T>C maps to NM_020771.3 R748R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:105198316 G>A maps to NM_020771.3 R748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:15621478 G>A maps to NM_012260.2 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:15604945 G>A maps to NM_012260.2 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:26508324 C>T maps to NM_000183.2 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:26502046 C>T maps to NM_000183.2 H225H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:26501645 C>T maps to NM_000183.2 R203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:26477302 A>T maps to NM_000183.2 R24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:26501656 C>T maps to NM_000183.2 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:26501644 C>T maps to NM_000183.2 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr2:26501518 C>T maps to NM_000183.2 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:1872924 G>A maps to NM_005326.4 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr12:96380881 A>C maps to NM_002108.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr12:96387587 C>T maps to NM_002108.2 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr12:96371776 G>A maps to NM_002108.2 S533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:96389600 C>A maps to NM_002108.2 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:96379923 G>A maps to NM_002108.2 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr12:96389529 G>A maps to NM_002108.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr12:96387921 G>A maps to NM_002108.2 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:96370430 G>A maps to NM_002108.2 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:96384197 C>T maps to NM_002108.2 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr12:96371812 G>A maps to NM_002108.2 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:35773542 G>A maps to NM_021175.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr19:35775747 G>A maps to NM_021175.2 W49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr5:153855394 G>A maps to NM_004821.2 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr5:153855434 T>A maps to NM_004821.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr4:174449921 C>T maps to NM_021973.2 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr20:7866478 C>T maps to NM_017545.2 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr20:7915257 G>A maps to NM_017545.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:7866457 G>A maps to NM_017545.2 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:119927540 C>T maps to ENST00000361035 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:119936441 G>A maps to ENST00000361035 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:119929328 C>T maps to ENST00000361035 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:119936447 G>A maps to ENST00000361035 Q360Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:119925618 C>T maps to ENST00000361035 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:119935284 G>A maps to ENST00000361035 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr1:119925536 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:119936433 C>T maps to ENST00000361035 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:119927498 A>G maps to ENST00000361035 Q141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:119936429 C>T maps to ENST00000361035 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:119927486 C>T maps to ENST00000361035 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:119929405 C>T maps to ENST00000361035 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:119927555 C>T maps to ENST00000361035 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:39890868 C>T maps to ENST00000310778 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr17:39881156 C>T maps to ENST00000310778 R604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr17:39884451 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:39888628 C>T maps to ENST00000310778 W189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr5:82948428 A>T maps to NM_001884.3 Y105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr5:82948512 G>A maps to NM_001884.3 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr5:82948506 A>G maps to NM_001884.3 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:82948550 G>A maps to NM_001884.3 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr5:82948467 C>T maps to NM_001884.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr5:82969276 A>C maps to NM_001884.3 Y22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:82937539 G>A maps to NM_001884.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:82940392 G>A maps to NM_001884.3 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:82937377 G>A maps to NM_001884.3 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:82948599 C>T maps to NM_001884.3 K48K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr1:156593851 G>A maps to NM_021817.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr15:89424927 C>T maps to NM_178232.2 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr15:89424759 C>T maps to NM_178232.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr15:89422477 G>A maps to NM_178232.2 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr15:89424915 C>T maps to NM_178232.2 E55E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr19:19369575 G>A maps to NM_023002.2 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:19371841 C>T maps to NM_023002.2 K88K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19369407 C>T maps to NM_023002.2 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19372291 C>T maps to NM_023002.2 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:46637730 G>A maps to NM_173811.3 H19H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr11:46625316 G>A maps to NM_173811.3 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr11:46637535 G>A maps to NM_173811.3 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:46625265 G>A maps to NM_173811.3 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:46637406 G>A maps to NM_173811.3 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr5:140053885 C>A maps to NM_002109.3 E496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr5:140057492 C>T maps to NM_002109.3 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:140059396 G>A maps to NM_002109.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:140056669 C>T maps to NM_002109.3 Q285Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:140062741 G>A maps to NM_002109.3 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr5:140076573 C>T maps to NM_012208.2 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr5:140073846 C>T maps to NM_012208.2 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:52217174 G>A maps to NM_001523.2 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:52217174 G>A maps to NM_001523.2 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr19:52222608 C>T maps to NM_001523.2 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:52222578 C>G maps to NM_001523.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:52220398 G>A maps to NM_001523.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:122626660 G>A maps to NM_005328.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr8:122627010 G>A maps to NM_005328.2 R333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:122626714 G>A maps to NM_005328.2 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr16:69143411 G>A maps to NM_005329.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:69148367 G>A maps to NM_005329.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr16:69148555 G>A maps to NM_005329.2 W350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:69143861 G>A maps to NM_005329.2 Q188Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:23417129 G>A maps to NM_017815.2 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:23417111 A>G maps to NM_017815.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:23416931 G>A maps to NM_017815.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:36110967 C>T maps to NM_015302.1 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr19:36106231 C>T maps to NM_015302.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr19:36109914 C>T maps to NM_015302.1 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:36110381 C>A maps to NM_015302.1 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr19:36108239 C>T maps to NM_015302.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr9:19070245 G>A maps to NM_017645.3 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:19058286 T>C maps to NM_017645.3 S826S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr23:152722638 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:152728075 G>A did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:152722005 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:17163693 C>A maps to NM_033417.1 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr19:17163669 C>T maps to NM_033417.1 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr5:156479462 C>T maps to NM_001173393.1 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:156479462 C>T maps to NM_001173393.1 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr5:156482404 G>A maps to NM_001173393.1 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:156479509 G>A maps to NM_001173393.1 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr5:156479462 C>T maps to NM_001173393.1 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:156479480 C>T maps to NM_001173393.1 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr5:156533878 G>A maps to NM_032782.3 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:156522377 G>A maps to NM_032782.3 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr5:156533971 C>T maps to NM_032782.3 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:156531713 G>A maps to NM_032782.3 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr11:5247986 G>A maps to NM_000518.4 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr11:5248027 G>A maps to NM_000518.4 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr11:5247806 C>T maps to NM_000518.4 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:5247935 C>T maps to NM_000518.4 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:5247976 G>A maps to NM_000518.4 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr11:5247938 C>T maps to NM_000518.4 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:5248188 C>T maps to NM_000518.4 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:5247893 C>T maps to NM_000518.4 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5247884 C>T maps to NM_000518.4 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr11:5255400 G>A maps to NM_000519.3 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr11:5291093 C>T maps to NM_005330.3 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:5289821 C>T maps to NM_005330.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:5290832 G>A maps to NM_005330.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:5289806 C>T maps to NM_005330.3 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:5290725 C>T maps to NM_005330.3 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:139722386 G>A maps to NM_001945.2 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:5269663 G>A maps to ENST00000440157 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:5269642 G>A maps to ENST00000440157 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr11:5275626 A>T maps to ENST00000399563 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr11:5275572 C>T maps to ENST00000399563 Q93Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:5274581 G>A maps to ENST00000399563 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:5274593 G>A maps to ENST00000399563 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:216425 G>A maps to NM_001003938.3 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:106822998 C>T maps to NM_012257.3 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr6:135307285 G>A maps to NM_006620.3 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:202970 G>A maps to NM_005332.2 Q21Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:11133032 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:11139764 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:11139885 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:11135391 A>G did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:153225812 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:153216279 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr23:153220910 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:153225278 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:153220574 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:153223332 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:153224143 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:153222160 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:153222161 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr23:153219121 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:153214804 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:153214805 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:153222122 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:153222119 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:153222904 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:153218264 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr23:153219096 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:153220599 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:153224841 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZG-06A-11D-A197-08 chr23:153227716 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:153217340 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:153221831 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr23:153223311 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:153219621 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:153222474 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr23:153221831 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:104461790 C>A maps to NM_013320.2 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr12:104461796 G>T maps to NM_013320.2 G129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr20:30672293 C>T maps to NM_002110.3 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr20:30672230 C>T maps to NM_002110.3 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:30662440 G>A maps to NM_002110.3 W115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:30686816 C>T maps to NM_002110.3 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr20:30689320 G>A maps to NM_002110.3 *527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr20:30667603 G>A maps to NM_002110.3 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr20:30686915 C>T maps to NM_002110.3 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:121351031 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr3:121351958 C>T maps to NM_005335.4 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr3:121353236 C>T maps to NM_005335.4 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:121350722 G>A maps to NM_005335.4 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:121353212 C>T maps to NM_005335.4 E248E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:121353215 C>T maps to NM_005335.4 E247E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr3:121353206 C>T maps to NM_005335.4 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:121350722 G>A maps to NM_005335.4 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr5:45262552 G>A maps to NM_021072.2 R715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr5:45645577 G>A maps to NM_021072.2 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr5:45396728 G>A maps to NM_021072.2 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:45396698 G>A maps to NM_021072.2 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr5:45645700 C>T maps to NM_021072.2 W145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr5:45262778 G>T maps to NM_021072.2 I639I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44Q-06A-11D-A25O-08 chr5:45262676 C>A maps to NM_021072.2 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr5:45262145 G>A maps to NM_021072.2 I850I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:45303698 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:45262427 C>T maps to NM_021072.2 Q756Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:45462052 G>A maps to NM_021072.2 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:45645517 G>A maps to NM_021072.2 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr5:45645577 G>A maps to NM_021072.2 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:45262406 C>T maps to NM_021072.2 P763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:45396680 G>A maps to NM_021072.2 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:45645577 G>A maps to NM_021072.2 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:45262580 G>A maps to NM_021072.2 S705S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:45262406 C>T maps to NM_021072.2 P763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr5:45262172 G>A maps to NM_021072.2 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:45262154 C>A maps to NM_021072.2 S847S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr5:45303829 G>A maps to NM_021072.2 Q497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:45462085 G>A maps to NM_021072.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr5:45262406 C>T maps to NM_021072.2 P763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr5:45262517 C>T maps to NM_021072.2 Q726Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr5:45262295 C>T maps to NM_021072.2 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:45645661 G>A maps to NM_021072.2 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:45695844 C>T maps to NM_021072.2 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:614008 C>T maps to NM_001194.3 D661D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:603795 C>T maps to NM_001194.3 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr19:603591 C>T maps to NM_001194.3 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:603588 C>T maps to NM_001194.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:603795 C>T maps to NM_001194.3 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:613252 C>T maps to NM_001194.3 I530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:155257824 C>T maps to NM_020897.1 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:155252279 G>A maps to NM_020897.1 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:155255657 C>T maps to NM_020897.1 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr15:73635896 G>A maps to NM_005477.2 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr15:73615109 G>A maps to NM_005477.2 S1108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr15:73635794 C>T maps to NM_005477.2 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr15:73615253 G>A maps to NM_005477.2 P1060P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr15:73621927 G>A maps to NM_005477.2 Q526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:73615778 C>T maps to NM_005477.2 G885G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr15:73622048 C>G maps to NM_005477.2 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr15:73615205 G>C maps to NM_005477.2 P1076P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr15:73615424 C>T maps to NM_005477.2 P1003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr15:73635980 G>A maps to NM_005477.2 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:73615103 C>T maps to NM_005477.2 G1110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:73636010 G>A maps to NM_005477.2 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:73659853 C>T maps to NM_005477.2 W253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:40336477 C>T maps to NM_001524.1 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:32089221 G>A maps to NM_001525.2 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr1:32084966 C>T maps to NM_001525.2 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:32089167 C>T maps to NM_001525.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:32084963 C>T maps to NM_001525.2 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:32086541 G>A maps to NM_001525.2 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:32084963 C>T maps to NM_001525.2 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:55113482 C>T maps to NM_001526.3 N90N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:55119932 G>A did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr6:55039511 C>T maps to NM_001526.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr6:55142314 G>A maps to NM_001526.3 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:55039501 C>T maps to NM_001526.3 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:55039414 C>T maps to NM_001526.3 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:55039519 G>A maps to NM_001526.3 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr6:55039579 C>T maps to NM_001526.3 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:55120097 C>T maps to NM_001526.3 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:55113587 C>T maps to NM_001526.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr6:55145170 G>A maps to NM_001526.3 W345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:55147134 C>T maps to NM_001526.3 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr6:55039447 G>A maps to NM_001526.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:55142284 G>A maps to NM_001526.3 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:55039573 C>T maps to NM_001526.3 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:36393500 C>T maps to NM_014266.3 I2I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:32794667 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr1:32796204 C>T maps to NM_004964.2 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:32782336 C>A maps to NM_004964.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr22:50686527 C>T maps to NM_032019.5 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr22:50686180 C>T maps to NM_032019.5 E454E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr22:50686338 C>T maps to NM_032019.5 E439E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:13525015 G>A maps to NM_024827.3 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr6:114281153 C>T maps to ENST00000398283 Q121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr5:141014469 G>A maps to NM_003883.3 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:240036808 G>A maps to NM_006037.3 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr2:240033330 G>A maps to NM_006037.3 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr2:240033240 G>A maps to NM_006037.3 T648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr2:239976469 G>A maps to NM_006037.3 S1016S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:239990239 G>A maps to NM_006037.3 F933F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:240078469 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:42156004 G>A maps to NM_001015053.1 F1065F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:42156612 G>A maps to NM_001015053.1 L994L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:42188139 C>T maps to NM_001015053.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr23:48665054 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:48674441 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:48681151 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:48663911 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:48681692 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:48681658 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr23:48681100 A>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:48674976 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:48666443 C>A did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr12:48189005 G>A maps to NM_015401.3 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr12:48189005 G>A maps to NM_015401.3 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:48188614 G>A maps to NM_015401.3 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:71787621 A>G did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:71787748 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:71684535 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:71710782 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:71549925 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:71708807 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:71681863 G>T did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr23:71684501 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr7:18975447 G>A maps to NM_178425.2 T940T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:18975553 C>T maps to NM_178425.2 L976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr7:18669045 C>T maps to NM_178425.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:19015504 G>A maps to NM_178425.2 E1033E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr7:18631224 A>T maps to NM_178425.2 K168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:18633626 G>A maps to NM_178425.2 K213K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:18875175 G>A maps to NM_178425.2 G851G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:19015471 C>T maps to NM_178425.2 G1022G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr7:18631202 G>A maps to NM_178425.2 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:18767288 C>T maps to NM_178425.2 H606H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:18687442 G>A maps to NM_178425.2 E357E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:18767249 T>G maps to NM_178425.2 A593A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:19015468 G>A maps to NM_178425.2 R1021R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr7:18687412 G>A maps to NM_178425.2 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr7:18631202 G>A maps to NM_178425.2 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr7:18705843 G>A maps to NM_178425.2 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr7:18705939 C>T maps to NM_178425.2 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr7:18767294 C>T maps to NM_178425.2 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:18624985 C>T maps to NM_178425.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:18705912 C>T maps to NM_178425.2 D515D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:18788652 G>A maps to NM_178425.2 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:50546440 C>T maps to NM_002112.3 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:50535043 G>A maps to NM_002112.3 R468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:50534744 G>A maps to NM_002112.3 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr15:50540489 G>A maps to NM_002112.3 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:50534752 G>A maps to NM_002112.3 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:50544915 G>A maps to NM_002112.3 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr15:50544900 G>A maps to NM_002112.3 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr15:50550612 C>T maps to NM_002112.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr15:50555431 C>T maps to NM_002112.3 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:50534693 G>A maps to NM_002112.3 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:50534735 G>A maps to NM_002112.3 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:50545817 G>A maps to NM_002112.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:50555458 C>T maps to NM_002112.3 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr15:50535101 G>A maps to NM_002112.3 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr15:50535124 G>A maps to NM_002112.3 Q441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:156714116 C>A maps to NM_001126050.1 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr6:22570478 G>A maps to NM_138574.2 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:22570322 G>A maps to NM_138574.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:22570397 C>T maps to NM_138574.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:22570049 C>T maps to NM_138574.2 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr19:4491832 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:4475532 C>T maps to ENST00000301284 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr15:83820056 T>C maps to NM_016073.2 K172K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:83808024 G>A maps to NM_016073.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:83826716 C>A maps to NM_016073.2 G80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:6968385 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:7023737 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr18:44635147 G>A maps to NM_032124.4 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr18:44656624 G>A maps to NM_032124.4 Q129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr9:116136430 G>A maps to NM_031219.2 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr9:116135908 G>A maps to NM_031219.2 D242D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:116136319 G>A maps to NM_031219.2 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:242174967 G>A maps to NM_005336.3 D982D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:242189354 G>A maps to NM_005336.3 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr2:242195760 G>A maps to NM_005336.3 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr2:242196122 T>C maps to NM_005336.3 K183K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:83599323 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:83591835 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:83724270 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:83588781 A>C did not map to a codon.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr1:236720518 G>A maps to NM_018072.5 P1777P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:236740196 C>T maps to NM_018072.5 R936R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr1:236749559 T>C maps to NM_018072.5 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:236735811 A>G maps to NM_018072.5 S1202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:236761207 G>A maps to NM_018072.5 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:236737996 C>G maps to NM_018072.5 A1097A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:236721627 T>A maps to NM_018072.5 K1705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:236732403 G>A maps to NM_018072.5 I1323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr1:236748363 C>T maps to NM_018072.5 Q734Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:780982 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:813753 G>A maps to NM_017802.3 G667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:825181 C>T maps to NM_017802.3 F820F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:825181 C>T maps to NM_017802.3 F820F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:796520 C>T maps to NM_017802.3 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr7:780535 C>T maps to NM_017802.3 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr7:796513 C>T maps to NM_017802.3 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:780475 C>T maps to NM_017802.3 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:825226 C>T maps to NM_017802.3 H835H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr7:769330 C>T maps to NM_017802.3 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr16:50136198 C>T maps to NM_182922.2 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:50100333 G>A maps to NM_182922.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr16:50138885 C>T maps to NM_182922.2 Q653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr16:50118189 C>T maps to NM_182922.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr16:50136243 C>A maps to NM_182922.2 A606A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr14:73989523 G>A maps to ENST00000334988 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:73985832 C>T maps to ENST00000334988 K321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:73989664 C>T maps to ENST00000334988 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr14:73962037 C>T maps to ENST00000334988 E846E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:73976136 G>A maps to ENST00000334988 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26D-06A-11D-A19A-08 chr14:73985813 C>A maps to ENST00000334988 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr14:31828258 G>A maps to ENST00000389961 N686N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr14:31855776 G>A maps to ENST00000389961 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:37234373 G>A maps to NM_019024.1 L1532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:37295974 C>A maps to NM_019024.1 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:37296033 A>G maps to NM_019024.1 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:37284582 G>A maps to NM_019024.1 F700F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:37235781 G>A maps to NM_019024.1 A1498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:37285624 G>A maps to NM_019024.1 I676I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr17:58134510 G>A maps to NM_022070.4 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr17:58121391 G>A maps to NM_022070.4 V1026V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:58128305 A>T maps to NM_022070.4 G774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:58137346 G>A maps to NM_022070.4 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr17:58121157 G>A maps to NM_022070.4 S1104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:58144811 G>A maps to NM_022070.4 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:145218743 C>T maps to NM_032450.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr8:145246703 C>T maps to NM_032450.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr8:145278099 C>T maps to NM_032450.2 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr8:145278090 C>T maps to NM_032450.2 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr8:145235382 G>A maps to NM_032450.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr5:40998260 C>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:40999859 G>A maps to ENST00000296803 L1503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:41009402 G>A maps to ENST00000296803 I1134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr5:41065469 G>A maps to ENST00000296803 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr5:41019028 G>A maps to ENST00000296803 L846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr5:41049520 G>A maps to ENST00000296803 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:41038975 C>T maps to ENST00000296803 G693G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:41048462 C>T maps to ENST00000296803 W549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr5:41018860 G>A maps to ENST00000296803 L870L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr5:41065496 G>A maps to ENST00000296803 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr5:41008721 G>A maps to ENST00000296803 I1199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr5:41038921 G>A maps to ENST00000296803 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr5:41038884 G>A maps to ENST00000296803 Q724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr5:41019026 C>T maps to ENST00000296803 L846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr5:41033238 G>A maps to ENST00000296803 F756F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr5:41033205 G>A maps to ENST00000296803 V767V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:40999859 G>A maps to ENST00000296803 L1503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:41061692 G>A maps to ENST00000296803 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:41061755 C>G maps to ENST00000296803 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20I-06A-11D-A196-08 chr5:41038948 G>A maps to ENST00000296803 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20I-06A-11D-A196-08 chr5:41058208 G>A maps to ENST00000296803 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:41064652 G>A maps to ENST00000296803 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:41004489 G>A maps to ENST00000296803 Y1385Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:41018472 G>A maps to ENST00000296803 I912I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:41055861 A>G maps to ENST00000296803 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:41004462 C>T maps to ENST00000296803 R1394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:41018870 G>A maps to ENST00000296803 S866S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:41065469 G>A maps to ENST00000296803 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr5:41039564 G>A maps to ENST00000296803 F683F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:41032917 G>A maps to ENST00000296803 F790F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:41058176 G>A maps to ENST00000296803 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr5:41018472 G>A maps to ENST00000296803 I912I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:41004874 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:41061812 G>A maps to ENST00000296803 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:41058245 G>A maps to ENST00000296803 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr5:41004525 G>A maps to ENST00000296803 I1373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr5:41065529 G>A maps to ENST00000296803 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr5:41061745 G>A maps to ENST00000296803 R181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:41009456 C>T maps to ENST00000296803 G1116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:41000371 G>A maps to ENST00000296803 Q1479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:41054919 G>A maps to ENST00000296803 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:41051192 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr5:41064580 G>A maps to ENST00000296803 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr5:41055888 G>A maps to ENST00000296803 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:41008721 G>A maps to ENST00000296803 I1199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr5:41000351 C>T maps to ENST00000296803 R1485R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr5:41054919 G>A maps to ENST00000296803 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr5:41049435 T>A maps to ENST00000296803 K483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:41004525 G>A maps to ENST00000296803 I1373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:41054940 C>T maps to ENST00000296803 E345E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr5:41012741 G>A maps to ENST00000296803 A1027A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr5:41038975 C>T maps to ENST00000296803 G693G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:41004525 G>A maps to ENST00000296803 I1373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:41019026 C>T maps to ENST00000296803 L846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:41038969 C>T maps to ENST00000296803 K695K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:41012730 C>T maps to ENST00000296803 W1031*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:41058293 G>A maps to ENST00000296803 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr5:41045889 G>A maps to ENST00000296803 F599F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:13128334 G>A maps to NM_015987.4 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:138734092 G>T maps to NM_014320.2 G166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr6:139498229 C>A maps to NM_016217.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr6:139488216 C>T maps to NM_016217.2 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr6:139488177 C>T maps to NM_016217.2 F343F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr6:139487973 G>A maps to NM_016217.2 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr14:31626486 G>A maps to NM_015382.2 R549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:31598271 G>A maps to NM_015382.2 V1435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr14:31583154 G>A maps to NM_015382.2 H1928H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr14:31614084 A>T maps to NM_015382.2 R853R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr14:31637528 G>A maps to NM_015382.2 Q533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:31597180 A>C maps to NM_015382.2 P1597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:31570517 C>T maps to NM_015382.2 L2521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr14:31578781 G>A maps to NM_015382.2 R2101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr14:31619268 G>A maps to NM_015382.2 I697I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:31604172 A>G maps to NM_015382.2 S1161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr14:31642961 G>A maps to NM_015382.2 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:31598523 G>A maps to NM_015382.2 S1351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr10:93256116 T>C maps to ENST00000446394 C560C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr10:93220271 C>T maps to ENST00000446394 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr10:93244935 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:45469357 G>A maps to NM_024602.5 F828F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr1:45475072 G>A maps to NM_024602.5 N319N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:45476264 G>A maps to NM_024602.5 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr1:45472387 G>A maps to NM_024602.5 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr7:43594323 C>T maps to NM_015052.3 L1548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr7:43484696 T>C maps to NM_015052.3 N642N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:43484246 G>A maps to NM_015052.3 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr7:43495938 G>A maps to NM_015052.3 V848V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr7:43477636 G>A maps to NM_015052.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr7:43519246 C>T maps to NM_015052.3 F1046F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:43436447 A>G maps to NM_015052.3 Q197Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:43483976 C>T maps to NM_015052.3 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:43591894 C>T maps to NM_015052.3 I1490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:43484423 G>A maps to NM_015052.3 G551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:43484093 C>T maps to NM_015052.3 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:43484483 C>T maps to NM_015052.3 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:43508658 G>A maps to NM_015052.3 L1018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:43484615 G>A maps to NM_015052.3 E615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:43580800 C>T maps to NM_015052.3 I1353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:43547679 G>A maps to NM_015052.3 R1272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:43484076 G>T maps to NM_015052.3 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:43508574 C>T maps to NM_015052.3 V990V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:43508544 C>T maps to NM_015052.3 S980S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:43447215 G>A maps to NM_015052.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:43590048 G>A maps to NM_015052.3 T1418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr7:43503333 C>T maps to NM_015052.3 A909A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr7:43591930 G>A maps to NM_015052.3 R1502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr7:43484276 G>A maps to NM_015052.3 E502E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:43351576 C>T maps to NM_015052.3 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:43594368 G>A maps to NM_015052.3 G1563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:43351591 C>T maps to NM_015052.3 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:43447228 C>T maps to NM_015052.3 Q234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:43484267 G>A maps to NM_015052.3 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr7:43484615 G>A maps to NM_015052.3 E615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:197090530 G>A maps to NM_020760.1 F1327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:197183396 C>T maps to NM_020760.1 R739R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:197194325 G>A maps to NM_020760.1 R182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:197208411 C>T maps to NM_020760.1 W123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr2:197183897 C>T maps to NM_020760.1 E572E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:197184146 G>A maps to NM_020760.1 I489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:197081766 T>A maps to NM_020760.1 R1487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:197208411 C>T maps to NM_020760.1 W123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:197183279 A>T maps to NM_020760.1 T778T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:197297970 G>A maps to NM_020760.1 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr2:197172777 C>T maps to NM_020760.1 R822R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:197183806 G>A maps to NM_020760.1 Q603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:197183390 C>T maps to NM_020760.1 G741G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:197183417 C>T maps to NM_020760.1 E732E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr2:197183522 C>T maps to NM_020760.1 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:197118737 C>T maps to NM_020760.1 E1145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:197183363 G>A maps to NM_020760.1 A750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:197171331 G>A maps to NM_020760.1 F898F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:197184086 C>T maps to NM_020760.1 E509E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:197066060 G>A maps to NM_020760.1 S1553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:197183411 C>T maps to NM_020760.1 G734G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:197208453 C>T maps to NM_020760.1 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:197298126 C>T maps to NM_020760.1 E7E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:197182091 A>G maps to NM_020760.1 G780G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr2:197122599 C>T maps to NM_020760.1 G1122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:124728597 G>A maps to NM_020733.1 I1048I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:124732112 G>A maps to NM_020733.1 L770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:124732622 G>A maps to NM_020733.1 S600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:124689555 G>A maps to NM_020733.1 F1362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr3:124739639 G>A maps to NM_020733.1 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:124692604 G>A maps to NM_020733.1 N1322N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:66703763 C>T maps to NM_033647.2 F352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr12:66700176 C>T maps to NM_033647.2 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr12:66725085 T>C maps to NM_033647.2 F941F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:96354525 C>T maps to NM_018063.3 R721R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:84339275 G>A maps to NM_133636.2 I1011I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr4:84376744 G>A maps to NM_133636.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr4:84367224 A>C maps to NM_133636.2 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:84370061 T>C maps to NM_133636.2 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr4:84367238 A>G maps to NM_133636.2 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:185940189 G>A maps to NM_001029887.1 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:185940950 C>T maps to NM_001029887.1 Y146Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:65147219 T>C maps to NM_014877.3 R766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:65105655 G>A maps to NM_014877.3 I1355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr17:65104785 G>A maps to NM_014877.3 Q1516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr17:65105285 G>A maps to NM_014877.3 L1479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:65116563 T>C maps to NM_014877.3 Q1265Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:65184495 G>A maps to NM_014877.3 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:65156471 G>A maps to NM_014877.3 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:65083038 G>A maps to NM_014877.3 S1800S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:65185746 G>A maps to NM_014877.3 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:100693424 C>T maps to NM_018437.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr3:50617355 C>T maps to NM_016173.3 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr3:50615279 G>A maps to NM_016173.3 W213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr3:50614941 C>T maps to NM_016173.3 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:124792319 C>T maps to NM_152722.4 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:124793775 G>A maps to NM_152722.4 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20I-06A-11D-A196-08 chr11:124793255 G>A maps to NM_152722.4 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:124794924 C>T maps to NM_152722.4 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr11:124794780 G>A maps to NM_152722.4 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr11:124792339 G>A maps to NM_152722.4 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:124794651 C>T maps to NM_152722.4 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:124805821 C>T maps to NM_152722.4 Q27Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr11:124794948 C>T maps to NM_152722.4 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr7:92826820 C>T maps to ENST00000453812 W395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:92826820 C>T maps to ENST00000453812 W395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:92848519 A>T maps to ENST00000453812 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:92838106 G>A maps to ENST00000453812 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr7:92826819 C>T maps to ENST00000453812 W395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:92844912 C>T maps to ENST00000453812 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:92848714 G>C maps to ENST00000453812 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:92844732 G>A maps to ENST00000453812 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr7:92837992 C>T maps to ENST00000453812 E327E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr7:92848780 G>A maps to NM_198151.1 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr7:92826840 G>A maps to ENST00000453812 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr23:65409640 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:65413475 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:65479995 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr23:65423390 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr23:65408328 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:65417616 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:65392414 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:65393458 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:65423251 G>A did not map to a codon.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr23:65474958 T>A did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:65392290 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:65392389 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:65486328 A>T did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:65412095 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:65390555 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:65478818 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:65486280 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr23:65476087 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr23:65486288 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:65392421 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:65420574 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:65390542 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:65486504 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr23:65486446 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr23:65411987 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:65413378 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:65480097 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:65476038 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:65479984 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:65413364 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:65480098 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:65414952 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr23:65409641 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:65486391 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:65409614 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:65476030 C>T did not map to a codon.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr23:65486410 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr23:65476087 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:65393460 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr23:65427070 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:65486493 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:65412045 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:65475997 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:65486410 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:65390522 G>A did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:65408297 C>T did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:65486365 C>T did not map to a codon.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr23:65423338 C>T did not map to a codon.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr23:65474948 C>T did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:65479979 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:93800689 C>T maps to NM_001098672.1 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr11:93806472 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr11:93822128 G>A maps to NM_001098672.1 G763G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:93808499 A>T maps to NM_001098672.1 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:93826759 G>A maps to NM_001098672.1 V796V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:93837821 C>T maps to NM_001098672.1 S937S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:93796734 G>A maps to NM_001098672.1 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:93806483 C>T maps to NM_001098672.1 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:93822029 G>A maps to NM_001098672.1 G730G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:93754683 G>A maps to NM_001098672.1 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:93779018 G>A maps to NM_001098672.1 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr11:93844972 G>A maps to NM_001098672.1 V1131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:93754683 G>A maps to NM_001098672.1 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:93845058 G>A maps to NM_001098672.1 *1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:93778991 G>A maps to NM_001098672.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:93778874 G>A maps to NM_001098672.1 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:93797566 G>A maps to NM_001098672.1 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:93754683 G>A maps to NM_001098672.1 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:93819206 C>T maps to NM_001098672.1 S644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:93839178 G>A maps to NM_001098672.1 G976G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr11:93779084 T>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:93800692 G>A maps to NM_001098672.1 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:93834496 A>G maps to NM_001098672.1 K857K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:124789831 C>T maps to NM_001037558.2 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr15:63986244 G>A maps to ENST00000261887 F1864F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:63966646 T>G maps to ENST00000261887 I2580I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr15:63948489 G>A maps to ENST00000261887 R3223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:63904617 G>A maps to ENST00000261887 Y4745Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr15:64067492 G>C maps to ENST00000261887 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr15:63908059 G>A maps to ENST00000261887 I4667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr15:63904508 G>A maps to ENST00000261887 R4782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr15:63932433 G>A maps to ENST00000261887 L3940L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr15:63920934 G>T maps to ENST00000261887 S4349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:63953992 G>A maps to ENST00000261887 Y3043Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr15:63935233 A>T maps to ENST00000261887 V3785V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr15:64005676 G>A maps to ENST00000261887 I1446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:63955209 G>A maps to ENST00000261887 I2958I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr15:63932497 G>A maps to ENST00000261887 S3918S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr15:63948489 G>A maps to ENST00000261887 R3223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q9-06A-11D-A19A-08 chr15:28482109 G>A maps to NM_004667.4 A1334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr15:28358282 G>A maps to NM_004667.4 F4722F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr15:28422224 G>A maps to NM_004667.4 I3101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr15:28502251 C>T maps to NM_004667.4 E824E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr15:28413669 G>A maps to NM_004667.4 S3432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr15:28420711 G>A maps to NM_004667.4 I3259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr15:28519456 G>A maps to NM_004667.4 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:28358366 G>A maps to NM_004667.4 I4694I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:28473472 G>A maps to NM_004667.4 F1785F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:28515963 G>A maps to NM_004667.4 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr15:28538061 C>A maps to NM_004667.4 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr15:28358291 G>A maps to NM_004667.4 F4719F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:28491993 G>A maps to NM_004667.4 L1095L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:28420711 G>A maps to NM_004667.4 I3259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr15:28424159 C>T maps to NM_004667.4 K3012K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr15:28362297 G>A maps to NM_004667.4 V4425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr15:28502310 G>A maps to NM_004667.4 L805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:28501247 G>A maps to NM_004667.4 L911L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr15:28358775 G>A maps to NM_004667.4 A4654A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr15:28525344 G>A maps to NM_004667.4 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr15:28419672 G>A maps to NM_004667.4 Q3309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr15:28419673 G>A maps to NM_004667.4 G3308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:28377942 C>A maps to NM_004667.4 L4088L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr15:28519528 G>A maps to NM_004667.4 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr15:28457651 G>A maps to NM_004667.4 N2288N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr15:28421698 C>T maps to NM_004667.4 R3187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr15:28519438 C>T maps to NM_004667.4 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr15:28491204 G>A maps to NM_004667.4 L1133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr15:28366575 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr15:28408299 C>T maps to NM_004667.4 G3562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:28501424 G>A maps to NM_004667.4 F852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:28443891 G>A maps to NM_004667.4 C2580C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr4:89579584 C>T maps to NM_014606.1 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:89574125 C>T maps to NM_014606.1 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:89576353 T>C maps to NM_014606.1 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr4:89588560 C>T maps to NM_014606.1 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:89608439 A>T maps to NM_014606.1 K883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:69750151 T>G maps to NM_022079.2 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:69726448 G>A maps to NM_022079.2 A639A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr4:89389520 T>A maps to NM_016323.2 L361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr4:89384698 C>T maps to NM_016323.2 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr4:89414188 T>A maps to NM_016323.2 Y720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr4:89326026 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr4:89326114 A>T maps to NM_017912.3 K394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr16:56976091 C>T maps to NM_014685.2 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:56973250 A>T maps to NM_014685.2 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:35674034 G>A maps to NM_022373.4 Q316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr3:193855628 C>T maps to NM_005524.2 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr3:193854429 A>T maps to NM_005524.2 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr3:57233910 C>T maps to NM_003865.2 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr3:57232421 G>A maps to NM_003865.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:57232438 G>A maps to NM_003865.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:72637869 G>A maps to ENST00000457859 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:72642919 G>A maps to ENST00000457859 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:72643515 G>A maps to ENST00000457859 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:72638913 G>A maps to ENST00000457859 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:72640429 G>A maps to ENST00000457859 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr5:73989523 T>A maps to NM_000521.3 L169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr17:80382278 C>T maps to NM_173620.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:80395113 C>T maps to NM_173620.2 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr17:80395107 G>A maps to NM_173620.2 K256K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:80391649 C>T maps to NM_173620.2 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr17:80382340 G>A maps to NM_173620.2 E52E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:43226787 G>A maps to NM_006460.2 Q77Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr17:43226692 A>C maps to NM_006460.2 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:43246725 C>A maps to NM_144608.1 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr17:43246476 G>A maps to NM_144608.1 E54E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr17:43246734 C>A maps to NM_144608.1 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:40105219 C>T maps to NM_014571.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:40097242 C>T maps to NM_014571.3 E52E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:26093144 G>A maps to NM_000410.3 Q283Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:145416930 C>T maps to NM_213653.3 Q426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:145416392 C>T maps to NM_213653.3 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:145416752 A>G maps to NM_213653.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:145415582 C>T maps to NM_213653.3 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:145415780 T>C maps to NM_213653.3 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:145416698 G>A maps to NM_213653.3 K348K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:145416920 G>A maps to NM_213653.3 W422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:91859873 G>A maps to NM_001017975.3 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:91784644 C>T maps to NM_001017975.3 L934L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:91740285 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:91816347 C>T maps to NM_001017975.3 W718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:91845775 C>T maps to NM_001017975.3 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:91727939 G>A maps to NM_001017975.3 Q1366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:91779568 C>T maps to NM_001017975.3 V1063V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:120352110 G>A maps to NM_000187.3 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr3:120394653 G>A maps to NM_000187.3 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr3:120352122 C>T maps to NM_000187.3 K353K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr3:120347262 G>A maps to NM_000187.3 F434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:120360504 C>T maps to NM_000187.3 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr3:120394692 C>T maps to NM_000187.3 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:120360504 C>T maps to NM_000187.3 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr3:120369646 G>A maps to NM_000187.3 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr3:120357374 G>A maps to NM_000187.3 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr3:120352101 C>T maps to NM_000187.3 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:120360534 G>A maps to NM_000187.3 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:120352143 G>A maps to NM_000187.3 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:120365843 C>T maps to NM_000187.3 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:120371456 C>T maps to NM_000187.3 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:120369646 G>A maps to NM_000187.3 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr7:81381565 C>T maps to NM_000601.4 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr7:81381528 G>A maps to NM_000601.4 R178*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D9-A149-06A-11D-A196-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-D9-A1JW-06A-11D-A19A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr7:81381565 C>T maps to NM_000601.4 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr7:81388077 G>A maps to NM_000601.4 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:81331938 C>T maps to NM_000601.4 W715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:81381562 G>A maps to NM_000601.4 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:81388080 C>T maps to NM_000601.4 W98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:81334774 T>C maps to NM_000601.4 R647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:81381550 T>C maps to NM_000601.4 K170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:81339533 C>T maps to NM_000601.4 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:81335622 C>T maps to NM_000601.4 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:81388020 G>T maps to NM_000601.4 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:81381514 C>T maps to NM_000601.4 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:81372744 G>A maps to NM_000601.4 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr4:3449239 C>T maps to ENST00000511533 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr4:3443793 C>T maps to ENST00000511533 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:3443790 C>T maps to ENST00000511533 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr4:3445874 G>A maps to ENST00000511533 K195K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr4:3446639 C>T maps to ENST00000511533 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr17:79663933 C>T maps to NM_004712.4 A596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr8:43014089 T>C maps to ENST00000458501 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr8:43048907 C>T maps to ENST00000458501 Y490Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr8:43037366 C>T maps to ENST00000458501 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:43054642 C>T maps to ENST00000458501 I641I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:210577890 C>T maps to NM_001170580.1 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:210761278 C>T maps to NM_001170580.1 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr1:210577938 C>T maps to NM_001170580.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:210577851 C>T maps to NM_001170580.1 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr3:42734362 G>A maps to NM_020707.3 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:42738350 G>A maps to NM_020707.3 I343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:42738518 G>A maps to NM_020707.3 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr3:42734362 G>A maps to NM_020707.3 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr3:42734254 C>T maps to NM_020707.3 E501E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:42738626 G>A maps to NM_020707.3 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:42739654 G>A maps to NM_020707.3 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:94450099 C>A maps to NM_002729.4 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:94454437 C>T maps to NM_002729.4 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:145629418 C>T maps to NM_022475.1 N419N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:145658961 G>A maps to NM_022475.1 P652P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr4:145573915 G>T maps to NM_022475.1 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:145579945 C>T maps to NM_022475.1 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr4:145636451 G>A maps to NM_022475.1 G516G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr4:145579945 C>T maps to NM_022475.1 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr4:145628355 C>T maps to NM_022475.1 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr4:145636514 C>T maps to NM_022475.1 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr4:145655995 A>T maps to NM_022475.1 K622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:145627779 G>A maps to NM_022475.1 W310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr4:145633212 G>A maps to NM_022475.1 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr4:145627717 C>T maps to NM_022475.1 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr14:100135228 G>A maps to NM_032425.4 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr14:100126722 T>A maps to NM_001127258.1 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr14:100126629 G>A maps to NM_001127258.1 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr14:100118832 C>A maps to NM_001127258.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:100118718 G>A maps to NM_001127258.1 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:100123420 C>T maps to NM_001127258.1 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:100129236 C>T maps to NM_001127258.1 N509N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr14:100129299 C>T maps to NM_001127258.1 F530F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:222717432 G>A maps to NM_024746.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr1:222713472 C>T maps to NM_024746.3 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:222696218 C>T maps to NM_024746.3 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:222713616 G>A maps to NM_024746.3 Y395Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr1:222696143 C>T maps to NM_024746.3 Q658Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:222715382 G>A maps to NM_024746.3 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:222717321 C>T maps to NM_024746.3 K177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr1:222705416 C>T maps to NM_024746.3 K538K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:222717363 C>T maps to NM_024746.3 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:222696059 C>T maps to NM_024746.3 K686K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:222717003 G>A maps to NM_024746.3 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:222717363 C>T maps to NM_024746.3 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:222721380 C>G maps to NM_024746.3 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:222700378 G>A maps to NM_024746.3 F579F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:222696017 C>T maps to NM_024746.3 R700R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:222713439 G>A maps to NM_024746.3 D454D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:222717465 G>A maps to NM_024746.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:222712033 G>A maps to NM_024746.3 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:108074058 G>A maps to NM_007072.2 W172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:108072295 C>T maps to NM_007072.2 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:108074058 G>A maps to NM_007072.2 W172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:108076802 G>A maps to NM_007072.2 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr3:108072514 G>A maps to NM_007072.2 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr3:108073995 G>A maps to NM_007072.2 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:108076873 G>A maps to NM_007072.2 W290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:100535201 G>T maps to NM_033055.2 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:100546059 C>T maps to NM_033055.2 Q371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr1:100546080 C>T maps to NM_033055.2 R378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:97218584 C>T maps to NM_032558.2 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:27671958 G>A maps to NM_152740.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:27689130 G>A maps to NM_152740.3 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:27570933 G>A maps to NM_152740.3 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:191117025 G>A maps to NM_014362.3 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:1961663 G>A maps to NM_001098202.1 T579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5KH-06A-11D-A27K-08 chr22:21800911 C>G maps to NM_015094.2 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5KH-06A-11D-A27K-08 chr22:21800995 C>A maps to NM_015094.2 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr22:21799327 C>T maps to NM_015094.2 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr22:21800467 G>A maps to NM_015094.2 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr22:21800779 C>T maps to NM_015094.2 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr22:21800593 C>T maps to NM_015094.2 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:21800536 C>T maps to NM_015094.2 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr14:62200958 G>A maps to ENST00000394997 K329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr14:62199182 C>A maps to ENST00000394997 S275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:102304786 C>T maps to ENST00000442724 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr19:46834509 C>T maps to NM_152795.2 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr19:46825114 C>T maps to NM_152795.2 F409F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr19:46832462 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr19:46811539 G>A maps to NM_152795.2 Q142Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:46825222 G>A maps to NM_152795.2 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr19:46832552 G>A maps to NM_152795.2 R510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr19:46811950 G>A maps to NM_152795.2 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:46808538 G>A maps to NM_152795.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:46832654 G>A maps to NM_152795.2 G544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr19:46807187 G>A maps to NM_152795.2 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr19:46825093 G>A maps to NM_152795.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr19:46828841 C>T maps to NM_152795.2 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:46825151 C>T maps to NM_152795.2 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q1-06A-21D-A196-08 chr12:51347823 C>T maps to NM_001109619.1 Q15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr11:119001633 C>T maps to NM_198971.1 D127D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr11:119003887 G>A maps to NM_198971.1 K366K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:119001504 C>T maps to NM_198971.1 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:130498345 G>A maps to NM_005340.5 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr9:35813317 G>A maps to NM_032593.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:35813501 G>A maps to NM_032593.2 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr9:35813655 G>A maps to NM_032593.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr6:126296112 T>C maps to NM_138571.4 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr7:75203129 C>T maps to NM_005338.4 Q227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:75189159 G>A maps to NM_005338.4 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:75221719 G>A maps to NM_005338.4 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:75178287 G>A maps to NM_005338.4 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:75192331 G>A maps to NM_005338.4 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:75182874 G>A maps to NM_005338.4 A724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr7:75182831 G>A maps to NM_005338.4 L739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr7:75182832 G>A maps to NM_005338.4 S738S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:75167504 G>A maps to NM_005338.4 T1034T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:75192535 G>A maps to NM_005338.4 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr7:75174474 G>A maps to NM_005338.4 S857S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:123338710 C>T maps to NM_003959.1 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:123341061 G>A maps to NM_003959.1 Q495Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr12:123344338 C>T maps to NM_003959.1 R809R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr12:123334489 C>T maps to NM_003959.1 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr1:114512712 G>A maps to ENST00000426820 L1040L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:114515827 T>C maps to ENST00000426820 A1180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:114516049 C>T maps to ENST00000426820 S1254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:114483055 C>T maps to ENST00000426820 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:114511150 C>T maps to ENST00000426820 V955V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:114500848 C>T maps to ENST00000426820 T710T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr1:114515734 C>T maps to ENST00000426820 S1149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:114510561 C>T maps to ENST00000426820 V923V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:139316455 G>A maps to NM_022740.4 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:139257938 G>A maps to NM_022740.4 L1111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:139299044 G>A maps to NM_022740.4 P659P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:139281518 G>A maps to NM_022740.4 V887V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr7:139313700 G>A maps to NM_022740.4 Q478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr7:139416419 G>A maps to NM_022740.4 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:139416467 G>A maps to NM_022740.4 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:139299122 C>T maps to NM_022740.4 R633R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:33308556 C>T maps to NM_005734.3 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr11:33374996 C>T maps to NM_005734.3 T1177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:33374801 C>T maps to NM_005734.3 L1112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr19:40890034 G>A maps to NM_144685.3 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:40889926 C>T maps to NM_144685.3 K195K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:40889915 C>T maps to NM_144685.3 W199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr22:19319021 G>A maps to NM_003325.3 R999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr22:19319034 G>A maps to NM_003325.3 I994I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:19348762 G>A maps to NM_003325.3 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:19385518 G>A maps to NM_003325.3 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:19346878 G>A maps to NM_003325.3 I738I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr22:19371174 G>A maps to NM_003325.3 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:19346935 G>A maps to NM_003325.3 S719S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr22:19344420 G>A maps to NM_003325.3 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr22:19373208 C>T maps to NM_003325.3 E388E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr22:19384455 G>A maps to NM_003325.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr6:27834653 G>C maps to NM_005322.2 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:27834833 C>T maps to NM_005322.2 K158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:27834935 C>T maps to NM_005322.2 K124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr6:27835109 C>T maps to NM_005322.2 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr6:27834899 C>T maps to NM_005322.2 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr6:27835040 G>A maps to NM_005322.2 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr6:27834782 C>T maps to NM_005322.2 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr6:27835010 G>A maps to NM_005322.2 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:27835052 C>T maps to NM_005322.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr6:26056137 G>A maps to NM_005319.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr6:26234617 G>A maps to NM_005320.2 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:26234972 A>T maps to NM_005320.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F2-06A-11D-A20D-08 chr6:26156923 G>T maps to NM_005321.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr6:26156896 G>A maps to NM_005321.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:26156974 G>A maps to NM_005321.2 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr6:26107904 C>T maps to NM_005323.3 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:26107853 C>T maps to NM_005323.3 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr6:25726740 C>T maps to NM_170745.3 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:26033691 G>A maps to NM_003513.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr6:26217324 C>T maps to NM_021052.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr6:25727445 C>T maps to NM_170610.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:25727285 C>T maps to NM_170610.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:25727180 C>T maps to NM_170610.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:26123985 G>A maps to NM_003526.2 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:26158579 G>A maps to NM_138720.1 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:26216778 C>T maps to NM_003518.3 K31K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr6:26252138 T>C maps to NM_003524.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr6:26252153 C>T maps to NM_003524.2 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:26273235 G>A maps to NM_003525.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr6:27100481 C>T maps to NM_021058.3 K16K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr6:27783081 C>T maps to NM_003521.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:26021001 G>A maps to NM_003529.2 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:26032059 G>A maps to NM_003537.3 Q77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:26032021 C>G maps to NM_003537.3 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:26031970 C>T maps to NM_003537.3 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr6:26046003 C>T maps to NM_003531.2 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr6:26197196 C>T maps to NM_003530.3 Q94Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:26271467 G>A maps to NM_003534.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:26271573 A>C maps to NM_003534.2 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:27839862 C>T maps to NM_003533.2 Q77Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:27858564 G>A maps to NM_003535.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:26104318 C>T maps to NM_003542.3 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr6:26104255 C>T maps to NM_003542.3 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr6:26189117 G>A maps to NM_003539.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr6:26189118 G>A maps to NM_003539.3 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:26247193 C>T maps to NM_003547.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:26247007 C>T maps to NM_003547.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:26285535 C>T maps to NM_003543.3 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:27792212 G>A maps to NM_021968.3 *104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:149858583 C>G maps to NM_003517.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:149858184 A>G maps to NM_003528.2 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr1:149783701 G>A maps to ENST00000427880 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr1:149783740 C>G maps to ENST00000427880 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:149784890 T>A maps to NM_001123375.2 K116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:149784912 C>T maps to NM_001123375.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:228612795 C>T maps to NM_003493.2 Q77Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr6:12125858 G>A maps to NM_002114.2 W1944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr6:12163946 C>T maps to NM_002114.2 G2470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr6:12164438 C>T maps to NM_002114.2 D2634D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr6:12121146 C>T maps to NM_002114.2 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:12123112 A>C maps to NM_002114.2 R1029R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:12120945 T>C maps to NM_002114.2 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr6:12123582 C>T maps to NM_002114.2 H1185H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:12122172 C>T maps to NM_002114.2 T715T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:12164526 C>T maps to NM_002114.2 L2664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:12121519 G>T maps to NM_002114.2 E498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:12121893 C>T maps to NM_002114.2 S622S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr6:12164379 C>T maps to NM_002114.2 L2615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:12124320 G>A maps to NM_002114.2 R1431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:12131131 C>T maps to NM_002114.2 R2114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:12124381 C>T maps to NM_002114.2 Q1452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr6:12122046 T>G maps to NM_002114.2 S673S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:12122503 C>T maps to NM_002114.2 L826L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:12125826 C>T maps to NM_002114.2 F1933F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr6:12120835 C>T maps to NM_002114.2 Q270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:12124261 C>T maps to NM_002114.2 R1412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr6:143093853 G>A maps to NM_006734.3 F674F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:143090868 A>C maps to NM_006734.3 V1669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:143093046 T>A maps to NM_006734.3 R943R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr6:143081030 T>A maps to NM_006734.3 R2132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr6:143081031 A>G maps to NM_006734.3 P2131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:143074867 G>A maps to NM_006734.3 S2239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:143091162 G>A maps to NM_006734.3 I1571I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:143074912 G>A maps to NM_006734.3 A2224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:143074501 G>A maps to NM_006734.3 P2361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:143092160 G>A maps to NM_006734.3 Q1239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:143093286 G>A maps to NM_006734.3 P863P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:143093091 G>A maps to NM_006734.3 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:143074684 G>A maps to NM_006734.3 S2300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:143091888 G>A maps to NM_006734.3 L1329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr6:143081307 G>A maps to NM_006734.3 F2039F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:143093025 G>A maps to NM_006734.3 S950S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:143074906 G>A maps to NM_006734.3 I2226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:42048623 G>A maps to NM_024503.3 S615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:42050327 C>T maps to NM_024503.3 E47E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr1:42045428 G>A maps to NM_024503.3 S1680S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:42048737 A>G maps to NM_024503.3 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr1:42049327 G>A maps to NM_024503.3 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:42047507 C>T maps to NM_024503.3 E987E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:42050192 G>A maps to NM_024503.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:42050036 G>A maps to NM_024503.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:42046370 C>T maps to NM_024503.3 T1366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:42049331 C>T maps to NM_024503.3 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:41976637 G>A maps to NM_024503.3 A2235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:41976847 G>A maps to NM_024503.3 H2165H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:42049343 G>A maps to NM_024503.3 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:42047702 G>A maps to NM_024503.3 F922F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:42049697 C>T maps to NM_024503.3 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:42049961 G>A maps to NM_024503.3 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:42049976 G>A maps to NM_024503.3 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr1:42047336 G>A maps to NM_024503.3 F1044F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:41978749 G>A maps to NM_024503.3 R2048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr1:42049976 G>A maps to NM_024503.3 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr1:42045926 G>A maps to NM_024503.3 P1514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr1:42049070 C>T maps to NM_024503.3 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:42041222 G>A maps to NM_024503.3 F1733F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:42045905 G>A maps to NM_024503.3 S1521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr1:42046220 C>T maps to NM_024503.3 L1416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr1:41976877 G>A maps to NM_024503.3 S2155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:42046640 G>A maps to NM_024503.3 S1276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:42047036 G>A maps to NM_024503.3 S1144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:42047557 G>A maps to NM_024503.3 L971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:42048689 G>A maps to NM_024503.3 I593I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:42049250 G>A maps to NM_024503.3 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:42050066 C>T maps to NM_024503.3 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:42050072 G>A maps to NM_024503.3 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:42050261 G>A maps to NM_024503.3 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:41978681 C>T maps to NM_024503.3 R2070R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:41976682 G>A maps to NM_024503.3 A2220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr2:234749970 C>T maps to NM_018410.3 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr2:234750116 G>A maps to NM_018410.3 R437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr2:234749334 G>A maps to NM_018410.3 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:234750087 G>A maps to NM_018410.3 C446C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:234750117 G>A maps to NM_018410.3 I436I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:234750387 A>T maps to NM_018410.3 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr10:71129365 C>T maps to ENST00000439900 N322N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:71075757 C>T maps to NM_033496.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:71119752 C>T maps to ENST00000439900 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr10:71142521 C>T maps to ENST00000439900 F550F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:71103626 C>T maps to ENST00000439900 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr10:71142302 C>T maps to ENST00000439900 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:75100491 G>A maps to NM_000189.4 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:75100425 G>A maps to NM_000189.4 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr2:75108958 G>A maps to NM_000189.4 Q564Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:75107649 C>T maps to NM_000189.4 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:75109254 C>T maps to NM_000189.4 D576D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr2:75115071 C>T maps to NM_000189.4 V754V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr2:75117983 C>T maps to NM_000189.4 F890F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:75115152 C>T maps to NM_000189.4 I781I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:75109338 C>T maps to NM_000189.4 F604F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr5:176314300 C>T maps to NM_002115.2 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr5:176308424 C>T maps to NM_002115.2 R835R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr5:176308832 G>A maps to NM_002115.2 I751I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr5:176308808 G>A maps to NM_002115.2 I759I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr5:176314515 G>A maps to NM_002115.2 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr5:176308796 G>A maps to NM_002115.2 I763I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:176308747 G>A maps to NM_002115.2 Q780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ES-06A-11D-A20D-08 chr5:176314704 C>T maps to NM_002115.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr5:176309024 C>T maps to NM_002115.2 G719G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:176308481 G>A maps to NM_002115.2 P816P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr5:176308502 G>A maps to NM_002115.2 I809I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:176314544 G>A maps to NM_002115.2 Q503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:176314545 T>C maps to NM_002115.2 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:70987057 G>A maps to NM_025130.3 K53K. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A29S-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr10:71020984 G>A maps to NM_025130.3 G769G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr10:71010323 C>T maps to NM_025130.3 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:71021020 C>T maps to NM_025130.3 F781F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:71017138 C>A maps to NM_025130.3 T663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:71010085 C>T maps to NM_025130.3 N537N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr10:71017108 C>T maps to NM_025130.3 V653V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:70986991 C>T maps to NM_025130.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:70987030 G>A maps to NM_025130.3 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:70987105 G>A maps to NM_025130.3 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:70992649 C>T maps to NM_025130.3 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:71008380 C>T maps to NM_025130.3 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:71005894 G>A maps to NM_025130.3 K312K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:71007301 C>T maps to NM_025130.3 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr19:37853242 C>T maps to NM_181786.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:37853798 C>T maps to NM_181786.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:37854457 C>T maps to NM_181786.2 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr19:37838724 G>A maps to NM_181786.2 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr6:29912167 A>C maps to ENST00000376806 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr6:31323217 G>C maps to ENST00000428231 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:31322988 G>A maps to ENST00000428231 Q373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:31237824 G>A maps to ENST00000383329 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr6:32917093 G>A maps to NM_006120.3 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr6:32918340 G>A maps to NM_006120.3 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:32905120 C>T maps to NM_002118.4 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:32975331 C>T maps to NM_002119.3 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:32974858 G>A maps to NM_002119.3 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr6:32975832 C>T maps to NM_002119.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:32975358 C>T maps to NM_002119.3 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:32975940 C>T maps to NM_002119.3 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr6:32782253 C>T maps to ENST00000452392 Q769Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:32782950 G>A maps to ENST00000452392 T684T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:32782214 C>T maps to ENST00000452392 R782R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr6:33036534 G>A maps to NM_033554.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr6:33036886 G>A maps to NM_033554.2 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr6:33048569 C>T maps to NM_002121.4 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr6:33052829 C>T maps to NM_002121.4 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr6:33052913 C>T maps to NM_002121.4 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:33052913 C>T maps to NM_002121.4 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:33052868 C>T maps to NM_002121.4 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr6:33053607 C>T maps to NM_002121.4 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr6:32609330 C>T maps to NM_002122.3 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr6:32609761 C>T maps to NM_002122.3 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:32605240 C>T maps to NM_002122.3 I2I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:32610393 G>A maps to NM_002122.3 E207E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:32609297 C>T maps to NM_002122.3 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr6:32609189 G>A maps to NM_002122.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr6:32713772 C>T maps to NM_020056.4 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:32714113 C>T maps to NM_020056.4 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:32713733 G>A maps to NM_020056.4 K166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr6:32713146 C>T maps to NM_020056.4 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:32714113 C>T maps to NM_020056.4 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:32713032 G>A maps to NM_020056.4 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:32713808 G>A maps to NM_020056.4 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr6:32712939 C>T maps to NM_020056.4 D29D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:32629235 T>G did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:32632737 G>A maps to ENST00000374943 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr6:32629960 G>A maps to ENST00000374943 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr6:32411074 C>T maps to NM_019111.4 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:32410360 T>C maps to NM_019111.4 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr6:32411031 C>T maps to NM_019111.4 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:32549499 C>T maps to NM_002124.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:32548625 C>T maps to NM_002124.2 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:32548562 G>A maps to NM_002124.2 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:32487312 C>T maps to NM_002125.3 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr6:29692181 C>T maps to NM_001098479.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:29797460 C>T maps to ENST00000376828 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr6:29795860 C>T maps to ENST00000376828 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:29796515 G>A maps to ENST00000376828 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr6:29796329 C>T maps to ENST00000376828 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:29797602 C>T maps to ENST00000376828 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:29797629 C>T maps to ENST00000376828 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:29795929 C>T maps to ENST00000376828 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr21:38137354 G>A maps to NM_000411.5 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr21:38309624 G>A maps to NM_000411.5 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr21:38302640 G>A maps to NM_000411.5 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:38302619 G>A maps to NM_000411.5 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:38309471 C>T maps to NM_000411.5 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr21:38132082 G>A maps to NM_000411.5 I580I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr21:38308997 G>A maps to NM_000411.5 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr21:38139567 C>T maps to NM_000411.5 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:53392717 C>T maps to NM_002126.4 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:53342916 C>T maps to NM_002126.4 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:53398086 C>T maps to NM_002126.4 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr3:148793735 G>A maps to NM_003071.3 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr3:148756979 G>A maps to NM_003071.3 S884S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:221057550 C>T maps to NM_021958.3 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:221057727 C>T maps to NM_021958.3 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:30125986 C>T maps to NM_178581.1 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:30142632 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr20:30126008 C>T maps to NM_178581.1 L104L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A2MJ-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr20:30154056 C>T maps to NM_178581.1 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr8:28908623 C>T maps to ENST00000444075 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr1:185970529 C>T maps to NM_031935.2 P1390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:186024594 C>T maps to NM_031935.2 S2311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr1:185892708 C>A maps to NM_031935.2 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr1:186088405 C>T maps to NM_031935.2 R3978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:186106058 C>T maps to NM_031935.2 V4524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:186113680 G>A maps to NM_031935.2 A4704A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:186158757 C>T maps to NM_031935.2 I5552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:185976274 C>T maps to NM_031935.2 G1497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:186083235 C>T maps to NM_031935.2 L3753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:186106693 C>T maps to NM_031935.2 I4549I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr1:186106751 C>T maps to NM_031935.2 Q4569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:186106979 G>A maps to NM_031935.2 R4600R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:185964215 C>T maps to NM_031935.2 Q1259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:186099732 C>T maps to NM_031935.2 T4378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:186158973 C>T maps to NM_031935.2 F5624F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:185986188 C>T maps to NM_031935.2 P1762P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:186022087 C>T maps to NM_031935.2 P2194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:186092167 C>T maps to NM_031935.2 L4105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:185902906 T>A maps to NM_031935.2 V593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr1:186072782 C>T maps to NM_031935.2 R3585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr1:186088326 A>G maps to NM_031935.2 A3951A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr1:185958750 C>T maps to NM_031935.2 A1060A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZH-06A-11D-A197-08 chr1:185704141 T>A maps to NM_031935.2 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:186083183 C>T maps to NM_031935.2 I3735I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:186088383 G>A maps to NM_031935.2 R3970R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr1:185963956 G>A maps to NM_031935.2 K1172K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:185902942 C>T maps to NM_031935.2 F605F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:186017873 G>A did not map to a codon.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:186106020 C>T maps to NM_031935.2 R4512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr15:77769934 C>T maps to NM_018200.2 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:77756656 C>T maps to NM_018200.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:3574508 C>T maps to NM_006339.2 H92H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:3578054 C>T maps to NM_006339.2 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:3578094 C>T maps to NM_006339.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:3574472 C>T maps to NM_006339.2 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:66308900 G>A maps to NM_003484.1 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr12:66308894 C>T maps to NM_003484.1 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:174253244 C>A maps to NM_002129.3 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:150154589 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:150156314 G>A did not map to a codon.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr1:34330331 G>A maps to NM_145205.4 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:34330139 G>A maps to NM_145205.4 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:34330037 G>A maps to NM_145205.4 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr1:24144067 G>A maps to NM_000191.2 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:24130997 C>T maps to NM_000191.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr1:24143196 G>A maps to NM_000191.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr6:55406859 T>A maps to NM_019036.2 K93*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D9-A6EC-06A-11D-A30X-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:55360231 G>A maps to NM_019036.2 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr6:55378889 C>T maps to NM_019036.2 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr6:55360291 G>A maps to NM_019036.2 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:55360231 G>A maps to NM_019036.2 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:55381320 C>T maps to NM_019036.2 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:55360231 G>A maps to NM_019036.2 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:55360231 G>A maps to NM_019036.2 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr5:74641437 C>A maps to NM_000859.2 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:74654480 G>C did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:74643087 C>T maps to NM_000859.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:43292653 A>C maps to NM_002130.6 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr1:120300002 G>A maps to NM_005518.3 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:120301900 C>T maps to NM_005518.3 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:120307173 C>T maps to NM_005518.3 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:120306939 G>A maps to NM_005518.3 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:120299954 G>A maps to NM_005518.3 D319D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:120293529 C>T maps to NM_005518.3 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:120298081 G>A maps to NM_005518.3 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:120301831 C>T maps to NM_005518.3 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:120307026 C>T maps to NM_005518.3 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:120293529 C>T maps to NM_005518.3 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr1:120293427 G>C maps to NM_005518.3 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr1:120295217 C>T maps to NM_005518.3 E458E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr1:120295915 C>T maps to NM_005518.3 Q427Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:120307134 C>T maps to NM_005518.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A264-06A-11D-A196-08 chr1:120301900 C>A maps to NM_005518.3 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr23:80375310 T>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:80370689 C>T did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:80371821 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr22:35660860 C>T maps to NM_001003681.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr22:35661463 C>T maps to NM_001003681.2 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr22:35679977 C>T maps to NM_001003681.2 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr19:1084304 G>T maps to NM_012292.2 V1008V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:1068552 C>T maps to NM_012292.2 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:1068552 C>T maps to NM_012292.2 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:1079800 C>T maps to NM_012292.2 Q492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:1068723 G>A maps to NM_012292.2 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:1068597 G>A maps to NM_012292.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr19:1079931 G>A maps to NM_012292.2 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr19:1080286 C>T maps to NM_012292.2 F579F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:1074871 G>A maps to NM_012292.2 R393R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:1079931 G>A maps to NM_012292.2 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:162910345 A>G maps to NM_001142556.1 E586E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr5:162911175 A>G maps to NM_001142556.1 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr5:162910052 A>G maps to NM_001142556.1 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:162902492 C>T maps to NM_001142556.1 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr22:35782754 C>T maps to NM_002133.2 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr22:35789527 C>T maps to NM_002133.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr16:4556931 C>T maps to NM_001127205.1 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr16:4559687 C>A maps to NM_001127205.1 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr16:4559639 G>A maps to NM_001127205.1 E278E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:173531280 C>T maps to NM_015980.3 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr5:173531262 C>T maps to NM_015980.3 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr18:61627561 C>A maps to NM_001123366.1 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr18:61620721 C>T maps to NM_001123366.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr18:61627534 C>T maps to NM_001123366.1 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr18:61627534 C>T maps to NM_001123366.1 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:124909092 C>T maps to NM_005519.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:124896586 C>T maps to NM_001105574.1 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr16:1741880 C>T maps to ENST00000382711 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr12:121431497 G>A maps to NM_000545.5 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:121437149 C>T maps to NM_000545.5 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:121431350 G>A maps to NM_000545.5 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:121416630 G>A maps to NM_000545.5 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:121437167 G>A maps to NM_000545.5 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr12:121416652 C>T maps to NM_000545.5 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:121416708 G>A maps to NM_000545.5 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:121426656 G>A maps to NM_000545.5 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr12:121431341 G>A maps to NM_000545.5 Q182Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:121416717 C>T maps to NM_000545.5 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr12:121431464 C>T maps to NM_000545.5 N223N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr17:36099440 C>T maps to NM_000458.2 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr17:36091760 C>T maps to NM_000458.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr17:36091654 G>A maps to NM_000458.2 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:36099563 C>T maps to NM_000458.2 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr17:36059180 T>C maps to NM_000458.2 E518E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr17:36104851 G>A maps to NM_000458.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:36099563 C>T maps to NM_000458.2 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr17:36064996 G>A maps to NM_000458.2 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:36091718 C>T maps to NM_000458.2 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr17:36091700 C>T maps to NM_000458.2 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr20:43042391 C>T maps to ENST00000338692 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr20:43052830 C>T maps to ENST00000338692 Q386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr20:43034710 A>G maps to ENST00000338692 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:43052704 C>T maps to ENST00000338692 Q344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr20:43042382 G>A maps to ENST00000338692 E175E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:43034830 C>T maps to ENST00000338692 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr20:43057086 C>T maps to ENST00000338692 N444N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:43043163 C>T maps to ENST00000338692 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:43057116 G>A maps to ENST00000338692 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:43058181 G>A maps to ENST00000338692 Q464Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:43052703 C>T maps to ENST00000338692 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:43058277 G>A maps to ENST00000338692 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:43043289 C>T maps to ENST00000338692 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr8:76465344 C>T maps to NM_004133.4 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3BZ-06A-12D-A196-08 chr8:76465281 A>C maps to NM_004133.4 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr8:76456160 G>T maps to NM_004133.4 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr8:76456044 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr8:76459857 G>A maps to NM_004133.4 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:76471253 C>T maps to NM_004133.4 Q359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:76471061 A>T maps to NM_004133.4 K295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr8:76465431 G>A maps to NM_004133.4 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:76471139 A>C maps to NM_004133.4 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr2:138771543 G>A maps to NM_006895.2 W241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr2:138724682 T>G maps to NM_001024074.2 *52E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr5:137088948 C>T maps to NM_006805.3 K269K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr12:54676896 A>G maps to NM_031157.2 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr12:54676929 T>C maps to NM_031157.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr13:53216986 C>T maps to NM_001011725.1 H120H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr7:26232186 A>G maps to NM_031243.2 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:178081270 G>A maps to NM_194247.2 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:21681205 G>A maps to NM_031314.2 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr1:12907965 C>T maps to NM_001013631.1 K59K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:12908028 G>A maps to NM_001013631.1 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:12907782 A>T maps to NM_001013631.1 Y120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:12907989 G>A maps to NM_001013631.1 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:12907851 C>T maps to NM_001013631.1 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:12908037 C>T maps to NM_001013631.1 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:12907575 C>T maps to NM_001013631.1 Q189Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:12908037 C>T maps to NM_001013631.1 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:12907287 G>A maps to NM_001013631.1 D285D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:12907497 C>T maps to NM_001013631.1 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:12907980 G>A maps to NM_001013631.1 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:12907539 C>T maps to NM_001013631.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12907434 C>T maps to NM_001013631.1 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12907473 C>T maps to NM_001013631.1 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12907881 C>T maps to NM_001013631.1 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr10:43882741 G>A maps to NM_001098204.1 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:43882356 T>G maps to NM_001098204.1 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr10:43882741 G>A maps to NM_001098204.1 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:179044566 G>A maps to NM_005520.2 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JB-06A-11D-A196-08 chr23:100667885 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr9:86585198 G>A maps to NM_031262.2 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr9:86588849 G>A maps to NM_031262.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr19:39330912 G>A maps to ENST00000221419 H352H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr19:39336516 C>T maps to ENST00000221419 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:39338029 G>A maps to ENST00000221419 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:39338074 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:39338016 G>A maps to ENST00000221419 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:39329541 C>T maps to ENST00000221419 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr19:8531249 C>T maps to NM_005968.3 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:8550626 C>T maps to NM_005968.3 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:8531249 C>T maps to NM_005968.3 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:23650087 G>A maps to ENST00000414299 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3BZ-06A-12D-A196-08 chr1:245018851 G>A maps to NM_031844.2 G742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr1:245018277 C>T maps to NM_031844.2 Q807Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:41779940 C>T maps to NM_007040.3 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr19:41770509 G>A maps to NM_007040.3 Q34Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr19:41798298 C>T maps to NM_007040.3 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr4:83349474 C>A maps to NM_031372.2 G190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:38809231 T>C maps to NM_138394.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:78671948 C>T maps to NM_004272.3 Q316Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr5:78734855 C>T maps to NM_004272.3 Q168Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr15:83544129 C>T maps to NM_199330.1 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr15:83561517 C>T maps to NM_199330.1 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr15:83532942 G>A maps to NM_199330.1 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:83527797 C>T maps to NM_199330.1 K170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:83527842 G>A maps to NM_199330.1 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr19:19042208 G>C maps to NM_004838.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:23745521 G>A maps to NM_020834.2 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr14:23745326 G>A maps to NM_020834.2 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:23746301 A>T maps to NM_020834.2 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:60299102 A>C maps to NM_015888.4 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:60328518 G>A maps to NM_015888.4 Q532Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:12878871 G>A maps to NM_013312.2 C390C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr19:12881843 C>T maps to NM_013312.2 E268E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr19:12883635 G>A maps to NM_013312.2 Q116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr19:12874529 G>A maps to NM_013312.2 S630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:12878889 C>T maps to NM_013312.2 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:12878641 A>G maps to NM_013312.2 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:12874529 G>A maps to NM_013312.2 S630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:12874529 G>A maps to NM_013312.2 S630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:57522115 C>T maps to NM_032495.5 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:150672617 C>T maps to NM_032132.4 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr22:30494851 C>T maps to NM_152510.2 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:27134226 G>A maps to NM_005522.4 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr7:27135279 C>T maps to NM_005522.4 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:27134280 G>A maps to NM_005522.4 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:27134412 C>T maps to NM_005522.4 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:27135419 G>A maps to NM_005522.4 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:27222488 G>A maps to NM_005523.5 Q290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr7:27140752 C>T maps to NM_006735.3 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr7:27140854 G>A maps to NM_006735.3 N207N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:27140890 C>T maps to NM_006735.3 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr7:27142095 C>T maps to NM_006735.3 E8E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:27140491 G>A maps to NM_006735.3 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr7:27148121 C>T maps to NM_153631.2 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:27149926 G>A maps to NM_153631.2 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:27150226 C>T maps to NM_153631.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:27148073 T>C maps to NM_153631.2 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:27147965 G>A maps to NM_153631.2 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr7:27169136 G>T maps to NM_002141.4 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr7:27169083 G>A maps to NM_002141.4 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr7:27187314 C>T maps to NM_024014.2 Q18Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:27185468 C>T maps to NM_024014.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr7:27187305 G>A maps to NM_024014.2 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:27204899 C>T maps to NM_152739.3 K59K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:27205055 C>G maps to NM_152739.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr7:27204713 G>A maps to NM_152739.3 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:46607774 C>T maps to NM_002144.3 K164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr17:46607148 G>A maps to NM_002144.3 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:46608053 G>A maps to NM_002144.3 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr17:46607720 C>T maps to NM_002144.3 W182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr17:46607130 C>T maps to NM_002144.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:46805733 G>A maps to NM_006361.5 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:46805892 C>T maps to NM_006361.5 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:46804307 C>T maps to NM_006361.5 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:46620504 G>A maps to NM_002145.3 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:46621988 G>A maps to NM_002145.3 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr17:46628421 C>T maps to NM_002146.4 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:46627845 C>T maps to NM_002146.4 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr17:46627736 G>A maps to NM_002146.4 Q419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:46628187 G>A maps to NM_002146.4 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:46627725 G>A maps to NM_002146.4 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:46628457 C>T maps to NM_002146.4 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:46655306 G>A maps to NM_024015.4 N125N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr17:46669789 G>A maps to NM_002147.3 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr17:46669654 G>A maps to NM_002147.3 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:46673890 C>A maps to NM_018952.4 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:46673891 C>T maps to NM_018952.4 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:46673837 C>T maps to NM_018952.4 E204E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr17:46685275 C>T maps to NM_004502.3 K194K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:46688172 G>A maps to NM_004502.3 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr17:46691955 G>A maps to NM_024016.3 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr17:46692051 G>A maps to NM_024016.3 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr17:46700459 G>A maps to NM_024017.4 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:46700314 G>A maps to NM_024017.4 Q234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:54379159 C>T maps to NM_017409.3 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr12:54367498 C>T maps to NM_014212.3 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:54369010 G>A maps to NM_014212.3 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:54367531 C>T maps to NM_014212.3 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:54348790 C>T maps to NM_173860.1 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:54348919 C>T maps to NM_173860.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr12:54448811 C>T maps to NM_153633.2 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:54448805 C>T maps to NM_153633.2 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:54427298 G>A maps to NM_018953.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr12:54427266 G>T maps to NM_018953.2 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr12:54423523 C>T maps to NM_004503.3 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:54423487 G>A maps to NM_004503.3 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr2:176983682 G>A maps to NM_002148.3 E249E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr2:176973653 G>T maps to NM_021192.2 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr2:176958157 C>T maps to NM_000523.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr2:177036545 C>T maps to NM_006898.4 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:177034348 G>A maps to NM_006898.4 Q169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:177036455 G>A maps to NM_006898.4 K251K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:177017651 G>A maps to NM_014621.2 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr2:177017508 C>T maps to NM_014621.2 Q203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr16:72094673 G>A maps to NM_005143.3 W369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr16:72094461 T>C maps to NM_005143.3 Y298Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr16:72094401 G>A maps to NM_005143.3 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr16:72094665 G>A maps to NM_005143.3 E366E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:72094209 G>A maps to NM_005143.3 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:21071421 T>C maps to NM_016287.3 R510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr1:33354741 C>T maps to NM_002143.2 D81D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:33359165 G>A maps to NM_002143.2 E140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr2:10559987 C>T maps to NM_002149.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:10560104 C>T maps to NM_002149.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr2:10560074 C>T maps to NM_002149.2 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:10560074 C>T maps to NM_002149.2 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr1:40149794 G>A maps to NM_016257.2 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:40149818 G>A maps to NM_016257.2 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:40149779 G>A maps to NM_016257.2 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:122292606 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr12:122296616 C>T maps to NM_002150.2 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:122294235 G>A maps to NM_002150.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr12:122295686 G>A maps to NM_002150.2 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:122281720 C>T maps to NM_002150.2 E283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:122277864 C>T maps to NM_002150.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:45793815 T>C maps to NM_032756.2 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:175413235 C>T maps to NM_000860.4 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr4:95220696 C>T maps to NM_014485.2 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:35551284 C>T maps to NM_182983.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr19:35551308 G>A maps to NM_182983.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:35550837 C>T maps to NM_182983.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:35551632 G>A maps to NM_182983.2 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:35556464 G>A maps to NM_182983.2 Q310Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:35556515 C>T maps to NM_182983.2 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:72110754 C>T maps to ENST00000228226 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr16:72110724 G>A maps to ENST00000228226 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:72110568 G>A maps to ENST00000228226 K249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:72107823 G>A maps to ENST00000228226 W50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr10:100190925 G>A maps to NM_000195.2 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr10:100195400 G>A maps to NM_000195.2 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:100195442 G>A maps to NM_000195.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:100177479 C>T maps to NM_000195.2 K648K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:100179852 G>A maps to NM_000195.2 F602F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr10:100183370 G>A maps to NM_000195.2 I529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr10:100189577 C>G maps to NM_000195.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr10:100177398 G>A maps to NM_000195.2 I675I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:100183636 G>A maps to NM_000195.2 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:148858067 C>T maps to NM_032383.3 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:148863267 C>T maps to NM_032383.3 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr3:148857935 C>T maps to NM_032383.3 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:148857890 C>T maps to NM_032383.3 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr22:26866779 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr22:26849354 A>C maps to NM_022081.4 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:26860446 G>A maps to NM_022081.4 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:18308238 G>A maps to NM_181507.1 S912S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr11:18303522 G>A maps to NM_181507.1 I1101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr10:103825887 G>A maps to NM_024747.4 W219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr10:103825818 C>T maps to NM_024747.4 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:84234440 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr4:84227367 G>A maps to NM_006665.5 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:84234384 G>A maps to NM_006665.5 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:84243432 G>A maps to NM_006665.5 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr4:84240599 G>A maps to NM_006665.5 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:84240498 G>T maps to NM_006665.5 S166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr4:84230556 G>A maps to NM_006665.5 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:84255860 G>A maps to NM_006665.5 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr10:100401654 C>T maps to NM_021828.4 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:100249932 G>A maps to NM_021828.4 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:100249953 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:100904147 G>A maps to NM_021828.4 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:100249953 C>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr10:100374729 G>A maps to NM_021828.4 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr10:100374729 G>A maps to NM_021828.4 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr11:6461514 C>T maps to NM_000613.2 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:6453221 G>A maps to NM_000613.2 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr11:6453012 G>A maps to NM_000613.2 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr11:6452877 G>A maps to NM_000613.2 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:6458754 G>A maps to NM_000613.2 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:6452883 G>A maps to NM_000613.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr8:21986203 G>A maps to NM_005144.4 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr8:21984958 G>T maps to NM_005144.4 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr8:21984859 G>C maps to NM_005144.4 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:21973257 G>A maps to NM_005144.4 F1175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr8:21982911 G>A maps to NM_005144.4 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:21978727 G>A maps to NM_005144.4 S739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:21985021 T>C maps to NM_005144.4 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:21977324 G>A maps to NM_005144.4 L975L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr8:21985246 G>A maps to NM_005144.4 H236H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:21976782 G>A maps to NM_005144.4 H997H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:192988398 C>T maps to NM_020386.3 R138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr3:192973510 C>T maps to NM_020386.3 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr3:192973510 C>T maps to NM_020386.3 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:63327631 C>A maps to NM_017878.1 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:63325899 C>T maps to NM_017878.1 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:63233674 C>T maps to NM_054108.3 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr11:63233659 G>A maps to NM_054108.3 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:63233659 G>A maps to NM_054108.3 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:63231067 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:63230975 C>T maps to NM_054108.3 *280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:63235894 G>A maps to NM_054108.3 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr11:63235894 G>A maps to NM_054108.3 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr11:63233659 G>A maps to NM_054108.3 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:63257785 T>C maps to NM_054108.3 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:63230975 C>T maps to NM_054108.3 *280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr19:49657462 C>T maps to NM_002152.2 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr19:49657366 C>T maps to NM_002152.2 E376E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr19:49657030 C>T maps to NM_002152.2 K488K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:49658203 C>T maps to NM_002152.2 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:49658452 C>T maps to NM_002152.2 W14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr3:186386821 C>T maps to NM_000412.2 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr3:186390649 C>T maps to NM_000412.2 H211H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:186395140 C>T maps to NM_000412.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:186392939 G>A maps to NM_000412.2 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr3:186395573 C>T maps to NM_000412.2 Q494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr3:186390583 G>A maps to NM_000412.2 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:186389427 C>T maps to NM_000412.2 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr3:11300947 C>T maps to NM_001098211.1 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr3:11301469 G>A maps to NM_001098211.1 K249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:11301226 C>T maps to NM_001098211.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:11301715 C>T maps to NM_001098211.1 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:11301955 G>A maps to NM_001098211.1 R411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr3:11301940 C>T maps to NM_001098211.1 H406H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:11301037 C>T maps to NM_001098211.1 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:11301358 G>A maps to NM_001098211.1 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr3:11300881 G>A maps to NM_001098211.1 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:11301358 G>A maps to NM_001098211.1 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:11301397 G>A maps to NM_001098211.1 E225E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:11301412 C>T maps to NM_001098211.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:11302086 G>A maps to NM_001098211.1 W455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr5:175110685 C>T maps to NM_001131055.1 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:175110436 C>T maps to NM_001131055.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr5:175111210 C>T maps to NM_001131055.1 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:175110673 C>T maps to NM_001131055.1 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:175111262 C>T maps to NM_001131055.1 Q343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr20:60794873 G>C maps to ENST00000317393 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:60791571 C>T maps to ENST00000317393 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr18:22048791 C>T maps to NM_021624.3 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr18:22056886 A>G maps to NM_021624.3 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr18:22057249 G>A maps to NM_021624.3 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:152187840 G>A maps to NM_001009931.1 S2088S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:152188089 T>C maps to NM_001009931.1 Q2005Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:152191365 G>A maps to NM_001009931.1 S913S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:152187519 G>A maps to NM_001009931.1 S2195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr1:152187879 T>G maps to NM_001009931.1 S2075S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:152188449 A>G maps to NM_001009931.1 T1885T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:152192666 G>A maps to NM_001009931.1 Q480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:152192217 G>A maps to NM_001009931.1 T629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:152188314 G>A maps to NM_001009931.1 S1930S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:152195618 C>T maps to NM_001009931.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:152191499 G>A maps to NM_001009931.1 Q869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:152185556 G>A maps to NM_001009931.1 Q2850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:152195624 T>C maps to NM_001009931.1 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:152192058 G>A maps to NM_001009931.1 S682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr1:152192184 G>A maps to NM_001009931.1 G640G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:152192202 G>A maps to NM_001009931.1 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:152185755 G>A maps to NM_001009931.1 S2783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr1:152188038 T>A maps to NM_001009931.1 A2022A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:152188254 G>A maps to NM_001009931.1 S1950S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:152188065 G>A maps to NM_001009931.1 S2013S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr1:152188317 G>C maps to NM_001009931.1 G1929G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:99118529 G>A maps to NM_005836.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:20824492 G>A maps to NM_022460.3 D261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:20838368 G>A maps to NM_022460.3 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr2:20818979 G>A maps to NM_022460.3 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:87570255 C>T maps to NM_012262.3 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr1:87380799 G>A maps to NM_012262.3 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:87570168 T>C maps to NM_012262.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:11401110 G>T maps to NM_005114.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:11400738 G>A maps to NM_005114.2 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:11400738 G>A maps to NM_005114.2 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr4:11401167 T>C maps to NM_005114.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr4:11401323 C>T maps to NM_005114.2 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:11401008 G>A maps to NM_005114.2 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr4:11401532 T>A maps to NM_005114.2 K33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr4:11401008 G>A maps to NM_005114.2 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr4:11401557 C>T maps to NM_005114.2 E24E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:11401212 G>A maps to NM_005114.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr16:22926814 C>T maps to NM_006043.1 R346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr16:22826333 C>T maps to NM_006043.1 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr16:22826359 G>A maps to NM_006043.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr16:22926570 C>T maps to NM_006043.1 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:22926336 G>A maps to NM_006043.1 E186E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:22926711 C>T maps to NM_006043.1 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr16:22926459 C>T maps to NM_006043.1 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr16:22826269 G>A maps to NM_006043.1 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:13400101 G>A maps to NM_006042.1 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:13503903 C>G maps to NM_006042.1 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:13400017 G>A maps to NM_006042.1 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:13400098 G>A maps to NM_006042.1 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr17:13399546 C>T maps to NM_006042.1 Q396Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:13503903 C>T maps to NM_006042.1 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:14248404 C>T maps to NM_006041.1 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:14248380 C>T maps to NM_006041.1 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr17:14205242 G>A maps to NM_006041.1 Q136Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr16:26147484 G>A maps to NM_006040.2 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr16:26147379 C>T maps to NM_006040.2 F394F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr16:26147191 C>T maps to NM_006040.2 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:26147154 G>A maps to NM_006040.2 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr16:26147109 G>A maps to NM_006040.2 K304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr16:26147373 G>A maps to NM_006040.2 K392K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:26147238 C>T maps to NM_006040.2 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:26147238 C>T maps to NM_006040.2 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr16:26147139 G>T maps to NM_006040.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr16:26147313 G>A maps to NM_006040.2 Q372Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr16:26147067 C>T maps to NM_006040.2 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:26147202 C>T maps to NM_006040.2 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:26147235 T>A maps to NM_006040.2 Y346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:26147539 C>T maps to NM_006040.2 Q448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr16:26147283 G>A maps to NM_006040.2 V362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr6:114378924 C>T maps to NM_153612.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:114378855 C>T maps to NM_153612.3 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr6:114378504 A>G maps to NM_153612.3 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr6:114379320 C>T maps to NM_153612.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr6:114378687 G>A maps to NM_153612.3 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr6:114378654 C>T maps to NM_153612.3 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:114378681 C>T maps to NM_153612.3 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:1961656 C>T maps to ENST00000454677 Q360Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:129026035 G>A maps to NM_004807.2 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr2:129026428 G>A maps to NM_004807.2 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr23:131762533 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:131762735 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:131762478 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:131762654 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:131762505 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr13:97484833 C>T maps to NM_153456.2 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr13:97485322 G>A maps to NM_153456.2 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr13:97484826 G>A maps to NM_153456.2 W264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr13:97484743 G>A maps to NM_153456.2 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr13:97485241 C>T maps to NM_153456.2 F402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr13:97484818 G>A maps to NM_153456.2 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:97484998 C>T maps to NM_153456.2 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:97485044 C>T maps to NM_153456.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr13:97485151 C>T maps to NM_153456.2 F372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr22:29139950 C>T maps to NM_172002.3 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr22:29139938 C>T maps to NM_172002.3 H102H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:5685009 G>A maps to NM_198706.1 Q28Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:5687363 G>A maps to NM_198706.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr17:40705283 G>A maps to NM_000413.2 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:53460831 C>T did not map to a codon.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr23:53458991 C>T did not map to a codon.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr4:88258514 G>A maps to NM_016245.3 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr11:43819885 G>A maps to NM_016142.2 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:88235054 G>A maps to NM_178135.3 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:88231450 G>T maps to NM_178135.3 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr4:88243984 G>A maps to NM_178135.3 I3I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:88235021 G>A maps to NM_178135.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:88243951 G>A maps to NM_178135.3 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:88243984 G>A maps to NM_178135.3 I3I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:49334993 C>T maps to NM_016246.2 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:49337583 G>A maps to NM_016246.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:82124622 C>T maps to NM_002153.2 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:82069200 T>C maps to NM_002153.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:82101928 G>A maps to NM_002153.2 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr16:82131704 G>A maps to NM_002153.2 W276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:82131752 G>A maps to NM_002153.2 Q292Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:82131917 G>A maps to NM_002153.2 W347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr9:99015187 C>T maps to NM_000197.1 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:99064371 C>T maps to NM_000197.1 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr9:99013702 G>A maps to NM_000197.1 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr5:118835026 C>T maps to NM_000414.3 Q330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr12:57167845 G>A maps to NM_003725.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44R-06A-41D-A25O-08 chr1:162762535 A>G maps to NM_016371.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr1:162769627 C>T maps to NM_016371.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:162767624 C>T maps to NM_016371.2 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:162767625 C>T maps to NM_016371.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:33173924 C>T maps to NM_014234.3 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:120056907 C>T maps to ENST00000235547 Y256Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:120057021 T>G maps to ENST00000235547 Y294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:120057060 C>T maps to ENST00000235547 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:120056761 C>T maps to ENST00000235547 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:120056586 G>A maps to ENST00000235547 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:120056667 G>A maps to ENST00000235547 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:120056997 G>A maps to ENST00000235547 W286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:120056925 G>A maps to ENST00000235547 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:119965008 C>T maps to NM_000198.3 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:119964867 C>T maps to NM_000198.3 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:119964987 C>T maps to NM_000198.3 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr1:119964636 G>A maps to NM_000198.3 W171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:119964531 C>T maps to NM_000198.3 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:119958095 C>T maps to NM_000198.3 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:119958173 G>A maps to NM_000198.3 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:119962182 C>T maps to NM_000198.3 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:119965158 G>A maps to NM_000198.3 W345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr16:30999284 C>T maps to NM_025193.3 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:84163305 G>A maps to NM_031463.4 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr16:84164716 G>A maps to NM_031463.4 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr8:145537688 C>A maps to NM_005526.2 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr8:145535747 C>T maps to NM_005526.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr8:145533466 C>T maps to NM_005526.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:145532614 C>T maps to NM_005526.2 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:145535765 C>T maps to NM_005526.2 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr6:122734773 C>T maps to NM_004506.3 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr21:45076492 G>A maps to NM_007031.1 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:45012193 G>A maps to NM_007031.1 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:56565287 G>A maps to NM_001080439.1 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:56536307 T>A did not map to a codon.
Sequencing variant TCGA-FS-A1YX-06A-11D-A197-08 chr17:56565263 G>A maps to NM_001080439.1 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:16268288 G>A maps to NM_032855.2 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:102550182 C>A maps to NM_001017963.2 E551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:102552568 A>T maps to NM_001017963.2 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:102605693 G>A maps to NM_001017963.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:102548766 G>A maps to NM_001017963.2 N712N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:102548619 G>A maps to NM_001017963.2 D761D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr6:44217788 C>A maps to NM_007355.2 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr6:44219203 C>T maps to NM_007355.2 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr6:44219204 C>T maps to NM_007355.2 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:44221313 T>C maps to NM_007355.2 S718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:104337626 C>T maps to NM_003299.1 Q668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:104327796 T>C maps to NM_003299.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr12:104326096 A>G maps to NM_003299.1 Q65Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:104327930 C>T maps to NM_003299.1 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr20:3722941 C>T maps to NM_052970.4 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr20:3725566 C>T maps to NM_052970.4 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:3728883 G>A maps to NM_052970.4 E232E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:3725569 G>A maps to NM_052970.4 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr20:3728910 G>A maps to NM_052970.4 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr21:15746237 G>A maps to NM_006948.4 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr21:15746246 G>A maps to NM_006948.4 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr6:31785398 C>T maps to NM_005345.5 F622F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr6:31779098 C>T maps to NM_005527.3 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:31778351 G>A maps to NM_005527.3 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:31779020 G>A maps to NM_005527.3 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:31779701 G>A maps to NM_005527.3 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:31779005 C>T maps to NM_005527.3 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr6:31779299 G>A maps to NM_005527.3 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:31778336 C>T maps to NM_005527.3 R471R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:31778459 G>A maps to NM_005527.3 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:31778531 C>T maps to NM_005527.3 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr14:65008496 C>T maps to NM_021979.3 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr14:65008502 C>T maps to NM_021979.3 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:65008859 C>T maps to NM_021979.3 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:132412461 C>T maps to NM_002154.3 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:128732670 C>T maps to ENST00000438626 I516I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr4:128717041 T>G maps to ENST00000438626 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:161496361 C>T maps to NM_002155.3 I638I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:122929031 C>T maps to NM_006597.3 K561K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:122930712 G>A maps to NM_006597.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr5:137906797 G>A maps to NM_004134.6 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:111784381 C>T maps to NM_001541.3 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr11:111784564 C>T maps to NM_001541.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr11:111784510 T>A maps to NM_001541.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:53751876 C>T maps to NM_006308.2 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr5:53751780 T>A maps to NM_006308.2 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:16342140 G>A maps to ENST00000375714 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:119631581 G>A maps to NM_014365.2 Q170Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr12:119617326 C>G maps to NM_014365.2 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:119631575 T>G maps to NM_014365.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:119631569 C>T maps to NM_014365.2 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr12:119617290 C>T maps to NM_014365.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr3:122474148 G>A maps to NM_024610.4 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr19:55789054 G>A maps to NM_012267.4 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr19:55789055 G>A maps to NM_012267.4 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr19:55776707 G>A maps to NM_012267.4 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr1:22157779 G>A maps to NM_005529.5 I3830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CE-06A-11D-A19A-08 chr1:22178170 G>A maps to NM_005529.5 P2342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:22216495 G>A maps to NM_005529.5 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:22203097 G>A maps to NM_005529.5 F911F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr1:22202147 G>A maps to NM_005529.5 S1092S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:22163356 G>A maps to NM_005529.5 L3431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:22176662 G>A maps to NM_005529.5 V2439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr1:22214553 G>A maps to NM_005529.5 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:22159010 G>A maps to NM_005529.5 L3728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:22204952 G>A maps to NM_005529.5 Q864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:22168861 G>T maps to NM_005529.5 S2974S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:22151092 G>C maps to NM_005529.5 P4227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:22159031 G>A maps to NM_005529.5 P3721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr1:22183634 G>A maps to NM_005529.5 T1816T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:22203097 G>A maps to NM_005529.5 F911F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:22169277 G>A maps to NM_005529.5 L2965L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:22188578 G>A maps to NM_005529.5 F1590F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:22214012 C>T maps to NM_005529.5 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:22175422 G>A maps to NM_005529.5 V2516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:22178047 G>A maps to NM_005529.5 V2383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr1:22158150 G>A maps to NM_005529.5 T3782T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:22169904 G>A maps to NM_005529.5 N2881N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr1:22176927 G>A maps to NM_005529.5 R2408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:22173090 G>A maps to NM_005529.5 A2722A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:22207307 G>A maps to NM_005529.5 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:22157779 G>A maps to NM_005529.5 I3830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:22157998 G>A maps to NM_005529.5 D3803D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:22182403 G>A maps to NM_005529.5 A1859A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:22205509 G>A maps to NM_005529.5 C816C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:22211864 G>A maps to NM_005529.5 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:22204956 G>A maps to NM_005529.5 P862P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:22202222 G>A maps to NM_005529.5 P1067P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr13:31711577 G>A maps to NM_006644.2 G818G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr13:31722560 A>G maps to NM_006644.2 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:20404708 C>T maps to NM_001098520.1 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:135593941 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:135593835 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr23:135593637 T>C did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:135582920 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:135591302 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr23:135584968 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr23:135586610 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:135593647 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:135581895 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:135582916 C>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:135592348 C>G did not map to a codon.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr23:135593318 C>T did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr23:135582868 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:70920058 G>A maps to NM_002159.2 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr5:63256408 G>A maps to NM_000524.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:63256337 G>A maps to NM_000524.2 F403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:63256841 C>T maps to NM_000524.2 K235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr5:63257241 C>T maps to NM_000524.2 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:63256577 C>T maps to NM_000524.2 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr5:63257241 C>T maps to NM_000524.2 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:63257039 G>A maps to NM_000524.2 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:63256643 G>A maps to NM_000524.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:63256577 C>T maps to NM_000524.2 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:63256910 C>T maps to NM_000524.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr5:63256523 C>T maps to NM_000524.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:63256304 G>A maps to NM_000524.2 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:63256379 G>A maps to NM_000524.2 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:63256408 G>A maps to NM_000524.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:63257111 C>T maps to NM_000524.2 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr5:63256278 C>T maps to NM_000524.2 *423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr6:78172691 G>A maps to NM_000863.1 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:78172712 G>A maps to NM_000863.1 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:78172484 G>A maps to NM_000863.1 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr6:78172886 C>T maps to NM_000863.1 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:23519748 G>A maps to NM_000864.4 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:23520334 G>A maps to NM_000864.4 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:23519644 G>T maps to NM_000864.4 Y356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:23519779 G>A maps to NM_000864.4 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:23520592 G>A maps to NM_000864.4 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:23519806 G>A maps to NM_000864.4 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:23519779 G>A maps to NM_000864.4 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:23520109 G>A maps to NM_000864.4 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:23520475 G>A maps to NM_000864.4 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr6:87725540 C>T maps to NM_000865.2 H163H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:87725390 C>T maps to NM_000865.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:87725873 C>T maps to NM_000865.2 H274H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:87725312 C>T maps to NM_000865.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr6:87725843 G>A maps to NM_000865.2 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr6:87725480 C>T maps to NM_000865.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:87725777 C>T maps to NM_000865.2 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr6:87725507 C>T maps to NM_000865.2 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:87725381 C>T maps to NM_000865.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr6:87725523 C>T maps to NM_000865.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr6:87725330 C>T maps to NM_000865.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:87725214 C>T maps to NM_000865.2 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr6:87725903 C>A maps to NM_000865.2 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:87725214 C>T maps to NM_000865.2 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:87725507 C>T maps to NM_000865.2 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:87726036 C>T maps to NM_000865.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:87725855 C>T maps to NM_000865.2 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr3:88040273 C>T maps to NM_000866.3 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr3:88040196 C>T maps to NM_000866.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:88040348 A>T maps to NM_000866.3 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:88040540 G>A maps to NM_000866.3 K214K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:88039931 G>A maps to NM_000866.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:88040765 G>A maps to NM_000866.3 R289R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D3-A2J8-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr13:47466723 C>T maps to NM_000621.3 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr13:47469887 G>A maps to NM_000621.3 R52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr13:47469825 C>T maps to NM_000621.3 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:47409367 G>A maps to NM_000621.3 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:47409493 C>T maps to NM_000621.3 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr13:47466612 G>A maps to NM_000621.3 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr13:47409283 G>A maps to NM_000621.3 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr13:47409562 C>T maps to NM_000621.3 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr13:47466684 C>T maps to NM_000621.3 W151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr2:231973941 C>T maps to NM_000867.4 Q245Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:231973838 T>A maps to NM_000867.4 K280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr2:231973407 C>T maps to NM_000867.4 E423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr23:114141516 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:114082661 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:114141162 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:114141242 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr23:114141363 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:114141939 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:114082604 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:114141242 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:114141516 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:114141389 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:114141242 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:114141203 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:114141607 T>A did not map to a codon.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr23:114141215 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:113961377 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:114141185 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:114141463 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:113965818 G>C did not map to a codon.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr23:114141467 A>G did not map to a codon.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr23:114082715 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr23:114141185 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr23:114141242 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:114141765 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:114141189 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:114141203 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:114082605 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:114141635 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr11:113857656 C>T maps to NM_213621.3 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:113852010 C>T maps to NM_213621.3 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr11:113849953 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:113860274 G>A maps to NM_213621.3 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:113860196 C>T maps to NM_213621.3 N421N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr11:113848643 G>A maps to NM_213621.3 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr11:113816708 C>T maps to NM_006028.3 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:113802574 C>T maps to NM_006028.3 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:113802505 G>A maps to NM_006028.3 W95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:113815349 C>T maps to NM_006028.3 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:113802128 G>A maps to NM_006028.3 K79K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:113803685 G>A maps to NM_006028.3 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:113815358 C>T maps to NM_006028.3 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr3:183777965 G>A maps to NM_130770.2 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:183777763 G>T maps to NM_130770.2 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:183773111 C>T maps to NM_130770.2 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:183774773 C>T maps to NM_130770.2 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:183777625 C>T maps to NM_130770.2 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:183777965 G>A maps to NM_130770.2 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:183778094 C>T maps to NM_130770.2 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:183778091 C>T maps to NM_130770.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:183756206 C>T maps to NM_001145143.1 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:183756206 C>T maps to NM_001145143.1 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:183756735 C>T maps to NM_001145143.1 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr3:183823755 C>T maps to NM_182589.2 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:183818414 C>T maps to NM_182589.2 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:183823659 G>A maps to NM_182589.2 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr3:183823941 C>T maps to NM_182589.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:183823976 C>T maps to NM_182589.2 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:183823956 C>T maps to NM_182589.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:183823755 C>T maps to NM_182589.2 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:183818294 C>T maps to NM_182589.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr3:183818417 G>A maps to NM_182589.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:183818288 C>T maps to NM_182589.2 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:183822694 C>T maps to NM_182589.2 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr5:147889409 A>G maps to NM_001040173.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:147928280 G>A maps to NM_001040173.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:147928262 C>T maps to NM_001040173.2 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:147928409 G>A maps to NM_001040173.2 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr5:147889485 G>A maps to NM_001040173.2 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:147830768 T>C maps to NM_001040169.2 E381E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr5:147889179 G>A maps to NM_001040173.2 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:147863900 C>T maps to NM_001040173.2 W373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr5:147889203 G>A maps to NM_001040173.2 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:147889194 G>A maps to NM_001040173.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr7:154876079 G>A maps to NM_024012.2 W319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:154876076 C>T maps to NM_024012.2 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:154876043 C>T maps to NM_024012.2 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:154876128 C>T maps to NM_024012.2 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr7:154875938 G>A maps to NM_024012.2 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:154863310 G>A maps to NM_024012.2 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:154876091 C>T maps to NM_024012.2 F323F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A2MS-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:154876091 C>T maps to NM_024012.2 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr7:154863262 C>T maps to NM_024012.2 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr7:154876079 G>A maps to NM_024012.2 W319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr7:154876004 C>T maps to NM_024012.2 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr7:154876070 C>T maps to NM_024012.2 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:154862650 C>T maps to NM_024012.2 T14T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-FW-A3TU-06A-11D-A23B-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:20005139 G>A maps to NM_000871.1 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:20005186 G>A maps to NM_000871.1 W281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:20005187 G>A maps to NM_000871.1 W281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr1:19992782 G>A maps to NM_000871.1 Q179Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr10:92508945 G>A maps to NM_019859.3 N315N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:92509191 G>A maps to NM_019859.3 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:92509302 C>T maps to NM_019859.3 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr10:92509228 C>T maps to NM_019859.3 W221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr10:92509350 C>T maps to NM_019859.3 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:92509248 G>A maps to NM_019859.3 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:92502256 C>T maps to NM_019859.3 K474K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr10:92509302 C>T maps to NM_019859.3 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr10:124266316 C>T maps to NM_002775.4 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr10:124266379 C>T maps to NM_002775.4 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr10:124271521 C>T maps to NM_002775.4 F405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr10:124266316 C>T maps to NM_002775.4 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:124249006 G>A maps to NM_002775.4 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr4:8304193 G>A maps to NM_053044.3 W352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr4:8293164 C>T maps to NM_053044.3 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:8307706 C>T maps to NM_053044.3 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr4:8293173 C>T maps to NM_053044.3 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr4:8288467 C>T maps to NM_053044.3 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:38839221 C>T maps to NM_153692.3 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr8:38845472 C>T maps to NM_153692.3 H429H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:38832574 G>A maps to NM_153692.3 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr8:38845589 G>A maps to NM_153692.3 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr4:3129174 C>T maps to NM_002111.6 I529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr4:3213789 C>T maps to NM_002111.6 L2183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:3189421 C>T maps to NM_002111.6 A1678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr4:3210517 C>T maps to NM_002111.6 S2057S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44R-06A-41D-A25O-08 chr4:3123133 T>C maps to NM_002111.6 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr4:3225269 G>A maps to NM_002111.6 L2536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:3134592 G>A maps to NM_002111.6 K816K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:3215734 C>T maps to NM_002111.6 L2275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr4:3123100 C>T maps to NM_002111.6 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr4:3213789 C>T maps to NM_002111.6 L2183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:3201561 C>T maps to NM_002111.6 S1824S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr4:3123106 T>C maps to NM_002111.6 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:3174061 C>T maps to NM_002111.6 L1294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:3235074 C>T maps to NM_002111.6 I2817I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr4:3234954 C>T maps to NM_002111.6 P2777P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr4:3208637 C>T maps to NM_002111.6 F2001F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:3221982 C>T maps to NM_002111.6 F2439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:3117818 C>T maps to NM_002111.6 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:3221982 C>T maps to NM_002111.6 F2439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr4:3134344 C>T maps to NM_002111.6 R765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:3227430 C>T maps to NM_002111.6 P2603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:3109018 C>T maps to NM_002111.6 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr4:3240314 C>T maps to NM_002111.6 F3011F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr4:3210517 C>T maps to NM_002111.6 S2057S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:3101016 C>T maps to NM_002111.6 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:3101049 C>T maps to NM_002111.6 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:3174070 C>T maps to NM_002111.6 L1297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:3174735 C>T maps to NM_002111.6 S1348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:3180141 C>T maps to NM_002111.6 I1527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:3188391 C>T maps to NM_002111.6 S1645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:3214417 C>T maps to NM_002111.6 F2252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr4:3230355 C>T maps to NM_002111.6 S2621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr21:33362476 C>T maps to NM_014586.1 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr21:33318447 G>A maps to NM_014586.1 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr21:33371034 C>T maps to NM_014586.1 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr21:33371422 C>T maps to NM_014586.1 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:33318441 C>T maps to NM_014586.1 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr21:33371037 C>T maps to NM_014586.1 F562F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr7:48007429 G>A maps to NM_004507.2 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr23:53617392 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr23:53674317 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr23:53592177 T>C did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:53595717 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:53575229 A>T did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr23:53652120 G>C did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:53565955 G>A did not map to a codon.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr23:53643933 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:53563539 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:53600724 A>G did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:53654415 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:53564553 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr23:53631698 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:53581757 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:53622155 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:53566727 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:53616538 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:53600920 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:53621487 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:53566767 C>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:53654435 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:53619422 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:53576161 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:53654424 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:53573411 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:53642792 T>G did not map to a codon.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr23:53576270 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:53652211 C>G did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:53585693 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:53642793 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:53581618 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr23:53620470 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr23:53577632 T>C did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:53610869 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:53613786 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:53617455 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:53630442 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:53657951 C>T did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr23:53563558 G>A did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:53573713 T>C did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:53611301 T>C did not map to a codon.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr12:111088038 C>T maps to NM_001040107.1 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:111098995 C>T maps to NM_001040107.1 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:111089094 G>A maps to NM_001040107.1 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:111099115 C>T maps to NM_001040107.1 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:50355823 G>A maps to NM_033158.4 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:50355942 G>A maps to NM_033158.4 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr7:123509070 C>T maps to NM_012269.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr7:123508935 C>T maps to NM_012269.2 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:123509187 G>A maps to NM_012269.2 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:123509238 A>G maps to NM_012269.2 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:123509271 C>T maps to NM_012269.2 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr7:123509271 C>T maps to NM_012269.2 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:123514849 C>T maps to NM_012269.2 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:123516851 G>A maps to NM_012269.2 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr16:70871610 C>T maps to NM_032821.2 G4407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr16:70889125 G>A maps to NM_032821.2 F4115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr16:71127814 G>A maps to NM_032821.2 R451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:70954604 C>T maps to NM_032821.2 G2557G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:71218806 G>A maps to NM_032821.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:70897081 G>A maps to NM_032821.2 F3824F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:70986509 G>A maps to NM_032821.2 V2114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr16:71103193 G>C maps to NM_032821.2 R650R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr16:70852319 C>T maps to NM_032821.2 S4860S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr16:70995864 G>A maps to NM_032821.2 Q1988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:71209533 G>A maps to NM_032821.2 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr16:70972584 G>A maps to NM_032821.2 A2308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr16:70926269 G>A maps to NM_032821.2 R3136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr16:71012906 C>T maps to NM_032821.2 R1515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr16:71015378 G>A maps to NM_032821.2 I1474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr16:70841836 G>A maps to NM_032821.2 I5003I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:70841527 C>T maps to NM_032821.2 E5106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:70908798 C>T maps to NM_032821.2 E3526E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:70954574 G>A maps to NM_032821.2 F2567F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr16:70954577 G>A maps to NM_032821.2 P2566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:70852310 G>A maps to NM_032821.2 F4863F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:70908325 C>T maps to NM_032821.2 E3609E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr16:71015378 G>A maps to NM_032821.2 I1474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr16:70896140 G>A maps to NM_032821.2 Q3862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:70895991 G>A maps to NM_032821.2 S3911S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:70916793 G>A maps to NM_032821.2 F3327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:70866800 G>A maps to NM_032821.2 L4616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:70841803 G>A maps to NM_032821.2 I5014I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:71026019 G>A maps to NM_032821.2 I1246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:71220704 G>A maps to NM_032821.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr16:70863535 C>T maps to NM_032821.2 E4698E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr16:71015452 G>A maps to NM_032821.2 Q1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:71127752 C>T maps to NM_032821.2 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr16:70954781 C>T maps to NM_032821.2 Q2498Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:71054097 G>A maps to NM_032821.2 S1103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:70954574 G>A maps to NM_032821.2 F2567F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:71012906 C>T maps to NM_032821.2 R1515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:70972644 C>T maps to NM_032821.2 K2288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:71218767 C>T maps to NM_032821.2 K87K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr16:70884482 C>T maps to NM_032821.2 K4172K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:70884500 C>T maps to NM_032821.2 L4166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:70926326 G>A maps to NM_032821.2 V3117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr16:70891770 G>A maps to NM_032821.2 I4043I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:71212845 C>T maps to NM_032821.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:70891682 G>A maps to NM_032821.2 L4073L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:70889125 G>A maps to NM_032821.2 F4115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr16:71218875 G>A maps to NM_032821.2 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr16:70972626 C>T maps to NM_032821.2 E2294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:70841626 G>A maps to NM_032821.2 I5073I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:70852283 G>A maps to NM_032821.2 I4872I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:71061498 C>T maps to NM_017558.3 R1016R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr16:71015462 G>A maps to NM_032821.2 I1446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr16:70977819 G>A maps to NM_032821.2 I2187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr16:70977756 G>A maps to NM_032821.2 L2208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr16:71015354 G>A maps to NM_032821.2 I1482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr16:71218809 C>T maps to NM_032821.2 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr16:70935002 C>T maps to NM_032821.2 L2983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:71103367 G>A maps to NM_032821.2 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:70998634 C>T maps to NM_032821.2 E1927E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr16:70954535 C>T maps to NM_032821.2 W2580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr16:70843822 G>A maps to NM_032821.2 Q4915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr16:71163557 G>A maps to NM_032821.2 F404F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:70841824 G>A maps to NM_032821.2 L5007L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:70871757 G>A maps to NM_032821.2 L4358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:70928353 G>A maps to NM_032821.2 F3081F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:71025229 C>T maps to NM_032821.2 V1285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:71025258 C>A maps to NM_032821.2 E1276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:71096191 G>A maps to NM_032821.2 P752P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:71103355 G>A maps to NM_032821.2 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:71163628 G>A maps to NM_032821.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:70908241 G>A maps to NM_032821.2 I3637I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:70954535 C>T maps to NM_032821.2 W2580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:71026019 G>A maps to NM_032821.2 I1246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:70897081 G>A maps to NM_032821.2 F3824F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:70926314 G>A maps to NM_032821.2 F3121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:70977741 G>A maps to NM_032821.2 L2213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr16:70954931 G>A maps to NM_032821.2 P2448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr1:43916980 T>A maps to NM_001190880.1 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr11:125769685 G>A maps to NM_001134793.1 Q141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:118925729 G>A maps to NM_001130991.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr11:118925229 C>T maps to NM_001130991.1 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:9621461 C>T maps to NM_001039613.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr9:95003156 A>G maps to ENST00000375660 C1090C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:95003198 G>A maps to ENST00000375660 S1076S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:95007261 A>G maps to ENST00000375660 F963F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:95021261 G>A maps to ENST00000375660 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr9:95048111 G>A maps to ENST00000375660 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:95004507 G>A maps to ENST00000375660 T1037T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr9:95021280 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:220267773 C>T maps to NM_018060.3 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr1:220275522 T>C maps to NM_018060.3 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:220316322 T>A maps to NM_018060.3 T866T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:220315267 C>T maps to NM_018060.3 F846F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:220298680 G>A maps to NM_018060.3 E581E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:220267641 C>T maps to NM_018060.3 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr4:88731792 G>A maps to NM_004967.3 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr4:88731889 T>C maps to NM_004967.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:88732863 G>A maps to NM_004967.3 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:88732725 C>T maps to NM_004967.3 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr4:88732572 G>A maps to NM_004967.3 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:82924512 G>A maps to NM_015525.2 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr6:82891738 A>T maps to NM_015525.2 S1194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:8167581 G>A maps to ENST00000422063 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:8181421 G>A maps to ENST00000422063 Q339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:8258069 G>A maps to ENST00000422063 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:8198254 T>A maps to ENST00000422063 K203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:8167501 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr7:8258107 G>A maps to ENST00000422063 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:8167709 G>A maps to ENST00000422063 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:8183560 C>T maps to ENST00000422063 E282E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:8196820 C>T maps to ENST00000422063 E243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:203690475 A>G maps to NM_138468.4 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:203693695 G>A maps to NM_138468.4 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr2:203693723 G>A maps to NM_138468.4 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr19:10394748 C>T maps to NM_000201.2 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr19:10394749 C>T maps to NM_000201.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr19:10394277 C>T maps to NM_000201.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:10395215 C>T maps to NM_000201.2 Q355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:62081229 G>A maps to NM_001099789.1 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr17:62080232 C>T maps to NM_001099789.1 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:62081207 G>A maps to NM_001099789.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:62082515 G>A maps to NM_001099789.1 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr19:10449496 G>A maps to NM_002162.3 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:10446488 C>T maps to NM_002162.3 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr19:10398008 G>A maps to NM_001544.3 W107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:10397702 C>T maps to NM_001544.3 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:10397993 C>T maps to NM_001544.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:10398443 C>T maps to NM_001544.3 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr19:10397969 G>A maps to NM_001544.3 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:10404812 G>A maps to NM_003259.3 Q603Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr6:52876950 G>T maps to NM_016513.4 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:52902751 G>A maps to NM_016513.4 N47N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr6:52905944 G>A maps to NM_016513.4 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr21:45657026 G>A maps to ENST00000400379 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr21:45656888 G>A maps to ENST00000400379 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr21:45655425 G>A maps to ENST00000400379 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:73016678 C>T maps to NM_001545.1 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CF-06A-11D-A196-08 chr2:8822643 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:8822543 C>T maps to NM_002166.4 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr10:94267331 C>T maps to NM_004969.3 K415K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr10:94223752 G>A maps to NM_004969.3 I832I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:94230031 G>A maps to NM_004969.3 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr10:94297303 G>A maps to NM_004969.3 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr10:94291657 G>A maps to NM_004969.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr10:94268590 G>A maps to NM_004969.3 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:94220953 G>A maps to NM_004969.3 F939F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:209101889 C>T maps to NM_005896.2 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:209110040 A>G did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr2:209108281 A>G maps to NM_005896.2 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5KH-06A-11D-A27K-08 chr2:209106742 G>A maps to NM_005896.2 D275D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr23:153053382 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:153055702 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:153055696 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:153056284 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr23:153055230 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:153053349 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:153053350 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:153052285 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr10:1087204 C>T maps to NM_004508.2 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:1065636 C>T maps to NM_033261.2 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:1066775 C>T maps to NM_033261.2 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr8:39781070 G>A maps to NM_002164.4 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:39780166 C>T maps to NM_002164.4 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:39781028 G>A maps to NM_002164.4 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:39780106 C>T maps to NM_002164.4 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:39785652 C>T maps to NM_002164.4 F387F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:39780142 G>A maps to NM_002164.4 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr8:39785613 G>A maps to NM_002164.4 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:39785359 C>T maps to NM_002164.4 Q290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:39775452 C>T maps to NM_002164.4 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr8:39785515 C>T maps to NM_002164.4 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr8:39845388 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr8:39862882 G>A maps to NM_194294.2 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr8:39871143 C>T maps to NM_194294.2 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:39806701 G>A maps to NM_194294.2 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:39840214 G>A maps to NM_194294.2 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr8:39847323 C>T maps to NM_194294.2 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr8:39872859 C>T maps to NM_194294.2 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr8:39872817 C>T maps to NM_194294.2 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr8:39806780 C>T maps to NM_194294.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr8:39873120 G>A maps to NM_194294.2 *421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:39821155 G>A maps to NM_194294.2 W56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr8:39847323 C>T maps to NM_194294.2 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:148584858 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:148568500 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:148579811 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:148568538 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:148585714 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:148579654 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:148579786 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:148564353 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr23:148578028 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:148582538 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr4:995789 C>T maps to NM_000203.3 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:998079 C>T maps to NM_000203.3 R621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr4:995527 G>T maps to NM_000203.3 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr9:131939647 G>A maps to NM_203434.2 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:131939644 G>A maps to NM_203434.2 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:6657268 G>T maps to NM_001193457.1 R481R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:6660112 G>A maps to NM_001193457.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr1:159023441 C>T maps to ENST00000295809 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr1:158988353 C>T maps to ENST00000295809 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:94578045 C>T maps to ENST00000448882 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:94578119 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr14:94568856 C>T maps to NM_206949.2 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:94594941 G>A maps to NM_032036.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:18285848 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:79129454 C>T maps to NM_006417.4 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:79102832 C>T maps to NM_006820.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:27992927 G>A maps to NM_022873.2 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr2:163124598 G>A maps to NM_022168.2 F935F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:163124039 C>T maps to NM_022168.2 K949K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:163128857 G>A maps to NM_022168.2 L832L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:163130397 G>A maps to NM_022168.2 I787I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:163144698 T>C maps to NM_022168.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:163134737 C>T maps to NM_022168.2 W581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr2:163134153 C>T maps to NM_022168.2 R605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:163133441 A>G maps to NM_022168.2 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:163138963 G>A maps to NM_022168.2 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr10:91162511 C>T maps to NM_001548.3 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:91162362 C>T maps to NM_001548.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr10:91163357 C>T maps to NM_001548.3 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr10:91143828 C>T maps to NM_001010987.2 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:91143183 G>A maps to NM_001010987.2 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:91143252 G>A maps to NM_001010987.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:91144030 T>C maps to NM_001010987.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:91144245 G>A maps to NM_001010987.2 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:91066441 C>T maps to NM_001547.4 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr10:91099143 C>T maps to NM_001549.4 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr10:91099110 C>T maps to NM_001549.4 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr10:91177850 C>T maps to NM_012420.2 Q299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:314349 C>T maps to ENST00000328221 S65S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D3-A3MU-06A-11D-A21A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr11:320741 C>T maps to NM_021034.2 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:320714 C>T maps to NM_021034.2 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:319852 G>A maps to NM_021034.2 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:298560 C>T maps to NM_001025295.1 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:298533 G>A maps to NM_001025295.1 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:25702437 G>A maps to NM_001145728.1 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:25699393 C>T maps to NM_001145728.1 K135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:25679771 C>T maps to NM_001145728.1 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr9:21206904 C>T maps to NM_002171.1 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:21207020 G>A maps to NM_002171.1 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:21367994 G>A maps to NM_006900.3 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr9:21367910 C>T maps to NM_006900.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr9:21239421 G>A maps to NM_002172.2 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr9:21239694 G>A maps to NM_002172.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr9:21239421 G>A maps to NM_002172.2 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:21239412 G>A maps to NM_002172.2 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:21239547 C>T maps to NM_002172.2 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr9:21239365 C>T maps to NM_002172.2 *190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr9:21216872 C>T maps to NM_002173.2 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr9:21216941 G>A maps to NM_002173.2 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:21217127 G>A maps to NM_002173.2 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:21216965 G>A maps to NM_002173.2 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr9:21217121 G>A maps to NM_002173.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr9:21217031 G>A maps to NM_002173.2 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr9:21217190 C>T maps to NM_002173.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr9:21217127 G>A maps to NM_002173.2 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr9:21217199 C>T maps to NM_002173.2 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:21216836 C>T maps to NM_002173.2 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:21217064 G>A maps to NM_002173.2 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr9:21227839 T>C maps to NM_021268.2 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:21227773 G>C maps to NM_021268.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:21384899 C>T maps to NM_000605.3 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:21384863 C>T maps to NM_000605.3 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr9:21166122 G>A maps to NM_002175.2 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr9:21166050 C>T maps to NM_002175.2 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr9:21166194 G>A maps to NM_002175.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr9:21166380 G>A maps to NM_002175.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr9:21187353 G>A maps to NM_021068.2 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr9:21305032 G>A maps to NM_002169.2 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:21305015 G>A maps to NM_002169.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr9:21304742 G>A maps to NM_002169.2 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:21350397 G>A maps to NM_021002.2 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:21350613 G>A maps to NM_021002.2 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:21350529 C>G maps to NM_021002.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:21350465 G>A maps to NM_021002.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr9:21350855 G>A maps to NM_021002.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:21202134 G>A maps to NM_021057.2 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr9:21201732 C>T maps to NM_021057.2 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr9:21201912 G>A maps to NM_021057.2 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:21201732 C>T maps to NM_021057.2 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr9:21409387 C>T maps to NM_002170.3 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr21:34617307 C>A maps to NM_207585.1 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr21:34635102 T>C maps to NM_207585.1 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr21:34619115 C>T maps to NM_207585.1 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr21:34621122 C>T maps to NM_207585.1 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:21077354 G>A maps to NM_002176.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:21077759 G>A maps to NM_002176.2 Q37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr9:21077569 C>T maps to NM_002176.2 W100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr9:21481522 C>T maps to NM_176891.4 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:21481606 G>A maps to NM_176891.4 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr12:68551977 C>T maps to NM_000619.2 W59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr12:68551790 G>A maps to NM_000619.2 Q90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr12:68551713 G>A maps to NM_000619.2 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:68551692 C>T maps to NM_000619.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr21:34793891 C>T maps to ENST00000381995 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr9:21141107 C>T maps to NM_002177.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr9:21141464 C>T maps to NM_002177.1 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr9:21141194 C>T maps to NM_002177.1 Q125Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:21141503 C>A maps to NM_002177.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:21141377 C>T maps to NM_002177.1 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr7:112112284 T>C maps to NM_001007245.2 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr7:112112350 C>T maps to NM_001007245.2 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr3:50326034 C>A maps to ENST00000336089 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:50326070 G>A maps to ENST00000336089 H531H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr3:50326109 G>A maps to ENST00000336089 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr3:129195588 C>T maps to NM_052985.2 A415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr3:129185820 C>T maps to NM_052985.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:129200534 C>T maps to NM_052985.2 Q602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:129221679 C>T maps to NM_052985.2 L885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:129238472 C>T maps to NM_052985.2 R1229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:129221685 C>T maps to NM_052985.2 S887S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:129202458 C>T maps to NM_052985.2 V646V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr3:129236372 C>T maps to NM_052985.2 S1160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr3:129233369 C>T maps to NM_052985.2 I1093I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:129168725 C>T maps to NM_052985.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:129185810 C>T maps to NM_052985.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:129237966 C>T maps to NM_052985.2 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr16:1616259 G>A maps to NM_014714.3 F601F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:1574817 G>A maps to NM_014714.3 V988V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr16:1652442 G>A maps to NM_014714.3 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:1633345 G>A maps to NM_014714.3 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:1573894 G>A maps to NM_014714.3 I1068I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr16:1634238 G>A maps to NM_014714.3 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr16:1621508 G>A maps to NM_014714.3 F517F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr16:1573572 G>A maps to NM_014714.3 F1133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr16:1573572 G>A maps to NM_014714.3 F1133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr16:1568273 G>A maps to NM_014714.3 I1375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:1634337 G>A maps to NM_014714.3 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:1657261 G>A maps to NM_014714.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr2:27672392 G>A maps to NM_015662.1 F1399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:27676351 G>A maps to NM_015662.1 R1284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:27700154 G>A maps to NM_015662.1 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:27667964 G>A maps to NM_015662.1 P1692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:27676932 C>T maps to NM_015662.1 G1209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr2:27700133 A>G maps to NM_015662.1 N425N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:27672912 G>A maps to NM_015662.1 V1334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:27672906 C>A maps to NM_015662.1 L1336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:27681042 G>A maps to NM_015662.1 I975I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:27693800 A>G maps to NM_015662.1 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:37154423 G>A maps to ENST00000453009 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr11:118428545 A>C maps to NM_020153.3 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr3:107885814 G>A maps to ENST00000457963 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:107932858 G>A maps to ENST00000457963 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr3:107885735 G>A maps to ENST00000457963 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr3:107885814 G>A maps to ENST00000457963 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:107937476 A>G maps to ENST00000457963 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:26978172 G>A maps to NM_025103.2 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:160000377 C>T maps to ENST00000483754 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:159986272 A>C maps to ENST00000483754 A888A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr13:21166489 C>T maps to NM_175605.3 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr13:21217680 T>A maps to NM_175605.3 S599S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:69354581 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:69366642 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:69353832 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:69385760 G>A did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:69370140 A>C did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:69370142 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr15:65621405 C>T maps to NM_004884.3 G762G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr15:65627165 G>A maps to NM_004884.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr15:65621441 G>A maps to NM_004884.3 S750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:65622077 G>A maps to NM_004884.3 F661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:65621279 G>A maps to NM_004884.3 A804A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr15:65627725 G>A maps to NM_004884.3 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:65667549 G>A maps to NM_004884.3 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:65622906 G>A maps to NM_004884.3 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:65667615 C>T maps to NM_004884.3 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:65621883 G>A maps to NM_004884.3 P683P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:65622703 G>A maps to NM_004884.3 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr15:65621769 G>A maps to NM_004884.3 F721F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:65621417 G>A maps to NM_004884.3 G758G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:65621787 C>T maps to NM_004884.3 K715K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:65623882 C>T maps to NM_004884.3 E421E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:65623987 G>A maps to NM_004884.3 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:65627692 G>A maps to NM_004884.3 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:65625742 A>G maps to NM_004884.3 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr15:65676526 G>A maps to NM_020962.1 A1191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr15:65678270 G>A maps to NM_020962.1 P1026P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr15:65682664 G>A maps to NM_020962.1 Q746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr15:65686868 G>A maps to NM_020962.1 Q532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr15:65687480 C>T maps to NM_020962.1 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:65678962 G>A maps to NM_020962.1 I959I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:65684547 G>A maps to NM_020962.1 G682G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:102811670 G>A maps to NM_001111285.1 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:102869511 G>A maps to NM_001111285.1 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr12:102811751 C>T maps to NM_001111285.1 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:102811658 C>T maps to NM_001111285.1 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:102811670 G>A maps to NM_001111285.1 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:102869433 C>T maps to NM_001111285.1 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr15:99500478 C>T maps to NM_000875.3 P1304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:99442802 C>T maps to NM_000875.3 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:99500586 C>T maps to NM_000875.3 F1340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr15:99500541 C>T maps to NM_000875.3 A1325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr15:99251217 C>T maps to NM_000875.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr15:99491829 C>A maps to NM_000875.3 I1205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:2161475 G>A maps to NM_001127598.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr17:47119627 C>T maps to NM_006546.3 N322N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr17:47123701 C>T maps to NM_006546.3 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:47118802 G>A maps to NM_006546.3 K294K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:47123313 G>A maps to NM_006546.3 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:47115559 G>A maps to NM_006546.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:47118856 C>T maps to NM_006546.3 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr17:47126799 G>A maps to NM_006546.3 R576R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:185407216 G>A maps to NM_006548.4 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr3:185375160 G>A maps to NM_006548.4 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:185364833 G>A maps to NM_006548.4 I562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:185404969 G>A maps to NM_006548.4 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr7:23391183 T>A maps to NM_006547.2 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:23352043 C>T maps to NM_006547.2 Q559Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:23401338 G>A maps to NM_006547.2 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:23508150 T>C maps to NM_006547.2 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr6:160485502 C>T maps to NM_000876.2 C1319C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr6:160468849 C>T maps to NM_000876.2 F752F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:160471584 C>T maps to NM_000876.2 L865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:160471554 C>T maps to NM_000876.2 T855T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:160468837 C>T maps to NM_000876.2 S748S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr6:160505108 C>T maps to NM_000876.2 C1987C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:45930192 G>A maps to NM_000596.2 E132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:45930312 G>A maps to NM_000596.2 W172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr2:217526681 C>T maps to NM_000597.2 I258I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D9-A6EC-06A-11D-A30X-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:38609375 G>A maps to NM_001552.2 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:217543704 G>A maps to NM_000599.3 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr2:217543761 C>T maps to NM_000599.3 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:217543704 G>A maps to NM_000599.3 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:53495899 G>A maps to NM_002178.2 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr4:57976073 G>A maps to NM_001553.1 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr9:38413338 G>A maps to NM_001007563.1 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr9:38411537 G>A maps to NM_001007563.1 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:38411495 G>A maps to NM_001007563.1 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:46733363 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:46663974 C>T maps to NM_001002915.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:46664003 C>T maps to NM_001002915.2 P80P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-FW-A3R5-06A-11D-A23B-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:46627528 A>G maps to NM_207393.1 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:46627207 C>T maps to NM_207393.1 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:46623586 T>A maps to NM_207393.1 *126Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:46623586 T>A maps to NM_207393.1 *126Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:46543618 G>A maps to NM_001002923.1 N42N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr19:46543782 T>G maps to NM_001002923.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr1:201195138 C>T maps to NM_001164586.1 L3558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:201185594 C>T maps to NM_001164586.1 P3103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr1:201196073 G>A maps to NM_001164586.1 L3617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr1:201195153 C>T maps to NM_001164586.1 P3563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr1:201190758 G>A maps to NM_001164586.1 T3362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:201190836 T>C maps to NM_001164586.1 S3388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr1:201195174 G>A maps to NM_001164586.1 R3570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:201195165 C>T maps to NM_001164586.1 Y3567Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:201196022 G>A maps to NM_001164586.1 V3600V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:201186445 C>T maps to NM_001164586.1 I3209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:201191882 C>T maps to NM_001164586.1 L3406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr1:201195015 G>A maps to NM_001164586.1 E3517E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:201184787 G>A maps to NM_001164586.1 W3039*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr1:201184808 G>A maps to NM_001164586.1 V3046V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr1:201184793 G>A maps to NM_001164586.1 K3041K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:201185870 G>A maps to NM_001164586.1 V3195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:201185663 G>A maps to NM_001164586.1 R3126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:201194980 C>T maps to NM_001164586.1 L3506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:201184949 C>T maps to NM_001164586.1 L3093L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:68702855 C>A maps to NM_002180.2 A574A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr11:68703892 G>T maps to NM_002180.2 E649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:68704545 G>A maps to NM_002180.2 K866K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:68675727 C>T maps to NM_002180.2 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:68704051 C>T maps to NM_002180.2 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:68696732 C>T maps to NM_002180.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:68701304 C>T maps to NM_002180.2 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:68702870 C>T maps to NM_002180.2 F579F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:68704305 C>T maps to NM_002180.2 A786A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:68703903 C>T maps to NM_002180.2 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr22:23915707 G>A maps to NM_020070.2 N129N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr22:23917245 C>T maps to NM_020070.2 W77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr22:23915530 G>A maps to NM_020070.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr22:23915599 G>A maps to NM_020070.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr22:23915668 C>A maps to NM_020070.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr22:23237553 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr22:23235903 G>A maps to ENST00000410090 Q78Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr22:23237603 G>A maps to ENST00000410090 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:51828704 G>A maps to NM_001101372.1 W166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr19:51832012 G>A maps to NM_001101372.1 *337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr23:130411012 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr23:130413157 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr23:130411867 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:130419793 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:130419412 A>T did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr23:130419215 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:130409259 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:130417023 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr23:130410936 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:130409143 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:130410154 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:130412579 G>A did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:130408774 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr23:130411074 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:130409491 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:130412035 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:130417073 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr23:130412494 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:130411079 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:130413298 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:130408769 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr23:130412482 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:130408834 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:130415672 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:130409592 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:130409176 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:130419850 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr23:130416469 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr23:130408804 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:130415850 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:130416703 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:130408836 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:130419290 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:130409618 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr23:130409560 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:130419973 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:130415298 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:130412579 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:130408082 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:130412482 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:130415713 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:130415850 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:130410049 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:130409646 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:130417204 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:130409705 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:130415819 C>T did not map to a codon.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr23:130409650 G>A did not map to a codon.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr23:130410994 A>C did not map to a codon.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr23:130411845 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:130416529 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:130419328 A>C did not map to a codon.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr23:130409048 A>T did not map to a codon.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr23:130410985 C>T did not map to a codon.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr23:130411012 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:130410922 G>A did not map to a codon.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr23:130419274 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr23:130416671 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr23:130408599 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr23:130412057 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr23:130419965 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:130407849 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:130408765 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:130409572 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:130409646 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:130419273 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:130419850 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:130419918 C>T did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr23:130410928 C>T did not map to a codon.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr23:130409480 G>C did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:130408591 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:130408826 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:130408987 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:130410049 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:130412676 A>C did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:130415214 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:130415672 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr23:130410927 C>T did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:130413281 G>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:151155688 C>T maps to NM_178822.4 G2220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr3:151166394 G>A maps to NM_178822.4 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:151155253 T>G maps to NM_178822.4 P2365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr3:151171224 C>T maps to NM_178822.4 W221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:151164104 G>A maps to NM_178822.4 Q1222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:151166010 G>A maps to NM_178822.4 F586F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:151164381 G>A maps to NM_178822.4 F1129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr3:151164726 C>T maps to NM_178822.4 R1014R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:151160908 C>T maps to NM_178822.4 R1942R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:151171406 C>T maps to NM_178822.4 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:151155679 G>A maps to NM_178822.4 T2223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:151164366 G>A maps to NM_178822.4 S1134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:151164699 G>A maps to NM_178822.4 I1023I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:151165793 G>A maps to NM_178822.4 Q659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr3:151166598 C>T maps to NM_178822.4 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:151155337 C>T maps to NM_178822.4 P2337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:151166801 G>A maps to NM_178822.4 Q323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:151160962 A>G maps to NM_178822.4 G1924G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr3:151155010 A>G maps to NM_178822.4 S2446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr3:151165545 C>T maps to NM_178822.4 R741R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr3:151165674 G>A maps to NM_178822.4 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr3:151164228 T>C maps to NM_178822.4 S1180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:151155952 G>A maps to NM_178822.4 V2132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:151165860 G>A maps to NM_178822.4 T636T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:151166598 C>T maps to NM_178822.4 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:151171417 G>A maps to NM_178822.4 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:151161508 G>A maps to NM_178822.4 S1742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:151164327 T>G maps to NM_178822.4 P1147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:151164711 C>T maps to NM_178822.4 R1019R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:151176434 G>A maps to NM_178822.4 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr3:151165536 G>A maps to NM_178822.4 F744F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr3:118644972 G>A maps to NM_152538.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:118645010 G>A maps to NM_152538.2 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:118824027 C>T maps to NM_152538.2 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:118621576 G>A maps to NM_152538.2 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:18554491 C>T maps to NM_032880.4 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr1:18702855 G>A maps to NM_032880.4 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:18618376 C>T maps to NM_032880.4 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:18703911 G>A maps to NM_032880.4 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr1:18661457 G>A maps to NM_032880.4 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:18554485 G>A maps to NM_032880.4 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr1:18702886 C>T maps to NM_032880.4 Q367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:18692033 C>T maps to NM_032880.4 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr1:18618467 C>T maps to NM_032880.4 Q98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:18554491 C>T maps to NM_032880.4 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:18691826 C>T maps to NM_032880.4 H217H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr1:18688693 C>T maps to NM_032880.4 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:18554485 G>A maps to NM_032880.4 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:18702886 C>T maps to NM_032880.4 Q367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr1:18691796 G>A maps to NM_032880.4 Q207Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:18692054 G>A maps to NM_032880.4 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:18691757 C>T maps to NM_032880.4 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:18554485 G>A maps to NM_032880.4 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:18691868 C>T maps to NM_032880.4 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:18692084 C>T maps to NM_032880.4 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:18618478 G>A maps to NM_032880.4 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:18691904 G>A maps to NM_032880.4 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr11:18737027 C>T maps to NM_173588.3 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr11:18745762 C>T maps to NM_173588.3 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr11:18736058 C>T maps to NM_173588.3 K548K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:18739490 C>T maps to NM_173588.3 E320E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr11:18745705 C>T maps to NM_173588.3 Q26Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr11:18730997 C>T maps to NM_173588.3 V978V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr11:18735420 G>A maps to NM_173588.3 A691A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:117131388 C>A maps to NM_001542.2 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:117150579 G>A maps to NM_001542.2 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr1:117158956 G>A maps to NM_001542.2 Q56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr1:117122035 G>A maps to NM_001542.2 I1124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:117156497 G>A maps to NM_001542.2 Q241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr1:117146636 G>A maps to NM_001542.2 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr21:41164018 G>A maps to NM_001080444.1 K347K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr21:41151062 G>A maps to NM_001080444.1 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr21:41143005 C>T maps to NM_001080444.1 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:160062788 G>A maps to NM_052868.2 R413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr1:160062369 G>A maps to NM_052868.2 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:159897631 G>A maps to NM_001135050.1 F1092F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:159898222 C>T maps to NM_001135050.1 V985V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr1:159897983 C>T maps to NM_001135050.1 W1065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:159900974 G>A maps to NM_001135050.1 G530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:159897580 G>A maps to NM_001135050.1 S1109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:159897574 G>A maps to NM_001135050.1 L1111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:159907536 C>T maps to NM_001135050.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:159907561 C>T maps to NM_001135050.1 W105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:159912789 G>A maps to NM_001135050.1 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr1:159899998 G>A maps to NM_001135050.1 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr1:159907561 C>T maps to NM_001135050.1 W105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:159904006 C>T maps to NM_001135050.1 K359K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:159898387 G>A maps to NM_001135050.1 P930P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:159897661 C>T maps to NM_001135050.1 V1082V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:159907539 G>A maps to NM_001135050.1 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr11:133807295 G>A maps to NM_014987.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:133795855 G>A maps to NM_014987.1 F604F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:133801383 G>C maps to NM_014987.1 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:133790958 G>A maps to NM_014987.1 P887P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:133795735 G>A maps to NM_014987.1 I644I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:133791009 C>T maps to NM_014987.1 K870K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:133790169 G>A maps to NM_014987.1 P1150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:133790337 G>A maps to NM_014987.1 I1094I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:133807340 T>C maps to NM_014987.1 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr11:133790091 C>T maps to NM_014987.1 R1176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:133807325 G>A maps to NM_014987.1 C208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:133790736 G>A maps to NM_014987.1 F961F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:133790478 G>A maps to NM_014987.1 F1047F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:133790484 G>A maps to NM_014987.1 F1045F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:133800930 G>A maps to NM_014987.1 V489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:133801029 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:133790577 C>T maps to NM_014987.1 E1014E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr11:133789668 C>T maps to NM_014987.1 P1317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:133799648 G>A maps to NM_014987.1 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:219920369 G>A maps to NM_002181.3 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:219920525 C>T maps to NM_002181.3 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:219920426 G>A maps to NM_002181.3 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:140041215 G>A maps to NM_006083.3 K475K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:140039371 C>T maps to NM_006083.3 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:140035471 C>T maps to NM_006083.3 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr5:140037239 G>A maps to NM_006083.3 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr12:99028091 G>A maps to NM_201612.1 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:99007634 G>A maps to NM_201612.1 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr9:111663952 G>A maps to NM_003640.3 V621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr9:111673344 C>T maps to NM_003640.3 K435K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr9:111643997 A>G maps to NM_003640.3 P1111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr9:111640355 G>A maps to NM_003640.3 A1258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr9:111693339 T>C maps to NM_003640.3 E29E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr8:42175287 C>T maps to NM_001556.2 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr8:42175251 C>T maps to NM_001556.2 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:42174334 C>T maps to NM_001556.2 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr8:42174316 C>T maps to NM_001556.2 I340I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:42162741 C>T maps to NM_001556.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr1:206658623 C>T maps to NM_014002.3 Q533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:206652285 G>A maps to NM_014002.3 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:206648314 C>T maps to NM_014002.3 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:206651541 C>T maps to NM_014002.3 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:206658623 C>T maps to NM_014002.3 Q533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:206651604 C>T maps to NM_014002.3 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:206664989 C>T maps to NM_014002.3 F581F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:206653843 C>T maps to NM_014002.3 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:206666434 C>T maps to NM_014002.3 Q639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr7:50468262 C>T maps to NM_006060.3 Q500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:50450283 G>A maps to NM_006060.3 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:50444267 G>A maps to NM_006060.3 E66E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:50450370 G>A maps to NM_006060.3 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr7:50468177 C>T maps to NM_006060.3 F471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr7:50450403 C>T maps to NM_006060.3 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr7:50455127 C>T maps to NM_006060.3 N225N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr7:50467742 C>T maps to NM_006060.3 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr7:50459561 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:50450370 G>A maps to NM_006060.3 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:50467664 G>A maps to NM_006060.3 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr7:50444450 C>T maps to NM_006060.3 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:214012516 G>A maps to ENST00000342002 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:213872806 C>T maps to ENST00000342002 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:213921668 C>T maps to ENST00000342002 E104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr2:213872224 G>A maps to ENST00000342002 F486F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:213872263 C>T maps to ENST00000342002 Q473Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:213872632 G>A maps to ENST00000342002 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:213872100 C>A maps to ENST00000342002 E528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:213872101 C>T maps to ENST00000342002 G527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:214012510 C>T maps to ENST00000342002 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:213921626 C>T maps to ENST00000342002 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:213872704 G>A maps to ENST00000342002 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr17:37922291 G>A maps to NM_012481.3 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:37922177 C>T maps to NM_012481.3 V465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:37988404 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr17:37922132 G>A maps to NM_012481.3 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:37949025 G>A maps to NM_012481.3 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:37922396 G>A maps to NM_012481.3 N392N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:37922669 G>A maps to NM_012481.3 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:56428478 C>T maps to NM_022465.3 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr12:56428793 C>T maps to NM_022465.3 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr12:56429090 C>T maps to NM_022465.3 V578V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:56427097 G>A maps to NM_022465.3 K330K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr12:56427046 C>T maps to NM_022465.3 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:124755639 G>A maps to NM_022466.5 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:124753637 C>T maps to NM_022466.5 Q306Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr11:117869500 C>T maps to NM_001558.3 H294H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:117869644 C>T maps to NM_001558.3 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr11:117869671 G>A maps to NM_001558.3 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr11:117870007 G>A maps to NM_001558.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr11:117866367 C>T maps to NM_001558.3 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:117864126 T>A did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr21:34660439 C>T maps to NM_000628.3 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr21:34660415 C>T maps to NM_000628.3 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:55879925 G>A maps to NM_000641.2 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr9:34656777 C>T maps to NM_001142784.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr9:34658539 C>T maps to NM_001142784.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:34655247 C>T maps to NM_001142784.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:34660507 G>A maps to NM_001142784.1 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:159708098 G>A maps to NM_000882.2 K88K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:159707981 C>T maps to NM_000882.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:158743782 G>A maps to NM_002187.2 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr5:158750202 G>A maps to NM_002187.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:158750329 G>A maps to NM_002187.2 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:18192970 G>A maps to NM_005535.1 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:18186628 G>A maps to NM_005535.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr19:18193074 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:18193030 G>A maps to NM_005535.1 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr19:18177378 G>A maps to NM_005535.1 R486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr19:18177379 G>A maps to NM_005535.1 C485C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:18191768 G>A maps to NM_005535.1 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr19:18182928 G>A maps to NM_005535.1 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:18170850 G>A maps to NM_005535.1 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:18170871 C>T maps to NM_005535.1 V605V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:18182979 C>T maps to NM_005535.1 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:131995465 C>T maps to NM_002188.2 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:117900880 T>G did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:117895131 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:117900491 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:117880925 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:117880926 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:117892164 A>G did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:114251823 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:114242620 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:114244153 G>T did not map to a codon.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr23:114245314 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:114245313 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:114249074 C>T did not map to a codon.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr23:114239876 A>C did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:114248385 G>A did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr23:114251823 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:142649121 G>A maps to NM_000585.3 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr10:6005799 G>A maps to NM_002189.3 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:6002492 C>T maps to NM_002189.3 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:6008123 G>A maps to NM_002189.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr15:81578107 G>A maps to NM_172217.3 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:81585005 C>T maps to NM_172217.3 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:81592523 C>T maps to NM_172217.3 Q953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:81593825 G>A maps to NM_172217.3 V1097V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr15:81578071 C>T maps to NM_172217.3 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:81565428 A>G did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr15:81591937 C>T maps to NM_172217.3 T757T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:81598277 C>A maps to NM_172217.3 A1150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr15:81600991 C>T maps to NM_172217.3 I1284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr15:81592111 C>T maps to NM_172217.3 S815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:52054083 G>A maps to NM_002190.2 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr6:52052501 G>A maps to NM_002190.2 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr6:52052519 G>A maps to NM_002190.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr6:52052558 G>A maps to NM_002190.2 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:52052495 C>T maps to NM_002190.2 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:52052447 C>T maps to NM_002190.2 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:148754099 G>A maps to NM_014443.2 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:148756468 C>T maps to NM_014443.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:88705705 C>T maps to NM_013278.3 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:88705456 G>A maps to NM_013278.3 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr16:88705576 C>T maps to NM_013278.3 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr13:21295855 C>T maps to NM_138284.1 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:52103712 G>T maps to NM_052872.3 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:52103574 G>A maps to NM_052872.3 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44R-06A-41D-A25O-08 chr22:17589455 C>T maps to NM_014339.5 R449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr22:17583050 C>T maps to NM_014339.5 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr22:17590262 C>T maps to NM_014339.5 F718F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr22:17589782 C>T maps to NM_014339.5 Y558Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:17578718 C>T maps to NM_014339.5 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:53890991 C>T maps to NM_018725.3 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:53883696 G>A maps to NM_018725.3 W34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:9974700 G>A maps to NM_153461.2 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr3:9970148 C>T maps to NM_153461.2 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:9960202 C>T maps to NM_153461.2 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:9962212 G>A maps to NM_153461.2 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:9974646 G>A maps to NM_153461.2 R582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:9959118 C>T maps to NM_153461.2 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:57135230 G>A maps to NM_017563.3 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr3:57143634 G>A maps to NM_017563.3 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:57132257 G>A maps to NM_017563.3 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr3:57143643 C>T maps to NM_017563.3 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr3:57132038 G>A maps to NM_017563.3 F564F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:57144328 G>A maps to NM_017563.3 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:57139950 G>A maps to NM_017563.3 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:57132038 G>A maps to NM_017563.3 F564F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr3:57154293 G>A maps to NM_017563.3 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr3:9953262 C>A maps to NM_153483.2 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:9952857 G>A maps to NM_153483.2 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:9953125 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:50436141 C>T maps to NM_001001694.2 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr11:112020876 T>A maps to NM_001562.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:71711487 C>T maps to NM_001145057.1 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:103006654 G>A maps to NM_003855.2 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:102992491 C>T maps to NM_003855.2 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:102984339 G>A maps to NM_003855.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:103001404 G>A maps to NM_003855.2 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:103013021 G>A maps to NM_003855.2 E434E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:102992407 G>A maps to NM_003855.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:102992413 G>A maps to NM_003855.2 K172K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:102992416 G>A maps to NM_003855.2 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:103068421 G>A maps to NM_003853.2 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:103040387 C>G maps to NM_003853.2 S63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:103067443 C>T maps to NM_003853.2 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr2:103061795 A>G maps to NM_003853.2 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr2:103068313 C>T maps to NM_003853.2 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr2:103068353 C>T maps to NM_003853.2 Q505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr2:103068367 C>T maps to NM_003853.2 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr2:103068391 C>T maps to NM_003853.2 F517F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr2:103068481 C>T maps to NM_003853.2 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr2:103068571 G>A maps to NM_003853.2 R577R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:103040466 G>A maps to NM_003853.2 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:103063557 C>T maps to NM_003853.2 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:103067329 C>T maps to NM_003853.2 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:103068523 G>A maps to NM_003853.2 V561V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:103061690 C>T maps to NM_003853.2 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:103040380 C>T maps to NM_003853.2 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr1:207010335 C>T maps to NM_153758.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr2:113541311 C>T maps to NM_000575.3 K12K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:113532691 C>T maps to NM_000575.3 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:113535610 G>A maps to NM_000575.3 Q190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr2:113537238 G>A maps to NM_000575.3 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:113588123 C>T maps to NM_000576.2 K208K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:113588048 G>A maps to NM_000576.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:113588000 G>A maps to NM_000576.2 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:113588000 G>A maps to NM_000576.2 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr2:113588928 C>T maps to NM_000576.2 K179K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:113587991 C>T maps to NM_000576.2 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:113588898 C>T maps to NM_000576.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:113588048 G>A maps to NM_000576.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr2:113832363 C>T maps to NM_032556.4 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr2:113832940 G>A maps to NM_032556.4 *153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:113832360 G>A maps to NM_032556.4 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr2:113832865 C>T maps to NM_032556.4 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:113831959 G>A maps to NM_032556.4 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:113832844 C>T maps to NM_032556.4 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:113832372 G>A maps to NM_032556.4 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:113832844 C>T maps to NM_032556.4 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:113832844 C>T maps to NM_032556.4 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:113832327 C>T maps to NM_032556.4 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:113832853 C>T maps to NM_032556.4 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:113832840 G>A maps to NM_032556.4 W120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:113832354 C>T maps to NM_032556.4 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr2:113819752 C>A maps to NM_173170.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr2:113819744 C>T maps to NM_173170.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr2:113820094 G>A maps to NM_173170.1 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:113820064 G>A maps to NM_173170.1 K93K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr2:113820196 C>T maps to NM_173170.1 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:113817029 G>A maps to NM_173170.1 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:113818500 G>A maps to NM_173170.1 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:113763638 C>T maps to NM_014440.1 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:113765560 C>T maps to NM_014440.1 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:113763578 G>A maps to NM_014440.1 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:113765449 G>A maps to NM_014440.1 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:113765533 C>T maps to NM_014440.1 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z4-06A-11D-A197-08 chr2:113764229 G>A maps to NM_014440.1 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:113763578 G>A maps to NM_014440.1 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr2:113765560 C>T maps to NM_014440.1 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:113676136 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:113670618 G>A maps to NM_014439.3 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr2:113670618 G>A maps to NM_014439.3 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:113675275 C>T maps to NM_014439.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr2:113675350 G>A maps to NM_014439.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:113674772 C>T maps to NM_014439.3 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:113676283 G>A maps to NM_014439.3 E185E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:113676316 G>A maps to NM_014439.3 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr2:113783803 C>T maps to NM_014438.3 Q89Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:113786541 G>A maps to NM_173178.1 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:113783692 C>T maps to NM_014438.3 W126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:113780346 C>T maps to NM_014438.3 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:113785659 C>T maps to NM_173178.1 K98K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:113783713 G>A maps to NM_014438.3 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr2:113786541 G>A maps to NM_173178.1 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:113786563 G>A maps to NM_173178.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr2:113785527 C>T maps to NM_173178.1 E142E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr2:113742454 C>T maps to NM_019618.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr2:113742457 G>A maps to NM_019618.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:113742472 C>T maps to NM_019618.2 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:113736263 C>T maps to NM_019618.2 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr2:113742457 G>A maps to NM_019618.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:113736845 G>A maps to NM_019618.2 W35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr2:102789290 A>T maps to NM_000877.2 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:102793101 G>A maps to NM_000877.2 W531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:102792978 G>A maps to NM_000877.2 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:102791179 C>T maps to NM_000877.2 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr2:102791056 C>T maps to NM_000877.2 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr2:102791116 C>T maps to NM_000877.2 F354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:102793023 C>T maps to NM_000877.2 F505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:102632497 G>A maps to NM_004633.3 K166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:102626051 G>A maps to NM_004633.3 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:102638676 C>T maps to NM_004633.3 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:102626189 C>T maps to NM_004633.3 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:102644760 G>A maps to NM_004633.3 W368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:102641100 G>A maps to NM_004633.3 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr2:102632510 A>T maps to NM_004633.3 K171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:102638685 C>T maps to NM_004633.3 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:102625057 G>A maps to NM_004633.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr3:190322007 C>T maps to NM_002182.3 H52H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr23:29973352 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr23:29938180 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:29973936 A>G did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:29972764 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:29973592 G>A did not map to a codon.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr23:29301162 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:29973842 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:29973484 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr23:29959831 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr23:29973426 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:29973501 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:29301112 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:29414515 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:29938168 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:29973334 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:29973591 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:29301169 T>C did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:29973376 G>A did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:29973461 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:104961394 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:104961394 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr23:105011053 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr23:104512070 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr23:104999312 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:105011476 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr23:104440226 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:104999227 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:104999228 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:105011266 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr23:105011255 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:104728344 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr23:104512201 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:104984616 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:104440254 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr23:105011104 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:104984678 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:104512185 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:103903603 C>T did not map to a codon.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr23:105011544 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:104961432 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:105011372 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:104440362 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:104512145 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:104999238 C>T did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr23:105011434 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:104440243 A>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:104999239 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:105011255 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:105011150 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:105011255 G>A did not map to a codon.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr23:105011019 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:102964477 C>T maps to NM_016232.4 I348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:102964508 C>T maps to NM_016232.4 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:102965683 G>A maps to NM_016232.4 G421G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A2GB-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:102968275 C>T maps to NM_016232.4 S522S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:102956710 A>C maps to NM_016232.4 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:102959822 G>A maps to NM_016232.4 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:102957190 G>A maps to NM_016232.4 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:102958746 G>A maps to NM_016232.4 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:102954759 C>T maps to NM_016232.4 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr2:102957280 G>A maps to NM_016232.4 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:102956584 G>A maps to NM_016232.4 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:102964546 G>A maps to NM_016232.4 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:102957178 C>T maps to NM_016232.4 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr2:102851420 C>T maps to NM_003854.2 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr2:102805608 C>T maps to NM_003854.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:102849573 C>T maps to NM_003854.2 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr2:102818035 G>A maps to NM_003854.2 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:102849489 G>A maps to NM_003854.2 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:102849528 G>A maps to NM_003854.2 E414E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:102851525 G>A maps to NM_003854.2 E489E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:102835428 G>A maps to NM_003854.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr2:113890348 C>T maps to NM_173841.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:113885269 G>A maps to NM_173841.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:113890432 C>T maps to NM_173841.2 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:113887168 C>T maps to NM_173841.2 Q48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:113885269 G>A maps to NM_173841.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:113890348 C>T maps to NM_173841.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr4:123372939 G>A maps to NM_000586.3 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr4:123377511 C>T maps to NM_000586.3 K28K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:123374863 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:207040733 C>A maps to NM_018724.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:207039926 G>A maps to NM_018724.3 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:207039848 C>T maps to NM_018724.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:207039875 G>A maps to NM_018724.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:207041866 G>A maps to NM_018724.3 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr6:137330501 G>A maps to NM_014432.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:137338106 G>A maps to NM_014432.2 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr6:137323264 C>T maps to NM_014432.2 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:137329865 C>T maps to NM_014432.2 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr6:137322979 G>A maps to NM_014432.2 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr3:136676960 G>A maps to NM_144717.3 Q2Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:136714373 C>T maps to NM_144717.3 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr3:136729034 T>C maps to NM_144717.3 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:136710871 C>T maps to NM_144717.3 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:136701037 C>T maps to NM_144717.3 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr3:136701037 C>T maps to NM_144717.3 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:136708325 C>T maps to NM_144717.3 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr3:136714337 G>A maps to NM_144717.3 W255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:123536881 C>T maps to NM_021803.2 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr4:123542115 G>A maps to NM_021803.2 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr4:123536857 C>T maps to NM_021803.2 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:123534023 G>A maps to NM_021803.2 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr16:27455915 C>T maps to NM_181079.4 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:27460579 G>A maps to NM_181079.4 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:27459904 G>A maps to NM_181079.4 W328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:27448860 A>C maps to NM_181079.4 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr16:27456004 G>A maps to NM_181079.4 W239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:27448832 G>A maps to NM_181079.4 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:27455990 G>A maps to NM_181079.4 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:27441436 G>A maps to NM_181079.4 Q37Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:68647153 G>A maps to NM_020525.4 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr1:24447456 G>A maps to NM_021258.2 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:24447644 G>A maps to NM_021258.2 Q459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:24447645 G>A maps to NM_021258.2 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:24448023 G>A maps to NM_021258.2 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:24463756 C>T maps to NM_021258.2 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:24447846 G>A maps to NM_021258.2 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr1:24454757 C>T maps to NM_021258.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:24447414 G>A maps to NM_021258.2 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr1:24454649 G>A maps to NM_021258.2 C217C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr1:67633821 C>T maps to NM_144701.2 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr1:67635190 G>A maps to NM_144701.2 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:67705955 C>T maps to NM_144701.2 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr1:207074885 G>A maps to NM_001185156.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr14:23844965 G>A maps to NM_022789.3 Q137Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr12:68595654 C>T maps to NM_018402.1 W162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:68619521 G>A maps to NM_018402.1 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:68619244 C>T maps to NM_018402.1 K69K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:68619437 G>T maps to NM_018402.1 Y33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr16:28515225 G>A maps to NM_145659.3 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr16:28515111 C>T maps to NM_145659.3 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:14159998 C>T maps to NM_004843.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:14150409 C>T maps to NM_004843.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:14162441 C>T maps to NM_004843.2 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:14157117 G>A maps to NM_004843.2 E307E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:14150598 G>A maps to NM_004843.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:14150714 G>A maps to NM_004843.2 W176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:14157365 G>A maps to NM_004843.2 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr19:39760174 G>A maps to NM_172138.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:39735075 C>T maps to ENST00000392072 W84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:24484344 G>A maps to NM_170743.2 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:24495952 G>A maps to NM_170743.2 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:24484057 G>A maps to NM_170743.2 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:24484156 G>A maps to NM_170743.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:24484324 G>A maps to NM_170743.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:24483952 C>T maps to NM_170743.2 K410K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:24483661 G>C maps to NM_170743.2 T507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr19:39787461 G>A maps to NM_172140.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:39787497 G>A maps to NM_172140.1 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:39787204 G>A maps to NM_172140.1 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:39788656 C>T maps to NM_172140.1 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:6066297 T>C maps to NM_000417.2 K92K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:6067911 C>T maps to NM_000417.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:6061851 G>A maps to NM_000417.2 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:6060044 G>A maps to NM_000417.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr10:6066300 C>T maps to NM_000417.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:6061851 G>A maps to NM_000417.2 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:6063630 C>T maps to NM_000417.2 W131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:6066261 C>T maps to NM_000417.2 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr22:37524183 G>A maps to ENST00000406505 Y541Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr22:37524693 G>A maps to ENST00000406505 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:37524377 G>A maps to ENST00000406505 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr22:37528504 C>T maps to ENST00000406505 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr22:37531453 G>A maps to ENST00000406505 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:37538545 C>T maps to ENST00000406505 W70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr22:37539644 G>T maps to ENST00000406505 S40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:37524321 C>T maps to ENST00000406505 E495E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr22:37524489 G>A maps to ENST00000406505 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr22:37524575 G>A maps to ENST00000406505 Q411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:70329077 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:70331330 C>G did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:70330369 T>C did not map to a codon.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr23:70328135 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:70329107 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr5:131396679 G>A maps to NM_000588.3 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr5:131398405 G>A maps to NM_000588.3 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:122657204 G>A maps to NM_001014336.1 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:55202112 C>T maps to NM_139017.4 Q417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:55178872 G>A maps to NM_139017.4 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:55195913 G>A maps to NM_139017.4 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr5:55206396 G>A maps to NM_139017.4 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:55212578 G>A maps to NM_139017.4 V642V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:55202045 T>C maps to NM_139017.4 D394D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr5:55155391 G>A maps to NM_139017.4 W40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr5:55192198 G>A maps to NM_139017.4 W265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:55195913 G>A maps to NM_139017.4 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:55202096 G>A maps to NM_139017.4 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr16:3117382 C>T maps to ENST00000416912 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:3119310 G>A maps to ENST00000416912 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:3119011 A>T maps to ENST00000416912 K121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:3119354 G>A maps to ENST00000416912 *235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:6256005 C>T maps to NM_033439.3 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:70688537 G>A maps to NM_152456.2 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:70693519 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:1471297 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:1477779 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:1467417 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr23:1460718 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr23:1460722 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:1501324 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:1497606 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:1464265 G>C did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:1475205 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:1499955 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:132018272 G>A maps to NM_000589.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr5:132018194 G>A maps to NM_000589.2 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr5:132010148 A>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:132018272 G>A maps to NM_000589.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr19:50399092 C>T maps to NM_172374.1 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr19:50398438 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:27375054 C>T maps to NM_000418.2 S794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr16:27375018 C>T maps to NM_000418.2 P782P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:3139680 G>A maps to NM_000564.3 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:3144437 C>T maps to NM_000564.3 W50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:3144437 C>T maps to NM_000564.3 W50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:3133935 C>T maps to NM_000564.3 W322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:3146587 C>T maps to NM_000564.3 K27K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:22767222 C>T maps to NM_000600.3 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:22769134 G>A maps to NM_000600.3 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:154422451 C>T maps to NM_000565.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr1:154408530 C>T maps to NM_000565.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:154403046 C>T maps to NM_000565.2 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:154420640 C>T maps to NM_000565.2 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr5:55237544 G>A maps to NM_002184.3 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:55265423 G>A maps to NM_002184.3 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr8:79710398 G>A maps to NM_000880.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr8:79652317 C>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:79710411 G>A maps to NM_000880.3 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:35873659 C>T maps to NM_002185.2 R206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr5:35876101 C>T maps to NM_002185.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr5:35876137 G>A maps to NM_002185.2 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr5:35873667 C>T maps to NM_002185.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr5:35874606 C>T maps to NM_002185.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:35873693 G>A maps to NM_002185.2 W217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:35874635 G>A maps to NM_002185.2 W264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr5:35876101 C>T maps to NM_002185.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr5:35875625 C>T maps to NM_002185.2 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:35861077 G>A maps to NM_002185.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:35876368 C>T maps to NM_002185.2 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:35873736 C>T maps to NM_002185.2 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:35876215 G>A maps to NM_002185.2 E336E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:35867440 C>T maps to NM_002185.2 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:35875625 C>T maps to NM_002185.2 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr5:35867482 C>T maps to NM_002185.2 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:35876083 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr5:35857147 C>T maps to NM_002185.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr5:35871188 C>T maps to NM_002185.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr5:35867476 G>A maps to NM_002185.2 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:35875625 C>T maps to NM_002185.2 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:35876117 C>T maps to NM_002185.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:35876215 G>A maps to NM_002185.2 E336E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr5:35876101 C>T maps to NM_002185.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:35857147 C>T maps to NM_002185.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:35874644 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:35876419 C>T maps to NM_002185.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:35861075 C>T maps to NM_002185.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:35876470 C>T maps to NM_002185.2 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:135229738 T>C maps to NM_000590.1 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:135228118 G>A maps to NM_000590.1 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:155239702 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:155235757 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr23:155237262 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:155235097 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:155233512 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr23:155233492 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:155239620 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:155233162 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr23:155233492 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:155235132 C>T did not map to a codon.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr23:155234226 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:121712023 C>T maps to ENST00000344209 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr3:121712425 C>T maps to ENST00000344209 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:121712077 C>T maps to ENST00000344209 E506E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr3:121712023 C>T maps to ENST00000344209 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:121725892 C>T maps to ENST00000344209 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr3:121724106 C>T maps to ENST00000344209 K121K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:121707228 C>T maps to ENST00000344209 R542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr3:121712740 G>A maps to ENST00000344209 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr3:121712794 G>A maps to ENST00000344209 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:121725943 G>A maps to ENST00000344209 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:121712386 G>A maps to ENST00000344209 H403H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:121720278 G>A maps to ENST00000344209 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:121712463 G>A maps to ENST00000344209 Q378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr3:121712359 G>A maps to ENST00000344209 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr3:121712467 G>A maps to ENST00000344209 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:121712467 G>A maps to ENST00000344209 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:121712500 C>T maps to ENST00000344209 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:121720676 C>T maps to ENST00000344209 W138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:121712533 G>A maps to ENST00000344209 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:121712146 C>T maps to ENST00000344209 E483E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:121712467 G>A maps to ENST00000344209 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:121725997 G>A maps to ENST00000344209 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:121712059 G>A maps to ENST00000344209 Y512Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:166890213 C>T maps to NM_199351.2 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr1:166927083 G>A maps to NM_199351.2 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr1:166927320 G>A maps to NM_199351.2 Q22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:166905894 G>A maps to NM_199351.2 C212C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:166926003 C>T maps to NM_199351.2 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:166927015 C>T maps to NM_199351.2 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:166927204 G>A maps to NM_199351.2 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:166905846 G>A maps to NM_199351.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:166926003 C>T maps to NM_199351.2 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:166904700 C>T maps to NM_199351.2 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:166891848 G>A maps to NM_199351.2 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr1:166926003 C>T maps to NM_199351.2 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:166896406 A>G maps to NM_199351.2 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:166891993 G>A maps to NM_199351.2 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:166891945 C>T maps to NM_199351.2 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:166904649 A>C maps to NM_199351.2 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr19:10794133 C>T maps to NM_017620.2 F593F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:10791922 C>T maps to NM_017620.2 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:10799882 C>T maps to NM_017620.2 S864S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:6629302 C>T maps to NM_001014795.1 H39H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:239079622 G>A maps to NM_030768.2 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr19:15233526 G>A maps to NM_006844.3 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:86389136 C>T maps to NM_006839.2 K286K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:131103601 C>T maps to NM_033416.1 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr2:131103833 C>T maps to NM_033416.1 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:131103619 C>T maps to NM_033416.1 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:43923096 C>T maps to NM_175882.2 D275D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:43923501 C>T maps to NM_175882.2 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr17:43922586 G>A maps to NM_175882.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:43922421 C>T maps to NM_175882.2 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:43922712 C>T maps to NM_175882.2 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:43922586 G>A maps to NM_175882.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:43922295 C>T maps to NM_175882.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:43922586 G>A maps to NM_175882.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr17:43923294 C>T maps to NM_175882.2 Y341Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr18:12028051 G>A maps to NM_014214.1 K167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr18:12028929 G>A maps to NM_014214.1 W230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr18:12030426 G>A maps to NM_014214.1 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr18:12009941 G>A maps to NM_014214.1 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr18:22029802 C>T maps to NM_018439.3 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr18:22023080 C>T maps to NM_018439.3 Q187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr18:22029901 C>T maps to NM_018439.3 N293N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr8:57878840 G>A maps to NM_017813.3 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:128040440 G>A maps to NM_000883.3 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr7:128034604 C>T maps to NM_000883.3 Q533Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:128035013 G>A maps to NM_000883.3 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr7:128038620 G>A maps to NM_000883.3 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr7:128038623 G>A maps to NM_000883.3 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr7:128040437 G>A maps to NM_000883.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr3:49065151 G>A maps to NM_000884.2 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:49061838 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:49065157 G>A maps to NM_000884.2 D172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:49065935 G>A maps to NM_000884.2 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr6:76734938 C>T maps to NM_001563.2 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr6:76751688 G>A maps to NM_001563.2 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:76751688 G>A maps to NM_001563.2 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr6:76712659 C>T maps to NM_001563.2 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:76751655 G>A maps to NM_001563.2 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:76660287 G>A maps to NM_001563.2 F605F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr6:76728557 G>A maps to NM_001563.2 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr6:76640842 G>A maps to NM_001563.2 F690F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr6:76657029 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:76751727 G>A maps to NM_001563.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:100949961 G>A maps to NM_016247.2 Y1087Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:100961712 C>T maps to NM_016247.2 Q947Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:100992529 C>T maps to NM_016247.2 Q241Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr3:100963419 G>A maps to NM_016247.2 F585F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:100962395 G>A maps to NM_016247.2 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:105048255 C>T maps to NM_032727.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:62579783 G>A maps to NM_176877.2 Q1507Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr1:62235070 C>T maps to NM_176877.2 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:62350029 G>A maps to NM_176877.2 K1027K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:62349915 C>T maps to NM_176877.2 I989I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:62582326 G>A maps to NM_176877.2 Q1593Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:62503681 T>A maps to NM_176877.2 T1331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:62349915 C>T maps to NM_176877.2 I989I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:62237270 C>T maps to NM_176877.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:62237271 C>T maps to NM_176877.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:62293126 C>T maps to NM_176877.2 R618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:62393400 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:62586893 C>T maps to NM_176877.2 F1644F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:62257018 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:62299447 G>A maps to NM_176877.2 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:62330130 G>A maps to NM_176877.2 E887E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:62579892 C>T maps to NM_176877.2 L1544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:62582305 G>A maps to NM_176877.2 E1586E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr1:62393436 T>G maps to NM_176877.2 P1202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:62299432 G>A maps to NM_176877.2 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr11:61912748 G>A maps to NM_001040694.1 E608E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:61912742 C>T maps to NM_001040694.1 I606I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:61897293 C>A maps to NM_001040694.1 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:61906361 C>T maps to NM_001040694.1 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr11:61897854 C>T maps to NM_001040694.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:105177965 G>T maps to ENST00000252520 E807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr14:105174325 C>T maps to ENST00000252520 S574S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr14:105174794 C>T maps to ENST00000252520 S586S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr14:105175701 C>T maps to ENST00000252520 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr14:105174857 C>T maps to ENST00000252520 S607S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:105169496 C>T maps to ENST00000252520 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:105173303 C>T maps to ENST00000252520 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:105180798 C>T maps to ENST00000252520 A1100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr13:111371711 C>T maps to NM_005537.3 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr13:111367819 C>T maps to NM_005537.3 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr13:111368023 C>T maps to NM_005537.3 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr4:184431570 T>A maps to NM_001564.2 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr7:120590959 C>T maps to NM_019071.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:120608052 C>T maps to NM_019071.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr12:6761505 G>A maps to NM_001127582.1 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:6760487 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:242644071 C>T maps to NM_032329.4 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:242644071 C>T maps to NM_032329.4 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:242664415 G>A maps to NM_032329.4 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:242644104 C>T maps to NM_032329.4 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:220439450 C>T maps to NM_002191.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:220440115 G>A maps to NM_002191.3 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr2:220437183 C>T maps to NM_002191.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:220439992 C>T maps to NM_002191.3 Y282Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr2:220440067 C>T maps to NM_002191.3 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:41729271 G>A maps to NM_002192.2 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr7:41729271 G>A maps to NM_002192.2 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:41739582 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:41729931 C>T maps to NM_002192.2 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr7:41729721 C>T maps to NM_002192.2 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr7:41730114 G>A maps to NM_002192.2 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:41729280 C>T maps to NM_002192.2 Q416Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr2:121106795 G>A maps to NM_002193.2 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr2:121107047 C>T maps to NM_002193.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr2:121106888 C>T maps to NM_002193.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:121107017 C>T maps to NM_002193.2 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:57843540 C>T maps to NM_005538.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:57828773 A>G maps to NM_005538.2 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:57843537 G>A maps to NM_005538.2 W264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:57843231 C>T maps to NM_005538.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:57828692 C>T maps to NM_005538.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:57828692 C>T maps to NM_005538.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:57828872 C>T maps to NM_005538.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:57843624 C>T maps to NM_005538.2 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:57849564 G>A maps to NM_031479.3 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr12:57850390 C>T maps to NM_031479.3 Y271Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr12:57850535 C>T maps to NM_031479.3 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:57849342 C>T maps to NM_031479.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr7:30795181 C>T maps to NM_006774.4 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr7:30793422 C>T maps to NM_006774.4 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:30791780 C>T maps to NM_006774.4 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:30791801 G>A maps to NM_006774.4 Q12Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:30793473 G>A maps to NM_006774.4 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:30793422 C>T maps to NM_006774.4 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:30795319 C>T maps to NM_006774.4 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr7:30795320 C>T maps to NM_006774.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr15:41365679 A>G maps to NM_017553.1 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr15:41371978 C>A maps to NM_017553.1 E351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr15:41348836 G>A maps to NM_017553.1 Q685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr15:41276080 G>A maps to NM_017553.1 P1372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:41276490 G>A maps to NM_017553.1 I1327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:41272543 G>A maps to NM_017553.1 S1516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr18:33077796 G>A maps to NM_001098817.1 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr2:206911277 G>A maps to NM_017759.4 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:206869259 G>A maps to NM_017759.4 L972L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:206869172 G>A maps to NM_017759.4 A1001A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:206921492 G>A maps to NM_017759.4 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:206869792 G>A maps to NM_017759.4 Q795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:30012802 C>T maps to NM_173618.1 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:30012297 C>T maps to NM_173618.1 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:30016747 C>T maps to NM_173618.1 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr2:99156090 C>T maps to NM_001134224.1 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:99169311 C>T maps to NM_001134224.1 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:99155367 C>T maps to NM_001134224.1 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:99156084 C>T maps to NM_001134224.1 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:99182196 C>T maps to NM_001134224.1 S754S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:143352382 T>C maps to NM_003866.2 E10E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:143129677 G>A maps to NM_003866.2 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr10:134563049 G>A maps to NM_005539.3 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr10:134563052 C>T maps to NM_005539.3 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:134579347 C>T maps to NM_005539.3 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr1:38351419 G>A maps to ENST00000373026 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:38328075 G>A maps to ENST00000373026 R965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:38343859 C>T maps to ENST00000373026 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:38338741 G>A maps to ENST00000373026 L763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:38353979 G>A maps to ENST00000373026 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:38330080 G>A maps to ENST00000373026 L923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr1:38331528 C>T maps to ENST00000373026 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:38331519 G>A maps to ENST00000373026 F889F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:38409516 G>A maps to ENST00000373026 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:234077949 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:234113017 C>T maps to ENST00000359570 P1074P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:234093123 C>T maps to ENST00000359570 S744S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr2:234077951 G>A maps to ENST00000359570 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:234079750 A>C maps to ENST00000359570 R648R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:234104084 G>A maps to ENST00000359570 K879K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:234098534 C>T maps to ENST00000359570 Q800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:234112975 C>T maps to ENST00000359570 I1060I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:234072437 C>T maps to ENST00000359570 I442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:234091089 C>T maps to ENST00000359570 S702S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:234072404 G>A maps to ENST00000359570 Q431Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:234113038 C>T maps to ENST00000359570 P1081P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:234106899 C>T maps to ENST00000359570 S951S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr9:139324150 G>A maps to NM_019892.3 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr9:139327673 G>A maps to NM_019892.3 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr9:139326423 G>A maps to NM_019892.3 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr10:121586481 C>T maps to NM_014937.2 F863F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:121551379 G>C did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr10:121556255 C>G maps to NM_014937.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr22:31522379 G>A maps to ENST00000331075 W430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr22:31524543 G>A maps to ENST00000331075 K699K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr22:31524261 C>T maps to ENST00000331075 F654F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:1411450 G>A maps to NM_016532.3 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr11:71941315 G>C did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:71946397 C>T maps to NM_001567.3 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:71939528 C>T maps to NM_001567.3 D128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:71940599 C>T maps to NM_001567.3 Q251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr11:71948479 C>T maps to NM_001567.3 F1064F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:71946937 C>T maps to NM_001567.3 S929S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:71945394 C>T maps to NM_001567.3 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:71946224 C>T maps to NM_001567.3 S827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr11:71941853 C>T maps to NM_001567.3 F404F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr11:71946392 C>T maps to NM_001567.3 L853L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:71940996 C>T maps to NM_001567.3 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:71942073 C>T maps to NM_001567.3 F446F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr11:71948209 C>T maps to NM_001567.3 A974A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr11:2182096 C>T maps to NM_001042376.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:2170540 G>A maps to NM_001042376.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:2170414 G>A maps to NM_001042376.2 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:15197502 C>T maps to NM_001031853.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:15222431 C>T maps to NM_001031853.3 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:15197304 G>A maps to NM_001031853.3 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:15212314 C>T maps to NM_001031853.3 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:15170713 G>A maps to NM_001031853.3 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr11:15260543 C>T maps to NM_001031853.3 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr11:15260487 C>T maps to NM_001031853.3 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:15267540 G>A maps to NM_001031853.3 V565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:15197631 G>A maps to NM_001031853.3 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:155093324 C>T maps to ENST00000344756 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr2:118864323 C>T maps to NM_016133.2 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:17927815 G>A maps to NM_005543.2 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr9:5233771 G>A maps to NM_002195.1 K105K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:67263911 G>A maps to NM_005478.3 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:5164203 C>T maps to NM_007179.2 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:5185413 C>T maps to NM_007179.2 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr20:20350317 C>T maps to NM_002196.2 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:20350425 C>T maps to NM_002196.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr20:20350122 C>T maps to NM_002196.2 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr19:7166348 T>A maps to NM_000208.2 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr19:7267491 G>A maps to NM_000208.2 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:7267764 G>A maps to NM_000208.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr19:7267509 G>A maps to NM_000208.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:7267803 C>T maps to NM_000208.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:7117303 G>A maps to NM_000208.2 F1304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:7117138 G>A maps to NM_000208.2 I1359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:7122739 C>T maps to NM_000208.2 Q1138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:7184364 G>A maps to NM_000208.2 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:7132256 C>T maps to NM_000208.2 P918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:7168045 T>A maps to NM_000208.2 R515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:7152744 G>A maps to NM_000208.2 F741F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr19:7168079 A>G maps to NM_000208.2 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr19:7267788 G>A maps to NM_000208.2 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:7152761 G>A maps to NM_000208.2 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr19:7172377 G>T maps to NM_000208.2 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:156813017 G>A maps to NM_014215.2 V968V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:156814413 C>T maps to NM_014215.2 E859E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr1:156819155 G>A maps to NM_014215.2 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:156814377 C>T maps to NM_014215.2 A871A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D3-A51R-06A-11D-A25O-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:156811949 T>C maps to NM_001007792.1 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:156811286 G>A maps to NM_014215.2 T1187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:156821857 G>A maps to NM_014215.2 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:156824045 C>T maps to NM_014215.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:156812212 G>A maps to NM_014215.2 R1072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:156811545 G>A maps to NM_014215.2 Y1146Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:156815087 C>T maps to NM_014215.2 R739R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:156812212 G>A maps to NM_014215.2 R1072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:156810769 C>T maps to NM_014215.2 P1263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:156823976 G>A maps to NM_014215.2 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:156813995 A>C maps to NM_014215.2 A938A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:156812212 G>A maps to NM_014215.2 R1072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:156811545 G>A maps to NM_014215.2 Y1146Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:156821912 G>A maps to NM_014215.2 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:156821104 G>A maps to NM_014215.2 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:156810787 G>A maps to NM_014215.2 L1257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:156812222 C>T maps to NM_014215.2 K1068K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:156814326 G>A maps to NM_014215.2 A888A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:156815024 G>A maps to NM_014215.2 F760F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:156816461 G>A maps to NM_014215.2 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:156816325 G>A maps to NM_014215.2 R599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:156811479 G>A maps to NM_014215.2 I1168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:156812212 G>A maps to NM_014215.2 R1072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:156810751 C>T maps to NM_014215.2 R1269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:156812900 G>A maps to NM_014215.2 S1007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:156814892 G>A maps to NM_014215.2 F804F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:156816440 C>T maps to NM_014215.2 V560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:156819152 G>A maps to NM_014215.2 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:156811533 C>T maps to NM_014215.2 G1150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:156816344 C>T maps to NM_014215.2 Q592Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:1516265 G>A maps to ENST00000389470 F1906F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr7:1516461 G>A maps to ENST00000389470 I1886I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr7:1522257 C>T maps to ENST00000389470 S1376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:1516265 G>A maps to ENST00000389470 F1906F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:1535813 G>A maps to ENST00000389470 A691A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr7:1527063 G>A maps to ENST00000389470 P994P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr7:1527397 G>A maps to ENST00000389470 P966P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:1542609 C>A maps to ENST00000389470 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr7:1526973 G>A maps to ENST00000389470 L1024L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr7:1526266 G>A maps to ENST00000389470 A1138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr7:1517261 C>T maps to ENST00000389470 W1830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:1516461 G>A maps to ENST00000389470 I1886I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:1522325 G>A maps to ENST00000389470 Q1354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr7:1538685 G>A maps to ENST00000389470 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr7:1518128 G>A maps to ENST00000389470 L1716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:1513980 G>A maps to ENST00000389470 I2098I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:1515938 G>A maps to ENST00000389470 C1982C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr7:1516075 G>A maps to ENST00000389470 L1937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:1513980 G>A maps to ENST00000389470 I2098I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:19682403 A>G maps to NM_018142.2 Q309Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:19703291 C>T maps to NM_018142.2 Q654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr4:106604162 G>A maps to NM_020395.3 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr17:59946487 G>A maps to NM_020748.2 Q1059*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr17:59962265 C>T maps to NM_020748.2 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:59958410 C>T maps to NM_020748.2 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:59968923 G>A maps to NM_020748.2 Q617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:153713832 C>T maps to ENST00000428986 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:153740200 C>T maps to ENST00000428986 T715T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:153730127 C>T maps to ENST00000428986 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr1:153732862 C>T maps to ENST00000428986 C439C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:153744397 C>T maps to ENST00000428986 S894S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:153721216 C>T maps to ENST00000428986 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:153724786 C>T maps to ENST00000428986 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:77702314 G>A maps to NM_033547.3 R29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:77702315 G>A maps to NM_033547.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:77594887 G>A maps to NM_033547.3 T901T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:62417061 G>A maps to NM_030628.1 Q164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:62417062 G>A maps to NM_030628.1 H163H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:62416552 G>A maps to NM_030628.1 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr11:62415319 C>G maps to NM_030628.1 G744G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:62414848 G>A maps to NM_030628.1 P901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:62415652 G>A maps to NM_030628.1 P633P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:62417455 G>A maps to NM_030628.1 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr11:62415913 G>A maps to NM_030628.1 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr13:51950220 C>T maps to NM_012141.2 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr13:51948810 G>A maps to NM_012141.2 N617N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr13:51952472 G>A maps to NM_012141.2 Q502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:212115246 G>A maps to NM_015434.3 S936S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr1:212208752 G>A maps to NM_015434.3 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:212180633 G>A maps to NM_015434.3 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:95869060 C>T maps to NM_017864.2 F603F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:95866067 G>A maps to NM_017864.2 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr8:95869076 C>T maps to NM_017864.2 Q609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr8:28633368 G>A maps to NM_018250.3 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:28695167 G>A maps to NM_018250.3 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:128564861 C>T maps to NM_015693.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr4:128627832 C>T maps to NM_015693.3 F660F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:128577863 T>G maps to NM_015693.3 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:128632130 C>T maps to NM_015693.3 I811I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:128564721 C>T maps to NM_015693.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:128595284 C>T maps to NM_015693.3 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:128595287 C>T maps to NM_015693.3 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:103002491 C>T maps to NM_014425.2 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:103014670 C>T maps to NM_014425.2 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr9:102866890 C>T maps to NM_014425.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr9:103035154 C>T maps to NM_014425.2 P527P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:49765025 G>A maps to NM_153273.3 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:49785287 G>A maps to NM_153273.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr3:49785290 G>A maps to NM_153273.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr3:48726086 G>A maps to ENST00000395509 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr3:48725996 G>A maps to ENST00000395509 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr3:48730483 G>A maps to ENST00000395509 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr3:48730484 G>A maps to ENST00000395509 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr6:33703226 G>A maps to NM_054111.4 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr6:33690841 C>T maps to NM_054111.4 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr6:33690634 G>A maps to NM_054111.4 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr6:33694520 C>T maps to NM_054111.4 E192E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:33693289 C>T maps to NM_054111.4 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:33695868 C>T maps to NM_054111.4 K136K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:154567811 C>T maps to NM_001130700.1 K53K. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A2GC-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:154520940 C>T maps to NM_001130700.1 K257K. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-ER-A193-06A-12D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr5:61832574 T>C maps to NM_001134779.1 G752G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:61811237 G>A maps to NM_001134779.1 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:61846258 C>T maps to NM_001134779.1 P812P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr5:61833061 C>T maps to NM_001134779.1 S772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:61802165 C>T maps to NM_001134779.1 I628I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:61779861 C>T maps to NM_001134779.1 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr1:44423213 C>T maps to NM_014652.3 F511F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:44422549 C>T maps to NM_014652.3 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:44433323 C>T maps to NM_014652.3 L954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:44433042 C>T maps to NM_014652.3 F890F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:44432450 C>T maps to NM_014652.3 F840F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr1:44426926 C>T maps to NM_014652.3 F779F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NF-06A-11D-A19A-08 chr1:44432249 C>T maps to NM_014652.3 L801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:44415558 C>T maps to NM_014652.3 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr14:24654437 G>A maps to ENST00000458132 H453H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr14:24653883 G>A maps to ENST00000458132 D536D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr14:24655609 G>A maps to ENST00000458132 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr14:24652821 G>A maps to ENST00000458132 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:24654166 G>A maps to ENST00000458132 Y476Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr14:24652709 G>A maps to ENST00000458132 F691F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr14:24652235 G>A maps to ENST00000458132 P789P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr14:24655588 G>T maps to ENST00000458132 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:24654768 G>A maps to ENST00000458132 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr14:24655567 G>A maps to ENST00000458132 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr14:24655657 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr13:98664588 C>T maps to NM_002271.4 F733F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr13:98637697 C>T maps to NM_002271.4 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr13:98671973 C>T maps to NM_002271.4 V1010V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:98666300 C>T maps to NM_002271.4 R738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr11:9455184 T>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:9446715 T>C maps to NM_006391.2 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:30787022 G>A maps to NM_006390.3 L965L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:30833520 G>A maps to NM_006390.3 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr12:30833475 G>A maps to NM_006390.3 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr12:30790081 G>A maps to NM_006390.3 I843I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:30824021 T>C maps to NM_006390.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr12:30784922 G>A maps to NM_006390.3 A974A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:30805970 G>A maps to NM_006390.3 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:201825034 C>T maps to NM_018085.4 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:201835968 C>T maps to NM_018085.4 V579V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:201840305 C>T maps to NM_018085.4 F809F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:46195342 G>A maps to NM_005897.2 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr9:95400562 C>G did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr9:95414915 G>A maps to NM_022755.5 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr2:237308113 C>T maps to ENST00000457693 W391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:237240103 C>T maps to ENST00000457693 Q765Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr2:237233336 C>T maps to ENST00000457693 R829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr2:237240133 G>A maps to ENST00000457693 V755V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:237285827 C>T maps to ENST00000457693 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:237233336 C>T maps to ENST00000457693 R829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:237405838 G>A maps to ENST00000457693 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr2:237272551 C>T maps to ENST00000457693 G588G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:237300693 C>T maps to ENST00000457693 Q453Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr2:237272551 C>T maps to ENST00000457693 G588G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:237246974 C>T maps to ENST00000457693 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr2:237300952 C>T maps to ENST00000457693 Q424Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:237233421 C>T maps to ENST00000457693 W801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:237240220 A>G maps to ENST00000457693 I726I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:237396807 G>A maps to ENST00000457693 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr2:237276885 G>A maps to ENST00000457693 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:237349718 C>T maps to ENST00000457693 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:237405805 G>A maps to ENST00000457693 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:113645326 G>A maps to ENST00000416617 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr12:113645371 A>T maps to ENST00000416617 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr7:2617905 C>T maps to NM_152558.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr7:2634550 C>T maps to NM_152558.3 Q461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:2611205 C>T maps to NM_152558.3 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:2638193 C>T maps to NM_152558.3 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr7:2645589 C>T maps to NM_152558.3 I608I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr3:51928923 G>A maps to NM_152397.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:51929124 G>A maps to NM_152397.2 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:51930910 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr3:51929064 G>A maps to NM_152397.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr3:51937093 C>T maps to NM_152397.2 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:51928920 G>A maps to NM_152397.2 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:51937084 C>T maps to NM_152397.2 K8K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:51929157 G>A maps to NM_152397.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr3:51895872 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:51895941 G>A maps to NM_203424.1 Q29Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:51864681 C>T maps to NM_001085479.1 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr3:51864709 C>T maps to NM_001085479.1 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:51864792 C>T maps to NM_001085479.1 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr3:51864456 G>A maps to NM_001085479.1 K35K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr3:197665516 G>A maps to NM_001134435.1 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:197670687 G>A maps to NM_001134435.1 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr15:67629323 G>A maps to NM_001031715.2 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr15:67709360 G>A maps to NM_001031715.2 R730R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr15:67713665 C>T maps to NM_001031715.2 V752V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:67571771 C>T maps to NM_001031715.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:67664822 C>T maps to NM_001031715.2 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr15:67665733 G>A maps to NM_001031715.2 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:67571771 C>T maps to NM_001031715.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:67681172 C>T maps to NM_001031715.2 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr15:67664975 G>A maps to NM_001031715.2 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr15:67709356 G>A maps to NM_001031715.2 W729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr15:67681241 C>T maps to NM_001031715.2 I510I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr15:67636458 G>A maps to NM_001031715.2 Q189Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:67629323 G>A maps to NM_001031715.2 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr3:158983179 C>T maps to NM_001042705.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:158983149 G>A maps to NM_001042705.2 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:158980378 C>G maps to NM_001197113.1 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:158980414 C>T maps to NM_001197113.1 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:19746702 C>T maps to NM_153208.1 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:19745081 C>T maps to NM_153208.1 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr15:91017135 C>T maps to NM_003870.3 S814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr15:91017316 C>T maps to NM_003870.3 Q843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:90999483 C>T maps to NM_003870.3 V571V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:91034750 C>T maps to NM_003870.3 Q1479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr15:91017135 C>T maps to NM_003870.3 S814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr15:91027478 C>T maps to NM_003870.3 V1272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr15:91009294 C>T maps to NM_003870.3 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:75896635 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:75970406 C>T maps to NM_006633.2 Q1134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:75866422 C>T maps to NM_006633.2 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:75954282 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:75964558 C>T maps to NM_006633.2 S911S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:75960999 G>A maps to NM_006633.2 Q893Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:75888725 C>T maps to NM_006633.2 Q295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:75927691 C>T maps to NM_006633.2 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:75969355 C>T maps to NM_006633.2 L1051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:75993945 G>A maps to NM_006633.2 K1447K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr1:156501014 G>A maps to NM_178229.4 I1376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr1:156508825 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:156542303 C>A maps to NM_178229.4 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:156507025 G>A maps to NM_178229.4 L1123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:156533597 C>T maps to NM_178229.4 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:156524172 C>T maps to NM_178229.4 Q434Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:156507043 G>A maps to NM_178229.4 I1117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr1:156521553 G>A maps to NM_178229.4 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:156504329 G>A maps to NM_178229.4 L1235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:156504510 G>A maps to NM_178229.4 L1174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:156498718 G>A maps to NM_178229.4 A1520A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:12977615 G>A maps to ENST00000429247 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:12950797 T>C maps to ENST00000429247 Q851Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:12977981 G>A maps to ENST00000429247 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr3:12977267 G>A maps to ENST00000429247 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:12977611 G>A maps to ENST00000429247 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:12954972 G>A maps to ENST00000429247 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr3:12953213 G>A maps to ENST00000429247 F777F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr3:12983361 G>A maps to ENST00000429247 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr23:53268416 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr23:53279584 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:53285071 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr23:53285069 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:53283774 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:53283775 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:53267475 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:53279923 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:53265597 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:53279875 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:53284081 G>A did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:53280173 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr23:53271019 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:176500 G>A maps to NM_001170738.1 K151K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr12:275030 G>A maps to NM_001170738.1 T982T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:278179 G>A maps to NM_001170738.1 W991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr12:247542 C>T maps to NM_001170738.1 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr12:274619 G>A maps to NM_001170738.1 K910K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:266292 G>A maps to NM_001170738.1 E752E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:266729 G>A maps to NM_001170738.1 Q771Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:247555 C>T maps to NM_001170738.1 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:271137 C>T maps to NM_001170738.1 I830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr12:248379 C>T maps to NM_001170738.1 A617A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:275030 G>A maps to NM_001170738.1 T982T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr7:123104988 G>A maps to NM_178827.4 V552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:123101416 C>T maps to NM_178827.4 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:123152384 G>A maps to NM_178827.4 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr7:123150012 C>T maps to NM_178827.4 K158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr7:123097525 C>T maps to NM_178827.4 W701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:123097515 G>A maps to NM_178827.4 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:123109327 C>T maps to NM_178827.4 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr7:123143006 C>T maps to NM_178827.4 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr7:123092934 G>A maps to NM_178827.4 I746I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr7:123136849 C>T maps to NM_178827.4 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:123101467 C>T maps to NM_178827.4 Q650Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr23:153284758 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:153278808 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:153284107 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr23:153282489 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:153284188 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:79607565 A>G maps to NM_001010844.1 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:10258729 C>T maps to NM_001570.3 Q301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:10280487 C>T maps to NM_001570.3 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:10261446 G>A maps to NM_001570.3 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:10280493 G>A maps to NM_001570.3 W512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:10276144 G>A maps to NM_001570.3 K425K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr3:10276208 G>T maps to NM_001570.3 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr3:10258704 T>C maps to NM_001570.3 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:10242053 G>A maps to NM_001570.3 W93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:10261404 C>T maps to NM_001570.3 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:10280487 C>T maps to NM_001570.3 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:10219699 G>A maps to NM_001570.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:10255054 G>A maps to NM_001570.3 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:10276307 C>T maps to NM_001570.3 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:66605262 C>T maps to NM_007199.2 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr12:66605283 C>T maps to NM_007199.2 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr12:66605283 C>T maps to NM_007199.2 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr12:44176256 A>G maps to NM_016123.3 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:44165128 C>T maps to NM_016123.3 Q90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr15:78770708 G>A maps to NM_004136.2 Q422Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr15:78764256 C>T maps to NM_004136.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr15:78775755 C>T maps to NM_004136.2 Q465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr4:185309929 G>A maps to NM_002199.3 A344A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DA-A1I8-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr4:185340706 G>A maps to NM_002199.3 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:46387735 G>A maps to NM_015649.1 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:46387736 G>A maps to NM_015649.1 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr19:46388612 C>A maps to NM_015649.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:46387946 G>T maps to NM_015649.1 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:46387757 G>A maps to NM_015649.1 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:50165505 C>T maps to NM_001571.5 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr19:50167993 G>A maps to NM_001571.5 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:50165464 C>T maps to NM_001571.5 W241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr6:401487 C>T maps to NM_002460.3 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:128588050 C>T maps to NM_001098629.1 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:209961872 G>A maps to NM_006147.2 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:209961872 G>A maps to NM_006147.2 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:209961956 C>T maps to NM_006147.2 E404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:209964128 A>C maps to NM_006147.2 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:209968731 C>T maps to NM_006147.2 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:209968650 G>A maps to NM_006147.2 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:209964071 G>A maps to NM_006147.2 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr1:209961986 G>A maps to NM_006147.2 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:613079 G>A maps to NM_004031.2 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr16:85954860 C>T maps to NM_002163.2 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:85952284 C>T maps to NM_002163.2 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr16:85952176 C>T maps to NM_002163.2 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:85936698 G>A maps to NM_002163.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr16:85954807 C>T maps to NM_002163.2 Q401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:85952164 G>A maps to NM_002163.2 E248E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr14:24632674 C>T maps to NM_006084.4 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:44223003 C>T maps to NM_019612.3 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:44223546 C>T maps to NM_019612.3 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:44223816 G>A maps to NM_019612.3 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:44224035 G>A maps to NM_019612.3 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:44223120 C>T maps to NM_019612.3 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:44222778 G>A maps to NM_019612.3 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:44223153 C>T maps to NM_019612.3 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr19:44223534 C>T maps to NM_019612.3 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr19:44099229 C>T maps to NM_001007561.2 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:44097395 C>T maps to NM_001007561.2 E218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr19:44096255 G>A maps to NM_001007561.2 H598H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr19:44096312 G>A maps to NM_001007561.2 F579F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:227662746 G>A maps to NM_005544.2 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr2:227661054 A>C maps to NM_005544.2 Y800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr2:227661606 G>A maps to NM_005544.2 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr13:110436663 G>A maps to NM_003749.2 T579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:107978057 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:107976576 G>A did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:107976622 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:107978306 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:107979389 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:107979467 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:107978023 C>G did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:107977126 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:107979254 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:107977072 T>C did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:107975912 C>G did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:107977624 C>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:107977899 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:107978024 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:107979431 G>A did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:107977538 G>T did not map to a codon.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr5:3599466 C>T maps to NM_024337.3 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr5:2748558 C>T maps to NM_033267.4 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr5:2749631 C>T maps to NM_033267.4 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:2749164 C>T maps to NM_033267.4 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:2749628 C>T maps to NM_033267.4 K174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr5:2748633 C>T maps to NM_033267.4 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr5:2749814 G>T maps to NM_033267.4 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:54318799 C>T maps to NM_024336.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr16:54319045 G>A maps to NM_024336.2 D249D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr5:1879855 C>T maps to NM_016358.2 K166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr16:54967725 C>T maps to NM_005853.5 Q465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:55363138 C>T maps to NM_024335.2 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:55361596 C>T maps to NM_024335.2 N171N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:55361545 C>T maps to NM_024335.2 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:74961579 C>T maps to NM_194279.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr15:89182722 C>T maps to NM_002201.4 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:89198720 C>T maps to NM_002201.4 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:156697009 G>A maps to NM_030980.1 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:156694029 G>A maps to NM_030980.1 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:156697216 G>A maps to NM_030980.1 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr5:50687118 G>A maps to NM_002202.2 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:50685492 C>T maps to NM_002202.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr5:50685525 C>T maps to NM_002202.2 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr15:74467237 G>A maps to NM_201526.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr15:74467762 C>T maps to NM_201526.1 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr15:74468479 C>T maps to NM_201526.1 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:74468380 G>A maps to NM_201526.1 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr15:74467804 C>T maps to NM_201526.1 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:74468299 G>A maps to NM_201526.1 K367K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:74468047 C>T maps to NM_201526.1 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:74467510 C>T maps to NM_201526.1 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:74467807 G>A maps to NM_201526.1 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:74468458 C>A maps to NM_201526.1 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:74467513 C>T maps to NM_201526.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:74426456 G>A maps to NM_001130137.1 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr20:13279934 C>G maps to NM_080826.1 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr20:13279724 C>T maps to NM_080826.1 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr20:13269301 G>A maps to NM_080826.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:77951262 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:77951250 G>A maps to NM_199296.2 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:77944600 C>T maps to NM_199296.2 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:77945044 C>T maps to NM_199296.2 Q329Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:77950758 G>A maps to NM_199296.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr14:77942258 C>T maps to NM_199296.2 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:128448567 C>T maps to NM_016048.2 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:128440888 C>T maps to NM_016048.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:55967751 G>A maps to NM_024710.2 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr19:55967742 G>A maps to NM_024710.2 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr19:55966691 C>T maps to NM_024710.2 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr7:16415866 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:35478530 A>C maps to NM_001008494.1 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr22:35481451 C>A maps to NM_001008494.1 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr22:35478598 C>T maps to NM_001008494.1 Y106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr22:35478634 G>A maps to NM_001008494.1 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr22:35480386 G>A maps to NM_001008494.1 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr22:35463172 C>T maps to NM_001008494.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr22:35481589 C>T maps to NM_001008494.1 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr22:35480374 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:128852946 C>T maps to ENST00000418265 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:18546080 G>A maps to NM_016368.4 I489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:18547640 C>T maps to NM_016368.4 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr20:33000323 C>T maps to ENST00000262650 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:33026302 C>T maps to ENST00000262650 D223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr20:33067433 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr16:47292639 G>A maps to NM_030790.3 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr16:47485328 G>A maps to NM_030790.3 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr16:47294473 G>A maps to NM_030790.3 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:304633 C>T maps to NM_032039.2 D74D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:304606 C>T maps to NM_032039.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr16:304618 C>T maps to NM_032039.2 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr16:314957 G>A maps to NM_032039.2 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr5:52216259 C>T maps to NM_181501.1 R752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:52145235 G>A maps to NM_181501.1 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:52240864 G>A maps to NM_181501.1 E1126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:52221112 C>T maps to NM_181501.1 P803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:52223418 C>T maps to NM_181501.1 I873I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr5:52183649 G>A maps to NM_181501.1 K259K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:52235710 C>T maps to NM_181501.1 L1074L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr5:52160893 G>A maps to NM_181501.1 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr5:52214622 C>T maps to NM_181501.1 Q684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:52211400 C>T maps to NM_181501.1 G655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:52240816 G>A maps to NM_181501.1 R1110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr5:52183737 C>T maps to NM_181501.1 R289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr1:145535785 C>T maps to NM_003637.3 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:145534129 G>A maps to NM_003637.3 Q545Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:145533059 G>A maps to NM_003637.3 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:145541454 C>T maps to NM_003637.3 S1081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:145539750 C>T maps to NM_003637.3 V1061V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:145535800 G>A maps to NM_003637.3 Q663Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:145532831 T>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:145531023 C>T maps to NM_003637.3 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr15:68628085 G>A maps to ENST00000423218 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr15:68617561 C>T maps to ENST00000423218 V743V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:68643712 C>T maps to ENST00000423218 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr15:68631853 G>A maps to ENST00000423218 N420N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr15:68657104 C>T maps to ENST00000423218 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr15:68641185 A>G maps to ENST00000423218 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:68643054 G>A maps to ENST00000423218 I320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr15:68643003 G>A maps to ENST00000423218 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr15:68624235 G>A maps to ENST00000423218 F577F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr15:68654003 G>A maps to ENST00000423218 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr15:68642964 G>A maps to ENST00000423218 F350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:68617471 G>A maps to ENST00000423218 V773V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:68643117 G>A maps to ENST00000423218 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:68650888 C>T maps to ENST00000423218 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:68661615 G>A maps to ENST00000423218 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:52344191 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:52379208 T>C maps to NM_002203.3 L1062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:52338038 C>T maps to NM_002203.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:52386419 C>A maps to NM_002203.3 L1179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr5:52344305 G>A maps to NM_002203.3 Q167Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:52353880 C>T maps to NM_002203.3 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:52361783 C>T maps to NM_002203.3 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:52374688 C>T maps to NM_002203.3 F971F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:42455744 G>A maps to NM_000419.3 A693A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr17:42449773 C>T maps to NM_000419.3 R1026R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr17:42451817 C>T maps to NM_000419.3 R988R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr17:42457167 G>A maps to NM_000419.3 F589F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q3-06A-11D-A196-08 chr17:48157684 C>T maps to NM_002204.2 P922P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:48151602 C>T maps to NM_002204.2 D447D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr17:48153709 C>T maps to NM_002204.2 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:48148253 T>C maps to NM_002204.2 Y237Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:48165181 C>T maps to NM_002204.2 A998A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:48149448 C>T maps to NM_002204.2 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr17:48154807 G>A maps to NM_002204.2 Q712Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:182339986 G>A maps to NM_000885.4 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:182363377 G>A maps to NM_000885.4 V523V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:182374407 C>T maps to NM_000885.4 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr2:182360542 A>G maps to NM_000885.4 L473L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A2GC-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:182395249 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:182399545 C>T maps to NM_000885.4 L963L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:182396418 C>T maps to NM_000885.4 F900F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:182396418 C>T maps to NM_000885.4 F900F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:182322467 G>A maps to NM_000885.4 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:182360569 G>A maps to NM_000885.4 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:182358139 C>T maps to NM_000885.4 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:182392092 G>A maps to NM_000885.4 E803E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr2:182360138 C>T maps to NM_000885.4 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr12:54799034 G>A maps to NM_002205.2 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr12:54797092 G>A maps to NM_002205.2 R598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr12:54797942 C>T maps to NM_002205.2 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:54796785 G>A maps to NM_002205.2 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr12:54798974 C>T maps to NM_002205.2 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr12:54798965 G>A maps to NM_002205.2 D403D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr12:54796798 G>A maps to NM_002205.2 I650I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:54798522 G>A maps to NM_002205.2 R461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr12:54799682 G>A maps to NM_002205.2 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:54797453 C>T maps to NM_002205.2 Q577Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:54798242 G>A maps to NM_002205.2 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr12:54797092 G>A maps to NM_002205.2 R598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr12:54791157 G>A maps to NM_002205.2 I1019I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:54791247 G>A maps to NM_002205.2 T989T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:54797987 G>A maps to NM_002205.2 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr12:54799658 C>A maps to NM_002205.2 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr12:54793712 G>A maps to NM_002205.2 L888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr2:173349577 C>T maps to ENST00000264106 R579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr2:173334103 G>A maps to ENST00000264106 W213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:173349973 C>T maps to ENST00000264106 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr2:173351767 G>A maps to ENST00000264106 E663E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr2:173349958 G>A maps to ENST00000264106 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr2:173352084 C>T maps to ENST00000264106 P727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr12:56090748 G>A maps to ENST00000347027 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:56086744 C>T maps to ENST00000347027 R953R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr12:56101442 G>A maps to ENST00000347027 D8D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr12:56088273 C>T maps to ENST00000347027 G814G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:56088047 G>A maps to ENST00000347027 S852S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr12:56087070 G>A maps to ENST00000347027 L900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:56089325 C>T maps to ENST00000347027 T705T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:56092630 G>T maps to ENST00000347027 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr12:56092221 G>A maps to ENST00000347027 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:56092215 G>A maps to ENST00000347027 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:56081757 C>T maps to ENST00000347027 W1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:56090697 G>A maps to ENST00000347027 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr12:56094070 G>A maps to ENST00000347027 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr12:56094761 G>A maps to ENST00000347027 C197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr12:56088579 G>A maps to ENST00000347027 V770V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr10:15647735 G>A maps to NM_003638.1 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr10:15714737 G>A maps to NM_003638.1 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr10:15697375 G>T maps to NM_003638.1 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr10:15559192 C>T maps to NM_003638.1 R1052R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:15639291 G>A maps to NM_003638.1 R709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr10:15729984 G>A maps to NM_003638.1 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:15649738 G>A maps to NM_003638.1 V567V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:15590552 G>A maps to NM_003638.1 I927I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:15600126 C>T maps to NM_003638.1 R904R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:15614329 G>A maps to NM_003638.1 I839I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:15646221 G>A maps to NM_003638.1 I701I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr10:15649690 G>A maps to NM_003638.1 F583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:15614284 G>A maps to NM_003638.1 L854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:15634240 G>A maps to NM_003638.1 F758F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:15614329 G>A maps to NM_003638.1 I839I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:37514926 G>A maps to NM_002207.2 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:37555366 C>T maps to NM_002207.2 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr3:37778456 C>T maps to NM_002207.2 F739F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:37670820 G>A maps to NM_002207.2 K611K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:37725430 C>T maps to NM_002207.2 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr16:31421741 G>A maps to ENST00000444228 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:31422167 G>A maps to ENST00000444228 W458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr16:31418928 G>A maps to ENST00000444228 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr16:31425821 C>T maps to ENST00000444228 L699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:31421726 C>T maps to ENST00000444228 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:31422500 A>T maps to ENST00000444228 R503R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:31437406 G>A maps to ENST00000444228 G1164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:31429641 C>T maps to ENST00000444228 F895F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:31418928 G>A maps to ENST00000444228 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr16:31422777 G>A maps to ENST00000444228 R565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr16:31427541 C>T maps to ENST00000444228 F780F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr16:31437361 G>A maps to ENST00000444228 K1149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr16:31418958 G>A maps to ENST00000444228 E292E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:31404689 C>T maps to ENST00000444228 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:31405602 G>A maps to ENST00000444228 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:31422419 C>T maps to ENST00000444228 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:31424181 C>T maps to ENST00000444228 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr16:31424256 C>T maps to ENST00000444228 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr17:3661059 G>A maps to NM_002208.4 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:3646902 C>T maps to NM_002208.4 E776E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:3643112 G>A maps to NM_002208.4 A836A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:3655000 G>A maps to NM_002208.4 F612F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr17:3680913 C>T maps to NM_002208.4 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:3661104 C>T maps to NM_002208.4 K305K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr17:3653742 G>A maps to NM_002208.4 Q643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr17:3635751 A>G maps to NM_002208.4 S888S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:3638193 G>A maps to NM_002208.4 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr17:3653761 G>A maps to NM_002208.4 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr16:30516614 C>T maps to NM_002209.2 T762T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr16:30522248 G>A maps to NM_002209.2 G889G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr16:30495204 C>T maps to NM_002209.2 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:30507441 C>T maps to NM_002209.2 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:30495177 C>T maps to NM_002209.2 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:30518176 G>A maps to NM_002209.2 K836K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:30495273 C>T maps to NM_002209.2 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:30532877 C>T maps to NM_002209.2 I1135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:30490432 C>T maps to NM_002209.2 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:30522200 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr16:30525121 C>T maps to NM_002209.2 F939F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr16:30507602 C>T maps to NM_002209.2 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr16:30516733 G>T maps to NM_002209.2 E773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:30516720 G>A maps to NM_002209.2 E768E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:30516771 C>T maps to NM_002209.2 F785F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr16:30510809 G>A maps to NM_002209.2 P715P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:30510707 G>A maps to NM_002209.2 R681R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:30531272 C>T maps to NM_002209.2 F1108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:30516711 C>T maps to NM_002209.2 I765I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr16:31332563 G>A maps to NM_001145808.1 R571R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr16:31284748 C>T maps to NM_001145808.1 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr16:31286949 C>T maps to NM_001145808.1 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:31286950 C>T maps to NM_001145808.1 Q314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr16:31341481 G>A maps to NM_001145808.1 V1020V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:31283224 C>T maps to NM_001145808.1 Q206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:31332895 G>A maps to NM_001145808.1 E651E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:31336346 C>T maps to NM_001145808.1 F787F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr16:31332868 G>A maps to NM_001145808.1 Q642Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr16:31335979 C>T maps to NM_001145808.1 I723I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:31341841 C>T maps to NM_001145808.1 L1065L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:31282317 C>T maps to NM_001145808.1 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:31284751 G>A maps to NM_001145808.1 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:31286971 C>T maps to NM_001145808.1 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:31342523 C>T maps to NM_001145808.1 P1106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:31342524 C>T maps to NM_001145808.1 L1107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr16:31308857 C>T maps to NM_001145808.1 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr16:31288248 C>T maps to NM_001145808.1 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr16:31287012 G>A maps to NM_001145808.1 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr2:187531504 C>T maps to NM_002210.3 I747I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:187455094 C>T maps to NM_002210.3 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr2:187519427 G>A maps to NM_002210.3 R519R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:187500839 C>T maps to NM_002210.3 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:187531933 T>A maps to NM_002210.3 V768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:187501807 C>T maps to NM_002210.3 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr16:31372415 G>A maps to NM_000887.3 W298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr16:31374046 G>A maps to NM_000887.3 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr16:31384572 G>A maps to NM_000887.3 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr16:31391097 G>A maps to NM_000887.3 R963R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr16:31383817 C>T maps to NM_000887.3 Y760Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:31383781 C>T maps to NM_000887.3 N748N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:31391139 G>A maps to NM_000887.3 L977L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:31391660 C>T maps to NM_000887.3 F1045F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr16:31391334 C>T maps to NM_000887.3 I1003I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr16:31372469 G>A maps to NM_000887.3 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:31367985 C>T maps to NM_000887.3 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:31374257 C>T maps to NM_000887.3 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr16:31374613 C>T maps to NM_000887.3 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:31374392 G>A maps to NM_000887.3 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr16:31383820 C>T maps to NM_000887.3 F761F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:31373211 C>T maps to NM_000887.3 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr16:31388539 C>T maps to NM_000887.3 Q915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:31392264 C>T maps to NM_000887.3 L1108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr16:31374269 C>T maps to NM_000887.3 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr16:31373953 C>T maps to NM_000887.3 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr16:31371383 C>T maps to NM_000887.3 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr16:31383008 C>T maps to NM_000887.3 P688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr16:31382969 G>A maps to NM_000887.3 V675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:31373953 C>T maps to NM_000887.3 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr16:31391890 C>T maps to NM_000887.3 F1074F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr16:31383008 C>T maps to NM_000887.3 P688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:31374055 C>T maps to NM_000887.3 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:31374538 G>A maps to NM_000887.3 W518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:31391693 C>T maps to NM_000887.3 V1056V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:31371684 C>T maps to NM_000887.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr10:33196014 T>A maps to NM_033668.2 G796G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:33190553 G>A maps to ENST00000374956 I819I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:33218798 C>T maps to ENST00000374956 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr23:70523326 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:70523172 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:70521711 A>G did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:70523547 G>A did not map to a codon.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr19:3942102 C>T maps to NM_170678.2 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:3939939 C>T maps to NM_170678.2 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:3937266 C>T maps to NM_170678.2 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:3941086 C>T maps to NM_170678.2 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr21:46330211 C>T maps to NM_000211.3 W45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr21:46323295 G>A maps to NM_000211.3 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr21:46306677 C>T maps to NM_000211.3 K740K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr21:46310001 C>T maps to NM_000211.3 Q516Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr21:46309893 C>T maps to NM_000211.3 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr21:46308785 G>A maps to NM_000211.3 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr21:46306656 C>T maps to NM_000211.3 W747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:46326872 C>T maps to NM_000211.3 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr17:45384949 C>T maps to NM_000212.2 R750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:45367594 C>T maps to NM_000212.2 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:45361893 C>T maps to NM_000212.2 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:45364509 G>A maps to NM_000212.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:45369599 C>T maps to NM_000212.2 I452I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr17:45360728 C>T maps to NM_000212.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr17:45384966 A>G maps to NM_000212.2 K755K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:45360901 C>T maps to NM_000212.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:45368324 C>T maps to NM_000212.2 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr17:45368357 C>A maps to NM_000212.2 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:63955796 G>T maps to ENST00000371092 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:63955868 G>A maps to ENST00000371092 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr17:73744962 G>A maps to NM_001005619.1 G1051G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:73738532 G>A maps to NM_001005619.1 K915K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:73725387 C>T maps to NM_001005619.1 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:73727397 G>A maps to NM_001005619.1 K388K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr17:73739905 C>T maps to NM_001005619.1 S1025S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr17:73745049 C>T maps to NM_001005619.1 H1080H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:73723293 C>T maps to NM_001005619.1 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr17:73739890 G>A maps to NM_001005619.1 G1020G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr17:73752698 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:73726335 G>A maps to NM_001005619.1 W251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:73727993 C>T maps to NM_001005619.1 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:73727999 C>T maps to NM_001005619.1 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:73736437 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:73738801 C>T maps to NM_001005619.1 L974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr17:73725384 C>T maps to NM_001005619.1 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:73739890 G>A maps to NM_001005619.1 G1020G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr17:73723751 C>T maps to NM_001005619.1 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr17:73724491 T>C maps to NM_001005619.1 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:73746841 C>T maps to NM_001005619.1 L1186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr17:73748357 G>A maps to NM_001005619.1 K1299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr17:73753114 G>A maps to NM_001005619.1 K1698K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:73727449 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:73746300 G>A maps to NM_001005619.1 K1142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:73748387 G>A maps to NM_001005619.1 E1309E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr17:73751163 G>A maps to NM_001005619.1 R1459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr17:73747166 C>T maps to NM_001005619.1 C1256C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:73727394 C>T maps to NM_001005619.1 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr3:124538621 G>A maps to NM_002213.3 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr3:124540213 G>A maps to NM_002213.3 H296H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr3:124578287 G>A maps to NM_002213.3 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:124567295 G>A maps to NM_002213.3 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:124567199 A>T maps to NM_002213.3 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr3:124536490 G>A maps to NM_002213.3 Q369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:124515541 C>T maps to NM_002213.3 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:124515328 G>A maps to NM_002213.3 C533C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:124567265 C>T maps to NM_002213.3 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr3:124492547 G>A maps to NM_002213.3 C635C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:124538681 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr3:124515334 G>A maps to NM_002213.3 N531N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:124515298 G>A maps to NM_002213.3 I543I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:124515319 G>A maps to NM_002213.3 F536F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr2:161029124 G>A maps to NM_000888.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:161025818 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:53594029 T>C maps to NM_000889.1 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:53589887 G>A maps to NM_000889.1 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:53594062 G>A maps to NM_000889.1 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:53594187 G>A maps to NM_000889.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr7:20421417 C>T maps to NM_002214.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr7:20406795 C>T maps to NM_002214.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:20418875 A>C maps to NM_002214.2 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr7:20421375 T>C maps to NM_002214.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr7:20421376 A>T maps to NM_002214.2 K277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr7:20418902 G>A maps to NM_002214.2 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr7:20418902 G>A maps to NM_002214.2 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr7:20445780 C>T maps to NM_002214.2 V670V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr7:20403339 C>T maps to NM_002214.2 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:20406639 C>T maps to NM_002214.2 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:20441432 A>G maps to NM_002214.2 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr13:102359247 G>A maps to NM_004791.1 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr3:52825872 G>A maps to NM_002215.2 G894G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr3:52812489 C>T maps to NM_002215.2 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr3:52812489 C>T maps to NM_002215.2 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:52812993 G>A maps to NM_002215.2 K114K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:52817047 C>T maps to NM_002215.2 R336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:52814382 C>T maps to NM_002215.2 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr3:52823753 C>T maps to NM_002215.2 I735I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:52816258 C>T maps to NM_002215.2 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:52820999 C>T maps to NM_002215.2 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:52816986 C>T maps to NM_002215.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:52825620 G>A maps to NM_002215.2 R861R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr3:52813517 C>T maps to NM_002215.2 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:52815969 C>T maps to NM_002215.2 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr3:52825797 G>A maps to NM_002215.2 R869R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:52816038 G>A maps to NM_002215.2 K257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:52825908 C>T maps to NM_002215.2 I906I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:52822005 C>T maps to NM_002215.2 F643F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr10:7745420 C>T maps to NM_002216.2 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:7750996 C>T maps to NM_002216.2 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr10:7762889 C>T maps to NM_002216.2 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:7759687 G>A maps to NM_002216.2 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:7763736 G>A maps to NM_002216.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:7772023 G>A maps to NM_002216.2 K463K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:7762926 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr10:7769727 G>T maps to NM_002216.2 G406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr10:7765478 C>T maps to NM_002216.2 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr10:7769000 G>A maps to NM_002216.2 W358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:7762922 G>A maps to NM_002216.2 Q245Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:7773904 A>T maps to NM_002216.2 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:7776938 G>A maps to NM_002216.2 Q614Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr10:7769756 G>A maps to NM_002216.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr3:52835083 C>T maps to NM_002217.3 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:52842609 G>A maps to NM_002217.3 T862T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:52830624 G>A maps to NM_002217.3 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:52842627 C>T maps to NM_002217.3 F868F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:52836468 C>T maps to NM_002217.3 I501I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr3:52852125 G>A maps to ENST00000485816 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:52848315 G>A maps to ENST00000485816 I850I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr3:52850925 C>T maps to ENST00000485816 K820K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:52858518 G>A maps to ENST00000485816 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:52854701 G>A maps to ENST00000485816 V593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:52858863 G>A maps to ENST00000485816 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr3:52857967 G>A maps to ENST00000485816 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:52858224 G>A maps to ENST00000485816 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:52848311 G>A maps to ENST00000485816 L852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr10:7679251 G>A maps to ENST00000256861 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:7611637 C>T maps to ENST00000256861 R714R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:7622016 G>A maps to ENST00000256861 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:7618857 G>A maps to ENST00000256861 I512I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr10:7679437 C>T maps to ENST00000256861 E135E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr10:7608104 G>A maps to ENST00000256861 A805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr10:7679269 G>A maps to ENST00000256861 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:7679269 G>A maps to ENST00000256861 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr10:7657989 G>A maps to ENST00000256861 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr10:7621821 G>A maps to ENST00000256861 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr10:7621866 G>A maps to ENST00000256861 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:7618551 G>A maps to ENST00000256861 F614F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:7621799 G>A maps to ENST00000256861 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:7621836 G>A maps to ENST00000256861 I433I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:7621968 G>A maps to ENST00000256861 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:7679434 C>T maps to ENST00000256861 K136K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:7683930 C>T maps to ENST00000256861 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr10:7608227 G>A maps to ENST00000256861 I764I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr10:7627960 G>A maps to ENST00000256861 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:54784963 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:54786194 C>T did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:54783452 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:54785237 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:54784274 T>G did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:54777625 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:54783973 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:54783978 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:54823446 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:54784029 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:54784030 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:54785276 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:54783526 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:54783452 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:54785291 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:54776453 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:54777750 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:54785279 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr5:156672893 C>T maps to NM_005546.3 F506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:156635901 G>A maps to NM_005546.3 K47K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:156636001 C>T maps to NM_005546.3 Q81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr5:156655357 C>T maps to NM_005546.3 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:156679615 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr5:156665144 G>A maps to NM_005546.3 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr5:156671377 C>T maps to NM_005546.3 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:156635958 G>A maps to NM_005546.3 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:156667158 C>T maps to NM_005546.3 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:156641208 G>A maps to NM_005546.3 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr5:156667189 C>T maps to NM_005546.3 Q324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:160850432 G>A maps to NM_017625.2 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr1:160851956 G>A maps to NM_017625.2 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr1:160851072 C>T maps to NM_017625.2 K145K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:160854649 G>A maps to NM_017625.2 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:160846563 G>A maps to NM_017625.2 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr1:160851025 C>T maps to NM_017625.2 W161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:160850441 G>A maps to NM_017625.2 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:160853248 C>T maps to NM_017625.2 K42K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:160921001 C>T maps to NM_080878.2 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr1:160920381 G>A maps to NM_080878.2 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:160920381 G>A maps to NM_080878.2 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:160920898 C>T maps to NM_080878.2 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:160917754 A>G maps to NM_080878.2 C263C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr1:160920976 C>T maps to NM_080878.2 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:160915040 G>A maps to NM_080878.2 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:160917802 G>A maps to NM_080878.2 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:160920887 C>T maps to NM_080878.2 W129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:78616620 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:78616611 C>A did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:78616620 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:78619029 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr23:78616939 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr2:231742192 C>T maps to NM_030926.4 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:231741645 C>T maps to NM_030926.4 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:231738191 C>T maps to NM_030926.4 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:231742780 C>T maps to NM_030926.4 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr2:231738152 C>T maps to NM_030926.4 R48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:231742768 C>T maps to NM_030926.4 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr20:3202488 C>T maps to NM_033453.2 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:3193980 G>A maps to NM_033453.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr20:3202494 C>T maps to NM_033453.2 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:3202494 C>T maps to NM_033453.2 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:93408147 G>A maps to NM_014216.4 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:93581430 G>A maps to NM_014216.4 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:226825420 G>A maps to NM_002221.3 R862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:226923416 G>A maps to NM_002221.3 A581A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:226924799 G>A maps to NM_002221.3 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:226827256 C>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:226923767 C>T maps to NM_002221.3 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:226923449 G>A maps to NM_002221.3 I570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:226822413 G>A maps to NM_002221.3 V933V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr1:226924619 G>A maps to NM_002221.3 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:41223579 G>A maps to NM_025194.2 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:41245434 C>T maps to NM_025194.2 I674I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr3:4808224 C>T maps to ENST00000356617 F1848F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr3:4853112 A>G maps to ENST00000356617 V2477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr3:4847917 G>A maps to ENST00000356617 G2411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:4735215 A>C maps to ENST00000356617 R1354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:4716798 C>T maps to ENST00000356617 F878F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:4725189 C>T maps to ENST00000356617 F1090F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:4732913 C>T maps to ENST00000356617 F1301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr3:4859856 C>T maps to ENST00000356617 I2651I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:4842137 C>T maps to ENST00000356617 L2319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:4706913 C>T maps to ENST00000356617 F545F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:4725213 G>A maps to ENST00000356617 E1098E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:4810402 C>T maps to ENST00000356617 L1974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:4735337 G>A maps to ENST00000356617 K1394K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr3:4732872 C>T maps to ENST00000356617 Q1288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:4702674 C>T maps to ENST00000356617 N381N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:4730286 C>T maps to ENST00000356617 L1267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:4732835 G>A maps to ENST00000356617 E1275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:4714906 C>T maps to ENST00000356617 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr3:4735307 C>T maps to ENST00000356617 V1384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr3:4878582 G>A maps to ENST00000356617 T2716T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr3:4725388 C>T maps to ENST00000356617 I1131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr12:26810791 C>T maps to NM_002223.2 E680E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:26709212 G>A maps to NM_002223.2 F1639F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:26868251 T>A maps to NM_002223.2 K279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:26572050 G>A maps to NM_002223.2 L2347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr12:26636831 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:26749937 G>A maps to NM_002223.2 L1378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:26592110 G>A maps to NM_002223.2 Q2198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:26731733 T>C maps to NM_002223.2 Q1514Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:26784915 G>A maps to NM_002223.2 F939F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:26636734 G>A maps to NM_002223.2 L1970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr6:33630346 C>T maps to ENST00000374316 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr6:33639929 G>A maps to ENST00000374316 L951L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:33652690 C>T maps to ENST00000374316 L1760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr6:33631627 C>T maps to ENST00000374316 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:33656526 C>T maps to ENST00000374316 F2221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:33641369 C>T maps to ENST00000374316 F977F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr6:33656170 C>T maps to ENST00000374316 F2177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr6:33632945 C>T maps to ENST00000374316 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr6:33643560 G>A maps to ENST00000374316 L1070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr6:33653891 C>T maps to ENST00000374316 F1910F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:33656077 C>T maps to ENST00000374316 F2146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:33623570 C>T maps to ENST00000374316 N63N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:33632885 C>T maps to ENST00000374316 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:33648128 C>T maps to ENST00000374316 F1416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr10:106074846 G>A maps to NM_033397.2 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:106074372 G>A maps to NM_033397.2 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr10:106075176 G>A maps to NM_033397.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr10:106074462 C>T maps to NM_033397.2 W449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr10:106074636 G>A maps to NM_033397.2 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:106075106 G>A maps to NM_033397.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:106074921 G>A maps to NM_033397.2 D296D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr10:106074291 G>A maps to NM_033397.2 F506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:106074665 G>A maps to NM_033397.2 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:106074291 G>A maps to NM_033397.2 F506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:106074623 G>A maps to NM_033397.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:106075176 G>A maps to NM_033397.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:106075308 G>A maps to NM_033397.2 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:106074330 G>A maps to NM_033397.2 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr2:96992827 C>T maps to ENST00000420728 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:96992897 C>T maps to ENST00000420728 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr16:19126059 C>T maps to NM_001034841.3 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr21:35247713 G>A maps to NM_003024.2 L1410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr21:35140023 C>T maps to NM_003024.2 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr21:35237481 C>G maps to NM_003024.2 S1306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr21:35186231 G>A maps to NM_003024.2 T861T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr21:35258648 G>A maps to NM_003024.2 T1634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr21:35122508 C>T maps to NM_003024.2 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:24507640 G>A maps to NM_006277.2 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:24522999 C>T maps to NM_006277.2 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr2:24426499 G>A maps to NM_006277.2 L1697L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:24435575 G>A maps to NM_006277.2 S1344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:24522948 C>T maps to NM_006277.2 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr15:40705278 G>A maps to NM_002225.3 K262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr15:40708538 C>A maps to NM_002225.3 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:40707678 C>T maps to NM_002225.3 Q323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:40710428 C>T maps to NM_002225.3 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:40710372 C>T maps to NM_002225.3 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:40699895 C>T maps to NM_002225.3 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:152882431 G>A maps to NM_005547.2 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:152882674 G>A maps to NM_005547.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:152883841 G>A maps to NM_005547.2 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:152883655 G>A maps to NM_005547.2 K461K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:152883860 C>T maps to NM_005547.2 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr1:152883847 G>A maps to NM_005547.2 Q525Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:152882512 G>A maps to NM_005547.2 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:152882554 G>A maps to NM_005547.2 Q94Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr1:152883655 G>A maps to NM_005547.2 K461K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:185270668 A>G maps to NM_006469.4 H264H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:185270668 A>G maps to NM_006469.4 H264H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:185269200 T>C maps to NM_006469.4 K477K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:128262740 A>G maps to NM_017969.2 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:128262587 G>A maps to NM_017969.2 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:128262701 C>T maps to NM_017969.2 Q259Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:150713565 C>T maps to NM_203395.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:150690256 G>A maps to NM_203395.2 K30K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:49244245 G>A maps to NM_182575.2 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr19:49244254 G>A maps to NM_182575.2 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:49244173 C>T maps to NM_182575.2 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:49248975 C>T maps to NM_182575.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr20:10624441 C>T maps to NM_000214.2 G814G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr20:10620151 G>A maps to NM_000214.2 I1217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr20:10633224 G>A maps to NM_000214.2 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:10630182 C>T maps to NM_000214.2 Q445Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr20:10630940 A>G maps to NM_000214.2 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr20:10621856 C>T maps to NM_000214.2 R984R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:10620598 G>A maps to NM_000214.2 F1068F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr20:10622122 C>T maps to NM_000214.2 K967K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr20:10639138 C>T maps to NM_000214.2 W224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr14:105612993 A>C maps to NM_002226.3 Y849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:105612286 A>G maps to NM_002226.3 C911C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr14:105615328 C>T maps to NM_002226.3 G617G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr14:105615337 G>A maps to NM_002226.3 S614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:105609478 G>A maps to NM_002226.3 A1090A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:9934916 C>T maps to NM_032492.3 Y136Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr3:9934781 C>T maps to NM_032492.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr1:65332742 G>A maps to NM_002227.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:65301107 G>A maps to NM_002227.2 L1114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:65301108 G>A maps to NM_002227.2 R1113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:65332752 G>A maps to NM_002227.2 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:65330538 G>A maps to NM_002227.2 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr9:5044463 C>T maps to NM_004972.3 R138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr9:5123073 C>T maps to NM_004972.3 L1044L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:5069173 C>T maps to NM_004972.3 F493F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr9:5064920 C>T maps to NM_004972.3 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr19:17951086 G>A maps to NM_000215.3 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:17949182 G>A maps to NM_000215.3 I486I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:17942509 G>A maps to NM_000215.3 L926L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:17943658 G>A maps to NM_000215.3 A810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:17943637 G>A maps to NM_000215.3 F817F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:17945446 G>A maps to NM_000215.3 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr4:6055814 G>A maps to NM_001099433.1 Q590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr4:6083464 C>T maps to NM_001099433.1 E324E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr4:6087145 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr4:6087146 C>T maps to NM_001099433.1 Q278Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:6055713 C>T maps to NM_144720.3 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:6042422 C>T maps to NM_001099433.1 K706K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr4:6064106 G>A maps to NM_001099433.1 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr4:6043933 C>T maps to NM_001099433.1 G683G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr4:6107568 C>T maps to NM_001099433.1 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:6051599 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:6055728 G>A maps to NM_144720.3 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:6055779 G>A maps to NM_001099433.1 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:6064098 G>A maps to NM_001099433.1 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:6081973 C>T maps to NM_001099433.1 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:6087173 C>T maps to NM_001099433.1 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr5:147040615 G>A maps to NM_014790.3 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr5:147016596 G>A maps to NM_014790.3 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:147020383 C>T maps to NM_014790.3 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:147019289 G>A maps to NM_014790.3 R479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:147020380 A>C maps to NM_014790.3 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:147040906 G>A maps to NM_014790.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr5:147020326 T>G maps to NM_014790.3 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:147012281 G>A maps to NM_014790.3 D579D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:147051360 C>T maps to NM_014790.3 K3K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr5:147030089 C>T maps to NM_014790.3 K216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:147040888 C>T maps to NM_014790.3 K83K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:147012259 G>A maps to NM_014790.3 R587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:147029950 G>A maps to NM_014790.3 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr5:147019212 G>A maps to NM_014790.3 D504D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:147027971 C>T maps to NM_014790.3 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr5:147024538 G>A maps to NM_014790.3 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:147040969 C>T maps to NM_014790.3 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:147040867 C>T maps to NM_014790.3 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr10:133954043 G>A maps to NM_001105521.2 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr10:133948553 T>C maps to NM_001105521.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:133967466 G>A maps to NM_001105521.2 R729R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr10:133967436 G>A maps to NM_001105521.2 K719K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr10:133930690 G>A maps to NM_001105521.2 E82E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:133930843 C>T maps to NM_001105521.2 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:133930885 C>T maps to NM_001105521.2 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr21:27071097 G>A maps to NM_021219.2 W168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr21:27086950 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr21:27062199 C>T maps to NM_021219.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr21:27066101 C>T maps to NM_021219.2 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr21:27071112 C>T maps to NM_021219.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr21:27071112 C>T maps to NM_021219.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr6:15501486 C>T maps to NM_004973.2 A765A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr6:15496652 C>T maps to NM_004973.2 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr6:15513249 C>T maps to NM_004973.2 T1080T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:15452402 C>T maps to NM_004973.2 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:15501379 C>T maps to NM_004973.2 L730L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr7:28220172 G>A maps to NM_175061.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:27880445 C>A maps to NM_175061.3 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr7:27880460 C>T maps to NM_175061.3 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:28220124 G>A maps to NM_175061.3 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:75928188 C>T maps to NM_001135049.1 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr14:75904778 C>T maps to NM_001135049.1 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:75928232 G>A maps to NM_001135049.1 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr14:75904814 G>T maps to NM_001135049.1 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr7:139810918 A>G maps to NM_030647.1 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr7:139799823 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr7:139833370 G>A maps to NM_030647.1 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr7:139820288 A>C maps to NM_030647.1 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:139826442 G>A maps to NM_030647.1 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:139790935 G>A maps to NM_030647.1 I928I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:139819009 C>T maps to NM_030647.1 E383E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr7:139824436 G>A maps to NM_030647.1 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr7:139818970 G>A maps to NM_030647.1 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:139818919 G>A maps to NM_030647.1 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr7:139824490 G>A maps to NM_030647.1 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:139826472 G>A maps to NM_030647.1 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:139796361 C>T maps to NM_030647.1 V789V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:139791649 C>T maps to NM_030647.1 K895K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:59954435 G>A maps to ENST00000356057 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:64968146 G>A maps to NM_032776.1 F1094F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr10:65024428 A>G maps to NM_032776.1 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr10:64968403 G>A maps to NM_032776.1 Q1009*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:64967069 T>C maps to NM_032776.1 T1453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:64966361 G>A maps to NM_032776.1 N1689N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:64968323 A>G maps to NM_032776.1 F1035F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr10:64977080 G>C maps to NM_032776.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:64974678 G>A maps to NM_032776.1 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:227920377 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr16:27225027 C>T maps to NM_001145348.1 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr16:27225028 C>T maps to NM_001145348.1 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr16:27231784 C>T maps to NM_001145348.1 H393H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr16:27224961 C>T maps to NM_001145348.1 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:74720106 A>G maps to NM_001081461.1 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:74719995 G>A maps to NM_001081461.1 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:74720087 G>A maps to NM_001081461.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:42127076 C>T maps to NM_005090.3 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:42127273 C>T maps to NM_005090.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr5:78610270 C>T maps to NM_152405.4 P752P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr5:78610163 C>T maps to NM_152405.4 Q717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:78608306 C>T maps to NM_152405.4 R684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:75227655 G>A maps to NM_020647.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:75227655 G>A maps to NM_020647.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:75227700 G>A maps to NM_020647.2 D178D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:75157288 C>T maps to NM_020647.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:75227616 C>T maps to NM_020647.2 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr8:75227729 C>A maps to NM_020647.2 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr20:42788511 C>T maps to NM_020433.4 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr20:42788352 C>T maps to NM_020433.4 K358K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr20:42788274 G>A maps to NM_020433.4 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr20:42806610 C>T maps to NM_175913.3 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr20:42788430 G>A maps to NM_020433.4 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:42747229 C>T maps to NM_020433.4 A401A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:42747235 C>T maps to NM_020433.4 E399E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:42788462 G>A maps to NM_020433.4 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr16:87678074 C>T maps to NM_020655.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr16:87677903 C>T maps to NM_020655.2 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr16:87678236 C>T maps to NM_020655.2 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr16:87723258 G>A maps to NM_020655.2 E431E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr16:87678068 C>T maps to NM_020655.2 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:87717834 C>T maps to NM_020655.2 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr16:87678074 C>T maps to NM_020655.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:87677873 G>A maps to NM_020655.2 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:87678641 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr16:87678629 C>T maps to NM_020655.2 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr16:87678311 G>A maps to NM_020655.2 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr14:24040601 T>A maps to NM_032452.2 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:24040511 G>A maps to NM_032452.2 C476C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr14:24040406 G>C maps to NM_032452.2 G511G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr8:143740338 C>T maps to NM_001077527.1 E533E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr8:143747282 G>A maps to NM_003724.2 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr11:96124979 C>T maps to NM_003772.3 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:2255217 C>T maps to NM_144616.3 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:2252648 C>T maps to NM_144616.3 E225E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:2252381 C>T maps to NM_144616.3 E314E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:23443309 G>A maps to NM_032876.4 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:59248100 C>T maps to NM_002228.3 Q214Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr19:18391904 G>T maps to NM_005354.4 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr17:39925851 C>A maps to NM_021991.2 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr17:39913717 G>A maps to NM_021991.2 S665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr17:39912103 G>A maps to NM_021991.2 P710P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr17:39912436 G>A maps to NM_021991.2 P692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:39920985 G>A maps to NM_021991.2 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:39923828 G>A maps to NM_021991.2 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:39913717 G>A maps to NM_021991.2 S665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:39921211 G>A maps to NM_021991.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:39913699 G>A maps to NM_021991.2 S671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:39914695 G>A maps to NM_021991.2 N576N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr17:39921202 G>A maps to NM_021991.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr17:39925417 C>T maps to NM_021991.2 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:39927938 C>T maps to NM_021991.2 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:39919276 G>A maps to NM_021991.2 I485I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr17:39913973 G>A maps to NM_021991.2 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:24358097 G>A maps to NM_181337.3 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr23:8507771 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:8507796 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr23:8503631 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr23:8503632 G>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:8565121 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:8501042 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:8538558 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:8522053 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr3:124103702 C>T maps to NM_001024660.3 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr3:124209607 G>A maps to NM_001024660.3 P1486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:124053167 G>A maps to NM_001024660.3 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr3:124437995 C>T maps to NM_001024660.3 F2880F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr3:124117546 C>T maps to NM_001024660.3 D723D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr3:123983538 T>G did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:124390669 C>T maps to NM_001024660.3 P2288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:124211648 G>A maps to NM_001024660.3 R1582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:124397058 C>T maps to NM_001024660.3 L2406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:124438106 G>A maps to NM_001024660.3 V2917V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:124103813 C>T maps to NM_001024660.3 F629F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr3:124149561 C>T maps to NM_001024660.3 S921S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr3:124196141 C>T maps to NM_001024660.3 S1382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:124209661 C>T maps to NM_001024660.3 S1504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:124413283 G>A maps to NM_001024660.3 W2504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:124437845 G>A maps to NM_001024660.3 Q2830Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:124181390 C>T maps to NM_001024660.3 T1312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr3:123987867 G>A maps to NM_001024660.3 E243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:124174097 G>A maps to NM_001024660.3 T1207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:124390732 C>T maps to NM_001024660.3 F2309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:123987690 C>T maps to NM_001024660.3 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr3:124149591 G>A maps to NM_001024660.3 R931R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:124416491 C>T maps to NM_001024660.3 S2584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:124053224 G>A maps to NM_001024660.3 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:124390555 G>A maps to NM_001024660.3 V2250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr3:124153236 C>T maps to NM_001024660.3 A969A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:124165123 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:124374465 G>C maps to NM_001024660.3 L1937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr3:124044921 C>T maps to NM_001024660.3 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr3:124044825 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr3:124393437 A>G maps to NM_001024660.3 A2390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr3:124153275 G>A maps to NM_001024660.3 E982E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr3:124438175 C>T maps to NM_001024660.3 P2940P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:124397084 G>A maps to NM_001024660.3 V2414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:124215214 C>T maps to NM_001024660.3 I1628I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr3:124436231 G>A maps to NM_001024660.3 K2805K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr3:124413297 C>T maps to NM_001024660.3 Q2509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:124201686 C>T maps to NM_001024660.3 S1406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:124303685 G>A maps to NM_007064.3 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:124351405 G>A maps to NM_001024660.3 T1772T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:124437989 C>T maps to NM_001024660.3 S2878S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr3:124415046 C>A maps to NM_001024660.3 C2548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:123946903 C>T maps to NM_001024660.3 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:123987906 C>T maps to NM_001024660.3 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:124351432 G>A maps to NM_001024660.3 G1781G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr3:124438106 G>A maps to NM_001024660.3 V2917V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr9:732593 T>C maps to NM_015158.2 P1074P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr19:11303657 G>A maps to NM_015493.6 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr19:11285167 C>A maps to NM_015493.6 V691V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr19:11283752 A>G maps to NM_015493.6 I713I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:11304038 G>A maps to NM_015493.6 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr19:11289037 G>A maps to NM_015493.6 F509F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:11289133 G>A maps to NM_015493.6 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:11285176 G>A maps to NM_015493.6 F688F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:11289037 G>A maps to NM_015493.6 F509F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr19:11280855 G>A maps to NM_015493.6 A768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:8397898 C>T maps to NM_198471.2 T645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:62739290 G>A maps to NM_181712.4 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:62740505 G>A maps to NM_181712.4 N90N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:62733963 G>A maps to NM_181712.4 A742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:62703960 G>A maps to NM_181712.4 S992S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:62739944 G>A maps to NM_181712.4 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr1:62739413 G>A maps to NM_181712.4 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:62740256 C>T maps to NM_181712.4 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:62739383 C>T maps to NM_181712.4 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:62737247 C>A maps to NM_181712.4 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:62718867 C>T maps to NM_181712.4 V851V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:62738909 C>T maps to NM_181712.4 K622K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:62739650 C>T maps to NM_181712.4 E375E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:62739692 C>T maps to NM_181712.4 E361E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:62739944 G>A maps to NM_181712.4 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:62739764 C>T maps to NM_181712.4 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:62739143 C>T maps to NM_181712.4 G544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr16:75681538 T>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:75675518 G>A maps to NM_001130089.1 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr17:40270411 G>A maps to NM_021078.2 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr17:40271324 G>A maps to NM_021078.2 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:40269425 G>A maps to NM_021078.2 I539I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:40266927 G>A maps to NM_021078.2 I667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:40271324 G>A maps to NM_021078.2 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr3:20136845 T>A maps to NM_003884.4 C174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:20136891 C>T maps to NM_003884.4 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:20189749 C>T maps to NM_003884.4 D724D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:20168971 C>T maps to NM_003884.4 F560F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:20193933 G>T maps to NM_003884.4 E806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr3:20153273 C>T maps to NM_003884.4 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:149922825 T>C maps to NM_007044.2 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr13:30805461 A>G maps to NM_032116.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr13:30784558 G>A maps to NM_032116.3 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr13:30782817 G>A maps to NM_032116.3 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr18:44625667 C>T maps to ENST00000356157 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr18:44584635 C>T maps to ENST00000356157 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr18:44595625 G>A maps to ENST00000356157 W270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr18:44580797 G>A maps to ENST00000356157 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr18:44579377 C>T maps to ENST00000356157 Q67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr18:44589356 C>T maps to ENST00000356157 D171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr16:57785578 C>T maps to NM_005886.2 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:57775704 C>T maps to NM_005886.2 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr16:57785892 T>G maps to NM_005886.2 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:57787412 C>T maps to NM_005886.2 Q387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr16:57789406 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:57775605 C>T maps to NM_005886.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr16:57778394 C>T maps to NM_005886.2 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr16:57787309 G>A maps to NM_005886.2 Q352Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr16:57790378 G>A maps to NM_005886.2 E610E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr16:57785889 C>T maps to NM_005886.2 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:15430673 C>T maps to NM_201628.2 F679F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:15382771 G>A maps to NM_201628.2 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:15370526 C>T maps to NM_201628.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:15386767 C>T maps to NM_201628.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:14925591 C>T maps to NM_201628.2 T33T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D3-A51R-06A-11D-A25O-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr10:102824050 G>A maps to NM_030929.4 W182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:102824123 G>A maps to NM_030929.4 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr10:102824141 C>T maps to NM_030929.4 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr10:102822603 C>T maps to NM_030929.4 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:127646675 G>A maps to NM_207335.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:127682110 G>A maps to NM_207335.2 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:127702958 C>T maps to NM_207335.2 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:127642488 G>A maps to NM_207335.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr3:127642654 C>T maps to NM_207335.2 Q251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:127642779 G>A maps to NM_207335.2 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:127646783 G>A maps to NM_207335.2 W416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr3:127642821 G>A maps to NM_207335.2 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr15:65369260 C>T maps to NM_001101362.2 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:65370430 G>A maps to NM_001101362.2 E426E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:32909367 G>A maps to NM_015483.2 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr7:32909535 A>G maps to NM_015483.2 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:32910036 A>C maps to NM_015483.2 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr11:105923627 C>T maps to NM_198439.2 V596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:105924092 G>A maps to NM_198439.2 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:105924521 G>A maps to NM_198439.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:47599197 A>T maps to NM_018095.4 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:42732405 C>T maps to NM_152393.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:42729764 C>T maps to NM_152393.2 C428C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:42729765 C>T maps to NM_152393.2 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr3:42733373 G>A maps to NM_152393.2 R585R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z4-06A-11D-A197-08 chr3:42728021 G>A maps to NM_152393.2 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZU-06A-12D-A196-08 chr3:42728090 C>T maps to NM_152393.2 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:42728210 C>T maps to NM_152393.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:42732371 C>T maps to NM_152393.2 F543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr13:41768228 G>A maps to NM_032138.4 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:41767907 G>A maps to NM_032138.4 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr3:67053840 G>A maps to NM_032505.2 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr3:67054065 G>A maps to NM_032505.2 Q225Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr3:67053690 G>A maps to NM_032505.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:67058397 C>T maps to NM_032505.2 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:67053898 C>T maps to NM_032505.2 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:67054578 A>C maps to NM_032505.2 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr3:67053664 C>T maps to NM_032505.2 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:67053898 C>T maps to NM_032505.2 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:85270736 G>A maps to NM_020122.4 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr2:85280375 T>G maps to NM_020122.4 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:5020774 G>A maps to NM_000217.2 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:5021485 C>T maps to NM_000217.2 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr12:5021980 C>A maps to NM_000217.2 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr12:5020558 T>G maps to NM_000217.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:5021545 C>T maps to NM_000217.2 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:5021485 C>T maps to NM_000217.2 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:5020951 C>T maps to NM_000217.2 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:5021209 C>T maps to NM_000217.2 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:5021122 G>A maps to NM_000217.2 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr12:5021215 G>A maps to NM_000217.2 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:5020936 G>A maps to NM_000217.2 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr12:5021405 C>T maps to NM_000217.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:111061364 A>G maps to NM_005549.2 N15N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:111060491 G>A maps to NM_005549.2 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr1:111060908 G>A maps to NM_005549.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:111060332 C>T maps to NM_005549.2 K359K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr1:111060905 G>A maps to NM_005549.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:111060962 C>T maps to NM_005549.2 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:111060587 C>T maps to NM_005549.2 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:111061259 C>T maps to NM_005549.2 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:111060470 G>A maps to NM_005549.2 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr1:111060614 G>A maps to NM_005549.2 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:111060401 G>A maps to NM_005549.2 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:111060401 G>A maps to NM_005549.2 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:111060341 G>A maps to NM_005549.2 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:111060398 C>T maps to NM_005549.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:111060797 G>A maps to NM_005549.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:111061283 C>T maps to NM_005549.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:111146753 G>A maps to NM_004974.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:111145994 C>T maps to NM_004974.2 E470E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:111146435 G>A maps to NM_004974.2 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr1:111215721 C>T maps to NM_002232.3 K570K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:111215757 C>T maps to NM_002232.3 T558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:111216507 G>A maps to NM_002232.3 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:111216543 G>A maps to NM_002232.3 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:111216660 C>G maps to NM_002232.3 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:111216888 G>A maps to NM_002232.3 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:111215775 G>A maps to NM_002232.3 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:111216201 G>A maps to NM_002232.3 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:111215757 C>T maps to NM_002232.3 T558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:30032767 G>A maps to NM_002233.2 F486F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr11:30034029 G>A maps to NM_002233.2 Q66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr11:30032278 C>T maps to NM_002233.2 V649V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr11:30034117 G>A maps to NM_002233.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:30032326 C>T maps to NM_002233.2 G633G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:30032407 C>T maps to NM_002233.2 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:5154926 G>A maps to NM_002234.2 E538E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:5154221 C>T maps to NM_002234.2 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:5155046 G>A maps to NM_002234.2 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr12:5153889 C>T maps to NM_002234.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:5154029 C>T maps to NM_002234.2 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:5155064 G>A maps to NM_002234.2 E584E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:5154290 C>T maps to NM_002234.2 I326I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:5153807 C>T maps to NM_002234.2 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:5154632 C>T maps to NM_002234.2 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:5154974 G>A maps to NM_002234.2 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:5154104 C>T maps to NM_002234.2 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr12:5153888 C>T maps to NM_002234.2 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:5154068 C>T maps to NM_002234.2 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:4920358 C>T maps to NM_002235.3 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:4919843 C>T maps to NM_002235.3 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:4920433 C>T maps to NM_002235.3 I409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr12:4919959 C>T maps to NM_002235.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:4920379 C>T maps to NM_002235.3 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:4920730 G>A maps to NM_002235.3 R508R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:4920739 C>T maps to NM_002235.3 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr12:4919803 C>T maps to NM_002235.3 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:4920517 C>T maps to NM_002235.3 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:4920724 G>A maps to NM_002235.3 R506R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr12:4919428 C>T maps to NM_002235.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:4919365 G>A maps to NM_002235.3 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:4920517 C>T maps to NM_002235.3 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr12:4919557 C>T maps to NM_002235.3 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:4920055 C>T maps to NM_002235.3 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:4920517 C>T maps to NM_002235.3 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:49573343 C>T maps to NM_031886.2 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:49574129 G>A maps to NM_031886.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr19:49574006 G>A maps to NM_031886.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr3:155838462 G>A maps to NM_172160.2 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:155838489 G>A maps to NM_172160.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:6158555 A>G maps to NM_003636.3 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr1:6155617 G>A maps to NM_003636.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:6147559 C>T maps to NM_003636.3 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr17:7827773 G>A maps to NM_004732.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr17:7827357 G>A maps to NM_004732.2 Y285Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:7827786 G>A maps to NM_004732.2 N219N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr20:47990038 G>T maps to NM_004975.2 P686P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr20:47989981 G>A maps to NM_004975.2 V705V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr20:47991499 G>A maps to NM_004975.2 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr20:47990023 G>A maps to NM_004975.2 Y691Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr20:47990377 G>A maps to NM_004975.2 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:47990437 C>T maps to NM_004975.2 Q553Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:47990998 G>A maps to NM_004975.2 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:47991331 C>T maps to NM_004975.2 W255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:47991121 C>T maps to NM_004975.2 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:47991181 G>A maps to NM_004975.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:47991319 C>T maps to NM_004975.2 K259K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr20:47991004 G>A maps to NM_004975.2 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr20:47991436 G>A maps to NM_004975.2 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr20:47991228 G>A maps to NM_004975.2 Q290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZG-06A-11D-A197-08 chr20:47990455 G>T maps to NM_004975.2 T547T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr20:47990860 G>A maps to NM_004975.2 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr20:48098602 G>A maps to NM_004975.2 Q139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:47990455 G>A maps to NM_004975.2 T547T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:48098735 G>A maps to NM_004975.2 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:47990860 G>A maps to NM_004975.2 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr8:73848252 G>A maps to NM_004770.2 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:73480283 C>T maps to NM_004770.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:73849113 C>T maps to NM_004770.2 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr8:73849971 C>T maps to NM_004770.2 F794F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:73480508 G>A maps to NM_004770.2 W180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:73480512 T>C maps to NM_004770.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr8:73850151 C>T maps to NM_004770.2 S854S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr8:73848693 C>T maps to NM_004770.2 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:73848771 G>A maps to NM_004770.2 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:73848828 C>T maps to NM_004770.2 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:73849560 G>A maps to NM_004770.2 E657E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:73848498 C>T maps to NM_004770.2 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:73848499 C>T maps to NM_004770.2 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:73848771 G>A maps to NM_004770.2 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:73480496 G>A maps to NM_004770.2 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr8:73848522 C>T maps to NM_004770.2 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:73480508 G>A maps to NM_004770.2 W180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr8:73480025 C>T maps to NM_004770.2 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr8:73849878 G>A maps to NM_004770.2 Q763Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr8:73848531 C>T maps to NM_004770.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:73848624 G>A maps to NM_004770.2 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:73848771 G>A maps to NM_004770.2 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:73848924 G>A maps to NM_004770.2 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:73849869 C>A maps to NM_004770.2 T760T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:73849857 C>A maps to NM_004770.2 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:73849944 C>T maps to NM_004770.2 S785S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:73848624 G>A maps to NM_004770.2 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr8:73848365 G>A maps to NM_004770.2 W259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:73849113 C>T maps to NM_004770.2 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr8:73849488 C>T maps to NM_004770.2 F633F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr8:73848345 C>T maps to NM_004770.2 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr8:73849101 C>A maps to NM_004770.2 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr8:73850316 C>G maps to NM_004770.2 T909T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr8:73848981 G>A maps to NM_004770.2 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr8:73480349 G>A maps to NM_004770.2 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr8:73848828 C>T maps to NM_004770.2 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr8:73848864 G>A maps to NM_004770.2 K425K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:73480154 G>A maps to NM_004770.2 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:73480280 G>A maps to NM_004770.2 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:73848366 G>A maps to NM_004770.2 W259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:73848915 G>A maps to NM_004770.2 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:73849488 C>T maps to NM_004770.2 F633F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:73849773 G>A maps to NM_004770.2 Q728Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:73848525 G>A maps to NM_004770.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr8:73849500 C>T maps to NM_004770.2 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr8:73849692 G>A maps to NM_004770.2 K701K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr8:73849623 C>T maps to NM_004770.2 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr8:73849077 G>A maps to NM_004770.2 R496R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:17793711 G>A maps to NM_001112741.1 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:17793885 G>A maps to NM_001112741.1 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:17794026 G>A maps to NM_001112741.1 R462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr11:17793306 G>A maps to NM_001112741.1 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:17793285 C>T maps to NM_001112741.1 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:17793945 C>T maps to NM_001112741.1 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:17757824 C>T maps to NM_001112741.1 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr11:17793720 C>T maps to NM_001112741.1 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr12:75444473 G>A maps to NM_139137.2 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CE-06A-11D-A19A-08 chr12:75444668 T>A maps to NM_139137.2 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr12:75442083 G>A maps to NM_139137.2 D543D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:75436944 T>G maps to NM_139137.2 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:75601361 G>A maps to NM_139137.2 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:75441936 C>T maps to NM_139137.2 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:75445022 G>A maps to NM_139137.2 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:75601754 C>T maps to NM_139137.2 K3K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:75444718 G>A maps to NM_139137.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr19:50827225 C>T maps to NM_004977.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr19:50823848 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr19:50826916 G>A maps to NM_004977.2 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:50823975 G>A maps to NM_004977.2 Q682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr19:50824030 G>A maps to NM_004977.2 P663P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:50823906 G>A maps to NM_004977.2 R705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr19:50826916 G>A maps to NM_004977.2 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:50826961 G>A maps to NM_004977.2 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr19:50826853 G>A maps to NM_004977.2 I452I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:50826955 G>A maps to NM_004977.2 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:50823901 G>A maps to NM_004977.2 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:50827027 G>A maps to NM_004977.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:50823955 T>C maps to NM_004977.2 E688E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:50826511 G>A maps to NM_004977.2 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:50826916 G>A maps to NM_004977.2 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:50827042 G>A maps to NM_004977.2 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:110766202 C>T maps to NM_004978.4 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:110774871 C>T maps to NM_004978.4 Q617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr1:110768750 C>T maps to NM_004978.4 F590F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:110754498 C>T maps to NM_004978.4 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:110765833 C>T maps to NM_004978.4 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:48826417 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:48819938 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:48826439 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:48826218 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:48823429 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:48826486 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr23:48823416 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:48823476 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:48826305 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:48823244 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr7:119915621 C>T maps to NM_012281.2 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:119915765 C>T maps to NM_012281.2 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:119915114 G>A maps to NM_012281.2 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:120381674 C>T maps to NM_012281.2 Q456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr7:119914790 G>A maps to NM_012281.2 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr7:119914937 C>T maps to NM_012281.2 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:119915780 C>T maps to NM_012281.2 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:120382598 C>T maps to NM_012281.2 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:119915231 G>A maps to NM_012281.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr7:119914769 G>A maps to NM_012281.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:119914838 C>T maps to NM_012281.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:119915288 G>A maps to NM_012281.2 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:119915534 G>A maps to NM_012281.2 E283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr7:119914694 G>C maps to NM_012281.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr7:120386039 G>A maps to NM_012281.2 T558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr1:112524286 G>A maps to ENST00000315987 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr1:112524805 C>T maps to ENST00000315987 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:112318746 C>T maps to ENST00000315987 T640T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:112525135 C>T maps to ENST00000315987 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:112525045 C>T maps to ENST00000315987 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:112319688 C>T maps to ENST00000315987 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:112524826 C>T maps to ENST00000315987 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr1:112525150 C>T maps to ENST00000315987 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr1:112525210 C>T maps to ENST00000315987 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:112524769 G>A maps to ENST00000315987 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr1:112524382 G>A maps to ENST00000315987 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:112329616 A>G maps to ENST00000315987 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:35821770 G>A maps to NM_000219.3 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr21:35821770 G>A maps to NM_000219.3 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:108867988 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:74168497 C>T maps to NM_005472.4 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:74168379 G>A maps to NM_005472.4 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:223918012 C>A maps to NM_080671.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:223918036 G>A maps to NM_080671.2 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:11053649 C>T maps to NM_002236.4 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr2:11053016 C>T maps to NM_002236.4 D155D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:11053070 G>A maps to NM_002236.4 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr2:11053718 C>T maps to NM_002236.4 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:11053985 C>T maps to NM_002236.4 P478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:11053631 C>T maps to NM_002236.4 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:11053301 C>T maps to NM_002236.4 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:11053058 G>A maps to NM_002236.4 W169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr2:11053559 C>T maps to NM_002236.4 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:49626146 G>A maps to NM_002237.3 N243N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr20:49626524 G>A maps to NM_002237.3 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:49626407 G>A maps to NM_002237.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:49620631 G>A maps to NM_002237.3 Q496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:49621208 C>T maps to NM_002237.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:49626344 C>T maps to NM_002237.3 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:49626503 G>A maps to NM_002237.3 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:49620805 G>A maps to NM_002237.3 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:49626803 G>A maps to NM_002237.3 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr20:49621268 G>A maps to NM_002237.3 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51K-06A-11D-A25O-08 chr18:77659209 G>A maps to NM_012283.1 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr18:77623909 C>T maps to NM_012283.1 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr18:77623969 C>T maps to NM_012283.1 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr18:77624239 C>T maps to NM_012283.1 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:42671466 G>A maps to NM_133329.5 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:42720425 G>A maps to NM_133329.5 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr16:84270875 G>A maps to NM_172347.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:84270430 T>A maps to NM_172347.2 K221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr16:84270722 G>A maps to NM_172347.2 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:84270908 G>A maps to NM_172347.2 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr16:84256350 G>A maps to NM_172347.2 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr16:84270533 C>T maps to NM_172347.2 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:84256407 C>T maps to NM_172347.2 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:84270551 C>T maps to NM_172347.2 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:84270629 C>T maps to NM_172347.2 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:84256590 G>A maps to NM_172347.2 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:84255834 G>A maps to NM_172347.2 I516I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:84270665 G>A maps to NM_172347.2 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr1:210857381 G>A maps to NM_172362.2 V737V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:211093129 C>T maps to NM_172362.2 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr1:211192451 G>A maps to NM_172362.2 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:211192538 G>A maps to NM_172362.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:210857018 C>T maps to NM_172362.2 S858S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:210948779 C>T maps to NM_172362.2 R674R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:211093210 C>T maps to NM_172362.2 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:210857018 C>T maps to NM_172362.2 S858S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:210977404 G>A maps to NM_172362.2 F522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:210856889 C>T maps to NM_172362.2 Q901Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:210970994 G>A maps to NM_172362.2 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:210856646 C>T maps to NM_172362.2 E982E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:210857018 C>T maps to NM_172362.2 S858S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:210970943 G>A maps to NM_172362.2 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:210977335 G>A maps to NM_172362.2 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:211192553 C>T maps to NM_172362.2 E201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr1:210970865 C>T maps to NM_172362.2 E633E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:210948695 C>T maps to NM_172362.2 R702R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:211093302 G>A maps to NM_172362.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:150644748 C>T maps to NM_000238.2 G970G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:150647447 G>A maps to NM_000238.2 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr7:150647469 G>T maps to NM_000238.2 I728I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr7:150649876 C>T maps to NM_000238.2 W398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr7:150647322 G>A maps to NM_000238.2 T777T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr7:150647238 C>A maps to NM_172056.1 A805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:150654534 G>A maps to NM_000238.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr7:150648677 G>A maps to NM_000238.2 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr7:150656678 G>A maps to NM_000238.2 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:150649662 G>A maps to NM_000238.2 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr7:150648101 G>A maps to NM_000238.2 I684I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:150656744 G>A maps to NM_000238.2 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr7:150648095 G>A maps to NM_000238.2 F686F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:150648755 C>T maps to NM_000238.2 E575E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr7:150648536 G>A maps to NM_000238.2 G648G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150647457 C>T maps to NM_000238.2 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr12:49943972 A>G maps to NM_012284.1 A593A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:49937233 G>A maps to NM_012284.1 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:49938130 G>A maps to NM_012284.1 E385E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr12:49948156 G>A maps to NM_012284.1 R652R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:49934910 G>A maps to NM_012284.1 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:49944053 C>T maps to NM_012284.1 Y620Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr12:49951465 G>A maps to NM_012284.1 W994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:49943338 C>T maps to NM_012284.1 H528H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr12:49935539 G>A maps to NM_012284.1 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:49942798 G>A maps to NM_012284.1 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr17:40332924 G>A maps to NM_012285.2 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:40315706 G>A maps to NM_012285.2 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr17:40328258 C>A maps to NM_012285.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr17:40312180 G>A maps to NM_012285.2 S977S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:40321536 G>A maps to NM_012285.2 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:40321671 G>A maps to NM_012285.2 F471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr17:40321525 C>T maps to NM_012285.2 W520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:40315252 G>A maps to NM_012285.2 P859P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr17:40328132 G>A maps to NM_012285.2 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr17:40327749 G>A maps to NM_012285.2 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:40322137 C>T maps to NM_012285.2 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr17:40323851 G>A maps to NM_012285.2 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:40312405 C>T maps to NM_012285.2 R902R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:40330367 G>A maps to NM_012285.2 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:40318549 G>A maps to NM_012285.2 F535F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr14:63269134 G>A maps to NM_139318.3 Y578Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr14:63453897 C>T maps to NM_139318.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr14:63175026 C>T maps to NM_139318.3 Q722Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr14:63453897 C>T maps to NM_139318.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr14:63473090 C>T maps to NM_139318.3 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr14:63316526 G>A maps to NM_139318.3 F471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr14:63447721 G>A maps to NM_139318.3 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr14:63453897 C>T maps to NM_139318.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr14:63174480 C>T maps to NM_139318.3 Q904Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr14:63447745 G>A maps to NM_139318.3 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr14:63447817 G>A maps to NM_139318.3 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:63468163 C>T maps to NM_139318.3 W106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr14:63174629 T>A maps to NM_139318.3 K855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:63447700 G>A maps to NM_139318.3 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:63453897 C>T maps to NM_139318.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr14:63174858 G>A maps to NM_139318.3 N778N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:63174723 C>T maps to NM_139318.3 E823E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:63175002 C>T maps to NM_139318.3 E730E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:63447649 C>T maps to NM_139318.3 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr14:63246484 G>A maps to NM_139318.3 F660F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:63447745 G>A maps to NM_139318.3 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr14:63417235 G>A maps to NM_139318.3 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr14:63453897 C>T maps to NM_139318.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:63453897 C>T maps to NM_139318.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr14:63316400 C>T maps to NM_139318.3 W513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr14:63416993 C>T maps to NM_139318.3 W409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr14:63174921 C>T maps to NM_139318.3 Q757Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:63174966 C>T maps to NM_139318.3 Q742Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:63175074 G>A maps to NM_139318.3 V706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr14:63269218 A>C maps to NM_139318.3 A550A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr14:63447727 C>T maps to NM_139318.3 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr14:63453897 C>T maps to NM_139318.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr14:63417256 A>G maps to NM_139318.3 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr14:63246517 G>A maps to NM_139318.3 V649V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:63174954 G>A maps to NM_139318.3 S746S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:63316526 G>A maps to NM_139318.3 F471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:63246598 G>A maps to NM_139318.3 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr14:63447646 G>A maps to NM_139318.3 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr14:63453897 C>T maps to NM_139318.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr17:61619791 G>A maps to NM_030779.2 R715R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr17:61622495 C>T maps to NM_030779.2 P854P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:61611488 C>T maps to NM_030779.2 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr17:61601707 C>T maps to NM_030779.2 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr17:61611503 C>T maps to NM_030779.2 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:61600839 C>T maps to NM_030779.2 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr17:61613047 C>T maps to NM_030779.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:61613364 C>T maps to NM_030779.2 F479F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr17:61622525 G>A maps to NM_030779.2 L864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:61601503 G>A maps to NM_030779.2 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:61611506 C>T maps to NM_030779.2 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:61623247 G>A maps to NM_030779.2 G990G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr17:61601674 G>A maps to NM_030779.2 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:163241345 G>A maps to NM_033272.2 I938I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr2:163374609 G>A maps to NM_033272.2 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:163374270 C>T maps to NM_033272.2 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:163302839 G>A maps to NM_033272.2 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:163374666 C>T maps to NM_033272.2 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr2:163291945 C>T maps to NM_033272.2 A572A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:163241342 G>A maps to NM_033272.2 S939S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:163374645 G>A maps to NM_033272.2 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:163374609 G>A maps to NM_033272.2 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:163302626 G>C maps to NM_033272.2 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:163693077 C>T maps to NM_033272.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:163292068 G>A maps to NM_033272.2 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr2:163292065 G>A maps to NM_033272.2 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr2:163374666 C>T maps to NM_033272.2 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr2:163291741 C>T maps to NM_033272.2 E640E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:163302788 G>A maps to NM_033272.2 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:163393519 G>A maps to NM_033272.2 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr2:163360984 G>A maps to NM_033272.2 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:163250929 C>T maps to NM_033272.2 R893R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:163369184 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:19575155 C>T maps to NM_144633.2 P963P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr3:19575435 C>T maps to NM_144633.2 Q1057*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr3:19559535 C>T maps to NM_144633.2 T863T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr5:170149736 G>A maps to NM_001034837.1 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr5:170149736 G>A maps to NM_001034837.1 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr5:170139861 C>T maps to NM_001034837.1 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr5:170139861 C>T maps to NM_001034837.1 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:170139869 G>A maps to NM_001034837.1 W25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:170145871 C>T maps to NM_001034837.1 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:169780939 T>C maps to NM_001034838.1 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:169780948 C>T maps to NM_001034838.1 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:103603286 G>A maps to NM_014591.4 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr2:95963200 G>A maps to NM_013434.4 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:96040907 C>T maps to NM_013434.4 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:21698994 T>G maps to NM_001035003.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:21305467 A>T maps to NM_147183.3 L21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:21305490 G>A maps to NM_147183.3 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:20884327 G>A maps to ENST00000382152 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr4:20852195 C>T maps to ENST00000382152 E86E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr11:128709328 C>T maps to NM_000220.2 Q289Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr11:128709567 G>A maps to NM_000220.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr11:128709562 G>A maps to NM_000220.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr11:128709264 G>T maps to NM_000220.2 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:128710120 C>T maps to NM_000220.2 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:128709859 G>A maps to NM_000220.2 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr11:128709667 C>T maps to NM_000220.2 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr11:128709904 G>A maps to NM_000220.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:128709190 C>T maps to NM_000220.2 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:160012040 C>T maps to NM_002241.4 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr1:160011518 G>A maps to NM_002241.4 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:160012187 G>T maps to NM_002241.4 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr1:160011860 G>A maps to NM_002241.4 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:160011956 G>A maps to NM_002241.4 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:160011956 G>A maps to NM_002241.4 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr11:17409611 G>A maps to NM_000525.3 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:17409116 G>A maps to NM_000525.3 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr11:17409005 G>A maps to NM_000525.3 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:17409005 G>A maps to NM_000525.3 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:17409614 G>A maps to NM_000525.3 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr17:21318659 C>T maps to NM_021012.4 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:21319631 C>T maps to NM_021012.4 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:21318785 C>T maps to NM_021012.4 N44N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:21318791 C>T maps to NM_021012.4 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr17:21319127 C>T maps to NM_021012.4 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr17:21319616 C>T maps to NM_021012.4 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:21318824 C>T maps to NM_021012.4 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:21319621 G>A maps to NM_021012.4 W323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:21318926 C>T maps to NM_021012.4 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr17:21319154 C>T maps to NM_021012.4 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:21319601 C>T maps to NM_021012.4 Y316Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr17:21319178 C>T maps to NM_021012.4 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr17:21319241 C>T maps to NM_021012.4 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:21318926 C>T maps to NM_021012.4 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:21318794 C>T maps to NM_021012.4 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:21318926 C>T maps to NM_021012.4 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:21319694 G>A maps to NM_021012.4 K347K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:21319146 C>T maps to NM_021012.4 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr17:21319616 C>T maps to NM_021012.4 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr17:21319154 C>T maps to NM_021012.4 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:21319496 C>T maps to NM_021012.4 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:21319127 C>T maps to NM_021012.4 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:48967556 C>T maps to NM_170720.1 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr19:48967908 C>T maps to NM_170720.1 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:48967991 C>T maps to NM_170720.1 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:48965200 C>T maps to NM_170720.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr21:39671263 C>T maps to NM_170736.1 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr21:39671686 C>T maps to NM_170736.1 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr21:39671359 C>T maps to NM_170736.1 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr21:39671338 A>G maps to NM_170736.1 Q52Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr21:39671203 C>T maps to NM_170736.1 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr21:39671971 C>T maps to NM_170736.1 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr21:39671515 G>A maps to NM_170736.1 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:39671461 G>A maps to NM_170736.1 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:39672163 C>T maps to NM_170736.1 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr21:39671593 G>A maps to NM_170736.1 E137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr17:68128683 C>T maps to NM_018658.1 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr17:68129131 C>A maps to NM_018658.1 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr17:68129476 C>T maps to NM_018658.1 Q417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:68171506 C>T maps to NM_000891.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:68171245 C>T maps to NM_000891.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr2:155711650 G>A maps to NM_002239.2 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:155566140 C>T maps to NM_002239.2 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:155566248 C>T maps to NM_002239.2 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr2:155555337 A>G maps to NM_002239.2 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:155711710 C>T maps to NM_002239.2 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:155555712 C>T maps to NM_002239.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:155566233 C>T maps to NM_002239.2 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:155555700 C>T maps to NM_002239.2 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:155711557 C>T maps to NM_002239.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr2:155711530 G>A maps to NM_002239.2 Q404Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr22:38823375 G>A maps to NM_152868.1 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5KH-06A-11D-A27K-08 chr22:38823852 C>T maps to NM_152868.1 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr22:38823279 G>A maps to NM_152868.1 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:38823897 G>A maps to NM_152868.1 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr22:38823738 C>T maps to NM_152868.1 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:38823003 G>A maps to NM_152868.1 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr22:38823567 G>A maps to NM_152868.1 H190H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr22:38823732 G>A maps to NM_152868.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:38822907 C>T maps to NM_152868.1 E410E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:38823762 G>A maps to NM_152868.1 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:128781539 A>G maps to NM_000890.3 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr11:128781896 G>A maps to NM_000890.3 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr11:128781413 G>A maps to NM_000890.3 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:128781824 C>T maps to NM_000890.3 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr11:128786601 C>T maps to NM_000890.3 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:128781893 G>A maps to NM_000890.3 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr11:128781566 C>T maps to NM_000890.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr11:128781788 C>T maps to NM_000890.3 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr11:128781737 C>T maps to NM_000890.3 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:128781493 G>A maps to NM_000890.3 W109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:128781929 G>A maps to NM_000890.3 Q254Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:128786427 C>T maps to NM_000890.3 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr11:128781674 G>A maps to NM_000890.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:128781737 C>T maps to NM_000890.3 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr21:39212974 G>A maps to NM_002240.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr21:39087306 C>T maps to NM_002240.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr21:39086775 C>T maps to NM_002240.2 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr21:39087193 C>T maps to NM_002240.2 W89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr21:39087042 G>A maps to NM_002240.2 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr21:39086775 C>T maps to NM_002240.2 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr21:39087252 G>A maps to NM_002240.2 N69N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:39087396 G>A maps to NM_002240.2 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr21:38997754 G>A maps to NM_002240.2 I326I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr12:21918971 C>T maps to NM_004982.2 W320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:21919241 G>A maps to NM_004982.2 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:21919283 C>T maps to NM_004982.2 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr12:21918680 T>G maps to NM_004982.2 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:21926376 C>T maps to NM_004982.2 Q58Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr12:21919271 G>A maps to NM_004982.2 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr12:21926283 G>A maps to NM_004982.2 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr1:160053978 G>A maps to NM_004983.2 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr1:233807110 G>A maps to NM_002245.3 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:233802527 C>T maps to NM_002245.3 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr1:233807083 G>A maps to NM_002245.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:233807021 C>T maps to NM_002245.3 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:233802401 C>T maps to NM_002245.3 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:233807122 G>A maps to NM_002245.3 K286K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:233807251 C>T maps to NM_002245.3 C329C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr1:233807104 C>T maps to NM_002245.3 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:233750216 G>A maps to NM_002245.3 W100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:233802599 C>A maps to NM_002245.3 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:233802527 C>T maps to NM_002245.3 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:233807176 C>T maps to NM_002245.3 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:233802488 C>T maps to NM_002245.3 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:233807081 C>T maps to NM_002245.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:233807092 C>T maps to NM_002245.3 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:233802605 G>A maps to NM_002245.3 E207E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr1:233807083 G>A maps to NM_002245.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:233802416 C>T maps to NM_002245.3 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:233807083 G>A maps to NM_002245.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr1:233807254 G>A maps to NM_002245.3 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:233750042 C>T maps to NM_002245.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:233749940 C>T maps to NM_002245.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:233807176 C>T maps to NM_002245.3 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:233750225 C>T maps to NM_002245.3 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:233807143 C>T maps to NM_002245.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:233807128 G>A maps to NM_002245.3 E288E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr14:88729551 C>T maps to NM_138318.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:88651880 A>C maps to NM_138318.2 *544E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:88652070 G>A maps to NM_138318.2 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr14:88693820 G>A maps to NM_138318.2 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr14:88729749 C>T maps to NM_138318.2 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr14:88729740 C>T maps to NM_138318.2 Q69Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:88652079 G>A maps to NM_138318.2 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:88652127 C>T maps to NM_138318.2 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:88652154 G>A maps to NM_138318.2 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:88652316 G>A maps to NM_138318.2 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr14:88652025 C>T maps to NM_138318.2 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:88729596 G>A maps to NM_138318.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr14:88729890 G>A maps to NM_138318.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr14:88652298 G>A maps to NM_138318.2 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr14:88693802 G>A maps to NM_138318.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:88651908 C>T maps to NM_138318.2 E534E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr14:88737115 C>T maps to NM_138318.2 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:88658670 G>A maps to NM_138318.2 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:88729614 G>A maps to NM_138318.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr14:90650770 C>T maps to NM_022054.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr14:90651052 G>A maps to NM_022054.2 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr14:90650962 C>T maps to NM_022054.2 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr14:90650905 C>T maps to NM_022054.2 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr14:90650587 C>T maps to NM_022054.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:90650926 C>T maps to NM_022054.2 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:90651115 G>A maps to NM_022054.2 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr14:90650905 C>T maps to NM_022054.2 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr20:43374694 C>T maps to ENST00000372861 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:43379007 G>A maps to ENST00000372861 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:43379196 C>T maps to ENST00000372861 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:39284207 G>A maps to NM_032115.3 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:39282992 G>A maps to NM_001135105.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr6:39282992 G>A maps to NM_001135105.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:39282977 C>T maps to NM_001135105.1 W297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:39284132 C>T maps to NM_032115.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr6:39267424 G>A maps to NM_031460.3 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr6:39271778 G>A maps to NM_031460.3 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr6:39267424 G>A maps to NM_031460.3 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr6:39271778 G>A maps to NM_031460.3 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:39271778 G>A maps to NM_031460.3 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:39271844 G>A maps to NM_031460.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr6:39272381 G>A maps to NM_031460.3 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr10:118969365 G>A maps to NM_181840.1 Q237Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:118969167 C>T maps to NM_181840.1 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr10:118969251 C>T maps to NM_181840.1 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:118957061 C>T maps to NM_181840.1 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:118960709 G>A maps to NM_181840.1 Q88Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:215259861 C>T maps to NM_001017425.2 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr1:215259777 C>T maps to NM_001017425.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:215345524 A>G maps to NM_001017425.2 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:215408271 C>T maps to NM_001017425.2 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:215298064 C>T maps to NM_001017425.2 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr1:215260014 C>A maps to NM_001017425.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:215259969 C>T maps to NM_001017425.2 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:215259777 C>T maps to NM_001017425.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:26950689 C>T maps to NM_002246.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr2:26951063 C>T maps to NM_002246.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:26950832 C>T maps to NM_002246.2 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:64064657 G>A maps to ENST00000422670 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:64065030 C>T maps to ENST00000422670 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr6:39159208 C>T maps to NM_003740.3 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr6:39162471 G>A maps to NM_003740.3 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:39162038 G>A maps to NM_003740.3 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr6:39159373 C>T maps to NM_003740.3 K264K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:39159208 C>T maps to NM_003740.3 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:39159433 C>T maps to NM_003740.3 W244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr6:39159496 G>A maps to NM_003740.3 Y223Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:39162038 G>A maps to NM_003740.3 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr6:39162077 G>A maps to NM_003740.3 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:39158830 C>T maps to NM_003740.3 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:39159079 C>T maps to NM_003740.3 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr19:38817596 C>T maps to NM_004823.1 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:38817435 C>T maps to NM_004823.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr8:140630644 G>A maps to NM_016601.2 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr8:140631243 G>A maps to NM_016601.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:140630499 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:140630512 C>T maps to NM_016601.2 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:140631106 G>A maps to NM_016601.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr8:140630563 G>A maps to NM_016601.2 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr8:140630563 G>A maps to NM_016601.2 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr8:140630830 G>A maps to NM_016601.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr8:140631106 G>A maps to NM_016601.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr8:140630785 C>T maps to NM_016601.2 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr8:140631298 G>A maps to NM_016601.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:140630506 G>A maps to NM_016601.2 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:78709043 G>A maps to NM_001161352.1 I855I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr10:78669807 G>A maps to NM_001161352.1 D1021D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr10:78637625 T>C maps to ENST00000404771 E1183E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr10:78850219 G>A maps to NM_001161352.1 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:78850192 C>T maps to NM_001161352.1 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:78944601 G>A maps to NM_001161352.1 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:78647062 G>T maps to NM_001161352.1 S1224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr10:78870047 G>A maps to NM_001161352.1 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:78647110 G>A maps to NM_001161352.1 S1208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:78647164 G>A maps to NM_001161352.1 S1190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:78846278 G>A maps to NM_001161352.1 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:78944601 G>A maps to NM_001161352.1 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:169810805 C>T maps to NM_004137.2 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:178543420 G>A maps to NM_005832.3 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr3:178560682 C>T maps to NM_005832.3 Y222Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr3:178546139 G>A maps to NM_005832.3 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr3:178560517 G>A maps to NM_005832.3 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:70824330 C>T maps to NM_014505.4 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:70824402 G>A maps to NM_014505.4 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr19:18096192 C>T maps to ENST00000222249 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:18092714 C>A maps to ENST00000222249 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr5:113740268 C>T maps to NM_021614.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:113822787 A>T maps to NM_021614.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr5:113698855 C>T maps to NM_021614.2 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:113698903 C>T maps to NM_021614.2 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:154744857 G>A maps to NM_002249.4 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:154794620 G>A maps to NM_002249.4 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:154705553 G>A maps to NM_002249.4 F505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:154705553 G>A maps to NM_002249.4 F505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:154687473 C>T maps to NM_002249.4 K569K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:154744506 G>A maps to NM_002249.4 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr19:44276175 G>A maps to NM_002250.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:44280755 C>T maps to NM_002250.2 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:44278615 G>A maps to NM_002250.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:44273935 G>A maps to NM_002250.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:2608861 G>A maps to NM_000218.2 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:2869091 C>T maps to NM_000218.2 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:2608861 G>A maps to NM_000218.2 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:2591880 C>T maps to NM_000218.2 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:2549160 C>T maps to NM_000218.2 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:2790145 C>T maps to NM_000218.2 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr11:2593263 C>T maps to NM_000218.2 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr11:2604735 C>T maps to NM_000218.2 C331C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr11:2606440 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:2592603 G>A maps to NM_000218.2 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:2610031 C>T maps to NM_000218.2 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr11:2606500 C>T maps to NM_000218.2 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr20:62076128 G>A maps to NM_172107.2 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr20:62076678 G>A maps to NM_172107.2 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr20:62038719 G>A maps to NM_172107.2 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr20:62076634 C>T maps to NM_172107.2 W157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr20:62039804 G>A maps to NM_172107.2 D616D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:62038245 G>A maps to NM_172107.2 I790I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:62045535 G>A maps to NM_172107.2 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:62039876 G>A maps to NM_172107.2 I592I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr20:62038653 C>T maps to NM_172107.2 E654E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:62039786 C>T maps to NM_172107.2 R622R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:62070962 G>A maps to NM_172107.2 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr20:62076609 C>T maps to NM_172107.2 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr8:133192440 C>T maps to NM_004519.2 W247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr8:133192439 C>T maps to NM_004519.2 W247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr8:133187714 G>A maps to NM_004519.2 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:133141595 G>A maps to NM_004519.2 P844P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:133198345 G>A maps to NM_004519.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr8:133141655 C>T maps to NM_004519.2 S824S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:133182619 C>T maps to NM_004519.2 W399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:133184931 C>T maps to NM_004519.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:133141969 G>A maps to NM_004519.2 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:133192487 G>A maps to NM_004519.2 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:133492515 C>T maps to NM_004519.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:133187813 G>A maps to NM_004519.2 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:133187825 G>A maps to NM_004519.2 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr8:133175740 C>T maps to NM_004519.2 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr8:133182619 C>T maps to NM_004519.2 W399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:133141655 C>T maps to NM_004519.2 S824S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:133142162 C>T maps to NM_004519.2 T655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:133192457 G>A maps to NM_004519.2 D241D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:133142180 C>T maps to NM_004519.2 R649R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:133153424 G>A maps to NM_004519.2 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr8:133141969 G>A maps to NM_004519.2 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr8:133153553 C>T maps to NM_004519.2 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr8:133152390 C>T maps to NM_004519.2 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:133141958 C>T maps to NM_004519.2 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:133141508 T>G maps to NM_004519.2 *873Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:133141901 C>T maps to NM_004519.2 V742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:133196569 C>T maps to NM_004519.2 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:133196596 G>A maps to NM_004519.2 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:133192418 G>A maps to NM_004519.2 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr8:133192440 C>T maps to NM_004519.2 W247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:41285928 C>T maps to NM_004700.3 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:41300674 G>A maps to NM_004700.3 K550K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:41285907 G>A maps to NM_004700.3 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:41300637 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:41298782 C>T maps to NM_004700.3 I537I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:41300650 C>T maps to NM_004700.3 F542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:41300651 C>T maps to NM_004700.3 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:41300770 G>C did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:41300636 A>C did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:41250025 C>T maps to NM_004700.3 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:41283873 C>T maps to NM_004700.3 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:41283849 C>T maps to NM_004700.3 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:41303366 G>A maps to NM_004700.3 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr6:73904752 G>A maps to NM_001160133.1 R824R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr6:73904446 C>T maps to NM_001160133.1 Y722Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr6:73751700 C>T maps to NM_001160133.1 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr6:73751700 C>T maps to NM_001160133.1 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:73900322 G>A maps to NM_001160133.1 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:73904845 C>T maps to NM_001160133.1 I855I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr6:73904809 G>A maps to NM_001160133.1 K843K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:73904752 G>A maps to NM_001160133.1 R824R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr6:73904455 C>T maps to NM_001160133.1 S725S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:73904962 G>A maps to NM_001160133.1 E894E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr6:73787060 C>T maps to NM_001160133.1 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:73879566 C>T maps to NM_001160133.1 R542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:73904928 G>A maps to NM_001160133.1 W883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr6:73904713 G>A maps to NM_001160133.1 Q811Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:73904254 C>T maps to NM_001160133.1 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:73904975 G>T maps to NM_001160133.1 E899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:73713654 G>A maps to NM_001160133.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr13:50589958 G>A maps to NM_173605.1 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr13:50589913 T>A maps to NM_173605.1 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr13:50589840 T>A maps to NM_173605.1 L71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr20:43723591 G>A maps to NM_002251.3 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:43723678 C>T maps to NM_002251.3 E471E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:99441547 T>G maps to NM_020697.2 Y447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr8:99441445 C>T maps to NM_020697.2 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr8:99441029 C>T maps to NM_020697.2 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:99441316 C>T maps to NM_020697.2 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:99441586 G>A maps to NM_020697.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:99441631 C>T maps to NM_020697.2 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr2:18113306 C>T maps to NM_002252.3 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:18113147 C>T maps to NM_002252.3 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr2:18112295 C>T maps to NM_002252.3 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr2:18112725 C>T maps to NM_002252.3 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:18113615 G>T maps to NM_002252.3 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr2:18112583 C>T maps to NM_002252.3 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:18113037 C>T maps to NM_002252.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:18113369 C>T maps to NM_002252.3 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr9:138678107 C>T maps to ENST00000298480 S1081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr9:138660730 C>T maps to ENST00000298480 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr9:138676457 C>T maps to ENST00000298480 L1007L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DA-A3F3-06A-11D-A20D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:138657526 C>T maps to ENST00000298480 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:138676385 C>T maps to ENST00000298480 F983F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr9:138641982 G>A maps to ENST00000298480 K98K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr9:138676725 C>T maps to ENST00000298480 S1049S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr9:138651644 G>A maps to ENST00000298480 W325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:138662852 G>A maps to ENST00000298480 E640E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:138670593 G>A maps to ENST00000298480 K885K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr9:138676635 C>T maps to ENST00000298480 I1019I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:138657007 C>T maps to ENST00000298480 F389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr9:138651665 C>T maps to ENST00000298480 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:196436862 C>T maps to NM_198503.2 W171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:196434427 G>A maps to NM_198503.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:196577387 G>A maps to NM_198503.2 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:196392206 G>A maps to NM_198503.2 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:196438156 C>T maps to NM_198503.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:196197464 T>A maps to NM_198503.2 V1099V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr1:196309669 C>T maps to NM_198503.2 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr1:196295880 C>A maps to NM_198503.2 E748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:196227399 C>T maps to NM_198503.2 R1045R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:196398829 G>A maps to NM_198503.2 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:196227390 T>C maps to NM_198503.2 E1048E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:196227594 C>T maps to NM_198503.2 W980*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:196458987 G>A maps to NM_198503.2 N85N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:196458977 C>A maps to NM_198503.2 G89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:196227609 G>A maps to NM_198503.2 I975I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:196300391 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:196395069 G>A maps to NM_198503.2 R345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr1:196438156 C>T maps to NM_198503.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:196461410 G>A maps to NM_198503.2 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:196311219 A>G maps to NM_198503.2 H514H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr1:196459047 G>A maps to NM_198503.2 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr1:196311222 G>A maps to NM_198503.2 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:196398760 G>A maps to NM_198503.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:196311243 C>T maps to NM_198503.2 K506K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:196395069 G>A maps to NM_198503.2 R345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:196398790 G>A maps to NM_198503.2 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:196197412 G>A maps to NM_198503.2 R1117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:196434427 G>A maps to NM_198503.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:196451490 C>T maps to NM_198503.2 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:196438153 T>C maps to NM_198503.2 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr1:196434427 G>A maps to NM_198503.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:196227450 G>A maps to NM_198503.2 H1028H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr8:36793059 G>A maps to NM_001031836.2 E1024E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr8:36793287 T>A maps to NM_001031836.2 S1100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr8:36675227 C>T maps to NM_001031836.2 F352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:36776395 C>T maps to NM_001031836.2 V859V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr8:36793307 G>A maps to NM_001031836.2 W1107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr8:36644918 C>T maps to NM_001031836.2 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr8:36780056 G>A maps to NM_001031836.2 G882G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr8:36793080 T>C maps to NM_001031836.2 D1031D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr8:36642032 C>T maps to NM_001031836.2 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr8:36793380 G>A maps to NM_001031836.2 R1131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr8:36698090 C>T maps to NM_001031836.2 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr8:110980535 G>A maps to NM_014379.2 N428N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr8:110980769 G>A maps to NM_014379.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr8:110980468 G>A maps to NM_014379.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr8:110984880 G>A maps to NM_014379.2 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:110984640 G>A maps to NM_014379.2 D279D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr8:110985003 C>T maps to NM_014379.2 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:110980598 G>A maps to NM_014379.2 I407I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:110980496 C>T maps to NM_014379.2 K441K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:110980463 C>T maps to NM_014379.2 K452K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr8:110986191 G>A maps to NM_014379.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr9:2718437 C>T maps to NM_133497.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr9:2718191 C>T maps to NM_133497.2 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:2729609 G>A maps to NM_133497.2 E507E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:2718584 G>A maps to NM_133497.2 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:24039766 G>A maps to NM_001142730.1 V752V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:7256413 C>T maps to NM_001002914.2 Y51Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr13:77459428 G>A maps to NM_138444.3 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr16:29922373 G>A maps to NM_178863.2 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr16:29923185 G>A maps to NM_178863.2 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:77734241 G>A maps to NM_023930.3 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:77728169 G>A maps to NM_023930.3 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr11:77728169 G>A maps to NM_023930.3 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:77728097 G>A maps to NM_023930.3 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:143586423 C>T maps to NM_020768.3 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:143586600 G>A maps to NM_020768.3 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr5:143586399 C>T maps to NM_020768.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:143586532 C>T maps to NM_020768.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr5:143853595 C>T maps to NM_020768.3 F402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:143853415 G>A maps to NM_020768.3 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:143853237 G>A maps to NM_020768.3 W283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:143853268 G>A maps to NM_020768.3 K293K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:143586771 C>T maps to NM_020768.3 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr22:37452390 C>T maps to ENST00000403888 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr2:201369527 G>A maps to NM_152387.2 D105D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr16:67325352 C>T maps to NM_001100915.1 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:67327492 T>C maps to NM_001100915.1 R724R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr16:67327543 C>T maps to NM_001100915.1 A707A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr16:67327543 C>T maps to NM_001100915.1 A707A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:67337156 G>A maps to NM_001100915.1 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:67325696 C>T maps to NM_001100915.1 V754V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr16:67354728 G>T maps to NM_001100915.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr16:67327804 C>T maps to NM_001100915.1 Q620Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:67333347 G>A maps to NM_001100915.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:67354557 G>A maps to NM_001100915.1 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:36449396 C>T maps to NM_173562.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:77885237 C>T maps to NM_001029859.1 Q121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:215793803 C>T maps to NM_016121.3 F764F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr1:215777579 G>A maps to NM_016121.3 Q415Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:215777492 C>T maps to NM_016121.3 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:45768147 C>T maps to NM_198404.2 E185E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr16:2732686 C>T maps to NM_018992.3 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr16:2732752 C>T maps to NM_018992.3 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:58486840 C>T maps to NM_153331.3 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CE-06A-11D-A19A-08 chr7:66104167 C>T maps to NM_153033.3 N273N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:66104086 C>T maps to NM_153033.3 H246H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr4:44176895 G>A maps to NM_198353.2 Q445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:44176878 G>A maps to NM_198353.2 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr4:44176893 C>T maps to NM_198353.2 Q445Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr4:44177175 G>A maps to NM_198353.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr4:44177154 G>A maps to NM_198353.2 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:44450351 G>A maps to NM_198353.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr4:44177028 C>T maps to NM_198353.2 W400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:44176932 C>T maps to NM_198353.2 E432E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr4:44449630 G>A maps to NM_198353.2 Q304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:103440207 G>A maps to NM_024089.2 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr13:103445759 G>A maps to NM_024089.2 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:108352017 G>T maps to NM_153705.4 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:48887537 G>A maps to NM_006801.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr22:38870561 C>T maps to NM_016657.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr22:38878538 T>C maps to NM_006855.2 *215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:23356987 C>T maps to NM_001009999.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:23398664 C>T maps to NM_001009999.2 Q533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:23357065 C>T maps to NM_001009999.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr1:23381646 C>T maps to NM_001009999.2 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr1:23381647 C>T maps to NM_001009999.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:67012769 C>T maps to NM_012308.2 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:67012809 C>T maps to NM_012308.2 R572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:66948823 T>A maps to NM_012308.2 L72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr12:122012473 G>A maps to ENST00000377071 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:121986881 G>A maps to ENST00000377071 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:121947465 C>T maps to ENST00000377071 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:121880144 G>A maps to ENST00000377071 P1033P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:121970720 G>A maps to ENST00000377071 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:121880393 C>T maps to ENST00000377071 L950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr12:121947408 C>T maps to ENST00000377071 E536E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr12:121878775 G>A maps to ENST00000377071 L1151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:121878616 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:121877843 G>A maps to ENST00000377071 I1215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr12:121970771 G>A maps to ENST00000377071 D290D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr12:121958816 G>T maps to ENST00000377071 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr12:121958817 C>T maps to ENST00000377071 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:122013720 G>A maps to ENST00000377071 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr12:121881907 C>T maps to ENST00000377071 P786P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:121932423 G>A maps to ENST00000377071 I564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:121947612 G>A maps to ENST00000377071 F468F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:122018774 G>A maps to ENST00000377071 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:86711262 G>T maps to NM_001146688.1 G1026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:86678278 C>T maps to NM_001146688.1 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:86697492 G>A maps to NM_001146688.1 K562K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr5:137756404 C>T maps to NM_016604.3 S1242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr5:137727396 C>T maps to NM_016604.3 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:137727453 C>T maps to NM_016604.3 T711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:137734049 G>A maps to NM_016604.3 E1005E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:137733917 C>T maps to NM_016604.3 P961P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:137727414 C>T maps to NM_016604.3 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr5:137763657 T>C maps to NM_016604.3 L1546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:137727468 C>T maps to NM_016604.3 S716S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr5:137756644 C>T maps to NM_016604.3 S1322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:44137311 C>G maps to NM_014663.2 V500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:44149398 C>T maps to NM_014663.2 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr1:44134854 C>T maps to NM_014663.2 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr19:5133942 G>A maps to NM_015015.2 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:5077384 C>T maps to NM_015015.2 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:5131468 C>T maps to NM_015015.2 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr19:5110694 C>T maps to NM_015015.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:5047611 C>T maps to NM_015015.2 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:5144377 C>T maps to NM_015015.2 F952F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:5039968 C>T maps to NM_015015.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:5047524 C>T maps to NM_015015.2 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr9:6984217 G>T maps to NM_015061.3 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:6849701 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:94731936 C>T maps to NM_018039.2 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:94731666 C>T maps to NM_018039.2 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:94759344 T>A maps to NM_001161630.1 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:94759476 G>A maps to NM_001161630.1 K252K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr12:459852 G>A maps to NM_001042603.1 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr12:402014 G>A maps to NM_001042603.1 P1592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr12:417099 G>A maps to NM_001042603.1 A1150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr12:416838 G>A maps to NM_001042603.1 P1237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:432785 G>A maps to NM_001042603.1 P710P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:493220 G>A maps to NM_001042603.1 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:438195 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:202715046 A>G maps to ENST00000367264 S790S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr1:202777349 A>C maps to ENST00000367264 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:202710799 G>A maps to ENST00000367264 L916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:202715367 G>A maps to ENST00000367264 F736F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:202702771 C>T maps to ENST00000367264 R1258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:202702924 G>A maps to ENST00000367264 L1207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:202710649 G>A maps to ENST00000367264 P966P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:202709806 G>A maps to ENST00000367264 L1063L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr1:202731856 G>A maps to ENST00000367264 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr23:53245344 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:53245322 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:53223706 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr23:53222221 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:53222466 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:53243944 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:53240719 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr23:53223566 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:53223911 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr24:21878555 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr24:21868681 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr24:21871432 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr24:21868068 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr24:21878325 G>C did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr24:21903331 G>A did not map to a codon.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr23:44922682 T>C did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:44966740 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:44950035 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:7752203 C>T maps to NM_001080424.1 S866S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:7753163 C>T maps to NM_001080424.1 R1156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr17:7748976 C>T maps to NM_001080424.1 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr17:7754525 C>T maps to NM_001080424.1 S1287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:7750889 C>T maps to NM_001080424.1 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:7753484 C>T maps to NM_001080424.1 S1221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:7753485 C>T maps to NM_001080424.1 L1222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr17:7752374 C>T maps to NM_001080424.1 T923T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:7749578 C>T maps to NM_001080424.1 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr17:7749461 C>T maps to NM_001080424.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr17:7752245 G>A maps to NM_001080424.1 R880R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr4:55961113 C>T maps to NM_002253.2 G942G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr4:55976876 C>T maps to NM_002253.2 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr4:55956161 C>T maps to NM_002253.2 R1051R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr4:55962485 G>A maps to NM_002253.2 R880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr4:55984966 C>T maps to NM_002253.2 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:55972086 G>A maps to NM_002253.2 I519I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:55964400 G>A maps to NM_002253.2 I804I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:55955949 C>T maps to NM_002253.2 W1071*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr4:55953823 C>T maps to NM_002253.2 E1204E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:55968568 G>A maps to NM_002253.2 I698I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:55981483 G>A maps to NM_002253.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr4:55955584 T>C maps to NM_002253.2 K1120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr4:55968658 C>T maps to NM_002253.2 T668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:55968073 G>A maps to NM_002253.2 F752F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr4:55972107 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr4:55948708 G>A maps to NM_002253.2 I1252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr4:55960993 G>A maps to NM_002253.2 S982S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:55984927 C>T maps to NM_002253.2 Q67Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:55961752 G>A maps to NM_002253.2 V936V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:55968568 G>A maps to NM_002253.2 I698I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:55976627 G>A maps to NM_002253.2 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr4:55972008 G>A maps to NM_002253.2 F545F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:55970895 A>T maps to NM_002253.2 L634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr4:55961005 C>T maps to NM_002253.2 V978V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr18:61006116 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:61018225 G>A maps to NM_002035.2 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:10600375 C>T maps to NM_203500.1 E493E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:10610577 G>A maps to NM_203500.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr7:142658180 C>T maps to NM_000420.2 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr7:142639970 G>A maps to NM_000420.2 I644I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr7:142658513 G>A maps to NM_000420.2 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:142651456 G>A maps to NM_000420.2 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:142658495 G>A maps to NM_000420.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:142640949 G>A maps to NM_000420.2 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr7:142650980 C>T maps to NM_000420.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:142650989 C>T maps to NM_000420.2 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:142654919 G>A maps to NM_000420.2 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:142655515 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:142649700 G>A maps to NM_000420.2 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:142650938 C>T maps to NM_000420.2 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:142641469 C>T maps to NM_000420.2 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:142651025 G>A maps to NM_000420.2 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:142650995 G>A maps to NM_000420.2 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr7:142651297 G>A maps to NM_000420.2 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:142650938 C>T maps to NM_000420.2 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr7:142655420 C>T maps to NM_000420.2 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr7:142658059 G>A maps to NM_000420.2 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:142655417 A>T maps to NM_000420.2 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr7:142649654 G>A maps to NM_000420.2 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr7:142638488 C>T maps to NM_000420.2 R683R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:142649654 G>A maps to NM_000420.2 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:142643343 G>A maps to NM_000420.2 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:142650989 C>T maps to NM_000420.2 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:142655513 C>T maps to NM_000420.2 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:142658102 G>A maps to NM_000420.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:91449938 G>A maps to NM_007035.3 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr12:91449338 G>A maps to NM_007035.3 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr12:91449443 C>T maps to NM_007035.3 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:91445200 C>T maps to NM_007035.3 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:73951814 A>G maps to ENST00000370385 C86C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:73952129 G>A maps to ENST00000370385 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:73935034 C>T maps to ENST00000370385 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:73935100 C>T maps to ENST00000370385 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:32498787 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:32495996 C>T maps to NM_006559.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr6:62611213 C>T maps to NM_152688.2 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr6:62687979 G>A maps to NM_152688.2 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr6:62995762 C>A maps to NM_152688.2 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:62688102 C>T maps to NM_152688.2 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:62604686 G>A maps to NM_152688.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:62757842 C>T maps to NM_152688.2 Q92Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:62687997 C>T maps to NM_152688.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:62887152 G>A maps to NM_152688.2 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr6:62604623 G>A maps to NM_152688.2 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr8:136470165 C>T maps to NM_006558.1 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:136594240 C>T maps to NM_006558.1 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:136569777 C>T maps to NM_006558.1 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr8:136619274 C>T maps to NM_006558.1 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:136533591 C>T maps to NM_006558.1 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:27317673 G>T maps to NM_006488.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr2:27317425 C>T maps to NM_000221.2 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr19:6418739 C>T maps to NM_003685.2 K251K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr19:6418801 G>A maps to NM_003685.2 Q231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:19570193 G>A maps to NM_015047.1 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:19568941 G>A maps to NM_015047.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr1:19577955 C>T maps to NM_015047.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:26960990 A>G maps to NM_014680.2 L1062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:26969290 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:26961607 A>G maps to NM_014680.2 P999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:26947000 G>A maps to NM_014680.2 F1799F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:26965340 G>A maps to NM_014680.2 Q481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:26965596 G>A maps to NM_014680.2 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr5:141307819 C>T maps to NM_014773.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr8:48353041 C>T maps to NM_001080394.1 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr8:48625417 C>T maps to NM_001080394.1 D724D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:48353038 C>T maps to NM_001080394.1 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:48625279 C>T maps to NM_001080394.1 V678V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr16:71961518 C>T maps to NM_014761.2 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr16:71950426 C>T maps to NM_014761.2 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:85682308 C>T maps to NM_014615.2 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:85690881 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr16:85667574 G>A maps to NM_014615.2 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:85694853 C>T maps to NM_014615.2 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr16:85704608 C>T maps to NM_014615.2 L1142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr17:73488709 C>T maps to ENST00000375248 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr17:73493243 C>T maps to ENST00000375248 I1130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr17:73493205 C>T maps to ENST00000375248 L1118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:73493868 C>T maps to ENST00000375248 L1145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr17:73484130 C>T maps to ENST00000375248 N176N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:73484955 C>T maps to ENST00000375248 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:73491704 C>T maps to ENST00000375248 F981F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:73492407 C>T maps to ENST00000375248 T1039T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:73487803 C>T maps to ENST00000375248 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:73489154 C>T maps to ENST00000375248 I692I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr17:73487203 C>T maps to ENST00000375248 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:73488761 C>T maps to ENST00000375248 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:73484037 C>T maps to ENST00000375248 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:73484038 C>T maps to ENST00000375248 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:73486829 C>T maps to ENST00000375248 V379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:73491368 C>T maps to ENST00000375248 S917S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:73491369 C>T maps to ENST00000375248 R918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr17:73492377 C>T maps to ENST00000375248 P1029P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:73482442 G>A maps to ENST00000375248 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr8:126073377 A>G maps to ENST00000377985 D494D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:126056249 G>A maps to ENST00000377985 P923P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:126091027 G>A maps to ENST00000377985 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:197403773 G>A maps to NM_014687.1 T876T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:197431410 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:197432025 A>G maps to NM_014687.1 D80D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr3:197427664 C>T maps to NM_014687.1 Q360Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:197427640 G>A maps to NM_014687.1 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr3:197427606 G>A maps to NM_014687.1 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:6865633 C>T maps to NM_014743.2 F1175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr4:6863950 C>T maps to NM_014743.2 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:6863956 C>T maps to NM_014743.2 P616P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr4:6865633 C>T maps to NM_014743.2 F1175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:6826399 C>T maps to NM_014743.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:6865639 C>A maps to NM_014743.2 P1177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr6:42830319 C>A maps to NM_015349.1 R808R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr6:42796514 C>T maps to NM_015349.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:42797105 T>G maps to NM_015349.1 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:42797891 G>A maps to NM_015349.1 Q607Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:42833144 C>T maps to NM_015349.1 S1067S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:42797153 G>A maps to NM_015349.1 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr6:42797268 C>T maps to NM_015349.1 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:42796337 C>T maps to NM_015349.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:42828036 A>G maps to NM_015349.1 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:42832751 C>T maps to NM_015349.1 G936G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:42828079 C>T maps to NM_015349.1 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:42833144 C>T maps to NM_015349.1 S1067S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr14:70171363 A>T maps to NM_014734.3 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr14:70170166 C>T maps to NM_014734.3 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:105346727 C>T maps to ENST00000453495 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:105360105 C>T maps to ENST00000453495 F1433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr14:75130446 A>G maps to NM_001039479.1 G816G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:75139617 G>A maps to NM_001039479.1 F446F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr14:75151288 G>A maps to NM_001039479.1 D37D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:75134174 G>A maps to NM_001039479.1 F679F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr14:75139650 G>A maps to NM_001039479.1 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:75150110 G>A maps to NM_001039479.1 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr6:24570192 G>A maps to NM_014809.3 T643T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:24582552 C>T maps to NM_014809.3 W372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:24551710 G>A maps to NM_014809.3 I997I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr6:24569075 G>A maps to NM_014809.3 F691F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:24596458 C>T maps to NM_014809.3 W148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:24551731 C>T maps to NM_014809.3 R990R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:24564559 G>A maps to NM_014809.3 I767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr6:24556955 A>G maps to NM_014809.3 G912G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr6:24596163 C>T maps to NM_014809.3 E246E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr6:24563738 C>T maps to NM_014809.3 R813R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:24596352 C>T maps to NM_014809.3 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr6:24551676 G>A maps to NM_014809.3 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr6:24576703 G>T maps to NM_014809.3 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr6:24596496 C>T maps to NM_014809.3 E135E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:24559265 G>A maps to NM_014809.3 F903F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:24596406 C>T maps to NM_014809.3 K165K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:24596512 C>T maps to NM_014809.3 W130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:24596613 G>A maps to NM_014809.3 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:24596739 G>A maps to NM_014809.3 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr6:24563609 C>T maps to NM_014809.3 K856K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr6:24596766 G>A maps to NM_014809.3 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr6:24551731 C>T maps to NM_014809.3 R990R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:35906720 C>T maps to NM_024874.4 K963K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:35926015 G>A maps to NM_024874.4 I439I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:36020053 G>A maps to NM_024874.4 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:35972518 C>T maps to NM_024874.4 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:35926015 G>A maps to NM_024874.4 I439I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:35936466 C>T maps to NM_024874.4 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:35944600 C>T maps to NM_024874.4 Q293Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr1:35900533 G>A maps to NM_024874.4 T1037T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:35932272 G>A maps to NM_024874.4 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:34833031 C>T maps to NM_014686.3 V731V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:34843721 C>T maps to NM_014686.3 D1025D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:34833127 G>A maps to NM_014686.3 Q763Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:34833097 T>G maps to NM_014686.3 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:34833007 C>T maps to NM_014686.3 S723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:34832668 C>T maps to NM_014686.3 S610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:34833031 C>T maps to NM_014686.3 V731V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr19:34833121 C>T maps to NM_014686.3 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr9:114154100 A>G maps to NM_001080398.1 V1210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:114187775 G>A maps to NM_001080398.1 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr9:114178581 G>A maps to NM_001080398.1 V756V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:114206666 G>A maps to NM_001080398.1 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr9:114176928 G>A maps to NM_001080398.1 I767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr9:114178560 G>A maps to NM_001080398.1 A763A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:114137452 C>G maps to NM_001080398.1 L1528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:114145513 G>A maps to NM_001080398.1 T1438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr9:114134035 G>A maps to NM_001080398.1 S1712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr20:36627678 G>A maps to NM_014657.1 Q902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:36641537 T>C maps to NM_014657.1 Q227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:36631065 G>A maps to NM_014657.1 H872H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr20:36641606 A>G maps to NM_014657.1 D204D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr20:36641846 G>A maps to NM_014657.1 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr20:36640160 G>A maps to NM_014657.1 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr20:36641211 A>T maps to NM_014657.1 L336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:36640942 G>A maps to NM_014657.1 Q426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:36641483 G>A maps to NM_014657.1 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:127770988 G>A maps to NM_014702.4 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:127768716 C>T maps to NM_014702.4 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:127767978 C>T maps to NM_014702.4 W495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr6:127767576 T>C maps to NM_014702.4 G629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr7:4830962 C>T maps to ENST00000450194 L1502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:4820811 C>T maps to ENST00000450194 I727I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr18:46146019 C>T maps to NM_001142397.1 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr18:46287843 C>T maps to NM_001142397.1 N387N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr18:46287927 C>T maps to NM_001142397.1 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:46385731 G>A maps to NM_001142397.1 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr18:46190190 C>T maps to NM_001142397.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr18:46190121 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr16:15704907 G>A maps to NM_014647.3 I1225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr16:15709849 A>G maps to NM_014647.3 C1030C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:15702249 G>A maps to NM_014647.3 L1360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr16:15719492 G>A maps to NM_014647.3 R563R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:43905574 C>T maps to NM_015284.2 R1457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:43905651 C>T maps to NM_015284.2 A1482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:43890866 C>T maps to NM_015284.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:43896197 G>A maps to NM_015284.2 E605E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:43903268 C>T maps to NM_015284.2 L1199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:43909141 C>T maps to NM_015284.2 D1974D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr1:43913863 G>A maps to NM_015284.2 G2327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:43896716 C>T maps to NM_015284.2 P725P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:43907441 C>T maps to NM_015284.2 V1666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:43891204 C>T maps to NM_015284.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr1:43896716 C>T maps to NM_015284.2 P725P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:43891736 C>T maps to NM_015284.2 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:43895511 C>T maps to NM_015284.2 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr1:43893784 C>T maps to NM_015284.2 V406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:43909389 C>T maps to NM_015284.2 F2017F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:43905597 G>A maps to NM_015284.2 G1464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:43898004 C>T maps to NM_015284.2 F880F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:47155321 G>A maps to NM_014774.2 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:47183624 G>A maps to NM_014774.2 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:47181972 G>A maps to NM_014774.2 R110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr1:47155264 C>T maps to NM_014774.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr1:47181972 G>A maps to NM_014774.2 R110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:3662420 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr16:85100907 C>T maps to NM_014732.2 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr16:85100991 G>A maps to NM_014732.2 K105K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:85100874 G>A maps to NM_014732.2 W66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr16:85105470 C>T maps to NM_014732.2 R138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr16:85105395 T>C maps to NM_014732.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:22643079 G>A maps to ENST00000446597 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr12:22678582 G>A maps to ENST00000446597 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:22623805 G>A maps to ENST00000446597 Q800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr16:27786389 C>T maps to NM_015202.2 P1478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr16:27772854 C>T maps to NM_015202.2 S1251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr16:27751960 C>T maps to NM_015202.2 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr16:27786296 C>T maps to NM_015202.2 S1447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:27720135 C>T maps to NM_015202.2 F500F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:27689172 C>T maps to NM_015202.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:27640068 C>T maps to NM_015202.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:3742986 C>T maps to NM_014704.3 G734G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:3761493 A>T maps to NM_014704.3 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr1:3742396 G>T maps to NM_014704.3 S763S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr1:3756224 C>A maps to NM_014704.3 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:3753954 G>A maps to NM_014704.3 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:42460145 G>A maps to NM_015058.1 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr13:42249369 G>A maps to NM_015058.1 R1464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr13:42265477 G>A maps to NM_015058.1 L1282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr13:42179405 C>T maps to NM_015058.1 K1628K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr13:42161770 G>A maps to NM_015058.1 R1716R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr13:42144659 G>A maps to NM_015058.1 D1851D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr13:42149908 G>A maps to NM_015058.1 P1779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr13:42404771 G>A maps to NM_015058.1 I531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr13:42293797 T>G maps to NM_015058.1 I1015I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr13:42179321 G>A maps to NM_015058.1 I1656I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:42185718 G>A maps to NM_015058.1 Q1624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:42295568 G>A maps to NM_015058.1 D967D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr13:42259189 G>A maps to NM_015058.1 Y1440Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr13:42407592 G>A maps to NM_015058.1 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr13:42295711 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr14:58955383 C>T maps to ENST00000354386 F1244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:58895131 T>C maps to ENST00000354386 N62N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr9:138376595 C>T maps to NM_014811.3 D80D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr9:138377522 C>T maps to NM_014811.3 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr9:138376397 C>T maps to NM_014811.3 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:138379982 C>T maps to NM_014811.3 V1209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr9:138377654 C>T maps to NM_014811.3 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr9:138376658 C>T maps to NM_014811.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:46667425 T>C maps to NM_001142673.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:46689397 C>T maps to NM_001142673.1 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:46693860 C>T maps to NM_001142673.1 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr17:2603695 G>A maps to NM_015229.3 R378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:2601308 G>A maps to NM_015229.3 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr17:2598353 G>A maps to NM_015229.3 F844F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr17:2605268 G>A maps to NM_015229.3 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr17:2597495 G>A maps to NM_015229.3 F965F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr12:55356340 G>A maps to NM_001098815.1 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:55361015 G>A maps to NM_001098815.1 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:55360173 G>A maps to NM_001098815.1 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr12:55367268 C>T maps to NM_001098815.1 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:55368261 G>A maps to NM_001098815.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:55357682 G>A maps to NM_001098815.1 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr17:6531815 A>G maps to NM_014804.2 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:6531875 G>A maps to NM_014804.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:6493148 G>A maps to NM_014804.2 I912I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:39880028 C>T maps to NM_015038.1 S1364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr1:39879437 G>A maps to NM_015038.1 E1167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:39877892 C>T maps to NM_015038.1 F652F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:39880100 A>G maps to NM_015038.1 L1388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:39876767 C>T maps to NM_015038.1 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:39878165 C>T maps to NM_015038.1 F743F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr18:8784468 C>T maps to ENST00000456698 Y813Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr18:8784546 C>T maps to ENST00000456698 L839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr18:8784534 C>T maps to ENST00000456698 T835T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr18:8784363 G>A maps to ENST00000456698 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr18:8798139 C>T maps to ENST00000456698 Q1082*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr18:8784804 C>T maps to ENST00000456698 I925I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr18:8784162 G>A maps to ENST00000456698 K711K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:8798181 C>T maps to ENST00000456698 R1096*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr18:8784327 C>T maps to ENST00000456698 P766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr18:8824714 C>T maps to ENST00000456698 S1388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr18:8718622 C>T maps to ENST00000456698 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr18:8826059 T>C maps to ENST00000456698 L1837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr19:19454709 C>T maps to NM_015329.3 C346C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr7:36373678 G>A maps to NM_001100425.1 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:36370646 G>A maps to NM_001100425.1 Q450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr16:67214000 G>A maps to NM_001040715.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr16:67213943 C>T maps to NM_001040715.1 Q190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr10:75553422 C>T maps to NM_015037.2 A797A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr10:75553446 C>T maps to NM_015037.2 P805P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr10:75548521 T>A maps to NM_015037.2 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr10:75552441 C>G maps to NM_015037.2 T715T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:75552345 A>G maps to NM_015037.2 T683T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:75550744 C>T maps to NM_015037.2 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr4:154541999 G>A maps to NM_001131007.1 K1220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr4:154510070 C>T maps to NM_001131007.1 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr4:154514995 C>T maps to NM_001131007.1 F656F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr4:154557688 C>T maps to NM_001131007.1 F1598F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:5457802 C>T maps to NM_015325.1 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr6:84904617 G>A maps to NM_014895.2 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr6:84862678 G>A maps to NM_014895.2 Q1072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr18:29496317 A>G maps to NM_014939.3 D178D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr18:29487476 A>T maps to NM_014939.3 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr18:29480919 A>G maps to NM_014939.3 D486D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:29493333 G>A maps to NM_014939.3 Q257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr15:79755471 C>T maps to NM_015206.2 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:79750540 T>G maps to NM_015206.2 S684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:79749388 C>T maps to NM_015206.2 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:79760659 G>A maps to NM_015206.2 L895L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr15:79755470 C>T maps to NM_015206.2 F787F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr15:79750336 C>T maps to NM_015206.2 V616V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr15:79749370 C>T maps to NM_015206.2 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:79748809 G>A maps to NM_015206.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr15:79760662 C>T maps to NM_015206.2 I896I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr15:79755662 G>A maps to NM_015206.2 Q851Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr15:79750312 G>A maps to NM_015206.2 R608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:79748962 C>T maps to NM_015206.2 C158C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:79760662 C>T maps to NM_015206.2 I896I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr15:79749346 G>A maps to NM_015206.2 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr12:105520089 C>T maps to NM_015275.1 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:34977563 C>T maps to NM_015297.1 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:34972407 G>A maps to NM_015297.1 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr9:34971591 C>T maps to NM_015297.1 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26D-06A-11D-A19A-08 chr9:34977181 C>A maps to NM_015297.1 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr4:123132085 C>T maps to NM_015312.3 Q695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr4:123249257 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr4:123280817 T>C maps to NM_015312.3 Y4914Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr4:123274078 C>T maps to NM_015312.3 R4624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:123230542 C>T maps to NM_015312.3 I3392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr4:123230599 G>A maps to NM_015312.3 G3411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:123277107 C>T maps to NM_015312.3 S4821S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:123271119 C>T maps to NM_015312.3 F4580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:123113459 T>G maps to NM_015312.3 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:123140655 T>C maps to NM_015312.3 L803L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:123161271 C>T maps to NM_015312.3 L1479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:123097014 G>T maps to NM_015312.3 G102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:123128702 G>C maps to NM_015312.3 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:123201108 C>G maps to NM_015312.3 S2924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr4:123264593 C>T maps to NM_015312.3 R4128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:123283251 C>T maps to NM_015312.3 G4956G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:141385294 G>A maps to NM_001080392.1 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr7:141385411 G>A maps to NM_001080392.1 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr7:141365101 G>A maps to NM_001080392.1 C279C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:34371686 A>G maps to NM_020702.3 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:34372143 G>A maps to NM_020702.3 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr9:34372239 C>T maps to NM_020702.3 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:175774787 G>A maps to NM_020444.3 R245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr15:81212553 C>T maps to NM_018689.1 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr15:81172150 C>T maps to NM_018689.1 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr15:81176683 C>T maps to NM_018689.1 H262H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr15:81212478 C>T maps to NM_018689.1 F614F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr15:81181887 G>A maps to NM_018689.1 W347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr15:81234614 G>A maps to NM_018689.1 E1212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:81172180 C>T maps to NM_018689.1 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr15:81230230 G>A maps to NM_018689.1 K1106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr15:81201496 G>A maps to NM_018689.1 Q549Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr15:81176590 C>T maps to NM_018689.1 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:81181833 C>T maps to NM_018689.1 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr15:81199034 G>A maps to NM_018689.1 E481E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:81172150 C>T maps to NM_018689.1 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:81212436 C>T maps to NM_018689.1 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr15:81201505 G>T maps to NM_018689.1 V552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:81221461 G>A maps to NM_018689.1 R853R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr23:118221519 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:118222374 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:118230537 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:118239073 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:118217041 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr23:118250482 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:118243073 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr23:118222292 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:118220959 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:118223551 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:118223409 C>T did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:118222827 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr23:118222853 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:118221311 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:118221965 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:118223172 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:118223173 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:118284319 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:118221260 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr23:118242373 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:118215319 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:118222374 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:118222242 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:118227656 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:118223490 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:118228049 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:118221190 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:118221191 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:118221687 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:118223314 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:118219347 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:118242360 C>T did not map to a codon.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr23:118221254 A>T did not map to a codon.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr23:118222544 C>T did not map to a codon.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr23:118239002 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:118215318 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr23:118215448 T>A did not map to a codon.
Sequencing variant TCGA-FS-A4F4-06A-12D-A25O-08 chr23:118284444 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:118221227 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:118228009 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:118230474 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:118230487 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:118221821 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:118221667 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:118221851 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:118221677 G>A did not map to a codon.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr23:118221775 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr23:118222589 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr4:57173804 G>T maps to NM_020722.1 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr4:57181314 C>T maps to NM_020722.1 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr4:57181782 C>T maps to NM_020722.1 S705S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr4:57189570 C>T maps to NM_020722.1 S1072S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr4:57181944 C>T maps to NM_020722.1 P759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:57182490 C>T maps to NM_020722.1 S941S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:57182491 C>T maps to NM_020722.1 Q942*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F4-06A-12D-A25O-08 chr4:57181812 C>T maps to NM_020722.1 V715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:57176869 C>T maps to NM_020722.1 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:57180318 C>T maps to NM_020722.1 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr4:57180912 G>A maps to NM_020722.1 W415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr4:57182232 C>T maps to NM_020722.1 S855S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr4:57181692 C>T maps to NM_020722.1 I675I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr10:24783480 C>T maps to NM_019590.3 Q578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr10:24762362 C>T maps to NM_019590.3 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr10:24833040 G>A maps to NM_019590.3 L1614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:24669946 G>A maps to NM_019590.3 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:24762677 G>A maps to NM_019590.3 R456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr10:24820870 G>A maps to NM_019590.3 T1065T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr10:24832140 G>A maps to NM_019590.3 T1314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr10:24833124 G>A maps to NM_019590.3 E1642E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr10:24508699 C>T maps to NM_019590.3 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:24835168 C>T maps to NM_019590.3 I1916I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr10:24831693 C>T maps to NM_019590.3 Q1203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:24822120 G>A maps to NM_019590.3 E1123E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:24834802 C>T maps to NM_019590.3 S1794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr10:24669853 C>T maps to NM_019590.3 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr10:24784105 G>A maps to NM_019590.3 R605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr10:24832929 C>T maps to NM_019590.3 F1577F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr10:24832986 G>A maps to NM_019590.3 G1596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr10:24721966 G>A maps to NM_019590.3 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr10:24813485 C>T maps to NM_019590.3 S897S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr10:24762209 C>A maps to NM_019590.3 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:24809156 G>A maps to NM_019590.3 V761V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr10:24833907 A>C did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:24816929 G>A maps to NM_019590.3 E988E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr10:24831851 G>A maps to NM_019590.3 W1218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr10:24813338 C>T maps to NM_019590.3 V848V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr10:24762677 G>A maps to NM_019590.3 R456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr10:24813599 C>T maps to NM_019590.3 S935S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr10:24669796 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:24669979 G>A maps to NM_019590.3 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:24809117 G>A maps to NM_019590.3 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:24816959 C>T maps to NM_019590.3 I998I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr10:24762770 C>T maps to NM_019590.3 H487H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:24762605 G>A maps to NM_019590.3 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:24762728 C>T maps to NM_019590.3 A473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:24813410 G>A maps to NM_019590.3 A872A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:24832641 G>A maps to NM_019590.3 E1481E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:24832665 G>A maps to NM_019590.3 G1489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:24834973 C>T maps to NM_019590.3 A1851A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:24835006 G>A maps to NM_019590.3 L1862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:24784105 G>A maps to NM_019590.3 R605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:24802348 C>T maps to NM_019590.3 I721I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr10:24669937 G>A maps to NM_019590.3 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr10:24813338 C>T maps to NM_019590.3 V848V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr6:138655748 G>A maps to NM_020340.4 L1922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr6:138655811 C>T maps to NM_020340.4 F1943F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr6:138628448 G>A maps to NM_020340.4 W1296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:138584479 G>A maps to NM_020340.4 K620K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:138619789 C>T maps to NM_020340.4 F1232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:138634994 T>C maps to NM_020340.4 L1422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:138584554 G>A maps to NM_020340.4 R645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:138584591 C>T maps to NM_020340.4 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr6:138601287 C>T maps to NM_020340.4 I816I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:138655862 C>T maps to NM_020340.4 T1960T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:138601143 C>T maps to NM_020340.4 F768F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:138640838 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:138657604 C>T maps to NM_020340.4 V2172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr3:128706456 A>C did not map to a codon.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr3:128697004 G>A maps to NM_020741.2 Q231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:128690106 G>A maps to NM_020741.2 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr3:128707653 G>A maps to NM_020741.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:128712087 G>A maps to NM_020741.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr17:44108898 G>A maps to NM_015443.3 P1087P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr17:44249328 G>A maps to NM_015443.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr17:44249329 G>A maps to NM_015443.3 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:44249419 G>A maps to NM_015443.3 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:44109021 G>A maps to NM_015443.3 P1046P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:44109634 G>A maps to NM_015443.3 T956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:44144013 G>A maps to NM_015443.3 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:44117170 G>T maps to NM_015443.3 P700P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr17:44110806 G>A maps to NM_015443.3 Q896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:44108898 G>A maps to NM_015443.3 P1087P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:44116453 G>A maps to NM_015443.3 P777P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:44249170 G>A maps to NM_015443.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr10:72307195 C>T maps to NM_014431.2 Y752Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr10:72297607 G>A maps to NM_014431.2 W423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr10:72298061 C>T maps to NM_014431.2 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr10:72298879 C>T maps to NM_014431.2 D534D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:72300952 C>T maps to NM_014431.2 T668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:72299397 G>A maps to NM_014431.2 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr10:72292519 C>T maps to NM_014431.2 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:72289706 C>T maps to NM_014431.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:72324220 C>T maps to NM_014431.2 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:72297606 G>A maps to NM_014431.2 W423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:72326434 G>A maps to NM_014431.2 R839R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:70775724 C>T maps to NM_015634.3 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:70775991 C>T maps to NM_015634.3 P562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:97278297 G>A maps to ENST00000421845 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:97279278 G>A maps to ENST00000421845 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:97274368 G>A maps to ENST00000421845 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:97271120 G>A maps to ENST00000421845 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:109735453 C>T maps to NM_020775.3 V635V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr1:109714589 C>T maps to NM_020775.3 N190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr1:109716107 C>T maps to NM_020775.3 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:109707301 G>A maps to NM_020775.3 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:109745595 C>T maps to NM_020775.3 L1002L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr1:109731787 G>A maps to NM_020775.3 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr1:109714517 C>T maps to NM_020775.3 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:109731706 A>G maps to NM_020775.3 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:109730817 G>A maps to NM_020775.3 W354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:109740599 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:109743401 G>A maps to NM_020775.3 K951K. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-GN-A266-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr7:86526896 C>T maps to NM_001142749.2 E870E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr7:86548561 G>A maps to NM_001142749.2 I488I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:86541411 G>A maps to NM_001142749.2 F715F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:86521201 C>T maps to NM_001142749.2 L956L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr7:86526905 G>A maps to NM_001142749.2 F867F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr7:86539311 C>T maps to NM_001142749.2 K725K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:86569380 G>A maps to NM_001142749.2 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr7:86539145 G>A maps to NM_001142749.2 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr18:34802117 G>A maps to NM_020776.1 K554K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr18:34740252 G>A maps to NM_020776.1 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr18:34415209 A>G maps to NM_020776.1 E36E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr18:34753041 C>T maps to NM_020776.1 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr15:52901076 G>A maps to NM_019600.2 S678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr15:52901655 A>T maps to NM_019600.2 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:101815100 C>T maps to NM_020802.2 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:101793383 C>T maps to NM_020802.2 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr11:101833616 G>A maps to NM_020802.2 K617K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:101818849 C>T maps to NM_020802.2 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:101815073 G>A maps to NM_020802.2 Q109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:101868334 G>A maps to NM_020802.2 K1105K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:232942559 G>A maps to NM_019090.2 G597G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:232942541 G>A maps to NM_019090.2 K591K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr1:232941650 C>T maps to NM_019090.2 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr1:232943051 G>A maps to NM_019090.2 V761V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:232941086 C>T maps to NM_019090.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:232942094 C>T maps to NM_019090.2 C442C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr3:113724547 G>A maps to NM_020817.1 Q559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr3:113699528 T>A maps to NM_020817.1 R759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr3:113737573 A>G maps to NM_020817.1 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:113729777 C>T maps to NM_020817.1 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:113737697 G>A maps to NM_020817.1 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:113724707 A>G maps to NM_020817.1 G505G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A3J7-06A-11D-A20D-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-ER-A19A-06A-21D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr3:113775238 C>T maps to NM_020817.1 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr3:113775247 C>G maps to NM_020817.1 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr3:113697112 G>A maps to NM_020817.1 F842F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr3:113753788 C>T maps to NM_020817.1 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:113753769 A>G did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:113772442 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:113772443 C>T maps to NM_020817.1 K43K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr14:93990336 C>T maps to ENST00000393153 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr14:94158198 G>A maps to ENST00000393153 Q2520Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr14:94156489 C>T maps to ENST00000393153 S2432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr14:94041525 G>A maps to ENST00000393153 G731G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:94120129 C>T maps to ENST00000393153 F2103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:94088531 G>A maps to ENST00000393153 T1673T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:94158135 C>T maps to ENST00000393153 I2499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr14:94079185 C>T maps to ENST00000393153 L1288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:94053161 G>A maps to ENST00000393153 K980K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr14:94046667 G>A maps to ENST00000393153 Q869Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr14:94158207 C>T maps to ENST00000393153 F2523F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr14:94046520 G>A maps to ENST00000393153 T820T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:94109962 C>T maps to ENST00000393153 I2049I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr14:94158279 C>T maps to ENST00000393153 A2547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr14:94173079 C>T maps to ENST00000393153 Q2602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:94083640 C>T maps to ENST00000393153 I1427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr14:94041414 G>A maps to ENST00000393153 E694E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr14:94044255 C>T maps to ENST00000393153 F760F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:94088192 C>T maps to ENST00000393153 I1560I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:94097237 C>T maps to ENST00000393153 S1922S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr14:93943985 G>A maps to ENST00000393153 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr14:94152931 G>A maps to ENST00000393153 A2339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr14:94007137 C>T maps to ENST00000393153 H495H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:94060034 G>A maps to ENST00000393153 R1014R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr14:94048565 G>A maps to ENST00000393153 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:94120310 C>T maps to ENST00000393153 A2135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr14:93962766 T>C maps to ENST00000393153 C241C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr14:93954021 G>A maps to ENST00000393153 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr14:94158219 G>A maps to ENST00000393153 A2527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr14:94084569 C>T maps to ENST00000393153 I1441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr14:94046613 G>A maps to ENST00000393153 K851K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr14:94063733 C>T maps to ENST00000393153 L1074L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:94069756 C>T maps to ENST00000393153 S1249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:94083535 C>T maps to ENST00000393153 C1392C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:94088531 G>A maps to ENST00000393153 T1673T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr14:94160745 C>T maps to ENST00000393153 T2573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr14:93943985 G>A maps to ENST00000393153 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr14:94139695 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:94152931 G>A maps to ENST00000393153 A2339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr14:94004400 G>T maps to ENST00000393153 G397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr8:95539166 G>A maps to NM_015496.3 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr8:95523658 G>A maps to NM_015496.3 P1048P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:95523742 G>A maps to NM_015496.3 L1020L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:95524275 G>A maps to NM_015496.3 T931T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr8:95504938 G>C maps to NM_015496.3 T1583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr8:95556101 G>A maps to NM_015496.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:95530058 G>A maps to NM_015496.3 L875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr8:95538605 C>T maps to NM_015496.3 G622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr8:95524311 G>A maps to NM_015496.3 I919I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:95550486 C>T did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr8:95511667 C>T maps to NM_015496.3 K1388K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr8:95556113 G>T maps to NM_015496.3 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr4:186083969 G>A maps to NM_020827.1 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:5754838 A>C did not map to a codon.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr9:5772726 C>T maps to ENST00000414202 S1260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr9:5763360 G>A maps to ENST00000414202 P778P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr9:5772612 C>T maps to ENST00000414202 S1222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr9:5757381 C>T maps to ENST00000414202 F641F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr10:30316688 C>T maps to NM_020848.2 G796G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr10:30336639 C>T maps to NM_020848.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr10:30318497 C>T maps to NM_020848.2 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr10:30316580 G>A maps to NM_020848.2 I832I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:30315734 G>A maps to NM_020848.2 P1114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:30336468 C>T maps to NM_020848.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:30316265 C>T maps to NM_020848.2 V937V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr10:30317231 C>T maps to NM_020848.2 K615K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr10:30318260 C>T maps to NM_020848.2 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr10:30315707 G>A maps to NM_020848.2 S1123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:30315536 C>T maps to NM_020848.2 G1180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr10:30336468 C>T maps to NM_020848.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr10:30316573 A>G maps to NM_020848.2 L835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:30315233 G>A maps to NM_020848.2 S1281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:30317816 G>A maps to NM_020848.2 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:30317558 C>T maps to NM_020848.2 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr10:30315629 C>T maps to NM_020848.2 R1149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr10:30317024 G>A maps to NM_020848.2 H684H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr10:30315748 G>A maps to NM_020848.2 Q1110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr10:30336618 C>T maps to NM_020848.2 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:30316292 C>T maps to NM_020848.2 W928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr10:30315095 C>T maps to NM_020848.2 R1327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr10:30318510 C>T maps to NM_020848.2 W189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:30316937 C>T maps to NM_020848.2 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:30318779 G>A maps to NM_020848.2 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:30315788 C>T maps to NM_020848.2 V1096V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:30336585 C>T maps to NM_020848.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr12:13229027 C>T maps to NM_020853.1 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:13220138 C>T maps to NM_020853.1 R351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:13229030 C>T maps to NM_020853.1 I532I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr12:13220138 C>T maps to NM_020853.1 R351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:13208815 C>T maps to NM_020853.1 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:13221608 C>T maps to NM_020853.1 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr12:13219708 C>T maps to NM_020853.1 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:13229021 C>T maps to NM_020853.1 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:59925254 A>G maps to NM_020854.3 R657R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:59912076 C>T maps to NM_020854.3 F567F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr18:59936120 G>A maps to NM_020854.3 G900G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr18:59972713 C>T maps to NM_020854.3 Q1200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr18:59911995 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr18:59931273 C>T maps to NM_020854.3 I801I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:59947645 C>T maps to NM_020854.3 A1007A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr2:226273631 G>A maps to NM_020864.1 E12E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:226447419 C>T maps to NM_020864.1 Y429Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51K-06A-11D-A25O-08 chr2:226378287 C>T maps to NM_020864.1 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr2:226446834 C>T maps to NM_020864.1 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr2:226447368 G>C maps to NM_020864.1 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr2:226446753 C>T maps to NM_020864.1 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:226378311 C>T maps to NM_020864.1 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:226447390 C>T maps to NM_020864.1 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:226447050 C>T maps to NM_020864.1 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:226447204 C>T maps to NM_020864.1 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:226447215 G>A maps to NM_020864.1 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:226446849 G>A maps to NM_020864.1 E239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:226446870 C>T maps to NM_020864.1 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr2:226447446 C>T maps to NM_020864.1 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:226446675 C>T maps to NM_020864.1 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:226447683 C>T maps to NM_020864.1 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:226516184 G>A maps to NM_020864.1 S622S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:33236534 G>A maps to NM_020888.2 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:33236282 C>T maps to NM_020888.2 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:108295123 A>G maps to NM_020890.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:108272528 C>T maps to NM_020890.2 Q791Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr9:100117248 C>T maps to ENST00000375206 Q1090*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:100090418 C>T maps to ENST00000375206 I776I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:100127969 C>T maps to ENST00000375206 I1321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr9:100071748 T>A maps to ENST00000375206 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr9:100119946 C>T maps to ENST00000375206 F1116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr9:100076901 C>T maps to ENST00000375206 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr9:100124120 C>T maps to ENST00000375206 S1214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr9:100124129 G>A maps to ENST00000375206 G1217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:100132243 C>T maps to ENST00000375206 P1399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:1348912 C>T maps to NM_020894.2 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:1343518 C>T maps to NM_020894.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr4:1369269 C>T maps to NM_020894.2 D469D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr4:1343497 C>T maps to NM_020894.2 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr4:1343461 C>T maps to NM_020894.2 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr9:35108109 G>A maps to NM_025182.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:35108109 G>A maps to NM_025182.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:35107467 G>A maps to NM_025182.2 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:7671209 G>A maps to NM_001080429.2 W152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:7677133 C>T maps to NM_001080429.2 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:7676683 G>A maps to NM_001080429.2 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:7675608 C>T maps to NM_001080429.2 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:7677205 G>A maps to NM_001080429.2 E636E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:7673058 C>T maps to NM_001080429.2 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:7675416 C>T maps to NM_001080429.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:7675817 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:7675992 C>T maps to NM_001080429.2 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:7677064 G>A maps to NM_001080429.2 V589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr19:7682654 G>A maps to NM_001080429.2 K1181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:7672754 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:138601949 G>A maps to NM_001164665.1 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr7:138601866 A>G maps to NM_001164665.1 G835G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr7:138602910 G>A maps to NM_001164665.1 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr7:138591806 C>T maps to NM_001164665.1 R1106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr7:138546010 G>A maps to NM_001164665.1 T1707T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr7:138529098 C>A maps to NM_001164665.1 P1805P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr7:138603045 C>A maps to NM_001164665.1 V442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:138603462 G>A maps to NM_001164665.1 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:138545920 G>A maps to NM_001164665.1 F1737F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:138546118 G>A maps to NM_001164665.1 S1671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:138579237 G>A maps to NM_001164665.1 S1294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:138601854 G>A maps to NM_001164665.1 I839I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr7:138529137 G>A maps to NM_001164665.1 A1792A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr7:138603645 G>A maps to NM_001164665.1 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:138596027 G>A maps to NM_001164665.1 S1003S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:138596018 G>A maps to NM_001164665.1 F1006F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A2MD-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:138603309 G>A maps to NM_001164665.1 F354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:138545962 G>A maps to NM_001164665.1 T1723T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:138546040 G>A maps to NM_001164665.1 L1697L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:138591707 C>T maps to NM_001164665.1 E1139E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:138546091 G>A maps to NM_001164665.1 I1680I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:138552729 G>A maps to NM_001164665.1 I1640I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:138566303 G>A maps to NM_001164665.1 F1353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:138591710 C>T maps to NM_001164665.1 V1138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:138591833 G>A maps to NM_001164665.1 T1097T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr7:138604143 G>A maps to NM_001164665.1 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:138602376 G>A maps to NM_001164665.1 P665P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-FW-A3R5-06A-11D-A23B-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:138522698 G>A maps to ENST00000413208 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:138566162 G>A maps to NM_001164665.1 I1400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:138591788 G>A maps to NM_001164665.1 I1112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr6:56915603 C>T maps to NM_020931.2 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr6:56919412 G>T maps to NM_020931.2 E706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr10:118711437 G>A maps to NM_001127211.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:118681008 G>A maps to NM_001127211.1 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr16:84520566 G>A maps to NM_020947.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr16:84529510 G>A maps to NM_020947.3 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr1:180904770 C>T maps to NM_020950.1 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr1:180886114 C>T maps to NM_020950.1 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:180885619 G>A maps to NM_020950.1 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr1:180905208 C>T maps to NM_020950.1 Q722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr18:43492289 G>A maps to NM_020964.2 F1316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr18:43447662 G>A maps to NM_020964.2 L2092L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr18:43446813 G>A maps to NM_020964.2 L2190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:43529512 G>A maps to NM_020964.2 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr18:43535082 G>A maps to NM_020964.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:43437822 A>T maps to NM_020964.2 S2479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr18:43437861 G>A maps to NM_020964.2 I2466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr18:43437837 C>T maps to NM_020964.2 R2474R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr18:43450555 C>T maps to NM_020964.2 Q2067Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:44692586 C>T maps to NM_001099294.1 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr22:44681323 G>A maps to NM_001099294.1 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:44681564 A>T maps to NM_001099294.1 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr19:18376006 G>T maps to NM_001145304.1 S781S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:18368547 G>A maps to NM_001145304.1 H1182H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:18376885 C>T maps to NM_001145304.1 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:18376105 C>T maps to NM_001145304.1 P748P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:18377053 G>A maps to NM_001145304.1 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:18368094 G>A maps to NM_001145304.1 T1333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:18368778 G>A maps to NM_001145304.1 S1105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:18368598 G>A maps to NM_001145304.1 T1165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr13:45589218 G>C did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr13:45594490 C>T maps to NM_018559.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:175231093 T>C maps to NM_001145314.1 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr4:175237392 T>A maps to NM_001145314.1 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:175224907 C>T maps to NM_001145314.1 Q98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr4:175225444 T>C maps to NM_001145314.1 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr2:176844544 T>C maps to NM_030650.1 E103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr2:176856981 G>A maps to NM_030650.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr14:77580456 C>T maps to NM_033426.2 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr14:77579931 G>T maps to NM_033426.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:1919979 C>T maps to ENST00000434971 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:1920399 A>T maps to ENST00000434971 L27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:1920051 C>T maps to ENST00000434971 K65K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr20:36869143 G>A maps to NM_001029864.1 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr20:36841512 G>A maps to NM_001029864.1 S1178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr20:36841569 G>A maps to NM_001029864.1 F1159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr20:36859608 G>A maps to NM_001029864.1 I622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:36869719 G>A maps to NM_001029864.1 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr20:36870277 C>T maps to NM_001029864.1 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:36848064 G>A maps to NM_001029864.1 V841V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:36869692 G>A maps to NM_001029864.1 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:36870250 G>A maps to NM_001029864.1 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr9:20990167 G>A maps to NM_017794.3 W1684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr9:20953017 T>C maps to NM_017794.3 S1362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr9:20990132 C>T maps to NM_017794.3 F1672F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr9:20907174 C>T maps to NM_017794.3 H884H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:20990234 T>C maps to NM_017794.3 N1706N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:20990195 C>G maps to NM_017794.3 L1693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:233514712 T>A maps to NM_032435.2 L654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:233515160 C>T maps to NM_032435.2 S803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:233518315 G>A maps to NM_032435.2 E990E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr1:233518132 G>A maps to NM_032435.2 R929R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:233518192 C>T maps to NM_032435.2 S949S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:233515106 G>A maps to NM_032435.2 G785G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:233512230 C>T maps to NM_032435.2 Q628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:233514854 C>T maps to NM_032435.2 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:233511737 G>A maps to NM_032435.2 R584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:233511737 G>A maps to NM_032435.2 R584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:233511737 G>A maps to NM_032435.2 R584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:233514854 C>T maps to NM_032435.2 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:233482260 G>A maps to NM_032435.2 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:233518168 C>T maps to NM_032435.2 I941I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:233514908 G>A maps to NM_032435.2 T719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:233482257 G>A maps to NM_032435.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:233514786 C>T maps to NM_032435.2 Q679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:233490630 C>T maps to NM_032435.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CF-06A-11D-A196-08 chr11:105880672 T>C maps to NM_032424.1 K209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr11:105880594 G>A maps to NM_032424.1 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr2:61345223 C>T maps to NM_001129993.1 D667D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:61308627 T>C maps to NM_001129993.1 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:61308591 G>T maps to NM_001129993.1 G226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr2:61298823 G>A maps to NM_001129993.1 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:61331071 T>C maps to NM_001129993.1 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr6:30652789 G>A maps to NM_133471.3 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr6:30653723 G>A maps to NM_133471.3 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:30652328 G>A maps to NM_133471.3 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr9:115337319 G>A maps to NM_133465.2 Q320Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr9:115337400 C>T maps to NM_133465.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:115336380 C>T maps to NM_133465.2 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr9:115422339 C>T maps to NM_133465.2 C714C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr9:115422087 C>T maps to NM_133465.2 Y630Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:115421589 C>T maps to NM_133465.2 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:115421616 C>T maps to NM_133465.2 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr8:22475236 C>T maps to NM_021174.5 V673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr8:22474991 C>T maps to NM_021174.5 P635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr8:22473054 C>T maps to NM_021174.5 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr8:22470616 C>T maps to NM_021174.5 Y224Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr8:22475242 C>A maps to NM_021174.5 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr8:22464831 C>T maps to NM_021174.5 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:113374803 G>A maps to NM_001009899.2 R1909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:113375878 G>A maps to NM_001009899.2 S1550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:113378866 A>T maps to NM_001009899.2 I554I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:113375884 G>A maps to NM_001009899.2 S1548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:113377996 G>A maps to NM_001009899.2 F844F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:113376430 G>A maps to NM_001009899.2 T1366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr23:73962839 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr23:73965441 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:73961407 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:73962419 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:73963929 C>A did not map to a codon.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr23:73963453 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr23:73960360 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr23:73963630 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr23:73963376 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:73960604 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:73963875 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr23:73961839 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:73961740 T>C did not map to a codon.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr23:73961965 A>C did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:73961063 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:73961451 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:73962508 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:73965442 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:73960800 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:73962827 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr23:73962140 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:73962823 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:73959936 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:73963896 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:73963192 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:73963426 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:73963787 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:73960457 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:73960925 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:73961992 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr23:73960578 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:73961096 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:73962771 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:73963454 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:73961339 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:73961523 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:73963842 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:73963187 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:73963437 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr23:73962070 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:73960451 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:73961103 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:73960627 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:73963454 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr23:73962508 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr23:73960046 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr23:73960457 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:73959289 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:73960000 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:73962588 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:73963782 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:73961114 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:73963454 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:73963905 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:73959965 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:73963607 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:73963875 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:73960240 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:73962554 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:73960533 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:73962654 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:73963265 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:73962794 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:73962752 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr23:73964129 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:73961512 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:73960441 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:73961672 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:73963706 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:73961641 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:73964092 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr23:73961691 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr23:73963797 C>T did not map to a codon.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr23:73960213 C>T did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:73963376 G>A did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:73963727 T>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr23:73962467 G>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:73962798 T>C did not map to a codon.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr23:73963412 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr23:73963686 A>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:73962839 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:73960272 T>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:73960617 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:73960770 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:73961517 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:73962515 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:73964161 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:73964162 G>A did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr23:73960343 C>T did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr23:73960907 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:73960919 T>C did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:73960340 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:73962249 C>T did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:73961169 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:73960520 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:73961965 A>C did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:73962339 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:73962508 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:73963779 G>A did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:73961063 C>T did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:73962140 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr23:73960867 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr23:73961367 G>A did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:73961696 C>T did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:73962430 G>A did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:73962836 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr9:5920143 A>C maps to NM_001017969.2 L1951*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:5924690 G>A maps to NM_001017969.2 L885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:5968634 G>A maps to NM_001017969.2 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:5924688 C>G maps to NM_001017969.2 L885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr9:5920073 A>G maps to NM_001017969.2 S1974S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:8871209 G>A maps to NM_020738.2 S1652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:8871125 G>A maps to NM_020738.2 P1680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:8871791 G>A maps to NM_020738.2 I1458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:8871203 G>A maps to NM_020738.2 S1654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:8930115 G>A maps to NM_020738.2 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr2:8871370 G>A maps to NM_020738.2 L1599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:8873708 G>A maps to NM_020738.2 R1306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr2:8871767 G>A maps to NM_020738.2 S1466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:94373211 C>T maps to NM_004523.3 Q290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr10:94368821 G>T maps to NM_004523.3 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:116857320 G>A maps to ENST00000259410 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:116856468 C>T maps to ENST00000259410 E430E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr9:116854269 C>T maps to ENST00000259410 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr9:116856656 G>A maps to ENST00000259410 Q395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:17764556 A>C maps to NM_022113.4 S1734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr6:17764703 G>A maps to NM_022113.4 I1685I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr6:17772249 A>G maps to NM_022113.4 P1455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:17850607 G>A maps to NM_022113.4 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr6:17817387 C>G maps to NM_022113.4 R621R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr6:17837155 G>A maps to NM_022113.4 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr6:17817357 G>A maps to NM_022113.4 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr6:17772168 G>A maps to NM_022113.4 A1482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:17794533 G>A maps to NM_022113.4 I1056I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr6:17764937 G>A maps to NM_022113.4 A1607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr8:28997621 G>A maps to NM_015254.3 V857V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr8:28988060 G>A maps to NM_015254.3 Q1022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:29025002 G>A maps to NM_015254.3 R349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr8:29043813 G>A maps to NM_015254.3 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr8:28997993 C>T maps to NM_015254.3 Q825Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:29043830 G>A maps to NM_015254.3 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:200572355 T>C maps to NM_014875.2 T659T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:200555349 T>C maps to NM_014875.2 L1040L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr1:200522522 C>T maps to NM_014875.2 W1647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:200534573 G>A maps to NM_014875.2 N1295N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr1:200559250 A>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:200571081 G>A maps to NM_014875.2 A698A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:200562860 G>A maps to NM_014875.2 I862I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr3:44879876 C>T maps to NM_020242.2 T1094T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr3:44844304 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr3:44856526 C>T maps to NM_020242.2 S836S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:44893302 T>G maps to NM_020242.2 L1277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr3:44893365 G>A maps to NM_020242.2 E1298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr3:44867636 C>T maps to NM_020242.2 Q886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr3:44847369 G>A maps to NM_020242.2 Q621Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr3:44852399 T>C maps to NM_020242.2 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr3:44867529 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:44881881 G>A maps to NM_020242.2 K1118K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr20:16355047 T>C maps to NM_024704.4 E1068E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:16360708 G>A maps to NM_024704.4 I646I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:16359498 G>A maps to NM_024704.4 Q1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr20:16493520 C>T maps to NM_024704.4 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:16359753 G>A maps to NM_024704.4 Q965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr20:16387033 G>A maps to NM_024704.4 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr20:16360168 G>A maps to NM_024704.4 F826F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-FW-A3R5-06A-11D-A23B-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:20996943 G>A maps to NM_020816.2 T921T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr1:20992746 C>T maps to NM_020816.2 R957R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:21040039 C>T maps to NM_020816.2 E129E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr1:21011405 G>A maps to NM_020816.2 P709P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:21009369 G>A maps to NM_020816.2 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:21036223 C>T maps to NM_020816.2 W193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:21011438 C>T maps to NM_020816.2 Q698Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:21014261 G>A maps to NM_020816.2 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:21009331 C>T maps to NM_020816.2 K759K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:21031350 G>A maps to NM_020816.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:21036144 C>T maps to NM_020816.2 E219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:20998467 G>A maps to NM_020816.2 I895I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:20998674 C>T maps to NM_020816.2 E826E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:21031192 C>T maps to NM_020816.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr1:21014159 G>A maps to NM_020816.2 F553F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:28112979 G>A maps to NM_031217.3 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:28058203 A>C maps to NM_031217.3 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr11:28090910 C>T maps to NM_031217.3 E495E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr11:28112953 A>T did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr17:43003833 G>A maps to ENST00000438933 A812A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr17:43011672 C>T maps to ENST00000438933 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr17:43006349 G>A maps to ENST00000438933 S532S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr17:43010090 G>A maps to ENST00000438933 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:43012706 G>A maps to ENST00000438933 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:72339223 C>T maps to NM_153209.3 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:72351366 T>C maps to NM_153209.3 G971G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:72350304 G>A maps to NM_153209.3 R771R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr17:72349660 G>A maps to NM_153209.3 W750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:72339244 C>T maps to NM_153209.3 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:72350631 G>A maps to NM_153209.3 R880R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:72346603 C>T maps to NM_153209.3 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:72347040 G>A maps to NM_153209.3 Q528Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:72350550 C>T maps to NM_153209.3 A853A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr17:72351339 C>T maps to NM_153209.3 P962P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr17:72340378 C>T maps to NM_153209.3 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr17:72351327 G>A maps to NM_153209.3 G958G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:72345459 G>A maps to NM_153209.3 Q395Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:72349018 G>A maps to NM_153209.3 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:72351060 C>T maps to NM_153209.3 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr17:72350658 G>A maps to NM_153209.3 R889R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr17:72340913 G>A maps to NM_153209.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr2:241727551 G>A maps to ENST00000373308 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:241715316 G>A maps to ENST00000373308 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr2:241682373 G>A maps to ENST00000373308 F1204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:241685219 G>A maps to ENST00000373308 F1103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:241683417 G>A maps to ENST00000373308 F1175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr2:241737088 G>A maps to ENST00000373308 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:241728670 G>A maps to ENST00000373308 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:241713622 G>A maps to ENST00000373308 Y338Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr2:241722493 G>A maps to ENST00000373308 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:241706373 C>A maps to ENST00000373308 E548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:241715277 C>T maps to ENST00000373308 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:241705142 G>A maps to ENST00000373308 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:241689930 G>A maps to ENST00000373308 P964P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr2:241658602 G>A maps to ENST00000373308 S1686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:10403296 C>T maps to ENST00000377086 Q1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr1:10399868 C>T maps to ENST00000377086 L1155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:10405969 C>T maps to ENST00000377086 L1252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:10364095 C>T maps to NM_183416.3 I951I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:10356643 C>T maps to ENST00000377086 I594I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:10386321 C>T maps to ENST00000377086 A943A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:10381873 C>T maps to ENST00000377086 L773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:10381866 C>A maps to ENST00000377086 A770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr1:10394661 G>A maps to ENST00000377086 R1003R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:10363558 C>T maps to NM_183416.3 A772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:4927034 C>T maps to NM_006612.5 A967A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:4927148 C>G maps to NM_006612.5 P1005P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr17:4923916 C>T maps to NM_006612.5 A627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:4927196 G>A maps to NM_006612.5 P1021P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:4906085 C>T maps to NM_006612.5 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:4927259 A>G maps to NM_006612.5 G1042G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr17:4927148 C>T maps to NM_006612.5 P1005P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:4923294 G>A maps to NM_006612.5 V557V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr5:137517383 T>C maps to NM_005733.2 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr10:91498210 C>T maps to ENST00000416354 Q1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr10:91497678 C>T maps to ENST00000416354 D1057D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr10:91497762 T>C maps to ENST00000416354 S1085S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr10:91497756 C>T maps to ENST00000416354 F1083F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:91474754 C>T maps to ENST00000416354 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr12:39696938 T>G did not map to a codon.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr12:39760858 T>C maps to ENST00000395670 Q236Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:39760927 T>C maps to ENST00000395670 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:39703440 A>G maps to ENST00000395670 S1409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr12:39752006 A>G maps to ENST00000395670 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:39760882 G>A maps to ENST00000395670 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:39734771 T>C maps to ENST00000395670 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr1:200946488 C>T maps to NM_017596.2 V1379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr1:200978067 C>T maps to NM_017596.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:200956194 G>A maps to NM_017596.2 F1181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:200960847 C>T maps to NM_017596.2 Q797Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:200960265 C>A maps to NM_017596.2 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:200965479 C>T maps to NM_017596.2 K707K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:200969849 C>T maps to NM_017596.2 E487E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr1:200972893 G>A maps to NM_017596.2 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr1:200967692 G>A maps to NM_017596.2 F632F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr1:200978519 C>T maps to NM_017596.2 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:200946497 C>A maps to NM_017596.2 S1376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:200960045 G>A maps to NM_017596.2 R896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr1:200971394 C>T maps to NM_017596.2 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:200969864 G>A maps to NM_017596.2 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:200943300 C>T maps to NM_017596.2 W1599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:200943301 C>T maps to NM_017596.2 W1599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:200956006 C>T maps to NM_017596.2 T1218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:200969849 C>T maps to NM_017596.2 E487E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:200950208 C>T maps to NM_017596.2 P1273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:200969711 G>A maps to NM_017596.2 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:200978067 C>T maps to NM_017596.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:200969076 G>A maps to NM_017596.2 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:200974768 G>A maps to NM_017596.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:200969849 C>T maps to NM_017596.2 E487E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:200967659 G>A maps to NM_017596.2 I643I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:200943843 G>T maps to NM_017596.2 S1591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:200969621 C>A maps to NM_017596.2 G527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:200969678 C>T maps to NM_017596.2 R508R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:200965371 C>T maps to NM_017596.2 R743R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:200967554 G>A maps to NM_017596.2 I678I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:200967677 G>A maps to NM_017596.2 A637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:200943940 C>T maps to NM_017596.2 W1559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:200950133 G>A maps to NM_017596.2 I1298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:200944035 G>A maps to NM_017596.2 I1527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:200960247 G>A maps to NM_017596.2 P828P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:200967692 G>A maps to NM_017596.2 F632F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:200948778 G>A maps to NM_017596.2 P1335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:29816467 G>A maps to NM_007317.1 T641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr16:29816328 C>A maps to NM_007317.1 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:29815379 G>A maps to NM_007317.1 K557K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:69727867 C>T maps to NM_138555.1 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr15:69728067 C>T maps to NM_138555.1 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr9:34256460 G>A maps to NM_194313.2 L1048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr9:34306348 T>C maps to NM_194313.2 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr9:34254446 C>T maps to NM_194313.2 R1346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr9:34259682 G>A maps to NM_194313.2 I512I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr9:34256067 C>T maps to NM_194313.2 T1179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:168440777 C>T maps to NM_030615.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:168445588 C>T maps to NM_030615.2 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr6:168443301 G>A maps to NM_030615.2 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr6:168443322 G>A maps to NM_030615.2 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:168431509 C>A maps to NM_030615.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr6:168440777 C>T maps to NM_030615.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr14:104642586 G>A maps to NM_015656.1 G1154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr14:104640151 C>T maps to NM_015656.1 A659A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:104642787 C>T maps to NM_015656.1 T1221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr14:104642883 G>A maps to NM_015656.1 Q1253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr14:104624132 C>T maps to NM_015656.1 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:104641647 C>T maps to NM_015656.1 F841F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:104640106 G>A maps to NM_015656.1 R644R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:104642394 C>T maps to NM_015656.1 A1090A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:104642754 C>T maps to NM_015656.1 L1210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:104643603 C>T maps to NM_015656.1 P1493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:245865805 G>A maps to NM_018012.3 E2075E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr1:245851522 C>T maps to NM_018012.3 R1746R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:245775267 G>A maps to NM_018012.3 G696G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:245848735 C>T maps to NM_018012.3 S817S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:245809552 C>T maps to NM_018012.3 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:245704167 G>A maps to NM_018012.3 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:245530266 C>T maps to NM_018012.3 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:245850439 C>T maps to NM_018012.3 I1385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:245849701 C>T maps to NM_018012.3 S1139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:245848729 G>A maps to NM_018012.3 G815G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:245849092 C>T maps to NM_018012.3 I936I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:245862272 C>T maps to NM_018012.3 L2038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:245852056 C>T maps to NM_018012.3 S1924S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:245848918 G>A maps to NM_018012.3 K878K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:245704089 G>T maps to NM_018012.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:245704204 C>T maps to NM_018012.3 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:86503461 G>A maps to NM_017576.1 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:86504116 G>A maps to NM_017576.1 R621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr9:86518862 A>G maps to NM_017576.1 N190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr9:86530215 G>A maps to NM_017576.1 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:86523439 G>A maps to NM_017576.1 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr9:86518516 G>A maps to NM_017576.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:61659024 G>A maps to NM_001098511.1 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr17:51900732 G>A maps to NM_032559.4 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr17:51900732 G>A maps to NM_032559.4 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr17:51900732 G>A maps to NM_032559.4 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr17:51900693 G>A maps to NM_032559.4 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr17:51900852 C>T maps to NM_032559.4 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr17:51900534 G>C maps to NM_032559.4 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr17:51900576 G>A maps to NM_032559.4 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr17:51902277 T>C maps to NM_032559.4 G628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:51900462 C>T maps to NM_032559.4 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:51901263 C>T maps to NM_032559.4 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:51901614 G>A maps to NM_032559.4 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr17:51901098 C>T maps to NM_032559.4 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:51900732 G>A maps to NM_032559.4 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:51901923 G>A maps to NM_032559.4 Q510Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:51900846 G>A maps to NM_032559.4 W151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr17:51901482 G>A maps to NM_032559.4 K363K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:51900708 C>T maps to NM_032559.4 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:51901476 G>A maps to NM_032559.4 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:51900576 G>A maps to NM_032559.4 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:51900577 G>T maps to NM_032559.4 E62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZU-06A-12D-A196-08 chr17:51901911 C>T maps to NM_032559.4 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:51901191 C>T maps to NM_032559.4 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:51902118 C>T maps to NM_032559.4 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:51902232 G>A maps to NM_032559.4 G613G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:51902355 G>A maps to NM_032559.4 E654E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr17:51901203 C>T maps to NM_032559.4 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr17:51901686 C>T maps to NM_032559.4 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:45227595 G>A maps to NM_006845.3 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr1:45232823 A>G maps to NM_006845.3 Q717Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:132051942 G>A maps to ENST00000403231 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:30898287 C>T maps to NM_004798.3 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:30898236 C>T maps to NM_004798.3 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr20:30904022 C>T maps to NM_004798.3 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:30898062 C>T maps to NM_004798.3 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:30898188 C>T maps to NM_004798.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:30919040 G>A maps to NM_004798.3 R721R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:26152310 G>A maps to NM_002254.6 S717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr2:26177194 G>A maps to NM_002254.6 I610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr2:26203832 C>T maps to NM_002254.6 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:26151894 G>A maps to NM_002254.6 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr2:26174710 G>A maps to NM_002254.6 F651F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:26204326 G>A maps to NM_002254.6 R154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr2:26178484 C>T maps to NM_002254.6 E565E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:26203481 C>T maps to NM_002254.6 E435E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:26203889 G>A maps to NM_002254.6 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:26204075 G>A maps to NM_002254.6 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:69626150 C>T did not map to a codon.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr23:69640027 G>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:69639985 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr23:69594072 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr23:69615625 C>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:69622481 A>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:69639973 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr5:154395848 G>A maps to NM_001099293.1 L810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:154395110 A>G maps to NM_001099293.1 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:154395497 C>T maps to NM_001099293.1 F693F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr5:154397003 G>A maps to NM_001099293.1 S1195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr5:154396922 C>T maps to NM_001099293.1 I1168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:154395875 G>A maps to NM_001099293.1 Q819Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr5:154395224 C>T maps to NM_001099293.1 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:154394580 C>T maps to NM_001099293.1 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr5:154395341 G>A maps to NM_001099293.1 W641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr5:154393532 G>A maps to NM_001099293.1 E38E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:154396922 C>T maps to NM_001099293.1 I1168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:154395296 G>A maps to NM_001099293.1 K626K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr5:154396481 C>T maps to NM_001099293.1 I1021I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:154395650 G>A maps to NM_001099293.1 R744R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr5:154395734 G>A maps to NM_001099293.1 K772K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:154394954 C>T maps to NM_001099293.1 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:154396865 G>A maps to NM_001099293.1 E1149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr5:154395272 G>A maps to NM_001099293.1 E618E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:154393844 G>A maps to NM_001099293.1 E142E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr12:57963425 G>A maps to NM_004984.2 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:57966371 C>T maps to NM_004984.2 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr12:57960967 G>A maps to NM_004984.2 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr12:57966361 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr12:57962771 C>T maps to NM_004984.2 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr12:57972124 G>A maps to NM_004984.2 Q846Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:57957250 C>T maps to NM_004984.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:57957964 C>T maps to NM_004984.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:57963332 G>A maps to NM_004984.2 K328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:57965878 C>T maps to NM_004984.2 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:57966028 G>A maps to NM_004984.2 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr12:57963425 G>A maps to NM_004984.2 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:57976383 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:57969033 C>T maps to NM_004984.2 S628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr2:149806889 G>A maps to NM_004522.1 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr2:149853800 C>T maps to NM_004522.1 Q683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr2:149806453 G>A maps to NM_004522.1 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr2:149840162 G>A maps to NM_004522.1 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr2:149806889 G>A maps to NM_004522.1 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:149840228 G>A maps to NM_004522.1 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr6:39512352 C>T maps to NM_145027.4 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr6:39328220 G>A maps to NM_145027.4 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:39607457 C>T maps to NM_145027.4 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr6:39693056 C>T maps to NM_145027.4 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr6:39507992 G>A maps to NM_145027.4 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:39325114 C>T maps to NM_145027.4 T706T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:90171865 C>T maps to NM_198525.2 P1272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:90185520 G>A maps to NM_198525.2 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr15:90189173 C>T maps to NM_198525.2 E624E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:90171979 C>T maps to NM_198525.2 Q1234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:90177087 C>T maps to NM_198525.2 T807T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr3:47308678 G>A maps to NM_182902.3 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:47307351 G>A maps to NM_182902.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:47298993 G>A maps to NM_182902.3 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:47284689 C>T maps to NM_182902.3 K520K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:47289519 G>A maps to NM_182902.3 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr1:169985726 T>G maps to NM_014970.2 I353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:169930249 G>A maps to NM_014970.2 R704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr6:33374648 C>T maps to NM_002263.3 S658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr6:33374157 C>T maps to NM_002263.3 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr8:145695005 C>T maps to NM_145754.2 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:145692695 C>T maps to NM_145754.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:145697782 G>A maps to NM_145754.2 V549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:145692662 G>A maps to NM_145754.2 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr16:57803755 G>A maps to NM_005550.3 Q351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr16:57803756 G>A maps to NM_005550.3 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr10:7811238 C>T maps to NM_012311.2 Q246Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr10:7816795 T>C maps to NM_012311.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr10:7817756 G>A maps to NM_012311.2 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr19:55286758 C>T maps to ENST00000291633 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:55281316 C>T maps to ENST00000291633 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr19:55290097 A>G maps to ENST00000291633 E233E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr19:55286632 T>C maps to ENST00000291633 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:55284956 C>T maps to ENST00000291633 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:55286851 C>T maps to ENST00000291633 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:55263937 C>T maps to NM_015868.2 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:55250024 C>T maps to NM_015868.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:55263176 C>T maps to NM_015868.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:55263167 C>T maps to NM_015868.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:55324583 C>T maps to ENST00000396289 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:55315352 C>T maps to ENST00000396289 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:55325197 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:55324655 C>T maps to ENST00000396289 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:55331324 C>T maps to ENST00000355608 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:55331456 C>T maps to ENST00000355608 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr19:55341404 G>A maps to NM_013289.2 E376E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr19:55330025 C>T maps to ENST00000355608 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:55330034 C>T maps to ENST00000355608 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:55331225 G>A maps to ENST00000355608 E138E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:55333101 C>T maps to ENST00000355608 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:55340882 C>A maps to NM_013289.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:55331424 C>T maps to ENST00000355608 Q205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr19:55331456 C>T maps to ENST00000355608 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:55340885 C>T maps to NM_013289.2 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr19:55331420 C>T maps to ENST00000355608 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:55362681 C>T maps to NM_006737.2 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr19:55378095 C>T maps to ENST00000355608 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr19:55377323 C>T maps to ENST00000355608 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:55377999 G>A maps to ENST00000355608 Q394Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:55377317 C>T maps to ENST00000355608 I353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:55378035 C>T maps to ENST00000355608 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:55247511 C>T maps to NM_153443.3 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr1:158063186 C>A maps to ENST00000368173 I526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr1:158059517 C>T maps to ENST00000368173 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:158063216 C>T maps to ENST00000368173 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:158064609 C>T maps to ENST00000368173 A674A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr1:158047895 C>T maps to ENST00000368173 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr1:158047896 C>T maps to ENST00000368173 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:36357401 C>T maps to NM_032123.5 F622F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:36350385 C>T maps to NM_199180.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:36357425 C>T maps to NM_032123.5 S630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr19:36349759 C>T maps to NM_199180.2 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr19:36351510 C>T maps to NM_199180.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:36357401 C>T maps to NM_032123.5 F622F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:36357192 C>T maps to NM_199180.2 F642F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:36357354 C>T maps to NM_199180.2 F696F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44R-06A-41D-A25O-08 chr11:126301338 C>T maps to NM_032531.3 A557A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr11:126314916 G>A maps to NM_032531.3 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr11:126396484 G>A maps to NM_032531.3 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:204159665 G>A maps to ENST00000306118 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr4:55564558 G>A maps to NM_000222.2 K149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:55564465 C>T maps to NM_000222.2 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:55602767 C>T maps to NM_000222.2 F863F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr4:55561753 C>T maps to NM_000222.2 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr12:88912641 T>C maps to NM_000899.4 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr12:88912536 G>A maps to NM_000899.4 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:88910189 G>A maps to NM_000899.4 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr13:33638083 C>T maps to NM_004795.3 Q934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr13:33628355 G>A maps to NM_004795.3 K424K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr13:33628070 A>G maps to NM_004795.3 K329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr13:33635750 G>A maps to NM_004795.3 V845V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr13:33638148 C>T maps to NM_004795.3 G955G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr13:33635582 C>T maps to NM_004795.3 F789F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr13:33638238 C>T maps to NM_004795.3 F985F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr13:33635798 C>T maps to NM_004795.3 F861F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr13:33635651 C>T maps to NM_004795.3 I812I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr13:33635750 G>A maps to NM_004795.3 V845V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr13:33635165 C>T maps to NM_004795.3 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr13:33635234 C>T maps to NM_004795.3 C673C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr13:33628013 C>T maps to NM_004795.3 D310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr13:33635670 G>T maps to NM_004795.3 E819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr13:33635003 C>T maps to NM_004795.3 S596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr13:33635226 C>T maps to NM_004795.3 R671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:33628010 C>T maps to NM_004795.3 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr13:33635387 G>A maps to NM_004795.3 G724G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr4:39439521 A>G maps to NM_175737.3 R504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:39439413 G>A maps to NM_175737.3 W468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr4:39439452 G>C maps to NM_175737.3 V481V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:39409222 C>T maps to NM_175737.3 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:39435942 G>A maps to NM_175737.3 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:104121126 C>T maps to ENST00000445352 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr14:104124052 G>A maps to ENST00000445352 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:66031184 C>T maps to NM_022822.2 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:66026256 C>T maps to NM_022822.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr19:45850769 G>A maps to NM_177417.2 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr6:43030860 G>A maps to NM_201523.1 Q173Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr6:43034128 C>T maps to NM_201523.1 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr6:43030827 G>A maps to NM_201523.1 K162K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr6:43041673 C>T maps to NM_201523.1 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:43034197 G>A maps to NM_201523.1 E260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:43039884 C>T maps to NM_201523.1 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:12995746 A>C maps to NM_006563.3 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr8:103664118 G>A maps to NM_005655.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:10192462 C>T maps to NM_003597.4 C456C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:10186389 T>A maps to NM_003597.4 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:10188297 C>T maps to NM_003597.4 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:74420309 G>A maps to NM_007249.4 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr13:74569124 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr13:74420000 G>A maps to NM_007249.4 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr13:74420438 G>A maps to NM_007249.4 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:130418344 C>T maps to NM_138693.2 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:126071117 G>A maps to NM_014079.3 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr1:44595356 C>T maps to NM_173484.3 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:44595389 G>A maps to NM_173484.3 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:44595868 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:44595755 G>A maps to NM_173484.3 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:44596313 C>T maps to NM_173484.3 F352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:44596232 C>T maps to NM_173484.3 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:44595254 G>A maps to NM_173484.3 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr4:38690507 G>A maps to NM_016531.5 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr9:110248118 C>T maps to NM_004235.4 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr9:110250263 C>T maps to NM_004235.4 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr9:110248118 C>T maps to NM_004235.4 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:73636694 C>T maps to NM_001730.3 Q320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:3822343 G>A maps to NM_001300.5 R252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:3823998 G>A maps to NM_001300.5 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:208030259 C>T maps to NM_003709.2 Q11Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:56291639 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:56310849 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr23:56296746 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr14:50199496 C>T maps to NM_172193.2 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:50210497 C>T maps to NM_172193.2 Q337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr7:129769349 C>T maps to NM_014997.3 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:129710497 G>A maps to NM_014997.3 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:129760664 C>T maps to NM_014997.3 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr7:129765757 C>T maps to NM_014997.3 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr6:42985299 C>T maps to NM_057161.2 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:42985013 C>T maps to NM_057161.2 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr16:87790030 C>A maps to NM_017566.3 G82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr1:18807969 G>A maps to NM_152375.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:18808296 C>T maps to NM_152375.2 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:18808287 G>A maps to NM_152375.2 E271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:18809328 C>T maps to NM_152375.2 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr1:18809065 C>A maps to NM_152375.2 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:18808728 C>T maps to NM_152375.2 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:18809343 C>T maps to NM_152375.2 F623F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:18807903 G>A maps to NM_152375.2 Q143Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:18809784 C>T maps to NM_152375.2 P770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:18809589 C>T maps to NM_152375.2 C705C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:18809631 C>T maps to NM_152375.2 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr1:18808314 G>A maps to NM_152375.2 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr1:18808383 G>A maps to NM_152375.2 Q303Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:18808266 C>T maps to NM_152375.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:18809472 G>A maps to NM_152375.2 K666K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:18809631 C>T maps to NM_152375.2 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:18807948 C>T maps to NM_152375.2 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:18809103 C>T maps to NM_152375.2 F543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr1:18809175 G>A maps to NM_152375.2 G567G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:18809385 C>T maps to NM_152375.2 F637F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr22:50988169 C>T maps to NM_138433.3 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr22:50987680 C>T maps to NM_138433.3 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr22:50987877 G>A maps to NM_138433.3 W428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:50987911 C>T maps to NM_138433.3 F439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:205308472 C>T maps to NM_018203.1 W202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr1:205308795 G>A maps to NM_018203.1 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr1:205308796 G>A maps to NM_018203.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:205306567 G>A maps to NM_018203.1 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:49212567 G>A maps to NM_173546.2 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr1:161068774 G>A maps to NM_152366.4 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr13:70371055 G>A maps to NM_020866.2 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr13:70275839 T>C maps to NM_020866.2 Q747Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:70314626 C>T maps to NM_020866.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:70514273 G>A maps to NM_020866.2 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr13:70681381 C>T maps to NM_020866.2 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr13:70413255 A>G maps to NM_020866.2 N422N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr13:70281852 G>A maps to NM_020866.2 L697L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr13:70371005 C>T maps to NM_020866.2 V501V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr13:70681624 C>T maps to NM_020866.2 W69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:40010861 A>G maps to NM_018143.1 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:202864776 G>A maps to NM_021633.2 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:202862509 C>A maps to NM_021633.2 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:117033290 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:117043428 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:117054224 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr23:117043959 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:117044001 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:117035815 C>T did not map to a codon.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr23:117043527 C>T did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:117043517 G>A did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:117079497 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:117033108 T>C did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:117054317 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:117079527 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr23:117106694 T>C did not map to a codon.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr23:117032926 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:117033354 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:117035834 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:117053533 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr23:117043542 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:117053534 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:117043776 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:117044001 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:117043930 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:117053559 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:117053616 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:117043589 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:117053492 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr23:117053614 T>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:117106746 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:117043418 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:117032884 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:117043966 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:117043650 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:117079531 G>A did not map to a codon.
Sequencing variant TCGA-ER-A197-06A-32D-A197-08 chr23:117043437 T>C did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:117043975 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:117053570 C>T did not map to a codon.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr23:117032950 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:117079507 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:117033004 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:117035814 T>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:117043326 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:117043327 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:117043517 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:117053513 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:117079485 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:117106776 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:117033026 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:117033270 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:117035909 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:117043302 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:117043418 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:117043959 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr23:117043466 C>T did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr18:30260435 G>A maps to NM_020805.1 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr18:30260387 C>T maps to NM_020805.1 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr18:30349750 G>A maps to NM_020805.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:30350422 G>A maps to NM_020805.1 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr18:30257203 G>A maps to NM_020805.1 R560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:30257203 G>A maps to NM_020805.1 R560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:30260456 C>T maps to NM_020805.1 T448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:30350065 G>A maps to NM_020805.1 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:30350521 G>A maps to NM_020805.1 F11F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-FW-A3TU-06A-11D-A23B-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:30321903 C>T maps to NM_020805.1 W352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:24006880 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr23:24006084 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:24007014 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:24006307 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:24006996 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:24006590 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:24024369 G>A did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr23:24006812 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:900522 C>T maps to NM_198317.2 F627F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr3:47385127 C>T maps to NM_025010.4 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr3:47374648 C>T maps to NM_025010.4 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:47385127 C>T maps to NM_025010.4 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:47361192 C>T maps to NM_025010.4 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:47371566 C>T maps to NM_025010.4 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:47385373 C>T maps to NM_025010.4 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:47371531 C>T maps to NM_025010.4 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:47371545 G>A maps to NM_025010.4 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr4:166226791 G>A maps to NM_001161521.1 K322K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr1:173725151 C>T maps to NM_014458.3 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:173702864 C>T maps to NM_014458.3 R13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr1:6659366 G>A maps to NM_014851.2 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr22:20819206 G>A maps to NM_032775.3 F350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:20825648 G>A maps to NM_032775.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr22:20825681 G>A maps to NM_032775.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr22:20819166 G>A maps to NM_032775.3 R364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr22:20819206 G>A maps to NM_032775.3 F350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr22:20812258 G>A maps to NM_032775.3 Q381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:20819665 G>A maps to NM_032775.3 Y197Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:20825708 G>A maps to NM_032775.3 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr22:20825680 G>A maps to NM_032775.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr2:170592501 G>A maps to NM_144711.5 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:170592399 G>A maps to NM_144711.5 W292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:183390262 C>T maps to NM_017644.3 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:183368596 C>T maps to NM_017644.3 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr15:86312414 C>T maps to NM_022480.3 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr15:86311556 G>A maps to NM_022480.3 F495F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:18779139 C>T maps to NM_018316.1 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:18775172 C>T maps to NM_018316.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:18778809 C>T maps to NM_018316.1 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr19:18779931 G>A maps to NM_018316.1 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:18775223 C>T maps to NM_018316.1 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr5:137045490 G>A maps to NM_017415.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:136964126 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr5:137045463 G>A maps to NM_017415.2 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:136969777 C>T maps to NM_017415.2 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:136974657 G>A maps to NM_017415.2 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:137028076 G>A maps to NM_017415.2 D141D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:239049907 C>T maps to NM_198582.3 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr2:239057732 C>T maps to NM_198582.3 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr6:53519496 G>A maps to NM_001003760.4 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr6:53519497 G>A maps to NM_001003760.4 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr6:53519614 G>A maps to NM_001003760.4 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:53519077 G>A maps to NM_001003760.4 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:53519767 G>A maps to NM_001003760.4 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr6:53519575 C>T maps to NM_001003760.4 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr6:97587154 C>T maps to NM_052904.3 I620I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr6:97562122 T>G maps to NM_052904.3 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:97424049 C>T maps to NM_052904.3 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr6:97562161 C>T maps to NM_052904.3 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:97562296 G>A maps to NM_052904.3 K422K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr11:75136524 C>T maps to NM_001039548.2 E429E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:84695402 C>T maps to NM_024731.2 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr16:84690631 C>T maps to NM_024731.2 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr8:124659188 G>A maps to NM_001081675.2 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:124663912 G>C maps to NM_001081675.2 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr8:124663819 G>A maps to NM_001081675.2 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr8:124664569 G>A maps to NM_001081675.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:124663867 G>A maps to NM_001081675.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr8:124658254 C>T maps to NM_001081675.2 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:124664731 G>A maps to NM_001081675.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:124664647 C>T maps to NM_001081675.2 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:86869524 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr23:86880699 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr23:86880700 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr23:86880674 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr23:86772917 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:86869443 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:86890698 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr23:86880624 G>T did not map to a codon.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr23:86868977 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:86890730 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:86772937 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr23:86868973 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:86773010 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:86888765 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:86877369 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:86887242 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:86921474 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:86869549 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr23:86887329 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr23:86887332 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:86772957 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:86890672 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:86888765 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:86887259 A>C did not map to a codon.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr23:86890588 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:86873069 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:86890620 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:86888816 G>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:86772974 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:86869512 G>A did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:86869003 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:86887276 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:86887277 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr4:39077584 G>A maps to NM_015990.4 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:39083652 G>A maps to NM_015990.4 Q304Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:183209861 G>A maps to NM_130446.2 I573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr3:183209741 C>T maps to NM_130446.2 R613R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:183217465 G>A maps to NM_130446.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr3:183210441 C>T maps to NM_130446.2 K468K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:183210291 G>A maps to NM_130446.2 I518I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:183226038 C>T maps to NM_130446.2 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:183209741 C>T maps to NM_130446.2 R613R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:183217612 G>A maps to NM_130446.2 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr7:23164756 T>C maps to NM_001031710.2 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr4:88085180 G>A maps to NM_020803.3 R530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr4:88085181 G>A maps to NM_020803.3 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr4:88084714 G>A maps to NM_020803.3 R607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:21334326 G>A maps to NM_018847.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr19:51323614 T>C maps to NM_002257.2 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:51323256 G>A maps to NM_002257.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:51322476 G>A maps to NM_002257.2 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:51518106 G>A maps to NM_001077500.1 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:51520526 G>A maps to NM_001077500.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:51518160 G>A maps to NM_001077500.1 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr19:51527934 G>A maps to NM_144947.1 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:51528012 G>A maps to NM_144947.1 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:51527367 G>A maps to NM_144947.1 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:51527505 G>A maps to NM_144947.1 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:51528039 C>T maps to NM_144947.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:51535132 C>T maps to NM_019598.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:51535144 G>A maps to NM_019598.2 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:51534142 G>A maps to NM_019598.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:51534091 C>T maps to NM_019598.2 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr19:51537261 G>C maps to NM_019598.2 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr19:51563193 G>A maps to NM_015596.1 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr19:51559966 G>A maps to NM_015596.1 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:51563168 G>A maps to NM_015596.1 Q141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:51563859 A>G maps to NM_015596.1 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:51563820 G>A maps to NM_015596.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:51582951 G>A maps to NM_022046.4 Q90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr19:51582164 G>A maps to NM_022046.4 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:51330338 G>A maps to NM_017509.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:51329057 C>T maps to NM_017509.2 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:51329957 A>T maps to NM_017509.2 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:51329168 G>A maps to NM_017509.2 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr19:51378016 G>A maps to NM_005551.3 W29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:51378007 G>A maps to NM_005551.3 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:51380009 G>A maps to NM_005551.3 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:51380288 C>T maps to NM_001002231.1 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:51378065 G>T maps to NM_005551.3 G46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr19:51361715 C>T maps to NM_001648.2 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:51362856 G>A maps to NM_001030047.1 W234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:51363229 T>C maps to NM_001648.2 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:51361293 G>A maps to NM_001648.2 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:51361524 G>A maps to NM_001648.2 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:51361365 C>T maps to NM_001648.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:51361365 C>T maps to NM_001648.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:51363301 C>T maps to NM_001648.2 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:51411945 A>G maps to NM_004917.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr19:51412003 G>A maps to NM_004917.3 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:51411874 C>T maps to NM_004917.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr19:51410323 G>A maps to NM_004917.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:51452286 G>A maps to NM_012427.4 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:51453181 G>A maps to NM_012427.4 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr19:51452021 G>A maps to NM_012427.4 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:51452021 G>A maps to NM_012427.4 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr19:51455844 G>A maps to NM_012427.4 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:51452008 G>A maps to NM_012427.4 Q205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr19:51470495 C>T maps to NM_001012964.1 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:51465128 G>A maps to NM_001012964.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:51462452 C>T maps to NM_001012964.1 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:51465128 G>A maps to NM_001012964.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:51466789 G>A maps to NM_001012964.1 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:51466677 G>A maps to NM_001012964.1 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr19:51470570 C>T maps to NM_001012964.1 E17E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:51465128 G>A maps to NM_001012964.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:51462447 C>T maps to NM_001012964.1 W236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:51483559 G>A maps to NM_005046.2 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:51483733 G>A maps to NM_005046.2 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:51485631 G>A maps to NM_005046.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:51483676 C>T maps to NM_005046.2 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr19:51503513 C>T maps to NM_144505.1 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CC-06A-11D-A19A-08 chr19:51499374 G>C maps to NM_144505.1 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CC-06A-11D-A19A-08 chr19:51499430 G>A maps to NM_144505.1 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:51503513 C>T maps to NM_144505.1 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:51503755 G>A maps to NM_144505.1 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:51499430 G>A maps to NM_144505.1 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr19:51501087 C>T maps to NM_144505.1 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:51503819 C>T maps to NM_144505.1 E75E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:51509945 G>T maps to NM_012315.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:51506441 G>A maps to NM_012315.1 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:51509897 G>A maps to NM_012315.1 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:51509960 A>T maps to NM_012315.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:187171544 C>T maps to ENST00000511608 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:187171538 G>A maps to ENST00000511608 W294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr4:187175879 C>T maps to ENST00000511608 I531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:187173247 C>T maps to ENST00000511608 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr4:187172639 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:187172986 G>A maps to ENST00000511608 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr4:187157995 G>A maps to ENST00000511608 K177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr4:187173247 C>T maps to ENST00000511608 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr4:187172453 C>T maps to ENST00000511608 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr12:10603143 C>T maps to NM_213658.2 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr12:10603137 C>T maps to NM_213658.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:10601877 C>T maps to NM_213658.2 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:10603647 C>T maps to NM_213658.2 Q36Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:10587970 G>A maps to NM_002260.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:10584712 G>A maps to NM_002260.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:10587103 C>T maps to NM_002260.3 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:10588009 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr12:10568305 G>A maps to NM_007333.2 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:10571031 T>A maps to NM_007333.2 K133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr12:10571008 C>T maps to NM_007333.2 E140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:10569273 G>A maps to NM_007333.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr12:10569333 C>T maps to NM_007333.2 W173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:10560949 G>A maps to NM_013431.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:10560268 G>A maps to NM_013431.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:10560277 G>A maps to NM_013431.2 R151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:10462071 G>A maps to ENST00000381908 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr12:10462029 G>A maps to ENST00000381908 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr12:9997103 C>T maps to NM_016523.1 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr12:9161634 G>A maps to NM_005810.3 W141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:9144892 G>A maps to NM_005810.3 W58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:9161638 G>A maps to NM_005810.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:139164441 C>T maps to NM_198508.2 Q312Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:139168325 G>A maps to NM_198508.2 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr12:10530801 C>T maps to NM_007360.3 W154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:10532317 C>T maps to NM_007360.3 W74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:10532305 G>A maps to NM_007360.3 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:10531182 G>A maps to NM_007360.3 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:241695762 C>T maps to NM_003679.3 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:241725502 C>T maps to NM_003679.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:241752098 G>A maps to NM_003679.3 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:135010602 G>A maps to ENST00000368572 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr10:135032399 C>T maps to ENST00000368572 F1583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:134999847 C>T maps to ENST00000368572 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:135038168 C>T maps to ENST00000368572 I1677I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:135015203 G>A maps to ENST00000368572 V1065V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:135027619 C>T maps to ENST00000368572 T1559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr10:135032557 G>A maps to ENST00000368572 K1610K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr10:135026240 C>T maps to ENST00000368572 R1422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:135020664 C>T maps to ENST00000368572 L1204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:135032538 G>A maps to ENST00000368572 W1604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:135015302 C>T maps to ENST00000368572 A1098A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:135012300 C>T maps to ENST00000368572 P763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr10:134981776 C>T maps to ENST00000368572 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:135020699 C>T maps to ENST00000368572 I1215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr3:186459944 G>A maps to NM_001102416.2 W587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr3:186459945 G>A maps to NM_001102416.2 W587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:186437988 G>A maps to NM_001102416.2 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:186445072 G>A maps to NM_001102416.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:186445087 G>A maps to NM_001102416.2 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr12:123068938 G>A maps to NM_014708.4 L1126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:123078866 A>G maps to NM_014708.4 K1430K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr12:123055669 C>T maps to NM_014708.4 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:123022895 G>T maps to NM_014708.4 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr12:123098304 C>T maps to NM_014708.4 S1958S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:123095384 C>T maps to NM_014708.4 L1854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:122182786 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr3:122156097 C>T maps to NM_002264.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:66036861 C>T maps to NM_002266.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:66040612 C>T maps to NM_002266.2 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:66033502 T>C maps to NM_002266.2 N35N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr13:50280403 C>T maps to NM_002267.3 K379K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr13:50306750 G>A maps to NM_002267.3 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:117053477 C>T maps to NM_002269.2 Q538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:32623922 C>T maps to NM_012316.4 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr1:32636330 C>T maps to NM_012316.4 Q483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:32622503 C>T maps to NM_012316.4 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr1:32628038 C>T maps to NM_012316.4 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr17:45750522 C>T maps to NM_002265.4 Q563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:45753817 C>T maps to NM_002265.4 P652P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr17:45735995 G>A maps to NM_002265.4 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr17:45730067 C>T maps to NM_002265.4 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:152733044 C>T maps to NM_001025231.1 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr1:152732492 T>C maps to NM_001025231.1 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:152732732 C>T maps to NM_001025231.1 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:152733734 G>A maps to NM_001025231.1 Q557Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:152733599 C>T maps to NM_001025231.1 D512D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr1:152732928 G>T maps to NM_001025231.1 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:152732819 C>T maps to NM_001025231.1 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr1:152733029 C>T maps to NM_001025231.1 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:152732711 C>T maps to NM_001025231.1 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:152733074 G>A maps to NM_001025231.1 Q337Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:152732972 C>T maps to NM_001025231.1 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:152732717 C>T maps to NM_001025231.1 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr1:152732717 C>T maps to NM_001025231.1 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:152733504 C>T maps to NM_001025231.1 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:152733509 G>A maps to NM_001025231.1 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr1:152732688 C>T maps to NM_001025231.1 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:152732645 G>A maps to NM_001025231.1 Q194Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:152733200 C>T maps to NM_001025231.1 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:47986433 G>A maps to NM_007059.2 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:47986449 G>A maps to NM_007059.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:47984042 G>A maps to NM_007059.2 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:149419621 G>A maps to NM_032534.2 Q192Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr7:149430367 C>T maps to NM_032534.2 P774P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr7:149428760 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:149426453 C>T maps to NM_032534.2 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:149420912 C>T maps to NM_032534.2 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:149428832 C>T maps to NM_032534.2 L739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:149430316 C>T maps to NM_032534.2 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:8272583 G>A maps to NM_213597.2 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr2:88327608 C>T maps to NM_016618.1 Q158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:29536300 C>T maps to NM_032045.4 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr22:29533585 C>T maps to NM_032045.4 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr22:29533537 C>T maps to NM_032045.4 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:10664941 C>T maps to NM_023008.3 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr19:10668487 G>A maps to NM_023008.3 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr19:10671069 G>A maps to NM_023008.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:10670360 G>A maps to NM_023008.3 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:10670351 G>A maps to NM_023008.3 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:91864911 G>A maps to NM_194456.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:91864730 G>A maps to NM_194456.1 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:75895756 A>C maps to NM_007043.6 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr12:53072495 C>T maps to NM_006121.3 W212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr12:53069057 G>A maps to NM_006121.3 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:53070201 C>T maps to NM_006121.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:53073658 G>A maps to NM_006121.3 N158N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:53073631 C>T maps to NM_006121.3 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr12:53072386 G>A maps to NM_006121.3 Q249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr12:53070225 G>A maps to NM_006121.3 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr12:53073597 G>A maps to NM_006121.3 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr12:53070081 G>A maps to NM_006121.3 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:53070219 C>T maps to NM_006121.3 K438K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:53070860 G>A maps to NM_006121.3 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:38975815 C>A maps to NM_000421.3 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:38978534 G>A maps to NM_000421.3 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr17:38976630 C>T maps to NM_000421.3 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:39021198 C>T maps to NM_000223.3 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr17:39017913 T>C maps to NM_000223.3 *495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr17:39019760 G>A maps to NM_000223.3 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:39022966 G>A maps to NM_000223.3 R158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr17:39023210 G>A maps to NM_000223.3 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:39019774 G>A maps to NM_000223.3 Q353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:39018823 G>A maps to NM_000223.3 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr17:39658666 C>T maps to NM_153490.2 E401E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:39659197 G>A maps to NM_153490.2 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr17:39661429 G>A maps to NM_153490.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr17:39659242 G>A maps to NM_153490.2 Y281Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:39742795 A>C maps to NM_000526.4 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:39740104 C>T maps to NM_000526.4 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr17:39670292 G>A maps to NM_002275.3 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:39672148 G>A maps to NM_002275.3 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr17:39671761 G>A maps to NM_002275.3 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:39673110 C>T maps to NM_002275.3 Q229Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:39672364 G>A maps to NM_002275.3 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr17:39672199 C>T maps to NM_002275.3 E321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr17:39673077 C>T maps to NM_002275.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:39671761 G>A maps to NM_002275.3 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:39674980 C>T maps to NM_002275.3 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr17:39672216 G>A maps to NM_002275.3 Q316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr17:39670313 C>T maps to NM_002275.3 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:39674839 G>A maps to NM_002275.3 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr17:39768658 G>A maps to NM_005557.3 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr17:39767695 G>A maps to NM_005557.3 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr17:39768427 G>A maps to NM_005557.3 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:39767895 C>T maps to NM_005557.3 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:39768499 C>T maps to NM_005557.3 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:39766712 C>A maps to NM_005557.3 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr17:39767644 G>A maps to NM_005557.3 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr17:39767379 G>A maps to NM_005557.3 Q292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:39767629 C>T maps to NM_005557.3 E246E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:39767898 G>A maps to NM_005557.3 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr17:39766662 G>C maps to NM_005557.3 Y400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:39776939 G>A maps to NM_000422.2 Y384Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:39777871 C>T maps to NM_000422.2 K269K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:39776927 C>T maps to NM_000422.2 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr17:39780587 G>A maps to NM_000422.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:39777065 G>A maps to NM_000422.2 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:39777259 G>A maps to NM_000422.2 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:53345615 C>T maps to NM_000224.2 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr12:53344587 C>T maps to NM_000224.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:53344143 C>T maps to NM_000224.2 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr12:53345287 G>A maps to NM_000224.2 Q227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:53345997 G>A maps to NM_000224.2 E348E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:53345627 C>T maps to NM_000224.2 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:39684154 C>T maps to NM_002276.4 W115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:39680681 C>T maps to NM_002276.4 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:39681450 G>A maps to NM_002276.4 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:39684283 G>A maps to NM_002276.4 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:39680672 G>A maps to NM_002276.4 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:39684412 G>A maps to NM_002276.4 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr12:53042058 G>A maps to NM_000423.2 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:53038982 C>T maps to NM_000423.2 K580K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:53045731 G>A maps to NM_000423.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:53045716 C>T maps to NM_000423.2 K70K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:53044160 C>T maps to NM_000423.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr12:53043751 C>T maps to NM_000423.2 E269E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:53044241 G>T maps to NM_000423.2 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:53041992 C>T maps to NM_000423.2 R362R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr12:53044202 C>T maps to NM_000423.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr12:53045767 G>A maps to NM_000423.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr17:39036115 C>T maps to NM_019010.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr17:39041296 G>A maps to NM_019010.2 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:39032651 G>A maps to NM_019010.2 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr17:39041305 G>A maps to NM_019010.2 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr17:39036925 C>T maps to NM_019010.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr17:38816300 C>T maps to NM_152349.2 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:38813977 C>T maps to NM_152349.2 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr17:38816459 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3CC-06A-11D-A19A-08 chr17:39092615 G>A maps to NM_015515.3 N80N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr17:39081697 C>T maps to NM_015515.3 Q350Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr17:38857514 C>T maps to NM_019016.2 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr17:38859624 C>T maps to NM_019016.2 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr17:38854566 C>T maps to NM_019016.2 K500K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:38857394 C>T maps to NM_019016.2 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:38859482 G>A maps to NM_019016.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr17:38855754 G>A maps to NM_019016.2 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr17:38854841 C>T maps to NM_019016.2 R474R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:38859630 G>A maps to NM_019016.2 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr17:38907295 G>A maps to NM_181534.3 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr17:38904546 C>T maps to NM_181534.3 E445E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr17:38911229 A>G maps to NM_181534.3 H98H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:38906651 G>A maps to NM_181534.3 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:38907518 G>A maps to NM_181534.3 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr17:38906747 G>A maps to NM_181534.3 H353H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:38910164 G>A maps to NM_181534.3 Q206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:38910714 G>A maps to NM_181534.3 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr17:38911121 G>A maps to NM_181534.3 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr17:38928355 G>A maps to NM_181539.4 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:38927433 T>A maps to NM_181539.4 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr17:38926624 C>T maps to NM_181539.4 E187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:38928299 G>C maps to NM_181539.4 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:38928355 G>A maps to NM_181539.4 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:38950196 G>A maps to NM_181535.3 H360H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr17:38953272 C>T maps to NM_181535.3 Q291Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr17:38955844 G>A maps to NM_181535.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:38955902 G>A maps to NM_181535.3 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:38955788 C>T maps to NM_181535.3 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:38949419 C>T maps to NM_181535.3 G413G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:38953467 C>T maps to NM_181535.3 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:38953242 G>A maps to NM_181535.3 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:53186073 C>T maps to ENST00000309505 E379E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr12:53189265 G>A maps to ENST00000309505 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:53189736 G>A maps to ENST00000309505 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:53185150 C>T maps to ENST00000309505 K458K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:53186063 G>A maps to ENST00000309505 Q383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr12:53189301 G>A maps to ENST00000309505 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:39552818 G>A maps to ENST00000393998 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr17:39552712 G>A maps to ENST00000393998 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr17:39551239 G>A maps to ENST00000393998 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:39553172 G>A maps to ENST00000393998 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr17:39550276 G>A maps to ENST00000393998 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:39551755 C>T maps to ENST00000393998 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr17:39551128 G>A maps to ENST00000393998 Y358Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:39552764 G>A maps to ENST00000393998 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr17:39552704 C>T maps to ENST00000393998 E187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:39553605 G>A maps to ENST00000393998 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:39553605 G>A maps to ENST00000393998 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:39550276 G>A maps to ENST00000393998 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr17:39620560 C>T maps to NM_002278.3 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:39616439 G>A maps to NM_002278.3 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr17:39623148 G>A maps to NM_002278.3 Y143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:39616370 G>A maps to NM_002278.3 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr17:39622141 G>C maps to NM_002278.3 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:39502484 G>A maps to NM_004138.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr17:39504770 C>T maps to NM_004138.2 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:39503170 G>A maps to NM_004138.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:39506773 C>T maps to NM_004138.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:39505677 G>A maps to NM_004138.2 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:39504770 C>T maps to NM_004138.2 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:39503325 C>T maps to NM_004138.2 W246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr17:39521721 G>A maps to ENST00000394004 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:39520159 G>A maps to ENST00000394004 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:39522798 G>A maps to ENST00000394004 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:39525714 C>T maps to ENST00000394004 E97E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:39525753 C>T maps to ENST00000394004 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:39522754 C>T maps to ENST00000394004 E186E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr17:39522859 G>A maps to ENST00000394004 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr17:39537397 C>T maps to NM_021013.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr17:39537355 C>T maps to NM_021013.3 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr17:39535637 G>A maps to NM_021013.3 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr17:39538267 C>T maps to NM_021013.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:39535884 C>T maps to NM_021013.3 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr17:39535983 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:39537337 C>T maps to NM_021013.3 E228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr17:39637058 C>T maps to NM_002280.4 E97E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:39636954 C>T maps to NM_002280.4 W132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr17:39635640 G>A maps to NM_002280.4 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:39637160 G>A maps to NM_002280.4 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:39637052 C>T maps to NM_002280.4 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr17:39637289 C>T maps to NM_002280.4 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr17:39635724 C>T maps to NM_002280.4 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:39642747 G>A maps to NM_003771.4 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr17:39646008 G>A maps to NM_003771.4 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr17:39643209 C>T maps to NM_003771.4 E400E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:39642729 G>A maps to NM_003771.4 T434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:39645936 C>T maps to NM_003771.4 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:39645852 G>A maps to NM_003771.4 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:39643314 G>A maps to NM_003771.4 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:39644898 C>T maps to NM_003771.4 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:39643905 G>A maps to NM_003771.4 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr17:39642765 G>A maps to NM_003771.4 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr17:39646002 C>T maps to NM_003771.4 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr17:39577165 C>T maps to NM_003770.4 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr17:39579050 G>A maps to NM_003770.4 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:39580745 G>A maps to NM_003770.4 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:39580463 C>T maps to NM_003770.4 E104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr17:39578664 G>A maps to NM_003770.4 Q252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr17:39577719 C>T maps to NM_003770.4 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:39578653 C>T maps to NM_003770.4 E255E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:39580691 G>A maps to NM_003770.4 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:39578668 C>T maps to NM_003770.4 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:39580345 C>A maps to NM_003770.4 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr17:39580550 A>G maps to NM_003770.4 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:39579059 C>T maps to NM_003770.4 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:39578647 G>A maps to NM_003770.4 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:39580292 G>A maps to NM_003770.4 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr17:39596777 C>T maps to NM_006771.3 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:39596765 G>A maps to NM_006771.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr17:39594367 G>A maps to NM_006771.3 N406N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr17:39594741 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:39595035 C>T maps to NM_006771.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr17:39594520 G>A maps to NM_006771.3 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr17:39122817 C>T maps to NM_213656.3 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:39118815 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:53202104 C>T maps to NM_002272.2 R440R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:53207851 G>A maps to NM_002272.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:53207449 C>T maps to NM_002272.2 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:53205629 C>T maps to NM_002272.2 Q272Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr12:53202188 C>T maps to NM_002272.2 Q412Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:53203181 C>T maps to NM_002272.2 K347K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr12:53207773 G>A maps to NM_002272.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:53201636 A>G maps to NM_002272.2 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr12:53201465 G>A maps to NM_002272.2 I510I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr17:39139368 C>T maps to NM_182497.3 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr17:39140423 G>A maps to NM_182497.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:39138606 C>T maps to NM_182497.3 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:39135198 G>A maps to NM_182497.3 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr12:52911919 G>A maps to NM_000424.3 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr12:52913596 G>A maps to NM_000424.3 Q162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr12:52908758 G>A maps to NM_000424.3 T580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:52913942 G>A maps to NM_000424.3 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:52908779 G>A maps to NM_000424.3 S573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:52911737 C>T maps to NM_000424.3 E290E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr12:52914056 G>A maps to NM_000424.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:52910458 G>A maps to NM_000424.3 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:52908823 G>A maps to NM_000424.3 R559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr12:52882227 C>T maps to NM_005554.3 K436K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:52884421 C>T maps to NM_005554.3 E336E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:52881883 C>T maps to NM_005554.3 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr12:52885418 G>A maps to NM_005554.3 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:52886438 G>A maps to NM_005554.3 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:52882263 C>T maps to NM_005554.3 K424K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:52886524 G>A maps to NM_005554.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr12:52885394 C>T maps to NM_005554.3 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr12:52885511 G>A maps to NM_005554.3 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:52881689 G>A maps to NM_005554.3 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr12:52882287 C>T maps to NM_005554.3 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr12:52886951 G>A maps to NM_005554.3 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr12:52845394 G>A maps to NM_005555.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:52842733 G>A maps to NM_005555.3 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:52845481 G>A maps to NM_005555.3 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:52841599 G>A maps to NM_005555.3 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr12:52842697 G>A maps to NM_005555.3 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:52841150 G>A maps to NM_005555.3 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr12:52841006 G>A maps to NM_005555.3 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:52840991 C>T maps to NM_005555.3 R559R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr12:52844239 C>T maps to NM_005555.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:52844212 G>A maps to NM_005555.3 D244D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr12:52862869 G>A maps to NM_173086.4 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr12:52867473 C>T maps to NM_173086.4 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:52865509 C>T maps to NM_173086.4 E254E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:52863031 G>A maps to NM_173086.4 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:52865920 G>A maps to NM_173086.4 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:52627349 G>A maps to NM_005556.3 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:52641959 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:52636806 C>T maps to NM_005556.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr12:52635398 T>A maps to NM_005556.3 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr12:52940107 G>A maps to NM_033448.2 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr12:52942550 C>T maps to NM_033448.2 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr12:52946768 G>A maps to NM_033448.2 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:52944021 C>T maps to NM_033448.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:52943862 C>T maps to NM_033448.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr12:52939382 C>T maps to NM_033448.2 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:52943958 C>T maps to NM_033448.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:52944000 C>T maps to NM_033448.2 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:52942559 G>A maps to NM_033448.2 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:52943996 G>A maps to NM_033448.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr12:52940248 C>A maps to NM_033448.2 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:52941944 G>A maps to NM_033448.2 Y323Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:52946816 C>T maps to NM_033448.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr12:52939361 G>A maps to NM_033448.2 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr12:52986726 C>T maps to NM_080747.2 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:52984625 C>T maps to NM_080747.2 K361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr12:52979798 C>T maps to NM_080747.2 G501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:52992683 C>T maps to NM_080747.2 K213K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr12:52992815 C>T maps to NM_080747.2 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:52992770 C>T maps to NM_080747.2 Q184Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:52979921 C>T maps to NM_080747.2 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:53001988 G>A maps to NM_175068.2 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:53011969 G>A maps to NM_175068.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr12:53002198 T>C maps to NM_175068.2 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr12:53002075 C>T maps to NM_175068.2 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr12:53011879 G>A maps to NM_175068.2 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:53002030 G>A maps to NM_175068.2 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:53005025 G>A maps to NM_175068.2 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:53010095 C>T maps to NM_175068.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:53005008 C>T maps to NM_175068.2 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:53011861 C>T maps to NM_175068.2 K149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:53007516 G>A maps to NM_175068.2 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:53007621 G>A maps to NM_175068.2 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr12:53005025 G>A maps to NM_175068.2 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr12:52961443 G>T maps to NM_175053.3 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr12:52964455 G>A maps to NM_175053.3 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:52967411 G>A maps to NM_175053.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr12:52963681 G>A maps to NM_175053.3 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr12:52963699 C>T maps to NM_175053.3 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr12:52967138 C>T maps to NM_175053.3 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:52966442 G>A maps to NM_175053.3 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr12:52966382 C>T maps to NM_175053.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr12:52963651 C>T maps to NM_175053.3 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr12:52967108 G>A maps to NM_175053.3 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:52962008 C>T maps to NM_175053.3 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:52827959 C>T maps to ENST00000252245 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr12:52827644 C>T maps to ENST00000252245 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr12:52828043 C>T maps to ENST00000252245 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr12:52826937 G>A maps to ENST00000252245 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr12:52827608 G>A maps to ENST00000252245 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:52820622 C>T maps to ENST00000252245 E519E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:52826856 C>T maps to ENST00000252245 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:52827872 G>A maps to ENST00000252245 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:52827608 G>A maps to ENST00000252245 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr12:53165684 T>A maps to NM_015848.4 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr12:53170595 T>C maps to NM_015848.4 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:53170559 G>A maps to NM_015848.4 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:53169377 G>A maps to NM_015848.4 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr12:53164931 G>A maps to NM_015848.4 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr12:53170628 C>T maps to NM_015848.4 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr12:53164826 C>T maps to NM_015848.4 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:53165937 G>A maps to NM_015848.4 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr12:53162535 G>A maps to NM_015848.4 S626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:53169179 G>A maps to NM_015848.4 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:53170523 C>T maps to NM_015848.4 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:53165750 C>T maps to NM_015848.4 R389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:53086389 C>T maps to NM_175078.2 E414E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr12:53085113 G>A maps to NM_175078.2 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr12:53091530 C>T maps to NM_175078.2 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr12:53086574 C>T maps to NM_175078.2 Q390Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:53097068 C>T maps to NM_175078.2 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr12:53096990 C>T maps to NM_175078.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr12:53237948 C>T maps to NM_173352.2 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:53237948 C>T maps to NM_173352.2 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr12:53238399 C>A maps to NM_173352.2 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr12:53237989 G>A maps to NM_173352.2 Q312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:53233555 C>T maps to NM_173352.2 E420E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:53240037 C>T maps to NM_173352.2 E233E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:53233609 C>T maps to NM_173352.2 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:53232923 C>T maps to NM_173352.2 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:53242381 C>T maps to NM_173352.2 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:53242525 C>T maps to NM_173352.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr12:53238381 C>T maps to NM_173352.2 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr12:53216810 G>A maps to NM_175834.2 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:53228032 G>A maps to NM_175834.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:53225323 C>T maps to NM_175834.2 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr12:53227900 G>A maps to NM_175834.2 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:53217760 C>T maps to NM_175834.2 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:53216909 C>T maps to NM_175834.2 K419K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr12:53217793 A>C maps to NM_175834.2 Y341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:53216852 G>A maps to NM_175834.2 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:53223902 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:53225194 C>T maps to NM_175834.2 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:53225269 C>T maps to NM_175834.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:53227576 G>A maps to NM_175834.2 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:53227585 G>A maps to NM_175834.2 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr12:53227585 G>A maps to NM_175834.2 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr12:53291250 C>T maps to NM_002273.3 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr12:53295760 G>A maps to NM_002273.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:53295760 G>A maps to NM_002273.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:52579233 C>T maps to NM_182507.2 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr12:52585451 G>A maps to NM_182507.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:52566019 G>A maps to NM_182507.2 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:52567413 C>T maps to NM_182507.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:52579320 G>A maps to NM_182507.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr12:52579169 G>A maps to NM_182507.2 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr12:52793819 G>A maps to NM_033033.3 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr12:52788965 G>A maps to NM_033033.3 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:52788965 G>A maps to NM_033033.3 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr12:52799827 G>A maps to NM_033033.3 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:52799830 G>A maps to NM_033033.3 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:52789549 C>T maps to NM_033033.3 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:52797501 C>T maps to NM_033033.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:52799752 G>T maps to NM_033033.3 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr12:52709726 C>T maps to NM_002282.3 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr12:52714915 G>A maps to NM_002282.3 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:52714915 G>A maps to NM_002282.3 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:52714915 G>A maps to NM_002282.3 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:52715035 G>A maps to NM_002282.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:52710323 G>A maps to NM_002282.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr12:52777538 C>T maps to NM_033045.3 W197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr12:52777486 G>A maps to NM_033045.3 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:52776839 C>T maps to NM_033045.3 E255E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr12:52779081 C>T maps to NM_033045.3 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:52778904 G>A maps to NM_033045.3 D155D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:52775174 C>T maps to NM_033045.3 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:52775246 G>A maps to NM_033045.3 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:52771865 G>A maps to NM_033045.3 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:52760975 G>A maps to NM_002283.3 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:52760976 G>A maps to NM_002283.3 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:52756078 G>A maps to NM_002283.3 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr12:52757038 G>A maps to NM_002283.3 Y314Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:52756676 G>A maps to NM_002283.3 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:52760877 G>A maps to NM_002283.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:52756739 C>T maps to NM_002283.3 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:52754804 G>A maps to NM_002283.3 V452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:52756697 G>A maps to NM_002283.3 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:52695780 C>T maps to NM_002284.3 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:52699157 G>A maps to NM_002284.3 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:52699472 C>T maps to NM_002284.3 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:52698735 C>T maps to NM_002284.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr17:39724858 G>A maps to NM_000226.3 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr17:39724517 G>A maps to NM_000226.3 I430I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr17:39725839 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:39726463 G>A maps to NM_000226.3 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr17:39726148 G>A maps to NM_000226.3 Q282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:39724825 C>T maps to NM_000226.3 K368K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:39725761 G>A maps to NM_000226.3 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr17:39723533 G>A maps to NM_000226.3 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:39724825 C>T maps to NM_000226.3 K368K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:39724454 G>A maps to NM_000226.3 I451I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:39197307 G>A maps to NM_030967.2 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:39197604 G>A maps to NM_030967.2 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CC-06A-11D-A19A-08 chr17:39191031 G>A maps to NM_030966.1 C14C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:39183032 C>T maps to NM_031957.1 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr21:45959364 G>A maps to NM_198691.2 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr21:45959991 G>A maps to NM_198691.2 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr21:45959787 C>T maps to NM_198691.2 Q82Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr21:45959319 A>G maps to NM_198691.2 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr21:45959331 G>A maps to NM_198691.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr21:46058020 C>T maps to NM_181688.1 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr21:46058032 C>T maps to NM_181688.1 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr21:46058074 G>A maps to NM_181688.1 Q247Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr21:46057912 C>T maps to NM_181688.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr21:46057510 C>T maps to NM_181688.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr21:46066995 C>T maps to NM_198692.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr21:46066503 G>A maps to NM_198692.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr21:46066509 G>T maps to NM_198692.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:46066851 C>T maps to NM_198692.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr21:46117838 C>T maps to NM_198699.1 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr21:46117232 C>T maps to NM_198699.1 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr21:46117694 C>A maps to NM_198699.1 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr21:46117526 C>T maps to NM_198699.1 C137C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:46117622 C>T maps to NM_198699.1 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:45970795 G>A maps to NM_198693.2 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:45978415 G>A maps to NM_198696.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr21:45994735 C>T maps to NM_198687.1 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr21:45994384 C>T maps to NM_198687.1 C250C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:45993751 C>T maps to NM_198687.1 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr21:46000281 G>A maps to NM_198694.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr21:46000350 G>A maps to NM_198694.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr21:46012326 C>T maps to NM_198688.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr21:46011786 G>T maps to NM_198688.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr21:46012257 G>A maps to NM_198688.2 D36D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr21:46021435 C>T maps to ENST00000380102 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr21:46020844 C>T maps to ENST00000380102 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:46021534 C>T maps to ENST00000380102 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr21:46032760 C>T maps to NM_198695.2 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr21:46032613 C>T maps to NM_198695.2 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr21:46032775 G>C maps to NM_198695.2 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr21:46032079 C>T maps to NM_198695.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr21:46032202 C>T maps to NM_198695.2 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr21:46032634 C>T maps to NM_198695.2 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr21:46047721 C>T maps to NM_198690.2 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr21:46047214 C>T maps to NM_198690.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr21:46047129 C>T maps to NM_198690.2 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr21:46047894 C>T maps to NM_198690.2 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:46047501 G>A maps to NM_198690.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr21:32253759 C>T maps to NM_175858.2 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr21:32253681 G>A maps to NM_175858.2 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:32253687 G>A maps to NM_175858.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr21:46101759 A>T maps to NM_181686.1 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:46101960 G>A maps to NM_181686.1 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr21:46086527 G>T maps to NM_181684.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr21:46086701 G>A maps to NM_181684.2 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:46086746 G>A maps to NM_181684.2 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr21:46077964 C>T maps to NM_198697.2 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr21:46078009 G>A maps to NM_198697.2 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr21:46078147 C>T maps to NM_198697.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr21:46074387 G>A maps to NM_198698.1 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr21:46074231 G>A maps to NM_198698.1 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr21:31768586 G>A maps to NM_181599.2 W61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr21:31768433 C>T maps to NM_181599.2 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr21:31744192 T>A maps to NM_181621.3 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr21:31744111 G>A maps to NM_181621.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr21:31797903 G>A maps to NM_181622.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr21:31797816 A>C maps to NM_181622.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr21:31802634 C>T maps to NM_181600.1 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr21:31812854 C>T maps to NM_181623.1 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:31813034 G>A maps to NM_181623.1 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr17:39471785 C>T maps to NM_031964.1 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr21:31864179 G>A maps to NM_181609.3 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr21:31869239 C>T maps to NM_181610.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:31869244 G>A maps to NM_181610.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr21:31869218 C>T maps to NM_181610.1 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr21:31869218 C>T maps to NM_181610.1 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr21:31933512 G>A maps to ENST00000437381 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr21:32410571 C>T maps to NM_001099219.1 *64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr21:32127609 G>C maps to NM_181619.1 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr21:32127549 A>G maps to NM_181619.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr21:32119352 G>A maps to NM_181617.1 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr21:31720771 G>A maps to NM_181624.1 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr21:31655067 G>A maps to NM_001085455.1 C61C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr21:31654497 C>T maps to NM_001085455.1 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:31654818 G>A maps to NM_001085455.1 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr21:31692179 C>T maps to NM_203405.1 E58E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr21:31691927 G>A maps to NM_203405.1 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:31692251 C>T maps to NM_203405.1 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr21:31709533 G>A maps to NM_001077711.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr21:31709431 G>A maps to NM_001077711.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:39165194 C>T maps to NM_031958.1 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr17:39156006 G>A maps to NM_031959.2 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr17:39156051 G>A maps to NM_031959.2 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr17:39155949 G>A maps to NM_031959.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:39155981 A>G maps to NM_031959.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:39150225 A>G maps to NM_033185.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:39274504 C>T maps to NM_033059.3 Q21Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:39279795 G>A maps to NM_031854.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr17:39279984 G>A maps to NM_031854.2 C130C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:39280337 G>A maps to NM_031854.2 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:39334188 G>A maps to ENST00000458321 C193C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:39334335 C>T maps to ENST00000458321 Q144Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr17:39324367 G>A maps to NM_033187.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr17:39316856 G>A maps to NM_032524.1 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr17:39316832 G>A maps to NM_032524.1 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr17:39305743 C>T maps to NM_033188.3 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr17:39305734 G>A maps to NM_033188.3 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:39240673 G>A maps to ENST00000377731 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr17:39253943 G>A maps to NM_031960.2 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr17:39254245 G>A maps to NM_031960.2 Q31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr17:39261978 C>T maps to NM_001146041.1 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44R-06A-41D-A25O-08 chr11:1606170 C>T maps to NM_001005922.1 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:1606188 C>T maps to NM_001005922.1 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:1606188 C>T maps to NM_001005922.1 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:71276977 C>T maps to ENST00000422553 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:71276848 G>A maps to ENST00000422553 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:71293787 G>A maps to ENST00000376535 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr11:71293628 G>A maps to ENST00000376535 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:71293715 G>A maps to ENST00000376535 S56S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D9-A6EC-06A-11D-A30X-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-DA-A1IC-06A-11D-A197-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-FW-A3R5-06A-11D-A23B-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-GN-A266-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr11:1628943 G>A maps to ENST00000359229 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44Q-06A-11D-A25O-08 chr11:1629537 G>A maps to NM_001012708.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:1629399 G>A maps to ENST00000359229 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:1629132 A>G maps to NM_001012708.2 C161C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr11:1629546 G>A maps to NM_001012708.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:1629393 C>T maps to ENST00000359229 K158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:1643026 C>T maps to ENST00000359229 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:1642984 G>A maps to ENST00000359229 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr11:1642681 G>A maps to NM_001012709.1 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:1643029 C>T maps to ENST00000359229 K98K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:1643248 G>A maps to ENST00000359229 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:1642705 G>A maps to NM_001012709.1 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:1642984 G>A maps to ENST00000359229 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr11:1651390 G>A maps to NM_001001480.2 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr11:1651303 T>C maps to NM_001001480.2 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:1651390 G>A maps to NM_001001480.2 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:1651678 C>T maps to NM_001001480.2 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:1718666 G>A maps to NM_001012416.1 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:71238543 C>T maps to NM_001012503.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:71238543 C>T maps to NM_001012503.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr11:71249286 C>T maps to ENST00000422553 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr11:71260044 C>T maps to NM_005553.3 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr11:71259855 C>T maps to NM_005553.3 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:71260053 C>T maps to NM_005553.3 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:31971121 G>A maps to NM_181604.1 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr21:31964964 C>T maps to ENST00000399871 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:39382962 C>T maps to NM_031961.2 C19C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:39382950 G>A maps to NM_031961.2 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr17:39406379 G>A maps to NM_033191.2 E136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:39406028 C>T maps to ENST00000431129 C19C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:39406379 G>A maps to NM_033191.2 E136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr17:39394566 C>T maps to NM_031963.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr17:39412101 C>T maps to ENST00000431129 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:25936328 G>A maps to ENST00000268763 G678G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:25924424 C>T maps to ENST00000268763 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr17:25932545 G>A maps to ENST00000268763 R512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:25936265 C>T maps to ENST00000268763 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:118199231 C>T maps to ENST00000339824 W190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr12:117962862 G>A maps to ENST00000339824 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:117968818 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:117923447 G>A maps to ENST00000339824 I756I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr12:117962700 G>A maps to ENST00000339824 F725F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr12:117923447 G>A maps to ENST00000339824 I756I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr12:118105429 C>T maps to ENST00000339824 K340K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr12:118293344 C>T maps to ENST00000339824 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr12:118199000 G>A maps to ENST00000339824 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:117962910 G>A maps to ENST00000339824 F655F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:117962928 G>A maps to ENST00000339824 A649A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:117962910 G>A maps to ENST00000339824 F655F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:118199078 C>T maps to ENST00000339824 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:117907477 C>T maps to ENST00000339824 W945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:117996323 G>A maps to ENST00000339824 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:117968818 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr12:117964917 T>C maps to ENST00000339824 E603E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr12:118198934 C>T maps to ENST00000339824 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:117977674 A>T maps to ENST00000339824 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr12:117962910 G>A maps to ENST00000339824 F655F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:118199027 G>A maps to ENST00000339824 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:118199000 G>A maps to ENST00000339824 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:117914312 C>T maps to ENST00000339824 E846E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:117923468 G>A maps to ENST00000339824 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:117962979 G>A maps to ENST00000339824 F632F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:117914375 C>T maps to ENST00000339824 Q825Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:117962700 G>A maps to ENST00000339824 F725F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr12:117962700 G>A maps to ENST00000339824 F725F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr12:118293377 G>A maps to ENST00000339824 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:117914342 G>A maps to ENST00000339824 I836I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:117922300 C>T maps to ENST00000339824 K790K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:117968807 C>T maps to ENST00000339824 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:117996323 G>A maps to ENST00000339824 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:118020102 G>A maps to ENST00000339824 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:118105315 G>A maps to ENST00000339824 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:118293377 G>A maps to ENST00000339824 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr12:118199090 C>T maps to ENST00000339824 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr12:118198895 G>A maps to ENST00000339824 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:117992997 G>A maps to ENST00000339824 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:118105312 G>A maps to ENST00000339824 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr12:117922324 G>A maps to ENST00000339824 I782I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr12:118199192 G>A maps to ENST00000339824 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr12:118199201 C>T maps to ENST00000339824 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr3:119190233 A>T maps to NM_152305.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr3:119190248 G>A maps to NM_152305.2 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:56134035 C>T maps to NM_001079521.1 V1085V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr14:56078981 C>T maps to NM_001079521.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr14:56133972 G>A maps to NM_001079521.1 Q1064Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr14:56119569 T>A maps to NM_001079521.1 L869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr14:56125296 C>T maps to NM_001079521.1 Q976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:134322945 C>T maps to NM_178554.4 E487E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:134323028 G>A maps to NM_178554.4 Q460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:134322756 G>A maps to NM_178554.4 F550F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:134327569 C>T maps to NM_178554.4 E337E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr3:134322981 G>A maps to NM_178554.4 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:134366312 G>A maps to NM_178554.4 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:134369697 C>T maps to NM_178554.4 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr2:143715283 G>A maps to NM_003937.2 E194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:143718221 C>T maps to NM_003937.2 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:143743578 G>A maps to NM_003937.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:143790871 C>T maps to NM_003937.2 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:143685262 G>A maps to NM_003937.2 W109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JB-06A-11D-A196-08 chr23:153130421 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:153132897 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr23:153128166 T>C did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:153130158 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:153130159 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5VV-06A-11D-A32N-08 chr23:153130846 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:153128945 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:153135266 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:153130593 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:153134069 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:153134070 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:153136578 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:153137757 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:153141285 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:153130812 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:153130443 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:153135650 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:153129834 G>A did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:153128220 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:153137768 C>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:153135270 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:153133546 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr1:62675552 G>A maps to NM_019079.4 E369E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:62672650 G>A maps to NM_019079.4 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:62676158 G>A maps to NM_019079.4 K571K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:62677025 G>C maps to NM_019079.4 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:62676101 C>A maps to NM_019079.4 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:62675516 C>T maps to NM_019079.4 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:62675615 G>A maps to NM_019079.4 E390E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:62672650 G>A maps to NM_019079.4 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr1:62672617 C>T maps to NM_019079.4 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:62672773 G>A maps to NM_019079.4 K158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:62675552 G>A maps to NM_019079.4 E369E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:62675714 G>A maps to NM_019079.4 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr14:50750673 G>A maps to NM_024884.2 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr20:42162711 C>T maps to NM_032107.4 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr20:42169605 G>A maps to NM_032107.4 G787G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr20:42143937 C>T maps to NM_032107.4 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:42143763 C>T maps to NM_032107.4 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:42169681 C>T maps to NM_032107.4 L813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr20:42168926 C>T maps to NM_032107.4 V748V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr20:42162940 C>T maps to NM_032107.4 F517F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr20:42162941 C>T maps to NM_032107.4 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr20:42168800 C>T maps to NM_032107.4 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:42162047 C>T maps to NM_032107.4 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr20:42169530 C>T maps to ENST00000373134 Q739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr20:42169608 G>A maps to NM_032107.4 K788K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr22:41620753 C>T maps to NM_031488.4 H400H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:41621802 C>T maps to NM_031488.4 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:130370509 C>T maps to NM_032438.2 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:130381272 C>T maps to NM_032438.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr6:130378611 G>A maps to NM_032438.2 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:130460843 C>T maps to NM_032438.2 F763F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr18:6093388 G>A maps to NM_173464.3 F446F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:5956287 G>A maps to NM_173464.3 I601I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr18:6093487 C>T maps to NM_173464.3 K413K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:6243369 C>T maps to NM_173464.3 W128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr18:6263963 A>G maps to NM_173464.3 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZG-06A-11D-A197-08 chr18:5969389 A>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:6239814 C>T maps to NM_173464.3 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:6243299 G>A maps to NM_173464.3 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:6244521 G>A maps to NM_173464.3 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:55025623 C>G did not map to a codon.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr15:63414105 T>A maps to NM_032857.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr8:71574086 G>A maps to NM_016027.2 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:201356023 G>A maps to NM_005558.3 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr1:201356011 C>T maps to NM_005558.3 E159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:201356203 C>T maps to NM_005558.3 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:201355552 G>A maps to NM_005558.3 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:201355639 C>T maps to NM_005558.3 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:201356011 C>T maps to NM_005558.3 E159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:6883974 C>T maps to NM_002286.5 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:6884442 G>T maps to NM_002286.5 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr12:6886535 A>G maps to NM_002286.5 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr23:153706297 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:153706644 T>G did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr19:54866918 G>A maps to NM_002287.3 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:54868145 G>A maps to NM_002287.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr19:54872568 G>T maps to NM_002287.3 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:54871679 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:54872607 T>C maps to NM_002287.3 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr19:54871656 G>A maps to NM_002287.3 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:54872706 C>T maps to NM_002287.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54872708 G>A maps to NM_002287.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54872760 C>T maps to NM_002287.3 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr19:54866903 G>A maps to NM_002287.3 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:55019220 G>A maps to NM_002288.3 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr12:48962943 G>T maps to NM_002289.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr12:48962889 C>T maps to NM_002289.2 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr12:48962901 G>A maps to NM_002289.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:48962955 C>T maps to NM_002289.2 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:48962325 G>A maps to NM_002289.2 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:48963761 G>A maps to NM_002289.2 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr18:7009356 C>T maps to NM_005559.2 W1294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr18:7015735 C>T maps to NM_005559.2 A1037A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr18:7023253 G>A maps to NM_005559.2 C870C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr18:6975950 G>A maps to NM_005559.2 L2158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr18:6992612 G>A maps to NM_005559.2 I1705I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr18:6992672 G>A maps to NM_005559.2 F1685F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:7011388 G>A maps to NM_005559.2 P1199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr18:7009356 C>T maps to NM_005559.2 W1294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr18:6958514 G>T maps to NM_005559.2 S2642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr18:6971938 C>T maps to NM_005559.2 L2272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr18:6965356 G>A maps to NM_005559.2 T2375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr18:6948507 G>A maps to NM_005559.2 S2868S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr18:6975026 G>A maps to NM_005559.2 F2166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr18:7024446 G>A maps to NM_005559.2 H807H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr18:6973111 G>A maps to NM_005559.2 L2240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr18:6983118 C>T maps to NM_005559.2 R1925R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr18:6956712 G>A maps to NM_005559.2 T2672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:6961659 C>T maps to NM_005559.2 T2517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr18:7042162 G>A maps to NM_005559.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr18:7049159 G>A maps to NM_005559.2 Q229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr18:6974990 G>A maps to NM_005559.2 F2178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr18:6978195 G>A maps to NM_005559.2 A2063A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr18:7080388 C>T maps to NM_005559.2 E43E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:6947244 G>A maps to NM_005559.2 R2921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:6965356 G>A maps to NM_005559.2 T2375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:7011415 C>T maps to NM_005559.2 T1190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:7042192 G>A maps to NM_005559.2 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr18:6956646 G>A maps to NM_005559.2 P2694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr18:6958647 G>A maps to NM_005559.2 Q2598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr6:129635943 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr6:129636652 C>T maps to NM_000426.3 P1196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr6:129781470 T>C did not map to a codon.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr6:129470194 G>A maps to NM_000426.3 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:129419559 G>A maps to NM_000426.3 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:129618903 C>T maps to NM_000426.3 F977F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr6:129774168 C>A maps to NM_000426.3 R2156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr6:129380962 G>A maps to NM_000426.3 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:129419328 C>T maps to NM_000426.3 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:129781439 A>G maps to NM_000426.3 K2321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr6:129634040 C>T maps to NM_000426.3 F1070F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr6:129837449 G>A maps to NM_000426.3 L3109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr6:129371156 G>A maps to NM_000426.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr6:129636685 C>T maps to NM_000426.3 T1207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:129637181 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:129637190 G>A maps to NM_000426.3 W1311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:129774191 G>A maps to NM_000426.3 K2163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:129824424 G>A maps to NM_000426.3 K2849K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr6:129371186 G>A maps to NM_000426.3 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr6:129704349 C>T maps to NM_000426.3 F1681F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:129833583 G>A maps to NM_000426.3 L2978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr6:129714401 T>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:129837341 C>T maps to NM_000426.3 L3073L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:129670502 G>A maps to NM_000426.3 R1499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr6:129722451 C>T maps to NM_000426.3 N1843N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:129371211 C>T maps to NM_000426.3 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr6:129636796 G>A maps to NM_000426.3 K1244K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr6:129636769 G>A maps to NM_000426.3 W1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr6:129637212 C>T maps to NM_000426.3 R1319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:129637031 C>T maps to NM_000426.3 I1287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr6:129833586 G>A maps to NM_000426.3 G2979G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr6:129636652 C>T maps to NM_000426.3 P1196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:129704355 G>A maps to NM_000426.3 K1683K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:129712753 G>A maps to NM_000426.3 R1730R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr6:129571258 C>T maps to NM_000426.3 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr6:129748922 G>A maps to NM_000426.3 K1964K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr18:21494381 G>A maps to ENST00000416669 R2448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr18:21501453 G>A maps to ENST00000416669 W2696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr18:21422578 C>T maps to ENST00000416669 S1158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr18:21330946 G>A maps to ENST00000416669 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr18:21526248 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr18:21437840 C>T maps to ENST00000416669 D1392D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:21484000 G>A maps to ENST00000416669 E2143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:21390429 G>A maps to ENST00000416669 R570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr18:21427575 G>A maps to ENST00000416669 R1362R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr18:21501543 G>A maps to ENST00000416669 R2726R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr18:21338392 G>A maps to ENST00000416669 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr18:21494462 G>A maps to ENST00000416669 V2475V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr18:21526118 C>T maps to ENST00000416669 G3076G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr18:21426416 C>T maps to ENST00000416669 I1294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr18:21469983 G>A maps to ENST00000416669 P1773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr18:21495272 C>T maps to ENST00000416669 F2557F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr18:21534609 T>C maps to ENST00000416669 *3336Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr18:21441764 G>A maps to ENST00000416669 G1528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr18:21526163 C>T maps to ENST00000416669 A3091A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:21330955 C>T maps to ENST00000416669 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr18:21343445 C>T maps to ENST00000416669 Q381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr18:21530062 C>T maps to ENST00000416669 I3196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr18:21478989 C>T maps to ENST00000416669 L1935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr18:21330955 C>T maps to ENST00000416669 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr18:21501011 C>T maps to ENST00000416669 D2681D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:21355828 C>T maps to ENST00000416669 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:21402244 G>A maps to ENST00000416669 G780G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:21419871 G>A maps to ENST00000416669 G1107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:21489198 C>T maps to ENST00000416669 I2368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:21523895 C>T maps to ENST00000416669 I3059I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr18:21501017 G>A maps to ENST00000416669 S2683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:112493821 C>T maps to NM_001105206.1 R514R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:112435332 G>A maps to NM_001105206.1 L1758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:112454585 G>A maps to NM_001105206.1 L1221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr6:112460973 G>A maps to NM_001105206.1 S1030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:112452236 G>A maps to NM_001105206.1 Q1301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr6:112476149 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr6:112522852 A>G maps to NM_001105206.1 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:112496545 G>A maps to NM_001105206.1 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr20:60911420 G>A maps to NM_005560.3 S766S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr20:60921781 G>A maps to NM_005560.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr20:60921782 G>A maps to NM_005560.3 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr20:60921787 G>A maps to NM_005560.3 Q381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:60904838 G>A maps to NM_005560.3 L1371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:60892006 G>A maps to NM_005560.3 I2528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:60909379 G>A maps to NM_005560.3 Y867Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:60888161 G>A maps to NM_005560.3 L2979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:60890243 G>A maps to NM_005560.3 I2629I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr20:60909352 C>A maps to NM_005560.3 L876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr20:60891787 G>A maps to NM_005560.3 L2565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr20:60893545 G>A maps to NM_005560.3 L2401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:60907632 G>A maps to NM_005560.3 S1141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:60886035 G>A maps to NM_005560.3 F3401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:60901998 G>A maps to NM_005560.3 L1712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:60902993 G>A maps to NM_005560.3 R1575R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:60921217 G>A maps to NM_005560.3 R446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:60886053 G>A maps to NM_005560.3 F3395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:60903379 G>A maps to NM_005560.3 V1523V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr20:60900497 C>T maps to NM_005560.3 Q1801Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr20:60910128 G>A maps to NM_005560.3 S810S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr20:60901735 C>T maps to NM_005560.3 V1765V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr20:60927132 G>A maps to NM_005560.3 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr20:60887985 G>A maps to NM_005560.3 V3012V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr20:60886297 G>A maps to NM_005560.3 T3336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr20:60904062 G>A maps to NM_005560.3 S1428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr20:60926761 G>A maps to NM_005560.3 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:60904228 G>A maps to NM_005560.3 F1400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:60908262 G>A maps to NM_005560.3 F1055F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:60903023 A>C maps to NM_005560.3 S1565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:60904291 G>A maps to NM_005560.3 V1379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:60908706 G>A maps to NM_005560.3 I978I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr20:60886749 C>T maps to NM_005560.3 P3242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr20:60889896 G>A maps to NM_005560.3 R2718R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr20:60926964 C>T maps to NM_005560.3 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr20:60904089 G>A maps to NM_005560.3 F1419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr7:107601668 G>A maps to NM_002291.2 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:107580510 G>A maps to NM_002291.2 S1228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:107576048 C>T maps to NM_002291.2 E1333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:107626733 G>A maps to NM_002291.2 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:107576057 C>T maps to NM_002291.2 E1330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:107594167 G>A maps to NM_002291.2 Y962Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:107626733 G>A maps to NM_002291.2 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:107618513 G>A maps to NM_002291.2 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:107603370 G>A maps to NM_002291.2 I612I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr7:107571870 G>T maps to NM_002291.2 T1489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:107600911 G>A maps to NM_002291.2 A764A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:107600244 G>A maps to NM_002291.2 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:107616284 A>G maps to NM_002291.2 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr3:49167661 A>C did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:49160883 G>A maps to NM_002292.3 F1326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:49168498 G>A maps to NM_002292.3 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:49168499 G>A maps to NM_002292.3 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:49159007 C>A maps to NM_002292.3 L1706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:49169617 G>A maps to NM_002292.3 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:49159720 G>A maps to NM_002292.3 I1552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:49161225 G>A maps to NM_002292.3 I1244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:49168415 G>A maps to NM_002292.3 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:49161986 G>A maps to NM_002292.3 C1056C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:49169763 G>A maps to NM_002292.3 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr3:49159019 T>C maps to NM_002292.3 L1702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr3:49162245 G>A maps to NM_002292.3 A999A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr3:49161486 G>A maps to NM_002292.3 R1157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:49165916 G>A maps to NM_002292.3 I664I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:49167283 G>A maps to NM_002292.3 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr3:49166460 G>A maps to NM_002292.3 R575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr3:49162317 G>A maps to NM_002292.3 D975D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr3:49168498 G>A maps to NM_002292.3 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr1:209807875 G>A maps to NM_000228.2 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr1:209796359 G>A maps to NM_000228.2 G841G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr1:209791951 G>T maps to NM_000228.2 A918A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:209807884 G>A maps to NM_000228.2 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:209797290 G>A maps to NM_000228.2 S677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:209799102 G>A maps to NM_000228.2 S622S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:209796984 C>T maps to NM_000228.2 Q741Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr1:209788681 C>T maps to NM_000228.2 E1151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr1:209796329 C>T maps to NM_000228.2 Q851Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:209805939 G>A maps to NM_000228.2 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:209796443 G>A maps to NM_000228.2 A813A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr1:209799003 G>A maps to NM_000228.2 I655I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:209801434 G>A maps to NM_000228.2 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:209788714 G>A maps to NM_000228.2 I1140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:209796338 C>T maps to NM_000228.2 R848R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:209823367 G>A maps to NM_000228.2 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:209823368 G>A maps to NM_000228.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr1:209789915 C>T maps to NM_000228.2 Q1094Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:209811882 C>T maps to NM_000228.2 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:209790844 G>A maps to NM_000228.2 L1046L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:209807848 C>T maps to NM_000228.2 Q169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:209807884 G>A maps to NM_000228.2 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:209823448 G>A maps to NM_000228.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr1:209796936 T>C maps to NM_000228.2 G757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr7:107703416 G>A maps to NM_007356.2 G1028G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr7:107671361 C>T maps to NM_007356.2 L1627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr7:107698334 C>T maps to NM_007356.2 G1107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:107674791 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr7:107717457 G>A maps to NM_007356.2 S685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:107664612 C>T maps to NM_007356.2 R1719R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:107704317 G>A maps to NM_007356.2 S983S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:107746956 G>A maps to NM_007356.2 Q218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr7:107684224 G>A maps to NM_007356.2 F1481F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:107703395 G>A maps to NM_007356.2 P1035P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr7:107704221 G>A maps to NM_007356.2 L1015L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr7:107704299 C>T maps to NM_007356.2 G989G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:107710210 C>G maps to NM_007356.2 P748P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr7:107671289 C>T maps to NM_007356.2 Q1651Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr7:107698334 C>T maps to NM_007356.2 G1107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:107732115 G>A maps to NM_007356.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr7:107720126 G>A maps to NM_007356.2 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr7:107718647 C>T maps to NM_007356.2 T667T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr1:182993135 G>A maps to NM_002293.3 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr1:183091339 C>T maps to NM_002293.3 P785P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:183083682 C>T maps to NM_002293.3 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr1:183072499 C>T maps to NM_002293.3 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:183097778 C>T maps to NM_002293.3 N1058N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:183085946 T>C maps to NM_002293.3 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:183111823 C>T maps to NM_002293.3 R1577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44R-06A-41D-A25O-08 chr1:183212406 C>T maps to NM_005562.2 Q1152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:183212513 C>A maps to NM_005562.2 T1187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:183204778 C>T maps to NM_005562.2 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:183190076 C>T maps to NM_005562.2 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:183196821 C>G maps to NM_005562.2 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:183206617 G>A maps to NM_005562.2 Q911Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr9:133960929 C>T maps to ENST00000355048 P1362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr9:133948705 G>A maps to ENST00000355048 R1164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:133901756 C>T maps to ENST00000355048 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:133961097 G>A maps to ENST00000355048 K1418K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:133961019 G>A maps to ENST00000355048 A1392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:133911687 G>A maps to ENST00000355048 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr9:133963160 G>A maps to ENST00000355048 L1490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr9:133942458 C>T maps to ENST00000355048 A820A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr9:133948192 C>T maps to ENST00000355048 L1130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr9:133907433 G>A maps to ENST00000355048 E227E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr9:133936603 C>T maps to ENST00000355048 Q781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:133948071 C>T maps to ENST00000355048 A1089A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr13:113965171 C>T maps to NM_005561.3 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr13:113975754 C>T maps to NM_005561.3 Q305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr3:182853631 C>T maps to NM_014398.3 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:182870234 C>T maps to NM_014398.3 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:182870194 G>A maps to NM_014398.3 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr3:182870234 C>T maps to NM_014398.3 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:182841907 G>A maps to NM_014398.3 I404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr2:211299264 G>A maps to NM_001136575.1 F382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr2:211300992 G>A maps to NM_001136575.1 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr2:211300993 G>A maps to NM_001136575.1 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:211302518 G>A maps to NM_001136575.1 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr7:55468952 C>T maps to NM_018697.3 H255H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:55467670 G>C maps to NM_018697.3 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr7:55466278 T>C maps to NM_018697.3 Y162Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:37431169 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:37526709 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:37431143 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr23:37514985 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:37518740 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:37515008 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr4:17606286 C>T maps to NM_015907.2 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr4:17609197 C>T maps to NM_015907.2 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr8:98828296 C>T maps to ENST00000378722 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:98837318 C>T maps to ENST00000378722 R318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:31214501 C>T maps to NM_006762.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:31212742 G>A maps to NM_006762.2 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:33673201 G>A maps to NM_133642.3 F639F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:33700228 G>A maps to NM_133642.3 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr22:33700405 G>A maps to NM_133642.3 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr22:33777976 G>A maps to NM_133642.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:34000544 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr22:33733714 G>A maps to NM_133642.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr22:33673081 C>T maps to NM_133642.3 W679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr22:33780258 C>T maps to NM_133642.3 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr22:33670591 G>A maps to NM_133642.3 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr22:33673210 G>A maps to NM_133642.3 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:34000533 G>A maps to NM_133642.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:33673201 G>A maps to NM_133642.3 F639F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:34046367 G>A maps to NM_133642.3 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr5:154181826 G>A maps to ENST00000377643 G659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr5:154190828 C>T maps to ENST00000377643 R956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:154190885 C>T maps to ENST00000377643 Q975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr5:154185510 C>T maps to ENST00000377643 Q873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr5:154173507 C>T maps to ENST00000377643 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr5:154193631 G>A maps to ENST00000377643 S1089S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:154181778 C>T maps to ENST00000377643 I643I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:129120746 C>T maps to NM_018078.2 C719C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:129120747 C>T maps to NM_018078.2 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr4:129127652 C>T maps to NM_018078.2 Q794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:129127672 C>A maps to NM_018078.2 T800T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr4:129120710 T>C maps to NM_018078.2 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr4:129128528 C>T maps to NM_018078.2 F846F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr4:129012228 C>T maps to NM_018078.2 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:50869445 G>A maps to ENST00000429001 E664E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr12:50854977 C>T maps to ENST00000429001 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:50860827 T>C maps to ENST00000429001 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr12:50867195 A>G did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:50855013 A>G maps to ENST00000429001 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr10:890980 G>A maps to NM_015155.1 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr10:871158 G>A maps to NM_015155.1 R444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr15:71124998 G>A maps to NM_018357.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr15:71124495 C>T maps to NM_018357.2 K457K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:71125131 C>T maps to NM_018357.2 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr15:71125350 G>A maps to NM_018357.2 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:71125437 C>T maps to NM_018357.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:71128714 C>T maps to NM_018357.2 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr4:113567582 A>T maps to ENST00000509061 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr5:145519824 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:45500237 C>T maps to NM_015340.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr3:45537799 G>A maps to NM_015340.3 T519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr3:45589003 C>T maps to NM_015340.3 N898N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:45557700 C>T maps to NM_015340.3 I659I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr3:45557691 G>A maps to NM_015340.3 Q656Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:45583411 C>T maps to NM_015340.3 F832F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:64738223 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:64734820 G>C did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr23:64753589 C>G did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:64744893 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:64743511 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:64744105 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr17:37046720 C>T maps to NM_006148.2 N71N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:18995022 G>A maps to NM_021267.3 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:18995023 G>A maps to NM_021267.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:18991212 G>A maps to NM_021267.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:18994942 G>A maps to NM_021267.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr1:150939672 G>A maps to NM_181746.2 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr1:150940568 G>A maps to NM_181746.2 R134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr1:150940569 G>A maps to NM_181746.2 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:150938686 T>C maps to NM_181746.2 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr1:150941452 A>G maps to NM_181746.2 D38D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:150939603 G>A maps to NM_181746.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr15:101041961 G>A maps to ENST00000394113 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr15:101031086 G>A maps to ENST00000394113 R86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:100996202 G>A maps to ENST00000394113 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr15:101042025 C>T maps to ENST00000394113 W21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr15:101016290 C>T maps to ENST00000394113 K214K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:100996190 G>A maps to ENST00000394113 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:101031136 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:8319472 C>T maps to NM_024552.2 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr12:50524369 C>T maps to NM_147190.2 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:169551551 C>T maps to ENST00000392687 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr2:169417814 G>A maps to ENST00000392687 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:169313053 C>T maps to ENST00000392687 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr2:169404120 G>A maps to ENST00000392687 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:169312970 T>C maps to ENST00000392687 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr2:169487542 C>T maps to ENST00000392687 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:169417791 C>T maps to ENST00000392687 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:169571509 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:169626018 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:169417814 G>A maps to ENST00000392687 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:169622101 G>A maps to ENST00000392687 W282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr16:28997972 C>T maps to NM_014387.3 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr7:73634320 G>A maps to NM_032464.2 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:73631185 G>A maps to NM_032464.2 Q42Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr6:150005365 G>A maps to NM_004690.2 R287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr6:150005366 G>A maps to NM_004690.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr6:150005420 C>T maps to NM_004690.2 W268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:21562820 G>A maps to NM_014572.2 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr13:21549191 G>T maps to NM_014572.2 P1028P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr13:21557731 G>A maps to NM_014572.2 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr13:21557378 G>A maps to NM_014572.2 S822S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr13:21562820 G>A maps to NM_014572.2 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr13:21563270 G>A maps to NM_014572.2 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr13:21562052 G>A maps to NM_014572.2 N622N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:203734719 G>A maps to NM_017773.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:203740493 G>C did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:203743175 G>A maps to NM_017773.3 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:30457354 G>A maps to NM_030915.3 K37K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:30480423 C>T maps to NM_030915.3 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:30457360 C>T maps to NM_030915.3 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:36982740 C>T maps to NM_004139.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:36982741 C>T maps to NM_004139.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:36997701 C>T maps to NM_004139.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:36999434 C>T maps to NM_004139.2 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:36997665 C>T maps to NM_004139.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr20:36993330 G>A maps to NM_004139.2 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr20:36993330 G>A maps to NM_004139.2 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:225609925 G>A maps to NM_194442.1 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr15:68123198 G>A maps to ENST00000380035 V853V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr15:68118327 T>C maps to ENST00000380035 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:68120256 C>T maps to ENST00000380035 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr6:80203404 C>T maps to NM_181714.3 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr6:80223456 G>A maps to NM_181714.3 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:80196869 G>A maps to NM_181714.3 Q649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr6:80196840 G>A maps to NM_181714.3 F658F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:80197077 G>A maps to NM_181714.3 F579F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr21:40795369 T>G maps to NM_152505.3 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr21:40795009 C>T maps to NM_152505.3 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr16:67974199 G>A maps to NM_000229.1 H310H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:152799974 G>A maps to NM_178348.2 Q9Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:152800130 C>T maps to NM_178348.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:152800037 C>T maps to NM_178348.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:152800121 C>T maps to NM_178348.2 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:152800130 C>T maps to NM_178348.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:152800277 C>T maps to NM_178348.2 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:152799962 G>A maps to NM_178348.2 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr1:152785192 C>T maps to NM_178349.1 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:152777801 G>A maps to NM_178351.3 C51C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr1:152777792 G>A maps to NM_178351.3 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:152759969 G>A maps to ENST00000417924 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:152759960 C>T maps to ENST00000417924 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:152760116 T>C maps to ENST00000417924 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:152760029 C>T maps to ENST00000417924 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:152760098 G>A maps to ENST00000417924 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr1:152748927 G>A maps to ENST00000417924 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:152748888 C>T maps to ENST00000417924 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:152748927 G>A maps to ENST00000417924 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr1:152748927 G>A maps to ENST00000417924 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:152748927 G>A maps to ENST00000417924 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:152748927 G>A maps to ENST00000417924 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:152748927 G>A maps to ENST00000417924 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr1:152671547 G>A maps to NM_178428.3 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:152648613 C>T maps to NM_178429.2 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:152648613 C>T maps to NM_178429.2 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:152648754 C>T maps to NM_178429.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:152595468 C>T maps to NM_178431.1 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:152586387 C>T maps to NM_178433.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:152573386 C>T maps to NM_178434.2 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:152552304 G>A maps to NM_032563.1 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:152552286 C>T maps to NM_032563.1 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:152552220 C>T maps to NM_032563.1 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:152552340 C>T maps to NM_032563.1 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:152552163 G>A maps to NM_032563.1 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:152552220 C>T maps to NM_032563.1 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr1:152552382 G>A maps to NM_032563.1 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:152552346 G>A maps to NM_032563.1 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:152552268 G>A maps to NM_032563.1 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:152538540 G>A maps to NM_178435.2 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr1:152538651 T>C maps to NM_178435.2 Q11Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:152538500 G>A maps to NM_178435.2 R62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:152538501 G>A maps to NM_178435.2 H61H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr1:152538651 T>C maps to NM_178435.2 Q11Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:152538543 G>A maps to NM_178435.2 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:152484099 C>A maps to NM_178438.4 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:152484250 C>T maps to NM_178438.4 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:32745776 G>A maps to ENST00000373562 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr1:32745281 G>A maps to ENST00000373562 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F4-06A-12D-A25O-08 chr1:32740399 G>T maps to ENST00000373562 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:32742025 T>G maps to ENST00000373562 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:32751280 C>T maps to ENST00000373562 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr1:32745524 C>T maps to ENST00000373562 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:30863145 C>T maps to NM_182551.3 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:30748455 C>T maps to NM_182551.3 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZH-06A-11D-A197-08 chr2:30785012 T>C maps to NM_182551.3 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr16:25172471 C>T maps to ENST00000380963 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr16:25172472 C>T maps to ENST00000380963 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:25182045 C>A maps to ENST00000380963 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr16:25172472 C>T maps to ENST00000380963 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr16:25186275 C>T maps to ENST00000380963 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:138416718 G>A maps to NM_002297.2 E149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:139847360 C>T maps to NM_178536.3 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:139847360 C>T maps to NM_178536.3 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr9:139847360 C>T maps to NM_178536.3 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:139656667 C>T maps to NM_203347.1 K164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr9:139658368 G>A maps to NM_203347.1 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:130913916 G>A maps to ENST00000373013 W94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr9:130911872 C>T maps to ENST00000373013 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr9:130914543 C>T maps to ENST00000373013 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:139641982 G>A maps to NM_198946.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:138555262 G>A maps to ENST00000277526 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:138556090 C>T maps to ENST00000277526 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:138557705 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:138556087 C>T maps to ENST00000277526 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:138555244 G>A maps to ENST00000277526 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:138556076 C>T maps to ENST00000277526 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr9:139879252 G>A maps to NM_207510.3 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:98715082 C>T maps to NM_001170765.1 Q236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr13:46708369 G>A maps to NM_002298.4 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr13:46708261 C>T maps to NM_002298.4 K542K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:46725187 A>C maps to NM_002298.4 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr13:46721148 G>A maps to NM_002298.4 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr5:169677817 G>C maps to NM_005565.3 Y465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:169720346 C>T maps to NM_005565.3 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:136575402 C>T maps to NM_002299.2 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr2:136570133 G>A maps to NM_002299.2 I700I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:136566964 G>A maps to NM_002299.2 F984F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr2:136570322 C>T maps to NM_002299.2 V637V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:136567237 G>A maps to NM_002299.2 F893F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr2:136570034 C>T maps to NM_002299.2 R733R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr2:136566573 C>A maps to NM_002299.2 E1115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:136566145 C>T maps to NM_002299.2 L1257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:136567204 C>T maps to NM_002299.2 R904R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:136567237 G>A maps to NM_002299.2 F893F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:136566151 C>T maps to NM_002299.2 R1255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:136564928 G>A maps to NM_002299.2 V1314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:136567039 C>T maps to NM_002299.2 L959L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:136567270 G>A maps to NM_002299.2 V882V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:136575459 G>A maps to NM_002299.2 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr2:136594358 G>A maps to NM_002299.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:136562525 G>A maps to NM_002299.2 A1425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr2:136570091 G>A maps to NM_002299.2 N714N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:136567393 G>A maps to NM_002299.2 I841I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:136594496 G>A maps to NM_002299.2 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:136570169 G>A maps to NM_002299.2 S688S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr2:136570040 C>T maps to NM_002299.2 G731G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:136566073 C>T maps to NM_002299.2 P1281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr2:136570388 C>T maps to NM_002299.2 E615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr2:136590680 C>T maps to NM_002299.2 Q240Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr2:136548426 G>A maps to NM_002299.2 R1712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr2:136545941 C>T maps to NM_002299.2 G1912G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:136566640 C>T maps to NM_002299.2 R1092R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:136561641 C>T maps to NM_002299.2 E1507E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:136562338 G>A maps to NM_002299.2 Q1488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:136564844 C>T maps to NM_002299.2 T1342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:136570067 G>A maps to NM_002299.2 S722S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:136575345 C>T maps to NM_002299.2 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:136575564 C>T maps to NM_002299.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr2:136567237 G>A maps to NM_002299.2 F893F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr2:136566277 G>A maps to NM_002299.2 I1213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr2:136566052 C>T maps to NM_002299.2 R1288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr2:136567096 C>T maps to NM_002299.2 G940G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr2:136594186 G>A maps to NM_002299.2 Q185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr2:136594187 G>A maps to NM_002299.2 H184H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:136567096 C>T maps to NM_002299.2 G940G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr15:66857167 C>T maps to NM_207338.2 W43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:66845567 C>T maps to NM_207338.2 E317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr15:66857160 C>A maps to NM_207338.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr15:66840938 G>A maps to NM_207338.2 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:103869428 G>A maps to NM_001113407.1 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr4:16510259 G>A maps to NM_001290.3 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:16597475 G>A maps to NM_001290.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr4:16513649 C>T maps to NM_001290.3 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr4:16510175 A>G maps to NM_001290.3 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:16510277 C>T maps to NM_001290.3 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:16590353 C>T maps to NM_001290.3 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr4:16760850 G>A maps to NM_001290.3 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:16504331 C>T maps to NM_001290.3 W352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr4:16504279 G>A maps to NM_001290.3 Q370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr4:16597412 C>T maps to NM_001290.3 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:88476309 C>T maps to NM_001171610.1 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr10:88478536 G>A maps to NM_001171610.1 A642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr10:88451794 C>T maps to NM_001171610.1 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:88466428 C>T maps to NM_007078.2 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr11:18485506 G>A did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:18498018 G>A maps to NM_144972.4 W227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr15:59499501 G>A maps to NM_033195.1 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:59499965 G>A maps to NM_033195.1 W276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr12:21807539 A>G maps to NM_002300.6 N22N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:18472616 C>T maps to NM_017448.3 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr11:18460141 G>A maps to NM_017448.3 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:75147667 C>T maps to NM_153486.3 Q333Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr16:75147555 C>T maps to NM_153486.3 E344E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr16:75148830 T>A maps to NM_153486.3 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:75146540 C>T maps to NM_153486.3 E439E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:11216157 G>A maps to NM_000527.4 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:11231067 C>T maps to NM_000527.4 T670T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr19:11211007 C>T maps to NM_000527.4 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:11224056 C>T maps to NM_000527.4 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:11223999 G>A maps to NM_000527.4 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:11224035 C>T maps to NM_000527.4 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:11240219 C>T maps to NM_000527.4 F807F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:11216250 G>A maps to NM_000527.4 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:11240291 C>T maps to NM_000527.4 T831T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:11231095 C>T maps to NM_000527.4 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:54475958 G>A maps to NM_001010978.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:54477831 C>T maps to NM_001010978.2 E108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:54474786 G>A maps to NM_001010978.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:22140990 C>T maps to NM_001013693.2 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:36057668 C>A maps to NM_174902.2 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:36248914 G>A maps to NM_174902.2 Q245Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:140270840 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:44893343 G>A maps to NM_032287.2 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr22:44893124 G>A maps to NM_032287.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr13:53307458 C>T maps to NM_007015.2 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr13:53307359 G>A maps to NM_007015.2 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr13:53313177 C>T maps to NM_007015.2 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:53286956 C>T maps to NM_007015.2 W172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr5:135286926 G>A maps to NM_002302.2 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:109002740 C>T maps to ENST00000515500 R173R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A29M-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:109088791 G>C maps to NM_016269.4 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:226075128 T>A maps to ENST00000419724 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:226127469 G>A maps to NM_003240.3 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr1:226127454 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr3:156763412 G>A maps to NM_001004316.2 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:156745893 A>T maps to NM_001004316.2 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr3:156763400 C>T maps to NM_001004316.2 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr3:156729225 G>A maps to NM_001004316.2 Q378Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:153177314 C>T maps to NM_001010857.1 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:153177278 G>A maps to NM_001010857.1 Q32Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:153177293 G>A maps to NM_001010857.1 K37K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:33752164 G>A maps to NM_181336.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:33744962 A>G maps to NM_181336.3 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CE-06A-11D-A19A-08 chr12:65564455 C>T maps to NM_014319.4 N360N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr12:65639997 C>T maps to NM_014319.4 Q877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:154966190 G>A maps to NM_018655.2 W36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr19:54966175 C>T maps to ENST00000431846 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:54968018 C>T maps to ENST00000431846 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:54966554 C>T maps to ENST00000431846 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:54969502 G>T maps to ENST00000431846 T681T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54963356 C>T maps to ENST00000431846 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:54974108 G>A maps to NM_198988.1 Q223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:54974109 G>A maps to NM_198988.1 H222H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:52245339 C>T maps to NM_138792.2 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr15:52258201 C>T maps to NM_138792.2 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:52242082 G>A maps to NM_138792.2 R574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:52239497 G>C maps to NM_138792.2 T629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:127892154 A>G maps to NM_000230.2 Q28Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:127894656 G>A maps to NM_000230.2 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:127894689 G>A maps to NM_000230.2 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr1:66083653 C>T maps to NM_002303.5 I740I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:66075954 G>A maps to NM_002303.5 E657E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr1:66064413 G>A maps to NM_002303.5 Q307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr1:66058372 C>T maps to NM_002303.5 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr1:66083653 C>T maps to NM_002303.5 I740I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr1:66062251 G>A maps to NM_002303.5 E275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:66067586 G>A maps to NM_002303.5 W449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:66075960 T>C maps to NM_002303.5 N659N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:66101926 T>C maps to NM_002303.5 G909G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr1:66083653 C>T maps to NM_002303.5 I740I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:66067138 C>T maps to NM_002303.5 I353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:66067283 C>T maps to NM_002303.5 R402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:66102400 C>T maps to NM_002303.5 F1067F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:66036255 C>T maps to NM_002303.5 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:66067185 G>A maps to NM_002303.5 W369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:66102238 C>T maps to NM_002303.5 F1013F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr1:66083653 C>T maps to NM_002303.5 I740I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:66102285 G>A maps to NM_002303.5 W1029*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:66075704 C>T maps to NM_002303.5 Q610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:66101938 G>A maps to NM_002303.5 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:66088587 G>A did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr1:66102124 G>A maps to NM_002303.5 E975E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:43224649 A>G maps to NM_022356.3 H271H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:43228089 A>G maps to NM_022356.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:43228101 G>A maps to NM_022356.3 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:43213058 T>A maps to NM_022356.3 R647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:189712006 G>A maps to NM_018192.3 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:189713144 C>T maps to NM_018192.3 E189E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:189706744 C>T maps to NM_018192.3 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr3:189692442 G>A maps to NM_018192.3 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:189705354 C>T maps to NM_018192.3 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:189690746 G>A maps to NM_018192.3 R539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr3:189689788 C>T maps to NM_018192.3 Q569Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr3:189713186 G>A maps to NM_018192.3 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr3:189688637 G>A maps to NM_018192.3 F620F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:189681854 G>A maps to NM_018192.3 I642I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:189675739 C>T maps to NM_018192.3 G696G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:189706759 G>A maps to NM_018192.3 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:189691730 C>T maps to NM_018192.3 K505K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:189711982 G>A maps to NM_018192.3 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr3:189692442 G>A maps to NM_018192.3 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:6946708 C>T maps to NM_014262.3 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr12:6943128 C>T maps to NM_014262.3 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:6946926 C>T maps to NM_014262.3 H580H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr12:6948168 G>A maps to NM_014262.3 R636R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6941023 G>A maps to NM_014262.3 E385E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr4:1843298 G>A maps to NM_012318.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr4:1843136 G>A maps to NM_012318.2 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr4:1818527 G>A maps to NM_012318.2 I619I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr4:1817423 C>T maps to NM_012318.2 K679K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr4:1821172 G>A maps to NM_012318.2 I545I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:1836643 G>A maps to NM_012318.2 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr12:51447631 C>T maps to ENST00000448283 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:51442930 C>T maps to ENST00000448283 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:2565152 C>T maps to NM_001040167.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:2565153 C>T maps to NM_001040167.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:2559869 C>T maps to NM_001040167.1 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:2564904 C>T maps to NM_001040167.1 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr7:2552876 G>A maps to NM_001166355.1 W45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:2559869 C>T maps to NM_001040167.1 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:63283157 C>T maps to NM_001142535.1 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:63283157 C>T maps to NM_001142535.1 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:63283052 G>A maps to NM_001142535.1 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:63273992 C>T maps to NM_001142535.1 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:63276444 C>T maps to NM_001142535.1 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:63273899 G>A maps to NM_001142535.1 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr11:63276044 G>A maps to NM_001142535.1 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:63276392 G>A maps to NM_001142535.1 W124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:63277356 C>T maps to NM_001142535.1 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:40095306 C>T maps to NM_013268.2 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr19:40093216 T>A maps to NM_013268.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:40197298 G>A maps to NM_203471.1 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:40197292 G>A maps to NM_203471.1 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr17:76972086 C>T maps to NM_005567.3 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr17:76967852 T>C maps to NM_005567.3 K521K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:76967690 G>A maps to NM_005567.3 P575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:39299542 G>A maps to NM_006149.3 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:39293029 G>A maps to NM_006149.3 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr19:39303138 G>A maps to NM_006149.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr19:39293029 G>A maps to NM_006149.3 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr19:39293022 G>A maps to NM_006149.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:236700858 T>A maps to NM_201545.1 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr1:236702355 G>A maps to NM_201545.1 E104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr17:25967795 C>T maps to NM_009587.2 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr17:25970615 C>T maps to NM_009587.2 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:25974436 C>T maps to NM_009587.2 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:25967723 G>A maps to NM_009587.2 E86E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:25974436 C>T maps to NM_009587.2 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr17:25974373 C>T maps to NM_009587.2 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:20358696 G>A maps to ENST00000324290 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr17:20354886 A>C maps to ENST00000324290 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr17:18389394 C>T maps to NM_001040078.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:95556970 G>A maps to NM_005097.2 W362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr10:95552550 G>A maps to NM_005097.2 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr10:95557001 C>T maps to NM_005097.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:95552499 G>A maps to NM_005097.2 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr10:95517913 A>T maps to NM_005097.2 R5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:95549900 C>T maps to NM_005097.2 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:95556848 C>T maps to NM_005097.2 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr10:95518008 A>G maps to NM_005097.2 K36K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr4:25005431 G>A maps to NM_018176.3 R427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr4:25005684 G>A maps to NM_018176.3 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:25005150 C>T maps to NM_018176.3 R520R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:25005843 G>A maps to NM_018176.3 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr4:25005141 G>A maps to NM_018176.3 F523F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr4:25005150 C>T maps to NM_018176.3 R520R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:25005662 G>A maps to NM_018176.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:25005546 G>A maps to NM_018176.3 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:25030199 C>T maps to NM_018176.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr4:25005713 G>A maps to NM_018176.3 Q333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:25030151 G>A maps to NM_018176.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr4:25005213 G>A maps to NM_018176.3 F499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr8:22013869 C>A maps to NM_139278.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:22006368 C>T maps to NM_139278.2 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:22005900 G>A maps to NM_139278.2 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr8:22011506 G>A maps to NM_139278.2 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:22006230 G>A maps to NM_139278.2 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr8:22009376 G>A maps to NM_139278.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr8:22013917 G>A maps to NM_139278.2 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:22006317 G>A maps to NM_139278.2 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:35617889 C>T maps to NM_139284.2 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr19:35616207 G>A maps to NM_139284.2 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:35616132 C>T maps to NM_139284.2 Q526Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:35617263 G>A maps to NM_139284.2 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr14:93178214 C>T maps to NM_005606.6 W232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr14:93178215 C>T maps to NM_005606.6 W232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:93179167 G>A maps to NM_005606.6 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:93185156 G>A maps to NM_005606.6 H57H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:71978210 G>T maps to NM_003667.2 V807V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:71977433 C>T maps to NM_003667.2 F548F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:71946957 C>T maps to NM_003667.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:71977916 C>T maps to NM_003667.2 S709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:71977856 C>T maps to NM_003667.2 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr12:71955581 C>T maps to NM_003667.2 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr12:71978150 C>T maps to NM_003667.2 F787F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr12:71971716 G>A maps to NM_003667.2 W407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:71898456 G>A maps to NM_003667.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:71977871 C>T maps to NM_003667.2 T694T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr12:71976279 C>T maps to NM_003667.2 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:71977811 G>A maps to NM_003667.2 T674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:71928963 C>T maps to NM_003667.2 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:202287251 C>T maps to NM_001017403.1 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:202288019 C>T maps to NM_001017403.1 S863S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:202245637 C>T maps to NM_001017403.1 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:202287437 C>T maps to NM_001017403.1 V669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:202287995 G>A maps to NM_001017403.1 A855A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:202287143 C>T maps to NM_001017403.1 I571I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:202163293 C>T maps to NM_001017403.1 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr1:202287104 C>T maps to NM_001017403.1 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:202283942 G>A maps to NM_001017403.1 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:202163308 G>A maps to NM_001017403.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:202288064 C>T maps to NM_001017403.1 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:202284010 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:202279387 G>A maps to NM_001017403.1 K490K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:202276530 T>C did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr1:202287115 G>A maps to NM_001017403.1 W562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:202197124 C>T maps to NM_001017403.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:202272433 G>A maps to NM_001017403.1 Q319Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:202287191 C>T maps to NM_001017403.1 F587F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:202287287 C>T maps to NM_001017403.1 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr6:63990432 C>T maps to NM_016571.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr6:63990573 C>T maps to NM_016571.2 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:64004950 C>T maps to ENST00000370658 Q9Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr6:63990573 C>T maps to NM_016571.2 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr6:63990573 C>T maps to NM_016571.2 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:63990033 C>T maps to NM_016571.2 Q474Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:63990144 G>A maps to NM_016571.2 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:63990069 G>A maps to NM_016571.2 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:63990432 C>T maps to NM_016571.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr6:63990432 C>T maps to NM_016571.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:63990951 C>T maps to NM_016571.2 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:63989955 C>T maps to NM_016571.2 E500E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr6:63990204 G>C maps to NM_016571.2 Y417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:63990483 C>T maps to NM_016571.2 K324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr6:63990441 C>T maps to NM_016571.2 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:63990546 G>A maps to NM_016571.2 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr6:63990387 G>A maps to NM_016571.2 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:206772887 G>A maps to NM_006893.2 H377H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr1:206770466 C>T maps to NM_006893.2 W457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:206767006 G>A maps to NM_006893.2 Q549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:206776554 C>T maps to NM_006893.2 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr1:206770520 T>C maps to NM_006893.2 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:206769162 G>A maps to NM_006893.2 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:206778856 G>A maps to NM_006893.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr2:48914907 G>A maps to NM_000233.3 S676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:48925815 G>A maps to NM_000233.3 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:48915315 G>A maps to NM_000233.3 F540F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:48915510 G>A maps to NM_000233.3 D475D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:48921444 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:48914994 C>T maps to NM_000233.3 R647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:48915275 G>A maps to NM_000233.3 R554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:48936094 C>T maps to NM_000233.3 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:48936160 C>T maps to NM_000233.3 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:48915057 G>A maps to NM_000233.3 F626F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr13:39952607 T>C maps to NM_005780.2 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:40175209 C>T maps to NM_005780.2 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr13:40175224 G>A maps to NM_005780.2 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:111874652 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:111874684 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:111914426 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:111903870 G>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:111914256 C>T did not map to a codon.
Sequencing variant TCGA-EB-A44Q-06A-11D-A25O-08 chr5:77805790 G>A maps to NM_005779.2 C82C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr5:77805874 C>T maps to NM_005779.2 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:77805808 G>A maps to NM_005779.2 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:104377185 G>A maps to NM_199000.2 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:104377341 G>A maps to NM_199000.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:9547720 G>A maps to NM_198560.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr3:9547825 C>T maps to NM_198560.2 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:9594045 G>A maps to NM_198560.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:9543969 G>A maps to NM_198560.2 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr3:9594069 G>A maps to NM_198560.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:9543895 C>T maps to NM_198560.2 *248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:35773575 C>T maps to NM_182548.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr6:35773710 C>T maps to NM_182548.3 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr6:35773632 C>T maps to NM_182548.3 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:35773457 T>A maps to NM_182548.3 L4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:35773725 C>T maps to NM_182548.3 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr6:35782488 C>T maps to NM_182548.3 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:35773695 C>T maps to NM_182548.3 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr6:35773803 C>T maps to NM_182548.3 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr6:35773743 C>T maps to NM_182548.3 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:35773581 C>T maps to NM_182548.3 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr10:126177015 C>T maps to NM_022126.3 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr10:126172719 C>T maps to NM_022126.3 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr17:35300122 C>T maps to NM_005568.3 Q306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:35300133 G>A maps to NM_005568.3 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:35297979 G>A maps to NM_005568.3 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:35300244 C>T maps to NM_005568.3 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:126794844 C>T maps to NM_004789.3 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr9:139089221 G>A maps to NM_014564.3 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr9:139089185 G>A maps to NM_014564.3 D398D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:139089575 C>T maps to NM_014564.3 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:180217585 C>T maps to NM_033343.3 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr1:180243485 C>T maps to NM_033343.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:180240973 G>A maps to NM_033343.3 W204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr12:113905967 C>T maps to NM_022363.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:113906999 G>A maps to NM_022363.2 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:113909183 C>T maps to NM_022363.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:124979497 G>T maps to NM_014368.3 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:124979470 G>A maps to NM_014368.3 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr1:75608910 C>T maps to NM_001001933.1 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr1:75608859 C>T maps to NM_001001933.1 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:75608859 C>T maps to NM_001001933.1 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:75609545 G>A maps to NM_001001933.1 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:75609554 C>T maps to NM_001001933.1 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr1:75608880 C>T maps to NM_001001933.1 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:197890586 G>A maps to NM_020204.2 K177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr1:197890484 G>A maps to NM_020204.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:197898139 C>T maps to NM_020204.2 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:197889292 G>A maps to NM_020204.2 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:197889253 C>T maps to NM_020204.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:197890484 G>A maps to NM_020204.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:39469177 C>T maps to NM_006859.2 R217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:30639957 C>T maps to NM_002309.3 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr22:30639705 C>T maps to NM_002309.3 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr22:30639669 C>T maps to NM_002309.3 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:30639681 C>T maps to NM_002309.3 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:30640035 C>T maps to NM_002309.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr5:38511922 C>T maps to NM_002310.5 W235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr5:38482086 C>T maps to NM_002310.5 G968G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:38490358 G>A maps to NM_002310.5 F700F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr5:38482696 G>A maps to NM_002310.5 V888V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr5:38527371 C>T maps to NM_002310.5 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr5:38482296 C>T maps to NM_002310.5 L898L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:38506052 C>T maps to NM_002310.5 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr5:38490384 G>A maps to NM_002310.5 R692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:38510689 C>T maps to NM_002310.5 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:38510698 G>A maps to NM_002310.5 N286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr5:38493840 G>A maps to NM_002310.5 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:38484965 C>T maps to NM_002310.5 V834V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:38523619 G>A maps to NM_002310.5 Y154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr19:48664687 G>T maps to NM_000234.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:48619176 G>A maps to NM_000234.1 R877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:48660361 G>A maps to NM_000234.1 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:48657185 G>A maps to NM_000234.1 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:48620927 G>A maps to NM_000234.1 S850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:48640928 G>A maps to NM_000234.1 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:48631187 C>T maps to NM_000234.1 V637V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:48665550 G>T maps to NM_000234.1 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr19:48634356 C>T maps to NM_000234.1 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:48654500 G>A maps to NM_000234.1 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:48654501 G>A maps to NM_000234.1 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:48643237 G>A maps to NM_000234.1 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:48660349 T>A maps to NM_000234.1 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr17:33319025 C>T maps to NM_013975.3 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr17:33316650 C>T maps to NM_013975.3 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:33317985 T>G maps to NM_013975.3 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:33316659 C>T maps to NM_013975.3 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:108861131 G>A maps to NM_001098268.1 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:108863373 G>A maps to NM_001098268.1 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:55106226 G>A maps to NM_006863.1 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:55107723 C>T maps to NM_006863.1 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:55106745 C>T maps to NM_006863.1 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:55106175 C>T maps to NM_006863.1 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:55106327 G>A maps to NM_006863.1 W90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr19:55106667 C>T maps to NM_006863.1 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:55105720 C>T maps to NM_006863.1 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:55110716 C>T maps to NM_006863.1 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:55106622 G>A maps to NM_006863.1 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:55106763 C>T maps to NM_006863.1 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr19:55106863 C>T maps to NM_006863.1 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr19:55112239 G>A maps to NM_006863.1 G476G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:55106694 A>G maps to NM_006863.1 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr19:55107840 C>T maps to NM_006863.1 F382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr19:55107287 C>T maps to NM_006863.1 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr19:55112224 C>T maps to NM_006863.1 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:55106214 C>T maps to NM_006863.1 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:55107733 C>T maps to NM_006863.1 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:55106128 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:55106175 C>T maps to NM_006863.1 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:55106193 G>A maps to NM_006863.1 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:55112233 C>T maps to NM_006863.1 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:55085957 C>T maps to NM_001130917.1 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:55086300 C>T maps to NM_001130917.1 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:55086444 G>A maps to NM_001130917.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr19:55085368 G>A maps to ENST00000396321 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:55085962 G>A maps to NM_001130917.1 W89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:55086444 G>A maps to NM_001130917.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr19:55085817 C>T maps to NM_001130917.1 Q41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:55086444 G>A maps to NM_001130917.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:55086387 C>T maps to NM_001130917.1 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:55086906 C>T maps to NM_001130917.1 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr19:55086486 G>A maps to NM_001130917.1 E214E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr19:55086897 G>A maps to NM_001130917.1 Q277Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:55086777 G>A maps to NM_001130917.1 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:55086444 G>A maps to NM_001130917.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:55087436 A>G maps to NM_001130917.1 Q372Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:55086466 C>T maps to NM_001130917.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:55086255 G>A maps to NM_001130917.1 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr19:55086318 A>C maps to NM_001130917.1 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr19:55086384 C>T maps to NM_001130917.1 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:55085365 C>T maps to ENST00000396321 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:55085804 C>T maps to NM_001130917.1 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr19:54803598 C>T maps to ENST00000251375 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:54802161 C>T maps to ENST00000251375 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:54803733 G>T maps to ENST00000251375 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr19:54802729 G>A maps to ENST00000251375 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:54803736 G>A maps to ENST00000251375 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr19:54803961 G>A maps to ENST00000251375 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr19:54802711 G>A maps to ENST00000251375 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr19:54803115 C>T maps to ENST00000251375 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:54803034 G>A maps to ENST00000251375 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:54804140 G>A maps to ENST00000251375 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr19:54803631 C>T maps to ENST00000251375 K64K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr19:54803595 C>T maps to ENST00000251375 E76E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr19:54803127 G>A maps to ENST00000251375 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54803166 G>A maps to ENST00000251375 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:54849441 G>A maps to NM_012276.3 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr19:54849718 C>T maps to NM_012276.3 Q101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:54849234 G>A maps to NM_012276.3 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:54848307 G>A maps to NM_012276.3 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:54848859 G>A maps to NM_012276.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:54849946 G>A maps to NM_012276.3 N25N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:54849934 G>A maps to NM_012276.3 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr19:54848869 G>A maps to NM_012276.3 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:54848303 G>A maps to NM_012276.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr19:54849321 G>A maps to NM_012276.3 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:54848878 G>A maps to NM_012276.3 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr19:54849691 G>A maps to NM_012276.3 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54848391 G>A maps to NM_012276.3 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54849489 G>A maps to NM_012276.3 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54849676 C>T maps to NM_012276.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54850342 G>A maps to NM_012276.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr19:54848199 G>A maps to NM_012276.3 H389H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr19:54849766 G>A maps to NM_012276.3 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr19:54823335 C>T maps to NM_021250.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr19:54818742 C>T maps to NM_021250.2 Q285Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:54822798 G>A maps to NM_021250.2 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:54822732 G>A maps to NM_021250.2 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr19:54822810 G>A maps to NM_021250.2 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:54823362 C>T maps to NM_021250.2 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:54823371 G>A maps to NM_021250.2 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr19:54823416 C>T maps to NM_021250.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr19:54823254 C>T maps to NM_021250.2 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:54818763 G>A maps to NM_021250.2 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:54823206 C>T maps to NM_021250.2 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:54822891 G>A maps to NM_021250.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:54822648 C>T maps to NM_181879.1 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54823362 C>T maps to NM_021250.2 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr19:54823362 C>T maps to NM_021250.2 G60G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D3-A2JF-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:54744788 C>T maps to ENST00000245620 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr19:54744938 C>T maps to ENST00000245620 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:54744716 G>A maps to ENST00000245620 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:54745566 G>A maps to ENST00000270464 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54746088 C>T maps to ENST00000407860 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr19:54745698 C>T maps to ENST00000270464 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:54745695 C>T maps to ENST00000270464 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:55144506 C>T maps to ENST00000427581 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr19:55143134 C>T maps to ENST00000427581 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr19:55145131 C>T maps to ENST00000427581 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:55143143 C>T maps to ENST00000427581 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:55143945 G>A maps to ENST00000427581 Q267Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr19:55143632 G>A maps to ENST00000427581 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr19:55145110 C>T maps to ENST00000427581 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:55144764 C>T maps to ENST00000427581 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:55143677 C>T maps to ENST00000427581 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:55143452 C>T maps to ENST00000427581 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:55146158 C>T maps to ENST00000427581 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:55143632 G>A maps to ENST00000427581 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:55146186 C>T maps to ENST00000427581 R536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr19:55145104 C>T maps to ENST00000427581 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:55143575 C>T maps to ENST00000427581 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:55146141 C>T maps to ENST00000427581 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr19:55142722 G>A maps to ENST00000427581 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:55147029 G>A maps to ENST00000427581 Q590Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr19:55144200 C>T maps to ENST00000427581 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr19:55143587 G>T maps to ENST00000427581 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr19:55144653 C>T maps to ENST00000427581 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:55144101 C>T maps to ENST00000427581 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:55144128 G>A maps to ENST00000427581 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr19:55144686 G>A maps to ENST00000427581 G429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr19:55143584 C>T maps to ENST00000427581 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:55143678 C>T maps to ENST00000427581 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr19:55144047 C>T maps to ENST00000427581 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:55144764 C>T maps to ENST00000427581 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:55146119 C>T maps to ENST00000427581 I513I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr19:55143158 A>G maps to ENST00000427581 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:55146104 C>T maps to ENST00000427581 H508H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr19:54782775 G>A maps to ENST00000391747 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr19:54782676 G>A maps to ENST00000391747 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:54782697 G>A maps to ENST00000391747 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:54783909 G>A maps to ENST00000391747 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:54783394 G>A maps to ENST00000391747 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:54784318 G>A maps to ENST00000391747 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54780681 G>A maps to ENST00000391747 Q504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54782273 G>A maps to ENST00000391747 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54782676 G>A maps to ENST00000391747 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54782697 G>A maps to ENST00000391747 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54783314 G>A maps to ENST00000391747 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54783814 C>T maps to ENST00000391747 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54784154 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54784339 G>A maps to ENST00000391747 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr19:54724985 G>A maps to NM_001081450.1 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54722247 C>T maps to NM_001081450.1 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr19:55175257 C>T maps to ENST00000391733 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr19:55179418 A>G maps to ENST00000391733 E433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:55175230 C>T maps to ENST00000391733 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:55177871 C>T maps to ENST00000391733 Q325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:55176614 G>A maps to ENST00000391733 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:55175266 G>A maps to ENST00000391733 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr19:55175308 G>A maps to ENST00000391733 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:55175925 C>T maps to ENST00000391733 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:55178169 G>A maps to ENST00000391733 Q338Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:55175227 C>T maps to ENST00000391733 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr19:55175853 G>A maps to ENST00000391733 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZU-06A-12D-A196-08 chr19:55176301 T>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:55174517 C>T maps to ENST00000391733 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:55177267 C>T maps to ENST00000391733 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:55179382 C>T maps to ENST00000391733 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:55175401 C>T maps to ENST00000391733 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:54758679 T>G maps to NM_001081442.1 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr19:54758781 C>T maps to NM_001081442.1 K357K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr19:54759988 C>T maps to NM_001081442.1 W191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:54759939 C>T maps to NM_001081442.1 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:54759987 C>T maps to NM_001081442.1 W191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:54760538 C>T maps to NM_001081442.1 E56E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:54760176 G>A maps to NM_001081442.1 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr19:54760056 T>G maps to NM_001081442.1 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr19:54759923 G>A maps to NM_001081442.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:54754775 G>A maps to NM_001081442.1 P550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54760538 C>T maps to NM_001081442.1 E56E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr19:51883891 G>A maps to NM_030657.3 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr19:51883822 C>T maps to NM_030657.3 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:51883762 G>A maps to NM_030657.3 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr19:51883514 C>T maps to NM_030657.3 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:51890685 G>A maps to NM_030657.3 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr12:50616038 G>C maps to NM_001113546.1 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr12:50615940 G>A maps to NM_001113546.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr4:41648258 G>A maps to NM_014988.2 R406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr4:41621391 G>A maps to NM_014988.2 E290E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr4:41648870 C>T maps to NM_014988.2 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:41648699 C>T maps to NM_014988.2 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr4:41648681 C>T maps to NM_014988.2 F479F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr4:41682051 G>A maps to NM_014988.2 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:41648678 C>T maps to NM_014988.2 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr4:41615514 T>C maps to NM_014988.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr4:41678478 G>A maps to NM_014988.2 Q789Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr4:41648741 C>T maps to NM_014988.2 F499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:41648537 G>A maps to NM_014988.2 K431K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:41608020 G>A maps to NM_014988.2 K162K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:41615664 G>A maps to NM_014988.2 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:41648594 C>T maps to NM_014988.2 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:41664892 G>A maps to NM_014988.2 V676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:41686443 G>A maps to NM_014988.2 G908G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:41689910 C>T maps to NM_014988.2 T997T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:41694355 C>T maps to NM_014988.2 R1061*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:41664931 G>A maps to NM_014988.2 S689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr3:45637069 C>T maps to NM_014240.2 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr3:45637070 C>T maps to NM_014240.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr3:45636772 C>T maps to NM_014240.2 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr20:62370075 C>T maps to NM_017806.2 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:62370243 C>T maps to NM_017806.2 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:73520477 G>A maps to NM_002314.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr7:73534931 G>A maps to NM_002314.2 K529K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr7:73513454 G>A maps to NM_002314.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:73522253 C>T maps to NM_002314.2 F373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:73513400 C>T maps to NM_002314.2 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr7:73521426 C>T maps to NM_002314.2 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr22:31674348 C>T maps to ENST00000438187 I644I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr22:31662018 C>T maps to NM_001031801.1 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr22:31674411 G>A maps to ENST00000438187 R665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr22:31663805 C>T maps to NM_001031801.1 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr22:31663833 C>T maps to NM_001031801.1 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr22:31658188 C>A maps to NM_001031801.1 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:31656015 C>T maps to NM_001031801.1 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr22:31669480 C>T maps to NM_001031801.1 I513I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr22:31672906 C>T maps to NM_001031801.1 I614I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr22:31656057 G>T maps to NM_001031801.1 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:31608408 G>A maps to NM_005569.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:31654357 G>A maps to NM_001031801.1 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:109276189 C>T maps to NM_001193484.1 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:109276205 G>T maps to NM_001193484.1 G85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:128415078 G>A maps to NM_017980.4 S47S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A2MD-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:26752947 G>A maps to NM_024674.4 *210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:26751876 G>A maps to NM_024674.4 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:26752888 C>T maps to NM_024674.4 Y190Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:26737875 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:105474267 G>A maps to NM_001004317.2 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr6:105526588 G>A maps to NM_001004317.2 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:74562681 C>T maps to NM_001024674.2 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:83858423 C>T maps to NM_194282.2 R520R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr4:83849305 G>A maps to NM_194282.2 V733V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr4:83858444 G>A maps to NM_194282.2 I513I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:81283034 G>A maps to NM_004664.2 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr12:81283034 G>A maps to NM_004664.2 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr12:81242077 C>T maps to NM_004664.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:226420282 G>A maps to ENST00000366807 I666I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:226453308 C>T maps to ENST00000366807 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:226420838 G>T maps to ENST00000366807 S644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr9:27949199 C>T maps to NM_152570.1 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:27949508 G>A maps to NM_152570.1 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:27949634 C>T maps to NM_152570.1 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:27950483 C>T maps to NM_152570.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:27949865 G>A maps to NM_152570.1 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:27949574 C>T maps to NM_152570.1 W365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:2291205 G>A maps to NM_001101391.1 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:2290686 G>A maps to NM_001101391.1 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:2290659 G>A maps to NM_001101391.1 F372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:151775057 G>A maps to NM_001004432.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:151773803 C>T maps to NM_001004432.2 G459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:151773935 G>A maps to NM_001004432.2 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:151773518 A>G maps to NM_001004432.2 I554I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:151775135 G>A maps to NM_001004432.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr1:151774898 G>A maps to NM_001004432.2 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:151774001 C>A maps to NM_001004432.2 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr15:101109544 G>A maps to NM_001040616.2 C724C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:101114333 G>A maps to NM_001040616.2 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr15:101109520 G>A maps to NM_001040616.2 F732F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:101109520 G>A maps to NM_001040616.2 F732F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:101114267 G>A maps to NM_001040616.2 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:101113901 G>A maps to NM_001040616.2 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:58855703 G>A maps to NM_000236.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:58855763 C>T maps to NM_000236.2 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr15:58840748 G>A maps to NM_000236.2 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr19:42930800 C>T maps to NM_005357.2 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:42931135 T>G maps to NM_005357.2 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr19:42931280 T>G maps to NM_005357.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:42914821 C>T maps to NM_005357.2 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr19:42930618 C>T maps to NM_005357.2 W228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr19:42907127 C>T maps to NM_005357.2 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr19:42930800 C>T maps to NM_005357.2 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:42910378 G>A maps to NM_005357.2 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr10:90435979 G>A maps to NM_001198829.1 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:90428402 C>T maps to NM_001198829.1 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:90429632 C>T maps to NM_001198829.1 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:90436021 G>A maps to NM_001198829.1 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:90433382 C>T maps to NM_001198829.1 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:90435979 G>A maps to NM_001198829.1 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:90435979 G>A maps to NM_001198829.1 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:90427137 C>T maps to NM_001198829.1 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:47101910 C>T maps to NM_006033.2 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr18:47101751 C>G maps to NM_006033.2 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr18:47088768 C>T maps to NM_006033.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr18:47107875 C>T maps to NM_006033.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:47110051 G>A maps to NM_006033.2 K428K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:185245281 G>A maps to NM_139248.2 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:185232217 G>C maps to NM_139248.2 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr3:185252756 G>T maps to NM_139248.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:185229331 C>T maps to NM_139248.2 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:185229468 G>A maps to NM_139248.2 Q371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:185232256 C>T maps to NM_139248.2 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr21:15561498 G>A maps to NM_198996.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr21:15558357 G>A maps to NM_198996.2 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr21:15561498 G>A maps to NM_198996.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr21:15524927 G>A maps to NM_198996.2 Q383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr21:15524927 G>A maps to NM_198996.2 Q383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr21:15561378 C>T maps to NM_198996.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr21:15517023 G>A maps to NM_198996.2 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr21:15579186 G>A maps to NM_198996.2 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr21:15561576 G>A maps to NM_198996.2 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:15561636 C>T maps to NM_198996.2 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr10:90356596 C>T maps to NM_001010939.2 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr10:90362397 G>A maps to NM_001010939.2 W263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:90503071 C>T maps to NM_001080518.1 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr10:90499823 G>A maps to NM_001080518.1 Q296Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr10:90490794 G>A maps to NM_001080518.1 W93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:90492286 C>T maps to NM_001080518.1 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:90528618 G>A maps to NM_001102469.1 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr10:90528661 C>T maps to NM_001102469.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr5:96432559 C>T maps to NM_153234.4 W172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr5:96460205 C>T maps to NM_153234.4 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:145492375 G>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:145492338 C>T maps to NM_153713.1 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:145498120 C>T maps to NM_153713.1 Q238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr17:18137690 G>A maps to NM_004140.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:18138460 C>T maps to NM_004140.3 D373D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:18138461 C>T maps to NM_004140.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:18143970 A>G maps to NM_004140.3 A762A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:18140907 C>T maps to NM_004140.3 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:18143907 C>T maps to NM_004140.3 P741P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr17:18139962 G>A maps to NM_004140.3 V465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr17:73567140 C>T maps to NM_001031803.1 F712F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr17:73559138 G>A maps to NM_001031803.1 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr17:73555365 C>T maps to NM_001031803.1 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:73566309 C>T maps to NM_001031803.1 H616H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:73559866 C>T maps to NM_001031803.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:73569201 C>T maps to NM_001031803.1 A856A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr17:73552143 C>T maps to NM_001031803.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:73554277 G>A maps to NM_001031803.1 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:73569339 C>T maps to NM_001031803.1 V902V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:73567140 C>T maps to NM_001031803.1 F712F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:73569258 G>A maps to NM_001031803.1 V875V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr17:73567826 C>T maps to NM_001031803.1 A752A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr17:73539581 G>A maps to NM_001031803.1 K25K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:73554624 C>T maps to NM_001031803.1 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:73566201 C>T maps to NM_001031803.1 F580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:73567065 C>T maps to NM_001031803.1 G687G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:73567143 C>T maps to NM_001031803.1 V713V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:73569207 C>T maps to NM_001031803.1 D858D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr17:73569691 G>A maps to NM_001031803.1 K952K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:57013216 G>A maps to NM_005570.3 Q297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:75116726 G>A maps to NM_021819.2 Q453Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr15:75105203 G>A maps to NM_021819.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:75108814 G>A maps to NM_021819.2 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:75114198 C>T maps to NM_021819.2 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr15:75105362 T>C maps to NM_021819.2 H56H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:75114198 C>T maps to NM_021819.2 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr15:75108594 G>A maps to NM_021819.2 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr15:75108808 C>T maps to NM_021819.2 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr15:75115899 G>A maps to NM_021819.2 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr5:176759164 G>A maps to NM_006816.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr5:176764724 G>A maps to NM_006816.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:176761404 C>A did not map to a codon.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr5:176764724 G>A maps to NM_006816.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:97403780 G>A maps to NM_001142292.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:97373550 G>A maps to NM_001142292.1 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:97400218 G>A maps to NM_001142292.1 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:97377633 G>A maps to NM_001142292.1 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr7:156480768 G>A maps to ENST00000354505 R489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:156480760 G>A maps to ENST00000354505 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr7:156476795 T>A maps to ENST00000354505 V524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr7:156556459 C>T maps to ENST00000354505 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr7:156589166 G>A maps to ENST00000354505 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:156518468 G>A maps to ENST00000354505 I393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:156619308 G>A maps to ENST00000354505 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr7:156549147 G>A maps to ENST00000354505 D232D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:49497572 C>T maps to NM_018113.2 E153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:49500747 G>T maps to NM_018113.2 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr6:70411842 G>A maps to NM_018368.3 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr5:36117839 G>A maps to NM_001007527.1 I433I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr5:36122394 A>T maps to NM_001007527.1 Y369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr5:36143316 G>A maps to NM_001007527.1 C45C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:36116683 G>A maps to NM_001007527.1 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:36116683 G>A maps to NM_001007527.1 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:36117839 G>A maps to NM_001007527.1 I433I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr3:8607122 C>T maps to NM_014583.2 C243C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:8609133 C>T maps to NM_014583.2 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:8590279 C>T maps to NM_014583.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:8590327 C>T maps to NM_014583.2 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:1004442 G>A maps to ENST00000262301 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:960942 G>A maps to ENST00000262301 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr16:919954 G>A maps to ENST00000262301 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr16:921329 G>A maps to ENST00000262301 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr16:920850 C>T maps to ENST00000262301 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:921173 G>A maps to ENST00000262301 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:961029 G>A maps to ENST00000262301 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr22:50942014 G>A maps to NM_033200.2 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:50944109 C>T maps to NM_033200.2 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:50941852 G>A maps to NM_033200.2 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:50944495 G>A maps to NM_033200.2 R248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:197762813 C>T maps to NM_001136049.2 H626H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:197723071 T>C maps to NM_001136049.2 C358C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:197765481 C>T maps to NM_001136049.2 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:156106055 C>T maps to NM_170707.2 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:156105072 C>T maps to NM_170707.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:156084912 G>A maps to NM_170707.2 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr1:156105738 C>T maps to NM_170707.2 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:126161726 C>A maps to NM_005573.3 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:2431605 C>T maps to NM_032737.2 E567E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr19:2438166 G>A maps to NM_032737.2 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:2433864 G>A maps to NM_032737.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr11:8248604 C>T maps to ENST00000428101 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:8248556 G>A maps to ENST00000428101 H171H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:33880940 C>T maps to NM_005574.3 Q215Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:33886332 G>A maps to NM_005574.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:16713426 G>A maps to ENST00000441439 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:16713468 G>A maps to ENST00000441439 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr12:16753611 G>T maps to ENST00000441439 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:16704167 G>C maps to ENST00000441439 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr12:16713472 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:76415945 G>A maps to ENST00000357063 P1216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr13:76432094 G>A maps to NM_015842.2 T1368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr13:76423254 T>A maps to ENST00000357063 S1327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:76432094 G>A maps to NM_015842.2 T1368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr13:76416005 A>G maps to ENST00000357063 Q1236Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr13:76423324 G>T maps to ENST00000357063 E1351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr13:76408474 C>T maps to ENST00000357063 Q990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr13:76415930 C>T maps to ENST00000357063 D1211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr13:76415294 C>T maps to ENST00000357063 A1141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr13:76423317 C>T maps to ENST00000357063 I1348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:76395318 C>T maps to ENST00000357063 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:76397895 C>T maps to ENST00000357063 Q876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:76397921 C>T maps to ENST00000357063 A884A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:76414571 C>T maps to ENST00000357063 Q1105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:76427473 G>A maps to ENST00000357063 P1467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr13:76374857 G>A maps to ENST00000357063 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr13:76397933 C>T maps to ENST00000357063 S888S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:201868628 C>T maps to NM_012134.2 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:201869435 C>T maps to NM_012134.2 E235E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:201869498 C>T maps to NM_012134.2 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:201869570 C>T maps to NM_012134.2 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:201915303 C>A maps to NM_012134.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:201868736 G>A maps to NM_012134.2 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:201868520 G>A maps to NM_012134.2 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr7:123302491 G>A maps to NM_207163.1 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr7:123296125 T>C maps to NM_207163.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:123302476 C>T maps to NM_207163.1 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:123302464 C>T maps to NM_207163.1 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:123302704 G>A maps to NM_207163.1 Q355Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:123302374 C>T maps to NM_207163.1 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:69168542 G>A maps to NM_198271.3 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:69168725 C>T maps to NM_198271.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:69168224 G>A maps to NM_198271.3 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr3:69171495 G>A maps to NM_198271.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr3:69171426 C>T maps to NM_198271.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr7:97822755 C>T maps to NM_014916.3 S993S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr7:97822686 G>T maps to NM_014916.3 S970S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:97823865 A>G maps to NM_014916.3 T1363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:97821024 G>A maps to NM_014916.3 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:97821333 C>T maps to NM_014916.3 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr7:97823515 C>T maps to NM_014916.3 L1247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:97814434 C>T maps to NM_014916.3 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:97822774 C>T maps to NM_014916.3 L1000L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:97821732 C>T maps to NM_014916.3 F652F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:97833004 C>T maps to NM_014916.3 S1409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:97832932 C>T maps to NM_014916.3 G1385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:97822950 C>T maps to NM_014916.3 T1058T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:97833286 C>T maps to NM_014916.3 S1424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:97823154 C>A maps to NM_014916.3 S1126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr7:97822164 C>T maps to NM_014916.3 V796V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:97800977 C>T maps to NM_014916.3 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr19:49012190 G>A maps to NM_001080434.1 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:49012223 C>T maps to NM_001080434.1 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr19:49000827 C>T maps to NM_001080434.1 P1195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:49004629 C>T maps to NM_001080434.1 W333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:49012211 C>T maps to NM_001080434.1 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:49012130 G>A maps to NM_001080434.1 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:49001171 G>A maps to NM_001080434.1 L1081L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:49013376 C>T maps to NM_001080434.1 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:49001493 C>T maps to NM_001080434.1 A973A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:49013313 G>A maps to NM_001080434.1 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:49000689 C>T maps to NM_001080434.1 L1241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:49001502 C>T maps to NM_001080434.1 E970E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:49001529 C>T maps to NM_001080434.1 G961G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:49006252 C>T maps to NM_001080434.1 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr19:49005810 G>A maps to NM_001080434.1 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:49012223 C>T maps to NM_001080434.1 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr1:165218837 G>A maps to NM_177398.3 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:165218846 G>A maps to NM_177398.3 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr1:165173260 G>A maps to NM_177398.3 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr1:165180004 C>T maps to NM_177398.3 E226E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr1:165218846 G>A maps to NM_177398.3 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:165183000 C>T maps to NM_177398.3 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:165218717 C>T maps to NM_177398.3 Q141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:165175191 G>A maps to NM_177398.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:165183024 G>A maps to NM_177398.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr1:165218846 G>A maps to NM_177398.3 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:165218717 C>T maps to NM_177398.3 Q141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:165218846 G>A maps to NM_177398.3 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:165218702 C>T maps to NM_177398.3 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:165218804 C>T maps to NM_177398.3 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:165183024 G>A maps to NM_177398.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr1:165218663 G>A maps to NM_177398.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:165175182 G>A maps to NM_177398.3 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:165218846 G>A maps to NM_177398.3 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:165179938 C>T maps to NM_177398.3 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:165179968 G>A maps to NM_177398.3 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:165175185 G>A maps to NM_177398.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:165183000 C>T maps to NM_177398.3 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr1:165173143 G>A maps to NM_177398.3 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:165173260 G>A maps to NM_177398.3 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:129453306 G>A maps to NM_001174147.1 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:129458636 C>T maps to NM_001174147.1 F372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr9:129453153 C>T maps to NM_001174147.1 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr9:129458636 C>T maps to NM_001174147.1 F372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:129458121 C>T maps to NM_001174147.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:100148713 C>T maps to ENST00000489752 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:96315502 C>T maps to NM_005575.2 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:96315503 C>T maps to NM_005575.2 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:96315550 C>T maps to NM_005575.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:96332161 C>T maps to NM_005575.2 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr5:96342188 C>T maps to NM_005575.2 Q669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr5:96315550 C>T maps to NM_005575.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr4:54364888 G>A maps to NM_001126328.1 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:54347997 G>A maps to NM_001126328.1 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr4:54343059 C>G maps to NM_001126328.1 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:54343014 T>C maps to NM_001126328.1 E599E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr13:28136561 G>A maps to NM_153371.3 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr13:28136653 A>G maps to NM_153371.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr13:28136617 G>A maps to NM_153371.3 R386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:28155801 C>T maps to NM_153371.3 Q13Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr13:28141845 G>A maps to NM_153371.3 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr13:28127487 G>A maps to NM_153371.3 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:28136758 G>A maps to NM_153371.3 Q339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:28136759 G>A maps to NM_153371.3 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr16:22545866 C>T maps to NM_001135865.1 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:135188410 C>T maps to ENST00000420621 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr2:207513415 C>T maps to NM_001102659.1 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:40172141 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:40172137 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr19:40172146 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:40172134 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:193128 G>A maps to NM_145651.2 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr19:19257565 C>T maps to ENST00000410050 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr19:19260220 C>T maps to ENST00000410050 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19257421 G>A maps to ENST00000410050 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr16:20855311 C>T maps to NM_030941.2 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr16:20857541 G>A did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr12:12618583 C>T maps to NM_058169.3 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr19:5705924 G>A maps to NM_004793.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:5719870 C>T maps to NM_004793.2 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:48381494 G>A maps to NM_031490.2 V672V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr8:12594426 T>A maps to NM_152271.3 K446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr8:12600737 G>A maps to NM_152271.3 Q259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:118140156 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:118148313 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:118109230 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:118123393 T>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:118151558 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:118145874 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr5:121409764 T>C maps to NM_002317.5 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr15:74219702 C>T maps to NM_005576.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr15:74235198 C>T maps to NM_005576.2 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr15:74219543 C>T maps to NM_005576.2 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr15:74241840 C>T maps to NM_005576.2 F548F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:74238811 C>T maps to NM_005576.2 F422F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:23198682 G>A maps to NM_002318.2 R189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr8:23167233 G>A maps to NM_002318.2 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr8:23225654 G>A maps to NM_002318.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr8:23167371 C>T maps to NM_002318.2 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr8:23225579 G>A maps to NM_002318.2 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:23191093 G>A maps to NM_002318.2 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr8:23177451 C>T maps to NM_002318.2 E472E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:23186039 C>T maps to NM_002318.2 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr8:23155594 G>A maps to NM_002318.2 H762H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr8:23191093 G>T maps to NM_002318.2 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:23177457 G>A maps to NM_002318.2 I470I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:74763571 G>A maps to NM_032603.2 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:74761310 C>A maps to NM_032603.2 V664V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr2:74761256 C>T maps to NM_032603.2 T682T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr10:100015376 G>A maps to NM_032211.6 S516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr10:100013500 C>T maps to NM_032211.6 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr10:100020800 C>T maps to NM_032211.6 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:100017475 C>T maps to NM_032211.6 Q397Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr10:100013539 C>T maps to NM_032211.6 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr6:160968931 C>T maps to NM_005577.2 K1731K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr6:161006177 G>A maps to NM_005577.2 R1397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr6:161016425 C>T maps to NM_005577.2 T1143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr6:160966475 G>A maps to NM_005577.2 L1798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr6:160999711 C>T maps to NM_005577.2 R1438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:160999687 A>C maps to NM_005577.2 P1446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr6:160999731 G>A maps to NM_005577.2 L1432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr6:160998267 G>A maps to NM_005577.2 R1511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr6:161020662 C>T maps to NM_005577.2 Q1052Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:160963745 C>T maps to NM_005577.2 W1831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:160977124 C>T maps to NM_005577.2 R1635R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:161006210 G>A maps to NM_005577.2 Q1386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr6:161020596 A>G maps to NM_005577.2 T1074T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:160978563 C>T maps to NM_005577.2 G1557G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr6:161071425 A>G maps to NM_005577.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr6:161012036 C>T maps to NM_005577.2 L1242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr6:161022054 G>A maps to NM_005577.2 V1007V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19T-06A-11D-A19A-08 chr6:160969512 G>A maps to NM_005577.2 Q1718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:161027680 G>A maps to NM_005577.2 I871I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:161071469 G>A maps to NM_005577.2 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:160961163 C>T maps to NM_005577.2 V1882V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr6:161006211 G>A maps to NM_005577.2 V1385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:160998244 G>A maps to NM_005577.2 V1518V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr9:113704151 C>T maps to NM_057159.2 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr9:113704253 G>A maps to NM_057159.2 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr9:113703965 G>A maps to NM_057159.2 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr9:113704359 C>T maps to NM_057159.2 W45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr9:113704019 C>T maps to NM_057159.2 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:113703936 C>T maps to NM_057159.2 W186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr9:113637907 G>A maps to NM_057159.2 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr9:113703935 C>T maps to NM_057159.2 W186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:113703755 G>A maps to NM_057159.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:19735325 A>G maps to NM_004720.5 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:85331548 G>A maps to NM_012152.2 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:85331158 C>T maps to NM_012152.2 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:85331487 G>A maps to NM_012152.2 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:85331710 C>T maps to NM_012152.2 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:85331095 C>T maps to NM_012152.2 K236K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:85331569 G>A maps to NM_012152.2 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:85331608 G>A maps to NM_012152.2 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr23:78011428 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:78011168 T>C did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:78010798 C>T did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:78010719 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr23:78010771 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:78010771 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:78011028 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:78010799 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr23:78011011 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:78010569 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:78011343 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:78011238 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:78010977 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:78011196 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr23:78010771 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z4-06A-11D-A197-08 chr23:78010398 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr23:78010793 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr23:78010804 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:78011250 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:78010771 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:78011428 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:78010383 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:78011170 C>T did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:78011007 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr13:48985881 C>T maps to NM_005767.5 K226K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:1494881 G>A maps to NM_024830.3 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr5:1474742 C>T maps to NM_024830.3 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:1494881 G>A maps to NM_024830.3 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:1494890 G>A maps to NM_024830.3 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr5:1463831 G>A maps to NM_024830.3 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:1474125 G>A maps to NM_024830.3 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr5:1495001 G>A maps to NM_024830.3 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:1494983 G>A maps to NM_024830.3 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:55562454 T>C maps to NM_017839.4 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr16:55608592 C>T maps to NM_017839.4 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr15:34657290 G>A maps to NM_153613.2 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr15:34656415 G>A maps to NM_153613.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr15:34657848 G>A maps to NM_153613.2 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr15:34657824 A>G maps to NM_153613.2 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:211952300 G>A maps to NM_014873.2 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr1:211956805 C>T maps to NM_014873.2 K164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:212002625 A>G maps to NM_014873.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr19:14273445 C>T maps to NM_001008701.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr19:14269965 C>T maps to NM_001008701.2 E700E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr19:14271493 G>A maps to NM_001008701.2 Q514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:14263228 G>A maps to NM_001008701.2 L1186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr19:14266209 C>T maps to NM_001008701.2 G1090G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr19:14266173 C>T maps to NM_001008701.2 K1102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:82408770 C>T maps to ENST00000370717 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:82408893 G>A maps to ENST00000370717 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:82447615 C>T maps to ENST00000370717 Q1091*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr1:82432133 C>T maps to ENST00000370717 F726F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:82434965 C>T maps to ENST00000370717 F872F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:82408932 G>A maps to ENST00000370717 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:82432109 C>T maps to ENST00000370717 I718I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:82434923 C>T maps to ENST00000370717 S858S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:82433840 C>T maps to ENST00000370717 H823H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:82456394 C>T maps to ENST00000370717 L1331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:82431862 G>A maps to ENST00000370717 R709R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:82435022 C>T maps to ENST00000370717 F891F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr1:82408686 G>A maps to ENST00000370717 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:82408944 G>A maps to ENST00000370717 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:82431754 C>T maps to ENST00000370717 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:82416786 G>A maps to ENST00000370717 V526V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A3AE-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:82409079 C>T maps to ENST00000370717 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:82447626 C>T maps to ENST00000370717 F1094F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr1:82408830 C>T maps to ENST00000370717 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr1:82372859 C>T maps to ENST00000370717 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:82433738 C>T maps to ENST00000370717 S789S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:82447512 C>T maps to ENST00000370717 F1056F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:82456471 G>A maps to ENST00000370717 K1356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:82416101 G>A maps to ENST00000370717 G476G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:82432205 C>T maps to ENST00000370717 N750N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:82447656 G>A maps to ENST00000370717 K1104K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:82436122 G>A maps to ENST00000370717 R949R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:82456237 C>T maps to ENST00000370717 I1278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:82372828 G>A maps to ENST00000370717 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:62813843 C>T maps to ENST00000506720 N885N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr4:62903525 G>A maps to ENST00000506720 G1223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:62897273 C>T maps to ENST00000506720 F1179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:62935857 T>C maps to ENST00000506720 S1325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr4:62598790 G>A maps to ENST00000506720 K306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr4:62599213 G>A maps to ENST00000506720 W447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:62897306 C>T maps to ENST00000506720 F1190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:62758606 C>A maps to ENST00000506720 R572R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr4:62849228 G>A maps to ENST00000506720 R1048R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr4:62758425 C>T maps to ENST00000506720 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:62813952 C>T maps to ENST00000506720 L922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr4:62363037 C>T maps to ENST00000506720 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr4:62903447 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:62845459 C>T maps to ENST00000506720 F995F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:62935950 C>T maps to ENST00000506720 D1356D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:62542621 C>T maps to ENST00000506720 Y184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:62599144 C>T maps to ENST00000506720 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:62903541 C>T maps to ENST00000506720 R1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr4:62845432 C>T maps to ENST00000506720 I986I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:11943101 C>T maps to ENST00000396099 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr2:11919761 G>A maps to ENST00000396099 Q322Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr2:11944619 C>T maps to ENST00000396099 C701C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:11911505 C>T maps to ENST00000396099 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr2:11905714 G>A maps to ENST00000396099 K22K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:11922583 C>T maps to ENST00000396099 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:11964769 C>T maps to ENST00000396099 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:11964793 C>T maps to ENST00000396099 F892F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:11905847 C>T maps to ENST00000396099 R67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr18:2926800 C>A maps to NM_014646.2 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr18:2931296 G>A maps to NM_014646.2 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:2940691 G>A maps to NM_014646.2 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr20:39983346 C>T maps to NM_022896.1 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:39984673 C>T maps to NM_022896.1 I601I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:39978903 C>T maps to NM_022896.1 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr20:39978915 G>A maps to NM_022896.1 E327E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr20:39978453 G>T maps to NM_022896.1 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:39978720 C>T maps to NM_022896.1 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:39987428 C>T maps to NM_022896.1 L827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:19805790 C>T maps to NM_000237.2 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:19805838 C>T maps to NM_000237.2 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:19811736 C>T maps to NM_000237.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr8:19805790 C>T maps to NM_000237.2 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr17:56320339 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr17:56345252 C>T maps to NM_006151.2 V679V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:56327780 G>A maps to NM_006151.2 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:56332313 C>T maps to NM_006151.2 I416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:56345270 G>A maps to NM_006151.2 W685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:56329577 G>A maps to NM_006151.2 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:56326424 C>G maps to NM_006151.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:56342159 C>G maps to NM_006151.2 Y448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr17:56329568 G>A maps to NM_006151.2 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr17:56344923 C>T maps to NM_006151.2 F636F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:56342231 C>T maps to NM_006151.2 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:56345177 G>A maps to NM_006151.2 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:56345294 C>T maps to NM_006151.2 F693F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr17:56344851 G>A maps to NM_006151.2 G612G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:56344923 C>T maps to NM_006151.2 F636F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr3:188242562 T>C maps to NM_005578.3 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:188584049 C>T maps to NM_005578.3 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:188592224 C>T maps to NM_005578.3 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr9:104048435 C>A maps to NM_017753.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:104048504 C>T maps to NM_017753.2 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:104032221 C>T maps to NM_017753.2 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:104048504 C>T maps to NM_017753.2 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr9:104079759 G>A maps to NM_017753.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:104048496 C>T maps to NM_017753.2 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr9:104048414 C>T maps to NM_017753.2 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr9:104075207 G>A maps to NM_017753.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:104032304 C>T maps to NM_017753.2 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:104048450 G>A maps to NM_017753.2 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:104075162 C>T maps to NM_017753.2 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:11470528 C>T maps to NM_001170635.1 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:11474441 C>T maps to NM_001170635.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr19:11474874 G>A maps to NM_001170635.1 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr19:11472103 G>A maps to NM_001170635.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:99771752 C>T maps to NM_014839.4 D493D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:99772124 C>T maps to NM_014839.4 P617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:99767389 T>A maps to NM_014839.4 Y301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:99771773 G>A maps to NM_014839.4 Q500Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:99767440 T>C maps to NM_014839.4 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:99422249 C>T maps to NM_001037317.1 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:99380379 G>A maps to NM_001037317.1 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:58322361 A>C maps to NM_004811.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:58338112 G>A maps to NM_004811.2 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr11:58317538 G>T maps to NM_004811.2 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:151271223 G>A maps to NM_006726.3 R2439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:151837861 C>T maps to NM_006726.3 W225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr4:151231396 G>A maps to NM_006726.3 V2622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr4:151682954 G>A maps to NM_006726.3 I1875I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr4:151791752 A>G maps to NM_006726.3 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:151835475 G>A maps to NM_006726.3 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr4:151773050 G>A maps to NM_006726.3 R1271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:151271218 G>A maps to NM_006726.3 A2440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr4:151203625 C>T maps to NM_006726.3 T2775T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr4:151788951 C>T maps to NM_006726.3 K879K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19T-06A-11D-A19A-08 chr4:151773036 C>T maps to NM_006726.3 E1275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr4:151271269 C>T maps to NM_006726.3 W2423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:151509256 G>A maps to NM_006726.3 S2102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr4:151818911 G>A maps to NM_006726.3 F661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr13:47315946 C>T maps to NM_001164211.1 V752V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:47286725 C>T maps to NM_001164211.1 R550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:114422877 G>A did not map to a codon.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr23:114357342 G>A did not map to a codon.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr23:114357725 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:114357667 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:114347893 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:114347893 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:114357449 G>A did not map to a codon.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr23:114422903 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:114357709 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr23:114418998 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr3:197518307 G>A maps to ENST00000425562 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:197559097 C>T maps to ENST00000425562 R338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:100176274 G>A maps to NM_002319.3 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr7:100179448 G>A maps to NM_002319.3 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:100175157 G>A maps to NM_002319.3 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr7:100176055 G>A maps to NM_002319.3 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr7:100179447 G>A maps to NM_002319.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr7:100179957 G>A maps to NM_002319.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr7:100175319 G>A maps to NM_002319.3 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr7:100179448 G>A maps to NM_002319.3 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:100176356 G>A maps to NM_002319.3 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr7:100176341 G>A maps to NM_002319.3 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:100172795 G>A maps to NM_002319.3 F662F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:802266 G>A maps to NM_145886.3 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:803366 G>A maps to NM_145886.3 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:803207 G>A maps to NM_145886.3 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:802335 G>A maps to NM_145886.3 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:803339 G>A maps to NM_145886.3 N181N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:804256 G>A maps to NM_145886.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr19:39805547 G>A maps to NM_020862.1 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:39798443 C>T maps to NM_020862.1 Q715Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:39804944 G>A maps to NM_020862.1 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr19:39805673 G>A maps to NM_020862.1 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr19:39804581 G>A maps to NM_020862.1 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:39804578 G>A maps to NM_020862.1 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:39804911 C>T maps to NM_020862.1 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:39798740 G>A maps to NM_020862.1 A616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:39804950 C>T maps to NM_020862.1 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:39805082 G>A maps to NM_020862.1 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr6:40360530 G>A maps to NM_020737.1 I507I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr6:40399670 G>A maps to NM_020737.1 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr6:40400323 G>A maps to NM_020737.1 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:40359792 C>T maps to NM_020737.1 T753T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:40399544 G>A maps to NM_020737.1 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:40359792 C>T maps to NM_020737.1 T753T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:40399580 C>T maps to NM_020737.1 R424R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:40400105 C>T maps to NM_020737.1 E249E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:40360131 C>T maps to NM_020737.1 W640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:40399838 G>A maps to NM_020737.1 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:40400045 C>T maps to NM_020737.1 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:40400411 G>A maps to NM_020737.1 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:40400162 G>A maps to NM_020737.1 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr6:40360101 C>T maps to NM_020737.1 K650K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr6:40359882 G>A maps to NM_020737.1 S723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:40400561 C>T maps to NM_020737.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:40360047 C>T maps to NM_020737.1 Q668Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr6:40360350 C>T maps to NM_020737.1 K567K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr6:40359879 G>A maps to NM_020737.1 F724F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr6:40360140 C>T maps to NM_020737.1 R637R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr6:40359792 C>T maps to NM_020737.1 T753T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:40400540 G>A maps to NM_020737.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:40360359 G>A maps to NM_020737.1 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:40400381 G>A maps to NM_020737.1 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:40400462 G>A maps to NM_020737.1 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:40400504 C>T maps to NM_020737.1 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:40359879 G>A maps to NM_020737.1 F724F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr6:40400354 C>T maps to NM_020737.1 W166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:36435785 C>T maps to NM_024509.1 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:36430512 C>T maps to NM_024509.1 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr19:36430467 G>A maps to NM_024509.1 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:36431364 C>T maps to NM_024509.1 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr19:36435674 C>T maps to NM_024509.1 I547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr11:66626526 C>T maps to NM_024036.4 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:66626555 C>T maps to NM_024036.4 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr14:42361151 A>G maps to NM_152447.3 A695A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:42361004 G>A maps to NM_152447.3 K646K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:42360872 T>C maps to NM_152447.3 C602C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:42360716 C>T maps to NM_152447.3 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr14:42356112 C>T maps to NM_152447.3 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:42361076 G>A maps to NM_152447.3 R670R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:42356403 C>T maps to NM_152447.3 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr14:42357006 T>A maps to NM_152447.3 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:4538662 G>A maps to NM_052972.2 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr19:4538803 G>A maps to NM_052972.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr19:4538413 G>A maps to NM_052972.2 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:4538734 G>A maps to NM_052972.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:4538830 G>A maps to NM_052972.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr19:4538227 G>A maps to NM_052972.2 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:4538268 G>A maps to NM_052972.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:4538434 G>A maps to NM_052972.2 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr19:4538052 G>A maps to NM_052972.2 Q315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:4538662 G>A maps to NM_052972.2 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:4538809 G>A maps to NM_052972.2 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:133848261 C>T maps to NM_144648.1 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr7:133943149 C>T maps to NM_144648.1 T780T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:133827911 C>T maps to NM_144648.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:133812131 C>T maps to NM_144648.1 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr7:133932391 C>T maps to NM_144648.1 Q690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:133884015 C>T maps to NM_144648.1 I530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr7:133948699 C>T maps to NM_144648.1 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr3:66431951 C>T maps to NM_015541.2 P907P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr3:66430758 G>A maps to NM_015541.2 P1070P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:66433778 C>T maps to NM_015541.2 V706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:66430725 C>T maps to NM_015541.2 G1081G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:66449434 C>T maps to NM_015541.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:66457824 G>A maps to NM_015541.2 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:66460623 G>A maps to NM_015541.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr3:66431076 C>T maps to NM_015541.2 G993G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr3:66434511 G>A maps to NM_015541.2 F658F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr3:66512875 C>T maps to NM_015541.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:66433742 C>T maps to NM_015541.2 G718G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:66433645 G>A maps to NM_015541.2 Q751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:113657298 C>T maps to NM_014813.1 G777G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:113638979 C>T maps to NM_014813.1 Q362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:59266362 C>T maps to NM_153377.3 L1117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:59271440 G>A maps to NM_153377.3 V759V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr12:59272617 G>A maps to NM_153377.3 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr12:59308074 G>A maps to NM_153377.3 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:59274657 C>G maps to NM_153377.3 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:59276765 G>A maps to NM_153377.3 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26D-06A-11D-A19A-08 chr12:59268353 C>T maps to NM_153377.3 G899G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr10:85991787 C>T maps to NM_015613.2 R589R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:86001151 C>T maps to NM_015613.2 W15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:85997354 G>A maps to NM_015613.2 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:85992411 C>T maps to NM_015613.2 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr10:85984281 G>A maps to NM_001017924.2 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:85982029 G>A maps to NM_001017924.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:85984272 G>A maps to NM_001017924.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr10:85982089 G>T maps to NM_001017924.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:85984122 C>T maps to NM_001017924.2 W286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:85984533 G>A maps to NM_001017924.2 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr10:85981711 C>T maps to NM_001017924.2 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:85984761 C>T maps to NM_001017924.2 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr10:85981768 G>A maps to NM_001017924.2 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr10:85981768 G>A maps to NM_001017924.2 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:85984755 G>A maps to NM_001017924.2 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:85985237 G>T maps to NM_001017924.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr4:110791012 C>T maps to NM_198506.2 Q325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr4:110791479 G>A maps to NM_198506.2 K480K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr4:110790879 T>C maps to NM_198506.2 D280D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:110791707 C>T maps to NM_198506.2 F556F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr4:110791134 C>T maps to NM_198506.2 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:110788860 C>T maps to NM_198506.2 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr4:110791064 G>A maps to NM_198506.2 W342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:25232331 G>A maps to ENST00000354454 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr12:25232683 G>A maps to ENST00000354454 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr12:25243070 C>T maps to ENST00000354454 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr12:25243106 C>T maps to ENST00000354454 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:25260918 G>A maps to ENST00000354454 E531E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr12:25256966 C>T maps to ENST00000354454 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:57578890 C>T maps to NM_002332.2 R2122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr12:57579530 C>T maps to NM_002332.2 F2227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr12:57604513 C>T maps to NM_002332.2 C4256C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr12:57604514 C>A maps to NM_002332.2 R4257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:57569797 C>T maps to NM_002332.2 I1300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr12:57598416 C>T maps to NM_002332.2 F3693F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:57577213 C>A maps to NM_002332.2 P1905P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:57573328 C>T maps to NM_002332.2 V1652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:57571293 C>T maps to NM_002332.2 H1427H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr12:57577162 C>T maps to NM_002332.2 G1888G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:57578923 C>T maps to NM_002332.2 P2133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:57594820 C>T maps to NM_002332.2 I3410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:57561242 C>T maps to NM_002332.2 F977F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr12:57574472 C>T maps to NM_002332.2 Q1804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:57569830 C>T maps to NM_002332.2 L1311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:57591967 C>T maps to NM_002332.2 P3104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:57601894 C>T maps to NM_002332.2 G3978G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:57601895 C>T maps to NM_002332.2 R3979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr12:57570935 C>T maps to NM_002332.2 I1368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:57585134 C>T maps to NM_002332.2 F2423F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr12:57585107 C>T maps to NM_002332.2 I2414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:57579530 C>T maps to NM_002332.2 F2227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:57574143 C>T maps to NM_002332.2 L1756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr12:57600502 C>T maps to NM_002332.2 D3946D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:57598217 C>T maps to NM_002332.2 F3659F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:57598913 C>T maps to NM_002332.2 T3739T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:57584758 C>T maps to NM_002332.2 I2401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:57591085 G>A maps to NM_002332.2 E3027E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr12:57578671 C>T maps to NM_002332.2 I2079I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr12:57589162 G>A maps to NM_002332.2 E2806E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:57569779 C>A maps to NM_002332.2 P1294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:57574472 C>T maps to NM_002332.2 Q1804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr12:57573151 C>T maps to NM_002332.2 I1593I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr12:57599030 C>T maps to NM_002332.2 I3778I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:57569315 C>T maps to NM_002332.2 S1207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:57587457 C>T maps to NM_002332.2 I2598I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:57589507 C>T maps to NM_002332.2 F2835F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:57600305 C>T maps to NM_002332.2 L3881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:57600439 C>T maps to NM_002332.2 S3925S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr12:57549948 C>T maps to NM_002332.2 Q434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr12:57552263 C>T maps to NM_002332.2 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr12:57574528 C>T maps to NM_002332.2 V1822V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr12:57584635 G>A maps to NM_002332.2 R2360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:23346334 C>T maps to NM_014045.3 Q581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:23344855 C>T maps to NM_014045.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:23345368 C>T maps to NM_014045.3 F404F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:23344335 C>T maps to NM_014045.3 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr14:23346597 C>T maps to NM_014045.3 P668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr6:150164122 T>C maps to NM_032832.5 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr8:105511566 A>G maps to NM_013437.4 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:105521197 T>G maps to NM_013437.4 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr8:105511742 G>A maps to NM_013437.4 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:105509255 G>A maps to NM_013437.4 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr8:105510107 G>A maps to NM_013437.4 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:141777558 C>T maps to NM_018557.2 Q634Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr2:141777597 C>T maps to NM_018557.2 R621R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr2:141215197 C>T maps to NM_018557.2 G3216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr2:141625351 G>A maps to NM_018557.2 I1462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:141081560 G>A maps to NM_018557.2 R4139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr2:141215030 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr2:141253290 C>T maps to NM_018557.2 L2959L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr2:141625351 G>A maps to NM_018557.2 I1462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:141243006 G>A maps to NM_018557.2 I3110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:141108563 G>A maps to NM_018557.2 I3898I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:141201962 G>A maps to NM_018557.2 I3410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr2:141110551 G>A maps to NM_018557.2 Q3874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr2:141460023 C>T maps to NM_018557.2 W2041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr2:141806609 G>A maps to NM_018557.2 F578F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:141245206 A>T maps to NM_018557.2 C3074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:141200148 C>T maps to NM_018557.2 T3446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:141215149 C>T maps to NM_018557.2 G3232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:141641522 C>T maps to NM_018557.2 W1344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:141072506 G>A maps to NM_018557.2 L4268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:141083388 G>A maps to NM_018557.2 I4094I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:141751567 G>A maps to NM_018557.2 N880N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:141777573 C>T maps to NM_018557.2 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:141130634 C>T maps to NM_018557.2 W3570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:141771292 A>G maps to NM_018557.2 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:141208192 C>T maps to NM_018557.2 W3334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:141773429 C>T maps to NM_018557.2 R675R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:141762936 G>A maps to NM_018557.2 Q824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr2:141460004 G>A maps to NM_018557.2 I2047I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr2:141607770 G>A maps to NM_018557.2 F1613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr2:142567967 G>A maps to NM_018557.2 Q29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:141130634 C>T maps to NM_018557.2 W3570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:141459359 C>T maps to NM_018557.2 T2119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:141598488 C>T maps to NM_018557.2 R1704R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:141055394 C>A maps to NM_018557.2 G4317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:141135811 C>T maps to NM_018557.2 G3525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:141457987 G>A maps to NM_018557.2 S2210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:141474302 G>A maps to NM_018557.2 I1947I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:141625218 G>A maps to NM_018557.2 Q1507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:141806609 G>A maps to NM_018557.2 F578F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr2:141272282 A>G maps to NM_018557.2 H2736H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:141032144 C>T maps to NM_018557.2 V4330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:141250218 C>T maps to NM_018557.2 R3026R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:141598491 G>A maps to NM_018557.2 V1703V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:141135826 G>A maps to NM_018557.2 F3520F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:141135847 C>T maps to NM_018557.2 Q3513Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:141680541 C>T maps to NM_018557.2 W1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:141214113 G>A maps to NM_018557.2 A3291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:141108404 G>A maps to NM_018557.2 I3951I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr2:141283911 G>A maps to NM_018557.2 T2590T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr2:141812715 G>A maps to NM_018557.2 F507F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:141128854 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:141777597 C>T maps to NM_018557.2 R621R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:141607743 C>T maps to NM_018557.2 W1622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:142567857 A>G maps to NM_018557.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:141143548 G>A maps to NM_018557.2 Q3482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:141264455 G>A maps to NM_018557.2 F2810F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:141747167 C>T maps to NM_018557.2 K901K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:141747169 T>A maps to NM_018557.2 K901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:141528473 G>A maps to NM_018557.2 Q1868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr2:141665548 G>A maps to NM_018557.2 P1139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:142004864 T>A maps to NM_018557.2 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:141665488 C>T maps to NM_018557.2 G1159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr2:141215149 C>T maps to NM_018557.2 G3232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:141215149 C>T maps to NM_018557.2 G3232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:141607770 G>A maps to NM_018557.2 F1613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:141459359 C>T maps to NM_018557.2 T2119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:141473638 A>G maps to NM_018557.2 L1976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:141122323 G>A maps to NM_018557.2 F3679F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:141709477 G>A maps to NM_018557.2 F973F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:141299510 G>A maps to NM_018557.2 F2408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:141607770 G>A maps to NM_018557.2 F1613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:141215149 C>T maps to NM_018557.2 G3232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:141232863 G>A maps to NM_018557.2 G3156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:141773429 C>T maps to NM_018557.2 R675R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:141122353 T>C did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:141777597 C>T maps to NM_018557.2 R621R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr2:141072528 T>G maps to NM_018557.2 G4260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr2:141751585 G>A maps to NM_018557.2 S874S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:141250218 C>T maps to NM_018557.2 R3026R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr2:141812739 C>T maps to NM_018557.2 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:141055536 C>T maps to NM_018557.2 G4269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:141110551 G>A maps to NM_018557.2 Q3874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:141092025 G>A maps to NM_018557.2 P4073P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:141739789 T>C maps to NM_018557.2 R942R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr2:141130634 C>T maps to NM_018557.2 W3570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:141128789 C>T maps to NM_018557.2 L3611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:141215074 G>A maps to NM_018557.2 A3257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:141215149 C>T maps to NM_018557.2 G3232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:141473642 G>A maps to NM_018557.2 F1974F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:141607770 G>A maps to NM_018557.2 F1613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:141709477 G>A maps to NM_018557.2 F973F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:141709477 G>A maps to NM_018557.2 F973F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:141128411 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:141773415 C>T maps to NM_018557.2 W680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:140990790 C>T maps to NM_018557.2 K4588K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:141294267 G>A maps to NM_018557.2 S2508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr2:141458188 C>T maps to NM_018557.2 G2143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr2:141986779 C>T maps to NM_018557.2 W274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:141215149 C>T maps to NM_018557.2 G3232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:141777597 C>T maps to NM_018557.2 R621R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr2:141294207 G>A maps to NM_018557.2 L2528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:141986780 C>T maps to NM_018557.2 W274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr2:170097741 G>A maps to NM_004525.2 V1267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr2:170042065 G>A maps to NM_004525.2 I3264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:170127603 G>A maps to NM_004525.2 F710F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr2:170003351 G>A maps to NM_004525.2 I4236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr2:170127588 G>A maps to NM_004525.2 S715S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:170058348 G>A maps to NM_004525.2 T2747T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:170151128 G>A maps to NM_004525.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:170011011 G>A maps to NM_004525.2 Q4085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:170058369 G>A maps to NM_004525.2 T2740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr2:169995203 G>A maps to NM_004525.2 L4467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:170063062 G>A maps to NM_004525.2 F2389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:170068589 C>T maps to NM_004525.2 R2056R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:170038100 G>A maps to NM_004525.2 H3342H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:170002289 G>A maps to NM_004525.2 R4319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:170044543 G>A maps to NM_004525.2 I3088I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:170115566 G>A maps to NM_004525.2 N827N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:170136032 G>A maps to NM_004525.2 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:170145542 G>A maps to NM_004525.2 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:170063572 G>A maps to NM_004525.2 F2219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr2:170009448 C>T maps to NM_004525.2 G4107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr2:170013929 G>A maps to NM_004525.2 S3990S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:170097678 C>T maps to NM_004525.2 W1288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr2:170032973 G>A maps to NM_004525.2 T3506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr2:170027070 T>C maps to NM_004525.2 E3790E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:170150721 G>A maps to NM_004525.2 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:170062005 G>A maps to NM_004525.2 Y2566Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:170063344 C>T maps to NM_004525.2 R2295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:170103478 G>A maps to NM_004525.2 Q976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:170115596 C>T maps to NM_004525.2 T817T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:170139473 C>T maps to NM_004525.2 Q360Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr2:170062080 G>A maps to NM_004525.2 F2541F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:169995846 G>A maps to NM_004525.2 I4434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:170058348 G>T maps to NM_004525.2 T2747T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:170070349 G>A maps to NM_004525.2 R1953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr2:170013887 G>A maps to NM_004525.2 S4004S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr4:186296787 C>T maps to ENST00000362004 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr4:186288399 C>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:186295300 C>T maps to ENST00000362004 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:33695654 C>T maps to NM_002333.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:33695696 C>T maps to NM_002333.3 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:33696317 G>A maps to NM_002333.3 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr19:33695570 C>T maps to NM_002333.3 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:33696188 C>T maps to NM_002333.3 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:33697952 C>T maps to NM_002333.3 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr11:46900680 G>A maps to ENST00000256991 P1045P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr11:46911510 G>A maps to ENST00000256991 P737P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr11:46911849 G>A maps to ENST00000256991 H676H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr11:46900851 G>A maps to ENST00000256991 S988S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr11:46920196 G>A maps to ENST00000256991 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:46911082 C>A maps to ENST00000256991 G743G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:46916347 G>A maps to ENST00000256991 F489F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:46917528 A>C maps to ENST00000256991 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr11:46914567 C>T maps to ENST00000256991 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:46890563 G>A maps to ENST00000256991 I1649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:46897154 G>A maps to ENST00000256991 T1304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr11:46895100 G>A maps to ENST00000256991 R1470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:46911082 C>T maps to ENST00000256991 G743G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr11:46880824 G>A maps to ENST00000256991 I1854I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:46898810 C>T maps to ENST00000256991 V1117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr11:46893150 G>A maps to ENST00000256991 I1584I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:46914640 C>T maps to ENST00000256991 W572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:68125189 G>A maps to NM_002335.2 K187K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:68181316 C>T maps to NM_002335.2 F888F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr11:68153958 C>T maps to NM_002335.2 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:68216285 C>T maps to NM_002335.2 I1532I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:68181199 C>T maps to NM_002335.2 F849F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:68191087 G>A maps to NM_002335.2 L1053L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:68216525 G>A maps to NM_002335.2 T1612T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:68115393 C>T maps to NM_002335.2 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:68201133 G>A maps to NM_002335.2 G1276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:68154021 C>T maps to NM_002335.2 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:68191150 C>A maps to NM_002335.2 V1074V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:68193602 C>T maps to NM_002335.2 V1195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:68181169 C>T maps to NM_002335.2 V839V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr11:68192665 C>T maps to NM_002335.2 L1111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr11:68207323 C>T maps to NM_002335.2 N1476N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr11:68193563 G>A maps to NM_002335.2 K1182K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:68153958 C>T maps to NM_002335.2 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:68125198 G>A maps to NM_002335.2 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:68115618 C>T maps to NM_002335.2 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:68193596 C>T maps to NM_002335.2 G1193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr22:25753277 G>A maps to NM_001135772.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr22:25753278 G>A maps to NM_001135772.1 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr22:25753392 G>A maps to NM_001135772.1 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr22:25755849 G>A maps to NM_001135772.1 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr12:12334020 C>T maps to NM_002336.2 E443E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:12277575 G>A maps to NM_002336.2 S1490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr12:12311841 G>A maps to NM_002336.2 C904C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr12:12315232 C>A maps to NM_002336.2 G725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:12279652 G>A maps to NM_002336.2 H1428H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr12:12317380 G>A maps to NM_002336.2 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:53741396 G>A maps to NM_004631.3 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:53736905 G>A maps to NM_004631.3 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:53723074 G>A maps to NM_004631.3 T757T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:53726198 G>A maps to NM_004631.3 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:53728232 G>A maps to NM_004631.3 F553F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:53729860 G>A maps to NM_004631.3 I545I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:53722918 G>A maps to NM_004631.3 S809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr4:3519814 G>A maps to NM_002337.2 Q233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr4:3519815 G>A maps to NM_002337.2 N232N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:44171033 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:44152286 G>A maps to NM_133259.3 L939L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr2:44187736 G>A maps to NM_133259.3 Q509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:44174914 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr6:53778707 G>A maps to NM_018214.4 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:53764568 C>T maps to NM_018214.4 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr6:53747711 G>A maps to NM_018214.4 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:70004468 G>A maps to NM_201550.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:70004426 G>A maps to NM_201550.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr12:70003787 G>A maps to NM_201550.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr5:195068 G>A maps to NM_001080478.1 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr5:194849 G>A maps to NM_001080478.1 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr3:194080932 G>A maps to NM_001135057.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr3:194081661 C>T maps to NM_001135057.2 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr3:194081289 C>T maps to NM_001135057.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:194080773 G>A maps to NM_001135057.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:194080083 G>A maps to NM_001135057.2 C569C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:194080125 G>A maps to NM_001135057.2 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:194081265 G>A maps to NM_001135057.2 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr3:194080632 G>A maps to NM_001135057.2 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:194081018 G>A maps to NM_001135057.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:194080212 G>A maps to NM_001135057.2 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:194080728 G>A maps to NM_001135057.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:25594644 C>T maps to NM_017640.5 V1003V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:25450224 T>G did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:25581585 C>T maps to NM_017640.5 P975P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr6:25581165 C>T maps to NM_017640.5 S919S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr14:24529202 C>T maps to NM_138360.3 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr14:24525588 C>T maps to NM_138360.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr14:24528490 C>T maps to NM_138360.3 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr14:24533495 C>T maps to NM_138360.3 T1007T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:24529922 C>T maps to NM_138360.3 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:24526128 C>T maps to NM_138360.3 Q320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:24529220 C>T maps to NM_138360.3 I637I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr14:24534934 T>C maps to NM_138360.3 G1167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr14:24523607 C>T maps to NM_138360.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:24537877 C>T maps to NM_138360.3 F1256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:24524793 G>A maps to NM_138360.3 W216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr14:24526175 C>T maps to NM_138360.3 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:24528490 C>T maps to NM_138360.3 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:24529223 C>T maps to NM_138360.3 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr7:102574539 C>T maps to NM_001031692.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:102574797 G>A maps to NM_001031692.2 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:102574368 G>A maps to NM_001031692.2 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:102575031 C>T maps to NM_001031692.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr7:102574539 C>T maps to NM_001031692.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr10:50122161 G>A maps to NM_001006939.3 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr10:50121549 G>A maps to NM_001006939.3 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:50121666 G>A maps to NM_001006939.3 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:50122128 G>A maps to NM_001006939.3 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:50122011 C>T maps to NM_001006939.3 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr10:50121762 G>A maps to NM_001006939.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr10:50121465 G>A maps to NM_001006939.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:50121723 G>A maps to NM_001006939.3 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr10:50121504 C>T maps to NM_001006939.3 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:50121984 G>A maps to NM_001006939.3 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:50121438 C>T maps to NM_001006939.3 W254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:50121612 C>T maps to NM_001006939.3 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:50121996 G>A maps to NM_001006939.3 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:50121482 G>A maps to NM_001006939.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr10:50122128 G>A maps to NM_001006939.3 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr10:50121702 G>A maps to NM_001006939.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:26999653 G>A maps to NM_022901.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr3:46580619 G>A maps to NM_024512.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr3:46586694 G>A maps to NM_024512.3 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:46568950 G>A maps to NM_024512.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:72083682 G>A maps to NM_207119.1 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:72061175 G>A maps to NM_207119.1 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:72136259 G>A maps to NM_207119.1 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr10:72100348 G>A maps to NM_207119.1 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr10:72100312 G>A maps to NM_207119.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr12:7022118 G>A maps to NM_201650.2 Q328Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr12:7019056 C>T maps to NM_201650.2 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:7015067 G>A maps to NM_201650.2 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:7021921 C>T maps to NM_201650.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr12:7021926 C>T maps to NM_201650.2 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:7014913 C>T maps to NM_201650.2 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:18507725 C>T maps to NM_145256.2 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:18507059 G>A maps to NM_145256.2 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:18507677 C>T maps to NM_145256.2 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:18507006 C>T maps to NM_145256.2 W256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr10:134161691 G>A maps to NM_030626.2 W253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:134147045 C>T maps to NM_030626.2 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:134158053 C>T maps to NM_030626.2 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr10:134161710 C>T maps to NM_030626.2 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr15:99828119 C>T maps to NM_144598.2 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr15:99892587 C>T maps to NM_144598.2 R203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:99828049 G>T maps to NM_144598.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr15:99874191 C>T maps to NM_144598.2 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:67241579 T>C maps to NM_001004055.1 Q200Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr21:45876568 C>T maps to NM_030891.3 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr21:45876901 C>T maps to NM_030891.3 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:45877171 C>T maps to NM_030891.3 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:45877192 C>T maps to NM_030891.3 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr21:45877285 C>T maps to NM_030891.3 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr18:7231750 C>T maps to NM_001105581.1 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:7231408 G>A maps to NM_001105581.1 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr18:7231693 G>A maps to NM_001105581.1 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:7231186 G>A maps to NM_001105581.1 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:7231408 G>A maps to NM_001105581.1 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr18:7231687 C>T maps to NM_001105581.1 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:7231888 C>T maps to NM_001105581.1 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr3:169578433 G>A maps to NM_024727.2 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:169579542 G>A maps to NM_024727.2 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:169579557 C>T maps to NM_024727.2 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:169557847 A>T maps to NM_024727.2 A527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr3:169572721 G>A maps to NM_024727.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:76370872 G>A maps to NM_001128922.1 G588G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:76371340 G>A maps to NM_001128922.1 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:76372306 C>T maps to NM_001128922.1 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:76371862 G>A maps to NM_001128922.1 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:76371223 C>T maps to NM_001128922.1 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:76372012 G>A maps to NM_001128922.1 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:76370749 G>A maps to NM_001128922.1 I629I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:76371304 G>A maps to NM_001128922.1 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:76372306 C>T maps to NM_001128922.1 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr11:76371808 G>A maps to NM_001128922.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:76372144 G>A maps to NM_001128922.1 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr11:76371964 G>A maps to NM_001128922.1 D224D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:76372278 G>A maps to NM_001128922.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:76370809 G>A maps to NM_001128922.1 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:76370953 G>A maps to NM_001128922.1 T561T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:76371826 C>T maps to NM_001128922.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr11:76372351 G>A maps to NM_001128922.1 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26D-06A-11D-A19A-08 chr11:76371967 T>C maps to NM_001128922.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr3:196386714 C>T maps to NM_198565.1 N67N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:196387756 C>T maps to NM_198565.1 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr3:196381499 C>T maps to NM_198565.1 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:196388523 C>T maps to NM_198565.1 I670I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:169514630 T>C maps to NM_001172779.1 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:169526513 G>A maps to NM_001172779.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr16:67418796 T>G maps to NM_018296.5 Y690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:67412535 C>T maps to NM_018296.5 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr16:67416105 G>A maps to NM_018296.5 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:44626398 C>T maps to NM_001006607.2 I1298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:44626152 G>A maps to NM_001006607.2 Q1216Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:44626248 G>A maps to NM_001006607.2 L1248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:62865264 G>A maps to NM_199340.2 L976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:62856231 G>A maps to NM_199340.2 F1344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:62856738 C>T maps to NM_199340.2 Q1175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr17:62856146 G>A maps to NM_199340.2 L1373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:62856306 G>A maps to NM_199340.2 P1319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:62893303 G>A maps to NM_199340.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:62856627 C>T maps to NM_199340.2 R1212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:62855805 G>T maps to NM_199340.2 P1486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr17:62855898 G>A maps to NM_199340.2 S1455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:62855837 G>A maps to NM_199340.2 Q1476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:62859105 G>A maps to NM_199340.2 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr17:62856285 C>T maps to NM_199340.2 K1326K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:62854926 C>T maps to NM_199340.2 T1593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr17:62850749 G>A maps to NM_199340.2 A1624A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr17:62856552 G>A maps to NM_199340.2 F1237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr17:30376283 G>A maps to ENST00000327564 L876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:30348368 C>G maps to ENST00000327564 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:30348288 C>T maps to ENST00000327564 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:30348606 C>T maps to ENST00000327564 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr17:30374873 G>T maps to ENST00000327564 S806S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:30348963 C>T maps to ENST00000327564 Q294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:30348995 C>T maps to ENST00000327564 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:30348593 C>T maps to ENST00000327564 N170N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr17:30376190 C>T maps to ENST00000327564 F845F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr3:26751900 G>A maps to NM_052953.2 Q246Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:26751813 G>A maps to NM_052953.2 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr3:26751402 C>T maps to NM_052953.2 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:26751306 C>T maps to NM_052953.2 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:26751885 C>T maps to NM_052953.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:26751373 C>T maps to NM_052953.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr7:127668929 G>A maps to NM_022143.4 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:70644644 G>A maps to NM_017768.4 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:46763233 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:46751382 G>A maps to ENST00000254454 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:46745897 C>T maps to ENST00000254454 E640E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr1:54417911 G>A maps to NM_052940.3 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:54417926 C>T maps to NM_052940.3 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr1:54418139 A>G maps to NM_052940.3 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:54417989 C>T maps to NM_052940.3 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr12:122685131 G>A maps to NM_001098519.1 K515K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr12:122669235 C>T maps to NM_001098519.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:122674685 C>T maps to NM_001098519.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr12:122687913 C>T maps to NM_001098519.1 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:122685384 C>T maps to NM_001098519.1 I571I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:122669283 C>T maps to NM_001098519.1 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr12:122677395 C>T maps to NM_001098519.1 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:79984866 C>A maps to NM_144999.2 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:45914245 G>A maps to NM_033413.3 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:3698135 C>T maps to NM_020710.2 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr1:3703793 G>A maps to NM_020710.2 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr17:17896149 G>A maps to NM_031294.3 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:17880974 C>T maps to NM_031294.3 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:17891357 C>T maps to NM_031294.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr17:17900815 G>A maps to NM_031294.3 E289E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr15:71302156 C>T maps to NM_017691.3 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr15:71196914 C>T maps to NM_017691.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:71256159 C>T maps to NM_017691.3 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:71300832 C>T maps to NM_017691.3 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:51021652 C>T maps to NM_001080457.1 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:51022174 T>C maps to NM_001080457.1 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr19:51021118 G>A maps to NM_001080457.1 I617I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:51022432 G>A maps to NM_001080457.1 N179N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:51021076 G>A maps to NM_001080457.1 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:51022660 C>T maps to NM_001080457.1 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr19:51021672 G>A maps to NM_001080457.1 Q433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:51022435 G>A maps to NM_001080457.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr19:51022165 G>A maps to NM_001080457.1 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:51022435 G>A maps to NM_001080457.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:51022507 G>A maps to NM_001080457.1 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:51021508 G>A maps to NM_001080457.1 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:51020866 C>T maps to NM_001080457.1 K701K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:40135943 G>A maps to NM_020929.1 D633D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:40136747 G>A maps to NM_020929.1 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:40136897 C>T maps to NM_020929.1 W315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr11:40136804 C>T maps to NM_020929.1 Q346Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr11:40137650 C>T maps to NM_020929.1 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:40135964 C>T maps to NM_020929.1 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:40137124 G>A maps to NM_020929.1 Q240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:40136711 G>A maps to NM_020929.1 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:40136876 C>T maps to NM_020929.1 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:40137096 C>T maps to NM_020929.1 W249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr11:40136258 G>A maps to NM_020929.1 I528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:40136897 C>T maps to NM_020929.1 W315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:40137124 G>A maps to NM_020929.1 Q240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:40137830 C>T maps to NM_020929.1 K4K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:40137563 C>T maps to NM_020929.1 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:40136855 C>A maps to NM_020929.1 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:40136876 C>T maps to NM_020929.1 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:40136780 C>T maps to NM_020929.1 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:40137721 G>A maps to NM_020929.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:40137106 G>A maps to NM_020929.1 Q246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr11:40137422 C>T maps to NM_020929.1 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr11:40137206 G>A maps to NM_020929.1 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr11:40136897 C>T maps to NM_020929.1 W315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:40136381 G>A maps to NM_020929.1 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:40137206 G>A maps to NM_020929.1 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr16:84189323 C>T maps to NM_178452.4 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:84203606 G>A maps to NM_178452.4 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:84205902 C>T maps to NM_178452.4 F522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr16:84188260 C>T maps to NM_178452.4 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr16:84203942 C>T maps to NM_178452.4 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:165514117 C>T maps to NM_001005214.3 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:165513877 G>A maps to NM_001005214.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:165513785 C>T maps to NM_001005214.3 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:165533027 G>A maps to NM_001005214.3 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:165533036 C>T maps to NM_001005214.3 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:56949441 C>T maps to NM_001005210.2 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:56949696 C>T maps to NM_001005210.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:56954887 C>T maps to NM_001005210.2 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:56949682 C>T maps to NM_001005210.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr11:56950113 C>T maps to NM_001005210.2 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr11:56954764 C>T maps to NM_001005210.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:56954887 C>T maps to NM_001005210.2 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:56949831 C>T maps to NM_001005210.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:56954854 C>T maps to NM_001005210.2 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:56949921 C>T maps to NM_001005210.2 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr11:541581 G>T maps to NM_198075.3 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:551783 T>A maps to NM_198075.3 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:540746 G>A maps to NM_198075.3 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:551918 C>T maps to NM_198075.3 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:541604 G>A maps to NM_198075.3 E82E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:552634 G>A maps to NM_198075.3 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:42837367 C>T maps to NM_153260.2 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr17:48460399 T>A maps to NM_018509.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:133627302 G>A maps to ENST00000250173 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr8:133623587 G>A maps to ENST00000250173 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr8:133627288 G>A maps to ENST00000250173 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr8:133627306 G>A maps to ENST00000250173 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr8:133673736 G>C maps to ENST00000250173 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr8:133669118 C>T maps to ENST00000250173 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:133650207 G>A maps to ENST00000250173 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:150034717 C>T maps to NM_023942.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr7:150034460 G>T maps to NM_023942.2 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:150033973 G>A maps to NM_023942.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr4:52861585 G>A maps to NM_001024611.1 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr4:52860909 G>A maps to NM_001024611.1 Q760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:52862275 G>A maps to NM_001024611.1 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr4:52861300 G>A maps to NM_001024611.1 S629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr4:52861054 G>A maps to NM_001024611.1 F711F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr4:52861711 C>T maps to NM_001024611.1 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:52860895 C>T maps to NM_001024611.1 G764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:52861264 G>A maps to NM_001024611.1 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr1:70477587 C>T maps to NM_020794.2 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr1:70446076 C>T maps to NM_020794.2 Q205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr1:70503804 A>T maps to NM_020794.2 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:70494041 G>A maps to NM_020794.2 E623E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr1:70291500 C>T maps to NM_020794.2 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5VV-06A-11D-A32N-08 chr1:70488951 G>A maps to NM_020794.2 Q525Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:70505211 G>A maps to NM_020794.2 R1197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:70555435 T>G maps to NM_020794.2 P1455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:70504777 C>T maps to NM_020794.2 Q1053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:70226018 C>T maps to NM_020794.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:70452013 C>T maps to NM_020794.2 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:70505116 C>T maps to NM_020794.2 L1166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:70478724 G>A maps to NM_020794.2 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:70225937 C>T maps to NM_020794.2 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:70505259 C>T maps to NM_020794.2 S1213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:70504701 C>T maps to NM_020794.2 V1027V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr1:70541980 G>A maps to NM_020794.2 Q1446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr1:70541981 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:70573451 G>A maps to NM_020794.2 R1483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr1:70257736 C>T maps to NM_020794.2 N67N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:70460304 T>C maps to NM_020794.2 N293N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:70488849 G>A maps to NM_020794.2 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:70541867 C>T maps to NM_020794.2 Q1409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:70478772 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr9:131670603 C>T maps to NM_001127244.1 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr9:131669899 C>T maps to NM_001127244.1 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr9:131670363 C>T maps to NM_001127244.1 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr9:131670801 G>A maps to NM_001127244.1 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr9:131670622 C>T maps to NM_001127244.1 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:131670756 C>T maps to NM_001127244.1 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:90049684 C>T maps to NM_015350.2 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:90048541 G>A maps to NM_015350.2 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:90048490 G>A maps to NM_015350.2 Q94Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:90050180 C>T maps to NM_015350.2 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:90048329 C>T maps to NM_015350.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr1:90179796 C>T maps to NM_032270.4 I556I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:90179559 T>C maps to NM_032270.4 C477C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:90398923 C>T maps to NM_001134479.1 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr19:7964027 G>A maps to NM_025061.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:7964849 C>T maps to NM_025061.3 F481F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr19:7964837 C>T maps to NM_025061.3 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr8:86042231 C>T maps to NM_033402.4 R569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:86044123 A>G maps to NM_033402.4 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr8:86043994 G>A maps to NM_033402.4 R589R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr8:86038925 C>T maps to NM_033402.4 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:86041442 C>T maps to NM_033402.4 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr8:86044156 C>T maps to NM_033402.4 F643F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:86049711 C>T maps to NM_033402.4 A781A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:238672404 C>T maps to NM_001137552.1 T683T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:238680783 C>A maps to ENST00000391999 R514R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr12:85518178 C>T maps to NM_001079910.1 Q1297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr12:85500320 G>A maps to NM_001079910.1 W1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:85554409 C>T maps to NM_001079910.1 A1580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr12:85492148 G>A maps to NM_001079910.1 L968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr12:85450856 G>A maps to NM_001079910.1 K762K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:85466850 C>T maps to NM_001079910.1 F954F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr12:85546092 C>T maps to NM_001079910.1 S1455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:85518213 C>A maps to NM_001079910.1 P1308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:85450848 C>T maps to NM_001079910.1 Q760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr12:85546800 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:74507519 C>T maps to NM_001105659.1 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:74507176 G>A maps to NM_001105659.1 Q480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:74575122 G>A maps to NM_001105659.1 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:74648260 G>A maps to NM_001105659.1 N178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:74506973 C>T maps to NM_001105659.1 E547E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:74492505 C>T maps to NM_001105659.1 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:74492523 A>G maps to NM_001105659.1 F616F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:74506958 A>G maps to NM_001105659.1 V552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:74507519 C>T maps to NM_001105659.1 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:74575134 C>T maps to NM_001105659.1 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:74492505 C>T maps to NM_001105659.1 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr3:169540092 C>T maps to NM_001080460.1 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:169540425 C>T maps to NM_001080460.1 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:169540284 C>T maps to NM_001080460.1 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr3:169540494 C>T maps to NM_001080460.1 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr3:169540642 C>T maps to NM_001080460.1 Q312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr3:169540521 G>A maps to NM_001080460.1 K271K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:169540260 C>T maps to NM_001080460.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:169539933 C>T maps to NM_001080460.1 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:169539940 C>T maps to NM_001080460.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:169540206 G>A maps to NM_001080460.1 K166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:169540248 C>T maps to NM_001080460.1 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:169540350 G>A maps to NM_001080460.1 Q214Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr3:169540326 G>A maps to NM_001080460.1 E206E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:169540425 C>T maps to NM_001080460.1 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr3:169539795 C>T maps to NM_001080460.1 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr15:101562660 C>T maps to NM_024652.3 I642I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr15:101595205 C>T maps to NM_024652.3 I1370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr15:101523786 C>T maps to NM_024652.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:101549205 C>T maps to NM_024652.3 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:101593216 C>T maps to NM_024652.3 A1260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:101569170 C>T maps to NM_024652.3 F899F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr15:101528918 C>T maps to NM_024652.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr15:101528918 C>T maps to NM_024652.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:101606017 G>A maps to NM_024652.3 L1792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr15:101593578 C>T maps to NM_024652.3 L1336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:101562663 C>T maps to NM_024652.3 I643I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr12:40687407 C>T maps to NM_198578.3 Y917Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr12:40657609 G>A maps to NM_198578.3 R521R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:40745495 C>T maps to NM_198578.3 L2179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr12:40689421 G>A maps to NM_198578.3 T1024T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:40687345 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:40745534 G>A maps to NM_198578.3 E2192E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:40699675 G>A maps to NM_198578.3 G1289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr12:40702472 C>T maps to NM_198578.3 L1388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr12:40692937 C>T maps to NM_198578.3 P1125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr12:40702499 T>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr12:40758796 A>T maps to NM_198578.3 I2445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:40689436 G>A maps to NM_198578.3 Q1029Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:40717019 C>T maps to NM_198578.3 A1856A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:40728918 C>T maps to NM_198578.3 L1970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:40716174 G>A maps to NM_198578.3 W1791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:3887641 C>T maps to NM_020873.5 I439I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr3:3887119 G>A maps to NM_020873.5 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr3:3887656 C>T maps to NM_020873.5 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr3:3886861 G>A maps to NM_020873.5 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:3886558 C>T maps to NM_020873.5 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:3886705 G>A maps to NM_020873.5 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:3887125 C>T maps to NM_020873.5 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:3887428 C>T maps to NM_020873.5 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:3887533 C>T maps to NM_020873.5 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:3888295 G>A maps to NM_020873.5 K657K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:3887536 A>G maps to NM_020873.5 E404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr3:3886712 C>T maps to NM_020873.5 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:3886861 G>A maps to NM_020873.5 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:3887075 C>T maps to NM_020873.5 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:3887224 C>T maps to NM_020873.5 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A264-06A-11D-A196-08 chr3:3887650 G>A maps to NM_020873.5 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:3887647 G>A maps to NM_020873.5 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:204587773 G>A maps to NM_201630.1 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:204587152 C>T maps to NM_201630.1 R656R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:204588391 G>A maps to NM_201630.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:204588310 C>T maps to NM_201630.1 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr1:204587038 C>T maps to NM_201630.1 R694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:204587209 G>A maps to NM_201630.1 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:204588010 G>A maps to NM_201630.1 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:204588112 C>T maps to NM_201630.1 Q336Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:204587953 G>A maps to NM_201630.1 F389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:6021913 C>T maps to NM_152611.3 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr20:6022300 C>T maps to NM_152611.3 E530E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr20:6025271 C>T maps to NM_152611.3 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr20:6022123 C>T maps to NM_152611.3 T589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:6022129 C>T maps to NM_152611.3 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:6022606 C>T maps to NM_152611.3 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:62455824 G>A maps to NM_203422.2 H52H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:80529997 C>T maps to NM_178839.4 W316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:80530035 C>T maps to NM_178839.4 W303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr2:80529462 C>T maps to NM_178839.4 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:80530935 G>A maps to NM_178839.4 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:80530635 G>A maps to NM_178839.4 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr5:138209493 C>T maps to NM_015564.2 W252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr5:138209933 G>A maps to NM_015564.2 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr5:138208983 C>T maps to NM_015564.2 R422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr10:68687177 C>T maps to NM_178011.3 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr10:68687115 C>T maps to NM_178011.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:68687189 C>T maps to NM_178011.3 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr10:68857448 G>A maps to NM_178011.3 T547T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:68688164 G>A maps to NM_178011.3 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:68857448 G>A maps to NM_178011.3 T547T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:68687036 C>T maps to NM_178011.3 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:68857448 G>A maps to NM_178011.3 T547T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:68688077 C>T maps to NM_178011.3 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr2:77745769 G>A maps to NM_001134745.1 Q409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:77745539 A>C maps to NM_001134745.1 Y485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr2:76975868 G>A maps to NM_001134745.1 I575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:76975906 G>A maps to NM_001134745.1 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:77746079 G>A maps to NM_001134745.1 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:76975988 G>A maps to NM_001134745.1 I535I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:77745842 G>A maps to NM_001134745.1 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr2:76975988 G>A maps to NM_001134745.1 I535I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:76975894 G>A maps to NM_001134745.1 R567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:130251787 C>T maps to NM_001005374.2 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:130255172 C>T maps to NM_001005374.2 I532I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:130219602 C>T maps to NM_001005374.2 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr9:130263418 G>A maps to NM_001005374.2 R681R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:54958912 G>A maps to NM_020678.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr3:54952854 C>T maps to NM_020678.2 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr3:54952521 C>T maps to NM_020678.2 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:54958919 G>A maps to NM_020678.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr3:54952650 G>A maps to NM_020678.2 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr3:54959204 G>A maps to NM_020678.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:54952602 G>A maps to NM_020678.2 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:54952851 G>A maps to NM_020678.2 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr3:54952851 G>A maps to NM_020678.2 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr3:54958889 G>A maps to NM_020678.2 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr3:54952868 T>A maps to NM_020678.2 K219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr3:54952851 G>A maps to NM_020678.2 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:54952569 G>A maps to NM_020678.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:54958994 G>A maps to NM_020678.2 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:54959230 G>A maps to NM_020678.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr3:54952860 G>A maps to NM_020678.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:1940341 C>T maps to NM_001163926.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:1943721 C>T maps to NM_001163926.1 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr12:1940100 G>A maps to NM_001163926.1 W23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr12:1943664 G>A maps to NM_001163926.1 Q297Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:1940296 C>T maps to NM_001163926.1 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:1943502 C>T maps to NM_001163926.1 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:71804596 G>A maps to NM_145309.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:102106287 C>T maps to NM_152892.1 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:102106641 C>T maps to NM_152892.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr7:102108810 G>A maps to NM_152892.1 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:115561417 G>A maps to NM_002338.3 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:115805320 G>A maps to NM_002338.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:115805177 G>A maps to NM_002338.3 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:194369448 G>A maps to NM_018385.2 R502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:194369449 G>A maps to NM_018385.2 H501H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:194379757 G>A maps to NM_018385.2 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:36859697 G>A maps to NM_032881.1 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:36859376 G>C maps to NM_032881.1 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr1:36859385 C>T maps to NM_032881.1 W115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr5:157178449 G>A maps to NM_173491.2 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:157178437 C>T maps to NM_173491.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:34712525 C>T maps to NM_001114093.1 F417F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr19:34712639 T>C maps to NM_001114093.1 Y455Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:34699852 C>T maps to NM_001114093.1 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:34712525 C>T maps to NM_001114093.1 F417F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr20:60701391 C>T maps to NM_144703.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr20:60705701 C>T maps to NM_144703.2 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr3:14239576 T>C maps to NM_014463.2 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr3:14239546 G>A maps to NM_014463.2 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:2328388 C>A maps to NM_016199.2 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:1908750 G>A maps to ENST00000381758 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:1908759 G>A maps to ENST00000381758 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr19:35753455 C>T maps to NM_205834.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr19:35757838 A>C maps to NM_205834.2 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr21:47627359 G>A maps to NM_002340.5 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr12:21242919 G>A maps to ENST00000381541 R622R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CC-06A-11D-A19A-08 chr12:21205149 T>G maps to ENST00000381541 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:21196485 A>T maps to ENST00000381541 K290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:21172305 C>T maps to ENST00000381541 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr12:21229491 C>T maps to ENST00000381541 S592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:21172302 C>T maps to ENST00000381541 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr12:21168706 C>T maps to ENST00000381541 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:21172236 G>A maps to ENST00000381541 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:21205141 C>T maps to ENST00000381541 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr12:21172236 G>A maps to ENST00000381541 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr12:21199993 C>T maps to ENST00000381541 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:21172236 G>A maps to ENST00000381541 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:21196325 C>T maps to ENST00000381541 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:21196346 C>T maps to ENST00000381541 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:21242928 C>T maps to ENST00000381541 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr12:21172236 G>A maps to ENST00000381541 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:21172236 G>A maps to ENST00000381541 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:21229479 G>A maps to ENST00000381541 R588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr12:21196277 G>A maps to ENST00000381541 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr12:21196325 C>T maps to ENST00000381541 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:21196325 C>T maps to ENST00000381541 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:21205028 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:21207552 T>C maps to ENST00000381541 Y529Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:21242994 C>T maps to ENST00000381541 F647F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:31555455 C>T maps to NM_007161.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr6:31541100 G>A maps to NM_000595.2 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:31541202 G>A maps to NM_000595.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr6:31541283 C>T maps to NM_000595.2 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr6:31541415 C>T maps to NM_000595.2 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr6:31541256 C>T maps to NM_000595.2 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:31540582 C>T maps to NM_000595.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:31540724 C>T maps to NM_000595.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:31541392 C>T maps to NM_000595.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:96429167 G>A maps to NM_000895.1 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:96421284 G>A maps to NM_000895.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:31550179 C>T maps to NM_002341.1 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:31550167 C>T maps to NM_002341.1 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr14:24785180 C>T maps to NM_181657.3 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:24780542 C>T maps to ENST00000336557 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr2:33525516 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr2:33518320 C>T maps to ENST00000354476 T1070T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:33477783 C>T maps to ENST00000354476 Y680Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr2:33173950 C>T maps to ENST00000354476 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:33487838 C>T maps to ENST00000354476 P823P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr2:33585817 A>G maps to ENST00000354476 E1386E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:33505207 G>A maps to ENST00000354476 W1033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:33572503 C>T maps to ENST00000354476 F1310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:33413824 C>T maps to ENST00000354476 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:33484667 C>T maps to ENST00000354476 P803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:33498837 G>A maps to ENST00000354476 R912R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:33623610 G>A maps to ENST00000354476 *1723*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-FS-A1Z3-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:33413644 G>A maps to ENST00000354476 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:33540298 G>A maps to ENST00000354476 Q1232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:33585683 C>T maps to ENST00000354476 Q1342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr2:33412022 C>T maps to ENST00000354476 V434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:33246024 A>G maps to ENST00000354476 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:33622329 G>A maps to ENST00000354476 T1656T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr14:74995672 G>A maps to NM_000428.2 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr14:75078536 C>T maps to NM_000428.2 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr14:75022392 G>A maps to NM_000428.2 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr14:75018995 G>A maps to NM_000428.2 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr14:75052642 C>T maps to NM_000428.2 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:74978062 G>A maps to NM_000428.2 I971I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:75017892 G>A maps to NM_000428.2 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:75078536 C>T maps to NM_000428.2 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr14:75022266 G>A maps to NM_000428.2 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr14:74975334 G>A maps to NM_000428.2 V1208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:74975995 G>A maps to NM_000428.2 S1116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:74976527 G>A maps to NM_000428.2 P1062P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:75017967 C>T maps to NM_000428.2 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:65321710 G>A maps to NM_001130144.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:65321711 G>A maps to NM_001130144.2 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr11:65321218 G>A maps to NM_001130144.2 Q273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:65313967 G>A maps to NM_001130144.2 F766F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr11:65315176 C>T maps to NM_001130144.2 G654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr11:65309085 G>A maps to NM_001130144.2 Q904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:65313967 G>A maps to NM_001130144.2 F766F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:65315421 G>A maps to NM_001130144.2 Y605Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr11:65309152 C>T maps to NM_001130144.2 G881G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:65318930 C>T maps to NM_001130144.2 E521E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:65319620 G>A maps to NM_001130144.2 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr19:41125250 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:41128897 G>T maps to ENST00000308370 A1242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr19:41113435 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:41129548 G>A maps to ENST00000308370 K1265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:6499961 C>T maps to NM_002342.1 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr3:46485062 G>A maps to NM_002343.3 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:46495813 G>A maps to NM_002343.3 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:46491347 C>T maps to NM_002343.3 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr3:46490374 C>T maps to NM_002343.3 E397E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:46496876 G>A maps to NM_002343.3 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:46487984 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr3:46480831 C>T maps to NM_002343.3 R621R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr3:46506327 G>A maps to NM_002343.3 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:41799416 G>A maps to NM_002344.5 R473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:41797933 G>A maps to NM_002344.5 F558F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr15:41797410 G>A maps to NM_002344.5 I640I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:41803692 C>T maps to NM_002344.5 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:41797461 C>T maps to NM_002344.5 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:249083 G>A maps to NM_201412.1 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr16:239274 G>A maps to NM_201412.1 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr7:139106911 C>T maps to NM_016019.2 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:48827943 G>A maps to ENST00000393227 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3BZ-06A-12D-A196-08 chr12:91502122 A>G maps to NM_002345.3 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr12:91502534 C>T maps to NM_002345.3 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:91502720 C>T maps to NM_002345.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:91502582 C>T maps to NM_002345.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:91502720 C>T maps to NM_002345.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:91498067 G>A maps to NM_002345.3 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:91502501 G>A maps to NM_002345.3 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr12:91502141 G>A maps to NM_002345.3 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:91502728 G>A maps to NM_002345.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:23417850 G>A maps to NM_001142546.1 S968S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:23418945 C>T maps to NM_001142546.1 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:23418815 G>A maps to NM_001142546.1 R647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:24936033 C>T maps to NM_001009909.2 Q158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr11:25100134 G>A maps to NM_001009909.2 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:25098951 G>A maps to NM_001009909.2 Q312Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:24784835 C>T maps to NM_001009909.2 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr11:25004712 C>A maps to NM_001009909.2 C213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:24759823 G>A maps to NM_001009909.2 E103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:24936032 C>T maps to NM_001009909.2 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr11:25071619 C>T maps to NM_001009909.2 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:114537897 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:114540848 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:114541097 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:114537893 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:114541217 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:31639821 C>T maps to ENST00000375873 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:31639770 C>T maps to ENST00000375873 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:31647022 C>T maps to NM_025262.3 W48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:31647023 C>T maps to NM_025262.3 W48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr6:31686914 G>A maps to NM_025261.1 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:31687067 G>A maps to NM_025261.1 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:31675735 G>A maps to ENST00000375834 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr6:31678183 G>A maps to NM_001003693.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:31675319 C>T maps to ENST00000375834 H46H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:143784629 C>T maps to ENST00000292430 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr8:143784536 G>A maps to ENST00000292430 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:143784662 G>A maps to ENST00000292430 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr2:160738734 C>T maps to NM_001198759.1 W382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr2:160738735 C>T maps to NM_001198759.1 W382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:160734850 C>T maps to NM_001198759.1 W586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:160735847 C>T maps to NM_001198759.1 E479E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:160714960 G>A maps to NM_001198759.1 G765G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:160688298 T>G did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:160706969 T>C maps to NM_001198759.1 L964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:160750530 C>A maps to NM_001198759.1 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:160741673 C>T maps to NM_001198759.1 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:160672033 G>A maps to NM_001198759.1 I1477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:160732020 G>A maps to NM_001198759.1 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr2:160755340 C>T maps to NM_001198759.1 W108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr2:160734988 G>A maps to NM_001198759.1 Y540Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:160667115 G>A maps to NM_001198759.1 I1540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr2:160692156 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:6626592 C>T maps to NM_004271.3 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:6625157 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:6626577 A>G maps to NM_004271.3 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr6:6626622 C>T maps to NM_004271.3 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr1:160788006 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:160786615 G>A maps to ENST00000263285 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr1:160769831 T>C maps to ENST00000263285 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:160793354 A>C maps to ENST00000263285 S533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr1:160784288 A>C maps to ENST00000263285 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:160788032 G>A maps to ENST00000263285 W456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:160771613 C>T maps to NM_001033667.1 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:160766090 C>T maps to ENST00000263285 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:160793253 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:160769729 G>A maps to ENST00000263285 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:160784447 G>A maps to ENST00000263285 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:160786539 C>G maps to ENST00000263285 S410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:160771658 C>T maps to NM_001033667.1 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:160784354 G>A maps to ENST00000263285 E292E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:160797599 C>T maps to ENST00000263285 F655F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr1:160769864 C>T maps to ENST00000263285 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr1:160769762 C>T maps to ENST00000263285 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:160766090 C>T maps to ENST00000263285 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:160784396 G>A maps to ENST00000263285 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:160786438 C>T maps to ENST00000263285 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:160784357 G>A maps to ENST00000263285 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:160793420 C>T maps to ENST00000263285 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:74903689 C>T maps to NM_015364.4 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr8:74917079 G>A maps to NM_015364.4 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:74917029 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:74922260 C>T maps to NM_015364.4 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:99907774 G>A maps to NM_174898.2 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q1-06A-21D-A196-08 chr2:99861802 G>T maps to NM_175735.3 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:99861748 C>T maps to NM_175735.3 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:99860565 C>T maps to NM_175735.3 W139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:99860573 G>A maps to NM_175735.3 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr2:99861919 C>T maps to NM_175735.3 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr8:56912055 C>T maps to NM_002350.2 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr8:56879415 G>A maps to NM_002350.2 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr8:56879361 C>T maps to NM_002350.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:56882294 G>A maps to NM_002350.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:56910936 G>A maps to NM_002350.2 K361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:56922569 G>A maps to NM_002350.2 W480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr8:56860175 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:56863068 C>T maps to NM_002350.2 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr8:56866537 G>A maps to NM_002350.2 W262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:143846517 G>A maps to NM_023946.2 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr8:143857011 G>A maps to NM_023946.2 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr8:143846091 G>A maps to NM_023946.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZY-06A-11D-A197-08 chr8:143846511 C>T maps to NM_023946.2 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:143846154 G>A maps to NM_023946.2 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr2:133403806 G>A maps to ENST00000409034 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:143831739 C>T maps to NM_205545.1 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:43967919 G>A maps to NM_014400.2 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:43965847 G>A maps to NM_014400.2 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr19:42342324 C>T maps to NM_173506.4 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:42341249 G>A maps to NM_173506.4 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:42342117 C>T maps to NM_173506.4 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:42341399 G>A maps to NM_173506.4 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:42342964 G>A maps to NM_173506.4 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:42341249 G>A maps to NM_173506.4 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:150327243 C>T maps to NM_194317.3 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr2:150069602 C>T maps to NM_177964.3 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:24120984 C>T maps to NM_007260.2 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr1:24119679 T>C maps to NM_007260.2 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:219347256 C>T maps to NM_138794.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:219385018 G>A maps to NM_138794.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:90347063 G>A maps to NM_020466.4 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr6:5216855 G>A maps to NM_001164840.1 R68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr12:25357092 C>T maps to NM_001001660.2 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:151133435 G>A maps to NM_212551.4 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:151134285 G>A maps to NM_212551.4 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:151133435 G>A maps to NM_212551.4 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:89815202 G>A maps to NM_198273.1 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:89815238 A>T maps to NM_198273.1 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr15:100269696 G>A maps to NM_152449.2 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr15:100269447 G>A maps to NM_152449.2 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr1:235907410 T>G maps to NM_000081.2 V2673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:235973316 T>C maps to NM_000081.2 K267K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:235950600 G>A maps to NM_000081.2 F1587F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:235973802 G>A maps to NM_000081.2 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr1:235967803 C>T maps to NM_000081.2 K1185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:235922486 G>A maps to NM_000081.2 S2222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:235891378 A>G maps to NM_000081.2 S3053S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:235887327 C>T maps to NM_000081.2 K3105K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:235950642 T>C maps to NM_000081.2 K1573K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:235866166 G>A maps to NM_000081.2 A3418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:235973732 G>A maps to NM_000081.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:235860521 G>A maps to NM_000081.2 S3475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:235929508 T>C maps to NM_000081.2 A1997A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr1:235860389 C>T maps to NM_000081.2 K3519K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:235955366 G>T maps to NM_000081.2 S1392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:235904727 G>A maps to NM_000081.2 S2784S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr11:10585850 C>T maps to NM_006691.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:10585562 C>T maps to NM_006691.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr11:10580717 G>A maps to NM_006691.3 N303N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr11:10585541 C>T maps to NM_006691.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr12:69743969 G>A maps to NM_000239.2 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr10:29578078 G>A maps to NM_032517.4 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:29580894 G>A maps to NM_032517.4 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr10:29599984 C>T maps to NM_032517.4 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:30915751 G>A maps to NM_183058.2 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:42445548 C>T maps to NM_144634.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr17:34263769 C>T maps to NM_020426.1 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr17:34263790 C>T maps to NM_020426.1 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:34266252 C>T maps to NM_020426.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr3:45872563 C>G did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr3:45874550 G>A maps to NM_020347.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr22:21348481 C>T maps to NM_006767.3 I513I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:21348892 A>T maps to NM_006767.3 A554A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr22:21348030 C>T maps to NM_006767.3 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:21340171 C>T maps to NM_006767.3 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr22:21340177 C>T maps to NM_006767.3 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr22:21350143 C>T maps to NM_006767.3 I684I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr8:20110388 G>A maps to NM_021020.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr10:102763364 C>G maps to NM_032429.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:102763646 C>T maps to NM_032429.2 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:102763706 C>T maps to NM_032429.2 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr12:9096119 G>A maps to NM_002355.2 N155N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr13:36049942 G>A maps to NM_005584.4 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:36049678 C>T maps to NM_005584.4 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr4:151504945 G>A maps to NM_006439.4 K255K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr4:151505188 G>A maps to NM_006439.4 E336E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr4:151505095 G>T maps to NM_006439.4 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr4:151504273 C>T maps to NM_006439.4 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr7:20199779 C>T maps to NM_182762.3 W68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:20197850 C>T maps to NM_182762.3 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr7:20197850 C>T maps to NM_182762.3 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:20199779 C>T maps to NM_182762.3 W68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:20198402 G>A maps to NM_182762.3 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:20198605 A>G maps to NM_182762.3 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:20198180 G>A maps to NM_182762.3 V601V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:20180763 G>A maps to NM_182762.3 A788A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr1:39549970 G>A maps to ENST00000361689 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:39934315 C>T maps to ENST00000361689 V5202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:39854047 C>T maps to ENST00000361689 A3116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr1:39788665 C>T maps to ENST00000361689 L1413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:39782104 T>C maps to ENST00000361689 A1169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:39801934 C>T maps to ENST00000289893 L1665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:39802079 A>T maps to ENST00000289893 K1714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:39818803 G>A maps to ENST00000361689 S1713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:39945527 C>T maps to ENST00000361689 S5251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:39945528 C>T maps to ENST00000361689 Q5252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr1:39801577 C>T maps to ENST00000289893 T1546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:39913437 C>T maps to ENST00000361689 F4553F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr1:39824448 C>T maps to ENST00000361689 A1946A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:39815238 C>T maps to ENST00000361689 H1573H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:39847727 C>T maps to ENST00000361689 L2522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:39824859 C>T maps to ENST00000361689 L1994L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:39763386 C>T maps to ENST00000361689 S822S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:39812800 G>A maps to ENST00000289893 Q2018Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:39765949 C>T maps to ENST00000361689 I855I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:39905144 C>T maps to ENST00000361689 I4081I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:39797698 C>T maps to ENST00000289893 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:39926464 C>T maps to ENST00000361689 S5115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:39823111 C>T maps to ENST00000361689 A1768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:39824416 C>T maps to ENST00000361689 Q1936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:39798745 T>C maps to ENST00000289893 P602P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr1:39835859 T>C did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:39893907 C>T maps to ENST00000361689 F3522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr1:39788335 C>T maps to ENST00000361689 S1367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:39788362 C>T maps to ENST00000361689 S1376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:39799708 C>T maps to ENST00000289893 S923S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:63918756 G>A maps to NM_014067.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr20:15967390 G>A maps to ENST00000310348 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr20:15210649 T>C maps to ENST00000310348 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr20:15210697 C>T maps to ENST00000310348 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:15967378 G>A maps to ENST00000310348 E331E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr20:15967370 G>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:15967390 G>A maps to ENST00000310348 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:14066289 C>T maps to ENST00000310348 Q63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:15843463 C>T maps to ENST00000310348 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:1976461 G>A maps to NM_003550.2 R556R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:2108855 G>A maps to NM_003550.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:2108854 G>A maps to NM_003550.2 Q398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr7:2262314 C>T maps to NM_003550.2 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr7:2255795 G>A maps to NM_003550.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:120981380 C>A maps to NM_002358.3 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:11736151 G>A maps to ENST00000376669 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:11735726 G>A maps to ENST00000376669 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:498502 G>A maps to NM_130760.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:504925 G>A maps to NM_130760.2 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:47308071 C>T maps to NM_003682.3 F880F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:47315488 C>T maps to NM_003682.3 S1157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:47304126 C>T maps to NM_003682.3 I555I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:47330883 C>T maps to NM_003682.3 F1328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:47299717 G>T maps to NM_003682.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:47303980 C>T maps to NM_003682.3 Q507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:47330564 G>A maps to NM_003682.3 E1301E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:47303196 C>T maps to NM_003682.3 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr4:1309273 C>A maps to ENST00000505177 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr4:1332302 C>T maps to ENST00000505177 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:1309240 C>T maps to ENST00000505177 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:1309273 C>T maps to ENST00000505177 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:1332317 C>T maps to ENST00000505177 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr1:166974496 C>T maps to NM_032858.1 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:166963284 C>T maps to NM_032858.1 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:166973516 G>A maps to NM_032858.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr1:166987156 G>A maps to NM_032858.1 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:166959059 G>A maps to NM_032858.1 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:166959041 G>A maps to NM_032858.1 K67K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:166961962 C>T maps to NM_032858.1 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:166973531 C>T maps to NM_032858.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:166959041 G>A maps to NM_032858.1 K67K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:166973432 G>A maps to NM_032858.1 K180K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:166990347 C>T maps to NM_032858.1 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:166991076 C>T maps to NM_032858.1 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr8:144511676 C>T maps to NM_201589.3 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q1-06A-21D-A196-08 chr20:39317283 C>T maps to NM_005461.3 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr7:1579890 C>T maps to NM_002360.3 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr19:35801451 C>T maps to NM_002361.3 R508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:35801492 C>T maps to NM_002361.3 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr19:35801483 C>T maps to NM_002361.3 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:35790526 G>A maps to NM_002361.3 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:35786519 C>T maps to NM_002361.3 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:35800924 C>T maps to NM_002361.3 F460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:35803182 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:152482128 G>A did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:152482211 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr23:152482451 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:152482274 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:152482822 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:152482446 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:152482457 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr23:152482816 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:152482328 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:152482398 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:151303171 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:151303811 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:151303924 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr23:151303976 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:151303401 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:151303935 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr23:151303843 A>C did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:151303094 G>A did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:151303314 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:151303791 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:151303318 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:151303486 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr23:151303171 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:151303973 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr23:151304039 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:151303506 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:151303845 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr23:151303952 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:151303156 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:151303171 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr23:151303156 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:151303918 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr23:151303260 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:151303198 C>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:151303860 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:151303873 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:151303882 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:151303924 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:151304044 A>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:151304070 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr23:151303863 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:151303336 C>T did not map to a codon.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr23:151303506 G>A did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:151303506 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:148798383 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr23:148798421 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:148797440 C>T did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:148798376 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:148797941 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr23:148798209 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr23:148797874 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:148797798 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:148798151 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:148798195 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr23:148798373 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr23:148797449 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:148796218 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:148798215 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:148798241 G>A did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:148797723 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr23:151900667 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:151899863 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr23:151900680 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr23:151900241 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:151900371 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:151900194 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:151900215 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:151900427 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:151899901 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:151899901 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:151899948 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:151900269 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:151900451 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:151900452 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:151899987 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr23:151900043 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:151900007 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:151900742 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:151900371 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:151900426 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:151900427 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:151900615 G>A did not map to a codon.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr23:151900151 G>A did not map to a codon.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr23:151900152 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:151900188 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:151900709 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr23:151900371 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:151900741 C>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:151900742 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:151900097 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:151900160 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:151900371 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr23:151900532 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr23:151935416 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr23:151935353 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr23:151935267 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:151935885 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr23:151935416 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr23:151935685 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:151935445 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr23:151935607 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr23:151935814 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:151935674 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:151935283 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:151935765 T>G did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:151935335 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:151935674 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:151935416 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:151935416 G>A did not map to a codon.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr23:151935696 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr23:151935534 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:151935258 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:151935343 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:151935416 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:151935934 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:151092602 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:151092697 G>A did not map to a codon.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr23:151092609 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:151092878 C>T did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:151092174 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr23:151092511 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr23:151092692 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr23:151092618 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:151092867 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr23:151092718 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:151092153 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr23:151092727 C>T did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:151092801 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:151092292 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:151092434 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:151092490 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:151092792 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:151092810 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:151093030 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:151092618 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:151092725 T>A did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:151283958 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:151283839 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:151283932 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr23:151283909 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr23:151283947 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr23:151283948 C>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:151283781 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:151283786 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr23:151283695 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:151283669 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:151869596 G>C did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:151869868 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:151869889 C>T did not map to a codon.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr23:151869751 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:151870034 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:151870035 C>T did not map to a codon.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr23:151869599 C>T did not map to a codon.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr23:151869779 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:151869894 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:151870015 G>C did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:151870059 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr23:151869683 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:151869868 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:151870041 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:151869912 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:151870129 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:151869562 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:151870059 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:151870033 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:151869815 T>G did not map to a codon.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr23:151869542 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:151869642 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr23:151869566 A>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:151870086 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr23:151870208 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:151869604 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:151869775 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:151869881 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:151870059 C>T did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:151869972 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr23:149013556 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:149013406 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:149013453 A>G did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:149013427 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:149013188 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr23:149013370 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr23:149013703 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:30269601 C>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:30269509 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr23:30269298 A>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:30269116 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:30269509 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:30269468 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr23:30269258 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:30269108 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr23:30268850 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:30268850 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:30269118 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:30269429 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:30269467 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:27840448 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:27839459 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:27839926 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:27839806 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:27840331 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:27839537 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:27839870 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:27840365 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr23:27839445 A>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:27839492 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:27839531 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:27839610 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:27840181 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:27840246 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:35820675 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr23:35821038 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:35820930 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:35820575 G>A did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:35821043 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:35821023 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:35820546 C>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:35820402 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr23:35820499 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:35820651 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:35820754 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr23:35821038 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr23:35820804 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr23:35820809 T>G did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:35820741 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr23:35820702 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:35821176 G>A did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr23:35820589 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:35820804 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr23:26157833 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr23:26157814 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr23:26157684 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:26157385 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr23:26157407 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr23:26157359 C>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:26157998 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:26157128 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:26157664 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:26157207 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:26157797 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:26157477 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:26157522 G>T did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:26158026 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:26157908 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:26157281 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:26157770 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:26158068 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:26157209 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:26157815 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:30237515 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr23:30237429 T>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:30236700 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:30237171 G>A did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:30237371 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:30237581 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:30237171 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:30237153 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:30237110 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:30237283 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:30236799 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr23:30237089 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3CE-06A-11D-A19A-08 chr23:30254166 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:30254047 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr23:30254636 C>T did not map to a codon.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr23:30254980 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:30254554 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:30254875 G>A did not map to a codon.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr23:30254884 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr23:30254463 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:30254885 A>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:30254403 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:30254510 C>T did not map to a codon.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr23:30254504 A>T did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:30254403 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:30260713 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:30260651 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr23:30261044 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:26213033 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr23:26212240 G>T did not map to a codon.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr23:26212797 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:26212305 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:26212335 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:26212922 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr23:26212390 C>T did not map to a codon.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr23:26212682 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr23:26212430 G>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:26212321 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:26212599 A>T did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:26212772 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:26212986 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:26212143 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:26213013 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:26212487 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr23:26212661 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr23:26212167 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:26212269 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr23:26212085 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:26212391 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr23:26213010 A>T did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:26212434 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:26212850 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:26212180 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr23:26212914 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:26212637 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:26212684 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:26212661 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:26212831 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:26212922 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:26212378 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:26213000 G>A did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:26212033 G>A did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:26212938 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr23:26211989 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr23:140993301 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr23:140996334 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr23:140993512 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:140994041 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr23:140994855 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:140994656 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr23:140993245 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr23:140993838 T>C did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:140994087 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr23:140995637 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:140994544 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:140994652 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:140994834 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:140995405 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:140995818 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:140995901 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr23:140995377 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr23:140996303 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:140993790 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr23:140994504 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:140996046 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:140995831 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr23:140995348 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr23:140995772 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr23:140995901 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:140993282 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:140993295 C>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:140994789 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr23:140995252 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:140993834 G>A did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:140993848 G>A did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:140994882 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr23:140994039 T>C did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:140994041 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:140994146 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr23:140995265 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr23:140995195 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:140995260 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr23:140994041 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:140995170 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:140995248 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:140995272 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:140995397 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:140995986 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:140996617 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:140993457 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:140996501 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:140996502 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr23:140996385 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:140993436 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:140995858 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:140996082 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:140996135 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:140996312 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:140996385 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:140996396 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:140993258 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:140993397 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:140993535 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:140994680 T>G did not map to a codon.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr23:140993590 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:140996572 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr23:140994420 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr23:140995391 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr23:140995818 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:140994329 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:140995047 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:140996435 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:140995067 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:140995423 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:140995858 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:140996285 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:140996396 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:140996487 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:140993480 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr23:140994717 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr23:140995047 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr23:140993561 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:140994566 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:140994574 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:140994841 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:140995273 C>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:140996140 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:140993840 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:140994320 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:140994882 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:140995455 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:140995509 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:140994252 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:140995237 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:140995272 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:140994870 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:140995997 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:140993875 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:140995476 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:140993202 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:140993338 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:140993282 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:140994603 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:140995047 G>A did not map to a codon.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr23:140995272 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:140993242 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr23:140995914 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:140996271 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr23:140994525 C>T did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:140993580 C>T did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:140993629 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:140994618 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:140995252 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:140994127 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr23:140993369 G>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr23:140993370 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr23:140994616 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr23:140995272 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:140993621 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:140993629 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:140995047 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:140995229 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:140996396 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr23:140994731 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:140995046 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:140993544 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:140993664 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:140994116 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:140994215 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:140994356 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:140994726 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:140994982 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:140995377 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:140995455 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:140995640 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:140995777 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:140995888 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:140995901 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:140995917 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:140996098 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:140996415 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:140996465 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:140995043 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:140995044 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:140993388 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:140993831 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:140994282 T>G did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:140995072 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:140995136 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:140995949 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:140996297 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:140996560 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:140995038 C>T did not map to a codon.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr23:140993590 C>T did not map to a codon.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr23:140993590 C>T did not map to a codon.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr23:140995726 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr23:140993487 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr23:140995047 G>A did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:140996028 C>T did not map to a codon.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr23:140994588 C>A did not map to a codon.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr23:140995696 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:141290860 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr23:141291723 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:141291334 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:141291304 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:141290875 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr23:141290790 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:141291748 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr23:141290728 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:141290664 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:141290825 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:141291346 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:141291313 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:141291412 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:141290959 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:141290766 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:141290968 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:141291238 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:141290736 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:141290914 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:141290911 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:141291490 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:141291745 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:141291014 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:141291538 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:141291568 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr23:141291320 G>A did not map to a codon.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr23:141290914 G>A did not map to a codon.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr23:141290959 C>T did not map to a codon.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr23:141291233 C>T did not map to a codon.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr23:141291129 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr23:141290978 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:141290857 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:141291459 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:141291765 G>A did not map to a codon.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr23:141290876 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:141290978 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:141290981 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:141291222 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr23:140969258 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:140969392 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:140983187 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr23:140984957 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:140984598 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr23:140985286 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:140985486 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:140953267 G>A did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:140969270 C>T did not map to a codon.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr23:140984542 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:140984621 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:140984915 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:140985152 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:140926197 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:140969286 T>C did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:140985540 A>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:140969393 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:140983290 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:140983077 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:140969391 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:140985040 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr23:140985454 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:140983091 C>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:140984963 A>C did not map to a codon.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr23:140984543 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr23:140985119 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:140969255 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:140953309 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:140969500 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:140985055 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:140969330 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:140985473 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:140984494 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr23:140953390 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z4-06A-11D-A197-08 chr23:140984914 T>G did not map to a codon.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr23:140985026 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:140969225 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:140984579 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:140983290 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:140926195 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:140969395 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:140984945 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:140985473 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr23:140969391 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:140969510 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:140983290 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:140984477 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:140984592 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr23:140969363 G>A did not map to a codon.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr23:140985305 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:51638415 A>G did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:51641706 G>A did not map to a codon.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr23:51638163 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr23:51643355 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:51641713 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:51644983 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr23:51639951 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:51641706 G>A did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr23:51640336 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr23:75648630 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr23:75648631 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:75650055 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:75649400 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:75648790 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:75649203 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:75649204 C>G did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr23:75650687 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:75650687 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr23:75649458 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:75650873 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:75650187 G>A did not map to a codon.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr23:75649674 A>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr23:75651012 A>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:75649269 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:75649545 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:75649611 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:75649368 G>A did not map to a codon.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr23:75649910 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:75003343 T>C did not map to a codon.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr23:75004549 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:75004477 C>T did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:75003385 C>T did not map to a codon.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr23:75004592 G>A did not map to a codon.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr23:75003615 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:75004258 C>A did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:75004583 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr23:75004286 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:75004516 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr23:75003329 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:75004775 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:75004314 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr23:75003315 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:75004813 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:75003414 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:75004022 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr23:75004634 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr23:75004444 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:75003385 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:75004185 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:75004534 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:75004630 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:75003604 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:75004124 G>A did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:75004185 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr23:75004217 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr23:75004144 C>T did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:75004234 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr23:55479005 G>C did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:55479299 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:55479044 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:55479461 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:55479462 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:23890500 G>A maps to NM_019066.4 Q797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr15:23890669 C>T maps to NM_019066.4 K740K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:23890510 G>A maps to NM_019066.4 T793T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr15:23890081 G>A maps to NM_019066.4 H936H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:23890861 C>T maps to NM_019066.4 E676E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:23889979 C>T maps to NM_019066.4 W970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr3:65349222 G>A maps to NM_001033057.1 R1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:65350613 C>T maps to NM_001033057.1 S1068S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:65415300 C>T maps to NM_001033057.1 V687V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:65607715 G>A maps to NM_001033057.1 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr3:65367726 G>A maps to NM_001033057.1 I842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:65350399 C>T maps to NM_001033057.1 R1097R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:65479265 C>T maps to NM_001033057.1 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:65376949 G>A maps to NM_001033057.1 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr3:65342697 G>T maps to NM_001033057.1 P1248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:65439005 C>T maps to NM_001033057.1 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:65342187 C>T maps to NM_001033057.1 R1418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:65439005 C>T maps to NM_001033057.1 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr3:65344737 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:65456127 G>A maps to NM_001033057.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr3:65364975 G>A maps to NM_001033057.1 I985I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:65377017 T>A maps to NM_001033057.1 K739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr3:65415351 C>T maps to NM_001033057.1 Q670Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr7:77708294 G>A maps to NM_012301.3 L1225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:77764515 G>A maps to NM_012301.3 P951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr7:77708387 G>A maps to NM_012301.3 I1194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:77764488 C>T maps to NM_012301.3 G960G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:77824278 G>A maps to NM_012301.3 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:77755154 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr7:77789393 G>A maps to NM_012301.3 F931F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr7:78256457 G>A maps to NM_012301.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr7:77708330 G>A maps to NM_012301.3 L1213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr7:77762377 C>T did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:77975260 G>A maps to NM_012301.3 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:77885577 G>A maps to NM_012301.3 Q577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:77973146 C>T maps to NM_012301.3 V452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:77797365 T>G maps to NM_012301.3 P821P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:77756672 G>A maps to NM_012301.3 F1088F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:77824341 C>T maps to NM_012301.3 T706T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:114165483 C>T maps to NM_001142782.1 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:114216002 C>T maps to NM_001142782.1 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:114184908 C>T maps to NM_001142782.1 I579I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr1:114201747 C>T maps to NM_001142782.1 D892D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:114123242 G>T maps to NM_001142782.1 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:114215981 C>T maps to NM_001142782.1 P1028P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A690-06A-11D-A30X-08 chr1:114123221 C>T maps to NM_001142782.1 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:49021604 A>G did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:49021313 T>C did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:49021368 C>T did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:49019250 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:53699255 C>T maps to NM_002370.2 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:77112975 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr23:77130978 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:77112284 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:77130971 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr23:77112988 G>T did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:77126356 C>T did not map to a codon.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr23:77112980 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr23:77112264 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr6:10764828 C>T maps to NM_005906.3 W576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:10796536 C>T maps to NM_005906.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr8:33342732 G>A maps to NM_032509.3 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr2:95713852 G>A maps to NM_002371.2 E81E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:120233966 G>A maps to ENST00000276681 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:120233970 C>T maps to ENST00000276681 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:110849248 G>A maps to NM_005434.4 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr18:56400683 C>T maps to NM_006785.2 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr18:56348518 C>T maps to NM_006785.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr18:56390460 C>T maps to NM_006785.2 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr18:56390421 T>G maps to NM_006785.2 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr18:56390483 G>T did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr9:72785458 G>A maps to NM_153267.4 E521E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:72724679 C>T maps to NM_153267.4 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr9:72659124 G>A maps to NM_153267.4 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr9:72723250 G>A maps to NM_153267.4 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr9:139749489 G>A maps to ENST00000392881 R375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr9:139751374 G>T maps to ENST00000392881 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr9:139749711 C>T maps to ENST00000392881 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:139748355 C>T maps to ENST00000392881 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr9:139749471 G>A maps to ENST00000392881 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr5:179201701 C>T maps to NM_014757.4 Q959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:179201800 C>T maps to NM_014757.4 L992L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:95826425 G>A maps to NM_032427.1 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr11:95712579 T>C maps to NM_032427.1 Q1001Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:95826060 G>A maps to NM_032427.1 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr11:95712377 A>G maps to NM_032427.1 L1069L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr4:140811905 G>A maps to ENST00000509479 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr4:140811107 C>T maps to ENST00000509479 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr4:140811491 G>A maps to ENST00000509479 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr4:140810908 G>A maps to ENST00000509479 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr4:140640578 G>A maps to ENST00000509479 F1105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:140810648 C>T maps to ENST00000509479 Q647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:140811506 G>A maps to ENST00000509479 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr4:140651713 G>A maps to ENST00000509479 F729F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr4:140810855 G>A maps to ENST00000509479 I578I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:140811107 C>T maps to ENST00000509479 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:140641355 C>T maps to ENST00000509479 T846T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr4:140811122 T>C maps to ENST00000509479 Q489Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:149639404 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1IB-06A-11D-A196-08 chr23:149642014 G>C did not map to a codon.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr23:149639277 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:149613848 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:149639730 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:149639731 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr6:119628139 C>T maps to NM_005907.2 W207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr6:119569519 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr6:119522417 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:119510859 G>A maps to NM_005907.2 A505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr6:119501110 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:119510834 G>A maps to NM_005907.2 R514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:117944940 C>T maps to NM_006699.3 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:117910831 C>T maps to NM_006699.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:117944838 C>T maps to NM_006699.3 R112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:139995979 C>T maps to NM_016219.3 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr1:26107602 G>A maps to NM_020379.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:26013025 C>T maps to NM_020379.2 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:26104699 C>T maps to NM_020379.2 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:26110159 C>T maps to NM_020379.2 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:26104627 C>T maps to NM_020379.2 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:26085090 G>A maps to NM_020379.2 W313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr5:109117300 T>C did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:109178086 C>T maps to NM_002372.2 N875N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:109159518 C>T maps to NM_002372.2 V849V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:109120468 C>T maps to NM_002372.2 F534F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:109183455 C>T maps to NM_002372.2 R981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:109103251 C>T maps to NM_002372.2 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr15:91455394 C>T maps to NM_006122.2 S744S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr15:91448629 C>T maps to NM_006122.2 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:91449171 C>T maps to NM_006122.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:91456114 C>T maps to NM_006122.2 V826V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr15:91462872 G>T maps to NM_006122.2 L1103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr15:91449692 C>T maps to NM_006122.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:91449186 C>T maps to NM_006122.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr15:91448659 C>T maps to NM_006122.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:12774559 C>T maps to NM_000528.3 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:12769288 G>A maps to NM_000528.3 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr19:12767423 G>A maps to NM_000528.3 F535F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:12760764 G>A maps to NM_000528.3 F743F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:12776226 G>A maps to NM_000528.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:12767498 G>A maps to NM_000528.3 F510F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr4:6580148 G>A maps to NM_015274.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:6611752 C>T maps to NM_015274.1 S745S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr4:6588814 C>T maps to NM_015274.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:6590782 C>T maps to NM_015274.1 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr4:6612844 C>T maps to NM_015274.1 F801F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:6590803 C>T maps to NM_015274.1 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:75652944 G>A maps to NM_006715.2 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr15:75654997 G>A maps to NM_006715.2 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:75651680 G>A maps to NM_006715.2 F678F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:75648740 G>A maps to NM_006715.2 F929F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:75652944 G>A maps to NM_006715.2 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:75651680 G>A maps to NM_006715.2 F678F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr15:75651148 C>T maps to NM_006715.2 R714R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:103585979 G>A maps to NM_005908.3 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:35929788 C>T maps to NM_022077.3 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:96053622 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:38265298 C>T maps to NM_001113482.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:38265328 C>T maps to NM_001113482.1 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:51426376 C>T maps to ENST00000273628 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:12483130 G>A maps to NM_018050.2 Q376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:12483665 A>T maps to NM_018050.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:12483518 G>A maps to NM_018050.2 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:12483125 G>A maps to NM_018050.2 Y377Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr23:43571119 G>A did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:43542826 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:43603699 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:43571158 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:43571144 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:43571966 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:43639592 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:43640712 T>C did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:43661465 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:43656434 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:43652796 G>A did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:43637954 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:43628570 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr23:43656392 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr23:43656390 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:43634451 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:43698124 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:43662610 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:43662604 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:43655066 C>T did not map to a codon.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr23:43655057 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:43627932 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:43652764 G>A did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr23:43639629 G>T did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:43634450 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr15:43817528 G>A maps to ENST00000382031 R1524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:43813931 C>A maps to ENST00000382031 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:43817594 G>A maps to ENST00000382031 A1546A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:43815728 G>A maps to ENST00000382031 Q924Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:43816734 C>T maps to ENST00000382031 Q1260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr15:43819241 C>T maps to ENST00000382031 L2095L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr15:43817993 G>A maps to ENST00000382031 K1679K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr15:43816166 C>T maps to ENST00000382031 I1070I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr15:43817096 C>T maps to ENST00000382031 D1380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:43821449 G>A maps to ENST00000382031 E2831E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:43817642 C>T maps to ENST00000382031 S1562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z4-06A-11D-A197-08 chr15:43817051 A>G maps to ENST00000382031 Q1365Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:43819303 G>A maps to ENST00000382031 W2116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:43821263 C>T maps to ENST00000382031 L2769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:43817882 G>A maps to ENST00000382031 Q1642Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:43813703 C>T maps to ENST00000382031 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:43817594 G>A maps to ENST00000382031 A1546A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr5:71489743 C>T maps to NM_005909.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr5:71500908 A>G did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:71494962 G>T maps to NM_005909.3 G1927G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:71492658 C>T maps to NM_005909.3 F1159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr5:71411609 C>T maps to NM_005909.3 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:71490075 C>T maps to NM_005909.3 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:71494884 G>T maps to NM_005909.3 V1901V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr5:71495433 C>T maps to NM_005909.3 L2084L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:71482454 C>T maps to NM_005909.3 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:71490408 C>T maps to NM_005909.3 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:71491386 C>T maps to NM_005909.3 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:71496141 C>G maps to NM_005909.3 T2320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr5:71495070 C>T maps to NM_005909.3 T1963T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:71494053 C>T maps to NM_005909.3 F1624F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:172944868 G>A maps to NM_199227.1 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:172926241 C>T maps to NM_199227.1 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr2:172930372 G>A maps to NM_199227.1 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr2:172928455 C>T maps to NM_199227.1 D72D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:172926304 C>T maps to NM_199227.1 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr2:172935783 T>C maps to NM_199227.1 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr20:33137833 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:117013839 C>T maps to NM_001085481.1 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:242161913 C>T maps to NM_001004343.2 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr19:17838019 C>T maps to NM_018174.4 P609P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:17837488 C>T maps to NM_018174.4 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr19:17831748 C>T maps to NM_018174.4 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr19:17837395 C>T maps to NM_018174.4 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:17838112 C>T maps to NM_018174.4 S640S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr2:210559008 G>A maps to NM_002374.3 P705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr2:210574779 C>T maps to NM_002374.3 T1625T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:210560568 C>T maps to NM_002374.3 I1225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:210559606 C>T maps to NM_002374.3 R905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:210570449 C>T maps to NM_002374.3 T1577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr2:210557649 C>T maps to NM_002374.3 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:210557361 C>T maps to NM_002374.3 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:210559986 C>T maps to NM_002374.3 S1031S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr2:210560313 C>T maps to NM_002374.3 L1140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr2:210557804 G>A maps to NM_002374.3 W304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:210559668 C>T maps to NM_002374.3 V925V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:210557910 C>T maps to NM_002374.3 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:210574719 C>T maps to NM_002374.3 T1605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:210595030 C>T maps to NM_002374.3 S1798S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr2:210574680 A>G maps to NM_002374.3 T1592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr15:66729178 C>T maps to NM_002755.3 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr15:66777373 G>A maps to NM_002755.3 W247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:66727568 C>T maps to NM_002755.3 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr15:66727556 C>T maps to NM_002755.3 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr15:66782951 A>C maps to NM_002755.3 *394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr19:4117551 G>A maps to NM_030662.3 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:4101103 C>T maps to NM_030662.3 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr17:21215476 C>T maps to NM_145109.2 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr17:21208385 G>A maps to NM_145109.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr17:21215554 C>T maps to NM_145109.2 D292D. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A2GJ-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr17:21215488 C>T maps to NM_145109.2 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr15:68020264 G>A maps to NM_145160.1 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:67985857 G>T maps to NM_145160.1 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr15:68040912 C>T maps to NM_145160.1 Q370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr15:67923224 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:67501924 G>A maps to NM_002758.3 K7K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:67515548 C>T maps to NM_002758.3 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr19:7975959 C>T maps to ENST00000425613 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr19:7968861 C>T maps to ENST00000425613 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:7977032 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr5:56174880 C>T maps to NM_005921.1 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:56178416 C>T maps to NM_005921.1 S1130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr5:56152576 G>A maps to NM_005921.1 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr19:40721042 C>T maps to NM_002446.3 S903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:40720928 C>T maps to NM_002446.3 F865F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:40719928 C>T maps to NM_002446.3 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr19:40710532 C>T maps to NM_002446.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:40720916 C>T maps to NM_002446.3 P861P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr19:40719063 C>T maps to NM_002446.3 I602I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:40698282 C>T maps to NM_002446.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:40719430 C>T maps to NM_002446.3 F615F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:40720955 C>T maps to NM_002446.3 F874F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:40698546 G>T maps to NM_002446.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:65375743 G>A maps to NM_002419.3 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:65366991 G>A maps to NM_002419.3 S693S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr11:65373426 G>A maps to NM_002419.3 Q577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:65367186 G>A maps to NM_002419.3 P628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:65380867 C>T maps to NM_002419.3 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:65375206 G>A maps to NM_002419.3 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:65374966 C>T maps to NM_002419.3 E421E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:65366004 A>T maps to NM_002419.3 P767P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:65373508 G>A maps to NM_002419.3 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:53879240 G>A maps to NM_001193511.1 D280D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr12:53880314 C>T maps to NM_001193511.1 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr12:53879189 C>T maps to NM_001193511.1 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr3:185167786 C>T maps to NM_004721.3 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:185155406 C>T maps to NM_004721.3 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr3:185190819 C>T maps to NM_004721.3 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr3:185198316 G>A maps to NM_004721.3 E933E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:185161268 C>T maps to NM_004721.3 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr3:185161231 G>C did not map to a codon.
Alternatively spliced codon TCGA-FS-A4F5-06A-11D-A25O-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:185146728 C>T maps to NM_004721.3 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:185165675 C>T maps to NM_004721.3 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:185198097 G>A maps to NM_004721.3 E860E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr17:43347909 A>G maps to ENST00000344686 P613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:43364705 G>A maps to ENST00000344686 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:43364172 G>A maps to ENST00000344686 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr17:43364099 G>A maps to ENST00000344686 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr23:19413208 C>A did not map to a codon.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr23:19378892 C>A did not map to a codon.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr23:19378893 C>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:19428061 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:19390896 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:19428073 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr23:19482431 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:19507024 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:19416365 C>T did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:19389504 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:19379466 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:19425326 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:19380928 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:19443745 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:19410590 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:19379478 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:19398346 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:19410162 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:19389541 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:19392707 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr23:19390814 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:19416400 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr23:19389080 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:19482480 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:19410550 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:19425357 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:19482365 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr2:128083323 T>A maps to NM_006609.3 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr2:128066207 G>A maps to NM_006609.3 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:128079619 A>C did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr17:61768529 C>T maps to NM_203351.1 Y458Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:61744304 T>C maps to NM_203351.1 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr17:61759135 C>T maps to NM_203351.1 N202N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr17:61744313 C>T maps to NM_203351.1 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr6:161513139 G>A maps to NM_005922.2 L1078L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:161470209 A>G maps to NM_005922.2 K302K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:161529836 C>T maps to NM_005922.2 F1394F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26D-06A-11D-A19A-08 chr6:161513083 C>T maps to NM_005922.2 Q1060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr6:161530836 G>A maps to NM_005922.2 E1429E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr6:137015309 C>T maps to NM_005923.3 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr6:136934290 G>A maps to NM_005923.3 L794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:136901502 C>T maps to NM_005923.3 W1151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:136913466 C>T maps to NM_005923.3 E1023E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:136977591 G>A maps to NM_005923.3 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:136980430 G>A maps to NM_005923.3 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:137041713 C>T maps to NM_005923.3 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:136944028 G>A maps to NM_005923.3 Q703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr6:136913364 G>A maps to NM_005923.3 I1057I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:137018413 G>A maps to NM_005923.3 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr6:136980465 G>A maps to NM_005923.3 Q473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr1:27687212 G>A maps to NM_004672.3 I679I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr1:27685036 G>A maps to NM_004672.3 L883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr1:27683181 G>A maps to NM_004672.3 S1141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:27688715 G>A maps to NM_004672.3 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:27683575 G>A maps to NM_004672.3 I1096I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:27684700 G>A maps to NM_004672.3 C962C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:27690810 G>A maps to NM_004672.3 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:91233484 G>A maps to NM_145331.1 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:91226366 T>C maps to NM_145331.1 E558E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:91257073 G>A maps to NM_145331.1 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:30747035 C>T maps to NM_005204.2 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:30749659 G>A maps to NM_005204.2 E433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr14:71199391 G>A maps to NM_033141.2 P912P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:71199748 G>A maps to NM_033141.2 P793P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr14:71209194 C>T maps to NM_033141.2 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr14:71197117 G>A maps to NM_033141.2 I1112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr14:71209196 G>A maps to NM_033141.2 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:71267525 T>C maps to NM_033141.2 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr14:71199481 C>T maps to NM_033141.2 E882E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr14:71267681 G>A maps to NM_033141.2 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:71209293 C>T maps to NM_033141.2 W447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr14:71202706 G>A maps to NM_033141.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr14:71205044 C>T maps to NM_033141.2 E587E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr14:71215674 G>A maps to NM_033141.2 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:71267480 G>A maps to NM_033141.2 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:71267771 G>A maps to NM_033141.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:71204984 C>T maps to NM_033141.2 K607K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr14:71216737 G>A maps to NM_033141.2 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr3:47894814 G>A maps to ENST00000426837 L2242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:47969823 G>A maps to ENST00000426837 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:47957453 G>A maps to ENST00000426837 F638F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:47913524 G>A maps to ENST00000426837 A1941A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr19:39100287 G>A maps to NM_001042600.1 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:39100578 G>A maps to NM_001042600.1 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:39096235 G>A maps to NM_001042600.1 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:39103297 G>A maps to NM_001042600.1 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:39096812 C>T maps to NM_001042600.1 K400K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:39104893 C>T maps to NM_001042600.1 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:39100551 G>A maps to NM_001042600.1 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:39090568 G>A maps to NM_001042600.1 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:39086355 C>T maps to NM_001042600.1 L731L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr19:39078450 T>C maps to NM_001042600.1 V801V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:39090784 G>A maps to NM_001042600.1 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:64564325 G>A maps to NM_004579.2 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:64563862 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:64559444 G>A maps to NM_004579.2 C676C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:64568599 G>A maps to NM_004579.2 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr2:39507458 G>A maps to NM_003618.2 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr2:39499518 G>A maps to NM_003618.2 S626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:39505595 C>A maps to NM_003618.2 G582G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr2:39485687 C>T maps to NM_003618.2 E783E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:102499088 G>A maps to NM_145686.2 E1090E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:102407206 T>A maps to NM_145686.2 L50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:102490541 A>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:102477312 C>T maps to NM_145686.2 N577N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:102490131 C>T maps to NM_145686.2 L928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:75298634 C>T maps to NM_033063.1 K637K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr11:75298568 C>T maps to NM_033063.1 K659K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:75319270 G>A maps to NM_033063.1 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr11:75299099 C>T maps to NM_033063.1 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:75298472 T>G maps to NM_033063.1 A691A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:75319243 C>T maps to NM_033063.1 E343E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:136677831 C>T maps to NM_001198609.1 E701E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:136687110 C>T maps to NM_001198609.1 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:136704881 C>T maps to NM_001198609.1 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:136667102 G>A maps to NM_001198609.1 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr6:136693710 C>T maps to NM_001198609.1 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:136683613 C>T maps to NM_001198609.1 E530E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:136742908 C>T maps to NM_001198609.1 K54K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:36644056 C>T maps to NM_018067.3 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr1:36638147 C>T maps to NM_018067.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:36638150 G>T maps to NM_018067.3 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr23:20062572 C>T did not map to a codon.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr23:20044016 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr23:20062505 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:20081555 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:20081556 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:20081641 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:20074886 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr23:20034250 T>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:20070999 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:20034405 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:20030587 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:20034415 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:20081588 C>T did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr23:20060744 C>T did not map to a codon.
Sequencing variant TCGA-GN-A26D-06A-11D-A19A-08 chr23:20134869 T>G did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:20134932 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:135302926 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:135313882 C>G did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:135309543 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr23:135328300 T>G did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:135323390 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr4:156294381 G>A maps to NM_001039580.1 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr4:156281453 G>A maps to NM_001039580.1 Q306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:156276981 C>T maps to NM_001039580.1 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:156277014 C>T maps to NM_001039580.1 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:156273855 G>A maps to NM_001039580.1 F571F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr22:22142677 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:22123582 G>A maps to NM_138957.2 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:86938512 C>T maps to NM_138982.2 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:87024364 C>T maps to NM_138982.2 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:86988959 G>A maps to NM_138982.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr4:86985429 C>A maps to NM_138982.2 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:87080461 C>T maps to NM_138982.2 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:87019692 G>A maps to NM_138982.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr22:50705393 G>A maps to NM_002751.5 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:50696676 C>T maps to NM_002969.3 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr6:36107149 G>A maps to NM_002754.3 *366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr6:36106190 G>A maps to NM_002754.3 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr6:36103815 C>T maps to NM_002754.3 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:36106166 G>A maps to NM_002754.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr6:36104506 C>T maps to NM_002754.3 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:36099122 C>T maps to NM_002754.3 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:36106767 G>A maps to NM_002754.3 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr6:36020473 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr6:36070421 C>T maps to NM_139012.2 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:36040748 C>T maps to NM_139012.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr8:144800413 C>T maps to NM_139021.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:144803007 G>A maps to NM_139021.2 Q305Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:144801551 C>T maps to NM_139021.2 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr8:144801596 C>T maps to NM_139021.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:144802953 C>T maps to NM_139021.2 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr14:55529628 C>T maps to NM_144578.3 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr16:30128289 G>A maps to NM_002746.2 N314N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr16:30129472 G>A maps to NM_002746.2 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr16:30128277 C>T maps to NM_002746.2 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr16:30133239 G>A maps to NM_002746.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr16:30129012 C>T maps to NM_002746.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:30133194 G>A maps to NM_002746.2 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr16:30129373 G>A maps to NM_002746.2 N218N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr16:30129472 G>A maps to NM_002746.2 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr18:48190681 G>A maps to NM_002747.3 Q118Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr18:48190585 C>T maps to NM_002747.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr18:48190636 C>T maps to NM_002747.3 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr18:48190558 C>T maps to NM_002747.3 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr18:48190849 C>T maps to NM_002747.3 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr18:48190729 C>T maps to NM_002747.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr18:48190771 G>A maps to NM_002747.3 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr18:48190834 C>T maps to NM_002747.3 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr18:48190867 C>T maps to NM_002747.3 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr18:48248338 C>T maps to NM_002747.3 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr18:48190459 G>A maps to NM_002747.3 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr18:48252353 C>T maps to NM_002747.3 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr15:52356249 G>T maps to NM_002748.3 E407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr15:52356224 C>T maps to NM_002748.3 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr15:52356225 C>T maps to NM_002748.3 R399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr17:19285535 C>T maps to NM_139034.2 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr17:19284079 C>T maps to NM_139034.2 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr10:49628256 C>T maps to NM_139049.1 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:45925617 C>T maps to NM_005456.2 Y524Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:45926267 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:45926794 C>T maps to NM_005456.2 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:45919641 C>A maps to NM_005456.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:45924118 C>T maps to NM_005456.2 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:45923602 C>T maps to NM_005456.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr11:45924250 C>T maps to NM_005456.2 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr22:51043436 C>T maps to ENST00000329492 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:51045389 C>T maps to ENST00000329492 S757S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:51040271 C>T maps to ENST00000329492 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:51041866 C>T maps to ENST00000329492 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr22:51044298 C>T maps to ENST00000329492 F686F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:1813666 G>A maps to NM_015133.3 T635T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr16:1816233 C>T maps to NM_015133.3 T880T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:1793461 C>T maps to NM_015133.3 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr16:1816260 C>T maps to NM_015133.3 S889S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr16:1810422 C>T maps to NM_015133.3 V448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:1779565 C>T maps to NM_015133.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:1815105 C>T maps to NM_015133.3 A790A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:1818311 C>T maps to NM_015133.3 S1224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr16:1816293 G>A maps to NM_015133.3 E900E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr16:1816054 C>T maps to NM_015133.3 I846I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr9:128347847 C>T maps to NM_001006617.1 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CF-06A-11D-A196-08 chr1:206905224 G>T maps to NM_032960.2 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:206902416 C>T maps to NM_032960.2 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:206902410 C>T maps to NM_032960.2 Q151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:206903357 C>T maps to NM_032960.2 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr1:206902125 C>T maps to NM_032960.2 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:50655028 C>T maps to NM_004635.3 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:112308965 T>C maps to NM_139078.1 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr15:42109903 G>A maps to NM_001128608.1 T631T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr15:42107931 C>T maps to NM_001128608.1 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr15:42111089 C>T maps to NM_001128608.1 R748R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:42113040 C>T maps to NM_001128608.1 S837S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:42116017 C>T maps to NM_001128608.1 F1330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:42105142 C>T maps to NM_001128608.1 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr20:31421625 C>T maps to NM_012325.2 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr20:31427586 G>A maps to NM_012325.2 K174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr18:32677440 C>T maps to NM_014268.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr17:44060586 G>A maps to NM_001123066.3 E139E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:44039837 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:44060997 C>T maps to NM_001123066.3 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:44067272 G>A maps to NM_001123066.3 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:44067302 C>T maps to NM_001123066.3 H414H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr17:44096041 G>A maps to NM_001123066.3 S687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:44060908 C>T maps to NM_001123066.3 Q247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr4:164506903 C>T maps to ENST00000514618 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr4:164506933 G>A maps to ENST00000514618 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:164506996 G>A maps to ENST00000514618 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr4:164450166 C>T maps to ENST00000514618 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr4:164506933 G>A maps to ENST00000514618 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:164507044 G>A maps to ENST00000514618 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr4:164507035 G>A maps to ENST00000514618 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr17:60813509 C>T maps to NM_152598.2 V573V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:60814520 G>A maps to NM_152598.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:60779114 C>T maps to NM_152598.2 S792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr17:60814082 C>T maps to NM_152598.2 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:60802362 C>G maps to NM_152598.2 V680V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:60814349 C>T maps to NM_152598.2 E293E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:60814505 T>A maps to NM_152598.2 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:60879060 G>A maps to NM_152598.2 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr17:60821839 C>T maps to NM_152598.2 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:16067684 C>T maps to NM_001102562.1 Q368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:16067686 G>A maps to NM_001102562.1 Q368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:8491501 T>A maps to NM_016496.4 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:8503360 C>A maps to NM_016496.4 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:8495717 C>T maps to NM_016496.4 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr19:8491630 C>T maps to NM_016496.4 Y105Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:126206348 C>T maps to NM_178450.3 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:126213903 G>A maps to NM_178450.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:126206431 G>A maps to NM_178450.3 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:217234481 G>A maps to NM_020814.2 Q168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:217124187 G>A maps to NM_020814.2 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:217142512 G>A maps to NM_020814.2 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:217142557 C>T maps to NM_020814.2 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:217124115 G>A maps to NM_020814.2 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr2:217142479 G>A maps to NM_020814.2 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:94109518 C>T maps to NM_017824.4 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr5:10415636 G>A maps to NM_005885.2 G668G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:10381948 A>G maps to NM_005885.2 Q76Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:10426587 C>T maps to NM_005885.2 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:10405767 C>T maps to NM_005885.2 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr5:10430028 T>A maps to NM_005885.2 L844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr2:160604790 A>G maps to NM_022826.2 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:45953749 G>A maps to NM_145021.4 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:58152598 C>T maps to NM_138396.4 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr12:58152033 C>T maps to NM_138396.4 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr12:58152072 C>T maps to NM_138396.4 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:32800308 T>C maps to NM_023009.5 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr2:119727732 C>T maps to NM_006770.3 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr2:119726832 C>T maps to NM_006770.3 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr2:119752008 G>A maps to NM_006770.3 E492E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:119731984 C>T maps to NM_006770.3 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr2:119727732 C>T maps to NM_006770.3 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr2:119739963 G>A maps to NM_006770.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:119727717 C>T maps to NM_006770.3 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:119739063 C>T maps to NM_006770.3 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:119726772 C>T maps to NM_006770.3 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:119726781 G>A maps to NM_006770.3 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:119727732 C>T maps to NM_006770.3 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr2:119727732 C>T maps to NM_006770.3 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:119739048 G>A maps to NM_006770.3 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr2:119727774 C>T maps to NM_006770.3 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:119727732 C>T maps to NM_006770.3 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:119748177 G>A maps to NM_006770.3 Q359Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr2:119732136 G>A maps to NM_006770.3 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr2:119727768 C>T maps to NM_006770.3 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr2:119735506 C>T maps to NM_006770.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:119739063 C>T maps to NM_006770.3 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:119729075 G>A maps to NM_006770.3 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr2:119699887 G>A maps to NM_006770.3 K4K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:119727714 G>A maps to NM_006770.3 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:119750853 G>A maps to NM_006770.3 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:119739063 C>T maps to NM_006770.3 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:220789324 C>T maps to NM_018650.3 H180H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:220805598 C>T maps to NM_018650.3 Q356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:220789324 C>T maps to NM_018650.3 H180H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZU-06A-12D-A196-08 chr1:220777409 T>G maps to NM_018650.3 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr1:220789318 T>C maps to NM_018650.3 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:220777407 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:220824044 G>A maps to NM_018650.3 Q518Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr11:63666125 C>A maps to NM_001039469.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:63672371 C>T maps to NM_001039469.2 F597F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:63668266 C>T maps to NM_001039469.2 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:63666287 C>T maps to NM_001039469.2 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr14:103958221 C>T maps to ENST00000335102 F588F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr14:103941513 T>C maps to ENST00000335102 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr14:103946815 C>T maps to ENST00000335102 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr14:103932025 C>T maps to ENST00000335102 Q248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:45805650 C>T maps to NM_031417.3 I674I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:45766590 C>T maps to NM_031417.3 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:45774923 C>T maps to NM_031417.3 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:45766590 C>T maps to NM_031417.3 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr19:45767987 G>A maps to NM_031417.3 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr12:57906612 G>A maps to NM_004990.2 G611G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:57884322 G>A maps to NM_004990.2 E222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr12:57884379 G>A maps to NM_004990.2 E241E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:57894286 C>T maps to NM_004990.2 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr12:57908736 G>A maps to NM_004990.2 R700R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:68737433 C>T maps to NM_001038603.2 Q544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr5:68715382 C>T maps to NM_001038603.2 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr16:71668225 G>A maps to NM_052858.3 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:71668132 G>A maps to NM_052858.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:71674494 G>A maps to NM_001017967.2 L266L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A3JA-06A-11D-A20D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr16:71668678 G>A maps to NM_052858.3 E393E. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-ER-A19G-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:71674740 G>A maps to NM_001017967.2 W348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:160328697 C>T maps to NM_002377.2 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr6:160328868 C>T maps to NM_002377.2 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:160328211 C>T maps to NM_002377.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:160328631 G>A maps to NM_002377.2 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:29454812 G>A maps to NM_052967.1 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:29455667 C>T maps to NM_052967.1 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr6:29454929 G>A maps to NM_052967.1 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:29455613 C>T maps to NM_052967.1 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:186943151 G>A maps to NM_001879.5 F567F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:186968108 C>T maps to NM_139125.3 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr3:186954275 G>A maps to NM_139125.3 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:187003810 G>A maps to NM_139125.3 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr3:186943151 G>A maps to NM_001879.5 F567F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:186947656 C>T maps to NM_001879.5 K444K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:186953726 C>T maps to NM_139125.3 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:186954119 C>T maps to NM_139125.3 K513K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr3:186974604 G>A maps to NM_139125.3 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:186974535 C>T maps to NM_139125.3 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:186953992 G>A maps to NM_139125.3 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:186954047 G>A maps to NM_139125.3 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr3:186954182 G>A maps to NM_139125.3 I492I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:11090803 C>T did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr1:11106673 G>A maps to NM_006610.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:11087496 C>T maps to NM_006610.2 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:11102954 C>T maps to NM_006610.2 W289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr1:11102947 G>A maps to NM_006610.2 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:12977551 T>A maps to NM_014975.2 S705S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:12977539 C>T maps to NM_014975.2 I701I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:12976546 C>T maps to NM_014975.2 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:12958461 C>T maps to NM_014975.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr19:12975901 C>T maps to NM_014975.2 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:12975889 G>A maps to NM_014975.2 K512K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:12976230 C>T maps to NM_014975.2 F580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:12980015 C>T maps to NM_014975.2 I970I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:12975862 C>T maps to NM_014975.2 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr19:12975979 C>T maps to NM_014975.2 F542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:12969362 G>A maps to NM_014975.2 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:12978675 C>T maps to NM_014975.2 A817A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:12979589 G>A maps to NM_014975.2 K900K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr1:46501425 G>A maps to NM_015112.2 K1695K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:46487734 C>T maps to NM_015112.2 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:46489569 C>T maps to NM_015112.2 F566F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:46496337 C>T maps to NM_015112.2 T871T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr1:46501230 T>G maps to NM_015112.2 L1630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:46499888 C>T maps to NM_015112.2 P1273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:46474036 C>T maps to NM_015112.2 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr19:18245445 C>T maps to NM_015016.1 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:18233515 C>T maps to NM_015016.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:18235112 C>T maps to NM_015016.1 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr19:18245775 C>T maps to NM_015016.1 F589F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr19:18249888 C>T maps to NM_015016.1 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:18248076 C>T maps to NM_015016.1 P638P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr19:18232548 C>T maps to NM_015016.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:18234052 C>T maps to NM_015016.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr5:66416868 C>T maps to NM_001164664.1 R562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:66396402 C>T maps to NM_001164664.1 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:66350256 T>C maps to NM_001164664.1 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:66460532 T>A maps to NM_001164664.1 V1842V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr5:66084621 G>A maps to NM_001164664.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr5:66084498 G>A maps to NM_001164664.1 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr5:66400333 C>T maps to NM_001164664.1 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr5:66459116 C>T maps to NM_001164664.1 S1370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr5:66449398 C>T maps to NM_001164664.1 L1213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:66409919 T>C maps to NM_001164664.1 F488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr5:66462575 C>T maps to NM_001164664.1 S2523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:66396277 C>T maps to NM_001164664.1 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:66459554 G>A maps to NM_001164664.1 R1516R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr5:66398378 C>T maps to NM_001164664.1 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:66460535 C>T maps to NM_001164664.1 L1843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:66462293 G>A maps to NM_001164664.1 T2429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr10:27458943 A>G maps to NM_001172303.1 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr10:27454412 T>A maps to NM_001172303.1 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr10:82045325 G>A maps to NM_000429.2 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:82034871 C>T maps to NM_000429.2 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:82039991 G>A maps to NM_000429.2 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:82034919 C>T maps to NM_000429.2 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr2:85770070 C>T maps to NM_005911.4 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr2:85770791 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr2:85769830 C>T maps to NM_005911.4 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:3779052 C>T maps to NM_002378.3 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr19:3778321 C>T maps to NM_002378.3 W462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr19:3784156 C>T maps to NM_002378.3 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:3778393 C>T maps to NM_002378.3 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr19:3779419 C>T maps to NM_002378.3 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:3779069 G>A maps to NM_002378.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:3783163 C>T maps to NM_002378.3 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:3784231 C>T maps to NM_002378.3 K85K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:31194578 C>T maps to NM_002379.3 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr8:98943538 C>T maps to ENST00000254898 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr8:98943550 G>A maps to ENST00000254898 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:99019815 G>A maps to ENST00000254898 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:99039821 C>T maps to ENST00000254898 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr8:98943538 C>T maps to ENST00000254898 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:20200318 T>A maps to NM_002381.4 K351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:20205940 G>A maps to NM_002381.4 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:20205628 C>T maps to NM_002381.4 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:20205994 G>A maps to NM_002381.4 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr2:20205775 G>A maps to NM_002381.4 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:20205895 G>A maps to NM_002381.4 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:20205859 G>A maps to NM_002381.4 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:43933078 G>A maps to ENST00000372754 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr20:43926852 G>A maps to ENST00000372754 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:43933246 G>A maps to ENST00000372754 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr20:43933111 C>T maps to ENST00000372754 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:43926897 G>A maps to ENST00000372754 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:43927044 G>A maps to ENST00000372754 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr20:43927065 C>T maps to ENST00000372754 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr5:138658192 C>T maps to ENST00000394800 S592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr5:138657651 C>T maps to ENST00000394800 A556A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr20:3846631 G>A maps to NM_020746.3 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr20:3844957 C>T maps to NM_020746.3 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr20:3838379 C>T maps to NM_020746.3 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:3846673 C>T maps to NM_020746.3 F501F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr16:29818723 G>A maps to NM_001042539.1 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr16:29818753 G>A maps to NM_001042539.1 K216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr16:29820897 G>A maps to NM_001042539.1 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr22:36013286 C>T maps to NM_203377.1 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr22:36007059 C>T maps to NM_203377.1 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:36007059 C>T maps to NM_203377.1 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr18:47803465 G>A maps to ENST00000424334 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr18:51729292 G>A maps to NM_015832.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr18:51731438 C>A maps to NM_003927.3 G211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr18:51729391 C>T maps to NM_015832.3 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:1578340 A>T maps to NM_003926.5 *292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:1581113 G>A maps to NM_003926.5 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:1578449 G>A maps to NM_003926.5 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:8953374 G>A maps to NM_145208.2 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:8953431 C>T maps to NM_145208.2 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:8953830 G>A maps to NM_145208.2 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:8953473 G>A maps to NM_145208.2 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:8953425 C>T maps to NM_145208.2 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr3:129156129 T>C maps to NM_003925.1 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:129155732 T>A maps to NM_003925.1 K252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr3:129152699 C>T maps to NM_003925.1 R468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:149227570 T>C maps to ENST00000404807 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr2:149247691 C>T maps to ENST00000404807 F1497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:149243351 C>T maps to ENST00000404807 L1196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:149240931 C>T maps to ENST00000404807 I924I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:149270437 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:149226732 C>T maps to ENST00000404807 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:149247565 C>T maps to ENST00000404807 I1455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:149221444 C>T maps to ENST00000404807 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:149226636 C>T maps to ENST00000404807 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:149226927 C>T maps to ENST00000404807 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr2:149227047 C>T maps to ENST00000404807 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:149243360 C>T maps to ENST00000404807 L1199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr2:149247508 C>T maps to ENST00000404807 P1436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:149247691 C>T maps to ENST00000404807 F1497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z4-06A-11D-A197-08 chr2:149248078 C>T maps to ENST00000404807 I1626I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZG-06A-11D-A197-08 chr2:149247827 C>T maps to ENST00000404807 Q1543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:149226883 C>T maps to ENST00000404807 Q458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:149227971 C>T maps to ENST00000404807 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:149260060 C>T maps to ENST00000404807 V1673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:149247109 G>A maps to ENST00000404807 Q1303Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:57919881 A>G maps to NM_052897.3 E377E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:57921366 C>T maps to NM_052897.3 S720S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:36784010 G>A maps to NM_016586.2 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr10:54530430 C>T maps to NM_000242.2 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:54530529 G>T maps to NM_000242.2 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:54528093 G>A maps to NM_000242.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:54528163 G>A maps to NM_000242.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr10:54528094 G>A maps to NM_000242.2 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr10:54531368 G>A maps to NM_000242.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr3:152150589 C>T maps to NM_021038.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:152173352 C>A maps to NM_021038.3 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr13:98009743 C>T maps to ENST00000376673 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:98018782 C>T maps to NM_144778.2 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NF-06A-11D-A19A-08 chr23:131573584 C>A did not map to a codon.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr6:20124762 G>A maps to NM_001080480.1 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr6:20109974 C>T maps to NM_001080480.1 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr6:20124681 G>T maps to NM_001080480.1 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:9002815 G>A maps to NM_138799.2 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:54678031 G>A maps to NM_024298.3 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:54684596 C>T maps to NM_024298.3 W249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54687452 G>A maps to NM_024298.3 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr18:74701950 G>A maps to NM_001025101.1 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr18:74728994 G>A maps to NM_001025101.1 D123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YX-06A-11D-A197-08 chr17:49279427 C>T maps to ENST00000389496 K361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZG-06A-11D-A197-08 chr17:49270311 A>G maps to ENST00000389496 R510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr16:84129264 G>A maps to NM_003791.2 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:84108246 G>A maps to NM_003791.2 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:84118694 G>A maps to NM_003791.2 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:21863440 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:21871588 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:21871529 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:21863444 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr18:13884884 G>A maps to NM_000529.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr18:13885331 G>A maps to NM_000529.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:13884967 G>A maps to NM_000529.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr18:13885331 G>A maps to NM_000529.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr18:13885118 G>A maps to NM_000529.2 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:13885421 G>A maps to NM_000529.2 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr18:13884925 G>A maps to NM_000529.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr18:13885394 C>T maps to NM_000529.2 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr18:13885412 G>A maps to NM_000529.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr18:13885094 G>A maps to NM_000529.2 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr18:13884967 G>A maps to NM_000529.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr18:13885331 G>A maps to NM_000529.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr20:54824079 C>T maps to ENST00000371389 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr20:54824279 C>T maps to ENST00000371389 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr20:54824477 C>T maps to ENST00000371389 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr20:54824279 C>T maps to ENST00000371389 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:54824489 C>T maps to ENST00000371389 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr20:54824279 C>T maps to ENST00000371389 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr20:54824280 C>T maps to ENST00000371389 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:54824048 C>T maps to ENST00000371389 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr20:54824810 G>A maps to ENST00000371389 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr20:54824258 C>T maps to ENST00000371389 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr20:54824489 C>T maps to ENST00000371389 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:54824438 C>T maps to ENST00000371389 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr20:54824303 C>T maps to ENST00000371389 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr20:54824660 C>T maps to ENST00000371389 C291C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:54824693 C>T maps to ENST00000371389 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr18:58038892 G>A maps to NM_005912.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr18:58038850 C>T maps to NM_005912.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr18:13826735 G>A maps to NM_005913.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr18:13826627 C>T maps to NM_005913.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr18:13826627 C>T maps to NM_005913.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr18:13826252 C>T maps to NM_005913.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr18:13826325 C>T maps to NM_005913.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr18:13825910 C>T maps to NM_005913.2 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr18:13826735 G>A maps to NM_005913.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:119185253 G>A maps to NM_006500.2 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:119182818 G>A maps to NM_006500.2 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr9:37888004 G>A maps to NM_033412.3 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr9:37888378 G>A maps to NM_033412.3 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr18:29339841 C>T maps to NM_001034172.2 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr18:29339731 C>T maps to NM_001034172.2 *298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr18:29340354 C>T maps to NM_001034172.2 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr18:29339868 C>T maps to NM_001034172.2 K252K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr18:29340392 G>A maps to NM_001034172.2 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr18:29340051 G>A maps to NM_001034172.2 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr18:29340132 C>T maps to NM_001034172.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr18:29340392 G>A maps to NM_001034172.2 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr23:103349513 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr23:103349040 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr23:103349041 G>A did not map to a codon.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr23:103349571 C>A did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr23:103349875 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:103349590 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:103349342 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:103349139 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr23:103349555 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr23:103349556 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:103349731 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:103349553 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:103349359 G>A did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:103349061 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr22:43533178 C>A maps to NM_173467.4 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:112418636 G>A maps to NM_001085377.1 F568F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:112458519 C>T maps to NM_001085377.1 E296E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr5:112720775 G>A maps to NM_001085377.1 R102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr5:112479057 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:112720812 G>A maps to NM_001085377.1 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:182759358 C>T maps to NM_020166.3 R421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:182763210 C>T maps to NM_020166.3 W358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr5:70900255 C>T maps to NM_022132.4 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:70952668 C>T maps to NM_022132.4 F558F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:70942102 T>A maps to NM_022132.4 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr6:31496961 G>A maps to NM_001011700.2 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr2:71351585 C>T maps to NM_032601.3 W43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:138669892 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:138669926 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr23:138678911 C>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:138701768 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr23:138669923 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr23:138680592 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:138697136 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr23:138670579 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:138668614 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr23:138729048 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:138698532 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:138697086 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:138698586 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr23:138708440 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:138664630 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:138708446 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:138687871 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:138697050 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:138667283 A>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:138698586 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:138684653 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:138684654 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:138729050 T>C did not map to a codon.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr23:138698586 C>T did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:138678841 C>T did not map to a codon.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr23:138698538 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr13:113714953 G>A maps to NM_001112732.1 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr13:113679036 C>T maps to NM_001112732.1 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr13:113730371 G>A maps to NM_001112732.1 Q524Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr13:113714962 C>T maps to NM_001112732.1 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:113740499 C>T maps to NM_001112732.1 S827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr3:183097193 G>A maps to NM_015078.2 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:183014922 G>A maps to NM_015078.2 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:182913011 C>T maps to NM_015078.2 T972T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr22:41077070 G>A maps to NM_005297.3 K136K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr22:41077040 G>A maps to NM_005297.3 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr6:100395746 G>A maps to NM_032503.2 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:100390824 C>T maps to NM_032503.2 W196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:100382356 G>A maps to NM_032503.2 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:100368878 G>A maps to NM_032503.2 I320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:100395840 C>T maps to NM_032503.2 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:100369019 C>T maps to NM_032503.2 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr6:100382374 C>T maps to NM_032503.2 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr6:100369010 C>T maps to NM_032503.2 Q276Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:100403861 G>A maps to NM_032503.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:100390993 G>A maps to NM_032503.2 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:100369010 C>T maps to NM_032503.2 Q276Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr6:100395828 G>A maps to NM_032503.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:100368899 G>A maps to NM_032503.2 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:100382356 G>A maps to NM_032503.2 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr6:100395840 C>T maps to NM_032503.2 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr6:100368899 G>A maps to NM_032503.2 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr6:100390895 C>T maps to NM_032503.2 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:100390946 C>T maps to NM_032503.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr6:100390824 C>T maps to NM_032503.2 W196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:150551358 A>G maps to NM_021960.4 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr10:13251259 C>T maps to NM_182751.2 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:13214475 C>T maps to NM_182751.2 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:13224991 C>T maps to NM_182751.2 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr10:13214664 T>G maps to NM_182751.2 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr10:13214475 C>T maps to NM_182751.2 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:13214674 C>T maps to NM_182751.2 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:127336174 C>T maps to NM_004526.2 I609I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr3:127335868 C>T maps to NM_004526.2 Q561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:127336839 C>T maps to NM_004526.2 F643F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:127325560 C>T maps to NM_004526.2 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:127334784 G>A maps to NM_004526.2 E503E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:127336234 C>T maps to NM_004526.2 A629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr3:127325560 C>T maps to NM_004526.2 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:127340601 C>T maps to NM_004526.2 L901L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr3:127318225 C>T maps to NM_004526.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr21:47692683 G>A maps to NM_003906.3 T752T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr21:47697594 G>A maps to NM_003906.3 H568H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr21:47699944 G>A maps to NM_003906.3 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr21:47660783 C>T maps to NM_003906.3 E1858E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:47692737 G>A maps to NM_003906.3 I734I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr21:47674388 G>A maps to NM_003906.3 L1351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr8:48878867 C>T maps to NM_182746.1 D318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr8:48874103 C>T maps to NM_182746.1 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:48887385 C>T maps to NM_182746.1 A743A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr22:35808548 C>T maps to NM_006739.3 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:35808653 C>T maps to NM_006739.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:35808530 C>T maps to NM_006739.3 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr22:35815966 G>A maps to NM_006739.3 R598R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:35812734 C>T maps to NM_006739.3 F506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:35799483 C>T maps to NM_006739.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:136627885 G>A maps to NM_005915.4 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:136620244 G>A maps to NM_005915.4 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr7:99693041 G>A maps to NM_005916.3 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr7:99697358 C>T maps to NM_005916.3 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr7:99695820 G>A maps to NM_005916.3 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:99693581 G>A maps to NM_005916.3 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:99697316 C>T maps to NM_005916.3 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:99693650 G>A maps to NM_005916.3 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr7:99696945 G>A maps to NM_005916.3 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:5948084 C>T maps to NM_032485.4 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:119245182 A>C maps to ENST00000316316 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr19:7589983 C>T maps to NM_020533.2 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr19:7593135 C>T maps to NM_020533.2 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr19:7593763 C>T maps to NM_020533.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:7594573 C>T maps to NM_020533.2 I445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:7595182 C>T maps to NM_020533.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:7595365 C>G maps to NM_020533.2 T518T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:7595173 C>T maps to NM_020533.2 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:85405367 G>A maps to NM_153259.2 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:85405262 G>A maps to NM_153259.2 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:85406602 G>A maps to NM_153259.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:85403714 G>A maps to NM_153259.2 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr8:6302914 C>T maps to NM_024596.3 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr8:6302682 C>T maps to NM_024596.3 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr8:6357404 T>C maps to NM_024596.3 I723I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:49952685 G>A maps to NM_001012300.1 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr5:94275876 G>A maps to NM_024717.4 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:94134741 C>T maps to NM_024717.4 G844G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:94230395 G>A maps to NM_024717.4 S599S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:94230509 C>T maps to NM_024717.4 R561R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr5:94288922 C>T maps to NM_024717.4 K327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr5:94275820 G>A maps to NM_024717.4 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr5:94230530 G>A maps to NM_024717.4 V554V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:94248650 G>A maps to NM_024717.4 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:94134765 C>T maps to NM_024717.4 W836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr5:94275829 G>A maps to NM_024717.4 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:94230395 G>A maps to NM_024717.4 S599S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr5:94278083 G>A maps to NM_024717.4 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr5:94259665 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr5:94224665 C>T maps to NM_024717.4 R617R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:94353076 G>A maps to NM_024717.4 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr5:94353069 C>A did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:94224665 C>T maps to NM_024717.4 R617R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr15:94983481 C>T maps to NM_018349.3 F721F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr15:94899427 G>A maps to NM_018349.3 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr15:95013639 C>T maps to NM_018349.3 F813F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:95013639 C>T maps to NM_018349.3 F813F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr15:94841703 G>A maps to NM_018349.3 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:94983424 G>A maps to NM_018349.3 W702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr15:94945244 C>T maps to NM_018349.3 F694F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:94986173 G>A maps to NM_018349.3 E745E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:95013639 C>T maps to NM_018349.3 F813F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr15:94928666 C>T maps to NM_018349.3 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr15:95020021 G>A maps to NM_018349.3 K856K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:94899421 G>A maps to NM_018349.3 W354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr15:95022244 G>A maps to NM_018349.3 K873K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr15:94945193 C>T maps to NM_018349.3 F677F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr15:94882562 C>T maps to NM_018349.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr15:94883459 C>T maps to NM_018349.3 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr15:94841673 C>T maps to NM_018349.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr15:95013582 C>T maps to NM_018349.3 P794P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:94841625 G>A maps to NM_018349.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:94888393 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:94927320 C>T maps to NM_018349.3 N551N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:94945193 C>T maps to NM_018349.3 F677F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:94858840 G>A maps to NM_018349.3 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:94928714 C>T maps to NM_018349.3 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:94884146 G>A maps to NM_018349.3 K321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:94899494 C>T maps to NM_018349.3 Q379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:119739362 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:30668265 G>A maps to NM_014641.2 S2082S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:30673674 G>A maps to NM_014641.2 S1095S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:30676090 G>A maps to NM_014641.2 F755F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:30680308 G>A maps to NM_014641.2 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:30672585 G>A maps to NM_014641.2 S1458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:30668354 G>A maps to NM_014641.2 L2053L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:30681795 G>A maps to NM_014641.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr6:30672021 A>T maps to NM_014641.2 S1646S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr6:30676072 C>T maps to NM_014641.2 E761E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:30671265 C>A maps to NM_014641.2 E1871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:30670991 A>G maps to NM_014641.2 G1918G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:30680737 G>A maps to NM_014641.2 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:30681076 G>A maps to NM_014641.2 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:30680704 G>A maps to NM_014641.2 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr6:41617375 C>T maps to NM_005586.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr6:41617423 G>A maps to NM_005586.3 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:41617480 G>A maps to NM_005586.3 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:114619727 C>T maps to NM_199072.4 Q238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr7:114619748 C>T maps to NM_199072.4 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr7:114619810 C>T maps to NM_199072.4 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr7:114619811 C>T maps to NM_199072.4 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr6:37619952 C>T maps to ENST00000297153 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr6:37618053 C>T maps to ENST00000297153 K480K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr6:37606050 C>T maps to ENST00000297153 G905G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr6:37606312 C>T maps to ENST00000297153 Q892Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr6:37631838 C>T maps to ENST00000297153 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr6:37612345 C>T maps to ENST00000297153 Q779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:37623613 G>A maps to ENST00000297153 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr6:37606429 G>A maps to ENST00000297153 L853L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:37626189 C>T maps to ENST00000297153 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr6:37631750 G>A maps to ENST00000297153 R67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:37619991 G>A maps to ENST00000297153 Y369Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:37631750 G>A maps to ENST00000297153 R67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:37619922 C>T maps to ENST00000297153 E392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr6:37606050 C>T maps to ENST00000297153 G905G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:37626153 G>A maps to ENST00000297153 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr6:37623547 C>T maps to ENST00000297153 W169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr14:47426820 G>A maps to NM_001113498.2 F615F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:47351310 G>A maps to NM_001113498.2 V784V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:47601015 G>A maps to NM_001113498.2 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:63833146 C>T maps to NM_005917.3 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:63821674 A>G maps to NM_005917.3 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr2:207629980 G>A maps to NM_001039845.1 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:207619910 C>T maps to NM_001039845.1 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:207615745 G>A maps to NM_001039845.1 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:207615785 C>T maps to NM_001039845.1 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:207619766 G>A maps to NM_001039845.1 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr2:207613771 C>T maps to NM_001039845.1 E396E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:207611010 C>T maps to NM_001039845.1 Q452Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:207620225 G>A maps to NM_001039845.1 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr2:207621695 C>T maps to NM_001039845.1 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:75686734 C>T maps to NM_005918.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:75695709 C>T maps to NM_005918.2 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NF-06A-11D-A19A-08 chr7:75694156 C>T maps to NM_005918.2 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:75689782 C>T maps to NM_005918.2 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr7:75695625 C>T maps to NM_005918.2 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr11:46405031 G>A maps to NM_001012333.1 K140K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr12:68720382 G>A maps to NM_020128.2 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr12:68707275 T>A maps to NM_017440.4 K556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr12:68717014 G>A maps to NM_017440.4 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:204518491 T>A maps to NM_002393.3 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr6:90365645 G>A maps to NM_014611.1 S5109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr6:90385231 G>A maps to NM_014611.1 R4238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:90402323 G>A maps to NM_014611.1 I3475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:90452921 G>A maps to NM_014611.1 F1465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr6:90482430 G>A maps to NM_014611.1 F648F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:90402773 G>A maps to NM_014611.1 S3325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr6:90491188 T>C maps to NM_014611.1 A524A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:90382347 G>A maps to NM_014611.1 L4516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:90411663 C>T maps to NM_014611.1 L2755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:90394611 G>A maps to NM_014611.1 L3938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr6:90424463 G>A maps to NM_014611.1 F2289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:90433233 G>A maps to NM_014611.1 N1925N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:90494816 G>A maps to NM_014611.1 R455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:90402560 G>A maps to NM_014611.1 A3396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:90402812 C>T maps to NM_014611.1 K3312K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:90432826 C>T maps to NM_014611.1 G1938G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr6:90421913 G>A maps to NM_014611.1 L2498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:90482424 G>A maps to NM_014611.1 F650F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr6:90411651 G>A maps to NM_014611.1 I2759I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr6:90405697 G>A maps to NM_014611.1 Q3133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr6:90405698 G>A maps to NM_014611.1 S3132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:90428500 C>G maps to NM_014611.1 L2102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr6:90468044 G>A maps to NM_014611.1 F877F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr6:90368014 G>A maps to NM_014611.1 S5032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:90397859 G>A maps to NM_014611.1 F3764F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:90433299 G>A maps to NM_014611.1 F1903F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:90504324 G>A maps to NM_014611.1 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr6:90438745 C>T maps to NM_014611.1 L1751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr6:90422394 G>A maps to NM_014611.1 L2443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr6:84025069 A>C maps to NM_002395.4 Y221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr6:83947537 C>T maps to NM_002395.4 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:84117512 G>A maps to NM_002395.4 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:84117512 G>A maps to NM_002395.4 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:84108093 C>T maps to NM_002395.4 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:84117512 G>A maps to NM_002395.4 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr6:84025036 A>T maps to NM_002395.4 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr6:84117512 G>A maps to NM_002395.4 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr6:84117512 G>A maps to NM_002395.4 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr6:84108147 A>T maps to NM_002395.4 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:84025042 C>T maps to NM_002395.4 E230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:84117512 G>A maps to NM_002395.4 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr18:48473490 C>T maps to NM_002396.4 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr18:48434449 A>G maps to NM_002396.4 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr18:48447031 G>T maps to NM_002396.4 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr18:48473475 G>A maps to NM_002396.4 R559R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:86160975 G>A maps to NM_001014811.1 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr11:86159198 G>A maps to NM_001014811.1 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr11:86267656 G>A maps to NM_001014811.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:86158196 G>A maps to NM_001014811.1 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:86382821 C>T maps to NM_001014811.1 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr6:42981044 C>A maps to NM_014623.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:37980287 C>T maps to NM_022756.4 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr3:168834003 C>T maps to NM_004991.3 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr3:168807882 C>T maps to NM_004991.3 K1102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr3:168810843 C>T maps to NM_004991.3 A1022A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:168834003 C>T maps to NM_004991.3 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:168833466 C>T maps to NM_004991.3 K731K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:168838946 G>A maps to NM_004991.3 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:168833466 C>T maps to NM_004991.3 K731K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr3:168845678 C>T maps to NM_004991.3 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr3:169099049 G>A maps to NM_004991.3 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:168834375 C>T maps to NM_004991.3 E428E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:168810795 G>A maps to NM_004991.3 F1038F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:168833625 C>T maps to NM_004991.3 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:169099127 G>A maps to NM_004991.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:168813033 C>G did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr3:168810795 G>A maps to NM_004991.3 F1038F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:168840515 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:168806892 C>T maps to NM_004991.3 R1160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:168849265 G>A maps to NM_004991.3 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:168834489 G>A maps to NM_004991.3 N390N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:169099229 G>A maps to NM_004991.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:168833568 G>A maps to NM_004991.3 L697L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:168861617 G>A maps to NM_004991.3 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:153296705 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:153296706 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr23:153296629 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:153296313 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr23:153296194 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr1:29542574 G>C maps to NM_016011.2 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:29533400 C>T maps to NM_016011.2 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:29520671 G>A maps to NM_016011.2 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr1:29557307 G>A maps to NM_016011.2 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr17:37563940 A>G maps to NM_004774.3 D1511D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:37576033 G>A maps to NM_004774.3 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:37580985 G>A maps to NM_004774.3 R249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JB-06A-11D-A196-08 chr23:70342381 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:70338618 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:70340914 T>G did not map to a codon.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr23:70345912 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:70356749 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:70339656 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:70346834 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:70344181 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr23:70341597 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:70342948 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:70350001 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:70343561 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:70356759 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:70352254 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr23:70356418 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:70348269 G>A did not map to a codon.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr23:70357679 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr23:70356321 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:70342949 C>T did not map to a codon.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr23:70357623 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr3:151082982 G>A maps to NM_053002.4 Q1023Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr3:151131059 C>T maps to NM_053002.4 R2057*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:151094936 G>A maps to NM_053002.4 T1394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr3:150877800 C>A maps to NM_053002.4 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:150906238 G>A maps to NM_053002.4 R575R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:150911422 A>G maps to NM_053002.4 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr3:150840631 G>A maps to NM_053002.4 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:151105620 G>A maps to NM_053002.4 Q1669Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:150908567 C>T maps to NM_053002.4 F606F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:151105866 C>T maps to NM_053002.4 S1751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:151095901 G>A maps to NM_053002.4 E1438E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:150903247 G>A maps to NM_053002.4 E542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr3:151073742 C>T maps to NM_053002.4 L824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:151105773 C>T maps to NM_053002.4 P1720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr3:151067845 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:151107897 C>T maps to NM_053002.4 F1826F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr3:151067890 C>T maps to NM_053002.4 L730L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr3:151134119 C>T maps to NM_053002.4 P2071P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr3:151102859 C>T maps to NM_053002.4 R1622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr3:151129184 A>T maps to NM_053002.4 A1975A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:150881819 C>T maps to NM_053002.4 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:151085968 G>A maps to NM_053002.4 A1125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:151094618 G>A maps to NM_053002.4 W1327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:150876534 C>T maps to NM_053002.4 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:151107867 C>T maps to NM_053002.4 L1816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr17:60072572 G>A maps to NM_005121.2 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:60106996 A>G maps to NM_005121.2 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:60062044 C>T maps to NM_005121.2 E886E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr17:60023954 A>T maps to NM_005121.2 V2133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr17:60060324 C>T maps to NM_005121.2 R1013R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr17:60030379 A>G maps to NM_005121.2 G2021G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr12:116434478 G>T maps to NM_015335.4 S933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:116444159 C>A maps to NM_015335.4 V765V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr12:116422132 A>C maps to NM_015335.4 R1461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:116445227 C>T maps to NM_015335.4 L742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:116434435 G>A maps to NM_015335.4 S947S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:116429485 G>A maps to NM_015335.4 P1091P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr12:116675501 G>A maps to NM_015335.4 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:116429467 G>A maps to NM_015335.4 P1097P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr12:116429500 G>A maps to NM_015335.4 P1086P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr12:116406783 A>C maps to NM_015335.4 P2062P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr23:40534568 T>C did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:40534534 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:40572217 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:40518792 C>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:40540120 A>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:40551482 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr22:20937219 C>T maps to NM_001003891.1 F501F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr22:20929470 C>T maps to NM_001003891.1 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr22:20929491 C>T maps to NM_001003891.1 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr22:20891472 C>T maps to NM_001003891.1 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:880116 G>A maps to NM_005481.2 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:873481 G>A maps to NM_005481.2 F624F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr19:873505 C>T maps to NM_005481.2 Q616Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:868157 G>A maps to NM_005481.2 H859H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:93535012 C>T maps to NM_004268.4 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:93530765 G>A maps to NM_004268.4 K403K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:93528226 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:93528227 T>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr11:93523910 C>T maps to NM_004268.4 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:93523910 C>T maps to NM_004268.4 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:28661300 C>T maps to NM_017638.2 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:41877042 G>A maps to NM_004275.3 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Z-06A-11D-A196-08 chr9:136210996 C>T maps to NM_133640.3 E132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr6:131927665 G>A maps to ENST00000403834 N446N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:131931275 G>A maps to ENST00000403834 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:131924267 C>T maps to ENST00000403834 R617R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:38183176 G>A maps to NM_014815.3 F547F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:38209598 G>T maps to NM_014815.3 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:38183161 G>A maps to NM_014815.3 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr17:38192009 C>T maps to NM_014815.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr19:50333966 T>A maps to NM_030973.3 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:50338358 C>T maps to NM_030973.3 F533F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:50335671 C>T maps to NM_030973.3 F494F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:50334627 C>T maps to NM_030973.3 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:50333402 C>A maps to NM_030973.3 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr14:71059683 G>A maps to ENST00000430055 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr14:71064453 G>A maps to ENST00000430055 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:156565769 G>A maps to NM_004270.4 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr5:156566259 A>G maps to NM_004270.4 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:43850171 C>T maps to NM_052877.3 K285K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr1:43853203 C>G maps to NM_052877.3 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:17394688 C>T maps to NM_018019.2 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:100211646 C>T maps to ENST00000338042 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr5:88018642 G>A maps to NM_002397.4 D400D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:88025140 C>T maps to NM_002397.4 Q286Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr5:88018699 G>A maps to NM_002397.4 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr1:156437892 G>A maps to NM_005920.2 D482D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr1:156438707 G>A maps to NM_005920.2 Q371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr16:3293452 C>T maps to NM_000243.2 G678G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr16:3306467 G>A maps to NM_000243.2 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr16:3293257 G>A maps to NM_000243.2 F743F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr16:3297183 C>T maps to NM_000243.2 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:3306548 C>T maps to NM_000243.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:3304434 C>T maps to NM_000243.2 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr16:3299631 G>A maps to NM_000243.2 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr16:3299466 C>T maps to NM_000243.2 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:3293194 C>T maps to NM_000243.2 G764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr5:126667026 G>A maps to NM_032446.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:126792923 C>T maps to NM_032446.2 L1113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr5:126790294 C>T maps to NM_032446.2 S1006S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:126734472 C>T maps to NM_032446.2 C255C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:126790294 C>T maps to NM_032446.2 S1006S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:126667075 C>T maps to NM_032446.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:126781203 C>T maps to NM_032446.2 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr5:126753434 C>T maps to NM_032446.2 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:126705671 G>A maps to NM_032446.2 W130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:126732422 C>T maps to NM_032446.2 D204D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:126746128 G>A maps to NM_032446.2 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:126784912 C>T maps to NM_032446.2 L993L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:126774212 G>A maps to NM_032446.2 G729G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr15:66257436 G>A maps to NM_032445.2 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr15:66262994 C>T maps to NM_032445.2 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:66223164 C>T maps to NM_032445.2 K468K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:66416265 G>A maps to NM_032445.2 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr15:66215173 G>A maps to NM_032445.2 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr15:66250031 G>A maps to NM_032445.2 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:3431120 G>A maps to ENST00000452816 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr1:3425708 C>T maps to ENST00000452816 Q561Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:3425765 G>A maps to ENST00000452816 F542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:3417828 G>A maps to ENST00000452816 C861C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:3428167 G>A maps to ENST00000452816 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:3440796 G>A maps to ENST00000452816 C240C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:42837754 A>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:42841326 A>G maps to ENST00000251268 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:42880503 A>G maps to ENST00000251268 P2705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr19:42848672 C>T maps to ENST00000251268 A623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:42840345 C>T maps to ENST00000251268 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr19:42848170 T>C maps to ENST00000251268 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:42875634 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:42880017 C>T maps to ENST00000251268 P2543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:42854466 C>T maps to ENST00000251268 S889S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:42839299 C>T maps to ENST00000251268 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:42861644 C>T maps to ENST00000251268 S1640S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:42837847 C>T maps to ENST00000251268 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:42867221 C>T maps to ENST00000251268 S2027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:42858151 C>T maps to ENST00000251268 S1329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr19:42848897 C>T maps to ENST00000251268 S670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr19:42848975 G>A maps to ENST00000251268 Q696Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:42853766 C>A maps to ENST00000251268 I805I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:42853767 C>T maps to ENST00000251268 Q806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:42880626 C>T maps to ENST00000251268 P2746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:42838217 C>T maps to ENST00000251268 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr19:42848888 C>T maps to ENST00000251268 F667F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr9:123367701 C>T maps to ENST00000426959 V562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr9:123453746 G>A maps to ENST00000426959 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:42150006 C>T maps to NM_152513.3 N636N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr22:42191743 G>A maps to NM_152513.3 Q1224Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:42149985 C>T maps to NM_152513.3 F629F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr22:42172207 C>T maps to NM_152513.3 R883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr22:42128252 C>T maps to NM_152513.3 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr22:42141921 C>T maps to NM_152513.3 A524A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr22:42174718 G>A maps to NM_152513.3 G906G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr22:42099375 C>T maps to NM_152513.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr22:42166715 C>T maps to NM_152513.3 F765F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr22:42166940 C>T maps to NM_152513.3 I840I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr22:42166926 T>C maps to NM_152513.3 L836L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:42128604 G>A maps to NM_152513.3 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr22:42154390 C>T maps to NM_152513.3 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr22:42114231 C>T maps to NM_152513.3 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:66667711 C>T maps to ENST00000407092 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:66795860 C>T maps to ENST00000407092 Q363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr15:37385868 G>T maps to NM_170675.2 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr15:37187013 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:37242592 G>A maps to NM_170675.2 Y303Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:37242538 G>A maps to NM_170675.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:37187001 C>A maps to NM_170677.2 G387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr19:47910354 G>A maps to NM_020160.1 I371I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:47918072 C>T maps to NM_020160.1 K166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:47910345 G>A maps to NM_020160.1 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr11:64572585 C>A maps to NM_130804.2 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr11:64571808 G>T maps to NM_130804.2 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:64575468 C>T maps to NM_130804.2 W188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr17:41738449 C>T maps to NM_004527.3 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:41738629 G>A maps to NM_004527.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:15652140 C>T maps to NM_005924.4 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:15666538 G>A maps to NM_005924.4 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr6:46800997 C>T maps to NM_005588.2 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr6:46806848 C>T maps to NM_005588.2 I739I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:46802450 G>A maps to NM_005588.2 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:46806749 G>A maps to NM_005588.2 G706G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:46806848 C>T maps to NM_005588.2 I739I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:46803190 C>T maps to NM_005588.2 D663D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr6:46806866 G>A maps to NM_005588.2 R745R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:46806800 C>T maps to NM_005588.2 I723I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr6:46797216 G>A maps to NM_005588.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:46803056 C>T maps to NM_005588.2 Q619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:46797135 G>T maps to NM_005588.2 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:46806722 C>T maps to NM_005588.2 I697I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr18:29790659 C>T maps to NM_005925.2 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr18:29797057 C>T maps to NM_005925.2 R622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr18:29793247 G>A maps to NM_005925.2 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr18:29793124 G>A maps to NM_005925.2 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr7:100028646 C>T maps to NM_019606.5 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:100029260 C>T maps to NM_019606.5 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr4:88766238 C>A maps to ENST00000395102 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:88766262 G>A maps to ENST00000395102 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr4:88766629 C>T maps to ENST00000395102 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:88767096 T>C maps to ENST00000395102 D390D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:88766622 C>T maps to ENST00000395102 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:112732864 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr2:112686786 T>A maps to NM_006343.2 L51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:112751958 G>A maps to NM_006343.2 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:112702605 C>T maps to NM_006343.2 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:112705121 C>T maps to NM_006343.2 S245S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A2ML-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr2:112785927 G>A maps to NM_006343.2 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:112702605 C>T maps to NM_006343.2 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:112751958 G>A maps to NM_006343.2 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:112786119 G>A maps to NM_006343.2 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:112786386 C>T maps to NM_006343.2 P982P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:112722774 G>A maps to NM_006343.2 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:112786131 C>T maps to NM_006343.2 I897I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr2:112785951 G>A maps to NM_006343.2 W837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr2:112785978 C>T maps to NM_006343.2 T846T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:112786131 C>T maps to NM_006343.2 I897I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:112755014 C>T maps to NM_006343.2 S522S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:112777018 C>T maps to NM_006343.2 F703F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr2:112751970 C>T maps to NM_006343.2 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr2:112751910 G>A maps to NM_006343.2 R460R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr15:81271618 G>A maps to NM_015154.1 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr15:81271601 G>A maps to NM_015154.1 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:90293985 G>A maps to NM_018670.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr15:90321453 C>T maps to NM_001039958.1 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:130138041 G>A maps to NM_002402.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr7:130135274 C>T maps to NM_002402.2 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr7:130137799 G>A maps to NM_002402.2 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:116340220 C>T maps to NM_001127500.1 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:116435842 C>T maps to NM_001127500.1 P1329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr7:116380979 C>T maps to NM_001127500.1 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:116339179 C>T maps to NM_001127500.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr7:116339803 G>A maps to NM_001127500.1 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr7:116411676 C>T maps to NM_001127500.1 F970F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr7:116409817 G>A maps to NM_001127500.1 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr7:116397780 G>A maps to NM_001127500.1 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:116380041 G>A maps to NM_001127500.1 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:116414987 C>T maps to NM_001127500.1 L1046L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr7:116371769 C>T maps to NM_001127500.1 R417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:116397717 G>A maps to NM_001127500.1 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:116414936 C>T maps to NM_001127500.1 Q1029*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:116422085 C>A maps to NM_001127500.1 A1207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr7:116339803 G>A maps to NM_001127500.1 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:116339545 C>T maps to NM_001127500.1 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:116411552 G>A maps to NM_001127500.1 W929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26D-06A-11D-A19A-08 chr7:116339557 C>G maps to NM_001127500.1 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr7:116397529 C>T maps to NM_001127500.1 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr17:81052055 C>T maps to NM_001004431.1 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr17:81042984 C>T maps to NM_001004431.1 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:2405513 G>A maps to NM_024086.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:2381127 T>A maps to NM_024086.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:2323265 A>T maps to NM_024086.3 *563K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr17:2323842 G>A maps to NM_024086.3 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:21464990 C>T maps to NM_001029991.1 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr14:21464745 G>T maps to NM_001029991.1 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr10:126454045 G>A maps to NM_212554.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:132396538 C>T maps to NM_014064.2 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:132397674 C>T maps to NM_014064.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr1:171755034 G>A maps to NM_015935.4 E310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:171761352 C>T maps to NM_015935.4 A557A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr4:119613140 A>T maps to NM_020961.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr4:119613141 C>T maps to NM_020961.2 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr17:60501660 G>A maps to NM_181725.3 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr17:60518078 C>T maps to NM_181725.3 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr7:128119281 G>A maps to NM_018396.2 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr18:2566950 G>T maps to NM_022840.3 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:170677746 C>T maps to NM_014168.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:15452785 G>A maps to NM_152396.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr3:15457400 G>A maps to NM_152396.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:56077724 G>A maps to NM_152637.2 W209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:21666635 C>T maps to NM_016025.3 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr16:21629266 C>T maps to NM_016025.3 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:82335560 G>A maps to NM_032246.3 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:82335977 G>A maps to NM_032246.3 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:1556353 G>A maps to NM_001174118.1 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr15:44107264 G>A maps to NM_005926.2 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:44105297 G>A maps to NM_005926.2 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:153432813 C>T maps to NM_005927.4 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:153432972 C>T maps to NM_005927.4 D263D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:153433111 C>T maps to NM_005927.4 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr5:153432801 C>T maps to NM_005927.4 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:170912660 G>A maps to NM_021647.6 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:8808043 C>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:8814652 G>A maps to NM_003480.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr2:228195473 G>A maps to NM_020194.4 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:228205010 C>T maps to NM_020194.4 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr15:89449928 C>T maps to NM_005928.2 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr15:89449880 G>A maps to NM_005928.2 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:8748816 G>A maps to NM_004225.2 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr8:8654903 G>A maps to NM_004225.2 P1032P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr8:8749116 A>C maps to NM_004225.2 Y484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr8:8749329 G>A maps to NM_004225.2 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr8:8749932 G>A maps to NM_004225.2 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr8:8748177 G>A maps to NM_004225.2 L797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr3:196737641 G>A maps to NM_005929.5 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:196737596 C>T maps to NM_005929.5 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:196754650 G>A maps to NM_005929.5 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:196749919 G>A maps to NM_005929.5 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr3:179096488 C>T maps to NM_033540.2 Q517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:179096427 C>T maps to NM_033540.2 I496I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr1:12057475 C>T maps to NM_014874.3 D199D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:12066608 C>T maps to NM_014874.3 I577I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:12062088 C>T maps to NM_014874.3 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:37876305 C>T maps to NM_002405.3 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr22:37882170 G>A maps to NM_002405.3 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:37882140 C>T maps to NM_002405.3 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:119217021 G>A maps to NM_031433.2 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:119217036 G>A maps to NM_031433.2 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr11:119214575 G>A maps to NM_031433.2 Y358Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:119214620 G>A maps to NM_031433.2 F343F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:119216621 G>A maps to NM_031433.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr3:158539802 C>T maps to NM_022736.2 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:158523176 C>T maps to NM_022736.2 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr3:158541954 C>T maps to NM_022736.2 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr3:158525196 C>T maps to NM_022736.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr4:2933362 G>A maps to NM_001146069.1 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr4:2933365 G>A maps to NM_001146069.1 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:2935554 G>A maps to NM_001146069.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr17:74774295 C>T maps to NM_024311.2 F404F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr1:40432816 C>T maps to NM_001136493.1 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr1:40432816 C>T maps to NM_001136493.1 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:40422862 C>T maps to NM_001136493.1 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:40430939 C>T maps to NM_001136493.1 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr1:40431538 G>A maps to NM_001136493.1 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr2:24239822 C>T maps to ENST00000338315 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:24239783 C>T maps to ENST00000338315 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:24245744 G>A maps to ENST00000338315 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr8:145736174 A>C did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:205549925 G>A maps to NM_181644.4 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:205554119 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr1:205553163 C>T maps to NM_181644.4 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:205549802 C>T maps to NM_181644.4 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:205549070 C>T maps to NM_181644.4 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:205561329 C>T maps to NM_181644.4 F404F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr1:205554034 G>A maps to NM_181644.4 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:205555196 G>A maps to NM_181644.4 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:205549070 C>T maps to NM_181644.4 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:205549799 C>T maps to NM_181644.4 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:205554034 G>A maps to NM_181644.4 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr1:205553163 C>T maps to NM_181644.4 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr12:53647945 G>T maps to NM_001170790.1 E550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr12:53646732 C>T maps to NM_001170790.1 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr12:53646603 C>T maps to NM_001170790.1 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:53647725 C>T maps to NM_001170790.1 I476I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:191302284 C>T maps to NM_017694.3 I510I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:191302197 C>T maps to NM_017694.3 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:191301864 C>T maps to NM_017694.3 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:191364931 G>C maps to NM_017694.3 A788A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr2:191354494 G>A maps to NM_017694.3 G598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr17:8701724 G>A maps to NM_152599.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:8700809 C>T maps to NM_152599.3 R543R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr4:677396 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:680022 C>T maps to ENST00000404286 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:680389 G>A maps to ENST00000404286 Y75Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr4:676657 G>A maps to ENST00000404286 I392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:128842792 C>G maps to NM_152778.2 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr2:103335118 G>A maps to NM_032718.3 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr2:103353173 C>T maps to NM_032718.3 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:103340267 G>A maps to NM_032718.3 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr2:103340157 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:103343330 G>A maps to NM_032718.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr15:42034888 C>T maps to ENST00000219905 V1626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr15:42041468 C>T maps to ENST00000219905 S1937S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr15:42019409 C>T maps to ENST00000219905 R1155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr15:42041982 C>T maps to ENST00000219905 Q2109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:42054351 G>A maps to ENST00000219905 K2561K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr15:42059093 C>T maps to ENST00000219905 L2987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr15:42042692 C>T maps to ENST00000219905 F2345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr15:42000028 C>T maps to ENST00000219905 N764N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr15:41961892 C>T maps to ENST00000219905 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr15:42041030 C>T maps to ENST00000219905 H1852H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr15:42050031 C>T maps to ENST00000219905 R2445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr15:42050031 C>T maps to ENST00000219905 R2445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:42058823 C>G maps to ENST00000219905 P2897P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr15:42059303 C>T maps to ENST00000219905 L3057L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr15:42035011 T>A maps to ENST00000219905 I1667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr15:42041409 C>T maps to ENST00000219905 Q1918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:141754618 C>T maps to ENST00000475668 S1075S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:141764244 C>T maps to ENST00000475668 I1469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr7:141758085 C>T maps to ENST00000475668 I1259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr7:141740607 C>T maps to ENST00000475668 I820I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr7:141722125 C>T maps to ENST00000475668 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:141747641 A>T maps to ENST00000475668 G852G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:141755435 C>T maps to ENST00000475668 L1131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr7:141758050 C>T maps to ENST00000475668 L1248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr7:141740593 C>T maps to ENST00000475668 R816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr7:141740640 G>A maps to ENST00000475668 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:141722208 C>T maps to ENST00000475668 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr7:141803217 C>T maps to ENST00000475668 F2722F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:141705446 G>A maps to ENST00000475668 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:141797418 C>T maps to ENST00000475668 F2574F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr7:141750582 G>A maps to ENST00000475668 E908E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A6L9-06A-11D-A32N-08 chr7:141760112 C>G maps to ENST00000475668 V1354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:141720876 C>T maps to ENST00000475668 H184H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:141758085 C>T maps to ENST00000475668 I1259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:141755447 G>A maps to ENST00000475668 G1135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr7:141752711 C>T maps to ENST00000475668 A1029A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:141727501 C>T maps to ENST00000475668 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:141752588 C>T maps to ENST00000475668 S988S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:141758085 C>T maps to ENST00000475668 I1259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:141731537 G>A maps to ENST00000475668 W510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:141731538 G>A maps to ENST00000475668 W510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr7:141755408 C>T maps to ENST00000475668 I1122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr7:141755435 C>T maps to ENST00000475668 L1131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr7:141755882 C>T maps to ENST00000475668 N1189N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:141734487 C>T maps to ENST00000475668 F602F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr7:141734598 C>T maps to ENST00000475668 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:141750660 G>A maps to ENST00000475668 L934L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr7:141802439 G>A maps to ENST00000475668 G2659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:141736636 C>T maps to ENST00000475668 A697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr7:141736729 C>T maps to ENST00000475668 F728F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr7:141758046 C>T maps to ENST00000475668 F1246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr7:141805689 G>A maps to ENST00000475668 *2755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:141797418 C>T maps to ENST00000475668 F2574F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:141764220 C>T maps to ENST00000475668 T1461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:141747668 G>A maps to ENST00000475668 T861T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:141754672 G>A maps to ENST00000475668 G1093G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:141760156 G>A maps to ENST00000475668 W1369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:141763351 G>A maps to ENST00000475668 R1437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:141758085 C>T maps to ENST00000475668 I1259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:141794438 C>T maps to ENST00000475668 L2443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:141794560 C>T maps to ENST00000475668 I2453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:141755372 C>T maps to ENST00000475668 L1110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr7:141752633 C>T maps to ENST00000475668 Y1003Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr7:141755486 G>A maps to ENST00000475668 W1148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:141797448 G>C maps to ENST00000475668 T2584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr7:141759378 G>A maps to ENST00000475668 G1309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr7:141747668 G>A maps to ENST00000475668 T861T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr7:141752621 C>T maps to ENST00000475668 V999V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr7:141754552 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:141756640 C>T maps to ENST00000475668 Q1198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr7:141722067 G>A maps to ENST00000475668 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr7:141802439 G>A maps to ENST00000475668 G2659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr7:141734622 C>T maps to ENST00000475668 N647N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr7:141758082 G>A maps to ENST00000475668 E1258E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr7:141796172 C>T maps to ENST00000475668 F2551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:141765191 C>T maps to ENST00000475668 P1514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:141740541 G>A maps to ENST00000475668 R798R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:141755471 G>A maps to ENST00000475668 R1143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:141765263 C>T maps to ENST00000475668 I1538I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:141796205 C>T maps to ENST00000475668 V2562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr7:141802439 G>A maps to ENST00000475668 G2659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr7:141736712 C>T maps to ENST00000475668 L723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr7:141802457 G>A maps to ENST00000475668 L2665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr7:141730553 G>A maps to ENST00000475668 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr5:180219416 G>A maps to NM_001114617.1 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:180219449 C>T maps to NM_001114617.1 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:50089302 C>T maps to NM_002408.3 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr14:50089056 T>C maps to NM_002408.3 C357C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr22:39884005 C>T maps to NM_001098270.1 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr22:39883738 C>T maps to NM_001098270.1 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr22:39883495 C>T maps to NM_001098270.1 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:39884212 C>T maps to NM_001098270.1 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr22:39884728 C>T maps to NM_001098270.1 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr22:39884671 C>T maps to NM_001098270.1 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr22:39884188 C>G maps to NM_001098270.1 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr22:39884938 C>T maps to NM_001098270.1 D529D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:39883675 C>T maps to NM_001098270.1 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:39884746 C>T maps to NM_001098270.1 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:99291552 C>T maps to NM_012214.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:99256383 G>A maps to NM_012214.2 Y403Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:179227053 G>A maps to NM_054013.3 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr5:179225962 G>A maps to NM_054013.3 I451I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr5:179228605 G>A maps to NM_054013.3 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr12:86373959 G>A maps to ENST00000393205 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:86373852 T>A maps to ENST00000393205 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr12:86373537 C>T maps to ENST00000393205 E351E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr12:86373090 C>T maps to ENST00000393205 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr12:86374017 G>A maps to ENST00000393205 H191H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr12:86373959 G>A maps to ENST00000393205 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:86373393 C>T maps to ENST00000393205 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:135206360 C>T maps to NM_002410.3 V723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr2:135076303 C>T maps to NM_002410.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr17:74902173 C>T maps to NM_198955.1 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr17:74922711 G>A maps to NM_198955.1 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:74944722 C>T maps to NM_198955.1 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr17:74934092 C>T maps to NM_198955.1 I493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:74922789 C>T maps to NM_198955.1 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:74928823 C>A maps to NM_198955.1 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr17:74901258 C>T maps to NM_198955.1 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:74901258 C>T maps to NM_198955.1 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:74936845 C>T maps to NM_198955.1 F597F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr7:88423704 G>A maps to NM_152706.2 Y184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:88424097 C>T maps to NM_152706.2 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:88424121 G>A maps to NM_152706.2 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr7:88424232 C>T maps to NM_152706.2 Q8Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:88423731 G>A maps to NM_152706.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:88423587 G>A maps to NM_152706.2 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr5:43280110 G>A maps to NM_153361.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:43246071 C>T maps to NM_153361.2 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:43280275 G>A maps to NM_153361.2 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:43246020 C>T maps to NM_153361.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr8:145753064 G>A maps to NM_001001795.1 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr7:22532978 G>C maps to ENST00000441815 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:22533206 G>A maps to ENST00000441815 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr10:103558829 G>A maps to NM_012215.3 P526P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:103550823 G>A maps to NM_012215.3 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:127414012 G>A maps to NM_007283.5 D207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr3:127441339 A>T maps to NM_007283.5 L111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr3:127413946 C>T maps to NM_007283.5 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr10:131506260 C>T maps to NM_002412.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:131506242 C>T maps to NM_002412.3 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:131506164 G>A maps to NM_002412.3 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr12:15035174 C>T maps to NM_001190839.1 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:4731624 C>T maps to NM_015246.2 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:4731633 C>T maps to NM_015246.2 I405I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:4731612 C>T maps to NM_015246.2 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:4700390 C>T maps to NM_015246.2 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr12:16510601 C>T maps to NM_145764.1 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:140616380 C>T maps to NM_002413.3 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:165623541 C>A maps to ENST00000367886 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:41281684 G>A maps to NM_006533.2 Q52Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr14:39717187 C>T maps to NM_054024.3 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr14:39722332 C>T maps to NM_054024.3 F615F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr14:39717187 C>T maps to NM_054024.3 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr14:39716703 G>A maps to NM_054024.3 W309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:39717190 G>A maps to NM_054024.3 Q471Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:39716428 T>C maps to NM_054024.3 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr14:39717064 G>A maps to NM_054024.3 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr1:222806470 T>C maps to NM_198551.2 P1119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:222802619 C>T maps to NM_198551.2 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr1:222837432 G>T maps to NM_198551.2 G1786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:222801983 C>T maps to NM_198551.2 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr18:19353596 C>T maps to NM_020774.2 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr18:19359526 T>C maps to NM_020774.2 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr18:19429315 C>T maps to NM_020774.2 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:1560201 C>T maps to NM_080875.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:1558804 C>T maps to NM_080875.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:1559298 C>T maps to NM_080875.2 D246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr1:1560756 C>T maps to NM_080875.2 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr1:1560563 C>T maps to NM_080875.2 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:1563760 C>G maps to NM_080875.2 A765A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:1565903 C>T maps to NM_080875.2 F1069F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:1563921 C>T maps to NM_080875.2 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr1:1560739 C>T maps to NM_080875.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:1562296 C>T maps to NM_080875.2 T501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr6:31378341 C>T maps to NM_000247.1 N31N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:31378942 C>T maps to NM_000247.1 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr6:109770952 G>A maps to NM_022765.3 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:109766439 G>A maps to NM_022765.3 A947A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:109768345 C>T maps to NM_022765.3 R719R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:109768429 G>A maps to NM_022765.3 A691A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:109769146 G>A maps to NM_022765.3 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr11:12183806 C>T maps to NM_014632.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr11:12280078 G>A maps to NM_014632.2 R1069R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr11:12247798 C>T maps to NM_014632.2 I590I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:12234919 C>T maps to NM_014632.2 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr11:12284033 C>T maps to NM_014632.2 F1114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:12270729 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:12225852 C>T maps to NM_014632.2 Y107Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:12225853 C>T maps to NM_014632.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr22:18300278 G>A maps to NM_015241.2 G1716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr22:18364024 G>A maps to NM_001136004.1 I762I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr22:18300932 G>A maps to NM_015241.2 P1498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr22:18384656 C>T maps to NM_015241.2 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr22:18305763 C>A maps to NM_015241.2 E1086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:18347653 A>C maps to NM_001136004.1 T996T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr22:18382264 G>A maps to NM_015241.2 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr22:18382264 G>A maps to NM_015241.2 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:18301667 G>A maps to NM_015241.2 P1253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr22:18347692 G>A maps to NM_015241.2 A859A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr22:18300782 G>A maps to NM_015241.2 S1548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr22:18354648 G>A maps to NM_015241.2 C794C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr22:18389392 G>A maps to NM_015241.2 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr22:18371809 G>A maps to NM_015241.2 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr22:18300617 G>A maps to NM_015241.2 S1603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr22:18314776 G>A maps to NM_015241.2 A966A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr22:18364024 G>A maps to NM_001136004.1 I762I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:18300146 G>A maps to NM_015241.2 C1760C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:18347478 G>A maps to NM_001136004.1 L1055L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr22:18347736 G>A maps to NM_015241.2 L845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr22:18273569 G>A maps to NM_015241.2 L1979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr11:12315205 G>A maps to NM_032867.2 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr11:12313729 G>A maps to NM_032867.2 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:12341345 C>T maps to NM_032867.2 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:12315610 C>T maps to NM_032867.2 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr11:12316174 C>T maps to NM_032867.2 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:12315463 G>A maps to NM_032867.2 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:12315718 G>A maps to NM_032867.2 Q247Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:12313834 C>T maps to NM_032867.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:12315808 C>T maps to NM_032867.2 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr22:38318089 G>A maps to NM_033386.2 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr22:38321961 C>T maps to NM_033386.2 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:38317993 C>T maps to NM_033386.2 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr22:38320718 C>T maps to NM_033386.2 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F4-06A-12D-A25O-08 chr22:38328585 G>A maps to NM_033386.2 E681E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F4-06A-12D-A25O-08 chr22:38328829 G>A maps to NM_033386.2 V723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F4-06A-12D-A25O-08 chr22:38329057 G>A maps to NM_033386.2 Q749Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr7:1474303 G>A maps to NM_182924.3 L881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:1484877 G>A maps to NM_182924.3 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:1484997 G>A maps to NM_182924.3 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr7:1479645 G>A maps to NM_182924.3 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:1481951 G>A maps to NM_182924.3 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:1488259 G>A maps to NM_182924.3 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr7:1474303 G>A maps to NM_182924.3 L881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:1484889 G>A maps to NM_182924.3 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr7:1477775 G>A maps to NM_182924.3 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr7:1487372 G>A maps to NM_182924.3 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:1478578 G>A maps to NM_182924.3 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:1489875 C>G maps to NM_182924.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr7:1474273 G>A maps to NM_182924.3 S891S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr7:1480264 C>T maps to NM_182924.3 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr6:31475298 G>T maps to NM_005931.3 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:31474868 C>T maps to NM_005931.3 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:10417592 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:10422959 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:10427725 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:10427797 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:10423069 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:10463688 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr23:38664491 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:107169962 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:107170185 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:107084037 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:107084241 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:107084266 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:107084267 A>C did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:107084243 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:107084244 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:107169344 C>T did not map to a codon.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr23:107170225 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:107147219 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:1251901 T>C did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:67394630 C>T maps to NM_020948.3 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr19:326548 G>A maps to NM_017550.1 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:308850 G>A maps to NM_017550.1 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:307126 G>A maps to NM_017550.1 P536P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:311856 G>A maps to NM_017550.1 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:327917 C>T maps to NM_017550.1 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:327145 A>T maps to NM_017550.1 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:334402 G>A maps to NM_017550.1 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr19:326590 G>A maps to NM_017550.1 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:313575 G>A maps to NM_017550.1 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr5:56219659 C>T maps to ENST00000381226 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr1:12089850 C>T maps to NM_021933.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:12090087 G>A maps to NM_021933.2 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:12082291 T>G maps to NM_021933.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12090105 C>T maps to NM_021933.2 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr17:4797554 C>T maps to NM_153827.4 P919P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr17:4789255 C>T maps to NM_153827.4 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr17:4798780 C>T maps to NM_153827.4 T1074T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:4789255 C>T maps to NM_153827.4 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:4789258 C>T maps to NM_153827.4 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr17:4789835 C>T maps to NM_153827.4 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr17:4789487 G>A maps to NM_153827.4 K256K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:4789757 C>T maps to NM_153827.4 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:4788844 C>T maps to NM_153827.4 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr7:7628178 C>T maps to NM_019005.3 F623F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:7645579 C>T maps to NM_019005.3 T803T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:7612813 C>T maps to NM_019005.3 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:7645636 C>T maps to NM_019005.3 N822N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr22:50925837 C>A maps to NM_017584.5 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr22:50927488 C>T maps to NM_017584.5 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr22:50926415 C>T maps to NM_017584.5 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr22:50926427 C>T maps to NM_017584.5 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr12:56847476 G>A maps to NM_012064.3 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:56848292 A>T maps to NM_012064.3 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:56847401 G>A maps to NM_012064.3 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:56847476 G>A maps to NM_012064.3 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:56847476 G>A maps to NM_012064.3 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr13:24433030 G>A maps to NM_005932.3 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:24455908 G>A maps to NM_005932.3 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:37969154 G>A maps to NM_001195296.1 Q358Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr14:38016169 G>A maps to NM_001195296.1 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:37969338 C>T maps to NM_001195296.1 Q420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:70014047 G>C maps to ENST00000448226 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:70014032 C>T maps to ENST00000448226 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:70014314 C>T maps to ENST00000448226 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:226413251 G>A maps to NM_031944.1 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:226413317 G>A maps to NM_031944.1 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:129903869 G>A maps to NM_002417.4 G2078G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr10:129907334 C>T maps to NM_002417.4 K923K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:129902336 G>A maps to NM_002417.4 P2589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:129904028 G>A maps to NM_002417.4 T2025T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:129905333 G>A maps to NM_002417.4 G1590G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:129905441 A>G maps to NM_002417.4 F1554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:129901360 G>A maps to NM_002417.4 L2915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:129902428 G>A maps to NM_002417.4 L2559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:129911696 G>A maps to NM_002417.4 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:129910433 G>A maps to NM_002417.4 S644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:129904175 G>A maps to NM_002417.4 I1976I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr10:129906971 G>A maps to NM_002417.4 F1044F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr10:129906067 G>A maps to NM_002417.4 L1346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr10:129911717 A>G maps to NM_002417.4 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr10:129901697 G>A maps to NM_002417.4 G2802G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr10:129914758 G>A maps to NM_002417.4 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:129921146 G>A maps to NM_002417.4 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:129906092 C>T maps to NM_002417.4 K1337K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:129903182 C>T maps to NM_002417.4 K2307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr10:129899737 C>T maps to NM_002417.4 E3163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr20:10393631 C>T maps to NM_170784.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr20:10393934 G>A maps to NM_170784.1 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:10393289 G>A maps to NM_170784.1 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:10393712 G>A maps to NM_170784.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr22:40819557 G>A maps to NM_020831.3 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr22:40820218 G>A maps to NM_020831.3 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr22:40827451 G>A maps to NM_020831.3 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr16:14341156 C>T maps to NM_014048.3 I680I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr16:14306220 C>T maps to NM_014048.3 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr16:14328109 C>T maps to NM_014048.3 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:14334137 G>A maps to NM_014048.3 K292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:14345760 C>T maps to NM_014048.3 Q766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:131072018 C>G maps to NM_013255.4 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr7:131012747 C>T maps to NM_013255.4 Y30Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:47042305 C>T maps to NM_003684.4 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:2037812 G>A maps to NM_017572.3 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:2041158 G>A maps to NM_199054.2 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:140156573 G>A maps to NM_013446.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:140156540 G>A maps to NM_013446.3 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr15:23811000 G>A maps to NM_005664.3 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr15:23812437 C>T maps to NM_005664.3 F503F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:23812122 G>A maps to NM_005664.3 K398K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr15:23811888 G>A maps to NM_005664.3 E320E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr15:23811096 C>T maps to NM_005664.3 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:23811087 G>A maps to NM_005664.3 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:23811027 C>T maps to NM_005664.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr17:56291735 G>A maps to NM_017777.3 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:56291645 G>A maps to NM_017777.3 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr17:56291166 G>A maps to NM_017777.3 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:28023457 G>A maps to NM_173576.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:28023640 C>T maps to NM_173576.2 E194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:27964477 G>A maps to NM_173576.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:28024254 G>A maps to NM_173576.2 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr22:50500042 C>T maps to NM_015166.3 W368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:50523256 G>A maps to NM_015166.3 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr22:50506906 G>A maps to NM_015166.3 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:50500074 G>A maps to NM_015166.3 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr3:158310306 C>T maps to NM_001195432.1 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr3:158317945 C>T maps to NM_001195432.1 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:158314671 C>T maps to NM_001195432.1 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr4:185616447 C>T maps to NM_024629.3 Q417Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr12:6859170 G>A maps to NM_005439.2 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr12:6859101 G>A maps to NM_005439.2 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr3:37070384 T>A maps to NM_000249.3 L507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr3:37081680 C>T maps to NM_000249.3 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:37055955 C>T maps to NM_000249.3 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr3:37035068 C>T maps to NM_000249.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr14:75513676 A>G maps to NM_001040108.1 S894S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr14:75514825 A>G maps to NM_001040108.1 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr14:75515206 G>C maps to NM_001040108.1 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:75514785 G>A maps to NM_001040108.1 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:75514207 G>A maps to NM_001040108.1 F717F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr16:74729604 C>T maps to NM_152649.2 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:74729604 C>T maps to NM_152649.2 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:74709641 C>T maps to NM_152649.2 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:74719432 G>A maps to NM_152649.2 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr16:74709292 G>A maps to NM_152649.2 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr16:74729418 G>A maps to NM_152649.2 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr16:74729211 G>A maps to NM_152649.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:74708867 G>A maps to NM_152649.2 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr11:118343919 C>T maps to NM_001197104.1 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr11:118373177 C>T maps to NM_001197104.1 R2191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:118362004 C>T maps to NM_001197104.1 S1597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr11:118355574 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:118365449 C>T maps to NM_001197104.1 S1777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr11:118374289 A>G maps to NM_001197104.1 P2561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:118344457 C>T maps to NM_001197104.1 R862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:118343023 C>T maps to NM_001197104.1 Q384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:118343787 C>T maps to NM_001197104.1 A638A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:118374106 C>T maps to NM_001197104.1 V2500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:118375416 T>A maps to NM_001197104.1 L2937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr11:118344457 C>T maps to NM_001197104.1 R862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:118373239 G>A maps to NM_001197104.1 R2211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr11:118363899 A>G maps to NM_001197104.1 L1711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr11:118372445 C>T maps to NM_001197104.1 R2127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:118344106 C>T maps to NM_001197104.1 R745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:118343601 C>T maps to NM_001197104.1 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr12:49434136 G>C maps to NM_003482.3 P2472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr12:49441819 C>T maps to NM_003482.3 R1388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:49433938 G>A maps to NM_003482.3 F2538F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr12:49444088 G>A maps to NM_003482.3 L1094L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr12:49420214 G>A maps to NM_003482.3 F5178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr12:49428388 G>A maps to NM_003482.3 N3472N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr12:49445206 G>A maps to NM_003482.3 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:49422928 G>A maps to NM_003482.3 F4722F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr12:49416070 G>A maps to NM_003482.3 G5468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:49435258 G>A maps to NM_003482.3 D2098D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:49442531 A>C maps to NM_003482.3 S1347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:49444277 G>A maps to NM_003482.3 S1031S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:49426046 G>A maps to NM_003482.3 S4147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:49424542 G>A maps to NM_003482.3 S4560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr12:49445230 G>A maps to NM_003482.3 P745P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:49434610 G>A maps to NM_003482.3 T2314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:49445152 G>A maps to NM_003482.3 S771S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:49445251 G>A maps to NM_003482.3 S738S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:49434301 G>A maps to NM_003482.3 S2417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:49445422 G>A maps to NM_003482.3 S681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr12:49425488 C>T maps to NM_003482.3 E4333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr12:49447821 G>A maps to NM_003482.3 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:49433791 G>A maps to NM_003482.3 F2587F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr12:49427579 G>A maps to NM_003482.3 L3636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:49433378 G>A maps to NM_003482.3 L2690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:49448350 G>A maps to NM_003482.3 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr12:49445854 G>A maps to NM_003482.3 S537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:49427387 G>A maps to NM_003482.3 F3700F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:49433989 G>A maps to NM_003482.3 S2521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:49444379 G>A maps to NM_003482.3 P997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr12:49418437 G>A maps to NM_003482.3 P5325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr12:49434219 G>A maps to NM_003482.3 Q2445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr7:151900065 G>A maps to ENST00000355193 R1349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr7:151855959 G>A maps to ENST00000355193 T3886T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Z-06A-11D-A196-08 chr7:151891140 A>T maps to ENST00000355193 L1538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr7:151970841 G>A maps to ENST00000355193 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:151845610 C>T maps to ENST00000355193 K4524K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:151970829 G>A maps to ENST00000355193 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:151970853 G>T maps to ENST00000355193 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:151851429 G>A maps to ENST00000355193 L4078L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:151877064 G>A maps to ENST00000355193 F2432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:151878413 C>T maps to ENST00000355193 Q2177Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:151873958 G>T maps to ENST00000355193 S2860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr7:151970805 G>A maps to ENST00000355193 D332D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:151877124 G>C maps to ENST00000355193 P2412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:151880142 G>C maps to ENST00000355193 P1727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:151962184 C>G maps to ENST00000355193 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr7:151845397 G>A maps to ENST00000355193 I4595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr7:151849907 C>T maps to ENST00000355193 L4193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr7:151846057 G>A maps to ENST00000355193 V4375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:151927039 G>A maps to ENST00000355193 Q982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:151874080 G>A maps to ENST00000355193 T2819T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:151962238 C>T maps to ENST00000355193 Q356Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr7:151945142 A>G maps to ENST00000355193 P792P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:36215909 C>T maps to NM_014727.1 P1150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr19:36221457 C>T maps to NM_014727.1 S1739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr19:36211032 C>T maps to NM_014727.1 Q262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:36223188 C>T maps to NM_014727.1 S1913S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:36218840 C>G maps to NM_014727.1 T1484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:36222830 C>T maps to NM_014727.1 P1820P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:36212369 C>T maps to NM_014727.1 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr19:36217191 G>A maps to NM_014727.1 W1314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:36219790 G>T did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:36218861 C>T maps to NM_014727.1 G1491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:36218862 C>T maps to NM_014727.1 Q1492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr19:36223528 G>T maps to NM_014727.1 E2027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr19:36218822 C>T maps to NM_014727.1 H1478H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:36218810 C>T maps to NM_014727.1 I1474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:36227702 C>T maps to NM_014727.1 F2424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:36228083 C>T maps to NM_014727.1 F2490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:36214783 C>T maps to NM_014727.1 L1070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:36224546 C>T maps to NM_014727.1 L2337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:36211904 C>T maps to NM_014727.1 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:104748149 C>T maps to NM_182931.2 S1082S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:104748311 T>C maps to NM_182931.2 T1136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:104715192 T>C maps to NM_182931.2 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:104753446 A>G maps to NM_182931.2 P1748P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:104722178 T>A maps to NM_182931.2 Y431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr7:104741912 T>C maps to NM_182931.2 F588F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:6270641 G>A maps to NM_005934.3 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:6230619 G>A maps to NM_005934.3 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr10:21962685 C>T maps to NM_004641.3 Q487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:20346497 C>G maps to NM_004529.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:20414348 G>A maps to NM_004529.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr6:168352765 C>T maps to ENST00000400822 Q1570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:168272949 C>T maps to ENST00000400822 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:168348569 C>T maps to ENST00000400822 A1189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:168352393 C>T maps to ENST00000400822 Q1446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:168265362 C>T maps to ENST00000400822 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr6:168352611 C>T maps to ENST00000400822 D1518D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:168265362 C>T maps to ENST00000400822 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:36865785 C>T maps to NM_005937.3 N170N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr17:36873074 T>C maps to NM_005937.3 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:36872947 T>G maps to NM_005937.3 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:36873769 C>T maps to NM_005937.3 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:36878936 A>G maps to NM_005937.3 T933T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr17:36876822 G>T did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr6:33768862 G>A maps to NM_002418.2 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr13:49795327 C>T maps to NM_001507.1 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr13:49795296 G>A maps to NM_001507.1 W275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr16:2257059 G>A maps to NM_022372.4 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr16:2258786 G>A maps to NM_022372.4 W297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr16:2258787 G>A maps to NM_022372.4 W297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr12:122620068 C>T maps to NM_014938.3 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr12:122622103 G>A maps to NM_014938.3 G707G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:122611826 G>A maps to NM_014938.3 W146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:122614160 C>T maps to NM_014938.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:122623074 C>T maps to NM_014938.3 I787I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr12:122622067 C>T maps to NM_014938.3 S695S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr12:122618088 C>T maps to NM_014938.3 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr7:73021318 G>A maps to NM_032951.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:73030422 G>T maps to NM_032951.2 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:73010569 C>T maps to NM_032951.2 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr7:73011983 G>A maps to NM_032951.2 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr7:73014011 G>A maps to NM_032951.2 N305N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:83948700 C>T maps to NM_012213.2 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:146560723 C>T maps to NM_172250.2 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr4:146576315 C>T maps to NM_172250.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr4:146576316 C>T maps to NM_172250.2 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:146576364 C>T maps to NM_172250.2 Q346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr4:146572220 T>G maps to NM_172250.2 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr12:110009484 G>A maps to NM_052845.3 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:45973087 C>T maps to NM_015506.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:45973168 C>T maps to NM_015506.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:53471726 G>A maps to NM_012329.2 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:53488739 G>A maps to NM_012329.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:4965102 C>T maps to NM_001100600.1 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:154866385 G>A maps to NM_007289.2 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr3:154886357 C>T maps to NM_007289.2 Q620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:154834732 T>C maps to NM_007289.2 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr3:154878181 G>A maps to NM_007289.2 W535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr3:154886389 C>T maps to NM_007289.2 S630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:154886308 C>T maps to NM_007289.2 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:154884715 C>T maps to NM_007289.2 P562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:154898229 G>A maps to NM_007289.2 K745K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:154860055 C>T maps to NM_007289.2 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr3:154858044 G>A maps to NM_007289.2 Q307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:2537755 G>A maps to NM_033467.3 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:2525361 G>A maps to NM_033467.3 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:2538437 C>T maps to NM_033467.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:2537692 G>A maps to NM_033467.3 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:2524135 C>T maps to NM_033467.3 G675G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:2537023 G>C maps to NM_033467.3 Y263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:2537723 C>T maps to NM_033467.3 W238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr1:2530139 G>A maps to NM_033467.3 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:135047231 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr11:102662224 C>T maps to NM_002421.3 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr11:102663420 G>A maps to NM_002421.3 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:102668785 C>T maps to NM_002421.3 W13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:102667463 G>A maps to NM_002421.3 Q186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:102668757 C>T maps to NM_002421.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr11:102668117 C>G maps to NM_002421.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr11:102643648 C>T maps to NM_002425.2 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:102650353 C>T maps to NM_002425.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:102651288 G>A maps to NM_002425.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr22:24123411 C>A maps to NM_005940.3 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr22:24122787 C>T maps to NM_005940.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr22:24125673 C>T maps to NM_005940.3 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:24125673 C>T maps to NM_005940.3 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:102742682 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:102743832 C>A maps to ENST00000326227 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:102743710 T>C maps to ENST00000326227 Q78Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:102733866 G>T maps to ENST00000326227 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr11:102737121 G>A maps to ENST00000326227 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr11:102825328 C>T maps to NM_002427.3 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr11:102819835 C>T maps to NM_002427.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:102826021 G>A maps to NM_002427.3 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr11:102820921 T>A maps to NM_002427.3 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:102819763 G>A maps to NM_002427.3 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr11:102825185 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:102824924 G>A maps to NM_002427.3 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:102826186 G>A maps to NM_002427.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:102819835 C>T maps to NM_002427.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr11:102826021 G>A maps to NM_002427.3 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr14:23311621 C>T maps to NM_004995.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr16:58072256 C>T maps to NM_002428.2 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:58079017 C>T maps to NM_002428.2 Q560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr16:58074456 G>A maps to NM_002428.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:58078992 C>T maps to NM_002428.2 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:58074567 C>T maps to NM_002428.2 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:58078923 C>T maps to NM_002428.2 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr8:89058939 C>T maps to NM_005941.4 G482G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr8:89180030 G>A maps to NM_005941.4 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:89086839 G>A maps to NM_005941.4 F405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr8:89128864 C>T maps to NM_005941.4 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:89086839 G>A maps to NM_005941.4 F405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:89198733 C>T maps to NM_005941.4 Q125Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr8:89128810 G>A maps to NM_005941.4 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:89128864 C>T maps to NM_005941.4 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:89086851 C>T maps to NM_005941.4 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr12:132329986 C>T maps to NM_016155.4 F399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr12:132323163 C>T maps to NM_016155.4 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr12:132334599 C>T maps to NM_016155.4 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:56231152 G>A maps to NM_002429.4 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:56233442 G>A maps to NM_002429.4 Y201Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:56231369 C>T maps to NM_002429.4 W386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:56235010 C>T maps to NM_002429.4 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:56236590 C>T maps to NM_002429.4 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr12:56230894 C>T maps to NM_002429.4 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr16:55522456 C>T maps to NM_004530.4 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr16:55532213 G>A maps to NM_004530.4 W541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr16:55517949 C>T maps to NM_004530.4 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr16:55523722 C>T maps to NM_004530.4 F389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr16:55539275 C>T maps to NM_004530.4 A635A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:55523611 C>T maps to NM_004530.4 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:55525833 C>T maps to NM_004530.4 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:55519265 C>T maps to NM_004530.4 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr11:102487565 C>T maps to NM_004771.3 W117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr11:102480669 G>A maps to NM_004771.3 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:102465481 G>A maps to NM_004771.3 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:102482567 C>T maps to NM_004771.3 Q147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:102464198 G>A maps to NM_004771.3 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:102480726 C>T maps to NM_004771.3 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:102495960 G>A maps to NM_004771.3 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:102495981 G>A maps to NM_004771.3 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:102496011 G>A maps to NM_004771.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:102496038 G>A maps to NM_004771.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:102465400 C>T maps to NM_004771.3 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:33834785 G>A maps to NM_006690.3 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:33834662 C>T maps to NM_006690.3 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:33834662 C>T maps to NM_006690.3 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:3100082 C>T maps to NM_022468.4 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:3100449 G>A maps to NM_022468.4 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr11:5013261 C>T maps to NM_021801.3 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr11:5010885 C>T maps to NM_021801.3 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr11:5010898 C>T maps to NM_021801.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:5009488 C>T maps to NM_021801.3 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr11:5010960 C>T maps to NM_021801.3 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:5010921 C>T maps to NM_021801.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:5010966 G>A maps to NM_021801.3 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:5010960 C>T maps to NM_021801.3 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:5013257 G>A maps to NM_021801.3 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5011050 C>T maps to NM_021801.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5011860 C>T maps to NM_021801.3 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5013341 C>T maps to NM_021801.3 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:5010966 G>A maps to NM_021801.3 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:5011074 G>A maps to NM_021801.3 W99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr11:102562685 C>T maps to NM_022122.2 K451K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:102573541 C>G maps to NM_022122.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:102564737 G>A maps to NM_022122.2 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:102710957 G>A maps to NM_002422.3 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:102711166 G>A maps to NM_002422.3 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:102712939 C>T maps to NM_002422.3 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:102711286 G>A maps to NM_002422.3 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:102709922 G>A maps to NM_002422.3 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr11:102709319 C>T maps to NM_002422.3 K397K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:102709862 C>T maps to NM_002422.3 K349K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:102711166 G>A maps to NM_002422.3 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:102713309 C>T maps to NM_002422.3 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr11:102398351 C>T maps to NM_002423.3 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:102394019 T>C maps to NM_002423.3 Q242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:102398511 C>T maps to NM_002423.3 W104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:102398303 C>T maps to NM_002423.3 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr11:102589229 G>A maps to NM_002424.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:102586044 G>A maps to NM_002424.2 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:44640908 G>A maps to NM_004994.2 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr4:90830521 G>A maps to NM_007351.2 W240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr4:90816650 C>T maps to NM_007351.2 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr4:90830521 G>A maps to NM_007351.2 W240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:90857242 G>A maps to NM_007351.2 K804K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr4:90856666 G>A maps to NM_007351.2 E612E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr4:90857302 T>G maps to NM_007351.2 Y824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr4:90816650 C>T maps to NM_007351.2 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:88702992 C>T maps to NM_024756.2 E516E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:88703673 A>G maps to NM_024756.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr10:88705379 G>A maps to NM_024756.2 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:88703313 C>T maps to NM_024756.2 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:88703832 G>A maps to NM_024756.2 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr22:28146982 G>A maps to NM_002430.2 R1295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr22:28192784 C>T maps to NM_002430.2 E1249E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:28194968 G>A maps to NM_002430.2 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:28193504 G>A maps to NM_002430.2 S1009S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr22:28146959 C>T maps to NM_002430.2 R1302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr22:28194968 G>A maps to NM_002430.2 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr22:28194067 G>A maps to NM_002430.2 Q822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:28193846 C>T maps to NM_002430.2 G895G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr22:28194581 C>T maps to NM_002430.2 S650S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:158811969 T>A maps to NM_002432.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:158817639 C>T maps to NM_002432.1 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:158813785 G>A maps to NM_002432.1 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:56726524 C>T maps to NM_018365.2 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:156799207 C>A maps to NM_005515.3 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:156798567 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:1491701 G>A maps to NM_001172223.1 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:1492537 G>A maps to NM_001172223.1 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:74386226 G>A maps to NM_018221.3 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr19:2076833 G>A maps to NM_130807.2 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:2076989 G>A maps to NM_130807.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr1:47079023 G>T maps to NM_145279.4 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:47078948 G>A maps to NM_145279.4 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:47075793 G>A maps to NM_145279.4 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:47080694 A>G maps to NM_145279.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:198415073 T>C maps to NM_015387.3 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr3:39543679 G>A maps to ENST00000311042 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:33795672 C>T maps to NM_017947.2 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:33779648 C>T maps to NM_017947.2 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr18:33800121 C>T maps to NM_017947.2 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:33785098 C>T maps to NM_017947.2 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:33785176 C>T maps to NM_017947.2 Q386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:39881526 G>A maps to ENST00000425303 N212N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr6:39895170 G>A maps to ENST00000425303 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:39883839 G>A maps to ENST00000425303 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:39895224 G>A maps to ENST00000425303 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:39880040 G>A maps to ENST00000425303 N316N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:39895170 G>A maps to ENST00000425303 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr5:52402950 C>A maps to NM_004531.3 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:52402944 G>A maps to NM_004531.3 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr20:49576503 G>A maps to NM_014484.3 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:49576005 G>A maps to NM_014484.3 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr20:49575822 C>T maps to NM_014484.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr6:29638085 G>A maps to NM_002433.4 W207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:29627394 C>T maps to NM_002433.4 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:29637981 G>A maps to NM_206811.3 K208K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr6:29625033 C>T maps to NM_002433.4 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:29627144 G>A maps to NM_002433.4 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr6:29627132 G>A maps to NM_002433.4 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:223559156 C>T maps to NM_058165.2 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr2:223559126 G>A maps to NM_058165.2 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:223554069 G>A maps to NM_058165.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:75431058 C>T maps to NM_025098.2 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:75442213 C>T maps to NM_025098.2 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr7:100839600 G>A maps to NM_178176.2 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:100843559 C>T maps to NM_178176.2 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr7:100843532 C>T maps to NM_178176.2 R90R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A29C-06A-21D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr7:100839229 G>A maps to NM_178176.2 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:100841578 C>T maps to NM_178176.2 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:100839561 G>A maps to NM_178176.2 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr7:100841985 G>A maps to NM_178176.2 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr2:74689940 G>A maps to NM_006302.2 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr2:74688899 G>A maps to NM_006302.2 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:49947859 G>A maps to NM_032355.3 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:49947862 C>T maps to NM_032355.3 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr16:77228346 C>T maps to NM_014940.2 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr16:77225522 G>A maps to NM_014940.2 E47E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr16:77232126 T>C maps to NM_014940.2 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr12:62926418 G>A maps to ENST00000393630 Q534Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr12:62931022 C>T maps to ENST00000393630 Q665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:62979269 C>T maps to ENST00000393630 C1633C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:62943453 C>A maps to ENST00000393630 S921S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:62954403 C>T maps to ENST00000393630 D1182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr12:62986504 C>T maps to ENST00000393630 S1711S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr3:108682410 C>T maps to NM_014429.3 R883R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr3:108819354 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:108778660 C>T maps to NM_014429.3 E341E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr3:108688521 G>A maps to NM_014429.3 F866F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr3:108776191 G>A maps to NM_014429.3 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr3:108751601 C>T maps to NM_014429.3 W510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr3:108833268 G>A maps to NM_014429.3 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:108818258 C>T maps to NM_014429.3 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr3:108724117 C>T maps to NM_014429.3 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr3:108773643 G>A maps to NM_014429.3 Q421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:108778651 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:108822723 G>A maps to NM_014429.3 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:108818306 G>A maps to NM_014429.3 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:108703567 C>T maps to NM_014429.3 W773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr3:108818306 G>A maps to NM_014429.3 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:108819337 G>A maps to NM_014429.3 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:108719406 G>A maps to NM_014429.3 I728I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:108818258 C>T maps to NM_014429.3 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:108682266 G>A maps to NM_014429.3 L931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr3:108682308 C>T maps to NM_014429.3 L917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:108682434 G>A maps to NM_014429.3 V875V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:108723675 C>T maps to NM_014429.3 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:108754253 C>T maps to NM_014429.3 E464E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:108813813 G>A maps to NM_014429.3 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:108813852 C>T maps to NM_014429.3 Q162Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:108818273 C>T maps to NM_014429.3 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:108819292 G>A maps to NM_014429.3 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:108833268 G>A maps to NM_014429.3 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:108682323 G>A maps to NM_014429.3 I912I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr3:108813852 C>T maps to NM_014429.3 Q162Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr22:31333579 G>A maps to ENST00000397641 T496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr22:31332499 G>A maps to ENST00000397641 Q579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:31328378 A>C maps to ENST00000397641 A936A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr22:31338097 C>T did not map to a codon.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr22:31330889 G>A maps to ENST00000397641 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr22:31337888 G>A maps to ENST00000397641 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:31331109 A>C maps to ENST00000397641 P617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr22:31333588 G>A maps to ENST00000397641 I493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr22:31333802 G>A maps to ENST00000397641 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:31330938 G>A maps to ENST00000397641 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:31337475 G>A maps to ENST00000397641 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr22:31331234 C>T maps to ENST00000397641 E604E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr22:31324110 G>A maps to ENST00000397641 A975A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:31337957 G>A maps to ENST00000397641 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:31331294 G>A maps to ENST00000397641 I584I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr21:37717256 T>C maps to ENST00000290384 D312D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:37710233 C>T maps to ENST00000290384 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:106224174 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:106186393 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:106185955 C>G did not map to a codon.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr23:106205310 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:106184801 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr23:106243182 C>A did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:106198236 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:106184785 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr15:79185882 C>T maps to NM_206839.1 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:102931836 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:102931921 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr1:2268179 G>A maps to NM_024848.1 F382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:2290104 C>T maps to NM_024848.1 Q265Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr9:124922254 G>T maps to NM_198469.2 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:57026445 C>T maps to NM_005372.1 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:220970083 C>T maps to NM_022746.3 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:220970050 C>T maps to NM_022746.3 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:220978452 C>T maps to NM_022746.3 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:220953376 C>T maps to NM_017898.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:220955231 C>A maps to NM_017898.3 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:220936283 C>A maps to NM_017898.3 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr1:220953377 C>T maps to NM_017898.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:220935158 C>T maps to NM_017898.3 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:134030968 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr23:14930382 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr23:14937838 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr23:14936886 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:14915260 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:14930467 C>A did not map to a codon.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr7:100211216 C>T maps to NM_023948.4 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:100212784 C>T maps to NM_023948.4 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr7:100210446 G>A maps to NM_023948.4 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:100212531 T>A maps to NM_023948.4 L185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr7:100212778 C>T maps to NM_023948.4 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr7:100212553 G>A maps to NM_023948.4 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr7:100212655 T>G did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:100210470 G>A maps to NM_023948.4 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:113232120 C>T maps to NM_020963.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:113232121 C>T maps to NM_020963.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr1:113238117 C>T maps to NM_020963.3 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:113231667 C>T maps to NM_020963.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:113232669 C>T maps to NM_020963.3 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:113240675 C>T maps to NM_020963.3 A753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:113232666 C>T maps to NM_020963.3 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr1:113232513 C>T maps to NM_020963.3 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:113231679 C>T maps to NM_020963.3 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr1:113241401 G>A maps to NM_020963.3 K858K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr22:50598105 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr22:50580514 G>A maps to NM_018995.2 R692R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr22:50582641 C>T maps to NM_018995.2 V825V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:50553639 G>A maps to NM_018995.2 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:50589165 C>T maps to NM_018995.2 I910I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr22:50552808 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr22:50563823 C>T maps to NM_018995.2 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:50596548 C>T maps to NM_018995.2 L1044L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:50599251 C>T maps to NM_018995.2 R1154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr22:50563978 G>A maps to NM_018995.2 G576G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr22:50537972 G>A maps to NM_018995.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr22:50546580 G>A maps to NM_018995.2 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr22:50563933 G>A maps to NM_018995.2 R561R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr22:50552965 T>C maps to NM_018995.2 N347N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr22:50580508 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr22:50580553 G>A maps to NM_018995.2 E705E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:50552914 C>T maps to NM_018995.2 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:50596571 C>T maps to NM_018995.2 A1051A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:50599868 G>A maps to NM_018995.2 E1209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr22:50530544 G>A maps to NM_018995.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr22:50547093 C>T maps to NM_018995.2 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr22:50589249 G>A maps to NM_018995.2 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr6:132645186 C>T maps to NM_015529.2 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr6:132645129 G>A maps to NM_015529.2 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr6:132641791 C>T maps to NM_015529.2 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr6:132636901 G>A maps to NM_015529.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:132645138 G>A maps to NM_015529.2 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr6:132649187 G>A maps to NM_015529.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:7487251 C>T maps to NM_004870.3 D24D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:7487252 C>T maps to NM_004870.3 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr9:13193233 G>A maps to ENST00000319217 R579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:13168522 G>A maps to ENST00000319217 I1032I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr9:13150677 G>A maps to ENST00000319217 L1154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr9:13162745 C>T maps to ENST00000319217 L1101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr9:13125265 G>A maps to ENST00000319217 Q1586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:13168488 G>A maps to ENST00000319217 R1044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:13133825 G>T maps to ENST00000319217 P1487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr9:13138030 G>A maps to ENST00000319217 V1375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:13125236 G>A maps to ENST00000319217 S1595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:13183509 G>A maps to ENST00000319217 I852I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr9:13110634 C>T maps to ENST00000319217 Q1943Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr9:13150515 G>A maps to ENST00000319217 I1208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr11:58978889 G>A maps to NM_001039396.1 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:58978763 C>T maps to NM_001039396.1 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:58978286 C>T maps to NM_001039396.1 K684K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:58980191 C>T maps to NM_001039396.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:58980035 C>T maps to NM_001039396.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:71377036 C>T maps to NM_005791.2 F646F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:71360429 C>T maps to NM_005791.2 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:71377055 C>T maps to NM_005791.2 Q653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:123641383 G>A maps to NM_022782.2 F1022F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr12:123646766 T>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:123687381 G>A maps to NM_022782.2 Q372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr15:75190016 G>A maps to NM_002435.1 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:43803539 C>T maps to NM_005373.2 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:43805032 C>T maps to NM_005373.2 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:43818334 G>A maps to NM_005373.2 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:43805059 C>T maps to NM_005373.2 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr1:43812472 C>T maps to NM_005373.2 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:43803533 C>T maps to NM_005373.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr19:4354995 C>T maps to ENST00000262967 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:4359203 G>A maps to ENST00000262967 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr19:4359233 C>T maps to ENST00000262967 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:56357779 G>A maps to ENST00000340482 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr17:56355338 C>T maps to ENST00000340482 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:56352920 G>A maps to ENST00000340482 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr17:56349179 C>T maps to ENST00000340482 R654R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:56350865 G>A maps to ENST00000340482 F542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr17:56357731 C>T maps to ENST00000340482 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:56355299 G>A maps to ENST00000340482 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:56350877 T>C maps to ENST00000340482 Q538Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr17:56355338 C>T maps to ENST00000340482 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr17:56352920 G>A maps to ENST00000340482 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr17:56355503 G>A maps to ENST00000340482 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:56349080 G>T maps to ENST00000340482 G687G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:56350259 G>A maps to ENST00000340482 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:56358050 G>A maps to ENST00000340482 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr23:154014500 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr23:154020427 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:154020552 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:154020552 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:154020510 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:154018293 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:154013345 T>G did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:154007561 C>A did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:154009979 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr17:41955275 G>A maps to NM_005374.3 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr17:41960579 G>A maps to NM_005374.3 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:41975674 G>A maps to NM_005374.3 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:41956705 G>A maps to NM_005374.3 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:41957311 C>T maps to NM_005374.3 Q397Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:41960588 G>A maps to NM_005374.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:41891595 G>T maps to ENST00000398393 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:41898294 C>T maps to ENST00000398393 Q297Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:41901337 G>A maps to ENST00000398393 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr17:41903165 G>A maps to ENST00000398393 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:41907409 G>A maps to ENST00000398393 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:202557633 T>C maps to NM_033066.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr14:67768119 G>A maps to NM_022474.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr14:67799543 G>A maps to NM_022474.2 Q633Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:24708139 G>A maps to ENST00000409253 Q367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr7:24703292 G>T maps to ENST00000409253 G288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:24689320 C>T maps to ENST00000409253 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr7:24663357 C>T maps to ENST00000409253 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:24703300 T>A maps to ENST00000409253 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr7:24663357 C>T maps to ENST00000409253 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:24690150 C>A maps to ENST00000409253 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:24705211 C>T maps to ENST00000409253 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:24663357 C>T maps to ENST00000409253 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:24681388 G>T maps to ENST00000409253 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:24689313 C>T maps to ENST00000409253 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr10:28408586 C>T maps to NM_173496.3 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr10:28347532 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:28413984 C>T maps to NM_173496.3 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr10:28347510 A>T maps to NM_173496.3 Y440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:28378744 A>G maps to NM_173496.3 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr10:28420536 C>T maps to NM_173496.3 E133E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr10:28409130 G>A maps to NM_173496.3 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr10:28409222 G>A maps to NM_173496.3 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:28348672 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:28409220 C>T maps to NM_173496.3 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:11889432 T>C maps to ENST00000344987 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr22:43898545 G>A maps to NM_001044370.1 K257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:30439116 C>T maps to NM_001584.2 W200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:30516868 C>T maps to NM_001584.2 K170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr11:30516964 G>A maps to NM_001584.2 F138F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-FS-A1Z3-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:17075094 C>T maps to NM_015134.2 Q743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr17:17049351 C>T maps to NM_015134.2 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr22:37420675 C>T maps to NM_021126.4 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr22:37420582 C>T maps to NM_021126.4 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr22:37425443 C>T maps to NM_021126.4 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr22:37420501 C>T maps to NM_021126.4 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:27535420 G>A maps to ENST00000405983 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:27532803 C>A maps to ENST00000405983 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr16:15501863 C>T maps to NM_001128423.1 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:18304779 C>T maps to NM_032683.2 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:161276687 T>C maps to ENST00000360451 Q96Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:161275689 C>T maps to ENST00000360451 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr11:118133682 C>T maps to NM_144765.2 W63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:118133291 C>T maps to NM_144765.2 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr11:118130815 C>T maps to NM_144765.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:181021440 T>C maps to NM_001531.2 H225H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:181022796 G>A maps to NM_001531.2 W323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:33684081 G>A maps to ENST00000445271 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr6:84799079 C>T maps to NM_138409.2 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:84799010 A>G maps to NM_138409.2 Q143Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:84798836 C>T maps to NM_138409.2 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:84799130 G>A maps to NM_138409.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:84799010 A>G maps to NM_138409.2 Q143Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr3:138116268 C>T maps to NM_001085049.1 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:17949595 G>A maps to NM_002438.2 W1320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr17:60757547 C>T maps to NM_006039.3 F772F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:60742215 C>T maps to NM_006039.3 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:60741972 G>A maps to NM_006039.3 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:60766289 G>A maps to NM_006039.3 E1101E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr17:60742069 C>T maps to NM_006039.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:60742189 C>T maps to NM_006039.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:60754831 C>T maps to NM_006039.3 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:60741969 G>A maps to NM_006039.3 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr17:60742019 G>A maps to NM_006039.3 W77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr17:60765982 G>A maps to NM_006039.3 G1061G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr17:60767562 G>A maps to NM_006039.3 Q1263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:60743814 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:60757547 C>T maps to NM_006039.3 F772F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:60754804 C>T maps to NM_006039.3 P670P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:60744151 C>T maps to NM_006039.3 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr17:60765903 G>A maps to NM_006039.3 W1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:60749031 G>A maps to NM_006039.3 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:60741963 G>A maps to NM_006039.3 Q58Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:60749488 G>A maps to NM_006039.3 E479E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:60757791 G>A maps to NM_006039.3 R817R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr11:94192582 G>A maps to NM_005591.3 I497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:94163118 G>A maps to NM_005591.3 S676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:94204873 G>A maps to NM_005591.3 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr2:216809588 G>A maps to NM_018000.2 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:6642900 C>T maps to NM_033296.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr11:68748440 C>T maps to NM_198923.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr11:68748251 C>T maps to NM_198923.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:68747513 C>T maps to NM_198923.2 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr11:68747576 C>T maps to NM_198923.2 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:68748122 C>T maps to NM_198923.2 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:3249786 G>C maps to ENST00000328215 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:3249789 G>A maps to ENST00000328215 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:3249747 G>A maps to ENST00000328215 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr11:3249684 C>T maps to ENST00000328215 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:3249927 G>C maps to ENST00000328215 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr11:68773054 G>A maps to NM_145015.4 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:18955493 G>A maps to NM_147199.3 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr11:18956091 A>G maps to NM_147199.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:18955470 C>T maps to NM_147199.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:18955512 G>A maps to NM_147199.3 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr11:18956223 G>A maps to NM_147199.3 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr11:18955509 G>A maps to NM_147199.3 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:18955841 G>A maps to NM_147199.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr11:18955728 C>T maps to NM_147199.3 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:18955509 G>A maps to NM_147199.3 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:18955395 G>A maps to NM_147199.3 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:18955509 G>A maps to NM_147199.3 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr11:18955620 G>A maps to NM_147199.3 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:18955788 G>A maps to NM_147199.3 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr11:18955656 G>A maps to NM_147199.3 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr11:18955620 G>A maps to NM_147199.3 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:18955413 C>T maps to NM_147199.3 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr11:18955428 C>T maps to NM_147199.3 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr11:18956223 G>A maps to NM_147199.3 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr11:18955686 G>A maps to NM_147199.3 Y215Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:18955500 G>A maps to NM_147199.3 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:18955458 G>A maps to NM_147199.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr11:18955650 G>A maps to NM_147199.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr11:18955458 G>A maps to NM_147199.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:18955476 C>T maps to NM_147199.3 Q285Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:18956157 C>T maps to NM_147199.3 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:18956241 G>A maps to NM_147199.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:18956271 C>T maps to NM_147199.3 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr11:18955521 G>A maps to NM_147199.3 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:18955628 G>A maps to NM_147199.3 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:18956172 G>A maps to NM_147199.3 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr11:18955500 G>A maps to NM_147199.3 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr11:19077106 G>A maps to NM_054030.2 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:19077100 G>A maps to NM_054030.2 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr11:19077216 G>A maps to NM_054030.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr11:19077322 G>A maps to NM_054030.2 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:19077394 G>A maps to NM_054030.2 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:19077591 G>A maps to NM_054030.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr11:19077843 G>A maps to NM_054030.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr11:19077841 C>T maps to NM_054030.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:19077313 G>A maps to NM_054030.2 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:19077646 G>A maps to NM_054030.2 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:18159570 C>T maps to NM_054031.3 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr11:18159525 C>T maps to NM_054031.3 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:18159651 G>A maps to NM_054031.3 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:18159339 C>T maps to NM_054031.3 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:18159063 C>T maps to NM_054031.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr11:18159525 C>T maps to NM_054031.3 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr11:18158856 C>T maps to NM_054031.3 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:18159408 C>T maps to NM_054031.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:18159570 C>T maps to NM_054031.3 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:18195624 C>T maps to NM_054032.3 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr11:18195096 C>T maps to NM_054032.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr11:18195348 G>A maps to NM_054032.3 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:18195505 C>T maps to NM_054032.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:18195093 C>T maps to NM_054032.3 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr11:18195624 C>T maps to NM_054032.3 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:18195408 C>T maps to NM_054032.3 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr19:13875468 A>T maps to NM_001031727.2 K23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr19:13876863 C>T maps to NM_001031727.2 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:34964772 C>T maps to NM_024864.3 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr18:48327811 C>T maps to NM_001127176.1 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr18:48327803 C>T maps to NM_001127176.1 W181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr18:48335728 G>A maps to NM_031939.3 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr18:48326494 G>A maps to NM_001127176.1 Q216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:48333183 G>A maps to NM_001127176.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr18:48331631 G>A maps to NM_001127176.1 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:48331679 G>A maps to NM_001127176.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:48335704 C>T maps to NM_031939.3 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr18:48327808 C>T maps to NM_001127176.1 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr4:78808384 G>A maps to NM_020236.3 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:78873664 C>T maps to NM_020236.3 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:78873664 C>T maps to NM_020236.3 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:66206156 G>A maps to NM_016050.3 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr11:66204360 G>A maps to NM_170739.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr17:79671402 C>T maps to NM_002949.3 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr17:79671403 C>T maps to NM_002949.3 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:79674063 C>T maps to NM_002949.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:44081882 G>A maps to NM_032111.2 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr8:55060095 C>T maps to NM_014175.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr6:160212104 C>A maps to NM_014161.3 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr6:43023882 G>A maps to NM_015950.3 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:43023882 G>A maps to NM_015950.3 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr6:43024175 G>A maps to NM_015950.3 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:68664141 G>A maps to NM_181514.1 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:154339538 G>T did not map to a codon.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr11:1977577 C>T maps to NM_021134.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:48447413 G>A maps to NM_016504.2 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:419070 G>C maps to NM_006428.4 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr16:418545 G>A maps to NM_006428.4 H177H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr3:131219360 G>A maps to ENST00000425847 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr7:42977018 C>T maps to NM_031903.2 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:86434389 C>G maps to NM_016622.3 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:54665993 G>A maps to NM_016491.3 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:54666248 C>T maps to NM_016491.3 C111C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:54681875 C>T maps to NM_016491.3 V351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr17:73895041 G>A maps to NM_032478.3 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:73900777 G>A maps to NM_032478.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr21:26976113 C>T maps to NM_080794.3 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr21:26965264 G>A maps to NM_080794.3 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:10363305 C>T maps to NM_146387.1 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:10369320 C>T maps to NM_146387.1 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:10367416 C>A maps to NM_146387.1 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr22:19423217 G>A maps to NM_003776.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr9:140446787 C>T maps to NM_032477.2 P85P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DA-A1HY-06A-11D-A19A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:224822311 C>T maps to NM_022915.3 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr17:36478142 C>T maps to NM_032351.3 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:36478091 C>T maps to NM_032351.3 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:36478148 C>T maps to NM_032351.3 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr15:89003038 G>A maps to NM_022163.3 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr15:89008962 A>T maps to NM_022163.3 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr3:179322376 T>C maps to NM_020409.2 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:64893059 C>T maps to NM_004927.3 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64893017 C>T maps to NM_004927.3 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6601547 G>A maps to NM_016497.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr14:23299431 C>T maps to NM_178336.2 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:151733956 A>T maps to NM_031420.2 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:151734007 G>A maps to NM_031420.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr1:151733935 G>A maps to NM_031420.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:151734887 G>A maps to NM_031420.2 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:174987583 C>T maps to NM_022100.2 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr1:36926371 C>T maps to NM_031280.3 E102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:43639615 G>A maps to ENST00000372118 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:84377271 G>A maps to NM_016067.2 K14K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr9:138395411 G>A maps to NM_016034.3 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:138395438 C>T maps to NM_016034.3 D117D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5KH-06A-11D-A27K-08 chr3:139065879 G>A maps to NM_020191.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:55926749 G>A maps to NM_016070.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:55917232 A>G maps to NM_016070.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:43906465 G>A maps to NM_032014.2 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:43906561 G>A maps to NM_032014.2 D80D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:43906396 G>A maps to NM_032014.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:15093986 C>T maps to NM_022497.3 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr20:3026875 C>T maps to NM_030811.3 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:71533936 G>A maps to ENST00000513900 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr5:71528293 G>A maps to ENST00000513900 C203C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:140710237 G>A maps to NM_053035.2 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:27908298 T>G maps to NM_021821.3 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr12:27863868 G>T maps to NM_021821.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr12:27908196 C>T maps to NM_021821.3 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:95756220 G>A maps to NM_031902.3 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr21:35514809 C>T maps to NM_032476.3 H96H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:73259492 G>T maps to NM_015971.3 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:105713765 C>T maps to NM_182640.2 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:105708939 C>T maps to NM_182640.2 R245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:125075622 G>A maps to NM_138777.3 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr9:125084877 C>T maps to NM_138777.3 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:24416694 T>C maps to NM_020662.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:19582530 C>T maps to NM_016183.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr11:10597929 C>T maps to NM_001098579.1 R887R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:10626043 G>A maps to NM_001098579.1 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:10622561 C>T maps to NM_001098579.1 V631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr11:10651258 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:10597932 C>T maps to NM_001098579.1 Q886Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr11:10615059 G>A maps to NM_001098579.1 S709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:10649567 C>T maps to NM_001098579.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr11:10649301 C>T maps to NM_001098579.1 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:10602093 C>T maps to NM_001098579.1 L792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:10647560 C>T maps to NM_001098579.1 Q431Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr11:10615059 G>A maps to NM_001098579.1 S709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:10615146 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:10673765 C>A maps to NM_001098579.1 G2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr11:10647548 C>T maps to NM_001098579.1 Q435Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:10647977 G>A maps to NM_001098579.1 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:10622576 C>T maps to NM_001098579.1 V626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:60230002 G>A maps to NM_152866.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:60229882 C>T maps to NM_152866.2 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:60235760 G>A maps to NM_152866.2 Q238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:60230594 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:60561512 C>T maps to NM_206893.3 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr11:60559751 G>A maps to NM_206893.3 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:60558556 G>A maps to NM_206893.3 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:60558511 G>A maps to NM_206893.3 K83K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:60558499 C>T maps to NM_206893.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr11:60565955 C>T maps to NM_206893.3 Q231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr11:60184159 G>A maps to NM_032597.3 G573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:60183349 T>A maps to NM_032597.3 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr11:60183852 G>A maps to NM_032597.3 W471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr11:60541314 G>A maps to NM_001098835.1 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr11:60541404 C>T maps to NM_001098835.1 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:60531205 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:59857197 C>T maps to NM_000139.4 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr11:59861535 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:59857902 C>A maps to NM_000139.4 S94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr11:59860949 G>A maps to NM_000139.4 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr11:59830064 G>A maps to NM_006138.4 W94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:59829942 C>T maps to NM_006138.4 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:59830029 C>T maps to NM_006138.4 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:60075591 C>T maps to NM_148975.1 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:60068514 A>G maps to NM_148975.1 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:60201272 C>T maps to NM_023945.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:59942972 A>G maps to NM_152852.1 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:59942972 A>G maps to NM_152852.1 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:59947393 G>A maps to NM_152852.1 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:59943006 C>T maps to NM_152852.1 Q139Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:59939726 C>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:59940506 G>A maps to NM_152852.1 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:60105269 C>T maps to NM_139249.2 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:60107350 C>T maps to NM_139249.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:60105284 C>T maps to NM_139249.2 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:60105275 C>T maps to NM_139249.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr11:60105225 C>T maps to NM_139249.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr11:60470918 G>A maps to NM_031457.1 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:60482844 C>T maps to NM_031457.1 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:60470891 C>T maps to NM_031457.1 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:60482805 C>T maps to NM_031457.1 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:60470894 C>T maps to NM_031457.1 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:60468528 C>T maps to NM_031457.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:60482507 G>A maps to NM_031457.1 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:17997859 T>G maps to NM_001105569.1 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:17998084 C>T maps to NM_001105569.1 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:17997964 C>T maps to NM_001105569.1 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:47639605 C>T maps to NM_000251.1 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:47710060 C>T maps to NM_000251.1 I926I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:47693881 C>T maps to NM_000251.1 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:47703665 C>T maps to NM_000251.1 V722V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:47656986 C>T maps to NM_000251.1 Q395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:47637471 C>A maps to NM_000251.1 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:47702401 C>T maps to NM_000251.1 I666I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:79974807 A>G maps to NM_002439.3 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:79970817 C>T maps to NM_002439.3 I348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:80021295 C>T maps to NM_002439.3 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:80037354 C>T maps to NM_002439.3 I547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr5:80171621 C>T maps to NM_002439.3 L1119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr5:79968678 T>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:76313940 C>T maps to NM_002440.2 Q404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:76349429 C>T maps to NM_002440.2 I677I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:76333260 G>T maps to NM_002440.2 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:31721349 C>T maps to ENST00000375742 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:31711765 C>T maps to ENST00000375742 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:31726609 G>T maps to ENST00000375742 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:31728483 C>T maps to ENST00000375742 F627F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr2:48030751 G>A maps to NM_000179.2 Q1122Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr12:120794703 C>T did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr12:120783432 G>A maps to NM_002442.2 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:120784123 G>A maps to NM_002442.2 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:120794810 C>T maps to NM_002442.2 K182K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:120785267 C>T maps to NM_002442.2 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr12:120791150 G>A maps to NM_002442.2 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:55478816 C>T maps to NM_138962.2 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:55704617 C>T maps to NM_138962.2 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr3:135871299 C>T maps to NM_018133.3 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:11783869 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr23:11782025 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:11790755 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:11790276 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:234774898 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:234774899 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:234775126 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:234774930 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:234775389 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:234774949 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr2:234774969 C>T did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:234775043 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:815779 G>A maps to NM_013404.4 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr16:816998 C>T maps to NM_013404.4 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:818648 G>A maps to NM_013404.4 E603E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:816367 C>T maps to NM_013404.4 Q370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr16:815752 G>A maps to NM_013404.4 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:814720 C>T maps to NM_013404.4 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:817442 C>T maps to NM_013404.4 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:818395 G>A maps to NM_013404.4 E546E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr16:824894 C>T maps to NM_001025190.1 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr16:825617 C>T maps to NM_001025190.1 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr16:823260 G>A maps to NM_001025190.1 F669F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr16:830709 G>A maps to NM_001025190.1 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:819601 G>A maps to NM_001025190.1 P996P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:825074 C>T maps to NM_001025190.1 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:825635 C>T maps to NM_001025190.1 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:51555798 C>T maps to NM_002443.2 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr10:51555753 G>A maps to NM_002443.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:51562351 G>A maps to NM_002443.2 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:51562357 G>A maps to NM_002443.2 K101K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:64955139 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:64959737 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr23:64959628 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:64957104 G>A did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:64957166 C>G did not map to a codon.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr23:64953081 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr8:16007769 G>A maps to ENST00000445506 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:16026230 C>T maps to ENST00000445506 E140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr8:16032717 G>A maps to ENST00000445506 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:16032768 G>A maps to ENST00000445506 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:15967635 G>A maps to ENST00000445506 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:16026356 C>T maps to ENST00000445506 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:16026221 G>A maps to ENST00000445506 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:16012620 G>A maps to ENST00000445506 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:16026356 C>T maps to ENST00000445506 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr8:15967686 C>T maps to ENST00000445506 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr8:16025992 G>A maps to ENST00000445506 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr8:16021676 C>T maps to ENST00000445506 Q256Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:15977990 G>A maps to ENST00000445506 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:15978097 G>A maps to ENST00000445506 R369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:16021576 G>A maps to ENST00000445506 Q290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr8:16001120 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:15978104 C>T maps to ENST00000445506 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:16026227 C>T maps to ENST00000445506 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr8:16026278 C>T maps to ENST00000445506 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:10159065 C>T maps to NM_012331.3 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr8:10159065 C>T maps to NM_012331.3 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr8:9912148 G>A maps to NM_012331.3 K41K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:65847547 C>T maps to NM_001031679.2 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:65857062 G>A maps to NM_001031679.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr12:65847586 G>A maps to NM_001031679.2 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:49723576 G>A maps to NM_020998.3 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr3:49722208 C>T maps to NM_020998.3 G577G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr3:49724852 C>G maps to NM_020998.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:49726070 G>A maps to NM_020998.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:49723381 G>A maps to NM_020998.3 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr3:49723119 G>A maps to NM_020998.3 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr3:49933250 G>A maps to NM_002447.2 V953V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr3:49933492 G>A maps to NM_002447.2 T899T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr3:49940160 C>T maps to NM_002447.2 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:49928019 C>T maps to NM_002447.2 R1236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:49928028 G>A maps to NM_002447.2 I1233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:49935641 G>A maps to NM_002447.2 F574F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:49928670 C>T maps to NM_002447.2 E1201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr3:49933672 G>T maps to NM_002447.2 A868A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr3:49933262 C>A maps to NM_002447.2 G949G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr3:49934756 G>A maps to NM_002447.2 T713T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr23:131203516 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:131206370 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr23:131197503 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr23:131197485 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:131202290 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:131203652 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:131202541 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:131206346 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:131202561 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:131197484 G>A did not map to a codon.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr2:190922135 G>A maps to NM_005259.2 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:190926977 C>G maps to NM_005259.2 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:190924967 G>A maps to NM_005259.2 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr5:174156264 C>T maps to NM_002449.4 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:174156246 C>T maps to NM_002449.4 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr16:56673227 C>T maps to NM_005946.2 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:56693045 G>A maps to ENST00000394501 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr14:105936542 C>T maps to NM_004689.3 I713I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr14:105936236 C>T maps to NM_004689.3 I635I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:62362537 G>A maps to NM_004739.2 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:62363301 A>C maps to NM_004739.2 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr11:62368096 G>A maps to NM_004739.2 N31N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:62361996 G>A maps to NM_004739.2 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:62363554 G>A maps to NM_004739.2 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:42936175 C>T maps to ENST00000405094 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr2:42836679 C>G maps to ENST00000405094 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:21816759 C>T maps to NM_002451.3 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr9:21816738 G>A maps to NM_002451.3 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:21859390 C>T maps to NM_002451.3 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr8:121518976 T>C maps to NM_022045.3 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:121457754 C>T maps to NM_022045.3 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:121509777 C>T maps to NM_022045.3 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr8:121457754 C>T maps to NM_022045.3 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr8:121476000 G>A maps to NM_022045.3 K349K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:47656244 G>A maps to NM_014342.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr23:154294260 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:154290180 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr8:98703285 C>T maps to NM_178812.3 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr8:98735187 C>T maps to NM_178812.3 Q535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:98718852 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:91503561 G>A maps to NM_006980.3 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr7:91502982 A>G maps to NM_006980.3 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr8:97258594 C>T maps to NM_015942.3 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr8:97270632 G>A maps to NM_015942.3 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:97258149 G>A maps to NM_015942.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr2:242036798 G>C maps to NM_182501.3 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:242039036 G>A maps to NM_182501.3 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:38281083 G>A maps to NM_005955.2 S662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:38281116 C>T maps to NM_005955.2 K651K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr1:38305671 G>A maps to NM_005955.2 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr15:65297274 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:65319170 G>T maps to NM_139242.3 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr15:65297206 T>C maps to NM_139242.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr15:65295426 A>C maps to NM_139242.3 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:66620086 A>G maps to NM_014637.3 Q258Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:135213097 C>T maps to NM_138384.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr14:64921457 C>T maps to NM_005956.3 P861P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr14:64909047 C>T maps to NM_005956.3 S688S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr14:64909104 C>T maps to NM_005956.3 H707H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:64898263 C>T maps to NM_005956.3 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr14:64884743 T>C did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr14:64898302 C>T maps to NM_005956.3 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr14:64921592 G>T maps to NM_005956.3 T906T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:64892500 G>A maps to NM_005956.3 W303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr6:151331021 C>T maps to NM_015440.3 S731S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:74438351 C>T maps to NM_006636.3 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr4:75167499 C>T maps to NM_001144978.1 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:75167516 C>T maps to NM_001144978.1 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr1:11856334 G>A maps to ENST00000376585 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr1:11855393 G>A maps to ENST00000376585 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:11854539 G>A maps to ENST00000376585 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr16:86575368 G>A maps to NM_001159377.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:86585793 G>A maps to NM_001159378.1 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:55481240 A>G maps to NM_002453.2 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:55489531 G>T maps to NM_002453.2 S84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:28011315 T>C maps to NM_152912.4 K185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr13:28014233 G>A maps to NM_152912.4 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:68478376 C>G maps to NM_004923.3 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:68514738 G>A maps to NM_004923.3 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr11:68517741 T>A maps to NM_004923.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr11:68517990 G>A maps to NM_004923.3 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr23:149809807 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:149787543 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:149831995 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:149828166 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:149839966 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:149809854 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr23:149807436 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr23:149814234 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr23:149767073 T>C did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:149828910 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:149826471 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr23:149924333 T>G did not map to a codon.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr23:149924334 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:149919205 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:149912856 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:149905726 G>C did not map to a codon.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr23:149887148 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:149931114 G>A did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:149912878 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:149905552 G>A maps to NM_001145862.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:149902773 G>A maps to NM_001145862.1 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:149902313 G>A maps to NM_001145862.1 F530F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ES-06A-11D-A20D-08 chr1:149904214 A>T maps to NM_001145862.1 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:149902811 G>A maps to NM_001145862.1 Q446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:149906992 G>A maps to NM_001145862.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:149903250 G>A maps to NM_001145862.1 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:149905337 G>A maps to NM_001145862.1 Q316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:149906992 G>A maps to NM_001145862.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U9-06A-11D-A32N-08 chr1:149907016 G>A maps to NM_001145862.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr5:32248158 G>A maps to NM_001040446.1 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:32230114 G>A maps to NM_001040446.1 V671V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:32230171 G>A maps to NM_001040446.1 I652I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:32248165 G>A maps to NM_001040446.1 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:32271027 G>C maps to NM_001040446.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr5:32230066 G>A maps to NM_001040446.1 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr3:9719702 C>T maps to NM_001077525.2 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:9719715 C>T maps to NM_001077525.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr3:9743587 C>T maps to NM_001077525.2 A628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:9724894 C>T maps to NM_001077525.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr3:9719741 G>A maps to NM_001077525.2 Q299Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr3:9730629 C>T maps to NM_001077525.2 R433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:31218059 G>A maps to NM_014967.4 G802G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:95580898 A>C maps to NM_016156.5 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr22:30374517 C>T maps to NM_021090.3 Q31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr22:30415990 C>T maps to NM_021090.3 V781V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr22:30416440 C>T maps to NM_021090.3 A931A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr22:30418656 C>T maps to NM_021090.3 F1132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr22:30415657 C>A maps to NM_021090.3 T670T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr22:30405058 T>G maps to NM_021090.3 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr22:30416767 G>A maps to NM_021090.3 Q1040Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr22:30419443 A>G did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:56573633 G>A maps to NM_004687.4 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr17:56581138 G>A maps to NM_004687.4 Q593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr17:56573455 G>A maps to NM_004687.4 Q683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr17:56582271 A>C maps to NM_004687.4 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:56572532 G>A maps to NM_004687.4 V990V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:56572418 G>A maps to NM_004687.4 I1028I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr17:56573597 G>A maps to NM_004687.4 N635N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr17:56573396 G>A maps to NM_004687.4 Y702Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr17:56589828 G>A maps to NM_004687.4 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr13:25832755 C>T maps to NM_004685.3 Q267Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:17218670 G>A maps to NM_004686.4 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr8:17169088 C>T maps to NM_004686.4 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr8:17198973 G>A maps to NM_004686.4 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:17198949 C>T maps to NM_004686.4 E218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:17230662 G>A maps to NM_004686.4 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr8:17218781 C>T maps to NM_004686.4 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:63557240 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:63574715 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr23:63574713 C>G did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:63563499 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr23:63557175 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:63579382 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:63564990 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:63574671 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:63488440 C>G did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:63555964 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr8:11162450 T>G maps to NM_015458.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr4:187455634 C>T maps to NM_005958.3 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:187455634 C>T maps to NM_005958.3 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:187455580 G>A maps to NM_005958.3 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr4:187454896 C>T maps to NM_005958.3 W333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr4:187455460 G>A maps to NM_005958.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr4:187455133 C>T maps to NM_005958.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr4:187455559 G>A maps to NM_005958.3 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:187455133 C>T maps to NM_005958.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr4:187455190 C>T maps to NM_005958.3 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr4:187455691 G>A maps to NM_005958.3 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr4:187455190 C>T maps to NM_005958.3 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr4:187455190 C>T maps to NM_005958.3 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr4:187454896 C>T maps to NM_005958.3 W333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr4:187455076 T>C maps to NM_005958.3 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr4:187455037 G>A maps to NM_005958.3 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr11:92715238 C>T maps to NM_005959.3 Q284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:92714775 C>T maps to NM_005959.3 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr11:92715222 C>T maps to NM_005959.3 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:92703055 C>T maps to NM_005959.3 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr11:92715351 G>A maps to NM_005959.3 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:92714790 C>T maps to NM_005959.3 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:92714928 C>T maps to NM_005959.3 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr6:74189657 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr6:74183274 C>T maps to NM_001123226.1 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:11307751 G>A maps to NM_004958.3 N385N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:11169427 C>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:11199664 G>A maps to NM_004958.3 S1641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:11264757 G>A maps to NM_004958.3 A1268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:11273515 G>A maps to NM_004958.3 I1075I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:11303280 G>A maps to NM_004958.3 F434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:11319448 A>C maps to NM_004958.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:11199411 G>A maps to NM_004958.3 H1693H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:11190723 G>A maps to NM_004958.3 I1825I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:11300597 G>A maps to NM_004958.3 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:11188074 G>A maps to NM_004958.3 Q2007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:11199425 G>A maps to NM_004958.3 L1689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:11293490 G>A maps to NM_004958.3 I795I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr1:11291000 G>A maps to NM_004958.3 S920S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:11177098 G>A maps to NM_004958.3 V2326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:11199664 G>A maps to NM_004958.3 S1641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:30824460 C>T maps to ENST00000439838 F319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:30629250 C>T maps to ENST00000358107 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr10:30625893 G>A maps to ENST00000358107 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:30602579 G>A maps to ENST00000358107 F699F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr10:30625815 G>A maps to ENST00000358107 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:135636299 G>A maps to NM_145808.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:237054610 C>T maps to NM_000254.2 F1062F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:237052583 G>A maps to NM_000254.2 R985R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr13:41797442 G>A maps to NM_004294.2 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:153314013 G>A maps to NM_019041.5 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr5:7900102 C>T maps to NM_024010.2 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:7891482 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr8:125716405 G>A maps to NM_014751.4 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr8:125597364 G>T maps to NM_014751.4 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr8:125568001 C>T maps to NM_014751.4 E516E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr4:100543902 C>T maps to ENST00000511045 S888S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:100543842 G>A maps to ENST00000511045 E868E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:100534067 A>C did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr4:100512908 G>A maps to ENST00000511045 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:100530111 C>T maps to ENST00000511045 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr8:17581342 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:17510999 C>T maps to NM_001001924.2 K1074K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr8:17573381 C>T maps to NM_001001924.2 E826E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:17503461 G>A maps to NM_001001924.2 F1262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr8:17513422 C>T maps to NM_001001924.2 R1019R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:17579353 G>A maps to NM_001001931.2 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:17611492 C>T maps to NM_001001924.2 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr13:30066810 G>A maps to NM_001033602.2 K1188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr13:29608161 G>A maps to NM_001033602.2 K792K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr13:29855895 G>A maps to NM_001033602.2 K910K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr13:29599852 C>T maps to NM_001033602.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr13:29608171 C>T maps to NM_001033602.2 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr13:29608251 C>T maps to NM_001033602.2 S822S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr13:29600556 T>A maps to NM_001033602.2 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr13:29599995 G>A maps to NM_001033602.2 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr13:29855946 G>A maps to NM_001033602.2 V927V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:29599078 C>T maps to NM_001033602.2 Q92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:29599242 G>A maps to NM_001033602.2 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr13:29599329 G>A maps to NM_001033602.2 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr13:29599842 G>A maps to NM_001033602.2 K346K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr13:29600622 G>A maps to NM_001033602.2 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr13:29933609 G>A maps to NM_001033602.2 K1049K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:29600442 C>T maps to NM_001033602.2 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr13:29933397 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr13:30062077 G>A maps to NM_001033602.2 E1157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr13:29600625 C>T maps to NM_001033602.2 I607I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr13:29599686 G>A maps to NM_001033602.2 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr13:29608131 G>A maps to NM_001033602.2 L782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr13:29600484 A>G maps to NM_001033602.2 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr13:29933549 G>A maps to NM_001033602.2 L1029L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr13:29600778 C>T maps to NM_001033602.2 I658I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:29598858 G>A maps to NM_001033602.2 K18K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:29599755 G>A maps to NM_001033602.2 E317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:29599803 G>A maps to NM_001033602.2 E333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:29599938 C>T maps to NM_001033602.2 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:29600268 G>A maps to NM_001033602.2 E488E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:29600727 C>T maps to NM_001033602.2 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr13:29599431 C>T maps to NM_001033602.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr13:29598954 C>T maps to NM_001033602.2 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr13:29600808 G>A maps to NM_001033602.2 V668V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr13:29601009 C>T maps to NM_001033602.2 F735F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr13:29599893 C>T maps to NM_001033602.2 H363H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr13:29600790 C>T maps to NM_001033602.2 P662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr13:29933543 G>A maps to NM_001033602.2 G1027G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:155182222 G>A maps to NM_002455.3 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:79284377 G>A maps to ENST00000512528 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr1:155160285 G>T maps to ENST00000425082 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:155160213 C>T maps to ENST00000425082 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:155159933 G>A maps to ENST00000425082 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr3:124632016 C>T maps to NM_033049.3 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:124635245 G>A maps to NM_033049.3 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:124646517 A>T maps to NM_033049.3 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr3:124641139 G>A maps to NM_033049.3 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:124630987 C>T maps to NM_033049.3 K404K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:124630954 C>T maps to NM_033049.3 K415K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:124627179 C>T maps to NM_033049.3 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:26587069 C>T maps to NM_001135091.1 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:26584714 C>T maps to NM_001135091.1 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:26582725 C>T maps to NM_001135091.1 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:26584714 C>T maps to NM_001135091.1 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr11:26582725 C>T maps to NM_001135091.1 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr11:26587198 C>T maps to NM_001135091.1 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:26586714 T>A maps to NM_001135091.1 K258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:26586931 C>T maps to NM_001135091.1 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:26586829 G>A maps to NM_001135091.1 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr19:9061147 G>A maps to NM_024690.2 S8766S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr19:8995692 C>T maps to NM_024690.2 G13765G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr19:9000159 G>A maps to NM_024690.2 L13533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr19:9064450 G>A maps to NM_024690.2 S7665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr19:9070972 C>T maps to NM_024690.2 E5491E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr19:9072271 G>A maps to NM_024690.2 T5058T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr19:9085553 C>T maps to NM_024690.2 T2087T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:9087494 C>T maps to NM_024690.2 G1440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:9089597 C>T maps to NM_024690.2 A739A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr19:9083585 C>T maps to NM_024690.2 S2743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr19:9068755 T>A maps to NM_024690.2 T6230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:9061714 G>A maps to NM_024690.2 S8577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:9084929 C>T maps to NM_024690.2 W2295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:9089081 G>A maps to NM_024690.2 F911F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr19:9067483 G>A maps to NM_024690.2 S6654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr19:9073984 G>A maps to NM_024690.2 T4487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr19:9065218 G>A maps to NM_024690.2 S7409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr19:9085313 C>T maps to NM_024690.2 P2167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr19:9057010 G>A maps to NM_024690.2 S10145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:9027567 G>A maps to NM_024690.2 T12192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:9059482 G>A maps to NM_024690.2 S9321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:9086189 C>T maps to NM_024690.2 L1875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr19:9008344 C>T maps to NM_024690.2 R13069R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CF-06A-11D-A196-08 chr19:9080449 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:9071242 C>T maps to NM_024690.2 E5401E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:9084929 C>T maps to NM_024690.2 W2295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:9058282 C>T maps to NM_024690.2 V9721V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:9072325 G>A maps to NM_024690.2 P5040P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr19:9058033 C>T maps to NM_024690.2 E9804E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr19:9064402 C>T maps to NM_024690.2 V7681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr19:9082793 G>A maps to NM_024690.2 T3007T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr19:9084491 G>A maps to NM_024690.2 S2441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr19:9089549 C>T maps to NM_024690.2 G755G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:9059610 G>A maps to NM_024690.2 Q9279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:9060262 C>T maps to NM_024690.2 V9061V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr19:9067503 C>A maps to NM_024690.2 E6648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr19:9050195 G>A maps to NM_024690.2 L10479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:9077719 C>T maps to NM_024690.2 V3242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr19:9083312 C>T maps to NM_024690.2 T2834T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr19:9074847 G>A maps to NM_024690.2 L4200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr19:9074857 C>T maps to NM_024690.2 E4196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:9002183 G>A maps to NM_024690.2 F13440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:9060430 C>T maps to NM_024690.2 R9005R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:9068395 G>A maps to NM_024690.2 S6350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:9068670 G>A maps to NM_024690.2 L6259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:9069838 C>T maps to NM_024690.2 G5869G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr19:9064855 C>T maps to NM_024690.2 R7530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:9062257 G>A maps to NM_024690.2 S8396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr19:9061795 C>T maps to NM_024690.2 P8550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:8997167 C>T maps to NM_024690.2 K13676K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:9006659 C>T maps to NM_024690.2 E13196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:9056479 C>T maps to NM_024690.2 E10322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:9063985 C>T maps to NM_024690.2 R7820R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:9072286 G>A maps to NM_024690.2 S5053S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:9070777 G>A maps to NM_024690.2 I5556I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:9071830 C>T maps to NM_024690.2 T5205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:9074986 C>T maps to NM_024690.2 V4153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr19:9062770 C>T maps to NM_024690.2 W8225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr19:9083531 G>A maps to NM_024690.2 F2761F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr19:9046737 C>T maps to NM_024690.2 V11631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr19:9047931 C>T maps to NM_024690.2 E11233E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr19:9068413 G>A maps to NM_024690.2 S6344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr19:9090788 C>T maps to NM_024690.2 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr19:9091670 G>A maps to NM_024690.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr19:8995662 C>T maps to NM_024690.2 K13775K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr19:9060352 C>T maps to NM_024690.2 T9031T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr19:9057802 C>T maps to NM_024690.2 E9881E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:9066037 C>T maps to NM_024690.2 T7136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:8995650 C>T maps to NM_024690.2 S13779S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:8999055 G>A maps to NM_024690.2 F13596F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:9064402 C>T maps to NM_024690.2 V7681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:9075391 C>T maps to NM_024690.2 R4018R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr19:9058105 G>A maps to NM_024690.2 T9780T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:9026202 G>A maps to NM_024690.2 V12261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:9046629 C>T maps to NM_024690.2 G11667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:9058048 G>A maps to NM_024690.2 I9799I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:9068305 G>A maps to NM_024690.2 S6380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:9089903 G>A maps to NM_024690.2 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr19:9064000 G>A maps to NM_024690.2 F7815F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr19:9077089 G>A maps to NM_024690.2 I3452I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:8994500 G>A maps to NM_024690.2 F13797F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:9007839 G>A maps to NM_024690.2 F13128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:9020784 G>A maps to NM_024690.2 G12439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:9049902 C>T maps to NM_024690.2 G10576G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:9066493 G>A maps to NM_024690.2 S6984S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:9091121 C>T maps to NM_024690.2 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:8995692 C>T maps to NM_024690.2 G13765G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:9005630 G>A maps to NM_024690.2 L13259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:9075210 G>A maps to NM_024690.2 L4079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:9076138 G>A maps to NM_024690.2 I3769I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:8994488 G>A maps to NM_024690.2 N13801N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr19:8995650 C>T maps to NM_024690.2 S13779S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr19:9058516 T>C maps to NM_024690.2 E9643E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr19:9088733 C>T maps to NM_024690.2 T1027T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr19:9089864 G>A maps to NM_024690.2 S650S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:8976422 C>T maps to NM_024690.2 K14135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:9046164 G>A maps to NM_024690.2 L11822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:9063835 G>A maps to NM_024690.2 S7870S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:9067426 C>T maps to NM_024690.2 E6673E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:9068659 G>A maps to NM_024690.2 I6262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:9070816 G>A maps to NM_024690.2 I5543I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr19:9058357 T>A maps to NM_024690.2 G9696G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr19:9075169 G>A maps to NM_024690.2 I4092I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr19:9063943 C>T maps to NM_024690.2 R7834R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr19:8982214 G>A maps to NM_024690.2 T14020T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:9059368 C>T maps to NM_024690.2 R9359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:9062065 G>A maps to NM_024690.2 S8460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:9062725 C>T maps to NM_024690.2 E8240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:9064408 G>A maps to NM_024690.2 P7679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:9065944 C>T maps to NM_024690.2 K7167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:9067147 C>T maps to NM_024690.2 S6766S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:9072285 G>A maps to NM_024690.2 L5054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:9076699 G>A maps to NM_024690.2 T3582T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:8995650 C>T maps to NM_024690.2 S13779S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:9046026 G>A maps to NM_024690.2 S11868S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:9066355 G>A maps to NM_024690.2 I7030I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:9072283 C>T maps to NM_024690.2 L5054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:9083501 C>T maps to NM_024690.2 T2771T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:9088508 G>A maps to NM_024690.2 F1102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr19:9000474 C>T maps to NM_024690.2 K13503K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr19:9090728 C>T maps to NM_024690.2 E362E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:9046167 A>C maps to NM_024690.2 S11821S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:9062911 A>C maps to NM_024690.2 T8178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:9068287 G>A maps to NM_024690.2 V6386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:9071965 C>A maps to NM_024690.2 V5160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:9072481 A>T maps to NM_024690.2 T4988T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:9074152 G>A maps to NM_024690.2 L4431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:9086273 G>A maps to NM_024690.2 L1847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:9091625 G>T maps to NM_024690.2 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:8994509 G>A maps to NM_024690.2 T13794T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:9005203 G>A maps to NM_024690.2 P13291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:9020005 T>G maps to NM_024690.2 R12497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:9063610 C>T maps to NM_024690.2 Q7945Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:9067810 G>A maps to NM_024690.2 P6545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:9072586 G>A maps to NM_024690.2 S4953S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:9076567 G>A maps to NM_024690.2 D3626D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr19:9056854 C>T maps to NM_024690.2 Q10197Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:9058152 G>A maps to NM_024690.2 L9765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:9075799 G>A maps to NM_024690.2 I3882I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:8976813 G>A maps to NM_024690.2 S14084S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:8999410 C>T maps to NM_024690.2 R13588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:9058381 C>T maps to NM_024690.2 G9688G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:9083312 C>T maps to NM_024690.2 T2834T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr19:9017364 C>T maps to NM_024690.2 R12653R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:9057985 G>A maps to NM_024690.2 S9820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:9077716 T>C maps to NM_024690.2 E3243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:9085474 G>A maps to NM_024690.2 Q2114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr19:9062965 G>A maps to NM_024690.2 S8160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr19:9076828 G>A maps to NM_024690.2 S3539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr19:9086534 C>T maps to NM_024690.2 V1760V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:9008191 C>T maps to NM_024690.2 R13120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:9061492 C>T maps to NM_024690.2 G8651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:9071104 C>T maps to NM_024690.2 S5447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:9088355 G>A maps to NM_024690.2 I1153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr19:9012860 G>A maps to NM_024690.2 F12861F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr19:9047541 C>T maps to NM_024690.2 R11363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr19:9084752 G>A maps to NM_024690.2 I2354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr19:9065736 G>A maps to NM_024690.2 Q7237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:8994428 G>A maps to NM_024690.2 V13821V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:9067633 C>T maps to NM_024690.2 K6604K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:9089864 G>A maps to NM_024690.2 S650S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr19:9087173 C>T maps to NM_024690.2 V1547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr19:9088961 G>A maps to NM_024690.2 T951T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:8997423 G>A maps to NM_024690.2 V13666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:9020066 C>A maps to NM_024690.2 L12476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:9058999 C>T maps to NM_024690.2 L9482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr19:9050169 C>T maps to NM_024690.2 K10487K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:9085682 C>T maps to NM_024690.2 R2044R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr19:8993391 C>T maps to NM_024690.2 R13899R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr19:8999467 C>T maps to NM_024690.2 W13569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr19:9059776 C>T maps to NM_024690.2 L9223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:9057355 C>T maps to NM_024690.2 T10030T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:9074893 G>A maps to NM_024690.2 S4184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr19:9056794 G>A maps to NM_024690.2 A10217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr19:9062443 G>A maps to NM_024690.2 T8334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr19:9069682 C>T maps to NM_024690.2 V5921V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr19:9059368 C>T maps to NM_024690.2 R9359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr19:9065878 G>A maps to NM_024690.2 P7189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr19:9082688 G>A maps to NM_024690.2 F3042F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:8999533 C>T maps to NM_024690.2 V13547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:9046065 C>T maps to NM_024690.2 G11855G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:9065347 C>T maps to NM_024690.2 E7366E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:9073480 G>A maps to NM_024690.2 F4655F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:9075931 C>T maps to NM_024690.2 V3838V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:9077275 G>A maps to NM_024690.2 T3390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:9086951 G>A maps to NM_024690.2 G1621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:9087821 C>T maps to NM_024690.2 K1331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:9076819 G>A maps to NM_024690.2 I3542I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr19:9074605 G>A maps to NM_024690.2 I4280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:9005616 G>A maps to NM_024690.2 T13263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:9057541 C>T maps to NM_024690.2 Q9968Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:9072100 C>T maps to NM_024690.2 K5115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:9083585 C>T maps to NM_024690.2 S2743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr19:9068620 T>A maps to NM_024690.2 S6275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr19:9014697 C>T maps to NM_024690.2 E12759E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr19:9062545 G>A maps to NM_024690.2 L8300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:9009650 C>T maps to NM_024690.2 G13025G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:9047994 G>A maps to NM_024690.2 V11212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:9048588 C>T maps to NM_024690.2 E11014E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:9063772 G>A maps to NM_024690.2 F7891F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:9067645 G>A maps to NM_024690.2 T6600T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:9071743 G>A maps to NM_024690.2 S5234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:8995963 G>A maps to NM_024690.2 S13759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:9048747 G>A maps to NM_024690.2 T10961T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:9064630 G>A maps to NM_024690.2 P7605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:9069547 C>T maps to NM_024690.2 R5966R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr19:9074695 C>T maps to NM_024690.2 T4250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:8982295 G>A maps to NM_024690.2 D13993D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:9060262 C>T maps to NM_024690.2 V9061V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:9065719 G>A maps to NM_024690.2 S7242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:9067237 G>A maps to NM_024690.2 I6736I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr19:9086882 G>A maps to NM_024690.2 T1644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:9083312 C>T maps to NM_024690.2 T2834T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:9087449 G>T maps to NM_024690.2 L1455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr19:9085007 C>T maps to NM_024690.2 K2269K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:9061312 C>T maps to NM_024690.2 R8711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:9088811 G>A maps to NM_024690.2 F1001F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:9015626 C>T maps to NM_024690.2 Q12732Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:9048012 C>T maps to NM_024690.2 G11206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:9056794 G>A maps to NM_024690.2 A10217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:9069613 G>A maps to NM_024690.2 S5944S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:9075412 G>A maps to NM_024690.2 S4011S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:9076486 C>T maps to NM_024690.2 K3653K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr19:9026202 G>A maps to NM_024690.2 V12261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:8994512 G>A maps to NM_024690.2 F13793F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:9057031 G>A maps to NM_024690.2 S10138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr19:9070066 G>A maps to NM_024690.2 I5793I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr19:9085829 A>T maps to NM_024690.2 V1995V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:9018508 C>T maps to NM_024690.2 L12555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:9049914 G>A maps to NM_024690.2 V10572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:9090077 C>T maps to NM_024690.2 G579G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr19:9061309 C>T maps to NM_024690.2 E8712E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:8976783 C>T maps to NM_024690.2 K14094K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:9018544 C>T maps to NM_024690.2 L12543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:9060157 C>T maps to NM_024690.2 L9096L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:9061168 G>A maps to NM_024690.2 S8759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:9064198 G>A maps to NM_024690.2 T7749T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:9065736 G>A maps to NM_024690.2 Q7237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:9075541 G>A maps to NM_024690.2 I3968I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:9089939 G>A maps to NM_024690.2 H625H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:9000145 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:8973574 G>A maps to NM_024690.2 F14247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:9049120 C>T maps to NM_024690.2 W10837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:9064720 G>A maps to NM_024690.2 S7575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:9068116 C>T maps to NM_024690.2 R6443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr19:9003658 G>T maps to NM_024690.2 L13327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr19:9026226 C>T maps to NM_024690.2 R12253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr19:9060703 G>A maps to NM_024690.2 I8914I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr19:9068068 G>A maps to NM_024690.2 T6459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr19:9062684 C>T maps to NM_024690.2 W8254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr19:9070153 A>C maps to NM_024690.2 T5764T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr19:9049611 G>A maps to NM_024690.2 S10673S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr19:9062584 C>T maps to NM_024690.2 E8287E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:9050243 C>G did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:9076828 G>A maps to NM_024690.2 S3539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr19:9069925 G>A maps to NM_024690.2 S5840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr19:9045921 G>A maps to NM_024690.2 S11903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:9014190 C>T maps to NM_024690.2 Q12819Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:9060271 G>A maps to NM_024690.2 S9058S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:9070015 A>G maps to NM_024690.2 T5810T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr19:9066115 G>A maps to NM_024690.2 P7110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr19:9074221 G>A maps to NM_024690.2 T4408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr19:9046599 C>T maps to NM_024690.2 R11677R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr19:9056804 C>T maps to NM_024690.2 W10214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr19:9057631 C>T maps to NM_024690.2 V9938V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr19:8993397 C>T maps to NM_024690.2 L13897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr19:8969338 G>A maps to NM_024690.2 S14335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr19:9019290 G>A maps to NM_024690.2 S12532S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr19:9086594 A>G maps to NM_024690.2 A1740A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr19:9065404 G>A maps to NM_024690.2 T7347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:9064312 G>A maps to NM_024690.2 P7711P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:9071323 C>T maps to NM_024690.2 V5374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:9074695 C>T maps to NM_024690.2 T4250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr19:9077725 G>A maps to NM_024690.2 T3240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:9060964 C>T maps to NM_024690.2 G8827G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr19:9063922 C>T maps to NM_024690.2 G7841G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:9049257 C>T maps to NM_024690.2 R10791R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:9059044 G>A maps to NM_024690.2 F9467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:9066586 C>T maps to NM_024690.2 L6953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:9082688 G>A maps to NM_024690.2 F3042F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:9086711 G>A maps to NM_024690.2 S1701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr19:9050136 G>A maps to NM_024690.2 V10498V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr19:9061108 C>T maps to NM_024690.2 T8779T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr19:9089933 G>A maps to NM_024690.2 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr19:9071824 T>G maps to NM_024690.2 T5207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:9047535 G>A maps to NM_024690.2 T11365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:9069394 C>T maps to NM_024690.2 G6017G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:9074545 C>T maps to NM_024690.2 E4300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:9076957 C>T maps to NM_024690.2 E3496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr19:9077821 G>A maps to NM_024690.2 I3208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F4-06A-12D-A25O-08 chr19:9059509 C>G maps to NM_024690.2 V9312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:9049491 G>A maps to NM_024690.2 A10713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:9059272 G>A maps to NM_024690.2 S9391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:9060391 C>T maps to NM_024690.2 K9018K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr19:9058951 C>T maps to NM_024690.2 E9498E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr19:9060019 G>A maps to NM_024690.2 S9142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr19:9076138 G>A maps to NM_024690.2 I3769I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr19:9060784 G>A maps to NM_024690.2 F8887F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:8971823 C>T maps to NM_024690.2 T14256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:8993435 G>A maps to NM_024690.2 L13885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:8997176 G>A maps to NM_024690.2 S13673S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9009647 C>T maps to NM_024690.2 E13026E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9048258 C>T maps to NM_024690.2 E11124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9048825 G>A maps to NM_024690.2 T10935T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9049947 G>A maps to NM_024690.2 F10561F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9056434 G>A maps to NM_024690.2 F10337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9057961 G>A maps to NM_024690.2 S9828S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9059449 G>A maps to NM_024690.2 S9332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9060568 G>A maps to NM_024690.2 L8959L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9061486 C>T maps to NM_024690.2 V8653V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9062044 G>A maps to NM_024690.2 F8467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9062074 C>T maps to NM_024690.2 R8457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9063592 C>T maps to NM_024690.2 R7951R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9063964 G>A maps to NM_024690.2 S7827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9064618 G>A maps to NM_024690.2 A7609A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9064666 G>A maps to NM_024690.2 S7593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9064855 C>T maps to NM_024690.2 R7530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9065395 G>A maps to NM_024690.2 S7350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9065467 G>A maps to NM_024690.2 I7326I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9065887 C>T maps to NM_024690.2 V7186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9067483 G>A maps to NM_024690.2 S6654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9067678 G>A maps to NM_024690.2 S6589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9068060 C>T maps to NM_024690.2 W6462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9069055 G>A maps to NM_024690.2 S6130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9069820 G>A maps to NM_024690.2 T5875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9070072 C>T maps to NM_024690.2 E5791E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9071251 G>A maps to NM_024690.2 I5398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9071512 G>A maps to NM_024690.2 T5311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9071764 G>A maps to NM_024690.2 V5227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9072127 G>A maps to NM_024690.2 A5106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9072406 C>T maps to NM_024690.2 L5013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9073561 C>T maps to NM_024690.2 G4628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9073720 C>T maps to NM_024690.2 G4575G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9074221 G>A maps to NM_024690.2 T4408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9074866 G>A maps to NM_024690.2 F4193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9075286 G>A maps to NM_024690.2 S4053S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9075382 G>A maps to NM_024690.2 S4021S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9076248 G>A maps to NM_024690.2 L3733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9076249 A>T maps to NM_024690.2 S3732S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9077158 C>T maps to NM_024690.2 W3429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9082625 C>T maps to NM_024690.2 R3063R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9082976 C>T maps to NM_024690.2 K2946K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9083066 G>A maps to NM_024690.2 T2916T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9085733 G>A maps to NM_024690.2 S2027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9085994 G>A maps to NM_024690.2 S1940S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9088429 G>A maps to NM_024690.2 L1129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9088838 G>A maps to NM_024690.2 L992L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9089882 C>T maps to NM_024690.2 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9090629 G>A maps to NM_024690.2 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr19:9059722 G>A maps to NM_024690.2 V9241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:9046788 C>T maps to NM_024690.2 T11614T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:9059695 G>A maps to NM_024690.2 A9250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:9063569 C>T maps to NM_024690.2 W7959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:9063955 G>A maps to NM_024690.2 T7830T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:9064482 G>A maps to NM_024690.2 Q7655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:9070954 C>T maps to NM_024690.2 K5497K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:9013881 C>T maps to NM_024690.2 G12836G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:9045612 G>A maps to NM_024690.2 T12006T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:9045876 C>T maps to NM_024690.2 W11918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:9048240 G>A maps to NM_024690.2 A11130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:9070393 C>T maps to NM_024690.2 T5684T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:9071722 G>A maps to NM_024690.2 S5241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:9072250 G>A maps to NM_024690.2 S5065S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:9072319 G>A maps to NM_024690.2 S5042S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:9073585 G>A maps to NM_024690.2 I4620I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:9083075 G>A maps to NM_024690.2 S2913S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr19:9071477 C>T maps to NM_024690.2 W5323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr19:9066397 G>A maps to NM_024690.2 L7016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr19:9064000 G>A maps to NM_024690.2 F7815F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:9019630 G>A maps to NM_024690.2 F12505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:9067507 C>T maps to NM_024690.2 R6646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:9061663 G>A maps to NM_024690.2 L8594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:9064378 G>A maps to NM_024690.2 S7689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:9087896 C>T maps to NM_024690.2 E1306E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:9049205 G>A maps to NM_024690.2 R10809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:9057631 C>T maps to NM_024690.2 V9938V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:9062542 G>A maps to NM_024690.2 N8301N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:9075169 G>A maps to NM_024690.2 I4092I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:9077593 G>A maps to NM_024690.2 S3284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:9083159 G>A maps to NM_024690.2 I2885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:9085016 G>A maps to NM_024690.2 F2266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:9070708 G>A maps to NM_024690.2 I5579I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr7:100694922 C>T maps to NM_001040105.1 Q4302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr7:100687011 C>T maps to NM_001040105.1 F4105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:100675719 C>T maps to NM_001040105.1 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr7:100674882 T>C maps to NM_001040105.1 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:100678419 A>G maps to NM_001040105.1 T1241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:100682776 T>C maps to NM_001040105.1 L2694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:100684680 T>G maps to NM_001040105.1 T3328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr7:100696389 C>T maps to NM_001040105.1 L4409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr7:100701292 C>T maps to NM_001040105.1 Q4484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:100678764 C>T maps to NM_001040105.1 I1356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:100685955 C>T maps to NM_001040105.1 T3753T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr7:100687041 G>A maps to NM_001040105.1 T4115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr7:100687038 C>A maps to NM_001040105.1 P4114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr7:100683507 C>T maps to NM_001040105.1 T2937T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:100686138 T>A maps to NM_001040105.1 T3814T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr7:100679670 C>T maps to NM_001040105.1 S1658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr7:100686261 C>T maps to NM_001040105.1 F3855F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:100681098 C>T maps to NM_001040105.1 I2134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:100696407 C>T maps to NM_001040105.1 R4415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:100679541 C>A maps to NM_001040105.1 T1615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr7:100677795 A>T maps to NM_001040105.1 P1033P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:100684179 A>G maps to NM_001040105.1 E3161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:100691289 G>A maps to NM_001040105.1 T4143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr7:100679880 T>C maps to NM_001040105.1 R1728R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:100685707 C>T maps to NM_001040105.1 Q3671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr7:100674975 G>A maps to NM_001040105.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:100682652 C>T maps to NM_001040105.1 T2652T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:100684575 G>A maps to NM_001040105.1 V3293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:100686969 C>T maps to NM_001040105.1 T4091T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr7:100683756 T>G maps to NM_001040105.1 T3020T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:100683576 C>T maps to NM_001040105.1 T2960T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:100678578 G>A maps to NM_001040105.1 E1294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr7:100691325 G>A maps to NM_001040105.1 G4155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr7:100679412 C>T maps to NM_001040105.1 S1572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:100679685 C>T maps to NM_001040105.1 I1663I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:100685694 G>A maps to NM_001040105.1 V3666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:100686591 G>A maps to NM_001040105.1 V3965V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr7:100674924 C>T maps to NM_001040105.1 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:100677147 G>C maps to NM_001040105.1 P817P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:100681920 G>C maps to NM_001040105.1 P2408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:100683330 C>A maps to NM_001040105.1 T2878T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:100683336 G>C maps to NM_001040105.1 P2880P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr7:100663451 G>A maps to NM_001040105.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:100679001 A>G maps to NM_001040105.1 S1435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr7:100675854 A>C maps to NM_001040105.1 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr7:100686663 G>A maps to NM_001040105.1 K3989K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr7:100685610 C>T maps to NM_001040105.1 T3638T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr7:100687011 C>T maps to NM_001040105.1 F4105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:100678233 C>T maps to NM_001040105.1 T1179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:100679637 G>A maps to NM_001040105.1 E1647E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:100680531 C>T maps to NM_001040105.1 T1945T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:100683360 C>T maps to NM_001040105.1 T2888T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:100684590 G>A maps to NM_001040105.1 T3298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:100685640 C>T maps to NM_001040105.1 T3648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:100679805 C>T maps to NM_001040105.1 A1703A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:100681200 C>G maps to NM_001040105.1 V2168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:100686279 C>T maps to NM_001040105.1 V3861V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:100686978 C>T maps to NM_001040105.1 T4094T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:100699523 C>T maps to NM_001040105.1 S4471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr7:100678056 C>A maps to NM_001040105.1 T1120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr7:100678764 C>T maps to NM_001040105.1 I1356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:1081658 G>A maps to ENST00000441003 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:1095662 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:1101121 C>T maps to ENST00000441003 L2507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:1093685 C>T maps to ENST00000441003 P1835P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:1095329 C>T maps to ENST00000441003 C2050C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:1104205 C>T maps to ENST00000441003 L2799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:1087446 G>A maps to ENST00000441003 V1066V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:1096454 C>T maps to ENST00000441003 I2160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr11:1097746 C>T maps to ENST00000441003 S2280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr11:1097791 C>T maps to ENST00000441003 S2295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:1096415 G>A maps to ENST00000441003 E2147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:1097740 C>T maps to ENST00000441003 I2278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr11:1097737 G>A maps to ENST00000441003 E2277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:1098760 C>T maps to ENST00000441003 A2377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr11:1093802 C>T maps to ENST00000441003 T1874T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:1093547 C>T maps to ENST00000441003 T1789T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:1081517 C>T maps to ENST00000441003 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr11:1090911 C>T maps to ENST00000441003 T1269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr11:1097803 C>A maps to ENST00000441003 C2299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr11:1080563 C>T maps to ENST00000441003 F402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr11:1098700 C>T maps to ENST00000441003 F2357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:1102136 G>A maps to ENST00000441003 V2591V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr11:1081529 G>A maps to ENST00000441003 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:1092164 G>A maps to ENST00000441003 G1328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:1103313 C>T maps to ENST00000441003 I2688I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr11:1099443 C>T maps to ENST00000441003 L2429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr11:1083139 C>T maps to ENST00000441003 S680S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr11:1097261 G>C maps to ENST00000441003 V2226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:1093536 A>T maps to ENST00000441003 K1786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:1077596 G>A did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:1104226 G>A maps to ENST00000441003 R2806R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr3:195453369 G>A maps to ENST00000447234 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:195453336 G>A maps to ENST00000447234 T621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr3:195453417 G>A maps to ENST00000447234 T648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr6:30955397 C>T maps to NM_001010909.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr6:30954875 C>T maps to NM_001010909.2 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr6:30955193 C>T maps to NM_001010909.2 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr6:30955082 C>T maps to NM_001010909.2 N377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:30954854 C>T maps to NM_001010909.2 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:30955001 C>T maps to NM_001010909.2 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:195501114 C>T maps to NM_018406.5 V4335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:195493606 G>A maps to NM_018406.5 F4515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr3:195498552 G>A maps to NM_018406.5 F4404F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:195479949 C>T maps to NM_018406.5 G5160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:195493585 G>A maps to NM_018406.5 S4522S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:195501129 G>A maps to NM_018406.5 F4330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:195505222 G>A maps to NM_018406.5 A4298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr3:195491985 C>T maps to NM_018406.5 W4602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr3:195490395 G>A maps to NM_018406.5 Q4721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr3:195538625 G>A maps to NM_018406.5 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:195501176 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:195505258 G>A maps to NM_018406.5 T4286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3BZ-06A-12D-A196-08 chr11:1264736 G>A maps to ENST00000447027 T2212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:1265951 G>A maps to ENST00000447027 T2617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:1272002 A>C maps to ENST00000447027 T4634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr11:1275418 C>T maps to ENST00000447027 I5108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr11:1271261 C>T maps to ENST00000447027 S4387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:1262885 G>A maps to ENST00000447027 R1595R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr11:1267247 G>A maps to ENST00000447027 R3049R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:1270361 G>A maps to ENST00000447027 T4087T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:1274169 G>A maps to ENST00000447027 S5062S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr11:1254363 G>A maps to ENST00000447027 V732V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:1267454 G>A maps to ENST00000447027 T3118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:1258300 G>A maps to ENST00000447027 K1071K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:1268567 G>A maps to ENST00000447027 E3489E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:1269215 G>A maps to ENST00000447027 T3705T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:1251273 G>A maps to ENST00000447027 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:1263989 G>A maps to ENST00000447027 G1963G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:1265444 G>A maps to ENST00000447027 T2448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:1266728 C>T maps to ENST00000447027 P2876P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr11:1260183 G>A maps to ENST00000447027 T1130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr11:1272381 C>T maps to ENST00000447027 L4761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr11:1265405 G>A maps to ENST00000447027 T2435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:1262684 G>A maps to ENST00000447027 G1528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:1270928 G>A maps to ENST00000447027 P4276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:1264084 G>A maps to ENST00000447027 W1995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:1257737 C>T maps to ENST00000447027 A1004A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr11:1019476 C>T maps to NM_005961.2 T1276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:1016746 A>G maps to NM_005961.2 T2018T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:1018432 A>G maps to NM_005961.2 T1456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr11:1030957 G>A maps to NM_005961.2 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:1015760 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:1016836 G>A maps to NM_005961.2 S1988S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:1029143 G>A maps to NM_005961.2 Q428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:1017367 G>A maps to NM_005961.2 S1811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:1020105 G>A maps to NM_005961.2 P1264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr11:1016836 G>A maps to NM_005961.2 S1988S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:1019290 C>T maps to NM_005961.2 G1338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr11:1021236 C>T maps to NM_005961.2 E1189E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr11:1017268 G>A maps to NM_005961.2 S1844S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr11:1018447 G>A maps to NM_005961.2 S1451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr11:1023554 G>A maps to NM_005961.2 C1160C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:71346527 C>T maps to NM_152291.2 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:71347537 T>C maps to NM_152291.2 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:71347171 C>T maps to NM_152291.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:71347240 C>T maps to NM_152291.2 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:55252024 G>A maps to NM_058173.2 *91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr12:55248900 G>A maps to NM_058173.2 Q20Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr12:55252001 C>T maps to NM_058173.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr12:55251989 G>A maps to NM_058173.2 W79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr14:57752954 C>T maps to ENST00000431972 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:20827451 G>A maps to NM_024544.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:20827740 G>A maps to NM_024544.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr19:1360162 C>T maps to NM_032853.3 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:1376565 C>T maps to NM_032853.3 R709R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:105449868 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:105449869 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr23:105449832 G>T did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:105450223 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr23:105450544 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:105450012 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr23:105450199 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:105450597 A>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:105450653 T>A did not map to a codon.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr23:105450037 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:105450437 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:105450678 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr23:105450601 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr23:105450818 G>T did not map to a codon.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr23:105450352 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:105451246 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:105450056 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:105450193 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr23:105449923 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:105450533 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:105449604 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:105450199 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr23:105449517 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr23:105449829 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:105450358 A>C did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:105450025 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:105451267 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:105449723 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr23:105450804 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:105450718 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr23:105450651 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr23:105451178 C>T did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:105450967 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr23:105449584 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr23:105450146 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr23:105449719 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:105449608 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:105450028 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:105450251 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:105450875 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:105451059 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:105450268 C>T did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:105449842 G>A did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:105449690 C>T did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:105450124 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:103348441 T>G maps to NM_001018116.1 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:65632504 C>T maps to NM_025128.4 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr11:65631969 C>T maps to NM_025128.4 F354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:65632591 C>T maps to NM_025128.4 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:113459612 C>T maps to ENST00000189978 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:113496636 G>A maps to ENST00000189978 W245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:113538217 G>A maps to ENST00000189978 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr9:113562763 G>A maps to ENST00000189978 Q708Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr9:113563066 C>T maps to ENST00000189978 Y809Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr9:113496630 C>T maps to ENST00000189978 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr9:113547962 C>T maps to ENST00000189978 I587I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr9:113445026 G>A maps to ENST00000189978 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:113496529 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:113496540 G>A maps to ENST00000189978 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:113562670 C>T maps to ENST00000189978 S677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:113562886 C>T maps to ENST00000189978 D749D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr9:113547962 C>T maps to ENST00000189978 I587I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr9:113538088 G>A maps to ENST00000189978 K408K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr9:113538239 C>T maps to ENST00000189978 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr6:49403219 G>A maps to NM_000255.3 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr6:49425442 G>A maps to NM_000255.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:45797396 G>A maps to NM_001128425.1 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:45798461 G>A maps to NM_001128425.1 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:45797755 C>T maps to NM_001128425.1 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr1:45799204 T>A maps to NM_001128425.1 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr16:88723967 C>T maps to NM_002461.1 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:88722521 G>A maps to NM_002461.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:88719737 G>A maps to NM_002461.1 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr16:88723976 G>C maps to NM_002461.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr16:88721185 A>G maps to NM_002461.1 N309N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:88719737 G>A maps to NM_002461.1 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:88723892 G>A maps to NM_002461.1 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr12:110013873 C>T maps to NM_001114185.1 D50D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr16:29859193 C>T maps to NM_017458.3 Q856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr16:29848074 C>T maps to NM_017458.3 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:29841947 C>T maps to NM_017458.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr16:29845322 C>T maps to NM_017458.3 N171N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:29841947 C>T maps to NM_017458.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:29856017 C>T maps to NM_017458.3 G613G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:29856065 C>T maps to NM_017458.3 P629P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr16:29853295 C>T maps to NM_017458.3 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:42824579 G>A maps to NM_001144925.1 E514E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr21:42830495 C>T maps to NM_001144925.1 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr21:42811672 C>T maps to NM_001144925.1 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr21:42815718 C>T maps to NM_001144925.1 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr21:42817403 C>T maps to NM_001144925.1 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr21:42824729 C>T maps to NM_001144925.1 F564F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:42762577 G>A maps to NM_002463.1 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr21:42754397 C>T maps to NM_002463.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr21:42771211 C>T maps to NM_002463.1 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr2:70164401 A>G maps to NM_002357.2 Q118Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:70143265 T>A maps to NM_002357.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr10:112044684 G>A maps to NM_130439.3 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:111967830 G>T maps to NM_130439.3 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:3229073 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr23:3238688 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr23:3242437 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr23:3240712 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr23:3242164 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:3229356 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr23:3238786 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:3242877 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:3228041 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:3238522 T>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:3241848 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:3248288 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr23:3229523 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:3241327 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:3241349 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr23:3228535 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr23:3248288 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:3228884 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:3235890 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:3235773 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:3238335 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:3238336 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr23:3229573 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr23:3239147 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr23:3239943 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr23:3239944 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr23:3241394 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr23:3240386 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:3235256 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:3240558 A>T did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:3229306 C>T did not map to a codon.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr23:3241140 C>T did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:3239113 C>T did not map to a codon.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr23:3261842 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr23:3240963 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:3228363 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:3241474 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:3241349 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:3242364 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr23:3229591 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr23:3238347 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr23:3240516 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr23:3228257 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr23:3240717 G>T did not map to a codon.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr23:3240032 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:3235331 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:3241149 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr23:3239261 C>T did not map to a codon.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr23:3240235 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:3228007 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:3229306 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:3240458 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:3240516 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:3240652 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:3241996 T>G did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:3228224 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:3242074 C>T did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:3238617 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:3235954 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:3239540 T>A did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr23:3248227 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr23:3229251 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr23:3239209 T>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:3238089 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:3241589 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:3241888 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:3248156 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:3229199 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:3239093 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:3240722 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:3240723 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr23:3228723 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr23:3238807 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:3238708 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:3239852 A>C did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr23:3242044 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:3229543 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:3261828 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:3238900 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr23:3228296 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr23:3235769 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:3227925 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:3228223 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:3229629 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr23:3238475 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:3229526 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:3241349 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:3242169 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:3248157 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:3239635 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr23:3235264 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:3239129 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:3241349 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr23:3228205 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr23:3228206 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:3229660 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:3238985 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr23:3241874 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:3240712 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:3241149 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:3241233 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:3227828 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:3228249 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:3241589 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr23:3240755 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:3235415 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:3241487 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr23:3229203 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:3241349 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:3240450 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:3241046 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:3227975 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:3238192 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr23:3239264 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr23:3240931 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr23:3241562 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:3228059 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:3236009 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:3238771 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:3241723 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:3229398 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:3235715 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:3241057 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr23:3239398 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:3228259 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:3242418 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:3248172 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:3248288 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr23:3241576 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:3228199 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:3239555 C>G did not map to a codon.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr23:3229291 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:3235705 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:3239626 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:3240466 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:3229629 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:3235666 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:3235705 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:3241567 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:3241568 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr23:3261694 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:3240121 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:3228778 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:3235705 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:3241640 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:3235750 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:3239093 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:3239850 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:3241043 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:3248729 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr23:3238495 C>T did not map to a codon.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr23:3261760 C>T did not map to a codon.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr23:3261785 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr23:3242383 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:3239244 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr23:3227969 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:3241349 C>T did not map to a codon.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr23:3241233 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr23:3240438 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr23:3240994 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:3228896 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:3235705 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:3235890 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:3241207 C>T did not map to a codon.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr23:3239522 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr23:3228148 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:3228959 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:3238413 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:3241037 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:3239521 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:3261813 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:3241069 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:3238771 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr23:3228496 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr23:3241355 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:3227865 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:3228098 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:3228263 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:3229529 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:3236041 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:3238440 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:3238444 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:3240416 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:3240610 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:3240870 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:3248120 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:3241460 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr23:3229095 G>A did not map to a codon.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr23:3241372 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:3239577 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:3235793 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:3235907 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:3238429 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:3240207 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:3240981 G>A did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:3240931 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr23:3242263 C>T did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:3241069 C>T did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:3248172 G>A did not map to a codon.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr23:3241017 C>T did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:3241105 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:1289772 G>A maps to NM_032348.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr1:1290449 C>T maps to NM_032348.2 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr1:1289860 G>A maps to NM_032348.2 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:1289285 C>T maps to NM_032348.2 K415K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:54377064 C>T maps to NM_001020818.1 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr6:135516935 C>T maps to NM_001130173.1 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr6:135517064 C>T maps to NM_001130173.1 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr6:135517064 C>T maps to NM_001130173.1 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:135517064 C>T maps to NM_001130173.1 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:135513575 C>T maps to NM_001130173.1 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:135518427 C>T maps to NM_001130173.1 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:135513629 C>T maps to NM_001130173.1 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr6:135517064 C>T maps to NM_001130173.1 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:4442856 A>G maps to NM_001105538.1 A1280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr17:4443767 C>T maps to NM_001105538.1 L1103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:4457549 G>A maps to NM_001105538.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr17:4455770 G>A maps to NM_001105538.1 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr17:4455541 G>A maps to NM_001105538.1 D261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr17:4458200 G>A maps to NM_001105538.1 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr17:4443222 G>A maps to NM_001105538.1 P1158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:67509629 G>A maps to NM_001080416.2 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:42341667 C>T maps to NM_002466.2 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr20:42331500 C>T maps to NM_002466.2 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr20:42344651 C>T maps to NM_002466.2 F676F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:42328578 C>T maps to NM_002466.2 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:42344685 C>T maps to NM_002466.2 L688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:102043043 G>A maps to NM_002465.2 K401K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:102023305 A>T maps to NM_002465.2 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:102038560 C>T maps to NM_002465.2 R318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:102054986 G>A maps to NM_002465.2 W660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:102069124 C>T maps to NM_002465.2 V955V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:102054993 C>T maps to NM_002465.2 I662I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:102069103 G>A maps to NM_002465.2 E948E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:102036331 G>A maps to NM_002465.2 K267K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:50957587 G>A maps to NM_004533.3 W659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:50958437 C>T maps to NM_004533.3 T696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr19:50939084 C>T maps to NM_004533.3 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:50962495 G>A maps to NM_004533.3 G908G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr19:50958491 C>T maps to NM_004533.3 F714F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:50939888 C>T maps to NM_004533.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr19:50957350 G>A maps to NM_004533.3 A608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:50961913 C>T maps to NM_004533.3 T803T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:50964890 C>T maps to NM_004533.3 T1008T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:50951488 G>A maps to NM_004533.3 Q438Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:50958515 C>T maps to NM_004533.3 S722S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:50944250 C>T maps to NM_004533.3 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr19:50947067 G>A maps to NM_004533.3 V376V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:50958830 G>A maps to NM_004533.3 K756K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:50958866 C>T maps to NM_004533.3 I768I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:50962181 C>T maps to NM_004533.3 P838P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:50954566 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr11:47364685 C>A maps to ENST00000399249 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:47354224 C>T maps to ENST00000399249 K1173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr11:47360952 C>T maps to ENST00000399249 G690G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr11:47364159 C>T maps to ENST00000399249 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:47364270 G>A maps to ENST00000399249 T494T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr11:47356605 C>T maps to ENST00000399249 V964V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:47358978 G>A maps to ENST00000399249 S855S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:203138067 C>T maps to NM_004997.2 G461G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:203140583 G>A maps to NM_004997.2 D240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:203140546 G>A maps to NM_004997.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:203144730 G>A maps to NM_004997.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:203143638 G>A maps to NM_004997.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr1:203143594 G>A maps to NM_004997.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:203143639 G>A maps to NM_004997.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:109840161 C>T maps to NM_001010985.2 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:109840098 G>A maps to NM_001010985.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:109840829 C>G maps to NM_001010985.2 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:109849467 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr13:77779698 T>C maps to NM_015057.4 L1208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr13:77718652 A>G maps to NM_015057.4 T2410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr13:77641723 G>A maps to NM_015057.4 F4149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr13:77730261 A>G maps to NM_015057.4 G2282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr13:77655573 G>A maps to NM_015057.4 S3802S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr13:77700587 G>A maps to NM_015057.4 F2583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr13:77661648 T>C maps to NM_015057.4 E3615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr13:77671817 G>A maps to NM_015057.4 P3157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr13:77754363 C>T maps to NM_015057.4 L1677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr13:77862313 G>A maps to NM_015057.4 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr13:77642738 G>A maps to NM_015057.4 F4044F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:77642738 G>A maps to NM_015057.4 F4044F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:77748453 G>A maps to NM_015057.4 L1881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:77799639 G>A maps to NM_015057.4 Y929Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr13:77642816 A>G maps to NM_015057.4 S4018S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:48602350 C>T maps to NM_032133.4 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:48603456 G>A maps to NM_032133.4 R709R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:48599399 G>A maps to NM_032133.4 G448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:48606152 G>A maps to NM_032133.4 G878G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:48605596 G>A maps to NM_032133.4 K834K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr17:48608749 C>T maps to NM_032133.4 P972P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:48602350 C>T maps to NM_032133.4 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:48601027 G>A maps to NM_032133.4 R549R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:48602368 G>A maps to NM_032133.4 R632R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr17:48601103 C>T maps to NM_032133.4 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr17:48599378 C>T maps to NM_032133.4 G441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:48603333 G>A maps to NM_032133.4 G668G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:48603615 G>A maps to NM_032133.4 E762E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:48606479 C>T maps to NM_032133.4 I928I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:48594703 G>A maps to NM_032133.4 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr17:48598576 C>T maps to NM_032133.4 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr1:40363544 G>T maps to NM_001033082.2 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr2:16086119 C>A maps to NM_005378.4 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5KH-06A-11D-A27K-08 chr2:16085649 G>T maps to NM_005378.4 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:16086191 G>A maps to NM_005378.4 K456K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr2:16085915 C>T maps to NM_005378.4 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:16086191 G>A maps to NM_005378.4 K456K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:16086110 T>A maps to NM_005378.4 Y429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr2:16085738 C>T maps to NM_005378.4 N305N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:16086020 C>T maps to NM_005378.4 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr6:153019123 C>T maps to NM_025107.2 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:153043112 C>T maps to NM_025107.2 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:153019225 C>T maps to NM_025107.2 N63N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:153042886 C>T maps to NM_025107.2 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:153042883 T>A maps to NM_025107.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:153043306 C>T maps to NM_025107.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:153043240 C>T maps to NM_025107.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr6:153043009 G>A maps to NM_025107.2 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:153043327 C>T maps to NM_025107.2 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:153043319 C>T maps to NM_025107.2 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:153043381 T>C maps to NM_025107.2 D234D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr3:38181466 C>T maps to NM_001172567.1 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr3:38182687 C>T maps to NM_001172567.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:38180250 T>C maps to NM_001172567.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr3:38182009 C>T maps to NM_001172567.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr3:38181484 C>T maps to NM_001172567.1 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr15:48443760 G>A maps to NM_016132.3 Y405Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr11:69063156 C>T maps to NM_138768.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:69063579 G>A maps to NM_138768.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr11:69063346 C>T maps to NM_138768.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:69063825 C>T maps to NM_138768.2 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:241069408 G>A maps to NM_138336.1 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:241069366 G>A maps to NM_138336.1 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr12:81110841 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:81112673 G>A maps to NM_005593.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:81111096 G>A maps to NM_005593.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:81112168 G>A maps to NM_005593.2 K178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:81111174 G>A maps to NM_005593.2 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:81111234 C>T maps to NM_005593.2 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:81111187 C>T maps to NM_005593.2 Q116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:81112694 G>A maps to NM_005593.2 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr12:81110910 C>T maps to NM_005593.2 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:81112828 G>A maps to NM_005593.2 *256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:81110910 C>T maps to NM_005593.2 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:81110976 G>A maps to NM_005593.2 E45E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr12:81101932 G>A maps to NM_002469.2 Q145Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr12:81101548 G>A maps to NM_002469.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:81102313 G>A maps to NM_002469.2 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:81101524 C>T maps to NM_002469.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr12:81101647 G>A maps to NM_002469.2 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:81101533 C>T maps to NM_002469.2 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q3-06A-11D-A196-08 chr17:10408755 G>A maps to NM_005963.3 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:10400484 C>T maps to NM_005963.3 Q1519Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:10400754 C>T maps to NM_005963.3 W1460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:10417206 G>A maps to NM_005963.3 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J6-06A-11D-A19A-08 chr17:10415495 T>C maps to NM_005963.3 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr17:10399578 C>T maps to NM_005963.3 R1648R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr17:10408195 C>T maps to NM_005963.3 R874R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr17:10419602 C>T maps to NM_005963.3 K87K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr17:10419638 G>A maps to NM_005963.3 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr17:10398349 C>T maps to NM_005963.3 K1788K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr17:10400667 C>T maps to NM_005963.3 K1489K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr17:10399659 C>T maps to NM_005963.3 K1621K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr17:10408496 C>T maps to NM_005963.3 Q806Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr17:10418207 C>T maps to NM_005963.3 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:10408303 G>A maps to NM_005963.3 F838F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:10409371 G>A maps to NM_005963.3 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:10412912 G>A maps to NM_005963.3 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr17:10419518 G>A maps to NM_005963.3 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:10411971 G>A maps to NM_005963.3 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:10408755 G>A maps to NM_005963.3 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:10395867 G>C maps to NM_005963.3 V1895V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:10401152 C>T maps to NM_005963.3 T1421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:10408517 G>A maps to NM_005963.3 F799F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr17:10406150 C>T maps to NM_005963.3 E1005E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr17:10399320 G>A maps to NM_005963.3 I1705I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:10405000 C>T maps to NM_005963.3 K1086K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr17:10404792 C>T maps to NM_005963.3 E1124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr17:10401062 C>T maps to NM_005963.3 R1451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:10408607 G>A maps to NM_005963.3 F769F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr17:10419599 G>A maps to NM_005963.3 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr17:10408559 C>T maps to NM_005963.3 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:10399788 C>T maps to NM_005963.3 R1578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:10408755 G>A maps to NM_005963.3 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr17:10404525 G>A maps to NM_005963.3 N1213N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:10415479 G>A maps to NM_005963.3 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr17:10404729 C>T maps to NM_005963.3 R1145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:10408782 G>A maps to NM_005963.3 I740I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:10411971 G>A maps to NM_005963.3 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:10395846 C>T maps to NM_005963.3 R1902R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:10406150 C>T maps to NM_005963.3 E1005E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:10400510 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:10408555 G>A maps to NM_005963.3 Q787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr17:10401152 C>T maps to NM_005963.3 T1421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr17:10401152 C>T maps to NM_005963.3 T1421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:10404774 C>T maps to NM_005963.3 R1130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr17:10411809 C>T maps to NM_005963.3 V589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:10398571 C>T maps to NM_005963.3 E1744E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:10401101 C>T maps to NM_005963.3 R1438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr17:10399284 A>G maps to NM_005963.3 V1717V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr17:10401164 G>A maps to NM_005963.3 S1417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr17:10411226 G>A maps to NM_005963.3 F648F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr17:10404513 C>T maps to NM_005963.3 V1217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr17:10415818 G>A maps to NM_005963.3 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:10408167 G>A maps to NM_005963.3 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:10399430 C>A maps to NM_005963.3 E1669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:10399731 G>A maps to NM_005963.3 I1597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr17:10397912 C>T maps to NM_005963.3 E1848E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr17:10408761 C>T maps to NM_005963.3 E747E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr17:10418200 G>A maps to NM_005963.3 Q173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr17:10408746 G>A maps to NM_005963.3 S752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr17:10406156 G>A maps to NM_005963.3 L1003L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:10401080 G>A maps to NM_005963.3 A1445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:10408707 G>A maps to NM_005963.3 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:10416276 G>A maps to NM_005963.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:10419893 C>T maps to NM_005963.3 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr17:10398580 G>A maps to NM_005963.3 I1741I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:10408333 C>T maps to NM_005963.3 V828V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:10412912 G>A maps to NM_005963.3 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr17:10401152 C>T maps to NM_005963.3 T1421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:10398394 C>T maps to NM_005963.3 L1773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:10399320 G>A maps to NM_005963.3 I1705I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:10405195 G>A maps to NM_005963.3 I1048I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:10411878 G>A maps to NM_005963.3 F566F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr17:10419276 G>A maps to NM_005963.3 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:8395692 C>T maps to ENST00000360416 E1531E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:8396122 A>G maps to ENST00000360416 L1477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:8409748 G>A maps to ENST00000360416 L1091L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:8424603 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:8397080 C>T maps to ENST00000360416 L1393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr17:8415803 G>A maps to ENST00000360416 Q973*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr17:8393839 G>A maps to ENST00000360416 L1568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:8417208 G>A maps to ENST00000360416 A836A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:8422106 G>A maps to ENST00000360416 I782I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr17:8396273 C>T maps to ENST00000360416 K1426K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr16:15851692 G>A maps to NM_001040114.1 I529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr16:15851692 G>T maps to NM_001040114.1 I529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr16:15851848 G>A maps to NM_001040114.1 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr16:15820734 C>T maps to NM_001040114.1 A1283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:15835745 C>T maps to NM_001040114.1 V848V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr16:15818206 C>T maps to NM_001040114.1 E1399E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:15841935 G>A maps to NM_001040114.1 P723P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:15851812 C>T maps to NM_001040114.1 K489K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:15872667 C>T maps to NM_001040114.1 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:15880531 G>A maps to NM_001040114.1 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:15818254 C>T maps to NM_001040114.1 S1383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:15841452 C>T maps to NM_001040114.1 A802A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr16:15813102 C>T maps to NM_001040114.1 E1722E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:15811115 C>T maps to NM_001040114.1 K1802K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:15829335 C>T maps to NM_001040114.1 R1138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:15850299 G>A maps to NM_001040114.1 F556F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr16:15853471 G>A maps to NM_001040114.1 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr16:15931848 C>T maps to NM_001040114.1 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr16:15829410 C>T maps to NM_001040114.1 K1113K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr16:15917241 C>T maps to NM_001040114.1 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr16:15851707 G>A maps to NM_001040114.1 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr16:15835402 C>A maps to NM_001040114.1 E933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:15815443 C>T maps to NM_001040114.1 R1478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:15826453 C>T maps to NM_001040114.1 E1213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:15829320 C>T maps to NM_001040114.1 K1143K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:15831418 C>T maps to NM_001040114.1 L1067L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:15917199 G>A maps to NM_001040114.1 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr16:15818850 T>C did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:15815374 C>T maps to NM_001040114.1 E1501E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:15835511 C>T maps to NM_001040114.1 K896K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr16:15831307 G>A maps to NM_001040114.1 A1104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr16:15853534 G>A maps to NM_001040114.1 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr16:15931779 G>A maps to NM_001040114.1 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr17:10209804 T>A maps to NM_003802.2 K1813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr17:10209805 C>T maps to NM_003802.2 G1812G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr17:10247201 C>A maps to NM_003802.2 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr17:10210315 C>T maps to NM_003802.2 V1745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr17:10253930 C>T maps to NM_003802.2 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr17:10267745 G>A maps to NM_003802.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:10212676 C>T maps to NM_003802.2 R1681R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr17:10235436 C>T maps to NM_003802.2 Q759Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr17:10215911 C>T maps to NM_003802.2 K1448K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:10243521 C>T maps to NM_003802.2 R667R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr17:10263491 C>T maps to NM_003802.2 Q173Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:10258026 G>A maps to NM_003802.2 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:10250065 C>T maps to NM_003802.2 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:10258089 C>T maps to NM_003802.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr17:10267772 G>A maps to NM_003802.2 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:10212946 C>T maps to NM_003802.2 K1619K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:10219108 C>T maps to NM_003802.2 V1295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:10247408 G>A maps to NM_003802.2 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:10263381 T>C maps to NM_003802.2 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:10258065 G>A maps to NM_003802.2 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr17:10209781 C>T maps to NM_003802.2 E1820E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr17:10216578 G>A maps to NM_003802.2 A1359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:10227385 G>A maps to NM_003802.2 L963L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:10267751 G>A maps to NM_003802.2 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr17:10206604 C>A maps to NM_003802.2 E1859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr17:10233819 G>A maps to NM_003802.2 L773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:10248822 G>A maps to NM_003802.2 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:10204912 C>T maps to NM_003802.2 R1925R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:10209805 C>T maps to NM_003802.2 G1812G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:10247363 G>A maps to NM_003802.2 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr17:10209910 C>T maps to NM_003802.2 Q1777Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr17:10224952 G>A maps to NM_003802.2 L1003L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:10212616 C>T maps to NM_003802.2 R1701R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:10233723 G>A maps to NM_003802.2 F805F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr17:10258026 G>A maps to NM_003802.2 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr17:10267765 G>A maps to NM_003802.2 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr17:10215379 C>T maps to NM_003802.2 W1460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:10209889 C>T maps to NM_003802.2 E1784E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:10222304 C>T maps to NM_003802.2 R1180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:10235457 G>A maps to NM_003802.2 S752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:10265790 G>A maps to NM_003802.2 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr17:10235496 G>A maps to NM_003802.2 F739F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:10216569 C>T maps to NM_003802.2 Q1362Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:10265492 C>T maps to NM_003802.2 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:10258307 G>A maps to NM_003802.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr17:10243689 C>T maps to NM_003802.2 G641G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr19:50781503 G>A maps to NM_001145809.1 E1330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr19:50721002 G>A maps to NM_001145809.1 E179E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr19:50713816 C>T maps to NM_001145809.1 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:50804989 C>T maps to NM_001145809.1 L1848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:50784855 C>T maps to NM_001145809.1 S1432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:50794223 A>G maps to NM_001145809.1 G1682G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr19:50774790 C>T maps to NM_001145809.1 S1053S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:50812329 C>T maps to NM_001145809.1 S1952S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:50795519 C>T maps to NM_001145809.1 A1710A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:50779268 C>T maps to NM_001145809.1 A1163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:50764856 C>A maps to NM_001145809.1 S850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19T-06A-11D-A19A-08 chr19:50735327 G>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr19:50784918 C>T maps to NM_001145809.1 R1453R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:50713816 C>T maps to NM_001145809.1 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:50735322 C>T maps to NM_001145809.1 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:50752300 C>T maps to NM_001145809.1 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:50781398 G>A maps to NM_001145809.1 R1295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:50813007 C>T maps to NM_001145809.1 S2024S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr3:108183484 C>T maps to NM_014981.1 V597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr3:108117570 G>A maps to NM_014981.1 S1702S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr3:108172896 C>T maps to NM_014981.1 Q805Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr3:108129436 G>A maps to NM_014981.1 N1516N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:108182075 G>T maps to NM_014981.1 I602I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:108219052 G>A maps to NM_014981.1 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:108229344 G>A maps to NM_014981.1 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr3:108149769 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:108229377 C>T maps to NM_014981.1 K20K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:108133251 G>A maps to NM_014981.1 A1344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:108175659 G>A maps to NM_014981.1 C717C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:108135741 G>A maps to NM_014981.1 L1309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:108117570 G>A maps to NM_014981.1 S1702S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:108117582 C>T maps to NM_014981.1 E1698E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:108135769 G>A maps to NM_014981.1 F1299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:108182069 A>G maps to NM_014981.1 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:108224660 C>T maps to NM_014981.1 W55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:108212015 G>A maps to NM_014981.1 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr3:108127246 C>T maps to NM_014981.1 E1520E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:108195300 G>A maps to NM_014981.1 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:108107885 G>A maps to NM_014981.1 I1842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:108107867 G>A maps to NM_014981.1 A1848A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:108147365 G>A maps to NM_014981.1 T1245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:108160066 C>T maps to NM_014981.1 W919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:108139933 C>T did not map to a codon.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr3:108112876 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:108159924 G>A maps to NM_014981.1 I966I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:108112946 C>T maps to NM_014981.1 Q1750Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:108129688 C>T maps to NM_014981.1 Q1432Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:108178242 C>T maps to NM_014981.1 V682V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr3:108112901 C>T maps to NM_014981.1 E1765E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:108220568 C>T maps to NM_014981.1 W130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr3:108110753 C>T maps to NM_014981.1 L1781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr3:108174624 G>A maps to NM_014981.1 S760S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr3:108129628 G>A maps to NM_014981.1 A1452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr3:108219034 C>T maps to NM_014981.1 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr3:108172971 C>T maps to NM_014981.1 G780G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:108220568 C>T maps to NM_014981.1 W130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr3:108175611 C>T did not map to a codon.
Multiple mappings detected for codon TCGA-D3-A1Q4-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr17:10440987 G>A maps to ENST00000399342 S20S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D3-A3ML-06A-11D-A21A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:10438616 G>A maps to NM_017534.5 I680I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:10448696 G>A maps to NM_017534.5 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr17:10436867 G>A maps to NM_017534.5 S754S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr17:10451189 G>A maps to NM_017534.5 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:10430365 A>G maps to NM_017534.5 F1293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr17:10428304 C>T maps to NM_017534.5 R1580R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:10442572 G>A maps to NM_017534.5 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:10429087 G>A maps to NM_017534.5 V1431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:10435087 C>T maps to NM_017534.5 K853K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr17:10427123 G>A maps to NM_017534.5 L1751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr17:10440748 G>A maps to NM_017534.5 F566F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:10431131 C>T maps to NM_017534.5 K1268K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:10433391 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:10428094 C>T maps to NM_017534.5 R1650R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:10440694 G>A maps to NM_017534.5 H584H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:10432384 C>T maps to NM_017534.5 E1122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:10439900 C>T maps to NM_017534.5 K640K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:10426965 C>T maps to NM_017534.5 E1773E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:10428594 C>T maps to NM_017534.5 K1536K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:10429021 C>T maps to NM_017534.5 R1453R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:10432294 G>A maps to NM_017534.5 I1152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr17:10444003 C>T maps to NM_017534.5 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr17:10440655 C>T maps to NM_017534.5 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:10428660 C>T maps to NM_017534.5 E1514E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:10432098 G>A maps to NM_017534.5 R1218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr17:10432921 G>A maps to NM_017534.5 L1026L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:10436681 C>T maps to NM_017534.5 L787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr17:10428304 C>T maps to NM_017534.5 R1580R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr17:10436639 G>A maps to NM_017534.5 F801F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr17:10433036 C>T maps to NM_017534.5 E987E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:10433054 C>T maps to NM_017534.5 V981V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr17:10428831 C>T maps to NM_017534.5 K1491K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr17:10428918 C>T maps to NM_017534.5 W1462*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A2MD-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:10440996 G>A maps to ENST00000399342 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:10447104 G>A maps to NM_017534.5 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:10432228 C>T maps to NM_017534.5 E1174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:10433036 C>T maps to NM_017534.5 E987E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:10444000 A>T maps to NM_017534.5 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:10432219 G>A maps to NM_017534.5 F1177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:10429968 C>T maps to NM_017534.5 R1378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr17:10426842 C>T maps to NM_017534.5 G1814G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:10429114 C>T maps to NM_017534.5 K1422K. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-ER-A193-06A-12D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr17:10428304 C>T maps to NM_017534.5 R1580R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr17:10432282 C>T maps to NM_017534.5 L1156L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-ER-A19J-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr17:10446475 A>T maps to NM_017534.5 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr17:10450800 C>T maps to NM_017534.5 W113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr17:10440700 C>T maps to NM_017534.5 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr17:10429183 C>T maps to NM_017534.5 L1399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr17:10427851 C>T maps to NM_017534.5 E1702E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:10439888 C>T maps to NM_017534.5 K644K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:10428304 C>T maps to NM_017534.5 R1580R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZY-06A-11D-A197-08 chr17:10428343 G>A maps to NM_017534.5 I1567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:10432093 C>T maps to NM_017534.5 V1219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr17:10432553 G>A maps to NM_017534.5 I1093I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:10427851 C>T maps to NM_017534.5 E1702E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:10440649 C>T maps to NM_017534.5 K599K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:10448672 G>A maps to NM_017534.5 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr17:10443320 C>T maps to NM_017534.5 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:10426690 C>T maps to NM_017534.5 K1837K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:10428870 C>T maps to NM_017534.5 K1478K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:10434960 G>A maps to NM_017534.5 Q896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:10432366 G>A maps to NM_017534.5 I1128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:10443994 C>T maps to NM_017534.5 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr17:10432569 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr17:10426899 G>A maps to NM_017534.5 T1795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr17:10450911 C>T maps to NM_017534.5 Q76Q. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-GN-A4U8-06A-11D-A32N-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr17:10441092 G>A maps to ENST00000399342 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:10430052 C>T maps to NM_017534.5 R1350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:10433054 C>T maps to NM_017534.5 V981V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-RP-A695-06A-11D-A30X-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr17:10441092 G>A maps to ENST00000399342 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:10543717 G>A maps to NM_002470.2 I786I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr17:10551930 G>A maps to NM_002470.2 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:10558351 G>A maps to NM_002470.2 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr17:10545579 G>A maps to NM_002470.2 Q646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr17:10541572 G>A maps to NM_002470.2 F1172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr17:10541358 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr17:10546181 G>A maps to NM_002470.2 F514F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr17:10552992 G>A maps to NM_002470.2 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:10535035 G>A maps to NM_002470.2 H1726H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:10543079 G>A maps to NM_002470.2 Q908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr17:10542695 G>A maps to NM_002470.2 A1007A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:10555829 G>A maps to NM_002470.2 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr17:10541695 C>T maps to NM_002470.2 A1131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:10546171 G>A maps to NM_002470.2 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:10543483 G>A maps to NM_002470.2 I837I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:10538189 G>A maps to NM_002470.2 A1441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:10543975 G>A maps to NM_002470.2 I731I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:10535963 C>T maps to NM_002470.2 V1595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr17:10542613 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:10543374 G>A maps to NM_002470.2 L874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:10533017 G>A maps to NM_002470.2 R1898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:10558264 G>A maps to NM_002470.2 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr17:10533709 C>T maps to NM_002470.2 K1784K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr17:10536919 G>A maps to NM_002470.2 L1545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:10551945 G>A maps to NM_002470.2 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:10532960 G>A maps to NM_002470.2 Q1917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr17:10541368 C>T maps to NM_002470.2 S1240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr17:10537448 C>T maps to NM_002470.2 E1469E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:10538688 C>T maps to NM_002470.2 E1389E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:10545977 G>A maps to NM_002470.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:10554889 G>A maps to NM_002470.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr17:10532970 G>A maps to NM_002470.2 I1913I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:10532970 G>A maps to NM_002470.2 I1913I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr17:10535909 G>A maps to NM_002470.2 I1613I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr17:10358063 C>T maps to NM_017533.2 W833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr17:10362663 G>A maps to NM_017533.2 F497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr17:10360794 C>T maps to NM_017533.2 Q613Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr17:10364236 C>T maps to NM_017533.2 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr17:10354167 G>A maps to NM_017533.2 Q1304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr17:10351323 C>T maps to NM_017533.2 R1592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr17:10360775 G>A maps to NM_017533.2 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:10362678 G>A maps to NM_017533.2 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:10355551 C>T maps to NM_017533.2 E1148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr17:10350412 G>A maps to NM_017533.2 L1696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr17:10357052 C>T maps to NM_017533.2 L947L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:10359018 G>A maps to NM_017533.2 Q696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr17:10357142 G>A maps to NM_017533.2 I917I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr17:10358012 C>T maps to NM_017533.2 E850E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:10351388 G>A maps to NM_017533.2 Q1571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr17:10366439 G>A maps to NM_017533.2 Q291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:10356593 G>A maps to NM_017533.2 L996L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:10358325 G>A maps to NM_017533.2 I789I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:10364278 G>A maps to NM_017533.2 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:10366422 C>T maps to NM_017533.2 K296K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr17:10355545 G>A maps to NM_017533.2 I1150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:10356591 C>T maps to NM_017533.2 L996L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr17:10350413 G>A maps to NM_017533.2 S1695S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr17:10352001 C>T maps to NM_017533.2 V1488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr17:10369673 G>A maps to NM_017533.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:10358974 C>T maps to NM_017533.2 R710R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:10348624 G>A maps to NM_017533.2 Q1742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:10362576 G>A maps to NM_017533.2 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:10355545 G>A maps to NM_017533.2 I1150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:10366924 G>A maps to NM_017533.2 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:10356642 C>T maps to NM_017533.2 V979V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:10363546 G>A maps to NM_017533.2 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:10358009 C>T maps to NM_017533.2 K851K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr17:10351248 C>T maps to NM_017533.2 R1617R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr17:10366250 G>A maps to NM_017533.2 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr17:10351275 C>T maps to NM_017533.2 E1608E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr17:10348439 C>T maps to NM_017533.2 L1773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr17:10361016 C>T maps to NM_017533.2 E539E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr17:10356642 C>T maps to NM_017533.2 V979V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr17:10356108 G>A maps to NM_017533.2 L1084L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr17:10355449 C>T maps to NM_017533.2 L1182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr17:10367884 C>T maps to NM_017533.2 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr17:10351245 G>A maps to NM_017533.2 I1618I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:10362606 G>A maps to NM_017533.2 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr17:10366195 G>A maps to NM_017533.2 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:10348604 G>A maps to NM_017533.2 I1748I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr17:10363346 G>A maps to NM_017533.2 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr17:10363533 G>A maps to NM_017533.2 Q418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:10353915 G>A maps to NM_017533.2 D1345D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:10357979 C>T maps to NM_017533.2 E861E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:10363549 C>T maps to NM_017533.2 E412E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr17:10362663 G>A maps to NM_017533.2 F497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:10356234 C>T maps to NM_017533.2 L1042L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr17:10360935 G>A maps to NM_017533.2 F566F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr17:10364278 G>A maps to NM_017533.2 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr17:10348322 C>T maps to NM_017533.2 G1812G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr17:10358394 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr14:23865959 C>T maps to NM_002471.3 E745E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr14:23862682 G>A maps to NM_002471.3 I991I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr14:23855196 C>T maps to NM_002471.3 R1701R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr14:23874313 G>A maps to NM_002471.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:23862724 C>T maps to NM_002471.3 V977V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr14:23868225 G>A maps to NM_002471.3 I534I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr14:23862254 G>A maps to NM_002471.3 S1039S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr14:23874031 C>T did not map to a codon.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr14:23865947 G>A maps to NM_002471.3 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr14:23868030 C>T maps to NM_002471.3 K599K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr14:23871968 G>A maps to NM_002471.3 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:23855610 G>A maps to NM_002471.3 L1624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:23865992 C>T maps to NM_002471.3 E734E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:23865998 G>A maps to NM_002471.3 I732I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:23866400 G>A maps to NM_002471.3 I676I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:23855139 G>A maps to NM_002471.3 S1720S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr14:23855280 G>A maps to NM_002471.3 I1673I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr14:23869929 G>A maps to NM_002471.3 F466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:23866822 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:23853899 C>T maps to NM_002471.3 K1772K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:23855814 C>T maps to NM_002471.3 E1556E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:23863003 C>T maps to NM_002471.3 E933E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr14:23870133 C>T maps to NM_002471.3 K398K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr14:23857129 G>A maps to NM_002471.3 I1454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr14:23867964 G>A maps to NM_002471.3 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:23857012 G>A maps to NM_002471.3 S1493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:23862721 C>T maps to NM_002471.3 K978K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:23868228 G>A maps to NM_002471.3 S533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:23872632 C>T maps to NM_002471.3 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr14:23862631 G>A maps to NM_002471.3 A1008A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr14:23863309 C>T maps to NM_002471.3 Q884Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr14:23858601 C>T maps to NM_002471.3 K1326K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:23851690 G>A maps to NM_002471.3 I1914I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:23855799 G>A maps to NM_002471.3 L1561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:23865590 C>T maps to NM_002471.3 E777E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:23865623 G>A maps to NM_002471.3 F766F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:23866397 G>A maps to NM_002471.3 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:23872984 C>T maps to NM_002471.3 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr14:23874459 G>A maps to NM_002471.3 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:23855676 G>A maps to NM_002471.3 S1602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr14:23865527 G>A maps to NM_002471.3 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr14:23896803 C>T maps to NM_000257.2 G626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr14:23894591 C>T maps to NM_000257.2 E774E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:23897103 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr14:23894187 C>T maps to NM_000257.2 G823G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr14:23883308 C>T maps to NM_000257.2 T1854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:23886166 G>A maps to NM_000257.2 S1518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:23898175 G>A maps to NM_000257.2 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:23886091 G>A maps to NM_000257.2 A1543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:23896073 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr14:23894118 C>T maps to NM_000257.2 E846E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr14:23885491 G>A maps to NM_000257.2 I1558I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr14:23902788 G>A maps to NM_000257.2 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr14:23897061 G>A maps to NM_000257.2 F540F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr14:23886452 G>A maps to NM_000257.2 S1476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:23895017 G>A maps to NM_000257.2 I724I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:23900865 G>A maps to NM_000257.2 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:23883042 C>T maps to NM_000257.2 E1905E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:23884278 G>A maps to NM_000257.2 A1828A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:23884990 C>T maps to NM_000257.2 K1668K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr14:23890223 C>T maps to NM_000257.2 R1093R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr14:23897714 G>A maps to NM_000257.2 I524I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr14:23883075 G>A maps to NM_000257.2 S1894S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:23893121 C>T maps to NM_000257.2 E972E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:23891522 G>A maps to NM_000257.2 S1037S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:23896992 G>A maps to NM_000257.2 F563F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr14:23886132 G>A maps to NM_000257.2 R1530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr14:23888690 C>A did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr14:23888758 C>T maps to NM_000257.2 K1262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr14:23887474 C>T maps to NM_000257.2 W1371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:23886740 G>A maps to NM_000257.2 L1442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:23886741 G>A maps to NM_000257.2 A1441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:23886855 G>A maps to NM_000257.2 A1403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:23892848 G>A maps to NM_000257.2 A1002A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:23895186 C>T maps to NM_000257.2 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:23896010 G>A maps to NM_000257.2 I673I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:23896923 C>T maps to NM_000257.2 V586V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:23897777 C>T maps to NM_000257.2 K503K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:23898556 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:23901875 G>A maps to NM_000257.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:23884449 C>T maps to NM_000257.2 K1771K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr14:23898175 G>A maps to NM_000257.2 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr20:33568415 C>T maps to NM_020884.3 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr20:33565765 C>T maps to NM_020884.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr20:33581264 G>A maps to NM_020884.3 L854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:33567513 C>T maps to NM_020884.3 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:33568445 C>A maps to NM_020884.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:33586700 G>A maps to NM_020884.3 E1433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr20:33578835 C>T maps to NM_020884.3 Q741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:33586700 G>A maps to NM_020884.3 E1433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr20:33578590 C>T maps to NM_020884.3 F718F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr20:33584225 G>A maps to NM_020884.3 Q1049Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr20:33578805 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr20:33589067 G>A maps to NM_020884.3 E1874E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:33565899 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:33572867 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:33577899 G>A maps to NM_020884.3 Q659Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:33588191 G>A maps to NM_020884.3 E1668E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:33587610 G>A maps to NM_020884.3 E1603E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q1-06A-21D-A196-08 chr17:10318881 G>A maps to NM_002472.2 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr17:10307676 C>T maps to NM_002472.2 E886E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr17:10317333 G>A maps to NM_002472.2 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr17:10299682 C>T maps to NM_002472.2 E1539E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:10314237 G>A maps to NM_002472.2 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:10317276 C>T maps to NM_002472.2 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr17:10304275 C>T maps to NM_002472.2 K1085K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:10298674 G>A maps to NM_002472.2 I1579I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr17:10304033 C>T maps to NM_002472.2 E1136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr17:10323472 C>T maps to NM_002472.2 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr17:10296177 C>T maps to NM_002472.2 G1811G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:10297721 G>A maps to NM_002472.2 L1670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr17:10304075 C>T maps to NM_002472.2 G1122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:10307883 G>A maps to NM_002472.2 I817I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr17:10321967 A>G maps to NM_002472.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:10304275 C>T maps to NM_002472.2 K1085K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:10304633 G>A maps to NM_002472.2 I1022I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:10315785 G>A maps to NM_002472.2 F439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:10317708 G>A maps to NM_002472.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr17:10314204 G>A maps to NM_002472.2 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:10315752 C>T maps to NM_002472.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:10312653 C>T maps to NM_002472.2 Q613Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:10317276 C>T maps to NM_002472.2 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr17:10303904 C>T maps to NM_002472.2 R1179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr17:10312746 C>T maps to NM_002472.2 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:10309359 C>T maps to NM_002472.2 R810R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:10318680 G>A maps to NM_002472.2 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:10318999 G>A maps to NM_002472.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:10322025 C>T maps to NM_002472.2 K149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:10296527 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:10300221 C>T maps to NM_002472.2 T1420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:10317724 G>A maps to NM_002472.2 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:10323466 C>T maps to NM_002472.2 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:10297709 C>T maps to NM_002472.2 L1674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:10299868 C>G did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:10303853 C>T maps to NM_002472.2 R1196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr17:10298449 C>T maps to NM_002472.2 K1654K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:10300302 C>T maps to NM_002472.2 K1393K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:10322007 G>A maps to NM_002472.2 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:10293806 C>T maps to NM_002472.2 K1926K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:10301819 C>T maps to NM_002472.2 Q1373Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:10299736 C>T maps to NM_002472.2 E1521E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr17:10309671 G>A maps to NM_002472.2 F738F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr17:10321976 G>A maps to NM_002472.2 Q166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:10297625 C>T maps to NM_002472.2 R1702R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr17:10312617 G>A maps to NM_002472.2 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:10297625 C>T maps to NM_002472.2 R1702R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr17:10323364 C>T maps to NM_002472.2 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr17:10304036 C>T maps to NM_002472.2 A1135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr17:10293782 G>A maps to NM_002472.2 I1934I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr17:10297625 C>T maps to NM_002472.2 R1702R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:10312758 G>A maps to NM_002472.2 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr17:10319022 G>A maps to NM_002472.2 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:10300302 C>T maps to NM_002472.2 K1393K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr17:10304633 G>A maps to NM_002472.2 I1022I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr17:10304275 C>T maps to NM_002472.2 K1085K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:10293917 C>T maps to NM_002472.2 E1889E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:10304275 C>T maps to NM_002472.2 K1085K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:10304662 G>A maps to NM_002472.2 L1013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:10312884 G>A maps to NM_002472.2 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:10315986 G>A maps to NM_002472.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:10315989 G>A maps to NM_002472.2 A401A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:10323456 G>A maps to NM_002472.2 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:10307676 C>T maps to NM_002472.2 E886E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:10312890 G>A maps to NM_002472.2 F534F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:10298470 C>T maps to NM_002472.2 R1647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:10321992 G>A maps to NM_002472.2 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr17:10300149 G>A maps to NM_002472.2 A1444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:10307661 T>C maps to NM_002472.2 Q891Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:10317784 G>A maps to NM_002472.2 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr22:36700072 G>A maps to NM_002473.4 F786F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr22:36684954 G>A maps to NM_002473.4 L1530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr22:36684955 G>A maps to NM_002473.4 A1529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr22:36689449 G>A maps to NM_002473.4 S1340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:36696965 C>T maps to NM_002473.4 R923R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr22:36692959 G>A maps to NM_002473.4 L1067L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:36691046 G>A maps to NM_002473.4 I1187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:36690307 C>A maps to NM_002473.4 E1223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr22:36688253 C>T maps to NM_002473.4 E1374E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr22:36702007 G>A maps to NM_002473.4 P709P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr22:36702034 G>A maps to NM_002473.4 G700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:36712699 G>A maps to NM_002473.4 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr22:36689449 G>A maps to NM_002473.4 S1340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr22:36700081 G>A maps to NM_002473.4 I783I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr22:36715636 G>A maps to NM_002473.4 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr22:36722678 C>T maps to NM_002473.4 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr22:36710237 G>A maps to NM_002473.4 I502I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr22:36700147 G>A maps to NM_002473.4 V761V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr22:36698616 G>A maps to NM_002473.4 T832T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr22:36685151 G>A maps to NM_002473.4 S1512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr22:36702082 G>A maps to NM_002473.4 D684D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:211163273 T>A maps to NM_079420.2 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:211163276 C>T maps to NM_079420.2 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:211163171 C>T maps to NM_079420.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:211163213 G>A maps to NM_079420.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr2:211167236 G>A maps to NM_079420.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:211163267 G>A maps to NM_079420.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr2:211159128 C>T maps to NM_079420.2 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr7:101259564 C>T maps to NM_138403.4 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:3253250 G>A maps to NM_006471.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:111350899 C>T maps to NM_000432.3 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:111348964 G>A maps to NM_000432.3 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:111348964 G>A maps to NM_000432.3 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr12:111350934 G>A maps to NM_000432.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr12:111351990 C>T maps to NM_000432.3 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr3:46904826 C>T maps to NM_000258.2 K18K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:46901046 G>A maps to NM_000258.2 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:46904856 G>A maps to NM_000258.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr3:46902186 G>A maps to NM_000258.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr3:46899901 C>T maps to NM_000258.2 E177E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:45299207 C>T maps to NM_002476.2 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr17:45299744 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:56553497 G>A maps to NM_079423.3 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:56548887 C>T maps to NM_002475.4 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:56548956 G>A maps to NM_002475.4 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:44179949 G>A maps to ENST00000457314 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:44178606 G>A maps to ENST00000457314 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr20:35176480 C>T maps to NM_006097.3 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr20:35173373 C>T maps to NM_006097.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr20:35177483 C>T maps to NM_006097.3 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:16145340 A>T maps to NM_013262.3 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr6:16143272 T>C maps to NM_013262.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr3:123376126 C>T maps to NM_053025.3 W1378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:123452975 C>T maps to NM_053025.3 E289E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:123401110 C>T maps to NM_053025.3 R1204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:123332999 C>T maps to NM_053025.3 V1899V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:123385167 G>A maps to NM_053025.3 F1243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr3:123451833 C>T maps to NM_053025.3 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:123512532 G>A maps to NM_053025.3 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr3:123419470 G>A maps to NM_053025.3 P948P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:123451842 G>A maps to NM_053025.3 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:123366087 G>A maps to NM_053025.3 I1534I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:123419175 G>A maps to NM_053025.3 L1047L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:123345667 C>T maps to NM_053025.3 W1745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:123385176 G>A maps to NM_053025.3 I1240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr3:123512532 G>A maps to NM_053025.3 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr3:123452894 G>A maps to NM_053025.3 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr3:123512532 G>A maps to NM_053025.3 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr3:123419848 C>T maps to NM_053025.3 G822G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:123512610 G>A maps to NM_053025.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr3:123444827 C>T maps to NM_053025.3 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr3:123339129 G>A maps to NM_053025.3 I1764I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr3:123512604 G>A maps to NM_053025.3 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr3:123367903 C>T maps to NM_053025.3 K1443K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr3:123457788 G>A maps to NM_053025.3 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:123512532 G>A maps to NM_053025.3 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:123332987 C>T maps to NM_053025.3 E1903E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:123345766 C>T maps to NM_053025.3 Q1712Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:123419461 G>A maps to NM_053025.3 V951V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:123456258 C>T maps to NM_053025.3 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:123376183 C>T maps to NM_053025.3 G1359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:123451914 G>A maps to NM_053025.3 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:30409457 C>T maps to NM_033118.3 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:30409530 C>T maps to NM_033118.3 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:30419643 C>T maps to NM_033118.3 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr20:30408202 G>A maps to NM_033118.3 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:30419643 C>T maps to NM_033118.3 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr20:30418839 G>A maps to NM_033118.3 K440K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:30419643 C>T maps to NM_033118.3 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr20:30408181 G>A maps to NM_033118.3 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:46763511 C>T maps to NM_182493.2 K552K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:46771905 G>A maps to NM_182493.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:46746677 G>A maps to NM_182493.2 R666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:46763012 G>A maps to NM_182493.2 N565N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:46771660 C>T maps to NM_182493.2 Q321Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:46781979 G>A maps to NM_182493.2 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr16:46781898 G>A maps to NM_182493.2 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr16:46781685 G>A maps to NM_182493.2 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:46744673 C>T maps to NM_182493.2 G714G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:46766492 C>T maps to NM_182493.2 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:46746654 G>A maps to NM_182493.2 F673F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:46781658 C>T maps to NM_182493.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:46781991 C>T maps to NM_182493.2 Q38Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:2683259 G>A maps to NM_001012418.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:2689107 C>A maps to NM_001012418.3 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr6:2685564 G>A maps to NM_001012418.3 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:2685800 G>A maps to NM_001012418.3 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:169492151 C>T maps to NM_018657.4 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr3:169496852 C>T maps to NM_018657.4 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr5:16701680 G>A maps to NM_012334.2 F941F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr5:16764484 G>A maps to NM_012334.2 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr5:16701830 G>A maps to NM_012334.2 L891L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr5:16711088 G>A maps to NM_012334.2 V699V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:18023653 G>T maps to ENST00000205890 E514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr17:18069780 G>A maps to ENST00000205890 W3298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr17:18022608 C>T maps to ENST00000205890 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr17:18055171 G>A maps to ENST00000205890 G2600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr17:18022890 C>T maps to ENST00000205890 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr17:18023418 G>A maps to ENST00000205890 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr17:18058013 C>T maps to ENST00000205890 S2723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5KH-06A-11D-A27K-08 chr17:18023160 C>T maps to ENST00000205890 Y349Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:18025410 C>T maps to ENST00000205890 P1099P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:18025411 C>T maps to ENST00000205890 L1100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:18045493 C>T maps to ENST00000205890 F1917F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:18023760 C>T maps to ENST00000205890 F549F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr17:18023637 G>A maps to ENST00000205890 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr17:18075513 C>T maps to ENST00000205890 F3420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr17:18046114 C>T maps to ENST00000205890 S1957S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:18042906 C>T maps to ENST00000205890 F1731F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:18042918 G>A maps to ENST00000205890 R1735R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr17:18022395 G>A maps to ENST00000205890 K94K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:18045050 C>T maps to ENST00000205890 V1872V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr17:18023244 C>T maps to ENST00000205890 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:18022635 C>T maps to ENST00000205890 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:18040974 C>T maps to ENST00000205890 I1619I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:18030146 C>T maps to ENST00000205890 L1303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:18034823 G>A maps to ENST00000205890 E1395E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr17:18022635 C>T maps to ENST00000205890 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:18054712 A>C maps to ENST00000205890 S2553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:18022155 G>A maps to ENST00000205890 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr17:18025416 C>T maps to ENST00000205890 P1101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:18022299 C>T maps to ENST00000205890 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:18030128 C>T maps to ENST00000205890 L1297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:18044403 G>A maps to ENST00000205890 R1826R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr17:18022437 G>A maps to ENST00000205890 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr17:18023614 C>T maps to ENST00000205890 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr17:18058686 G>A maps to ENST00000205890 L2800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr17:18025674 C>T maps to ENST00000205890 S1187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr13:109459055 G>A maps to NM_015011.1 K235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr13:109535435 G>A maps to NM_015011.1 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr13:109704765 G>A maps to NM_015011.1 K975K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr13:109704684 G>A maps to NM_015011.1 S948S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr13:109318402 C>T maps to NM_015011.1 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr13:109772716 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr13:109859072 T>C maps to NM_015011.1 A1822A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr13:109793692 C>T maps to NM_015011.1 S1689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr13:109318279 C>T maps to NM_015011.1 I3I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr13:109379903 C>T maps to NM_015011.1 N138N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:109318450 C>T maps to NM_015011.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:109707874 C>T maps to NM_015011.1 V1067V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr13:109459110 C>T maps to NM_015011.1 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr17:27493523 G>A maps to NM_078471.3 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:27401844 G>A maps to NM_078471.3 S2036S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr17:27437630 G>A maps to NM_078471.3 I970I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr17:27437623 G>A maps to NM_078471.3 L973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr17:27448184 G>A maps to NM_078471.3 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:27414025 G>A maps to NM_078471.3 L1880L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr17:27493684 G>A maps to NM_078471.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr17:27493685 G>A maps to NM_078471.3 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr17:27445448 G>A maps to NM_078471.3 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr17:27425430 C>T maps to NM_078471.3 E1271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr17:27493345 G>A maps to NM_078471.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr17:27442391 G>A maps to NM_078471.3 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:27493256 G>A maps to NM_078471.3 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr17:27442116 C>T maps to NM_078471.3 R773R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr22:26423016 G>A maps to ENST00000407587 P2361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr22:26173698 C>G maps to ENST00000407587 V675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr22:26219541 G>A maps to ENST00000407587 E866E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr22:26423472 C>T maps to ENST00000407587 S2513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr22:26239720 C>T maps to ENST00000407587 T1078T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr22:26291228 G>A maps to ENST00000407587 R1552R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr22:26423016 G>A maps to ENST00000407587 P2361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr22:26164227 C>T maps to ENST00000407587 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr22:26422497 C>T maps to ENST00000407587 T2188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr22:26423382 C>T maps to ENST00000407587 N2483N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr22:26222394 G>A maps to ENST00000407587 V907V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr22:26423568 C>A maps to ENST00000407587 P2545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:26422698 C>T maps to ENST00000407587 F2255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr22:26242216 G>A maps to ENST00000407587 R1175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr22:26165192 G>A maps to ENST00000407587 W439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr22:26423112 G>A maps to ENST00000407587 V2393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr22:26222467 T>C did not map to a codon.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr22:26242183 G>A maps to ENST00000407587 R1164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr22:26423484 C>T maps to ENST00000407587 I2517I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr22:26165046 C>T maps to ENST00000407587 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr22:26228957 C>T maps to ENST00000407587 P1020P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:26176128 C>T maps to ENST00000407587 F727F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:26164827 G>A maps to ENST00000407587 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr22:26422902 G>A maps to ENST00000407587 L2323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:26348302 C>T maps to ENST00000407587 R1964*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr22:26423106 C>T maps to ENST00000407587 S2391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr22:26219583 C>T maps to ENST00000407587 I880I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr22:26173716 G>A maps to ENST00000407587 G681G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr22:26231384 C>T maps to ENST00000407587 F1063F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr22:26294332 G>A maps to ENST00000407587 R1578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr22:26299722 G>A maps to ENST00000407587 W1693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr22:26299752 G>A maps to ENST00000407587 Q1703Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr22:26422686 C>T maps to ENST00000407587 A2251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr22:26423625 G>A maps to ENST00000407587 K2564K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr22:26228957 C>T maps to ENST00000407587 P1020P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr22:26348361 C>T maps to ENST00000407587 F1983F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr22:26422461 G>A maps to ENST00000407587 L2176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:26224820 G>A maps to ENST00000407587 Q957Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:26228957 C>T maps to ENST00000407587 P1020P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:26294329 G>A maps to ENST00000407587 K1577K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:26423025 G>A maps to ENST00000407587 G2364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr22:26270263 G>A maps to ENST00000407587 K1323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr22:26423112 G>A maps to ENST00000407587 V2393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr22:26294332 G>A maps to ENST00000407587 R1578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr22:26423592 G>A maps to ENST00000407587 G2553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:26423415 G>A maps to ENST00000407587 L2494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr22:26422410 G>A maps to ENST00000407587 R2159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr22:26168437 C>T maps to ENST00000407587 V612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr22:26286817 C>T maps to ENST00000407587 A1472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr22:26219622 C>T maps to ENST00000407587 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr22:26164455 G>A maps to ENST00000407587 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr22:26219547 G>A maps to ENST00000407587 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr22:26348334 C>T maps to ENST00000407587 I1974I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr22:26224751 C>T maps to ENST00000407587 S934S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr22:26242162 G>A maps to ENST00000407587 Q1157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr22:26242246 G>A maps to ENST00000407587 Q1185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr22:26165121 G>A maps to ENST00000407587 E415E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr22:26423511 C>T maps to ENST00000407587 I2526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr22:26423595 G>A maps to ENST00000407587 R2554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:26157079 C>T maps to ENST00000407587 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:26164845 C>T maps to ENST00000407587 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:26165031 G>A maps to ENST00000407587 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:26176113 G>A maps to ENST00000407587 V722V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:26294332 G>A maps to ENST00000407587 R1578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:26343784 C>T maps to ENST00000407587 L1915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:26346379 G>A maps to ENST00000407587 E1934E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:26422809 G>A maps to ENST00000407587 R2292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:26422851 G>A maps to ENST00000407587 R2306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr22:26239705 C>T maps to ENST00000407587 S1073S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr22:26164845 C>T maps to ENST00000407587 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:26164821 C>T maps to ENST00000407587 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:26194047 G>A maps to ENST00000407587 A837A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:26422716 G>A maps to ENST00000407587 R2261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:26423568 C>T maps to ENST00000407587 P2545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr22:26273948 G>A maps to ENST00000407587 R1418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr17:34881061 T>C maps to NM_001163735.1 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr17:34856790 A>C maps to NM_001163735.1 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:34856751 G>A maps to NM_001163735.1 A765A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr17:34859797 G>A maps to NM_001163735.1 F656F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:57430815 C>T maps to NM_005379.2 Q705Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr12:57441806 G>A maps to NM_005379.2 Q66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr12:57424937 C>T maps to NM_005379.2 G790G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:57430833 C>T maps to NM_005379.2 Q699Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:57431349 G>A maps to NM_005379.2 F679F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr12:57430740 C>T maps to NM_005379.2 W730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:57423649 G>A maps to NM_005379.2 P866P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr12:57424049 C>T maps to NM_005379.2 R845R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:57431349 G>A maps to NM_005379.2 F679F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr12:57424844 C>T maps to NM_005379.2 Q821Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:57423013 G>A maps to NM_005379.2 F969F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:57432320 G>A maps to NM_005379.2 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:57437679 C>T maps to NM_005379.2 Q284Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:57437747 G>A maps to NM_005379.2 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:57423347 C>T maps to NM_005379.2 L916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:192251957 C>T maps to NM_001130158.1 Y521Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:192194744 A>C maps to NM_001130158.1 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:192252041 C>T maps to NM_001130158.1 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:192272863 C>T maps to NM_001130158.1 F860F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr2:192252017 C>T maps to NM_001130158.1 A541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr2:192194690 C>T maps to NM_001130158.1 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr17:1375288 G>A maps to NM_001080779.1 Q645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr17:1381190 C>A maps to NM_001080779.1 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:1371775 G>A maps to NM_001080779.1 A875A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:1372851 C>T maps to NM_001080779.1 R861R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr17:31039086 G>A maps to NM_015194.1 F680F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:31039004 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr17:31107693 G>A maps to NM_015194.1 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr17:30980902 C>T maps to NM_015194.1 K851K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:30932225 G>A maps to NM_015194.1 Q915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:30821871 T>A maps to NM_015194.1 K976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:59523927 G>T maps to NM_004998.2 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:59494599 G>A maps to NM_004998.2 F541F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:59470627 C>T maps to NM_004998.2 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:59497636 A>G maps to NM_004998.2 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:8615458 C>T maps to NM_012335.3 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr19:8590432 C>T maps to NM_012335.3 K928K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr19:8587369 G>A maps to NM_012335.3 P1037P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr19:8618260 C>T maps to NM_012335.3 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr19:8610596 G>A maps to NM_012335.3 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:8616641 G>A maps to NM_012335.3 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:8590432 C>T maps to NM_012335.3 K928K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:8604854 G>A maps to NM_012335.3 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr19:8616665 C>T maps to NM_012335.3 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:8604836 C>T maps to NM_012335.3 K562K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr19:8595445 C>T maps to NM_012335.3 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:8618076 C>T maps to NM_012335.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:8595249 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:8620542 G>A maps to NM_012335.3 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:8601134 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:8610560 G>A maps to NM_012335.3 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:8615557 C>T maps to NM_012335.3 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:8619416 C>T maps to NM_012335.3 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr7:45005408 G>A maps to NM_033054.2 I736I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:45010580 C>T maps to NM_033054.2 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:45006395 C>T maps to NM_033054.2 K608K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:45005695 G>A maps to NM_033054.2 P711P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:45006320 G>A maps to NM_033054.2 V633V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:45014787 G>A maps to NM_033054.2 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:45006305 G>A maps to NM_033054.2 F638F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr7:45016597 G>A maps to NM_033054.2 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr7:45015127 C>T maps to NM_033054.2 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:45009348 G>A maps to NM_033054.2 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:45009749 G>A maps to NM_033054.2 F407F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr12:109863821 C>T maps to NM_001101421.3 I583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:109862584 G>A maps to NM_001101421.3 R543R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:109865367 G>A maps to NM_001101421.3 R626R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:109834263 G>A maps to NM_001101421.3 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:109876413 G>A maps to NM_001101421.3 R745R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr12:109853351 G>A maps to NM_001101421.3 K492K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:109881336 A>T maps to NM_001101421.3 K887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:109826555 C>T maps to NM_001101421.3 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr12:109844616 C>T maps to NM_001101421.3 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:109844601 G>A maps to NM_001101421.3 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:109865298 G>A maps to NM_001101421.3 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr12:109876413 G>A maps to NM_001101421.3 R745R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr12:109847372 G>A maps to NM_001101421.3 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr10:26463296 G>A maps to NM_017433.4 K1368K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr10:26243816 G>A maps to NM_017433.4 E61E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr10:26243816 G>A maps to NM_017433.4 E61E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr10:26463419 G>A maps to NM_017433.4 K1409K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:26462876 G>A maps to NM_017433.4 R1228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20I-06A-11D-A196-08 chr10:26465721 C>T maps to NM_017433.4 V1462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:26310490 C>T maps to NM_017433.4 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:26457765 G>A maps to NM_017433.4 Q1079Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:26459363 C>T maps to NM_017433.4 V1098V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:26462591 G>A maps to NM_017433.4 R1133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr10:26462930 G>A maps to NM_017433.4 E1246E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr10:26463485 G>A maps to NM_017433.4 Q1431Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:26500876 C>T maps to NM_017433.4 L1612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:26434393 G>A maps to NM_017433.4 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr10:26359143 G>A maps to NM_017433.4 Q425Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr10:26500831 C>T maps to NM_017433.4 Y1597Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr10:26491912 T>A maps to NM_017433.4 L1536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:26462972 G>A maps to NM_017433.4 R1260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:26377301 C>T maps to NM_017433.4 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:26455031 C>T maps to NM_017433.4 P1012P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:26490202 C>T maps to NM_017433.4 Q1519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr10:26465655 C>T maps to NM_017433.4 F1440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:26459366 G>A maps to NM_017433.4 R1099R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr10:26359272 T>G maps to NM_017433.4 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr10:26315365 C>T maps to NM_017433.4 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:26312974 G>A maps to NM_017433.4 Q252Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:26446394 C>T maps to NM_017433.4 R984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:26465769 C>T maps to NM_017433.4 L1478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:26462936 G>A maps to NM_017433.4 R1248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:26315455 G>A maps to NM_017433.4 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr10:26500831 C>T maps to NM_017433.4 Y1597Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr2:171375993 C>T maps to NM_138995.3 S1173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr2:171376041 G>A maps to NM_138995.3 E1189E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr2:171358319 G>A maps to NM_138995.3 R1105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr2:171256756 C>T maps to NM_138995.3 F617F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr2:171323155 G>A maps to NM_138995.3 L983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr2:171073889 C>T maps to NM_138995.3 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:171355152 G>A maps to NM_138995.3 E1022E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr2:171323056 G>A maps to NM_138995.3 Q950Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:171243659 C>T maps to NM_138995.3 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:171356172 C>T maps to NM_138995.3 Y1048Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:171259450 C>T maps to NM_138995.3 I741I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr2:171258174 A>C maps to NM_138995.3 T701T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr2:171055879 G>A maps to NM_138995.3 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:171055855 G>A maps to NM_138995.3 K47K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:171323128 G>A maps to NM_138995.3 L974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr15:52668713 G>A maps to ENST00000358212 F750F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr15:52681551 T>C maps to ENST00000358212 K517K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr15:52672076 G>A maps to ENST00000358212 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr15:52681451 G>A maps to ENST00000358212 Q551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr15:52664449 G>A maps to ENST00000358212 F896F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr15:52672095 C>T maps to ENST00000358212 E674E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr18:47373528 C>T maps to NM_001080467.2 R1482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr18:47480802 G>A maps to NM_001080467.2 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr18:47406755 G>A maps to NM_001080467.2 L1039L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr18:47432957 G>A maps to NM_001080467.2 R749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr18:47511175 G>A maps to NM_001080467.2 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr18:47398566 C>T maps to NM_001080467.2 P1191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr18:47479644 G>A maps to NM_001080467.2 I579I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr18:47479692 A>T maps to NM_001080467.2 G563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr18:47480802 G>A maps to NM_001080467.2 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr18:47518740 G>A maps to NM_001080467.2 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:47438482 G>A maps to NM_001080467.2 A717A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr18:47455913 C>T maps to NM_001080467.2 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr18:47463662 G>A maps to NM_001080467.2 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr18:47432961 G>A maps to NM_001080467.2 F747F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr18:47527696 G>A maps to NM_001080467.2 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr18:47488731 G>A maps to NM_001080467.2 I483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:47563359 G>A maps to NM_001080467.2 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr18:47566543 G>A maps to NM_001080467.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr18:47421393 G>A maps to NM_001080467.2 L988L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr18:47463689 C>T maps to NM_001080467.2 S610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr18:47581730 G>A maps to NM_001080467.2 I15I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr18:47511086 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr18:47506852 C>T maps to NM_001080467.2 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:47379866 C>T maps to NM_001080467.2 V1391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:47398566 C>T maps to NM_001080467.2 P1191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:47463689 C>T maps to NM_001080467.2 S610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:47500802 G>A maps to NM_001080467.2 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:47506909 G>A maps to NM_001080467.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:47511091 G>A maps to NM_001080467.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr18:47527696 G>A maps to NM_001080467.2 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:47421508 G>A maps to NM_001080467.2 S949S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:47563305 G>A maps to NM_001080467.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3BZ-06A-12D-A196-08 chr15:52567821 G>A maps to NM_018728.3 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr15:52497303 G>A maps to NM_018728.3 S1526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr15:52505445 G>A maps to NM_018728.3 Y1360Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr15:52556395 G>A maps to NM_018728.3 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:52497105 G>A maps to NM_018728.3 F1592F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr15:52539764 G>A maps to NM_018728.3 Q591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:52531998 G>A maps to NM_018728.3 I878I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr15:52539150 G>A maps to NM_018728.3 R648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:52521416 C>T maps to NM_018728.3 K1040K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr15:52498024 G>A maps to NM_018728.3 Q1509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr15:52564869 C>T maps to NM_018728.3 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:52534249 G>A maps to NM_018728.3 R851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:52536614 G>A maps to NM_018728.3 F776F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:52553135 G>A maps to NM_018728.3 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr15:52517714 G>A maps to NM_018728.3 F1074F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr15:52534394 T>A maps to NM_018728.3 A802A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr15:52543595 A>G maps to NM_018728.3 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr15:52497126 C>T maps to NM_018728.3 A1585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr15:52517714 G>A maps to NM_018728.3 F1074F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:52556488 G>A maps to NM_018728.3 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:52571155 G>A maps to NM_018728.3 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr6:76558069 C>T maps to ENST00000428345 Y300Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:76576247 C>T maps to ENST00000428345 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr11:76924903 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:76903202 C>T maps to NM_000260.3 L1344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:76910699 G>A maps to NM_000260.3 A1563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:76893103 C>T maps to NM_000260.3 F1004F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:76877190 C>T maps to NM_000260.3 Q594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:76912661 C>T maps to NM_000260.3 T1674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr11:76910720 C>T maps to NM_000260.3 F1570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:76868389 G>A maps to NM_000260.3 K267K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr11:76877111 G>A maps to NM_000260.3 E567E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:76924924 C>T maps to NM_000260.3 P2153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr11:76909606 G>A maps to NM_000260.3 E1503E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:76910663 G>A maps to NM_000260.3 A1551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:76868004 G>A maps to NM_000260.3 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr11:76886425 C>T maps to NM_000260.3 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:76867914 G>A maps to NM_000260.3 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:76874014 C>T maps to NM_000260.3 I557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr11:76910693 G>A maps to NM_000260.3 R1561R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr11:76872131 C>T maps to NM_000260.3 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr11:76877190 C>T maps to NM_000260.3 Q594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:76924903 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:76893037 G>A maps to NM_000260.3 L982L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:76886425 C>T maps to NM_000260.3 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:76885806 C>T maps to NM_000260.3 F647F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:76893485 G>A maps to NM_000260.3 W1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:76868004 G>A maps to NM_000260.3 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:76900451 C>T maps to NM_000260.3 A1189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:76900490 C>T maps to NM_000260.3 F1202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:76919503 C>T maps to NM_000260.3 F1962F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:76867786 G>A maps to NM_000260.3 W184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr11:76893587 G>A maps to NM_000260.3 E1076E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:76893016 G>A maps to NM_000260.3 R975R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr11:76872113 C>T maps to NM_000260.3 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr2:128345965 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr2:128387247 G>A maps to ENST00000389524 K1525K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:128390865 G>A maps to ENST00000389524 V1788V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:128341876 C>T maps to ENST00000389524 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr2:128346006 C>T maps to ENST00000389524 I577I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:128327433 C>T maps to ENST00000389524 Q181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr2:128351212 C>T maps to ENST00000389524 F746F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:128341879 C>T maps to ENST00000389524 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:128341880 C>T maps to ENST00000389524 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:128351212 C>T maps to ENST00000389524 F746F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr2:128341870 C>T maps to ENST00000389524 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:128335721 C>T maps to ENST00000389524 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:128327390 G>A maps to ENST00000389524 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:128381867 C>T maps to ENST00000389524 V1314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:128331610 C>T maps to ENST00000389524 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:128322867 C>T maps to ENST00000389524 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:128341840 G>A maps to ENST00000389524 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:128342408 C>T maps to ENST00000389524 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:128341803 G>A maps to ENST00000389524 W484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:128331609 C>T maps to ENST00000389524 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:128363454 C>T maps to ENST00000389524 T792T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr2:128392734 G>A maps to ENST00000389524 R1893R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:128389970 C>T maps to ENST00000389524 V1775V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr15:72146817 G>A maps to ENST00000424560 L2153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr15:72192091 G>A maps to ENST00000424560 Q1136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr15:72192296 C>G maps to ENST00000424560 V1067V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr15:72141212 G>A maps to ENST00000424560 T2341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr15:72208773 A>G maps to ENST00000424560 I874I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr15:72119126 G>A maps to ENST00000424560 L2552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr15:72119127 G>A maps to ENST00000424560 F2551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:72324875 C>T maps to ENST00000424560 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr15:72190601 T>C maps to ENST00000424560 S1414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr15:72144481 G>A maps to ENST00000424560 R2227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr15:72193564 G>A maps to ENST00000424560 F1039F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:17295732 C>T maps to NM_004145.3 T811T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:17213279 C>T maps to NM_004145.3 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:17265204 C>T maps to NM_004145.3 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:17306162 C>A maps to NM_004145.3 A1309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr19:17305745 G>A maps to NM_004145.3 K1170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr19:17305746 G>T maps to NM_004145.3 E1171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr19:17283772 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:17311625 C>T maps to NM_004145.3 F1517F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:17308651 C>T maps to NM_004145.3 S1366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr19:17212877 C>T maps to NM_004145.3 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr19:17306051 C>T maps to NM_004145.3 P1272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:17311448 C>T maps to NM_004145.3 A1458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:17317978 C>T maps to NM_004145.3 F1850F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:17213223 C>T maps to NM_004145.3 Q233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:171605700 C>T maps to NM_000261.1 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr1:171605583 C>T maps to NM_000261.1 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:171605733 C>T maps to NM_000261.1 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:171621210 T>G maps to NM_000261.1 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:171605337 T>C maps to NM_000261.1 E414E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:171621334 C>T maps to NM_000261.1 E139E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:171621637 C>T maps to NM_000261.1 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:171605127 C>T maps to NM_000261.1 K484K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:171607852 C>T maps to NM_000261.1 W205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr1:171605570 G>A maps to NM_000261.1 Q337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr1:171605571 G>A maps to NM_000261.1 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:171605289 G>A maps to NM_000261.1 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:171605340 G>A maps to NM_000261.1 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr17:12656506 C>T maps to NM_001146312.1 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr17:12656635 C>A maps to NM_001146312.1 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:12626275 G>A maps to NM_001146312.1 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr17:12666900 C>T maps to NM_001146312.1 F967F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr17:12656626 C>T maps to NM_001146312.1 V674V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr17:12656203 G>A maps to NM_001146312.1 W533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:12656423 C>T maps to NM_001146312.1 Q607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:12656299 C>T maps to NM_001146312.1 F565F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:12666654 G>A maps to NM_001146312.1 G885G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:12666630 G>A maps to NM_001146312.1 G877G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:12666804 G>A maps to NM_001146312.1 W935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr17:12626206 G>A maps to NM_001146312.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr17:12655754 C>T maps to NM_001146312.1 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:12647609 G>A maps to NM_001146312.1 E276E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr17:12639553 G>A maps to NM_001146312.1 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:12655975 G>A maps to NM_001146312.1 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:12656185 G>A maps to NM_001146312.1 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr17:12647603 G>A maps to NM_001146312.1 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr17:12649389 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr17:12656203 G>A maps to NM_001146312.1 W533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:12618857 C>T maps to NM_001146312.1 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr17:12666525 C>T maps to NM_001146312.1 I842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:12656326 G>A maps to NM_001146312.1 E574E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:12666900 C>T maps to NM_001146312.1 F967F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:12666918 C>T maps to NM_001146312.1 L973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr17:12647615 C>A maps to NM_001146312.1 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr17:12666525 C>T maps to NM_001146312.1 I842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:12656047 C>T maps to NM_001146312.1 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr17:12656534 A>T maps to NM_001146312.1 K644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:17741472 G>A maps to NM_002478.4 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr10:95161229 G>A maps to NM_013451.3 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr10:95111306 G>A maps to NM_013451.3 R1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr10:95085654 C>T maps to NM_013451.3 R1733R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr10:95111580 G>A maps to NM_013451.3 F1168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr10:95119733 G>A maps to NM_013451.3 G992G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:95111580 G>A maps to NM_013451.3 F1168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:95088580 G>A maps to NM_013451.3 I1690I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:95129434 G>A maps to NM_013451.3 F852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:95169407 C>T maps to NM_013451.3 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr10:95076543 C>T maps to NM_013451.3 T1875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:95076570 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:95191273 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:95134594 C>T maps to NM_013451.3 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr10:95107488 G>A maps to NM_013451.3 I1378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr10:95097622 C>T maps to NM_013451.3 G1462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr10:95147613 C>T maps to NM_013451.3 E546E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr10:95076516 G>A maps to NM_013451.3 I1884I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:95159187 G>A maps to NM_013451.3 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:95093535 C>T maps to NM_013451.3 Q1566Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:203054834 C>T maps to NM_002479.4 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:203054894 G>A maps to NM_002479.4 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:203054975 C>T maps to NM_002479.4 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr18:3151781 G>A maps to NM_003803.3 R585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr18:3079234 G>A maps to NM_003803.3 V1530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:3151752 G>A maps to NM_003803.3 F594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr18:3215038 G>A maps to NM_003803.3 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:3134817 G>A maps to NM_003803.3 I738I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr18:3116373 C>T maps to NM_003803.3 Q1086Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:3067448 G>A maps to NM_003803.3 F1623F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr18:3119870 G>A maps to NM_003803.3 V1038V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr18:3141960 C>T maps to NM_003803.3 E667E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr18:3215170 G>A maps to NM_003803.3 Y17Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr18:3141981 G>A maps to NM_003803.3 P660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr18:3149149 T>C maps to NM_003803.3 E631E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr8:2048768 C>T maps to NM_003970.2 F848F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr8:2063805 C>T maps to NM_003970.2 R1079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr8:2037889 G>A maps to NM_003970.2 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:2000353 C>T maps to NM_003970.2 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:2089089 C>T maps to NM_003970.2 Q1331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:2077142 C>T maps to NM_003970.2 L1241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr8:2054310 G>A maps to NM_003970.2 K974K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:2044138 C>T maps to NM_003970.2 S726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr8:2056619 C>T maps to NM_003970.2 P1014P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr8:1998936 C>T maps to NM_003970.2 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr8:2048801 G>A maps to NM_003970.2 W859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr8:2057228 G>A maps to NM_003970.2 K1029K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:2033404 G>A maps to NM_003970.2 Q509Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr8:2044252 C>T maps to NM_003970.2 P764P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:2024296 C>T maps to NM_003970.2 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr8:2054074 C>T maps to NM_003970.2 I926I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:2020458 C>T maps to NM_003970.2 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:2020476 G>A maps to NM_003970.2 E282E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr8:2021455 C>T maps to NM_003970.2 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr1:24408646 G>A maps to ENST00000330966 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:24411062 C>T maps to ENST00000330966 W623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr1:24387572 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:24434502 C>T maps to ENST00000330966 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr1:24424458 C>T maps to ENST00000330966 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:24408640 G>A maps to ENST00000330966 N711N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:24413233 C>T maps to ENST00000330966 E567E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:24417293 C>T maps to ENST00000330966 R476R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:24392448 G>A maps to ENST00000330966 Q1159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:24411108 G>A maps to ENST00000330966 Q608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:24387572 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:24406640 G>A maps to ENST00000330966 S818S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:24388475 C>T maps to ENST00000330966 G1301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:24383874 G>A maps to ENST00000330966 P1434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:24426246 C>T maps to ENST00000330966 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:24432552 G>A maps to ENST00000330966 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:24398486 C>T maps to ENST00000330966 K996K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:24394473 C>T maps to ENST00000330966 W1115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:24433594 G>A maps to ENST00000330966 Q125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:24388526 C>T maps to ENST00000330966 L1284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:24390595 C>T maps to ENST00000330966 G1199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:24433685 C>T maps to ENST00000330966 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr1:24419473 G>A maps to ENST00000330966 F352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:137223043 A>G maps to NM_006790.2 Q489Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:137217679 G>A maps to NM_006790.2 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:75399718 G>A maps to NM_021245.2 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr10:75391750 C>T maps to NM_021245.2 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:75397609 T>C maps to NM_021245.2 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:75397642 C>T maps to NM_021245.2 K37K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr10:75399721 C>T maps to NM_021245.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:75393767 G>A maps to NM_021245.2 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr4:120079241 C>T maps to NM_016599.3 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr10:69881854 G>A maps to NM_032578.2 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr10:69948660 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:69966577 G>A maps to NM_032578.2 K1237K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr10:69926171 C>T maps to NM_032578.2 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:69918340 G>A maps to NM_032578.2 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr10:69948795 C>T maps to NM_032578.2 I946I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr10:69881311 C>T maps to NM_032578.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:69881561 C>T maps to NM_032578.2 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr10:69881389 C>T maps to NM_032578.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr19:46394006 G>A maps to NM_001012643.2 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:40085591 G>A maps to NM_015460.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr3:40211496 G>A maps to NM_015460.2 W262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr3:40231955 T>C did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:40231803 G>A maps to NM_015460.2 R505R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:40291795 G>A maps to NM_015460.2 R782R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:40231917 C>T maps to NM_015460.2 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:40231731 G>A maps to NM_015460.2 R481R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr1:59142728 C>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:59147775 G>A maps to NM_001085487.1 Q314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:59126877 G>A maps to NM_001085487.1 I764I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:59147986 A>G maps to NM_001085487.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr16:31141912 C>T maps to NM_182958.2 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:31131549 C>T maps to NM_182958.2 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:47893178 C>T maps to NM_007067.4 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr8:41798674 G>A maps to NM_006766.3 A908A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr8:41812836 G>A maps to NM_006766.3 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:41801327 G>A maps to NM_006766.3 I722I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr8:41791729 G>A maps to NM_006766.3 P1336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:41906402 C>T maps to NM_006766.3 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:41790360 G>A maps to NM_006766.3 Q1793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:41790310 G>A maps to NM_006766.3 T1809T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr8:41834819 G>A maps to NM_006766.3 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:41832275 G>A maps to NM_006766.3 I476I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr8:41792308 G>T maps to NM_006766.3 S1143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr8:41791255 G>A maps to NM_006766.3 V1494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr8:41845063 G>A maps to NM_006766.3 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr10:76739022 C>T maps to NM_012330.2 Y719Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr10:76784906 C>T maps to NM_012330.2 V1188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr10:76784907 C>T maps to NM_012330.2 L1189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr10:76790633 C>T maps to NM_012330.2 Q2018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:76735651 C>T maps to NM_012330.2 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:76603187 C>T maps to NM_012330.2 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:76784831 A>C maps to NM_012330.2 S1163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:76780391 C>T maps to NM_012330.2 L894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr10:76739016 C>T maps to NM_012330.2 G717G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr10:76735663 C>T maps to NM_012330.2 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr10:76789961 T>C maps to NM_012330.2 L1794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr10:76788640 G>A maps to NM_012330.2 E1353E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:76739022 C>T maps to NM_012330.2 Y719Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:76744935 C>T maps to NM_012330.2 F824F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr20:62839673 G>A maps to NM_004535.2 R375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr20:62839563 G>T maps to NM_004535.2 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:62839556 C>T maps to NM_004535.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:62851142 C>T maps to NM_004535.2 F683F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:62839343 G>A maps to NM_004535.2 E265E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr20:62839625 G>A maps to NM_004535.2 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr20:62839220 C>T maps to NM_004535.2 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr20:62871695 C>T maps to NM_004535.2 F1087F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr20:62842671 A>T maps to NM_004535.2 K469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:62839223 C>T maps to NM_004535.2 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:62839328 G>A maps to NM_004535.2 E260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:1842994 C>T maps to ENST00000399161 T1002T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr2:1893183 C>T maps to ENST00000399161 R783R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:1805527 G>A maps to ENST00000399161 I1072I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:1926202 C>T maps to ENST00000399161 K446K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr2:1893231 C>T maps to ENST00000399161 V767V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:1926982 C>T maps to ENST00000399161 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:1926907 G>A maps to ENST00000399161 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:1926268 G>A maps to ENST00000399161 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:1926199 G>A maps to ENST00000399161 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:1926535 G>A maps to ENST00000399161 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:1893141 G>A maps to ENST00000399161 S797S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:1926163 C>T maps to ENST00000399161 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:1926226 G>A maps to ENST00000399161 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:1926912 T>A maps to ENST00000399161 K210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr2:1906930 G>A maps to ENST00000399161 Y651Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr2:1906968 C>A maps to ENST00000399161 E639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:1926253 C>T maps to ENST00000399161 G429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr2:1843099 C>T maps to ENST00000399161 G967G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr2:1805524 C>T maps to ENST00000399161 K1073K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:1891350 G>A maps to ENST00000399161 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:1893042 C>T maps to ENST00000399161 R830R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:1914013 G>A maps to ENST00000399161 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:1926340 C>T maps to ENST00000399161 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:1926805 C>T maps to ENST00000399161 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:1983497 G>A maps to ENST00000399161 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr2:1893249 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:59074698 C>T maps to NM_198055.1 Q315Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr19:59080694 C>A maps to NM_198055.1 E241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr19:59081863 G>A maps to NM_198055.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr19:59081864 G>A maps to NM_198055.1 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr16:48595626 A>T maps to NM_153029.3 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:48580146 G>A maps to NM_153029.3 F748F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:48580146 G>A maps to NM_153029.3 F748F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr4:40123873 C>T maps to NM_018177.3 P1381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:40104725 C>T maps to NM_018177.3 Q421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:40104812 G>T maps to NM_018177.3 G450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr4:40123585 T>A maps to NM_018177.3 S1285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:40123360 T>A maps to NM_018177.3 T1210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr13:33017746 G>A maps to NM_033111.3 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:33016597 G>A maps to NM_033111.3 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:177548665 C>T maps to NM_015111.1 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:177547339 C>T maps to NM_015111.1 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr21:30255338 T>C maps to NM_013240.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr21:30255314 A>G maps to NM_013240.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:153197786 G>A did not map to a codon.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr4:80246959 C>T maps to NM_032693.2 E24E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:80246971 A>T maps to NM_032693.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:80246800 C>T maps to NM_032693.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:80246881 C>T maps to NM_032693.2 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr4:80246767 C>T maps to NM_032693.2 Q88Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:80246503 C>T maps to NM_032693.2 E176E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr4:140272704 C>T maps to NM_057175.3 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr13:41933025 C>T maps to NM_024561.4 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr13:41932626 T>C maps to NM_001110798.1 C425C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr12:112481006 G>A maps to NM_024953.3 F753F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr12:112499074 A>G maps to NM_024953.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:112498128 A>T maps to NM_024953.3 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:112528545 G>A maps to NM_024953.3 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr12:112486127 C>T maps to NM_024953.3 R616R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:112506772 G>A maps to NM_024953.3 Q354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:112516048 G>A maps to NM_024953.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:112481521 C>T maps to NM_024953.3 G719G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:112509801 C>T maps to NM_024953.3 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:112491379 A>G maps to NM_024953.3 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr12:112492208 G>A maps to NM_024953.3 I537I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:112467424 C>T maps to NM_024953.3 G943G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr14:57876123 A>T maps to NM_001011713.2 K327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr9:88631452 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:88611378 C>T maps to NM_024635.3 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr11:63719956 C>T maps to NM_024771.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr4:76861191 C>T maps to NM_014435.3 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:89882178 C>T maps to NM_005467.3 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr11:89868802 C>T maps to NM_005467.3 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr11:89891352 C>T maps to NM_005467.3 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:89892442 G>A maps to NM_005467.3 W309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:89896571 G>A maps to NM_005467.3 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr11:89907059 A>C maps to NM_005467.3 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:89916123 C>T maps to NM_005467.3 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:89924812 T>C maps to NM_005467.3 N707N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:89880512 T>C maps to NM_005467.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr11:89891346 G>A maps to NM_005467.3 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:89896701 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr11:89868838 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr11:64821041 C>T maps to ENST00000340252 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr11:64825927 G>A maps to ENST00000340252 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:64825870 G>A maps to ENST00000340252 D41D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:64825816 C>T maps to ENST00000340252 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:64825816 C>T maps to ENST00000340252 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64815822 C>T maps to ENST00000340252 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64825981 C>T maps to ENST00000340252 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:175184860 C>T maps to NM_207015.2 I474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr3:175184917 C>T maps to NM_207015.2 F493F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:175293878 C>T maps to NM_207015.2 I568I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:174814907 C>T maps to NM_207015.2 H124H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:175473075 C>T maps to NM_207015.2 Q687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:175520889 C>T maps to NM_207015.2 Q763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:175473131 C>T maps to NM_207015.2 I705I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:175189488 G>A maps to NM_207015.2 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr3:175520795 C>T maps to NM_207015.2 N731N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:174974279 C>T maps to NM_207015.2 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:174815069 G>A maps to NM_207015.2 K178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:175473110 G>A maps to NM_207015.2 K698K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr12:57485768 C>T maps to NM_005967.3 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr12:57486349 C>T maps to NM_005967.3 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr12:57110375 G>A maps to NM_001113203.1 S1646S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:57112046 G>A maps to NM_001113203.1 S1089S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr12:57111977 G>A maps to NM_001113203.1 S1112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:57111704 G>A maps to NM_001113203.1 P1203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:57112115 G>A maps to NM_001113203.1 S1066S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:57110417 G>A maps to NM_001113203.1 A1632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr12:57112328 G>A maps to NM_001113203.1 S995S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:57111329 G>A maps to NM_001113203.1 P1328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr12:57111128 G>A maps to NM_001113203.1 I1395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr12:57111266 G>A maps to NM_001113203.1 L1349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr12:57110777 G>A maps to NM_001113203.1 S1512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:57112019 G>A maps to NM_001113203.1 S1098S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:57114890 G>A maps to NM_001113203.1 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:59668384 G>A maps to NM_199290.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:59668298 G>A maps to NM_199290.3 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:59668334 C>T maps to NM_199290.3 Q69Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr17:59668250 C>T maps to NM_199290.3 W97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr17:59668250 C>T maps to NM_199290.3 W97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr19:13248976 C>T maps to NM_052876.2 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:13246833 C>T maps to NM_052876.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:13246314 C>T maps to NM_052876.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr9:138905066 G>A maps to NM_144653.3 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:138903367 G>A maps to NM_144653.3 T586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:1696782 G>A maps to ENST00000344463 Y21Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:1688035 G>A maps to ENST00000344463 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:1686833 G>A maps to ENST00000344463 Q368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:71166154 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:71189503 C>T maps to NM_018161.4 R288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:71185491 C>T maps to NM_018161.4 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr16:66839686 G>A maps to ENST00000359087 F499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:66844304 G>A maps to ENST00000359087 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr4:164050414 G>A maps to NM_138386.2 F373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr4:164066931 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr22:42456377 G>A maps to NM_000262.2 R381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr22:42456378 G>A maps to NM_000262.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr22:42463798 G>A maps to NM_000262.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr17:40695667 C>T maps to NM_000263.3 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:40689424 T>A maps to NM_000263.3 Y131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:40690484 C>T maps to NM_000263.3 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:40693177 C>T maps to NM_000263.3 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:5083626 A>G maps to NM_016256.3 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr17:42084742 G>A maps to NM_153006.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr9:130825873 G>A maps to NM_197956.3 Q273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:130825766 G>A maps to NM_197956.3 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:70307128 C>T maps to NM_004536.2 W214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:70308418 G>A maps to NM_004536.2 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:70308412 C>T maps to NM_004536.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:70308364 G>A maps to NM_004536.2 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr13:101714436 C>T maps to NM_052867.2 K1546K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr13:101712205 C>T maps to NM_052867.2 T1623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr13:101997759 C>T maps to NM_052867.2 W219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr13:101890180 G>A maps to NM_052867.2 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr13:101759917 G>A maps to NM_052867.2 F833F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr13:101733928 G>A maps to NM_052867.2 L1278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr13:101717759 G>A maps to NM_052867.2 L1534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr13:101717760 G>A maps to NM_052867.2 V1533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr13:101742292 G>A maps to NM_052867.2 F1098F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr13:101756702 G>A maps to NM_052867.2 F944F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr13:101755618 G>A maps to NM_052867.2 V987V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr13:101742247 G>A maps to NM_052867.2 S1113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:101710318 C>T maps to NM_052867.2 R1665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:101717858 G>A maps to NM_052867.2 L1501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr13:101712205 C>T maps to NM_052867.2 T1623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr13:101776978 G>A maps to NM_052867.2 T724T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr13:101733961 G>A maps to NM_052867.2 G1267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr13:101759869 A>G maps to NM_052867.2 F849F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr13:101717829 G>A maps to NM_052867.2 L1510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr13:101717856 C>T maps to NM_052867.2 L1501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr13:101890117 G>A maps to NM_052867.2 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr13:101890180 G>A maps to NM_052867.2 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr13:101727001 C>T maps to NM_052867.2 K1322K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr13:101777033 T>G did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr13:101944442 G>A maps to NM_052867.2 N315N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:101710324 G>A maps to NM_052867.2 P1663P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:101720308 G>A maps to NM_052867.2 H1469H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:101759872 G>A maps to NM_052867.2 N848N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:101776984 C>T maps to NM_052867.2 K722K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr13:101712205 C>T maps to NM_052867.2 T1623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr13:101742292 G>A maps to NM_052867.2 F1098F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr7:105894855 A>T maps to NM_005746.2 L395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr12:7945675 G>A maps to NM_024865.2 K94K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:7947345 G>A maps to NM_024865.2 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:46417819 C>T maps to NM_001029861.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:46417849 C>T maps to NM_001029861.2 E34E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3BZ-06A-12D-A196-08 chr19:13988289 G>T maps to NM_001098622.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:13988434 C>T maps to NM_001098622.1 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:13988319 C>T maps to NM_001098622.1 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:13988107 C>T maps to NM_001098622.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr19:13988376 C>T maps to NM_001098622.1 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr20:25597013 G>A maps to NM_152667.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr23:72434321 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr23:72433835 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:72434265 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr23:72434150 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:72433928 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr23:72434150 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr23:72434218 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:72433364 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:72433612 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:72433250 T>C did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr23:72433892 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:72433163 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:72433727 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:72433934 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:72433158 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:72433505 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:72433460 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:72433979 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr23:72433253 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr23:72433254 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:72433382 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:72432950 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:72433430 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr23:72433603 T>G did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:72434031 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:72434183 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:72433703 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:72433196 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:72434243 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:72434303 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:72434305 T>C did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:72433934 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr23:92926849 G>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:92928073 T>C did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:92926789 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:92927120 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:92927627 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:92927394 A>G did not map to a codon.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr23:92928260 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:92927585 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:92928217 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:92926782 T>C did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:92927222 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr23:92926917 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr11:2991031 C>G did not map to a codon.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr11:2981037 G>A maps to ENST00000399624 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr4:89618587 T>C maps to NM_153757.2 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:47996235 G>A maps to NM_003827.2 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:47996741 G>A maps to NM_003827.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:102760136 C>T maps to ENST00000455523 W349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:144658648 T>C maps to ENST00000276844 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:144659270 G>A maps to ENST00000276844 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:50868797 G>A maps to NM_004851.1 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:50863085 G>A maps to NM_004851.1 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:50863040 G>A maps to NM_004851.1 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr19:50864340 G>A maps to NM_004851.1 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:80436781 C>T maps to ENST00000374611 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:789654 G>A maps to NM_022493.1 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr16:789654 G>A maps to NM_022493.1 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:782335 G>A maps to NM_022493.1 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:60747313 G>A maps to NM_024611.4 H277H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr18:55269715 G>A maps to NM_004539.3 V462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr18:55273958 A>G maps to NM_004539.3 C342C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr18:55274436 G>A maps to NM_004539.3 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:55273871 C>T maps to NM_004539.3 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr11:78147745 G>A maps to NM_024678.4 F468F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:78277272 G>A maps to NM_024678.4 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:18079795 C>T maps to NM_001160176.1 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:34152964 C>T maps to NM_024662.2 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:34145399 C>T maps to NM_024662.2 Q336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:34129801 C>T maps to NM_024662.2 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr11:34160823 C>T maps to NM_024662.2 A766A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:34152949 C>T maps to NM_024662.2 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:34149086 C>T maps to NM_024662.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr11:34162703 C>T maps to NM_024662.2 P887P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:34152953 C>T maps to NM_024662.2 Q466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:34135385 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:34145357 C>T maps to NM_024662.2 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:55997950 C>T maps to NM_020378.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:3533402 C>T maps to NM_024845.2 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr8:18257720 C>T maps to NM_000015.2 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr8:18257575 G>A maps to NM_000015.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr8:18257755 A>T maps to NM_000015.2 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:18258355 C>T maps to NM_000015.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:18257720 C>T maps to NM_000015.2 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr8:18257758 C>T maps to NM_000015.2 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:18257551 G>A maps to NM_000015.2 K13K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:18257560 G>A maps to NM_000015.2 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:18258340 G>A maps to NM_000015.2 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:18257840 C>T maps to NM_000015.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:18258226 C>T maps to NM_000015.2 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:50334540 G>A maps to NM_012191.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr3:50334156 G>A maps to NM_012191.2 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr3:50334615 G>A maps to NM_012191.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr3:50334687 G>A maps to NM_012191.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:50334495 G>A maps to NM_012191.2 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr4:2062818 C>T maps to ENST00000423729 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZY-06A-11D-A197-08 chr17:72768378 G>A maps to NM_015654.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:201782367 A>G maps to ENST00000367296 G1774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:201777202 G>A maps to ENST00000367296 Q1257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:201777277 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr1:201750363 G>A maps to ENST00000367296 K530K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:201779105 C>T maps to ENST00000367296 T1478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:201752809 C>T maps to ENST00000367296 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:201778346 C>T maps to ENST00000367296 L1421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr1:201780772 C>A maps to ENST00000367296 R1614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr11:20057618 C>T maps to ENST00000396087 S984S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr11:19955286 G>A maps to ENST00000396087 E522E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr11:20129300 C>T maps to ENST00000396087 L2370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr11:19967989 C>T maps to ENST00000396087 I753I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:19970321 C>T maps to ENST00000396087 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:20065597 C>T maps to ENST00000396087 D1016D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr11:19955583 C>G maps to ENST00000396087 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr11:19914093 C>T maps to ENST00000396087 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:20129300 C>T maps to ENST00000396087 L2370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:20077462 C>T maps to ENST00000396087 T1620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:19955097 C>T maps to ENST00000396087 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:19735411 C>T maps to ENST00000396087 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:20122582 C>T maps to ENST00000396087 I2153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr12:78573379 T>A maps to NM_014903.4 L1790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr12:78225315 G>A maps to NM_014903.4 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr12:78522584 T>C maps to NM_014903.4 P1460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr12:78516169 C>T maps to NM_014903.4 L1400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:78452853 C>T maps to NM_014903.4 I865I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:78562596 C>T maps to NM_014903.4 A1644A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr12:78400985 T>C maps to NM_014903.4 T556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:78513167 C>T maps to NM_014903.4 S1064S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:78516157 C>T maps to NM_014903.4 V1396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr12:78400286 C>T maps to NM_014903.4 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr12:78593242 G>A maps to NM_014903.4 W2194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:78574769 G>A maps to NM_014903.4 R1857R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:78400325 C>T maps to NM_014903.4 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:78513212 C>T maps to NM_014903.4 I1079I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:78513720 C>T maps to NM_014903.4 R1249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:78513131 C>T maps to NM_014903.4 P1052P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:78594371 G>A did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:78444684 C>T maps to NM_014903.4 S758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:15432683 C>T maps to NM_015909.2 R1668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr2:15470727 G>A maps to NM_015909.2 P1447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:15307435 G>A maps to NM_015909.2 S2284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:15448366 G>A maps to NM_015909.2 F1590F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:15674760 C>A maps to NM_015909.2 G218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:15432746 G>A maps to NM_015909.2 I1647I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:15470889 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:15319126 G>A maps to NM_015909.2 I2275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr2:15557751 G>A maps to NM_015909.2 L888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:15608548 G>A maps to NM_015909.2 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:15427213 G>A maps to NM_015909.2 F1707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr13:36241667 G>A maps to ENST00000400445 G2853G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr13:36046663 C>T maps to ENST00000400445 I2192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:35716404 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr13:36125085 C>T maps to ENST00000400445 F2241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr13:36241520 C>T maps to ENST00000400445 C2804C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr13:35733925 A>G maps to ENST00000400445 K1206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr13:35735897 T>C maps to ENST00000400445 G1291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr13:35738573 C>T maps to ENST00000400445 S1387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr13:35615184 G>A maps to ENST00000400445 W137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr13:35731358 G>A maps to ENST00000400445 W932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr13:35716466 T>C maps to ENST00000400445 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr13:36223796 C>T maps to ENST00000400445 F2571F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr13:35716492 C>G maps to ENST00000400445 T808T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr13:35756555 G>A maps to ENST00000400445 L1574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr13:35747689 C>T maps to ENST00000400445 Q1505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr13:35630183 G>A maps to ENST00000400445 W337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:35644167 C>T maps to ENST00000400445 Q455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:35716441 C>T maps to ENST00000400445 F791F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr13:36229803 C>T maps to ENST00000400445 I2739I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr13:35619163 C>T maps to ENST00000400445 R203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:203991365 C>T maps to NM_001114132.1 L995L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:204058525 C>T maps to NM_001114132.1 H2281H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:203976773 G>T maps to NM_001114132.1 G690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr2:203972707 A>G maps to NM_001114132.1 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:203991545 G>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:204002980 C>T maps to NM_001114132.1 I1525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:203980783 C>T maps to NM_001114132.1 Y832Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:204031987 C>T maps to NM_001114132.1 R1939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr3:47049363 G>A maps to NM_015175.1 R2522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr3:47045636 C>T maps to NM_015175.1 R1984R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr3:47041162 C>T maps to NM_015175.1 S1249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:47043883 C>T maps to NM_015175.1 F1725F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:47036848 G>T maps to NM_015175.1 G542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:47036850 A>T maps to NM_015175.1 G542G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:47030211 G>A maps to NM_015175.1 K35K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:47042834 C>T maps to NM_015175.1 A1517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:47050060 C>T maps to NM_015175.1 L2644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:47045730 C>T maps to NM_015175.1 Q2016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr3:47047316 C>T maps to NM_015175.1 Q2261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr3:47033333 C>T maps to NM_015175.1 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:47049158 G>A maps to NM_015175.1 K2493K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:47031039 C>T maps to NM_015175.1 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:47043883 C>T maps to NM_015175.1 F1725F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr3:47039690 C>T maps to NM_015175.1 T1031T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:47043252 C>T maps to NM_015175.1 L1573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr1:19981519 G>A maps to NM_182744.2 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr8:90958505 C>T maps to NM_002485.4 Q644Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr8:90982698 A>G maps to NM_002485.4 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:16893806 G>A maps to NM_017940.3 V902V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr1:16895718 C>T maps to NM_017940.3 E821E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:16892176 G>A maps to NM_017940.3 S1006S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:16902894 G>A maps to NM_017940.3 S662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:16893824 A>G maps to NM_017940.3 D896D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:16891402 C>T maps to NM_017940.3 K1026K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:16914224 G>A maps to NM_017940.3 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:16902776 G>A maps to NM_017940.3 Q702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:16907353 G>A maps to NM_017940.3 Q493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:16907279 G>A maps to NM_017940.3 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:145302734 C>T maps to NM_001039703.4 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:145301741 C>T maps to NM_001039703.4 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:145299841 C>T maps to NM_001039703.4 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:145304539 C>T maps to NM_001039703.4 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:145304476 C>T maps to NM_001039703.4 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:148004556 G>A maps to ENST00000310701 F924F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:148004571 C>T maps to ENST00000310701 Q919Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr1:148594438 A>G maps to NM_001170755.1 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:148591245 G>A maps to NM_001170755.1 Q437Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr1:21799390 G>A maps to NM_032264.2 Q239Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:21798169 C>T maps to NM_032264.2 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:21799381 G>A maps to NM_032264.2 E236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr1:21807432 G>A maps to NM_032264.2 K464K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:144816613 C>T maps to NM_001037675.2 V506V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:144828543 C>T maps to NM_001037675.2 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:41346378 C>T maps to NM_005899.3 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr17:41346488 C>T maps to NM_005899.3 I549I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:41343547 C>T maps to NM_005899.3 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr17:41349034 C>T maps to NM_005899.3 T646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:102705103 G>A maps to NM_032041.2 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:102701626 G>A maps to NM_032041.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:102731542 G>A maps to NM_032041.2 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr11:113085145 G>A maps to ENST00000316851 Q323Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr11:113102985 G>A maps to ENST00000316851 T444T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A29E-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:113103519 C>T maps to ENST00000316851 F501F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr11:113103513 G>A maps to ENST00000316851 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr11:113131019 C>T maps to ENST00000316851 T701T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:113140985 G>A maps to ENST00000316851 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:113130933 C>T maps to ENST00000316851 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr11:113103072 G>A maps to ENST00000316851 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:113075044 C>T maps to ENST00000316851 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:113075225 C>T maps to ENST00000316851 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:113085139 G>A maps to ENST00000316851 E321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:113085148 C>T maps to ENST00000316851 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:113105809 C>G maps to ENST00000316851 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:113146033 G>A maps to ENST00000316851 T833T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:113076846 C>A maps to ENST00000316851 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr21:22790800 T>C maps to NM_004540.2 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr21:22696802 C>T maps to NM_004540.2 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr21:22906899 G>A maps to NM_004540.2 E775E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr21:22746187 G>A maps to NM_004540.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr21:22841001 C>T maps to NM_004540.2 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:19337343 G>A maps to NM_004386.2 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr19:19339380 G>A maps to NM_004386.2 W984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:19339056 G>A maps to NM_004386.2 L876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:19334878 C>T maps to NM_004386.2 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr19:19338384 C>T maps to NM_004386.2 T652T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:19335123 C>T maps to NM_004386.2 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:19338711 C>T maps to NM_004386.2 F761F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:19339200 G>A maps to NM_004386.2 G924G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:19356150 G>A maps to NM_004386.2 P1174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:19345816 C>T maps to NM_004386.2 P1054P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:19351454 C>T maps to NM_004386.2 I1151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19337745 C>T maps to NM_004386.2 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19339086 C>T maps to NM_004386.2 A886A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19339335 C>T maps to NM_004386.2 F969F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19339422 C>T maps to NM_004386.2 T998T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19349164 C>T maps to NM_004386.2 R1118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:19338858 C>T maps to NM_004386.2 V810V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr19:19329754 G>A maps to NM_004386.2 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:19327835 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:19351454 C>T maps to NM_004386.2 I1151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:19351432 G>A maps to NM_004386.2 W1144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr12:6636084 C>T maps to NM_014865.3 F921F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr12:6639006 C>T maps to NM_014865.3 L1240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr12:6637022 C>T maps to NM_014865.3 I996I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr12:6624076 G>A maps to NM_014865.3 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6635478 C>T maps to NM_014865.3 P836P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr12:6618899 C>T maps to NM_014865.3 R49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr12:6631171 C>T maps to NM_014865.3 I641I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr11:134047152 G>A maps to NM_015261.2 I994I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:134048798 G>A maps to NM_015261.2 A864A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:134051016 G>A maps to NM_015261.2 I838I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr11:134047119 G>A maps to NM_015261.2 L1005L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr11:134076552 G>A maps to NM_015261.2 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr4:17829962 C>T maps to NM_022346.3 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:17843953 C>A maps to NM_022346.3 S959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr4:17832624 T>C maps to NM_022346.3 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:158486164 G>A maps to NM_017760.5 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:158439231 G>A maps to NM_017760.5 T1033T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:158447920 G>T maps to NM_017760.5 S845S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:158472758 G>A maps to NM_017760.5 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr2:97017714 C>T maps to NM_015341.3 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr22:50957716 C>T maps to NM_001185011.1 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr22:50961484 C>T maps to NM_001185011.1 Q524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr22:50956400 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:50956059 C>T maps to NM_001185011.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr9:100405572 T>C maps to NM_002486.4 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:39691121 C>T maps to NM_001001414.1 Q229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:39691001 C>T maps to NM_001001414.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:39691305 C>T maps to NM_001001414.1 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:39691305 C>T maps to NM_001001414.1 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:36026642 C>T maps to NM_001014839.1 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:36028898 C>T maps to NM_001014839.1 F494F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr1:36030873 C>T maps to NM_001014839.1 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:36026843 C>T maps to NM_001014839.1 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr3:172351309 G>A maps to NM_001146276.1 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:172351765 G>A maps to NM_001146276.1 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr3:172351836 A>G maps to NM_001146276.1 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:172351849 G>A maps to NM_001146276.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:172351690 G>A maps to NM_001146276.1 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:183543711 C>T maps to NM_001127651.2 W137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:183539971 G>A maps to NM_001127651.2 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr1:183543645 G>A maps to NM_001127651.2 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:183546756 G>A maps to NM_001127651.2 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:183532328 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:183543645 G>A maps to NM_001127651.2 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:183529291 C>T maps to NM_001127651.2 E469E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr22:37271915 C>T maps to NM_013416.3 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr22:37273672 G>A maps to NM_000631.4 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:37268388 A>G maps to NM_013416.3 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr22:37271912 C>T maps to NM_013416.3 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:37268427 G>A maps to NM_013416.3 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr22:37273837 C>T maps to NM_000631.4 N331N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:37272104 C>T maps to NM_013416.3 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:136664567 G>T maps to NM_006153.4 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:106471560 C>T maps to NM_001004720.2 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:106509457 C>T maps to NM_001004720.2 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr2:183859597 G>A maps to NM_205842.1 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr12:54930764 C>T maps to NM_005337.4 I1037I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:54936460 C>T maps to NM_005337.4 L1126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr12:54925125 G>A maps to NM_005337.4 Q863Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr12:54917263 G>A maps to NM_005337.4 E655E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr12:54936444 G>T maps to NM_005337.4 V1120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr12:54911363 C>T maps to NM_005337.4 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr12:54936378 C>T maps to NM_005337.4 F1098F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr12:54920344 G>A maps to NM_005337.4 T730T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:54920356 C>T maps to NM_005337.4 I734I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr12:54912695 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:54911345 C>T maps to NM_005337.4 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:54901692 C>T maps to NM_005337.4 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:54932735 C>T maps to NM_005337.4 S1084S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr12:54926003 G>A maps to NM_005337.4 K944K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:54913089 G>A maps to NM_005337.4 V533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:54917218 G>A maps to NM_005337.4 K640K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:54925123 C>T maps to NM_005337.4 Q863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:54929985 C>T maps to NM_005337.4 L1010L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr12:54912490 C>T maps to NM_005337.4 I465I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr12:54922054 G>A maps to NM_005337.4 Q800Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr12:54925357 C>T maps to NM_005337.4 P896P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr12:54911715 C>T maps to NM_005337.4 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:54905869 C>T maps to NM_005337.4 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:54917707 C>T maps to NM_005337.4 Y708Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr12:54894363 C>T maps to NM_005337.4 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:54901635 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:54905627 G>A maps to NM_005337.4 W259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:54925569 C>T maps to NM_005337.4 I914I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr12:54917206 C>T maps to NM_005337.4 I636I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:54920356 C>T maps to NM_005337.4 I734I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:54922087 C>A maps to NM_005337.4 A811A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr2:133541239 G>A maps to NM_207363.2 T1048T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr2:133542790 C>T maps to NM_207363.2 K531K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr2:133541611 C>T maps to NM_207363.2 V924V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr2:133547742 G>A maps to NM_207363.2 C315C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr2:133489531 G>A maps to NM_207363.2 Q1741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:133489376 G>A maps to NM_207363.2 S1792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:133540837 G>A maps to NM_207363.2 S1182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:133542817 C>T maps to NM_207363.2 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr2:133543087 C>T maps to NM_207363.2 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:133539544 C>T maps to NM_207363.2 T1613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:133538681 T>C maps to NM_207363.2 G1664G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:133540480 G>A maps to NM_207363.2 I1301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:133539520 G>A maps to NM_207363.2 L1621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:133489580 G>A maps to NM_207363.2 T1724T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr2:133486511 G>A maps to NM_207363.2 S1819S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:133539544 C>T maps to NM_207363.2 T1613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:133542790 C>T maps to NM_207363.2 K531K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:133540321 G>A maps to NM_207363.2 S1354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:133542205 T>A maps to NM_207363.2 A726A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:133542541 C>T maps to NM_207363.2 V614V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:133543014 G>A maps to NM_207363.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr2:133540480 G>A maps to NM_207363.2 I1301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr12:50186671 C>T maps to NM_001037806.3 K1146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr12:50186632 G>A maps to NM_001037806.3 P1159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:50188993 G>A maps to NM_001037806.3 I883I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:50187174 C>T maps to NM_001037806.3 E1100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:50189509 G>A maps to NM_001037806.3 S711S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:50185642 G>A maps to NM_001037806.3 S1328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:50186345 G>A maps to NM_001037806.3 T1225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:50188918 C>T maps to NM_001037806.3 E908E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:50189359 C>T maps to NM_001037806.3 V761V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:50190430 G>A maps to NM_001037806.3 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:48719487 G>A maps to NM_016453.2 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr3:48719936 T>G maps to NM_016453.2 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:48716110 G>A maps to NM_016453.2 F617F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:232320839 G>A maps to NM_005381.2 S571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:232321447 G>A maps to NM_005381.2 F533F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:232320839 G>A maps to NM_005381.2 S571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:232325243 C>T maps to NM_005381.2 K281K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:3193343 C>T maps to NM_020170.3 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:3205963 C>T maps to NM_020170.3 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:3193406 C>T maps to NM_020170.3 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:3198861 C>T maps to NM_020170.3 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:3207466 G>A maps to NM_020170.3 Q544Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:3205975 G>A maps to NM_020170.3 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr19:3205997 C>T maps to NM_020170.3 R424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:24930525 C>T maps to NM_003743.4 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:24929946 C>T maps to NM_003743.4 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:24916134 C>T maps to NM_003743.4 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:24930583 C>T maps to NM_003743.4 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:24930084 C>T maps to NM_003743.4 S582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:24930669 G>A maps to NM_003743.4 K777K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:24920555 C>T maps to NM_003743.4 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr8:71036963 G>A maps to NM_006540.2 S1351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr8:71060646 G>A maps to NM_006540.2 F822F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:71036136 G>A maps to NM_006540.2 S1425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr20:46265097 C>T maps to NM_181659.2 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr20:46277838 C>T maps to NM_181659.2 Q1213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:46268360 C>T maps to NM_181659.2 S916S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:46281231 C>T maps to NM_181659.2 S1343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:46276049 C>T maps to NM_181659.2 P1162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:46264392 C>T maps to NM_181659.2 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr20:46256462 C>T maps to NM_181659.2 Q231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr20:46265034 C>T maps to NM_181659.2 S635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr10:51584897 C>T maps to NM_001145260.1 Q349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:44692185 G>A maps to NM_020967.2 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr20:44691022 A>C maps to NM_020967.2 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr20:44692185 G>A maps to NM_020967.2 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr20:44691163 G>A maps to NM_020967.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:44699027 G>A maps to NM_020967.2 D62D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:44691436 G>A maps to NM_020967.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:33330825 G>A maps to NM_014071.2 V1078V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:33345527 G>A maps to NM_014071.2 N341N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr20:33329490 C>T maps to NM_014071.2 E1523E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:33345245 G>A maps to NM_014071.2 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:33331094 G>A maps to NM_014071.2 Q989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:33364246 G>A maps to NM_014071.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr20:33329385 G>A maps to NM_014071.2 S1558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr20:33337510 G>C maps to NM_014071.2 V829V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr20:33345455 C>G maps to NM_014071.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:33345248 G>A maps to NM_014071.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr6:126242090 C>T maps to NM_181782.4 I749I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:126243889 A>G maps to NM_181782.4 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr17:15983349 A>G maps to ENST00000395857 S1159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr17:15965062 C>A maps to ENST00000395857 E1860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:15965135 G>A maps to ENST00000395857 A1835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr17:16089913 G>A maps to ENST00000395857 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr12:124821308 G>A maps to NM_006312.4 L2042L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr12:124870392 C>T maps to NM_006312.4 R639R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr12:124848236 G>C maps to NM_006312.4 A972A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:124835139 G>A maps to NM_006312.4 S1286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr12:124827584 G>A maps to NM_006312.4 P1641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:124968246 G>A maps to NM_006312.4 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:124979719 G>A maps to NM_006312.4 Y26Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:124824628 C>T maps to NM_006312.4 Q1877Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr12:124817776 A>G maps to NM_006312.4 G2225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr12:124911289 A>G maps to NM_006312.4 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr12:124841212 G>A maps to NM_006312.4 P1079P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr12:124841296 C>T maps to NM_006312.4 G1051G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:124846819 G>A maps to NM_006312.4 P983P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:124848314 G>A maps to NM_006312.4 T946T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:124915204 G>A maps to NM_006312.4 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr12:124824945 G>A maps to NM_006312.4 S1801S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr12:124848329 C>T maps to NM_006312.4 R941R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr19:55417932 G>A maps to NM_004829.5 K41K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:55420730 C>T maps to NM_004829.5 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:55418118 G>C maps to NM_004829.5 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:55420850 C>T maps to NM_004829.5 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:55423542 T>G maps to NM_004829.5 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:55423578 C>T maps to NM_004829.5 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr19:55421411 C>T maps to NM_004829.5 D223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:55420754 G>A maps to NM_004829.5 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:41304017 A>C maps to NM_004828.3 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr6:31557859 G>A maps to NM_147130.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:31560468 G>A maps to NM_147130.2 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr6:31557874 G>A maps to NM_147130.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:132985377 C>T maps to NM_014286.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr1:160321842 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:160326851 C>T maps to NM_015331.2 Q606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr18:2595413 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr18:2578002 C>T maps to NM_006101.2 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr18:2590051 C>T maps to NM_006101.2 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr16:15761166 C>T maps to NM_001143979.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr13:80125152 C>T maps to NM_019080.2 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr13:80122488 C>T maps to NM_019080.2 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr15:23931428 G>A maps to NM_002487.2 H312H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr15:23931647 G>A maps to NM_002487.2 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:23931539 G>A maps to NM_002487.2 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr15:23931539 G>A maps to NM_002487.2 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:23931488 G>A maps to NM_002487.2 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr15:23931404 C>T maps to NM_002487.2 E320E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr15:23931500 C>T maps to NM_002487.2 Q288Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:23931437 G>A maps to NM_002487.2 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr15:23931500 C>T maps to NM_002487.2 Q288Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr15:29561249 C>T maps to NM_138704.2 K220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:140109370 C>T maps to NM_001144026.1 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:140109370 C>T maps to NM_001144026.1 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr9:140108685 C>T maps to NM_001144026.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:140110459 C>T maps to NM_001144026.1 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:140108291 C>T maps to NM_001144026.1 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr9:140109352 C>T maps to NM_001144026.1 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:43809111 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:134274297 G>A maps to NM_006096.3 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr8:134256627 C>T maps to NM_006096.3 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:134258870 G>A maps to NM_006096.3 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr8:134274294 G>A maps to NM_006096.3 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:134296508 A>G maps to NM_006096.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr8:134256627 C>T maps to NM_006096.3 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:21486621 G>A maps to NM_201537.1 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr14:21491037 G>A maps to NM_201537.1 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:21490297 C>T maps to NM_201537.1 Q89Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr14:21486173 G>A maps to NM_201537.1 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr20:35317154 G>A maps to ENST00000373803 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr20:35293685 G>A maps to ENST00000373803 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr20:35315938 C>A maps to ENST00000373803 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr16:58537757 C>T maps to NM_001130487.1 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr16:58538173 C>T maps to NM_001130487.1 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr16:58543092 G>A maps to NM_001130487.1 Q323Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr16:58542879 C>T maps to NM_001130487.1 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:149931401 C>A maps to NM_001543.4 P838P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:149925011 C>A maps to NM_001543.4 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:149918881 C>T maps to NM_001543.4 N510N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr5:149914540 C>T maps to NM_001543.4 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:149901076 C>T maps to NM_001543.4 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:149929307 C>T maps to NM_001543.4 F795F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr5:149907733 C>T maps to NM_001543.4 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr10:75566504 G>A maps to NM_003635.3 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:75567891 G>A maps to NM_003635.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:118975245 C>T maps to NM_004784.2 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr4:118975377 C>T maps to NM_004784.2 Q105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:119154281 G>A maps to NM_004784.2 G645G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:118975688 C>G maps to NM_004784.2 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:118975703 T>G maps to NM_004784.2 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:119161731 G>A maps to NM_004784.2 V724V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr4:118975721 C>T maps to NM_004784.2 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr4:119064800 C>T maps to NM_004784.2 Q501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr4:118975866 C>T maps to NM_004784.2 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:119064784 G>A maps to NM_004784.2 E495E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:118975305 C>T maps to NM_004784.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr4:115767074 C>G maps to NM_022569.1 S673S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr4:115997727 C>T maps to NM_022569.1 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr4:115792004 C>T maps to NM_022569.1 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr4:115856430 T>G maps to NM_022569.1 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr4:115767137 G>A maps to NM_022569.1 F652F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:115767137 G>A maps to NM_022569.1 F652F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:115997280 G>A maps to NM_022569.1 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr4:115856475 C>T maps to NM_022569.1 Q474Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr4:115769494 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr4:115997907 G>A maps to NM_022569.1 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr4:115998158 G>A maps to NM_022569.1 R12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr4:115997859 G>A maps to NM_022569.1 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr4:115760581 C>T maps to NM_022569.1 W746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr4:115998158 G>A maps to NM_022569.1 R12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:115997367 C>T maps to NM_022569.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:115997964 C>T maps to NM_022569.1 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:115997879 G>A maps to NM_022569.1 Q105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:19638110 C>T maps to ENST00000436926 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19638101 C>T maps to ENST00000436926 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr22:42483171 T>C maps to NM_002490.3 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:4768258 C>T maps to NM_005002.4 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr12:4758312 C>T maps to NM_005002.4 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr15:41680720 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr15:41679740 G>A maps to NM_016013.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19T-06A-11D-A19A-08 chr5:60369036 G>A maps to NM_174889.4 W71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:97339080 G>A maps to NM_014165.3 Q143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr6:97339237 C>T maps to NM_014165.3 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr7:140402710 C>T maps to NM_004546.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:201950310 C>T maps to NM_002491.2 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr3:120315214 C>T maps to NM_004547.5 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:120319968 C>T maps to NM_004547.5 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:179334801 C>T maps to NM_002492.2 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:179333832 C>T maps to NM_002492.2 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:32572893 G>A maps to NM_002493.3 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr19:14682740 G>A maps to NM_004146.4 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:14682755 G>A maps to NM_004146.4 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr19:14676959 G>A maps to NM_004146.4 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:125555408 C>T maps to NM_005005.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:161180450 C>T maps to NM_004550.4 Q313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:47605939 C>T maps to NM_004551.2 D234D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:1390910 C>T maps to NM_024407.4 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:67803945 C>T maps to NM_002496.3 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:67800475 C>T maps to NM_002496.3 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:67378901 C>T maps to NM_007103.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:67379624 C>T maps to NM_007103.3 F399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:67379640 C>A maps to NM_007103.3 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr18:9124965 A>T maps to NM_021074.4 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr21:44323506 C>T maps to NM_021075.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr21:44324000 C>T maps to NM_021075.3 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:44323748 C>T maps to NM_021075.3 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr2:152471029 C>T maps to NM_001164507.1 P3787P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:152382698 C>T maps to NM_001164507.1 A7341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:152514604 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr2:152584255 G>A maps to NM_001164507.1 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:152432772 G>A maps to NM_001164507.1 I5600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr2:152500559 C>T maps to NM_001164507.1 W2576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:152419196 G>A maps to NM_001164507.1 F6273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:152496541 T>C maps to NM_001164507.1 R2906R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:152512756 A>G maps to NM_001164507.1 T2135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:152512942 C>T maps to NM_001164507.1 G2073G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr2:152394722 C>T maps to NM_001164507.1 G6976G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr2:152348942 G>A maps to NM_001164507.1 P8277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:152482131 C>T maps to NM_001164507.1 W3456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:152432772 G>A maps to NM_001164507.1 I5600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:152566274 C>T maps to NM_001164507.1 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr2:152373029 C>T maps to NM_001164507.1 L7616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:152528984 G>A maps to NM_001164507.1 V1399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr2:152500475 C>T maps to NM_001164507.1 V2604V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:152471011 G>A maps to NM_001164507.1 I3793I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:152410365 C>T maps to NM_001164507.1 R6534R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:152500514 C>T maps to NM_001164507.1 K2591K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:152424922 G>A maps to NM_001164507.1 Y5881Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:152474839 C>T maps to NM_001164507.1 T3675T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:152534255 C>T maps to NM_001164507.1 W1199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:152512906 G>A maps to NM_001164507.1 P2085P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:152388398 C>T maps to NM_001164507.1 R7143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:152410458 C>T maps to NM_001164507.1 K6503K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr2:152534273 C>T maps to NM_001164507.1 K1193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:152506827 C>T maps to NM_001164507.1 E2431E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:152520313 C>T maps to NM_001164507.1 L1837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr2:152424919 C>T maps to NM_001164507.1 R5882R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:152512942 C>T maps to NM_001164507.1 G2073G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr2:152370930 C>T maps to NM_001164507.1 R7676R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:152484209 T>A maps to NM_001164507.1 K3324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:152466491 C>T maps to NM_001164507.1 W4054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:152520286 G>A maps to NM_001164507.1 F1846F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:152550914 C>T maps to NM_001164507.1 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:152490362 C>T maps to NM_001164507.1 R3073R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:152427046 G>A maps to NM_001164507.1 I5694I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:152507369 T>C maps to NM_001164507.1 Q2315Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:152522713 G>A maps to NM_001164507.1 Q1641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:152499776 G>A maps to NM_001164507.1 Q2683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:152529134 G>A maps to NM_001164507.1 L1349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:152374873 C>T maps to NM_001164507.1 L7586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:152579985 T>C maps to NM_001164507.1 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:152350315 C>T maps to NM_001164507.1 V8215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:152420118 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:152492815 C>T maps to NM_001164507.1 K3009K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr2:152422107 C>T maps to NM_001164507.1 K6091K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr2:152496874 C>T maps to NM_001164507.1 Q2893Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr2:152506889 G>A maps to NM_001164507.1 L2411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr2:152527581 G>A maps to NM_001164507.1 S1487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr2:152467038 G>A maps to NM_001164507.1 I4003I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:152550863 G>A maps to NM_001164507.1 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:152515620 G>A maps to NM_001164507.1 P2011P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr2:152490353 T>C maps to NM_001164507.1 K3076K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:152512465 C>T maps to NM_001164507.1 V2189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr2:152426747 C>T maps to NM_001164507.1 Q5759Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:152394449 C>T maps to NM_001164507.1 W7013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:152423745 C>T maps to NM_001164507.1 W6031*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:152468713 G>A maps to NM_001164507.1 L3931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:152470821 G>A maps to NM_001164507.1 Q3857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:152490374 G>A maps to NM_001164507.1 I3069I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:152496919 G>A maps to NM_001164507.1 P2878P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:152520313 C>T maps to NM_001164507.1 L1837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:152521993 C>T maps to NM_001164507.1 E1697E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:152553712 C>T maps to NM_001164507.1 Q473Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:152554066 G>A maps to NM_001164507.1 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:152512672 C>T maps to NM_001164507.1 Q2163Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr2:152541387 G>A maps to NM_001164507.1 S913S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr2:152419207 G>A maps to NM_001164507.1 R6270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:152359375 C>T maps to NM_001164507.1 G7953G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:152370117 C>T maps to NM_001164507.1 R7739R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:152527696 C>T maps to NM_001164507.1 W1449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:152553213 G>A maps to NM_001164507.1 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr2:152514586 G>A maps to NM_001164507.1 S2031S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:21101731 G>A maps to ENST00000430741 I830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr10:21098759 C>T maps to ENST00000430741 Q864Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:21309072 C>T maps to NM_213569.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr10:21115399 C>T maps to ENST00000430741 K615K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr10:21148695 A>C maps to ENST00000430741 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr10:21250657 G>A maps to NM_213569.2 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:21097532 G>A maps to ENST00000430741 F891F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:21115399 C>T maps to ENST00000430741 K615K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr10:21074699 C>T maps to ENST00000430741 A1009A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:21250657 G>A maps to NM_213569.2 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:21101728 C>T maps to ENST00000430741 V831V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:21185940 A>C maps to ENST00000430741 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:21101731 G>A maps to ENST00000430741 I830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:21108350 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr10:21129778 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr10:21101827 G>A maps to ENST00000430741 G798G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr10:21076193 G>A maps to ENST00000430741 G937G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:21101836 C>T maps to ENST00000430741 K795K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr10:21134297 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:21112211 C>T maps to ENST00000430741 E629E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:21250666 G>A maps to NM_213569.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr10:21120196 C>T maps to ENST00000430741 G533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:21158758 C>T maps to ENST00000430741 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:21097532 G>A maps to ENST00000430741 F891F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr10:21074777 G>A maps to ENST00000430741 I983I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr10:21120196 C>T maps to ENST00000430741 G533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr10:21139335 C>T maps to ENST00000430741 K368K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:21169767 G>A maps to ENST00000430741 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:21120488 C>T maps to ENST00000430741 E491E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:21158758 C>T maps to ENST00000430741 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr10:21124455 C>A maps to ENST00000430741 E479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:21101785 C>T maps to ENST00000430741 R812R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:21129739 C>T maps to ENST00000430741 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr8:91937823 C>T maps to NM_022351.4 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:84014683 G>A maps to NM_019065.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:84024220 G>A maps to NM_019065.2 Q194Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:32258569 G>A maps to NM_031232.3 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr12:8242618 G>A maps to NM_015509.3 E61E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:8234961 C>T maps to NM_015509.3 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:8245338 C>T maps to NM_015509.3 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr12:97306519 A>G maps to NM_001135175.1 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr12:97345794 A>T maps to NM_001135175.1 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:56122118 G>T maps to ENST00000508342 T1312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr15:56155187 C>T maps to ENST00000508342 E618E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:56207724 G>A maps to ENST00000508342 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr15:56155175 G>A maps to ENST00000508342 I622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr18:55992271 C>T maps to NM_001144967.1 H186H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr18:55992272 C>T maps to NM_001144967.1 Q187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr18:56008974 C>T maps to NM_001144967.1 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr18:56063467 G>A maps to NM_001144967.1 V965V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr18:56024450 C>T maps to NM_001144967.1 D578D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr18:56008368 C>T maps to NM_001144967.1 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr22:29886370 G>A maps to NM_021076.3 V914V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr22:29885167 G>A maps to NM_021076.3 E513E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:29881754 G>A maps to NM_021076.3 W376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr22:29885806 G>A maps to NM_021076.3 V726V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:29885002 G>A maps to NM_021076.3 E458E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:29885662 G>A maps to NM_021076.3 E678E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr22:29885293 G>A maps to NM_021076.3 K555K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:29885059 G>A maps to NM_021076.3 E477E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:29886151 G>A maps to NM_021076.3 K841K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr22:29879463 G>A maps to NM_021076.3 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:29886022 G>A maps to NM_021076.3 K798K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr8:24813675 C>T maps to ENST00000221169 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr8:24813810 C>T maps to ENST00000221169 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:24811136 G>A maps to ENST00000221169 Q448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:24813303 C>T maps to ENST00000221169 Q242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:24811209 G>A maps to ENST00000221169 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr8:24771738 C>T maps to NM_005382.2 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:24775486 A>T maps to NM_005382.2 K707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr8:24772256 C>T maps to NM_005382.2 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr8:24776031 G>A maps to NM_005382.2 E888E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr8:24771611 G>A maps to NM_005382.2 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr8:24775239 G>A maps to NM_005382.2 E624E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:24775311 G>A maps to NM_005382.2 V648V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr8:24775338 G>A maps to NM_005382.2 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr8:24775233 G>T maps to NM_005382.2 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:24775278 G>A maps to NM_005382.2 E637E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:24774852 G>A maps to NM_005382.2 K495K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:24772224 A>T maps to NM_005382.2 K307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:72241921 G>A maps to NM_173808.2 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:72058605 T>G maps to NM_173808.2 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr1:72163760 C>T maps to NM_173808.2 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:75647320 G>A maps to NM_024608.2 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr15:75644679 C>T maps to NM_024608.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:75641614 G>A maps to NM_024608.2 W123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr8:11628988 C>T maps to NM_145043.2 H11H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr8:11629027 G>A maps to NM_145043.2 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:11637288 C>T maps to NM_145043.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr8:11640908 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr4:178272599 C>T maps to NM_018248.2 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr4:178281683 C>T maps to NM_018248.2 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr4:170428877 G>A maps to ENST00000507142 I633I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:170506613 G>A maps to ENST00000507142 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:170498182 G>A maps to ENST00000507142 Q306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:27326179 G>A maps to ENST00000396636 R643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:27385791 G>A maps to ENST00000396636 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:27326369 G>A maps to ENST00000396636 H624H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:27393972 G>A maps to ENST00000396636 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr3:27346344 G>A maps to ENST00000396636 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:27333046 G>A maps to ENST00000396636 F468F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:27343199 G>A maps to ENST00000396636 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr3:27326099 T>G maps to ENST00000396636 V669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:130871528 C>T maps to NM_024800.4 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:130873926 G>A maps to NM_024800.4 L308L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A2M6-06A-12D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:130947504 C>T maps to NM_024800.4 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:130851630 G>A maps to NM_024800.4 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr1:211840481 C>T maps to NM_002497.2 K359K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr1:211842668 G>A maps to NM_002497.2 Y257Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:52718861 G>A maps to NM_002498.2 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr3:52780207 G>A maps to NM_003157.4 R566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr3:52802596 G>A maps to NM_003157.4 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:52800229 G>A maps to NM_003157.4 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr13:52646131 C>T maps to NM_199289.1 E624E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr13:52676395 C>T maps to NM_199289.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr13:52639699 C>T maps to NM_199289.1 W657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr13:52639551 G>A maps to NM_199289.1 I706I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr13:52684495 A>G maps to NM_199289.1 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:52660490 C>T maps to NM_199289.1 W467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:52682523 G>A maps to NM_199289.1 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr13:52639698 C>T maps to NM_199289.1 W657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:127101922 C>T maps to NM_001166171.1 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr9:127089716 C>T maps to NM_001166171.1 H239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr17:27061925 G>A maps to NM_178170.2 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr17:27066201 G>A maps to NM_178170.2 W467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:75567737 G>A maps to NM_033116.4 I653I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr14:75587854 G>A maps to NM_033116.4 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr14:75587838 T>A maps to NM_033116.4 K146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr14:75574129 G>A maps to NM_033116.4 R415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr14:75570663 G>A maps to NM_033116.4 Q538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr14:75587220 G>A maps to NM_033116.4 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:75563920 G>A maps to NM_033116.4 T685T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:21250980 G>A maps to NM_006157.3 G510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr11:20939744 G>A maps to NM_006157.3 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:20805241 C>T maps to NM_006157.3 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr11:21592417 C>T maps to NM_006157.3 Q697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:20940876 A>T maps to NM_006157.3 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr11:21581771 G>A maps to NM_006157.3 W608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:20948934 C>T maps to NM_006157.3 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:20805359 C>T maps to NM_006157.3 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:20805233 A>T maps to NM_006157.3 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:20939732 C>T maps to NM_006157.3 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr11:20869158 G>A maps to NM_006157.3 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:20959374 G>A maps to NM_006157.3 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr11:20869164 G>A maps to NM_006157.3 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr12:44913943 C>T maps to NM_001145107.1 E798E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:44915950 G>A maps to NM_001145107.1 F719F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:73528760 C>T maps to NM_002499.3 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:73409064 G>A maps to NM_002499.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:73575395 G>C maps to NM_002499.3 V1118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr15:73593716 G>A maps to NM_002499.3 R1407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:156640235 C>T maps to NM_006617.1 G1248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:156641392 G>A maps to NM_006617.1 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:156642500 G>A maps to NM_006617.1 C493C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:156641392 G>A maps to NM_006617.1 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:156642845 G>A maps to NM_006617.1 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:156640163 G>A maps to NM_006617.1 P1272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:156642356 C>T maps to NM_006617.1 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:156640514 G>A maps to NM_006617.1 S1155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:5494463 C>A maps to NM_001047160.1 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr18:70450982 C>T maps to NM_153181.2 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr18:70417352 G>A maps to NM_153181.2 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr18:70451054 G>A maps to NM_153181.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:70461372 G>A maps to NM_153181.2 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr18:70526247 C>T maps to NM_153181.2 W93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr18:70532131 C>T maps to NM_153181.2 W43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr18:70451048 C>T maps to NM_153181.2 E243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr18:70417685 G>A maps to NM_153181.2 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr18:70417712 C>T maps to NM_153181.2 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:70526178 G>A maps to NM_153181.2 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:70526219 G>A maps to NM_153181.2 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr16:47162259 G>A maps to NM_018092.3 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:47143406 A>G maps to NM_018092.3 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:47117341 G>A maps to NM_018092.3 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:47143562 G>A maps to NM_018092.3 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:31827672 C>T maps to NM_000434.3 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr6:31828334 C>A maps to NM_000434.3 G227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr6:31827573 G>A maps to NM_000434.3 Y390Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr6:31829866 C>T maps to NM_000434.3 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr6:31827642 G>A maps to NM_000434.3 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr2:233899574 C>T maps to NM_005383.2 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:233897452 C>T maps to NM_005383.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:233899190 G>A maps to NM_005383.2 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:233899724 C>T maps to NM_005383.2 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:233899344 C>T maps to NM_005383.2 R241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:233899664 C>T maps to NM_005383.2 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr2:233899635 C>T maps to NM_005383.2 Q338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:233898926 C>T maps to NM_005383.2 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:74716819 C>T maps to NM_006656.5 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr11:74716558 C>T maps to NM_006656.5 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:74716850 C>T maps to NM_006656.5 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:242756231 C>T maps to NM_001167599.1 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:242758340 G>A maps to NM_001167599.1 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:242757512 C>T maps to NM_001167599.1 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:242755719 C>T maps to NM_001167599.1 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:242755875 C>T maps to NM_001167599.1 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr10:105331478 C>T maps to NM_004210.4 N183N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:105330818 C>T maps to NM_004210.4 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:105331391 C>T maps to NM_004210.4 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:105344434 G>A maps to NM_004210.4 E264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr17:7226329 G>A maps to NM_032442.2 L844L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:7227008 G>A maps to NM_032442.2 V765V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr17:7221240 G>A maps to NM_032442.2 F1357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:7230807 G>A maps to NM_032442.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:7230053 G>A maps to NM_032442.2 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:7226168 G>A maps to NM_032442.2 V870V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:7227206 G>A maps to NM_032442.2 I729I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr17:7221918 A>G maps to NM_032442.2 S1253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:7227236 G>A maps to NM_032442.2 F719F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr17:7222488 G>A maps to NM_032442.2 S1188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:7222443 G>A maps to NM_032442.2 F1203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:7229761 G>A maps to NM_032442.2 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr17:7230053 G>A maps to NM_032442.2 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:182543374 T>C maps to NM_002500.2 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr2:182543038 C>T maps to NM_002500.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr2:182542990 C>T maps to NM_002500.2 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr2:182542603 G>A maps to NM_002500.2 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:182543236 C>T maps to NM_002500.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr2:182543522 C>T maps to NM_002500.2 W22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:37762255 G>A maps to NM_006160.3 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr12:55420828 C>T maps to NM_021191.2 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:55420621 G>A maps to NM_021191.2 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr12:55420930 C>T maps to NM_021191.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:55421005 G>A maps to NM_021191.2 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:55420281 G>A maps to NM_021191.2 W20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr12:55421209 C>T maps to NM_021191.2 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr12:55420885 C>T maps to NM_021191.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr12:55420918 G>A maps to NM_021191.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:55420484 C>T maps to NM_021191.2 R88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:55420281 G>A maps to NM_021191.2 W20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:55420885 C>T maps to NM_021191.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr12:55421050 C>T maps to NM_021191.2 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr12:55420819 C>T maps to NM_021191.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr12:55420513 G>A maps to NM_021191.2 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:55421209 C>T maps to NM_021191.2 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr12:55420714 G>A maps to NM_021191.2 Q164Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr7:31378591 C>T maps to NM_022728.2 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr7:31378642 C>T maps to NM_022728.2 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr7:31378225 G>A maps to NM_022728.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:31378318 G>A maps to NM_022728.2 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:31378623 G>A maps to NM_022728.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr7:31377985 G>A maps to NM_022728.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:71332736 G>A maps to NM_020999.3 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:71332739 G>A maps to NM_020999.3 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr1:78383315 A>G maps to NM_144573.3 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr1:78383921 G>A maps to NM_144573.3 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:78392510 T>A maps to NM_144573.3 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:78395050 C>T maps to NM_144573.3 Y305Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr17:29557908 C>T maps to NM_001042492.2 Q1055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:29652876 C>A maps to NM_001042492.2 Y1625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr17:29665141 C>T maps to NM_001042492.2 I2268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr17:29556132 C>T maps to NM_001042492.2 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:29527481 G>T maps to NM_001042492.2 G311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr17:29654620 C>T maps to NM_001042492.2 I1791I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:29509638 C>T maps to NM_001042492.2 Q282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:29553537 G>A maps to NM_001042492.2 W696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:29557325 G>A maps to NM_001042492.2 T1013T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr17:29483086 C>T maps to NM_001042492.2 Y49Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr17:29562693 G>A maps to NM_001042492.2 W1258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:29533314 C>T maps to NM_001042492.2 R440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:29546049 C>T maps to NM_001042492.2 Q519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:29533314 C>T maps to NM_001042492.2 R440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:29562965 C>T maps to NM_001042492.2 L1301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:29654711 C>T maps to NM_001042492.2 Q1822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr17:29486062 T>A maps to NM_001042492.2 Y80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:29559100 C>T maps to NM_001042492.2 Q1070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:29665052 C>T maps to NM_001042492.2 Q2239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:29665052 C>T maps to NM_001042492.2 Q2239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:29662003 G>A maps to NM_001042492.2 Q1987Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:29683976 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:29562640 C>T maps to NM_001042492.2 R1241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr17:29701166 C>T maps to NM_001042492.2 I2838I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:29548866 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:29654857 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:29654857 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:29486026 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:29679307 C>A maps to NM_001042492.2 P2497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:29554565 G>A maps to NM_001042492.2 W784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:29554566 G>A maps to NM_001042492.2 W784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr17:29576110 C>T maps to NM_001042492.2 R1362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:29553500 C>T maps to NM_001042492.2 Q684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:29527589 C>T maps to NM_001042492.2 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:29562631 G>T maps to NM_001042492.2 E1238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr17:29556482 G>A maps to NM_001042492.2 Q950Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:29679365 C>T maps to NM_001042492.2 R2517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr22:30069409 G>C maps to NM_181832.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr22:30050713 G>A maps to NM_181832.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr22:42793935 G>A maps to NM_145912.5 D197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr22:42793926 C>T maps to NM_145912.5 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr22:42783015 G>A maps to NM_145912.5 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:42807449 G>A maps to NM_145912.5 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:42807590 C>T maps to NM_145912.5 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr1:204938096 G>A maps to ENST00000367172 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr1:204946813 C>T maps to ENST00000367172 Q613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr1:204949555 G>A maps to ENST00000367172 E745E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:204923357 G>A maps to ENST00000367172 K86K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:204951080 C>T maps to ENST00000367172 V801V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr1:204985600 G>A maps to ENST00000367172 E1326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:204951004 G>A maps to ENST00000367172 W776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:204971856 C>T maps to ENST00000367172 I1197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:204966397 C>T maps to ENST00000367172 P1068P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:204949558 C>T maps to ENST00000367172 I746I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:204948604 C>T maps to ENST00000367172 Y698Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:204913472 C>T maps to ENST00000367172 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr1:204942403 C>A maps to ENST00000367172 S379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:204981967 G>A maps to ENST00000367172 K1262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr1:204985597 G>A maps to ENST00000367172 K1325K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:204948165 C>T maps to ENST00000367172 I649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:204943418 G>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:204944444 G>A maps to ENST00000367172 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:204951122 C>T maps to ENST00000367172 S815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:204953221 G>A maps to ENST00000367172 W846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:204943917 A>T maps to ENST00000367172 K509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr16:69681273 C>T maps to NM_138713.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr16:69725733 C>A maps to NM_138713.2 S669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr16:69727949 C>T maps to NM_138713.2 Q1408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:69693671 C>T maps to NM_138713.2 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr16:69718850 C>T maps to NM_138713.2 C584C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:69727478 C>T maps to NM_138713.2 Q1251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:69727232 C>T maps to NM_138713.2 Q1169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:77208903 C>T maps to NM_172387.1 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr18:77170532 C>T maps to NM_172387.1 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:77170467 C>T maps to NM_172387.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:77211022 C>T maps to NM_172387.1 I540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr18:77221366 G>A did not map to a codon.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr18:77170937 T>C maps to NM_172387.1 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr20:50139726 G>A maps to NM_012340.3 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr20:50133367 G>A maps to NM_012340.3 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr20:50140169 G>A maps to NM_012340.3 Q204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:50140413 G>A maps to NM_012340.3 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr20:50140317 G>C maps to NM_012340.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:50049126 C>T maps to NM_012340.3 T733T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:50140002 G>A maps to NM_012340.3 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:50140112 G>A maps to NM_012340.3 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:50092035 G>A maps to NM_012340.3 V498V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr20:50140305 G>A maps to NM_012340.3 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:50159026 G>A maps to NM_012340.3 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr20:50140112 G>A maps to NM_012340.3 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr16:28975099 C>T maps to NM_032815.3 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr16:68191930 C>T maps to NM_173165.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr16:68225517 C>T maps to NM_173165.2 G982G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr16:68225518 C>T maps to NM_173165.2 Q983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr16:68217228 G>A maps to NM_173165.2 K686K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr16:68156439 C>A maps to NM_173165.2 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:68156100 C>T maps to NM_173165.2 P105P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A20C-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:24839800 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:24845680 C>T maps to NM_001136022.1 P809P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr14:24839701 A>G maps to NM_001136022.1 G429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:24839716 G>A maps to NM_001136022.1 E434E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:24839277 G>A maps to NM_001136022.1 W288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr12:54686205 C>T maps to NM_001136023.1 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:54686970 G>A maps to NM_001136023.1 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:54686622 C>T maps to NM_001136023.1 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr12:54686864 G>A maps to NM_001136023.1 Q139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:54686415 C>T maps to NM_001136023.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:54686322 C>T maps to NM_001136023.1 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:54686865 G>A maps to NM_001136023.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr12:54687051 G>A maps to NM_001136023.1 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:54686832 G>A maps to NM_001136023.1 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr12:54686211 G>A maps to NM_001136023.1 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr17:46134782 G>A maps to ENST00000362042 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr17:46135679 A>G maps to ENST00000362042 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:46128818 C>T maps to ENST00000362042 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:46135823 C>T maps to ENST00000362042 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:46136642 C>T maps to ENST00000362042 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:46134779 C>T maps to ENST00000362042 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:46136123 C>T maps to ENST00000362042 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:178095821 C>T maps to NM_006164.3 R503R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:178096112 G>A maps to NM_006164.3 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr7:26224889 G>A maps to NM_004289.6 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:26217609 C>G maps to NM_004289.6 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:61554128 C>T maps to NM_001145512.1 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:61848984 C>T maps to NM_001145512.1 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr9:14307336 C>T maps to ENST00000397581 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:3381894 G>A maps to ENST00000269778 W72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:3449010 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr19:3434308 C>T maps to ENST00000269778 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr19:3452489 G>A maps to ENST00000269778 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr19:3434309 C>T maps to ENST00000269778 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U9-06A-11D-A32N-08 chr19:3382149 C>T maps to ENST00000269778 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr19:13184813 G>A maps to ENST00000397661 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr19:13186432 C>T maps to ENST00000397661 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr19:13136079 C>T maps to ENST00000397661 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr19:13184816 C>T maps to ENST00000397661 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr19:13192605 G>A maps to ENST00000397661 Q397Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:13136079 C>T maps to ENST00000397661 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:13201180 C>T maps to ENST00000397661 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr19:13135902 C>T maps to ENST00000397661 N32N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:13192545 C>T maps to ENST00000397661 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr19:13192527 C>T maps to ENST00000397661 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr4:103504092 C>T maps to NM_003998.3 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:103459046 C>T maps to NM_003998.3 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:103459028 C>T maps to NM_003998.3 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr4:103517388 C>T maps to NM_003998.3 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr10:104157398 C>T maps to NM_001077494.1 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr10:104156227 C>T maps to NM_001077494.1 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr10:104157368 C>T maps to NM_001077494.1 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:104159899 C>T maps to NM_001077494.1 I511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr14:35872464 G>A maps to NM_020529.2 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:35872484 G>A maps to NM_020529.2 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr19:39396104 C>T maps to NM_002503.3 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr19:39396029 C>T maps to NM_002503.3 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:39398052 C>T maps to NM_002503.3 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:39396065 C>T maps to NM_002503.3 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr19:39396029 C>T maps to NM_002503.3 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:36381328 G>A maps to ENST00000352614 Q376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr19:36387123 G>A maps to ENST00000352614 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr19:36387016 G>A maps to ENST00000352614 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr6:44227797 G>A maps to NM_004556.2 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5KH-06A-11D-A27K-08 chr6:44227995 C>T maps to NM_004556.2 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr6:31525546 C>T maps to NM_005007.3 A159A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A2MH-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:145662196 G>A maps to NM_013432.4 F611F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:145667671 G>A maps to NM_013432.4 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:145667650 C>T maps to NM_013432.4 E241E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:145662288 G>A maps to NM_013432.4 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:101576281 C>T maps to NM_031419.3 P694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr3:101572056 C>T maps to NM_031419.3 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr11:129753056 G>A maps to NM_006165.3 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:129748211 G>A maps to NM_006165.3 V526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr11:129756295 G>A maps to NM_006165.3 C140C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:129756217 G>A maps to NM_006165.3 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:129739559 C>A maps to NM_006165.3 G1145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:129734736 G>A maps to NM_006165.3 I1286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:129747255 G>A maps to NM_006165.3 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:129744078 G>A maps to NM_006165.3 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr11:129739547 G>A maps to NM_006165.3 V1149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:34263104 G>A maps to NM_021100.4 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr20:34263026 C>A maps to NM_021100.4 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr9:33354887 A>G maps to NM_002504.4 K957K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:33366685 C>T maps to NM_002504.4 I1033I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr9:33328582 C>T maps to NM_002504.4 F637F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr9:33364753 C>T maps to NM_002504.4 L1007L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:33352708 T>C maps to NM_002504.4 T907T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr4:47887672 G>A maps to NM_152995.4 R556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr4:47907309 G>A maps to NM_152995.4 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:77732920 C>T maps to NM_021257.3 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:233785140 C>T maps to NM_019850.2 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:233839558 C>T maps to NM_019850.2 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:233839537 C>T maps to NM_019850.2 W21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:233835020 T>A maps to NM_019850.2 K96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:233839558 C>T maps to NM_019850.2 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:233746932 C>T maps to NM_019850.2 R600R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:115829101 G>A maps to NM_002506.2 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:115829227 C>T maps to NM_002506.2 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:115828984 C>T maps to NM_002506.2 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:115829394 G>A maps to NM_002506.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:115828825 C>T maps to NM_002506.2 W197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr17:47583928 C>T maps to NM_002507.3 N159N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:47583853 C>T maps to NM_002507.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:47587924 G>A maps to NM_002507.3 Q240Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:47590130 G>A maps to NM_002507.3 E348E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:102632524 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:25761669 G>A maps to NM_018297.3 R542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:25781207 G>A maps to NM_018297.3 N247N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:25805595 G>A maps to NM_018297.3 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:25781077 G>A maps to NM_018297.3 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:25775391 G>A maps to NM_018297.3 R411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:25775391 G>A maps to NM_018297.3 R411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:103870498 G>A maps to NM_139173.3 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:103912819 G>A maps to NM_139173.3 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr4:103988683 A>T maps to NM_178833.4 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:219942889 G>A maps to NM_024782.2 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr1:160340655 C>T maps to NM_005598.3 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr1:160340838 C>T maps to NM_005598.3 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:160340880 C>T maps to NM_005598.3 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:160340541 C>T maps to NM_005598.3 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:18121868 G>A maps to NM_198586.2 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr13:39613750 C>T maps to NM_001012754.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr16:618056 C>T maps to ENST00000293874 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr16:618190 C>T maps to ENST00000293874 F796F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:618155 C>T maps to ENST00000293874 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:17743840 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:17746423 A>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:17744380 A>C did not map to a codon.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr23:17746033 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:17746876 T>C did not map to a codon.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr23:17710500 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:17745907 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:17710467 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:17744106 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:17744465 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:17744271 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:17744271 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:17746075 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:17742490 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:17744402 T>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:17744949 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:17745856 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:17744327 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:17743769 G>A did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:17742433 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr23:71358755 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr23:71359491 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:71359706 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:71358660 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:71360302 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr23:71360110 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:71360220 A>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:71359741 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:71359250 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr23:71360042 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:71360567 A>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr23:71359489 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:71360098 A>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:71360215 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:49466623 G>A maps to NM_032316.3 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:236143952 C>T maps to NM_002508.2 G1076G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:236143953 C>T did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr1:236212000 G>A maps to NM_002508.2 Q172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:236175236 G>A maps to NM_002508.2 F837F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:236192895 G>A maps to NM_002508.2 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr1:236154239 G>A maps to NM_002508.2 P958P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:236157082 G>A maps to NM_002508.2 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:236205348 G>A maps to NM_002508.2 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:236154254 C>T maps to NM_002508.2 K953K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr1:236143949 G>A maps to NM_002508.2 N1077N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:236205561 C>T maps to NM_002508.2 W261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:236205562 C>T maps to NM_002508.2 W261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr14:52534764 C>T maps to NM_007361.3 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr14:52493940 G>A maps to NM_007361.3 A884A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr14:52477676 G>T maps to NM_007361.3 A1213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:52485932 G>A maps to NM_007361.3 F958F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr14:52481897 G>A maps to NM_007361.3 Q1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr14:52508838 G>A maps to NM_007361.3 N603N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr14:52505567 G>A maps to NM_007361.3 F718F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:52485932 G>A maps to NM_007361.3 F958F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:52496388 C>T maps to NM_007361.3 P759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:52508882 G>A maps to NM_007361.3 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:52521020 G>A maps to NM_007361.3 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr14:52535601 G>A maps to NM_007361.3 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr14:52496388 C>T maps to NM_007361.3 P759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr14:51238083 G>A maps to NM_020921.3 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr14:51224443 A>G maps to NM_020921.3 L1102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr14:51196402 G>A maps to NM_020921.3 S1972S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr14:51204892 G>A maps to NM_020921.3 Q1914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr14:51239807 G>A maps to NM_020921.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr14:51190267 G>A maps to NM_020921.3 L2105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:51259444 G>A maps to NM_020921.3 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr14:51224101 G>A maps to NM_020921.3 R1216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr14:51243723 G>A maps to NM_020921.3 N203N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr14:51226702 G>A maps to NM_020921.3 G757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr14:51223777 G>A maps to NM_020921.3 L1324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr14:51223835 G>A maps to NM_020921.3 F1304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr14:51224285 G>A maps to NM_020921.3 D1154D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:51224953 G>A maps to NM_020921.3 L932L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:675179 C>T maps to NM_016533.4 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr20:25481559 G>A maps to NM_025176.4 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr20:25459692 G>A maps to NM_025176.4 V689V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:25460859 C>A maps to NM_025176.4 T618T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr20:25459647 G>A maps to NM_025176.4 P704P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr20:25471997 G>A maps to NM_025176.4 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr20:25471998 G>C maps to NM_025176.4 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr20:25439081 G>A maps to NM_025176.4 A1260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:25460820 G>A maps to NM_025176.4 D631D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr15:23052733 G>A maps to NM_144599.4 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:23049281 G>A maps to NM_144599.4 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:48037600 C>T maps to NM_207330.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr4:48036945 G>A maps to NM_207330.1 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr8:99208210 G>A maps to NM_024759.1 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr8:99217346 G>A maps to NM_024759.1 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr8:99208228 G>A maps to NM_024759.1 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:24768660 C>T maps to NM_020448.4 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:24768669 C>T maps to NM_020448.4 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:24782683 C>T maps to NM_020448.4 Q232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:24795474 G>C did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr5:156899457 G>A maps to NM_001099287.1 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:156899469 G>A maps to NM_001099287.1 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:156899649 C>G maps to NM_001099287.1 Y361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:156890237 C>T maps to NM_001099287.1 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:156899772 C>T maps to NM_001099287.1 F402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr5:156898685 C>T maps to NM_001099287.1 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr5:37022474 C>T maps to NM_133433.3 L1853L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr5:37006514 T>A maps to NM_133433.3 V1304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr5:37007539 A>T maps to NM_133433.3 L1401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr5:37049279 C>T maps to NM_133433.3 S2277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:36984970 C>A maps to NM_133433.3 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr5:36976494 C>T maps to NM_133433.3 Q496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr5:36976076 T>C maps to NM_133433.3 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:37048730 C>A maps to NM_133433.3 T2239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr5:37064711 C>T maps to NM_133433.3 I2711I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:37044567 C>T maps to NM_133433.3 L2076L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:37051981 C>T maps to NM_133433.3 F2352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr5:36986308 T>C maps to NM_133433.3 S1009S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr22:29966481 G>A maps to NM_003634.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr22:29957587 C>T maps to NM_003634.2 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:29956780 C>T maps to NM_003634.2 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:107521576 G>A maps to NM_015469.1 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr3:52526455 G>A maps to NM_007184.3 E1491E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr3:52514213 C>T maps to NM_007184.3 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:52512202 T>C maps to NM_007184.3 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr3:52524838 C>T maps to NM_007184.3 F1244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr3:52521643 G>A maps to NM_007184.3 W712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:52524781 C>T maps to NM_007184.3 F1225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr3:52510542 C>T maps to NM_007184.3 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr3:52523639 C>T maps to NM_007184.3 V1134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr3:52521916 C>T maps to NM_007184.3 F803F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr3:52525524 C>T maps to NM_007184.3 T1300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:52511652 C>T maps to NM_007184.3 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:52522225 C>T maps to NM_007184.3 I906I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr3:52507757 C>T maps to NM_007184.3 H226H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:161089988 T>C maps to NM_005600.2 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr1:31655410 G>T maps to NM_024522.2 Y166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr1:31658141 C>T maps to NM_024522.2 W75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:31656840 G>A maps to NM_024522.2 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr6:124604233 C>T maps to NM_001040214.1 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:125112495 C>T maps to NM_001040214.1 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr6:124604233 C>T maps to NM_001040214.1 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:125112495 C>T maps to NM_001040214.1 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr8:63659633 C>T maps to NM_173688.2 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr8:63659648 C>T maps to NM_173688.2 Y144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr23:119068485 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr23:119072752 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr23:119070326 C>T did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr23:119077538 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:119068456 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr6:28227577 C>T maps to NM_001007531.1 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr16:50667451 C>T maps to NM_033119.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:50659400 C>T maps to NM_033119.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:50667568 G>A maps to NM_033119.3 E430E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr16:50664179 G>T maps to NM_033119.3 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr16:50583351 C>T maps to NM_033119.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:1032301 C>T maps to NM_033120.2 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr5:1032325 G>A maps to NM_033120.2 Q67Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr5:1033490 A>C maps to NM_033120.2 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr5:1033571 C>T maps to NM_033120.2 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:51875430 G>A maps to NM_005601.3 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr19:51875054 G>A maps to NM_005601.3 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:51875729 C>T maps to NM_005601.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr19:51875257 G>A maps to NM_005601.3 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:51875761 G>A maps to NM_005601.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr3:23952323 G>A maps to NM_020345.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr23:118726447 G>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:118724537 G>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:118725045 A>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr3:42660521 C>T maps to NM_005385.3 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:36987097 G>A maps to NM_001079668.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr20:21492578 G>A maps to NM_002509.2 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr20:21492947 C>T maps to NM_002509.2 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr20:21492583 G>A maps to NM_002509.2 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr14:37051551 G>A maps to NM_014360.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr4:13545654 C>A maps to NM_001189.3 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:85419045 C>T maps to NM_006168.2 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr4:85414692 G>A maps to NM_006168.2 Q285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:85416950 C>T maps to NM_006168.2 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr4:85414681 C>T maps to NM_006168.2 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:85419213 G>A maps to NM_006168.2 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:33466920 G>A maps to NM_018096.3 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:33464653 G>A maps to NM_018096.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr17:33466947 G>T maps to NM_018096.3 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:173999059 C>T maps to NM_014932.2 P813P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:7318296 C>T maps to NM_020795.2 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr17:7318892 C>T maps to NM_020795.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr17:7311997 C>T maps to NM_020795.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr17:7318838 C>T maps to NM_020795.2 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr17:7318901 G>A maps to NM_020795.2 Q370Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:7318371 G>A maps to NM_020795.2 K314K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr17:7320604 C>T maps to NM_020795.2 F665F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr23:70389909 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:70389543 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:70389544 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr23:70387189 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:70389875 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:70375107 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:70387353 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:70375178 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:70387218 C>T did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:70386991 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:6069431 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:5811553 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:5947422 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:5811618 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:6069226 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:5811553 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:5821215 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:6069278 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr23:5811150 C>T did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:5811129 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:5811468 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:6069259 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr23:5811687 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:5821746 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:5811414 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:5811308 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:5811247 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:6069441 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:5827206 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:5827207 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:5811038 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:5821358 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:5821664 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:5821283 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:5821215 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:5821347 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr23:5811247 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:6069207 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:6069465 G>A did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr23:5811090 C>T did not map to a codon.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr23:5811553 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:5811150 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr23:5821653 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr24:16835114 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr24:16734008 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr24:16734108 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr24:16734174 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr24:16734200 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr24:16734077 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr24:16734106 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:26490648 C>T maps to NM_016231.4 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:26495638 C>T maps to NM_016231.4 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr5:65058796 C>T maps to NM_020726.4 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:65081738 T>C did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:3614472 C>T maps to ENST00000448023 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr16:3594307 C>T maps to ENST00000448023 G977G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:3611770 G>A maps to ENST00000448023 F696F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:3614226 C>T maps to ENST00000448023 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr16:3614280 G>A maps to ENST00000448023 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:3611704 G>A maps to ENST00000448023 I718I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr16:3600436 C>T maps to ENST00000448023 V850V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:3613899 C>T maps to ENST00000448023 R393R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr16:3602200 C>T maps to ENST00000448023 E828E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:3607625 G>A maps to ENST00000448023 S736S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:3614463 G>A maps to ENST00000448023 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:3614673 G>A maps to ENST00000448023 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:32463320 A>G maps to NM_021209.4 L801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr2:32461351 G>A maps to NM_021209.4 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr2:32476104 G>A maps to NM_021209.4 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr2:32475630 C>T maps to NM_021209.4 R434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:32476017 G>A maps to NM_021209.4 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:32475891 G>A maps to NM_021209.4 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:32474889 C>T maps to NM_021209.4 G681G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr2:32476323 G>A maps to NM_021209.4 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr16:57113006 C>T maps to NM_032206.3 A1709A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr16:57059625 C>T maps to NM_032206.3 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:57060141 G>A maps to NM_032206.3 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:57070086 G>A maps to NM_032206.3 R901R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:57113138 G>A maps to NM_032206.3 A1724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:57059745 G>A maps to NM_032206.3 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:57054812 C>T maps to NM_032206.3 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:57054813 C>T maps to NM_032206.3 Q64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:57099123 G>A maps to NM_032206.3 R1385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:57060582 C>T maps to NM_032206.3 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr16:57093399 C>T maps to NM_032206.3 F1314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr16:57056214 C>T maps to NM_032206.3 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:57054866 G>A maps to NM_032206.3 E81E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:57062237 C>T maps to NM_032206.3 A728A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:57062238 C>T maps to NM_032206.3 R729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr16:57060687 G>A maps to NM_032206.3 K611K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr16:57075939 C>T maps to NM_032206.3 Q1026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr16:57111869 C>T maps to NM_032206.3 A1673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr16:57100494 C>T maps to NM_032206.3 Q1431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr16:57060213 C>T maps to NM_032206.3 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:57060873 C>T maps to NM_032206.3 P673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr16:57075433 C>T maps to NM_032206.3 Q993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr16:57071175 C>T maps to NM_032206.3 T927T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr16:57088713 C>T maps to NM_032206.3 T1186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr17:5485278 C>T maps to NM_033004.3 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr17:5462773 C>T maps to NM_033004.3 E414E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr17:5463181 G>A maps to NM_033004.3 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr17:5445199 C>T maps to NM_033004.3 P892P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:5456731 G>A maps to NM_033004.3 R834R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:5461948 G>A maps to NM_033004.3 I689I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:5434014 G>A maps to NM_033004.3 F1102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr17:5461996 G>A maps to NM_033004.3 F673F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr17:5461921 C>T maps to NM_033004.3 R698R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:5425005 C>T maps to NM_033004.3 L1207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:5433987 G>A maps to NM_033004.3 P1111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:5445202 C>T maps to NM_033004.3 Q891Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr17:5418808 G>A maps to NM_033004.3 I1362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:5461921 C>T maps to NM_033004.3 R698R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:5418188 C>T maps to NM_033004.3 W1436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr17:5462152 G>A maps to NM_033004.3 F621F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:5456812 G>A maps to NM_033004.3 T807T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr17:5463220 G>A maps to NM_033004.3 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr17:5462136 G>A maps to NM_033004.3 Q627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:5462794 G>A maps to NM_033004.3 F407F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:5421207 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr17:5462257 G>A maps to NM_033004.3 F586F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr17:5461921 C>T maps to NM_033004.3 R698R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:5436227 C>T maps to NM_033004.3 T1070T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:5486047 C>T maps to NM_033004.3 Q130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr17:5485359 G>A maps to NM_033004.3 Y157Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:5445345 A>G maps to NM_033004.3 L844L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:5424221 C>T maps to NM_033004.3 G1298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr11:7982492 G>A maps to NM_176821.3 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:7981463 G>A maps to NM_176821.3 F565F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:7981921 G>A maps to NM_176821.3 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr11:7982252 G>A maps to NM_176821.3 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:7981856 C>T maps to NM_176821.3 R434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:7981481 C>T maps to NM_176821.3 R559R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:7981921 G>A maps to NM_176821.3 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:7982420 G>A maps to NM_176821.3 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:7984964 C>T maps to NM_176821.3 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr11:7981880 G>A maps to NM_176821.3 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr11:7982348 C>T maps to NM_176821.3 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:7982195 C>T maps to NM_176821.3 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:7981505 C>T maps to NM_176821.3 Q551Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:7981880 G>A maps to NM_176821.3 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr11:7982612 G>A maps to NM_176821.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:7981751 G>A maps to NM_176821.3 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:7981577 C>T maps to NM_176821.3 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:7984934 G>A maps to NM_176821.3 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr19:56329408 C>T maps to NM_145007.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:56321558 G>T maps to NM_145007.3 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr19:56321663 G>A maps to NM_145007.3 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr19:56329459 C>T maps to NM_145007.3 K27K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr19:56329468 C>T maps to NM_145007.3 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:56321639 A>C maps to NM_145007.3 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr19:56321201 G>A maps to NM_145007.3 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:56329291 C>T maps to NM_145007.3 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:56321021 C>T maps to NM_145007.3 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:56303781 G>A maps to NM_145007.3 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr19:56321366 G>A maps to NM_145007.3 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:56320493 G>A maps to NM_145007.3 F494F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:56321525 G>A maps to NM_145007.3 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:56329300 A>G maps to NM_145007.3 D80D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:56321672 C>T maps to NM_145007.3 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr19:56320961 G>A maps to NM_145007.3 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:56321525 G>A maps to NM_145007.3 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56297164 C>T maps to NM_145007.3 L976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56300730 G>A maps to NM_145007.3 Q850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56320559 G>A maps to NM_145007.3 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56320979 G>A maps to NM_145007.3 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr19:56321129 C>T maps to NM_145007.3 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr19:56329285 G>A maps to NM_145007.3 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:56297161 G>A maps to NM_145007.3 I977I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr19:54307239 G>A maps to ENST00000391773 L852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr19:54313226 G>A maps to ENST00000391773 F562F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr19:54327416 G>T maps to ENST00000391773 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr19:54299234 G>A maps to ENST00000391773 F993F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:54314132 C>T maps to ENST00000391773 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:54313049 C>T maps to ENST00000391773 Q621Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:54313568 C>T maps to ENST00000391773 G448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr19:54327214 A>G maps to ENST00000391773 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr19:54299279 C>T maps to ENST00000391773 L978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:54313361 G>A maps to ENST00000391773 F517F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:54313964 C>T maps to ENST00000391773 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:54314234 C>A maps to ENST00000391773 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:54313964 C>T maps to ENST00000391773 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:54314063 G>A maps to ENST00000391773 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr19:54312869 G>A maps to ENST00000391773 S681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54313097 G>A maps to ENST00000391773 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54313817 G>A maps to ENST00000391773 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54314321 C>T maps to ENST00000391773 E197E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:54307218 G>A maps to ENST00000391773 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:54312890 C>T maps to ENST00000391773 G674G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr19:56443601 G>A maps to NM_176810.2 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:56424096 C>T maps to NM_176810.2 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:56423514 G>A maps to NM_176810.2 F556F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:56424570 G>A maps to NM_176810.2 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:56423088 C>T maps to NM_176810.2 R698R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr19:56423634 G>A maps to NM_176810.2 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:56421972 G>A maps to NM_176810.2 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:56422053 G>A maps to NM_176810.2 C719C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:56423184 C>T maps to NM_176810.2 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:56424165 G>A maps to NM_176810.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:56424492 C>T maps to NM_176810.2 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:56424263 G>A maps to NM_176810.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr19:56423097 G>A maps to NM_176810.2 I695I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:56424492 C>T maps to NM_176810.2 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:56443521 G>A maps to NM_176810.2 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:56423349 C>T maps to NM_176810.2 R611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr19:56424468 C>T maps to NM_176810.2 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:56413447 G>A maps to NM_176810.2 F914F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:56424462 C>T maps to NM_176810.2 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr19:56410230 C>T maps to NM_176810.2 V954V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:56443521 G>A maps to NM_176810.2 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:56423733 G>A maps to NM_176810.2 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:56424492 C>T maps to NM_176810.2 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:56424368 T>A maps to NM_176810.2 K272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:56423232 G>A maps to NM_176810.2 F650F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr19:56424102 C>T maps to NM_176810.2 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr19:56443521 G>A maps to NM_176810.2 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr19:56424335 C>A maps to NM_176810.2 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:56424405 C>T maps to NM_176810.2 Q259Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56416315 C>T maps to NM_176810.2 E870E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56419204 C>T maps to NM_176810.2 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56423463 G>A maps to NM_176810.2 V573V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56424592 C>T maps to NM_176810.2 W197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:56423184 C>T maps to NM_176810.2 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr19:56424570 G>A maps to NM_176810.2 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:56416474 C>T maps to NM_176810.2 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:56423743 C>T maps to NM_176810.2 W480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:7091609 G>A maps to NM_176822.3 Q1023Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:7063790 C>T maps to NM_176822.3 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:7083620 G>A maps to NM_176822.3 L954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr11:7063997 C>T maps to NM_176822.3 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr11:7070913 C>T maps to NM_176822.3 I712I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:7070919 C>T maps to NM_176822.3 F714F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:7064762 C>T maps to NM_176822.3 N502N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:7064874 C>T maps to NM_176822.3 R540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:7064300 G>A maps to NM_176822.3 W348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:7064276 C>T maps to NM_176822.3 Y340Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr11:7064039 C>T maps to NM_176822.3 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:7063787 G>A maps to NM_176822.3 Q177Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:7079534 G>A maps to NM_176822.3 E829E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:7079012 G>A maps to NM_176822.3 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:7065200 C>T maps to NM_176822.3 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:7079043 T>C maps to NM_176822.3 L810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:7063706 C>T maps to NM_176822.3 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:7091573 C>T maps to NM_176822.3 I1011I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr11:7064318 T>C maps to NM_176822.3 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:7059990 G>A maps to NM_176822.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:7064874 C>T maps to NM_176822.3 R540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:7091657 G>A maps to NM_176822.3 K1039K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr11:7070919 C>T maps to NM_176822.3 F714F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:7065068 G>A maps to NM_176822.3 K604K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:7092535 C>T maps to NM_176822.3 F1093F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr11:7081196 G>A maps to NM_176822.3 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr19:55492997 G>A maps to NM_017852.3 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr19:55494628 G>A maps to NM_017852.3 E521E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr19:55501986 G>A maps to NM_017852.3 V885V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr19:55494040 G>A maps to NM_017852.3 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:55493563 G>A maps to NM_017852.3 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr19:55505684 G>A maps to NM_017852.3 K919K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr19:55493635 G>A maps to NM_017852.3 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:55494100 G>A maps to NM_017852.3 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:55494713 C>T maps to NM_017852.3 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:55501422 G>A maps to NM_017852.3 W800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr19:55508801 G>A maps to NM_017852.3 V999V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:55494376 C>T maps to NM_017852.3 F437F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:55494433 G>A maps to NM_017852.3 Q456Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:55501974 G>A maps to NM_017852.3 G881G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:55512130 G>A maps to NM_017852.3 L1018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:55493644 C>T maps to NM_017852.3 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr19:55495042 G>A maps to NM_017852.3 K659K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:55501870 T>C maps to NM_017852.3 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:55512190 C>T maps to NM_017852.3 N1038N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr19:55508783 C>T maps to NM_017852.3 P993P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr19:55493977 C>T maps to NM_017852.3 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:55496492 T>C maps to NM_017852.3 G703G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:55501546 C>T maps to NM_017852.3 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:55481538 G>A maps to NM_017852.3 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:55493557 G>A maps to NM_017852.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:55493983 G>A maps to NM_017852.3 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:55494139 C>T maps to NM_017852.3 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:55496417 C>T maps to NM_017852.3 S678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:55501473 C>T maps to NM_017852.3 N817N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:55492997 G>A maps to NM_017852.3 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:55494751 C>T maps to NM_017852.3 N562N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr1:247592991 G>A maps to NM_004895.4 G754G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:247587773 G>A maps to NM_004895.4 E343E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:247587956 C>T maps to NM_004895.4 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:247587447 C>T maps to NM_004895.4 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:247588556 C>T maps to NM_004895.4 I604I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:247587446 C>T maps to NM_004895.4 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:247588694 C>T maps to NM_004895.4 F650F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr1:247588826 G>A maps to NM_004895.4 E694E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr1:247592892 G>A maps to NM_004895.4 V721V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr1:247587437 G>A maps to NM_004895.4 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr1:247587725 G>A maps to NM_004895.4 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr1:247588670 C>T maps to NM_004895.4 F642F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:247597440 C>T maps to NM_004895.4 F788F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr1:247587300 G>T maps to NM_004895.4 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr1:247599358 G>T maps to NM_004895.4 V862V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:247582212 C>T maps to NM_004895.4 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:247588670 C>T maps to NM_004895.4 F642F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:247608118 C>T maps to NM_004895.4 L1003L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:247599272 T>C maps to NM_004895.4 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:247587614 C>T maps to NM_004895.4 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:247588112 G>A maps to NM_004895.4 G456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:247587758 G>A maps to NM_004895.4 K338K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:247588514 C>T maps to NM_004895.4 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:247587737 C>T maps to NM_004895.4 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:247586553 G>A maps to NM_004895.4 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:247586559 C>T maps to NM_004895.4 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:247588832 G>A maps to NM_004895.4 K696K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:247587587 C>T maps to NM_004895.4 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:247588010 G>A maps to NM_004895.4 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:247588500 C>T maps to NM_004895.4 Q586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:247587995 C>T maps to NM_004895.4 I417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:247588526 G>A maps to NM_004895.4 K594K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:247597404 G>A maps to NM_004895.4 W776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr1:247587644 C>T maps to NM_004895.4 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:247582290 G>A maps to NM_004895.4 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:247587614 C>T maps to NM_004895.4 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:247588448 C>T maps to NM_004895.4 F568F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr1:247587437 G>A maps to NM_004895.4 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:247588397 G>A maps to NM_004895.4 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:247587614 C>T maps to NM_004895.4 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:247582116 C>T maps to NM_004895.4 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:247587230 G>A maps to NM_004895.4 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:247587806 C>T maps to NM_004895.4 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:247587812 G>A maps to NM_004895.4 E356E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:247588019 G>A maps to NM_004895.4 Q425Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:247588199 G>A maps to NM_004895.4 E485E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:247597449 C>T maps to NM_004895.4 S791S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:247608108 C>T maps to NM_004895.4 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr1:247592885 G>A did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr1:247587455 G>A maps to NM_004895.4 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:247588670 C>T maps to NM_004895.4 F642F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:247588184 G>A maps to NM_004895.4 Q480Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:247588541 G>A maps to NM_004895.4 K599K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr19:56369883 C>T maps to NM_134444.4 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:56373426 G>A maps to NM_134444.4 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr19:56363679 G>A maps to NM_134444.4 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr19:56369073 G>A maps to NM_134444.4 Q105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr19:56373456 C>T maps to NM_134444.4 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:56382201 C>T maps to NM_134444.4 F788F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:56363514 C>T maps to NM_134444.4 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr19:56363517 G>A maps to NM_134444.4 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:56369539 C>T maps to NM_134444.4 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:56369626 C>T maps to NM_134444.4 Q290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr19:56363445 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:56370066 G>A maps to NM_134444.4 K436K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:56382294 G>A maps to NM_134444.4 L819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:56388523 G>A maps to NM_134444.4 E896E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:56370414 G>A maps to NM_134444.4 A552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:56373426 G>A maps to NM_134444.4 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:56369457 C>T maps to NM_134444.4 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:56369792 G>A maps to NM_134444.4 W345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:56369415 C>T maps to NM_134444.4 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:56369415 C>T maps to NM_134444.4 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:56369319 T>A maps to NM_134444.4 Y187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:56370474 C>T maps to NM_134444.4 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:56369766 C>T maps to NM_134444.4 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr19:56369304 C>T maps to NM_134444.4 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr19:56369316 C>T maps to NM_134444.4 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr19:56369850 C>T maps to NM_134444.4 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:56390160 T>C maps to NM_134444.4 L900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56369376 C>T maps to NM_134444.4 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56369415 C>T maps to NM_134444.4 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56369442 C>T maps to NM_134444.4 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56372892 C>T maps to NM_134444.4 S666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56373450 G>A maps to NM_134444.4 T704T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56392834 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56392910 C>T maps to NM_134444.4 T981T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:56369962 C>T maps to NM_134444.4 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:56373426 G>A maps to NM_134444.4 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:56369415 C>T maps to NM_134444.4 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:56369595 C>T maps to NM_134444.4 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr19:56539224 G>A maps to NM_153447.4 R542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:56538552 C>T maps to NM_153447.4 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr19:56515138 C>T maps to NM_153447.4 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr19:56549441 C>T maps to NM_153447.4 I889I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:56539824 G>A maps to NM_153447.4 G742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:56549441 C>T maps to NM_153447.4 I889I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:56515324 G>A maps to NM_153447.4 E102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:56572881 G>A maps to NM_153447.4 W1197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:56539830 C>T maps to NM_153447.4 F744F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr19:56515138 C>T maps to NM_153447.4 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:56538861 C>T maps to NM_153447.4 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr19:56530711 T>C maps to NM_153447.4 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:56539217 G>A maps to NM_153447.4 W540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:56539476 C>T maps to NM_153447.4 F626F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:56539224 G>A maps to NM_153447.4 R542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr19:56539551 C>T maps to NM_153447.4 V651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:56515250 C>T maps to NM_153447.4 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr19:56539218 G>A maps to NM_153447.4 W540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:56515405 C>A maps to NM_153447.4 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:56539224 G>A maps to NM_153447.4 R542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr19:56539770 C>T maps to NM_153447.4 S724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr19:56539359 C>T maps to NM_153447.4 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:56539029 C>T maps to NM_153447.4 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr19:56549389 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:56565004 T>C maps to NM_153447.4 L1044L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:56539575 G>A maps to NM_153447.4 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56520205 G>A maps to NM_153447.4 K165K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56538969 G>A maps to NM_153447.4 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56544946 C>T maps to NM_153447.4 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56565063 G>A maps to NM_153447.4 R1063R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr19:56572833 C>T maps to NM_153447.4 V1181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr19:56549391 C>T maps to NM_153447.4 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:56539824 G>A maps to NM_153447.4 G742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:282770 C>T maps to NM_138329.1 D725D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr11:284541 C>T maps to NM_138329.1 L814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:281032 C>T maps to NM_138329.1 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr19:55450299 G>A maps to ENST00000446217 F657F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr19:55439136 C>T maps to ENST00000446217 W967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr19:55452980 G>A maps to ENST00000446217 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr19:55451703 C>T maps to ENST00000446217 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:55450445 C>A maps to ENST00000446217 E609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:55441954 G>A maps to ENST00000446217 L936L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:55451373 C>T maps to ENST00000446217 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:55451436 G>A maps to ENST00000446217 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:55441916 C>T maps to ENST00000446217 W948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:55451793 A>T maps to ENST00000446217 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:55451637 C>T maps to ENST00000446217 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr19:55449491 T>C maps to ENST00000446217 K711K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:55451187 G>A maps to ENST00000446217 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:55451187 G>A maps to ENST00000446217 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr19:55451637 C>T maps to ENST00000446217 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr19:55445870 G>A maps to ENST00000446217 F847F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:55450449 C>T maps to ENST00000446217 Q607Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:55450857 G>A maps to ENST00000446217 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr19:55452998 G>A maps to ENST00000446217 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:55447722 G>A maps to ENST00000446217 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:55450785 G>A maps to ENST00000446217 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:55451004 G>A maps to ENST00000446217 F422F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:55451412 C>T maps to ENST00000446217 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:55451818 C>T maps to ENST00000446217 W151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:55447702 G>A maps to ENST00000446217 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr19:55451436 G>A maps to ENST00000446217 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:55447702 G>A maps to ENST00000446217 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr19:55447765 C>T maps to ENST00000446217 R749R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr19:55452869 C>T maps to ENST00000446217 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:55451280 C>T maps to ENST00000446217 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr19:55449587 C>T maps to ENST00000446217 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:55439063 G>A maps to ENST00000446217 L992L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:55444992 C>T maps to ENST00000446217 G890G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:55450702 C>T maps to ENST00000446217 W523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:55450995 G>A maps to ENST00000446217 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:55451340 G>A maps to ENST00000446217 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr19:55449587 C>T maps to ENST00000446217 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr19:56481908 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr19:56499233 C>A maps to NM_176811.2 P1034P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:56466092 G>A maps to NM_176811.2 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr19:56459348 G>A maps to NM_176811.2 W27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr19:56459285 A>G maps to NM_176811.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:56482008 C>T maps to NM_176811.2 S827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:56482033 C>T maps to NM_176811.2 L836L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr19:56485146 G>A maps to NM_176811.2 W888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:56466461 G>A maps to NM_176811.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:56477620 C>T maps to NM_176811.2 I752I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:56473561 G>A maps to NM_176811.2 A724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:56481918 C>T maps to NM_176811.2 D797D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr19:56467103 C>T maps to NM_176811.2 F560F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:56485017 G>A maps to NM_176811.2 S845S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:56466512 C>T maps to NM_176811.2 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr19:56466476 C>T maps to NM_176811.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr19:56481908 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:56466864 C>T maps to NM_176811.2 Q481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:56467271 C>T maps to NM_176811.2 I616I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:56487501 G>A maps to NM_176811.2 L903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr19:56487664 C>T maps to NM_176811.2 L958L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:56467271 C>T maps to NM_176811.2 I616I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:56487618 C>T maps to NM_176811.2 I942I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr19:56459267 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:56467046 G>A maps to NM_176811.2 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr19:56466569 C>T maps to NM_176811.2 F382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:56466020 G>A maps to NM_176811.2 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:56466710 G>A maps to NM_176811.2 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:56467421 C>T maps to NM_176811.2 F666F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56466992 C>T maps to NM_176811.2 F523F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56467448 C>T maps to NM_176811.2 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56477605 G>A maps to NM_176811.2 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56485098 G>A maps to NM_176811.2 L872L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56490831 G>A maps to NM_176811.2 L983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:56466545 G>A maps to NM_176811.2 E374E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:56477725 G>A maps to NM_176811.2 R787R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:56465888 G>A maps to NM_176811.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr19:56241294 G>A maps to NM_176820.2 F632F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr19:56244332 C>T maps to NM_176820.2 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:56223889 C>T maps to NM_176820.2 G856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:56243945 C>T maps to NM_176820.2 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:56244617 G>A maps to NM_176820.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr19:56244383 G>A maps to NM_176820.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:56226515 G>A maps to NM_176820.2 S802S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:56243459 T>C maps to NM_176820.2 V579V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:56223853 T>A maps to NM_176820.2 I868I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:56244086 G>A maps to NM_176820.2 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr19:56223314 G>A maps to NM_176820.2 T898T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:56220292 C>T maps to NM_176820.2 R987R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56226560 G>A maps to NM_176820.2 S787S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56243489 G>A maps to NM_176820.2 F569F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:56243720 C>T maps to NM_176820.2 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr19:56244575 C>T maps to NM_176820.2 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr19:56244086 G>A maps to NM_176820.2 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:119054037 C>T maps to NM_024618.2 L940L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:119053010 C>T maps to NM_024618.2 L855L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:119053961 C>T maps to NM_024618.2 L914L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr6:142409672 C>T maps to NM_002511.2 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr6:142399865 G>A maps to NM_002511.2 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr6:142396922 G>A maps to NM_002511.2 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr6:142399727 A>G maps to NM_002511.2 N245N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:142409429 G>A maps to NM_002511.2 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:142399931 G>A maps to NM_002511.2 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr6:142399799 G>A maps to NM_002511.2 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr3:160952971 G>A maps to ENST00000472947 Q183Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:49233062 C>T maps to ENST00000393198 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:1820658 C>T maps to NM_002513.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr16:1821166 G>A maps to NM_002513.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:169199981 G>A maps to NM_013330.3 R322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:152138506 G>A maps to NM_004688.2 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:10042713 C>T maps to NM_022787.3 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:183253890 G>A maps to NM_015039.2 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr1:183255899 G>A maps to NM_015039.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr3:139297736 C>T maps to ENST00000296202 W90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr3:139297772 G>A maps to ENST00000296202 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr3:139279986 G>A maps to ENST00000296202 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:139297868 G>A maps to ENST00000296202 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:139297776 C>T maps to ENST00000296202 W77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:139297760 A>C maps to ENST00000296202 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:139297745 C>T maps to ENST00000296202 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:139292485 C>T maps to ENST00000296202 Q110Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:139297844 C>T maps to ENST00000296202 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:139297787 C>T maps to ENST00000296202 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:139297844 C>T maps to ENST00000296202 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:139297757 C>T maps to ENST00000296202 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr16:4511822 G>A maps to NM_020677.3 D286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:101099713 G>A maps to NM_001011717.1 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:101099713 G>A maps to NM_001011717.1 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr2:101099724 G>A maps to NM_001011717.1 *154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:43138777 T>C maps to NM_021079.3 H27H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr10:15154794 C>G maps to ENST00000378143 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:56471486 G>A maps to NM_006681.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:232390101 G>A maps to NM_006056.4 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr2:232390032 G>A maps to NM_006056.4 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:232390017 G>A maps to NM_006056.4 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q3-06A-11D-A196-08 chr5:151771826 A>G maps to NM_020167.4 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:151775056 G>A maps to NM_020167.4 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr5:151784665 C>T maps to NM_020167.4 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:151784029 G>A maps to NM_020167.4 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr5:151784008 G>A maps to NM_020167.4 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:151784639 C>T maps to NM_020167.4 W12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr5:151784536 G>A maps to NM_020167.4 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr5:151771937 G>A maps to NM_020167.4 D354D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:151771996 G>A maps to NM_020167.4 Q335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:151771997 G>A maps to NM_020167.4 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:151784281 G>A maps to NM_020167.4 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:151784347 G>A maps to NM_020167.4 N109N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:151784320 G>A maps to NM_020167.4 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:151784107 G>A maps to NM_020167.4 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:151784401 G>A maps to NM_020167.4 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:151784539 G>A maps to NM_020167.4 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:151771985 G>A maps to NM_020167.4 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:151784179 C>T maps to NM_020167.4 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:151784263 G>A maps to NM_020167.4 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr5:151771976 C>T maps to NM_020167.4 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr5:151784167 G>A maps to NM_020167.4 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:36150758 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:114167418 G>A maps to NM_006169.2 K47K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr11:114168874 G>A maps to NM_006169.2 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr11:114168748 C>T maps to NM_006169.2 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:114168874 G>A maps to NM_006169.2 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr11:114182985 G>A maps to NM_006169.2 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26D-06A-11D-A19A-08 chr11:114182785 G>T maps to NM_006169.2 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr5:43628343 C>T maps to NM_182977.2 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr5:43628325 G>A maps to NM_182977.2 K267K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr5:43619148 C>T maps to NM_182977.2 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:43650654 T>A maps to NM_182977.2 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr5:43651922 C>T maps to NM_182977.2 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:43659397 C>T maps to NM_182977.2 I860I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr5:43613101 T>C maps to NM_182977.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:43628322 C>T maps to NM_182977.2 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr16:69782868 G>A maps to NM_014062.1 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr16:69788586 C>A maps to NM_014062.1 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:69782978 C>A maps to NM_014062.1 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:69778778 G>A maps to NM_014062.1 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr16:69778901 G>A maps to NM_014062.1 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr7:144098465 G>A maps to ENST00000467773 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr7:144098262 C>T maps to ENST00000467773 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:144097405 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr7:144098646 C>T maps to ENST00000467773 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr7:144098193 C>A maps to ENST00000467773 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr7:144097382 C>T maps to ENST00000467773 K289K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:144098262 C>T maps to ENST00000467773 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:144098544 G>A maps to ENST00000467773 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr1:880949 G>A maps to NM_015658.3 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:888656 G>A maps to NM_015658.3 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:888563 G>A maps to NM_015658.3 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:889263 G>A maps to NM_015658.3 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:881015 G>A maps to NM_015658.3 F645F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:883569 G>A maps to NM_015658.3 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:888593 G>A maps to NM_015658.3 C321C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:892589 G>A maps to NM_015658.3 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr10:96112661 T>C maps to NM_022451.9 K283K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:96110004 G>A maps to NM_022451.9 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr10:96101486 T>A maps to NM_022451.9 I529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr10:96106292 G>A maps to NM_022451.9 C426C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:132636058 C>T maps to NM_024078.1 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr12:132632302 C>T maps to NM_024078.1 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:30492618 G>A maps to NM_006092.2 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:30492117 C>T maps to NM_006092.2 W305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr7:30492183 G>A maps to NM_006092.2 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:30492006 G>A maps to NM_006092.2 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:30491124 G>A maps to NM_006092.2 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr7:30491985 G>A maps to NM_006092.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr16:50733427 C>T maps to NM_022162.1 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:50733667 C>T maps to NM_022162.1 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:50765675 C>T maps to NM_022162.1 F1023F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:50733553 C>T maps to NM_022162.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:50733552 C>T maps to NM_022162.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:50759400 C>T maps to NM_022162.1 L962L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:50753904 C>T maps to NM_022162.1 S900S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:50745126 G>A maps to NM_022162.1 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:50753890 C>T maps to NM_022162.1 R896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:50744601 G>A maps to NM_022162.1 W260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr16:50759471 G>A maps to NM_022162.1 L985L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr16:50763801 C>T maps to NM_022162.1 L1014L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:50741773 G>A maps to NM_022162.1 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:50744590 C>T maps to NM_022162.1 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:50756562 G>A maps to NM_022162.1 G915G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:50757271 G>A maps to NM_022162.1 K953K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr16:50763779 C>T maps to NM_022162.1 A1006A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:54672216 G>A maps to NM_005450.4 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:54671847 C>T maps to NM_005450.4 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr2:10729251 G>A maps to NM_024894.2 V587V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr2:10717815 C>T maps to NM_024894.2 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr17:65720283 G>A maps to NM_015462.3 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr17:65732797 C>T maps to NM_015462.3 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr22:38086702 G>T did not map to a codon.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr18:31803073 C>T maps to NM_003787.4 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr18:31537406 G>A maps to NM_003787.4 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr18:31538327 G>A maps to NM_003787.4 R371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr18:31537397 G>A maps to NM_003787.4 I440I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr18:31523037 C>T maps to NM_003787.4 E511E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr18:31599281 C>T maps to NM_003787.4 K352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr18:31537409 C>T maps to NM_003787.4 K436K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr18:31685103 G>A maps to NM_003787.4 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:31463234 G>A maps to NM_003787.4 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:31709924 G>A maps to NM_003787.4 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr9:33463376 G>A maps to NM_022917.4 I1019I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr9:33470069 G>A maps to NM_022917.4 Y166Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr9:33468038 G>A maps to NM_022917.4 D471D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:33470117 G>A maps to NM_022917.4 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr9:33468378 G>A maps to NM_022917.4 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr9:33465233 G>A maps to NM_022917.4 F884F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr9:33466066 A>G did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr9:33468750 C>T maps to NM_022917.4 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:33464951 G>A maps to NM_022917.4 R902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:33466939 G>A maps to NM_022917.4 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:33467230 G>A maps to NM_022917.4 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr9:95077334 C>T maps to NM_017948.5 K524K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:95078255 G>A maps to NM_017948.5 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:6589207 G>A maps to NM_024654.4 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:6605138 A>G maps to NM_024654.4 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:6589099 C>T maps to NM_024654.4 G593G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:103921621 G>A maps to ENST00000405356 R637R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr10:103921609 C>T maps to ENST00000405356 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr10:103916801 C>T maps to ENST00000405356 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:156746967 C>T maps to NM_138400.1 I428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:156752582 C>T maps to NM_138400.1 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:156746922 C>T maps to NM_138400.1 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:156752694 T>C maps to NM_138400.1 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:156759008 C>A maps to NM_138400.1 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr7:156759008 C>A maps to NM_138400.1 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr7:156743168 C>T maps to NM_138400.1 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr16:14970249 G>T maps to ENST00000456867 G797G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:14970342 C>T maps to ENST00000456867 I828I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr16:14970279 C>T maps to ENST00000456867 I807I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr16:14980715 C>T maps to ENST00000456867 G1107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr16:14968901 C>T maps to ENST00000456867 I688I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:18554962 G>A maps to NM_001004060.1 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:18532157 G>A maps to NM_001004060.1 T734T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:18544464 G>A maps to NM_001004060.1 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A264-06A-11D-A196-08 chr16:18549972 G>A maps to NM_001004060.1 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr16:16355469 C>T maps to ENST00000263012 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr23:70511789 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr23:70516738 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr23:70511802 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:70514278 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr23:70511696 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:70519837 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:70514087 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:70519860 C>T did not map to a codon.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr23:70514158 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:70511717 C>T did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:70518651 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr4:2940993 C>A maps to NM_003703.1 E799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:2952879 G>A maps to NM_003703.1 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:2941318 C>T maps to NM_003703.1 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:2955285 G>A maps to NM_003703.1 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr4:2943383 G>A maps to NM_003703.1 F708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:6669262 C>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:6669312 G>A maps to ENST00000382421 F613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:6666413 C>G maps to ENST00000382421 P761P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr20:2635509 C>T maps to NM_006392.2 N162N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr20:2636274 C>T maps to NM_006392.2 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr20:2636009 C>T maps to NM_006392.2 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr2:203165001 C>T maps to NM_015934.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr2:203142700 C>T maps to NM_015934.3 Q51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr2:203149090 C>T maps to NM_015934.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:203157612 T>A maps to NM_015934.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:117665446 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:117685230 C>T maps to ENST00000338101 R949R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr12:117660636 G>A maps to ENST00000338101 F1320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr12:117768778 C>T maps to ENST00000338101 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:117665377 G>A maps to ENST00000338101 F1192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:117723977 G>A maps to ENST00000338101 I407I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr12:117665401 G>A maps to ENST00000338101 T1184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr12:117768499 G>A maps to ENST00000338101 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr12:117664495 G>A maps to ENST00000338101 F1266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:117768310 C>T maps to ENST00000338101 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr12:117718529 C>T maps to ENST00000338101 E508E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr12:117685242 C>T maps to ENST00000338101 L945L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:117718613 C>T maps to ENST00000338101 W480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:117696833 C>T maps to ENST00000338101 G823G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:117768529 C>T maps to ENST00000338101 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:117768565 G>A maps to ENST00000338101 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:117672547 G>A maps to ENST00000338101 F1053F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:117723923 C>T maps to ENST00000338101 Q425Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:117672436 C>T maps to ENST00000338101 L1090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:117725961 C>T maps to ENST00000338101 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:117728168 G>A maps to ENST00000338101 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:117768796 C>T maps to ENST00000338101 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:117660558 C>T maps to ENST00000338101 E1346E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:117665346 G>A maps to ENST00000338101 L1203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:117696203 C>T maps to ENST00000338101 R843R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:117685179 G>A maps to ENST00000338101 F966F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:117749354 C>A maps to ENST00000338101 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:117768202 C>T maps to ENST00000338101 K224K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr12:117768499 G>A maps to ENST00000338101 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr12:117718652 G>A maps to ENST00000338101 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:117681135 G>A maps to ENST00000338101 L1010L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:117696829 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:117768313 G>A maps to ENST00000338101 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:117718538 C>T maps to ENST00000338101 Q505Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:117703282 G>A maps to ENST00000338101 S658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:117768658 C>T maps to ENST00000338101 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr12:117665422 C>T maps to ENST00000338101 W1177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr12:117665377 G>A maps to ENST00000338101 F1192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr12:117660591 G>A maps to ENST00000338101 T1335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:117768184 C>T maps to ENST00000338101 K230K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr12:117665377 G>A maps to ENST00000338101 F1192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:117768217 C>T maps to ENST00000338101 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr12:117696932 C>T maps to ENST00000338101 V790V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr12:117768406 C>T maps to ENST00000338101 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:117662893 G>A maps to ENST00000338101 L1285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:117665423 C>T maps to ENST00000338101 W1177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:117669775 G>A maps to ENST00000338101 V1166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:117685227 G>A maps to ENST00000338101 I950I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:117691444 C>T maps to ENST00000338101 V916V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:117691540 G>A maps to ENST00000338101 F884F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:117710336 C>T maps to ENST00000338101 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:117665423 C>T maps to ENST00000338101 W1177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:117703243 G>A maps to ENST00000338101 Y671Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:117710300 G>A maps to ENST00000338101 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr12:117691546 G>A maps to ENST00000338101 V882V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:117672445 G>A maps to ENST00000338101 I1087I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr12:117664507 C>T maps to ENST00000338101 L1262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:162335312 C>T maps to NM_014697.2 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:162325112 G>A maps to NM_014697.2 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:162337145 G>A maps to NM_014697.2 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:162124241 C>T maps to NM_014697.2 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:162313647 G>A maps to NM_014697.2 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:162324975 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:162337097 C>T maps to NM_014697.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:26084379 C>A did not map to a codon.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr17:26108130 G>A maps to NM_000625.4 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:26096158 G>A maps to NM_000625.4 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:26105946 G>A maps to NM_000625.4 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr17:26115903 C>T maps to NM_000625.4 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:26085933 C>T maps to NM_000625.4 Q1109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:26108067 G>A maps to NM_000625.4 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:26101375 C>T maps to NM_000625.4 W461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:26101375 C>T maps to NM_000625.4 W461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:26085918 G>A maps to NM_000625.4 F1114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr7:150696116 A>G maps to NM_000603.4 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr7:150697608 G>A maps to NM_000603.4 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:150696301 C>T maps to NM_000603.4 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:150707275 C>T maps to NM_000603.4 F862F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:150695476 G>A maps to NM_000603.4 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr7:150695755 G>A maps to NM_000603.4 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:150696052 G>A maps to NM_000603.4 W279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr7:150698428 C>T maps to NM_000603.4 I448I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:150698464 C>T maps to NM_000603.4 F460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr7:150695527 C>G maps to NM_000603.4 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150693610 C>T maps to NM_000603.4 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr7:150692296 G>A maps to NM_000603.4 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr19:50059049 C>T maps to NM_015953.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr19:50060401 G>A maps to NM_015953.3 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr2:169681218 G>A maps to NM_001171631.1 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:169690822 G>A maps to NM_001171631.1 K164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:169690823 G>T maps to NM_001171631.1 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:169711902 G>A maps to NM_001171631.1 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:169707601 G>A maps to NM_001171631.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr9:139417599 G>A maps to NM_017617.3 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr9:139407551 C>T maps to NM_017617.3 A796A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:139396257 G>A maps to NM_017617.3 P1860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr9:139396749 G>A maps to NM_017617.3 P1786P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr9:139391863 G>A maps to NM_017617.3 I2109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr9:139391770 G>A maps to NM_017617.3 C2140C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr9:139401832 G>A maps to NM_017617.3 S1189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:139391458 G>A maps to NM_017617.3 I2244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr9:139393585 G>A maps to NM_017617.3 D2020D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr9:139390978 C>T maps to NM_017617.3 Q2404Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr9:139412640 G>A maps to NM_017617.3 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:139390780 G>A maps to NM_017617.3 S2470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:139391251 C>T maps to NM_017617.3 R2313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr1:120468307 G>A maps to NM_024408.2 G1377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:120471785 G>A maps to NM_024408.2 C1235C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:120465313 G>A maps to NM_024408.2 L1649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:120510781 G>A maps to NM_024408.2 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr1:120496232 G>A maps to NM_024408.2 C766C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:120539836 T>C maps to NM_024408.2 K178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:120458984 G>T maps to NM_024408.2 A2120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:120497736 G>T maps to NM_024408.2 P715P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr1:120548029 G>A maps to NM_024408.2 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr1:120548054 T>C maps to NM_024408.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:120464977 G>A maps to NM_024408.2 I1698I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:120468082 C>T maps to NM_024408.2 G1452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:120469124 G>A maps to NM_024408.2 P1334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr1:120465349 G>A maps to NM_024408.2 D1637D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr1:120458414 G>A maps to NM_024408.2 I2310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:120458024 G>A maps to NM_024408.2 T2440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:120512161 G>A maps to NM_024408.2 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:120459206 G>A maps to NM_024408.2 P2046P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:120466291 G>A maps to NM_024408.2 S1609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:120483291 G>A maps to NM_024408.2 L1023L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:120512203 G>A maps to NM_024408.2 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr1:145273370 T>C maps to ENST00000454606 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:15271901 G>A maps to NM_000435.2 A2179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:15290070 C>T maps to NM_000435.2 E1161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:15300168 A>G maps to NM_000435.2 N369N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:15273332 C>T maps to NM_000435.2 V1952V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:15302454 C>T maps to NM_000435.2 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr19:15276317 G>A maps to NM_000435.2 I1892I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:15272506 G>A maps to NM_000435.2 L1978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:15300082 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15276852 C>T maps to NM_000435.2 E1804E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15296160 G>A maps to NM_000435.2 R735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15296161 G>A maps to NM_000435.2 A734A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr19:15276260 G>A maps to NM_000435.2 I1911I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:15276215 G>A maps to NM_000435.2 I1926I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr6:32187405 C>T maps to NM_004557.3 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:32169935 G>A maps to NM_004557.3 F1224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:32188875 C>T maps to NM_004557.3 Q226Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:32190477 G>A maps to NM_004557.3 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:32189025 G>A maps to NM_004557.3 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:32188578 C>T maps to NM_004557.3 Q292Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:32190849 C>T maps to NM_004557.3 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr6:32172031 C>T maps to NM_004557.3 G1000G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr6:32190332 G>A maps to NM_004557.3 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr6:32190333 G>A maps to NM_004557.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:32187387 G>A maps to NM_004557.3 F497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr6:32188537 C>T maps to NM_004557.3 W306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:32170079 C>T maps to NM_004557.3 K1176K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr6:32180660 C>T maps to NM_004557.3 Q822Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:32185011 G>A maps to NM_004557.3 I552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:32187405 C>T maps to NM_004557.3 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:32169986 G>A maps to NM_004557.3 V1207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:32188209 G>A maps to NM_004557.3 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr6:32165330 T>C maps to NM_004557.3 E1599E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:32188209 G>A maps to NM_004557.3 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr6:32180269 C>T maps to NM_004557.3 Q887Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr17:79914550 G>A maps to NM_178493.5 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr17:79913409 G>A maps to NM_178493.5 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:79914582 G>A maps to NM_178493.5 Q311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:79913409 G>A maps to NM_178493.5 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:79913409 G>A maps to NM_178493.5 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:79914535 C>T maps to NM_178493.5 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr17:79914799 C>T maps to NM_178493.5 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr8:120429132 G>A maps to NM_002514.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:120435356 C>T maps to NM_002514.3 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:120430337 C>T maps to NM_002514.3 Y117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr14:26949326 C>T maps to ENST00000449198 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr14:26918049 C>T maps to ENST00000449198 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr14:26917365 C>T maps to ENST00000449198 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr14:26917977 G>A maps to ENST00000449198 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr14:26917299 G>A maps to ENST00000449198 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr14:26949268 G>A maps to ENST00000449198 R138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:26917425 C>T maps to ENST00000449198 K438K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr14:26917278 C>T maps to ENST00000449198 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:26917526 G>A maps to ENST00000449198 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr14:26918121 C>T maps to ENST00000449198 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:26917314 G>A maps to ENST00000449198 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr14:26917476 G>A maps to ENST00000449198 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr14:26917365 C>T maps to ENST00000449198 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr14:26917299 G>A maps to ENST00000449198 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr14:26941527 G>A maps to ENST00000449198 Q190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr14:26917365 C>T maps to ENST00000449198 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr19:46443426 G>A maps to NM_002516.2 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr19:46443357 A>G maps to NM_002516.2 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:100118198 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr23:100105230 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:100118163 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:100104845 C>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:100125713 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:100105278 T>A did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:100105196 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr23:100125712 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:100104885 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:100104390 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:100117281 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr23:100104846 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:100105172 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:100117457 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:100125743 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:100103675 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr6:155749974 G>A maps to NM_015718.2 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr6:155732480 C>T maps to NM_015718.2 W441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:155757581 G>A maps to NM_015718.2 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:155732416 C>T maps to NM_015718.2 R462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:155764547 G>A maps to NM_015718.2 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr6:155761094 C>T maps to NM_015718.2 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:155761160 G>A maps to NM_015718.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr6:155732401 C>T maps to NM_015718.2 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:89224396 C>T maps to NM_016931.3 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr11:89155088 G>A maps to NM_016931.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:89184967 G>A maps to NM_016931.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:89135700 C>T maps to NM_016931.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr11:89182644 G>A maps to NM_016931.3 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:89166024 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr15:69320682 C>T maps to NM_024505.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr15:69347813 C>T maps to NM_024505.3 Q714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr15:69335038 G>A maps to NM_024505.3 W514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr15:69335039 G>A maps to NM_024505.3 W514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr15:69318984 G>A maps to NM_024505.3 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr15:69325613 C>T maps to NM_024505.3 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr15:69347776 G>A maps to NM_024505.3 E701E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr15:69335130 C>T maps to NM_024505.3 Q545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr15:69318945 G>A maps to NM_024505.3 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:69329396 C>T maps to NM_024505.3 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:69329471 C>T maps to NM_024505.3 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:69329426 G>T maps to NM_024505.3 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr15:69223035 C>T maps to NM_001184780.1 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:69320592 C>T maps to NM_024505.3 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:69329378 G>A maps to NM_024505.3 W400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:69329483 C>T maps to NM_024505.3 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:69348987 G>A maps to NM_024505.3 K750K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:69325562 C>T maps to NM_024505.3 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr9:140328736 C>T maps to NM_006647.1 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr9:140325753 C>T maps to NM_006647.1 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:2029902 G>A maps to NM_172168.1 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr19:47535944 C>T maps to NM_002517.2 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:47548452 G>A maps to NM_002517.2 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:47535944 C>T maps to NM_002517.2 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:47535944 C>T maps to NM_002517.2 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:47548650 G>A maps to NM_002517.2 Q505Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr19:47535944 C>T maps to NM_002517.2 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:47535944 C>T maps to NM_002517.2 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr19:47542690 G>A maps to NM_002517.2 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:101587466 G>A maps to NM_002518.3 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:101611998 C>T maps to NM_002518.3 V810V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:101564764 C>T maps to NM_002518.3 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:101611914 C>T maps to NM_002518.3 S782S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:101580568 C>T maps to NM_002518.3 C216C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:101564794 C>T maps to NM_002518.3 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:101598754 C>T maps to NM_002518.3 I515I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr14:34269591 C>T maps to NM_001164749.1 S693S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr14:34269612 G>A maps to NM_001164749.1 G700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:34270071 C>T maps to NM_001164749.1 F853F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:34247773 G>A maps to NM_001164749.1 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr14:34269585 C>T maps to NM_001164749.1 F691F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:34029358 G>A maps to NM_001164749.1 Q167Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:34247713 G>A maps to NM_001164749.1 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr11:66192410 C>T maps to NM_178864.3 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:66191398 C>T maps to NM_178864.3 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:66192361 C>T maps to NM_178864.3 P667P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:66192013 G>A maps to NM_178864.3 E551E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:66190193 G>A maps to NM_178864.3 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:66189690 G>A maps to NM_178864.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr11:66190382 A>G maps to NM_178864.3 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr11:66190352 C>T maps to NM_178864.3 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr11:66191068 C>T maps to NM_178864.3 Q277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:66189621 C>T maps to NM_178864.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:66190154 C>T maps to NM_178864.3 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:66189690 G>A maps to NM_178864.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:66192131 C>T maps to NM_178864.3 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:66191884 C>T maps to NM_178864.3 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr11:66191082 G>A maps to NM_178864.3 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:108032497 G>A maps to NM_002519.2 S1105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr11:108064741 G>A maps to NM_002519.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr8:53853378 C>T maps to NM_005285.3 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:53853271 C>T maps to NM_005285.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr20:62737563 G>A maps to NM_005286.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr20:62737682 G>A maps to NM_005286.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr20:62737656 G>A maps to NM_005286.2 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr18:21141429 G>A maps to NM_000271.4 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr18:21121118 G>A maps to NM_000271.4 S809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr18:21121365 G>A maps to NM_000271.4 T759T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:21119922 G>A maps to NM_000271.4 L883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr7:44574087 G>A maps to NM_013389.2 S708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr7:44574125 G>A maps to NM_013389.2 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr7:44578459 C>T maps to NM_013389.2 Q512Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:44556396 G>A maps to NM_013389.2 L1169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:44579890 G>A maps to NM_013389.2 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:44555715 C>T maps to NM_013389.2 R1227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:44561317 C>T maps to NM_013389.2 S982S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:44575516 G>A maps to NM_013389.2 I635I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr7:44578822 C>T maps to NM_013389.2 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:44553138 A>C maps to NM_013389.2 A1329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:44575476 G>A maps to NM_013389.2 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:44573050 G>A maps to NM_013389.2 S796S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:44579356 C>T maps to NM_013389.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:44579758 G>A maps to NM_013389.2 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:44578438 C>T maps to NM_013389.2 K519K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:44579782 C>T maps to NM_013389.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr7:44579080 G>A maps to NM_013389.2 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:44561401 C>A maps to NM_013389.2 V954V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr7:44575875 G>A maps to NM_013389.2 F611F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr7:44578513 G>A maps to NM_013389.2 F494F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr7:44579068 G>A maps to NM_013389.2 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:44553213 C>T maps to NM_013389.2 Q1304Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:44555715 C>T maps to NM_013389.2 R1227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:44560391 C>T maps to NM_013389.2 V1036V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:44560655 C>T maps to NM_013389.2 V1005V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:44579080 G>A maps to NM_013389.2 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:44579752 G>A maps to NM_013389.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:44561763 G>A maps to NM_013389.2 T905T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:44579080 G>A maps to NM_013389.2 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr7:44556924 C>T maps to NM_013389.2 L1083L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:44573116 C>T maps to NM_013389.2 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr7:44578780 G>A maps to NM_013389.2 F405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:139937427 G>A maps to ENST00000371600 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:139935264 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr20:57290243 C>T maps to NM_024663.3 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr20:57274284 C>T maps to NM_024663.3 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr20:57288559 C>T maps to NM_024663.3 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:45681378 G>T maps to NM_006310.3 V613V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr12:53900649 C>T maps to NM_003717.2 W84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr12:53900650 C>T maps to NM_003717.2 W84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:72025857 G>A maps to ENST00000277942 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:72025965 C>T maps to ENST00000277942 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:72026112 G>A maps to ENST00000277942 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr4:73012781 C>T maps to NM_004885.2 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:72994358 G>A maps to NM_004885.2 W119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:73003784 G>A maps to NM_004885.2 K221K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:73012964 C>T maps to NM_004885.2 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:73013192 C>T maps to NM_004885.2 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:73013081 C>T maps to NM_004885.2 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:73013234 C>T maps to NM_004885.2 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr4:73013453 G>A maps to NM_004885.2 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr4:73012772 C>T maps to NM_004885.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr4:73013132 C>T maps to NM_004885.2 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:73013234 C>T maps to NM_004885.2 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:110919262 G>A maps to NM_000272.3 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr2:110881625 G>A maps to NM_000272.3 F648F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:110901147 G>A maps to NM_000272.3 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:132415579 G>A maps to ENST00000393156 I722I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:132438566 T>C maps to ENST00000393156 K167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:132407934 G>A maps to ENST00000393156 L956L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr3:132423120 C>T maps to ENST00000393156 W482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:132403492 C>A maps to ENST00000393156 E1159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:132409387 G>A maps to ENST00000393156 Q893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:5924433 G>A maps to NM_015102.2 L1320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:5964794 G>A maps to NM_015102.2 F675F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr1:6027357 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr1:5947472 G>A maps to NM_015102.2 V786V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:5927848 G>A maps to NM_015102.2 L1141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:5964856 G>A maps to NM_015102.2 Q655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:5925287 G>A maps to NM_015102.2 L1230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:5947472 G>A maps to NM_015102.2 V786V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:5923955 G>A maps to NM_015102.2 S1378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr1:6007207 G>A maps to NM_015102.2 Q359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr19:36340037 C>T maps to NM_004646.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr19:36334397 C>T maps to NM_004646.3 P770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr19:36342371 C>T maps to NM_004646.3 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:36342488 T>G maps to NM_004646.3 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:36340479 G>A maps to NM_004646.3 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr19:36322263 C>T maps to NM_004646.3 E1107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr19:36333296 G>A maps to NM_004646.3 L830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:36333362 C>T maps to NM_004646.3 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:36339881 G>A maps to NM_004646.3 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr19:36330310 G>A maps to NM_004646.3 A979A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr19:36330277 G>A maps to NM_004646.3 V990V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr19:36342506 C>T maps to NM_004646.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr19:36330411 C>T maps to NM_004646.3 Q971Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr19:36322273 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:36322206 C>T maps to NM_004646.3 Q1126Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:36330465 G>A maps to NM_004646.3 T953T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:36330509 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:36332716 G>A maps to NM_004646.3 T905T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:36340551 C>T maps to NM_004646.3 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:36342176 G>A maps to NM_004646.3 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr1:179533842 G>A maps to NM_014625.2 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:179523636 C>T maps to NM_014625.2 W256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:179526182 C>T maps to NM_014625.2 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:179523624 C>T maps to NM_014625.2 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:179520385 C>T maps to NM_014625.2 Q358Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:179533881 G>A maps to NM_014625.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr1:179530462 G>A maps to NM_014625.2 R138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr16:15045784 C>G maps to NM_006985.2 S319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr1:182794923 C>T maps to NM_030769.1 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:182787805 C>T maps to NM_030769.1 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr17:79573812 G>A maps to NM_017921.2 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr17:79539069 G>A maps to NM_017921.2 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr17:79556065 G>A maps to NM_017921.2 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr5:170834759 C>T maps to NM_002520.6 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:106819105 G>A maps to ENST00000503451 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:106848585 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:106861356 C>T maps to ENST00000503451 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr4:106879637 A>G maps to ENST00000503451 Q437Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr1:11907371 C>T maps to NM_006172.3 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:11918269 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:11918409 G>A maps to NM_002521.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr1:153665856 C>T maps to NM_000906.3 L1051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:153660535 C>T maps to NM_000906.3 I752I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:153659520 G>A maps to NM_000906.3 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:153665652 C>T maps to NM_000906.3 R1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:153653109 C>T maps to NM_000906.3 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:153656274 C>T maps to NM_000906.3 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:153665652 C>T maps to NM_000906.3 R1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr1:153665652 C>T maps to NM_000906.3 R1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:153652231 C>T maps to NM_000906.3 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:153661464 C>T maps to NM_000906.3 S818S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:153661482 G>A maps to NM_000906.3 A824A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr9:35800422 C>T maps to NM_003995.3 D387D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:35792845 C>T maps to NM_003995.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr9:35793934 C>T maps to NM_003995.3 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:35800026 C>T maps to NM_003995.3 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:35801079 C>T maps to NM_003995.3 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:35802511 C>T maps to NM_003995.3 Q575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr9:35805667 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr9:35805668 T>A did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr5:32774911 G>A maps to ENST00000265074 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr5:32712193 G>A maps to ENST00000265074 E104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:32724810 C>T maps to ENST00000265074 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:32739084 C>T maps to ENST00000265074 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:32774911 G>A maps to ENST00000265074 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:50385295 G>A maps to NM_006545.4 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:142605 G>A maps to ENST00000399953 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:167368 G>A maps to ENST00000399953 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr16:148259 G>A maps to ENST00000399953 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:34888269 C>T maps to NM_207172.1 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr7:34851446 C>T maps to NM_207172.1 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:34851464 C>T maps to NM_207172.1 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr7:34889185 A>G maps to NM_207172.1 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr7:34867077 C>T maps to NM_207172.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:34888188 G>A maps to NM_207172.1 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:34884511 G>A maps to NM_207172.1 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:34889260 C>T maps to NM_207172.1 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr7:34884511 G>A maps to NM_207172.1 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:34851455 C>T maps to NM_207172.1 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:34867175 G>A maps to NM_207172.1 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:34851464 C>T maps to NM_207172.1 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:34874055 G>A maps to NM_207172.1 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:34724192 C>T maps to NM_207172.1 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:34874043 C>T maps to NM_207172.1 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:34698053 C>T maps to NM_207172.1 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr7:34724228 T>A maps to NM_207172.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:34851468 C>T maps to NM_207172.1 Q158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr7:34851464 C>T maps to NM_207172.1 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:34867059 C>T maps to NM_207172.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr7:34888236 C>T maps to NM_207172.1 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr7:34851419 C>T maps to NM_207172.1 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr7:34724189 C>T maps to NM_207172.1 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr7:34698171 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:34889215 G>A maps to NM_207172.1 E355E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr7:34698053 C>T maps to NM_207172.1 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr7:34724174 G>A maps to NM_207172.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:34851464 C>T maps to NM_207172.1 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr7:34851464 C>T maps to NM_207172.1 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr7:34851443 C>A maps to NM_207172.1 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:34888122 C>T maps to NM_207172.1 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:34888230 C>T maps to NM_207172.1 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:34889176 G>A maps to NM_207172.1 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr15:73889471 G>A maps to NM_012428.3 D110D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:78445620 G>A maps to NM_002522.3 Q330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr7:98254456 C>T maps to NM_002523.2 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr7:98254309 C>T maps to NM_002523.2 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:98254282 C>T maps to NM_002523.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr7:98249157 C>T maps to NM_002523.2 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr7:98254432 G>A maps to NM_002523.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr7:98256640 C>T maps to NM_002523.2 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:98256640 C>T maps to NM_002523.2 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:98256592 G>A maps to NM_002523.2 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:98257928 C>T maps to NM_002523.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr7:98257817 C>T maps to NM_002523.2 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr7:98254426 C>T maps to NM_002523.2 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr22:39218643 G>A maps to NM_014293.2 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:39218643 G>A maps to NM_014293.2 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:39224439 C>T maps to NM_014293.2 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr22:39219261 G>A maps to NM_014293.2 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:25266432 C>T maps to NM_022150.3 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr7:25266531 G>A maps to NM_022150.3 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr7:25266387 C>T maps to NM_022150.3 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr7:24325032 C>T maps to NM_000905.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:24324906 G>T maps to NM_000905.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:164247433 G>A maps to NM_000909.4 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr4:164246547 C>T maps to NM_000909.4 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:164246484 G>A maps to NM_000909.4 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:164246628 G>A maps to NM_000909.4 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:164246628 G>A maps to NM_000909.4 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:164247475 G>A maps to NM_000909.4 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:164247319 G>A maps to NM_000909.4 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr4:164246514 C>T maps to NM_000909.4 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr4:164247610 A>G maps to NM_000909.4 D32D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr4:164247556 C>T maps to NM_000909.4 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr4:156135507 C>T maps to NM_000910.2 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:156135364 C>T maps to NM_000910.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr4:156136185 C>T maps to NM_000910.2 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr4:156136098 C>T maps to NM_000910.2 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:156136011 C>T maps to NM_000910.2 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:156136173 G>A maps to NM_000910.2 K361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:156135438 G>A maps to NM_000910.2 W116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:156135354 C>T maps to NM_000910.2 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:156135567 G>A maps to NM_000910.2 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:156135818 G>A maps to NM_000910.2 W243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:156135318 C>T maps to NM_000910.2 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:156136173 G>A maps to NM_000910.2 K361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:156136098 C>T maps to NM_000910.2 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr4:156135759 C>T maps to NM_000910.2 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:156135201 G>A maps to NM_000910.2 E37E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:156135672 C>T maps to NM_000910.2 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:156135765 G>A maps to NM_000910.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr4:156135354 C>T maps to NM_000910.2 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr4:164271505 C>T maps to NM_006174.2 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr4:164272237 C>T maps to NM_006174.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr4:164272438 G>A maps to NM_006174.2 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr4:164272411 C>T maps to NM_006174.2 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:164271931 C>T maps to NM_006174.2 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:164272237 C>T maps to NM_006174.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr4:164272411 C>T maps to NM_006174.2 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr4:164272297 G>A maps to NM_006174.2 K291K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:164272153 C>A maps to NM_006174.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:164271862 C>T maps to NM_006174.2 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:164272254 G>A maps to NM_006174.2 W277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:164271658 C>T maps to NM_006174.2 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr6:3015826 C>T maps to NM_000904.3 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:30322749 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:30327362 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:30327044 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:38253336 C>T maps to NM_021724.3 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:23997549 G>T maps to NM_005126.4 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:23996175 C>T maps to NM_005126.4 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:24003558 C>T maps to NM_005126.4 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:50882434 C>T maps to NM_007121.4 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:50882335 C>T maps to NM_007121.4 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:50881014 C>T maps to NM_007121.4 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr19:50882383 C>T maps to NM_007121.4 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:47290145 C>A maps to NM_005693.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:47282909 C>T maps to NM_005693.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr11:47283528 C>T maps to NM_005693.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr12:100926344 G>A maps to ENST00000392986 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr12:100928737 C>T maps to ENST00000392986 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:119528943 C>T maps to NM_022002.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:119536040 C>T maps to NM_022002.2 F468F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:119526123 G>A maps to NM_022002.2 W48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:15057666 G>A maps to NM_003298.3 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr6:108499446 T>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:108497821 C>T maps to ENST00000368983 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr6:108497890 C>T maps to ENST00000368983 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:108502807 C>T maps to ENST00000368983 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr6:108492755 C>T maps to ENST00000368983 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr6:108502053 C>T maps to ENST00000368983 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr15:72109898 G>A maps to NM_014249.2 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr15:72109898 G>A maps to NM_014249.2 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:72105970 A>G maps to NM_014249.2 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr15:72104814 C>T maps to NM_014249.2 N237N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr5:92929448 C>T maps to NM_005654.4 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr5:92929367 C>T maps to NM_005654.4 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:92923969 C>T maps to NM_005654.4 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:96880661 G>A maps to NM_021005.3 Q352Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr19:17351501 G>A maps to NM_005234.3 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr5:142689667 G>A maps to NM_001024094.1 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:142779582 G>A maps to NM_001024094.1 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:142779717 C>T maps to NM_001024094.1 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr4:149075933 G>A maps to ENST00000511528 I715I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr4:149115959 G>A maps to ENST00000511528 R655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:149357070 C>T maps to ENST00000511528 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:149356725 T>C maps to ENST00000511528 Q429Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:149075852 G>T maps to ENST00000511528 P742P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:149073663 C>T maps to ENST00000511528 T826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:149075933 G>A maps to ENST00000511528 I715I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr12:52448609 T>G maps to ENST00000360284 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:52451273 C>T maps to ENST00000360284 V554V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr12:52450362 C>T maps to ENST00000360284 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:52451237 C>T maps to ENST00000360284 A542A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr2:157183339 G>A maps to NM_006186.3 I417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:157183324 C>T maps to NM_006186.3 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:157186668 G>A maps to NM_006186.3 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:157186236 C>T maps to NM_006186.3 Q154Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:157186170 G>A maps to NM_006186.3 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr9:102590755 C>T maps to NM_173200.1 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:102607112 C>T maps to NM_173200.1 V490V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:102609856 C>T maps to NM_173200.1 I542I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:127245120 C>T maps to NM_004959.4 K434K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr9:127253504 C>T maps to NM_004959.4 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr9:127262842 G>A maps to NM_004959.4 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:127262836 G>A maps to NM_004959.4 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:199996998 G>A maps to NM_205860.1 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:200090048 C>T maps to NM_205860.1 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:200080355 G>A maps to NM_205860.1 Q379Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:200143152 C>T maps to NM_205860.1 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:200017831 C>T maps to NM_205860.1 N332N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:200017309 C>T maps to NM_205860.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:200090048 C>T maps to NM_205860.1 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:200143283 G>A maps to NM_205860.1 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:200080415 G>A maps to NM_205860.1 K399K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:200017918 G>A maps to NM_205860.1 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:200090063 C>T maps to NM_205860.1 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:200008807 C>T maps to NM_205860.1 H29H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:200143253 A>G maps to NM_205860.1 E514E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:200017897 C>T maps to NM_205860.1 F354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:127298173 G>A maps to NM_033334.2 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:127300561 C>T maps to NM_033334.2 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr9:127298250 G>A maps to NM_033334.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:127300525 G>A maps to NM_033334.2 Y223Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:127302412 C>T maps to NM_033334.2 E165E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr10:115350519 C>T maps to ENST00000369358 K1599K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr10:115365968 G>T maps to ENST00000369358 R1267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:115349448 C>T maps to ENST00000369358 R1696R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:115411666 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr10:115389532 C>T maps to ENST00000369358 K626K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr10:115350561 G>A maps to ENST00000369358 F1585F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:115389427 C>T maps to ENST00000369358 R661R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:115393909 C>T maps to ENST00000369358 Q496Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr10:115374690 T>C maps to ENST00000369358 E1039E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr10:115391666 C>T maps to ENST00000369358 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr10:115411615 C>T maps to ENST00000369358 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:115391683 C>A maps to ENST00000369358 G558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:115406705 C>T maps to ENST00000369358 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:115412771 G>A maps to ENST00000369358 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:115384620 G>A maps to ENST00000369358 F779F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:115256529 G>A maps to NM_002524.3 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:115256578 C>A maps to NM_002524.3 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:115258668 A>G did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:144919302 G>A maps to NM_178564.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:144919434 G>A maps to NM_178564.3 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr8:144918152 G>A maps to NM_178564.3 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr7:107834553 G>A maps to ENST00000379032 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:107872916 G>A maps to ENST00000379032 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr7:107834799 A>T maps to ENST00000379032 I512I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:107807504 C>T maps to ENST00000379032 W1109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr7:107872848 G>A maps to ENST00000379032 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:52290998 G>A maps to NM_002525.2 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:52344245 C>T maps to NM_002525.2 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:52293522 G>A maps to NM_002525.2 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:52343947 G>A maps to NM_002525.2 R114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:52343948 G>A maps to NM_002525.2 Y113Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:52264052 G>A maps to NM_002525.2 A892A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:129348934 C>T maps to ENST00000393231 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr8:32505268 C>T maps to NM_013959.3 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr8:32621853 G>A maps to NM_013956.3 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr8:32463201 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:32621460 G>A maps to NM_013956.3 E493E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr8:32505724 T>C maps to NM_013959.3 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:32621577 G>A maps to NM_013956.3 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:32621313 C>T maps to NM_013956.3 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr8:32611947 C>T maps to NM_013956.3 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:32505584 T>C maps to NM_013959.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:32585530 C>T maps to NM_013956.3 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:32617768 C>T maps to NM_013956.3 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr8:32621490 C>T maps to NM_013956.3 F503F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:32505808 C>T maps to NM_013959.3 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:32613920 G>A maps to NM_013956.3 K273K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:32453406 C>T maps to NM_013956.3 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:31498132 C>T maps to NM_013962.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:32505268 C>T maps to NM_013959.3 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:32585566 C>T maps to NM_013956.3 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:32472035 C>T maps to NM_013956.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr5:139422084 C>T maps to NM_013982.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr5:139251406 G>A maps to NM_013982.2 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:139251313 G>A maps to NM_013982.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr5:139232075 C>T maps to NM_013982.2 G503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr10:84718704 G>A maps to ENST00000404547 K386K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:84711312 C>T maps to ENST00000404547 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr10:84738843 G>A maps to ENST00000404547 R517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr10:84718753 A>T maps to ENST00000404547 K403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:83635815 C>T maps to ENST00000404547 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:84738843 G>A maps to ENST00000404547 R517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr10:84718704 G>A maps to ENST00000404547 K386K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr10:84745000 C>T maps to ENST00000404547 I601I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr10:84738861 G>A maps to ENST00000404547 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:84118498 G>A maps to ENST00000404547 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr10:84738846 C>T maps to ENST00000404547 I518I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr10:84498389 C>T maps to ENST00000404547 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:84711288 C>T maps to ENST00000404547 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr10:83635776 G>A maps to ENST00000404547 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr21:16340212 G>A maps to NM_003489.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr21:16339139 A>T maps to NM_003489.3 V458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:16339672 G>A maps to NM_003489.3 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr12:2943929 G>A maps to NM_031474.2 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:2936808 C>T maps to NM_031474.2 Q245Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr11:9009763 G>A maps to NM_020645.2 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr23:105178360 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:105075049 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:105137832 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:105150461 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:105153172 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr23:105178249 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr23:105139464 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:105197108 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:105179202 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:105169002 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr23:105153187 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:105152851 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr23:105152737 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr23:105152792 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:105168802 G>A did not map to a codon.
Sequencing variant TCGA-EE-A17Z-06A-11D-A196-08 chr23:105178258 G>C did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:105181564 A>T did not map to a codon.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr23:105193600 T>A did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr23:105168760 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:105150442 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr23:105153187 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:105137868 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr23:105168831 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr23:105168888 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr23:105168905 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:105184002 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:105178248 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:105189953 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr23:105132292 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:105152765 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr23:105137923 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr23:105179257 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:105137921 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:105139434 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:105150409 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:105142615 G>A did not map to a codon.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr23:105152842 C>T did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:105167251 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:105153630 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr23:105189980 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr23:105183927 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr23:105150501 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:105189953 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:105150461 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:105152871 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:105153048 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:105167205 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:105168910 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:105150503 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:105167131 G>A did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr23:105153271 G>A did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr23:105193628 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:105179308 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr23:105153108 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:24551934 G>A maps to NM_006177.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:24552050 G>A maps to NM_006177.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:24552051 G>A maps to NM_006177.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:30658015 G>A maps to NM_007243.1 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:30657976 G>A maps to NM_007243.1 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:67920137 C>T maps to NM_198443.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:33486587 G>A maps to NM_003873.5 T638T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:33491906 C>T maps to NM_003873.5 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr10:33545361 T>G maps to NM_003873.5 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr10:33481309 C>T maps to NM_003873.5 W654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:33475372 C>T maps to NM_003873.5 K702K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr10:33469204 G>A maps to NM_003873.5 I857I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr10:33545301 C>T maps to NM_003873.5 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr10:33469009 C>T maps to NM_003873.5 E922E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr10:33552607 G>A maps to NM_003873.5 Y208Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:33502595 G>A maps to NM_003873.5 D444D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:33552742 G>A maps to NM_003873.5 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:33481251 C>T maps to NM_003873.5 W673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:33502445 G>A maps to NM_003873.5 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:33502472 G>A maps to NM_003873.5 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr2:206608068 C>T maps to NM_201266.1 I478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr2:206630208 G>A maps to NM_201266.1 E773E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:206659622 G>A maps to NM_201266.1 L879L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:206590787 C>T maps to NM_201266.1 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr2:206610480 G>A maps to NM_201266.1 G551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:206605370 C>T maps to NM_201266.1 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:206580964 C>T maps to NM_201266.1 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:206659664 C>T maps to NM_201266.1 S893S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:206562289 G>A maps to NM_201266.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr2:206659640 C>T maps to NM_201266.1 G885G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr2:206659775 G>A maps to NM_201266.1 E930E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:206610474 C>T maps to NM_201266.1 F549F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:206628458 C>T maps to NM_201266.1 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:206580991 C>T maps to NM_201266.1 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:206608233 G>A maps to NM_201266.1 K533K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr2:206641045 C>T maps to NM_018534.3 Y839Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr6:24145855 C>T maps to NM_080723.4 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:24145990 G>A maps to NM_080723.4 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:24134689 G>A maps to NM_080723.4 E45E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:24134671 C>T maps to NM_080723.4 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:24145855 C>T maps to NM_080723.4 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr20:333859 C>T maps to NM_024958.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr20:334185 C>T maps to NM_024958.2 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:50724556 G>A maps to ENST00000404971 F971F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr2:50850703 G>A maps to ENST00000404971 Y327Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:51255168 C>T maps to ENST00000404971 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:50765610 C>T maps to ENST00000404971 V681V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D3-A51R-06A-11D-A25O-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:51255021 G>A maps to ENST00000404971 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr2:51254886 C>T maps to ENST00000404971 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:51254829 G>A maps to ENST00000404971 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr2:50733642 C>T maps to ENST00000404971 Q869Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:51254949 G>A maps to ENST00000404971 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:50780136 C>T maps to ENST00000404971 R489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr2:50779743 G>A maps to ENST00000404971 F620F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:50318476 G>A maps to ENST00000404971 I1274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:51255177 G>A maps to ENST00000404971 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr2:50765511 C>T maps to ENST00000404971 K714K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr2:50758400 G>A maps to ENST00000404971 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:50779773 C>T maps to ENST00000404971 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:51253596 G>A maps to ENST00000404971 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:50464100 C>T maps to ENST00000404971 T1164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr2:50724508 C>T maps to ENST00000404971 G987G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:50282131 G>A maps to ENST00000404971 R1297*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-FW-A3R5-06A-11D-A23B-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:51253596 G>A maps to ENST00000404971 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:51254946 G>A maps to ENST00000404971 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:50724619 C>T maps to ENST00000404971 K950K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:50765706 C>T maps to ENST00000404971 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:51255006 G>A maps to ENST00000404971 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr2:50573967 G>A maps to NM_138735.2 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr2:50699454 C>T maps to ENST00000404971 Q1115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:64418794 G>A maps to NM_015080.3 A950A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:64416263 G>A maps to NM_015080.3 L1075L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:64375231 G>A maps to NM_015080.3 T1525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:64375246 G>A maps to NM_015080.3 V1520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:64421194 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:64402787 C>T maps to NM_015080.3 R1180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:64453330 C>T maps to NM_015080.3 E313E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:64421180 G>A maps to NM_015080.3 V801V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr11:64419052 G>A maps to NM_015080.3 I864I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr11:64390347 C>T maps to NM_015080.3 A1350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr11:64453287 G>A maps to NM_015080.3 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64390362 G>A maps to NM_015080.3 S1345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64397936 G>A maps to NM_015080.3 R1232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64417929 G>A maps to NM_015080.3 L1033L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64427843 C>T maps to NM_015080.3 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:64374928 C>T maps to NM_015080.3 V1626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr14:80328033 G>A maps to NM_004796.4 R971R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr14:79175876 C>T maps to NM_004796.4 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr14:79746864 C>T maps to ENST00000440563 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:80328214 C>T maps to NM_004796.4 Q1032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr14:80130179 G>A maps to NM_004796.4 E795E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:79181282 C>T maps to NM_004796.4 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr14:79175786 G>A maps to NM_004796.4 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:79117587 C>T maps to NM_004796.4 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:79423657 G>A maps to NM_004796.4 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:79181201 C>T maps to NM_004796.4 N215N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:79181111 G>A maps to NM_004796.4 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr14:79181307 C>T maps to NM_004796.4 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr14:79181465 A>G maps to NM_004796.4 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr14:79270137 G>A maps to NM_004796.4 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr14:79454458 T>C maps to NM_004796.4 S706S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr14:79432482 C>T maps to NM_004796.4 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr14:79181156 C>T maps to NM_004796.4 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr14:79434616 T>C maps to NM_004796.4 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:79433633 G>A maps to NM_004796.4 W581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr14:80158558 C>T maps to NM_001105250.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr5:176631247 C>T maps to NM_022455.4 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:176637325 T>A maps to NM_022455.4 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr5:176721286 C>T maps to NM_022455.4 S2306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:176638324 C>T maps to NM_022455.4 S975S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:176719085 C>T maps to NM_022455.4 L2130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:176709572 C>T maps to NM_022455.4 T2000T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr5:176721949 G>A maps to NM_022455.4 W2527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr5:176696737 C>T maps to NM_022455.4 F1813F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr5:176638264 T>C maps to NM_022455.4 V955V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:176638708 C>T maps to NM_022455.4 D1103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:176707783 C>T maps to NM_022455.4 F1947F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:176636776 C>T maps to NM_022455.4 D459D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr5:176700721 G>A maps to NM_022455.4 E1853E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr23:152037543 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:152037580 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:152034496 C>T did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:152037406 C>T did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:152037407 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr20:1424411 G>A maps to ENST00000476071 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr20:1447409 C>T maps to ENST00000476071 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr8:59547753 G>A maps to NM_001144772.1 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr8:59508132 A>G maps to NM_001144772.1 Y657Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr8:59511824 T>C maps to NM_001144772.1 K548K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr8:59515880 G>A maps to NM_001144772.1 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr8:59515916 C>T maps to NM_001144772.1 E330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:27244393 T>C maps to NM_145080.3 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr16:27238130 G>A maps to NM_145080.3 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:6611114 G>A maps to NM_017755.5 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:6620226 G>A maps to NM_017755.5 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr5:6611114 G>A maps to NM_017755.5 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr5:6632737 G>A maps to NM_017755.5 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:6600041 C>T maps to NM_017755.5 R767R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:93813944 C>T maps to NM_022072.3 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:46810567 C>T maps to NM_199044.2 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:46810470 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr1:46818684 G>A maps to NM_199044.2 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:46810804 C>T maps to NM_199044.2 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:72717956 G>A maps to NM_148956.2 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr7:72718302 G>A maps to NM_148956.2 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr7:72718004 G>A maps to NM_148956.2 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr7:72717595 C>T maps to NM_018044.3 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:72717688 G>A maps to NM_148956.2 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr10:18874970 G>A maps to NM_182543.2 Q277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:18840780 G>A maps to NM_182543.2 Q348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:40778151 G>A maps to NM_024677.4 W304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr4:40796464 G>A maps to NM_024677.4 Q418Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr4:40810325 G>A maps to NM_024677.4 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr4:40810394 G>A maps to NM_024677.4 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr4:40810383 C>T maps to NM_024677.4 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:40778244 G>A maps to NM_024677.4 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:40126933 C>T maps to NM_032526.1 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:40131881 G>A maps to NM_032526.1 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr1:40126861 G>A maps to NM_032526.1 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:40129047 C>T maps to NM_032526.1 K164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:18757620 C>T maps to ENST00000455492 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr2:18766202 G>A maps to ENST00000455492 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:18767595 C>T maps to ENST00000455492 W138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr2:18766226 C>T maps to ENST00000455492 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:18765452 C>T maps to ENST00000455492 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr2:18766241 G>A maps to ENST00000455492 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr2:18768804 C>T maps to ENST00000455492 K28K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr2:18764167 C>T maps to ENST00000455492 V406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr2:18765812 G>A maps to ENST00000455492 Y307Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:18765521 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:18765452 C>T maps to ENST00000455492 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:18745385 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:18765359 G>A maps to ENST00000455492 F372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr7:33063711 C>T maps to NM_001002010.1 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:33059299 A>T maps to NM_001002010.1 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:39985092 C>A maps to NM_052935.4 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr17:39992140 G>A maps to NM_052935.4 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:39985107 G>A maps to NM_052935.4 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:52562555 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:52568561 G>A maps to NM_022908.2 N36N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:52563344 G>A maps to NM_001134231.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr3:52561703 G>A maps to NM_001134231.1 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:104171642 G>A maps to NM_001031701.2 F537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr12:104171813 G>A maps to NM_001031701.2 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:104179184 G>A maps to NM_001031701.2 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:104187198 G>A maps to NM_001031701.2 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:104190779 G>A maps to NM_001031701.2 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr12:104174100 C>T maps to NM_001031701.2 W457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr12:104190779 G>A maps to NM_001031701.2 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr6:86197191 G>A maps to NM_002526.2 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:86181078 C>T maps to NM_002526.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr6:86197122 G>A maps to NM_002526.2 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:17207001 G>C maps to ENST00000379552 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:5604141 C>T maps to NM_001102654.1 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:5604141 C>T maps to NM_001102654.1 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:5604141 C>T maps to NM_001102654.1 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr12:5603427 C>T maps to NM_001102654.1 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:5603409 C>T maps to NM_001102654.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:5603721 C>T maps to NM_001102654.1 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:5603769 G>A maps to NM_001102654.1 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:5603667 G>A maps to NM_001102654.1 Q109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:49564674 G>A maps to NM_006179.4 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr16:2093625 A>T maps to NM_002528.5 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr16:2097827 G>A maps to NM_002528.5 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr16:2096347 G>A maps to NM_002528.5 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:132177685 C>T maps to NM_001144058.1 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:132184490 C>T maps to NM_001144058.1 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:131781524 G>A maps to NM_001144058.1 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:2522768 C>T maps to NM_006181.1 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:96104249 C>T maps to NM_021229.3 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr12:96180893 G>A maps to NM_021229.3 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr12:96076519 C>T maps to NM_021229.3 W491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:96059655 G>A maps to NM_021229.3 F560F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:96063852 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:96059664 C>T maps to NM_021229.3 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:96076519 C>T maps to NM_021229.3 W491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr19:49173970 G>A maps to NM_145807.1 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr19:49167499 G>T maps to NM_145807.1 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:49167854 G>A maps to NM_145807.1 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:49166723 G>A maps to NM_145807.1 D367D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:49166768 C>T maps to NM_145807.1 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:107867517 G>A maps to NM_001113226.1 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr1:107973429 C>T maps to NM_001113226.1 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:107937868 G>A maps to NM_001113226.1 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:108023380 C>T maps to NM_001113226.1 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:108023381 C>T maps to NM_001113226.1 Q514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr1:107867109 C>T maps to NM_001113226.1 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:107867319 C>T maps to NM_001113226.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr1:107866962 C>T maps to NM_001113226.1 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr9:135102364 G>A maps to NM_032536.2 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:135073589 C>T maps to NM_032536.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr9:135073873 G>A maps to NM_032536.2 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:156837937 C>T maps to NM_002529.3 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:156844178 C>T maps to NM_002529.3 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:156845905 C>T maps to NM_002529.3 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:156851295 C>T maps to NM_002529.3 A751A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:156844393 G>A maps to NM_002529.3 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:156848977 C>T maps to NM_002529.3 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:156834184 C>T maps to NM_002529.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:156849840 C>T maps to NM_002529.3 I699I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:156851340 G>A maps to NM_002529.3 R766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:156834552 G>A maps to NM_002529.3 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:156834178 G>A maps to NM_002529.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:156843533 C>T maps to NM_002529.3 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:156843674 C>T maps to NM_002529.3 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:156845884 C>T maps to NM_002529.3 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:87359969 C>T maps to NM_006180.3 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr9:87482206 T>C maps to NM_006180.3 H498H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:87339158 G>A maps to NM_006180.3 Q247Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:87482335 G>A maps to NM_006180.3 K541K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr15:88679835 A>T maps to NM_001012338.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr15:88669547 G>A maps to NM_001012338.1 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr15:88472451 G>A maps to NM_001012338.1 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr15:88423560 C>T maps to NM_001012338.1 V758V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:88483955 G>A maps to NM_001012338.1 I538I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr15:88476247 G>A maps to NM_001012338.1 F628F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:88524487 C>T maps to NM_001007156.1 Q563Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr15:88476382 C>T maps to NM_001012338.1 K583K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr15:88420242 A>G maps to NM_001012338.1 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr15:88423522 C>T maps to NM_001012338.1 W771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:88423557 G>A maps to NM_001012338.1 I759I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:88476247 G>A maps to NM_001012338.1 F628F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr15:88483883 C>A maps to NM_001012338.1 P562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr15:88669598 G>A maps to NM_001012338.1 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr15:88476250 C>T maps to NM_001012338.1 K627K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr15:88522626 G>A maps to NM_001007156.1 I596I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:88420240 C>T maps to NM_001012338.1 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:88472475 C>T maps to NM_001012338.1 V693V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:88476367 C>T maps to NM_001012338.1 E588E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:88476385 C>T maps to NM_001012338.1 R582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:88669547 G>A maps to NM_001012338.1 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:88678497 C>T maps to NM_001012338.1 K346K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:88423517 G>A maps to NM_001012338.1 Q773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:88680698 G>A maps to NM_001012338.1 N186N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:88726710 C>T maps to NM_001012338.1 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr15:88423593 G>A maps to NM_001012338.1 F747F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr12:86276089 G>A maps to NM_006183.3 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:61341149 C>T maps to NM_002531.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:61341150 C>T maps to NM_002531.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr20:61340783 G>A maps to NM_002531.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr20:61386056 C>T maps to NM_002531.2 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:61391528 G>A maps to NM_002531.2 R389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:11802204 G>A maps to NM_012344.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr2:11802192 G>A maps to NM_012344.3 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:11802345 G>A maps to NM_012344.3 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:11809799 G>A maps to NM_012344.3 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:106460687 C>T maps to NM_014840.2 K626K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:106480592 G>A maps to NM_014840.2 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr12:106461155 C>T maps to NM_014840.2 K470K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:106460734 G>A maps to NM_014840.2 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr12:106461485 G>A maps to NM_014840.2 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:106461651 C>T maps to NM_014840.2 W305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr12:106461155 C>T maps to NM_014840.2 K470K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:106460849 G>A maps to NM_014840.2 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:106461005 C>T maps to NM_014840.2 R520R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr12:106460744 G>A maps to NM_014840.2 F607F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:106461461 C>T maps to NM_014840.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:205272819 G>A maps to ENST00000441520 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:205273168 G>A maps to ENST00000441520 I476I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:205277744 G>A maps to ENST00000441520 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr1:205273081 G>A maps to ENST00000441520 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:205272646 G>A maps to ENST00000441520 S650S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:205280896 G>A maps to ENST00000441520 H140H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:205273114 C>T maps to ENST00000441520 K494K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:205272733 G>A maps to ENST00000441520 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:205272895 G>A maps to ENST00000441520 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:205273192 C>T maps to ENST00000441520 E468E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:205273429 C>T maps to ENST00000441520 E389E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr7:151074235 G>A maps to ENST00000355851 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr7:151052944 C>T maps to ENST00000355851 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:151073880 C>T maps to ENST00000355851 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr7:151072974 C>T maps to ENST00000355851 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr16:10855240 C>T maps to NM_002484.2 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr16:10861803 A>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:10850584 C>T maps to NM_002484.2 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr16:1836595 C>T maps to NM_012225.2 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:1838654 C>T maps to NM_012225.2 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:32328365 T>C maps to NM_025152.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:49416798 C>T maps to NM_006184.5 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:17316983 C>T maps to ENST00000458064 H38H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:17323409 C>T maps to ENST00000458064 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:205687457 T>A maps to NM_022731.4 K228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr1:205696888 G>A maps to NM_022731.4 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr1:205696888 G>A maps to NM_022731.4 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:27269435 C>T maps to NM_006600.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:110255462 G>A maps to NM_032869.3 A509A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr7:44530079 G>A maps to NM_015332.3 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:44444177 G>T maps to NM_015332.3 S216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr23:51076065 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr10:74884002 G>A maps to NM_015901.4 E130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr3:131100666 C>T maps to NM_152395.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr16:4743801 C>T maps to NM_032349.3 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr1:145587473 T>C maps to NM_001012758.2 Q202Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr9:34339150 G>A maps to NM_147173.1 W38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr16:56485105 C>A maps to NM_007006.2 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr16:56485054 G>A maps to NM_007006.2 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:63996738 C>T maps to NM_032344.2 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr6:34256605 G>C maps to NM_006703.2 S148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr12:93793085 C>T maps to NM_199040.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:93793085 C>T maps to NM_199040.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:77775525 C>T maps to NM_001105663.1 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:77775585 C>T maps to NM_001105663.1 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr16:77775735 C>T maps to NM_001105663.1 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr16:77769817 G>T maps to NM_001105663.1 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr16:77775564 C>T maps to NM_001105663.1 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:163298689 A>T maps to NM_145697.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:163310152 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr1:163317605 G>A maps to NM_145697.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr1:163307841 C>T maps to NM_145697.2 N156N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:163295906 C>T maps to NM_145697.2 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:163295963 G>A maps to NM_145697.2 K41K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr13:45554048 C>T maps to NM_012345.2 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr17:27613813 G>A maps to NM_020772.2 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr17:27613814 G>A maps to NM_020772.2 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr11:71732259 G>A maps to ENST00000393695 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:71721863 G>A maps to ENST00000393695 Q1569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:71727570 G>A maps to ENST00000393695 C381C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:71726465 G>A maps to ENST00000393695 Q701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:71724482 G>A maps to ENST00000393695 L1362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:71724777 G>A maps to ENST00000393695 A1263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr11:71720189 C>T maps to ENST00000393695 Q1633Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U9-06A-11D-A32N-08 chr11:71724438 C>T maps to ENST00000393695 L1376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr14:73822357 G>A maps to NM_001005743.1 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr14:73753938 C>T maps to NM_001005743.1 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr14:73749085 T>C maps to NM_001005743.1 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr14:73783130 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:41188698 T>G maps to NM_004756.3 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr19:41186950 G>A maps to NM_004756.3 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:41186938 G>A maps to NM_004756.3 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:69136223 G>A maps to NM_020401.2 G920G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:229613412 G>A maps to NM_018230.2 Q563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:229631306 A>C maps to NM_018230.2 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:17649489 G>A maps to ENST00000430136 I510I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr6:17637498 G>A maps to ENST00000430136 T814T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:17675477 G>A maps to ENST00000430136 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:37342741 G>A maps to NM_153485.1 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:37350280 T>C maps to NM_153485.1 Q270Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:37309284 G>A maps to NM_153485.1 Q905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr5:37318089 C>A maps to NM_153485.1 E769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr5:37341335 A>G maps to NM_153485.1 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr5:37294508 G>A maps to NM_153485.1 F1284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:47837084 G>A maps to NM_015231.1 H544H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:47827778 C>T maps to NM_015231.1 K844K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:47804705 G>A maps to NM_015231.1 D1345D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:47843340 C>T maps to NM_015231.1 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr11:47827790 G>A maps to NM_015231.1 F840F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:47833672 G>A maps to NM_015231.1 F728F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr9:131735485 C>T maps to NM_015354.1 F387F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:131745610 T>C maps to NM_015354.1 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:131768354 C>T maps to NM_015354.1 T1632T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr9:131761555 C>T maps to NM_015354.1 F1207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr9:131752414 C>T maps to NM_015354.1 N850N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr9:131742985 G>A maps to NM_015354.1 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr9:131745238 C>T maps to NM_015354.1 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:131745226 C>T maps to NM_015354.1 V572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr7:135261108 C>T maps to NM_015135.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:135315145 C>T maps to NM_015135.2 Q1663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr7:135269643 C>T maps to NM_015135.2 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr7:135328087 C>T maps to NM_015135.2 P1847P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr7:135282768 C>T maps to NM_015135.2 S696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:135286116 G>T did not map to a codon.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr3:13360632 G>A maps to NM_024923.2 P1834P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:13361446 G>A maps to NM_024923.2 F1733F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr3:13401822 G>T maps to NM_024923.2 R701R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:13367351 G>A maps to NM_024923.2 A1529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr3:13381750 G>A maps to NM_024923.2 I1092I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr3:13393591 G>A maps to NM_024923.2 H907H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:13415265 C>T maps to NM_024923.2 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:13368906 G>A maps to NM_024923.2 P1439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr3:13363297 C>T maps to NM_024923.2 T1651T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr3:13368918 G>A maps to NM_024923.2 I1435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr3:13370431 G>A maps to NM_024923.2 S1375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr3:13367411 G>A maps to NM_024923.2 S1509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:13417925 G>A maps to NM_024923.2 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:13379372 G>A maps to NM_024923.2 I1172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:13438929 G>A maps to NM_024923.2 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:13381494 G>A maps to NM_024923.2 I1110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr3:13378340 G>A maps to NM_024923.2 F1210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:13361446 G>A maps to NM_024923.2 F1733F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:13363278 G>A maps to NM_024923.2 L1658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:13363723 G>A maps to NM_024923.2 F1628F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:13363828 G>A maps to NM_024923.2 T1593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:13381425 G>A maps to NM_024923.2 I1133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:13381783 G>A maps to NM_024923.2 F1081F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:13381425 G>A maps to NM_024923.2 I1133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr1:154112300 G>A maps to NM_207308.2 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:154090290 C>T maps to NM_207308.2 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr1:154108431 C>T maps to NM_207308.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:154029407 C>T maps to NM_207308.2 Q1041Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr1:154026823 C>T maps to NM_207308.2 Q1121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:154067455 C>T maps to NM_207308.2 Q714Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:154042923 C>T maps to NM_207308.2 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:154026784 C>T maps to NM_207308.2 G1134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:154031058 C>T maps to NM_207308.2 E987E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:154072488 A>C maps to NM_207308.2 A650A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr1:154112301 A>G maps to NM_207308.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:154027278 C>T maps to NM_207308.2 E1090E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:154018577 C>T maps to NM_207308.2 R1221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:154090245 A>T maps to NM_207308.2 V525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:154072473 C>T maps to NM_207308.2 K655K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:154026847 G>A maps to NM_207308.2 I1113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr1:154108434 G>A maps to NM_207308.2 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:154042843 C>T maps to NM_207308.2 W820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:134062708 T>G maps to ENST00000451030 P1152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr9:134073011 C>A maps to ENST00000451030 P1378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr9:134074073 C>T maps to ENST00000451030 V1732V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr9:134073038 C>T maps to ENST00000451030 P1387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:134073809 C>T maps to ENST00000451030 S1644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr9:134026040 C>G maps to ENST00000451030 A723A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr9:134020012 C>T maps to ENST00000451030 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr9:134073005 T>C maps to ENST00000451030 T1376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr9:134073740 C>T maps to ENST00000451030 T1621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr2:184024280 C>T maps to NM_138285.3 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:184025780 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q3-06A-11D-A196-08 chr12:102512167 A>G maps to NM_024057.2 Y43Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:150057736 G>A maps to NM_198887.1 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:45574413 T>C maps to NM_007172.3 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:77055371 G>A maps to ENST00000458189 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr4:77065564 G>A maps to ENST00000458189 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:77036569 G>A maps to ENST00000458189 V492V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:77057347 G>A maps to ENST00000458189 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:77055430 G>A maps to ENST00000458189 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr4:77053727 T>C maps to ENST00000458189 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:50412605 G>A maps to NM_012346.4 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:50411633 G>A maps to NM_012346.4 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:50411879 G>A maps to NM_012346.4 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr23:106397397 T>A did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:106397461 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr23:106396493 T>C did not map to a codon.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr23:106396511 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr23:106397457 C>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:106396729 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr17:73227515 C>T maps to NM_024844.3 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr17:73214301 C>T maps to NM_024844.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:73214292 C>T maps to NM_024844.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:5307545 G>A maps to NM_002532.3 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr17:5308442 G>A maps to NM_002532.3 I326I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr16:56868112 G>A maps to NM_014669.3 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr16:56857656 A>C maps to NM_014669.3 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:56868647 C>T maps to NM_014669.3 F580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr16:56867142 G>A maps to NM_014669.3 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:3723979 A>C maps to NM_016320.4 T1075T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:3735137 G>A maps to NM_016320.4 I829I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr11:3720320 G>A maps to NM_016320.4 Q1334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:3781852 G>A maps to NM_016320.4 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr13:25887864 C>T maps to NM_014089.3 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr13:25901093 C>T maps to NM_014089.3 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr13:25882030 C>T maps to NM_014089.3 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr16:28549462 C>T maps to NM_001042483.1 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr16:67904741 C>T maps to NM_005796.1 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr16:67902280 C>T maps to NM_005796.1 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr1:224477256 C>A maps to NM_002533.2 E502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr1:224482015 G>A maps to NM_002533.2 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr1:224418996 A>C maps to NM_002533.2 G819G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:224482087 G>A maps to NM_002533.2 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:224455760 A>G maps to NM_002533.2 F719F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:224477368 G>A maps to NM_002533.2 H464H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:224475509 T>C maps to NM_002533.2 E587E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:224437952 G>A maps to NM_002533.2 P750P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:224475602 G>A maps to NM_002533.2 F556F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:224473769 G>A maps to NM_002533.2 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:16860406 C>T maps to ENST00000438489 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:16861219 C>T maps to ENST00000438489 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:16860934 C>T maps to ENST00000438489 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:16860304 G>A maps to ENST00000438489 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr19:16860406 C>T maps to ENST00000438489 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:16923626 G>A maps to ENST00000438489 K1453K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:16861093 C>G maps to ENST00000438489 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr19:16860970 C>T maps to ENST00000438489 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:16910869 T>C maps to ENST00000438489 F1211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:16918481 C>T maps to ENST00000438489 L1274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:16860715 C>T maps to ENST00000438489 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:16899850 G>A maps to ENST00000438489 K930K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr19:16910719 G>A maps to ENST00000438489 G1161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:16884102 C>T maps to ENST00000438489 P859P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr19:16908555 G>A maps to ENST00000438489 S1106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:16918625 C>T maps to ENST00000438489 V1322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:16860283 C>T maps to ENST00000438489 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:16884081 C>T maps to ENST00000438489 F852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:16918925 G>A maps to ENST00000438489 W1422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:16872876 G>A maps to ENST00000438489 G687G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr19:16861033 C>T maps to ENST00000438489 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:16875869 G>A maps to ENST00000438489 R759R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:16883982 C>T maps to ENST00000438489 F819F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:16860200 T>C maps to ENST00000438489 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:16860847 C>T maps to ENST00000438489 I465I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:16860952 C>T maps to ENST00000438489 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:16908678 C>T maps to ENST00000438489 S1147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:16910719 G>A maps to ENST00000438489 G1161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:16918925 G>A maps to ENST00000438489 W1422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:16925941 G>A maps to ENST00000438489 E1499E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:16860910 G>A maps to ENST00000438489 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr11:62562462 C>T maps to NM_006362.4 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr11:62569485 G>A maps to NM_006362.4 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr23:101576785 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:101581399 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:101615543 T>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:101620164 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:101620168 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr23:102339390 T>C did not map to a codon.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:102338595 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:102337211 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:102339302 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr23:102338426 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:102337211 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:102334947 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:102338548 G>A did not map to a codon.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr23:102337258 C>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:102339392 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:102333496 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:102338551 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr23:102339394 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr23:102333531 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr23:102334394 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr23:102339343 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:102338147 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:102332622 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr23:102334769 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:102333541 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:102337761 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:102334162 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:102334966 C>G did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:102338565 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:102335529 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:102337933 G>C did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:102335093 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr23:102338383 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:102339405 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:102334725 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:102337986 T>C did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:102337714 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:101092586 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr23:101097734 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:101095993 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr23:101096476 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:101097731 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:101092551 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:101092579 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:101096485 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr23:101095998 T>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr23:101096530 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:101096499 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr17:704266 C>T maps to NM_022463.3 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr19:17571429 C>T maps to NM_138454.1 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:17571378 G>A maps to NM_138454.1 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:17571609 C>T maps to NM_138454.1 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr19:17571377 G>A maps to NM_138454.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:8475375 C>T maps to NM_152745.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:8790999 G>A maps to NM_152745.2 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:8790858 G>A maps to NM_152745.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr7:8790843 C>T maps to NM_152745.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:8790864 C>T maps to NM_152745.2 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:139429217 C>T maps to NM_007226.2 K23K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:139428492 C>T maps to NM_007226.2 *265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr2:139428554 G>A maps to NM_007226.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:139428829 G>A maps to NM_007226.2 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr2:139428695 C>T maps to NM_007226.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr2:139428989 C>T maps to NM_007226.2 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr2:139428890 C>T maps to NM_007226.2 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:139428695 C>T maps to NM_007226.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:139429022 C>T maps to NM_007226.2 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:47656121 G>A maps to ENST00000513748 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr12:57619022 C>T maps to NM_007224.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr12:57619167 C>T maps to NM_007224.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:57619154 G>A maps to NM_007224.3 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:57619146 C>T maps to NM_007224.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:57619433 C>T maps to NM_007224.3 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:57619442 C>T maps to NM_007224.3 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr20:23334888 C>T maps to NM_013248.2 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr14:24878673 C>T maps to NM_025081.2 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr14:24885106 C>T maps to NM_025081.2 L1384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr14:24885223 C>T maps to NM_025081.2 S1423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr14:24884797 G>A maps to NM_025081.2 E1281E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr14:24885106 C>T maps to NM_025081.2 L1384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr14:24879217 C>T maps to NM_025081.2 Q740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr14:24884614 C>T maps to NM_025081.2 S1220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:24877604 C>T maps to NM_025081.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:24878172 C>T maps to NM_025081.2 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:24885235 C>T maps to NM_025081.2 I1427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr14:24885031 C>T maps to NM_025081.2 A1359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr14:24884116 C>T maps to NM_025081.2 I1054I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr14:24886411 G>A maps to NM_025081.2 R1819R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:24884434 C>T maps to NM_025081.2 F1160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:24886129 C>T maps to NM_025081.2 A1725A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr14:24885811 C>T maps to NM_025081.2 I1619I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr14:24883900 C>T maps to NM_025081.2 P982P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr14:24884731 C>T maps to NM_025081.2 S1259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr14:24878919 C>T maps to NM_025081.2 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr14:24877292 G>A maps to NM_025081.2 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr14:24877085 G>A maps to NM_025081.2 K70K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:24877583 C>T maps to NM_025081.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:24878112 C>T maps to NM_025081.2 I371I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:24880575 G>A maps to NM_025081.2 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:24885321 G>A maps to NM_025081.2 W1456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:24885580 G>A maps to NM_025081.2 R1542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:24885901 C>T maps to NM_025081.2 F1649F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:24886120 C>T maps to NM_025081.2 F1722F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:113346561 C>T maps to NM_001032409.1 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr12:113346561 C>T maps to NM_001032409.1 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:113346510 G>A maps to NM_001032409.1 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:113425084 C>T maps to NM_016817.2 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:113442791 C>T maps to NM_016817.2 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:113445715 G>A maps to NM_016817.2 R621R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr12:113425018 C>T maps to NM_016817.2 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:113436178 G>A maps to NM_016817.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:113424926 C>T maps to NM_016817.2 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:113425117 G>A maps to NM_001032731.1 K151K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:113435490 G>A maps to NM_016817.2 W265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:113448258 C>T maps to NM_016817.2 I710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr12:113446900 C>T maps to NM_016817.2 I635I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr12:113425018 C>T maps to NM_016817.2 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:113442791 C>T maps to NM_016817.2 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr12:113444368 G>A maps to NM_016817.2 K540K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr12:113386913 G>A maps to NM_006187.2 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:113405370 C>T maps to NM_006187.2 I946I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr12:113407509 C>T maps to NM_006187.2 L1068L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr12:113405392 C>T maps to NM_006187.2 Q954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:113400488 C>T maps to NM_006187.2 A622A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:113403601 C>T maps to NM_006187.2 L819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr12:113403829 C>T maps to NM_006187.2 A895A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr12:113405250 C>T maps to NM_006187.2 S906S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr12:113405853 G>A maps to NM_006187.2 E993E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:113382386 G>A maps to NM_006187.2 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:113405797 C>T maps to NM_006187.2 L975L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr12:113400696 C>T maps to NM_006187.2 R692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr12:113384615 C>T maps to NM_006187.2 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr12:113398966 C>T maps to NM_006187.2 F583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:113388724 C>T maps to NM_006187.2 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:113388766 C>T maps to NM_006187.2 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:113403695 C>T maps to NM_006187.2 Q851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:113405328 G>A maps to NM_006187.2 R932R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:113388610 C>T maps to NM_006187.2 I496I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:113407526 G>A maps to NM_006187.2 R1073R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:121458606 G>A maps to NM_003733.2 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:121458627 C>T maps to NM_003733.2 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:121469307 G>A maps to NM_003733.2 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:121469307 G>A maps to NM_003733.2 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:121471315 C>T maps to NM_003733.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:121469307 G>A maps to NM_003733.2 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:121469316 C>T maps to NM_003733.2 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr12:121469307 G>A maps to NM_003733.2 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr12:121458597 G>A maps to NM_003733.2 F437F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr12:121471315 C>T maps to NM_003733.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:121458438 C>T maps to NM_003733.2 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr15:64982718 G>A maps to ENST00000403937 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:151739671 C>T maps to ENST00000321531 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:151739672 C>T maps to ENST00000321531 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr1:151740680 C>T maps to ENST00000321531 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr10:105657311 G>A maps to NM_024928.4 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr10:105642576 G>A maps to NM_024928.4 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:192550391 C>T maps to NM_001031716.2 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:56622897 C>T maps to NM_024068.3 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr9:138438730 G>A maps to NM_014582.2 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr9:138439042 C>T maps to NM_014582.2 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:138438673 G>A maps to NM_014582.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr9:138439056 G>A maps to NM_014582.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:138441152 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr9:136082649 C>T maps to NM_014581.2 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:136083926 C>T maps to NM_014581.2 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:228432087 C>T maps to NM_001098623.1 A1099A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:228547306 C>T maps to NM_052843.2 T6238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr1:228556586 C>T maps to NM_001098623.1 S6644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:228462333 G>A maps to NM_001098623.1 E1915E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:228505800 G>A maps to NM_001098623.1 T4686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:228562328 C>T maps to NM_001098623.1 A7513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:228558432 C>T maps to NM_001098623.1 F6740F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr1:228481084 G>A maps to NM_001098623.1 R3633R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:228469826 G>A maps to NM_001098623.1 R2797R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:228505764 G>A maps to NM_001098623.1 Q4674Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:228520615 C>T maps to NM_001098623.1 F5236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:228494857 C>T maps to NM_001098623.1 L4061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr1:228559340 C>T maps to NM_001098623.1 T6954T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr1:228529148 C>T maps to NM_001098623.1 I5956I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr1:228434304 G>A maps to NM_001098623.1 L1278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:228553832 C>T maps to NM_001098623.1 A6374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:228475407 G>T maps to NM_001098623.1 R3186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:228451913 C>T maps to NM_001098623.1 A1561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:228456378 G>A maps to NM_001098623.1 S1670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:228509043 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:228547870 G>A maps to NM_052843.2 E6426E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:228554255 G>T maps to NM_001098623.1 L6444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr1:228433279 C>T maps to NM_001098623.1 V1216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr1:228451886 C>T maps to NM_001098623.1 A1552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:228433369 C>T maps to NM_001098623.1 S1246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:228466963 C>T maps to NM_001098623.1 P2405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:228505629 C>T maps to NM_001098623.1 A4629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:228437924 C>T maps to NM_001098623.1 F1431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:228451838 G>A maps to NM_001098623.1 K1536K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr1:228494758 G>A maps to NM_001098623.1 Q4028Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:228437820 C>T maps to NM_001098623.1 R1397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:228473845 C>T maps to NM_001098623.1 F3024F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:228473857 C>T maps to NM_001098623.1 I3028I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:228528803 C>T maps to NM_001098623.1 F5902F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:228538554 C>T maps to NM_001098623.1 F6110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:228444557 C>T maps to NM_001098623.1 Q1506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:228523939 G>A maps to NM_001098623.1 A5502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:228524703 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:228547873 G>A maps to NM_052843.2 A6427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:228505435 C>T maps to NM_001098623.1 P4611P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:228509754 G>A maps to NM_001098623.1 A5071A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:228565641 C>T maps to NM_001098623.1 L7838L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:228474642 G>A maps to NM_001098623.1 R3149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:228509637 C>T maps to NM_001098623.1 F5032F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:228475870 G>A maps to NM_001098623.1 K3307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr1:228482116 G>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:228524723 G>A maps to NM_001098623.1 K5519K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr1:228452072 C>T maps to NM_001098623.1 S1614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr1:228403513 C>T maps to NM_001098623.1 I693I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:228503686 G>A maps to NM_001098623.1 E4384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:228504467 G>A maps to NM_001098623.1 Q4448Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:228482033 C>T maps to NM_001098623.1 I3771I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:228548353 C>T maps to NM_052843.2 T6587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:228563784 C>A maps to NM_001098623.1 T7621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr1:228399630 G>A maps to NM_001098623.1 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr1:228482538 G>A maps to NM_001098623.1 T3818T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:228505788 C>T maps to NM_001098623.1 I4682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:228556532 C>T maps to NM_001098623.1 S6626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:228469850 G>A maps to NM_001098623.1 G2805G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr1:228476515 G>T maps to NM_001098623.1 L3422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:228553784 C>T maps to NM_001098623.1 S6358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:228402554 C>T maps to NM_001098623.1 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:228461636 C>A maps to NM_001098623.1 A1768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:228473971 G>A maps to NM_001098623.1 R3066R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:228479638 G>A maps to NM_001098623.1 E3460E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:228479752 G>A maps to NM_001098623.1 Q3498Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:228481216 C>T maps to NM_001098623.1 A3677A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:228505602 G>A maps to NM_001098623.1 P4620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:228509172 G>A maps to NM_001098623.1 V4877V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:228509412 G>A maps to NM_001098623.1 L4957L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:228509865 C>T maps to NM_001098623.1 A5108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:228525784 C>T maps to NM_001098623.1 T5647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:228526037 G>A maps to NM_001098623.1 E5683E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:228547303 G>A maps to NM_052843.2 E6237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:228556047 C>T maps to NM_001098623.1 V6566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:228559457 C>T maps to NM_001098623.1 A6993A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:228560540 C>T maps to NM_001098623.1 P7354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:228562352 G>A maps to NM_001098623.1 L7521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:228432123 G>A maps to NM_001098623.1 G1111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:228481132 G>A maps to NM_001098623.1 L3649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:228529195 G>A maps to NM_001098623.1 W5972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:228461501 C>T maps to NM_001098623.1 C1723C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:220431638 G>A maps to NM_015311.2 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:220435579 C>T maps to NM_015311.2 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:220420889 C>T maps to NM_015311.2 G1487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:220429979 G>A maps to NM_015311.2 F797F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:220420864 G>A maps to NM_015311.2 L1496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:220431774 G>A maps to NM_015311.2 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:220430135 G>A maps to NM_015311.2 F745F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr2:220424196 G>A maps to NM_015311.2 Y992Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:133053842 G>A maps to ENST00000262283 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr8:133036940 G>A maps to ENST00000262283 N619N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr8:133053896 G>A maps to ENST00000262283 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:133051335 G>A maps to ENST00000262283 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr8:133044279 G>A maps to ENST00000262283 F505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:133053348 G>A maps to ENST00000262283 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:133044177 G>A maps to ENST00000262283 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr8:133053348 G>A maps to ENST00000262283 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr15:28202873 C>T maps to NM_000275.2 K548K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr15:28259951 G>A maps to NM_000275.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr15:28259930 G>A maps to NM_000275.2 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5KH-06A-11D-A27K-08 chr15:28000614 C>T maps to NM_000275.2 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr15:28196951 G>A maps to NM_000275.2 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:28326951 G>A maps to NM_000275.2 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:28116380 G>A maps to NM_000275.2 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:48906538 G>A maps to NM_001014446.1 Q10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr4:48906530 T>C maps to NM_001014446.1 K12K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:48894820 G>A maps to NM_001014446.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:48894787 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr5:68809846 C>T maps to NM_002538.2 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:68805378 G>A maps to NM_002538.2 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:5925698 C>T maps to NM_001097622.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr7:5923526 C>T maps to NM_001097622.1 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:128691356 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:128723829 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:128723830 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:128691383 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:128691375 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:128709928 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:128710348 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:128692674 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:128674730 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:128696420 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:128695238 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr23:128724182 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr4:71068510 G>A maps to NM_017855.3 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr4:71068892 G>A maps to NM_017855.3 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:10583844 G>A maps to NM_002539.1 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:10583693 G>A maps to NM_002539.1 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:103573082 C>T maps to NM_024410.3 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:103572925 C>T maps to NM_024410.3 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr8:103572847 G>A maps to NM_024410.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26D-06A-11D-A19A-08 chr8:103572782 C>T maps to NM_024410.3 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr9:131246221 A>G maps to NM_153435.1 Q395Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:131247669 C>T maps to NM_153435.1 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr9:131256910 C>T maps to NM_153435.1 I689I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr1:86852688 C>A maps to ENST00000370567 G8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:86818610 T>G maps to ENST00000370567 I579I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:86847983 G>A maps to ENST00000370567 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr11:198576 C>T maps to NM_053280.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr15:76019448 C>T maps to NM_175881.3 H131H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:76019595 C>T maps to NM_175881.3 Y180Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:474624 C>T maps to NM_182577.2 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:474702 G>A maps to NM_182577.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:474629 G>A maps to NM_182577.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr17:8243449 G>A maps to NM_153007.4 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr17:8243539 C>A maps to NM_153007.4 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr17:8243740 C>T maps to NM_153007.4 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr17:8249103 G>A maps to NM_153007.4 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr23:123871003 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr23:123871025 T>C did not map to a codon.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr23:123615659 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr23:124029835 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr23:123805604 T>G did not map to a codon.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr23:123805539 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr23:123518063 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr23:123699396 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr23:123870901 G>T did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:124028168 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:124028169 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr23:123587287 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr23:123518236 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:123657235 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:123663787 A>T did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:123526146 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr23:123514579 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr23:123615713 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:123556298 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:123556362 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:123657310 G>A did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:123518400 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:123525925 A>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:123587256 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:123787508 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:123839061 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:123778992 C>A did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:123517892 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr23:123514832 C>A did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:123554599 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr23:123785785 T>G did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:123540247 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:123519761 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:123525978 C>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:123556264 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:123637532 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:123779111 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:123779112 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:123839006 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:123587291 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr23:123556328 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr23:123785915 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr23:123654523 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr23:123775803 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:123518350 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:123556261 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:123805591 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:124097544 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:123539079 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:123556121 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:123779146 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:123515009 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:123838899 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr23:123785873 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr23:123870876 T>C did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:123630864 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr23:123680789 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:123654621 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:124097410 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:123615779 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:123699396 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:123514520 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr23:123654523 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:123554566 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:123514526 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:123838891 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:123630926 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:123657414 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr23:123517661 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:123654408 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr23:123519726 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:123657418 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:123805562 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:123539076 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:123515033 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:123663717 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:123518360 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr23:123657237 C>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:123539080 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:123587261 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:123657238 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:123775762 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:123517539 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr23:123654523 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:123787497 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:123554566 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:123839006 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:123518536 C>T did not map to a codon.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr23:123699395 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:123805561 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr23:123514402 C>T did not map to a codon.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr23:123775739 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:123556194 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:123787497 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr23:123518111 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:123518569 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr23:123519812 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr23:123870806 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr23:123518419 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:123554650 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:123785910 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:123871002 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:124029936 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr23:123514861 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:123515038 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:123519850 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:123540241 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:123556374 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:123615707 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:123695633 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:123779148 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:124097410 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:124097437 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:123514579 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:123517666 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:123540269 G>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:123787620 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:124028186 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:123654523 C>T did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:123785910 C>T did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:123838974 G>A did not map to a codon.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr23:123556450 G>A did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:123615809 T>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr5:167420092 G>A maps to NM_001122679.1 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:167517615 G>A maps to NM_001122679.1 W518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr5:167673922 T>C maps to NM_001122679.1 N1984N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr5:167631398 G>A maps to NM_001122679.1 G1190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr5:167489206 C>T maps to NM_001122679.1 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:167653128 C>T maps to NM_001122679.1 R1706R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:167645263 C>T maps to NM_001122679.1 C1447C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:167645206 C>T maps to NM_001122679.1 I1428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:167645620 T>A maps to NM_001122679.1 P1566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr5:167517604 G>A maps to NM_001122679.1 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr5:167626001 C>T maps to NM_001122679.1 S1006S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:167420182 C>T maps to NM_001122679.1 F394F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr5:167631410 C>T maps to NM_001122679.1 F1194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr5:167631593 C>T maps to NM_001122679.1 P1255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr5:167420047 C>T maps to NM_001122679.1 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr5:167489215 G>A maps to NM_001122679.1 K487K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr5:167551954 G>A maps to NM_001122679.1 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:167674648 G>A maps to NM_001122679.1 L2226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:167675293 G>A maps to NM_001122679.1 K2441K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:167687291 G>A maps to NM_001122679.1 V2470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr5:167625887 C>T maps to NM_001122679.1 S968S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:167645245 G>A maps to NM_001122679.1 A1441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:167420137 C>T maps to NM_001122679.1 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:167553801 G>A maps to NM_001122679.1 G751G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr5:167642212 C>G maps to NM_001122679.1 P1329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:167675101 C>T maps to NM_001122679.1 I2377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr5:167420155 C>T maps to NM_001122679.1 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr5:167630769 C>T maps to NM_001122679.1 F1160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:167625869 C>T maps to NM_001122679.1 I962I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:167517610 G>A maps to NM_001122679.1 E516E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:167517658 C>T maps to NM_001122679.1 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:167625887 C>T maps to NM_001122679.1 S968S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:167626900 C>T maps to NM_001122679.1 S1056S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:167645875 C>T maps to NM_001122679.1 T1651T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:167674012 G>A maps to NM_001122679.1 G2014G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:167675203 C>T maps to NM_001122679.1 T2411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:167489212 G>A maps to NM_001122679.1 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr5:167625869 C>T maps to NM_001122679.1 I962I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr5:167420054 C>T maps to NM_001122679.1 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr4:183694732 C>T maps to NM_001080477.1 S1667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr4:183600826 C>T maps to NM_001080477.1 F445F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr4:183601488 G>A maps to NM_001080477.1 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr4:183714424 G>A maps to NM_001080477.1 R2200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr4:183672950 A>C did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr4:183675572 C>T maps to NM_001080477.1 N1351N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr4:183676245 C>T maps to NM_001080477.1 R1576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:183600988 G>A maps to NM_001080477.1 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr4:183594299 C>T maps to NM_001080477.1 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr4:183714430 G>A maps to NM_001080477.1 T2202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr4:183676208 C>T maps to NM_001080477.1 T1563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr4:183714467 C>T maps to NM_001080477.1 R2215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:183675764 C>T maps to NM_001080477.1 V1415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:183245250 C>T maps to NM_001080477.1 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:183650187 G>A maps to NM_001080477.1 R813R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:183673090 C>T maps to NM_001080477.1 V1256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr4:183600835 C>T maps to NM_001080477.1 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr4:183600988 G>A maps to NM_001080477.1 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:183675765 C>T maps to NM_001080477.1 L1416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:183601410 G>A maps to NM_001080477.1 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:183600817 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr4:183651351 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr4:183600826 C>T maps to NM_001080477.1 F445F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr4:183658197 C>T maps to NM_001080477.1 Q1069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:183675992 G>A maps to NM_001080477.1 G1491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr4:183675686 G>A maps to NM_001080477.1 V1389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:183600871 G>A maps to NM_001080477.1 R460R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:183664515 C>T maps to NM_001080477.1 F1191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:183673090 C>T maps to NM_001080477.1 V1256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:183694753 C>T maps to NM_001080477.1 I1674I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:183713527 C>T maps to NM_001080477.1 T1901T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:183713752 C>T maps to NM_001080477.1 V1976V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:183714622 G>A maps to NM_001080477.1 S2266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr4:183650331 G>A maps to NM_001080477.1 K861K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr4:183714412 C>T maps to NM_001080477.1 F2196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr4:183721182 C>T maps to NM_001080477.1 F2593F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr4:183600988 G>A maps to NM_001080477.1 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr4:183717906 G>A maps to NM_001080477.1 W2444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr4:183600826 C>T maps to NM_001080477.1 F445F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr4:183717788 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr4:183673099 G>A maps to NM_001080477.1 G1259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr4:183245229 G>A maps to NM_001080477.1 K19K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr4:183675896 C>T maps to NM_001080477.1 Y1459Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr4:183574951 G>A maps to NM_001080477.1 Q339Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:183673093 C>T maps to NM_001080477.1 V1257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:183694774 C>T maps to NM_001080477.1 I1681I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:183696239 G>A maps to NM_001080477.1 L1746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:183713540 C>T maps to NM_001080477.1 R1906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:183721182 C>T maps to NM_001080477.1 F2593F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr4:183673090 C>T maps to NM_001080477.1 V1256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr4:183675623 C>T maps to NM_001080477.1 I1368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr4:183600940 C>T maps to NM_001080477.1 I483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr4:183721335 G>A maps to NM_001080477.1 E2644E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr4:183721335 G>A maps to NM_001080477.1 E2644E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr11:78399180 G>A maps to NM_001098816.2 V1726V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:78380300 G>A maps to NM_001098816.2 I2363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr11:78372616 G>A maps to NM_001098816.2 L2476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr11:78413361 G>A maps to NM_001098816.2 I1432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr11:78413142 G>A maps to NM_001098816.2 L1505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr11:78423557 C>T maps to NM_001098816.2 K1341K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:78443558 G>A maps to NM_001098816.2 I980I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr11:78433747 G>A maps to NM_001098816.2 F1255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:78443362 G>A maps to NM_001098816.2 Q1046*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:78380702 C>T maps to NM_001098816.2 G2229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:78423525 C>T did not map to a codon.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr11:78440595 G>A maps to NM_001098816.2 I1077I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr11:78433783 G>A maps to NM_001098816.2 L1243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:78419498 G>A maps to NM_001098816.2 I1372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr11:78369243 C>T maps to NM_001098816.2 G2723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr11:78412974 C>T maps to NM_001098816.2 R1561R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:78369593 G>A maps to NM_001098816.2 L2607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:78497943 G>A maps to NM_001098816.2 I788I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:78516397 G>A maps to NM_001098816.2 F706F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:78383098 C>T maps to NM_001098816.2 W1924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:78369176 C>A maps to NM_001098816.2 E2746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:78380297 C>T maps to NM_001098816.2 G2364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:78516337 G>A maps to NM_001098816.2 I726I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:78369602 G>A maps to NM_001098816.2 L2604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:78380675 C>T maps to NM_001098816.2 R2238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:78383098 C>T maps to NM_001098816.2 W1924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:78433819 G>A maps to NM_001098816.2 A1231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:78440508 G>A maps to NM_001098816.2 F1106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:78440598 C>T maps to NM_001098816.2 R1076R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:78443369 C>T maps to NM_001098816.2 P1043P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:78516337 G>A maps to NM_001098816.2 I726I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr11:78440568 G>A maps to NM_001098816.2 F1086F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:78440625 C>T maps to NM_001098816.2 R1067R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr11:78440604 G>A maps to NM_001098816.2 V1074V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr11:78443552 C>T maps to NM_001098816.2 Q982Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:78369252 C>T maps to NM_001098816.2 W2720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr11:78443471 G>A maps to NM_001098816.2 P1009P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:78369258 C>T maps to NM_001098816.2 R2718R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:13757011 T>C did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:13778280 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:13764498 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:13764498 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:13762614 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:13778413 C>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr7:44746845 C>T maps to ENST00000444676 I900I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr7:44741165 C>T maps to ENST00000444676 L877L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:44706362 C>T maps to ENST00000444676 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:44713423 C>T maps to ENST00000444676 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:44715810 C>T maps to NM_001003941.2 F423F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:44734096 C>T maps to ENST00000444676 I545I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr7:44746875 A>T maps to ENST00000444676 P910P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:44715756 C>T maps to NM_001003941.2 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:44714018 G>A maps to ENST00000444676 E281E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:44713489 C>T maps to ENST00000444676 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr7:44685011 C>T maps to ENST00000444676 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr10:50960187 C>T maps to NM_018245.2 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr10:50959931 C>T maps to NM_018245.2 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr10:50958943 G>A maps to NM_018245.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:50955094 C>A maps to NM_018245.2 G383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:50964926 G>A maps to NM_018245.2 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:50946067 G>A maps to NM_018245.2 I814I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:50960762 C>T maps to NM_018245.2 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:50952094 G>A maps to NM_018245.2 T602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:50954807 G>A maps to NM_018245.2 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr10:50952112 G>A maps to NM_018245.2 I596I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr10:50944402 C>T maps to NM_018245.2 Q918Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:50946013 G>A maps to NM_018245.2 I832I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:50953879 C>T maps to NM_018245.2 W480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:50946287 C>T maps to NM_018245.2 A780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:50959004 C>T maps to NM_018245.2 W259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:50959018 G>A maps to NM_018245.2 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:50964977 G>A maps to NM_018245.2 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:50954831 C>T maps to NM_018245.2 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:50964914 G>A maps to NM_018245.2 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr12:123463463 G>A maps to ENST00000228922 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:123463550 C>T maps to ENST00000228922 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:61443800 C>T maps to NM_007346.2 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr20:61441913 C>T maps to NM_007346.2 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr20:61444778 C>T maps to NM_007346.2 P604P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:61444718 C>T maps to NM_007346.2 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:72003051 G>A maps to NM_024576.3 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:72006409 C>T maps to NM_024576.3 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr6:72011391 C>T maps to NM_024576.3 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:72006512 C>T maps to NM_024576.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:9798867 A>G maps to NM_016820.3 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:95152204 G>T maps to NM_033014.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:70779215 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:70779459 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:70782855 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:70787442 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:70783275 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:70781707 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:70781689 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:70782756 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:70775854 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr23:70784519 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:70784461 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:70764431 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:70787582 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:74692131 G>A maps to NM_152635.1 R496R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr10:74658713 G>A maps to NM_152635.1 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:74684189 G>A maps to NM_152635.1 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr10:74690313 G>C maps to NM_152635.1 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:74658704 G>A maps to NM_152635.1 W115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:74673192 C>T maps to NM_152635.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:74658689 G>A maps to NM_152635.1 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:175006600 T>C maps to ENST00000409546 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr10:15103829 C>T maps to NM_018324.2 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:15107689 G>A maps to NM_018324.2 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:15107689 G>A maps to NM_018324.2 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr10:15115179 G>A maps to NM_018324.2 K303K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:15115134 G>A maps to NM_018324.2 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr9:138011441 C>T maps to NM_014279.4 H274H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:138011384 C>T maps to NM_014279.4 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:9965320 C>T maps to NM_058164.2 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:9968507 G>A maps to NM_058164.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:9968029 A>G maps to NM_058164.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:9967557 G>C maps to NM_058164.2 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:9968152 C>T maps to NM_058164.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:9965149 C>T maps to NM_058164.2 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3BZ-06A-12D-A196-08 chr1:102270069 A>G maps to ENST00000338858 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:102296229 G>A maps to ENST00000338858 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:102296229 G>A maps to ENST00000338858 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr1:102269863 C>T maps to ENST00000338858 W456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr1:102269985 C>T maps to ENST00000338858 K415K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:102270069 A>G maps to ENST00000338858 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:102290666 C>T maps to ENST00000338858 E189E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:102269928 G>A maps to ENST00000338858 F434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr13:53624464 C>T maps to NM_006418.3 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:53624758 G>A maps to NM_006418.3 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr13:53624635 G>A maps to NM_006418.3 W421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:7507105 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr11:7530872 C>A maps to NM_198474.3 Y221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:7530739 T>A maps to NM_198474.3 L177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr11:7530731 G>A maps to NM_198474.3 K174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr9:127570174 G>A maps to NM_182487.2 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr9:127572459 G>A maps to NM_182487.2 G576G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr9:127572525 C>T maps to NM_182487.2 V598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:127563898 C>T maps to NM_182487.2 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr9:127561589 G>A maps to NM_182487.2 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:127561571 G>A maps to NM_182487.2 K157K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr9:127566400 G>A maps to NM_182487.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:161953992 G>A maps to ENST00000451379 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr1:161953686 G>A maps to ENST00000451379 F678F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr1:161976239 C>T maps to ENST00000451379 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:161970011 C>T maps to ENST00000451379 Q281Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:161969921 C>T maps to ENST00000451379 E311E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:161953800 C>T maps to ENST00000451379 E640E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:161953593 G>A maps to ENST00000451379 I709I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr1:161987261 G>A maps to ENST00000451379 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:161954025 G>A maps to ENST00000451379 I565I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr1:161954615 C>T maps to ENST00000451379 R544R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:114523736 C>T maps to NM_020190.2 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:114524267 C>T maps to NM_020190.2 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:114523090 C>T maps to NM_020190.2 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:137814848 C>T maps to NM_175747.2 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr6:137814842 G>A maps to NM_175747.2 H155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:10313408 C>T maps to NM_002543.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:10313504 C>T maps to NM_002543.3 W148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr12:10312594 G>A maps to NM_002543.3 Q236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:58996365 G>A maps to NM_145243.3 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:58946768 C>T maps to NM_145243.3 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:58946723 C>T maps to NM_145243.3 T496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:59004618 G>A maps to NM_145243.3 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:76813932 C>T maps to NM_006189.1 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:53081289 G>A maps to NM_004498.1 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr15:53081457 G>A maps to NM_004498.1 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr18:55143789 C>T maps to NM_004852.2 R450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr18:55104090 C>T maps to NM_004852.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:55104009 G>A maps to NM_004852.2 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr18:55143861 C>T maps to NM_004852.2 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:55104003 C>T maps to NM_004852.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr18:55143777 G>A maps to NM_004852.2 K446K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:55143861 C>T maps to NM_004852.2 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:74079007 G>A maps to NM_001080507.2 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr6:74079100 G>A maps to NM_001080507.2 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:74078977 C>T maps to NM_001080507.2 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:193361861 C>T maps to NM_130837.2 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:98105808 C>T maps to NM_033207.3 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:98108054 C>T maps to NM_033207.3 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:132527114 G>A maps to NM_002545.3 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr11:132812918 G>A maps to NM_002545.3 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:132307125 G>A maps to NM_002545.3 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:132527176 G>A maps to NM_002545.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr11:132306019 C>T maps to NM_002545.3 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:67273530 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:67316725 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr23:67518910 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:67426471 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:67333081 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:67283897 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:67293002 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:67502951 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr8:145111917 G>A maps to ENST00000360660 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr8:145112554 G>A maps to ENST00000360660 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:145111540 G>A maps to ENST00000360660 F608F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:145113013 G>A maps to ENST00000360660 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr8:145110729 G>A maps to ENST00000360660 Q737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:145109473 G>A maps to ENST00000360660 F892F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:145111948 G>A maps to ENST00000360660 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr8:145113013 G>A maps to ENST00000360660 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:145109542 G>A maps to ENST00000360660 P869P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:145111879 C>T maps to ENST00000360660 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:145114839 G>A maps to ENST00000360660 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:145111555 G>A maps to ENST00000360660 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr23:153416415 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:153420074 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:153421960 A>C did not map to a codon.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr23:153416404 C>T did not map to a codon.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr23:153416284 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:153421924 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:153420165 C>T did not map to a codon.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr23:153421871 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:153418574 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:153421921 C>T did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:153496228 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:153458975 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:153490620 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr7:128415808 G>A maps to NM_001708.2 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:128413858 G>A maps to NM_001708.2 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr10:88417908 C>T maps to NM_001030015.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr10:88415937 G>A maps to NM_001030015.2 W57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:88419741 C>T maps to NM_001030015.2 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:88418295 C>T maps to NM_001030015.2 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:88418311 C>T maps to NM_001030015.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:88417788 G>A maps to NM_001030015.2 Q108Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:88417800 C>T maps to NM_001030015.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:88418323 C>T maps to NM_001030015.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:88418307 C>T maps to NM_001030015.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr10:88417914 G>A maps to NM_001030015.2 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:47749897 G>A maps to ENST00000489301 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:47776107 G>A maps to ENST00000489301 K325K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:29189626 C>T maps to NM_000911.3 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:29189311 G>A maps to NM_000911.3 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:29189341 C>T maps to NM_000911.3 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr8:54142249 G>A maps to NM_000912.3 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:54163573 G>A maps to NM_000912.3 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:54142357 G>A maps to NM_000912.3 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr8:54142012 G>A maps to NM_000912.3 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr8:54142186 C>T maps to NM_000912.3 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:54142225 G>A maps to NM_000912.3 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:54141919 G>A maps to NM_000912.3 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr8:54141973 C>T maps to NM_000912.3 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr8:54142117 G>A maps to NM_000912.3 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:54142291 C>T maps to NM_000912.3 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:54147436 C>T maps to NM_000912.3 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr8:54163387 G>A maps to NM_000912.3 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr20:62729884 C>T maps to NM_000913.3 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr20:62724271 C>T maps to NM_000913.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr20:62724141 C>T maps to NM_000913.3 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr20:62729388 C>T maps to NM_000913.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:62729257 C>T maps to NM_000913.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:62729719 C>T maps to NM_000913.3 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:154411104 G>A maps to NM_001145279.1 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr6:154360945 C>T maps to NM_001145279.1 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr6:154412477 C>T maps to NM_001145279.1 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:154412558 T>G maps to NM_001145279.1 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:154411257 C>T maps to NM_001145279.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:203467962 G>A maps to NM_014359.3 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:203472061 C>T maps to NM_014359.3 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:203465351 C>T maps to NM_014359.3 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:203472694 C>T maps to NM_014359.3 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr10:13151268 C>T maps to NM_021980.4 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr11:6891671 C>G maps to NM_001004460.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:6891350 C>T maps to NM_001004460.1 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:6891758 G>A maps to NM_001004460.1 K258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:6891437 C>T maps to NM_001004460.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:6891509 C>T maps to NM_001004460.1 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:6891545 C>T maps to NM_001004460.1 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr11:6891545 C>T maps to NM_001004460.1 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:6891191 G>T maps to NM_001004460.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:6891860 C>T maps to NM_001004460.1 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:6891434 C>T maps to NM_001004460.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr11:7960356 G>A maps to NM_001003745.1 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:7960902 G>A maps to NM_001003745.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:7960950 C>T maps to NM_001003745.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr11:7960995 C>T maps to NM_001003745.1 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr11:7961031 G>A maps to NM_001003745.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr11:7960725 G>A maps to NM_001003745.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr11:7960716 C>T maps to NM_001003745.1 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:7960425 G>A maps to NM_001003745.1 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:6898402 G>A maps to NM_207186.2 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr11:6898246 C>T maps to NM_207186.2 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:6898225 G>A maps to NM_207186.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:6898378 C>T maps to NM_207186.2 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:6898759 G>A maps to NM_207186.2 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr11:6898648 C>T maps to NM_207186.2 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr11:6897919 C>T maps to NM_207186.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:6898504 C>T maps to NM_207186.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr11:6867566 C>T maps to ENST00000379831 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:6867533 G>A maps to ENST00000379831 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:6867365 C>T maps to ENST00000379831 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:6867101 C>T maps to ENST00000379831 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:6867806 G>A maps to ENST00000379831 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:6867227 C>T maps to ENST00000379831 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:6867197 C>T maps to ENST00000379831 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr11:6867320 C>T maps to ENST00000379831 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:6867338 G>A maps to ENST00000379831 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:6867614 G>A maps to ENST00000379831 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:6866951 C>T maps to ENST00000379831 I17I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:7950065 G>A maps to NM_001004461.1 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:7950002 C>T maps to NM_001004461.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr11:7949600 G>A maps to NM_001004461.1 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr11:7950065 G>A maps to NM_001004461.1 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:7950044 G>A maps to NM_001004461.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:7950068 G>A maps to NM_001004461.1 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr12:55615122 C>T maps to NM_001005280.1 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr12:55615074 G>A maps to NM_001005280.1 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr12:55615428 C>T maps to NM_001005280.1 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:55614900 C>T maps to NM_001005280.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:55615671 C>T maps to NM_001005280.1 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:55615095 C>T maps to NM_001005280.1 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:55615185 C>T maps to NM_001005280.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:55615026 C>T maps to NM_001005280.1 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr12:55614882 T>A maps to NM_001005280.1 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:55615377 G>A maps to NM_001005280.1 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr11:55735630 A>T maps to NM_001005491.1 C103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr11:55735765 G>A maps to NM_001005491.1 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:55735474 G>A maps to NM_001005491.1 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:55735217 A>T maps to NM_001005491.1 L241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:55735135 G>A maps to NM_001005491.1 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:55735288 C>T maps to NM_001005491.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr11:55735288 C>T maps to NM_001005491.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:55735129 G>A maps to NM_001005491.1 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:55735465 G>A maps to NM_001005491.1 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr11:55735332 G>A maps to NM_001005491.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr11:55735159 C>T maps to NM_001005491.1 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55735075 G>A maps to NM_001005491.1 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55735153 C>T maps to NM_001005491.1 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:55735093 G>A maps to NM_001005491.1 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:55735474 G>A maps to NM_001005491.1 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr11:55735636 C>T maps to NM_001005491.1 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:29408331 C>T maps to NM_013941.2 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:29408289 C>T maps to NM_013941.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:29408454 C>T maps to NM_013941.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:29408526 C>T maps to NM_013941.2 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:29408541 C>T maps to NM_013941.2 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr6:29408526 C>T maps to NM_013941.2 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:29408454 C>T maps to NM_013941.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr6:29408517 C>T maps to NM_013941.2 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:29407833 C>T maps to NM_013941.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:29408205 G>A maps to NM_013941.2 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:29408388 C>T maps to NM_013941.2 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:29408445 G>A maps to NM_013941.2 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr14:22102461 C>T maps to NM_001005466.1 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr14:22102350 G>A maps to NM_001005466.1 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr14:22102212 G>A maps to NM_001005466.1 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr14:22102905 G>A maps to NM_001005466.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr14:22102461 C>T maps to NM_001005466.1 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:22102950 G>A maps to NM_001005466.1 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:22102965 G>A maps to NM_001005466.1 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:22102212 G>A maps to NM_001005466.1 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:22102845 G>A maps to NM_001005466.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:22102212 G>A maps to NM_001005466.1 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr14:22102908 G>A maps to NM_001005466.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr14:22102950 G>A maps to NM_001005466.1 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:22102440 G>A maps to NM_001005466.1 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:22102644 G>A maps to NM_001005466.1 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr14:22102919 G>A maps to NM_001005466.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:22102491 G>A maps to NM_001005466.1 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:22102943 G>A maps to NM_001005466.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr14:22102950 G>A maps to NM_001005466.1 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:22038383 G>A maps to NM_001005465.1 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:22038554 G>A maps to NM_001005465.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:22038388 G>A maps to NM_001005465.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr14:22037999 C>T maps to NM_001005465.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr11:123886914 C>T maps to NM_001004462.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr11:123886940 C>T maps to NM_001004462.1 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr11:123887039 C>T maps to NM_001004462.1 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr11:123886823 G>A maps to NM_001004462.1 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr11:123887210 G>A maps to NM_001004462.1 R310R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A29D-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr11:123886811 C>T maps to NM_001004462.1 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr11:123886904 C>T maps to NM_001004462.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr11:123886829 C>T maps to NM_001004462.1 I183I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A3J5-06A-11D-A20D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:123887066 C>T maps to NM_001004462.1 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr11:123886367 C>T maps to ENST00000375021 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:123886952 C>T maps to NM_001004462.1 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:123909435 G>A maps to NM_001004463.1 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:123909027 G>A maps to NM_001004463.1 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr11:123909393 G>A maps to NM_001004463.1 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr11:123909483 C>T maps to NM_001004463.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:123908928 C>T maps to NM_001004463.1 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr11:123909234 C>T maps to NM_001004463.1 Q158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:123908964 A>C maps to NM_001004463.1 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr11:123909596 G>A maps to NM_001004463.1 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr11:123909159 G>A maps to NM_001004463.1 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:123909372 G>A maps to NM_001004463.1 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:123909188 G>A maps to NM_001004463.1 Q174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr11:123909219 G>A maps to NM_001004463.1 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:123908940 G>A maps to NM_001004463.1 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr11:123908940 G>A maps to NM_001004463.1 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:123908862 G>A maps to NM_001004463.1 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:123908901 C>T maps to NM_001004463.1 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:123908973 G>A maps to NM_001004463.1 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:123909108 C>T maps to NM_001004463.1 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:123909510 G>A maps to NM_001004463.1 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:123909621 G>A maps to NM_001004463.1 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:123901063 C>T maps to ENST00000375021 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr11:123901066 G>A maps to ENST00000375021 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr11:123901096 C>T maps to ENST00000375021 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:123901120 G>A maps to ENST00000375021 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr11:123900445 G>A maps to NM_001004464.1 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr11:123900997 C>T maps to ENST00000375021 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr11:123900574 T>G maps to NM_001004464.1 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:123900445 G>A maps to NM_001004464.1 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr11:123900475 G>A maps to NM_001004464.1 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:123901220 C>T maps to ENST00000375021 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:123901225 G>A maps to ENST00000375021 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr11:123900817 C>T maps to ENST00000375021 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr11:123901063 C>T maps to ENST00000375021 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:123900508 C>T maps to NM_001004464.1 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr11:123894486 C>T maps to NM_001001953.1 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr11:123893830 C>T maps to NM_001001953.1 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:123893748 C>T maps to NM_001001953.1 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr11:123894486 C>T maps to NM_001001953.1 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:123894207 C>T maps to NM_001001953.1 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:123894516 C>T maps to NM_001001953.1 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr11:123894486 C>T maps to NM_001001953.1 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr19:15918097 G>A maps to NM_013940.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr19:15918634 G>A maps to NM_013940.2 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:15918181 G>A maps to NM_013940.2 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:15918297 G>A maps to NM_013940.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:15918415 C>T maps to NM_013940.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:15918157 A>T maps to NM_013940.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:15917965 C>T maps to NM_013940.2 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:15918160 G>A maps to NM_013940.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:15918811 G>A maps to NM_013940.2 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr19:15918001 G>A maps to NM_013940.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:15917947 G>A maps to NM_013940.2 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15918199 G>A maps to NM_013940.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr19:15839269 G>A maps to NM_013939.2 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr19:15839065 C>T maps to NM_013939.2 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:15839074 C>T maps to NM_013939.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:15838867 C>T maps to NM_013939.2 N5N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr19:15839539 C>T maps to NM_013939.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:15838852 C>A did not map to a codon.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr19:15839083 C>T maps to NM_013939.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr19:15838912 C>T maps to NM_013939.2 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr19:15839500 C>T maps to NM_013939.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr19:15852387 C>T maps to NM_013938.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:15852273 C>T maps to NM_013938.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:15852288 C>T maps to NM_013938.1 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:15852288 C>T maps to NM_013938.1 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:15852408 C>T maps to NM_013938.1 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:15852645 G>A maps to NM_013938.1 W148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:15853086 G>A maps to NM_013938.1 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:15852310 C>T maps to NM_013938.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr19:15852519 C>T maps to NM_013938.1 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:15853086 G>A maps to NM_013938.1 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:15852477 C>T maps to NM_013938.1 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:16060467 C>T maps to NM_001004465.1 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:16059925 C>T maps to NM_001004465.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:16059903 C>T maps to NM_001004465.1 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:16060701 G>A maps to NM_001004465.1 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr19:16060410 C>T maps to NM_001004465.1 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr19:16059876 C>T maps to NM_001004465.1 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:16059903 C>T maps to NM_001004465.1 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:16060263 C>T maps to NM_001004465.1 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:16060458 C>T maps to NM_001004465.1 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr19:16059903 C>T maps to NM_001004465.1 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr19:16060701 G>A maps to NM_001004465.1 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:16060707 G>A maps to NM_001004465.1 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:16059903 C>T maps to NM_001004465.1 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:16060098 C>T maps to NM_001004465.1 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:16060701 G>A maps to NM_001004465.1 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:16059912 C>T maps to NM_001004465.1 Y32Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr19:15904950 C>T maps to NM_001004466.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr19:15905607 C>T maps to NM_001004466.1 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:15905562 G>A maps to NM_001004466.1 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:15905070 C>T maps to NM_001004466.1 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:15905709 C>T maps to NM_001004466.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr19:15905070 C>T maps to NM_001004466.1 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr19:15905601 G>A maps to NM_001004466.1 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15905625 C>T maps to NM_001004466.1 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:15905006 G>A maps to NM_001004466.1 W50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:15905668 G>T maps to NM_001004466.1 G271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:159410432 G>A maps to NM_012351.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:159410498 G>A maps to NM_012351.2 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:159409835 C>T maps to NM_012351.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:159410432 G>A maps to NM_012351.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:159410222 C>T maps to NM_012351.2 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:159409673 C>T maps to NM_012351.2 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:159410102 C>T maps to NM_012351.2 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:159409868 G>A maps to NM_012351.2 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:159409880 G>A maps to NM_012351.2 Q111Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:159410279 G>A maps to NM_012351.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:159410024 C>T maps to NM_012351.2 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:159409835 C>T maps to NM_012351.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr1:159410435 C>T maps to NM_012351.2 N296N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:159410141 C>T maps to NM_012351.2 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:159409766 C>T maps to NM_012351.2 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:159409967 C>T maps to NM_012351.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:159283513 G>A maps to NM_001004467.1 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:159283645 G>A maps to NM_001004467.1 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:159283696 G>A maps to NM_001004467.1 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:159283588 G>A maps to NM_001004467.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr1:159284410 G>A maps to NM_001004467.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:159283705 C>T maps to NM_001004467.1 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:159283942 G>A maps to NM_001004467.1 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:159283489 G>A maps to NM_001004467.1 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:159283795 G>A maps to NM_001004467.1 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:159283651 C>T maps to NM_001004467.1 Q266Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:159284215 G>A maps to NM_001004467.1 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr1:159284413 G>A maps to NM_001004467.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:159284245 G>A maps to NM_001004467.1 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:159283828 G>A maps to NM_001004467.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr1:159284041 G>A maps to NM_001004467.1 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:159283828 G>A maps to NM_001004467.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:159283540 C>T maps to NM_001004467.1 Q303Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:159284431 G>A maps to NM_001004467.1 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:159284311 G>A maps to NM_001004467.1 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:159505704 G>A maps to NM_001004469.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:159505098 C>T maps to NM_001004469.1 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:159505365 C>T maps to NM_001004469.1 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:159505785 C>T maps to NM_001004469.1 K4K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr1:159505083 G>A maps to NM_001004469.1 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr1:159505704 G>A maps to NM_001004469.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr1:159505704 G>A maps to NM_001004469.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:159505353 G>A maps to NM_001004469.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:159505395 G>A maps to NM_001004469.1 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:159505182 C>T maps to NM_001004469.1 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:158435993 C>T maps to NM_001004473.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr1:158435860 C>T maps to NM_001004473.1 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:158435545 C>T maps to NM_001004473.1 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:158435677 C>T maps to NM_001004473.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:158436013 C>T maps to NM_001004473.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr1:158436016 C>T maps to NM_001004473.1 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr1:158435596 G>A maps to NM_001004473.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr1:158436085 C>A maps to NM_001004473.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr1:158436235 G>A maps to NM_001004473.1 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:158435392 C>T maps to NM_001004473.1 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:158435932 C>T maps to NM_001004473.1 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:158435386 C>T maps to NM_001004473.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:158436034 C>T maps to NM_001004473.1 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:158436034 C>T maps to NM_001004473.1 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:158436070 C>T maps to NM_001004473.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:158436190 C>T maps to NM_001004473.1 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:158435860 C>T maps to NM_001004473.1 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:158436121 C>T maps to NM_001004473.1 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:158435981 C>T maps to NM_001004473.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158435690 C>T maps to NM_001004473.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158435834 C>T maps to NM_001004473.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr1:158435896 C>A maps to NM_001004473.1 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:158435974 C>T maps to NM_001004473.1 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:158435444 C>T maps to NM_001004473.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:158389888 G>A maps to NM_001004476.1 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:158390017 C>T maps to NM_001004476.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:158390227 T>G maps to NM_001004476.1 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:158390182 G>A maps to NM_001004476.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:158390503 C>T maps to NM_001004476.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:158390394 G>A maps to NM_001004476.1 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:158390470 G>A maps to NM_001004476.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:158390473 G>A maps to NM_001004476.1 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:158389855 G>A maps to NM_001004476.1 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:158390563 G>A maps to NM_001004476.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:158390563 G>A maps to NM_001004476.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:158390029 G>A maps to NM_001004476.1 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:158389801 G>A maps to NM_001004476.1 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:158390614 G>A maps to NM_001004476.1 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:158390139 G>A maps to NM_001004476.1 Q173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:56031457 C>T maps to NM_206899.1 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:56031541 C>T maps to NM_206899.1 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr12:56031319 T>C maps to NM_206899.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:56030905 C>T maps to NM_206899.1 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:56031538 C>T maps to NM_206899.1 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:56031271 C>T maps to NM_206899.1 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr12:56031196 C>T maps to NM_206899.1 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr12:56031406 C>T maps to NM_206899.1 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:56031520 C>T maps to NM_206899.1 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:57995987 C>T maps to NM_001004471.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:57995972 G>A maps to NM_001004471.2 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr11:57995729 G>A maps to NM_001004471.2 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:57996161 C>T maps to NM_001004471.2 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr11:57995810 G>A maps to NM_001004471.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr11:57995414 G>A maps to NM_001004471.2 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr11:57995779 G>A maps to NM_001004471.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:158450224 C>T maps to NM_001004472.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr1:158449912 C>T maps to NM_001004472.1 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:158449726 G>A maps to NM_001004472.1 Q20Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr1:158450491 T>G maps to NM_001004472.1 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:158449870 C>T maps to NM_001004472.1 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:158449912 C>T maps to NM_001004472.1 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:158449900 A>G maps to NM_001004472.1 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr1:158450620 A>G maps to NM_001004472.1 Q318Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:158449783 C>T maps to NM_001004472.1 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:158450326 C>T maps to NM_001004472.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:158449912 C>T maps to NM_001004472.1 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr1:158449855 C>T maps to NM_001004472.1 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:123847741 G>A maps to NM_001004474.1 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:123848275 G>A maps to NM_001004474.1 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:123847717 G>A maps to NM_001004474.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:123848248 G>A maps to NM_001004474.1 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr11:123847810 G>A maps to NM_001004474.1 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:123847939 C>T maps to NM_001004474.1 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr11:123848155 G>A maps to NM_001004474.1 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr11:123848356 C>T maps to NM_001004474.1 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:123847639 G>A maps to NM_001004474.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:123847608 G>A maps to NM_001004474.1 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:123848077 G>A maps to NM_001004474.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:123848170 C>T maps to NM_001004474.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:123848335 C>T maps to NM_001004474.1 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:123848224 G>A maps to NM_001004474.1 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:123848275 G>A maps to NM_001004474.1 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr1:158368941 G>A maps to NM_001004475.1 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:158369154 G>A maps to NM_001004475.1 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:158368869 G>A maps to NM_001004475.1 H129H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:158368947 G>A maps to NM_001004475.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr1:158368575 C>T maps to NM_001004475.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:158368794 G>A maps to NM_001004475.1 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr1:158368833 C>A maps to NM_001004475.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:158368848 G>A maps to NM_001004475.1 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:158368446 C>T maps to NM_001004475.1 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr1:158369214 G>A maps to NM_001004475.1 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr1:158368848 G>A maps to NM_001004475.1 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158368776 G>A maps to NM_001004475.1 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158369139 G>A maps to NM_001004475.1 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:158368902 C>T maps to NM_001004475.1 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:59481030 C>T maps to NM_001005324.1 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:59481006 G>A maps to NM_001005324.1 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr11:58034421 C>T maps to NM_207374.3 Q303Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr11:58034640 G>A maps to NM_207374.3 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:58035225 G>A maps to NM_207374.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr11:58034853 G>A maps to NM_207374.3 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:58034484 G>A maps to NM_207374.3 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:58034436 C>T maps to NM_207374.3 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:58034457 G>A maps to NM_207374.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:58035194 G>A maps to NM_207374.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:158548960 C>T maps to NM_001004477.1 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:158548717 C>T maps to NM_001004477.1 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:158549410 G>A maps to NM_001004477.1 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr1:158548822 G>A maps to NM_001004477.1 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr1:158549332 G>A maps to NM_001004477.1 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:158548900 C>T maps to NM_001004477.1 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:158548771 C>T maps to NM_001004477.1 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:158549164 C>T maps to NM_001004477.1 E175E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:158549149 G>A maps to NM_001004477.1 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr1:158549155 C>T maps to NM_001004477.1 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:158548960 C>T maps to NM_001004477.1 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:158549605 G>A maps to NM_001004477.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:158548891 G>A maps to NM_001004477.1 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158549182 G>A maps to NM_001004477.1 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr1:158576413 C>T maps to NM_001004478.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr1:158576821 G>A maps to NM_001004478.1 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:158576566 C>T maps to NM_001004478.1 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr1:158576308 C>T maps to NM_001004478.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:158576482 G>A maps to NM_001004478.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:158577106 G>A maps to NM_001004478.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr1:158576413 C>T maps to NM_001004478.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:158577041 C>T maps to NM_001004478.1 Q272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:158577043 G>A maps to NM_001004478.1 Q272Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:158576824 C>T maps to NM_001004478.1 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr1:158577106 G>A maps to NM_001004478.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:158576413 C>T maps to NM_001004478.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr1:158576269 C>T maps to NM_001004478.1 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr1:158576830 C>T maps to NM_001004478.1 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158577133 G>A maps to NM_001004478.1 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr1:158576654 C>T maps to NM_001004478.1 Q143*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D3-A3MU-06A-11D-A21A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr6:29394884 A>G maps to NM_013937.2 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr6:29394893 A>T maps to NM_013937.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:29395052 G>A maps to NM_013937.2 D122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:29394863 G>A maps to NM_013937.2 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:29395301 G>A maps to NM_013937.2 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:29395010 C>T maps to NM_013937.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:20665880 C>T maps to NM_001005503.1 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr14:20665796 C>T maps to NM_001005503.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr14:20665715 C>T maps to NM_001005503.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:20665542 C>T maps to NM_001005503.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:20665670 G>A maps to NM_001005503.1 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:20666201 C>T maps to NM_001005503.1 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr14:20665949 C>T maps to NM_001005503.1 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr14:20665682 C>T maps to NM_001005503.1 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr14:20666087 C>T maps to NM_001005503.1 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr14:20665812 T>C maps to NM_001005503.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr14:20666237 C>T maps to NM_001005503.1 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr14:20666513 G>A maps to NM_001005503.1 K340K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr14:20666111 C>T maps to NM_001005503.1 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr14:20665808 C>T maps to NM_001005503.1 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:20665658 C>T maps to NM_001005503.1 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:20666273 G>A maps to NM_001005503.1 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:20666270 C>T maps to NM_001005503.1 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr22:16449681 G>A maps to NM_001005239.1 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:16449126 G>A maps to NM_001005239.1 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:19377811 C>T maps to NM_001013354.1 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:19378111 C>T maps to NM_001013354.1 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr14:19377715 C>T maps to NM_001013354.1 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr14:19378111 C>T maps to NM_001013354.1 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr14:19378108 G>A maps to NM_001013354.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr14:19378042 C>T maps to NM_001013354.1 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr14:19378101 G>A maps to NM_001013354.1 W170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr14:19378042 C>T maps to NM_001013354.1 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:19378099 G>T maps to NM_001013354.1 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr14:19377760 G>A maps to NM_001013354.1 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr14:20710961 C>T maps to NM_001004479.1 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr14:20711324 G>A maps to NM_001004479.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:20711636 C>T maps to NM_001004479.1 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr14:20711057 C>T maps to NM_001004479.1 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:20711003 C>T maps to NM_001004479.1 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr14:20711658 C>T maps to NM_001004479.1 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:20711876 C>T maps to NM_001004479.1 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr14:20711183 C>T maps to NM_001004479.1 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:20711300 G>A maps to NM_001004479.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:20711558 C>T maps to NM_001004479.1 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr14:20692215 C>T maps to NM_001004480.1 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr14:20692341 C>T maps to NM_001004480.1 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:20692827 G>A maps to NM_001004480.1 K320K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:20692320 C>T maps to NM_001004480.1 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr14:20692621 C>T maps to NM_001004480.1 R252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:20692515 C>T maps to NM_001004480.1 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:20691972 C>T maps to NM_001004480.1 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:20691873 C>T maps to NM_001004480.1 F2F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr14:20691987 G>A maps to NM_001004480.1 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr14:20692326 C>T maps to NM_001004480.1 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:248004379 G>A maps to NM_001001959.1 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:248004808 G>A maps to NM_001001959.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr1:248004538 G>A maps to NM_001001959.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr1:248005105 G>A maps to NM_001001959.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr1:248004238 G>A maps to NM_001001959.1 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:248004730 G>A maps to NM_001001959.1 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:248005012 G>A maps to NM_001001959.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:248004538 G>A maps to NM_001001959.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:248004481 G>A maps to NM_001001959.1 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248004717 G>A maps to NM_001001959.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248005087 C>T maps to NM_001001959.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248005099 G>A maps to NM_001001959.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr1:248004796 G>A maps to NM_001001959.1 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:248004277 C>T maps to NM_001001959.1 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:29364961 T>C maps to NM_013936.3 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr6:29365201 C>T maps to NM_013936.3 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:29364562 C>T maps to NM_013936.3 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:29364592 G>A maps to NM_013936.3 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:29364562 C>T maps to NM_013936.3 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:29364622 C>T maps to NM_013936.3 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:29365267 G>A maps to NM_013936.3 E264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr6:29364949 C>T maps to NM_013936.3 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:29342599 C>A maps to NM_030959.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:29342883 G>A maps to ENST00000396806 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:29342251 C>T maps to NM_030959.2 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:29342737 C>T maps to ENST00000396806 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:29342164 C>T maps to NM_030959.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr6:29342554 C>T maps to NM_030959.2 Q170Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr6:29342983 C>T maps to ENST00000396806 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:29342695 G>A maps to ENST00000396806 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr10:45799183 G>A maps to NM_001004297.2 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:45799153 G>A maps to NM_001004297.2 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:45799153 G>A maps to NM_001004297.2 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr10:45799225 G>A maps to NM_001004297.2 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:45799174 G>A maps to NM_001004297.2 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:45799189 C>T maps to NM_001004297.2 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:45799330 C>T maps to NM_001004297.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:45799375 G>A maps to NM_001004297.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr10:45799174 G>A maps to NM_001004297.2 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr9:107367089 C>T maps to NM_001004481.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:107367599 G>A maps to NM_001004481.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:107367194 G>A maps to NM_001004481.1 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr9:107367137 G>A maps to NM_001004481.1 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:107367520 G>A maps to NM_001004481.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:107367629 G>A maps to NM_001004481.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:107367887 G>A maps to NM_001004481.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr9:107367266 G>A maps to NM_001004481.1 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr9:107298149 C>T maps to NM_001001961.1 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr9:107299019 G>A maps to NM_001001961.1 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr9:107298473 G>A maps to NM_001001961.1 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr9:107298800 G>A maps to NM_001001961.1 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr9:107298149 C>T maps to NM_001001961.1 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:107298404 C>T maps to NM_001001961.1 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:107299019 G>A maps to NM_001001961.1 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr9:107298473 G>A maps to NM_001001961.1 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr9:107298602 G>A maps to NM_001001961.1 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr9:107298473 G>A maps to NM_001001961.1 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:107298817 G>A maps to NM_001001961.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:107298449 G>A maps to NM_001001961.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:107298515 G>A maps to NM_001001961.1 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr9:107298815 C>T maps to NM_001001961.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:107298473 G>A maps to NM_001001961.1 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr9:107289151 G>A maps to NM_001001919.1 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr9:107288689 G>A maps to NM_001001919.1 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:107289148 G>A maps to NM_001001919.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr9:107288827 G>A maps to NM_001001919.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:107288806 C>T maps to NM_001001919.1 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr9:107288986 G>A maps to NM_001001919.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr9:107289475 G>A maps to NM_001001919.1 N5N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr9:107289112 G>A maps to NM_001001919.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr9:107289286 G>A maps to NM_001001919.1 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:107288854 G>A maps to NM_001001919.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr9:107288986 G>A maps to NM_001001919.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr9:107289415 G>A maps to NM_001001919.1 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr9:107288806 C>T maps to NM_001001919.1 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr9:107288806 C>T maps to NM_001001919.1 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr9:107289148 G>A maps to NM_001001919.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr9:107289415 G>A maps to NM_001001919.1 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:107288830 G>A maps to NM_001001919.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:107288839 G>A maps to NM_001001919.1 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:107289352 G>A maps to NM_001001919.1 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:107288830 G>A maps to NM_001001919.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr9:107288959 G>A maps to NM_001001919.1 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr9:107360961 G>A maps to NM_001004482.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr9:107361388 G>A maps to NM_001004482.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr9:107360782 C>T maps to NM_001004482.1 K304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr9:107361415 G>A maps to NM_001004482.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr9:107361331 G>A maps to NM_001004482.1 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr9:107360980 G>A maps to NM_001004482.1 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr9:107361664 C>T maps to NM_001004482.1 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:107360935 C>T maps to NM_001004482.1 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:107361190 G>A maps to NM_001004482.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:107361306 G>A maps to NM_001004482.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:107361654 G>A maps to NM_001004482.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr9:107361076 G>A maps to NM_001004482.1 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr9:107331456 G>A maps to NM_001004483.1 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:107331528 C>T maps to NM_001004483.1 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr9:107331486 C>T maps to NM_001004483.1 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr9:107331699 C>T maps to NM_001004483.1 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:107331636 C>T maps to NM_001004483.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:107331531 C>T maps to NM_001004483.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:107331555 G>A maps to NM_001004483.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:107332281 C>T maps to NM_001004483.1 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:107331513 G>A maps to NM_001004483.1 K22K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:107331798 G>A maps to NM_001004483.1 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr9:107331654 C>T maps to NM_001004483.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:107331703 C>T maps to NM_001004483.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr9:107331675 C>T maps to NM_001004483.1 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr9:107332053 G>A maps to NM_001004483.1 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr9:107331798 G>A maps to NM_001004483.1 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr9:107332095 C>T maps to NM_001004483.1 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr9:107380041 G>A maps to NM_001001956.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr9:107380039 C>T maps to NM_001001956.1 W149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr9:107380179 G>A maps to NM_001001956.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr9:107380128 G>A maps to NM_001001956.1 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:107379816 G>A maps to NM_001001956.1 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr9:107457502 G>A maps to NM_001004484.1 K267K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr9:107457247 C>T maps to NM_001004484.1 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr9:107457244 G>A maps to NM_001004484.1 W181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:107457337 A>G maps to NM_001004484.1 E212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:107457421 G>A maps to NM_001004484.1 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:107456938 C>T maps to NM_001004484.1 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr9:107267322 G>A maps to NM_001004485.1 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr9:107266617 C>T maps to NM_001004485.1 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr9:107266585 C>T maps to NM_001004485.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:107267136 C>T maps to NM_001004485.1 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:107266962 C>T maps to NM_001004485.1 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:107266989 G>A maps to NM_001004485.1 W149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr9:107267205 C>T maps to NM_001004485.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr9:107266728 C>T maps to NM_001004485.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr9:107267484 C>T maps to NM_001004485.1 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr9:107266869 C>T maps to NM_001004485.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr9:107266962 C>T maps to NM_001004485.1 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr9:107267484 C>T maps to NM_001004485.1 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:107267484 C>T maps to NM_001004485.1 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:107266683 C>T maps to NM_001004485.1 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:107267145 G>A maps to NM_001004485.1 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr1:247836238 A>G maps to NM_001005487.1 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:247836217 G>A maps to NM_001005487.1 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:247835854 C>T maps to NM_001005487.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:247836112 C>T maps to NM_001005487.1 K77K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr1:247836166 G>A maps to NM_001005487.1 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:247836280 C>T maps to NM_001005487.1 Q21Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:247836292 C>T maps to NM_001005487.1 K17K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:247836166 G>A maps to NM_001005487.1 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:247835467 C>T maps to NM_001005487.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:247836115 C>T maps to NM_001005487.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:247835509 C>T maps to NM_001005487.1 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr23:130678460 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr23:130678509 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:130678410 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:130678867 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:130678814 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:130678878 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr23:130678392 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:130678431 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:130678702 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr23:130678656 T>G did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:130678232 C>T did not map to a codon.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr23:130678949 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:130678527 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:130678592 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:130678424 C>T did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:130678967 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:35869519 C>T maps to NM_001004487.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:35869519 C>T maps to NM_001004487.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr1:247978617 G>A maps to NM_001001966.1 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:247978232 A>G maps to NM_001001966.1 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr1:247978791 G>A maps to NM_001001966.1 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:247978179 G>A maps to NM_001001966.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr1:247978755 G>A maps to NM_001001966.1 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr1:248512159 C>T maps to NM_001001918.1 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:248512921 C>T maps to NM_001001918.1 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:248512474 C>T maps to NM_001001918.1 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:248512879 G>A maps to NM_001001918.1 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:248512711 C>T maps to NM_001001918.1 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:248512702 C>T maps to NM_001001918.1 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:248512231 C>T maps to NM_001001918.1 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:248512184 C>T maps to NM_001001918.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:248512562 C>T maps to NM_001001918.1 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:248512198 C>T maps to NM_001001918.1 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:248512471 G>A maps to NM_001001918.1 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:248512474 C>T maps to NM_001001918.1 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:248512861 G>A maps to NM_001001918.1 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:248512474 C>T maps to NM_001001918.1 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr1:248512747 C>T maps to NM_001001918.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:248845032 G>A maps to NM_001004734.1 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:248845248 G>A maps to NM_001004734.1 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:248845269 G>A maps to NM_001004734.1 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr1:248845068 G>T maps to NM_001004734.1 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:248845269 G>A maps to NM_001004734.1 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr1:248844732 C>T maps to NM_001004734.1 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248845323 G>A maps to NM_001004734.1 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr6:29275263 G>A maps to NM_030946.1 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:29274702 C>T maps to NM_030946.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:29275192 C>T maps to NM_030946.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:29275143 C>T maps to NM_030946.1 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:29274810 G>A maps to NM_030946.1 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr6:29274588 C>T maps to NM_030946.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:29274633 C>T maps to NM_030946.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:29275125 C>T maps to NM_030946.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:29275209 C>T maps to NM_030946.1 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr6:29274666 G>A maps to NM_030946.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:3119591 G>A maps to NM_014565.2 Q226Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr17:3119690 C>T maps to NM_014565.2 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:3119114 C>T maps to NM_014565.2 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr17:3119588 C>T maps to NM_014565.2 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr17:3119771 C>T maps to NM_014565.2 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr17:3119771 C>T maps to NM_014565.2 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr17:3118943 G>A maps to NM_014565.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr17:3119099 C>T maps to NM_014565.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:3119771 C>T maps to NM_014565.2 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr17:3100898 G>A maps to NM_012352.1 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr17:3101679 C>T maps to NM_012352.1 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr17:3100892 C>T maps to NM_012352.1 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr9:125391382 G>A maps to NM_001004450.1 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:125391721 G>A maps to NM_001004450.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr9:125390893 G>C maps to NM_001004450.1 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr9:125390911 C>T maps to NM_001004450.1 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr9:125391364 G>A maps to NM_001004450.1 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr9:125391721 G>A maps to NM_001004450.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr9:125391514 C>T maps to NM_001004450.1 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr1:247921573 G>A maps to NM_012353.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:247920928 G>A maps to NM_012353.2 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:247921024 G>A maps to NM_012353.2 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:247921672 G>A maps to NM_012353.2 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:247921396 G>A maps to NM_012353.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:247921003 C>T maps to NM_012353.2 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:247921396 G>A maps to NM_012353.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:247921543 G>A maps to NM_012353.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:247921189 G>A maps to NM_012353.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr1:247921189 G>A maps to NM_012353.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:247921672 G>A maps to NM_012353.2 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:247921396 G>A maps to NM_012353.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:247921585 C>T maps to NM_012353.2 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr17:2996196 G>A maps to NM_002548.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr17:2995980 G>A maps to NM_002548.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr17:2995981 G>A maps to NM_002548.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:2996029 G>A maps to NM_002548.2 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:2996056 G>T maps to NM_002548.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:2996211 G>A maps to NM_002548.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:2996155 G>A maps to NM_002548.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr17:2996151 G>A maps to NM_002548.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr17:2995981 G>A maps to NM_002548.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr17:2995651 G>A maps to NM_002548.2 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:2996104 G>A maps to NM_002548.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:2995948 G>A maps to NM_002548.2 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:3301101 G>A maps to NM_003553.2 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr17:3301278 G>A maps to NM_003553.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr17:3301560 G>A maps to NM_003553.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:3300825 C>T maps to NM_003553.2 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:3336172 G>A maps to NM_003554.1 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr17:3336751 G>A maps to NM_003554.1 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr16:3254842 C>T maps to NM_012360.1 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr16:3254554 C>T maps to NM_012360.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr16:3254566 C>T maps to NM_012360.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr16:3254266 G>A maps to NM_012360.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr16:3254363 C>T maps to NM_012360.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:3254245 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:3254584 C>T maps to NM_012360.1 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr16:3254872 C>T maps to NM_012360.1 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:3254584 C>T maps to NM_012360.1 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr16:3254554 C>T maps to NM_012360.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr16:3254842 C>T maps to NM_012360.1 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:3254527 C>T maps to NM_012360.1 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr16:3255166 G>A maps to NM_012360.1 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr16:3254665 C>T maps to NM_012360.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr16:3254602 C>T maps to NM_012360.1 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr16:3255037 C>T maps to NM_012360.1 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr16:3254554 C>T maps to NM_012360.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr16:3255007 C>T maps to NM_012360.1 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:3254554 C>T maps to NM_012360.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:3255032 C>T maps to NM_012360.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr17:3030566 G>A maps to ENST00000381953 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:3030611 G>A maps to ENST00000381953 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr17:3030146 C>T maps to ENST00000381953 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:3030131 A>G maps to ENST00000381953 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:3030188 C>T maps to ENST00000381953 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr17:3030349 G>A maps to ENST00000381953 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr17:3030146 C>T maps to ENST00000381953 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr17:3030710 G>A maps to ENST00000381953 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:3030698 G>A maps to ENST00000381953 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr17:3030584 G>A maps to ENST00000381953 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr17:3030056 G>A maps to ENST00000381953 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr17:3030533 G>A maps to ENST00000381953 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr19:15198337 C>T maps to NM_001004713.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr19:15198368 C>T maps to NM_001004713.1 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr19:15198754 G>A maps to NM_001004713.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr19:15198406 C>T maps to NM_001004713.1 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr19:15198808 C>T maps to NM_001004713.1 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:15198368 C>T maps to NM_001004713.1 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:15197947 G>A maps to NM_001004713.1 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr19:15198322 G>A maps to NM_001004713.1 W149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:15198721 C>T maps to NM_001004713.1 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr9:125239734 A>C maps to NM_001004451.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:125239943 G>A maps to NM_001004451.1 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:125240163 G>A maps to NM_001004451.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr9:125239278 G>A maps to NM_001004451.1 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:125239571 G>A maps to NM_001004451.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:125240166 G>A maps to NM_001004451.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:125239752 G>A maps to NM_001004451.1 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr9:125240019 G>A maps to NM_001004451.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr9:125240121 G>A maps to NM_001004451.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:125239413 G>A maps to NM_001004451.1 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:125240121 G>A maps to NM_001004451.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr9:125239893 G>A maps to NM_001004451.1 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:125273214 C>T maps to ENST00000444856 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:125273979 C>T maps to NM_054107.1 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:125273160 C>T maps to ENST00000444856 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:125273982 T>G maps to NM_054107.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr9:125273172 C>T maps to ENST00000444856 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:125273118 C>T maps to ENST00000444856 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:125273118 C>T maps to ENST00000444856 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:125273185 C>T maps to ENST00000444856 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr9:125273976 G>A maps to NM_054107.1 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr9:125273722 C>T maps to NM_054107.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:125273454 C>T maps to ENST00000444856 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr9:125282297 G>A maps to NM_001004452.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr9:125281529 C>T maps to ENST00000444856 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:125282144 C>T maps to NM_001004452.1 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr9:125282297 G>A maps to NM_001004452.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr9:125281757 C>T maps to ENST00000444856 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr9:125281757 C>T maps to ENST00000444856 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:125281454 C>T maps to ENST00000444856 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr9:125281919 C>T maps to NM_001004452.1 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:125281490 G>A maps to ENST00000444856 Q190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:125281524 C>T maps to ENST00000444856 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:125282012 C>T maps to NM_001004452.1 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:125282297 G>A maps to NM_001004452.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr9:125282216 C>T maps to NM_001004452.1 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr9:125281919 C>T maps to NM_001004452.1 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr9:125562643 G>A maps to NM_080859.1 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr9:125563090 C>A maps to NM_080859.1 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr9:125563177 C>T maps to NM_080859.1 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:125563282 G>A maps to NM_080859.1 W294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr9:125562577 C>T maps to NM_080859.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr9:125424368 C>T maps to ENST00000373686 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:125424131 C>T maps to ENST00000373686 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:125424092 C>T maps to ENST00000373686 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:125424584 C>T maps to ENST00000373686 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr9:125424311 C>T maps to ENST00000373686 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:125424092 C>T maps to ENST00000373686 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr9:125424774 C>T maps to ENST00000373686 Q311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:125437534 C>T maps to NM_001005234.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr9:125437716 C>T maps to NM_001005234.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr9:125437506 C>T maps to NM_001005234.1 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:125437890 C>T maps to NM_001005234.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:125438073 C>T maps to NM_001005234.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr9:125438136 C>T maps to NM_001005234.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr9:125437782 C>T maps to NM_001005234.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:125437962 G>A maps to NM_001005234.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:125486999 C>T maps to NM_001005235.1 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr9:125486831 C>T maps to NM_001005235.1 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr9:125486369 C>T maps to NM_001005235.1 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr9:125486327 C>T maps to NM_001005235.1 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr9:125486789 C>T maps to NM_001005235.1 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr9:125486804 C>T maps to NM_001005235.1 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:125486594 G>A maps to NM_001005235.1 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:125487018 C>T maps to NM_001005235.1 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr9:125486450 C>T maps to NM_001005235.1 Y61Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr9:125512977 C>G maps to ENST00000373684 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:125512860 C>T maps to ENST00000373684 H281H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:125512227 C>T maps to ENST00000373684 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr9:125512248 G>A maps to ENST00000373684 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:125512452 G>A maps to ENST00000373684 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:125512428 G>A maps to ENST00000373684 Q137Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr9:125512185 C>T maps to ENST00000373684 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr9:125513034 G>A maps to ENST00000373684 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:125512488 C>T maps to ENST00000373684 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr9:125330663 G>A maps to NM_001004454.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr9:125330723 G>A maps to NM_001004454.1 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr9:125329867 G>A maps to NM_001004454.1 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr9:125330012 C>T maps to NM_001004454.1 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr9:125330435 G>A maps to NM_001004454.1 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:125330654 G>A maps to NM_001004454.1 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr9:125330186 G>A maps to NM_001004454.1 C190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr9:125330618 G>A maps to NM_001004454.1 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr9:125330654 G>A maps to NM_001004454.1 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:125330749 T>G maps to NM_001004454.1 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:125330480 G>A maps to NM_001004454.1 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr9:125330474 G>A maps to NM_001004454.1 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr9:125330477 G>A maps to NM_001004454.1 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr9:125330255 G>A maps to NM_001004454.1 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr9:125330003 G>A maps to NM_001004454.1 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr9:125330714 G>A maps to NM_001004454.1 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:125330003 G>A maps to NM_001004454.1 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr19:9204417 C>T maps to ENST00000305465 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr19:9204843 G>A maps to ENST00000305465 K311K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr19:9204237 C>T maps to ENST00000305465 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr19:9204507 G>A maps to ENST00000305465 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:9204399 C>T maps to ENST00000305465 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:9204288 C>T maps to ENST00000305465 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:9204519 C>T maps to ENST00000305465 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:9204288 C>T maps to ENST00000305465 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr19:9204330 C>T maps to ENST00000305465 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9204042 G>A maps to ENST00000305465 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9204288 C>T maps to ENST00000305465 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9204489 G>A maps to ENST00000305465 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:9204810 G>A maps to ENST00000305465 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr9:125288861 G>A maps to ENST00000359439 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:125288699 C>T maps to ENST00000359439 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr9:125289467 G>A maps to ENST00000359439 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr9:125289539 G>A maps to ENST00000359439 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr9:125288711 G>A maps to ENST00000359439 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr9:125288800 G>A maps to ENST00000359439 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:125288789 G>A maps to ENST00000359439 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:125288810 G>A maps to ENST00000359439 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr9:125316062 C>T maps to NM_001004457.1 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr9:125316095 C>T maps to NM_001004457.1 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr9:125316062 C>T maps to NM_001004457.1 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:125316140 C>T maps to NM_001004457.1 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:125315496 A>T maps to NM_001004457.1 K17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr9:125316095 C>T maps to NM_001004457.1 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr9:125316095 C>T maps to NM_001004457.1 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr9:125316020 C>T maps to NM_001004457.1 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:125315489 G>A maps to NM_001004457.1 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:125316008 C>G maps to NM_001004457.1 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr9:125315726 C>T maps to NM_001004457.1 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr9:125377549 C>T maps to NM_012364.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:125377354 C>T maps to NM_012364.1 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr9:125377768 C>T maps to NM_012364.1 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr9:125377537 C>T maps to NM_012364.1 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr9:125377495 C>T maps to NM_012364.1 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr9:125377153 C>T maps to NM_012364.1 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr9:125377420 C>T maps to NM_012364.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr9:125377204 C>T maps to NM_012364.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr9:125377894 G>A maps to NM_012364.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr9:125377327 C>T maps to NM_012364.1 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr11:57982332 C>T maps to NM_001004458.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr11:57983139 G>A maps to NM_001004458.1 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:57982548 C>T maps to NM_001004458.1 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:57982296 C>T maps to NM_001004458.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:57983037 C>T maps to NM_001004458.1 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:57983037 C>T maps to NM_001004458.1 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:57983133 G>A maps to NM_001004458.1 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:57982704 C>T maps to NM_001004458.1 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:57971428 G>A maps to NM_001004459.1 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:57970738 C>T maps to NM_001004459.1 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:57970828 G>A maps to NM_001004459.1 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:57970780 G>A maps to NM_001004459.1 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:57970951 G>A maps to NM_001004459.1 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:143793006 G>A maps to NM_001004135.1 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr7:143793075 G>A maps to NM_001004135.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:143792394 G>A maps to NM_001004135.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr7:143792931 C>T maps to NM_001004135.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:143793045 G>A maps to NM_001004135.1 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr7:143792811 C>T maps to NM_001004135.1 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr7:143792313 G>A maps to NM_001004135.1 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:143793114 G>A maps to NM_001004135.1 W305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:143793081 A>C maps to NM_001004135.1 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr7:143792739 C>T maps to NM_001004135.1 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:143792595 C>T maps to NM_001004135.1 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:143792643 G>A maps to NM_001004135.1 W148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr7:143793009 G>A maps to NM_001004135.1 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr7:143792331 C>T maps to NM_001004135.1 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:143792874 G>A maps to NM_001004135.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:143792859 C>T maps to NM_001004135.1 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:143793108 C>T maps to NM_001004135.1 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr7:143792751 C>T maps to NM_001004135.1 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr7:143793022 C>T maps to NM_001004135.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr7:143792628 G>A maps to NM_001004135.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr7:143792730 C>T maps to NM_001004135.1 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr7:143827122 G>A maps to NM_001001659.1 K306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr7:143827038 C>T maps to NM_001001659.1 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:143827080 G>A maps to NM_001001659.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:143826573 G>A maps to NM_001001659.1 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr7:143826895 G>T maps to NM_001001659.1 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr7:143826489 A>C maps to NM_001001659.1 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr7:143826660 C>T maps to NM_001001659.1 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:143827080 G>A maps to NM_001001659.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr7:143827119 G>A maps to NM_001001659.1 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr7:143826606 C>T maps to NM_001001659.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr7:143826660 C>T maps to NM_001001659.1 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr7:143807497 C>T maps to NM_001005480.2 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:143807334 C>T maps to NM_001005480.2 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:143806933 C>T maps to NM_001005480.2 Q87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:143807249 G>A maps to NM_001005480.2 W192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr7:143807475 G>A maps to NM_001005480.2 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:143807205 C>T maps to NM_001005480.2 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:143807310 G>A maps to NM_001005480.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:143806752 C>T maps to NM_001005480.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:143806714 C>T maps to NM_001005480.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr7:143807349 G>A maps to NM_001005480.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr7:143806794 G>A maps to NM_001005480.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:143806806 C>T maps to NM_001005480.2 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr7:143806794 G>A maps to NM_001005480.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:143807052 C>T maps to NM_001005480.2 C126C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:143807589 G>A maps to NM_001005480.2 Q305Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr7:143807055 C>T maps to NM_001005480.2 H127H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr7:143807481 G>A maps to NM_001005480.2 Q269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:143807592 G>A maps to NM_001005480.2 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:143807592 G>A maps to NM_001005480.2 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr7:143771929 G>A maps to NM_001004488.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr7:143771405 C>T maps to NM_001004488.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:143772037 C>T maps to NM_001004488.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:143771557 G>A maps to NM_001004488.1 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr7:143771344 C>T maps to NM_001004488.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr7:143771755 G>A maps to NM_001004488.1 W148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr7:143771368 C>T maps to NM_001004488.1 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr7:143771443 C>T maps to NM_001004488.1 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:143771347 C>T maps to NM_001004488.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:143771683 C>T maps to NM_001004488.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:143771941 C>T maps to NM_001004488.1 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr7:143772112 G>A maps to NM_001004488.1 K267K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr7:143771380 G>A maps to NM_001004488.1 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr7:143771521 C>T maps to NM_001004488.1 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr7:143771344 C>T maps to NM_001004488.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr7:143771512 C>T maps to NM_001004488.1 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:143771317 G>A maps to NM_001004488.1 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:143771992 C>T maps to NM_001004488.1 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr7:143771515 C>T maps to NM_001004488.1 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:143772187 G>A maps to NM_001004488.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr7:143771782 C>T maps to NM_001004488.1 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr7:143771431 G>A maps to NM_001004488.1 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr7:143748156 C>T maps to NM_012365.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr7:143748393 C>T maps to NM_012365.1 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:143748027 C>T maps to NM_012365.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:143747550 C>T maps to NM_012365.1 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:143748192 C>A maps to NM_012365.1 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr7:143747859 G>A maps to NM_012365.1 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr7:143747526 C>T maps to NM_012365.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:143747772 C>T maps to NM_012365.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr7:143748222 C>T maps to NM_012365.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:143748357 G>A maps to NM_012365.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:143748372 G>A maps to NM_012365.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:143747577 G>A maps to NM_012365.1 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:143747939 G>A maps to NM_012365.1 W149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr7:143747898 C>T maps to NM_012365.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:143748114 G>A maps to NM_012365.1 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr7:143747506 C>T maps to NM_012365.1 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr7:143747583 C>T maps to NM_012365.1 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:143747605 C>T maps to NM_012365.1 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:143748222 C>T maps to NM_012365.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:143748285 C>T maps to NM_012365.1 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr7:143747526 C>T maps to NM_012365.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:143747997 C>T maps to NM_012365.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:143747526 C>T maps to NM_012365.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr7:143956658 C>T maps to NM_001005328.1 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr7:143956684 G>A maps to NM_001005328.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr7:143956031 C>T maps to NM_001005328.1 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:143956631 G>A maps to NM_001005328.1 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:99474347 G>A maps to NM_001005276.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:99473783 G>A maps to NM_001005276.1 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr7:99474421 G>A maps to NM_001005276.1 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr7:99474422 G>A maps to NM_001005276.1 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr7:99474578 G>A maps to NM_001005276.1 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:6806801 C>T maps to NM_001004489.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:6806561 C>T maps to NM_001004489.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr11:6806692 G>A maps to NM_001004489.2 W142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:6806561 C>T maps to NM_001004489.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:6806717 C>T maps to NM_001004489.2 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:6806669 C>T maps to NM_001004489.2 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:6790140 C>T maps to NM_001004490.1 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:6789888 C>T maps to NM_001004490.1 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr11:6789369 G>A maps to NM_001004490.1 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:6790089 G>A maps to NM_001004490.1 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:6789483 C>T maps to NM_001004490.1 K235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:248128815 C>T maps to NM_001004491.1 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr1:248129235 A>G maps to NM_001004491.1 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:248128866 C>T maps to NM_001004491.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:248129310 C>T maps to NM_001004491.1 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:248128656 C>T maps to NM_001004491.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:248129295 C>T maps to NM_001004491.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr11:74800539 G>A maps to NM_001005285.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:74800545 G>A maps to NM_001005285.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:74799831 G>A maps to NM_001005285.1 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:74800092 G>A maps to NM_001005285.1 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:74800155 G>C maps to NM_001005285.1 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:74800530 G>A maps to NM_001005285.1 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr11:74799927 G>A maps to NM_001005285.1 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr1:247614942 C>T maps to NM_001004492.1 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr1:247615086 G>A maps to NM_001004492.1 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:247614627 A>G maps to NM_001004492.1 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:247614804 G>A maps to NM_001004492.1 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:247614960 G>A maps to NM_001004492.1 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:247614471 G>A maps to NM_001004492.1 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:247614639 C>T maps to NM_001004492.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:247614624 G>A maps to NM_001004492.1 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:247614654 G>A maps to NM_001004492.1 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:247614801 G>A maps to NM_001004492.1 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:247614804 G>T maps to NM_001004492.1 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr6:27879791 G>A maps to NM_033057.2 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr6:27879875 G>A maps to NM_033057.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr6:27879785 G>A maps to NM_033057.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr6:29054620 G>A maps to NM_001005226.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:29054842 G>A maps to NM_001005226.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr6:29054545 A>T maps to NM_001005226.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:29054566 G>A maps to NM_001005226.2 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr6:29054719 G>A maps to NM_001005226.2 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:29054101 G>A maps to NM_001005226.2 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:29054974 G>A maps to NM_001005226.2 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr6:29054446 C>T maps to NM_001005226.2 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr6:29054668 G>A maps to NM_001005226.2 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr6:27925444 C>T maps to NM_012367.1 Q143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:27925359 C>T maps to NM_012367.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:27925896 G>A maps to NM_012367.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:27925213 C>T maps to NM_012367.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:27925785 C>T maps to NM_012367.1 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:27925617 C>T maps to NM_012367.1 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:27925684 C>T maps to NM_012367.1 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr6:27925335 C>T maps to NM_012367.1 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr6:27925896 G>A maps to NM_012367.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:27925635 C>T maps to NM_012367.1 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:3406125 C>T maps to NM_012368.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr16:3406857 G>A maps to NM_012368.2 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:3406251 C>T maps to NM_012368.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:3406278 C>T maps to NM_012368.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr16:3406125 C>T maps to NM_012368.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr16:3406743 G>A maps to NM_012368.2 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr1:247694991 G>A maps to NM_198074.4 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:247695300 C>T maps to NM_198074.4 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr1:247695393 C>T maps to NM_198074.4 Q140Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:247695138 G>A maps to NM_198074.4 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:247695300 C>T maps to NM_198074.4 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:247695726 G>A maps to NM_198074.4 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:247695696 C>T maps to NM_198074.4 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:247694967 G>A maps to NM_198074.4 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:247695747 G>A maps to NM_198074.4 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:247695663 G>A maps to NM_198074.4 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:247695675 G>A maps to NM_198074.4 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:247695168 G>A maps to NM_198074.4 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:247694919 C>T maps to NM_198074.4 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:247694931 C>T maps to NM_198074.4 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:247695171 G>A maps to NM_198074.4 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:247695030 G>A maps to NM_198074.4 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:6913245 G>A maps to NM_003700.1 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:6913715 G>A maps to NM_003700.1 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:6913604 G>A maps to NM_003700.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:6913458 G>A maps to NM_003700.1 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:6913092 C>T maps to NM_003700.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:6912876 G>A maps to NM_003700.1 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr11:6913200 G>A maps to NM_003700.1 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr11:6913088 G>A maps to NM_003700.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr11:6913593 G>A maps to NM_003700.1 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:6912852 C>T maps to NM_003700.1 K293K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:6913200 G>A maps to NM_003700.1 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr11:6943158 G>A maps to NM_001004684.1 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:6942546 G>A maps to NM_001004684.1 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr11:6942267 G>A maps to NM_001004684.1 Q12Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr11:6942378 C>T maps to NM_001004684.1 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:6942667 C>T maps to NM_001004684.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr11:6943200 A>G maps to NM_001004684.1 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:143657344 C>T maps to NM_012369.2 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr7:143657150 C>T maps to NM_012369.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr7:143657491 G>A maps to NM_012369.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:143657713 C>T maps to NM_012369.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:143657854 C>T maps to NM_012369.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:143657917 G>A maps to NM_012369.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:143657980 G>A maps to NM_012369.2 W306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr7:143657941 G>A maps to NM_012369.2 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:143657185 G>A maps to NM_012369.2 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:143657980 G>A maps to NM_012369.2 W306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:143657111 C>T maps to NM_012369.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:143657389 G>A maps to NM_012369.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr7:143657953 G>A maps to NM_012369.2 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr7:143657555 C>T maps to NM_012369.2 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:143657089 G>A maps to NM_012369.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:143657917 G>A maps to NM_012369.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr7:143657173 G>A maps to NM_012369.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr7:143657683 G>T maps to NM_012369.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr7:143633110 C>T maps to NM_001004685.1 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr7:143633248 C>T maps to NM_001004685.1 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr7:143632996 C>T maps to NM_001004685.1 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr7:143632411 C>T maps to NM_001004685.1 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:143633203 G>A maps to NM_001004685.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:143633089 G>A maps to NM_001004685.1 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:143633242 G>A maps to NM_001004685.1 E306E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:143632522 C>T maps to NM_001004685.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:143632868 C>T maps to NM_001004685.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:143633221 G>A maps to NM_001004685.1 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:143632573 A>C maps to NM_001004685.1 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr7:143632378 C>T maps to NM_001004685.1 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr7:143632537 C>T maps to NM_001004685.1 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr7:143633089 G>A maps to NM_001004685.1 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr7:143632351 G>A maps to NM_001004685.1 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:143633132 C>T maps to NM_001004685.1 Q270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:143632967 C>T maps to NM_001004685.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:143632471 C>T maps to NM_001004685.1 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr7:143632999 C>T maps to NM_001004685.1 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:247752312 C>T maps to NM_001001915.1 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:247752200 C>T maps to NM_001001915.1 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:247752473 G>A maps to NM_001001915.1 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr1:247751945 C>T maps to NM_001001915.1 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:247752527 C>T maps to NM_001001915.1 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:247752419 C>T maps to NM_001001915.1 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:247751855 C>T maps to NM_001001915.1 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:247752440 C>T maps to NM_001001915.1 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:247752383 C>T maps to NM_001001915.1 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:247752383 C>T maps to NM_001001915.1 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:247752548 G>A maps to NM_001001915.1 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:247751792 G>A maps to NM_001001915.1 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:247752050 C>T maps to NM_001001915.1 C130C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:247752287 C>T maps to NM_001001915.1 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:247751843 G>A maps to NM_001001915.1 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:247752386 G>A maps to NM_001001915.1 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:247752383 C>T maps to NM_001001915.1 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:247752335 C>T maps to NM_001001915.1 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:247751765 G>A maps to NM_001001915.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:247751769 C>T maps to NM_001001915.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:247752560 G>A maps to NM_001001915.1 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:247751666 G>A maps to NM_001001915.1 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:247752346 T>A maps to NM_001001915.1 L229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:247769159 G>A maps to NM_001001914.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:247769189 C>T maps to NM_001001914.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:247769159 G>A maps to NM_001001914.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:247769279 C>T maps to NM_001001914.1 H131H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:247769792 G>A maps to NM_001001914.1 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:247769225 C>T maps to NM_001001914.1 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:247769027 C>T maps to NM_001001914.1 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr1:247769765 G>A maps to NM_001001914.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:247769714 C>T maps to NM_001001914.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:247769030 C>T maps to NM_001001914.1 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:247769750 C>T maps to NM_001001914.1 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:247769792 G>A maps to NM_001001914.1 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr1:247769723 C>T maps to NM_001001914.1 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:247769024 C>T maps to NM_001001914.1 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:247769765 G>A maps to NM_001001914.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:247769159 G>A maps to NM_001001914.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr1:247769210 C>T maps to NM_001001914.1 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:247769159 G>A maps to NM_001001914.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:247769531 C>T maps to NM_001001914.1 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr1:248685144 C>T maps to NM_001013355.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:248685727 C>T maps to NM_001013355.1 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:248685813 C>T maps to NM_001013355.1 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:248685081 C>T maps to NM_001013355.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:248685081 C>T maps to NM_001013355.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:248685415 C>T maps to NM_001013355.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr1:248685543 C>T maps to NM_001013355.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:248685727 C>T maps to NM_001013355.1 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:248685609 C>T maps to NM_001013355.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:248685693 C>T maps to NM_001013355.1 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:248685813 C>T maps to NM_001013355.1 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr1:248685627 G>A maps to NM_001013355.1 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr1:248685663 G>A maps to NM_001013355.1 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:248685004 C>T maps to NM_001013355.1 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248684976 G>A maps to NM_001013355.1 K10K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248685414 C>T maps to NM_001013355.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:248685265 T>C maps to NM_001013355.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr6:29430418 G>A maps to NM_030883.3 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:29429563 C>T maps to NM_030883.3 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:29430157 C>T maps to NM_030883.3 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:29430457 G>A maps to NM_030883.3 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:29429566 C>T maps to NM_030883.3 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:29430157 C>T maps to NM_030883.3 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:29430157 C>T maps to NM_030883.3 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:29430208 G>A maps to NM_030883.3 Q221Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr6:29430095 C>T maps to NM_030883.3 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:29556431 G>A maps to NM_007160.3 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:29556056 C>T maps to NM_007160.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:29556053 C>T maps to NM_007160.3 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:29556419 G>A maps to NM_007160.3 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr6:29555765 C>T maps to NM_007160.3 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:29556176 G>A maps to NM_007160.3 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr6:29555738 C>T maps to NM_007160.3 S6S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-FR-A69P-06A-21D-A30X-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:29142131 G>A maps to NM_030905.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:29141897 C>T maps to NM_030905.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr6:29141753 C>T maps to NM_030905.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:29142017 C>T maps to NM_030905.2 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:29142131 G>A maps to NM_030905.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:29142317 G>A maps to NM_030905.2 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr6:29142224 G>A maps to NM_030905.2 Q271Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:29141648 C>T maps to NM_030905.2 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:29141897 C>T maps to NM_030905.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:29142317 G>A maps to NM_030905.2 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:29142194 C>T maps to NM_030905.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr6:29079810 C>T maps to NM_001005216.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr6:29080494 C>T maps to NM_001005216.2 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr6:29080494 C>T maps to NM_001005216.2 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr6:29080272 C>T maps to NM_001005216.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr6:29080299 C>T maps to NM_001005216.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:29079994 C>T maps to NM_001005216.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:29080167 C>T maps to NM_001005216.2 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr6:29080338 C>T maps to NM_001005216.2 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr6:29079826 C>T maps to NM_001005216.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:29079900 C>T maps to NM_001005216.2 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr6:29079939 G>A maps to NM_001005216.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:114090527 G>A maps to ENST00000374428 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr9:114090047 G>A maps to ENST00000374428 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr9:114090350 G>A maps to ENST00000374428 D150D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr9:114090455 C>G maps to ENST00000374428 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr9:114090032 G>A maps to ENST00000374428 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr9:114089897 G>A maps to ENST00000374428 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:114090532 A>G maps to ENST00000374428 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:248263420 C>T maps to NM_175911.2 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:248263417 G>A maps to NM_175911.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr1:248263372 G>A maps to NM_175911.2 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr1:248263603 C>T maps to NM_175911.2 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:248263294 C>T maps to NM_175911.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:248262766 C>A maps to NM_175911.2 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:248263567 G>A maps to NM_175911.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:248262847 G>A maps to NM_175911.2 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:248263492 C>T maps to NM_175911.2 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:248262955 C>T maps to NM_175911.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr1:248262934 C>T maps to NM_175911.2 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:248262874 C>T maps to NM_175911.2 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr1:248262874 C>T maps to NM_175911.2 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:248263016 C>T maps to NM_175911.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248263315 C>T maps to NM_175911.2 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr1:248201712 C>T maps to NM_001004686.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr1:248202231 C>T maps to NM_001004686.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr1:248202231 C>T maps to NM_001004686.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:248202483 G>A maps to NM_001004686.2 Q305Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:248201643 C>T maps to NM_001004686.2 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:248202402 C>T maps to NM_001004686.2 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:248202498 G>A maps to NM_001004686.2 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:248201877 C>T maps to NM_001004686.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:248201643 C>T maps to NM_001004686.2 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr1:248202225 G>A maps to NM_001004686.2 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248202489 C>T maps to NM_001004686.2 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:248201643 C>T maps to NM_001004686.2 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:248201601 C>T maps to NM_001004686.2 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:248224084 C>T maps to NM_001004687.1 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:248224277 C>T maps to NM_001004687.1 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr1:248224273 G>A maps to NM_001004687.1 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:248224162 C>T maps to NM_001004687.1 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:248224642 T>C maps to NM_001004687.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr1:248224855 G>A maps to NM_001004687.1 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:248224840 C>G maps to NM_001004687.1 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:248224162 C>T maps to NM_001004687.1 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:248224757 C>T maps to NM_001004687.1 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:248112287 C>T maps to NM_001001963.1 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:248112453 C>T maps to NM_001001963.1 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:248112605 C>T maps to NM_001001963.1 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:248112260 C>T maps to NM_001001963.1 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:248112191 C>T maps to NM_001001963.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:248112338 C>T maps to NM_001001963.1 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:248112602 G>A maps to NM_001001963.1 W148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:248112254 C>T maps to NM_001001963.1 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:248112614 G>A maps to NM_001001963.1 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:248112854 G>A maps to NM_001001963.1 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:248112191 C>T maps to NM_001001963.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:248112359 C>T maps to NM_001001963.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:248112260 C>T maps to NM_001001963.1 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:248112158 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:248112733 G>A maps to NM_001001963.1 W192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr1:248112338 C>T maps to NM_001001963.1 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248112356 C>T maps to NM_001001963.1 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:248112536 C>T maps to NM_001001963.1 C126C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:248112933 C>T maps to NM_001001963.1 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:248112948 C>T maps to NM_001001963.1 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:248343364 C>T maps to NM_001004688.1 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:248343667 C>T maps to NM_001004688.1 C127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:248343913 C>T maps to NM_001004688.1 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:248344279 C>T maps to NM_001004688.1 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:248343328 C>T maps to NM_001004688.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr1:248343736 C>T maps to NM_001004688.1 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:248344171 G>A maps to NM_001004688.1 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:248343835 C>T maps to NM_001004688.1 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:248343913 C>T maps to NM_001004688.1 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:248343835 C>T maps to NM_001004688.1 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:248344126 C>T maps to NM_001004688.1 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr1:248343370 C>T maps to NM_001004688.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248343310 C>T maps to NM_001004688.1 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr1:248344288 C>T maps to NM_001004688.1 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:248343781 C>T maps to NM_001004688.1 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr1:248367007 C>T maps to NM_001004689.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:248366437 C>T maps to NM_001004689.1 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:248366446 C>T maps to NM_001004689.1 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:248366377 G>A maps to NM_001004689.1 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:248366968 C>T maps to NM_001004689.1 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:248366743 C>T maps to NM_001004689.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:248366470 C>T maps to NM_001004689.1 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr1:248367253 G>A maps to NM_001004689.1 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:248366743 C>T maps to NM_001004689.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr1:248366968 C>T maps to NM_001004689.1 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr1:248367244 C>A maps to NM_001004689.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248366641 C>T maps to NM_001004689.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr1:248367223 G>A maps to NM_001004689.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:248366959 G>A maps to NM_001004689.1 K197K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr1:248366452 C>T maps to NM_001004689.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:248402451 C>T maps to NM_017504.1 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:248402763 C>T maps to NM_017504.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:248402547 C>T maps to NM_017504.1 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:248402871 C>T maps to NM_017504.1 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr1:248403000 C>T maps to NM_017504.1 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:248402697 G>A maps to NM_017504.1 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:248402325 G>A maps to NM_017504.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:248402322 C>T maps to NM_017504.1 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr1:248402268 C>T maps to NM_017504.1 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:248402601 G>A maps to NM_017504.1 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:248402793 C>T maps to NM_017504.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248402394 C>T maps to NM_017504.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248402532 A>C maps to NM_017504.1 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:248403084 G>A maps to NM_017504.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr1:248308754 C>T maps to NM_001004690.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:248308788 C>T maps to NM_001004690.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:248309249 C>T maps to NM_001004690.1 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr1:248308493 G>A maps to NM_001004690.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr1:248308754 C>T maps to NM_001004690.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:248308484 C>T maps to NM_001004690.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr1:248308634 C>T maps to NM_001004690.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:248308484 C>T maps to NM_001004690.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:248308532 C>T maps to NM_001004690.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr1:248309048 C>T maps to NM_001004690.1 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:248308991 C>T maps to NM_001004690.1 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:248308622 C>A maps to NM_001004690.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:248487738 G>A maps to NM_001004691.1 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:248487420 G>A maps to NM_001004691.1 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr1:248487312 G>A maps to NM_001004691.1 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:248487801 G>A maps to NM_001004691.1 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:248487414 G>A maps to NM_001004691.1 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:248487006 G>A maps to NM_001004691.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr1:248487834 G>A maps to NM_001004691.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:248487243 G>A maps to NM_001004691.1 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248487738 G>A maps to NM_001004691.1 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248487828 G>A maps to NM_001004691.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr9:35957486 C>T maps to NM_019897.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr9:35958056 G>A maps to NM_019897.2 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:35957933 G>A maps to NM_019897.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr9:35957966 A>G maps to NM_019897.2 N43N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr9:35957390 C>T maps to NM_019897.2 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:248570110 G>A maps to NM_030904.1 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr1:248569573 G>A maps to NM_030904.1 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:248570146 G>A maps to NM_030904.1 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:248570068 G>A maps to NM_030904.1 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:248569978 C>T maps to NM_030904.1 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:248569429 C>T maps to NM_030904.1 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:248570314 C>T maps to NM_030904.1 Y340Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:248569330 C>T maps to NM_030904.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:248569978 C>T maps to NM_030904.1 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr1:248756772 G>A maps to NM_001004693.1 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr1:248756643 G>A maps to NM_001004693.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:248757030 G>A maps to NM_001004693.1 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:248756756 G>A maps to NM_001004693.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:248756280 G>A maps to NM_001004693.1 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:248756988 G>A maps to NM_001004693.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:248756718 G>A maps to NM_001004693.1 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:248757030 G>A maps to NM_001004693.1 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr1:248756583 G>A maps to NM_001004693.1 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248756927 G>A maps to NM_001004693.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:248756343 G>A maps to NM_001004693.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:248756415 G>A maps to NM_001004693.1 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:248790027 G>A maps to NM_001001964.1 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:248789504 G>A maps to NM_001001964.1 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:248789895 G>A maps to NM_001001964.1 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr1:248790285 C>T maps to NM_001001964.1 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:248790396 G>A maps to NM_001001964.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr1:248458364 G>A maps to NM_001004692.1 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:248458451 G>T maps to NM_001004692.1 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:248458388 G>A maps to NM_001004692.1 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:248458210 G>A maps to NM_001004692.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:248458247 G>A maps to NM_001004692.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:248458169 G>A maps to NM_001004692.1 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr1:248457918 C>T maps to NM_001004692.1 *321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:248458010 C>T maps to NM_001004692.1 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:248458340 G>A maps to NM_001004692.1 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:248458607 G>A maps to NM_001004692.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr1:248458415 G>A maps to NM_001004692.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248458787 G>A maps to NM_001004692.1 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr1:248616136 C>T maps to NM_001004136.1 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr1:248616136 C>T maps to NM_001004136.1 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:248616172 C>T maps to NM_001004136.1 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:248616208 G>A maps to NM_001004136.1 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:248616136 C>T maps to NM_001004136.1 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr1:248616304 C>T maps to NM_001004136.1 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr1:248617057 G>A maps to NM_001004136.1 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:248616136 C>T maps to NM_001004136.1 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:248616301 C>T maps to NM_001004136.1 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:248616347 C>T maps to NM_001004136.1 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr1:248616436 C>T maps to NM_001004136.1 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:248616127 C>T maps to NM_001004136.1 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:248616436 C>T maps to NM_001004136.1 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:248616439 C>T maps to NM_001004136.1 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:248616388 C>T maps to NM_001004136.1 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248616151 C>T maps to NM_001004136.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248616430 G>A maps to NM_001004136.1 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:248814047 G>A maps to NM_001001824.1 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr1:248814038 G>A maps to NM_001001824.1 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:248814047 G>A maps to NM_001001824.1 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:248813306 C>T maps to NM_001001824.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr1:248637451 G>A maps to NM_001005495.1 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:248637394 C>T maps to NM_001005495.1 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:248637571 G>A maps to NM_001005495.1 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:248637181 G>A maps to NM_001005495.1 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:248637403 C>T maps to NM_001005495.1 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:248637322 C>T maps to NM_001005495.1 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:248637008 C>T maps to NM_001005495.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:248637187 C>T maps to NM_001005495.1 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr1:248637244 C>T maps to NM_001005495.1 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248637505 C>T maps to NM_001005495.1 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr1:248637520 G>A maps to NM_001005495.1 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:248637007 C>T maps to NM_001005495.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:248436399 G>A maps to NM_001004695.1 C239C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr1:248436939 G>A maps to NM_001004695.1 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr1:248436864 C>T maps to NM_001004695.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr1:248436219 C>T maps to NM_001004695.1 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:248436381 C>T maps to NM_001004695.1 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:248436939 G>A maps to NM_001004695.1 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:248436957 G>A maps to NM_001004695.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:248436969 C>T maps to NM_001004695.1 W49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:248436936 G>A maps to NM_001004695.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:248437020 G>A maps to NM_001004695.1 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:248437020 G>A maps to NM_001004695.1 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:248436182 G>A maps to NM_001004695.1 Q312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr1:248436228 C>T maps to NM_001004695.1 K296K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:248436600 G>A maps to NM_001004695.1 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr1:248437020 G>A maps to NM_001004695.1 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248436696 C>T maps to NM_001004695.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248437011 G>A maps to NM_001004695.1 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248437014 C>T maps to NM_001004695.1 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:248436939 G>A maps to NM_001004695.1 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr1:248436261 G>A maps to NM_001004695.1 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr1:248737332 G>A maps to NM_001001821.1 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:248737509 G>A maps to NM_001001821.1 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:248737305 G>A maps to NM_001001821.1 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:248737704 G>A maps to NM_001001821.1 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:248737509 G>A maps to NM_001001821.1 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:248737527 C>T maps to NM_001001821.1 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:248737442 G>A maps to NM_001001821.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:248737704 G>A maps to NM_001001821.1 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:248737701 G>A maps to NM_001001821.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr1:248801911 C>G maps to NM_001001827.1 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:248525013 C>T maps to NM_001004696.1 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:248525316 C>T maps to NM_001004696.1 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:248525706 C>T maps to NM_001004696.1 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr1:248525785 A>T maps to NM_001004696.1 K302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:248525724 C>T maps to NM_001004696.1 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:248525115 C>T maps to NM_001004696.1 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr1:248525856 G>A maps to NM_001004696.1 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr1:248525496 G>A maps to NM_001004696.1 E205E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:248525163 C>T maps to NM_001004696.1 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:248524929 C>T maps to NM_001004696.1 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:248525235 C>T maps to NM_001004696.1 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr1:248525017 C>T maps to NM_001004696.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:248524929 C>T maps to NM_001004696.1 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr1:248652005 C>T maps to NM_001004697.1 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:248651954 C>T maps to NM_001004697.1 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:248651999 G>A maps to NM_001004697.1 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:248551190 C>T maps to NM_001005471.1 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:248551787 G>A maps to NM_001005471.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:248551787 G>A maps to NM_001005471.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:248551040 C>T maps to NM_001005471.1 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:248551610 G>A maps to NM_001005471.1 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:248551094 C>T maps to NM_001005471.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr1:248551478 G>A maps to NM_001005471.1 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr1:248551382 C>T maps to NM_001005471.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248551091 C>T maps to NM_001005471.1 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248551787 G>A maps to NM_001005471.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:248551787 G>A maps to NM_001005471.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr1:248084414 C>T maps to NM_001005522.1 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:248084810 C>T maps to NM_001005522.1 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:248084465 G>A maps to NM_001005522.1 W49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:248084477 C>T maps to NM_001005522.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:248084414 C>T maps to NM_001005522.1 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:248085242 C>T maps to NM_001005522.1 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:248084810 C>T maps to NM_001005522.1 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:248084495 C>T maps to NM_001005522.1 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:248084537 C>T maps to NM_001005522.1 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:248084464 G>A maps to NM_001005522.1 W49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:248084465 G>A maps to NM_001005522.1 W49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248084348 C>T maps to NM_001005522.1 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248084465 G>A maps to NM_001005522.1 W49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:248084426 C>T maps to NM_001005522.1 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:248084318 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:180582421 G>A maps to NM_206880.1 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:180582832 G>A maps to NM_206880.1 E297E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr5:180582586 C>T maps to NM_206880.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:180582493 C>T maps to NM_206880.1 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:180582583 C>T maps to NM_206880.1 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr6:29012268 C>T maps to NM_030903.3 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:29012609 G>A maps to NM_030903.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr6:29012268 C>T maps to NM_030903.3 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:29012352 G>A maps to NM_030903.3 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:29012133 G>A maps to NM_030903.3 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:29012514 G>A maps to NM_030903.3 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr6:29012640 G>C maps to NM_030903.3 Y104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:29012045 T>A maps to NM_030903.3 K303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:29012766 G>A maps to NM_030903.3 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:29012874 G>A maps to NM_030903.3 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr6:29012133 G>A maps to NM_030903.3 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:29012009 T>A maps to NM_030903.3 K315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:29012268 C>T maps to NM_030903.3 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:29012880 C>T maps to NM_030903.3 E24E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:29012268 C>T maps to NM_030903.3 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:248059070 C>T maps to NM_001001957.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr1:248059442 C>T maps to NM_001001957.2 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:248059640 C>T maps to NM_001001957.2 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:248058986 C>T maps to NM_001001957.2 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:248059193 C>T maps to NM_001001957.2 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:248058923 C>T maps to NM_001001957.2 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:248059199 C>T maps to NM_001001957.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:248059535 C>T maps to NM_001001957.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr1:248059343 G>A maps to NM_001001957.2 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:248059073 C>T maps to NM_001001957.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:248058927 C>T maps to NM_001001957.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:248059175 C>T maps to NM_001001957.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:248058950 C>T maps to NM_001001957.2 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:248059529 C>T maps to NM_001001957.2 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr1:248059073 C>T maps to NM_001001957.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248059418 C>T maps to NM_001001957.2 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:248059199 C>T maps to NM_001001957.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:248058926 C>T maps to NM_001001957.2 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:247654806 C>T maps to NM_001004698.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:247655349 G>A maps to NM_001004698.2 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:247655218 C>T maps to NM_001004698.2 Q264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr1:247654770 C>T maps to NM_001004698.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:247654917 G>A maps to NM_001004698.2 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr1:247654917 G>A maps to NM_001004698.2 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:247654917 G>A maps to NM_001004698.2 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr1:247655376 G>A maps to NM_001004698.2 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr5:180166587 C>T maps to NM_001001657.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr5:180166749 G>A maps to NM_001001657.1 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr5:180166980 G>A maps to NM_001001657.1 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr5:180166710 C>T maps to NM_001001657.1 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:180166275 G>T maps to NM_001001657.1 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr5:180166144 C>T maps to NM_001001657.1 W305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr5:180166280 G>A maps to NM_001001657.1 Q260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr5:180166377 C>T maps to NM_001001657.1 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:180166986 C>T maps to NM_001001657.1 E24E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:180166599 G>A maps to NM_001001657.1 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:180166620 G>A maps to NM_001001657.1 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:8841863 C>T maps to NM_001004699.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr19:8841476 C>T maps to NM_001004699.1 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:8842007 C>T maps to NM_001004699.1 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:8841698 C>T maps to NM_001004699.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:8841645 C>T maps to NM_001004699.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr19:8841457 C>G maps to NM_001004699.1 S23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr19:8841569 C>T maps to NM_001004699.1 Y60Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr19:8841899 C>A maps to NM_001004699.1 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:8841698 C>T maps to NM_001004699.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:8841989 C>T maps to NM_001004699.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:8841429 C>T maps to NM_001004699.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:8841875 C>T maps to NM_001004699.1 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:8841860 C>T maps to NM_001004699.1 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr19:8841818 G>A maps to NM_001004699.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr19:8841875 C>T maps to NM_001004699.1 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:8841698 C>T maps to NM_001004699.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr19:8842007 C>T maps to NM_001004699.1 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr19:8841729 C>T maps to NM_001004699.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:3195150 G>A maps to ENST00000397187 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr17:3195210 G>A maps to ENST00000397187 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:3195660 C>T maps to ENST00000397187 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:3195489 G>A maps to ENST00000397187 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:3195498 G>A maps to ENST00000397187 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr17:3181815 G>A maps to NM_002551.3 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr17:3181518 G>A maps to NM_002551.3 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr17:3181359 G>A maps to NM_002551.3 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:3181659 G>A maps to NM_002551.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr17:3181590 G>A maps to NM_002551.3 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:3181449 G>A maps to NM_002551.3 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr17:3324754 C>T maps to NM_012373.2 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5KH-06A-11D-A27K-08 chr17:3324274 C>A maps to NM_012373.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:55136372 G>A maps to NM_001005275.1 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:55135991 C>T maps to NM_001005275.1 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:55135499 G>A maps to NM_001005275.1 Q47Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr11:55136057 G>A maps to NM_001005275.1 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:55136057 G>A maps to NM_001005275.1 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:55136138 G>A maps to NM_001005275.1 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:55135917 C>T maps to NM_001005275.1 Q187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:55136057 G>A maps to NM_001005275.1 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:55136057 G>A maps to NM_001005275.1 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:55136192 C>T maps to NM_001005275.1 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:55135935 C>T maps to NM_001005275.1 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr11:55135888 G>A maps to NM_001005275.1 W177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr11:55136339 G>A maps to NM_001005275.1 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr11:55136265 C>T maps to NM_001005275.1 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55135646 C>T maps to NM_001005275.1 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55136210 C>T maps to NM_001005275.1 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr11:55110708 C>T maps to NM_001005274.1 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr11:55110927 C>T maps to NM_001005274.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr11:55110738 G>A maps to NM_001005274.1 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:55110798 C>T maps to NM_001005274.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:55111341 C>T maps to NM_001005274.1 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:55110912 G>A maps to NM_001005274.1 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:55110738 G>A maps to NM_001005274.1 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55110891 C>T maps to NM_001005274.1 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55111095 C>T maps to NM_001005274.1 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55111165 C>T maps to NM_001005274.1 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr11:55111081 C>T maps to NM_001005274.1 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr11:55111309 C>T maps to NM_001005274.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:48510937 G>A maps to NM_001005512.2 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr11:48510812 C>T maps to NM_001005512.2 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:48510658 C>T maps to NM_001005512.2 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:48511189 C>T maps to NM_001005512.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr11:48511045 C>T maps to NM_001005512.2 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:48511027 G>A maps to NM_001005512.2 Q228Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:48510679 C>T maps to NM_001005512.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:48510797 C>T maps to NM_001005512.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:48510355 G>A maps to NM_001005512.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr11:48510478 G>A maps to NM_001005512.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:48510892 G>A maps to NM_001005512.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr11:48510797 C>T maps to NM_001005512.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr11:48511050 C>A maps to NM_001005512.2 S236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:48510355 G>A maps to NM_001005512.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr11:48510448 G>A maps to NM_001005512.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr11:51411636 G>A maps to NM_001005272.3 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr11:51411636 G>A maps to NM_001005272.3 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:51412002 C>T maps to NM_001005272.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:51412083 G>A maps to NM_001005272.3 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr11:51411636 G>A maps to NM_001005272.3 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:51411753 G>A maps to NM_001005272.3 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:51411971 G>A maps to NM_001005272.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr11:51412062 G>A maps to NM_001005272.3 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:51411989 G>A maps to NM_001005272.3 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:51411636 G>A maps to NM_001005272.3 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:51411975 G>A maps to NM_001005272.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr11:51412062 G>A maps to NM_001005272.3 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr11:51411645 G>A maps to NM_001005272.3 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr11:51411975 G>A maps to NM_001005272.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:51412362 G>A maps to NM_001005272.3 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:51412230 G>A maps to NM_001005272.3 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:51412218 G>A maps to NM_001005272.3 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr11:48238843 C>T maps to NM_001005470.1 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr11:48238550 C>T maps to NM_001005470.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr11:48238933 C>T maps to NM_001005470.1 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr11:48239104 T>C maps to NM_001005470.1 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:48239236 G>A maps to NM_001005470.1 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:48238585 C>T maps to NM_001005470.1 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:48238843 C>T maps to NM_001005470.1 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:48238672 C>T maps to NM_001005470.1 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:48239194 C>T maps to NM_001005470.1 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:48238597 C>T maps to NM_001005470.1 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr11:48238696 G>A maps to NM_001005470.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:48239289 G>A maps to NM_001005470.1 *310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr11:48239032 G>A maps to NM_001005470.1 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr11:48238567 C>T maps to NM_001005470.1 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr11:48238576 C>T maps to NM_001005470.1 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:48238597 C>T maps to NM_001005470.1 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr11:55371519 G>A maps to NM_001004700.1 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:55371060 G>A maps to NM_001004700.1 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr11:55371783 C>T maps to NM_001004700.1 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55371087 G>A maps to NM_001004700.1 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr11:55371060 G>A maps to NM_001004700.1 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:55371372 G>A maps to NM_001004700.1 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr11:50003383 G>A maps to NM_001005270.2 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr11:50003440 C>T maps to NM_001005270.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:50003707 G>A maps to NM_001005270.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr11:50004007 G>A maps to NM_001005270.2 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr11:50003707 G>A maps to NM_001005270.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr11:50003707 G>A maps to NM_001005270.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr11:50003857 G>A maps to NM_001005270.2 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr11:50003770 G>A maps to NM_001005270.2 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr11:50003707 G>A maps to NM_001005270.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:50003146 C>T maps to NM_001005270.2 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:50003386 C>T maps to NM_001005270.2 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr11:49974627 C>T maps to NM_001001955.2 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:49974402 G>A maps to NM_001001955.2 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr11:49974660 G>A maps to NM_001001955.2 E229E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr11:49974792 C>A maps to NM_001001955.2 Y273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:49974423 C>T maps to NM_001001955.2 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:49973997 A>T maps to NM_001001955.2 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:49974879 G>A maps to NM_001001955.2 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr11:49974864 G>A maps to NM_001001955.2 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:49974045 C>T maps to NM_001001955.2 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:49974456 C>T maps to NM_001001955.2 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F4-06A-12D-A25O-08 chr11:49974837 G>A maps to NM_001001955.2 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:55322600 C>T maps to NM_001001920.1 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr11:55322837 G>A maps to NM_001001920.1 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr11:55321910 C>T maps to NM_001001920.1 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:55322892 T>C maps to NM_001001920.1 *371Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:55322522 C>T maps to NM_001001920.1 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:55321880 C>T maps to NM_001001920.1 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:55322768 C>T maps to NM_001001920.1 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:55322136 C>T maps to NM_001001920.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr11:55321880 C>T maps to NM_001001920.1 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55322558 C>T maps to NM_001001920.1 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55322828 G>A maps to NM_001001920.1 Q349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr11:55321931 T>C maps to NM_001001920.1 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:55322604 T>C maps to NM_001001920.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr11:55321880 C>T maps to NM_001001920.1 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:55339779 C>T maps to NM_001004701.2 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:55340151 G>A maps to NM_001004701.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:55339782 C>T maps to NM_001004701.2 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:55340394 C>T maps to NM_001004701.2 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:55340346 C>T maps to NM_001004701.2 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:55340493 G>A maps to NM_001004701.2 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:55340502 G>A maps to NM_001004701.2 W300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr11:55340394 C>T maps to NM_001004701.2 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:55340151 G>A maps to NM_001004701.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr11:55340088 G>A maps to NM_001004701.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr11:55340451 G>A maps to NM_001004701.2 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55339668 G>A maps to NM_001004701.2 K22K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55340172 C>T maps to NM_001004701.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55340190 C>T maps to NM_001004701.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr11:55339944 C>T maps to NM_001004701.2 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr11:48346752 C>T maps to NM_001004702.1 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr11:48347130 C>T maps to NM_001004702.1 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:48346605 C>T maps to NM_001004702.1 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:48347188 C>T maps to NM_001004702.1 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:48347046 C>T maps to NM_001004702.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr11:48346899 G>A maps to NM_001004702.1 E136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr11:48347412 G>A maps to NM_001004702.1 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:48347055 C>T maps to NM_001004702.1 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:48346902 C>T maps to NM_001004702.1 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:48347199 C>T maps to NM_001004702.1 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:48346605 C>T maps to NM_001004702.1 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:48346950 G>A maps to NM_001004702.1 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:48346653 G>A maps to NM_001004702.1 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:48347298 C>T maps to NM_001004702.1 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:48346605 C>T maps to NM_001004702.1 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr11:48346605 C>T maps to NM_001004702.1 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:48347283 C>T maps to NM_001004702.1 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:48346563 C>T maps to NM_001004702.1 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:48346986 C>T maps to NM_001004702.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:48346752 C>T maps to NM_001004702.1 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:48347049 C>T maps to NM_001004702.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:48346902 C>T maps to NM_001004702.1 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr11:48347262 G>A maps to NM_001004702.1 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:48347199 C>T maps to NM_001004702.1 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:48346521 C>T maps to NM_001004702.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:48346902 C>T maps to NM_001004702.1 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:48346899 G>A maps to NM_001004702.1 E136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:48347430 C>T maps to NM_001004702.1 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:48346752 C>T maps to NM_001004702.1 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:48347199 C>T maps to NM_001004702.1 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:48346779 C>T maps to NM_001004702.1 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:48346752 C>T maps to NM_001004702.1 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:51515850 C>T maps to NM_001004703.1 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr11:51515427 C>A maps to NM_001004703.1 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:51515286 G>A maps to NM_001004703.1 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:51515754 C>T maps to NM_001004703.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:51515760 C>T maps to NM_001004703.1 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr11:51515532 C>T maps to NM_001004703.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:51515547 C>T maps to NM_001004703.1 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:51515763 C>T maps to NM_001004703.1 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:51515754 C>T maps to NM_001004703.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:51515859 G>T maps to NM_001004703.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr11:51515382 C>T maps to NM_001004703.1 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:51516171 G>A maps to NM_001004703.1 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:51515946 C>T maps to NM_001004703.1 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:55432651 C>T maps to NM_001004704.1 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr11:55433565 G>A maps to NM_001004704.1 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:55432968 G>A maps to NM_001004704.1 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:55433040 C>T maps to NM_001004704.1 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:55432974 C>T maps to NM_001004704.1 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr11:55433517 G>A maps to NM_001004704.1 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:55433514 G>A maps to NM_001004704.1 E291E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55432785 C>T maps to NM_001004704.1 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:55433218 C>T maps to NM_001004704.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:56233032 C>T maps to NM_012374.1 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:56232663 T>G maps to NM_012374.1 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:56232597 C>T maps to NM_012374.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr17:56232786 G>A maps to NM_012374.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr17:56232642 C>T maps to NM_012374.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:56233248 C>T maps to NM_012374.1 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:56232606 C>T maps to NM_012374.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr17:56232786 G>A maps to NM_012374.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr17:56232591 C>T maps to NM_012374.1 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:56232591 C>T maps to NM_012374.1 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr17:56232981 C>T maps to NM_012374.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr11:59245543 C>T maps to NM_001004705.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:59245654 C>T maps to NM_001004705.1 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:59245603 G>A maps to NM_001004705.1 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:59245603 G>A maps to NM_001004705.1 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr11:59245399 C>T maps to NM_001004705.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:59245627 C>T maps to NM_001004705.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:59245504 C>T maps to NM_001004705.1 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:59245615 C>T maps to NM_001004705.1 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:59245654 C>T maps to NM_001004705.1 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:59244991 C>T maps to NM_001004705.1 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:59271749 G>A maps to NM_001004706.1 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr11:59271950 G>A maps to NM_001004706.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:59271452 C>T maps to NM_001004706.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr11:59271158 G>A maps to NM_001004706.1 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:59271299 C>T maps to NM_001004706.1 D84D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:59271746 G>A maps to NM_001004706.1 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:59271503 C>T maps to NM_001004706.1 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:59271962 C>T maps to NM_001004706.1 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr17:56247768 C>T maps to NM_001004707.3 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:56247039 G>A maps to NM_001004707.3 W8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:56247327 C>T maps to NM_001004707.3 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:56247768 C>T maps to NM_001004707.3 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:56247057 C>T maps to NM_001004707.3 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:56247837 C>T maps to NM_001004707.3 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr17:56247027 G>A maps to NM_001004707.3 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr17:56247705 G>A maps to NM_001004707.3 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr11:123811256 C>T maps to NM_001001965.1 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:123810614 C>T maps to NM_001001965.1 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:123811240 G>A maps to NM_001001965.1 K306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:123811204 G>A maps to NM_001001965.1 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:123810751 C>T maps to NM_001001965.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:123810343 C>T maps to NM_001001965.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:123811213 C>T maps to NM_001001965.1 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr11:123810406 C>T maps to NM_001001965.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:123810367 G>A maps to NM_001001965.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:123810814 C>T maps to NM_001001965.1 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:59225272 C>T maps to NM_001004708.1 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:59224810 C>T maps to NM_001004708.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:59224978 C>T maps to NM_001004708.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:59224870 G>A maps to NM_001004708.1 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:59224645 C>T maps to NM_001004708.1 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr11:59225122 G>A maps to NM_001004708.1 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:59224522 C>T maps to NM_001004708.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:59224645 C>T maps to NM_001004708.1 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr11:59283137 C>T maps to NM_001004711.1 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr11:59283083 G>A maps to NM_001004711.1 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:59282708 G>A maps to NM_001004711.1 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:59283137 C>T maps to NM_001004711.1 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:59282882 C>T maps to NM_001004711.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr11:59282666 C>T maps to NM_001004711.1 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:59283137 C>T maps to NM_001004711.1 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr11:59282475 C>T maps to NM_001004711.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr11:59282861 G>A maps to NM_001004711.1 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:59282475 C>T maps to NM_001004711.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr11:59283137 C>T maps to NM_001004711.1 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr14:22134222 G>A maps to NM_001001912.1 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr14:22134165 G>A maps to NM_001001912.1 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:22133913 C>T maps to NM_001001912.1 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr14:22134150 C>T maps to NM_001001912.1 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:22133574 C>T maps to NM_001001912.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:22134219 C>T maps to NM_001001912.1 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:22133613 C>T maps to NM_001001912.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr14:22134222 G>A maps to NM_001001912.1 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr14:22133481 C>T maps to NM_001001912.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:22134222 G>A maps to NM_001001912.1 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr14:22134222 G>A maps to NM_001001912.1 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr14:22133358 G>A maps to NM_001001912.1 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr14:22133643 C>T maps to NM_001001912.1 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr14:22134090 C>T maps to NM_001001912.1 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:22134063 C>T maps to NM_001001912.1 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:22134093 C>T maps to NM_001001912.1 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:22134150 C>T maps to NM_001001912.1 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr15:102358667 C>T maps to NM_001001674.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:102358667 C>T maps to NM_001001674.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:102359048 C>T maps to NM_001001674.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr15:102359036 T>A maps to NM_001001674.1 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:102358694 C>T maps to NM_001001674.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:102358520 C>T maps to NM_001001674.1 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr15:102346755 C>T maps to NM_001005326.1 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr15:102346731 C>T maps to NM_001005326.1 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr15:102346077 C>T maps to NM_001005326.1 D52D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr15:102345963 C>T maps to NM_001005326.1 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr14:20404562 G>A maps to NM_001004063.2 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr14:20404490 G>A maps to NM_001004063.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr14:20404151 G>A maps to NM_001004063.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr14:20404751 G>A maps to NM_001004063.2 W309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr14:20404457 C>T maps to NM_001004063.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:20403869 G>A maps to NM_001004063.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr14:20404481 C>T maps to NM_001004063.2 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr14:20404676 C>T maps to NM_001004063.2 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr14:20404571 T>A maps to NM_001004063.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr14:20404733 C>T maps to NM_001004063.2 N303N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:20404556 C>T maps to NM_001004063.2 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr14:20404451 C>T maps to NM_001004063.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr14:20404751 G>A maps to NM_001004063.2 W309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:20404130 C>T maps to NM_001004063.2 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr14:20404055 C>T maps to NM_001004063.2 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr14:20404439 G>A maps to NM_001004063.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr14:20404493 C>T maps to NM_001004063.2 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr14:20404049 C>T maps to NM_001004063.2 N75N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:20404028 C>T maps to NM_001004063.2 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:20404037 C>T maps to NM_001004063.2 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr14:20404439 G>A maps to NM_001004063.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:20404457 C>T maps to NM_001004063.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr14:20404751 G>A maps to NM_001004063.2 W309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr14:20502847 G>A maps to NM_001004714.1 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr14:20502083 G>A maps to NM_001004714.1 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr14:20502003 T>C maps to NM_001004714.1 *305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr14:20502074 G>A maps to NM_001004714.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:20502632 C>T maps to NM_001004714.1 W95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:20502845 C>T maps to NM_001004714.1 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:20502401 A>G maps to NM_001004714.1 N172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr14:20502083 G>A maps to NM_001004714.1 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr14:20502701 G>A maps to NM_001004714.1 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:20502785 G>A maps to NM_001004714.1 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr14:20502701 G>A maps to NM_001004714.1 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr14:20502266 G>A maps to NM_001004714.1 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:20502662 G>A maps to NM_001004714.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:20502812 G>A maps to NM_001004714.1 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr14:20482420 C>T maps to NM_001004712.1 *311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:20482617 G>A maps to NM_001004712.1 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr14:20482944 C>T maps to NM_001004712.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr14:20482452 C>T maps to NM_001004712.1 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr14:20483166 G>A maps to NM_001004712.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr14:20483166 G>A maps to NM_001004712.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr14:20482617 G>A maps to NM_001004712.1 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr14:20483004 C>T maps to NM_001004712.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr14:20483094 G>A maps to NM_001004712.1 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:20483094 G>A maps to NM_001004712.1 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr14:20483166 G>A maps to NM_001004712.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:20444426 G>A maps to NM_001005486.1 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr14:20444676 C>T maps to NM_001005486.1 Q334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr14:20444069 C>T maps to NM_001005486.1 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr14:20443907 C>T maps to NM_001005486.1 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr14:20444709 C>T maps to NM_001005486.1 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr14:20443886 C>T maps to NM_001005486.1 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr14:20443797 C>T maps to NM_001005486.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr14:20444708 C>T maps to NM_001005486.1 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr14:20586323 C>T maps to NM_001004715.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:20586467 C>T maps to NM_001004715.1 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr14:20586245 G>A maps to NM_001004715.1 Q227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr14:20585693 C>T maps to NM_001004715.1 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr14:20586317 G>A maps to NM_001004715.1 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:20586398 G>A maps to NM_001004715.1 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr14:20586305 C>T maps to NM_001004715.1 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr14:20586008 C>A maps to NM_001004715.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr14:20585705 A>T maps to NM_001004715.1 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:20585855 C>T maps to NM_001004715.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:20586275 C>T maps to NM_001004715.1 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr14:20586335 G>A maps to NM_001004715.1 K257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr14:20586389 C>T maps to NM_001004715.1 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F4-06A-12D-A25O-08 chr14:20585750 C>T maps to NM_001004715.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:20586116 C>T maps to NM_001004715.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr14:20344761 C>T maps to NM_001005501.1 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr14:20344608 C>T maps to NM_001005501.1 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr14:20345184 A>G maps to NM_001005501.1 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr14:20344737 C>T maps to NM_001005501.1 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:20344608 C>T maps to NM_001005501.1 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr14:20344608 C>T maps to NM_001005501.1 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:20344869 C>T maps to NM_001005501.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr14:20344983 G>A maps to NM_001005501.1 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr14:20345253 C>T maps to NM_001005501.1 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:20345322 G>A maps to NM_001005501.1 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr14:20344830 C>T maps to NM_001005501.1 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:20344629 C>T maps to NM_001005501.1 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr14:20345322 G>A maps to NM_001005501.1 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr14:20344905 C>T maps to NM_001005501.1 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr14:20345157 C>T maps to NM_001005501.1 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:20345328 G>A maps to NM_001005501.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr14:20344608 C>T maps to NM_001005501.1 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr14:20345307 A>C maps to NM_001005501.1 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr14:20389532 C>T maps to NM_001005483.1 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr14:20389529 C>T maps to NM_001005483.1 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr14:20389661 G>A maps to NM_001005483.1 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr14:20389661 G>A maps to NM_001005483.1 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr14:20389397 C>T maps to NM_001005483.1 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr14:20389661 G>A maps to NM_001005483.1 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:20389256 G>A maps to NM_001005483.1 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:20388833 C>A maps to NM_001005483.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:20388834 C>T maps to NM_001005483.1 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr14:20388825 C>T maps to NM_001005483.1 Q21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr14:20389532 C>T maps to NM_001005483.1 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr14:20388833 C>T maps to NM_001005483.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr14:20388834 C>T maps to NM_001005483.1 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr14:20389634 G>A maps to NM_001005483.1 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr14:20389661 G>A maps to NM_001005483.1 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr14:20388953 G>A maps to NM_001005483.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:20389079 C>T maps to NM_001005483.1 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr14:20389661 G>A maps to NM_001005483.1 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr14:20389634 G>A maps to NM_001005483.1 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr14:20389661 G>A maps to NM_001005483.1 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:20389046 C>T maps to NM_001005483.1 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:20389661 G>A maps to NM_001005483.1 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:20389169 C>T maps to NM_001005483.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:20389397 C>T maps to NM_001005483.1 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr14:20389634 G>A maps to NM_001005483.1 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr14:20528637 G>A maps to NM_001004717.1 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr14:20528283 C>T maps to NM_001004717.1 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr14:20528829 C>T maps to NM_001004717.1 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:20528835 C>T maps to NM_001004717.1 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:20528748 C>T maps to NM_001004717.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr14:20528334 C>T maps to NM_001004717.1 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr14:20528799 C>T maps to NM_001004717.1 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr14:20528835 C>T maps to NM_001004717.1 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr14:20528334 C>T maps to NM_001004717.1 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:20528283 C>T maps to NM_001004717.1 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:20528838 C>T maps to NM_001004717.1 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr14:20528637 G>A maps to NM_001004717.1 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr14:20248804 G>A maps to NM_001005500.1 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr14:20248810 G>A maps to NM_001005500.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr14:20248885 C>T maps to NM_001005500.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr14:20248627 C>T maps to NM_001005500.1 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr14:20248747 G>A maps to NM_001005500.1 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr14:20248615 C>T maps to NM_001005500.1 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr14:20249038 G>A maps to NM_001005500.1 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:20249050 C>T maps to NM_001005500.1 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:20248663 C>T maps to NM_001005500.1 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:20249098 C>T maps to NM_001005500.1 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr14:20249140 C>T maps to NM_001005500.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr14:20248759 C>T maps to NM_001005500.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:20248609 C>T maps to NM_001005500.1 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr14:20248609 C>T maps to NM_001005500.1 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:20249185 C>T maps to NM_001005500.1 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:20248885 C>T maps to NM_001005500.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr14:20249059 C>T maps to NM_001005500.1 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:20248729 A>T maps to NM_001005500.1 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr14:20248825 C>T maps to NM_001005500.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr14:20248588 G>A maps to NM_001005500.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr14:20248546 G>A maps to NM_001005500.1 E22E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr14:20248714 C>T maps to NM_001005500.1 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr15:22369153 C>T maps to NM_001004719.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr15:22369021 G>A maps to NM_001004719.2 W149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr15:22368703 C>T maps to NM_001004719.2 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr15:22368967 C>T maps to NM_001004719.2 H131H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:22369417 C>T maps to NM_001004719.2 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr15:22369003 C>T maps to NM_001004719.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:22368643 C>T maps to NM_001004719.2 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr15:22369003 C>T maps to NM_001004719.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr15:22369378 C>T maps to NM_001004719.2 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr15:22368757 C>T maps to NM_001004719.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr15:22368757 C>T maps to NM_001004719.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr15:22369004 C>T maps to NM_001004719.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr15:22368757 C>T maps to NM_001004719.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:22369067 C>T maps to NM_001004719.2 R165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:22369237 T>G maps to NM_001004719.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:22369417 C>T maps to NM_001004719.2 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:22368628 C>T maps to NM_001004719.2 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr14:20296401 C>T maps to NM_001004723.1 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:20295936 G>A maps to NM_001004723.1 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr14:20295981 C>T maps to NM_001004723.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr14:20296158 C>T maps to NM_001004723.1 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr14:20296086 G>A maps to NM_001004723.1 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:20295861 C>T maps to NM_001004723.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr14:20295870 G>A maps to NM_001004723.1 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr14:20296338 C>T maps to NM_001004723.1 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr14:20296332 C>T maps to NM_001004723.1 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:20296488 G>A maps to NM_001004723.1 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr14:20295861 C>T maps to NM_001004723.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr15:22382672 C>T maps to NM_001005241.1 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr15:22382675 C>T maps to NM_001005241.1 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:22382570 T>A maps to NM_001005241.1 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:22383096 C>T maps to NM_001005241.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:22382582 C>T maps to NM_001005241.1 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr15:22383167 G>A maps to NM_001005241.1 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr15:22382954 C>T maps to NM_001005241.1 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr15:22382822 G>A maps to NM_001005241.1 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr15:22382675 C>T maps to NM_001005241.1 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr15:22383167 G>A maps to NM_001005241.1 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr15:22382690 C>T maps to NM_001005241.1 Y73Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr15:22382939 C>T maps to NM_001005241.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:22382561 G>A maps to NM_001005241.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr15:22382813 C>T maps to NM_001005241.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:22383002 C>T maps to NM_001005241.1 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr15:22382582 C>T maps to NM_001005241.1 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr15:22383179 C>T maps to NM_001005241.1 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr15:22383269 A>T maps to NM_001005241.1 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:22382612 C>T maps to NM_001005241.1 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:22382675 C>T maps to NM_001005241.1 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:22382696 C>T maps to NM_001005241.1 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:22383056 G>A maps to NM_001005241.1 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:22383131 C>T maps to NM_001005241.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:22383179 C>T maps to NM_001005241.1 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:22382582 C>T maps to NM_001005241.1 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:22383335 C>T maps to NM_001005241.1 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr14:20612313 C>T maps to NM_001004724.1 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr14:20612118 C>T maps to NM_001004724.1 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr14:20612592 G>A maps to NM_001004724.1 K233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr14:20612571 G>A maps to NM_001004724.1 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:20612790 G>A maps to NM_001004724.1 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:20612076 C>T maps to NM_001004724.1 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:20612526 C>T maps to NM_001004724.1 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:20612137 T>C maps to NM_001004724.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr14:20612148 C>T maps to NM_001004724.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:20612397 C>T maps to NM_001004724.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr14:20612335 C>T maps to NM_001004724.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr14:20612526 C>T maps to NM_001004724.1 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr14:20612736 G>A maps to NM_001004724.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:20612410 C>T maps to NM_001004724.1 Q173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr14:20612004 C>T maps to NM_001004724.1 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr14:20612379 T>C maps to NM_001004724.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr14:20612775 G>A maps to NM_001004724.1 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr14:20612307 T>C maps to NM_001004724.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr14:20612004 C>T maps to NM_001004724.1 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr14:20612022 C>T maps to NM_001004724.1 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr14:20612571 G>A maps to NM_001004724.1 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr14:20612187 C>T maps to NM_001004724.1 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr11:55406439 T>C maps to NM_001004124.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:55406570 C>T maps to NM_001004124.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr14:20215792 C>T maps to NM_172194.1 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr14:20216252 C>T maps to NM_172194.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr14:20215585 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr14:20216335 G>A maps to NM_172194.1 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr14:20216059 C>T maps to NM_172194.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr14:20216440 C>T maps to NM_172194.1 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:20216059 C>T maps to NM_172194.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:20216404 C>T maps to NM_172194.1 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr14:20215843 C>T maps to NM_172194.1 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr14:20216050 C>T maps to NM_172194.1 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:20215666 C>T maps to NM_172194.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:20216257 C>T maps to NM_172194.1 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:48328649 G>A maps to NM_001004725.1 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:48328685 G>A maps to NM_001004725.1 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:48327914 C>T maps to NM_001004725.1 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:48328205 G>A maps to NM_001004725.1 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:48327959 C>T maps to NM_001004725.1 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:48328208 C>T maps to NM_001004725.1 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr11:48328316 C>T maps to NM_001004725.1 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:48328679 C>T maps to NM_001004725.1 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr11:55418846 C>T maps to NM_001004059.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:55419206 C>T maps to NM_001004059.2 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr11:55418856 C>T maps to NM_001004059.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:55418846 C>T maps to NM_001004059.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:55418411 T>C maps to NM_001004059.2 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:55419020 C>T maps to NM_001004059.2 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:55418501 C>T maps to NM_001004059.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr11:55418999 G>A maps to NM_001004059.2 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr11:55418673 C>T maps to NM_001004059.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:48285606 C>T maps to NM_001004726.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:48286275 G>A maps to NM_001004726.1 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:48286017 C>T maps to NM_001004726.1 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr11:48285552 C>T maps to NM_001004726.1 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr11:48286287 G>A maps to NM_001004726.1 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:48286155 C>T maps to NM_001004726.1 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr11:48285897 C>T maps to NM_001004726.1 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:48286287 G>A maps to NM_001004726.1 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr11:48285723 C>T maps to NM_001004726.1 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:48286078 C>T maps to NM_001004726.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr11:48286260 G>A maps to NM_001004726.1 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:48285447 C>T maps to NM_001004726.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:48286020 C>T maps to NM_001004726.1 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:48266816 C>T maps to NM_001004727.1 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:48267035 C>T maps to NM_001004727.1 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:48266897 G>A maps to NM_001004727.1 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr11:48266759 C>T maps to NM_001004727.1 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:48267002 G>A maps to NM_001004727.1 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr11:48267356 C>A maps to NM_001004727.1 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:48266724 C>T maps to NM_001004727.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr11:48267209 C>T maps to NM_001004727.1 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:48266729 C>T maps to NM_001004727.1 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:48266969 C>T maps to NM_001004727.1 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:48267326 G>A maps to NM_001004727.1 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:48267531 C>T maps to NM_001004727.1 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:48267269 C>T maps to NM_001004727.1 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr11:48266759 C>T maps to NM_001004727.1 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:48267209 C>T maps to NM_001004727.1 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:48267269 C>T maps to NM_001004727.1 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr11:48267518 G>A maps to NM_001004727.1 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:48266804 C>T maps to NM_001004727.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:48267328 G>A maps to NM_001004727.1 W225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:48267362 C>T maps to NM_001004727.1 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:48267542 G>A maps to NM_001004727.1 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr11:48267470 G>A maps to NM_001004727.1 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:4976682 G>A maps to NM_001004748.1 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr11:4976793 G>A maps to NM_001004748.1 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr11:4976193 G>A maps to NM_001004748.1 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:4976460 G>A maps to NM_001004748.1 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:4976460 G>A maps to NM_001004748.1 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:4976475 G>A maps to NM_001004748.1 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr11:4976282 G>A maps to NM_001004748.1 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr11:4976898 G>A maps to NM_001004748.1 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:4976591 G>A maps to NM_001004748.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr11:4976232 C>T maps to NM_001004748.1 K237K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr11:4976301 G>A maps to NM_001004748.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr11:4976682 G>A maps to NM_001004748.1 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:4976412 G>A maps to NM_001004748.1 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr11:4968180 G>A maps to NM_001005329.1 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr11:4967580 G>A maps to NM_001005329.1 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:4967670 G>A maps to NM_001005329.1 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr11:4968128 A>G maps to NM_001005329.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:4967847 G>A maps to NM_001005329.1 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:4968015 G>A maps to NM_001005329.1 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:4967862 G>A maps to NM_001005329.1 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr11:4967466 C>T maps to NM_001005329.1 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:4967847 G>A maps to NM_001005329.1 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:4968015 G>A maps to NM_001005329.1 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr11:4967514 G>A maps to NM_001005329.1 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr11:4967637 G>A maps to NM_001005329.1 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr11:4967487 G>A maps to NM_001005329.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:4967973 G>A maps to NM_001005329.1 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:4967978 G>A maps to NM_001005329.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:4968015 G>A maps to NM_001005329.1 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:4968026 G>A maps to NM_001005329.1 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr11:4929510 G>A maps to NM_001004749.1 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:4928682 C>T maps to NM_001004749.1 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:4928634 C>T maps to NM_001004749.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:4929222 G>A maps to NM_001004749.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:4928610 C>T maps to NM_001004749.1 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:4929090 G>A maps to NM_001004749.1 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:4928916 A>T maps to NM_001004749.1 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:4929510 G>A maps to NM_001004749.1 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:4929303 G>A maps to NM_001004749.1 K235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:4929498 G>A maps to NM_001004749.1 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:4929414 G>A maps to NM_001004749.1 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:4929232 C>T maps to NM_001004749.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr11:4929261 G>A maps to NM_001004749.1 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr11:4928736 C>T maps to NM_001004749.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr11:4928634 C>T maps to NM_001004749.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:4928847 G>A maps to NM_001004749.1 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr11:4929003 C>T maps to NM_001004749.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:4928889 C>T maps to NM_001004749.1 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:5345386 G>A maps to NM_033180.4 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr11:5345044 A>T maps to NM_033180.4 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:5344708 G>A maps to NM_033180.4 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:5344687 G>A maps to NM_033180.4 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:5344768 C>T maps to NM_033180.4 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:5344894 G>A maps to NM_033180.4 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:5345272 C>T maps to NM_033180.4 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:5345203 C>T maps to NM_033180.4 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:5345281 G>A maps to NM_033180.4 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr11:5345085 G>A maps to NM_033180.4 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr11:5344999 G>A maps to NM_033180.4 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5344753 G>A maps to NM_033180.4 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5344951 G>A maps to NM_033180.4 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:5345395 G>A maps to NM_033180.4 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr11:5322816 G>A maps to NM_033179.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr11:5322609 G>A maps to NM_033179.2 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr11:5322672 G>A maps to NM_033179.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:5322816 G>A maps to NM_033179.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:5322327 G>A maps to NM_033179.2 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:5322300 C>T maps to NM_033179.2 K292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:5322876 G>A maps to NM_033179.2 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:5322390 C>T maps to NM_033179.2 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:5322888 G>A maps to NM_033179.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:5322939 G>A maps to NM_033179.2 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr11:5322696 G>A maps to NM_033179.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5323134 G>A maps to NM_033179.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:5322888 G>A maps to NM_033179.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:5364199 G>A maps to NM_001005567.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr11:5364733 G>A maps to NM_001005567.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:5364315 G>A maps to NM_001005567.1 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr11:5364501 G>A maps to NM_001005567.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:5364667 G>A maps to NM_001005567.1 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:5364247 G>A maps to NM_001005567.1 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:5364577 G>A maps to NM_001005567.1 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:5364700 C>T maps to NM_001005567.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:5363816 C>T maps to NM_001005567.1 *313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr11:5364610 C>T maps to NM_001005567.1 K48K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5363816 C>T maps to NM_001005567.1 *313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5363911 G>A maps to NM_001005567.1 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5364115 G>A maps to NM_001005567.1 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:5364109 G>T maps to NM_001005567.1 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr11:5372796 G>A maps to NM_001004750.1 K20K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:5373573 C>T maps to NM_001004750.1 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:5373624 G>A maps to NM_001004750.1 Q296Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:5373573 C>T maps to NM_001004750.1 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:5373183 G>A maps to NM_001004750.1 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr11:5373573 C>T maps to NM_001004750.1 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:5373579 C>T maps to NM_001004750.1 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:5373195 C>T maps to NM_001004750.1 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:5373042 C>T maps to NM_001004750.1 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:5373579 C>T maps to NM_001004750.1 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:5372814 C>T maps to NM_001004750.1 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:5373573 C>T maps to NM_001004750.1 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:4661751 G>A maps to NM_001004751.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:4661529 C>T maps to NM_001004751.2 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr11:4661868 C>T maps to NM_001004751.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr11:4661721 C>T maps to NM_001004751.2 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:4661697 C>T maps to NM_001004751.2 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:4661091 C>T maps to NM_001004751.2 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:4661401 C>T maps to NM_001004751.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:4661928 C>T maps to NM_001004751.2 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr11:4661091 C>T maps to NM_001004751.2 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:4661820 C>T maps to NM_001004751.2 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr11:4661964 C>T maps to NM_001004751.2 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:4661313 C>T maps to NM_001004751.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:4661505 G>A maps to NM_001004751.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:4661091 C>T maps to NM_001004751.2 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr11:4661313 C>T maps to NM_001004751.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:4661106 C>T maps to NM_001004751.2 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:4674283 C>T maps to NM_152430.3 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:4674659 C>T maps to NM_152430.3 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr11:4674526 C>T maps to NM_152430.3 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:4674659 C>T maps to NM_152430.3 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:4673995 C>T maps to NM_152430.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:4674056 C>T maps to NM_152430.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:4674250 C>T maps to NM_152430.3 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr11:4674040 C>T maps to NM_152430.3 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:4674277 C>G maps to NM_152430.3 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr11:4673830 G>A maps to NM_152430.3 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:4674253 C>T maps to NM_152430.3 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:4674268 C>T maps to NM_152430.3 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr11:4703602 G>A maps to NM_030774.3 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:4703401 G>A maps to NM_030774.3 H180H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr11:4703440 G>A maps to NM_030774.3 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:4703638 G>A maps to NM_030774.3 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:4703458 C>T maps to NM_030774.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:4703812 G>A maps to NM_030774.3 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:4703800 G>A maps to NM_030774.3 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr11:4703074 G>A maps to NM_030774.3 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr11:4703845 G>A maps to NM_030774.3 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr11:4703473 G>A maps to NM_030774.3 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:4703086 G>A maps to NM_030774.3 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:4703416 G>A maps to NM_030774.3 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:4703602 G>A maps to NM_030774.3 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:4703722 G>A maps to NM_030774.3 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:4703857 G>A maps to NM_030774.3 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:4790961 A>T maps to ENST00000380383 Y69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr11:4790451 G>A maps to ENST00000380383 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr11:4791138 G>A maps to ENST00000380383 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:4790820 G>A maps to ENST00000380383 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:4790955 G>A maps to ENST00000380383 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:4791006 G>A maps to ENST00000380383 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:4790700 C>T maps to ENST00000380383 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:4790451 G>A maps to ENST00000380383 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:4790427 G>A maps to ENST00000380383 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:4790994 G>A maps to ENST00000380383 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:4843235 G>A maps to NM_001004753.1 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr11:4842791 C>T maps to NM_001004753.1 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr11:4842966 C>T maps to NM_001004753.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr11:4843346 C>T maps to NM_001004753.1 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:4843415 C>T maps to NM_001004753.1 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr11:4842791 C>T maps to NM_001004753.1 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr11:4842867 C>T maps to NM_001004753.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:4843133 C>T maps to NM_001004753.1 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:4843319 C>T maps to NM_001004753.1 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:4843254 C>T maps to NM_001004753.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr11:4945254 G>A maps to NM_001005237.1 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:4945020 G>A maps to NM_001005237.1 H183H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr11:4944918 A>G maps to NM_001005237.1 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:4945446 G>A maps to NM_001005237.1 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:4945446 G>A maps to NM_001005237.1 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:4945290 C>T maps to NM_001005237.1 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:4944990 G>A maps to NM_001005237.1 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:4935974 G>A maps to NM_001005238.1 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:4936440 C>T maps to NM_001005238.1 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr11:4936634 G>A maps to NM_001005238.1 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:4936875 C>T maps to NM_001005238.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:4936569 G>A maps to NM_001005238.1 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:4936470 G>A maps to NM_001005238.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:4936692 G>A maps to NM_001005238.1 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:4935984 C>T maps to NM_001005238.1 Q303Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr11:5462627 G>A maps to NM_001005288.2 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:5462429 G>A maps to NM_001005288.2 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr11:5461832 C>A maps to NM_001005288.2 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:5462138 G>A maps to NM_001005288.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr11:5462078 C>T maps to NM_001005288.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:5461817 G>A maps to NM_001005288.2 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:5462549 G>A maps to NM_001005288.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:5462681 C>T maps to NM_001005288.2 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:5462527 G>A maps to NM_001005288.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:5462651 C>T maps to NM_001005288.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr11:5461847 C>T maps to NM_001005288.2 K299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:5462096 G>A maps to NM_001005288.2 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5462036 C>T maps to NM_001005288.2 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:5462078 C>T maps to NM_001005288.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr11:5475539 C>T maps to NM_001004754.2 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:5474882 C>T maps to NM_001004754.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:5474972 C>T maps to NM_001004754.2 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr11:5475248 C>T maps to NM_001004754.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr11:5474873 G>A maps to NM_001004754.2 E52E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:5020781 C>T maps to NM_001004755.1 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:5020352 C>T maps to NM_001004755.1 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:5020376 C>T maps to NM_001004755.1 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:5021039 C>T maps to NM_001004755.1 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr11:5020223 G>A maps to NM_001004755.1 W4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:5021081 C>T maps to NM_001004755.1 N290N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:5020310 C>T maps to NM_001004755.1 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:5021141 C>T maps to NM_001004755.1 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:5020829 T>C maps to NM_001004755.1 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr11:5020322 T>A maps to NM_001004755.1 Y37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr11:5021012 G>A maps to NM_001004755.1 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr11:5021147 G>A maps to NM_001004755.1 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5020565 G>A maps to NM_001004755.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5020751 C>T maps to NM_001004755.1 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:5021141 C>T maps to NM_001004755.1 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:5411368 C>T maps to NM_001004756.2 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr11:5411146 C>T maps to NM_001004756.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr11:5410795 C>T maps to NM_001004756.2 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr11:5411278 C>T maps to NM_001004756.2 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr11:5411113 C>T maps to NM_001004756.2 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:5411089 C>T maps to NM_001004756.2 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:5410855 C>T maps to NM_001004756.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:5411134 C>T maps to NM_001004756.2 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:5410946 G>T maps to NM_001004756.2 G107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr11:5443519 C>T maps to NM_001004757.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr11:5444246 C>T maps to NM_001004757.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:5443435 C>T maps to NM_001004757.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:5443498 G>A maps to NM_001004757.2 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:5444353 C>T maps to NM_001004757.2 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr11:5444293 G>A maps to NM_001004757.2 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:5443744 C>T maps to NM_001004757.2 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:5443627 C>T maps to NM_001004757.2 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr11:5444329 G>A maps to NM_001004757.2 Q300Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr11:5444159 C>T maps to NM_001004757.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr11:5443450 C>T maps to NM_001004757.2 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr11:5444059 C>T maps to NM_001004757.2 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5444074 C>T maps to NM_001004757.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr11:4869853 C>T maps to NM_001004758.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:4869931 G>A maps to NM_001004758.1 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:4869889 G>A maps to NM_001004758.1 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:4869670 G>A maps to NM_001004758.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:4869963 G>A maps to NM_001004758.1 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr11:4869498 A>G maps to NM_001004758.1 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr11:4869931 G>A maps to NM_001004758.1 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:4869781 C>A maps to NM_001004758.1 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:4870102 G>A maps to NM_001004758.1 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:4869963 G>A maps to NM_001004758.1 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:4870119 G>A maps to NM_001004758.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:4869658 G>A maps to NM_001004758.1 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:4869574 G>A maps to NM_001004758.1 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:4869591 G>A maps to NM_001004758.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr11:4903485 C>T maps to NM_001004759.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr11:4903713 G>A maps to NM_001004759.1 W222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:4903428 C>T maps to NM_001004759.1 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:4903170 C>T maps to NM_001004759.1 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr11:4903599 C>T maps to NM_001004759.1 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:4903170 C>T maps to NM_001004759.1 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:4903320 C>T maps to NM_001004759.1 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr11:4904097 G>A maps to NM_001004759.1 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr11:4903887 C>T maps to NM_001004759.1 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:4903792 C>T maps to NM_001004759.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr11:4903908 C>T maps to NM_001004759.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:4903371 C>T maps to NM_001004759.1 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:4903120 C>T maps to NM_001004759.1 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:4903185 C>T maps to NM_001004759.1 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:4903248 C>T maps to NM_001004759.1 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr11:5221879 C>T maps to NM_001004760.2 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:5221246 G>A maps to NM_001004760.2 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr11:5221054 G>A maps to NM_001004760.2 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr11:5221879 C>T maps to NM_001004760.2 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr11:5221879 C>T maps to NM_001004760.2 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:5221816 G>A maps to NM_001004760.2 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:5221078 G>A maps to NM_001004760.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:5221177 G>A maps to NM_001004760.2 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:5221054 G>A maps to NM_001004760.2 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:5221141 A>G maps to NM_001004760.2 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5221754 C>T maps to NM_001004760.2 W59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr11:5221450 C>T maps to NM_001004760.2 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:5221692 G>A maps to NM_001004760.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr11:5221390 G>A maps to NM_001004760.2 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:5172900 C>T maps to NM_012375.2 Q233Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:5172774 G>A maps to NM_012375.2 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr11:5172741 G>A maps to NM_012375.2 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr11:5173353 C>T maps to NM_012375.2 K82K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr11:5172909 A>T maps to NM_012375.2 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:5173013 G>A maps to NM_012375.2 Q196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr11:5173107 C>T maps to NM_012375.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:5173449 G>A maps to NM_012375.2 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:5172831 G>A maps to NM_012375.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5172951 G>A maps to NM_012375.2 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5173284 G>A maps to NM_012375.2 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:5172774 G>A maps to NM_012375.2 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:5173509 C>T maps to NM_012375.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:5142613 G>A maps to NM_001005222.2 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:5153041 G>A maps to NM_001005160.2 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr11:5153158 G>A maps to NM_001005160.2 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:5153365 C>T maps to NM_001005160.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr11:5153119 G>A maps to NM_001005160.2 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr11:5153500 G>A maps to NM_001005160.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:5153286 G>A maps to NM_001005160.2 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:5153287 G>T maps to NM_001005160.2 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5153218 G>A maps to NM_001005160.2 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5153545 G>A maps to NM_001005160.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:6190815 G>A maps to NM_001004052.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:6191049 G>A maps to NM_001004052.1 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr11:6191109 G>A maps to NM_001004052.1 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:6191298 G>A maps to NM_001004052.1 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr11:6190585 C>T maps to NM_001004052.1 *324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:6191207 G>A maps to NM_001004052.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:6191511 G>A maps to NM_001004052.1 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:6191298 G>A maps to NM_001004052.1 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:6190734 G>A maps to NM_001004052.1 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:4389048 G>A maps to NM_001005161.3 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:4389042 G>A maps to NM_001005161.3 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:4389276 G>A maps to NM_001005161.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:4389396 C>T maps to NM_001005161.3 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:4389180 C>T maps to NM_001005161.3 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:4388922 C>T maps to NM_001005161.3 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr11:4388942 G>A maps to NM_001005161.3 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr11:4389345 G>A maps to NM_001005161.3 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:4389378 G>A maps to NM_001005161.3 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:4389389 G>A maps to NM_001005161.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:4389396 C>T maps to NM_001005161.3 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr11:4389396 C>T maps to NM_001005161.3 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:4388942 G>A maps to NM_001005161.3 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:5602504 C>T maps to NM_001005162.2 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:5602594 C>T maps to NM_001005162.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:5602594 C>T maps to NM_001005162.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr11:5602786 C>T maps to NM_001005162.2 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr11:5602624 C>T maps to NM_001005162.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5602588 G>A maps to NM_001005162.2 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:5510697 C>T maps to NM_001005163.2 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr11:5510607 C>T maps to NM_001005163.2 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:5510313 T>C maps to NM_001005163.2 Y126Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:5510607 C>T maps to NM_001005163.2 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:5510838 G>A maps to NM_001005163.2 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr11:5510824 G>T maps to NM_001005163.2 G297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:5510205 C>T maps to NM_001005163.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr11:5510550 G>A maps to NM_001005163.2 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:5510514 C>T maps to NM_001005163.2 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:5510718 C>T maps to NM_001005163.2 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr11:5079909 C>T maps to NM_001005164.2 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:5080593 C>T maps to NM_001005164.2 W88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:5079888 C>T maps to NM_001005164.2 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr11:5079888 C>T maps to NM_001005164.2 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:5079936 T>A maps to NM_001005164.2 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:5080803 C>T maps to NM_001005164.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:5079888 C>T maps to NM_001005164.2 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:5080029 G>A maps to NM_001005164.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr11:5080815 G>A maps to NM_001005164.2 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5080722 G>A maps to NM_001005164.2 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:5080740 G>A maps to NM_001005164.2 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr11:5080386 G>A maps to NM_001005164.2 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:5905956 C>T maps to NM_001005165.1 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr11:5906157 G>A maps to NM_001005165.1 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr11:5905701 C>T maps to NM_001005165.1 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr11:5905794 C>T maps to NM_001005165.1 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:5906187 C>T maps to NM_001005165.1 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:5905803 C>T maps to NM_001005165.1 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr11:5905797 A>G maps to NM_001005165.1 Q92Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:5905918 C>T maps to NM_001005165.1 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr11:5862974 G>A maps to ENST00000379946 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:5862461 G>A maps to ENST00000379946 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:5862812 G>A maps to ENST00000379946 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr11:5862629 T>C maps to ENST00000379946 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr11:5862251 G>A maps to ENST00000379946 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:5862782 G>A maps to ENST00000379946 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr11:5862233 T>C maps to ENST00000379946 K302K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:5862869 G>A maps to ENST00000379946 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr11:5862770 G>A maps to ENST00000379946 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:5863070 G>A maps to ENST00000379946 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr11:5863034 G>A maps to ENST00000379946 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr11:5862203 G>A maps to ENST00000379946 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr11:5862437 G>A maps to ENST00000379946 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:5862488 G>A maps to ENST00000379946 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr11:5862626 C>T maps to ENST00000379946 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:5878392 G>A maps to NM_001005168.1 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr11:5878596 G>A maps to NM_001005168.1 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:5878023 C>T maps to NM_001005168.1 Q303Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:5878410 G>A maps to NM_001005168.1 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:5878019 G>A maps to NM_001005168.1 R305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr11:5878392 G>A maps to NM_001005168.1 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:5878509 G>A maps to NM_001005168.1 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:5878767 G>A maps to NM_001005168.1 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:5878068 G>A maps to NM_001005168.1 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr11:5566204 G>A maps to NM_001005289.1 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:5566168 G>A maps to NM_001005289.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:5566261 G>A maps to NM_001005289.1 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr11:5565832 G>A maps to NM_001005289.1 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:5566282 G>A maps to NM_001005289.1 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:5565952 G>A maps to NM_001005289.1 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:5566729 G>A maps to NM_001005289.1 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:5566204 G>A maps to NM_001005289.1 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr11:5565994 G>A maps to NM_001005289.1 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr11:5566689 G>A maps to NM_001005289.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5566225 G>A maps to NM_001005289.1 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr11:5566420 G>A maps to NM_001005289.1 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:4616182 G>A maps to ENST00000450052 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr11:4608338 G>A maps to NM_001005170.2 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:4608386 C>T maps to NM_001005170.2 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:4608957 C>T maps to NM_001005170.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:4608407 C>T maps to NM_001005170.2 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:4608101 G>A maps to NM_001005170.2 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:5068544 C>T maps to NM_001001916.2 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:5068651 G>A maps to NM_001001916.2 Q299Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:5068651 G>A maps to NM_001001916.2 Q299Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:5068606 C>T maps to NM_001001916.2 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:5068516 C>T maps to NM_001001916.2 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5068441 C>T maps to NM_001001916.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr11:4510972 C>T maps to NM_001005171.2 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:4510322 C>T maps to NM_001005171.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr11:4511074 G>A maps to NM_001005171.2 *315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:4510978 C>T maps to NM_001005171.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr11:4510906 C>T maps to NM_001005171.2 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr11:4510459 C>T maps to NM_001005171.2 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr11:4511005 C>T maps to NM_001005171.2 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr11:4510276 C>T maps to NM_001005171.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:4471396 C>T maps to NM_001005172.2 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:4470610 C>T maps to NM_001005172.2 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr11:4471396 C>T maps to NM_001005172.2 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:4470715 C>T maps to NM_001005172.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:4470781 C>T maps to NM_001005172.2 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:4471495 C>T maps to NM_001005172.2 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:4471210 C>T maps to NM_001005172.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:4471396 C>T maps to NM_001005172.2 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr11:4471174 C>T maps to NM_001005172.2 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr11:4471471 C>T maps to NM_001005172.2 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:4470634 G>A maps to NM_001005172.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr11:4471057 C>T maps to NM_001005172.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:6008118 C>T maps to NM_001005173.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:6007439 G>A maps to NM_001005173.2 Q241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr11:6007635 G>A maps to NM_001005173.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:6007920 G>A maps to NM_001005173.2 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:6008028 C>T maps to NM_001005173.2 W44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:6008151 C>T maps to NM_001005173.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr11:6007407 G>A maps to NM_001005173.2 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:6007821 G>A maps to NM_001005173.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:6007899 G>A maps to NM_001005173.2 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr11:6007626 G>A maps to NM_001005173.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:6007700 G>A maps to NM_001005173.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:6007659 C>T maps to NM_001005173.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:6007701 G>A maps to NM_001005173.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:6008109 G>A maps to NM_001005173.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:4566476 C>T maps to NM_001004137.1 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr11:4566965 T>C maps to NM_001004137.1 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr11:4567251 C>T maps to NM_001004137.1 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:4567140 C>T maps to NM_001004137.1 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:4566491 C>T maps to NM_001004137.1 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:4566872 C>T maps to NM_001004137.1 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr11:4566872 C>T maps to NM_001004137.1 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:4566770 C>T maps to NM_001004137.1 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr11:4566515 C>T maps to NM_001004137.1 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr11:4566908 G>A maps to NM_001004137.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:4566872 C>T maps to NM_001004137.1 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr11:4567352 G>A maps to NM_001004137.1 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:4566560 C>T maps to NM_001004137.1 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr11:4566959 C>T maps to NM_001004137.1 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:4566713 C>T maps to NM_001004137.1 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:4566770 C>T maps to NM_001004137.1 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:4566770 C>T maps to NM_001004137.1 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:4566515 C>T maps to NM_001004137.1 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr11:4567173 C>T maps to NM_001004137.1 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr11:4567274 C>T maps to NM_001004137.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:4566680 C>T maps to NM_001004137.1 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:4567271 C>T maps to NM_001004137.1 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr11:5809340 G>A maps to NM_001001913.1 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr11:5809911 G>A maps to NM_001001913.1 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr11:5809911 G>A maps to NM_001001913.1 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr11:5809488 C>A maps to NM_001001913.1 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:5809917 C>T maps to NM_001001913.1 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:5809572 A>G maps to NM_001001913.1 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:5809377 A>T maps to NM_001001913.1 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:5842146 C>T maps to NM_001005174.1 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:5841678 C>T maps to NM_001005174.1 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:5842047 C>T maps to NM_001005174.1 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:5842473 G>A maps to NM_001005174.1 Q303Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:5842092 C>T maps to NM_001005174.1 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:5841840 G>A maps to NM_001005174.1 K92K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5841609 C>T maps to NM_001005174.1 I15I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5842089 C>T maps to NM_001005174.1 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5842128 G>A maps to NM_001005174.1 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5842168 C>T maps to NM_001005174.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr11:5776681 A>T maps to NM_001005175.2 K238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:5776233 G>A maps to NM_001005175.2 W88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:5776644 G>A maps to NM_001005175.2 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:5776590 G>A maps to NM_001005175.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:5776068 C>T maps to NM_001005175.2 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:5776098 G>A maps to NM_001005175.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:5776575 G>A maps to NM_001005175.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:5776410 G>A maps to NM_001005175.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5776015 C>T maps to NM_001005175.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5776053 G>A maps to NM_001005175.2 W28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:5776209 C>T maps to NM_001005175.2 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:5776782 C>T maps to NM_001005175.2 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:5776644 G>T maps to NM_001005175.2 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:5799129 C>T maps to NM_001001922.2 K245K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr11:5799459 A>T maps to NM_001001922.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:5799756 G>A maps to NM_001001922.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:5799162 C>T maps to NM_001001922.2 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:5799717 C>T maps to NM_001001922.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:4825160 G>A maps to ENST00000380382 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:4825357 A>G maps to ENST00000380382 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:4825532 G>A maps to ENST00000380382 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr11:4825217 G>A maps to ENST00000380382 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:4825010 C>T maps to ENST00000380382 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:4824860 G>A maps to ENST00000380382 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:4825414 G>A maps to ENST00000380382 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:4825160 G>A maps to ENST00000380382 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:4825175 G>A maps to ENST00000380382 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr11:4825175 G>A maps to ENST00000380382 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:4824731 G>A maps to ENST00000380382 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr11:4825097 G>A maps to ENST00000380382 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:4825118 G>A maps to ENST00000380382 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:4825531 G>A maps to ENST00000380382 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr11:6220758 C>T maps to NM_001005178.1 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:6048712 G>A maps to NM_001001917.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr11:6048592 G>A maps to NM_001001917.2 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:6048685 G>A maps to NM_001001917.2 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:6048318 G>A maps to NM_001001917.2 Q206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:6048772 G>A maps to NM_001001917.2 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:5968623 C>T maps to NM_001003443.2 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:5968695 C>T maps to NM_001003443.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:5968908 C>T maps to NM_001003443.2 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:5969166 C>T maps to NM_001003443.2 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:5969178 T>G maps to NM_001003443.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:5969064 C>T maps to NM_001003443.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:5968869 C>T maps to NM_001003443.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr11:5969508 G>A maps to NM_001003443.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr11:5968821 C>T maps to NM_001003443.2 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr11:5968866 C>T maps to NM_001003443.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:5968800 C>T maps to NM_001003443.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr11:5968692 C>T maps to NM_001003443.2 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr11:5968869 C>T maps to NM_001003443.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:5969064 C>T maps to NM_001003443.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr11:6023652 G>A maps to NM_001005179.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:6024366 C>T maps to NM_001005179.2 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:6023832 G>A maps to NM_001005179.2 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:6024000 G>A maps to NM_001005179.2 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:6024231 C>T maps to NM_001005179.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:6024168 G>A maps to NM_001005179.2 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:6023367 G>A maps to NM_001005179.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr11:6023601 C>T maps to NM_001005179.2 W259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:6023313 C>T maps to NM_001005179.2 K355K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:6023379 G>A maps to NM_001005179.2 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:5758615 C>T maps to NM_001005180.2 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:5757808 C>T maps to NM_001005180.2 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:5757958 C>T maps to NM_001005180.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:5758198 A>G maps to NM_001005180.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:5758024 C>T maps to NM_001005180.2 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5757958 C>T maps to NM_001005180.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5758567 G>A maps to NM_001005180.2 E274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:5758090 C>T maps to NM_001005180.2 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:6129416 C>T maps to NM_001005181.1 Q137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr11:6129416 C>T maps to NM_001005181.1 Q137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:6129685 A>G maps to NM_001005181.1 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:6129061 C>T maps to NM_001005181.1 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:6129496 C>T maps to NM_001005181.1 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:6129373 C>T maps to NM_001005181.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr11:6129256 C>T maps to NM_001005181.1 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr11:6129274 C>T maps to NM_001005181.1 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr11:6129064 C>T maps to NM_001005181.1 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:59211495 C>T maps to NM_001004728.1 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:59211054 C>T maps to NM_001004728.1 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:59210721 G>A maps to NM_001004728.1 Q27Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr11:59211054 C>T maps to NM_001004728.1 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr11:59211400 C>T maps to NM_001004728.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:59211504 G>A maps to NM_001004728.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:59211348 C>T maps to NM_001004728.1 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:59211123 C>T maps to NM_001004728.1 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr11:59211108 C>T maps to NM_001004728.1 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr11:59211108 C>T maps to NM_001004728.1 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:59211054 C>T maps to NM_001004728.1 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:59190057 C>T maps to NM_001001954.1 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:59189523 G>A maps to NM_001001954.1 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr11:59189493 C>T maps to NM_001001954.1 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr11:59190345 G>A maps to NM_001001954.1 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr11:59189502 C>T maps to NM_001001954.1 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr11:59189676 G>A maps to NM_001001954.1 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:97806255 C>T maps to NM_054106.1 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:97806480 C>T maps to NM_054106.1 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:97806207 C>T maps to NM_054106.1 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:97806858 G>A maps to NM_054106.1 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr3:97806703 A>T maps to NM_054106.1 K230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:97806366 G>A maps to NM_054106.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr3:97806363 C>T maps to NM_054106.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:97806870 C>T maps to NM_054106.1 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr11:56757026 C>T maps to NM_001005323.1 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:56757008 G>A maps to NM_001005323.1 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr11:56757062 C>T maps to NM_001005323.1 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr11:56756480 C>T maps to NM_001005323.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:56757089 G>A maps to NM_001005323.1 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr11:56756747 G>A maps to NM_001005323.1 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:56756600 C>T maps to NM_001005323.1 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr11:56757302 G>A maps to NM_001005323.1 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:56756909 C>T maps to NM_001005323.1 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr11:56757089 G>A maps to NM_001005323.1 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr11:56757296 G>A maps to NM_001005323.1 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:56757089 G>A maps to NM_001005323.1 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:56757302 G>A maps to NM_001005323.1 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:56757089 G>A maps to NM_001005323.1 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:56756837 C>T maps to NM_001005323.1 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:56757002 T>A maps to NM_001005323.1 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:56757302 G>A maps to NM_001005323.1 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:56756471 C>T maps to NM_001005323.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:56756465 C>T maps to NM_001005323.1 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:56757188 C>T maps to NM_001005323.1 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:56756618 C>T maps to NM_001005323.1 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:56756660 G>A maps to NM_001005323.1 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:56756660 G>A maps to NM_001005323.1 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:59132524 C>T maps to NM_001004729.1 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:59131939 G>A maps to NM_001004729.1 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:59131999 G>A maps to NM_001004729.1 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:59132056 G>A maps to NM_001004729.1 W42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:59132521 G>A maps to NM_001004729.1 Q197Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:56409858 G>A maps to NM_001002925.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:56409012 C>T maps to NM_001002925.1 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:56408979 C>T maps to NM_001002925.1 W312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:56408985 G>A maps to NM_001002925.1 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:56409000 C>T maps to NM_001002925.1 K305K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:56409162 G>A maps to NM_001002925.1 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:56409242 G>A maps to NM_001002925.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr11:56431805 C>T maps to NM_001004730.1 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:56432088 C>T maps to NM_001004730.1 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:56431805 C>T maps to NM_001004730.1 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr11:56431598 G>T maps to NM_001004730.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:56431748 G>A maps to NM_001004730.1 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr11:56431304 G>A maps to NM_001004730.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:56431415 C>T maps to NM_001004730.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:55798784 G>A maps to NM_001001921.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr11:55798784 G>A maps to NM_001001921.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr11:55798796 C>T maps to NM_001001921.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:55798646 C>T maps to NM_001001921.1 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:55798446 C>T maps to NM_001001921.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:55797986 C>T maps to NM_001001921.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:55798436 C>T maps to NM_001001921.1 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:55797980 G>A maps to NM_001001921.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr11:55798784 G>A maps to NM_001001921.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr11:55798784 G>A maps to NM_001001921.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr11:55798325 C>T maps to NM_001001921.1 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr14:21623431 G>A maps to NM_001004731.1 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr14:21623857 G>A maps to NM_001004731.1 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr14:21623512 G>A maps to NM_001004731.1 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr14:21623848 G>A maps to NM_001004731.1 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:21623644 G>A maps to NM_001004731.1 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr14:21624049 G>A maps to NM_001004731.1 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:21623356 G>A maps to NM_001004731.1 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr14:21623767 C>T maps to NM_001004731.1 K139K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr14:21624049 G>A maps to NM_001004731.1 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr11:58207357 G>A maps to NM_001004733.2 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr11:58207171 G>A maps to NM_001004733.2 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:58207444 G>A maps to NM_001004733.2 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr11:58206829 G>A maps to NM_001004733.2 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:58207291 G>A maps to NM_001004733.2 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr11:58207171 G>A maps to NM_001004733.2 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr11:58206829 G>A maps to NM_001004733.2 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr11:58206721 C>T maps to NM_001004733.2 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr11:58207444 G>A maps to NM_001004733.2 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:58207357 G>A maps to NM_001004733.2 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:58207537 G>A maps to NM_001004733.2 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:58206841 G>A maps to NM_001004733.2 N261N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:58207171 G>A maps to NM_001004733.2 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:58126512 G>A maps to NM_001005489.1 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr11:58125657 C>T maps to NM_001005489.1 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr11:58125705 G>A maps to NM_001005489.1 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr11:58125888 G>A maps to NM_001005489.1 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:58125747 G>A maps to NM_001005489.1 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:58125747 G>A maps to NM_001005489.1 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:58126224 G>A maps to NM_001005489.1 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr11:58126509 G>A maps to NM_001005489.1 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:58125675 G>A maps to NM_001005489.1 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr11:58125669 C>T maps to NM_001005489.1 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr11:58190128 G>A maps to NM_001005566.2 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr11:58190181 G>A maps to NM_001005566.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:58190497 G>A maps to NM_001005566.2 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:58189846 C>T maps to NM_001005566.2 Q296Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:58189834 C>T maps to NM_001005566.2 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:58189861 C>T maps to NM_001005566.2 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:58190467 G>A maps to NM_001005566.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:58190554 G>A maps to NM_001005566.2 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:58190554 G>A maps to NM_001005566.2 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr11:58274945 G>A maps to NM_001005218.1 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:58275542 G>A maps to NM_001005218.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:58274927 G>A maps to NM_001005218.1 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:58170216 G>A maps to NM_001005469.1 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr11:58170744 C>T maps to NM_001005469.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr11:58170429 G>A maps to NM_001005469.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr11:58170228 G>A maps to NM_001005469.1 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:58170030 G>A maps to NM_001005469.1 N284N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:58170117 G>A maps to NM_001005469.1 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:58170405 C>T maps to NM_001005469.1 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:58170447 G>A maps to NM_001005469.1 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr9:125551447 C>T maps to NM_001001923.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr9:125551210 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:125551738 G>A maps to NM_001001923.1 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr9:125551885 C>T maps to NM_001001923.1 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr11:55541797 G>A maps to NM_001001967.1 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr11:55541104 C>T maps to NM_001001967.1 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:55541374 G>A maps to NM_001001967.1 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:55541557 C>T maps to NM_001001967.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr11:55541584 C>T maps to NM_001001967.1 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:55541557 C>T maps to NM_001001967.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:55541212 C>T maps to NM_001001967.1 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:55541771 C>T maps to NM_001001967.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr11:55541092 C>T maps to NM_001001967.1 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr11:55541797 G>A maps to NM_001001967.1 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr11:55541317 C>T maps to NM_001001967.1 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:55541017 C>T maps to NM_001001967.1 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:55541557 C>T maps to NM_001001967.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:55541104 C>T maps to NM_001001967.1 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:55541557 C>T maps to NM_001001967.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr11:55540934 C>T maps to NM_001001967.1 Q8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr11:55540912 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55541131 C>T maps to NM_001001967.1 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr11:55541017 C>T maps to NM_001001967.1 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr11:55541281 C>T maps to NM_001001967.1 D123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:55563261 C>T maps to NM_001004735.1 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:55563153 G>A maps to NM_001004735.1 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:55563234 C>T maps to NM_001004735.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:55563789 C>T maps to NM_001004735.1 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:55563135 C>T maps to NM_001004735.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr11:55563222 C>T maps to NM_001004735.1 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr11:55563507 G>A maps to NM_001004735.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:55563900 G>A maps to NM_001004735.1 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:55563360 G>A maps to NM_001004735.1 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:55563222 C>T maps to NM_001004735.1 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:55563801 C>T maps to NM_001004735.1 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr11:55563174 C>T maps to NM_001004735.1 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:55563222 C>T maps to NM_001004735.1 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55563285 G>A maps to NM_001004735.1 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:55563807 C>T maps to NM_001004735.1 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:55606460 C>T maps to NM_001005496.1 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:55606439 G>A maps to NM_001005496.1 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr11:55607075 G>A maps to NM_001005496.1 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:55606439 G>A maps to NM_001005496.1 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:55607045 C>T maps to NM_001005496.1 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:55606709 C>T maps to NM_001005496.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55606457 C>T maps to NM_001005496.1 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55606481 G>A maps to NM_001005496.1 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55606646 G>A maps to NM_001005496.1 Q140Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55606745 C>T maps to NM_001005496.1 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55606841 C>T maps to NM_001005496.1 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:55606784 G>A maps to NM_001005496.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:55587969 C>T maps to ENST00000395203 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:55587693 C>T maps to ENST00000395203 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:55587329 C>T maps to ENST00000395203 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:55587953 C>T maps to ENST00000395203 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:55587575 C>T maps to ENST00000395203 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr11:55587293 C>T maps to ENST00000395203 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:55587476 C>T maps to ENST00000395203 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr11:55587125 T>C maps to ENST00000395203 N9N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:55587293 C>T maps to ENST00000395203 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:55587575 C>T maps to ENST00000395203 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:55587653 C>T maps to ENST00000395203 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55587557 C>T maps to ENST00000395203 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55587767 C>T maps to ENST00000395203 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55587929 C>T maps to ENST00000395203 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr11:55587702 C>T maps to ENST00000395203 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:55761807 G>A maps to NM_003697.1 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr11:55761207 C>T maps to NM_003697.1 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:55761408 C>T maps to NM_003697.1 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr11:55761195 C>T maps to NM_003697.1 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:55761195 C>T maps to NM_003697.1 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:55761696 G>A maps to NM_003697.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr11:55761570 G>A maps to NM_003697.1 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:55761861 C>T maps to NM_003697.1 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:55761237 C>T maps to NM_003697.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr11:55761195 C>T maps to NM_003697.1 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr11:55761807 G>A maps to NM_003697.1 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr11:55761180 C>T maps to NM_003697.1 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:55761645 C>T maps to NM_003697.1 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr11:55761612 G>A maps to NM_003697.1 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55762065 G>A maps to NM_003697.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:55761291 C>T maps to NM_003697.1 Q270Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:97851870 G>A maps to NM_001005338.1 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr3:97852269 C>T maps to NM_001005338.1 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:97852044 C>T maps to NM_001005338.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:97852245 G>A maps to NM_001005338.1 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr3:97851870 G>A maps to NM_001005338.1 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:97852245 G>A maps to NM_001005338.1 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr3:97852161 G>A maps to NM_001005338.1 Q207Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr3:97851966 C>T maps to NM_001005338.1 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:97851840 G>A maps to NM_001005338.1 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr3:97868312 C>T maps to NM_001005514.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr3:97868546 C>T maps to NM_001005514.1 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr3:97868477 C>T maps to NM_001005514.1 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:97868999 C>T maps to NM_001005514.1 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:97868351 G>A maps to NM_001005514.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:97888088 C>T maps to NM_001005515.1 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:97888211 C>T maps to NM_001005515.1 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:97888247 G>A maps to NM_001005515.1 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:97888016 C>T maps to NM_001005515.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:97887584 C>G maps to NM_001005515.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr3:97888043 C>T maps to NM_001005515.1 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr3:97888286 C>T maps to NM_001005515.1 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:97887659 C>T maps to NM_001005515.1 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr3:97888469 T>A maps to NM_001005515.1 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr3:97888368 C>T maps to NM_001005515.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:98002429 G>A maps to NM_001005482.1 K233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:98001919 C>T maps to NM_001005482.1 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:98001871 C>T maps to NM_001005482.1 N47N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr3:98002147 G>A maps to NM_001005482.1 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr3:98002375 C>T maps to NM_001005482.1 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr3:97983955 G>A maps to NM_001005479.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr3:97983155 C>T maps to NM_001005479.1 Q10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:97983346 C>T maps to NM_001005479.1 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:97983874 G>A maps to NM_001005479.1 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr3:97983133 C>T maps to NM_001005479.1 F2F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:97983781 C>T maps to NM_001005479.1 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:97983577 C>T maps to NM_001005479.1 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:97983424 C>T maps to NM_001005479.1 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr3:97983880 A>G maps to NM_001005479.1 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr11:55703684 G>A maps to NM_006637.1 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr11:55703450 G>A maps to NM_006637.1 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr11:55703609 C>T maps to NM_006637.1 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:55703180 A>G maps to NM_006637.1 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:55703735 C>T maps to NM_006637.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:55703402 G>A maps to NM_006637.1 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr11:55944191 G>A maps to NM_001005492.1 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:55944455 C>T maps to NM_001005492.1 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:55944626 C>T maps to NM_001005492.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr11:55944404 C>T maps to NM_001005492.1 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr11:55944230 C>T maps to NM_001005492.1 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:98188563 G>A maps to NM_001004736.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:98188479 C>T maps to NM_001004736.2 H20H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:98188458 C>T maps to NM_001004736.2 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:98188533 C>T maps to NM_001004736.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr3:98188671 C>T maps to NM_001004736.2 N84N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr3:98188782 C>T maps to NM_001004736.2 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:98189038 C>T maps to NM_001004736.2 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:98189115 G>A maps to NM_001004736.2 E232E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:98216787 G>A maps to NM_001004737.1 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:98216595 G>A maps to NM_001004737.1 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:98216778 C>T maps to NM_001004737.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr3:98109619 C>T maps to NM_001005516.1 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr3:98109667 A>G maps to NM_001005516.1 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:98109976 C>T maps to NM_001005516.1 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr3:98072975 C>T maps to NM_001005517.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr3:98073359 C>T maps to NM_001005517.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr3:98072975 C>T maps to NM_001005517.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:98072717 C>T maps to NM_001005517.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:98073563 G>A maps to NM_001005517.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:98073320 C>T maps to NM_001005517.1 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:98072951 C>T maps to NM_001005517.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr3:98072933 C>A maps to NM_001005517.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr3:98072732 C>T maps to NM_001005517.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:98072951 C>T maps to NM_001005517.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr3:98073320 C>T maps to NM_001005517.1 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr11:55579694 C>T maps to NM_001004738.1 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr11:55579280 C>T maps to NM_001004738.1 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:55579001 C>T maps to NM_001004738.1 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr11:55578950 G>A maps to NM_001004738.1 K3K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:55579832 G>A maps to NM_001004738.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:55579280 C>T maps to NM_001004738.1 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:55579580 C>T maps to NM_001004738.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:55579089 C>T maps to NM_001004738.1 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:55578977 C>T maps to NM_001004738.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr11:55579817 G>A maps to NM_001004738.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr11:55579127 C>T maps to NM_001004738.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr11:55579694 C>T maps to NM_001004738.1 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55578977 C>T maps to NM_001004738.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55579460 G>A maps to NM_001004738.1 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:55579025 C>T maps to NM_001004738.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:55579439 C>T maps to NM_001004738.1 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr11:55594777 C>T maps to NM_001004739.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:55595227 C>T maps to NM_001004739.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:55595332 C>T maps to NM_001004739.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr11:55594879 C>T maps to NM_001004739.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:55594972 C>T maps to NM_001004739.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr11:55594729 C>T maps to NM_001004739.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr11:55594879 C>T maps to NM_001004739.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr11:55594873 C>T maps to NM_001004739.1 Y60Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:55595368 C>T maps to NM_001004739.1 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr11:55595524 C>T maps to NM_001004739.1 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr11:55595041 C>T maps to NM_001004739.1 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr11:55594879 C>T maps to NM_001004739.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55595212 G>A maps to NM_001004739.1 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55595368 C>T maps to NM_001004739.1 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr11:56380099 C>T maps to NM_001004740.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:56380267 G>A maps to NM_001004740.1 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr11:56380723 G>A maps to NM_001004740.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:56380969 G>A maps to NM_001004740.1 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr11:56380654 C>T maps to NM_001004740.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr11:56380165 G>A maps to NM_001004740.1 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr11:56380879 C>T maps to NM_001004740.1 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:56380306 C>T maps to NM_001004740.1 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:56380900 G>A maps to NM_001004740.1 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:56380567 G>A maps to NM_001004740.1 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:56380879 C>T maps to NM_001004740.1 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:56380885 G>A maps to NM_001004740.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:56380879 C>T maps to NM_001004740.1 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:56344633 G>A maps to NM_001004741.1 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:56344693 G>A maps to NM_001004741.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr11:56344978 A>G maps to NM_001004741.1 Y73Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr11:56344873 C>T maps to NM_001004741.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr11:56344873 C>A maps to NM_001004741.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr11:56344609 C>T maps to NM_001004741.1 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:56344323 G>A maps to NM_001004741.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr11:56344432 G>A maps to NM_001004741.1 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:56344942 G>A maps to NM_001004741.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:56345098 C>T maps to NM_001004741.1 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:56344462 C>T maps to NM_001004741.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr11:56345161 G>A maps to NM_001004741.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:56345059 G>A maps to NM_001004741.1 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr11:56310478 G>A maps to NM_001005245.1 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:56310240 G>A maps to NM_001005245.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr11:56310121 G>A maps to NM_001005245.1 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr11:56310252 G>A maps to NM_001005245.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr11:56310097 G>A maps to NM_001005245.1 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:56310286 G>A maps to NM_001005245.1 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:56310628 G>A maps to NM_001005245.1 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr11:56310478 G>A maps to NM_001005245.1 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:56310097 G>A maps to NM_001005245.1 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr11:56309816 C>T maps to NM_001005245.1 *306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:56310478 G>A maps to NM_001005245.1 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr11:56309821 C>T maps to NM_001005245.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr11:56237837 A>G maps to NM_001004742.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:56237850 G>A maps to NM_001004742.1 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:56237475 G>A maps to NM_001004742.1 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:56237349 G>A maps to NM_001004742.1 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr11:56237850 G>A maps to NM_001004742.1 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:56237552 G>A maps to NM_001004742.1 R141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:56237334 G>A maps to NM_001004742.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:56237166 C>T maps to NM_001004742.1 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:56237943 G>A maps to NM_001004742.1 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:56258183 G>A maps to NM_001005282.1 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr11:56258813 G>A maps to NM_001005282.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:56258735 C>T maps to NM_001005282.1 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr11:56258594 G>A maps to NM_001005282.1 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr11:56230547 G>A maps to NM_001004743.1 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr11:56229950 C>T maps to NM_001004743.1 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr11:56230571 G>A maps to NM_001004743.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:56230009 G>A maps to NM_001004743.1 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:56230223 G>A maps to NM_001004743.1 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:56230745 G>A maps to NM_001004743.1 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr11:56230397 C>T maps to NM_001004743.1 W160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:56230592 G>A maps to NM_001004743.1 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr11:7818468 C>T maps to NM_153444.1 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr11:7817637 C>T maps to NM_153444.1 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr11:7818387 G>A maps to NM_153444.1 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:7817637 C>T maps to NM_153444.1 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:7817658 C>T maps to NM_153444.1 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:7818246 G>A maps to NM_153444.1 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:7818440 G>A maps to NM_153444.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:7817685 C>T maps to NM_153444.1 K268K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:7818000 G>A maps to NM_153444.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:7818246 G>A maps to NM_153444.1 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr11:7817652 G>A maps to NM_153444.1 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr11:7818402 G>A maps to NM_153444.1 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:7818402 G>A maps to NM_153444.1 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:7817730 G>A maps to NM_153444.1 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:7818039 G>A maps to NM_153444.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:7847258 C>T maps to NM_153445.1 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:7846843 G>A maps to NM_153445.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr11:7847390 G>A maps to NM_153445.1 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr11:7847264 G>A maps to NM_153445.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:7846916 G>A maps to NM_153445.1 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:7847333 G>A maps to NM_153445.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:7847216 G>A maps to NM_153445.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:7847258 C>T maps to NM_153445.1 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:7847180 G>A maps to NM_153445.1 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:7846790 G>A maps to NM_153445.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:7847057 C>T maps to NM_153445.1 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:7847180 G>A maps to NM_153445.1 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:7846727 G>A maps to NM_153445.1 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:56184841 G>A maps to NM_001004744.1 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr11:56185522 G>A maps to NM_001004744.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr11:56185690 G>A maps to NM_001004744.1 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:56185303 C>T maps to NM_001004744.1 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:56185321 G>A maps to NM_001004744.1 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:56184862 G>A maps to NM_001004744.1 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr11:56185027 C>T maps to NM_001004744.1 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:56185600 C>T maps to NM_001004744.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr11:56184907 G>A maps to NM_001004744.1 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:56043920 C>T maps to NM_001004745.1 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr11:56043404 C>T maps to NM_001004745.1 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr11:56043506 T>C maps to NM_001004745.1 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:56043276 T>C maps to NM_001004745.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr11:56043122 G>A maps to NM_001004745.1 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:56043653 C>T maps to NM_001004745.1 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:56043179 C>T maps to NM_001004745.1 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:56043527 C>T maps to NM_001004745.1 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr11:56000187 A>G maps to NM_001004746.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:55999842 C>T maps to NM_001004746.1 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:55999926 G>A maps to NM_001004746.1 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:56000148 A>G maps to NM_001004746.1 Y171Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:56000153 G>A maps to NM_001004746.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:55999752 G>A maps to NM_001004746.1 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr11:55999779 G>A maps to NM_001004746.1 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr11:56020496 C>T maps to NM_001004747.1 H274H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:56020260 C>T maps to NM_001004747.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:56020178 C>T maps to NM_001004747.1 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:56019944 T>A maps to NM_001004747.1 Y90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr11:56019897 C>T maps to NM_001004747.1 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:56020466 G>A maps to NM_001004747.1 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:56020265 C>T maps to NM_001004747.1 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:56019764 G>A maps to NM_001004747.1 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:56019908 G>A maps to NM_001004747.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:56020049 C>T maps to NM_001004747.1 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:56020497 C>T maps to NM_001004747.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:29323093 C>T maps to NM_030876.5 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr6:29323093 C>T maps to NM_030876.5 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:29323234 G>A maps to NM_030876.5 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr6:29323093 C>T maps to NM_030876.5 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr6:29323339 G>A maps to NM_030876.5 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr6:29323678 C>T maps to NM_030876.5 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:29323339 G>A maps to NM_030876.5 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:29323780 C>T maps to NM_030876.5 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:29323780 C>T maps to NM_030876.5 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr11:55681167 C>T maps to NM_001001960.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:55681305 G>A maps to NM_001001960.1 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:55681862 G>A maps to NM_001001960.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:55681497 G>A maps to NM_001001960.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr11:55681146 C>T maps to NM_001001960.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr11:55681515 G>A maps to NM_001001960.1 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55681548 C>T maps to NM_001001960.1 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55681680 G>A maps to NM_001001960.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr11:6816405 G>A maps to NM_003696.2 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr11:6816726 C>T maps to NM_003696.2 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:6816666 C>T maps to NM_003696.2 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:6816381 G>A maps to NM_003696.2 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr11:6816291 G>A maps to NM_003696.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr11:6816324 G>A maps to NM_003696.2 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:6816141 C>T maps to NM_003696.2 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr11:6816324 G>A maps to NM_003696.2 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:6816285 G>A maps to NM_003696.2 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:143701622 C>T maps to NM_001005281.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:143701532 C>T maps to NM_001005281.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr7:143701562 G>A maps to NM_001005281.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr7:143701835 C>T maps to NM_001005281.1 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:143701589 C>T maps to NM_001005281.1 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:143701709 C>T maps to NM_001005281.1 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:143701691 C>T maps to NM_001005281.1 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:143701181 C>T maps to NM_001005281.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:143701556 C>T maps to NM_001005281.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:143701557 C>T maps to NM_001005281.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:143701352 G>A maps to NM_001005281.1 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:240969246 G>A maps to NM_001005853.1 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:240969585 G>A maps to NM_001005853.1 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:240969753 G>A maps to NM_001005853.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr2:240969564 G>A maps to NM_001005853.1 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:240969588 G>A maps to NM_001005853.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:240969783 T>G maps to NM_001005853.1 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:240969564 G>A maps to NM_001005853.1 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr2:240968961 C>T maps to NM_001005853.1 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr2:240969564 G>A maps to NM_001005853.1 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr2:240969564 G>A maps to NM_001005853.1 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:240969786 G>A maps to NM_001005853.1 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:240985396 G>A maps to NM_173351.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr2:240984889 G>A maps to NM_173351.1 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:240985396 G>A maps to NM_173351.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:240984547 C>T maps to NM_173351.1 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:240985207 G>A maps to NM_173351.1 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:240985279 C>T maps to NM_173351.1 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:240985477 C>T maps to NM_173351.1 E4E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr2:240984586 C>T maps to NM_173351.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:55715105 C>T maps to NM_001005182.1 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr12:55714841 C>T maps to NM_001005182.1 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr12:55714466 C>T maps to NM_001005182.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr12:55714508 C>T maps to NM_001005182.1 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr12:55714514 C>T maps to NM_001005182.1 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:55715294 G>A maps to NM_001005182.1 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:55715295 A>T maps to NM_001005182.1 K305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:55715320 G>A maps to NM_001005182.1 *313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr12:55715320 G>A maps to NM_001005182.1 *313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:55715216 A>G maps to NM_001005182.1 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr12:55714499 G>A maps to NM_001005182.1 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:55714562 C>T maps to NM_001005182.1 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:55714601 C>A maps to NM_001005182.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr12:55846719 C>T maps to NM_054105.1 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr12:55846758 C>T maps to NM_054105.1 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr12:55846617 C>T maps to NM_054105.1 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:55846761 C>T maps to NM_054105.1 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:55846821 T>C maps to NM_054105.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:55846077 C>T maps to NM_054105.1 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:55846191 C>T maps to NM_054105.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr12:55846587 T>C maps to NM_054105.1 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:55846692 G>A maps to NM_054105.1 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr12:55846692 G>A maps to NM_054105.1 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:55846191 C>T maps to NM_054105.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:55846719 C>T maps to NM_054105.1 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:55846839 C>T maps to NM_054105.1 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr12:55846666 C>T maps to NM_054105.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:55846719 C>T maps to NM_054105.1 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr12:55846761 C>T maps to NM_054105.1 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr12:55846581 G>A maps to NM_054105.1 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr12:55725660 C>T maps to NM_054104.1 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr12:55726418 G>A maps to NM_054104.1 *312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:55726245 C>T maps to NM_054104.1 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:55726215 C>T maps to NM_054104.1 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:55725852 C>T maps to NM_054104.1 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:55725660 C>T maps to NM_054104.1 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr12:55725573 C>T maps to NM_054104.1 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:55725783 C>T maps to NM_054104.1 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:55725966 C>T maps to NM_054104.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:55725633 C>G maps to NM_054104.1 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:55725660 C>T maps to NM_054104.1 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:55726101 C>T maps to NM_054104.1 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:55725552 G>A maps to NM_054104.1 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr12:55726245 C>T maps to NM_054104.1 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr12:55945441 C>T maps to NM_001005494.1 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr12:55945168 C>T maps to NM_001005494.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr12:55945195 G>A maps to NM_001005494.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:55945369 T>G maps to NM_001005494.1 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:55945720 C>T maps to NM_001005494.1 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:55945640 C>T maps to NM_001005494.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:55945169 C>T maps to NM_001005494.1 Q54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:55945750 C>T maps to NM_001005494.1 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr12:55945753 C>G maps to NM_001005494.1 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr12:55945507 C>T maps to NM_001005494.1 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:55945400 C>T maps to NM_001005494.1 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr12:55945094 C>T maps to NM_001005494.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr12:55945061 C>T maps to NM_001005494.1 Q18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr12:55945189 C>T maps to NM_001005494.1 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr12:55688320 C>T maps to NM_001005493.1 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:55688380 C>T maps to NM_001005493.1 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr12:55688986 G>A maps to NM_001005493.1 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr12:55688890 G>A maps to NM_001005493.1 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:55688938 G>A maps to NM_001005493.1 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:55688680 G>A maps to NM_001005493.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr12:55795200 C>T maps to NM_001005518.1 Q297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr12:55794743 C>T maps to NM_001005518.1 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:55795007 G>A maps to NM_001005518.1 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr12:55795115 G>A maps to NM_001005518.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:55794707 C>T maps to NM_001005518.1 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:55794782 C>T maps to NM_001005518.1 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr12:55794497 G>A maps to NM_001005518.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:55795196 G>A maps to NM_001005518.1 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:55794907 T>A maps to NM_001005518.1 L199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr12:55795007 G>A maps to NM_001005518.1 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr12:55795217 C>T maps to NM_001005518.1 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:55794836 C>T maps to NM_001005518.1 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr12:55794836 C>T maps to NM_001005518.1 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:55886238 C>T maps to NM_001005519.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr12:55886277 G>A maps to NM_001005519.1 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr12:55886838 C>T maps to NM_001005519.1 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:55886344 C>T maps to NM_001005519.1 Q67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr12:55886781 C>T maps to NM_001005519.1 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:55886865 C>T maps to NM_001005519.1 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr12:55863457 G>A maps to NM_001005499.1 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr12:55863874 C>T maps to NM_001005499.1 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:55863831 G>A maps to NM_001005499.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr12:55863780 G>A maps to NM_001005499.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:55863874 C>T maps to NM_001005499.1 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr12:55863874 C>T maps to NM_001005499.1 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:55863784 G>A maps to NM_001005499.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:55863265 G>A maps to NM_001005499.1 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:55863028 G>A maps to NM_001005499.1 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:55863178 G>A maps to NM_001005499.1 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr12:55863589 G>A maps to NM_001005499.1 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:55863469 G>A maps to NM_001005499.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:55863244 G>A maps to NM_001005499.1 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:55863685 G>A maps to NM_001005499.1 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:55863844 G>A maps to NM_001005499.1 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr12:55863283 G>A maps to NM_001005499.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:55863136 C>T maps to NM_001005499.1 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr12:55641154 C>T maps to NM_001005490.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr12:55641163 C>T maps to NM_001005490.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr12:55641545 C>T maps to NM_001005490.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr12:55641805 C>T maps to NM_001005490.1 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:55641395 G>T maps to NM_001005490.1 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr12:55758905 C>T maps to NM_001005497.1 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:55759805 G>A maps to NM_001005497.1 Q304Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:55759517 C>T maps to NM_001005497.1 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:55759584 C>T maps to NM_001005497.1 Q231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:55759739 C>T maps to NM_001005497.1 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr12:55759589 G>A maps to NM_001005497.1 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:55759262 C>T maps to NM_001005497.1 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr12:55759589 G>A maps to NM_001005497.1 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:55759598 C>G maps to NM_001005497.1 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:55759079 G>A maps to NM_001005497.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr12:55820222 G>A maps to NM_001005183.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr12:55820222 G>A maps to NM_001005183.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr12:55820417 G>A maps to NM_001005183.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:55820948 G>A maps to NM_001005183.1 K304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:55820231 C>T maps to NM_001005183.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr12:55820216 C>T maps to NM_001005183.1 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:55820738 C>T maps to NM_001005183.1 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:55820222 G>A maps to NM_001005183.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr1:247875286 G>A maps to NM_001005286.1 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr1:247875469 C>T maps to NM_001005286.1 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:247876009 G>A maps to NM_001005286.1 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:247876017 A>G maps to NM_001005286.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:247875553 G>A maps to NM_001005286.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:247875598 G>A maps to NM_001005286.1 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:247875598 G>A maps to NM_001005286.1 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:247875553 G>A maps to NM_001005286.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:247875958 C>T maps to NM_001005286.1 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr1:247875757 C>T maps to NM_001005286.1 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr1:247875286 G>A maps to NM_001005286.1 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:247875733 G>A maps to NM_001005286.1 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr1:247875199 G>A maps to NM_001005286.1 N286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:247875847 C>T maps to NM_001005286.1 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:247875286 G>A maps to NM_001005286.1 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:247875319 G>C maps to NM_001005286.1 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:247875376 C>T maps to NM_001005286.1 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr1:158669704 G>A maps to NM_001005279.1 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:158670426 G>A maps to NM_001005279.1 R6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr1:158670151 G>A maps to NM_001005279.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:158669719 C>G maps to NM_001005279.1 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:158669535 T>A maps to NM_001005279.1 K303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:158670294 G>A maps to NM_001005279.1 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:158669860 G>A maps to NM_001005279.1 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:158670040 G>A maps to NM_001005279.1 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:158670268 G>A maps to NM_001005279.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158669800 G>A maps to NM_001005279.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:158686960 A>C maps to ENST00000368146 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:158687227 C>T maps to ENST00000368146 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:158687227 C>T maps to ENST00000368146 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:158687236 C>T maps to ENST00000368146 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr1:158686993 G>A maps to ENST00000368146 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:158687788 G>A maps to ENST00000368146 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:158687446 G>A maps to ENST00000368146 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:158687359 G>A maps to ENST00000368146 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr1:158687161 C>T maps to ENST00000368146 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr1:158687446 G>A maps to ENST00000368146 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr1:158687446 G>A maps to ENST00000368146 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr1:158687209 C>T maps to ENST00000368146 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:158724724 C>T maps to NM_001005184.1 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:158724892 C>T maps to NM_001005184.1 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:158725173 G>A maps to NM_001005184.1 W190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr1:158724802 C>T maps to NM_001005184.1 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:158725429 C>T maps to NM_001005184.1 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:158725231 C>T maps to NM_001005184.1 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:158725173 G>A maps to NM_001005184.1 W190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:158724704 C>T maps to NM_001005184.1 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:158725282 G>A maps to NM_001005184.1 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:158725525 C>T maps to NM_001005184.1 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:158725525 C>T maps to NM_001005184.1 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr1:158724850 C>T maps to NM_001005184.1 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:158725000 C>T maps to NM_001005184.1 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:123676142 G>A maps to NM_001005325.1 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:123676244 G>A maps to NM_001005325.1 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:123676664 C>T maps to NM_001005325.1 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:123676124 C>T maps to NM_001005325.1 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:123676603 G>A maps to NM_001005325.1 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:123676700 G>A maps to NM_001005325.1 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr11:123676379 G>A maps to NM_001005325.1 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:123676124 C>T maps to NM_001005325.1 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr1:158736436 G>A maps to NM_001005185.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:158736022 C>T maps to NM_001005185.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:158736238 G>A maps to NM_001005185.1 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:158736271 G>A maps to NM_001005185.1 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:158735658 G>A maps to NM_001005185.1 Q272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:158736455 C>T maps to NM_001005185.1 W6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr1:158735545 C>T maps to NM_001005185.1 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr1:158735839 G>A maps to NM_001005185.1 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:158736178 G>A maps to NM_001005185.1 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:158735578 C>T maps to NM_001005185.1 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr1:158746810 G>A maps to NM_001005278.1 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:158746891 G>A maps to NM_001005278.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:158746636 C>T maps to NM_001005278.1 K263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158746636 C>T maps to NM_001005278.1 K263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr1:158747290 G>A maps to NM_001005278.1 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:57799098 C>T maps to NM_001005186.2 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:57798741 C>T maps to NM_001005186.2 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:57798954 C>T maps to NM_001005186.2 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:57799104 G>A maps to NM_001005186.2 W227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:57799155 C>T maps to NM_001005186.2 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:57799035 C>T maps to NM_001005186.2 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:57799014 T>G maps to NM_001005186.2 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr14:21109316 C>T maps to NM_001001968.1 Q178Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:21109684 G>A maps to NM_001001968.1 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:21109808 G>A maps to NM_001001968.1 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr14:21108992 T>C maps to NM_001001968.1 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr14:21109262 C>T maps to NM_001001968.1 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:21109736 G>A maps to NM_001001968.1 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr11:123814340 G>A maps to NM_001005187.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr11:123814359 G>A maps to NM_001005187.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:123814344 G>A maps to NM_001005187.1 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:123813630 C>T maps to NM_001005187.1 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:123813675 G>A maps to NM_001005187.1 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr11:123814337 C>A maps to NM_001005187.1 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr11:123814338 C>T maps to NM_001005187.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:123814014 G>A maps to NM_001005187.1 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:123814359 G>A maps to NM_001005187.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:123813840 C>T maps to NM_001005187.1 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:123814470 G>A maps to NM_001005187.1 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr11:123813960 C>T maps to NM_001005187.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:123814491 G>A maps to NM_001005187.1 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:123814494 G>A maps to NM_001005187.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:123813798 G>A maps to NM_001005187.1 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:123814125 G>A maps to NM_001005187.1 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:123813960 C>T maps to NM_001005187.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr7:142750297 C>T maps to NM_001001667.1 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr7:142750169 C>T maps to NM_001001667.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:142750117 C>T maps to NM_001001667.1 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:142750144 C>T maps to NM_001001667.1 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:142749509 C>T maps to NM_001001667.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:142750180 C>T maps to NM_001001667.1 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:142750297 C>T maps to NM_001001667.1 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:142749773 C>T maps to NM_001001667.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:142749487 C>T maps to NM_001001667.1 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr7:142749643 C>T maps to NM_001001667.1 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:142749481 C>T maps to NM_001001667.1 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:142750031 C>T maps to NM_001001667.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:142749748 C>T maps to NM_001001667.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:123624611 G>A maps to NM_001005188.1 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:123624512 G>A maps to NM_001005188.1 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:123624668 G>A maps to NM_001005188.1 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr11:123624404 C>T maps to NM_001005188.1 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:123624386 G>A maps to NM_001005188.1 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:123624785 C>T maps to NM_001005188.1 W147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:158516941 C>T maps to NM_001005189.1 Q318Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr1:158517835 C>T maps to NM_001005189.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:158517793 G>A maps to NM_001005189.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:158517127 G>A maps to NM_001005189.1 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:158517163 G>A maps to NM_001005189.1 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:158517199 C>T maps to NM_001005189.1 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr1:158517879 G>A maps to NM_001005189.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:158517121 G>A maps to NM_001005189.1 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:158517796 G>A maps to NM_001005189.1 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:158517070 G>A maps to NM_001005189.1 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr19:14952488 G>A maps to NM_001005190.1 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:14952071 C>A maps to NM_001005190.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:14952515 G>A maps to NM_001005190.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:14991801 C>G maps to NM_030901.1 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:14991699 G>A maps to NM_030901.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:14991525 G>A maps to NM_030901.1 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:14938506 G>A maps to NM_017506.1 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:14938705 G>A maps to NM_017506.1 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr19:14938288 G>A maps to NM_017506.1 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:14910906 G>A maps to NM_198944.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr19:14910267 C>T maps to NM_198944.1 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:14910369 G>A maps to NM_198944.1 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:15052341 C>T maps to NM_012377.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:15052500 C>T maps to NM_012377.1 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:15053070 C>T maps to NM_012377.1 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:15052947 C>T maps to NM_012377.1 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:15053175 G>A maps to NM_012377.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:15053061 C>T maps to NM_012377.1 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:15053166 C>T maps to NM_012377.1 Y289Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:15052941 C>T maps to NM_012377.1 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15052500 C>T maps to NM_012377.1 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15052767 C>T maps to NM_012377.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15053253 C>T maps to NM_012377.1 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:15053049 C>T maps to NM_012377.1 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr19:9297089 C>T maps to NM_175883.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:9296534 C>T maps to NM_175883.2 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr19:9296615 C>T maps to NM_175883.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:9296798 C>T maps to NM_175883.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:9296798 C>T maps to NM_175883.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9296534 C>T maps to NM_175883.2 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:9296696 G>A maps to NM_175883.2 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr19:9324634 C>T maps to NM_001005191.2 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr19:9325374 G>A maps to NM_001005191.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:9325045 G>A maps to NM_001005191.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:9325294 G>A maps to NM_001005191.2 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:9325378 G>A maps to NM_001005191.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:9325032 G>A maps to NM_001005191.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:9325099 G>A maps to NM_001005191.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:9324871 G>A maps to NM_001005191.2 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:9324982 G>A maps to NM_001005191.2 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:9325174 G>A maps to NM_001005191.2 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9324871 G>A maps to NM_001005191.2 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr19:9325378 G>A maps to NM_001005191.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:9324649 G>A maps to NM_001005191.2 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr19:9362114 C>T maps to NM_001079935.1 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:9361895 G>A maps to NM_001079935.1 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:9361871 C>T maps to NM_001079935.1 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr19:9361871 C>T maps to NM_001079935.1 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:9361910 C>T maps to NM_001079935.1 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:9362288 G>A maps to NM_001079935.1 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:9362471 G>A maps to NM_001079935.1 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:9361850 C>T maps to NM_001079935.1 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr19:9362279 C>T maps to NM_001079935.1 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9362177 C>T maps to NM_001079935.1 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:9362520 T>C maps to NM_001079935.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr19:9362303 C>T maps to NM_001079935.1 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr19:9362582 G>A maps to NM_001079935.1 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:9362375 C>T maps to NM_001079935.1 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:9225791 G>A maps to ENST00000293614 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr19:9226423 G>A maps to ENST00000293614 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:9225964 G>A maps to ENST00000293614 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr19:9226361 G>A maps to ENST00000293614 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:9226250 G>A maps to ENST00000293614 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:9226316 C>T maps to ENST00000293614 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:9225704 G>A maps to ENST00000293614 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr19:9226037 G>A maps to ENST00000293614 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:9226319 C>T maps to ENST00000293614 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9225551 C>T maps to ENST00000293614 E296E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:9225995 G>A maps to ENST00000293614 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:9213397 G>A maps to NM_001005193.1 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:9213796 C>T maps to NM_001005193.1 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:9213385 G>A maps to NM_001005193.1 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:9212985 G>A maps to NM_001005193.1 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:9213976 C>T maps to NM_001005193.1 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:9213733 G>A maps to NM_001005193.1 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:9213397 G>A maps to NM_001005193.1 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:9213688 C>T maps to NM_001005193.1 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr19:9213649 C>T maps to NM_001005193.1 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:9213112 C>T maps to NM_001005193.1 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9213013 C>T maps to NM_001005193.1 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9213418 G>A maps to NM_001005193.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:9213058 G>A maps to NM_001005193.1 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr19:9213733 G>A maps to NM_001005193.1 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:9237047 G>A maps to NM_001001958.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:9237443 G>A maps to NM_001001958.1 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:9237092 G>A maps to NM_001001958.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:9237101 G>A maps to NM_001001958.1 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr19:9237430 G>A maps to NM_001001958.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9237431 G>A maps to NM_001001958.1 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr11:124440011 G>A maps to NM_001005194.1 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:124440110 C>T maps to NM_001005194.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:124440101 C>T maps to NM_001005194.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:124440632 C>T maps to NM_001005194.1 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr11:124440362 A>C maps to NM_001005194.1 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:124440710 G>A maps to NM_001005194.1 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:124440854 A>T maps to NM_001005194.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr11:124413390 G>A maps to NM_001005195.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:124413466 G>A maps to NM_001005195.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:124413459 G>A maps to NM_001005195.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:124413322 G>A maps to NM_001005195.1 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr11:124413430 C>T maps to NM_001005195.1 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:124413430 C>T maps to NM_001005195.1 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:124413022 G>A maps to NM_001005195.1 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr11:124413367 G>A maps to NM_001005195.1 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:124413289 C>T maps to NM_001005195.1 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr11:124412728 G>A maps to NM_001005195.1 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr11:124412727 G>A maps to NM_001005195.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:124412746 C>T maps to NM_001005195.1 E268E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:124413289 C>T maps to NM_001005195.1 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:124413430 C>T maps to NM_001005195.1 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr11:124413010 G>A maps to NM_001005195.1 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:124253152 G>A maps to NM_001005468.1 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr11:124252579 G>A maps to NM_001005468.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr11:124253092 G>A maps to NM_001005468.1 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:124253218 G>A maps to NM_001005468.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:124252918 G>A maps to NM_001005468.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:124252918 G>A maps to NM_001005468.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:124253152 G>A maps to NM_001005468.1 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr11:124253092 G>A maps to NM_001005468.1 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:124252336 C>T maps to NM_001005468.1 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:124252918 G>A maps to NM_001005468.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:124252336 C>T maps to NM_001005468.1 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr11:124252579 G>A maps to NM_001005468.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:124252336 C>T maps to NM_001005468.1 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:124253008 G>A maps to NM_001005468.1 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:124253035 G>A maps to NM_001005468.1 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:124252579 G>A maps to NM_001005468.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr11:124266938 G>A maps to NM_001005467.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr11:124267016 G>A maps to NM_001005467.1 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:124267061 G>A maps to NM_001005467.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:124267100 G>A maps to NM_001005467.1 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:124266728 G>A maps to NM_001005467.1 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:124266626 G>A maps to NM_001005467.1 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr11:124266608 G>A maps to NM_001005467.1 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:124267100 G>A maps to NM_001005467.1 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr11:124266337 G>A maps to NM_001005467.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr11:124294668 C>T maps to NM_001005196.1 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:124293852 C>T maps to NM_001005196.1 K305K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:124294692 G>A maps to NM_001005196.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:124294221 G>A maps to NM_001005196.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:124293857 G>A maps to NM_001005196.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr11:124294728 G>A maps to NM_001005196.1 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:124294170 G>A maps to NM_001005196.1 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr11:124293963 G>A maps to NM_001005196.1 N268N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:124293999 G>A maps to NM_001005196.1 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:124294683 G>A maps to NM_001005196.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:124294022 G>A maps to NM_001005196.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:124294074 C>T maps to NM_001005196.1 E231E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:124294728 G>A maps to NM_001005196.1 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr11:124310858 C>T maps to NM_012378.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:124310894 G>A maps to NM_012378.1 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:124310840 G>A maps to NM_012378.1 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:124310339 G>A maps to NM_012378.1 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:124310639 G>A maps to NM_012378.1 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr11:124310276 G>A maps to NM_012378.1 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:124310204 G>T maps to NM_012378.1 Y259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:124310336 G>A maps to NM_012378.1 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:124310912 G>A maps to NM_012378.1 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:124310102 C>T maps to NM_012378.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr11:124310903 G>A maps to NM_012378.1 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr11:124310603 G>A maps to NM_012378.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:124180059 G>A maps to NM_001002917.1 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:124179849 C>T maps to NM_001002917.1 E271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:124180161 G>A maps to NM_001002917.1 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr11:124180575 G>A maps to NM_001002917.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:124180575 G>A maps to NM_001002917.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:124180578 G>A maps to NM_001002917.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:124179771 C>T maps to NM_001002917.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:124180575 G>A maps to NM_001002917.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr11:124180449 G>A maps to NM_001002917.1 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr11:124180458 G>A maps to NM_001002917.1 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr11:124180566 C>T maps to NM_001002917.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr11:124180605 C>T maps to NM_001002917.1 Q19Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:124179771 C>T maps to NM_001002917.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:124180491 G>A maps to NM_001002917.1 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:124180002 G>A maps to NM_001002917.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:124180488 G>A maps to NM_001002917.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:124180568 G>A maps to NM_001002917.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:124180578 G>A maps to NM_001002917.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr11:124180407 G>A maps to NM_001002917.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:124179882 G>A maps to NM_001002917.1 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:124190009 G>A maps to NM_001002918.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:124189247 G>A maps to NM_001002918.1 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:124189784 G>A maps to NM_001002918.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:124189814 G>T maps to NM_001002918.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:124190006 G>A maps to NM_001002918.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr11:124189433 G>A maps to NM_001002918.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:124189214 C>T maps to NM_001002918.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr11:124189424 A>G maps to NM_001002918.1 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr11:124189544 G>A maps to NM_001002918.1 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:124189925 G>A maps to NM_001002918.1 Y56Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:124189784 G>A maps to NM_001002918.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:124189202 C>T maps to NM_001002918.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:124190018 C>A maps to NM_001002918.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr11:124189889 G>A maps to NM_001002918.1 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:124189829 C>T maps to NM_001002918.1 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr11:124190054 G>A maps to NM_001002918.1 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:124189534 G>A maps to NM_001002918.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:124189844 C>T maps to NM_001002918.1 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr11:124190053 G>A maps to NM_001002918.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:123777539 C>T maps to NM_001005197.1 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:123777515 C>T maps to NM_001005197.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr11:123777608 G>A maps to NM_001005197.1 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:123777308 C>T maps to NM_001005197.1 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr11:124095621 C>T maps to NM_001007249.1 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr11:56058502 G>A maps to NM_001005199.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:56057982 G>A maps to NM_001005199.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr11:56058442 G>A maps to NM_001005199.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:56058352 G>A maps to NM_001005199.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:56058259 G>A maps to NM_001005199.1 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:56057638 G>A maps to NM_001005199.1 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr11:55872985 C>A maps to NM_001005200.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:55873405 G>A maps to NM_001005200.1 E296E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:55872769 G>A maps to NM_001005200.1 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr11:55872706 C>T maps to NM_001005200.1 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:55873193 C>T maps to NM_001005200.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:55873147 C>T maps to NM_001005200.1 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr11:55872667 C>T maps to NM_001005200.1 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:55873108 C>T maps to NM_001005200.1 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr11:55872952 C>T maps to NM_001005200.1 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:55872590 C>T maps to NM_001005200.1 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:55873318 C>T maps to NM_001005200.1 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:55872769 G>A maps to NM_001005200.1 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr11:55872706 C>T maps to NM_001005200.1 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:55872559 C>T maps to NM_001005200.1 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:55872763 C>T maps to NM_001005200.1 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr11:55872985 C>T maps to NM_001005200.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr11:55873408 G>A maps to NM_001005200.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr11:55873331 C>T maps to NM_001005200.1 Q272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55872835 C>T maps to NM_001005200.1 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55872952 C>T maps to NM_001005200.1 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55873177 C>T maps to NM_001005200.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:55872556 C>T maps to NM_001005200.1 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr11:55890126 C>T maps to NM_001005201.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:55890036 C>T maps to NM_001005201.1 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:55890315 C>T maps to NM_001005201.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr11:55889997 C>T maps to NM_001005201.1 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr11:55890552 G>A maps to NM_001005201.1 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:55890507 C>T maps to NM_001005201.1 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr11:55890327 G>A maps to NM_001005201.1 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:55890024 C>T maps to NM_001005201.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:55890099 G>A maps to NM_001005201.1 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr11:55890036 C>T maps to NM_001005201.1 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:55890036 C>T maps to NM_001005201.1 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:55890552 G>A maps to NM_001005201.1 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr11:55890036 C>T maps to NM_001005201.1 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:55890639 G>A maps to NM_001005201.1 K264K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55890738 G>A maps to NM_001005201.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:55889946 C>T maps to NM_001005201.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:55861193 C>T maps to NM_001003750.1 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr11:55861031 G>A maps to NM_001003750.1 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:55861121 C>T maps to NM_001003750.1 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:55861679 T>A maps to NM_001003750.1 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr11:55860824 C>T maps to NM_001003750.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:55861529 C>T maps to NM_001003750.1 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55860968 C>T maps to NM_001003750.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55861394 C>T maps to NM_001003750.1 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:55860915 C>T maps to NM_001003750.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:55861550 C>T maps to NM_001003750.1 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:56128022 C>T maps to NM_001005205.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:56127901 C>T maps to NM_001005205.1 Y60Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:56128588 G>A maps to NM_001005205.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:56128423 G>A maps to NM_001005205.1 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:56128603 G>A maps to NM_001005205.1 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:56128030 G>A maps to NM_001005205.1 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr11:56128351 C>T maps to NM_001005205.1 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:56128657 C>T maps to NM_001005205.1 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr11:55905071 C>T maps to NM_001004064.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr11:55905122 C>T maps to NM_001004064.1 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:55904456 T>G maps to NM_001004064.1 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:55904474 G>A maps to NM_001004064.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:55904564 G>A maps to NM_001004064.1 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr11:55905176 G>A maps to NM_001004064.1 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:55905008 G>A maps to NM_001004064.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:55905101 G>A maps to NM_001004064.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:55905008 G>A maps to NM_001004064.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55904768 G>A maps to NM_001004064.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr11:56113717 C>T maps to NM_001002907.1 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr11:56114095 C>T maps to NM_001002907.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:56113648 G>A maps to NM_001002907.1 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:56114056 C>T maps to NM_001002907.1 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr11:56113753 C>T maps to NM_001002907.1 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:56113936 C>T maps to NM_001002907.1 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:56113717 C>T maps to NM_001002907.1 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:56114290 G>A maps to NM_001002907.1 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr11:56085889 G>A maps to NM_001005202.1 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr11:56086267 G>A maps to NM_001005202.1 K162K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr11:56086282 C>T maps to NM_001005202.1 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:56086228 C>T maps to NM_001005202.1 Y149Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:56085841 C>T maps to NM_001005202.1 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:56085889 G>A maps to NM_001005202.1 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:56086048 G>A maps to NM_001005202.1 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:56086402 G>A maps to NM_001005202.1 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:56086642 G>A maps to NM_001005202.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:56085985 C>T maps to NM_001005202.1 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:56085817 C>T maps to NM_001005202.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:56086444 C>T maps to NM_001005202.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr11:55927076 G>A maps to NM_001004058.2 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:55927700 G>A maps to NM_001004058.2 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr11:55927514 G>A maps to NM_001004058.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:55927274 G>A maps to NM_001004058.2 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:55927451 G>A maps to NM_001004058.2 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr11:55927528 G>A maps to NM_001004058.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:55927076 G>A maps to NM_001004058.2 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55926893 G>T maps to NM_001004058.2 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:55927400 G>A maps to NM_001004058.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:48919554 C>T maps to NM_001005203.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:48920004 C>T maps to NM_001005203.2 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr12:48919740 G>A maps to NM_001005203.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr12:48921756 G>A maps to NM_001005203.2 W317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:48919932 C>T maps to NM_001005203.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:48920046 C>T maps to NM_001005203.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr12:48920221 T>C maps to NM_001005203.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr12:48919455 C>T maps to NM_001005203.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr12:48919449 C>T maps to NM_001005203.2 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr12:48919932 C>T maps to NM_001005203.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr12:48919932 C>T maps to NM_001005203.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr12:48920046 C>T maps to NM_001005203.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:48921755 G>A maps to NM_001005203.2 W317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:48919968 C>T maps to NM_001005203.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:48919719 C>T maps to NM_001005203.2 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr7:142724009 G>A maps to NM_001001658.1 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:142723676 G>A maps to NM_001001658.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr7:142724186 G>A maps to NM_001001658.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:142723400 C>T maps to NM_001001658.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:142723526 C>T maps to NM_001001658.1 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr7:142723334 C>T maps to NM_001001658.1 E295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:142723738 G>A maps to NM_001001658.1 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:142724186 G>A maps to NM_001001658.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr7:142723946 C>T maps to NM_001001658.1 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:142723340 G>A maps to NM_001001658.1 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:142723784 C>T maps to NM_001001658.1 W145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:142723785 C>T maps to NM_001001658.1 W145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:142723367 G>A maps to NM_001001658.1 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:142724036 G>A maps to NM_001001658.1 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr7:141619379 G>A maps to NM_001001656.1 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr7:141618809 C>T maps to NM_001001656.1 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr7:141619574 C>T maps to NM_001001656.1 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr7:141619379 G>A maps to NM_001001656.1 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr7:141619140 C>T maps to NM_001001656.1 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:141619140 C>T maps to NM_001001656.1 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr7:141618713 C>T maps to NM_001001656.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr7:141618857 C>T maps to NM_001001656.1 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:141618824 G>A maps to NM_001001656.1 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:141618749 C>T maps to NM_001001656.1 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:141618980 C>T maps to NM_001001656.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr7:141619574 C>T maps to NM_001001656.1 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:141619259 G>A maps to NM_001001656.1 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:141619610 C>T maps to NM_001001656.1 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr7:141619379 G>A maps to NM_001001656.1 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:141619541 C>T maps to NM_001001656.1 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr7:141618722 C>T maps to NM_001001656.1 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr7:141619421 G>A maps to NM_001001656.1 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:141619379 G>A maps to NM_001001656.1 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr7:141619580 G>A maps to NM_001001656.1 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr7:141618884 C>T maps to NM_001001656.1 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr11:56468738 G>A maps to NM_001013358.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:56468462 C>T maps to NM_001013358.1 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:56468463 C>T maps to NM_001013358.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr11:56468588 C>T maps to NM_001013358.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:56468243 G>A maps to NM_001013358.1 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:56510723 G>A maps to NM_001005284.1 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr11:56511233 C>T maps to NM_001005284.1 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:56510336 C>T maps to NM_001005284.1 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr11:56510998 G>A maps to NM_001005284.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:56510579 G>A maps to NM_001005284.1 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:56511254 G>A maps to NM_001005284.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:56510324 C>T maps to NM_001005284.1 Q321Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:56510345 C>T maps to NM_001005284.1 E314E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:56511146 C>T maps to NM_001005284.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:56510579 G>A maps to NM_001005284.1 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:56510822 G>A maps to NM_001005284.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr11:56510998 G>A maps to NM_001005284.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:56510999 G>A maps to NM_001005284.1 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr11:56511056 G>A maps to NM_001005284.1 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:56510378 G>A maps to NM_001005284.1 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:56510575 G>A maps to NM_001005284.1 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:56511245 C>T maps to NM_001005284.1 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:56511254 G>A maps to NM_001005284.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:56510405 G>C maps to NM_001005284.1 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:57886004 G>A maps to NM_001005211.1 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr11:57886067 G>A maps to NM_001005211.1 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:57886847 C>T maps to NM_001005211.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr11:57886004 G>A maps to NM_001005211.1 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:57886367 G>A maps to NM_001005211.1 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr11:57886004 G>A maps to NM_001005211.1 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:57886004 G>A maps to NM_001005211.1 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A690-06A-11D-A30X-08 chr11:57886444 G>A maps to NM_001005211.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr12:55524100 T>A maps to NM_001005243.1 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:55523680 G>A maps to NM_001005243.1 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:55523968 C>T maps to NM_001005243.1 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:55523902 C>T maps to NM_001005243.1 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:55523812 C>T maps to NM_001005243.1 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr12:55524208 C>T maps to NM_001005243.1 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr11:57947791 G>A maps to NM_001005212.3 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:57947698 T>A maps to NM_001005212.3 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr11:57947245 C>T maps to NM_001005212.3 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:57947812 C>T maps to NM_001005212.3 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr11:57947581 C>T maps to NM_001005212.3 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:57947581 C>T maps to NM_001005212.3 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr11:57958135 G>A maps to NM_001005283.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:57958000 C>T maps to NM_001005283.2 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:57958678 C>T maps to NM_001005283.2 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:57958402 G>A maps to NM_001005283.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:57958531 G>A maps to NM_001005283.2 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:57958624 C>T maps to NM_001005283.2 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:57958681 C>T maps to NM_001005283.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:57958436 C>T maps to NM_001005283.2 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr11:57958048 C>T maps to NM_001005283.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr11:57958775 C>T maps to NM_001005283.2 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr11:57958363 C>T maps to NM_001005283.2 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr11:57958816 G>A maps to NM_001005283.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:122079437 G>A maps to NM_032790.3 K267K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:122079086 C>T maps to NM_032790.3 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:122079401 C>T maps to NM_032790.3 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr7:102087366 C>T maps to NM_032831.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr7:102087294 C>T maps to NM_032831.2 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:69482349 A>G maps to NM_153451.2 C117C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:69482295 A>T maps to NM_153451.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr1:52850900 G>A maps to NM_004153.3 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr1:52849184 G>A maps to NM_004153.3 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:52850380 G>A maps to NM_004153.3 I532I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr1:52859235 G>A maps to NM_004153.3 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr1:52838930 G>A maps to NM_004153.3 P836P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:201785740 G>A maps to NM_006190.4 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U9-06A-11D-A32N-08 chr2:201798643 G>T maps to NM_006190.4 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr6:88321921 C>T maps to NM_181837.2 Q277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr6:88318857 C>T maps to NM_181837.2 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:103808891 G>C maps to NM_181747.3 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:117087380 C>T maps to NM_000607.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr9:117086342 G>A maps to NM_000607.2 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr9:117085965 C>T maps to NM_000607.2 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:117087419 C>T maps to NM_000607.2 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:117094121 G>A maps to NM_000608.2 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr17:38079369 G>A maps to NM_139280.2 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr12:58114029 G>A maps to NM_006812.3 E583E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr12:58112149 C>T maps to NM_006812.3 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:58113909 C>T maps to NM_006812.3 V543V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:58113945 G>A maps to NM_006812.3 Q555Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:58111978 C>T maps to NM_006812.3 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:59361106 G>A maps to NM_002556.2 R550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr11:59348977 C>T maps to NM_002556.2 K576K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr11:59344406 G>A maps to NM_002556.2 R718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:59368784 G>A maps to NM_002556.2 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr22:31137151 C>T maps to NM_030758.3 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr22:31286917 G>C maps to NM_030758.3 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr22:31091507 C>T maps to NM_030758.3 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr22:31091279 C>T maps to NM_030758.3 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr22:31266587 C>T maps to NM_030758.3 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:31286728 G>A maps to NM_030758.3 E546E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:31286902 G>A maps to NM_030758.3 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr22:31091408 G>A maps to NM_030758.3 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr3:31710153 C>T maps to NM_017784.4 K692K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr3:31725456 G>A maps to NM_017784.4 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr3:31774766 G>A maps to NM_017784.4 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:31789437 G>A maps to NM_017784.4 Q302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:31789438 G>A maps to NM_017784.4 H301H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:31789432 C>G maps to NM_017784.4 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:31710234 G>A maps to NM_017784.4 F665F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:31712335 C>T maps to NM_017784.4 A622A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:31917962 G>A maps to NM_017784.4 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr3:31789437 G>A maps to NM_017784.4 Q302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr3:125249391 C>T maps to NM_022776.4 W737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:125298757 A>T maps to NM_022776.4 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:125271247 G>T maps to NM_022776.4 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr18:21883640 G>A maps to NM_080597.2 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr18:21819271 A>C maps to NM_080597.2 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:21743220 G>A maps to NM_080597.2 P925P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr20:60861676 C>T maps to NM_144498.1 D345D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr20:60856131 C>T maps to NM_144498.1 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr20:60864339 C>T maps to NM_144498.1 D401D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr20:60847269 C>T maps to NM_144498.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr20:60854353 G>A maps to NM_144498.1 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr20:60847230 C>T maps to NM_144498.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:60854365 C>T maps to NM_144498.1 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:60854377 C>T maps to NM_144498.1 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr7:24870476 G>A maps to NM_015550.2 Y598Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr7:24901283 G>A maps to NM_015550.2 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr7:24874317 C>T maps to NM_015550.2 R511R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:24874209 C>T maps to NM_015550.2 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:24901382 C>T maps to NM_015550.2 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr11:3111845 G>A maps to NM_020896.3 S780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr11:3115486 G>A maps to NM_020896.3 Q567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:3125454 G>A maps to NM_020896.3 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:3122902 G>A maps to NM_020896.3 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:179214105 C>T maps to ENST00000392505 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr2:179255918 C>T maps to ENST00000392505 P832P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr2:179255832 C>T maps to ENST00000392505 Q804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:179238630 C>T maps to ENST00000392505 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:179248803 C>T maps to ENST00000392505 S663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr2:179260238 C>T maps to ENST00000392505 R945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:179238681 C>T maps to ENST00000392505 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr17:45890657 G>A maps to NM_145798.2 R571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:45888180 G>T maps to NM_145798.2 I586I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:45888201 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr17:45886792 G>A maps to NM_145798.2 V644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr17:45895674 G>A maps to NM_145798.2 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr17:45885689 G>A maps to NM_145798.2 G832G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:76791506 G>A maps to NM_020841.4 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr12:76767207 G>A maps to NM_020841.4 F611F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr12:76749710 G>A maps to NM_020841.4 L876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:52226375 C>T maps to ENST00000428468 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:52249659 C>T maps to ENST00000428468 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:54600296 G>A maps to NM_130771.3 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:54598536 G>A maps to NM_130771.3 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:54600242 G>A maps to NM_130771.3 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:36887762 G>A maps to ENST00000356637 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:36884633 T>C maps to ENST00000356637 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr14:20915793 C>T maps to NM_017807.3 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:190615319 A>T maps to NM_022353.2 L410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr2:190618688 G>A maps to NM_022353.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:83992992 C>T maps to NM_013370.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr16:83998924 C>T maps to NM_013370.3 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:83992976 C>T maps to NM_013370.3 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:83994349 C>T maps to NM_013370.3 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:83998948 C>T maps to NM_013370.3 I340I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr22:30659889 C>T maps to NM_020530.3 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:30659889 C>T maps to NM_020530.3 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr22:30659928 C>T maps to NM_020530.3 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr5:38921763 C>T maps to NM_003999.2 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:38881696 G>A maps to NM_003999.2 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr5:38881792 G>A maps to NM_003999.2 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr5:38904065 A>T maps to NM_003999.2 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr5:38925304 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr5:38904068 G>A maps to NM_003999.2 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr5:38933077 G>A maps to NM_003999.2 R824R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:38884130 G>A maps to NM_003999.2 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:38885466 C>T maps to NM_003999.2 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:38876417 G>A maps to NM_003999.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:38884196 C>T maps to NM_003999.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:38923309 G>A maps to NM_003999.2 R608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:38925387 C>T maps to NM_003999.2 F709F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:38917672 G>A maps to NM_003999.2 W437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:38904050 G>A maps to NM_003999.2 W353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:38904468 C>T maps to NM_003999.2 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:38884058 G>A maps to NM_003999.2 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:38886288 C>T maps to NM_003999.2 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr5:38869196 C>T maps to NM_003999.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z4-06A-11D-A197-08 chr5:38881843 G>A maps to NM_003999.2 W132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:38876375 C>T maps to NM_003999.2 H49H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:38886149 G>A maps to NM_003999.2 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:38924683 G>A maps to NM_003999.2 K677K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:38925447 G>A maps to NM_003999.2 T729T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr5:38904525 G>A maps to NM_003999.2 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:38883965 C>T maps to NM_003999.2 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:38884064 G>A maps to NM_003999.2 Q185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:99961248 C>T maps to ENST00000457907 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:99961428 C>T maps to ENST00000457907 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:99961764 G>A maps to ENST00000457907 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:99961683 G>A maps to ENST00000457907 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr3:195955679 G>A maps to NM_152672.5 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:195955748 G>A maps to NM_152672.5 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:195953990 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:195944802 G>A maps to NM_152672.5 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr23:38262955 C>T did not map to a codon.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr23:38260573 C>A did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr23:38240679 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr23:38271194 T>A did not map to a codon.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr23:38262969 C>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:38262947 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr16:21737936 C>T maps to ENST00000286149 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr16:21698897 A>T maps to ENST00000286149 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr16:21771857 G>A maps to ENST00000286149 W1153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:21747592 C>T maps to ENST00000286149 I785I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:21693133 C>T maps to ENST00000286149 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:21721276 G>A maps to ENST00000286149 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:21709177 G>A maps to ENST00000286149 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:21739614 T>C maps to ENST00000286149 C704C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr16:21698750 C>T maps to ENST00000286149 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:21690355 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:21712327 G>A maps to ENST00000286149 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:21698750 C>T maps to ENST00000286149 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr16:21730462 C>T maps to ENST00000286149 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:26781364 G>A maps to NM_194248.2 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr2:26696414 C>T maps to NM_194248.2 R1143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:26688824 G>A maps to NM_194248.2 V1540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:26690041 G>A maps to NM_194248.2 F1429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr2:26700539 C>T maps to NM_194248.2 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:26702453 C>T maps to NM_194248.2 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr2:26699020 G>A maps to NM_194248.2 F947F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:26706494 C>T maps to NM_194248.2 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr2:26707370 G>A maps to NM_194248.2 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:26699764 G>A maps to NM_194248.2 F890F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:26680943 G>A maps to ENST00000403946 L1986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr2:26739410 C>T maps to NM_194248.2 W128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:26739394 G>A maps to NM_194248.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:26781397 C>T maps to NM_194248.2 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr2:26703110 C>T maps to NM_194248.2 R624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:26703656 C>T maps to NM_194248.2 S600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr2:26705272 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr2:26717845 G>A maps to NM_194248.2 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr2:26698903 T>A maps to NM_194248.2 K957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr3:161221393 C>T maps to NM_001080440.1 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr3:161221561 G>A maps to NM_001080440.1 Q422Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:161221264 G>A maps to NM_001080440.1 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:161214599 G>A maps to NM_001080440.1 W2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:161214885 C>T maps to NM_001080440.1 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr3:161221357 T>C maps to NM_001080440.1 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:161221585 C>T maps to NM_001080440.1 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:161214669 C>T maps to NM_001080440.1 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:161214771 C>T maps to NM_001080440.1 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:161214804 C>T maps to NM_001080440.1 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:161214864 C>T maps to NM_001080440.1 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:161220113 G>A maps to NM_001080440.1 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:161221690 C>T maps to NM_001080440.1 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr3:161221471 C>T maps to NM_001080440.1 Y392Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr4:4199726 C>T maps to NM_177998.1 Q278Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:4214695 G>A maps to NM_177998.1 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:4199693 C>T maps to NM_177998.1 W289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr4:4190620 C>T maps to NM_177998.1 W583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr4:4199348 G>A maps to NM_177998.1 I404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr4:4190619 C>T maps to NM_177998.1 W583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr4:4199273 G>A maps to NM_177998.1 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr4:4199453 G>A maps to NM_177998.1 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr4:4190643 C>T maps to NM_177998.1 E575E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr17:72920942 G>A maps to NM_178160.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:72920756 G>A maps to NM_178160.2 K10K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:72926629 C>T maps to NM_178160.2 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:72926629 C>T maps to NM_178160.2 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:72926962 C>T maps to NM_178160.2 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:72926902 G>A maps to NM_178160.2 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:72926995 C>T maps to NM_178160.2 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:72926671 G>A maps to NM_178160.2 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:72937620 G>A maps to NM_178233.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:72945423 C>T maps to NM_178233.1 F568F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:72937999 C>T maps to NM_178233.1 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:72943323 C>T maps to NM_178233.1 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:72937887 G>A maps to NM_178233.1 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr17:72937809 C>T maps to NM_178233.1 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:72937551 G>A maps to NM_178233.1 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:72938119 C>T maps to NM_178233.1 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:72943524 G>A maps to NM_178233.1 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:72937728 C>T maps to NM_178233.1 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr20:16729069 C>T maps to NM_020157.2 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:241078667 G>A maps to NM_148961.3 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:241078631 G>A maps to NM_148961.3 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:76932723 G>A maps to NM_032109.2 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr11:63764667 C>T maps to ENST00000422031 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:146071733 G>C maps to ENST00000447906 S397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:146076604 G>A maps to ENST00000447906 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:146067418 G>A maps to ENST00000447906 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr4:146065532 T>C maps to ENST00000447906 R492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:48780998 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:48791868 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr23:69282556 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:69283108 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr23:69282950 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:69282857 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:69283081 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr23:69283109 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr23:69283110 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr23:69283209 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:69282508 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:69282578 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:69283115 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:69283058 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr15:31776363 G>A maps to ENST00000382902 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr15:31779659 C>T maps to ENST00000382902 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr15:31851328 G>A maps to ENST00000382902 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:31819473 C>T maps to ENST00000382902 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr15:31851205 G>A maps to ENST00000382902 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr15:31862356 C>T maps to ENST00000382902 Q65Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr15:31779420 C>T maps to ENST00000382902 W449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr15:31819488 C>T maps to ENST00000382902 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:149942997 G>A maps to NM_020205.2 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:149943099 G>A maps to NM_020205.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:63282712 G>A maps to NM_014562.3 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:63282748 C>T maps to NM_014562.3 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr14:57271052 G>A maps to NM_021728.2 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr14:57268929 G>A maps to NM_021728.2 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr14:57268779 C>T maps to NM_021728.2 Q189Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr14:57268989 G>T maps to NM_021728.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr14:57269061 C>T maps to NM_021728.2 K95K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr14:57270959 G>A maps to NM_021728.2 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr14:57268563 G>A maps to NM_021728.2 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:57268470 C>T maps to NM_021728.2 W292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:1945385 C>T maps to NM_080822.2 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:29617456 C>T maps to NM_183378.2 W703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr12:29640713 G>A maps to NM_183378.2 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr12:29608201 C>T maps to NM_183378.2 W806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:29617509 G>A maps to NM_183378.2 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:29648365 C>T maps to NM_183378.2 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr11:7722017 A>T maps to NM_198185.2 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:7723022 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr11:7721944 G>A maps to NM_198185.2 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:7723014 G>A maps to NM_198185.2 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:111964029 G>A maps to ENST00000369728 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:111968009 G>A maps to ENST00000369728 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:111966311 G>A maps to ENST00000369728 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:111964219 G>A maps to ENST00000369728 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:111957817 G>A maps to ENST00000369728 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:111957658 G>A maps to ENST00000369728 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:111964020 G>A maps to ENST00000369728 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:111965555 G>A maps to ENST00000369728 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:111966269 G>A maps to ENST00000369728 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:111969147 G>A maps to ENST00000369728 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:65561596 C>T maps to NM_004561.2 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:65561574 G>A maps to NM_004561.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr20:18022286 C>T maps to NM_021220.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr14:23240111 C>T maps to NM_005015.3 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:23235849 C>T maps to NM_005015.3 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:41850260 G>A maps to NM_000436.3 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:41850281 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:41801133 G>A maps to NM_000436.3 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:42990068 C>T maps to NM_148962.4 K417K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr13:97639497 G>A maps to NM_080818.3 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:97639218 G>A maps to NM_080818.3 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr13:97639851 C>T maps to NM_080818.3 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:16312570 C>T maps to NM_138381.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr8:107718675 G>A maps to NM_001198533.1 E309E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:107722881 C>T maps to NM_001198533.1 R553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr8:107691492 G>A maps to NM_001198533.1 Q92Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:107704999 C>T maps to NM_001198533.1 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr8:107705018 C>T maps to NM_001198533.1 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr8:107722925 G>A maps to NM_001198533.1 R567R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr3:25833012 C>T maps to NM_017897.2 Q168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:38278448 C>T maps to NM_005109.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr3:38284239 C>T maps to NM_005109.2 R361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:38289196 C>T maps to NM_005109.2 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr3:38291484 C>T maps to NM_005109.2 R451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:8809177 C>T maps to NM_000916.3 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:8809231 G>A maps to NM_000916.3 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:8794893 G>A maps to NM_000916.3 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:8794833 C>A maps to NM_000916.3 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:8794752 C>T maps to NM_000916.3 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr17:3806912 G>A maps to NM_002558.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr17:3806588 G>A maps to NM_002558.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:3801320 C>T maps to NM_002558.2 E372E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:3801116 C>T maps to NM_002558.2 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr12:133195512 G>A maps to NM_170683.2 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:57115695 G>A maps to NM_002559.2 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr11:57137454 C>T maps to NM_002559.2 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:57114887 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr11:57115698 C>T maps to NM_002559.2 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:57117371 G>A maps to NM_002559.2 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:57117372 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:57135873 C>T maps to NM_002559.2 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:57137379 C>T maps to NM_002559.2 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:121654978 C>A maps to NM_002560.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:121660777 C>T maps to NM_002560.2 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:3593722 C>T maps to ENST00000435558 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:3595051 G>C maps to ENST00000435558 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:3595084 C>T maps to ENST00000435558 W47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr22:21377653 T>C maps to NM_005446.3 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr22:21377587 C>T maps to NM_005446.3 D221D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr22:21377662 C>T maps to NM_005446.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr12:121603180 C>G maps to NM_002562.5 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:121622586 C>T maps to NM_002562.5 G590G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr12:121622598 T>C maps to NM_002562.5 P594P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:121605370 C>T maps to NM_002562.5 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:121593886 C>T maps to NM_002562.5 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr23:78216280 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:78216490 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:78216754 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:78216113 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:78216315 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:78216953 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr23:78216688 C>G did not map to a codon.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr23:78216808 T>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:78217035 A>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:78216790 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:78217005 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:78216643 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:78216633 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:78216490 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:78216490 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:78217000 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr23:78216947 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:151056102 G>A maps to NM_022788.3 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:151056564 G>A maps to NM_022788.3 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:151056273 G>A maps to NM_022788.3 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:151056489 C>T maps to NM_022788.3 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:151056189 G>A maps to NM_022788.3 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr3:151055901 T>A maps to NM_022788.3 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr3:151046190 C>T maps to NM_176894.2 W218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr3:151046627 G>A maps to NM_176894.2 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr3:151046681 A>C maps to NM_176894.2 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr3:150931936 G>A maps to NM_014879.3 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:150931714 A>T maps to NM_014879.3 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr3:150931666 C>T maps to NM_014879.3 W146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr3:150931771 G>A maps to NM_014879.3 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:150931447 C>T maps to NM_014879.3 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:150931470 T>A maps to NM_014879.3 K212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:150931651 G>A maps to NM_014879.3 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:150931471 C>T maps to NM_014879.3 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:150931681 C>T maps to NM_014879.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:72945978 C>T maps to NM_176071.1 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr11:72946178 C>T maps to NM_176071.1 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:72945941 C>T maps to NM_176071.1 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:72945203 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:72945845 C>T maps to NM_176071.1 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr11:72945203 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:72945397 G>A maps to NM_176071.1 W65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:72945665 C>T maps to NM_176071.1 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:72946125 C>T maps to NM_176071.1 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:72945977 C>T maps to NM_176071.1 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:72946295 C>T maps to NM_176071.1 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr23:69478474 A>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:69478690 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr11:73007868 C>T maps to NM_004154.3 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr11:73008405 G>A maps to NM_004154.3 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:73007961 C>T maps to NM_004154.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:1584686 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:1584845 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:1584800 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:1585080 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:1585081 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:1585281 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:1585059 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:1584668 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:1584395 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:1585247 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr23:1584750 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:1584423 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:1584753 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:1584833 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:1584899 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:1585100 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:1584507 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr23:1584447 G>A did not map to a codon.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr23:1584833 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr10:74813220 G>C maps to NM_000917.3 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:131554250 G>A maps to NM_001142599.1 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr5:131530616 A>C did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:131543475 G>A maps to NM_001142599.1 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:73979286 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr11:74015354 C>T maps to NM_182904.3 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr11:74013506 G>A maps to NM_182904.3 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr11:74013521 G>A maps to NM_182904.3 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:74013502 G>A maps to NM_182904.3 Q160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:73988183 C>T maps to NM_182904.3 W394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:73997401 C>T maps to NM_182904.3 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:74015354 C>T maps to NM_182904.3 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:74009361 C>T maps to NM_182904.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr11:73997012 G>A maps to NM_182904.3 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr17:79804385 G>C maps to NM_000918.3 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr17:79805118 C>T maps to NM_000918.3 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:49038931 G>A maps to NM_177938.2 K166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:49028018 C>T maps to NM_177938.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:49044309 G>A maps to NM_177938.2 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:56504386 C>T maps to NM_006191.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:73627594 C>T maps to NM_025155.1 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:73638352 C>T maps to NM_025155.1 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr11:73620447 C>T maps to NM_025155.1 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr8:101733712 C>T maps to NM_002568.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr8:101717162 G>A maps to NM_002568.3 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr8:101730086 G>A maps to NM_002568.3 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr20:43561047 G>A maps to NM_001124756.1 W435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:43545458 C>T maps to NM_001124756.1 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:43559288 C>T maps to NM_001124756.1 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr20:43545479 C>T maps to NM_001124756.1 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr13:25671145 G>A maps to NM_030979.2 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr13:25670377 C>T maps to NM_030979.2 Y14Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr13:25671850 G>A maps to NM_030979.2 R505R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr13:25670977 C>T maps to NM_030979.2 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:25671517 C>T maps to NM_030979.2 N394N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr13:25671070 G>A maps to NM_030979.2 Q245Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:40034557 G>A maps to NM_001135653.1 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:40036967 G>A maps to NM_001135653.1 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:40035299 A>G maps to NM_001135653.1 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:90691563 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:90691121 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:90691122 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:90691347 G>C did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr14:23793408 C>T maps to NM_004643.3 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr14:23792247 T>C maps to NM_004643.3 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr16:88932316 G>A maps to NM_001080487.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr6:163483306 G>A maps to NM_152410.2 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:163235238 C>T maps to NM_152410.2 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr6:163235303 C>T maps to NM_152410.2 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr4:20728951 C>T maps to ENST00000503585 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr11:65987257 G>A maps to NM_018026.2 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr11:65983684 C>A maps to NM_018026.2 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:66000510 C>T maps to NM_018026.2 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr11:65983616 C>T maps to NM_018026.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:66006667 C>G maps to NM_018026.2 P783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:66006655 C>T maps to NM_018026.2 S779S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr11:66008960 C>T maps to NM_018026.2 P831P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:66010696 C>T maps to NM_018026.2 P946P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr11:65983734 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:65988657 C>T maps to NM_018026.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:105836194 G>A maps to ENST00000458164 Q253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:105849722 C>T maps to ENST00000458164 T551T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr14:105843124 C>T maps to ENST00000458164 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr6:34499544 C>T maps to NM_020804.3 D402D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr6:34496596 G>A maps to NM_020804.3 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:34496491 C>T maps to NM_020804.3 H98H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:34496572 C>T maps to NM_020804.3 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:34499442 C>T maps to NM_020804.3 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr22:43272326 G>A maps to NM_001184970.1 Y388Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr22:43272197 G>T maps to NM_001184970.1 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:17548895 G>A maps to NM_013358.2 W68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:17548874 G>A maps to NM_013358.2 E61E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:17559375 C>T maps to NM_013358.2 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:17557155 C>T maps to NM_013358.2 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:17531717 C>T maps to NM_013358.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:17550868 C>T maps to NM_013358.2 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:17559459 C>T maps to NM_013358.2 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:17552624 C>T maps to NM_013358.2 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:17402194 A>G maps to NM_007365.2 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:17413096 G>A maps to NM_007365.2 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr1:17420165 C>T maps to NM_007365.2 W142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:17420060 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:17431501 C>T maps to NM_007365.2 W49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr1:17395640 G>A maps to NM_007365.2 I632I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr1:17409123 G>A maps to NM_007365.2 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:17405781 G>A maps to NM_007365.2 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:17411113 G>A maps to NM_007365.2 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:17422448 C>T maps to NM_007365.2 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:17606924 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:17593284 C>T maps to NM_016233.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr1:17597609 G>A maps to NM_016233.2 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr1:17597429 G>A maps to NM_016233.2 W296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:17575649 C>T maps to NM_016233.2 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr1:17593215 G>A maps to NM_016233.2 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr1:17601260 C>T maps to NM_016233.2 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:17607260 G>A maps to NM_016233.2 R577R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:17607178 G>A maps to NM_016233.2 W550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr1:17607260 G>A maps to NM_016233.2 R577R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:17596842 C>T maps to NM_016233.2 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:17599923 C>T maps to NM_016233.2 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:17603052 C>T maps to NM_016233.2 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:17592199 G>A maps to NM_016233.2 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr1:17609360 G>A maps to NM_016233.2 G594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:17599902 G>A maps to NM_016233.2 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr1:17681060 C>T maps to NM_012387.2 Q397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr1:17657556 C>T maps to NM_012387.2 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:17657565 C>T maps to NM_012387.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr1:17657607 G>A maps to NM_012387.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:17668438 G>A maps to NM_012387.2 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:17690063 C>T maps to NM_012387.2 F602F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr1:17690147 C>T maps to NM_012387.2 I630I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr1:17657607 G>A maps to NM_012387.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:17657535 C>T maps to NM_012387.2 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:17668546 C>T maps to NM_012387.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:17668879 G>A maps to NM_012387.2 Q306Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr1:17672606 G>A maps to NM_012387.2 E340E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:17690198 C>T maps to NM_012387.2 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:17698793 C>T maps to NM_207421.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:17727762 G>A maps to NM_207421.3 K638K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:17723615 G>A maps to NM_207421.3 K556K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:17721593 G>A maps to NM_207421.3 E495E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:17699607 C>T maps to NM_207421.3 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:138454249 G>A maps to NM_002571.2 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr19:39876821 C>A maps to NM_019088.2 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:39879935 C>T maps to NM_019088.2 E149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:39879776 G>A maps to NM_019088.2 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:39879777 G>A maps to NM_019088.2 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:39877417 C>T maps to NM_019088.2 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:2583501 G>A maps to NM_000430.3 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:2570416 G>A maps to NM_000430.3 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr1:26316032 G>A maps to NM_000437.3 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:26301044 G>A maps to NM_000437.3 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:26311003 G>A maps to NM_000437.3 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:81888982 G>A maps to NM_018440.3 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr8:81897256 C>A maps to NM_018440.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr8:81897448 G>A maps to NM_018440.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:49455969 C>T did not map to a codon.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr23:55116529 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr23:55103075 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:55103944 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:55103884 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:49597194 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr23:49597217 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:49597175 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:49597217 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:49598450 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr23:55247080 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:55249118 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:55247855 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:55249138 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:103234195 A>G maps to NM_000277.1 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:103234184 G>A maps to NM_000277.1 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr12:103288624 G>A maps to NM_000277.1 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:103234199 C>T maps to NM_000277.1 K431K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr12:103310869 C>T maps to NM_000277.1 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:103249037 C>T maps to NM_000277.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:103260387 G>A maps to NM_000277.1 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr12:103288525 C>T maps to NM_000277.1 K113K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr4:57325559 T>G maps to NM_001079525.1 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:57318117 C>T maps to NM_001079525.1 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:43556006 T>A maps to NM_006451.4 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr5:138700375 C>T maps to NM_001033112.1 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr5:138700375 C>T maps to NM_001033112.1 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr2:71429638 C>T maps to NM_020459.1 K27K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:77070062 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:77085396 C>T maps to NM_001128620.1 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr11:77034361 G>A maps to NM_001128620.1 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:77066758 C>T maps to NM_001128620.1 Q242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr3:196554125 C>T maps to NM_002577.4 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr3:196529916 A>G maps to NM_002577.4 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr23:110366491 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:110435808 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:110439847 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:110390986 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:110391070 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr23:110366396 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:110439806 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:110439123 A>C did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:110385364 C>T did not map to a codon.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr23:110439089 C>T did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:110459747 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:110439145 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:110366387 T>C did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:110439089 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:39668370 C>T maps to NM_005884.3 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:39667318 C>T maps to NM_005884.3 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:39660288 C>T maps to NM_005884.3 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr15:40564468 C>T maps to NM_020168.4 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:40566413 C>T maps to NM_020168.4 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr20:9547013 T>G maps to NM_177990.2 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr20:9624790 G>A maps to NM_177990.2 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr20:9525014 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr20:9523274 C>T maps to NM_177990.2 R654R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:9525084 C>T maps to NM_177990.2 R600R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr20:9523304 G>A maps to NM_177990.2 F644F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr20:9560904 G>A maps to NM_177990.2 Q293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr20:9546737 G>A maps to NM_177990.2 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:9561100 A>C maps to NM_177990.2 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:9525084 C>T maps to NM_177990.2 R600R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr20:9561211 G>A maps to NM_177990.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr20:9624796 T>G maps to NM_177990.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:9538326 G>A maps to NM_177990.2 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:9546683 C>T maps to NM_177990.2 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr20:9538275 G>A maps to NM_177990.2 I574I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr20:9560929 C>T maps to NM_177990.2 Q284Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:9523337 C>T maps to NM_177990.2 V633V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr20:9561043 G>A maps to NM_177990.2 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr20:9624958 C>T maps to NM_177990.2 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:9543668 G>A maps to NM_177990.2 V495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:9547018 G>A maps to NM_177990.2 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:9523343 G>A maps to NM_177990.2 I631I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr20:9520186 G>A maps to NM_177990.2 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr20:9525084 C>T maps to NM_177990.2 R600R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr20:9546701 G>A maps to NM_177990.2 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr20:9523343 G>A maps to NM_177990.2 I631I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:9547018 G>A maps to NM_177990.2 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:9561571 G>A maps to NM_177990.2 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:9561340 C>T maps to NM_177990.2 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr20:9561478 C>T maps to NM_177990.2 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr20:9547010 C>T maps to NM_177990.2 Q337Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr20:9561217 C>T maps to NM_177990.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr20:9525014 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:9523352 G>A maps to NM_177990.2 S628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:9560896 C>T maps to NM_177990.2 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:9560964 G>A maps to NM_177990.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr20:9520183 G>A maps to NM_177990.2 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr16:23646879 T>C maps to NM_024675.3 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:23625359 G>A maps to NM_024675.3 Q1056*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:23619258 G>A maps to NM_024675.3 L1092L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:23647608 G>A maps to NM_024675.3 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr4:169812120 G>A maps to NM_001166108.1 E671E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr4:169589388 C>T maps to NM_001166108.1 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:169632816 G>A maps to NM_001166108.1 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:169825026 G>A maps to NM_001166108.1 G864G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr4:169812090 C>T maps to NM_001166108.1 A661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:169611809 C>T maps to NM_001166108.1 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr4:169604157 G>A maps to NM_001166108.1 K388K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr4:169632732 C>A maps to NM_001166108.1 A541A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-FS-A4FC-06A-11D-A24R-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:169432678 G>A maps to NM_001166108.1 E8E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:169432735 C>T maps to NM_001166108.1 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:169432900 G>A maps to NM_001166108.1 K82K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:169433293 C>T maps to NM_001166108.1 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr19:746735 G>A maps to NM_002579.2 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr19:736043 G>A maps to NM_002579.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:731130 C>T maps to NM_002579.2 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:746456 C>T maps to NM_002579.2 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:746417 C>T maps to NM_002579.2 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:727598 G>A maps to NM_002579.2 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:112705476 C>T maps to ENST00000413420 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:112705125 C>A maps to ENST00000413420 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr9:112694225 C>T maps to NM_007203.4 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:112705446 G>A maps to ENST00000413420 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44Q-06A-11D-A25O-08 chr1:100152487 T>C maps to NM_017734.4 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:100127915 G>A maps to NM_017734.4 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:100154748 G>A maps to NM_017734.4 E311E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:100155312 C>T maps to NM_017734.4 P499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:102285615 A>G maps to NM_000919.3 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:102343269 C>T maps to NM_000919.3 I708I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr5:102363937 T>C maps to NM_000919.3 F914F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr5:102338739 G>A maps to NM_000919.3 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr5:102361014 G>A maps to NM_000919.3 W889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:102309920 C>T maps to NM_000919.3 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:102340890 A>G maps to NM_000919.3 K588K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:35456110 C>T maps to NM_015430.2 G542G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:35463161 G>A maps to NM_015430.2 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:35492366 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:35492218 G>A maps to NM_015430.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:35457604 G>A maps to NM_015430.2 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr11:35456128 G>A maps to NM_015430.2 D536D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr12:56721153 G>A maps to NM_001127460.2 Q305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44Q-06A-11D-A25O-08 chr12:56721415 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:56722377 G>A maps to NM_001127460.2 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:56718093 G>A maps to NM_001127460.2 R638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr13:28862196 C>T maps to NM_175854.7 Q821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr13:28830606 C>T maps to NM_175854.7 I393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr10:91371713 C>T maps to NM_148977.1 E265E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:3870337 C>T maps to NM_153638.2 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr20:3899432 C>A maps to NM_153638.2 S551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:167995998 G>A maps to NM_024594.2 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr1:2445458 G>A maps to ENST00000425477 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:2452229 G>A maps to ENST00000425477 Q188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:2458005 G>A maps to ENST00000425477 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:2444430 G>A maps to ENST00000425477 V549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:93913145 G>A maps to NM_015368.3 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:93913319 C>T maps to NM_015368.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:93913320 C>T maps to NM_015368.3 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:93912977 C>T maps to NM_015368.3 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:93911539 C>T maps to NM_015368.3 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:93911599 C>T maps to NM_015368.3 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr11:124489647 C>T maps to NM_052959.2 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:124489710 G>A maps to NM_052959.2 K353K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:124489197 G>A maps to NM_052959.2 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:124489500 G>A maps to NM_052959.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr11:124489452 C>T maps to NM_052959.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr10:135195146 C>T maps to NM_152911.2 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr10:135197567 C>T maps to NM_152911.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:135197710 C>T maps to NM_152911.2 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr5:78964809 C>T maps to NM_173797.3 D389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:78941000 C>T maps to NM_173797.3 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr5:78915895 C>T maps to NM_173797.3 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:78915543 C>T maps to NM_173797.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr5:6748697 C>T maps to NM_006999.4 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr5:6746460 C>T maps to NM_006999.4 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:6750519 C>T maps to NM_006999.4 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:6753011 C>T maps to NM_006999.4 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:39589263 C>T maps to NM_001004318.2 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:39600742 G>A maps to NM_001004318.2 R434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:39597621 C>T maps to NM_001004318.2 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:39597621 C>T maps to NM_001004318.2 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr19:39597639 C>T maps to NM_001004318.2 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr19:39591435 C>T maps to NM_001004318.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr19:39589287 G>A maps to NM_001004318.2 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:39597621 C>T maps to NM_001004318.2 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr14:73727415 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:73716791 G>A maps to ENST00000427855 K145K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:73726127 C>T maps to ENST00000427855 P620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:73717619 C>T maps to ENST00000427855 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:73720566 C>T maps to ENST00000427855 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr14:73721247 C>A maps to ENST00000427855 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr14:73721589 C>T maps to ENST00000427855 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:73731422 G>A maps to ENST00000427855 Q1038Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr14:73718531 C>T maps to ENST00000427855 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:97002295 C>T maps to NM_032632.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr14:97009113 G>T maps to NM_032632.3 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr7:4899798 A>T maps to NM_020144.4 L548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr7:4899854 G>A maps to NM_020144.4 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:4900112 C>T maps to NM_020144.4 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:60988876 C>T maps to NM_022894.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:61009066 C>T maps to NM_022894.3 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:61019307 C>T maps to NM_022894.3 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:61002229 C>T maps to NM_022894.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:60995609 C>T maps to NM_022894.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:61021870 G>A maps to NM_022894.3 K672K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr9:118949535 C>T maps to NM_002581.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr9:118982243 C>T maps to NM_002581.3 P649P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr9:119106878 T>G maps to NM_002581.3 A1223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr9:118982327 C>T maps to NM_002581.3 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:118950201 G>A maps to NM_002581.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:118982234 C>T maps to NM_002581.3 S646S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:118950480 C>A maps to NM_002581.3 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:119033602 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:119097239 C>T maps to NM_002581.3 F1166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:118949434 C>T maps to NM_002581.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:118949874 C>T maps to NM_002581.3 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:118997652 G>A maps to NM_002581.3 G823G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:118997907 C>T maps to NM_002581.3 F908F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr9:119028243 T>C maps to NM_002581.3 C947C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr9:118982378 C>T maps to NM_002581.3 F694F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr9:118974125 C>T maps to NM_002581.3 S611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr9:119115030 C>T maps to NM_002581.3 F1337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr9:118949586 C>T maps to NM_002581.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:119065204 C>T maps to NM_002581.3 I1041I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:118950189 C>T maps to NM_002581.3 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr9:119158840 C>T maps to NM_002581.3 D1610D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:118949538 G>A maps to NM_002581.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr9:118969758 G>A maps to NM_002581.3 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr9:118997907 C>T maps to NM_002581.3 F908F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr9:118950282 G>A maps to NM_002581.3 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr9:118950270 G>A maps to NM_002581.3 K418K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr9:119106929 G>A maps to NM_002581.3 V1240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:118949992 C>T maps to NM_002581.3 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr9:118950330 G>A maps to NM_002581.3 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr9:118997907 C>T maps to NM_002581.3 F908F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr9:118997544 C>T maps to NM_002581.3 F787F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr9:118969824 G>A maps to NM_002581.3 E523E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr9:119097171 C>T maps to NM_002581.3 L1144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:118969758 G>A maps to NM_002581.3 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:118997856 C>T maps to NM_002581.3 D891D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:119106954 C>T maps to NM_002581.3 Q1249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:119124923 C>T maps to NM_002581.3 S1467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr9:118982374 G>A maps to NM_002581.3 W693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr9:119106833 C>T maps to NM_002581.3 F1208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr9:119109483 G>A maps to NM_002581.3 L1320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr9:119115985 A>T maps to NM_002581.3 K1421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:118969824 G>A maps to NM_002581.3 E523E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr9:119129969 C>T maps to NM_002581.3 I1514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr1:176659393 C>T maps to NM_020318.2 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr1:176734897 C>T maps to NM_020318.2 L1416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr1:176668452 G>A maps to NM_020318.2 L988L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr1:176760577 G>A maps to NM_020318.2 L1660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:176734807 C>T maps to NM_020318.2 I1386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:176526252 C>T maps to NM_020318.2 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr1:176563732 G>A maps to NM_020318.2 K331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:176760565 C>T maps to NM_020318.2 P1656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:176738852 C>T maps to NM_020318.2 S1478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:176525685 G>A maps to NM_020318.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:176668503 C>T maps to NM_020318.2 I1005I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:176758968 G>A maps to NM_020318.2 L1580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:176525475 C>T maps to NM_020318.2 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:176681087 C>T maps to NM_020318.2 L1257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr1:176679228 C>T maps to NM_020318.2 Q1190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:176564104 C>T maps to NM_020318.2 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr1:176525944 C>T maps to NM_020318.2 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:176525626 C>T maps to NM_020318.2 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:176640216 C>T maps to NM_020318.2 T701T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:176668302 C>A maps to NM_020318.2 Y938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:176734924 G>A maps to NM_020318.2 R1425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:176661332 C>T maps to NM_020318.2 Q835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:176525556 C>A maps to NM_020318.2 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:176526075 G>A maps to NM_020318.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr1:176661397 C>T maps to NM_020318.2 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:176809388 C>T maps to NM_020318.2 S1761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:176668461 G>A maps to NM_020318.2 K991K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr1:176668692 G>T maps to NM_020318.2 V1068V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:176681029 C>T maps to NM_020318.2 P1237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:176564601 G>A maps to NM_020318.2 W621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:176564611 G>A maps to NM_020318.2 R624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:176681098 G>A maps to NM_020318.2 E1260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:176709185 C>T maps to NM_020318.2 F1335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:176758950 C>T maps to NM_020318.2 L1574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:176525626 C>T maps to NM_020318.2 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:176668360 C>T maps to NM_020318.2 Q958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:176738852 C>T maps to NM_020318.2 S1478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:176740313 G>A maps to NM_020318.2 R1571R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:176762723 C>T maps to NM_020318.2 I1683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:176525626 C>T maps to NM_020318.2 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:176525475 C>T maps to NM_020318.2 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:176762783 G>A maps to NM_020318.2 W1703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:176564116 C>T maps to NM_020318.2 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:176661406 C>T maps to NM_020318.2 S859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr1:176679242 G>A maps to NM_020318.2 R1194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:176709323 G>A maps to NM_020318.2 Q1381Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr1:176740148 C>T maps to NM_020318.2 L1516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:176709236 C>T maps to NM_020318.2 I1352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:176661283 C>T maps to NM_020318.2 F818F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:176525994 C>T maps to NM_020318.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr1:176661301 C>T maps to NM_020318.2 A824A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:176671741 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:176563948 C>A maps to NM_020318.2 C403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:176564266 G>A maps to NM_020318.2 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:176526271 C>T maps to NM_020318.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:176563711 G>A maps to NM_020318.2 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:176564035 C>T maps to NM_020318.2 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:176564036 C>T maps to NM_020318.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:176668410 C>T maps to NM_020318.2 F974F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:176708835 G>A maps to NM_020318.2 E1291E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:176762774 G>A maps to NM_020318.2 L1700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:176809403 G>A maps to NM_020318.2 K1766K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr1:176525493 G>A maps to NM_020318.2 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:176668533 G>A maps to NM_020318.2 G1015G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr1:176659411 G>A maps to NM_020318.2 K759K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:176640162 C>T maps to NM_020318.2 F683F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:176671741 G>A did not map to a codon.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:176668692 G>A maps to NM_020318.2 V1068V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr10:89504778 C>T maps to NM_001015880.1 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:79847851 C>T maps to NM_001040202.1 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:79856295 A>G maps to NM_001040202.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:79847830 G>A maps to NM_001040202.1 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr4:79845035 G>C maps to NM_001040202.1 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:79860261 G>A maps to NM_001040202.1 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:3021894 C>T maps to NM_152341.3 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr15:69692347 A>G maps to NM_017705.3 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr15:69672242 C>T maps to NM_017705.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr15:69652436 C>T maps to NM_017705.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr1:156214932 C>T maps to NM_024897.2 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:156216477 G>A maps to NM_198406.1 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:26189652 G>A maps to NM_178422.5 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr6:52268562 C>T maps to ENST00000361841 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:142681298 T>A maps to NM_198504.2 K294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:142681065 G>A maps to NM_198504.2 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q3-06A-11D-A196-08 chr10:34759191 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr10:34663807 C>T maps to NM_019619.3 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr10:34400330 G>A maps to NM_019619.3 V1279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr10:34606231 C>T maps to NM_019619.3 G959G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:34648194 G>A maps to NM_019619.3 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr10:34573159 G>A maps to NM_019619.3 R1030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr10:34759084 G>A maps to NM_019619.3 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr10:34673109 A>G maps to NM_019619.3 N321N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:34558810 G>A maps to NM_019619.3 R1068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr2:206364751 C>T maps to ENST00000406610 L1059L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:206480476 C>T maps to ENST00000406610 D1186D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr2:206166305 G>A maps to ENST00000406610 T837T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:206166305 G>A maps to ENST00000406610 T837T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:206305093 G>A maps to ENST00000406610 R914R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr2:206166305 G>A maps to ENST00000406610 T837T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:206166389 G>A maps to ENST00000406610 R865R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:205990427 C>T maps to ENST00000406610 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:206166305 G>A maps to ENST00000406610 T837T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:206023507 C>T maps to ENST00000406610 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:206023510 C>T maps to ENST00000406610 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr2:206023564 C>T maps to ENST00000406610 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr20:49366991 C>T maps to NM_032521.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:49366358 C>T maps to NM_032521.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr18:77917845 G>A maps to NM_032510.3 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr6:161781174 G>A maps to NM_004562.2 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr6:162864377 G>A maps to NM_004562.2 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr6:161771199 G>A maps to NM_004562.2 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:162683584 C>T maps to NM_004562.2 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:162622219 C>T maps to NM_004562.2 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:161771214 C>T maps to NM_004562.2 Q438Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:162394440 G>A maps to NM_004562.2 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:162683578 G>A maps to NM_004562.2 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:162864440 G>A maps to NM_004562.2 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:8025433 C>T maps to NM_001123377.1 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr3:183551568 G>A maps to NM_018622.5 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr3:183551529 G>A maps to NM_018622.5 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr4:75938091 G>A maps to NM_015393.3 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr4:75937637 G>A maps to NM_015393.3 W16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr4:75938325 G>A maps to NM_015393.3 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr16:14711452 G>A maps to NM_002582.2 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:14711452 G>A maps to NM_002582.2 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr16:14645905 G>A maps to NM_002582.2 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr1:226564967 C>A maps to NM_001618.3 T594T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:226564856 G>A maps to NM_001618.3 F631F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:226570803 G>T maps to NM_001618.3 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:226578130 G>A maps to NM_001618.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:226570803 G>A maps to NM_001618.3 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr1:226566964 G>A maps to NM_001618.3 H541H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr8:145059796 C>T maps to NM_032789.3 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr8:145057634 G>A maps to NM_032789.3 Q708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:145058971 G>A maps to NM_032789.3 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:145058972 G>A maps to NM_032789.3 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:145059329 G>A maps to NM_032789.3 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr8:145059110 G>T maps to NM_032789.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr12:3921429 G>A maps to NM_020367.4 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:3935325 G>A maps to NM_020367.4 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr7:139724491 G>A maps to NM_022750.2 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr7:139724422 G>A maps to NM_022750.2 S681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:139727206 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr7:139757830 C>T maps to NM_022750.2 K110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:139724439 G>A maps to NM_022750.2 Q676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:139756821 G>A maps to NM_022750.2 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:139756881 G>A maps to NM_022750.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:139741512 G>A maps to NM_022750.2 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr7:139754563 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr3:122422608 C>T maps to NM_017554.2 S1034S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:122418558 T>C maps to NM_017554.2 D386D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr3:122399741 C>T maps to NM_017554.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:122404131 C>T maps to NM_017554.2 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:122399900 C>T maps to NM_017554.2 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:122422656 C>T maps to NM_017554.2 L1050L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr3:122411235 C>T maps to NM_017554.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr3:122334615 C>T maps to NM_152615.1 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:122353913 G>A maps to NM_001113523.1 K540K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:122335956 G>T maps to NM_001113523.1 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr3:122335961 G>A maps to NM_001113523.1 Q317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr15:65553250 G>A maps to NM_017851.4 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr15:65558941 G>A maps to NM_017851.4 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:65559097 C>T maps to NM_017851.4 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr14:20823074 G>T maps to NM_005484.3 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:51979197 C>T maps to NM_001003931.2 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:51982486 C>T maps to NM_001003931.2 V538V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr3:51980192 C>T maps to NM_001003931.2 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr13:25029200 G>A maps to NM_006437.3 S904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr13:25044067 G>A maps to NM_006437.3 F670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr13:25058813 C>T maps to NM_006437.3 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:25073474 T>C maps to NM_006437.3 Q147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr13:25029326 G>A maps to NM_006437.3 P862P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr13:25029161 G>A maps to NM_006437.3 F917F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr13:25026554 G>A maps to NM_006437.3 A1001A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr13:25027757 G>A maps to NM_006437.3 I931I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr15:72551975 G>A maps to NM_020214.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr15:72534536 G>A maps to NM_020214.2 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr15:72534537 G>A maps to NM_020214.2 F555F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr5:50137823 T>C maps to ENST00000505697 D830D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr5:50056162 C>T maps to ENST00000505697 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr5:50129835 C>A maps to ENST00000505697 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:50117066 C>T maps to ENST00000505697 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:50056192 G>A maps to ENST00000505697 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:50091142 C>T maps to ENST00000505697 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr5:50091241 T>C maps to ENST00000505697 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:50118183 C>T maps to ENST00000505697 R604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:50055531 G>A maps to ENST00000505697 E80E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:50056162 C>T maps to ENST00000505697 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:50118200 G>A maps to ENST00000505697 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr5:50120752 G>A maps to ENST00000505697 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:122274909 G>A maps to NM_031458.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:122274966 C>T maps to NM_031458.2 E52E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr3:122274840 G>A maps to NM_031458.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:122255867 G>A maps to NM_031458.2 I641I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr3:122259598 G>A maps to NM_031458.2 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:122247234 G>A maps to NM_031458.2 F847F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:55223544 G>A maps to NM_152268.3 Y430Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:55223871 G>A maps to NM_152268.3 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr1:55223652 G>A maps to NM_152268.3 Y394Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:55224057 G>A maps to NM_152268.3 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:55224552 G>A maps to NM_152268.3 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:12534870 C>T maps to NM_018222.4 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:12518125 C>T maps to NM_018222.4 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:12530147 C>T maps to NM_018222.4 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:44514922 C>T maps to NM_001003828.1 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr22:44579262 C>T maps to NM_001137606.1 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr22:44602266 G>A maps to NM_001137606.1 K319K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr22:44579271 G>A maps to NM_001137606.1 E21E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr22:44585030 C>T maps to NM_001137606.1 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:44585088 C>A maps to NM_001137606.1 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr22:44594523 C>A maps to NM_001137606.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr23:150832718 G>A did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:150844504 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr23:150842490 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr23:150842499 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:150780152 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:150832596 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:150840953 G>A did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:150839560 G>A did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:150842616 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:150817137 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:150832762 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:150791501 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:150840849 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr23:150840218 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr23:150791501 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:150832596 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:150840951 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:150832596 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:150840118 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:150832598 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:150840203 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:150832763 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:150839662 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:150828183 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:150832762 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr23:150791486 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:150828251 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:150828305 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:150832796 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:150839560 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:150789485 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:150773144 G>A did not map to a codon.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr23:150839575 T>C did not map to a codon.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr23:150773186 T>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:150840151 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:150832697 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:150773145 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:150841034 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr23:150832775 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr23:150842479 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:150773145 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:150817105 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:150828305 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:150840203 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:150840932 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:150842648 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:150842657 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:150844495 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:150793949 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:150840163 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:150840190 T>A did not map to a codon.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr23:150841076 G>A did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:150789426 T>C did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:150832781 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2J6-06A-11D-A19A-08 chr2:242066277 C>T maps to ENST00000358649 P684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:242075322 G>A maps to ENST00000358649 D423D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr2:242072320 G>A maps to ENST00000358649 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr2:242054768 G>A maps to ENST00000358649 P1044P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:242065956 G>A maps to ENST00000358649 V791V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:242051779 G>A maps to ENST00000358649 I1143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:242051689 G>A maps to ENST00000358649 I1173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:242062229 G>A maps to ENST00000358649 Q997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:242065898 G>A maps to ENST00000358649 R811*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:242080010 C>T maps to ENST00000358649 W118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:242046055 C>T maps to ENST00000358649 G1306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:242072400 G>A maps to ENST00000358649 R451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:242047621 G>C maps to ENST00000358649 T1216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:242054729 G>A maps to ENST00000358649 S1057S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:242082348 G>A maps to ENST00000358649 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr11:125648650 G>A maps to NM_212555.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:59406623 G>A maps to NM_152716.2 Q730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:59406624 G>A maps to NM_152716.2 P729P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr11:59420466 C>A maps to NM_152716.2 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:59420042 C>G maps to NM_152716.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:59406584 G>A maps to NM_152716.2 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:31740814 G>A maps to NM_014323.2 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr22:31740334 A>G maps to NM_014323.2 C418C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr22:31741168 G>A maps to NM_014323.2 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:31740841 G>A maps to NM_014323.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:80014942 C>T maps to NM_002583.2 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr20:21695182 C>T maps to NM_006192.3 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:21689304 A>G maps to NM_006192.3 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr20:21687289 G>A maps to NM_006192.3 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:102566349 C>T maps to NM_003987.3 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr10:102587324 C>T maps to NM_003987.3 A401A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:102584734 A>G maps to ENST00000370296 Q389Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr10:102568880 C>T maps to NM_003987.3 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:102541063 C>T maps to NM_003987.3 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr2:223161825 G>A maps to NM_181459.3 H64H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:127253581 G>A maps to NM_006193.2 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr7:127254548 C>T maps to NM_006193.2 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr7:127253885 G>A maps to NM_006193.2 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr7:127253840 G>A maps to NM_006193.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr7:127254540 G>T maps to NM_006193.2 S136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr7:127255463 C>T maps to NM_006193.2 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:127253906 G>A maps to NM_006193.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr7:127254562 G>A maps to NM_006193.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr9:36882076 G>A maps to NM_016734.1 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr9:36966611 G>A maps to NM_016734.1 D238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr9:36882067 G>A maps to NM_016734.1 Y315Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:36846858 G>A maps to NM_016734.1 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:19027169 C>T maps to NM_002584.2 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:18961013 C>T maps to NM_002584.2 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:19062343 C>T maps to NM_002584.2 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:18961633 G>A maps to NM_002584.2 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:19062481 C>T maps to NM_002584.2 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:114004338 G>A maps to NM_003466.3 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:113999597 C>T maps to NM_003466.3 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:113993112 G>A maps to NM_003466.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:114002155 G>A maps to NM_003466.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:113999205 G>A maps to NM_003466.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:113999621 G>A maps to NM_003466.3 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:37145461 C>T maps to NM_006194.3 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr7:154754117 G>A maps to NM_007349.3 V680V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:154738109 C>T maps to NM_007349.3 L1053L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:154747268 G>A maps to NM_007349.3 F874F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:154738115 G>A maps to NM_007349.3 F1051F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr8:27668611 C>T maps to NM_018492.2 W212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr10:70056086 C>A maps to NM_022129.3 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr10:70048752 G>A maps to NM_022129.3 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:70044032 G>A maps to NM_022129.3 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:70051921 G>A maps to NM_022129.3 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr10:70048380 G>A maps to NM_022129.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:52584442 G>A maps to ENST00000296302 L1631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:52623164 A>G maps to ENST00000296302 D962D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr3:52675974 A>T maps to ENST00000296302 L361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:52620638 A>T maps to ENST00000296302 Y1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:52643484 A>T maps to ENST00000296302 L804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr3:52597487 C>T maps to ENST00000296302 K1299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr3:52610694 G>A maps to ENST00000296302 R1185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr3:52643767 G>A maps to ENST00000296302 R710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:52643746 T>A maps to ENST00000296302 K717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:52649472 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:52620569 G>A maps to ENST00000296302 V1086V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr3:52610699 C>T maps to ENST00000296302 W1183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:52643873 A>G maps to ENST00000296302 D674D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:52668784 G>A maps to ENST00000296302 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:164789375 G>A maps to NM_002585.2 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:164761827 G>A maps to NM_002585.2 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:164781387 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:164776781 G>T maps to NM_002585.2 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr1:164761830 G>A maps to NM_002585.2 K122K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:164761878 G>A maps to NM_002585.2 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:164769099 C>T maps to NM_002585.2 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:164761750 C>T maps to NM_002585.2 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr1:164769003 C>T maps to NM_002585.2 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr1:164769115 C>T maps to NM_002585.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:32155123 C>A maps to NM_002586.4 G307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:128723126 C>T maps to ENST00000373487 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:19681039 G>A maps to NM_025245.1 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:19675742 G>A maps to NM_025245.1 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr19:19680374 G>A maps to NM_025245.1 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19681592 G>A maps to NM_025245.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:19681072 G>A maps to NM_025245.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr19:19681607 G>A maps to NM_025245.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:154923759 C>T maps to NM_020524.2 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:154919210 G>A maps to NM_020524.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr1:154919183 G>A maps to NM_020524.2 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:154918535 C>T maps to NM_020524.2 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr1:154918697 G>A maps to NM_020524.2 D484D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr11:66631274 G>A maps to NM_022172.2 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr11:66620009 C>T maps to NM_022172.2 Q575Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr11:66639328 G>A maps to NM_022172.2 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:66631372 G>A maps to NM_022172.2 Q414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:66638891 G>A maps to NM_022172.2 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr11:66633741 G>A maps to NM_022172.2 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:70314982 T>C maps to NM_006196.3 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:53856348 C>T maps to NM_005016.5 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:47360065 G>A maps to NM_020528.2 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr3:51994625 G>A maps to NM_033010.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr13:100861599 C>T maps to NM_000282.3 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr13:100982854 C>T maps to NM_000282.3 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr13:100925545 C>T maps to NM_000282.3 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr13:100807309 C>T maps to NM_000282.3 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr3:136002689 G>A maps to NM_001178014.1 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:135969366 G>A maps to NM_001178014.1 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:136048786 C>T maps to NM_001178014.1 A533A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:136035826 C>T maps to NM_001178014.1 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:135975434 C>T maps to NM_001178014.1 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr5:141248666 G>A maps to NM_032420.2 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:141242886 G>A maps to NM_032420.2 F1003F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr5:141244202 G>A maps to NM_032420.2 Q565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:141244781 G>A maps to NM_032420.2 Q372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:141244782 G>T maps to NM_032420.2 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:141243291 G>A maps to NM_032420.2 I868I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:141243201 G>A maps to NM_032420.2 A898A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:141248676 G>A maps to NM_032420.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr5:141243087 G>A maps to NM_032420.2 S936S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr5:141242727 G>A maps to NM_002587.3 T1056T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:141243237 G>A maps to NM_032420.2 Y886Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:141248532 G>A maps to NM_032420.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr5:141248396 G>A maps to NM_032420.2 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr4:134072764 G>A maps to NM_032961.1 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr4:134072857 G>A maps to NM_032961.1 E521E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr4:134072068 C>T maps to NM_032961.1 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr4:134073034 G>T maps to NM_032961.1 G580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr4:134072585 C>T maps to NM_032961.1 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:134073472 C>T maps to NM_032961.1 S726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:134073097 C>T maps to NM_032961.1 T601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr4:134071429 T>C maps to NM_032961.1 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:134072296 C>T maps to NM_032961.1 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:134073280 C>T maps to NM_032961.1 D662D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:134073481 C>T maps to NM_032961.1 F729F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:91132450 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:91132451 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:91090557 T>C did not map to a codon.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr23:91456429 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:91090713 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:91133280 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:91133868 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:91873616 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:91134200 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:91132993 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:91642773 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:91090779 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:91090802 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:91132679 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:91090779 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:91132486 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:91091008 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:91642776 A>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:91723301 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:91134172 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:91873420 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:91090670 C>T did not map to a codon.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr23:91090983 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr24:5605534 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr24:4925488 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr24:4966927 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr24:5605717 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr24:4968153 C>T did not map to a codon.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr24:5605453 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr24:4966927 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr24:5605902 C>T did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr24:4925191 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr24:4925488 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr24:5605783 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr24:4925236 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr24:4968741 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr24:4925193 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr24:5605942 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr24:5605693 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr24:4925126 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr24:4925049 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr24:4925236 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr24:4968577 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr24:4924938 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr24:4925456 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr24:4966351 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr24:4968064 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr24:5605449 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr5:141335157 C>T maps to NM_016580.2 R753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr5:141335817 G>A maps to NM_016580.2 F533F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:141337074 C>T maps to NM_016580.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr5:141335151 G>A maps to NM_016580.2 A755A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr5:141335628 A>G maps to NM_016580.2 N596N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:141335403 C>T maps to NM_016580.2 W671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:141325254 C>T maps to NM_016580.2 E1082E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:141336441 C>T maps to NM_016580.2 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr5:141335514 G>A maps to NM_016580.2 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:141336750 G>A maps to NM_016580.2 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr5:141335229 G>A maps to NM_016580.2 F729F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr10:55581881 C>T maps to NM_001142763.1 T1875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr10:55943311 G>A maps to NM_001142763.1 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J6-06A-11D-A19A-08 chr10:55996589 G>A maps to NM_001142763.1 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:55582004 G>A maps to NM_001142763.1 C1834C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3BZ-06A-12D-A196-08 chr10:55587279 G>A maps to NM_001142763.1 R1419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr10:55568841 C>T maps to NM_001142769.1 R1661R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr10:55996642 G>A maps to NM_001142763.1 Q314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr10:55582727 C>T maps to NM_001142763.1 R1593R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr10:55568841 C>T maps to NM_001142769.1 R1661R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr10:55583111 G>A maps to NM_001142763.1 F1465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr10:55943311 G>A maps to NM_001142763.1 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr10:55912999 G>A maps to NM_001142763.1 I553I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:55569294 C>T maps to NM_001142769.1 K1510K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr10:55943353 C>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:55944944 G>A maps to NM_001142763.1 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr10:55583111 G>A maps to NM_001142763.1 F1465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:55569123 G>A maps to NM_001142769.1 I1567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr10:55583012 C>T maps to NM_001142763.1 E1498E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr10:55945004 A>T maps to NM_001142763.1 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:55566673 G>A maps to ENST00000373965 R1574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:55582415 G>A maps to NM_001142763.1 I1697I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:55943266 G>A maps to NM_001142763.1 F514F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:55955460 C>T maps to NM_001142763.1 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:56138693 G>A maps to NM_001142763.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:55587286 C>T maps to NM_001142763.1 K1416K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:55626548 C>T maps to NM_001142763.1 E1195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:56089364 G>A maps to NM_001142763.1 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr10:55582493 A>G maps to NM_001142763.1 F1671F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:55973764 C>T maps to NM_001142763.1 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr10:55591181 C>T maps to NM_001142763.1 K1370K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr10:55755465 C>T maps to NM_001142763.1 P942P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr10:55839162 C>T maps to NM_001142763.1 G678G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr10:55566673 G>A maps to ENST00000373965 R1574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr10:55568778 C>T maps to NM_001142769.1 R1682R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:55698692 G>A maps to NM_001142763.1 I1090I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:55583057 C>T maps to NM_001142763.1 R1483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr10:55569294 C>T maps to NM_001142769.1 K1510K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:55569252 C>T maps to NM_001142769.1 E1524E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:55591214 G>A maps to NM_001142763.1 I1359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:55955562 A>G maps to NM_001142763.1 F400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr10:55582478 G>A maps to NM_001142763.1 F1676F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr10:55582772 C>T maps to NM_001142763.1 Q1578Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr10:55591293 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr10:55700728 A>C maps to NM_001142763.1 P1048P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr10:55996642 G>A maps to NM_001142763.1 Q314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:55849823 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:55912972 G>A maps to NM_001142763.1 I562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr10:55566485 C>T maps to ENST00000373965 L1636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr10:55568559 C>T maps to NM_001142769.1 Q1755Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr10:55780073 A>G maps to NM_001142763.1 L882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr10:55698674 C>T maps to NM_001142763.1 V1096V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr10:55600204 C>T maps to NM_001142763.1 V1291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:55944920 C>T maps to NM_001142763.1 R476R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr10:55591293 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:55569294 C>T maps to NM_001142769.1 K1510K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:55719574 C>T maps to NM_001142763.1 E1018E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:55782876 G>A maps to NM_001142763.1 S772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:55955502 C>T maps to NM_001142763.1 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr10:55566608 C>T maps to ENST00000373965 L1595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr10:55569294 C>T maps to NM_001142769.1 K1510K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr10:55826534 G>A maps to NM_001142763.1 A739A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr10:55944965 C>T maps to NM_001142763.1 Q461Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr10:56138574 G>A maps to NM_001142763.1 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr13:58299280 C>T maps to NM_001040429.2 S1111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr13:58299217 C>T maps to NM_001040429.2 F1090F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr13:58240914 G>A maps to NM_001040429.2 R915R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44R-06A-41D-A25O-08 chr13:58208164 C>T maps to NM_001040429.2 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:58298821 C>T maps to NM_001040429.2 F958F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:58299274 G>A maps to NM_001040429.2 R1109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr13:58208593 C>T maps to NM_001040429.2 I638I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr13:58207408 C>T maps to NM_001040429.2 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr13:58206727 C>T maps to NM_001040429.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr13:58206799 G>A maps to NM_001040429.2 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr13:58208368 G>A maps to NM_001040429.2 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr13:58207510 A>G maps to NM_001040429.2 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:58207024 C>T maps to NM_001040429.2 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:58207132 C>T maps to NM_001040429.2 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:58208269 G>A maps to NM_001040429.2 T530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:58208803 C>T maps to NM_001040429.2 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:58209160 G>A maps to NM_001040429.2 Q827Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:58240848 G>A maps to NM_001040429.2 G893G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr13:58240624 C>T maps to NM_001040429.2 P863P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr4:138442608 C>T maps to NM_019035.3 E994E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr4:138452018 C>T maps to NM_019035.3 Q408Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr4:138442626 C>T maps to NM_019035.3 K988K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr4:138450989 G>A maps to NM_019035.3 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr4:138442314 G>A maps to NM_019035.3 I1092I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:138451228 G>A maps to NM_019035.3 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:138452126 C>T maps to NM_019035.3 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:138452387 G>A maps to NM_019035.3 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:138451043 G>A maps to NM_019035.3 S733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:138451724 C>T maps to NM_019035.3 E506E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:138451922 C>T maps to NM_019035.3 R440R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:138452417 C>T maps to NM_019035.3 E275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr4:138452552 G>A maps to NM_019035.3 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:138451646 G>A maps to NM_019035.3 I532I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr4:138442416 G>A maps to NM_019035.3 A1058A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:138453103 G>A maps to NM_019035.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr4:138449931 G>A maps to NM_019035.3 Q844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:138451031 C>T maps to NM_019035.3 R737R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr4:138451934 G>A maps to NM_019035.3 I436I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:138442554 G>A maps to NM_019035.3 F1012F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr4:138453043 G>A maps to NM_019035.3 R67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:138442437 C>T maps to NM_019035.3 Q1051Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr4:138451271 G>A maps to NM_019035.3 I657I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:138451271 G>A maps to NM_019035.3 I657I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:138451961 C>T maps to NM_019035.3 K427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:138452405 C>T maps to NM_019035.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:138453098 T>C maps to NM_019035.3 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:138442336 C>T maps to NM_019035.3 W1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:138452771 G>A maps to NM_019035.3 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr4:138442554 G>A maps to NM_019035.3 F1012F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr4:138452989 C>A maps to NM_019035.3 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr4:138442599 C>T maps to NM_019035.3 G997G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:99551603 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:99662086 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:99662259 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr23:99597062 A>G did not map to a codon.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr23:99661579 C>A did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr23:99551611 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:99551702 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:99551715 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:99597040 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:99605675 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:99605698 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:99657803 C>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:99661936 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:99657659 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:99551283 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:99661774 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:99551453 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:99551529 A>G did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:99662086 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:99662303 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr23:99662808 T>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:99551336 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:99551855 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:99658618 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:99661606 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:99662310 C>T did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr23:99663265 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:99661933 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr13:61987204 G>A maps to NM_022843.3 Q343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr13:61987196 C>T maps to NM_022843.3 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr13:61986626 G>A maps to NM_022843.3 F535F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:61986203 G>A maps to NM_022843.3 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr13:61986194 C>T maps to NM_022843.3 V679V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr13:61987196 C>T maps to NM_022843.3 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr13:61986626 G>A maps to NM_022843.3 F535F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr13:61985636 T>G maps to NM_022843.3 I865I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr13:61985741 G>C maps to NM_022843.3 P830P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:61987409 G>A maps to NM_022843.3 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr13:61987730 G>A maps to NM_022843.3 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr4:30725410 C>T maps to NM_001173523.1 F789F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr4:30724765 G>A maps to NM_001173523.1 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr4:30724720 G>T maps to NM_001173523.1 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:31144344 G>A maps to NM_001173523.1 E1214E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:31144213 C>T maps to NM_001173523.1 Q1171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr13:53420309 G>A maps to NM_002590.2 I754I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr13:53420334 C>T maps to NM_002590.2 W746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr13:53422091 C>T maps to NM_002590.2 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr13:53418922 C>T maps to NM_002590.2 R995R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr13:53422433 G>A maps to NM_002590.2 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr13:53422532 G>A maps to NM_002590.2 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr13:53420447 G>A maps to NM_002590.2 F708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr13:53419611 G>A maps to NM_002590.2 S929S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr13:53418960 G>A maps to NM_002590.2 Q983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr13:67801774 G>C maps to NM_203487.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr13:66878978 C>T maps to NM_203487.2 V1174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr13:67800394 G>A maps to NM_203487.2 F726F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr13:67800010 G>T maps to NM_203487.2 A854A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:66878843 C>T maps to NM_203487.2 L1219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:67801996 G>A maps to NM_203487.2 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr5:140166399 T>C maps to NM_018900.2 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr5:140166144 C>T maps to NM_018900.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr5:140389332 C>T maps to NM_018909.2 F888F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:140166990 C>T maps to NM_018900.2 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:140166201 C>T maps to NM_018900.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr5:140167134 C>T maps to NM_018900.2 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140168283 C>T maps to NM_031410.1 F803F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140389233 C>T maps to NM_018909.2 S855S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:140166765 C>T maps to NM_018900.2 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:140165976 G>A maps to NM_018900.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:140389332 C>T maps to NM_018909.2 F888F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr5:140389473 G>A maps to NM_018909.2 Q935Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:140167740 C>T maps to NM_018900.2 F622F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:140167830 G>A maps to NM_018900.2 K652K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:140167177 C>T maps to NM_018900.2 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr5:140165895 G>A maps to NM_018900.2 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140167038 C>T maps to NM_018900.2 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140167677 G>A maps to NM_018900.2 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140167992 G>A maps to NM_018900.2 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140358574 G>A maps to NM_018909.2 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140362059 C>T maps to NM_018909.2 S818S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:140166225 C>T maps to NM_018900.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr5:140362114 C>T maps to NM_018909.2 Q837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr5:140236475 C>T maps to NM_018901.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:140237414 C>T maps to NM_018901.2 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr5:140236202 C>T maps to NM_018901.2 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr5:140236220 G>A maps to NM_018901.2 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:140237444 G>C maps to NM_018901.2 A604A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr5:140237183 C>G maps to NM_018901.2 Y517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr5:140236502 G>A maps to NM_018901.2 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:140236229 G>A maps to NM_018901.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr5:140235980 C>T maps to NM_018901.2 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr5:140237489 C>T maps to NM_018901.2 I619I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:140237228 C>T maps to NM_018901.2 F532F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr5:140235761 C>T maps to NM_018901.2 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr5:140248702 G>A maps to NM_018902.3 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:140248702 G>A maps to NM_018902.3 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:140250916 G>A maps to NM_018902.3 A743A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:140248957 C>T maps to NM_018902.3 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:140248819 C>T maps to NM_018902.3 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:140249704 C>T maps to NM_018902.3 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr5:140250550 C>T maps to NM_018902.3 F621F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr5:140249596 C>T maps to NM_018902.3 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:140249014 C>T maps to NM_018902.3 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:140250439 G>A maps to NM_018902.3 V584V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:140248879 C>T maps to NM_018902.3 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:140250529 G>A maps to NM_018902.3 A614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr5:140249776 G>A maps to NM_018902.3 Q363Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:140248954 G>A maps to NM_018902.3 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:140250187 C>T maps to NM_018902.3 D500D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:140249573 C>T maps to NM_018902.3 Q296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140250109 C>T maps to NM_018902.3 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140250253 G>A maps to NM_018902.3 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140250718 C>T maps to NM_018902.3 A677A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140251066 T>C maps to NM_018902.3 N793N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:140250853 G>A maps to NM_018902.3 W722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr5:140248789 C>T maps to NM_018902.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:140248750 C>T maps to NM_018902.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr5:140249987 C>T maps to NM_018902.3 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr5:140249047 C>T maps to NM_018902.3 N120N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr5:140255407 C>T maps to NM_018903.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr5:140255200 C>T maps to NM_018903.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr5:140256595 G>A maps to NM_018903.2 E513E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:140255383 C>T maps to NM_018903.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:140255188 C>T maps to NM_018903.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140256430 C>T maps to NM_018903.2 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr5:140255749 C>T maps to NM_018903.2 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr5:140257348 G>A maps to NM_018903.2 P764P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:140257012 G>A maps to NM_018903.2 K652K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr5:140255407 C>T maps to NM_018903.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:140257384 T>A maps to NM_018903.2 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr5:140256013 G>A maps to NM_018903.2 Q319Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:140255068 C>T maps to NM_018903.2 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr5:140255089 C>T maps to NM_018903.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140256430 C>T maps to NM_018903.2 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr5:140262122 C>T maps to NM_018904.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr5:140262122 C>T maps to NM_018904.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr5:140262023 G>A maps to NM_018904.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr5:140262443 G>A maps to NM_018904.2 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr5:140263980 C>T maps to NM_018904.2 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:140262443 G>A maps to NM_018904.2 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr5:140264093 T>C maps to NM_018904.2 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr5:140263790 C>T maps to NM_018904.2 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr5:140262056 C>T maps to NM_018904.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140262170 G>A maps to NM_018904.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140262209 G>A maps to NM_018904.2 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr5:140263724 G>A maps to NM_018904.2 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr5:140263865 G>A maps to NM_018904.2 E671E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:140262119 G>A maps to NM_018904.2 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr5:140262587 C>A maps to NM_018904.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:140262386 C>T maps to NM_018904.2 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:140263829 G>A maps to NM_018904.2 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr5:140263655 G>A maps to NM_018904.2 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:140261918 A>C maps to NM_018904.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:140263049 C>T maps to NM_018904.2 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr5:140264036 C>T maps to NM_018904.2 T728T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:140263217 C>T maps to NM_018904.2 F455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140262461 G>A maps to NM_018904.2 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140262587 C>T maps to NM_018904.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140262635 G>A maps to NM_018904.2 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr5:140175769 G>A maps to NM_018905.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:140175304 A>G maps to NM_018905.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:140174818 C>T maps to NM_018905.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:140174569 G>A maps to NM_018905.2 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140174611 C>T maps to NM_018905.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:140176492 C>T maps to NM_018905.2 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:140175769 G>A maps to NM_018905.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:140176534 G>A maps to NM_018905.2 T662T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:140175943 G>A maps to NM_018905.2 K465K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:140174899 C>T maps to NM_018905.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:140176162 G>A maps to NM_018905.2 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:140176855 C>T maps to NM_018905.2 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:140174806 G>A maps to NM_018905.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr5:140174680 C>T maps to NM_018905.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr5:140174596 C>T maps to NM_018905.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140174611 C>T maps to NM_018905.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140175832 G>A maps to NM_018905.2 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140176786 G>A maps to NM_018905.2 G746G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr5:140176903 G>A maps to NM_018905.2 E785E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:140175832 G>A maps to NM_018905.2 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr5:140176021 C>T maps to NM_018905.2 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr5:140175877 C>T maps to NM_018905.2 I443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr5:140183148 G>A maps to NM_018906.2 Q789Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr5:140182107 C>T maps to NM_018906.2 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr5:140182266 G>A maps to NM_018906.2 V495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr5:140182155 C>T maps to NM_018906.2 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr5:140183148 G>A maps to NM_018906.2 Q789Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:140181450 T>C maps to NM_018906.2 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:140183193 A>G maps to NM_031497.1 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr5:140181132 C>T maps to NM_018906.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr5:140181795 C>T maps to NM_018906.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:140183127 C>T maps to NM_018906.2 S782S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr5:140181711 C>T maps to NM_018906.2 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:140182680 G>A maps to NM_018906.2 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:140182657 C>T maps to NM_018906.2 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr5:140182635 G>A maps to NM_018906.2 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:140182998 G>A maps to NM_018906.2 L739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:140181150 G>A maps to NM_018906.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:140181906 C>T maps to NM_018906.2 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:140181268 G>T maps to NM_018906.2 G163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140181385 C>T maps to NM_018906.2 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140182107 C>T maps to NM_018906.2 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140182155 C>T maps to NM_018906.2 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140182170 C>T maps to NM_018906.2 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140182443 C>T maps to NM_018906.2 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140182557 G>A maps to NM_018906.2 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140182884 C>T maps to NM_018906.2 I701I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr5:140182206 C>T maps to NM_018906.2 F475F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr5:140181516 G>A maps to NM_018906.2 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:140183019 G>A maps to NM_018906.2 G746G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr5:140187362 G>A maps to NM_018907.2 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr5:140188691 G>A maps to NM_018907.2 T640T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr5:140188661 G>A maps to NM_018907.2 E630E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:140188115 G>A maps to NM_018907.2 V448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr5:140186942 G>T maps to NM_018907.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:140188433 C>T maps to NM_018907.2 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr5:140188682 G>A maps to NM_018907.2 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr5:140187257 C>T maps to NM_018907.2 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:140187041 C>T maps to NM_018907.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr5:140188124 C>T maps to NM_018907.2 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:140188691 G>A maps to NM_018907.2 T640T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:140188814 G>A maps to NM_018907.2 R681R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:140188874 C>T maps to NM_018907.2 I701I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr5:140187998 G>A maps to NM_018907.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140187041 C>T maps to NM_018907.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140187260 G>A maps to NM_018907.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140187671 A>C maps to NM_018907.2 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140188163 G>A maps to NM_018907.2 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140189124 C>T maps to NM_018907.2 Q785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:140189009 G>A maps to NM_018907.2 G746G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:140189033 G>A maps to NM_018907.2 R754R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:140187122 C>T maps to NM_018907.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr5:140188613 G>A maps to NM_018907.2 G614G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr5:140202107 T>C maps to NM_018908.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr5:140203276 C>T maps to NM_018908.2 T639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr5:140202562 G>A maps to NM_018908.2 K401K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:140203522 G>A maps to NM_018908.2 R721R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr5:140203174 G>A maps to NM_018908.2 W605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:140203216 C>T maps to NM_018908.2 I619I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr5:140201560 C>T maps to NM_018908.2 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr5:140203024 G>A maps to NM_018908.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140202439 G>A maps to NM_018908.2 E360E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:140203744 C>A maps to NM_031501.1 P795P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:140203618 G>A maps to NM_018908.2 R753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr5:140203663 C>T maps to NM_018908.2 L768L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:140202247 T>G maps to NM_018908.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:140203456 G>A maps to NM_018908.2 L699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:140201626 C>T maps to NM_018908.2 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:140202181 G>A maps to NM_018908.2 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:140202853 G>A maps to NM_018908.2 V498V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:140202748 G>A maps to NM_018908.2 V463V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:140202274 G>A maps to NM_018908.2 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr5:140202745 C>T maps to NM_018908.2 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140201488 C>T maps to NM_018908.2 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140202460 C>T maps to NM_018908.2 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140203018 C>T maps to NM_018908.2 F553F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr5:140202424 C>T maps to NM_018908.2 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:140203618 G>A maps to NM_018908.2 R753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr5:140207898 C>T maps to NM_018909.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr5:140209736 G>A maps to NM_018909.2 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr5:140209337 C>T maps to NM_018909.2 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:140209067 G>A maps to NM_018909.2 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:140209781 C>T maps to NM_018909.2 I702I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr5:140208417 G>T maps to NM_018909.2 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr5:140208002 C>T maps to NM_018909.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr5:140209874 G>A maps to NM_018909.2 T733T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr5:140208002 C>T maps to NM_018909.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr5:140209337 C>T maps to NM_018909.2 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140207945 C>T maps to NM_018909.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr5:140207807 C>T maps to NM_018909.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:140208806 C>T maps to NM_018909.2 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:140207945 C>T maps to NM_018909.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr5:140208959 G>A maps to NM_018909.2 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:140207720 C>T maps to NM_018909.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:140210015 T>C maps to NM_018909.2 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:140208830 G>A maps to NM_018909.2 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr5:140208461 C>T maps to NM_018909.2 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:140208797 G>A maps to NM_018909.2 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr5:140207819 C>T maps to NM_018909.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140208797 G>A maps to NM_018909.2 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140209451 G>A maps to NM_018909.2 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140209643 G>A maps to NM_018909.2 E656E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:140209658 G>A maps to NM_018909.2 A661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr5:140208959 G>A maps to NM_018909.2 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:140208431 C>T maps to NM_018909.2 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr5:140215080 G>A maps to NM_018910.2 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr5:140215338 G>A maps to NM_018910.2 Q457Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr5:140214285 G>A maps to NM_018910.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr5:140214183 G>A maps to NM_018910.2 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr5:140214117 G>A maps to NM_018910.2 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr5:140215567 C>T maps to NM_018910.2 Q534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr5:140216148 C>G maps to NM_018910.2 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:140214324 G>A maps to NM_018910.2 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:140214165 G>A maps to NM_018910.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr5:140216016 G>A maps to NM_018910.2 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:140214072 C>T maps to NM_018910.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr5:140216070 C>T maps to NM_018910.2 I701I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr5:140215866 G>A maps to NM_018910.2 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140214888 T>C maps to NM_018910.2 H307H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140215332 C>T maps to NM_018910.2 F455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140216076 C>T maps to NM_018910.2 A703A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A264-06A-11D-A196-08 chr5:140214936 C>T maps to NM_018910.2 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:140214294 C>T maps to NM_018910.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:140215257 G>A maps to NM_018910.2 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr5:140215876 C>T maps to NM_018910.2 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr5:140223008 C>T maps to NM_018911.2 I701I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr5:140222070 C>T maps to NM_018911.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr5:140221175 C>T maps to NM_018911.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr5:140222315 G>A maps to NM_018911.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr5:140221277 G>A maps to NM_018911.2 K124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr5:140221469 G>A maps to NM_018911.2 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr5:140223140 G>A maps to NM_018911.2 V745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:140222918 G>A maps to NM_018911.2 E671E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140220977 G>A maps to NM_018911.2 W24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:140221067 G>A maps to NM_018911.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:140223340 G>A maps to NM_031856.1 W812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:140220998 C>T maps to NM_018911.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:140221175 C>T maps to NM_018911.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:140223218 C>T maps to NM_018911.2 A771A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:140221049 C>T maps to NM_018911.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:140222567 C>T maps to NM_018911.2 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:140222696 G>A maps to NM_018911.2 V597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr5:140222472 C>T maps to NM_018911.2 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr5:140223212 C>T maps to NM_018911.2 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140222036 C>T maps to NM_018911.2 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140222216 C>T maps to NM_018911.2 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140222492 G>A maps to NM_018911.2 E529E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140222681 G>A maps to NM_018911.2 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:140222567 C>T maps to NM_018911.2 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr5:140228283 C>T maps to NM_031857.1 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:140229540 C>T maps to NM_031857.1 N487N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr5:140228397 G>A maps to NM_031857.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr5:140228406 C>T maps to NM_031857.1 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr5:140228337 G>A maps to NM_031857.1 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:140229264 C>T maps to NM_031857.1 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr5:140230101 G>A maps to NM_031857.1 Q674Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140229535 G>T maps to NM_031857.1 E486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:140230392 C>T maps to NM_031857.1 A771A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr5:140230084 C>T maps to NM_031857.1 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr5:140229693 C>T maps to NM_031857.1 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:140229678 C>T maps to NM_031857.1 F533F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:140228403 G>A maps to NM_031857.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:140229474 G>A maps to NM_031857.1 K465K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:140228436 G>A maps to NM_031857.1 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr5:140229999 G>A maps to NM_031857.1 T640T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr5:140230191 C>T maps to NM_031857.1 I704I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140230470 G>A maps to NM_031857.1 G797G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr5:140229504 C>T maps to NM_031857.1 F475F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:140228406 C>T maps to NM_031857.1 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr5:140230314 G>A maps to NM_031857.1 V745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr5:140308741 C>T maps to NM_018898.3 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:140307997 C>T maps to NM_018898.3 I507I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr5:140308246 T>C maps to NM_018898.3 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr5:140308408 A>G maps to NM_018898.3 P644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr5:140307490 C>T maps to NM_018898.3 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:140307247 C>T maps to NM_018898.3 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:140307290 C>T maps to NM_018898.3 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr5:140307349 G>A maps to NM_018898.3 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:140306914 G>A maps to NM_018898.3 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:140308885 G>A maps to NM_018898.3 G803G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:140307835 C>T maps to NM_018898.3 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr5:140307700 C>T maps to NM_018898.3 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140307139 C>T maps to NM_018898.3 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140308562 C>T maps to NM_018898.3 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:140307559 C>T maps to NM_018898.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr5:140347661 C>T maps to NM_018899.5 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:140348597 G>A maps to NM_018899.5 R749R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr5:140348015 G>A maps to NM_018899.5 G555G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140347415 C>T maps to NM_018899.5 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr5:140348393 G>A maps to NM_018899.5 V681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr5:140346635 G>A maps to NM_018899.5 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr5:140346713 G>A maps to NM_018899.5 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:140348393 G>A maps to NM_018899.5 V681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr5:140348540 G>A maps to NM_018899.5 K730K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:140347256 C>T maps to NM_018899.5 D302D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:140348165 C>T maps to NM_018899.5 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:140347040 G>A maps to NM_018899.5 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr5:140346977 G>A maps to NM_018899.5 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr5:140347958 C>T maps to NM_018899.5 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr5:140346521 C>T maps to NM_018899.5 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr5:140346809 C>T maps to NM_018899.5 Y153Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140348027 G>A maps to NM_018899.5 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140348123 C>T maps to NM_018899.5 F591F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140348337 C>T maps to NM_018899.5 R663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140348694 C>T maps to NM_018899.5 R782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140348708 C>T maps to NM_018899.5 S786S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr5:140347862 G>A maps to NM_018899.5 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:140431405 C>T maps to NM_013340.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr5:140433457 G>A maps to NM_013340.2 R801R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr5:140433457 G>A maps to NM_013340.2 R801R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:140431588 C>T maps to NM_013340.2 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:140432971 G>A maps to NM_013340.2 Q639Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr5:140433394 C>T maps to NM_013340.2 F780F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140433457 G>A maps to NM_013340.2 R801R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:140432833 G>A maps to NM_013340.2 V593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr5:140433184 C>T maps to NM_013340.2 F710F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:140432251 G>A maps to NM_013340.2 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr5:140431405 C>T maps to NM_013340.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:140431115 C>T maps to NM_013340.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:140432227 C>T maps to NM_013340.2 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr5:140432251 G>A maps to NM_013340.2 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr5:140431768 C>T maps to NM_013340.2 H238H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr5:140431931 C>T maps to NM_013340.2 Q293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr5:140432779 C>T maps to NM_013340.2 D575D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr5:140431132 G>A maps to NM_013340.2 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140431663 G>A maps to NM_013340.2 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140431711 C>T maps to NM_013340.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140431855 G>A maps to NM_013340.2 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140432510 C>T maps to NM_013340.2 Q486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140433100 A>G maps to NM_013340.2 R682R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140433409 G>A maps to NM_013340.2 G785G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:140431462 G>A maps to NM_013340.2 K136K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr5:140432590 G>A maps to NM_013340.2 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr5:140574497 C>T maps to NM_018930.3 F791F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr5:140573297 C>T maps to NM_018930.3 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr5:140573264 G>A maps to NM_018930.3 K380K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:140572442 C>T maps to NM_018930.3 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:140572901 C>T maps to NM_018930.3 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr5:140572658 C>T maps to NM_018930.3 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140573496 C>T maps to NM_018930.3 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:140573705 C>T maps to NM_018930.3 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:140572733 G>A maps to NM_018930.3 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr5:140573102 C>T maps to NM_018930.3 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr5:140573666 C>T maps to NM_018930.3 F514F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr5:140574089 C>T maps to NM_018930.3 T655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr5:140573477 C>T maps to NM_018930.3 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr5:140572752 T>C maps to NM_018930.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:140573021 G>A maps to NM_018930.3 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr5:140572787 C>T maps to NM_018930.3 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:140573630 C>T maps to NM_018930.3 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr5:140573033 C>A maps to NM_018930.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:140574377 C>T maps to NM_018930.3 Y751Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140572148 C>T maps to NM_018930.3 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140573666 C>T maps to NM_018930.3 F514F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr5:140573285 G>A maps to NM_018930.3 E387E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:140580519 C>T maps to NM_018931.2 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:140580927 C>T maps to NM_018931.2 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr5:140579361 G>A maps to NM_018931.2 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:140579976 C>T maps to NM_018931.2 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:140579976 C>T maps to NM_018931.2 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr5:140579526 C>T maps to NM_018931.2 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:140581614 G>A maps to NM_018931.2 T756T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:140580483 A>G maps to NM_018931.2 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:140579976 C>T maps to NM_018931.2 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr5:140579466 G>A maps to NM_018931.2 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr5:140579559 G>A maps to NM_018931.2 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140580265 C>T maps to NM_018931.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140580504 G>A maps to NM_018931.2 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140580591 C>T maps to NM_018931.2 A415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140580723 C>T maps to NM_018931.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140580799 C>T maps to NM_018931.2 Q485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140581302 C>T maps to NM_018931.2 R652R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140581365 C>T maps to NM_018931.2 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr5:140590308 G>A maps to NM_018932.3 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr5:140590314 C>T maps to NM_018932.3 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr5:140589045 G>A maps to NM_018932.3 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:140589168 G>A maps to NM_018932.3 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:140589278 G>A maps to NM_018932.3 W267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr5:140589324 C>T maps to NM_018932.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:140588760 G>A maps to NM_018932.3 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:140588985 C>T maps to NM_018932.3 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:140590623 G>A maps to NM_018932.3 R715R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr5:140588664 G>A maps to NM_018932.3 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:140589759 G>A maps to NM_018932.3 G427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:140590231 C>T maps to NM_018932.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr5:140590602 C>T maps to NM_018932.3 F708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140590254 G>A maps to NM_018932.3 V592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:140589585 G>A maps to NM_018932.3 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr5:140588529 C>T maps to NM_018932.3 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr5:140589519 C>T maps to NM_018932.3 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr5:140589519 C>T maps to NM_018932.3 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr5:140594276 G>A maps to NM_018933.2 E194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr5:140595191 C>T maps to NM_018933.2 P499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:140594387 C>T maps to NM_018933.2 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:140594579 C>T maps to NM_018933.2 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:140594834 G>A maps to NM_018933.2 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:140594624 C>T maps to NM_018933.2 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr5:140595299 C>T maps to NM_018933.2 D535D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:140595047 C>T maps to NM_018933.2 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:140595071 C>T maps to NM_018933.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:140595677 C>T maps to NM_018933.2 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:140595818 C>T maps to NM_018933.2 F708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:140596016 C>T maps to NM_018933.2 F774F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr5:140596016 C>T maps to NM_018933.2 F774F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140594351 C>T maps to NM_018933.2 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140594624 C>T maps to NM_018933.2 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr5:140594474 C>T maps to NM_018933.2 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr5:140594855 G>A maps to NM_018933.2 Q387Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr5:140603400 G>A maps to NM_018934.2 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr5:140605399 C>T maps to NM_018934.2 Q775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140604186 C>T maps to NM_018934.2 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140605095 C>T maps to NM_018934.2 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140605444 C>T maps to NM_018934.2 R790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:140603832 C>T maps to NM_018934.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:140605428 G>A maps to NM_018934.2 G784G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:140604585 G>A maps to NM_018934.2 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:140603127 C>T maps to NM_018934.2 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:140603808 G>A maps to NM_018934.2 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:140604279 C>T maps to NM_018934.2 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZG-06A-11D-A197-08 chr5:140604054 T>C maps to NM_018934.2 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140604453 C>T maps to NM_018934.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140605213 C>T maps to NM_018934.2 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr5:140626249 T>C maps to NM_018935.2 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:140625808 C>T maps to NM_018935.2 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr5:140625541 G>A maps to NM_018935.2 E132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:140626591 C>T maps to NM_018935.2 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr5:140626825 C>T maps to NM_018935.2 F560F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140625497 C>T maps to NM_018935.2 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:140626349 A>C maps to NM_018935.2 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:140626177 C>T maps to NM_018935.2 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:140625679 C>T maps to NM_018935.2 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:140625497 C>T maps to NM_018935.2 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr5:140625712 G>A maps to NM_018935.2 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:140625946 G>A maps to NM_018935.2 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:140626637 C>T maps to NM_018935.2 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr5:140626405 C>T maps to NM_018935.2 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr5:140625712 G>A maps to NM_018935.2 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr5:140626759 C>T maps to NM_018935.2 F538F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr5:140626825 C>T maps to NM_018935.2 F560F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140625475 G>A maps to NM_018935.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140626687 C>T maps to NM_018935.2 F514F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140627269 C>T maps to NM_018935.2 F708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr5:140625337 C>T maps to NM_018935.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q1-06A-21D-A196-08 chr5:140564440 G>A maps to NM_020957.1 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr5:140563276 G>A maps to NM_020957.1 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:140562589 C>T maps to NM_020957.1 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr5:140564311 G>A maps to NM_020957.1 S726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:140564326 C>T maps to NM_020957.1 P731P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr5:140562469 C>T maps to NM_020957.1 N112N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:140562667 C>T maps to NM_020957.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:140564422 G>A maps to NM_020957.1 E763E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr5:140563207 G>A maps to NM_020957.1 E358E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr5:140562934 G>A maps to NM_020957.1 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:140562214 C>A maps to NM_020957.1 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:140563510 C>T maps to NM_020957.1 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140563282 C>T maps to NM_020957.1 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:140563714 C>T maps to NM_020957.1 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:140563714 C>T maps to NM_020957.1 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr5:140562299 T>C maps to NM_020957.1 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:140475312 C>T maps to NM_018936.2 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr5:140474739 G>A maps to NM_018936.2 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr5:140476314 G>A maps to NM_018936.2 K647K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:140474859 G>A maps to NM_018936.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr5:140475555 C>T maps to NM_018936.2 F394F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:140475756 C>T maps to NM_018936.2 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:140476749 G>A maps to NM_018936.2 R792R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr5:140475256 C>T maps to NM_018936.2 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140476482 C>T maps to NM_018936.2 F703F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr5:140474799 G>A maps to NM_018936.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr5:140475591 G>A maps to NM_018936.2 V406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:140474610 C>T maps to NM_018936.2 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:140474697 C>T maps to NM_018936.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr5:140475054 G>T maps to NM_018936.2 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr5:140475535 C>T maps to NM_018936.2 Q388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:140474496 G>A maps to NM_018936.2 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:140476701 C>T maps to NM_018936.2 F776F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:140475306 C>T maps to NM_018936.2 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:140475960 C>T maps to NM_018936.2 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:140476710 G>A maps to NM_018936.2 Q779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:140475180 G>A maps to NM_018936.2 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr5:140475642 C>T maps to NM_018936.2 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:140475555 C>T maps to NM_018936.2 F394F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:140476764 C>T maps to NM_018936.2 F797F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr5:140475750 C>T maps to NM_018936.2 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:140476701 C>T maps to NM_018936.2 F776F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140474452 C>T maps to NM_018936.2 Q27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140475123 G>A maps to NM_018936.2 E250E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140475756 C>T maps to NM_018936.2 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr5:140474817 C>T maps to NM_018936.2 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:140475256 C>T maps to NM_018936.2 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:140475300 G>A maps to NM_018936.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr5:140476314 G>A maps to NM_018936.2 K647K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr5:140482554 C>T maps to NM_018937.2 F774F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr5:140480436 C>T maps to NM_018937.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr5:140480553 G>A maps to NM_018937.2 Q107Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:140480268 G>A maps to NM_018937.2 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:140482080 C>G maps to NM_018937.2 G616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:140480580 C>T maps to NM_018937.2 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:140482602 G>A maps to NM_018937.2 R790R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr5:140480551 C>T maps to NM_018937.2 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr5:140482335 C>T maps to NM_018937.2 F701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr5:140480580 C>T maps to NM_018937.2 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:140482014 C>T maps to NM_018937.2 G594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:140480964 G>A maps to NM_018937.2 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:140481048 A>G maps to NM_018937.2 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr5:140480652 G>A maps to NM_018937.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr5:140480754 G>A maps to NM_018937.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:140481408 C>T maps to NM_018937.2 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:140480502 G>A maps to NM_018937.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr5:140482366 C>A maps to NM_018937.2 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr5:140481795 C>G maps to NM_018937.2 Y521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:140480850 G>A maps to NM_018937.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140480343 G>A maps to NM_018937.2 E37E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140480397 G>A maps to NM_018937.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140480412 C>T maps to NM_018937.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140480799 G>A maps to NM_018937.2 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140481609 C>T maps to NM_018937.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140481951 C>T maps to NM_018937.2 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:140481153 G>A maps to NM_018937.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:140480964 G>A maps to NM_018937.2 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr5:140480877 G>A maps to NM_018937.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr5:140481399 C>T maps to NM_018937.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr5:140501747 G>A maps to NM_018938.2 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr5:140502953 C>T maps to NM_018938.2 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr5:140503256 C>T maps to NM_018938.2 F559F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr5:140502953 C>T maps to NM_018938.2 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:140501837 G>A maps to NM_018938.2 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr5:140503919 G>A maps to NM_018938.2 R780R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr5:140502261 C>T maps to NM_018938.2 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:140503403 C>T maps to NM_018938.2 A608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr5:140502681 C>T maps to NM_018938.2 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:140501928 C>T maps to NM_018938.2 Q117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:140503113 C>T maps to NM_018938.2 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr5:140503943 C>T maps to NM_018938.2 F788F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:140503307 C>T maps to NM_018938.2 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:140503928 G>A maps to NM_018938.2 K783K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr5:140503256 C>T maps to NM_018938.2 F559F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr5:140502641 C>T maps to NM_018938.2 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr5:140502320 G>T maps to NM_018938.2 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr5:140503274 G>A maps to NM_018938.2 Q565Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr5:140503928 G>A maps to NM_018938.2 K783K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140501769 C>A maps to NM_018938.2 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140501993 C>T maps to NM_018938.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140503380 C>T maps to NM_018938.2 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr5:140516368 C>T maps to NM_015669.2 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr5:140515367 C>T maps to NM_015669.2 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr5:140516848 C>A maps to NM_015669.2 P611P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr5:140517364 G>A maps to NM_015669.2 G783G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:140516692 C>T maps to NM_015669.2 F559F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:140516389 C>T maps to NM_015669.2 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:140515462 G>A maps to NM_015669.2 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:140516389 C>T maps to NM_015669.2 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr5:140516152 G>A maps to NM_015669.2 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:140516605 G>A maps to NM_015669.2 V530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:140515441 C>T maps to NM_015669.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:140517376 C>T maps to NM_015669.2 A787A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:140515441 C>T maps to NM_015669.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:140516329 C>T maps to NM_015669.2 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr5:140516599 C>T maps to NM_015669.2 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr5:140517310 C>T maps to NM_015669.2 F765F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:140516398 G>A maps to NM_015669.2 E461E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:140517364 G>A maps to NM_015669.2 G783G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr5:140516536 G>A maps to NM_015669.2 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140515441 C>T maps to NM_015669.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140515801 C>T maps to NM_015669.2 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140516977 C>T maps to NM_015669.2 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr5:140531208 C>T maps to NM_018939.2 F457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr5:140530479 G>A maps to NM_018939.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:140530707 C>T maps to NM_018939.2 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:140531955 C>T maps to NM_018939.2 F706F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:140531346 C>T maps to NM_018939.2 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr5:140531313 G>A maps to NM_018939.2 Q492Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:140529984 G>A maps to NM_018939.2 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr5:140530092 A>T maps to NM_018939.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:140531511 C>T maps to NM_018939.2 F558F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:140531412 C>T maps to NM_018939.2 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:140529942 G>A maps to NM_018939.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:140531412 C>T maps to NM_018939.2 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr5:140531412 C>T maps to NM_018939.2 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:140531766 G>A maps to NM_018939.2 K643K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr5:140531955 C>T maps to NM_018939.2 F706F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr5:140530768 C>T maps to NM_018939.2 Q311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:140531511 C>T maps to NM_018939.2 F558F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:140530116 G>A maps to NM_018939.2 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr5:140531679 C>T maps to NM_018939.2 G614G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:140531001 C>T maps to NM_018939.2 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140530608 C>T maps to NM_018939.2 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140531184 C>T maps to NM_018939.2 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140532153 C>T maps to NM_018939.2 F772F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:140531241 C>T maps to NM_018939.2 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:140530065 T>C maps to NM_018939.2 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr5:140552766 C>T maps to NM_018940.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:140553171 C>T maps to NM_018940.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:140553180 C>T maps to NM_018940.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:140554512 C>T maps to NM_018940.2 F699F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr5:140553522 G>A maps to NM_018940.2 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:140553282 C>T maps to NM_018940.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:140553765 C>T maps to NM_018940.2 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:140554533 C>T maps to NM_018940.2 F706F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:140553297 C>T maps to NM_018940.2 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:140554779 G>A maps to NM_018940.2 Q788Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:140553106 C>T maps to NM_018940.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr5:140554377 C>T maps to NM_018940.2 A654A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:140553801 G>A maps to NM_018940.2 E462E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr5:140554533 C>T maps to NM_018940.2 F706F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr5:140554242 C>T maps to NM_018940.2 A609A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr5:140553894 C>T maps to NM_018940.2 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr5:140552430 G>A maps to NM_018940.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr5:140554260 C>T maps to NM_018940.2 F615F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140553996 C>T maps to NM_018940.2 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:140553445 C>T maps to NM_018940.2 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr5:140554095 C>T maps to NM_018940.2 F560F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:140559699 G>A maps to NM_019120.2 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:140559771 G>A maps to NM_019120.2 R719R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:140558184 G>A maps to NM_019120.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:140559666 C>T maps to NM_019120.2 A684A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:140558521 C>T maps to NM_019120.2 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:140558544 C>T maps to NM_019120.2 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:140558794 C>T maps to NM_019120.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:140558554 C>T maps to NM_019120.2 Q314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:140558862 C>T maps to NM_019120.2 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:140558931 C>T maps to NM_019120.2 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:140559123 C>T maps to NM_019120.2 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:140558521 C>T maps to NM_019120.2 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:140558691 G>A maps to NM_019120.2 E359E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr5:140559297 C>T maps to NM_019120.2 F561F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:140558184 G>A maps to NM_019120.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:140558496 G>A maps to NM_019120.2 K294K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140558037 G>A maps to NM_019120.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:140558811 G>A maps to NM_019120.2 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr5:140558773 C>T maps to NM_019120.2 Q387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr5:140710394 C>T maps to NM_018912.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr5:140712149 G>A maps to NM_018912.2 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr5:140712497 C>T maps to NM_018912.2 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:140712329 G>A maps to NM_018912.2 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:140885025 C>T maps to NM_018915.2 A850A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:140890535 C>T maps to NM_018915.2 T865T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr5:140710500 T>C maps to NM_018912.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:140710475 C>T maps to NM_018912.2 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:140711003 C>T maps to NM_018912.2 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:140711993 C>T maps to NM_018912.2 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:140712560 C>T maps to NM_018912.2 F770F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:140712377 C>T maps to NM_018912.2 I709I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:140712560 C>T maps to NM_018912.2 F770F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr5:140710991 C>T maps to NM_018912.2 Y247Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr5:140711937 C>T maps to NM_018912.2 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:140711177 C>T maps to NM_018912.2 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:140712377 C>T maps to NM_018912.2 I709I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr5:140792873 G>A maps to NM_018913.2 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr5:140794563 C>T maps to NM_018913.2 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:140795000 C>T maps to NM_018913.2 F753F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:140794692 C>T maps to NM_018913.2 Q651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:140792982 C>T maps to NM_018913.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr5:140794688 C>T maps to NM_018913.2 A649A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:140793902 C>T maps to NM_018913.2 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr5:140795000 C>T maps to NM_018913.2 F753F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140793596 C>T maps to NM_018913.2 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140794787 C>T maps to NM_018913.2 F682F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr5:140803133 C>T maps to NM_018914.2 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr5:140801021 C>T maps to NM_018914.2 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:140802647 C>T maps to NM_018914.2 F618F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr5:140801792 G>A maps to NM_018914.2 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr5:140801460 C>T maps to NM_018914.2 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140801195 C>T maps to NM_018914.2 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr5:140801405 G>A maps to NM_018914.2 E204E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr5:140801495 C>T maps to NM_018914.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr5:140810550 C>T maps to NM_003735.2 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140811978 C>T maps to NM_003735.2 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140812011 C>T maps to NM_003735.2 I562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:140810529 C>A maps to NM_003735.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:140810550 C>T maps to NM_003735.2 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:140812224 G>A maps to NM_003735.2 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:140812287 C>T maps to NM_003735.2 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:140812572 C>T maps to NM_003735.2 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr5:140811681 C>T maps to NM_003735.2 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr5:140718654 C>T maps to NM_018915.2 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr5:140720649 C>T maps to NM_018915.2 F704F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr5:140719074 C>T maps to NM_018915.2 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:140719002 G>A maps to NM_018915.2 K155K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr5:140720217 C>A maps to NM_018915.2 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr5:140720784 C>T maps to NM_018915.2 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44R-06A-41D-A25O-08 chr5:140719815 T>C maps to NM_018915.2 D426D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr5:140718681 C>T maps to NM_018915.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:140720280 C>T maps to NM_018915.2 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr5:140719378 C>T maps to NM_018915.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:140720538 G>A maps to NM_018915.2 R667R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:140720190 C>T maps to NM_018915.2 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:140720292 C>T maps to NM_018915.2 G585G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:140718609 G>A maps to NM_018915.2 W24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:140719101 G>A maps to NM_018915.2 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr5:140718669 C>T maps to NM_018915.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr5:140720634 G>A maps to NM_018915.2 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr5:140720640 C>T maps to NM_018915.2 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr5:140720247 C>T maps to NM_018915.2 D570D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr5:140719539 C>T maps to NM_018915.2 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140718687 G>A maps to NM_018915.2 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140719137 G>A maps to NM_018915.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140719242 G>A maps to NM_018915.2 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140719695 C>T maps to NM_018915.2 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr5:140724181 G>A maps to NM_018916.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr5:140725561 C>T maps to NM_018916.3 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:140725538 C>T maps to NM_018916.3 Q647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr5:140724440 C>T maps to NM_018916.3 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr5:140725828 G>A maps to NM_018916.3 A743A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr5:140723812 G>A maps to NM_018916.3 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:140723605 C>T maps to NM_018916.3 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr5:140723998 C>T maps to NM_018916.3 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:140724379 G>A maps to NM_018916.3 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr5:140725726 C>T maps to NM_018916.3 I709I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:140723891 C>T maps to NM_018916.3 Q98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:140725213 G>A maps to NM_018916.3 G538G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:140725156 C>T maps to NM_018916.3 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:140724814 G>A maps to NM_018916.3 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:140725258 G>A maps to NM_018916.3 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr5:140725945 G>A maps to NM_018916.3 Q782Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr5:140724646 C>T maps to NM_018916.3 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr5:140737079 C>T maps to NM_018917.2 S771S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:140734829 G>A maps to NM_018917.2 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:140736452 C>T maps to NM_018917.2 I562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr5:140735747 C>T maps to NM_018917.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:140736452 C>T maps to NM_018917.2 I562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:140734934 C>T maps to NM_018917.2 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr5:140736305 C>T maps to NM_018917.2 I513I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:140736305 C>T maps to NM_018917.2 I513I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:140736845 C>T maps to NM_018917.2 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:140736122 C>T maps to NM_018917.2 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:140736705 C>T maps to NM_018917.2 Q647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:140736893 G>A maps to NM_018917.2 T709T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr5:140734910 C>T maps to NM_018917.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140735501 C>T maps to NM_018917.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140736824 C>T maps to NM_018917.2 D686D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140736878 C>T maps to NM_018917.2 F704F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140737028 C>T maps to NM_018917.2 S754S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr5:140736452 C>T maps to NM_018917.2 I562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr5:140736131 T>A maps to NM_018917.2 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr5:140744364 C>T maps to NM_018918.2 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr5:140745582 C>T maps to NM_018918.2 I562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:140744028 C>T maps to NM_018918.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr5:140745192 C>T maps to NM_018918.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr5:140746179 G>T maps to NM_018918.2 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140746203 C>T maps to NM_018918.2 I769I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:140746158 C>T maps to NM_018918.2 S754S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:140744286 C>T maps to NM_018918.2 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:140745252 C>T maps to NM_018918.2 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:140745588 C>T maps to NM_018918.2 Y564Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:140746221 C>T maps to NM_018918.2 Y775Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:140746170 C>T maps to NM_018918.2 S758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr5:140744592 C>T maps to NM_018918.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr5:140744721 G>A maps to NM_018918.2 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:140745900 C>T maps to NM_018918.2 I668I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr5:140744697 G>A maps to NM_018918.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140744772 C>T maps to NM_018918.2 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140746017 C>T maps to NM_018918.2 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr5:140745856 C>T maps to NM_018918.2 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:140745252 C>T maps to NM_018918.2 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr5:140745252 C>T maps to NM_018918.2 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr5:140754525 C>T maps to NM_018919.2 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr5:140754312 C>T maps to NM_018919.2 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:140755113 C>T maps to NM_018919.2 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:140753700 C>T maps to NM_018919.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr5:140756032 C>T maps to NM_018919.2 Q795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:140754525 C>T maps to NM_018919.2 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:140754585 G>A maps to NM_018919.2 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:140754856 C>T maps to NM_018919.2 R403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr5:140755683 C>T maps to NM_018919.2 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:140755005 C>T maps to NM_018919.2 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:140754839 C>A maps to NM_018919.2 S397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140755242 G>A maps to NM_018919.2 W531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140755959 C>T maps to NM_018919.2 F770F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr5:140755050 G>A maps to NM_018919.2 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:140754489 C>T maps to NM_018919.2 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:140764611 C>T maps to NM_018920.2 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:140764712 C>T maps to NM_018920.2 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:140764875 C>T maps to NM_018920.2 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr5:140764775 C>T maps to NM_018920.2 F770F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:140764448 C>T maps to NM_018920.2 T661T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr5:140763815 C>T maps to NM_018920.2 P450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:140764152 C>T maps to NM_018920.2 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr5:140762957 G>A maps to NM_018920.2 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140764586 C>T maps to NM_018920.2 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr5:140774626 C>T maps to NM_032088.1 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44R-06A-41D-A25O-08 chr5:140773912 C>T maps to NM_032088.1 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:140774693 C>T maps to NM_032088.1 Q772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140772559 G>A maps to NM_032088.1 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140772577 C>T maps to NM_032088.1 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:140772877 C>T maps to NM_032088.1 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:140772571 C>T maps to NM_032088.1 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:140772814 C>T maps to NM_032088.1 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:140772778 C>T maps to NM_032088.1 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr5:140773222 C>T maps to NM_032088.1 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:140774189 C>T maps to NM_032088.1 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140772916 C>T maps to NM_032088.1 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140773897 C>T maps to NM_032088.1 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr5:140774692 C>T maps to NM_032088.1 P771P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr5:140773096 C>T maps to NM_032088.1 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr5:140784765 C>T maps to NM_018921.2 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr5:140784330 C>T maps to NM_018921.2 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr5:140784210 C>T maps to NM_018921.2 Y564Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:140784597 C>T maps to NM_018921.2 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140784825 C>T maps to NM_018921.2 I769I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:140784597 C>T maps to NM_018921.2 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:140784003 C>T maps to NM_018921.2 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr5:140784276 C>T maps to NM_018921.2 Y586Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr5:140784277 C>T maps to NM_018921.2 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr5:140784792 C>T maps to NM_018921.2 S758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:140783811 C>T maps to NM_018921.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:140784765 C>T maps to NM_018921.2 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:140784345 C>T maps to NM_018921.2 F609F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:140783937 C>T maps to NM_018921.2 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr5:140783202 C>T maps to NM_018921.2 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr5:140784825 C>T maps to NM_018921.2 I769I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140782716 C>T maps to NM_018921.2 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr5:140784474 C>T maps to NM_018921.2 P652P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr5:140731359 C>T maps to NM_018922.2 F511F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr5:140729877 C>T maps to NM_018922.2 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:140731311 G>T maps to NM_018922.2 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr5:140730861 C>T maps to NM_018922.2 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr5:140730570 C>T maps to NM_018922.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr5:140730571 C>T maps to NM_018922.2 Q249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140730168 C>T maps to NM_018922.2 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:140730112 A>T maps to NM_018922.2 K96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr5:140731170 C>T maps to NM_018922.2 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:140730450 C>T maps to NM_018922.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr5:140729980 C>T maps to NM_018922.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:140731996 C>T maps to NM_018922.2 Q724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:140731806 C>T maps to NM_018922.2 F660F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr5:140730564 T>A maps to NM_018922.2 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:140731170 C>T maps to NM_018922.2 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr5:140731425 G>A maps to NM_018922.2 Q533Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr5:140731708 T>C maps to NM_018922.2 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140729880 C>T maps to NM_018922.2 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140731806 C>T maps to NM_018922.2 F660F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140731944 G>A maps to NM_018922.2 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140732106 G>A maps to NM_018922.2 E760E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr5:140741426 C>T maps to NM_018923.2 F575F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr5:140739822 C>T maps to NM_018923.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr5:140740931 G>A maps to NM_018923.2 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr5:140741396 C>T maps to NM_018923.2 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr5:140741693 C>T maps to NM_018923.2 F664F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:140740019 C>T maps to NM_018923.2 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:140740376 G>A maps to NM_018923.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:140741261 C>T maps to NM_018923.2 F520F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140741048 C>T maps to NM_018923.2 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr5:140750786 G>T maps to NM_018924.2 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:140751496 G>A maps to NM_018924.2 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr5:140751262 C>T maps to NM_018924.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:140752072 C>T maps to NM_018924.2 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr5:140751466 G>A maps to NM_018924.2 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:140751424 C>T maps to NM_018924.2 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:140751568 C>T maps to NM_018924.2 D536D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr5:140751046 G>T maps to NM_018924.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140751019 C>T maps to NM_018924.2 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:140751142 C>T maps to NM_018924.2 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr5:140751505 C>T maps to NM_018924.2 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:140750110 C>T maps to NM_018924.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:140751952 C>T maps to NM_018924.2 F664F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr5:140751046 G>A maps to NM_018924.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZG-06A-11D-A197-08 chr5:140750026 C>G maps to NM_018924.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr5:140751611 T>C maps to NM_018924.2 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140750161 G>A maps to NM_018924.2 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140751505 C>T maps to NM_018924.2 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140751520 C>T maps to NM_018924.2 F520F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140752117 C>T maps to NM_018924.2 S719S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr5:140751382 C>G maps to NM_018924.2 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:140752213 C>T maps to NM_018924.2 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr5:140752180 C>T maps to NM_018924.2 L740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr5:140769604 C>T maps to NM_003736.2 S718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:140768881 G>A maps to NM_003736.2 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr5:140768287 C>T maps to NM_003736.2 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr5:140768842 G>A maps to NM_003736.2 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:140768737 C>T maps to NM_003736.2 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr5:140769553 C>T maps to NM_003736.2 F701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140769169 C>T maps to NM_003736.2 F573F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr5:140788485 C>T maps to NM_018926.2 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr5:140789040 C>T maps to NM_018926.2 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr5:140789352 C>T maps to NM_018926.2 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr5:140788197 C>T maps to NM_018926.2 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:140790066 C>T maps to NM_018926.2 F766F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140788366 C>T maps to NM_018926.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr5:140788197 C>T maps to NM_018926.2 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr5:140788612 C>T maps to NM_018926.2 R282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:140789034 C>T maps to NM_018926.2 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140789313 C>T maps to NM_018926.2 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:140798556 G>A maps to NM_018927.2 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr5:140799339 C>T maps to NM_018927.2 V638V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:140799444 G>A maps to NM_018927.2 P673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:140858106 C>T maps to NM_002588.2 P808P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:140857374 C>T maps to NM_002588.2 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:140865915 C>T maps to NM_018928.2 H392H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:140866989 C>T maps to NM_018928.2 L750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr5:140865108 C>T maps to NM_018928.2 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:140865195 C>T maps to NM_018928.2 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr5:140866629 G>A maps to NM_018928.2 T630T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr5:140865165 T>C maps to NM_018928.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140866222 C>T maps to NM_018928.2 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr5:140870658 C>T maps to NM_018929.2 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:140870105 C>T maps to NM_018929.2 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:140870567 C>A maps to NM_018929.2 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr5:140870981 G>A maps to NM_018929.2 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:140870543 C>T maps to NM_018929.2 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:140869592 C>T maps to NM_018929.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr5:140870696 A>G maps to NM_018929.2 T630T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:120409609 C>T maps to NM_001029996.3 F507F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:120369264 C>T maps to NM_001029996.3 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr2:120369227 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:120385250 C>T maps to NM_001029996.3 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:120383217 G>A maps to NM_001029996.3 E204E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:120385304 G>A maps to NM_001029996.3 K245K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr2:120362781 A>G maps to NM_001029996.3 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:120383232 G>A maps to NM_001029996.3 K209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:120369296 G>A maps to NM_001029996.3 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:120387521 C>T maps to NM_001029996.3 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr11:82877447 C>T maps to NM_015885.3 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr11:82868660 C>T maps to NM_015885.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:82879497 C>T maps to NM_015885.3 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:82880376 C>T maps to NM_015885.3 V1000V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr11:82880147 C>G maps to NM_015885.3 S924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:82880377 C>T maps to NM_015885.3 Q1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:74733311 C>T maps to NM_032673.2 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr17:36895319 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:36894822 G>A maps to NM_007144.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr13:113835475 G>A maps to ENST00000246505 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr13:113838774 G>A maps to ENST00000246505 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr20:44569572 C>T maps to NM_022104.3 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr20:56139562 G>A maps to NM_002591.3 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr20:56136487 C>T maps to NM_002591.3 N7N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr20:56140120 C>T maps to NM_002591.3 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr20:56139562 G>A maps to NM_002591.3 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr20:56140646 C>T maps to NM_002591.3 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:56139562 G>A maps to NM_002591.3 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:56140547 G>A maps to NM_002591.3 K519K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr20:56140565 C>T maps to NM_002591.3 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr20:56137869 G>A maps to NM_002591.3 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr20:56140096 T>A maps to NM_002591.3 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr20:56138724 C>G maps to NM_002591.3 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr20:56140832 C>T maps to NM_002591.3 A614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr20:56137860 C>T maps to NM_002591.3 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr20:56138105 C>T maps to NM_002591.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr20:56138760 C>T maps to NM_002591.3 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:56140523 C>T maps to NM_002591.3 I511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr20:56137165 C>T maps to NM_002591.3 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:56138688 G>A maps to NM_002591.3 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:56140523 C>T maps to NM_002591.3 I511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr20:56138730 G>A maps to NM_002591.3 W303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr20:56140853 G>A maps to NM_002591.3 Q621Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr20:56137914 C>T maps to NM_002591.3 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr14:24566226 C>T maps to NM_004563.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr7:82538320 G>A maps to NM_033026.5 L4437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr7:82581592 G>A maps to NM_033026.5 I2892I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr7:82764398 G>A maps to NM_033026.5 R823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:82474747 G>A maps to NM_033026.5 Q4629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr7:82581190 A>G maps to NM_033026.5 T3026T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr7:82580213 G>A maps to NM_033026.5 R3230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr7:82585450 C>T maps to NM_033026.5 G1606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr7:82785302 C>T maps to NM_033026.5 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:82579667 C>T maps to NM_033026.5 K3412K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:82580150 G>A maps to NM_033026.5 I3251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr7:82595500 C>T maps to NM_033026.5 E1201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr7:82584642 T>A maps to NM_033026.5 K1876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr7:82595632 C>T maps to NM_033026.5 V1157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr7:82763772 C>T maps to NM_033026.5 K1031K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr7:82580558 C>T maps to NM_033026.5 V3115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr7:82585180 C>T maps to NM_033026.5 E1696E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:82785575 C>T maps to NM_033026.5 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr7:82390044 C>T maps to NM_033026.5 K5066K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:82389989 G>A maps to NM_033026.5 R5085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:82538282 C>T maps to NM_033026.5 R4449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:82584274 C>T maps to NM_033026.5 Q1998Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr7:82545690 G>A maps to NM_033026.5 Q3871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr7:82585470 T>A maps to NM_033026.5 K1600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr7:82764423 G>A maps to NM_033026.5 S814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:82580167 G>A maps to NM_033026.5 R3246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:82584292 C>T maps to NM_033026.5 K1992K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:82579262 T>C maps to NM_033026.5 V3547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:82532039 C>T maps to NM_033026.5 G4485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:82544026 G>A maps to NM_033026.5 F4425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:82544602 C>T maps to NM_033026.5 R4233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:82764180 G>A maps to NM_033026.5 S895S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:82580372 C>T maps to NM_033026.5 T3177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:82764150 G>A maps to NM_033026.5 F905F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:82785167 C>T maps to NM_033026.5 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:82544593 G>A maps to NM_033026.5 L4236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:82545064 G>A maps to NM_033026.5 L4079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr7:82546171 G>A maps to NM_033026.5 T3710T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr7:82584100 C>T maps to NM_033026.5 R2056R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:82579778 G>A maps to NM_033026.5 T3375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr7:82584825 G>A maps to NM_033026.5 R1815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr7:82545019 G>A maps to NM_033026.5 F4094F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr7:82585207 T>C maps to NM_033026.5 K1687K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr7:82580555 C>T maps to NM_033026.5 R3116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:82545019 G>A maps to NM_033026.5 F4094F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:82580134 A>G maps to NM_033026.5 L3257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:82785563 G>A maps to NM_033026.5 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr7:82579079 G>A maps to NM_033026.5 S3608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr7:82583280 G>A maps to NM_033026.5 R2330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr7:82784602 G>A maps to NM_033026.5 Q452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:82545019 G>A maps to NM_033026.5 F4094F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:82595632 C>T maps to NM_033026.5 V1157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:82595440 G>A maps to NM_033026.5 I1221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:82785053 T>C maps to NM_033026.5 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr7:82582543 G>A maps to NM_033026.5 S2575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr7:82582183 G>A maps to NM_033026.5 S2695S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:82581415 C>T maps to NM_033026.5 R2951R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr7:82585033 C>T maps to NM_033026.5 P1745P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr7:82585783 C>T maps to NM_033026.5 E1495E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr7:82764633 C>T maps to NM_033026.5 Q744Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:82764398 G>A maps to NM_033026.5 R823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:82785101 C>T maps to NM_033026.5 Q285Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:82585843 C>T maps to NM_033026.5 R1475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr7:82784257 G>A maps to NM_033026.5 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:82476561 C>T maps to NM_033026.5 G4552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:82545448 C>T maps to NM_033026.5 Q3951Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:82584100 C>T maps to NM_033026.5 R2056R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr7:82457227 C>T maps to NM_033026.5 W4768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr7:82579778 G>A maps to NM_033026.5 T3375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:82388007 C>T maps to NM_033026.5 G5104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:82579733 G>A maps to NM_033026.5 I3390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr7:82579499 C>T maps to NM_033026.5 V3468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr7:82784477 C>T maps to NM_033026.5 Q493Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr7:82580168 G>A maps to NM_033026.5 F3245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr7:82579433 C>T maps to NM_033026.5 R3490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr7:82583365 C>T maps to NM_033026.5 V2301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr7:82585078 G>A maps to NM_033026.5 S1730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr7:82545685 G>A maps to NM_033026.5 T3872T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr7:82585612 C>T maps to NM_033026.5 E1552E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr7:82764657 T>C maps to NM_033026.5 K736K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr7:82785401 G>A maps to NM_033026.5 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr7:82583808 G>A maps to NM_033026.5 Q2154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr7:82784660 C>T maps to NM_033026.5 K432K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr7:82545738 G>A maps to NM_033026.5 R3855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr7:82579457 C>T maps to NM_033026.5 W3482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr7:82580576 G>A maps to NM_033026.5 S3109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr7:82583449 G>A maps to NM_033026.5 I2273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr7:82545808 A>G maps to NM_033026.5 R3831R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr7:82581310 C>T maps to NM_033026.5 G2986G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr7:82582165 C>T maps to NM_033026.5 E2701E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:82763745 A>T maps to NM_033026.5 P1040P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr7:82582357 C>T maps to NM_033026.5 Q2637Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr7:82455958 C>T maps to NM_033026.5 L4787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr7:82586110 C>T maps to NM_033026.5 K1386K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr7:82585752 T>G maps to NM_033026.5 R1506R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:82467538 C>T maps to NM_033026.5 G4739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:82545018 G>A maps to NM_033026.5 L4095L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:82578908 G>A maps to NM_033026.5 P3665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:82578962 G>A maps to NM_033026.5 L3647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:82584931 C>T maps to NM_033026.5 L1779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:82585474 C>T maps to NM_033026.5 K1598K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:82595398 G>A maps to NM_033026.5 L1235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:82785260 C>T maps to NM_033026.5 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr7:82584436 C>T maps to NM_033026.5 E1944E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:82430891 C>T maps to NM_033026.5 Q4983Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:82545859 C>T maps to NM_033026.5 K3814K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:82585210 C>T maps to NM_033026.5 Q1686Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:82763877 C>T maps to NM_033026.5 V996V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr7:82453630 G>A maps to NM_033026.5 S4839S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr7:82581796 G>A maps to NM_033026.5 L2824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr7:82585618 C>T maps to NM_033026.5 G1550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr7:82784309 G>A maps to NM_033026.5 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:17871516 C>T maps to NM_006197.3 V1852V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr8:17883058 C>T maps to NM_006197.3 L1981L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr8:17863887 A>G maps to NM_006197.3 Q1648Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:17823919 C>T maps to NM_006197.3 F1053F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:17819628 C>T maps to NM_006197.3 T803T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:52733156 C>T maps to NM_052937.2 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr8:52732985 T>C maps to NM_052937.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr20:62904951 A>T maps to NM_018257.2 *362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:62904718 C>T maps to NM_018257.2 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr20:5099320 G>A maps to NM_002592.2 Q108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr20:5100228 G>A maps to NM_002592.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:101311500 C>T maps to NM_020357.1 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:101311500 C>T maps to NM_020357.1 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr21:47775380 C>T maps to NM_006031.5 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr21:47783510 G>A maps to NM_006031.5 E757E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr21:47805829 G>A maps to NM_006031.5 R1132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr21:47831554 C>T maps to NM_006031.5 I1856I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr21:47860046 C>T maps to NM_006031.5 L3109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr21:47821562 G>A maps to NM_006031.5 S1630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr21:47831554 C>T maps to NM_006031.5 I1856I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr21:47831555 C>T maps to NM_006031.5 Q1857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr21:47819661 C>T maps to NM_006031.5 L1581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr21:47831638 G>A maps to NM_006031.5 K1884K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr21:47860832 G>A maps to NM_006031.5 K3153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr21:47832827 C>T maps to NM_006031.5 T2024T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr21:47744192 G>A maps to NM_006031.5 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr21:47817389 C>T maps to NM_006031.5 N1476N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr21:47754534 C>T maps to NM_006031.5 H164H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr21:47831941 C>T maps to NM_006031.5 S1985S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr21:47831872 C>T maps to NM_006031.5 P1962P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr21:47836464 C>T maps to NM_006031.5 P2211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr21:47819662 C>T maps to NM_006031.5 Q1582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr21:47783489 G>A maps to NM_006031.5 T750T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr21:47835984 T>C maps to NM_006031.5 G2051G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr21:47847570 C>T maps to NM_006031.5 D2452D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr21:47831714 C>T maps to NM_006031.5 L1910L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr21:47864621 A>G maps to NM_006031.5 P3285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr21:47831638 G>A maps to NM_006031.5 K1884K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CC-06A-11D-A19A-08 chr14:71572020 G>T maps to NM_014982.2 G2055G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:71575514 C>T maps to NM_014982.2 Q2166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Z-06A-11D-A196-08 chr14:71540340 T>C maps to NM_014982.2 P1644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:71555959 C>T maps to NM_014982.2 F1830F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr14:71576564 C>T maps to NM_014982.2 I2313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:71443821 C>T maps to NM_014982.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr14:71518711 C>T maps to NM_014982.2 F1520F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:71428978 C>T maps to NM_014982.2 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:71543006 C>T maps to NM_014982.2 V1736V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:71543099 C>T maps to NM_014982.2 L1767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr14:71575702 C>T maps to NM_014982.2 N2228N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr14:71542943 G>A maps to NM_014982.2 E1715E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:71543096 C>T maps to NM_014982.2 Y1766Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr14:71575606 C>T maps to NM_014982.2 S2196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr14:71568759 C>T maps to NM_014982.2 A1881A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:71485758 C>T maps to NM_014982.2 V1010V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:71511996 C>T maps to NM_014982.2 R1339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:71575493 C>T maps to NM_014982.2 R2159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:233394692 C>T maps to NM_014801.3 Q305Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:233296140 G>A maps to NM_014801.3 A1135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:233225829 C>T maps to NM_014801.3 V1351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:233270914 G>A maps to NM_014801.3 I1227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr1:233122098 G>A maps to NM_014801.3 S1993S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:233231575 G>A maps to NM_014801.3 L1291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:233313565 C>T maps to NM_014801.3 K1085K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:233398768 C>T maps to NM_014801.3 K98K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:233297092 C>T maps to NM_014801.3 W1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:233394137 C>T maps to NM_014801.3 W490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:233398891 C>T maps to NM_014801.3 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr1:233344345 G>A maps to NM_014801.3 A927A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:233134933 C>T maps to NM_014801.3 G1840G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:233152690 T>C maps to NM_014801.3 Q1605Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:233296050 C>T maps to NM_014801.3 E1165E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:233394845 C>T maps to NM_014801.3 K254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:233134870 C>T maps to NM_014801.3 W1861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:233275578 G>A maps to NM_014801.3 F1180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:233134018 G>A maps to NM_014801.3 S1923S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr1:233152876 C>T maps to NM_014801.3 T1543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:233270785 G>A maps to NM_014801.3 F1270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:233394211 G>A maps to NM_014801.3 Q466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:233122149 C>A maps to NM_014801.3 L1976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:233394617 G>A maps to NM_014801.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:233394590 C>T maps to NM_014801.3 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:233225829 C>T maps to NM_014801.3 V1351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr1:233152678 C>T maps to NM_014801.3 R1609R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr1:233334684 C>T maps to NM_014801.3 K1022K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:233161125 C>T maps to NM_014801.3 R1457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:233394725 G>A maps to NM_014801.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:233394983 C>T maps to NM_014801.3 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:233275578 G>A maps to NM_014801.3 F1180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:233134072 C>T maps to NM_014801.3 Q1905Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr1:233160981 G>A maps to NM_014801.3 I1505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:233134125 C>A maps to NM_014801.3 G1888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:233190031 G>A maps to NM_014801.3 R1445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:233270845 G>A maps to NM_014801.3 F1250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:233275578 G>A maps to NM_014801.3 F1180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:233296027 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:233297092 C>T maps to NM_014801.3 W1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:233335966 G>A maps to NM_014801.3 F969F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:233372590 C>T maps to NM_014801.3 R786R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:233372722 C>T maps to NM_014801.3 E742E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:233394086 C>T maps to NM_014801.3 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:233190031 G>A maps to NM_014801.3 R1445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr11:65396094 C>T maps to NM_032223.2 F1244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:65396305 C>T maps to NM_032223.2 F1276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:65392944 C>T maps to NM_032223.2 P1033P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:65385972 C>T maps to NM_032223.2 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:65396320 C>T maps to NM_032223.2 L1281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:65385972 C>T maps to NM_032223.2 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr11:65396094 C>T maps to NM_032223.2 F1244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:65396365 C>T maps to NM_032223.2 A1296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr7:100204224 G>A maps to NM_002593.3 E304E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:142607684 G>A maps to NM_013363.3 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:142567293 G>A maps to NM_013363.3 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:142537227 G>A maps to NM_013363.3 F399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:142542440 C>T maps to NM_013363.3 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr3:142561822 G>A maps to NM_013363.3 D172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr21:41301011 G>A maps to NM_006198.2 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr21:41301005 C>T maps to NM_006198.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr21:41301005 C>T maps to NM_006198.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr21:41300985 C>T maps to NM_006198.2 Q47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr1:161254231 C>T maps to NM_001102566.1 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr5:95728986 C>T maps to NM_000439.4 E660E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr5:95761619 T>C maps to NM_000439.4 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:95761541 C>T maps to NM_000439.4 W126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr5:95730585 C>T maps to NM_000439.4 K622K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr5:95735808 C>T maps to NM_000439.4 W426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr5:95746678 C>T maps to NM_000439.4 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:95735808 C>T maps to NM_000439.4 W426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:95746663 G>A maps to NM_000439.4 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:95746477 G>A maps to NM_000439.4 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr5:95729010 C>T maps to NM_000439.4 G652G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr5:95746537 C>T maps to NM_000439.4 E345E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr5:95733108 C>T maps to NM_000439.4 W551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:95734735 G>A maps to NM_000439.4 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:95734736 G>A maps to NM_000439.4 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr5:95728974 G>A maps to NM_000439.4 S664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:95728850 T>A maps to NM_000439.4 K706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr5:95735891 T>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:95764943 G>A maps to NM_000439.4 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:95746552 G>A maps to NM_000439.4 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:95746651 C>T maps to NM_000439.4 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr20:17434547 C>T maps to NM_002594.2 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:17446090 C>T maps to NM_002594.2 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:17462537 G>A maps to NM_002594.2 Q580Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:17434577 G>A maps to NM_002594.2 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:1487052 C>T maps to NM_017573.3 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr9:78641899 G>A maps to NM_001190482.1 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr9:78784739 G>A maps to NM_001190482.1 R580R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr9:78796370 G>A maps to NM_001190482.1 R687R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr9:78711012 A>T maps to NM_001190482.1 K368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr9:78799587 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:78749102 G>A maps to NM_001190482.1 W429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:78547380 C>T maps to NM_001190482.1 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:78601054 G>A maps to NM_001190482.1 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:78638697 C>T maps to NM_001190482.1 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:78784739 G>A maps to NM_001190482.1 R580R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr9:78804603 C>T maps to NM_001190482.1 C856C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr9:78808171 G>A maps to NM_006200.3 A882A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr9:78784739 G>A maps to NM_001190482.1 R580R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr9:78547380 C>T maps to NM_001190482.1 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr9:78804139 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:78547308 G>A maps to NM_001190482.1 K69K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:78796446 C>T maps to NM_001190482.1 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr9:78804139 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr9:78804037 C>A maps to NM_001190482.1 C803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:78794542 C>T maps to NM_001190482.1 G644G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr9:78547338 G>A maps to NM_001190482.1 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr15:101933622 G>A maps to NM_002570.3 Q334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr15:101929706 G>A maps to NM_002570.3 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:101858554 C>T maps to NM_002570.3 G845G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:101905175 G>A maps to NM_138325.2 F643F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr15:101983762 G>A maps to NM_002570.3 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr15:101853489 G>A maps to NM_138320.1 A929A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:101865214 C>T maps to NM_002570.3 G738G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:101865229 G>A maps to NM_002570.3 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:101971536 C>T maps to NM_002570.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr11:117100224 G>A maps to NM_004716.2 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:117089787 G>A maps to NM_004716.2 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:117089802 G>A maps to NM_004716.2 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:117100448 G>A maps to NM_004716.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr11:117100313 G>A maps to NM_004716.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:55521729 C>T maps to NM_174936.3 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:55505575 C>T maps to NM_174936.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:55525298 C>T maps to NM_174936.3 T548T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:55518041 C>T maps to NM_174936.3 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr1:55525202 G>A maps to NM_174936.3 G516G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr1:55518435 G>A maps to NM_174936.3 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:55512299 G>A maps to NM_174936.3 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:53851149 C>T maps to NM_021213.3 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:53852168 C>T maps to NM_021213.3 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr5:148743681 C>T maps to NM_024028.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:148743656 C>T maps to NM_024028.3 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr5:148742245 C>T maps to NM_024028.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:195965645 G>A maps to NM_005017.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:195975102 G>A maps to NM_005017.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr3:195965606 G>A maps to NM_005017.2 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:24597495 A>C did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:24625907 A>G did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:24637165 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:24608150 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr23:24605401 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:24608155 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:24637201 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:24608279 C>A did not map to a codon.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr23:24625971 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:24580540 T>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:24608225 C>T did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:24665155 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr17:79864636 G>A maps to NM_001184917.1 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr17:79864053 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:79863006 G>A maps to NM_001184917.1 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:186413500 C>T maps to ENST00000340129 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:186415665 C>T maps to ENST00000340129 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:242794826 G>A maps to NM_005018.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:167405097 C>A maps to NM_145859.1 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr10:105177553 G>A maps to NM_014976.1 V592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr10:105187112 C>T maps to NM_014976.1 F1111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:105184907 C>T maps to NM_014976.1 S977S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr10:105184766 G>A maps to NM_014976.1 A930A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr10:105203820 G>A maps to NM_014976.1 K1758K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr10:105184742 G>A maps to NM_014976.1 L922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr10:105179416 C>A maps to NM_014976.1 G743G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:105174065 C>T maps to NM_014976.1 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:105162876 C>T maps to NM_014976.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:170892151 C>T maps to NM_002598.3 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:34900063 A>G did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:34912483 C>T maps to NM_032346.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:112645009 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr5:271858 C>T maps to NM_013232.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr3:33868068 C>T maps to NM_001162429.1 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:33877621 C>G maps to NM_001162429.1 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:33893999 C>T maps to NM_001162429.1 S559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:125582720 G>A maps to NM_005388.4 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr9:125582720 G>T maps to NM_005388.4 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:56428589 C>T maps to NM_152401.2 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr11:771390 G>A maps to NM_182612.2 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:773624 G>A maps to NM_182612.2 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr6:165863796 T>C maps to NM_001130690.1 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr6:165846587 C>T maps to NM_001130690.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr6:165827141 C>T maps to NM_001130690.1 R375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr6:165746616 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:165801864 G>A maps to NM_001130690.1 F578F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr6:165832184 G>A maps to NM_001130690.1 D312D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:178879163 G>A maps to NM_016953.3 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:178494140 C>T maps to NM_016953.3 R932R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:178494269 C>T maps to NM_016953.3 V889V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:178534250 C>T maps to NM_016953.3 R844R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:178769881 G>A maps to NM_016953.3 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:178936258 G>A maps to NM_016953.3 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:178936630 C>T maps to NM_016953.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr3:57542495 G>A maps to NM_177966.5 E130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr3:57543411 C>T maps to NM_177966.5 Q436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:183070692 C>T maps to NM_005019.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:183094849 G>A maps to NM_005019.3 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:183070749 C>T maps to NM_005019.3 E289E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:183050709 G>A maps to NM_005019.3 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:183104925 C>T maps to NM_005019.3 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:183066171 G>A maps to NM_005019.3 F389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:183050709 G>A maps to NM_005019.3 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr2:183066286 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:183095837 G>A maps to NM_005019.3 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:183066171 G>A maps to NM_005019.3 F389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:183104877 C>T maps to NM_005019.3 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:183104895 C>T maps to NM_005019.3 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:183104954 G>T maps to NM_005019.3 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr12:54969375 C>T maps to NM_000924.3 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:54966503 C>T maps to NM_000924.3 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr12:54943751 G>A maps to NM_000924.3 W32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:54963329 G>A maps to NM_000924.3 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:54968956 C>T maps to NM_000924.3 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:54968986 G>A maps to NM_000924.3 E390E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:54969363 C>T maps to NM_000924.3 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr12:54971042 C>T maps to NM_000924.3 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:54967153 C>T maps to NM_000924.3 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:54963141 C>T maps to NM_000924.3 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:54971042 C>T maps to NM_000924.3 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr7:32109933 G>A maps to NM_001191057.1 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr7:31890259 C>T maps to NM_001191057.1 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:31877506 C>T maps to NM_001191057.1 K353K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr7:32091192 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr7:31864596 G>A maps to NM_001191057.1 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:31918726 G>A maps to NM_001191057.1 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:31855583 C>T maps to NM_001191057.1 G589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr7:31890331 G>A maps to NM_001191057.1 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:32109930 C>T maps to NM_001191057.1 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:31918628 C>T maps to NM_001191057.1 Q135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:31864524 G>A maps to NM_001191057.1 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:31864482 C>T maps to NM_001191057.1 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:31918622 C>T maps to NM_001191057.1 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:31890268 G>A maps to NM_001191057.1 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:31864596 G>A maps to NM_001191057.1 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:31862735 C>T maps to NM_001191057.1 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr7:31887693 G>A maps to NM_001191057.1 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:32091188 C>T maps to NM_001191057.1 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:31877577 G>A maps to NM_001191057.1 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr7:31862789 C>T maps to NM_001191057.1 P493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:32109987 C>T maps to NM_001191057.1 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr7:32091188 C>T maps to NM_001191057.1 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr7:31862771 G>A maps to NM_001191057.1 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:31864569 G>A maps to NM_001191057.1 F439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:31876799 G>A maps to NM_001191057.1 F399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:31876827 C>T maps to NM_001191057.1 W390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:31920406 C>T maps to NM_001191057.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:32109933 G>A maps to NM_001191057.1 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:31890253 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:31855718 C>T maps to NM_001191057.1 E544E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr7:31864515 G>A maps to NM_001191057.1 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:72288507 G>A maps to NM_002599.3 L916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr11:72289952 C>T maps to NM_002599.3 T819T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr11:72292004 G>A maps to NM_002599.3 I686I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:72296628 G>A maps to NM_002599.3 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:72289952 C>G maps to NM_002599.3 T819T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr11:72297155 G>A maps to NM_002599.3 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:72290352 G>A maps to NM_002599.3 F777F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr12:20833090 G>A maps to NM_000921.3 L1104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr12:20786683 G>A maps to NM_000921.3 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:20774241 G>A maps to NM_000921.3 W479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr12:20833082 C>T maps to NM_000921.3 Q1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:20799790 G>A maps to NM_000921.3 L824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:20832982 G>A maps to NM_000921.3 R1068R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr12:20766444 C>T maps to NM_000921.3 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr12:20766633 G>A maps to NM_000921.3 K423K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:20782848 C>T maps to NM_000921.3 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:20801752 C>T maps to NM_000921.3 F899F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr12:20799775 G>A maps to NM_000921.3 G819G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr11:14808176 C>T maps to NM_000922.3 Y408Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:14840738 C>T maps to NM_000922.3 C597C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:14891082 G>A maps to NM_000922.3 W1072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr19:10568588 G>A maps to NM_001111307.1 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr19:10574557 C>T maps to NM_001111307.1 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr19:10574566 C>T maps to NM_001111307.1 F614F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:10568681 C>T maps to NM_001111307.1 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:10578041 C>T maps to NM_001111307.1 F802F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:10577708 C>T maps to NM_001111307.1 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr19:10578248 C>T maps to NM_001111307.1 S871S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr19:10574551 C>T maps to NM_001111307.1 I609I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:10541624 C>A maps to NM_001111308.1 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:66713310 G>A maps to NM_001037341.1 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:66838169 C>T maps to NM_001037341.1 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:66384347 C>T maps to NM_001037341.1 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:66384347 C>T maps to NM_001037341.1 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:66829100 C>T maps to NM_001037341.1 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:66829100 C>T maps to NM_001037341.1 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr19:18332976 C>T maps to NM_000923.3 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr19:18333018 G>A maps to NM_000923.3 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:18324246 G>A maps to NM_000923.3 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:18321933 G>A maps to NM_000923.3 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr19:18330169 A>T maps to NM_000923.3 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:18331233 C>T maps to NM_000923.3 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr19:18333099 C>T maps to NM_000923.3 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr19:18324185 G>T maps to NM_000923.3 R534R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:18330166 C>T maps to NM_000923.3 E281E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:18331126 G>A maps to NM_000923.3 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:18331248 C>T maps to NM_000923.3 Q224Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:18329176 G>A maps to NM_000923.3 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr5:58511676 G>A maps to NM_001104631.1 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:58271612 G>A maps to NM_001104631.1 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr1:144918964 T>A maps to NM_014644.4 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:144852489 G>A maps to NM_014644.4 L2337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:144879432 C>T maps to NM_014644.4 Q1339Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:144918871 G>A maps to NM_014644.4 H438H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:144882664 G>A maps to NM_014644.4 L1118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:145015919 G>A maps to NM_001198832.1 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:144863440 G>A maps to NM_014644.4 L1988L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:144917868 A>G maps to NM_014644.4 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:144882703 G>A maps to NM_014644.4 L1105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:144879495 G>A maps to NM_014644.4 R1318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:144854638 C>T maps to NM_014644.4 R2277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:144859816 G>A maps to NM_014644.4 S2089S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:144923701 C>T maps to NM_014644.4 E252E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:144874725 C>A maps to NM_014644.4 E1628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:144864154 G>A maps to NM_014644.4 S1980S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:144867969 C>T maps to NM_014644.4 G1823G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:144864150 G>A maps to NM_014644.4 Q1982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:144946720 C>T maps to NM_014644.4 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:144882799 G>A maps to NM_014644.4 I1073I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:144867987 C>T maps to NM_014644.4 Q1817Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:144916679 G>A maps to NM_014644.4 Q559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:144879264 G>A maps to NM_014644.4 P1395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr1:144917887 G>A maps to NM_014644.4 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:144882454 A>G maps to NM_014644.4 D1188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:144886116 G>A maps to NM_014644.4 F1039F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:145075736 G>A maps to NM_022359.5 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr1:145015919 G>A maps to NM_001198832.1 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:144918897 G>A maps to NM_014644.4 R430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:144856916 G>A maps to NM_014644.4 L2190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr4:120528040 G>A maps to NM_001083.3 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr4:120419757 A>G maps to NM_001083.3 *876R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr4:120463729 G>A maps to NM_001083.3 R486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr5:149262996 G>A maps to NM_000440.2 I710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:149276014 G>A maps to NM_000440.2 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:149324044 G>A maps to NM_000440.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr5:149286901 G>A maps to NM_000440.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr5:149324128 G>A maps to NM_000440.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:149263074 G>A maps to NM_000440.2 I684I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:149274850 G>A maps to NM_000440.2 A541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:149323975 G>A maps to NM_000440.2 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr4:657926 C>T maps to NM_000283.3 I682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr4:651249 G>A maps to NM_000283.3 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:657902 G>A maps to NM_000283.3 K674K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr4:651210 C>T maps to NM_000283.3 N443N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr4:619504 G>A maps to NM_000283.3 E30E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr4:654257 G>A maps to NM_000283.3 K490K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr4:658004 C>T maps to NM_000283.3 I708I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr4:659045 C>T maps to NM_000283.3 V732V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr4:650078 C>T maps to NM_000283.3 Q369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr4:619540 G>A maps to NM_000283.3 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr4:628566 C>T maps to NM_000283.3 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:619828 C>T maps to NM_000283.3 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:629673 C>T maps to NM_000283.3 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:652760 G>A maps to NM_000283.3 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr4:619804 C>T maps to NM_000283.3 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr10:95400235 G>A maps to NM_006204.3 R553R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr10:95380649 C>T maps to NM_006204.3 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:95372904 G>A maps to NM_006204.3 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr10:95372778 C>T maps to NM_006204.3 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:95380679 C>T maps to NM_006204.3 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:95386416 C>T maps to NM_006204.3 I320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:95400675 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr10:95380489 C>T maps to NM_006204.3 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:95385363 A>T maps to NM_006204.3 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:95400235 G>A maps to NM_006204.3 R553R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr10:95372613 C>T maps to NM_006204.3 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:95400220 G>A maps to NM_006204.3 W548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:95380734 C>T maps to NM_006204.3 Q241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:95372853 G>A maps to NM_006204.3 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:95380459 C>T maps to NM_006204.3 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr2:232602837 G>A maps to NM_002601.2 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr17:79620251 A>G maps to ENST00000331056 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:15134400 G>A maps to NM_006205.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr6:136475306 G>A maps to NM_018945.3 E191E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:136502372 G>A maps to NM_018945.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:136502373 A>T maps to NM_018945.3 K320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ES-06A-11D-A20D-08 chr6:136476823 C>T maps to NM_018945.3 H213H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr6:136500191 G>A maps to NM_018945.3 Q287Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:136476859 G>A maps to NM_018945.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr15:85661060 G>A maps to NM_002605.2 E575E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr15:85657156 A>G maps to NM_002605.2 E413E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr15:85666318 G>T maps to NM_002605.2 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:76700599 G>A maps to NM_003719.3 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:76721605 G>A maps to NM_003719.3 K811K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr5:76627229 G>A maps to NM_003719.3 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr5:76645266 G>A maps to NM_003719.3 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:76715590 G>T did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr5:76621383 G>A maps to NM_003719.3 K140K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr21:44171280 C>T maps to NM_002606.2 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr21:44174107 C>T maps to NM_002606.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr22:39626233 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr22:39631876 C>T maps to NM_002608.2 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr22:39627770 G>A maps to NM_002608.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr22:39621781 C>T maps to NM_002608.2 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:39629527 C>T maps to NM_002608.2 E54E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr4:157689053 C>T maps to NM_016205.2 K264K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:157771462 C>T maps to NM_016205.2 W75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:157771500 C>T maps to NM_016205.2 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr4:157771500 C>T maps to NM_016205.2 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr11:103780426 G>A maps to NM_025208.4 R370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr11:103814204 C>T maps to NM_025208.4 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr11:103797714 T>A maps to NM_025208.4 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:103866849 G>A maps to NM_025208.4 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:55140785 G>A maps to NM_006206.4 W549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:55155062 A>G maps to ENST00000507166 E684E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr4:55139808 C>T maps to NM_006206.4 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:55127442 C>T maps to NM_006206.4 N77N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:55129978 C>T maps to NM_006206.4 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:55156544 G>A maps to ENST00000507166 V742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr4:55139829 C>T maps to NM_006206.4 I497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:55129832 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:55133824 G>A maps to NM_006206.4 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr4:55154999 T>C maps to ENST00000507166 S663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr4:55136798 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:55139808 C>T maps to NM_006206.4 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr4:55152069 C>T maps to ENST00000507166 I594I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr5:149511643 G>A maps to NM_002609.3 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr5:149511572 C>T maps to NM_002609.3 E404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:149497275 G>A maps to NM_002609.3 P1014P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr5:149498405 G>A maps to NM_002609.3 I936I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:149497197 A>C maps to NM_002609.3 G1040G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:149513467 G>A maps to NM_002609.3 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:149509531 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr5:149505122 G>A maps to NM_002609.3 I564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr5:149495376 C>T maps to NM_002609.3 P1090P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr5:149501581 C>T maps to NM_002609.3 E735E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:149499581 G>A maps to NM_002609.3 F897F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:149506169 G>A maps to NM_002609.3 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:149509437 C>T maps to NM_002609.3 Q487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:149513290 G>A maps to NM_002609.3 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:149506145 G>A maps to NM_002609.3 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr8:17447049 G>A maps to NM_006207.2 K43K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:17491703 G>A maps to NM_006207.2 W307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:17500138 G>A maps to NM_006207.2 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr8:17491610 C>T maps to NM_006207.2 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:19368087 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:19369386 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:19373503 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr23:19373554 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:19377729 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:19377617 G>T did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr4:96761520 T>C maps to NM_005390.4 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr4:96761471 G>T maps to NM_005390.4 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr4:96761936 G>A maps to NM_005390.4 W212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:96761321 C>T maps to NM_005390.4 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:96762041 C>T maps to NM_005390.4 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:96761621 C>T maps to NM_005390.4 N107N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:58417665 C>A maps to NM_000925.3 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:34991823 C>T maps to NM_003477.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr16:335409 G>A maps to NM_006849.2 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:336884 G>A maps to NM_006849.2 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:335681 A>G maps to NM_006849.2 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:333321 C>T maps to NM_006849.2 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr15:44053691 T>C maps to NM_005313.4 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:44055281 C>T maps to NM_005313.4 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:44053649 G>A maps to NM_005313.4 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:44062467 C>T maps to NM_005313.4 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr7:148701008 G>A maps to NM_004911.4 F605F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr7:148701083 G>A maps to NM_004911.4 I580I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr7:148716089 G>A maps to NM_004911.4 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr7:148716090 G>A maps to NM_004911.4 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:148702419 G>A maps to NM_004911.4 F445F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:148702428 G>A maps to NM_004911.4 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr7:148702401 G>A maps to NM_004911.4 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:148701263 G>T maps to NM_004911.4 P520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:148701260 C>T maps to NM_004911.4 K521K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr7:148701134 G>A maps to NM_004911.4 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:122849383 C>T maps to NM_006810.3 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr3:122842983 C>T maps to NM_006810.3 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:10937288 G>T maps to ENST00000381611 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:10929931 G>A maps to ENST00000381611 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:10927438 G>A maps to ENST00000381611 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr16:20376826 C>T maps to NM_174924.1 W384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:20380831 G>A maps to NM_174924.1 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr16:20380936 G>A maps to NM_174924.1 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr16:20384132 G>A maps to NM_174924.1 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:20380951 G>A maps to NM_174924.1 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:20376748 C>T maps to NM_174924.1 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr16:20384231 G>A maps to NM_174924.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr16:20376850 G>A maps to NM_174924.1 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr16:20387404 G>A maps to NM_174924.1 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr16:20381011 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr16:20396090 C>T maps to NM_174924.1 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:20384348 G>A maps to NM_174924.1 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr16:20387404 G>A maps to NM_174924.1 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:20376775 G>A maps to NM_174924.1 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:20387404 G>A maps to NM_174924.1 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:173460627 C>T maps to ENST00000392571 N434N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr17:48185984 C>T maps to NM_002611.3 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:48182767 C>T maps to NM_002611.3 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr23:24546234 C>T did not map to a codon.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr23:24521591 A>G did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:24521543 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:24523414 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:24549802 C>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:24549803 C>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:24517000 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr7:95222119 G>A maps to NM_002612.3 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:95222230 G>A maps to NM_002612.3 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:95224384 G>A maps to NM_002612.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:95222230 G>A maps to NM_002612.3 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr10:96997711 A>G maps to NM_020992.2 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:97028576 C>T maps to NM_020992.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:97006990 G>A maps to NM_020992.2 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:186435443 G>A maps to NM_014476.4 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:186427718 C>A maps to NM_014476.4 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:186429495 G>A maps to NM_014476.4 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr4:186456495 C>T maps to NM_014476.4 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:131607088 C>T maps to NM_003687.3 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr5:131607148 C>T maps to NM_003687.3 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr4:95583615 T>C maps to NM_006457.3 F543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr4:95575609 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:95494538 C>T maps to NM_006457.3 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:176915134 G>A maps to NM_005451.3 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:94934857 C>T maps to NM_001161778.1 Q250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr8:94935235 C>T maps to NM_001161778.1 Q376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr8:94935030 C>T maps to NM_001161778.1 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:94935498 C>T maps to NM_001161778.1 H463H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr8:94934463 G>A maps to NM_001161778.1 K118K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr16:66919775 A>G maps to NM_020786.2 *530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:66918540 C>T maps to NM_020786.2 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:66919224 G>A maps to NM_020786.2 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr16:66918892 C>T maps to NM_020786.2 Q236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:66919185 C>T maps to NM_020786.2 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:2636801 C>T maps to NM_002613.3 H417H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:2636723 C>T maps to NM_002613.3 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr1:13933737 C>G maps to NM_006474.4 A122A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-ER-A2ND-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr16:70190454 C>A maps to NM_017990.3 I771I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr16:70166092 G>A maps to NM_017990.3 W296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr16:70166105 C>T maps to NM_017990.3 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr16:70190388 C>T maps to NM_017990.3 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr16:70176284 C>T maps to NM_017990.3 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr16:70172810 C>T maps to NM_017990.3 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:70154550 C>T maps to NM_017990.3 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:39871031 G>A maps to NM_001100399.1 S829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:39929622 G>T maps to NM_001100399.1 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr4:39881416 C>T maps to NM_001100399.1 G641G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr4:39876032 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q3-06A-11D-A196-08 chr13:33268437 C>A maps to ENST00000400481 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr13:33332293 G>A maps to ENST00000400481 K1042K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr13:33261420 C>T maps to ENST00000400481 R452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr13:33327525 C>T maps to ENST00000400481 S931S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr13:33270998 C>T maps to ENST00000400481 A520A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr13:33344515 A>C maps to ENST00000400481 P1294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:26998698 T>G did not map to a codon.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr10:27009215 C>T maps to NM_014317.3 H179H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr6:107780384 C>T maps to NM_020381.3 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr6:107475897 G>A maps to NM_020381.3 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr13:28498645 C>T maps to NM_000209.3 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:28498597 G>A maps to NM_000209.3 E204E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr16:15098187 C>T maps to NM_015027.2 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr21:45168937 C>T maps to NM_003681.4 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr21:45173470 C>G maps to NM_003681.4 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:38061866 T>C maps to ENST00000442465 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr20:1961355 C>T maps to NM_024411.4 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:1961226 C>T maps to NM_024411.4 K169K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr20:1961244 G>A maps to NM_024411.4 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:1961235 C>T maps to NM_024411.4 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:1961115 G>A maps to NM_024411.4 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:1961397 G>A maps to NM_024411.4 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:1963715 C>T maps to NM_024411.4 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr20:1961562 C>T maps to NM_024411.4 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr5:32058183 C>T maps to NM_178140.2 I725I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr5:32090174 G>A maps to NM_178140.2 S2207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr5:32053901 C>T maps to NM_178140.2 R605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr5:32074046 C>T maps to NM_178140.2 L945L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr5:32053981 T>G maps to NM_178140.2 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr5:31983491 C>T maps to NM_178140.2 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:32088002 G>A maps to NM_178140.2 P1483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr5:32090402 G>A maps to NM_178140.2 L2283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr5:32058174 G>A maps to NM_178140.2 K722K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr5:32074433 G>A maps to NM_178140.2 W1074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:32087294 T>A maps to NM_178140.2 P1247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:32089223 C>T maps to NM_178140.2 L1890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:31983536 G>A maps to NM_178140.2 E251E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:32087273 G>A maps to NM_178140.2 G1240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:32087282 G>A maps to NM_178140.2 G1243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr5:32088005 G>A maps to NM_178140.2 R1484R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:32074472 G>A maps to NM_178140.2 L1087L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:32061117 C>T maps to NM_178140.2 Q777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:31799633 C>T maps to NM_178140.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:31799780 C>T maps to NM_178140.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:32090918 G>A maps to NM_178140.2 T2455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:31983419 G>A maps to NM_178140.2 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:32088467 G>A maps to NM_178140.2 P1638P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr5:31799633 C>T maps to NM_178140.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:32073986 G>A maps to NM_178140.2 G925G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr5:32087978 C>T maps to NM_178140.2 V1475V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:31983413 G>A maps to NM_178140.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr5:32088111 C>T maps to NM_178140.2 L1520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:32071493 C>T maps to NM_178140.2 T846T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:32087273 G>A maps to NM_178140.2 G1240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr5:31799633 C>T maps to NM_178140.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:119059485 C>T maps to ENST00000392817 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:119059486 C>T maps to ENST00000392817 R466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:119060200 G>A maps to ENST00000392817 *572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr23:153073990 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr23:153069985 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr23:153070592 C>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:153069940 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr23:153069984 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:153073941 G>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:153073942 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:153069973 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr23:153073825 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:153070216 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr23:153069218 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr23:153070561 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr23:153070562 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:153070123 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:153070249 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:153070965 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:153069132 G>A did not map to a codon.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr23:153069992 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:153068891 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr23:153069031 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr23:153070078 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr23:153071016 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:153072225 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:153069652 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:102781560 G>A maps to NM_001195263.1 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:102789775 G>A maps to NM_001195263.1 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr10:102783209 G>A maps to NM_001195263.1 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:102789949 G>A maps to NM_001195263.1 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr10:119043054 C>T maps to NM_173791.3 E1063E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr10:119044224 C>T maps to NM_173791.3 S673S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr10:119044790 A>G maps to NM_173791.3 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:119044644 G>A maps to NM_173791.3 P533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr10:119044941 G>A maps to NM_173791.3 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr10:119049714 G>A maps to NM_173791.3 R415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:119044545 G>A maps to NM_173791.3 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:145762275 A>T maps to NM_002614.3 K485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:47653013 G>A maps to NM_005764.3 N51N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:73433560 C>T maps to NM_015009.1 W719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:73432953 C>T maps to NM_015009.1 W921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:73433841 G>A maps to NM_015009.1 F625F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:73432572 T>C maps to NM_015009.1 T1048T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:73433157 C>T maps to NM_015009.1 Q853Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:73432518 T>A maps to NM_015009.1 V1066V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:41831770 C>T maps to NM_013377.3 Q9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr12:41967334 C>T maps to NM_001164595.1 I918I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:41961617 G>T maps to NM_001164595.1 E501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr12:41949534 G>A maps to NM_001164595.1 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:41966224 C>T maps to NM_001164595.1 N548N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:41957444 G>A maps to NM_001164595.1 E487E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:41966779 G>A maps to NM_001164595.1 K733K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr12:41966311 C>T maps to NM_001164595.1 P577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr12:41967415 G>A maps to NM_001164595.1 E945E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:41967283 C>T maps to NM_001164595.1 I901I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:41585334 C>T maps to NM_001164595.1 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:41900268 G>A maps to NM_001164595.1 K285K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:41961631 G>A maps to NM_001164595.1 E505E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:41966704 G>A maps to NM_001164595.1 R708R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:41967190 C>T maps to NM_001164595.1 L870L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:41967583 G>A maps to NM_001164595.1 K1001K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr12:41966398 C>T maps to NM_001164595.1 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:156879666 C>T maps to NM_001080471.1 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:156875115 G>A maps to NM_001080471.1 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr1:156876098 T>A maps to NM_001080471.1 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:156880482 G>A maps to NM_001080471.1 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:156882721 G>A maps to NM_001080471.1 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:156874578 C>T maps to NM_001080471.1 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:156874587 C>T maps to NM_001080471.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:156874632 C>T maps to NM_001080471.1 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:156882655 G>A maps to NM_001080471.1 V768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:156883007 C>T maps to NM_001080471.1 H815H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr1:156873747 C>T maps to NM_001080471.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr1:156880095 G>A maps to NM_001080471.1 K583K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr1:156873813 G>A maps to NM_001080471.1 W32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:156875148 G>A maps to NM_001080471.1 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr12:118582478 C>T maps to NM_002567.2 H145H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:22777792 C>T maps to NM_144962.2 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr8:22777732 C>T maps to NM_144962.2 W74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr8:22777733 C>T maps to NM_144962.2 W74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:22675179 G>A maps to NM_144962.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr6:4116157 C>A maps to NM_206836.2 E379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr2:216904054 C>T maps to NM_018441.5 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr2:216914080 G>A maps to NM_018441.5 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr2:216914081 G>A maps to NM_018441.5 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:216923646 G>A maps to NM_018441.5 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr1:32096300 G>A maps to NM_012392.3 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:32098174 G>A maps to NM_012392.3 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:32098207 G>A maps to NM_012392.3 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr7:94293523 C>T maps to NM_001172437.1 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr7:94293207 G>A maps to NM_001172437.1 *189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr19:57325465 C>T maps to NM_006210.2 G1448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr19:57327718 G>A maps to NM_006210.2 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr19:57328093 G>A maps to NM_006210.2 F572F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:57325195 G>A maps to NM_006210.2 A1538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:57325216 G>A maps to NM_006210.2 I1531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr19:57326050 C>T maps to NM_006210.2 L1253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:57326830 C>T maps to NM_006210.2 R993R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:57328837 G>A maps to NM_006210.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:57326278 G>A maps to NM_006210.2 F1177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:57325314 G>A maps to NM_006210.2 Q1499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr19:57326416 C>T maps to NM_006210.2 R1131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:57325126 C>T maps to NM_006210.2 E1561E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:57329129 G>A maps to NM_006210.2 Y282Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:57325060 C>T maps to NM_006210.2 Q1583Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:57326491 G>A maps to NM_006210.2 I1106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:57326575 G>A maps to NM_006210.2 T1078T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:57325216 G>A maps to NM_006210.2 I1531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:57325936 G>A maps to NM_006210.2 F1291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:57327957 G>A maps to NM_006210.2 Q618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr19:57325402 C>T maps to NM_006210.2 E1469E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr19:57327325 C>T maps to NM_006210.2 R828R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:57327994 C>T maps to NM_006210.2 G605G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:57334190 C>T maps to NM_006210.2 W165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr19:57328177 G>A maps to NM_006210.2 F544F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr19:57325237 C>T maps to NM_006210.2 L1524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr19:57330037 G>A maps to NM_006210.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr19:57326133 G>A maps to NM_006210.2 R1226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:57327955 C>T maps to NM_006210.2 Q618Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:57333045 G>A maps to NM_006210.2 D214D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:57328786 G>A maps to NM_006210.2 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:57334190 C>T maps to NM_006210.2 W165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr14:56755312 C>T maps to NM_021255.2 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr14:56755152 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr14:56757135 T>C maps to NM_021255.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr14:56757086 C>T maps to NM_021255.2 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:56763865 C>T maps to NM_021255.2 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:56763338 C>T maps to NM_021255.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr14:56763439 C>T maps to NM_021255.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr11:66239883 C>T maps to NM_145065.2 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:66241260 C>T maps to NM_145065.2 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:52096926 C>T maps to NM_015946.4 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:52096557 C>T maps to NM_015946.4 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:52096728 C>T maps to NM_015946.4 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:52096833 A>T maps to NM_015946.4 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr17:4576955 G>A maps to ENST00000301396 T676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:4576308 G>A maps to ENST00000301396 P803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:4576308 G>A maps to ENST00000301396 P803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:4578166 G>A maps to ENST00000301396 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr17:4578570 G>A maps to ENST00000301396 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr17:4575135 G>A maps to ENST00000301396 P1194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr17:4575321 G>A maps to ENST00000301396 P1132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:17409589 G>A maps to NM_148172.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr17:17425607 G>A maps to NM_148172.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:17425607 G>A maps to NM_148172.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr8:57354229 C>T maps to NM_001135690.1 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr8:57354175 G>A maps to NM_001135690.1 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:57354136 G>A maps to NM_001135690.1 N166N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr8:57354052 C>T maps to NM_001135690.1 K194K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:57354436 C>T maps to NM_001135690.1 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:57358377 G>A maps to NM_001135690.1 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr8:57354304 G>A maps to NM_001135690.1 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:57354067 G>A maps to NM_001135690.1 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:57354073 C>T maps to NM_001135690.1 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:57354217 G>A maps to NM_001135690.1 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:57358376 G>A maps to NM_001135690.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:33980918 G>A maps to NM_000285.3 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr19:33892681 G>A maps to NM_000285.3 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:34003557 G>A maps to NM_000285.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr17:8053141 G>A maps to NM_002616.2 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr17:8049411 C>T maps to NM_002616.2 R694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr17:8049420 G>A maps to NM_002616.2 A691A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:8045720 C>T maps to NM_002616.2 E1105E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:8049306 G>A maps to NM_002616.2 V729V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:8051092 G>A maps to NM_002616.2 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:8051348 C>T maps to NM_002616.2 E400E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr17:8052954 G>A maps to NM_002616.2 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr17:8049362 T>A maps to NM_002616.2 K711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:8049771 G>A maps to NM_002616.2 A652A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr17:8049753 G>A maps to NM_002616.2 T658T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr2:239165599 G>A maps to NM_022817.2 I676I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr2:239164310 C>T maps to NM_022817.2 Q769Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:239176772 C>T maps to NM_022817.2 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:239162200 G>A maps to NM_022817.2 P821P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:239162250 G>A maps to NM_022817.2 R805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:239169516 G>A maps to NM_022817.2 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:239161915 C>T maps to NM_022817.2 G916G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr2:239155102 A>T maps to NM_022817.2 I1227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:239161975 G>A maps to NM_022817.2 F896F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr2:239180103 G>A maps to NM_022817.2 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:7887211 C>T maps to ENST00000377532 G741G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:7887367 C>T maps to ENST00000377532 F793F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:7890144 C>T maps to ENST00000377532 S1046S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:7870506 C>T maps to ENST00000377532 Q461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:7844969 A>G maps to ENST00000377532 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:7895933 C>T maps to ENST00000377532 A1109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr1:7861236 T>C maps to ENST00000377532 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:7863105 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:7887694 C>T maps to ENST00000377532 P902P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:138417524 G>A maps to NM_022121.4 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:138413250 G>A maps to NM_022121.4 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr22:30974943 C>T maps to NM_014303.2 K521K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr22:30980646 G>A maps to NM_014303.2 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:30974829 G>A maps to NM_014303.2 I559I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr22:30976583 G>A maps to NM_014303.2 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:152640636 G>A maps to NM_004564.2 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr4:152593946 G>A maps to NM_004564.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:152629190 G>A maps to NM_004564.2 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:152638130 G>A maps to NM_004564.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:92129125 G>A maps to NM_000466.2 P870P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:92147276 G>A maps to NM_000466.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:92146607 G>A maps to NM_000466.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr7:92151511 G>A maps to NM_000466.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:7546944 G>A maps to NM_080662.2 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr17:33904983 G>A maps to NM_000286.2 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr17:33904920 C>T maps to NM_000286.2 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr1:10689674 C>A maps to NM_004565.2 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr1:10683171 C>T maps to NM_004565.2 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:10684461 C>T maps to NM_004565.2 Q185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:45935739 G>A maps to NM_057174.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:45932503 G>A maps to NM_057174.2 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr11:45935478 G>A maps to NM_057174.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:160252836 G>A maps to NM_002857.3 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:160252887 G>A maps to NM_002857.3 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:77895943 G>A maps to NM_001172087.1 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:77895646 G>A maps to NM_001172087.1 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr22:18567992 C>T maps to NM_017929.5 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:18566337 G>A maps to NM_017929.5 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr22:18568001 C>T maps to NM_017929.5 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:143793362 C>A maps to NM_003630.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:7362671 C>T maps to NM_001131023.1 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr12:7361077 C>T maps to NM_001131023.1 Q418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr12:7362644 C>T maps to NM_001131023.1 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr12:7362645 C>T maps to NM_001131023.1 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:7360658 C>T maps to NM_001131023.1 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:7354847 C>T maps to NM_001131023.1 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr3:179605527 G>A maps to NM_016559.1 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:179593206 G>A maps to NM_016559.1 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr3:179533711 C>T maps to NM_016559.1 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:179525586 G>A maps to NM_016559.1 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:179537747 C>T maps to NM_016559.1 W280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:179525580 C>T maps to NM_016559.1 A519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:179526209 C>T maps to NM_016559.1 G456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:179597798 G>A maps to NM_016559.1 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr6:42946033 G>A maps to NM_000287.3 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:42942622 G>A maps to NM_000287.3 Q346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:137191065 A>G maps to NM_000288.3 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:74847171 C>T maps to NM_002619.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:74847219 C>T maps to NM_002619.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:74846986 C>T maps to NM_002619.2 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:74719087 C>A maps to NM_002620.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr17:8167624 C>T maps to NM_012393.2 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr17:8169315 C>T maps to NM_012393.2 I894I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:8158941 C>T maps to NM_012393.2 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr17:8159862 C>T maps to NM_012393.2 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:8172022 C>T maps to NM_012393.2 S1185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr17:8161173 T>C maps to NM_012393.2 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:161070582 G>T maps to NM_012394.3 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:54960283 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:54978456 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr23:54978346 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:55020373 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr23:54975518 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:54984786 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:54971907 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:54982605 G>A did not map to a codon.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr23:54985313 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr23:54964044 A>G did not map to a codon.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr1:207240855 C>T maps to NM_006212.2 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr10:6255622 C>T maps to NM_004566.3 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr10:6255622 C>T maps to NM_004566.3 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:6258673 C>T maps to NM_004566.3 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr10:6258673 C>T maps to NM_004566.3 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr3:48563045 G>A maps to NM_004567.2 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:48573727 C>T maps to NM_004567.2 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:48576722 G>A maps to NM_004567.2 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:48563045 G>A maps to NM_004567.2 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr3:48572950 G>A maps to NM_004567.2 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr21:45739289 C>T maps to NM_002626.4 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr21:45742853 C>A maps to NM_002626.4 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr21:45733005 C>T maps to NM_002626.4 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr21:45732068 C>T maps to NM_002626.4 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr21:45739289 C>T maps to NM_002626.4 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr21:45746144 C>T maps to NM_002626.4 F731F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:48501969 C>T maps to NM_001166686.1 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr12:48537891 G>A maps to NM_001166686.1 G719G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr12:48535531 C>A maps to NM_001166686.1 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr10:3162142 C>T maps to NM_002627.3 V530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr10:3155368 C>T maps to NM_002627.3 Q405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr10:3151551 C>T maps to NM_002627.3 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:61017143 C>T maps to ENST00000422676 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:61018704 C>T maps to ENST00000422676 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:61015962 G>A maps to ENST00000422676 W243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr7:44105076 G>A maps to NM_000290.3 Q18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:44102377 C>T maps to NM_000290.3 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr23:77224484 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:77224715 G>T did not map to a codon.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr23:77224664 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr23:77224406 T>C did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:133294598 C>T maps to NM_001170543.1 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr2:197755584 G>A maps to NM_024989.3 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:197757951 C>T maps to NM_024989.3 K315K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:197707545 A>T maps to NM_024989.3 Y843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:3832620 C>T maps to NM_014489.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr11:3845363 C>T maps to NM_014489.2 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:37829085 C>T maps to NM_033419.3 K311K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:37840879 G>A maps to NM_033419.3 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr17:37840879 G>A maps to NM_033419.3 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:37844114 G>A maps to NM_033419.3 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr17:37829899 G>A maps to NM_033419.3 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr6:28268648 C>T maps to NM_032507.3 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr6:28268986 C>T maps to NM_032507.3 V452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:28251875 C>T maps to NM_032507.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr6:28269286 C>T maps to NM_032507.3 C552C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr6:28269229 C>T maps to NM_032507.3 F533F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:28268884 C>T maps to NM_032507.3 N418N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:28264675 C>T maps to NM_032507.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:249211568 G>A maps to NM_170725.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:249211019 C>T maps to NM_170725.2 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:50723687 G>A maps to ENST00000515869 F959F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr10:50724500 G>A maps to ENST00000515869 D688D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr10:50723758 C>A maps to ENST00000515869 E936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr10:50724533 A>G maps to ENST00000515869 H677H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr15:34395928 C>T maps to NM_152595.4 F399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr15:34396488 A>G maps to NM_152595.4 *586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:230468617 C>T maps to ENST00000321327 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:230486706 G>A maps to ENST00000321327 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:230492690 G>A maps to ENST00000321327 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr6:41712204 G>A maps to NM_002630.3 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:41712479 G>A maps to NM_002630.3 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr6:41715030 C>T maps to NM_002630.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr6:41712503 C>T maps to NM_002630.3 K34K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr6:41704715 G>A maps to NM_002630.3 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr6:41712138 G>A maps to NM_002630.3 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:41710161 G>A maps to NM_002630.3 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr6:41705560 G>A maps to NM_002630.3 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:41704678 G>A maps to NM_002630.3 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr6:41712539 G>A maps to NM_002630.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr8:97847234 C>T maps to ENST00000325141 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:10479547 C>T maps to NM_002631.2 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr1:10468149 C>T maps to NM_002631.2 Q158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:10460535 C>T maps to NM_002631.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:10477452 C>T maps to NM_002631.2 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:10479550 C>T maps to NM_002631.2 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:10477455 C>T maps to NM_002631.2 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:10477452 C>T maps to NM_002631.2 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:10479766 C>T maps to NM_002631.2 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:10477119 C>T maps to NM_002631.2 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr14:75416245 G>A maps to ENST00000405431 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:77369646 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:77373638 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:77381285 G>C did not map to a codon.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr6:49754579 G>A maps to NM_138733.4 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:49754105 G>A maps to NM_138733.4 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:49754495 G>A maps to NM_138733.4 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:49754543 C>T maps to NM_138733.4 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:49753679 G>A maps to NM_138733.4 I407I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:49754783 C>T maps to NM_138733.4 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:49754783 C>T maps to NM_138733.4 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:49753679 G>A maps to NM_138733.4 I407I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:49754852 C>T maps to NM_138733.4 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:49754131 G>A maps to NM_138733.4 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:49754645 G>A maps to NM_138733.4 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:49754726 T>C maps to NM_138733.4 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:49753820 C>T maps to NM_138733.4 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr6:49754588 C>T maps to NM_138733.4 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr6:49754645 G>A maps to NM_138733.4 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:49754168 G>A maps to NM_138733.4 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:49754363 C>T maps to NM_138733.4 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr6:49754579 G>A maps to NM_138733.4 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr6:49753702 G>A maps to NM_138733.4 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:49754615 G>A maps to NM_138733.4 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:49753679 G>A maps to NM_138733.4 I407I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:49754486 C>T maps to NM_138733.4 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:49754825 G>A maps to NM_138733.4 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr19:17628556 G>A maps to NM_012088.2 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr19:46522827 C>T maps to NM_005091.2 W122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr19:15586958 C>T maps to NM_052890.3 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:15586706 A>G maps to NM_052890.3 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr19:15586667 G>A maps to NM_052890.3 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:15587069 G>A maps to NM_052890.3 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr19:15586355 G>A maps to NM_052890.3 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:15586355 G>A maps to NM_052890.3 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:15586976 G>A maps to NM_052890.3 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:15586349 C>T maps to NM_052890.3 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:15586582 G>A maps to NM_052890.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr19:15587189 C>T maps to NM_052890.3 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15579515 C>T maps to NM_052890.3 R563R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15586490 G>A maps to NM_052890.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15587018 G>A maps to NM_052890.3 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:153279642 G>A maps to NM_052891.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:153277426 C>T maps to NM_052891.1 K124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr1:153275000 G>A maps to NM_052891.1 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:153271691 C>T maps to NM_052891.1 Q248Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:153270490 G>A maps to NM_052891.1 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:153270485 G>A maps to NM_052891.1 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:153270485 G>A maps to NM_052891.1 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:153276336 C>T maps to NM_052891.1 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:153279642 G>A maps to NM_052891.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:153276395 G>A maps to NM_052891.1 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:153276365 G>A maps to NM_052891.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:153309738 C>T maps to NM_020393.2 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:153309723 G>A maps to NM_020393.2 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:153309708 G>A maps to NM_020393.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:153309672 G>A maps to NM_020393.2 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:153314217 T>C maps to NM_020393.2 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr1:153312981 C>T maps to NM_020393.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:153320360 C>T maps to NM_020393.2 W16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:153312969 G>A maps to NM_020393.2 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:64095112 C>T maps to NM_002633.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:64125270 C>T maps to NM_002633.2 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:64095184 C>T maps to NM_002633.2 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:64120091 C>T maps to NM_002633.2 I518I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:64120032 C>T maps to NM_002633.2 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:64095130 C>T maps to NM_002633.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:64089130 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr6:83885737 G>A maps to ENST00000416472 H385H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr9:70999393 C>T maps to NM_021965.3 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr9:71006610 G>T maps to NM_021965.3 G287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:71114246 G>A maps to NM_021965.3 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:71002415 C>T maps to NM_021965.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr16:2264142 G>A maps to NM_001042371.2 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:18453693 C>T maps to NM_017712.2 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr15:99514378 G>A maps to NM_001102612.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr15:99512802 C>T maps to NM_001102612.2 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:100999492 G>A maps to NM_000926.4 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr11:100999687 C>T maps to NM_000926.4 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:100962566 G>A maps to NM_000926.4 I610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:100999087 C>T maps to NM_000926.4 K238K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr11:100920672 T>C maps to NM_000926.4 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr11:100922293 G>A maps to NM_000926.4 R740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:100999144 C>T maps to NM_000926.4 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr11:100933231 G>A maps to NM_000926.4 Q720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr11:100922293 G>A maps to NM_000926.4 R740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:100920693 G>A maps to NM_000926.4 F818F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:100999519 C>T maps to NM_000926.4 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:118377141 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:118370368 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr4:129193637 G>A maps to NM_006320.4 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr17:76396764 C>T maps to NM_024419.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:76395591 C>T maps to NM_024419.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:76400048 C>T maps to NM_024419.3 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr17:76399760 T>G maps to NM_024419.3 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr17:76395525 G>A maps to NM_024419.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr17:76399922 C>T maps to NM_024419.3 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr6:12749948 C>T maps to NM_030948.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:13283703 C>T maps to NM_030948.1 I520I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr6:12718975 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:12749885 G>A maps to NM_030948.1 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr6:13053618 G>A maps to NM_030948.1 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:13182883 G>A maps to NM_030948.1 E210E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:13206216 C>T maps to NM_030948.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr6:144095217 C>T maps to NM_001100164.1 R485R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr6:144070140 C>T maps to NM_001100164.1 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:144128270 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:144081763 G>A maps to NM_001100164.1 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr6:144086701 C>T maps to NM_001100164.1 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr20:58381144 G>A maps to NM_080672.3 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr20:58381144 G>A maps to NM_080672.3 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:58322814 C>T maps to NM_080672.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr20:58416568 G>A maps to NM_080672.3 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr20:58322849 G>A maps to NM_080672.3 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr20:58348418 G>A maps to NM_080672.3 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:58342388 C>T maps to NM_080672.3 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:58381186 C>T maps to NM_080672.3 F422F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:28800499 C>T maps to NM_023923.3 R430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr1:28785770 T>G did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:28793199 C>T maps to NM_023923.3 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr1:28792353 C>A maps to NM_023923.3 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr5:125939353 G>T maps to NM_032177.3 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:47482518 G>A maps to NM_002634.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr12:7079697 C>T maps to NM_001144831.1 Q3Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:7079363 G>A maps to NM_001144831.1 H69H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr12:9083323 G>A maps to ENST00000433083 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:9074315 C>A maps to ENST00000433083 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr12:9072354 C>T maps to ENST00000433083 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr12:9086522 C>T maps to ENST00000433083 V747V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr1:33797948 G>A maps to ENST00000419414 F606F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:33799693 G>A maps to ENST00000419414 F586F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr1:33840972 G>A maps to ENST00000419414 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:169824617 A>G did not map to a codon.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr3:169840472 G>A maps to NM_024947.3 V616V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:22065202 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:22129636 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:22239737 T>C did not map to a codon.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr23:22095763 T>C did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:22129678 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr23:22117213 C>G did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:22117196 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:22112103 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:22263513 C>T did not map to a codon.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr23:22231042 G>A did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:22196405 C>T did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:22196406 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr6:33380096 T>G maps to NM_024165.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr6:33382065 A>T maps to NM_024165.2 K267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:33383372 C>T maps to NM_024165.2 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:33383016 A>G maps to NM_024165.2 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr17:27248743 G>A maps to NM_001033561.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:27240100 G>A maps to NM_001033561.1 C496C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr17:27240250 A>G maps to NM_001033561.1 H446H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:27250965 G>A maps to NM_001033561.1 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:27233233 C>T maps to NM_001033561.1 Q994Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr17:27254013 G>A maps to NM_001033561.1 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:6680348 C>T maps to NM_153812.2 R210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:6680320 C>T maps to NM_153812.2 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:11022695 G>A maps to ENST00000303905 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:11022441 C>T maps to ENST00000303905 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:11076226 G>A maps to ENST00000303905 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:11076095 C>T maps to ENST00000303905 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr7:11076095 C>T maps to ENST00000303905 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr5:133914514 G>A maps to ENST00000448712 K687K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr5:133909397 C>T maps to ENST00000448712 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:133895525 C>T maps to ENST00000448712 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:133873697 C>G maps to ENST00000448712 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:46913780 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:46918376 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:46845160 A>C did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:46915588 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:46913939 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:46857533 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:46887369 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:46913812 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr4:129752965 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:129764142 C>T maps to NM_199320.2 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr4:129783052 C>T maps to NM_199320.2 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr4:129764135 C>T maps to NM_199320.2 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr4:129783277 C>T maps to NM_199320.2 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr4:129782941 G>A maps to NM_199320.2 E355E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr9:123631464 G>C maps to NM_015651.1 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:123620470 G>A maps to NM_015651.1 C498C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr9:96418821 C>T maps to NM_005392.3 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr9:96437254 C>T maps to NM_005392.3 S891S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:96429432 C>T maps to NM_005392.3 V753V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr9:96428030 G>A maps to NM_005392.3 E667E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:96420454 C>T maps to NM_005392.3 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr9:96425205 G>T maps to NM_005392.3 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr20:34430608 C>T maps to NM_016436.4 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr20:34505529 C>T maps to NM_016436.4 F650F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr20:34526951 C>T maps to NM_016436.4 S878S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr20:34505529 C>T maps to NM_016436.4 F650F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr20:34519237 G>T maps to NM_016436.4 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:34501988 C>T maps to NM_016436.4 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr8:133816951 C>T maps to ENST00000395386 Q273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:133829220 T>C maps to ENST00000395386 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:133844531 T>A maps to ENST00000395386 S600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr11:45975104 G>T maps to ENST00000257821 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr11:46001478 T>G maps to ENST00000257821 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr11:45987069 G>A maps to ENST00000257821 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr11:45959821 A>G maps to ENST00000257821 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:45987078 G>A maps to ENST00000257821 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr11:45987051 G>A maps to ENST00000257821 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:45312174 G>A maps to NM_138415.3 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr22:45279177 G>A maps to NM_138415.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr22:45312396 G>T maps to NM_138415.3 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr22:45278977 C>T maps to NM_138415.3 Q528Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr22:45289407 G>A maps to NM_138415.3 Q297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:45279061 C>T maps to NM_138415.3 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:45309884 G>A maps to NM_138415.3 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr22:45316358 C>T maps to NM_138415.3 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:45309845 G>A maps to NM_138415.3 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr22:45309860 G>A maps to NM_138415.3 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr22:45309779 G>A maps to NM_138415.3 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr17:7140085 C>A maps to NM_024297.2 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:7139345 G>A maps to NM_024297.2 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:64422955 C>T maps to NM_015153.2 P1824P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:64394363 T>C maps to NM_015153.2 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:64395689 C>T maps to NM_015153.2 F689F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr6:64421504 C>T maps to NM_015153.2 L1341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:64394786 G>A maps to NM_015153.2 E388E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:64408416 T>C maps to NM_015153.2 S968S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr23:133547592 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:133551251 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr23:133551266 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:52456877 T>C maps to ENST00000454052 C301C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr3:52454955 C>T maps to ENST00000454052 Q151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:52457305 C>T maps to ENST00000454052 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr3:52456778 G>A maps to ENST00000454052 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:54020142 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:53965626 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:54037564 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:54048695 C>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:53966797 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:54022211 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:54014279 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr23:54037694 A>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:54048723 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:54014368 C>G did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:54048723 G>A did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:54011531 C>T did not map to a codon.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr23:54020144 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr6:79668244 G>A maps to NM_017934.5 S1243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:79664601 A>G maps to NM_017934.5 L1328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:71877457 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr23:71822119 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:71813012 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:71840727 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr23:71825179 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:71825250 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr23:71840660 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:71840644 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:71870316 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:71840657 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr23:71870318 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:71804145 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:71825147 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:71925050 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:71895920 T>G did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr23:71822082 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:71830923 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:71915727 T>A did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:71895930 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr23:71840573 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr23:71887292 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:71802345 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:71825459 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:71825460 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:71842983 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:71843060 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:71872431 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:71887251 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:71843001 C>A did not map to a codon.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr23:71887313 C>T did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:71895929 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:18913296 A>C did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:18959708 A>C did not map to a codon.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr23:18958110 A>G did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:18942595 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr23:18944673 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:18972392 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:18942231 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:18963269 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr23:18924612 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:18911700 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr23:18936812 C>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:18969318 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr23:18954221 T>C did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:18923921 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr23:18959727 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr16:47630347 C>T maps to NM_000293.2 N423N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr16:47703277 C>T maps to NM_000293.2 I860I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:47627448 C>T maps to NM_000293.2 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:47621610 C>T maps to NM_000293.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:47723056 G>A maps to NM_000293.2 L912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:47730371 G>A maps to NM_000293.2 Q992Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:47730389 C>T maps to NM_000293.2 I998I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr16:47699900 C>T maps to NM_001031835.2 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr16:47495299 G>A maps to NM_000293.2 W13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr16:47732460 C>T maps to NM_000293.2 Q1036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr16:47627448 C>T maps to NM_000293.2 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr7:56149603 C>T maps to NM_006213.3 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:56149358 C>T maps to NM_006213.3 E294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:30762460 C>T maps to NM_000294.2 R44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:30764753 C>T maps to NM_000294.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:76424915 T>C maps to NM_007350.3 Q202Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr11:118498621 C>T maps to NM_015157.2 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:118499022 G>A maps to NM_015157.2 W495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr11:118502727 T>C maps to NM_015157.2 R733R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr11:118516206 T>C maps to NM_015157.2 P1085P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:118498462 C>T maps to NM_015157.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr11:118498843 C>T maps to NM_015157.2 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:111632455 A>G maps to NM_001134438.1 E542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:111685507 G>A maps to NM_001134438.1 L1042L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr3:111603274 C>T maps to NM_001134438.1 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:111693352 G>A maps to NM_001134438.1 R1235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr3:111604057 G>A maps to NM_001134438.1 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:111603640 G>A maps to NM_001134438.1 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:111603907 C>T maps to NM_001134438.1 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:111688686 A>T maps to NM_001134438.1 K1156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr3:111603064 G>A maps to NM_001134438.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:111685505 T>C maps to NM_001134438.1 L1042L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:111632512 T>G maps to NM_001134438.1 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:111667825 G>A maps to NM_001134438.1 T845T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:111671487 C>T maps to NM_001134438.1 R901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:111693358 G>A maps to NM_001134438.1 W1237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:43979573 G>A maps to NM_198850.3 N637N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr18:60646129 C>T maps to NM_194449.2 F1540F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr18:60646445 C>T maps to NM_194449.2 R1646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr18:60497325 C>T maps to NM_194449.2 V545V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr16:71683446 C>T maps to NM_015020.2 L1106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:71748506 G>A maps to NM_015020.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr16:71683302 G>A maps to NM_015020.2 P1154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr16:71710359 G>A maps to NM_015020.2 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr16:71690520 T>C maps to NM_015020.2 S781S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr16:71683203 C>T maps to NM_015020.2 E1187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr16:71748506 G>A maps to NM_015020.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:71715667 G>A maps to NM_015020.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:71736600 G>A maps to NM_015020.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:71748698 A>G did not map to a codon.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr16:71697868 G>A maps to NM_015020.2 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr16:71697893 G>A maps to NM_015020.2 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:41748159 G>A maps to NM_003924.3 N203N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr4:41750450 G>A maps to NM_003924.3 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:41748192 C>G maps to NM_003924.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr4:41750495 A>T maps to NM_003924.3 Y44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:41750414 C>T maps to NM_003924.3 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr4:41748138 C>T maps to NM_003924.3 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr4:41748081 G>A maps to NM_003924.3 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr11:609394 C>T maps to ENST00000264555 S1313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr11:609395 C>T maps to ENST00000264555 L1314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr11:605664 C>T maps to ENST00000264555 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:607765 C>T maps to ENST00000264555 V770V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr11:609256 C>T maps to ENST00000264555 A1267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:607120 C>T maps to ENST00000264555 F555F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr11:587262 C>T maps to ENST00000264555 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:605144 C>T maps to ENST00000264555 I393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:587400 C>A maps to ENST00000264555 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr11:591434 C>T maps to ENST00000264555 R158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:609184 C>T maps to ENST00000264555 P1243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr1:114254403 C>A maps to NM_006608.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:114280738 G>A maps to NM_006608.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:114280738 G>A maps to NM_006608.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr10:13336469 G>A maps to NM_006214.3 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr10:13337533 G>A maps to NM_006214.3 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr10:13330473 G>A maps to NM_006214.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:13325818 G>A maps to NM_006214.3 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:131702714 C>T maps to NM_001100876.1 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr9:131696296 C>T maps to NM_001100876.1 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:22079003 C>T maps to NM_014759.3 E285E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:22078982 G>A maps to NM_014759.3 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:22079093 G>A maps to NM_014759.3 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:22079282 C>T maps to NM_014759.3 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:60994166 G>A maps to NM_032439.3 W70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:75757660 T>G maps to NM_015886.3 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr8:75761469 C>T maps to NM_015886.3 Y253Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:75756214 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr6:36931062 C>T maps to NM_153370.2 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:36929676 G>A maps to NM_153370.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr6:36929688 C>T maps to NM_153370.2 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr6:36929689 C>T maps to NM_153370.2 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr6:36922607 C>T maps to NM_153370.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr20:43804673 C>T maps to NM_002638.3 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr20:43804763 C>T maps to NM_002638.3 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:43804673 C>T maps to NM_002638.3 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:43804763 C>T maps to NM_002638.3 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:43804763 C>T maps to NM_002638.3 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr20:43804652 C>T maps to NM_002638.3 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:43803610 G>A maps to NM_002638.3 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr10:99410888 C>T maps to ENST00000416867 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr4:25265403 T>C maps to NM_018323.3 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr4:25278736 T>C maps to NM_018323.3 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr4:25270158 T>C maps to NM_018323.3 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q3-06A-11D-A196-08 chr22:21080784 C>T maps to NM_058004.2 R1604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr22:21159334 G>A maps to NM_058004.2 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr22:21150438 G>A maps to NM_058004.2 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr22:21150439 G>A maps to NM_058004.2 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr22:21088362 G>A maps to NM_058004.2 N1282N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr22:21159289 G>A maps to NM_058004.2 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr22:21073015 G>A maps to NM_058004.2 F1679F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:21065060 G>A maps to NM_058004.2 I1945I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr22:21088120 G>A maps to NM_058004.2 L1297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr22:21088121 G>A maps to NM_058004.2 T1296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:21174863 G>A maps to NM_058004.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr22:21087379 G>A maps to NM_058004.2 P1331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:21107418 G>A maps to NM_058004.2 F889F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:21174038 G>A maps to NM_058004.2 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr22:21173973 C>T maps to NM_058004.2 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:21157581 G>A maps to NM_058004.2 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:21165308 G>A maps to NM_058004.2 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:151276086 G>A maps to NM_002651.2 Q496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:151288330 G>A maps to NM_002651.2 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:151280270 G>A maps to NM_002651.2 R333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:151288046 A>G did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr18:44426690 A>C maps to NM_004671.2 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:44470762 T>C maps to NM_004671.2 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr1:145578321 C>A maps to NM_006099.3 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:145580512 C>T maps to NM_006099.3 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr1:145580315 C>T maps to NM_006099.3 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:145585606 C>T maps to NM_006099.3 I624I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:145578692 C>T maps to NM_006099.3 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr19:4024106 C>T maps to NM_015897.2 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:4024061 G>A maps to NM_015897.2 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr13:73409494 A>G maps to NM_006346.2 E404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr13:73491274 C>A maps to NM_006346.2 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr13:73401868 A>G did not map to a codon.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr22:38461088 C>T maps to NM_012407.3 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:38469032 C>T maps to NM_012407.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr22:38463713 G>T maps to NM_012407.3 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:38468551 A>T maps to NM_012407.3 K209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr2:229890518 C>T maps to NM_017933.4 Q192Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:229890440 C>T maps to NM_017933.4 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr2:229890440 C>T maps to NM_017933.4 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:229890638 G>A maps to NM_017933.4 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:229890677 G>A maps to NM_017933.4 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr2:229890743 C>T maps to NM_017933.4 W117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr2:229890686 G>A maps to NM_017933.4 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:229890617 G>A maps to NM_017933.4 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr2:229890443 G>A maps to NM_017933.4 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr15:65116063 C>T maps to ENST00000333425 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr15:65112121 C>A maps to ENST00000333425 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr15:65110165 C>T maps to ENST00000333425 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr15:65110471 G>A maps to ENST00000333425 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:65113579 C>T maps to ENST00000333425 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr23:15344094 T>C did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:15342952 G>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:15344086 G>T did not map to a codon.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr4:517459 C>T maps to NM_001127178.1 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:520927 C>T maps to NM_001127178.1 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:524290 C>T maps to NM_001127178.1 D776D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:509862 C>T maps to NM_001127178.1 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr4:517459 C>T maps to NM_001127178.1 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:520863 C>T maps to NM_001127178.1 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:517372 C>T maps to NM_001127178.1 F580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:527690 C>T maps to NM_001127178.1 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr14:68060609 G>A maps to NM_004569.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr14:68059434 G>A maps to NM_004569.3 Q131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:77620210 G>A maps to NM_005482.2 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr1:77672385 G>A maps to NM_005482.2 R60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:77620245 G>A maps to NM_005482.2 Q292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr17:16120578 C>G maps to NM_004278.3 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:16221108 C>T maps to NM_004278.3 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:160000968 G>A maps to NM_145167.2 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr1:160000283 G>A maps to NM_145167.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:59814234 G>A maps to NM_176787.4 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:59770100 G>A maps to NM_176787.4 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr9:35094309 G>A maps to NM_032634.2 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:35092158 G>A maps to NM_032634.2 F575F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr9:35095415 G>A maps to NM_032634.2 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr9:35089443 G>A maps to NM_032634.2 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:35093435 G>A maps to NM_032634.2 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr16:624314 C>T maps to NM_148920.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr16:624571 C>T maps to NM_148920.1 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:624337 C>T maps to NM_148920.1 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:624463 C>T maps to NM_148920.1 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr16:624742 C>T maps to NM_148920.1 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:633624 C>T maps to NM_148920.1 V758V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:207103752 G>A maps to NM_002644.3 S735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr1:207110449 G>A maps to NM_002644.3 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:207103719 G>A maps to NM_002644.3 F746F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:207110676 G>A maps to NM_002644.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:207110998 C>T maps to NM_002644.3 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:207105085 C>T maps to NM_002644.3 R690R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:207110998 C>T maps to NM_002644.3 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:207105094 C>T maps to NM_002644.3 E687E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:207110998 C>T maps to NM_002644.3 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:207109155 C>T maps to NM_002644.3 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:207105031 G>A maps to NM_002644.3 S708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:207112695 C>T maps to NM_002644.3 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:207108074 C>T maps to NM_002644.3 K465K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr17:26887111 G>A maps to NM_033198.3 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:26881985 C>T maps to NM_033198.3 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:26887180 G>A maps to NM_033198.3 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:26881492 G>A maps to NM_033198.3 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr20:44048993 C>T maps to NM_015937.4 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:44047557 C>T maps to NM_015937.4 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:44052928 C>T maps to NM_015937.4 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr20:44049271 C>T maps to NM_015937.4 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:44050116 C>T maps to NM_015937.4 H376H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr20:44048199 C>T maps to NM_015937.4 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr20:33173344 G>A maps to NM_080476.4 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:33162997 G>A maps to NM_080476.4 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr1:27120995 C>T maps to NM_017837.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:27120623 C>T maps to NM_017837.2 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:27121058 C>T maps to NM_017837.2 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:27124181 C>T maps to NM_017837.2 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:34893582 C>T maps to NM_178517.3 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:196678713 G>A maps to NM_025163.2 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr19:49949822 G>A maps to NM_017916.2 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr19:49950643 G>A maps to NM_017916.2 Q188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:111941230 G>A maps to NM_138789.3 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr10:98408469 G>A maps to NM_152309.2 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr10:98469423 C>T maps to NM_152309.2 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr10:98362053 C>T maps to NM_152309.2 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:98388182 C>T maps to NM_152309.2 K481K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:98355378 C>T maps to NM_152309.2 R791R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:98380282 G>A maps to NM_152309.2 P589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:98408568 C>T maps to NM_152309.2 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:98408550 G>A maps to NM_152309.2 N350N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:17140198 A>G maps to NM_002645.2 L1010L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:17190961 G>A maps to NM_002645.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:17135969 G>A maps to NM_002645.2 Q1087*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr11:17139150 G>A maps to NM_002645.2 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr11:17158168 G>A maps to NM_002645.2 Q570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:17167465 C>G maps to NM_002645.2 V528V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:17143760 A>G maps to NM_002645.2 D877D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:17139103 C>T maps to NM_002645.2 T1050T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:17190304 A>G maps to NM_002645.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr1:204438312 C>T maps to NM_002646.3 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr1:204412634 C>T maps to NM_002646.3 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr1:204438516 G>A maps to NM_002646.3 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:204433192 C>A maps to NM_002646.3 V419V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:204433168 C>T maps to NM_002646.3 K427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:204426915 G>A maps to NM_002646.3 I551I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:204425174 C>T maps to NM_002646.3 K584K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr1:204433650 G>A maps to NM_002646.3 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr1:204438447 G>A maps to NM_002646.3 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr1:204418339 G>A maps to NM_002646.3 F773F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr1:204438345 G>A maps to NM_002646.3 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:204410670 G>A maps to NM_002646.3 S1059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr12:18747450 C>T maps to NM_004570.4 F1304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr12:18435239 G>A maps to NM_004570.4 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr12:18478004 C>T maps to NM_004570.4 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr12:18793379 T>G maps to NM_004570.4 S1359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:18466970 G>A maps to NM_004570.4 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:18499701 C>T maps to NM_004570.4 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:18435578 G>A maps to NM_004570.4 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:18435665 G>A maps to NM_004570.4 W217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:18691165 C>T maps to NM_004570.4 Q1093*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:18644458 C>T maps to NM_004570.4 N879N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:18435354 T>C maps to NM_004570.4 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:18552691 G>A maps to NM_004570.4 W701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:18658278 C>T maps to NM_004570.4 I1028I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr12:18573873 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr12:18691165 C>T maps to NM_004570.4 Q1093*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:18715675 G>A maps to NM_004570.4 L1169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:18691146 G>A maps to NM_004570.4 G1086G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:18762520 G>A maps to NM_004570.4 E1339E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:18491418 G>T maps to NM_004570.4 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr12:18691146 G>A maps to NM_004570.4 G1086G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:18715675 G>A maps to NM_004570.4 L1169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr12:18658386 G>A maps to NM_004570.4 G1064G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr12:18573874 T>C maps to NM_004570.4 S731S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr18:39623704 T>C maps to ENST00000398870 F705F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr18:39647476 G>A maps to ENST00000398870 Q884Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:39542543 C>T maps to ENST00000398870 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr3:178921432 A>T maps to NM_006218.2 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr3:178919219 C>T maps to NM_006218.2 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:138376565 G>A maps to NM_006219.1 Q970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:138474785 G>A maps to NM_006219.1 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr3:138417773 C>T maps to NM_006219.1 W582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:138461458 A>G maps to NM_006219.1 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:138453616 G>A maps to NM_006219.1 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr3:138402619 C>T maps to NM_006219.1 K775K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:9781282 C>T maps to ENST00000361110 A620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:9776046 C>T maps to ENST00000361110 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:106513252 C>T maps to NM_002649.2 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:106508131 C>T maps to NM_002649.2 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:106508752 C>T maps to NM_002649.2 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:106508674 C>T maps to NM_002649.2 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:106509118 C>A maps to NM_002649.2 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:106509676 G>A maps to NM_002649.2 A557A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:106508614 G>A maps to NM_002649.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr7:106509798 G>A maps to NM_002649.2 W598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:106508297 C>T maps to NM_002649.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:106508122 C>T maps to NM_002649.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:67592092 C>T maps to ENST00000396611 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr5:67589535 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr5:67589625 T>G maps to ENST00000396611 Y463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr5:67589196 A>T maps to ENST00000396611 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr5:67576527 C>T maps to ENST00000396611 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:67576470 C>T maps to ENST00000396611 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:18273087 G>A maps to NM_005027.2 Q326Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:18273313 C>T maps to NM_005027.2 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:18274114 C>T maps to NM_005027.2 Q445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:18273851 C>T maps to NM_005027.2 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:130449248 G>A maps to NM_014602.2 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr3:130398287 G>A maps to NM_014602.2 T1316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr3:130463912 G>A maps to NM_014602.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr17:8808202 G>A maps to NM_001142633.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:8793302 G>A maps to NM_001142633.1 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr17:8794120 G>A maps to NM_001142633.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:8788074 G>A maps to NM_001142633.1 I718I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr17:8784241 C>T maps to NM_001142633.1 K825K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr17:8784274 G>A maps to NM_001142633.1 P814P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr17:8808178 G>C maps to NM_001142633.1 Y109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:8808163 G>A maps to NM_001142633.1 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A264-06A-11D-A196-08 chr17:8785144 G>A maps to NM_001142633.1 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:8784238 G>A maps to NM_001142633.1 I826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr17:8738760 G>A maps to NM_001010855.2 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr17:8726793 G>A maps to NM_001010855.2 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr17:8726802 C>T maps to NM_001010855.2 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:8706698 G>A maps to NM_001010855.2 S718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:8738706 G>A maps to NM_001010855.2 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:8741158 G>A maps to NM_001010855.2 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:8726720 G>A maps to NM_001010855.2 Q537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:8738696 G>A maps to NM_001010855.2 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr17:8738706 G>A maps to NM_001010855.2 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr17:8732305 C>T maps to NM_001010855.2 W297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr17:8739898 C>T maps to NM_001010855.2 Q142Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:8731915 C>T maps to NM_001010855.2 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr2:209142371 C>T maps to NM_015040.3 Q185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:209188918 C>T maps to NM_015040.3 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:209217484 C>T maps to NM_015040.3 F1941F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr2:209150621 T>C maps to NM_015040.3 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:209190147 C>T maps to NM_015040.3 S871S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:209190192 C>T maps to NM_015040.3 N886N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:209165795 C>T maps to NM_015040.3 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:209179021 C>T maps to NM_015040.3 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:209190804 C>T maps to NM_015040.3 L1090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr2:209200544 G>T maps to NM_015040.3 E1429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:99995511 G>A maps to NM_013439.2 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:99971760 C>T maps to NM_013439.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:99972024 C>T maps to NM_013439.2 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr7:99971892 C>T maps to NM_013439.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:99956643 G>A maps to ENST00000413850 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:99956640 C>T maps to ENST00000413850 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr7:99956403 C>T maps to ENST00000413850 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr6:37140844 C>T maps to ENST00000373507 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr6:37138791 C>T maps to ENST00000373507 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:37140802 C>T maps to ENST00000373507 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:37140844 C>T maps to ENST00000373507 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:48772545 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:48771523 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr23:48771761 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:48776076 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:48776077 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:50355388 C>T maps to NM_001001852.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr22:50356708 C>T maps to NM_001001852.3 D305D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr22:50356709 C>T maps to NM_001001852.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr19:9949113 C>T maps to NM_006221.2 R21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:9949199 G>A maps to NM_006221.2 Q49Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:20964585 C>T maps to NM_032409.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:20972133 G>T maps to NM_032409.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:77006656 G>A maps to NM_017439.3 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:76940675 C>T maps to NM_017439.3 *855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr7:77006656 G>A maps to NM_017439.3 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr7:76984541 G>A maps to NM_017439.3 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:77004406 G>A maps to NM_017439.3 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:77006656 G>A maps to NM_017439.3 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr7:142836719 C>T maps to NM_002652.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:142829227 C>T maps to NM_002652.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:142836647 G>A maps to NM_002652.2 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:142836686 C>T maps to NM_002652.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr10:22880590 G>T maps to NM_005028.4 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr10:22830847 G>A maps to NM_005028.4 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:22839617 G>A maps to NM_005028.4 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:57985149 C>T maps to NM_024779.4 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:57994596 C>T maps to NM_024779.4 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr12:57987899 C>T maps to NM_024779.4 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:57988950 C>G maps to NM_024779.4 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:151214995 C>T maps to NM_001135638.1 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:151206686 C>T maps to NM_001135638.1 N218N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:151205034 C>T maps to NM_001135638.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:71532594 G>A maps to NM_003558.2 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr9:71509439 G>A maps to NM_003558.2 E219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr9:71491665 C>T maps to NM_003558.2 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:71555571 C>T maps to NM_003558.2 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr9:71549833 G>A maps to NM_003558.2 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr19:3661968 G>A maps to NM_012398.2 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:3656498 G>A maps to NM_012398.2 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr19:3653440 G>A maps to NM_012398.2 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:3643269 G>A maps to NM_012398.2 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:3644154 G>A maps to NM_012398.2 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:3643365 G>A maps to NM_012398.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:3641755 C>T maps to NM_012398.2 Q578Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:3664861 G>A maps to NM_012398.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:3653368 G>A maps to NM_012398.2 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:3648693 G>A maps to NM_012398.2 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:3661038 G>A maps to NM_012398.2 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:130688230 G>A maps to NM_001135219.1 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:130688149 G>A maps to NM_001135219.1 N253N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:27380579 C>T maps to NM_016518.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr17:27383230 C>T maps to NM_016518.2 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:27383202 C>T maps to NM_016518.2 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:27381693 C>T maps to NM_016518.2 Y264Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr17:27380538 A>T maps to NM_016518.2 K196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:15477784 A>G did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:15408312 G>C did not map to a codon.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr22:32019696 G>A maps to NM_014338.3 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr22:32017036 G>A maps to ENST00000422296 Y432Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr17:1438751 A>G maps to ENST00000313486 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:1444892 G>A maps to ENST00000313486 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:67262927 G>T maps to NM_004910.2 T821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:67270060 G>A maps to NM_004910.2 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:67262361 G>A maps to NM_004910.2 F899F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr11:67267575 G>A maps to NM_004910.2 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:67260518 G>A maps to NM_004910.2 I1119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr11:67265105 G>A maps to NM_004910.2 P609P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr11:67270000 C>T maps to NM_004910.2 W89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:67261496 G>A maps to NM_004910.2 I968I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr12:123482011 G>A maps to NM_020845.2 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr12:123477211 G>A maps to NM_020845.2 F746F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr12:123471919 G>A maps to NM_020845.2 F1107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr12:123489976 G>A maps to NM_020845.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:123481384 G>A maps to NM_020845.2 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:123482005 C>T maps to NM_020845.2 K446K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr12:123485330 G>A maps to NM_020845.2 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr12:123494520 G>A maps to NM_020845.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:123498442 G>A maps to NM_020845.2 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:123481276 G>A maps to NM_020845.2 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr12:123489904 G>A maps to NM_020845.2 D278D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:123481975 G>A maps to NM_020845.2 F456F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:123489862 C>T maps to NM_020845.2 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:123498382 G>A maps to NM_020845.2 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr17:6387072 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:6358672 G>A maps to NM_031220.3 F970F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:6428718 G>A maps to NM_031220.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr17:6371586 G>A maps to NM_031220.3 P616P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr17:6367077 G>A maps to NM_031220.3 V760V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:6386952 G>A maps to NM_031220.3 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr10:3181111 G>C maps to ENST00000380989 V968V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr5:134364828 G>A maps to NM_002653.4 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr4:111542322 G>A maps to NM_153426.1 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr4:111539352 G>A maps to NM_153426.1 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr4:111539382 C>T maps to NM_153426.1 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:103990561 C>T maps to NM_005029.3 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr12:130846059 C>T maps to NM_004764.4 I628I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr12:130831090 G>T maps to NM_004764.4 G165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr12:130830320 C>T maps to NM_004764.4 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:130846098 G>A maps to NM_004764.4 R641R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr12:130855735 C>T maps to NM_004764.4 I779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:130830988 C>T maps to NM_004764.4 Q131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:130840206 A>T maps to NM_004764.4 K467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:130833934 C>T maps to NM_004764.4 Q296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:22212891 G>A maps to NM_001135721.1 W932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:22161611 C>T maps to NM_001135721.1 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr8:22175703 C>T maps to NM_001135721.1 S773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr8:22175739 G>A maps to NM_001135721.1 V785V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr8:22145100 C>G maps to NM_001135721.1 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr22:25115474 C>T maps to NM_001008496.2 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr22:25119214 G>A maps to NM_001008496.2 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr22:25144948 C>T maps to NM_001008496.2 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:25152460 C>T maps to NM_001008496.2 E189E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:25152643 G>A maps to NM_001008496.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:25144918 C>T maps to NM_001008496.2 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:25145726 C>T maps to NM_001008496.2 W383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr11:94318640 T>C maps to NM_152431.2 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:94352940 G>A maps to NM_152431.2 V728V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr11:94326772 C>T maps to NM_152431.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:94341757 C>T maps to NM_152431.2 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:68382855 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:68381748 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:68382406 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:68382129 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:68381535 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:108673045 G>A maps to NM_014819.4 C671C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:108714062 G>A maps to NM_014819.4 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr16:2163264 G>T maps to NM_001009944.2 S961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr16:2163266 G>A maps to NM_001009944.2 G960G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr16:2149653 G>A maps to NM_001009944.2 S3347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr16:2168110 G>A maps to NM_001009944.2 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:2140796 G>A maps to NM_001009944.2 L4006L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:2161120 G>A maps to NM_001009944.2 F1349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:2159290 G>A maps to NM_001009944.2 A1959A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:2162885 G>A maps to NM_001009944.2 L1022L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr16:2159101 C>T maps to NM_001009944.2 S2022S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:2160337 G>A maps to NM_001009944.2 I1610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr16:2160598 G>A maps to NM_001009944.2 F1523F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr16:2152831 G>A maps to NM_001009944.2 T2977T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr16:2153633 G>A maps to NM_001009944.2 I2808I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr16:2140132 G>A maps to NM_001009944.2 S4169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr16:2161783 G>A maps to NM_001009944.2 S1128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr16:2162789 G>A maps to NM_001009944.2 L1054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:2150296 G>A maps to NM_001009944.2 A3194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr16:2153648 G>A maps to NM_001009944.2 G2803G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr16:2140375 G>A maps to NM_001009944.2 Y4118Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:47968882 G>A maps to NM_138295.3 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr7:47882568 C>T maps to NM_138295.3 L1812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:47921603 G>A maps to NM_138295.3 D1115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr7:47876653 G>A maps to NM_138295.3 F1936F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr7:47894812 G>A maps to NM_138295.3 P1547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:47866970 C>T maps to NM_138295.3 E2277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr7:47880162 C>T maps to NM_138295.3 V1816V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr7:47930264 G>A maps to NM_138295.3 S850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr7:47814749 C>T maps to NM_138295.3 K2847K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr7:47879172 C>T maps to NM_138295.3 V1880V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr7:47921618 C>T maps to NM_138295.3 G1110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:47880063 G>A maps to NM_138295.3 I1849I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:47832322 G>A maps to NM_138295.3 L2810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:47852819 C>T maps to NM_138295.3 E2415E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:47925485 G>A maps to NM_138295.3 A1001A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:47874792 G>A maps to NM_138295.3 L1998L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:47930225 G>A maps to NM_138295.3 F863F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:47852762 G>A maps to NM_138295.3 G2434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr7:47874751 G>A maps to NM_138295.3 S2011S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:47884603 G>C maps to NM_138295.3 S1742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr7:47840381 G>A maps to NM_138295.3 F2686F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr7:47894628 C>T maps to NM_138295.3 R1570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:47894496 G>A maps to NM_138295.3 P1614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr7:47854964 T>A maps to NM_138295.3 G2352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr7:47886646 G>A maps to NM_138295.3 S1661S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:47876551 G>A maps to NM_138295.3 L1970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:47882630 G>A maps to NM_138295.3 L1792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:47925323 C>T maps to NM_138295.3 E1055E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:47897421 G>A maps to NM_138295.3 L1457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr16:81142813 G>A maps to NM_052892.3 I2356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:81197303 G>A maps to NM_052892.3 A1126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr16:81175101 C>T maps to NM_052892.3 A1739A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr16:81150980 C>T maps to NM_052892.3 R2255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr16:81155283 G>A maps to NM_052892.3 L2172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr16:81193306 C>A maps to NM_052892.3 T1272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:81134835 G>A maps to NM_052892.3 F2423F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:81151064 G>A maps to NM_052892.3 I2227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr16:81190502 C>T maps to NM_052892.3 V1362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:81181054 C>T maps to NM_052892.3 W1679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:81134868 G>A maps to NM_052892.3 I2412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:81142879 C>T maps to NM_052892.3 W2334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:81181948 G>A maps to NM_052892.3 F1589F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:81241151 G>A maps to NM_052892.3 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:81253726 C>T maps to NM_052892.3 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:81249949 G>A maps to NM_052892.3 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:81134868 G>A maps to NM_052892.3 I2412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:81214827 G>A maps to NM_052892.3 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr16:81253797 C>A maps to NM_052892.3 G60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:81134756 G>A maps to NM_052892.3 R2450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr16:81253735 G>A maps to NM_052892.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:81211532 G>A maps to NM_052892.3 P772P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:81213264 G>A maps to NM_052892.3 R749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr16:81181921 C>T maps to NM_052892.3 L1598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr16:81219191 G>A maps to NM_052892.3 T634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr16:81241208 G>A maps to NM_052892.3 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr16:81164148 C>T maps to NM_052892.3 R1986R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr16:81222603 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr16:81249940 G>A maps to NM_052892.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:81134855 G>A maps to NM_052892.3 L2417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:81167171 G>A maps to NM_052892.3 I1951I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:81181900 G>A maps to NM_052892.3 F1605F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr16:81232477 G>A maps to NM_052892.3 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:88973228 C>T maps to NM_000297.2 F545F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr4:88967889 C>T maps to NM_000297.2 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr4:88996692 C>T maps to NM_000297.2 S918S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr10:102058344 G>A maps to NM_016112.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:102048185 G>A maps to NM_016112.2 S795S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:102048185 G>A maps to NM_016112.2 S795S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr10:102059379 G>A maps to NM_016112.2 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr10:102054387 G>A maps to NM_016112.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr10:102089770 G>A maps to NM_016112.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:102051117 C>T maps to NM_016112.2 G649G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:102057326 G>A maps to NM_016112.2 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:137230202 C>T maps to ENST00000230643 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr5:137228268 T>C maps to ENST00000230643 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:42282531 C>T maps to NM_138370.2 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:42284373 C>T maps to NM_138370.2 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr22:46656930 G>T maps to NM_006071.1 T763T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr22:46655682 G>A maps to NM_006071.1 S1179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr22:46653537 G>A maps to NM_006071.1 S1894S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr22:46657455 C>T maps to NM_006071.1 R588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr22:46656234 C>T maps to NM_006071.1 R995R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:46656897 C>T maps to NM_006071.1 Q774Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr22:46658001 C>T maps to NM_006071.1 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr22:46655877 C>T maps to NM_006071.1 W1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr22:46655878 C>T maps to NM_006071.1 W1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr22:46655115 T>C maps to NM_006071.1 K1368K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr22:46657116 C>T maps to NM_006071.1 K701K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr22:46657626 C>T maps to NM_006071.1 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr22:46657851 G>A maps to NM_006071.1 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr22:46658277 C>T maps to NM_006071.1 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr22:46655700 C>T maps to NM_006071.1 R1173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr22:46658037 C>T maps to NM_006071.1 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr22:46657908 C>T maps to NM_006071.1 K437K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr22:46653006 G>A maps to NM_006071.1 F2071F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr22:46657020 G>A maps to NM_006071.1 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:46653855 G>A maps to NM_006071.1 I1788I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr22:46658226 G>A maps to NM_006071.1 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:51910840 G>A maps to NM_138694.3 S851S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr6:51918900 G>A maps to NM_138694.3 I633I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr6:51497503 G>A maps to NM_138694.3 R3842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:51890746 C>T maps to NM_138694.3 V1287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:51920405 A>G maps to NM_138694.3 Y605Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:51889492 C>T maps to NM_138694.3 V1705V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr6:51524126 G>A maps to NM_138694.3 H3599H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr6:51890236 G>A maps to NM_138694.3 F1457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr6:51889699 C>T maps to NM_138694.3 L1636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:51907680 C>A maps to NM_138694.3 E1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:51612695 G>A maps to NM_138694.3 R3240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:51586801 A>G maps to NM_170724.2 A3391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:51503725 A>C maps to NM_138694.3 G3809G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:51889717 C>A maps to NM_138694.3 G1630G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:51923237 C>T maps to NM_138694.3 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:51934294 G>A maps to NM_138694.3 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr6:51889855 G>A maps to NM_138694.3 S1584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:51890233 G>A maps to NM_138694.3 S1458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr6:51918862 C>T maps to NM_138694.3 W646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:51613140 G>A maps to NM_138694.3 L3091L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr6:51491839 G>A maps to NM_138694.3 R3914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:51918900 G>A maps to NM_138694.3 I633I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr6:51774189 G>A maps to NM_138694.3 S2191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr6:51497447 G>A maps to NM_138694.3 I3860I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:51900433 G>A maps to NM_138694.3 V1061V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:51923198 C>T maps to NM_138694.3 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr6:51799085 G>A maps to NM_138694.3 I1981I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:51512898 G>A maps to NM_138694.3 S3776S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:51944769 G>A maps to NM_138694.3 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:51935804 G>A maps to NM_138694.3 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr8:110457015 C>T maps to ENST00000426474 L1640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr8:110451186 G>A maps to ENST00000426474 A1274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr8:110457191 C>T maps to ENST00000426474 F1698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr8:110453597 G>A maps to ENST00000426474 G1398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr8:110510902 T>C maps to ENST00000426474 C3578C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:110523105 C>T maps to ENST00000426474 F3833F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr8:110509205 G>A maps to ENST00000426474 G3462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:110447417 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:110454287 G>A maps to ENST00000426474 G1419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr8:110376845 G>A maps to ENST00000426474 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr8:110431367 G>A maps to ENST00000426474 T801T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr8:110457650 C>T maps to ENST00000426474 I1851I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr8:110497337 C>T maps to ENST00000426474 I3214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr8:110509205 G>A maps to ENST00000426474 G3462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:110397838 G>A maps to ENST00000426474 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:110460498 C>T maps to ENST00000426474 I1968I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:110510896 G>A maps to ENST00000426474 G3576G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:110489604 G>A maps to ENST00000426474 K3023K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:110489616 C>T maps to ENST00000426474 A3027A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr8:110503253 C>T maps to ENST00000426474 F3346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr8:110497313 C>T maps to ENST00000426474 F3206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:110505900 G>A maps to ENST00000426474 G3416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr8:110408343 C>T maps to ENST00000426474 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr8:110457191 C>T maps to ENST00000426474 F1698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:110406673 T>C maps to ENST00000426474 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:110465060 C>T maps to ENST00000426474 L2208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:110487397 G>A maps to ENST00000426474 W2886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:110408290 C>T maps to ENST00000426474 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:110453034 G>A maps to ENST00000426474 R1351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:110376774 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr8:110457017 G>T maps to ENST00000426474 L1640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:110431367 G>A maps to ENST00000426474 T801T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:110447557 C>T maps to ENST00000426474 I1160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr8:110397838 G>A maps to ENST00000426474 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr8:110516655 G>A maps to ENST00000426474 V3644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:110510692 C>T maps to ENST00000426474 S3534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:110477409 G>A maps to ENST00000426474 P2783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr8:110397850 G>A maps to ENST00000426474 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr8:110520386 G>A maps to ENST00000426474 G3764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:110464990 C>T maps to ENST00000426474 F2184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr8:110401306 G>C did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr8:110504138 G>A maps to ENST00000426474 G3384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:110416852 C>T maps to ENST00000426474 R482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:110520419 G>A maps to ENST00000426474 L3775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr8:110431436 C>T maps to ENST00000426474 F824F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr8:110530531 C>T maps to ENST00000426474 F3943F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr8:110432828 T>C maps to ENST00000426474 N869N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr8:110487356 T>C maps to ENST00000426474 I2872I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr8:110424510 G>A maps to ENST00000426474 G701G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr8:110453034 G>A maps to ENST00000426474 R1351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr8:110509187 C>T maps to ENST00000426474 A3456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:110402699 C>T maps to ENST00000426474 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:110439351 G>A maps to ENST00000426474 W989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:110477421 C>T maps to ENST00000426474 G2787G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:110478891 C>T maps to ENST00000426474 F2833F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:110489535 C>T maps to ENST00000426474 F3000F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:110535019 G>A maps to ENST00000426474 V4078V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:110477070 C>T maps to ENST00000426474 F2670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:110453507 C>T maps to ENST00000426474 S1368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr8:110478891 C>T maps to ENST00000426474 F2833F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr8:110447479 C>T maps to ENST00000426474 S1134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr8:110431367 G>A maps to ENST00000426474 T801T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr8:110453597 G>A maps to ENST00000426474 G1398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr8:110527487 G>A maps to ENST00000426474 W3882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr8:110530693 G>A maps to ENST00000426474 E3997E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr8:110478891 C>T maps to ENST00000426474 F2833F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr8:110457461 C>T maps to ENST00000426474 F1788F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr8:79510759 C>T maps to NM_181839.1 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:123039007 G>A maps to ENST00000368446 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:123046338 G>A maps to ENST00000368446 *88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:43243232 C>T maps to NM_181805.1 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:155265515 C>T maps to ENST00000423816 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:155263134 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:155264091 G>A maps to ENST00000423816 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:155264115 G>A maps to ENST00000423816 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:155264142 G>A maps to ENST00000423816 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:155263258 G>A maps to ENST00000423816 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr15:72502029 G>A maps to ENST00000419739 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr15:72501044 G>A maps to ENST00000419739 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr15:72502750 G>A maps to ENST00000419739 Y179Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:72492919 G>A maps to ENST00000419739 Q536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:14578388 C>T maps to NM_213560.1 Q588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:14557314 C>T maps to NM_213560.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:14574745 T>C maps to NM_213560.1 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:14580206 C>T maps to NM_213560.1 F683F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:14562689 C>T maps to NM_213560.1 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:14581442 G>A maps to NM_213560.1 E837E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:14568909 C>T maps to NM_213560.1 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:14581590 G>A maps to NM_213560.1 R857R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:14574502 G>T maps to NM_213560.1 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr1:89250364 G>A maps to NM_006256.2 E343E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr1:89150310 G>A maps to NM_006256.2 Q16Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr1:89237542 C>T maps to NM_006256.2 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr9:131475653 C>T maps to NM_013355.3 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:131476551 C>T maps to NM_013355.3 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:131480860 C>T maps to NM_013355.3 A694A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr11:125281706 C>T maps to NM_022062.2 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr11:125267784 C>T maps to NM_022062.2 Q139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:125301155 G>A maps to NM_022062.2 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:125237848 C>T maps to NM_022062.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:201282610 C>T maps to NM_000299.3 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr1:201294147 C>T maps to NM_000299.3 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:201263088 G>A maps to NM_000299.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:201287818 C>T maps to NM_000299.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:201252991 C>T maps to NM_000299.3 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZU-06A-12D-A196-08 chr1:201286701 C>T maps to NM_000299.3 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:201286863 C>T maps to NM_000299.3 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:201287785 G>A maps to NM_000299.3 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:201294247 C>T maps to NM_000299.3 R693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:201297942 G>A maps to NM_000299.3 R741R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:33030889 G>A maps to NM_004572.3 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr12:32945414 C>T maps to NM_004572.3 K863K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:32994047 G>A maps to NM_004572.3 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:33031216 G>A maps to NM_004572.3 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:33030832 C>T maps to NM_004572.3 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:32974394 G>A maps to NM_004572.3 S680S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:32975517 C>T maps to NM_004572.3 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:32996149 C>T maps to NM_004572.3 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:32949218 G>A maps to NM_004572.3 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:32955373 C>T maps to NM_004572.3 R754R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:33031072 C>T maps to NM_004572.3 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:33030931 G>A maps to NM_004572.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr12:32994095 G>A maps to NM_004572.3 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:33031366 C>T maps to NM_004572.3 E149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:32974421 G>A maps to NM_004572.3 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:33031375 C>T maps to NM_004572.3 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr12:33030949 G>A maps to NM_004572.3 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:32945631 G>A maps to NM_004572.3 S841S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:32993999 G>A maps to NM_004572.3 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:33021995 C>T maps to NM_004572.3 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:33031000 G>A maps to NM_004572.3 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:32945369 G>A maps to NM_004572.3 S878S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr12:32945414 C>T maps to NM_004572.3 K863K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr12:33030883 C>T maps to NM_004572.3 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr12:33031216 G>A maps to NM_004572.3 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr12:32996155 C>T maps to NM_004572.3 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:32945426 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:32975412 C>T maps to NM_004572.3 R653R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:33031216 G>A maps to NM_004572.3 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr11:397655 G>A maps to NM_007183.2 K354K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr11:404550 G>A maps to NM_007183.2 E792E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:404556 C>T maps to NM_007183.2 F794F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:399128 G>A maps to NM_007183.2 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr11:399047 G>A maps to NM_007183.2 Q375Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr11:400003 G>A maps to NM_007183.2 K437K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr2:159490798 C>T maps to NM_003628.3 P520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr2:159530489 G>A maps to NM_003628.3 Q1035Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:159519536 C>T maps to NM_003628.3 D780D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:159481682 C>T maps to NM_003628.3 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:159530251 C>T maps to NM_003628.3 D996D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:159499092 C>T maps to NM_003628.3 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:119331933 C>T maps to NM_015900.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:119343986 G>A maps to NM_015900.2 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr3:119328328 G>A maps to NM_015900.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr3:119328346 C>T maps to NM_015900.2 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:119336968 G>A maps to NM_015900.2 K286K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr4:110638854 G>A maps to NM_030821.4 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:110650854 G>A maps to NM_030821.4 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:74714266 C>T maps to NM_032562.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:74714431 G>A maps to NM_032562.2 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:74695434 G>A maps to NM_032562.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:74695421 G>A maps to NM_032562.2 Q181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:74700993 G>A maps to NM_032562.2 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr10:74700939 G>A maps to NM_032562.2 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:68289708 C>T maps to NM_012320.3 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:63357682 G>A maps to NM_001128203.1 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:63357817 T>C maps to NM_001128203.1 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr1:20305230 G>A maps to NM_001161728.1 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:20501648 C>T maps to NM_001105572.1 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:20440675 C>T maps to ENST00000442610 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:20466685 C>T maps to NM_022819.3 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr1:20474839 C>T maps to NM_022819.3 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:20469972 G>A maps to NM_022819.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:20471156 C>T maps to NM_022819.3 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr22:31532892 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr22:31534275 C>T maps to NM_015715.3 W256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr22:31533711 A>G maps to NM_015715.3 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:31532913 G>A maps to NM_015715.3 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr22:31536232 G>A maps to NM_015715.3 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr22:31536283 C>T maps to NM_015715.3 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr22:31536155 C>T maps to NM_015715.3 W62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr22:31533696 C>T maps to NM_015715.3 Q355Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr22:31533738 G>A maps to NM_015715.3 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr22:31536100 G>A maps to NM_015715.3 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:31532916 G>A maps to NM_015715.3 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:31533828 C>T maps to NM_015715.3 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr22:31533831 C>T maps to NM_015715.3 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr1:186901933 C>T maps to NM_024420.2 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:186946726 A>G maps to NM_024420.2 E589E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:186880478 C>T maps to NM_024420.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr1:186863339 C>T maps to NM_024420.2 N125N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:186880419 C>T maps to NM_024420.2 Q153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:48565293 G>A maps to NM_003706.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:48609801 G>A maps to NM_001159322.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:48565341 G>A maps to NM_003706.2 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr19:48578066 G>A maps to NM_003706.2 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:48565281 G>A maps to NM_003706.2 F410F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr15:42363463 C>T maps to NM_178034.3 W578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr15:42379611 C>T maps to NM_178034.3 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr15:42362986 G>T maps to NM_178034.3 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:42363513 C>T maps to NM_178034.3 E561E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:42364023 G>A maps to NM_178034.3 F507F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:42364500 C>T maps to NM_178034.3 E469E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:42374581 G>A maps to NM_178034.3 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr15:42363336 G>A maps to NM_178034.3 D620D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr15:42363654 C>T maps to NM_178034.3 K556K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:42375968 C>T maps to NM_178034.3 E160E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr15:42375497 C>T maps to NM_178034.3 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr15:42379496 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:42375932 C>T maps to NM_178034.3 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:42379883 G>A maps to NM_178034.3 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:42375521 C>T maps to NM_178034.3 K182K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr15:42292361 G>A maps to NM_001080490.1 Y235Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:42276095 C>T maps to NM_001080490.1 K792K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:42280280 G>A maps to NM_001080490.1 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:42287556 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:42287589 G>A maps to NM_001080490.1 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:42287670 G>A maps to NM_001080490.1 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:42285015 G>A maps to NM_001080490.1 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:42302334 C>T maps to NM_001080490.1 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:42282376 G>A maps to NM_001080490.1 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:42298261 G>A maps to NM_001080490.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:42280265 C>T maps to NM_001080490.1 R575R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:42299961 C>A maps to NM_001080490.1 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr15:42282346 C>T maps to NM_001080490.1 K490K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:42279562 C>T maps to NM_001080490.1 P585P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:42285036 G>A maps to NM_001080490.1 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr15:42436654 G>A maps to ENST00000397272 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr15:42436184 G>A maps to ENST00000397272 A713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr15:42437806 G>A maps to ENST00000397272 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:42439348 G>A maps to ENST00000397272 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr15:42436717 G>A maps to ENST00000397272 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:42434729 G>A maps to ENST00000397272 A777A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:42434765 G>A maps to ENST00000397272 F765F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:42437979 C>T maps to ENST00000397272 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:42439522 C>T maps to ENST00000397272 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:20417109 C>T maps to NM_000929.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:20412624 G>A maps to NM_000929.2 E30E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr1:20412720 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr22:38508284 G>A maps to NM_003560.2 I768I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr22:38541617 G>A maps to NM_003560.2 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr22:38536041 G>A maps to NM_003560.2 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr22:38541527 G>A maps to NM_003560.2 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr22:38516830 G>A maps to NM_003560.2 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:38530994 C>T maps to NM_003560.2 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:38531036 G>A maps to NM_003560.2 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr22:38509601 G>A maps to NM_003560.2 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:46675801 G>A maps to NM_001168357.1 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr6:46675874 C>T maps to NM_001168357.1 W298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr6:46684774 G>A maps to NM_001168357.1 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr6:46675831 C>T maps to NM_001168357.1 Q312Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F4-06A-12D-A25O-08 chr6:46679258 C>A maps to NM_001168357.1 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:46672296 C>T maps to NM_001168357.1 *442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr2:160898620 A>C maps to NM_007366.4 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:160901447 G>A maps to NM_007366.4 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr2:160843732 C>T maps to NM_007366.4 E657E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:160901662 C>A maps to NM_007366.4 G39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:160901447 G>A maps to NM_007366.4 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:160798467 G>A maps to NM_007366.4 L1405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:160884795 C>T maps to NM_007366.4 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:160833801 G>A maps to NM_007366.4 I798I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:160833814 C>T maps to NM_007366.4 W794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:160879357 C>T maps to NM_007366.4 W371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:160843669 G>A maps to NM_007366.4 F678F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:160869881 C>T maps to NM_007366.4 W519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr2:160824066 G>A maps to NM_007366.4 L963L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:160801486 C>T maps to NM_007366.4 R1358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:160843795 G>A maps to NM_007366.4 H636H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:160862249 G>A maps to NM_007366.4 Q583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:160873223 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:160901447 G>A maps to NM_007366.4 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:160824072 C>A maps to NM_007366.4 G961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr2:160889545 C>T maps to NM_007366.4 E255E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr2:160808036 G>A maps to NM_007366.4 T1118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:26910387 G>A maps to NM_001031689.2 F535F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:26919512 A>T maps to NM_001031689.2 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr9:26925928 G>A maps to NM_001031689.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr9:26925889 G>A maps to NM_001031689.2 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr9:26925890 G>A maps to NM_001031689.2 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:133700463 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:59807961 T>G maps to NM_173801.3 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr4:84026066 C>T maps to NM_001130715.1 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:145464077 G>A maps to NM_001029869.1 Q151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr8:57079134 G>A maps to NM_002655.2 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr8:57079506 G>A maps to NM_002655.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:57078987 G>A maps to NM_002655.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr8:57079665 G>A maps to NM_002655.2 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:57079197 A>G maps to NM_002655.2 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:57079554 G>A maps to NM_002655.2 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:144262863 C>T maps to NM_001080951.1 K363K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:144263445 C>T maps to NM_001080951.1 K169K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr6:144263748 C>T maps to NM_001080951.1 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:30784536 G>A maps to NM_002657.3 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr20:30784500 G>A maps to NM_002657.3 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr20:30784308 G>A maps to NM_002657.3 F479F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr20:30784637 G>A maps to NM_002657.3 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr20:30789888 G>A maps to NM_002657.3 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:30784908 G>A maps to NM_002657.3 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:42050646 G>A maps to NM_000930.3 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:75673107 C>T maps to NM_002658.3 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:75673309 C>T maps to NM_002658.3 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:75673752 G>A maps to NM_002658.3 K232K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:75674609 G>A maps to NM_002658.3 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:44171763 G>A maps to NM_002659.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:28865906 C>T maps to NM_153021.4 L1453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr2:28865848 C>T maps to NM_153021.4 I1433I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:28719004 C>T maps to NM_153021.4 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr2:28849368 G>A maps to NM_153021.4 E1218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:28796088 C>T maps to NM_153021.4 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:28828718 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:28843481 G>A maps to NM_153021.4 G1133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr2:28843764 C>T maps to NM_153021.4 N1149N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr2:28804975 G>A maps to NM_153021.4 K536K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr2:28804999 G>A maps to NM_153021.4 E544E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:28852028 G>A maps to NM_153021.4 G1265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr2:28752247 G>A maps to NM_153021.4 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:28719004 C>T maps to NM_153021.4 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr2:28843797 G>A maps to NM_153021.4 W1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:28761175 C>T maps to NM_001170585.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:28828727 C>T maps to NM_153021.4 L990L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr2:28800972 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:28763256 C>T maps to NM_153021.4 C241C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:28823675 G>A maps to NM_153021.4 E825E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr2:28719004 C>T maps to NM_153021.4 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr2:28854913 C>T maps to NM_153021.4 S1303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr2:28775808 G>A maps to NM_153021.4 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:28854958 G>A maps to NM_153021.4 A1318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:28816582 C>T maps to NM_153021.4 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr2:28828808 C>T maps to NM_153021.4 T1017T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:28805324 G>A maps to NM_153021.4 R562R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:28828805 G>A maps to NM_153021.4 W1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:28865887 G>A maps to NM_153021.4 R1446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:28823693 C>G maps to NM_153021.4 V831V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:28823694 C>T maps to NM_153021.4 Q832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:28827595 C>T maps to NM_153021.4 F977F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:28796067 C>T maps to NM_153021.4 I443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:14688710 A>G maps to NM_024829.5 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:14664329 G>A maps to NM_024829.5 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:14693724 C>T maps to NM_024829.5 K177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:14706182 C>T maps to NM_024829.5 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:14693811 T>C maps to NM_024829.5 K148K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr12:113826403 C>T maps to NM_173542.3 F581F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:113824828 G>A maps to NM_173542.3 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:113825581 G>C maps to NM_173542.3 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:113821968 C>T maps to NM_173542.3 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q9-06A-11D-A19A-08 chr20:8665705 G>A maps to NM_015192.2 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr20:8717763 G>A maps to NM_015192.2 K711K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr20:8713957 C>T maps to NM_015192.2 F654F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:8678390 C>T maps to NM_015192.2 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:8698343 C>T maps to NM_015192.2 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:8755293 G>A maps to NM_015192.2 Q1013Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr20:8665693 C>T maps to NM_015192.2 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr20:8713957 C>T maps to NM_015192.2 F654F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:8609077 G>A maps to NM_015192.2 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:8713927 G>A maps to NM_015192.2 G644G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr20:8769118 C>T maps to NM_015192.2 V1045V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr20:8770195 C>T maps to NM_015192.2 Q1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr20:8782783 C>T maps to NM_182734.1 Q1169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr20:8678348 G>A maps to NM_015192.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:8626762 G>A maps to NM_015192.2 E133E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr20:8770194 C>T maps to NM_015192.2 I1103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr20:8770909 T>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:8678294 C>T maps to NM_015192.2 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr20:8862494 G>A maps to NM_015192.2 *1217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:8665651 G>A maps to NM_015192.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:8698472 C>T maps to NM_015192.2 F497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr15:40581029 G>A maps to NM_004573.2 T1148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:40591080 G>A maps to NM_004573.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:40594353 C>T maps to NM_004573.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr15:40594798 G>A maps to NM_004573.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr15:40588497 G>A maps to NM_004573.2 A565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:40590441 G>A maps to NM_004573.2 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:40589052 G>A maps to NM_004573.2 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr15:40594550 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr15:40599843 G>A maps to NM_004573.2 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr15:40591080 G>A maps to NM_004573.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr15:40581115 G>A maps to NM_004573.2 Q1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr15:40581116 G>A maps to NM_004573.2 F1119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr15:40590103 G>A maps to NM_004573.2 I404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:40589766 C>T maps to NM_004573.2 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr15:40590507 C>T maps to NM_004573.2 E357E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:40599852 G>A maps to NM_004573.2 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr15:40591076 G>A maps to NM_004573.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr11:64021913 C>T maps to NM_000932.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:64028930 C>T maps to NM_000932.2 I597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr11:64026179 G>T maps to NM_000932.2 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:64023200 C>T maps to NM_000932.2 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:64030186 C>T maps to NM_000932.2 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:64029441 C>T maps to NM_000932.2 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr11:64023221 C>T maps to NM_000932.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr11:64022395 C>T maps to NM_000932.2 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:64026158 C>T maps to NM_000932.2 I409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr20:9424640 C>T maps to NM_001172646.1 I926I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr20:9417794 G>A maps to NM_001172646.1 K920K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr20:9459569 G>A maps to NM_001172646.1 A1166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr20:9318683 C>T maps to NM_001172646.1 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr20:9416234 G>A maps to NM_001172646.1 K851K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:9351932 C>T maps to NM_001172646.1 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr20:9401955 C>T maps to NM_001172646.1 Q723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:9365043 C>T maps to NM_001172646.1 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:9391703 C>T maps to NM_001172646.1 Q674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr20:9391682 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr20:9453990 C>T maps to NM_001172646.1 F1158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:9438106 C>T maps to NM_001172646.1 Q1015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:9353041 C>T maps to NM_001172646.1 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr20:9457374 C>T maps to NM_000933.3 S1157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr20:9438075 C>T maps to NM_001172646.1 L1004L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:9402009 T>C maps to NM_001172646.1 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr20:9440328 C>T maps to NM_001172646.1 I1040I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr20:9438075 C>T maps to NM_001172646.1 L1004L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr20:9404487 C>T maps to NM_001172646.1 Q805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr20:9360768 C>T maps to NM_001172646.1 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr20:9438099 C>T maps to NM_001172646.1 I1012I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr20:9404486 C>T maps to NM_001172646.1 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr20:9319683 G>A maps to NM_001172646.1 K123K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr20:9319684 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr20:9404510 C>T maps to NM_001172646.1 S812S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr20:9424677 G>T did not map to a codon.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr20:9449274 C>T maps to NM_001172646.1 A1102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr20:9434088 G>A maps to NM_001172646.1 E992E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:9317853 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:9353692 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:9364962 C>T maps to NM_001172646.1 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:9374248 G>A maps to NM_001172646.1 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:9434088 G>A maps to NM_001172646.1 E992E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:9317804 C>T maps to NM_001172646.1 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:9416234 G>A maps to NM_001172646.1 K851K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr20:9453991 C>T maps to NM_001172646.1 L1159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr20:9317804 C>T maps to NM_001172646.1 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr20:9404514 C>T maps to NM_001172646.1 R814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:38051221 G>A maps to NM_001130964.1 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:43196224 G>A maps to NM_133373.3 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr17:43196355 G>A maps to NM_133373.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:43196365 G>A maps to NM_133373.3 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr17:43194046 C>T maps to NM_133373.3 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:219487533 G>A maps to ENST00000432688 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:219483368 G>A maps to ENST00000432688 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:219492821 C>T maps to ENST00000432688 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:219499292 G>A maps to ENST00000432688 Q644Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr2:219486274 C>T maps to ENST00000432688 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr10:95931162 C>T maps to ENST00000371380 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr10:95791099 G>A maps to ENST00000371380 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:96058136 T>C maps to ENST00000371380 S1723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:95791318 C>T maps to ENST00000371380 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:96058370 C>T maps to ENST00000371380 P1801P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr10:95791084 C>T maps to ENST00000371380 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:96058175 T>G maps to ENST00000371380 S1736S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:95791618 G>A maps to ENST00000371380 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:95791692 T>A maps to ENST00000371380 L297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:95848985 G>A maps to NM_001165979.1 E45E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:96073090 C>T maps to ENST00000371380 T2028T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr10:95791711 C>T maps to ENST00000371380 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:95791423 C>T maps to ENST00000371380 N207N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr10:95791354 G>A maps to ENST00000371380 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr10:96081674 C>T maps to ENST00000371380 N2120N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr10:95791307 C>T maps to ENST00000371380 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr10:95791099 G>A maps to ENST00000371380 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr10:96022311 G>A maps to ENST00000371380 S1292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr10:96066278 C>T maps to ENST00000371380 F1906F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr10:96068342 C>T maps to ENST00000371380 R1964*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr10:96028693 G>A maps to ENST00000371380 L1430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr10:96043625 G>A maps to ENST00000371380 K1625K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:96064323 G>A maps to ENST00000371380 K1848K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr10:96058181 T>G maps to ENST00000371380 P1738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:95791483 G>A maps to ENST00000371380 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:96014662 C>T maps to ENST00000371380 I1137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr10:95792001 G>A maps to ENST00000371380 W400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:95791483 G>A maps to ENST00000371380 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:95892154 G>A maps to ENST00000371380 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:96025693 C>T maps to ENST00000371380 S1420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:39792091 C>T maps to NM_002660.2 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:39793701 C>T maps to NM_002660.2 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr20:39791896 C>T maps to NM_002660.2 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr20:39792110 C>T maps to NM_002660.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr20:39792067 C>T maps to NM_002660.2 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr20:39794388 C>T maps to NM_002660.2 I574I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:39793584 C>T maps to NM_002660.2 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:81965258 G>A maps to NM_002661.2 K913K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:81990322 C>T maps to NM_002661.2 S1198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:81971474 C>T maps to NM_002661.2 S1055S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr16:81891955 C>T maps to NM_002661.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr16:81942190 C>T maps to NM_002661.2 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:81971414 C>T maps to NM_002661.2 G1035G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:81960688 G>A maps to NM_002661.2 W807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:81934315 G>A maps to NM_002661.2 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:81944271 C>T maps to NM_002661.2 F627F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr16:81944271 C>T maps to NM_002661.2 F627F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr16:81888100 C>T maps to NM_002661.2 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr16:81969852 C>T maps to NM_002661.2 L974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr16:81944271 C>T maps to NM_002661.2 F627F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr16:81979867 G>A maps to NM_002661.2 L1190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:81929529 G>A maps to NM_002661.2 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:81902884 C>T maps to NM_002661.2 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:81914534 G>A maps to NM_002661.2 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:155215184 G>A maps to ENST00000340059 T594T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:155200112 A>G maps to ENST00000340059 F1242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:155215136 G>A maps to ENST00000340059 S610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:155311830 G>A maps to ENST00000340059 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr3:155215190 C>T maps to ENST00000340059 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:155199388 G>A maps to ENST00000340059 L1484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr3:155241703 G>T maps to ENST00000340059 C472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:155200811 C>T maps to ENST00000340059 G1009G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:155203268 C>T maps to ENST00000340059 R958R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:155271911 G>A maps to ENST00000340059 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:155215206 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr3:155200025 C>T maps to ENST00000340059 T1271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr3:155200040 G>A maps to ENST00000340059 T1266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr3:155232637 G>A maps to ENST00000340059 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:155314036 C>T maps to ENST00000340059 K58K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr3:155314052 C>T maps to ENST00000340059 W53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:155200084 G>A maps to ENST00000340059 L1252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:155267629 C>T maps to ENST00000340059 G424G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A2A6-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr3:155199128 G>A maps to ENST00000340059 L1570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr3:155199995 G>A maps to ENST00000340059 P1281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:155303855 G>A maps to ENST00000340059 Q188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:155314090 G>A maps to ENST00000340059 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:155200523 C>T maps to ENST00000340059 V1105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:155211981 G>A maps to ENST00000340059 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:155200052 C>T maps to ENST00000340059 S1262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:155200481 C>T maps to ENST00000340059 G1119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:155203475 C>T maps to ENST00000340059 K889K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:155199878 G>A maps to ENST00000340059 T1320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:155282848 T>C maps to ENST00000340059 E296E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19T-06A-11D-A19A-08 chr3:155199620 G>A maps to ENST00000340059 N1406N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:155203355 C>T maps to ENST00000340059 R929R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr3:155200265 C>T maps to ENST00000340059 E1191E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr3:155203355 C>T maps to ENST00000340059 R929R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:155198855 G>A maps to ENST00000340059 H1661H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:155203355 C>T maps to ENST00000340059 R929R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr3:155210561 G>A maps to ENST00000340059 Q743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr3:155211993 G>A maps to ENST00000340059 N694N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:155200580 T>C maps to ENST00000340059 P1086P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:155282899 C>T maps to ENST00000340059 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:2418729 C>T maps to NM_014638.2 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:2428309 C>T maps to NM_014638.2 A659A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:2435904 C>T maps to NM_014638.2 S1168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:2408074 G>A maps to NM_014638.2 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:2411248 C>T maps to NM_014638.2 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:2418757 C>T maps to NM_014638.2 Q353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:2436318 C>T maps to NM_014638.2 L1306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:2421227 G>A maps to NM_014638.2 E479E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:2418401 C>T maps to NM_014638.2 C291C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:198949554 C>T maps to NM_006226.3 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:198948639 T>C maps to NM_006226.3 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr2:198950721 C>T maps to NM_006226.3 P827P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:198949005 G>A maps to NM_006226.3 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:198949101 C>T maps to NM_006226.3 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:198950622 C>T maps to NM_006226.3 I794I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:198949056 C>T maps to NM_006226.3 N272N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr2:198950127 G>A maps to NM_006226.3 E629E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:198948910 C>T maps to NM_006226.3 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:198950187 C>T maps to NM_006226.3 I649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:198950721 C>T maps to NM_006226.3 P827P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:198948747 G>A maps to NM_006226.3 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:17051374 G>A maps to NM_001144382.1 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:17053501 G>A maps to NM_001144382.1 K884K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr3:17084433 G>A maps to NM_001144382.1 Q1025Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:17052664 G>A maps to NM_001144382.1 V605V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr3:17052709 C>T maps to NM_001144382.1 I620I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:17051446 C>T maps to NM_001144382.1 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:17053117 C>T maps to NM_001144382.1 I756I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr3:17053048 C>T maps to NM_001144382.1 V733V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:17084421 C>T maps to NM_001144382.1 I1021I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:17053426 C>T maps to NM_001144382.1 S859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:17056315 C>T maps to NM_001144382.1 V973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr3:17052778 C>T maps to NM_001144382.1 S643S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr3:17056373 C>T maps to NM_001144382.1 L993L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:17109538 G>A maps to NM_001144382.1 W1058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:17052325 C>T maps to NM_001144382.1 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:17053021 C>T maps to NM_001144382.1 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr3:17052314 C>T maps to NM_001144382.1 Q489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:17109547 C>T maps to NM_001144382.1 T1061T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr3:17109537 G>A maps to NM_001144382.1 W1058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:17109457 C>T maps to NM_001144382.1 F1031F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:17056384 C>T maps to NM_001144382.1 I996I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr3:17053543 C>T maps to NM_001144382.1 S898S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:17052325 C>T maps to NM_001144382.1 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:17053360 C>T maps to NM_001144382.1 F837F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:17052415 A>G maps to NM_001144382.1 K522K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr3:17052040 C>T maps to NM_001144382.1 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr3:17051875 C>T maps to NM_001144382.1 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:205505 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:111426915 C>T maps to ENST00000312791 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr3:111426915 C>T maps to ENST00000312791 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:111427001 C>T maps to ENST00000312791 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr3:111426860 C>T maps to ENST00000312791 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:111394211 C>T maps to ENST00000312791 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:111426818 G>A maps to ENST00000312791 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr5:41382220 C>T maps to NM_001005473.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr5:41510610 C>T maps to NM_001005473.2 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr5:41382220 C>T maps to NM_001005473.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:41381968 G>A maps to NM_001005473.2 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:41382376 G>A maps to NM_001005473.2 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:41382220 C>T maps to NM_001005473.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:41313844 G>A maps to NM_001005473.2 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr5:41313872 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr5:41382220 C>T maps to NM_001005473.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr12:18847963 C>T maps to ENST00000266505 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:18852824 C>T maps to ENST00000266505 E359E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr12:18841058 G>A maps to ENST00000266505 Q519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr12:18847927 C>T maps to ENST00000266505 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:18849174 C>T maps to ENST00000266505 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:18854443 C>T maps to ENST00000266505 K336K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:18858150 G>A maps to ENST00000266505 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:18858168 C>T maps to ENST00000266505 Q265Q. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-ER-A195-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:18847963 C>T maps to ENST00000266505 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:18889169 C>T maps to ENST00000266505 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr12:18854659 C>T maps to ENST00000266505 K305K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:18865910 C>T maps to ENST00000266505 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:18876380 G>A maps to ENST00000266505 F77F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-GF-A6C8-06A-12D-A30X-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:18854437 C>T maps to ENST00000266505 K338K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr3:171321002 G>A maps to NM_002662.3 P1030P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:171320909 A>G maps to NM_002662.3 V1061V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr3:171320998 G>A maps to NM_002662.3 R1032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:171395395 G>A maps to NM_002662.3 F652F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:171455441 G>A maps to NM_002662.3 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr3:171377079 G>A maps to NM_002662.3 F784F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr17:4711378 G>A maps to NM_002663.3 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr17:4725981 C>T maps to NM_002663.3 L875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:4713309 C>T maps to NM_002663.3 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr17:4726005 C>T maps to NM_002663.3 P883P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr17:4722095 C>T maps to NM_002663.3 I717I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:4722406 C>T maps to NM_002663.3 S734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:4720325 C>T maps to NM_002663.3 F559F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:4711583 C>T maps to NM_002663.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr17:4725969 C>T maps to NM_002663.3 S871S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr17:4711408 G>A maps to NM_002663.3 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:4714186 C>T maps to NM_002663.3 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr17:4711684 C>T maps to NM_002663.3 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:4722874 C>T maps to NM_002663.3 F820F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr17:4714153 C>T maps to NM_002663.3 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr17:4721599 C>T maps to NM_002663.3 F643F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:4726071 C>T maps to NM_002663.3 H905H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr17:4720286 C>T maps to NM_002663.3 V546V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:40877666 C>T maps to NM_012268.2 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:40883697 C>T maps to NM_012268.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:40883977 G>A maps to NM_012268.2 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:40884016 C>T maps to NM_012268.2 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:40873680 C>T maps to NM_012268.2 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr19:40883998 C>T maps to NM_012268.2 F464F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:105396384 G>A maps to NM_138790.2 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:242451696 C>T maps to NM_152666.2 W154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr1:242253347 C>T maps to NM_152666.2 Q473Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:242287769 C>T maps to NM_152666.2 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:242253242 C>T maps to NM_152666.2 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:242383349 G>A maps to NM_152666.2 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:242271140 C>T maps to NM_152666.2 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:242287897 G>A maps to NM_152666.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:242264024 G>T maps to NM_152666.2 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:242383334 G>A maps to NM_152666.2 H230H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:242383355 G>A maps to NM_152666.2 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:242383364 C>T maps to NM_152666.2 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr1:242253242 C>T maps to NM_152666.2 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:17109300 G>A maps to NM_178836.3 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr8:144995803 G>A maps to NM_201380.2 L2866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr8:144995804 G>A maps to NM_201380.2 I2865I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr8:145001454 G>A maps to NM_201380.2 Q1406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr8:144998506 C>A maps to NM_201380.2 E2001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr8:144992530 G>A maps to NM_201380.2 L3957L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:144990868 G>A maps to NM_201380.2 L4511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:144990869 G>A maps to NM_201380.2 A4510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr8:144994510 G>A maps to NM_201380.2 R3297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:144991292 G>A maps to NM_201380.2 F4369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr8:145006585 G>A maps to NM_201380.2 A790A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr8:144997100 C>T maps to NM_201380.2 L2469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr8:145006820 C>G maps to NM_201380.2 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:144994913 G>A maps to NM_201380.2 V3162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr8:145001237 G>A maps to NM_201380.2 L1421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr8:144995048 C>T maps to NM_201380.2 L3117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr8:145003927 G>A maps to NM_201380.2 L1074L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:144993557 G>A maps to NM_201380.2 P3614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:145006847 G>A maps to NM_201380.2 Y727Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr8:144993386 G>A maps to NM_201380.2 P3671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:144995942 G>A maps to NM_201380.2 L2819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr8:144998069 C>T maps to NM_201380.2 E2146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr8:144998603 C>T maps to NM_201380.2 A1968A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:144998576 G>A maps to NM_201380.2 A1977A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:144990956 G>A maps to NM_201380.2 I4481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr8:144992921 C>T maps to NM_201380.2 T3826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:144991292 G>A maps to NM_201380.2 F4369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:144992837 G>A maps to NM_201380.2 A3854A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr8:144995303 G>A maps to NM_201380.2 V3032V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:144996173 G>A maps to NM_201380.2 H2742H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr8:145003383 C>T maps to NM_201380.2 K1186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:144994642 G>A maps to NM_201380.2 L3253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:144996938 C>T maps to NM_201380.2 K2523K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr8:144995444 G>A maps to NM_201380.2 D2985D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr8:144999674 C>T maps to NM_201380.2 E1611E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr8:144997234 G>A maps to NM_201380.2 Q2425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:144995678 G>A maps to NM_201380.2 A2907A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:144995894 G>A maps to NM_201380.2 I2835I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:145001727 G>A maps to NM_201380.2 L1339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:145006618 G>A maps to NM_201380.2 F779F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr8:144994259 C>A maps to NM_201380.2 V3380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:144996878 G>A maps to NM_201380.2 F2543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr8:144998534 G>A maps to NM_201380.2 I1991I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr8:144993599 G>A maps to NM_201380.2 R3600R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr2:68607560 C>T maps to NM_002664.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:68622907 G>A maps to NM_002664.2 W338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:68607868 C>T maps to NM_002664.2 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:68615583 C>T maps to NM_002664.2 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:68620322 G>A maps to NM_002664.2 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr2:68607988 G>A maps to NM_002664.2 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:68607988 G>A maps to NM_002664.2 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:68621294 G>A maps to NM_002664.2 E301E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:68607928 C>T maps to NM_002664.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:68620304 G>A maps to NM_002664.2 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:67864444 G>A maps to NM_016445.1 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr10:124189306 C>T maps to NM_021622.4 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:124152832 C>T maps to NM_021622.4 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:38775470 C>T maps to NM_021623.1 N8N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:49364934 G>A maps to NM_020904.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr19:49362158 G>A maps to NM_020904.2 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:49344404 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:49362197 G>A maps to NM_020904.2 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr19:49363626 G>A maps to NM_020904.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:49362197 G>A maps to NM_020904.2 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:49362254 G>A maps to NM_020904.2 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr19:49355504 G>A maps to NM_020904.2 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U9-06A-11D-A32N-08 chr19:49340605 G>A maps to NM_020904.2 V760V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:19418702 C>T maps to ENST00000429027 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:19418703 C>T maps to ENST00000429027 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CF-06A-11D-A196-08 chr12:19522625 G>C did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:19512470 C>T maps to ENST00000429027 F1153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr12:19418702 C>T maps to ENST00000429027 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:204197268 C>A maps to ENST00000367191 R1011R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:204197304 C>T maps to ENST00000367191 Q999Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:204226885 G>A maps to ENST00000367191 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr1:204236632 G>A maps to ENST00000367191 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr11:16838741 G>A maps to ENST00000448080 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:16873844 A>G maps to ENST00000448080 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:17035711 G>T maps to ENST00000448080 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:16822594 G>A maps to ENST00000448080 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr11:16847785 C>T maps to ENST00000448080 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:16838382 C>T maps to ENST00000448080 G610G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:16838577 G>A maps to ENST00000448080 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:16823226 G>A maps to ENST00000448080 S765S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr11:16876446 G>A maps to ENST00000448080 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:16822586 C>T maps to ENST00000448080 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:16812686 G>A maps to ENST00000448080 P936P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:16838403 C>T maps to ENST00000448080 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:16838748 G>A maps to ENST00000448080 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:16810705 C>T maps to ENST00000448080 G1099G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:16812572 C>T maps to ENST00000448080 V974V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:16816493 C>T maps to ENST00000448080 E827E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:16816046 C>T maps to ENST00000448080 A911A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr11:16816141 G>A maps to ENST00000448080 R880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:30101625 C>T maps to ENST00000440706 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:45567770 G>A maps to ENST00000256692 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr12:45567148 G>A maps to ENST00000256692 R334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:45567851 C>T maps to ENST00000256692 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:131897828 C>T maps to ENST00000409158 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr19:30164946 C>T maps to ENST00000436066 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr19:30165195 C>T maps to ENST00000436066 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:96166769 C>T maps to NM_024613.3 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:96166838 G>A maps to NM_024613.3 K189K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr6:151161773 G>A maps to NM_001029884.1 R1300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:151054897 C>T maps to NM_001029884.1 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:151152721 G>A maps to NM_001029884.1 K825K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr6:151121945 C>T maps to NM_001029884.1 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr6:151152181 C>T maps to NM_001029884.1 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr6:151121945 C>T maps to NM_001029884.1 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr6:151152310 G>A maps to NM_001029884.1 R688R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr6:151130833 G>A maps to NM_001029884.1 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:39914775 C>T maps to NM_022835.2 S1001S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr19:39914449 C>T maps to NM_022835.2 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:39913838 G>A maps to NM_022835.2 G715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr19:39907044 C>T maps to NM_022835.2 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:39911636 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:39913433 C>T maps to NM_022835.2 T580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:39914712 C>T maps to NM_022835.2 I980I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:39905797 G>A maps to NM_022835.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr19:39911622 C>T maps to NM_022835.2 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr14:65209766 C>T maps to ENST00000394691 P1002P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr14:65210189 G>A maps to ENST00000394691 R1143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:65210243 G>A maps to ENST00000394691 E1161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr14:65209039 C>T maps to ENST00000394691 L935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:65207890 G>A maps to ENST00000394691 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr14:65209874 C>T maps to ENST00000394691 P1038P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr14:65209910 C>T maps to ENST00000394691 V1050V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr16:67315970 C>T maps to NM_001129729.1 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr16:67321006 C>T maps to NM_001129729.1 S1010S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:67322295 C>T maps to NM_001129729.1 P1149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr16:67314415 T>C maps to NM_001129729.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr16:67313979 C>T maps to NM_001129729.1 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr16:67320514 C>T maps to NM_001129729.1 F900F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr5:173028 G>A maps to NM_052909.3 Q1000Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:173181 G>A maps to NM_052909.3 K1051K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr5:143612 C>T maps to NM_052909.3 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:161968 C>T maps to NM_052909.3 F497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr5:157007 C>T maps to NM_052909.3 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr5:163321 G>A maps to NM_052909.3 G689G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:144941 G>A maps to NM_052909.3 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:154997 C>T maps to NM_052909.3 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:163454 C>T maps to NM_052909.3 Q734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr5:163579 C>T maps to NM_052909.3 S775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr5:182230 C>T maps to NM_052909.3 S1203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:145001 C>T maps to NM_052909.3 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:161926 G>A maps to NM_052909.3 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:161960 C>T maps to NM_052909.3 Q495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:6529667 C>T maps to NM_198681.2 R700R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:6532640 C>T maps to NM_198681.2 W419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:6529655 G>A maps to NM_198681.2 I704I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:6527631 C>T maps to NM_198681.2 S1081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:6528516 G>A maps to NM_198681.2 A870A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr1:6534164 G>A maps to NM_198681.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:6529205 C>T maps to NM_198681.2 E792E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:6528453 G>A maps to NM_198681.2 S891S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:6530406 C>T maps to NM_198681.2 K640K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:6534222 G>A maps to NM_198681.2 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:6421473 C>T maps to NM_001144856.1 R28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:6427489 G>A maps to NM_001144856.1 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr12:6424799 C>T maps to NM_001144856.1 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:6426817 A>T maps to NM_001144856.1 K325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr12:6427489 G>A maps to NM_001144856.1 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6422853 C>T maps to NM_001144856.1 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6422907 G>A maps to NM_001144856.1 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6428017 C>T maps to NM_001144856.1 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr12:6421436 C>T maps to NM_001144856.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:93139297 G>A maps to NM_001004330.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr12:93139258 C>T maps to NM_001004330.2 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr14:68029190 C>T maps to NM_020715.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr14:68053855 C>A maps to NM_020715.2 P1333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr14:68028983 G>A maps to NM_020715.2 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr14:68008658 T>C maps to NM_020715.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:68028920 C>T maps to NM_020715.2 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:68048917 G>A maps to NM_020715.2 L1139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr14:68029203 C>T maps to NM_020715.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr14:68044783 G>A maps to NM_020715.2 V873V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr14:68028699 C>T maps to NM_020715.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr14:68029229 C>T maps to NM_020715.2 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr2:43926990 C>T maps to NM_172069.3 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr2:43970995 C>T maps to NM_172069.3 T1141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr2:43968179 C>T maps to NM_172069.3 S1073S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:43927644 C>T maps to NM_172069.3 S516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr2:43922288 T>A maps to NM_172069.3 L143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr2:43927267 C>T maps to NM_172069.3 Q391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:43939476 C>T maps to NM_172069.3 S805S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:43958683 C>T maps to NM_172069.3 S962S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:43953529 C>T maps to NM_172069.3 I887I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:43953566 C>T maps to NM_172069.3 L900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:43926861 C>T maps to NM_172069.3 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:43947863 T>A maps to NM_172069.3 Y839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:43927365 C>T maps to NM_172069.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr2:43933473 C>T maps to NM_172069.3 T580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:43927011 C>T maps to NM_172069.3 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:43937378 T>G maps to NM_172069.3 G708G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:43947854 G>A maps to NM_172069.3 K836K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:43971010 T>C maps to NM_172069.3 F1146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr2:43939500 C>T maps to NM_172069.3 T813T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr17:40822653 G>A maps to NM_024927.4 H497H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:43555384 G>A maps to NM_014798.2 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr17:43552899 G>A maps to NM_014798.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr17:43552887 G>A maps to NM_014798.2 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:43535769 G>A maps to NM_014798.2 Y448Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr17:43552887 G>A maps to NM_014798.2 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:16060314 C>T maps to ENST00000420314 I1085I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:16054324 C>T maps to ENST00000420314 F689F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr2:208773275 G>A maps to NM_001080475.2 Q638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:208773279 G>A maps to NM_001080475.2 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:208773294 G>A maps to NM_001080475.2 F631F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:208841834 G>A maps to NM_001080475.2 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr2:208841903 G>A maps to NM_001080475.2 F339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:208841612 G>A maps to NM_001080475.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:208773294 G>A maps to NM_001080475.2 F631F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:909346 G>A maps to ENST00000379409 K575K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:150129667 C>T maps to ENST00000443480 H202H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:150129668 C>T maps to ENST00000443480 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:150131312 C>T maps to ENST00000443480 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:150131291 C>T maps to ENST00000443480 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:150129121 C>T maps to ENST00000443480 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:150131105 C>T maps to ENST00000443480 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr1:150128400 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:65152170 C>A maps to NM_025201.4 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr15:65157783 C>T maps to NM_025201.4 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr6:161143575 G>A maps to NM_000301.3 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:161139392 G>A maps to NM_000301.3 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr6:161152885 C>T maps to NM_000301.3 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr6:161139847 C>T maps to NM_000301.3 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr6:161160198 G>A maps to NM_000301.3 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr6:161152795 G>A maps to NM_000301.3 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:161160102 C>T maps to NM_000301.3 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:161173177 C>T maps to NM_000301.3 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:161134068 G>A maps to NM_000301.3 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:161157940 G>A maps to NM_000301.3 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:161127553 G>A maps to NM_000301.3 E55E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:161173177 C>T maps to NM_000301.3 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr6:161152885 C>T maps to NM_000301.3 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:161174017 C>T maps to NM_000301.3 R786R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:161135944 A>T maps to NM_000301.3 K223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:161132107 G>C did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:161162402 C>T maps to NM_000301.3 V693V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:161173183 C>T maps to NM_000301.3 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:161143530 G>A maps to NM_000301.3 K396K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr6:161132169 A>G maps to NM_000301.3 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr15:90213232 G>A maps to NM_002666.4 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr15:90210241 C>T maps to NM_002666.4 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr15:90210253 G>A maps to NM_002666.4 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr19:4839242 G>A maps to NM_005817.4 A422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr19:4852124 G>A maps to NM_005817.4 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:4844712 G>A maps to NM_005817.4 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:4859642 A>G maps to NM_005817.4 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:4839364 G>A maps to NM_005817.4 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:4847813 G>A maps to NM_005817.4 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr19:4511994 G>A maps to NM_001080400.1 I645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr19:4512462 G>A maps to NM_001080400.1 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:4512687 G>A maps to NM_001080400.1 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:4513344 G>A maps to NM_001080400.1 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:4510788 G>A maps to NM_001080400.1 A1047A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr19:4510977 G>A maps to NM_001080400.1 F984F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr19:4513644 C>T maps to NM_001080400.1 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:4511295 A>G maps to NM_001080400.1 T878T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:4511346 C>T maps to NM_001080400.1 V861V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:4511330 G>A maps to NM_001080400.1 Q867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:4513458 C>T maps to NM_001080400.1 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:4517587 C>T maps to NM_001080400.1 E43E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:4511781 C>T maps to NM_001080400.1 K716K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:4511781 C>T maps to NM_001080400.1 K716K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:4513254 G>A maps to NM_001080400.1 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:4513542 G>A maps to NM_001080400.1 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr19:4513233 C>T maps to NM_001080400.1 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr19:4512033 C>T maps to NM_001080400.1 K632K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:4512126 G>T maps to NM_001080400.1 T601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:4511418 C>T maps to NM_001080400.1 L837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:4510755 G>T maps to NM_001080400.1 T1058T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:4511238 C>T maps to NM_001080400.1 G897G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr19:4512738 C>T maps to NM_001080400.1 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:4511187 C>T maps to NM_001080400.1 K914K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr19:4511664 C>T maps to NM_001080400.1 G755G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr19:4523746 C>T maps to NM_001013706.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr19:4529247 C>T maps to NM_001013706.2 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:4534035 C>T maps to NM_001013706.2 Q17Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:4523731 G>A maps to NM_001013706.2 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:4525643 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:4525710 C>T maps to NM_001013706.2 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr16:23695366 C>T maps to NM_005030.3 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr16:23700595 C>T maps to NM_005030.3 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr16:23700834 C>T maps to NM_005030.3 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr5:57751415 G>A maps to NM_006622.2 V525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:57753145 C>T maps to NM_006622.2 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:57755645 G>A maps to NM_006622.2 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:45268512 A>G maps to NM_004073.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:45267364 C>T maps to NM_004073.2 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:45267295 C>T maps to NM_004073.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr4:128812329 G>A maps to NM_014264.4 Q638Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:128814497 T>G maps to NM_014264.4 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:128814690 G>C maps to NM_014264.4 L782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:128814467 C>T maps to NM_014264.4 F739F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr1:12010497 G>A maps to ENST00000376369 E176E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CF-06A-11D-A196-08 chr1:12025607 C>T maps to ENST00000376369 T561T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:12018691 C>T maps to ENST00000376369 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:12008120 C>T maps to ENST00000376369 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:12034861 C>T maps to ENST00000376369 P774P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:12032951 C>T maps to ENST00000376369 V689V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:12020720 C>T maps to ENST00000376369 Q379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:12012791 G>A maps to ENST00000376369 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:12012792 G>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:12030737 C>T maps to ENST00000376369 I636I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:145822081 G>A maps to NM_182943.2 T221T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A2MJ-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:100855616 C>T maps to NM_001084.4 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr7:100849576 G>T maps to NM_001084.4 S734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr7:100853382 G>A maps to NM_001084.4 I558I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr7:100853623 G>A maps to NM_001084.4 F534F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr23:103042836 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:103041537 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:103041538 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:49029804 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr23:49029589 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr23:49028419 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:155458437 G>A maps to NM_002669.2 A495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr4:155461992 G>A maps to NM_002669.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:155461948 G>A maps to NM_002669.2 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:142403005 G>A maps to NM_001172312.1 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:142430401 T>C maps to NM_001172312.1 N563N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr3:142403095 T>G maps to NM_001172312.1 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:142408620 G>A maps to NM_001172312.1 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:114864163 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:114877743 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:114869285 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:114880810 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr23:114871203 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr23:114879410 T>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr23:114863526 A>C did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:146233882 G>A maps to NM_021105.2 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr3:146167064 G>A maps to ENST00000497985 N264N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr3:146166995 G>A maps to ENST00000497985 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:146177692 C>T maps to ENST00000497985 W73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:7296235 G>A maps to NM_020360.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr3:146307568 C>T maps to NM_001085420.1 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:146307598 C>T maps to NM_001085420.1 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr20:44531168 G>A maps to NM_006227.2 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr20:44533685 C>T maps to NM_006227.2 E259E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr20:31826003 C>T maps to NM_130852.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr20:31828180 C>T maps to NM_130852.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:31828037 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr20:31829238 C>T maps to NM_130852.2 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr20:31829205 C>T maps to NM_130852.2 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:31825927 C>T maps to NM_130852.2 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:31825523 C>T maps to NM_130852.2 Q3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr19:17476400 C>T maps to NM_031310.1 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr19:17476310 C>T maps to NM_031310.1 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:17476535 G>A maps to NM_031310.1 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:17471374 G>A maps to NM_031310.1 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:17487998 G>A maps to NM_031310.1 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:17476391 G>A maps to NM_031310.1 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr19:17476971 A>G maps to NM_031310.1 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr19:17476670 C>T maps to NM_031310.1 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:17487896 G>A maps to NM_031310.1 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:17488004 G>A maps to NM_031310.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:17476121 T>G maps to NM_031310.1 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U9-06A-11D-A32N-08 chr19:17476977 G>A maps to NM_031310.1 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr17:37264481 C>T maps to NM_020405.4 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr17:37265217 G>A maps to NM_020405.4 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:37296030 C>T maps to NM_020405.4 W44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:37265576 C>T maps to NM_020405.4 W108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:37265617 G>A maps to NM_020405.4 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr10:20453446 C>T maps to NM_032812.7 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr10:20436729 C>T maps to NM_032812.7 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:20357115 C>T maps to NM_032812.7 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr10:20568654 G>A maps to NM_032812.7 A499A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr10:20465932 C>T maps to NM_032812.7 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:20357115 C>T maps to NM_032812.7 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr10:20290866 C>T maps to NM_032812.7 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr10:20453482 C>T maps to NM_032812.7 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:20466003 G>A maps to NM_032812.7 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:20453416 G>A maps to NM_032812.7 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr10:20290821 G>A maps to NM_032812.7 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:20534355 C>T maps to NM_032812.7 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr10:20432346 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr3:126708281 C>T maps to NM_032242.3 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr3:126708269 C>T maps to NM_032242.3 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:126748744 C>T maps to NM_032242.3 P1633P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:126741133 C>T maps to NM_032242.3 L1415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:126708044 C>T maps to NM_032242.3 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr3:126749211 C>T maps to NM_032242.3 Q1730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr3:126736491 C>T maps to NM_032242.3 S1167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:126748897 G>C maps to NM_032242.3 L1684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:126707642 C>T maps to NM_032242.3 N69N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr3:126739069 C>T maps to NM_032242.3 I1307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:126751235 C>T maps to NM_032242.3 P1746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:126736440 C>T maps to NM_032242.3 P1150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:208216435 G>A maps to NM_025179.3 I1329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr1:208234041 G>A maps to NM_025179.3 I909I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:208217961 G>A maps to NM_025179.3 I1255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr1:208215666 G>A maps to NM_025179.3 L1354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:208216534 G>A maps to NM_025179.3 L1296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:208390340 G>C maps to NM_025179.3 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:208234098 G>A maps to NM_025179.3 I890I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:208207907 G>A maps to NM_025179.3 V1598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:208215513 G>A maps to NM_025179.3 L1405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:208390427 G>A maps to NM_025179.3 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr1:208218051 C>T maps to NM_025179.3 S1225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:208200647 C>T maps to NM_025179.3 R1875R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:208215708 T>A maps to NM_025179.3 V1340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr23:153696527 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr23:153694360 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr23:153692582 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:153693374 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:153694495 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:153697285 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:153691742 G>T did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:153697249 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:153696821 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:153696179 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:153695624 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr23:153697518 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:153699654 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:153698862 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:153689748 T>G did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:153693441 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:153695451 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:153695452 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr23:153692628 G>A did not map to a codon.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr23:153688985 A>G did not map to a codon.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr23:153689067 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:153690569 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:153689548 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr23:153694838 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:153696707 C>T did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr23:153697400 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:153694311 C>T did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:153692026 G>A did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:153692616 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr7:132192612 G>A maps to NM_020911.1 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr7:131844262 G>A maps to NM_020911.1 S1543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr7:131832689 G>A maps to NM_020911.1 S1611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:131912261 G>A maps to NM_020911.1 I610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:131831448 G>A maps to NM_020911.1 I1625I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr7:131866241 G>A maps to NM_020911.1 I1130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr7:131866145 G>A maps to NM_020911.1 I1162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:131831325 C>T maps to NM_020911.1 G1666G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:131831358 C>T maps to NM_020911.1 V1655V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:132192810 G>A maps to NM_020911.1 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:131859575 G>A maps to NM_020911.1 F1326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:131859611 G>A maps to NM_020911.1 F1314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr7:131866370 C>T maps to NM_020911.1 E1087E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr7:131883254 G>A maps to NM_020911.1 I909I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:131844298 C>T maps to NM_020911.1 K1531K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:131849005 G>A maps to NM_020911.1 I1465I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:131853304 C>T maps to NM_020911.1 V1348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:131831285 G>A maps to NM_020911.1 R1680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:131848930 G>A maps to NM_020911.1 L1490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr7:131908288 G>A maps to NM_020911.1 P698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:132192576 G>A maps to NM_020911.1 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:131831316 C>T maps to NM_020911.1 G1669G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:131878934 G>A maps to NM_020911.1 I914I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr7:131831316 C>A maps to NM_020911.1 G1669G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:131864563 G>A maps to NM_020911.1 F1252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr7:131878934 G>A maps to NM_020911.1 I914I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:131878937 C>T maps to NM_020911.1 Q913Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:131866223 G>A maps to NM_020911.1 F1136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:131887527 G>A maps to NM_020911.1 F821F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr7:131825482 G>A maps to NM_020911.1 L1771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr7:132192879 C>T maps to NM_020911.1 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr7:132192909 G>A maps to NM_020911.1 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr7:131830011 C>T maps to NM_020911.1 E1697E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr7:131883356 C>T maps to NM_020911.1 K875K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr7:132192468 G>A maps to NM_020911.1 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:131817885 G>A maps to NM_020911.1 S1837S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:131870131 G>A maps to NM_020911.1 I1028I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:131859575 G>A maps to NM_020911.1 F1326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:131865362 G>A maps to NM_020911.1 I1207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr7:132193152 G>A maps to NM_020911.1 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr7:131866241 G>A maps to NM_020911.1 I1130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr7:131878832 G>A maps to NM_020911.1 L948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr7:131888139 C>T maps to NM_020911.1 V779V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr7:131844316 G>A maps to NM_020911.1 I1525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr7:131883272 A>T maps to NM_020911.1 P903P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr7:131908384 C>T maps to NM_020911.1 V666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:131864563 G>A maps to NM_020911.1 F1252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:131864653 G>A maps to NM_020911.1 S1222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:131878823 G>A maps to NM_020911.1 F951F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:131908342 G>A maps to NM_020911.1 V680V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:132193080 C>T maps to NM_020911.1 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr7:132192423 C>T maps to NM_020911.1 Q343Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:131925886 C>T maps to NM_020911.1 Q514Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr7:131912222 G>A maps to NM_020911.1 I623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:48457769 G>A maps to NM_001130082.1 H1155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr3:48455199 G>A maps to NM_001130082.1 L1472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:48457564 G>A maps to NM_001130082.1 V1164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:48452430 T>C maps to NM_001130082.1 L1754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr3:48448228 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr3:48448229 C>T maps to NM_001130082.1 W2076*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:48465164 C>A maps to NM_001130082.1 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:48454339 G>A maps to NM_001130082.1 T1555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:48451457 C>T maps to NM_001130082.1 E1878E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:48461453 G>A maps to NM_001130082.1 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr3:48453375 T>A maps to NM_001130082.1 K1715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr3:48456264 G>A maps to NM_001130082.1 N1384N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:48451735 G>A maps to NM_001130082.1 L1858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:48461414 G>A maps to NM_001130082.1 S760S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:48465261 G>A maps to NM_001130082.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr3:48456734 G>A maps to NM_001130082.1 V1272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr3:48448476 G>A maps to NM_001130082.1 L2037L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr22:50722086 G>A maps to NM_012401.2 I838I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr22:50728359 G>A maps to NM_012401.2 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:50719184 A>C maps to NM_012401.2 S1327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:50719571 G>A maps to NM_012401.2 Q1237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr22:50716103 G>A maps to NM_012401.2 V1704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:50728407 G>A maps to NM_012401.2 D202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr22:50719521 G>A maps to NM_012401.2 F1253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr22:50720717 C>T maps to NM_012401.2 T1004T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr22:50720042 G>A maps to NM_012401.2 P1158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr22:50719196 C>T maps to NM_012401.2 L1323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr22:50720693 C>T maps to NM_012401.2 Q1012Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:50719042 G>A maps to NM_012401.2 F1350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr22:50724695 G>A maps to NM_012401.2 Q595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr22:50722062 G>A maps to NM_012401.2 S846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr22:50717096 G>A maps to NM_012401.2 I1525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr22:50721177 G>A maps to NM_012401.2 P983P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr22:50719036 G>A maps to NM_012401.2 S1352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr22:50719042 G>A maps to NM_012401.2 F1350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:50719832 G>A maps to NM_012401.2 I1206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:50722330 G>A maps to NM_012401.2 G784G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:153032886 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:153032757 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:153037320 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:153033716 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:153041611 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr23:153036992 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:153035693 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:153039544 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr23:153043032 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:94562987 C>T maps to NM_005761.1 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr12:94673363 C>T maps to NM_005761.1 F1238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:94575304 C>T maps to NM_005761.1 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:94673246 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr12:94641879 C>T maps to NM_005761.1 Q864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr12:94634386 C>T maps to NM_005761.1 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:94642107 C>T maps to NM_005761.1 Q900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26D-06A-11D-A19A-08 chr12:94637741 A>T maps to NM_005761.1 R777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr12:94692558 G>A maps to NM_005761.1 W1409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:129304872 G>A maps to NM_015103.2 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr3:129293199 G>A maps to NM_015103.2 C888C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr3:129302424 G>A maps to NM_015103.2 A742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr3:129284278 G>A maps to NM_015103.2 A1475A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:129286602 C>T maps to NM_015103.2 W1304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:129290065 G>A maps to NM_015103.2 F1139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:129288797 G>A maps to NM_015103.2 I1251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:129293292 G>A maps to NM_015103.2 S857S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:129278530 G>A maps to NM_015103.2 F1743F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:129276009 G>A maps to NM_015103.2 I1834I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr3:129276009 G>A maps to NM_015103.2 I1834I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:129276018 G>A maps to NM_015103.2 Y1831Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:129276033 C>T maps to NM_015103.2 K1826K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:129278590 C>T maps to NM_015103.2 K1723K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:129279546 C>T maps to NM_015103.2 E1671E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:129284779 G>A maps to NM_015103.2 I1424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:205811875 C>T maps to NM_152491.4 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr1:205819152 G>T maps to NM_152491.4 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:205814610 G>A maps to NM_152491.4 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:205812793 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:205813318 G>A maps to NM_152491.4 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr1:205801882 G>A maps to NM_152491.4 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:205814566 G>A maps to NM_152491.4 H125H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:205813989 C>T maps to NM_152491.4 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:205813962 G>A maps to NM_152491.4 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:205813995 C>T maps to NM_152491.4 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:205814602 C>T maps to NM_152491.4 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:205817043 G>A maps to NM_152491.4 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:205813228 C>T maps to NM_152491.4 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:89855889 G>A maps to NM_001010853.1 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:89868144 C>T maps to NM_001010853.1 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr20:56227492 G>A maps to NM_020182.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr20:56227582 G>A maps to NM_020182.3 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr20:56227488 G>A maps to NM_020182.3 Q162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:56227471 G>A maps to NM_020182.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr20:56227600 G>A maps to NM_020182.3 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr20:56234730 G>A maps to NM_020182.3 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:56234688 G>A maps to NM_020182.3 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:156203420 G>A maps to NM_007221.3 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr16:72162588 G>A maps to NM_031293.2 T685T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr16:72170666 C>A maps to NM_031293.2 E324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr16:72164553 C>T maps to NM_031293.2 R505R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:72156855 G>A maps to NM_031293.2 R909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:72184566 G>A maps to NM_031293.2 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr16:72157518 G>A maps to NM_031293.2 P873P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:72163054 C>T maps to NM_031293.2 R620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr16:72188325 C>T maps to NM_031293.2 E66E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:72164189 C>T maps to NM_031293.2 K568K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr16:72188247 G>A maps to NM_031293.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr16:72198809 C>T maps to NM_031293.2 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:72170367 C>T maps to NM_031293.2 K394K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr16:72174406 C>T maps to NM_031293.2 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr16:72184518 C>T maps to NM_031293.2 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr16:72164553 C>T maps to NM_031293.2 R505R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:72156855 G>A maps to NM_031293.2 R909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr16:72188352 C>T maps to NM_031293.2 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr15:74290559 C>T maps to NM_033238.2 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr15:74290466 G>A maps to NM_033238.2 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:74328123 C>T maps to NM_033239.2 A774A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:74328124 C>T maps to NM_033239.2 Q775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr15:74328255 C>T maps to NM_033239.2 I818I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:74328021 C>T maps to NM_033239.2 S740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr15:74327979 A>G maps to NM_033239.2 R726R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr15:74328054 C>T maps to NM_033239.2 A751A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr15:74327595 G>A maps to NM_033239.2 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr15:74327547 C>T maps to NM_033239.2 S582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr15:74290541 C>T maps to NM_033238.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr22:41979974 G>A maps to NM_002676.2 S154S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D9-A6EC-06A-11D-A30X-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr22:41980373 G>A maps to NM_002676.2 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr8:82355684 T>C did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr8:82355665 G>A maps to NM_002677.3 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:82357171 G>A maps to NM_002677.3 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr8:82357093 G>A maps to NM_002677.3 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr8:82356830 G>A maps to NM_002677.3 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:82357105 G>A maps to NM_002677.3 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr17:15162438 G>A maps to NM_000304.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr9:139306960 G>A maps to NM_015160.1 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:139313498 C>T maps to NM_015160.1 R402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr9:139317676 G>A maps to NM_015160.1 K513K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr9:139313548 C>T maps to NM_015160.1 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr2:190670412 T>C maps to NM_000534.4 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr2:190719500 A>G maps to NM_000534.4 G501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:6026543 G>A maps to NM_000535.5 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr7:6026895 G>A maps to NM_000535.5 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr7:6045616 G>A maps to NM_000535.5 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:6027009 G>A maps to NM_000535.5 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr7:6026708 G>A maps to NM_000535.5 R563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:154897655 G>A maps to NM_006556.3 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:152937352 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr23:152936208 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr23:152939615 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr23:152938024 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr23:152938025 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:152936626 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr23:152936405 C>T did not map to a codon.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr2:219204767 C>A maps to NM_015488.4 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:219206853 C>T maps to NM_015488.4 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:219204528 G>A maps to NM_015488.4 W87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr2:219204779 C>T maps to NM_015488.4 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:50370392 G>A maps to NM_007254.3 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr19:50365693 G>A maps to NM_007254.3 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr19:50367222 G>A maps to NM_007254.3 Q248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:50370416 G>A maps to NM_007254.3 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:50368641 C>T maps to NM_007254.3 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:50367232 C>T maps to NM_007254.3 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:160239610 C>T maps to NM_173516.1 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:160229781 C>T maps to NM_173516.1 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:160240381 C>T maps to NM_173516.1 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr6:160239685 C>T maps to NM_173516.1 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:160240298 C>T maps to NM_173516.1 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr6:160240297 C>T maps to NM_173516.1 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:160221849 C>T maps to NM_173516.1 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr10:118306869 G>A maps to NM_000936.2 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr10:118314900 G>A maps to NM_000936.2 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr10:118315527 G>C maps to NM_000936.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr10:118314747 C>T maps to NM_000936.2 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:118320012 C>T maps to NM_000936.2 N382N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:118306878 C>T maps to NM_000936.2 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:118307870 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:118313318 G>A maps to NM_000936.2 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr10:118365032 G>A maps to NM_006229.2 K436K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:118351421 C>T maps to NM_006229.2 N63N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:118351307 C>T maps to NM_006229.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:118360594 C>T maps to NM_006229.2 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:118385530 C>T maps to NM_005396.4 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:118394430 C>T maps to NM_005396.4 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:118389457 G>A maps to NM_005396.4 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr10:118202571 C>T maps to NM_001011709.2 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:118196346 C>T maps to NM_001011709.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:118203961 C>T maps to NM_001011709.2 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr14:74180021 G>A maps to NM_006029.4 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr8:26365943 G>A maps to NM_007257.5 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:26365725 C>T maps to NM_007257.5 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:26365907 G>A maps to NM_007257.5 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr23:152226195 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:152226133 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr23:152226398 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:152225434 A>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:152225435 C>T did not map to a codon.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr23:152225666 G>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:152226783 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr23:152225781 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:152226766 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:152226002 C>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr23:152226734 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:152226666 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr23:152159272 T>C did not map to a codon.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr23:152158842 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:152159203 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:152158822 C>A did not map to a codon.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr23:152159671 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:152158807 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr23:152159671 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:152159967 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:152159166 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr23:152159824 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:152159654 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:152159754 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:152159857 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:152159170 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:152159383 C>T did not map to a codon.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr23:152159651 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:46973884 G>A maps to NM_018215.3 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr19:46998607 G>A maps to NM_020709.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr19:46997129 C>T maps to NM_020709.1 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:46997225 G>A maps to NM_020709.1 S499S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A2GO-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:46998299 C>T maps to ENST00000377652 S137S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A2MJ-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:46998335 G>A maps to ENST00000377652 G149G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A2MR-06A-11D-A196-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-EE-A3JE-06A-11D-A20D-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-EE-A3JE-06A-11D-A20D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr19:46998437 G>A maps to ENST00000377652 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr19:46997519 G>A maps to NM_020709.1 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:46997546 C>T maps to NM_020709.1 E392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr14:39650382 C>T maps to NM_002687.3 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:39650382 C>T maps to NM_002687.3 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr14:39650091 T>C maps to NM_002687.3 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr14:39645287 C>T maps to NM_002687.3 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:28196900 G>A maps to NM_006228.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr8:28196744 C>T maps to NM_006228.3 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr14:20942961 C>T maps to NM_000270.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:20943075 C>T maps to NM_000270.3 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr14:20943057 C>T maps to NM_000270.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:20943274 G>A maps to NM_000270.3 Q172Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:20943235 C>T maps to NM_000270.3 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr6:36259244 G>A maps to ENST00000457797 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:36270113 C>T maps to ENST00000457797 Q419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr6:36270246 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:36269983 C>T maps to ENST00000457797 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:36270121 C>T maps to ENST00000457797 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:36274123 G>A maps to ENST00000457797 V481V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:36259148 C>T maps to ENST00000457797 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:36269677 C>T maps to ENST00000457797 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:821703 C>T maps to NM_020376.3 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr22:44342111 C>T maps to NM_025225.2 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:44328957 G>C maps to NM_025225.2 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:44323028 C>T maps to NM_025225.2 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:7894013 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr23:7868852 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr23:7870111 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr22:44280190 C>T maps to ENST00000216177 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:44285211 G>A maps to ENST00000216177 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr22:44282288 G>A maps to ENST00000216177 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:44282249 C>T maps to ENST00000216177 W294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr22:44280202 C>T maps to ENST00000216177 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:44280178 G>A maps to ENST00000216177 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:7614809 C>T maps to NM_001166111.1 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:7620633 C>T maps to NM_001166111.1 A1036A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:7601354 C>G maps to NM_001166111.1 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:7621578 C>T maps to NM_001166111.1 I1093I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:7614992 C>T maps to NM_001166111.1 F612F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:7623820 G>A maps to NM_001166111.1 G1171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:7622069 C>T maps to NM_001166111.1 Y1109Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:7605064 C>T maps to NM_001166111.1 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:7619497 C>T maps to NM_001166111.1 I851I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr19:7606271 C>T maps to NM_001166111.1 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:7614986 C>T maps to NM_001166111.1 S610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:7625907 C>T maps to NM_001166111.1 A1285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:7616318 C>T maps to NM_001166111.1 F761F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:7618779 C>T maps to NM_001166111.1 P770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr9:140409900 G>A maps to NM_001098537.1 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr9:140373552 G>A maps to NM_001098537.1 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr9:140392597 C>T maps to NM_001098537.1 W619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:140389595 C>T maps to NM_001098537.1 V672V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr9:140441760 G>T maps to NM_001098537.1 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr9:140357202 A>T maps to NM_001098537.1 Y1142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr9:140358794 G>A maps to NM_001098537.1 I1051I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr9:140435108 G>A maps to NM_001098537.1 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr9:140389553 G>A maps to NM_001098537.1 A686A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:140396113 C>T maps to NM_001098537.1 R513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:140414483 G>A maps to NM_001098537.1 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:140438246 G>A maps to NM_001098537.1 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr9:140438179 T>A maps to NM_001098537.1 K121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr7:108154960 T>C maps to NM_015723.2 E325E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:108143004 G>A maps to NM_015723.2 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:108143005 G>A maps to NM_015723.2 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:108137999 G>A maps to NM_015723.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr7:108155290 G>A maps to NM_015723.2 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:55920891 G>A maps to NM_033109.3 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:89790783 C>T maps to NM_006813.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:52185053 G>A maps to NM_015426.4 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr3:52130634 G>A maps to NM_015426.4 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr3:52130635 T>A maps to NM_015426.4 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr3:52130713 G>A maps to NM_015426.4 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr3:52183353 G>A maps to NM_015426.4 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:89853417 G>C maps to NM_172240.2 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:53543376 C>T maps to NM_153703.4 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr1:53535823 C>T maps to NM_153703.4 N147N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:53544159 G>A maps to NM_153703.4 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:53544333 C>T maps to NM_153703.4 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:53547715 G>A maps to NM_153703.4 Q623Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:53544405 G>A maps to NM_153703.4 E456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr19:14046616 G>A maps to NM_024825.3 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:14043521 C>T maps to NM_024825.3 W512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:131195647 A>G maps to NM_001018111.2 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:131189132 C>T maps to NM_001018111.2 W538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:131191021 C>T maps to NM_001018111.2 K436K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:131195770 C>T maps to NM_001018111.2 K174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr3:127379872 C>T maps to NM_015720.2 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr3:127379359 G>A maps to NM_015720.2 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr23:84622722 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr23:84614581 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:84537225 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:84537323 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:84561287 G>C did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:84606373 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:84563163 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:84560873 C>T did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:84561283 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr23:84634307 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:84560887 A>C did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:84586073 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:84562248 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr23:84561250 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:84622754 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:84585957 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:84562248 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:84606426 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr23:84634305 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:84560878 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:84634332 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:84559433 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:84569508 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:84560874 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:84634288 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:84562261 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:84586002 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr23:84537295 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr23:84560825 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:84537305 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr23:84561240 T>C did not map to a codon.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr23:84634243 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:84570717 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:84561242 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F4-06A-12D-A25O-08 chr23:84634217 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr23:84563206 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:84537234 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:84537276 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:84559347 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:84585979 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:84606390 T>G did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr20:30816215 C>T maps to NM_015352.1 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr20:30822424 C>T maps to NM_015352.1 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:30803148 C>T maps to NM_015352.1 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:30797940 C>T maps to NM_015352.1 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr21:46685453 G>A maps to NM_133635.4 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr21:46696961 G>A maps to NM_133635.4 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr21:46705835 G>A maps to NM_133635.4 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr21:46687371 G>A maps to NM_015227.4 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr1:166819621 C>G maps to NM_017542.3 T602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:166818658 C>T maps to NM_017542.3 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:151400734 G>A maps to NM_015100.3 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:151400395 G>A maps to NM_015100.3 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:151378398 G>A maps to NM_015100.3 Q1038*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:151380946 A>T maps to NM_015100.3 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:151377412 A>G maps to NM_015100.3 S1366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr23:24859899 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr23:24734547 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:24742540 A>G did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:24759605 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:24828028 G>A did not map to a codon.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr23:24734548 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:65062069 C>T maps to NM_002689.2 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:65046213 C>T maps to NM_002689.2 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:65046387 C>T maps to NM_002689.2 R217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:65046371 G>A maps to NM_002689.2 Q211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZU-06A-12D-A196-08 chr11:65036174 T>A maps to NM_002689.2 L110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr11:65061711 C>T maps to NM_002689.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr8:42220188 C>G maps to NM_002690.1 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr19:50906832 C>T maps to ENST00000391817 I407I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:50918103 G>A maps to ENST00000391817 K833K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr19:50906826 C>T maps to ENST00000391817 Y405Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:50918805 C>T maps to ENST00000391817 S918S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:50902209 C>T maps to ENST00000391817 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr19:50905594 C>T maps to ENST00000391817 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:50909674 G>A maps to ENST00000391817 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr19:50912808 C>T maps to ENST00000391817 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr19:50912865 C>T maps to ENST00000391817 S725S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:50906814 C>T maps to ENST00000391817 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:50909686 C>T maps to ENST00000391817 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:50905328 G>A maps to ENST00000391817 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:50905349 C>T maps to ENST00000391817 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:44156454 G>A maps to NM_006230.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:74323980 C>T maps to NM_006591.1 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:74329800 C>T maps to NM_006591.1 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:74329632 C>T maps to NM_006591.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:74324007 C>T maps to NM_006591.1 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:67120852 G>A maps to NM_021173.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:26680768 A>T maps to NM_015584.3 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr22:42998026 G>A maps to ENST00000415122 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr22:42981922 C>T maps to ENST00000415122 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr22:42988045 G>A maps to ENST00000415122 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:133218811 G>A maps to ENST00000455752 F1711F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr12:133241934 G>A maps to ENST00000455752 A810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr12:133225927 G>A maps to ENST00000455752 A1326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:133252320 C>T maps to ENST00000455752 W369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:133254193 G>A maps to ENST00000455752 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:133236095 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:133225984 G>A maps to ENST00000455752 P1307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr12:133209065 G>A maps to ENST00000455752 V2058V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:133218417 A>T maps to ENST00000455752 L1734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr12:133219875 G>A maps to ENST00000455752 A1498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:133253987 C>G maps to ENST00000455752 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:133233742 G>A maps to ENST00000455752 F1190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr12:133226277 G>A maps to ENST00000455752 A1263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr15:89870212 C>T maps to NM_002693.2 K505K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr15:89867053 G>A maps to NM_002693.2 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr15:89867054 G>T maps to NM_002693.2 P716P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr15:89869919 G>A maps to NM_002693.2 A545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr15:89873431 G>A maps to NM_002693.2 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:89866724 G>A maps to NM_002693.2 P725P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:62487035 T>C maps to NM_007215.3 E282E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr17:62474034 G>A maps to NM_007215.3 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:62492549 C>T maps to NM_007215.3 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:43581766 C>T maps to NM_006502.2 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:43582290 T>C maps to NM_006502.2 H713H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:43565572 C>T maps to NM_006502.2 Q211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr18:51820380 C>T maps to NM_007195.2 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr18:51820449 T>C maps to NM_007195.2 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:51818290 C>T maps to NM_007195.2 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:74865162 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:103339388 G>A maps to NM_013274.3 R517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:103339569 G>A maps to NM_013274.3 F456F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:103345860 G>A maps to NM_013274.3 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr10:103340152 G>A maps to NM_013274.3 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:44119558 C>G did not map to a codon.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr4:2083369 G>A maps to NM_181808.2 F766F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:2083369 G>A maps to NM_181808.2 F766F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:2132986 G>A maps to NM_181808.2 Q588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr4:2074696 G>A maps to NM_181808.2 Q839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr4:2195029 G>A maps to NM_181808.2 Q308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:2132986 G>A maps to NM_181808.2 Q588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr3:121208659 G>A maps to ENST00000393672 R1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr3:121208659 G>A maps to ENST00000393672 R1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:121215715 C>T maps to ENST00000393672 Q875Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr3:121264613 G>A maps to ENST00000393672 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:121251893 G>A maps to ENST00000393672 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr2:86255068 G>A maps to NM_015425.3 S1667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:86257384 C>T maps to NM_015425.3 K1571K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:86272787 C>T maps to NM_015425.3 R946R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:86272889 G>A maps to NM_015425.3 I912I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:86266484 G>A maps to NM_015425.3 L1281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:86258506 G>A maps to NM_015425.3 I1508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:86327249 G>A maps to NM_015425.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:86310219 G>A maps to NM_015425.3 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:86310220 G>A maps to NM_015425.3 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr2:86267561 G>A maps to NM_015425.3 F1231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:113326336 C>T maps to NM_019014.4 V644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr2:113325560 A>G maps to NM_019014.4 R588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:37493677 C>T maps to NM_022490.1 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:7417411 T>C maps to NM_000937.4 T1943T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:7405229 C>T maps to NM_000937.4 V787V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr17:7400321 C>T maps to NM_000937.4 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:7404344 C>T maps to NM_000937.4 S656S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:7405247 C>T maps to NM_000937.4 V793V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr17:7401486 C>T maps to NM_000937.4 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr17:7401000 C>A maps to NM_000937.4 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:7401450 C>T maps to NM_000937.4 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr17:7401453 C>T maps to NM_000937.4 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr17:7402800 C>T maps to NM_000937.4 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr4:57890232 C>A maps to NM_000938.1 P973P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:57873036 C>T maps to NM_000938.1 R425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:57883316 T>C maps to NM_000938.1 A688A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr4:57871873 C>T maps to NM_000938.1 F402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr16:57503879 C>T maps to NM_032940.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr2:128608248 G>A maps to NM_004805.3 Q89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr2:128608249 G>A maps to NM_004805.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:1093966 C>T maps to NM_002695.3 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr19:1090090 G>A maps to NM_002695.3 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:1091853 C>T maps to NM_002695.3 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr22:38355369 C>T maps to ENST00000407936 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr3:184086000 G>A maps to NM_006232.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:184085979 C>T maps to NM_006232.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr19:36604964 G>A maps to NM_006233.4 C89C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr10:79762057 G>A maps to NM_007055.3 I752I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr10:79745091 C>T maps to NM_007055.3 Q1026Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:79778948 G>A maps to NM_007055.3 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:79781440 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr10:79785849 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:79781315 A>T maps to NM_007055.3 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:79782127 G>A maps to NM_007055.3 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:79767570 G>A maps to NM_007055.3 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:79767571 G>A maps to NM_007055.3 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr10:79781923 G>A maps to NM_007055.3 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr10:79739920 G>A maps to NM_007055.3 F1334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr10:79741290 G>A maps to NM_007055.3 A1262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr10:79762036 G>A maps to NM_007055.3 I759I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr12:106772117 C>T maps to NM_018082.5 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr12:106890666 G>A maps to NM_018082.5 G985G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:106772060 T>G maps to NM_018082.5 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr8:22107919 C>T maps to NM_001722.2 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr8:22107733 C>T maps to NM_001722.2 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:22105495 C>T maps to NM_001722.2 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr8:22105715 C>T maps to NM_001722.2 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:22107730 C>T maps to NM_001722.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr16:22334248 C>T maps to NM_018119.2 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr16:22337115 C>T maps to NM_018119.2 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr16:22337116 C>T maps to NM_018119.2 Q462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr16:22314309 C>T maps to NM_018119.2 D7D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:22328450 C>T maps to NM_018119.2 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:22319542 G>A maps to NM_018119.2 Q54Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr16:101618 C>T maps to NM_016310.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr19:621258 G>A maps to NM_005035.3 F813F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr19:629845 G>A maps to NM_005035.3 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:625221 G>A maps to NM_005035.3 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr7:72413672 C>T maps to ENST00000434423 F1047F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:72413897 C>T maps to ENST00000434423 T1122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:72400634 C>T maps to ENST00000434423 R421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr7:72416745 C>T maps to ENST00000434423 A1241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:72413720 C>T maps to ENST00000434423 V1063V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr7:75050948 G>A maps to ENST00000257665 T1104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:75048687 C>T maps to ENST00000257665 A1169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr7:75053410 G>A maps to ENST00000257665 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr7:53103939 C>T maps to NM_182595.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:53103786 C>T maps to NM_182595.3 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:53103939 C>T maps to NM_182595.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:53104166 G>A maps to NM_182595.3 W268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr7:53103786 C>T maps to NM_182595.3 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr7:53104212 C>T maps to NM_182595.3 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:53103885 C>T maps to NM_182595.3 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr7:53103699 C>T maps to NM_182595.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:53103576 G>A maps to NM_182595.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:53103870 C>T maps to NM_182595.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr7:53103888 G>A maps to NM_182595.3 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr7:53103597 C>T maps to NM_182595.3 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:53103675 G>A maps to NM_182595.3 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:53103957 C>T maps to NM_182595.3 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr7:53103783 G>A maps to NM_182595.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr7:53103831 G>A maps to NM_182595.3 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr7:53103666 C>T maps to NM_182595.3 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:53103815 G>A maps to NM_182595.3 W151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:53103996 G>A maps to NM_182595.3 Q211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:53104230 G>A maps to NM_182595.3 Q289Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:53103957 C>T maps to NM_182595.3 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:53104242 C>T maps to NM_182595.3 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:53103870 C>T maps to NM_182595.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:53103535 C>T maps to NM_182595.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:53103792 C>T maps to NM_182595.3 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr7:53103408 C>T maps to NM_182595.3 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr7:53104125 C>T maps to NM_182595.3 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr7:53103885 C>T maps to NM_182595.3 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr7:53104224 C>T maps to NM_182595.3 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr7:53103786 C>T maps to NM_182595.3 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:53103653 G>A maps to NM_182595.3 W97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:53103786 C>T maps to NM_182595.3 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:53104212 C>T maps to NM_182595.3 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:53104047 C>T maps to NM_182595.3 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:53103597 C>T maps to NM_182595.3 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:53103786 C>T maps to NM_182595.3 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr7:53103402 G>A maps to NM_182595.3 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr7:53103831 G>A maps to NM_182595.3 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr7:53103888 G>A maps to NM_182595.3 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:53103402 G>A maps to NM_182595.3 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr1:46659579 G>A maps to ENST00000371986 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr1:46657985 C>T maps to ENST00000371986 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:46655137 G>A maps to NM_017739.3 S629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr9:134393830 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr9:134387466 G>A maps to NM_007171.3 V364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr9:134382803 C>T maps to NM_007171.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr9:134385343 C>T maps to NM_007171.3 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr9:134390881 C>T maps to NM_007171.3 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:134387517 C>G maps to NM_007171.3 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr14:77750142 G>A maps to NM_013382.5 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:77765074 G>A maps to NM_013382.5 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:77778330 G>A maps to NM_013382.5 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:94931552 G>A maps to NM_000446.5 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:94940785 G>A maps to NM_000446.5 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:94928407 G>A maps to NM_000446.5 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:94931642 G>A maps to NM_000446.5 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:94935615 C>T maps to NM_000446.5 W254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:94993239 C>T maps to NM_000940.2 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:95019471 G>A maps to NM_000940.2 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:94996711 C>T maps to NM_000940.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr7:94991697 G>A maps to NM_000940.2 N294N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:99142336 C>T maps to NM_015029.2 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr8:99146829 G>C maps to NM_015029.2 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:99152403 C>T maps to NM_015029.2 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:99168298 C>T maps to NM_015029.2 P693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr8:99162718 C>T maps to NM_015029.2 R637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr8:99148714 C>T maps to NM_015029.2 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr19:30106214 G>T maps to NM_006627.2 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:30099603 C>T maps to NM_006627.2 D16D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:30106193 C>T maps to NM_006627.2 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:30104820 C>T maps to NM_006627.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:119378808 G>A maps to NM_022135.2 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:119379155 G>A maps to NM_022135.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:119367314 G>A maps to NM_022135.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr6:105609452 A>T maps to NM_022361.4 L111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:105609340 C>T maps to NM_022361.4 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:105609475 G>A maps to NM_022361.4 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr6:105609424 C>T maps to NM_022361.4 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr6:105607651 G>A maps to NM_022361.4 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr23:48371040 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:48372728 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr23:48372735 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:48372688 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:48374288 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:48372723 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:48372656 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr13:38160303 C>T maps to NM_006475.2 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:38171376 C>T maps to NM_006475.2 K54K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr13:38143518 C>T maps to NM_006475.2 E783E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:38137470 C>T maps to NM_006475.2 *837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr13:38154774 C>T maps to NM_006475.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr13:38156622 G>A maps to NM_006475.2 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr7:124503643 T>A maps to NM_015450.2 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:124503574 G>A maps to NM_015450.2 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr7:124469350 G>A maps to NM_015450.2 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr8:43172525 G>A maps to NM_001005365.2 K335K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr8:43211923 C>T maps to NM_001005365.2 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr8:43147878 C>T maps to NM_001005365.2 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr8:43157197 C>T maps to NM_001005365.2 Q260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:43147878 C>T maps to NM_001005365.2 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:43159889 C>T maps to NM_001005365.2 N294N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr8:43211926 G>A maps to NM_001005365.2 Q462Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr18:14542740 G>A maps to ENST00000444806 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr18:14542878 G>A maps to ENST00000444806 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr18:14511959 G>A maps to ENST00000444806 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:14542914 C>T maps to ENST00000444806 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:14542689 G>A maps to ENST00000444806 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:14542980 C>T maps to ENST00000444806 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr18:14542923 C>T maps to ENST00000444806 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr18:14542923 C>T maps to ENST00000444806 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr18:14542671 G>A maps to ENST00000444806 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr18:14542998 G>A maps to ENST00000444806 H49H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr18:14534952 C>T maps to ENST00000444806 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:14982957 C>T maps to NM_174981.3 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:15013745 G>A maps to NM_174981.3 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:131976358 C>T maps to NM_001083538.1 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr2:132021466 G>A maps to NM_001083538.1 K813K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:131984448 G>A maps to NM_001083538.1 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr2:131976430 C>T maps to NM_001083538.1 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:132021751 C>T maps to NM_001083538.1 I908I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:131976460 G>A maps to NM_001083538.1 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:132021550 C>T maps to NM_001083538.1 S841S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:132021551 C>T maps to NM_001083538.1 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:132021640 C>T maps to NM_001083538.1 L871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:131984463 G>A maps to NM_001083538.1 K293K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:131976358 C>T maps to NM_001083538.1 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:132021796 C>T maps to NM_001083538.1 F923F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:132021763 C>T maps to NM_001083538.1 I912I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:131976307 G>A maps to NM_001083538.1 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr2:132021833 C>T maps to NM_001083538.1 L936L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:132021631 G>A maps to NM_001083538.1 G868G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:132021838 G>A maps to NM_001083538.1 E937E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:131976448 C>T maps to NM_001083538.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:131976229 C>T maps to NM_001083538.1 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr2:132021631 G>A maps to NM_001083538.1 G868G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:132021436 C>T maps to NM_001083538.1 I803I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:131984463 G>A maps to NM_001083538.1 K293K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr2:132021424 G>A maps to NM_001083538.1 E799E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr2:130831873 G>A maps to NM_001099771.2 I1057I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr2:130877881 G>A maps to NM_001099771.2 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr2:130832797 C>T maps to NM_001099771.2 Q749Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:130878043 C>T maps to NM_001099771.2 K15K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:130832281 C>T maps to NM_001099771.2 L921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr2:130832616 G>A maps to NM_001099771.2 L810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:130832986 C>T maps to NM_001099771.2 R686R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr2:130832616 G>A maps to NM_001099771.2 L810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:130877704 G>A maps to NM_001099771.2 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:130869620 C>T maps to NM_001099771.2 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:130877803 C>T maps to NM_001099771.2 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:130877770 G>A maps to NM_001099771.2 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:130832581 C>T maps to NM_001099771.2 Q821Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:130832995 C>T maps to NM_001099771.2 V683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr2:130832584 G>A maps to NM_001099771.2 T820T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:130877833 G>A maps to NM_001099771.2 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:130832467 G>A maps to NM_001099771.2 V859V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:130832995 C>T maps to NM_001099771.2 V683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr2:130832539 G>A maps to NM_001099771.2 A835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr2:130833112 G>A maps to NM_001099771.2 I644I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:19553511 C>T maps to NM_001005356.2 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr14:19573099 G>T maps to NM_001005356.2 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr14:19553799 C>T maps to NM_001005356.2 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:19553721 C>T maps to NM_001005356.2 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr14:19566059 C>T maps to NM_001005356.2 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:19553733 C>T maps to NM_001005356.2 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:19553769 C>T maps to NM_001005356.2 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:19553544 G>A maps to NM_001005356.2 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr14:19553824 C>T maps to NM_001005356.2 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:19553748 G>A maps to NM_001005356.2 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr14:19553589 G>A maps to NM_001005356.2 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr14:19573108 C>T maps to NM_001005356.2 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:19553748 G>A maps to NM_001005356.2 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:19566051 C>T maps to NM_001005356.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr14:19553733 C>T maps to NM_001005356.2 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr22:16279247 C>T maps to NM_001136213.1 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr22:16279247 C>T maps to NM_001136213.1 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr22:16279247 C>T maps to NM_001136213.1 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr22:16287420 G>A maps to NM_001136213.1 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr22:16266987 C>T maps to NM_001136213.1 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr22:16279247 C>T maps to NM_001136213.1 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr22:16266987 C>T maps to NM_001136213.1 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr22:16279247 C>T maps to NM_001136213.1 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:16279247 C>T maps to NM_001136213.1 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr22:16279247 C>T maps to NM_001136213.1 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr22:16287789 G>A maps to NM_001136213.1 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr22:16279247 C>T maps to NM_001136213.1 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:16279247 C>T maps to NM_001136213.1 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr22:16266987 C>T maps to NM_001136213.1 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr22:16287414 C>T maps to NM_001136213.1 W157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr22:16266987 C>T maps to NM_001136213.1 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr22:16279247 C>T maps to NM_001136213.1 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr22:16279247 C>T maps to NM_001136213.1 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr22:16279258 G>A maps to NM_001136213.1 Q322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr22:16266987 C>T maps to NM_001136213.1 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr22:16279247 C>T maps to NM_001136213.1 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr22:16287489 C>T maps to NM_001136213.1 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:16287328 C>T maps to NM_001136213.1 W186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:16287711 C>T maps to NM_001136213.1 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:16287789 G>A maps to NM_001136213.1 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr22:16279247 C>T maps to NM_001136213.1 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr22:16287390 G>A maps to NM_001136213.1 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:16279247 C>T maps to NM_001136213.1 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr14:20019836 G>A maps to ENST00000439503 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:20019998 C>T maps to ENST00000439503 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:20019935 C>T maps to ENST00000439503 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr3:87311362 C>T maps to NM_001122757.1 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:87313584 G>A maps to NM_001122757.1 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A264-06A-11D-A196-08 chr3:87309091 C>T maps to NM_001122757.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:111228320 C>T maps to NM_006235.2 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr11:111228229 C>T maps to NM_006235.2 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:111225261 C>T maps to NM_006235.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr1:167343505 C>T maps to NM_002697.3 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr1:167343472 C>T maps to NM_002697.3 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:42621503 G>A maps to ENST00000342301 D62D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr19:42599533 G>A maps to ENST00000342301 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:42600012 G>A maps to ENST00000342301 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:42626696 C>T maps to ENST00000342301 E15E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:42599548 C>T maps to ENST00000342301 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:120175795 C>T maps to NM_014352.2 Q168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:120187959 G>A maps to NM_014352.2 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr11:120175803 C>T maps to NM_014352.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:120180243 C>T maps to NM_014352.2 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:120188028 C>T maps to NM_014352.2 N409N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:99283556 C>T maps to NM_005604.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr2:105473140 C>T maps to NM_006236.1 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:82763887 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:82764187 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:82763741 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:82763471 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:82763703 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:82763826 G>T did not map to a codon.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr4:147561242 C>T maps to NM_004575.2 H171H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr4:147561590 G>A maps to NM_004575.2 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr5:145719370 G>A maps to NM_002700.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:145719178 G>A maps to NM_002700.2 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:145719772 G>A maps to NM_002700.2 E261E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr5:145719649 G>A maps to NM_002700.2 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:128428509 G>A maps to NM_001159542.1 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr8:128428623 G>A maps to NM_001159542.1 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr8:128428545 A>G maps to NM_001159542.1 E145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr8:128428575 G>A maps to NM_001159542.1 Q155Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr8:128428287 G>A maps to NM_001159542.1 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr5:93076864 C>T maps to NM_153216.1 Q135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:93076822 G>A maps to NM_153216.1 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:93076969 G>A maps to NM_153216.1 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:93076585 G>A maps to NM_153216.1 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr12:51586220 G>A maps to NM_002702.3 Q95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr12:51586221 G>A maps to NM_002702.3 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:39504008 C>T maps to NM_007252.3 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:39379266 C>T maps to NM_007252.3 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:39504251 G>A maps to NM_007252.3 E681E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr7:39472824 C>T maps to NM_007252.3 I392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:39504281 C>T maps to NM_007252.3 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:39472833 G>A maps to NM_007252.3 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:39379266 C>T maps to NM_007252.3 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:39125629 C>T maps to NM_007252.3 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr7:39243876 C>T maps to NM_007252.3 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr7:39243877 C>T maps to NM_007252.3 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr7:39247155 C>T maps to NM_007252.3 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr7:39504140 G>A maps to NM_007252.3 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:39247155 C>T maps to NM_007252.3 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr7:39500185 G>A maps to NM_007252.3 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:39491253 C>T maps to NM_007252.3 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:39247055 C>T maps to NM_007252.3 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:39504227 G>A maps to NM_007252.3 E673E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:39503969 C>T maps to NM_007252.3 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:39504113 G>A maps to NM_007252.3 Q635Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr7:39472824 C>T maps to NM_007252.3 I392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:106317464 G>A maps to ENST00000357415 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:106345443 G>A maps to ENST00000357415 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:10221438 C>T maps to NM_001040664.2 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:54771129 G>A maps to NM_003711.2 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:57002659 G>A maps to NM_003713.4 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:56989551 C>T maps to NM_003713.4 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:57002770 G>A maps to NM_003713.4 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:282247 G>A maps to NM_177543.1 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:291297 C>G maps to NM_003712.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:291324 C>T maps to NM_003712.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:288022 G>A maps to NM_177543.1 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:291315 G>A maps to NM_003712.2 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr10:122348836 C>T maps to NM_001030059.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:122334745 C>T maps to NM_001030059.1 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:122280584 C>T maps to NM_001030059.1 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr10:122273433 C>T maps to NM_001030059.1 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr9:134165419 C>T maps to NM_032728.3 D12D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr9:134165542 T>G maps to NM_032728.3 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr9:134165395 C>T maps to NM_032728.3 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr22:46628086 G>A maps to NM_001001928.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr22:46614164 C>T maps to NM_001001928.2 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:46614224 C>T maps to NM_001001928.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr22:46594429 C>T maps to NM_001001928.2 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:46615853 C>T maps to NM_001001928.2 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr6:35392546 C>T maps to NM_006238.4 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr6:35392116 C>T maps to NM_006238.4 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:35392530 C>T maps to NM_006238.4 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:35392491 C>T maps to NM_006238.4 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr3:12458653 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr3:12447429 G>A maps to NM_015869.4 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:12458486 C>T maps to NM_015869.4 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:12422908 C>T maps to NM_015869.4 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:12421417 C>T maps to NM_015869.4 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:12458441 C>T maps to NM_015869.4 I353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:12447417 G>A maps to NM_015869.4 E219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr3:12421305 C>T maps to NM_015869.4 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:23815317 A>G maps to NM_013261.3 S596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:23803488 G>A maps to NM_013261.3 F719F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:23830200 C>T maps to NM_013261.3 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr4:23815707 G>A maps to NM_013261.3 F466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr4:23833375 T>A did not map to a codon.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr4:23816007 A>C maps to NM_013261.3 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:23830059 C>T maps to NM_013261.3 K240K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:23816228 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr5:149216495 G>A maps to NM_133263.3 G826G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:149216112 C>T maps to NM_133263.3 R699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr5:149216010 C>T maps to NM_133263.3 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:149212370 G>A maps to NM_133263.3 K245K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr15:75341000 C>T maps to NM_021823.3 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:18836212 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:18845508 A>G did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:18845469 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:18822163 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:18836171 A>T did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:18775835 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:18824655 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:18822093 C>T did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:18842118 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr4:76788486 T>A maps to NM_006239.2 K579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:76785631 G>A maps to NM_006239.2 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:76805838 C>T maps to NM_006239.2 E218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr4:76788532 C>T maps to NM_006239.2 R563R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr4:76808003 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr4:76794330 G>A maps to NM_006239.2 I485I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr4:76794404 G>A maps to NM_006239.2 R461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:76781930 G>A maps to NM_006239.2 F717F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:76797799 C>A maps to NM_006239.2 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr4:76793175 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:76794279 C>T maps to NM_006239.2 K502K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:76811166 G>A maps to NM_006239.2 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr11:70201879 C>T maps to NM_003626.2 G817G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr11:70201880 C>T maps to NM_003626.2 R818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:70185378 C>T maps to NM_003626.2 G558G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr11:70208221 C>T maps to NM_003626.2 A868A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr11:70184523 C>T maps to NM_003626.2 D512D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:70194462 C>T maps to NM_003626.2 S700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:70171014 G>A maps to NM_003626.2 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:70185378 C>G maps to NM_003626.2 G558G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:70208468 C>T maps to NM_003626.2 L914L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:70171011 C>G maps to NM_003626.2 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:70118403 C>T maps to NM_003626.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:70178154 G>A maps to NM_003626.2 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr12:81688663 G>A maps to NM_003625.2 Q959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:81660751 T>A maps to NM_003625.2 G1178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr12:81719571 G>A maps to NM_003625.2 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:81751896 C>T maps to NM_003625.2 R579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr12:82147925 C>T maps to NM_003625.2 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:81734988 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:81719571 G>A maps to NM_003625.2 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:81746929 C>T maps to NM_003625.2 Q654Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr12:81768448 C>T maps to NM_003625.2 E410E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:81657126 G>A maps to NM_003625.2 Q1200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr12:81693151 A>C maps to NM_003625.2 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:82070581 C>G maps to NM_003625.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:81661829 C>T maps to NM_003625.2 W1116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:81675179 C>T maps to NM_003625.2 W1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:81738457 C>T maps to NM_003625.2 R749R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:81769582 G>A maps to NM_003625.2 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:82147810 G>A maps to NM_003625.2 Q64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:81751996 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:81678082 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr12:81675115 G>T maps to NM_003625.2 C1044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:49633252 C>T maps to NM_003660.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:49633324 G>T did not map to a codon.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr1:203040845 C>T maps to ENST00000367238 F1096F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:203024736 C>T maps to ENST00000367238 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr1:203020941 A>T maps to ENST00000367238 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr1:203024754 C>T maps to ENST00000367238 S654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:203025995 C>T maps to ENST00000367238 I754I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:203029379 C>T maps to ENST00000367238 A852A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:203040860 C>T maps to ENST00000367238 A1101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:27841287 C>T maps to NM_003622.3 L810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:27799044 A>T maps to NM_003622.3 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:27829446 C>T maps to NM_003622.3 F499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:27832955 C>T maps to NM_003622.3 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:27841340 C>T maps to NM_003622.3 V827V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr12:27811781 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr12:27832572 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:7647018 C>T maps to NM_003621.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:7661051 T>G maps to NM_003621.2 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:42836512 C>T maps to NM_016488.6 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr12:42768706 C>G maps to NM_016488.6 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr12:42839993 C>T maps to NM_016488.6 Q418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:44839449 C>T maps to NM_021130.3 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr1:143767484 A>G maps to NM_001123068.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:143767509 G>A maps to NM_001123068.1 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:143767518 G>A maps to NM_001123068.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:143767517 G>A maps to NM_001123068.1 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:143767607 C>A maps to NM_001123068.1 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:143767509 G>A maps to NM_001123068.1 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:122359605 C>T maps to NM_000943.4 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr5:122365029 C>T maps to NM_000943.4 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:122361628 C>T maps to NM_000943.4 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:81109469 C>T maps to NM_005729.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:170470972 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:170492690 T>C maps to NM_004792.2 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:170460736 C>T maps to NM_004792.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr2:170470976 A>T maps to NM_004792.2 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:170488368 C>T maps to NM_004792.2 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:43130568 G>A maps to NM_006347.3 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:36823753 G>A maps to NM_016059.4 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr6:36823600 G>A maps to NM_016059.4 Y163Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr22:22040809 C>T maps to NM_148175.2 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NF-06A-11D-A19A-08 chr22:22049075 C>T maps to NM_148175.2 F434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr22:22036805 C>T maps to NM_148175.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:22039148 C>T maps to NM_148175.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:149833341 A>G maps to NM_139126.2 C392C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:149855852 G>A maps to NM_139126.2 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:109748350 G>A maps to NM_001111298.2 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr6:109748296 C>T maps to NM_001111298.2 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:43827032 G>A maps to NM_001130858.2 Q1381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:43827024 G>A maps to NM_001130858.2 Y1383Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr15:43827033 G>A maps to NM_001130858.2 I1380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr15:43873489 G>A maps to NM_001130858.2 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr5:102537322 G>A maps to ENST00000451606 G1275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr5:102526636 C>T maps to ENST00000451606 S1184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:102469212 C>T maps to ENST00000451606 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr5:102493922 G>A maps to ENST00000451606 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:4935289 C>T maps to NM_002705.4 K1122K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr16:4934358 C>A maps to NM_002705.4 E1433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr16:4944541 C>T maps to NM_002705.4 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr16:4938189 C>T maps to NM_002705.4 R809R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:4935870 G>A maps to NM_002705.4 Q929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:4935160 G>A maps to NM_002705.4 N1165N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:4934161 C>T maps to NM_002705.4 K1498K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:4945318 C>T maps to NM_002705.4 R395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:4945267 C>T maps to NM_002705.4 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:4952412 C>T maps to NM_002705.4 E144E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr16:4937168 C>T maps to NM_002705.4 Q858Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr16:4934734 C>T maps to NM_002705.4 E1307E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr16:4949106 C>T maps to NM_002705.4 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:4933849 C>T maps to NM_002705.4 A1602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:4947741 C>T maps to NM_002705.4 W302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:4947742 C>T maps to NM_002705.4 W302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:4935358 C>T maps to NM_002705.4 K1099K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:60712654 G>A maps to NM_177952.2 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:58678185 G>A maps to NM_003620.3 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr17:58740831 C>T maps to NM_003620.3 T579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:57057590 G>A maps to NM_014906.3 R489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr17:57043130 C>T maps to NM_014906.3 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr17:57057491 G>A maps to NM_014906.3 E456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:57058256 G>A maps to NM_014906.3 G711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr22:22277638 G>A maps to NM_014634.3 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:22285611 G>A maps to NM_014634.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr2:27610019 A>G maps to NM_177983.1 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:27606281 G>A maps to NM_177983.1 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:27605341 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr2:27607719 G>A maps to NM_177983.1 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:63225926 G>A maps to NM_020700.1 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr12:63328471 G>A maps to NM_020700.1 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:63226042 T>A maps to NM_020700.1 K88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr12:63131335 G>A maps to NM_020700.1 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:113255383 C>T maps to NM_005167.5 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr1:113253413 G>A maps to NM_005167.5 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:113253641 C>T maps to NM_005167.5 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:113253677 G>A maps to NM_005167.5 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:89199392 G>A maps to NM_152542.3 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr3:160786641 C>T maps to NM_139245.2 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr3:160786713 C>T maps to NM_139245.2 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr3:160786632 C>T maps to NM_139245.2 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:160783335 G>A maps to NM_139245.2 K240K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:160786677 G>A maps to NM_139245.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr3:160474203 G>A maps to NM_139245.2 W36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr3:160474482 G>A maps to NM_139245.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:52281708 C>T maps to NM_144641.2 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:52283763 C>T maps to NM_144641.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr19:46003762 G>A maps to NM_001080401.1 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr11:73941313 C>T maps to NM_016147.1 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:161137199 C>A maps to NM_001122764.1 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:161138346 G>A maps to NM_001122764.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr11:67166014 G>A maps to NM_001008709.1 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:67167055 C>A maps to NM_001008709.1 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:29016844 T>C maps to NM_002709.2 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:29006833 C>T maps to NM_002709.2 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:111162495 G>A maps to NM_002710.2 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:30573709 G>A maps to NM_002714.2 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr6:30572208 C>T maps to NM_002714.2 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:30569808 G>A maps to NM_002714.2 R873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:30572208 C>T maps to NM_002714.2 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:30036911 T>C maps to NM_021959.2 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr6:30036458 C>T maps to NM_021959.2 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:80203598 G>A maps to NM_001143885.1 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:80266637 G>A maps to NM_001143885.1 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:80266606 C>A maps to NM_001143885.1 G117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:202396217 G>A maps to ENST00000367270 W251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:202411595 G>T maps to ENST00000367270 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:202533585 C>T maps to ENST00000367270 L890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:202391753 C>T maps to ENST00000367270 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:55614868 C>T maps to NM_017607.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:55610166 G>A maps to NM_017607.2 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr14:104212808 G>A maps to NM_015316.2 Q351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr14:104206787 G>A maps to NM_015316.2 A655A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:104206766 G>A maps to NM_015316.2 T662T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr14:104208205 G>A maps to NM_015316.2 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:104206790 G>A maps to NM_015316.2 P654P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr14:104208523 C>T maps to NM_015316.2 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr14:104206310 G>T maps to NM_015316.2 A814A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr19:45885982 G>A maps to NM_001142502.1 D750D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr19:45885814 C>T maps to NM_001142502.1 Q806Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:45899950 G>A maps to NM_001142502.1 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:45895344 G>A maps to NM_001142502.1 P536P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr19:45895245 G>A maps to NM_001142502.1 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:45885982 G>A maps to NM_001142502.1 D750D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:38741972 C>A maps to NM_033256.1 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:38743535 G>A maps to NM_033256.1 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr6:150464596 G>A maps to NM_030949.2 W90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:150464462 G>A maps to NM_030949.2 E45E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr15:41120752 C>T maps to NM_001130143.1 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:41120710 C>T maps to NM_001130143.1 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:41108450 C>T maps to NM_001130143.1 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr15:41120746 C>T maps to NM_001130143.1 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr19:49376549 C>T maps to NM_014330.3 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr19:49377074 T>C maps to NM_014330.3 D195D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr19:49377920 C>T maps to NM_014330.3 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:49378992 C>T maps to NM_014330.3 I596I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:204380329 G>A maps to NM_032833.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:204378970 G>A maps to NM_032833.3 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:204379327 A>T maps to NM_032833.3 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:204379630 G>A maps to NM_032833.3 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:145724213 C>A maps to NM_032902.5 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr8:145722741 G>A maps to NM_032902.5 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:145722798 C>T maps to NM_032902.5 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr8:145724399 G>A maps to NM_032902.5 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr8:145724423 G>A maps to NM_032902.5 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr20:37547164 G>A maps to NM_015568.2 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr20:37536551 G>A maps to NM_015568.2 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:37534637 C>T maps to NM_015568.2 Y241Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:37534638 C>T maps to NM_015568.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr20:37547010 G>A maps to NM_015568.2 W469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:37536823 G>A maps to NM_015568.2 E394E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr20:37546849 C>T maps to NM_015568.2 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr20:37464765 C>T maps to NM_015568.2 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr20:37534724 C>T maps to NM_015568.2 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:37534655 C>T maps to NM_015568.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:37547011 G>A maps to NM_015568.2 W469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:54975915 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr12:54975865 C>T maps to NM_006741.3 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:54974739 C>T maps to NM_006741.3 K166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr17:37791979 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:37786250 C>T maps to ENST00000394271 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr17:37786256 G>A maps to ENST00000394271 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr17:37791920 G>A maps to ENST00000394271 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr2:182928483 G>A maps to ENST00000280295 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr2:182852600 G>A maps to ENST00000280295 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr2:182850860 G>A maps to ENST00000280295 K8K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr3:195256632 A>G maps to NM_006241.4 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:195245817 G>A maps to NM_006241.4 Q190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr7:113517930 G>A maps to NM_002711.3 T1072T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr7:113518197 C>T maps to NM_002711.3 V983V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr7:113519210 G>A maps to NM_002711.3 Q646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:113518602 G>A maps to NM_002711.3 S848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:113559024 C>T maps to NM_002711.3 Q9Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr7:113518302 C>T maps to NM_002711.3 T948T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:113518302 C>T maps to NM_002711.3 T948T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:113518089 C>T maps to NM_002711.3 E1019E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:113558484 G>A maps to NM_002711.3 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:113518659 C>T maps to NM_002711.3 R829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr7:113519544 G>A maps to NM_002711.3 F534F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr7:113518395 G>A maps to NM_002711.3 S917S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr7:113518266 G>A maps to NM_002711.3 I960I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:113518302 C>T maps to NM_002711.3 T948T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:113519034 G>A maps to NM_002711.3 T704T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:8998782 G>A maps to NM_024607.2 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr8:8998396 G>A maps to NM_024607.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:8998384 G>A maps to NM_024607.2 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:8998359 G>A maps to NM_024607.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:8999143 G>A maps to NM_024607.2 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr10:93389688 G>A maps to NM_005398.4 R317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:93390067 G>A maps to NM_005398.4 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr20:58514302 G>A maps to NM_006242.3 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr20:58514629 G>A maps to NM_006242.3 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:58514656 G>A maps to NM_006242.3 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:49143443 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr23:49143506 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:49142940 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:49143277 C>T did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:49142437 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:242099827 C>A maps to NM_002712.1 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:242105765 C>T maps to NM_002712.1 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr7:94913413 C>T maps to NM_001166160.1 F1127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr7:94881169 G>A maps to NM_001166160.1 R831R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr7:94913479 C>T maps to NM_001166160.1 S1149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:94539709 T>A maps to NM_001166160.1 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:94879549 C>T maps to NM_001166160.1 I793I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:94913328 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr7:94881389 C>T maps to NM_001166160.1 T871T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:94913449 C>T maps to NM_001166160.1 S1139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:94539928 G>A maps to NM_001166160.1 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:94540531 C>T maps to NM_001166160.1 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:94898019 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:94913332 C>T maps to NM_001166160.1 I1100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:48221006 G>A maps to NM_032595.3 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:48226560 C>T maps to NM_032595.3 R438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr17:48222507 A>G maps to NM_032595.3 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr5:133541809 G>A maps to NM_002715.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:52705249 T>A maps to NM_014225.5 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:52716049 C>T maps to NM_014225.5 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:52719260 C>T maps to NM_014225.5 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:111636042 T>G maps to NM_181699.2 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:26221325 C>T maps to NM_001177591.1 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr8:26218497 C>T maps to NM_001177591.1 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr5:145979964 C>T maps to ENST00000394414 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr5:145969653 C>T maps to ENST00000394414 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:145969629 G>A maps to ENST00000394414 I470I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:146077635 G>A maps to ENST00000394414 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr5:146017868 C>T maps to ENST00000394414 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr5:146030137 C>T maps to ENST00000394414 W265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:6335387 C>T maps to NM_181876.2 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr4:6325199 C>T maps to NM_181876.2 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr4:6349648 G>A maps to NM_181876.2 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr4:6349732 G>A maps to NM_181876.2 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr4:6380248 G>A maps to NM_181876.2 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:6374376 C>T maps to NM_181876.2 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:6374388 C>T maps to NM_181876.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:6473932 C>T maps to NM_020416.3 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr4:6380218 G>A maps to NM_181876.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:6325220 G>A maps to NM_181876.2 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:6374256 C>T maps to NM_181876.2 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:135801249 A>G maps to NM_002718.4 R925R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:301558 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:302649 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr23:299623 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:295188 C>G did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:295199 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:295173 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:295176 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr23:322178 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:295176 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr14:35560352 G>A maps to NM_017917.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr9:131899967 C>T maps to NM_178001.2 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr9:131891280 C>T maps to NM_178001.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr9:131885395 C>T maps to NM_178001.2 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:131891298 G>A maps to NM_178001.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr9:131885398 C>T maps to NM_178001.2 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr9:131909679 C>T maps to NM_178001.2 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr1:212515561 G>A maps to NM_006243.3 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:212530018 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr1:212519228 G>T maps to NM_006243.3 G220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr1:212533978 G>C did not map to a codon.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr11:64699324 C>T maps to NM_006244.3 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64698930 C>T maps to NM_006244.3 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:102323170 C>T maps to NM_002719.3 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr14:102348515 C>T maps to NM_002719.3 R105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr4:101947216 A>T maps to NM_000944.4 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:101947022 C>T maps to NM_000944.4 *522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:22355617 A>G maps to ENST00000397775 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:22370922 C>T maps to ENST00000397775 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr2:68413776 G>A maps to ENST00000406334 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:104356957 G>A maps to NM_147180.2 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:104357119 C>T maps to NM_147180.2 K31K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:104356975 G>A maps to NM_147180.2 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr16:30095041 C>A maps to NM_002720.1 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr18:9557370 G>A maps to NM_001042388.1 R680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:9588786 G>A maps to NM_001042388.1 N120N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr3:73114651 C>T maps to NM_174907.2 Q345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr14:94708236 C>T maps to NM_058237.1 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr14:94716612 A>G maps to NM_058237.1 E572E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr14:94674842 C>T maps to NM_058237.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr14:94712007 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr14:94697045 C>T maps to NM_058237.1 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr14:94712812 C>T maps to NM_058237.1 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr14:94722886 G>A maps to NM_058237.1 V652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:94722889 G>A maps to NM_058237.1 R653R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:94731787 C>T maps to NM_058237.1 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr14:94708699 C>T maps to NM_058237.1 D407D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:94700009 C>T maps to NM_058237.1 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:94718185 C>T maps to NM_058237.1 F606F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:46878976 C>T maps to NM_006247.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:127951859 A>T maps to NM_001123355.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr9:127915951 G>A maps to NM_001123355.1 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr9:127923118 C>G did not map to a codon.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr9:127911957 G>A maps to NM_001123355.1 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:127915937 C>T maps to NM_001123355.1 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr9:127915933 G>A maps to NM_001123355.1 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr22:42003274 G>A maps to NM_015704.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr10:103901747 C>T maps to NM_015062.3 F1161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:103899828 C>A maps to NM_015062.3 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr10:103907119 C>T maps to NM_015062.3 S1457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:103899554 C>T maps to NM_015062.3 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:103901606 C>T maps to NM_015062.3 P1114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr10:103909753 T>C maps to NM_015062.3 L1655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:103897785 C>T maps to NM_015062.3 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:103908593 C>T maps to NM_015062.3 F1546F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:103908621 C>T maps to NM_015062.3 R1556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:40544324 G>T maps to ENST00000372783 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:32122886 A>G maps to NM_138717.1 Q94Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr6:32123667 C>T maps to NM_138717.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr12:110989647 C>A maps to NM_139283.1 G117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr12:110983802 G>A maps to NM_139283.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr12:110983803 G>A maps to NM_139283.1 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr12:110983767 T>G maps to NM_139283.1 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr10:47087365 C>T maps to NM_005972.4 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr10:47087211 C>T maps to NM_005972.4 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr10:47087904 C>T maps to NM_005972.4 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr10:47087022 C>T maps to NM_005972.4 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44Q-06A-11D-A25O-08 chr10:47087304 C>T maps to NM_005972.4 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr10:47086947 G>A maps to NM_005972.4 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr10:47087157 G>A maps to NM_005972.4 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:47087589 G>A maps to NM_005972.4 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:47086911 C>T maps to NM_005972.4 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:47087409 C>T maps to NM_005972.4 H209H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr10:47087320 C>T maps to NM_005972.4 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:47087076 C>T maps to NM_005972.4 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr10:47086992 G>A maps to NM_005972.4 K70K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:47087775 G>A maps to NM_005972.4 K331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr10:47087208 C>T maps to NM_005972.4 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr10:47087169 C>T maps to NM_005972.4 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr10:47087532 G>A maps to NM_005972.4 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:47087229 G>A maps to NM_005972.4 W149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:47087787 C>T maps to NM_005972.4 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr10:47087349 C>T maps to NM_005972.4 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:47087478 C>T maps to NM_005972.4 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:77679197 G>A maps to NM_025078.4 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:19653761 C>T maps to NM_017765.2 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:48931590 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr19:8555574 C>T maps to NM_032152.4 G603G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr19:8563368 C>T maps to NM_032152.4 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:8564196 C>T maps to NM_032152.4 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:8563692 G>A maps to NM_032152.4 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:8563971 G>A maps to NM_032152.4 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr19:8564340 C>T maps to NM_032152.4 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:8563992 G>A maps to NM_032152.4 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:8564172 G>A maps to NM_032152.4 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr22:22890500 G>A maps to NM_206954.1 F506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr22:22890773 C>T maps to NM_206954.1 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr22:22892524 G>A maps to NM_206954.1 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr22:22892368 C>T maps to NM_206954.1 W244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:22892157 G>A maps to NM_206954.1 Q315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:22893199 C>T maps to NM_206954.1 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr22:22890989 G>A maps to NM_206954.1 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:22890773 C>T maps to NM_206954.1 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:22892236 G>A maps to NM_206954.1 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr22:22890728 G>A maps to NM_206954.1 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:12854552 C>T maps to NM_023013.2 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:12853447 C>T maps to NM_023013.2 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:12854240 C>T maps to NM_023013.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:12853409 C>T maps to NM_023013.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:12854486 C>T maps to NM_023013.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr1:12856063 G>A maps to NM_023013.2 K448K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:12853513 G>A maps to NM_023013.2 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:12854297 G>A maps to NM_023013.2 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:12855982 C>T maps to NM_023013.2 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:12856117 G>A maps to NM_023013.2 E466E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:12855736 C>T maps to NM_023013.2 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:12855632 C>T maps to NM_023013.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr1:12854495 C>T maps to NM_023013.2 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:12854213 C>T maps to NM_023013.2 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:12854297 G>A maps to NM_023013.2 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:12855637 G>A maps to NM_023013.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12854105 G>A maps to NM_023013.2 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12854284 G>A maps to NM_023013.2 W170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12854465 G>A maps to NM_023013.2 E230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12855781 C>T maps to NM_023013.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12855899 C>T maps to NM_023013.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12856144 G>A maps to NM_023013.2 *475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:12855944 C>T maps to NM_023013.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:12954862 C>T maps to NM_001039361.3 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:12954862 C>T maps to NM_001039361.3 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:12954981 G>A maps to NM_001039361.3 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12954981 G>A maps to NM_001039361.3 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:12887685 T>C maps to NM_001146344.1 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:12887370 C>T maps to NM_001146344.1 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:12887329 C>T maps to NM_001146344.1 W176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:12887685 T>C maps to NM_001146344.1 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr1:12887370 C>T maps to NM_001146344.1 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:12887273 G>A maps to NM_001146344.1 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr1:12887484 G>A maps to NM_001146344.1 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr1:12887685 T>C maps to NM_001146344.1 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:12887502 C>T maps to NM_001146344.1 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:12887586 C>T maps to NM_001146344.1 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:12887391 G>A maps to NM_001146344.1 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:12884946 C>T maps to NM_001146344.1 W388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:12887175 C>T maps to NM_001146344.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr1:12887328 C>T maps to NM_001146344.1 W176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:12887381 G>A maps to NM_001146344.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:12884918 G>A maps to NM_001146344.1 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr1:12835841 C>T maps to NM_001080830.1 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr1:12835270 A>C maps to NM_001080830.1 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr1:12835081 C>T maps to NM_001080830.1 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:12836087 G>A maps to NM_001080830.1 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:12837393 C>T maps to NM_001080830.1 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr1:12837291 C>T maps to NM_001080830.1 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:12835748 T>C maps to NM_001080830.1 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:12837297 T>C maps to NM_001080830.1 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:12835994 G>A maps to NM_001080830.1 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:12836147 G>A maps to NM_001080830.1 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:12835237 G>A maps to NM_001080830.1 E76E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:12837675 G>A maps to NM_001080830.1 R462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:12835988 G>A maps to NM_001080830.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:12835934 T>C maps to NM_001080830.1 C179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr1:12835841 C>T maps to NM_001080830.1 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:12835721 G>A maps to NM_001080830.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:12835799 G>A maps to NM_001080830.1 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:12835153 C>T maps to NM_001080830.1 C48C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:12835721 G>A maps to NM_001080830.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:12837393 C>T maps to NM_001080830.1 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12836063 C>T maps to NM_001080830.1 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12837369 C>T maps to NM_001080830.1 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:12836231 C>T maps to NM_001080830.1 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:12836234 C>T maps to NM_001080830.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:13448285 G>A maps to NM_001024661.1 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:13716881 C>T maps to NM_001099851.1 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr1:13716848 C>T maps to NM_001099851.1 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:13475030 G>A maps to NM_001099850.1 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:13695884 C>T maps to NM_001099850.1 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:13695910 G>A maps to NM_001099850.1 Q352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:13695857 G>A maps to NM_001099850.1 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr1:13695884 C>T maps to NM_001099850.1 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr1:12920099 C>T maps to NM_023014.1 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:12921096 G>A maps to NM_023014.1 E296E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:12921315 C>T maps to NM_023014.1 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:12921471 C>T maps to NM_023014.1 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:12919568 G>A maps to NM_023014.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:12919001 G>A maps to NM_023014.1 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:12921555 G>A maps to NM_023014.1 R449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:12921090 C>T maps to NM_023014.1 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:12919634 C>T maps to NM_023014.1 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:12919917 C>T maps to NM_023014.1 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr1:12921345 C>T maps to NM_023014.1 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr1:12921270 C>T maps to NM_023014.1 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:12919787 T>C maps to NM_023014.1 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:12920099 C>T maps to NM_023014.1 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:13036555 C>T maps to NM_001100631.1 Q210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr1:13036629 G>A maps to NM_001100631.1 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr1:12943101 G>A maps to NM_001009611.2 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:12943053 C>T maps to NM_001009611.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:12943140 C>T maps to NM_001009611.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:12943110 T>C maps to NM_001009611.2 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:12943143 A>G maps to NM_001009611.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:12943182 G>A maps to NM_001009611.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:12941847 C>T maps to ENST00000376192 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:12943131 G>A maps to NM_001009611.2 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:12943160 G>A maps to NM_001009611.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:12943089 G>A maps to NM_001009611.2 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:12939709 G>A maps to ENST00000376192 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:12943107 T>C maps to NM_001009611.2 E36E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr1:12939628 G>A maps to ENST00000376192 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:13001313 C>T maps to ENST00000415464 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr1:13001274 C>T maps to ENST00000415464 Q136Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:13001292 C>T maps to ENST00000415464 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:13001262 C>T maps to ENST00000415464 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:13001292 C>T maps to ENST00000415464 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:13001208 C>T maps to ENST00000415464 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:13001262 C>T maps to ENST00000415464 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:12979743 C>T maps to NM_001012277.1 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:12979809 C>T maps to NM_001012277.1 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:12979686 C>T maps to NM_001012277.1 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12979734 G>A maps to NM_001012277.1 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr10:135165826 C>T maps to ENST00000423766 Y114Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:11506222 G>A maps to NM_005039.3 Q272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:11545981 T>A maps to NM_006248.3 K344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:11548454 C>T maps to NM_006248.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr12:11546315 G>A maps to NM_006248.3 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr12:11420864 T>C maps to NM_006249.4 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr12:11422582 C>T maps to NM_006249.4 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr12:11422548 A>G maps to NM_006249.4 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr12:11422549 G>A maps to NM_006249.4 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:11420936 G>A maps to NM_006249.4 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr12:11462313 G>A maps to NM_002723.3 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:11461465 G>A maps to NM_002723.3 Q151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:11461220 T>C maps to NM_002723.3 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr12:11461397 G>A maps to NM_002723.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JB-06A-11D-A196-08 chr15:91517846 G>T maps to NM_003981.2 R440R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr15:91519979 G>A maps to NM_003981.2 R377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr15:91517853 C>T maps to NM_003981.2 E437E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr15:91523620 T>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr15:91512730 G>A maps to NM_003981.2 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:156756878 C>T maps to NM_005973.4 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:156752096 C>T maps to NM_005973.4 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:156756842 C>T maps to NM_005973.4 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:74538646 T>G maps to NM_001077620.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:74538647 C>T maps to NM_001077620.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr11:82560192 T>C maps to NM_199418.2 Q294Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:106553105 G>A maps to NM_001198.3 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:106553489 G>A maps to NM_001198.3 R485R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:106543593 G>A maps to NM_001198.3 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr6:106553249 G>A maps to NM_001198.3 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:106543593 G>A maps to NM_001198.3 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:106553273 C>T maps to NM_001198.3 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr6:106552700 A>T maps to NM_001198.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:106547182 C>T maps to NM_001198.3 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:106552988 C>T maps to NM_001198.3 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr6:106554850 G>A maps to NM_001198.3 E656E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr6:106553561 C>T maps to NM_001198.3 A509A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:106552874 C>T maps to NM_001198.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:106553750 G>A maps to NM_001198.3 K572K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr11:129785641 G>A maps to NM_020228.2 P817P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr11:129782021 G>A maps to NM_020228.2 I984I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr11:129814663 A>C did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:129814866 C>T maps to NM_020228.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:129795049 G>A maps to NM_020228.2 F539F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr11:129817268 G>A maps to NM_199438.1 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:129814707 G>A maps to NM_020228.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:129780500 G>A maps to NM_020228.2 L1015L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:129795111 G>A maps to NM_020228.2 Q519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:129784871 G>A maps to NM_020228.2 F860F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:129817090 G>A maps to NM_020228.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:129781994 G>A maps to NM_020228.2 A993A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:45204595 C>T maps to NM_020229.2 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:45204436 C>T maps to NM_020229.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:45226311 C>T maps to NM_020229.2 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:133556641 C>T maps to NM_021619.2 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:133540057 C>T maps to NM_021619.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr8:70981780 G>A maps to NM_024504.2 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:70981504 G>A maps to NM_024504.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr8:70981528 C>T maps to NM_024504.2 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:70981483 G>A maps to NM_024504.2 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:70982035 C>T maps to NM_024504.2 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:70980554 G>A maps to NM_024504.2 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:70978469 C>A maps to NM_024504.2 E395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr8:70970970 C>T maps to NM_024504.2 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:70981498 C>T maps to NM_024504.2 E199E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:70981483 G>A maps to NM_024504.2 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:70981620 G>A maps to NM_024504.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr21:43243679 G>A maps to NM_022115.3 H951H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr21:43242387 G>A maps to NM_022115.3 I955I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:43221840 C>T maps to NM_022115.3 S1361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr21:43243671 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr21:43240523 G>A maps to NM_022115.3 I1055I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr21:43221639 C>T maps to NM_022115.3 Q1428Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:43259927 G>A maps to NM_022115.3 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:43274921 G>A maps to NM_022115.3 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr21:43281848 G>A maps to NM_022115.3 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:3328854 C>T maps to NM_022114.3 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:3328995 C>T maps to NM_022114.3 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr1:3342246 C>T maps to NM_022114.3 N1014N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr1:3319547 C>T maps to NM_022114.3 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr1:3321446 G>A maps to NM_022114.3 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:3328302 C>T maps to NM_022114.3 F514F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:3342732 C>T maps to NM_022114.3 I1076I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr1:3331183 G>A maps to NM_022114.3 R888R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:3334519 C>T maps to NM_022114.3 S940S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:3102722 C>T maps to NM_022114.3 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:3328935 C>T maps to NM_022114.3 F725F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:3329121 C>T maps to NM_022114.3 P787P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:3348586 G>A maps to NM_022114.3 G1193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:3348616 G>A maps to NM_022114.3 E1203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr1:3321338 C>T maps to NM_022114.3 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:3328401 C>T maps to NM_022114.3 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:3342180 G>A maps to NM_022114.3 S992S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:3342630 G>A maps to NM_022114.3 G1042G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:3347450 C>T maps to NM_022114.3 I1100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr1:14107475 T>G maps to NM_012231.4 S1062S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr1:14075929 G>A maps to NM_012231.4 E153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:14108621 C>T maps to NM_012231.4 A1444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr1:14057583 C>T maps to NM_012231.4 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:14107220 C>T maps to NM_012231.4 P977P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:14107256 C>T maps to NM_012231.4 L989L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr1:14104970 C>T maps to NM_012231.4 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr1:14107070 C>T maps to NM_012231.4 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr12:108147757 G>A maps to NM_012406.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr12:108147758 G>A maps to NM_012406.3 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:108145330 G>A maps to NM_012406.3 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr12:108150663 T>G maps to NM_012406.3 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:121631532 G>A maps to NM_018699.2 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:121774620 G>A maps to NM_018699.2 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:121631513 G>A maps to NM_018699.2 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:121774680 C>T maps to NM_018699.2 K64K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:90124942 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:90141870 G>A maps to NM_001098173.1 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:81123398 C>T maps to NM_001099403.1 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:81123449 C>T maps to NM_001099403.1 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:81123332 C>T maps to NM_001099403.1 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr5:23522893 G>A maps to NM_020227.2 W261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr5:23527797 G>T maps to NM_020227.2 R867R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr5:23523410 G>A maps to NM_020227.2 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr5:23527650 C>T maps to NM_020227.2 H818H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:23524448 G>A maps to NM_020227.2 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:23526444 C>T maps to NM_020227.2 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr5:23522774 C>T maps to NM_020227.2 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr5:23524610 G>A maps to NM_020227.2 W373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr5:23527653 C>T maps to NM_020227.2 L819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr5:23527764 G>A maps to NM_020227.2 G856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr5:23526582 C>T maps to NM_020227.2 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:23522482 G>A maps to NM_020227.2 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:23526564 C>T maps to NM_020227.2 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:23527764 G>A maps to NM_020227.2 G856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:23524457 C>T maps to NM_020227.2 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr5:23527857 C>T maps to NM_020227.2 P887P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:23527701 G>A maps to NM_020227.2 R835R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:23522419 G>A maps to NM_020227.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:23526471 C>T maps to NM_020227.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:23509676 G>A maps to NM_020227.2 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:23522419 G>A maps to NM_020227.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:23526505 C>T maps to NM_020227.2 Q437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr5:23527497 G>A maps to NM_020227.2 Q767Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:23509189 G>A maps to NM_020227.2 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:23522828 C>T maps to NM_020227.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:23526573 G>A maps to NM_020227.2 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:23526957 G>A maps to NM_020227.2 R587R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr5:23524491 C>T maps to NM_020227.2 Q334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:12911707 C>T maps to NM_181738.1 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:23697365 C>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr11:64088218 C>T maps to NM_012094.3 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:203452497 C>T maps to NM_201348.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr1:203452497 C>T maps to NM_201348.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr6:105729673 C>T maps to NM_002726.4 W595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:105736769 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:105771584 C>T maps to NM_002726.4 E424E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:105733415 G>A maps to NM_002726.4 I498I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:105726129 C>T maps to NM_002726.4 V674V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr20:47249085 G>A maps to NM_020820.3 S1453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr20:47273651 C>T maps to NM_020820.3 E683E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:47273668 G>A maps to NM_020820.3 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr20:47258998 G>A maps to NM_020820.3 I1210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:47274763 G>A maps to NM_020820.3 I628I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:47249067 G>T maps to NM_020820.3 A1459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:47309288 G>A maps to NM_020820.3 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:47262528 G>A maps to NM_020820.3 A1124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:47268116 G>A maps to NM_020820.3 F824F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr20:47244111 C>T maps to NM_020820.3 K1637K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr20:47305232 C>T maps to NM_020820.3 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr20:47260956 C>T maps to NM_020820.3 E1197E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr20:47246066 G>A maps to NM_020820.3 A1562A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr20:47267557 G>A maps to NM_020820.3 F897F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr20:47292787 C>T maps to NM_020820.3 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:47267429 A>C did not map to a codon.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr20:47317391 G>A maps to NM_020820.3 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:47274754 C>T maps to NM_020820.3 Q631Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:47274757 G>A maps to NM_020820.3 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:47361636 G>A maps to NM_020820.3 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:47267431 C>T maps to NM_020820.3 E939E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr20:47276591 C>T maps to NM_020820.3 E582E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:47253039 G>A maps to NM_020820.3 V1376V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:47274730 G>A maps to NM_020820.3 I639I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr8:69009414 T>A maps to NM_024870.2 G844G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:68956811 G>T maps to NM_024870.2 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:69020453 G>A maps to NM_024870.2 V942V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr8:68956772 T>G maps to NM_024870.2 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:68993057 G>A maps to NM_024870.2 K621K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr8:69005847 C>T maps to NM_024870.2 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr8:68992729 G>A maps to NM_024870.2 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr8:69136816 G>A maps to NM_024870.2 A1577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:68939497 C>T maps to NM_024870.2 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:68972988 A>G maps to NM_024870.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr8:69002859 C>T maps to NM_024870.2 I720I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:69002928 G>A maps to NM_024870.2 R743R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:69021712 C>T maps to NM_024870.2 L1001L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:68989630 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:69030802 G>A maps to NM_024870.2 R1115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr8:69020426 C>T maps to NM_024870.2 F933F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr8:68939479 G>A maps to NM_024870.2 R155R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A2GI-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:69020508 C>T maps to NM_024870.2 Q961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr8:69033270 G>A maps to NM_024870.2 R1237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr8:68864760 C>T maps to NM_024870.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:69033270 G>A maps to NM_024870.2 R1237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:68989693 T>C maps to NM_024870.2 F544F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:69021804 C>T maps to NM_024870.2 G1031G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:69136816 G>A maps to NM_024870.2 A1577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr8:69030802 G>A maps to NM_024870.2 R1115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr8:69033154 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:68950440 C>T maps to NM_024870.2 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:68984783 G>A maps to NM_024870.2 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr8:69033270 G>A maps to NM_024870.2 R1237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr8:69046487 C>T maps to NM_024870.2 Q1321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr8:68965371 G>A maps to NM_024870.2 W328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr8:69129883 C>T maps to NM_024870.2 I1546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr8:68972997 T>C maps to NM_024870.2 N441N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr8:69033270 G>A maps to NM_024870.2 R1237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:68950479 G>T maps to NM_024870.2 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:68950491 C>T maps to NM_024870.2 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:68968188 C>T maps to NM_024870.2 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:68984805 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:69000000 G>A maps to NM_024870.2 Q690Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:69002946 G>A maps to NM_024870.2 T749T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-GN-A262-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr8:69021651 G>A maps to NM_024870.2 G980G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr8:69046462 G>A maps to NM_024870.2 A1312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr8:68950471 G>T maps to NM_024870.2 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr10:72358264 G>A maps to NM_005041.4 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr10:72358717 C>T maps to NM_005041.4 E253E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:72358729 G>A maps to NM_005041.4 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:72358522 G>A maps to NM_005041.4 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr10:72358236 G>A maps to NM_005041.4 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:72358285 G>A maps to NM_005041.4 C397C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:72358711 C>T maps to NM_005041.4 E255E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:72360604 G>A maps to NM_005041.4 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:72358405 C>T maps to NM_005041.4 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr11:57157408 G>A maps to NM_002728.4 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:57155260 G>A maps to NM_002728.4 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:57156617 G>A maps to NM_002728.4 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:57145276 C>T maps to NM_006093.3 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr11:57148169 G>A maps to NM_006093.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr11:57147107 G>A maps to NM_006093.3 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:186277190 G>A maps to NM_005807.3 G780G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:186277043 G>A maps to NM_005807.3 K731K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:186276032 G>A maps to NM_005807.3 K394K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:186266057 C>T maps to NM_005807.3 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:186276032 G>A maps to NM_005807.3 K394K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:186266006 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:186276692 G>A maps to NM_005807.3 K614K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:186276716 G>A maps to NM_005807.3 K622K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:186266057 C>T maps to NM_005807.3 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:186276149 G>A maps to NM_005807.3 K433K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:186269232 C>T maps to NM_005807.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr1:186277994 G>A maps to NM_005807.3 T1048T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:186276563 C>T maps to NM_005807.3 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:186281958 T>A maps to NM_005807.3 V1350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:186266027 C>T maps to NM_005807.3 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:186276026 T>C maps to NM_005807.3 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:186281400 G>A maps to NM_005807.3 T1296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr12:11035669 G>A maps to NM_006250.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:11034872 G>A maps to NM_006250.2 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr13:28562732 G>A maps to NM_001105577.1 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr13:28562650 C>A maps to NM_001105577.1 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr13:28562651 C>T maps to NM_001105577.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr20:62203459 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr20:62200239 G>A maps to NM_001037335.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr20:62192809 G>A maps to NM_001037335.2 T2282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr20:62194564 G>A maps to NM_001037335.2 F1870F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr20:62195260 G>A maps to NM_001037335.2 L1638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:62194399 G>A maps to NM_001037335.2 G1925G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr20:62194488 G>A maps to NM_001037335.2 L1896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:62196570 G>A maps to NM_001037335.2 L1202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr20:62195149 G>A maps to NM_001037335.2 I1675I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:62192593 G>A maps to NM_001037335.2 F2329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr20:62193695 G>A maps to NM_001037335.2 S2114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr20:62195583 G>A maps to NM_001037335.2 Q1531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr20:62192982 G>A maps to NM_001037335.2 P2269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:62191962 G>A maps to NM_001037335.2 L2457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:62196997 A>T maps to NM_001037335.2 A1059A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:62200345 G>A maps to NM_001037335.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:62192270 G>A maps to NM_001037335.2 L2386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr20:62194213 G>A maps to NM_001037335.2 F1987F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr20:62200604 G>A maps to NM_001037335.2 N328N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr20:62190679 G>A maps to NM_001037335.2 L2623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:62195449 G>C maps to NM_001037335.2 P1575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:62200327 G>A maps to NM_001037335.2 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr20:62198412 G>A maps to NM_001037335.2 H766H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:62192545 G>A maps to NM_001037335.2 A2345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:62195401 G>A maps to NM_001037335.2 P1591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:62203492 G>A maps to NM_001037335.2 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:62193671 C>A maps to NM_001037335.2 L2122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:62197147 G>A maps to NM_001037335.2 S1009S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr20:62198991 G>A maps to ENST00000370091 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr20:62199886 C>T maps to NM_001037335.2 K518K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr20:62192524 C>T maps to NM_001037335.2 L2352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr12:42854183 C>T maps to NM_153026.2 G641G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:42853643 C>T maps to NM_153026.2 K821K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:42858581 G>A maps to NM_153026.2 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3BZ-06A-12D-A196-08 chr3:64139007 G>A maps to NM_198859.3 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:64133274 G>A maps to NM_198859.3 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:64085071 C>T maps to NM_198859.3 R730R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr3:64085041 G>A maps to NM_198859.3 S740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr3:64085190 G>A maps to NM_198859.3 R691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr3:64133289 G>A maps to NM_198859.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:64133292 G>A maps to NM_198859.3 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr3:64142933 G>A maps to NM_198859.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:64084891 G>A maps to NM_198859.3 F790F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:49034473 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr12:57146013 G>A maps to NM_000946.2 Y23Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr6:57246933 G>T maps to NM_000947.2 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:57246858 C>T maps to NM_000947.2 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr14:94203660 G>A maps to NM_178013.3 I95I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A2MI-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:94203636 G>A maps to NM_178013.3 S103S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-FW-A3R5-06A-11D-A23B-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:94203636 G>A maps to NM_178013.3 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:40764628 G>A maps to NM_206907.3 F489F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:40764856 C>T maps to NM_206907.3 W450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:57169961 G>A maps to NM_006252.3 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr1:57157099 T>C maps to NM_006252.3 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:57170072 C>T maps to NM_006252.3 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:57170073 C>T maps to NM_006252.3 R407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:57161733 C>T maps to NM_006252.3 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr1:57171823 G>A maps to NM_006252.3 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr1:57140108 G>A maps to NM_006252.3 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:57158173 C>T maps to NM_006252.3 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:57169989 A>T maps to NM_006252.3 K379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:120110192 C>T maps to NM_006253.4 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:146639509 G>A maps to NM_005399.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:146638496 G>A maps to NM_005399.3 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:14213633 G>A maps to NM_002730.3 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:84662425 G>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr9:71628483 G>A maps to NM_002732.3 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr9:71628456 C>T maps to NM_002732.3 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr9:71628162 G>A maps to NM_002732.3 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr9:71628153 G>A maps to NM_002732.3 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr9:71628659 G>A maps to NM_002732.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr9:71628255 G>A maps to NM_002732.3 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:71628483 G>A maps to NM_002732.3 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:71628927 G>A maps to NM_002732.3 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr9:71628114 G>A maps to NM_002732.3 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:71628096 G>A maps to NM_002732.3 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr9:71628336 G>A maps to NM_002732.3 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:71628096 G>A maps to NM_002732.3 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:71628129 C>T maps to NM_002732.3 K293K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:71628474 C>T maps to NM_002732.3 Q178Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:71628816 C>T maps to NM_002732.3 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr9:71628009 C>T maps to NM_002732.3 E333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:71628843 G>A maps to NM_002732.3 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:49397340 G>A maps to NM_002733.3 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:49397576 C>T maps to NM_002733.3 Q222Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:151372660 G>A maps to NM_016203.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:151265867 G>A maps to NM_016203.3 D389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:151372706 G>A maps to NM_016203.3 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr7:151273499 G>A maps to NM_016203.3 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr2:219694898 C>T maps to NM_017431.2 W145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:219695066 C>T maps to NM_017431.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr2:219694841 C>T maps to NM_017431.2 Q164Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:219694766 C>T maps to NM_017431.2 Q189Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:219695036 C>T maps to NM_017431.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:219696074 C>T maps to NM_017431.2 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:219695544 C>T maps to NM_017431.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:219695514 T>C maps to NM_017431.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:219693281 C>T maps to NM_017431.2 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:219695496 C>T maps to NM_017431.2 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr17:66526523 C>T maps to NM_212472.1 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:66522026 C>T maps to NM_212472.1 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr7:635806 C>T maps to NM_002735.2 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:750995 G>A maps to NM_002735.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:750992 G>A maps to NM_002735.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:750980 G>A maps to NM_002735.2 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:751022 G>A maps to NM_002735.2 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr7:590234 C>T maps to NM_002735.2 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr7:590186 C>T maps to NM_002735.2 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:751016 C>T maps to NM_002735.2 K42K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr7:720201 G>A maps to NM_002735.2 Y113Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr7:106797451 C>T maps to NM_002736.2 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr7:106685402 G>A maps to NM_002736.2 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr17:64299124 C>T maps to NM_002737.2 H52H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:64734895 C>T maps to NM_002737.2 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr17:64641629 G>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:64738835 G>A maps to NM_002737.2 T494T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr16:24135268 C>T maps to NM_002738.6 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr16:24104249 G>A maps to NM_002738.6 W223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:24183664 C>T maps to NM_002738.6 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr16:24231415 G>A maps to NM_212535.2 E666E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:24196821 C>T maps to NM_002738.6 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr16:24166006 C>T maps to NM_002738.6 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:24196443 C>T maps to NM_002738.6 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr16:24202505 G>A maps to NM_002738.6 E606E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:24135196 G>A maps to NM_002738.6 K320K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:24196454 G>A maps to NM_002738.6 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:24196455 A>T maps to NM_002738.6 K520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr16:24192137 C>T maps to NM_002738.6 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:24124305 G>A maps to NM_002738.6 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr16:24226116 A>T maps to NM_002738.6 K668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr16:24105561 C>T maps to NM_002738.6 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:24166057 G>A maps to NM_002738.6 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:53226260 C>T maps to NM_212539.1 F670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:53217544 C>T maps to NM_212539.1 D245D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:53220036 C>T maps to NM_212539.1 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:53222762 G>A maps to NM_212539.1 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:53223126 C>T maps to NM_212539.1 V536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:46372339 C>T maps to NM_005400.2 F567F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:46313412 C>T maps to NM_005400.2 R502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:46237592 G>A maps to NM_005400.2 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:46411914 C>G maps to NM_005400.2 T703T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:46203595 C>T maps to NM_005400.2 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:46237646 C>T maps to NM_005400.2 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:46237647 C>T maps to NM_005400.2 Q477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:54395855 C>T maps to NM_002739.3 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr19:54385798 C>T maps to NM_002739.3 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:54394985 G>A maps to NM_002739.3 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:54401229 C>T maps to NM_002739.3 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:54395021 G>A maps to NM_002739.3 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:54394985 G>A maps to NM_002739.3 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:54395021 G>A maps to NM_002739.3 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:54403690 C>T maps to NM_002739.3 I464I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:54395021 G>A maps to NM_002739.3 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr19:54392968 C>T maps to NM_002739.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:54403500 C>T maps to NM_002739.3 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:54386422 C>T maps to NM_002739.3 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54395000 C>T maps to NM_002739.3 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54395846 G>A maps to NM_002739.3 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54403939 G>A maps to NM_002739.3 E504E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:54395783 G>A maps to NM_002739.3 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:54403936 G>A maps to NM_002739.3 K503K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:54403500 C>T maps to NM_002739.3 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr14:61924336 C>T maps to NM_006255.3 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:62016440 C>T maps to NM_006255.3 F648F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr14:61995921 C>T maps to NM_006255.3 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:61919966 C>T maps to NM_006255.3 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr3:170009646 A>G maps to NM_002740.5 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:169998139 T>C maps to NM_002740.5 D277D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:169999000 C>A maps to NM_002740.5 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr3:169940534 C>T maps to NM_002740.5 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:169985706 C>T maps to NM_002740.5 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr10:6506327 C>T maps to NM_006257.2 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr10:6539197 C>T maps to NM_006257.2 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:6498774 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr10:6528044 G>A maps to NM_006257.2 N284N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr10:6553001 C>T maps to NM_006257.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:6553127 C>T maps to NM_006257.2 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr10:6506357 G>A maps to NM_006257.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr10:6521088 G>A maps to NM_006257.2 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:6521088 G>A maps to NM_006257.2 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:6553136 G>A maps to NM_006257.2 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:6472819 C>T maps to NM_006257.2 W639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:6527201 G>A maps to NM_006257.2 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:6527996 C>T maps to NM_006257.2 Q300Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:6540401 G>A maps to NM_006257.2 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:6498689 T>C maps to NM_006257.2 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr10:6553058 G>A maps to NM_006257.2 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr10:6549449 C>T maps to NM_006257.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:6483971 C>T maps to NM_006257.2 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:6484040 G>A maps to NM_006257.2 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:6553067 G>A maps to NM_006257.2 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:6472804 C>T maps to NM_006257.2 R644R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:6540413 G>A maps to NM_006257.2 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr19:11558264 C>T maps to ENST00000436195 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr19:11558518 G>A maps to ENST00000436195 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:2105450 C>T maps to NM_002744.4 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:2103819 G>A maps to NM_002744.4 E426E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:2103566 C>T maps to NM_002744.4 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:2082314 C>T maps to NM_002744.4 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:30066931 G>A maps to NM_002742.2 I733I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:30046449 G>A maps to NM_002742.2 I911I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:47204180 G>A maps to ENST00000449438 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr19:47192934 G>A maps to ENST00000449438 I610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr19:47192805 G>A maps to ENST00000449438 F653F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:47177967 G>A maps to ENST00000449438 R827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:47177968 G>A maps to ENST00000449438 L826L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr19:47197354 G>A maps to ENST00000449438 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:37507064 G>A maps to NM_005813.3 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr8:48805885 G>A maps to NM_006904.6 L1220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr8:48691181 G>A maps to NM_006904.6 F3896F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:48772228 C>T maps to NM_006904.6 Q2049Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr8:48855780 G>A maps to NM_006904.6 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr8:48842430 C>T maps to NM_006904.6 K678K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:48801779 G>A maps to NM_006904.6 L1358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:48801780 G>A maps to NM_006904.6 L1357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:48809736 G>A maps to NM_006904.6 F1194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:48751728 G>A maps to NM_006904.6 I2510I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:48839793 G>T maps to NM_006904.6 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZG-06A-11D-A197-08 chr8:48840366 A>G maps to NM_006904.6 I741I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr8:48713416 G>A maps to NM_006904.6 I3350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:48752647 G>A maps to NM_006904.6 F2460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:48866230 G>A maps to NM_006904.6 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr8:48769851 G>A maps to NM_006904.6 R2157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr8:48805807 G>A maps to NM_006904.6 G1246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr10:54040558 G>T maps to NM_001098512.1 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:54040659 C>T maps to NM_001098512.1 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr10:54053572 C>A maps to NM_001098512.1 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:54048560 A>G maps to NM_001098512.1 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:54040671 C>T maps to NM_001098512.1 H494H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:54011353 C>T maps to NM_001098512.1 F352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr10:54040659 C>T maps to NM_001098512.1 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr10:54042049 C>T maps to NM_001098512.1 I546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr10:54031111 C>T maps to NM_001098512.1 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr10:54049985 G>A maps to NM_001098512.1 W618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:54031198 C>T maps to NM_001098512.1 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:54040659 C>T maps to NM_001098512.1 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr4:82031726 C>T maps to NM_006259.1 Q605Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr4:82073115 G>A maps to NM_006259.1 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:82125880 C>T maps to NM_006259.1 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr4:82090824 G>A maps to NM_006259.1 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:82125918 G>A maps to NM_006259.1 Q95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:82013575 C>T maps to NM_006259.1 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr4:82063962 G>A maps to NM_006259.1 F464F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:82031726 C>T maps to NM_006259.1 Q605Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:82070041 G>A maps to NM_006259.1 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:82027082 G>A maps to NM_006259.1 P649P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:102040046 C>T maps to NM_024653.3 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:102040025 C>T maps to NM_024653.3 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:76062873 G>A maps to NM_004705.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:76063410 G>A maps to NM_004705.2 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:3592648 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:3592715 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:3592714 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:3530318 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr23:3592738 C>A did not map to a codon.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr23:3592739 C>T did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:3592751 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:22294637 G>A maps to ENST00000397199 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:22294706 G>A maps to ENST00000397199 D46D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr6:22287666 G>A maps to ENST00000397199 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr6:22287759 C>T maps to ENST00000397199 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:238475778 C>T maps to NM_015893.1 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:238475736 G>A maps to NM_015893.1 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:238475778 C>T maps to NM_015893.1 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr2:238475736 G>A maps to NM_015893.1 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:238475805 C>T maps to NM_015893.1 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:238475806 C>T maps to NM_015893.1 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:120353907 G>A maps to NM_004248.2 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr10:120354744 C>T maps to NM_004248.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:120353730 G>A maps to NM_004248.2 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:120354501 G>A maps to NM_004248.2 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:120354452 G>A maps to NM_004248.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr5:35070304 G>A maps to NM_000949.4 Y202Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr5:35065711 G>A maps to NM_000949.4 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:35065775 G>A maps to NM_000949.4 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:35065472 C>T maps to NM_000949.4 E529E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr5:35065850 G>A maps to NM_000949.4 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr5:35065775 G>A maps to NM_000949.4 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr5:35065427 C>T maps to NM_000949.4 K544K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr5:35065415 C>T maps to NM_000949.4 K548K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:35084644 G>A maps to NM_000949.4 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:35070247 C>T maps to NM_000949.4 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:35065573 G>A maps to NM_000949.4 Q496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:35065574 G>A maps to NM_000949.4 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:35072784 G>A maps to NM_000949.4 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr5:35065985 G>A maps to NM_000949.4 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr5:35086389 C>T maps to NM_000949.4 K41K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:35070310 C>T maps to NM_000949.4 Q200Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:35066065 C>A maps to NM_000949.4 E332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr5:35065217 G>A maps to NM_000949.4 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr5:35066003 C>T maps to NM_000949.4 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:50187244 C>T maps to NM_001536.3 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:50188093 C>T maps to NM_001536.3 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr21:48081833 C>T maps to NM_206962.1 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr21:48064318 C>T maps to NM_206962.1 N82N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr21:48068503 C>T maps to NM_206962.1 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr21:48064249 C>T maps to NM_206962.1 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr21:48068378 T>C maps to NM_206962.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr11:20414468 C>T maps to NM_005788.3 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:20486070 C>T maps to NM_005788.3 I442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:20424496 C>T maps to NM_005788.3 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:20486070 C>T maps to NM_005788.3 I442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr14:23395485 G>A maps to NM_006109.3 D211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr14:23393226 G>A maps to NM_006109.3 H455H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr14:23393689 G>A maps to NM_006109.3 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:68382242 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr16:68389639 C>T maps to NM_019023.2 F555F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:68386188 C>T maps to NM_019023.2 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr16:68349950 C>T maps to NM_019023.2 H23H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:3659211 C>T maps to NM_019854.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:4705643 G>A maps to NM_012409.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr20:4705310 G>A maps to NM_012409.2 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:4705196 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr20:4705301 G>A maps to NM_012409.2 W35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr2:128186125 C>T maps to ENST00000409048 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:128186466 G>A maps to ENST00000409048 W478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr2:128179006 C>T maps to ENST00000409048 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr2:128186092 C>T maps to ENST00000409048 C353C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:128183745 A>G maps to ENST00000409048 Q241Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr20:33764013 C>T maps to NM_006404.3 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr20:33764076 C>T maps to NM_006404.3 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr20:33760001 C>T maps to NM_006404.3 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:33764013 C>A maps to NM_006404.3 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:33764244 G>A maps to NM_006404.3 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr22:18907077 C>T maps to NM_016335.4 V379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr22:18905842 G>A maps to NM_016335.4 N471N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:18909851 G>A maps to NM_016335.4 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:36297624 C>T maps to NM_021232.1 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:36297474 C>T maps to NM_021232.1 R362R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr19:36297575 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr19:36303158 C>T maps to NM_021232.1 E205E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:36304129 C>T maps to NM_021232.1 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:36297435 T>C maps to NM_021232.1 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:36303124 G>A maps to NM_021232.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:36293155 G>A maps to NM_021232.1 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr19:36303434 G>A maps to NM_021232.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr19:36304171 C>T maps to NM_021232.1 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:71821913 C>T maps to NM_001126128.1 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr2:68873114 T>C maps to NM_138964.2 N54N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr2:68882299 G>A maps to NM_138964.2 E258E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr2:68882248 C>T maps to NM_138964.2 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:68873195 C>T maps to NM_138964.2 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:68882233 C>T maps to NM_138964.2 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:68882033 C>T maps to NM_138964.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr20:5283168 G>A maps to NM_144773.2 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr20:5294826 G>A maps to NM_144773.2 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:5294688 G>A maps to NM_144773.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:5295003 C>T maps to NM_144773.2 Q4Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr20:5283168 G>A maps to NM_144773.2 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr20:5282885 C>A maps to NM_144773.2 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr20:5283060 C>T maps to NM_144773.2 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr20:5282979 G>A maps to NM_144773.2 C287C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr20:5283042 C>T maps to NM_144773.2 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:5294652 C>T maps to NM_144773.2 W121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:5283060 C>T maps to NM_144773.2 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr20:5283225 C>T maps to NM_144773.2 K205K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr20:5294769 C>T maps to NM_144773.2 K82K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr20:5283027 C>T maps to NM_144773.2 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:5282925 G>A maps to NM_144773.2 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:5283144 G>A maps to NM_144773.2 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr20:5294808 G>A maps to NM_144773.2 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:5282925 G>A maps to NM_144773.2 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr20:5282769 C>T maps to NM_144773.2 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:5294865 G>A maps to NM_144773.2 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:5283144 G>A maps to NM_144773.2 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr20:5294826 G>A maps to NM_144773.2 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr20:5282937 G>A maps to NM_144773.2 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:5283084 G>A maps to NM_144773.2 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr20:5282925 G>A maps to NM_144773.2 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr20:5294790 G>A maps to NM_144773.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr20:5282925 G>A maps to NM_144773.2 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:5283348 C>T maps to NM_144773.2 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:5282895 G>A maps to NM_144773.2 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:5283060 C>T maps to NM_144773.2 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:5294910 G>A maps to NM_144773.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr20:5282925 G>A maps to NM_144773.2 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr20:5294604 G>A maps to NM_144773.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr20:5282886 G>A maps to NM_144773.2 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr20:5283194 G>A maps to NM_144773.2 Q216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr20:5283369 G>A maps to NM_144773.2 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr4:71275482 C>T maps to NM_021225.4 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr4:71275300 C>T maps to NM_021225.4 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr4:71275344 G>A maps to NM_021225.4 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:71275638 A>C maps to NM_021225.4 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:71275269 C>T maps to NM_021225.4 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:71275269 C>T maps to NM_021225.4 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:71275398 G>A maps to NM_021225.4 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:71265026 C>T maps to NM_021225.4 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:71275273 C>T maps to NM_021225.4 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr4:15987391 G>A maps to NM_006017.2 I757I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:15991444 G>A maps to NM_006017.2 P662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr2:95942370 C>T maps to NM_144707.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:95950776 C>T maps to NM_144707.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:95947734 G>A maps to NM_144707.2 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:95951397 C>T maps to NM_144707.2 P629P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:95944835 G>A maps to NM_144707.2 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:95954680 C>T maps to NM_144707.2 S814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:95954255 G>A maps to NM_144707.2 W787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:95954256 G>A maps to NM_144707.2 W787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:95941748 T>G maps to NM_144707.2 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:95941805 G>A maps to NM_144707.2 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:95943130 C>T maps to NM_144707.2 H264H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:95954274 C>T maps to NM_144707.2 I793I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:95944533 T>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr2:95944470 G>A maps to NM_144707.2 E351E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr2:95947007 C>T maps to NM_144707.2 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:95947689 G>A maps to NM_144707.2 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr2:95952586 C>T maps to NM_144707.2 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr2:95945598 C>T maps to NM_144707.2 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr5:177421178 C>T maps to NM_006261.4 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:177419862 A>T maps to NM_006261.4 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:93611824 G>A maps to NM_000313.3 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr3:93646165 A>G maps to NM_000313.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:37633524 C>T maps to NM_007198.3 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:37633524 C>T maps to NM_007198.3 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr1:214170486 T>C maps to NM_002763.3 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:214171386 C>T maps to NM_002763.3 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:214171452 G>A maps to NM_002763.3 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr1:214170184 A>T maps to NM_002763.3 K103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:214209111 C>T maps to NM_002763.3 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr1:214209047 C>T maps to NM_002763.3 A695A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:214178551 C>T maps to NM_002763.3 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr1:214171137 C>T maps to NM_002763.3 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:75330485 G>A maps to ENST00000445876 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:75329427 C>T maps to ENST00000445876 Q370Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:75330267 C>T maps to ENST00000445876 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:75323698 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:75330246 C>T maps to ENST00000445876 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:75330435 C>T maps to ENST00000445876 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr14:75323587 T>C maps to ENST00000445876 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr13:113826187 G>A maps to ENST00000342783 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr13:113814379 G>A maps to ENST00000342783 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr13:113826021 G>A maps to ENST00000342783 W291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:113814418 G>A maps to ENST00000342783 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr10:13629109 C>T maps to NM_003675.3 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr1:150310700 G>A maps to NM_004698.2 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:150316933 C>T maps to NM_004698.2 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr19:54627238 C>T maps to NM_015629.3 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:54634856 C>A maps to NM_015629.3 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr19:54625308 C>T maps to NM_015629.3 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54625918 C>T maps to NM_015629.3 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54626874 C>T maps to NM_015629.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:116045452 G>A maps to NM_004697.3 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr9:116046645 C>T maps to NM_004697.3 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:116038898 T>C maps to NM_004697.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:153512912 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:50037687 G>A maps to NM_001031698.1 K808K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr12:50036040 G>A maps to NM_001031698.1 R614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr6:4032431 C>T maps to NM_003913.4 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:4057354 C>T maps to NM_003913.4 F889F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:4032371 C>T maps to NM_003913.4 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:4032431 C>T maps to NM_003913.4 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:4031810 T>G maps to NM_003913.4 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr20:62626270 G>A maps to NM_012469.3 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr20:62626387 C>T maps to NM_012469.3 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:62658387 C>T maps to NM_012469.3 A694A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr17:1577965 G>A maps to NM_006445.3 N1023N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:1582091 G>A maps to NM_006445.3 H561H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:1577737 G>A maps to NM_006445.3 F1099F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:1579043 C>A maps to NM_006445.3 L914L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:1585292 C>T maps to NM_006445.3 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:1559772 G>A maps to NM_006445.3 F1902F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:1562736 G>A maps to NM_006445.3 F1684F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:1577110 G>A maps to NM_006445.3 I1125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:1558804 G>A maps to NM_006445.3 A1942A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:1579317 C>T maps to NM_006445.3 R861R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr12:49691294 C>T maps to ENST00000451891 N384N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:42689949 C>T maps to NM_000322.4 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr6:42689565 G>A maps to NM_000322.4 N169N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr23:106884132 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:106882635 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:106885594 G>T did not map to a codon.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr23:106888462 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:18067240 G>A maps to NM_175886.2 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:18066979 T>C maps to NM_175886.2 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr7:18066520 G>A maps to NM_175886.2 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr7:18066663 A>G maps to NM_175886.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:18067129 G>A maps to NM_175886.2 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr7:18066928 G>A maps to NM_175886.2 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:18066901 G>A maps to NM_175886.2 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr7:18067300 G>A maps to NM_175886.2 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:18066817 C>T maps to NM_175886.2 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:12838919 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:12838867 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:12840890 C>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:12827409 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr17:74307766 A>G maps to NM_002766.2 N338N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:74326655 G>A maps to NM_002766.2 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:74309913 G>A maps to NM_002766.2 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr17:74328482 G>A maps to NM_002766.2 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:74307760 G>A maps to NM_002766.2 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:18769193 C>T maps to NM_002767.2 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:57274952 C>T maps to NM_018304.3 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr17:57275068 C>T maps to NM_018304.3 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr19:50105141 C>T maps to NM_020719.1 F1580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr19:50118188 C>T maps to NM_020719.1 F1649F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr19:50100153 C>T maps to NM_020719.1 L854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr19:50099389 C>T maps to NM_020719.1 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr19:50099085 C>T maps to NM_020719.1 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:50097747 G>C maps to NM_020719.1 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:50099988 C>T maps to NM_020719.1 P799P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr19:50099718 C>T maps to NM_020719.1 S709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr19:50099913 C>T maps to NM_020719.1 T774T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr19:50102986 C>T maps to NM_020719.1 S1379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr12:53839806 C>A maps to NM_018457.3 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr16:30664258 T>C maps to NM_024031.2 C113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr16:30666433 G>A maps to NM_024031.2 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr16:30664423 G>A maps to NM_024031.2 E168E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:30664711 C>T maps to NM_024031.2 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr16:30664294 C>T maps to NM_024031.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr16:30666247 C>T maps to NM_024031.2 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr17:46030477 C>T maps to NM_024320.2 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr5:120022370 G>A maps to NM_016644.1 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr5:120022370 G>A maps to NM_016644.1 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:120022241 C>T maps to NM_016644.1 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:120022370 G>A maps to NM_016644.1 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr5:120022106 G>A maps to NM_016644.1 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr5:120022041 C>T maps to NM_016644.1 Q162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:120021884 G>A maps to NM_016644.1 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:42814735 C>T maps to NM_199285.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:42814693 G>A maps to NM_199285.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:42813930 C>T maps to NM_199285.2 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr19:42813816 G>A maps to NM_199285.2 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:42814486 C>T maps to NM_199285.2 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:42813858 C>T maps to NM_199285.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:240981427 G>A maps to NM_001080835.1 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr2:240981460 G>A maps to NM_001080835.1 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:240981436 G>A maps to NM_001080835.1 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:240981418 G>A maps to NM_001080835.1 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:5783675 G>A maps to NM_001134316.1 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:5784032 G>A maps to NM_001134316.1 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:138724852 C>T maps to NM_001134659.1 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:138724462 G>A maps to NM_001134659.1 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr3:138724852 C>T maps to NM_001134659.1 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:138724462 G>A maps to NM_001134659.1 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:138738945 G>A maps to NM_001013650.2 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr3:138738774 A>T maps to NM_001013650.2 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr3:138739083 T>C maps to NM_001013650.2 E140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr3:138738753 G>A maps to NM_001013650.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:138738705 C>T maps to NM_001013650.2 *266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:138762973 G>A maps to NM_001134657.1 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:138762805 G>A maps to NM_001134657.1 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr3:138762970 C>T maps to NM_001134657.1 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr3:138763080 G>A maps to NM_001134657.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:138762817 G>A maps to NM_001134657.1 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr3:138763090 C>T maps to NM_001134657.1 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:30525942 G>T maps to NM_025263.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr12:10999769 G>A maps to NM_007244.2 H99H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:10999760 G>A maps to NM_007244.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:45130908 G>A maps to ENST00000352766 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr22:45122506 C>T maps to ENST00000352766 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr22:45110519 C>T maps to ENST00000352766 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:45128246 C>T maps to ENST00000352766 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:45128159 C>T maps to ENST00000352766 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr11:36467959 G>A maps to NM_001160167.1 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:126887406 T>C maps to ENST00000330542 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44R-06A-41D-A25O-08 chr5:126860241 T>G maps to ENST00000330542 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:37312577 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:37312439 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr23:37312547 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr23:37312718 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr23:37312577 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:37312708 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr19:50086931 C>T maps to NM_000951.2 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr19:50086974 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr23:150868506 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:150868589 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:150868506 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:150869276 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:150869277 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:150868979 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr23:150868495 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:150868528 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:150869196 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:150868548 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:150869198 C>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:150869254 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:150868506 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr23:150869196 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:150869164 G>A did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:150868506 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:150868627 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:150868514 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:150868556 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:150869195 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:150868526 T>C did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:150869306 G>A did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:150869414 G>A did not map to a codon.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr23:150869163 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:32874862 G>A maps to NM_024081.4 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr16:29825238 C>T maps to NM_145239.2 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:29824854 C>T maps to NM_145239.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:29824998 C>T maps to NM_145239.2 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr3:9991655 C>T maps to NM_207351.3 K48K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr3:9991022 C>T maps to NM_207351.3 E259E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr3:9989668 C>T maps to NM_207351.3 W396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr3:9991427 G>A maps to NM_207351.3 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr1:170688912 G>A maps to NM_022716.2 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:170688894 G>A maps to NM_022716.2 K90K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:132484531 C>T maps to NM_016307.3 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:132483026 C>T maps to NM_016307.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr7:142459657 C>T maps to ENST00000486171 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:142459657 C>T maps to ENST00000486171 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:142459672 G>A maps to ENST00000486171 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr7:142459846 C>T maps to ENST00000486171 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr7:142458514 C>T maps to ENST00000486171 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:142459669 G>A maps to ENST00000486171 E96E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:142459672 G>A maps to ENST00000486171 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr7:142457352 C>T maps to ENST00000486171 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr7:142459786 C>T maps to ENST00000486171 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr7:142460360 G>A maps to ENST00000486171 K192K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:142458517 C>T maps to ENST00000486171 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:142460756 C>T maps to ENST00000486171 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr7:142458472 C>T maps to ENST00000486171 P36P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A3JI-06A-11D-A21A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr7:142457352 C>T maps to ENST00000486171 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:142457352 C>T maps to ENST00000486171 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:142459744 C>T maps to ENST00000486171 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr7:142457349 G>A maps to ENST00000486171 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr7:142458484 C>T maps to ENST00000486171 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr7:142459648 G>A maps to ENST00000486171 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr7:142459846 C>T maps to ENST00000486171 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:142459672 G>A maps to ENST00000486171 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr6:27216905 G>A maps to NM_005865.3 W122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr6:27222475 C>T maps to NM_005865.3 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:27222526 C>T maps to NM_005865.3 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:27222595 G>A maps to NM_005865.3 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:27222580 G>A maps to NM_005865.3 Q420Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr6:27215683 G>T maps to NM_005865.3 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:27218584 G>A maps to NM_005865.3 K197K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:27220705 G>A maps to NM_005865.3 Q376Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr6:27216651 G>A maps to NM_005865.3 W88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:27216675 C>T maps to NM_005865.3 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr7:142481159 C>T maps to ENST00000311757 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:142481279 C>T maps to ENST00000311757 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr7:142479963 G>A maps to ENST00000311757 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr7:142481282 C>T maps to ENST00000311757 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr7:142481315 T>C maps to ENST00000311757 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr7:142479987 C>T maps to ENST00000311757 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:2871028 C>T maps to NM_006799.2 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr16:2870992 C>T maps to NM_006799.2 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr16:2906156 C>T maps to NM_022119.3 K69K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:2903973 G>A maps to NM_022119.3 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:2903999 G>A maps to NM_022119.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:2905649 G>A maps to NM_022119.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr11:86519057 C>T maps to NM_007173.4 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:86518724 C>T maps to NM_007173.4 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr11:86519506 G>C maps to NM_007173.4 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:33796704 C>T maps to NM_007343.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr16:2836099 C>T maps to NM_152891.2 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr16:2836099 C>T maps to NM_152891.2 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:84233585 C>T maps to NM_153362.2 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr6:84233462 A>G maps to NM_153362.2 Q101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr6:84233585 C>T maps to NM_153362.2 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:84233840 G>A maps to NM_153362.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:84233615 G>C maps to NM_153362.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:84234161 C>T maps to NM_153362.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:84233939 G>A maps to NM_153362.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:84233840 G>A maps to NM_153362.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr16:31150731 G>A maps to NM_173502.3 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr16:31151831 C>T maps to NM_173502.3 W716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:31150653 C>T maps to NM_173502.3 E791E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:31155071 C>T maps to NM_173502.3 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:31155152 G>A maps to NM_173502.3 D242D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr7:141537834 G>A maps to NM_001008270.2 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:141537045 G>A maps to NM_001008270.2 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr7:141537834 G>A maps to NM_001008270.2 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr7:141536272 G>A maps to NM_001008270.2 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:141536281 C>T maps to NM_001008270.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr1:228004921 C>T maps to NM_183062.2 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr1:228003821 C>T maps to NM_183062.2 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:228033809 C>A maps to NM_183062.2 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr1:228003848 G>A maps to NM_183062.2 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:228005125 G>A maps to NM_183062.2 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:228033872 C>T maps to NM_183062.2 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:228003911 C>T maps to NM_183062.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:228003848 G>A maps to NM_183062.2 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr1:228005002 G>A maps to NM_183062.2 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:228003848 G>A maps to NM_183062.2 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:228033737 C>T maps to NM_183062.2 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:228003821 C>T maps to NM_183062.2 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr3:46874577 G>A maps to NM_182702.1 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr3:46874470 C>T maps to NM_182702.1 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:46874577 G>A maps to NM_182702.1 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:46784426 G>A maps to ENST00000331814 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr4:152203359 G>A maps to NM_183375.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:152204437 G>A maps to NM_183375.2 K217K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:152204438 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:46758960 G>A maps to NM_013270.4 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:46755771 C>T maps to NM_013270.4 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr3:46753879 C>T maps to NM_013270.4 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr3:46754495 C>T maps to NM_013270.4 E272E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:46753845 G>A maps to NM_013270.4 Q350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:31097482 G>A maps to NM_001039503.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr16:31095587 G>A maps to NM_001039503.2 F498F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr16:58320098 C>T maps to NM_001080492.1 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr16:58319855 C>T maps to NM_001080492.1 W169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:58314307 C>T maps to NM_001080492.1 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr16:58314214 C>T maps to NM_001080492.1 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:58314172 G>A maps to NM_001080492.1 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr16:58319856 C>T maps to NM_001080492.1 W169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr16:58314232 C>T maps to NM_001080492.1 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr8:10388837 C>T maps to NM_198464.3 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:10388882 C>T maps to NM_198464.3 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:10395999 G>A maps to NM_198464.3 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr8:10388873 C>T maps to NM_198464.3 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr8:10396059 G>A maps to NM_198464.3 W272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:31144210 C>T maps to NM_002773.3 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:31144656 G>A maps to NM_002773.3 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:31143542 C>T maps to NM_002773.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr19:691995 G>A maps to NM_214710.3 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:686996 G>A maps to NM_214710.3 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr10:25226280 G>A maps to NM_020200.5 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:25160959 G>A maps to NM_020200.5 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:25226181 C>T maps to NM_020200.5 K90K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr15:55916538 C>T did not map to a codon.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr15:55919240 G>A maps to NM_173814.4 I964I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr15:55931907 G>A maps to NM_173814.4 I752I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr15:55929374 G>A maps to NM_173814.4 H872H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr15:55931934 C>T maps to NM_173814.4 R743R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:55931946 G>A maps to NM_173814.4 F739F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr15:56032808 G>A maps to NM_173814.4 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr15:55931946 G>A maps to NM_173814.4 F739F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr15:55921200 C>T maps to NM_173814.4 G875G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:55912416 G>A maps to NM_173814.4 T1082T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:843545 G>A maps to NM_002777.3 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:150998084 C>T maps to NM_021222.1 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr9:79267402 G>A maps to NM_015225.2 G2851G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr9:79323952 G>C maps to NM_015225.2 Y1079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr9:79465506 C>T maps to NM_015225.2 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr9:79326061 G>A maps to NM_015225.2 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr9:79322953 G>A maps to NM_015225.2 S1412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr9:79441573 G>A maps to NM_015225.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:79322149 G>A maps to NM_015225.2 V1680V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:79252383 C>T maps to NM_015225.2 R2971R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:79320802 C>T maps to NM_015225.2 V2129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr9:79320202 C>T maps to NM_015225.2 P2329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr9:79322452 C>T maps to NM_015225.2 Q1579Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr9:79325623 G>A maps to NM_015225.2 F522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr9:79244196 G>A maps to NM_015225.2 F3020F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:79323127 C>T maps to NM_015225.2 G1354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:79325872 G>A maps to NM_015225.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr9:79323694 G>A maps to NM_015225.2 T1165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr9:79461488 C>T maps to NM_015225.2 K150K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr9:79321226 G>T maps to NM_015225.2 S1988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:79320583 A>G maps to NM_015225.2 G2202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:79321507 G>A maps to NM_015225.2 P1894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:79321834 C>T maps to NM_015225.2 E1785E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr9:79465512 G>C maps to NM_015225.2 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr9:79318511 G>A maps to NM_015225.2 Q2673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr9:79324222 T>C maps to NM_015225.2 P989P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr9:79320712 T>C maps to NM_015225.2 E2159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr9:79318668 C>T maps to NM_015225.2 T2620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr9:79267525 A>T maps to NM_015225.2 L2810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr9:79323835 C>T maps to NM_015225.2 V1118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr9:79461539 C>T maps to NM_015225.2 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr9:79324196 G>T maps to NM_015225.2 S998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr9:79325113 G>A maps to NM_015225.2 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr9:79323880 G>A maps to NM_015225.2 N1103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:79324105 C>T maps to NM_015225.2 G1028G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:79325626 G>A maps to NM_015225.2 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:79326247 C>T maps to NM_015225.2 Q314Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr9:79321789 C>T maps to NM_015225.2 W1800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr9:79321790 C>T maps to NM_015225.2 W1800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:79267531 G>A maps to NM_015225.2 I2808I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr9:79322299 A>G maps to NM_015225.2 D1630D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr9:79326148 G>A maps to NM_015225.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:40902446 T>C maps to NM_181882.2 Q604Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr19:40902140 G>A maps to NM_181882.2 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:40900622 C>T maps to NM_181882.2 K1212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:40900361 C>T maps to NM_181882.2 E1299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:40901189 G>A maps to NM_181882.2 L1023L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:40902512 G>A maps to NM_181882.2 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:40901360 G>A maps to NM_181882.2 L966L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:40902440 C>T maps to NM_181882.2 P606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr19:40900775 C>T maps to NM_181882.2 G1161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:73588777 G>A maps to ENST00000373120 H144H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:73594157 G>A maps to ENST00000373120 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:73587851 C>T maps to ENST00000373120 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:73590881 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr9:80921374 C>T maps to ENST00000421149 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr9:80923394 C>T maps to ENST00000421149 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:80916930 G>A maps to ENST00000421149 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:80919827 C>T maps to ENST00000421149 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:80921350 G>A maps to ENST00000421149 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:143763495 C>T maps to ENST00000301258 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr10:104165190 G>A maps to NM_002779.3 F746F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:104172316 G>A maps to NM_002779.3 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr10:104173587 C>T maps to NM_002779.3 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr10:104176549 G>T maps to NM_002779.3 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:104174840 G>A maps to NM_002779.3 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:104176660 G>A maps to NM_002779.3 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr10:104165106 C>T maps to NM_002779.3 R774R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr10:104174891 G>A maps to NM_002779.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:104175789 C>T maps to NM_002779.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:104176756 G>A maps to NM_002779.3 D13D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:104164978 G>A maps to NM_002779.3 F786F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:104170844 G>A maps to NM_002779.3 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:104174891 G>A maps to NM_002779.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:104176567 G>T maps to NM_002779.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:104165166 C>T maps to NM_002779.3 G754G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:139189357 C>T maps to NM_032289.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr5:139216476 C>T maps to NM_032289.2 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr5:139197083 G>A maps to NM_032289.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:139193049 C>T maps to NM_032289.2 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr5:139217313 C>T maps to NM_032289.2 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:139192923 G>A maps to NM_032289.2 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:139216446 C>T maps to NM_032289.2 F485F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:139221944 C>T maps to NM_032289.2 A734A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr5:139193049 C>T maps to NM_032289.2 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:139221956 G>A maps to NM_032289.2 G738G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr5:139189294 G>A maps to NM_032289.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr8:18432753 C>T maps to ENST00000440756 L843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr8:18729959 C>T maps to ENST00000440756 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:18729233 G>A maps to ENST00000440756 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:18413763 C>T maps to ENST00000440756 K963K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:18725191 G>A maps to ENST00000440756 F542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:18729422 C>T maps to ENST00000440756 Q317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:18725305 G>A maps to ENST00000440756 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:113940599 C>T maps to NM_012455.2 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr2:113950936 C>T maps to NM_012455.2 F674F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A6L9-06A-11D-A32N-08 chr2:113955150 C>T maps to NM_012455.2 G799G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:113940401 G>A maps to NM_012455.2 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:113940512 C>T maps to NM_012455.2 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:113950645 G>T maps to NM_012455.2 V620V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr2:113950694 C>T maps to NM_012455.2 R637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:113940065 C>T maps to NM_012455.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:113951443 G>A maps to NM_012455.2 G700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:113955446 C>T maps to NM_012455.2 Q861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:113940599 C>T maps to NM_012455.2 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:113950849 C>T maps to NM_012455.2 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:113943682 G>A maps to NM_012455.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr2:113956457 C>T maps to NM_012455.2 S922S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr2:113940170 C>T maps to NM_012455.2 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:113940134 G>A maps to NM_012455.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:113940518 G>A maps to NM_012455.2 Q162Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:113940668 G>A maps to NM_012455.2 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:113940806 G>A maps to NM_012455.2 E258E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:113943682 G>A maps to NM_012455.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:113955457 G>A maps to NM_012455.2 T864T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:113940557 G>A maps to NM_012455.2 E175E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr14:73640348 C>T maps to NM_000021.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr14:73640348 C>T maps to NM_000021.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr14:73637677 C>T maps to NM_000021.3 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr1:227069742 C>T maps to ENST00000391872 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:227077814 C>T maps to ENST00000391872 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:227069664 C>T maps to ENST00000391872 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:227071563 C>T maps to ENST00000391872 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:227081807 C>T maps to ENST00000391872 C424C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr19:43383678 G>A maps to NM_006905.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:43376027 C>T maps to NM_006905.2 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:43382317 G>A maps to NM_006905.2 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr19:43382077 G>A maps to NM_006905.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:43372271 G>A maps to NM_006905.2 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr19:43373112 G>A maps to NM_006905.2 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:43383709 G>A maps to NM_006905.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:43372343 A>T maps to NM_006905.2 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:43382350 C>T maps to NM_006905.2 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:43376048 C>T maps to NM_006905.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:43373160 G>C maps to NM_006905.2 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:43382350 C>T maps to NM_006905.2 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr19:43376021 G>A maps to NM_006905.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr19:43519393 G>A maps to ENST00000306308 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:43528945 G>A maps to ENST00000306308 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:43523095 G>A maps to ENST00000306308 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:43519496 G>A maps to ENST00000306308 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:43523024 G>A maps to ENST00000306308 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:43519496 G>A maps to ENST00000306308 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr19:43519292 G>T maps to ENST00000306308 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:43519496 G>A maps to ENST00000306308 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:43579632 C>T maps to NM_031246.3 Q194Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:43586712 G>A maps to NM_031246.3 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr19:43586676 C>T maps to NM_031246.3 W15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:43579634 G>A maps to NM_031246.3 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:43585351 C>T maps to ENST00000449000 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:43576026 C>T maps to NM_031246.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:43585318 C>T maps to ENST00000449000 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr19:43579719 C>T maps to NM_031246.3 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:43576026 C>T maps to NM_031246.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:43576026 C>T maps to NM_031246.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:43585143 G>A maps to ENST00000449000 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J6-06A-11D-A19A-08 chr19:43243059 G>A maps to NM_021016.3 Y82Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:43233933 G>A maps to NM_021016.3 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr19:43243029 C>T maps to NM_021016.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:43233374 G>A maps to NM_021016.3 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:43243227 G>A maps to NM_021016.3 N26N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr19:43243086 C>T maps to NM_021016.3 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:43236936 G>A maps to NM_021016.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr19:43233380 G>A maps to NM_021016.3 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr19:43234161 C>T maps to NM_021016.3 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:43233404 C>T maps to NM_021016.3 K371K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr19:43237164 C>T maps to NM_021016.3 E160E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:43237122 C>G maps to NM_021016.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr19:43237056 G>A maps to NM_021016.3 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:43237140 G>A maps to NM_021016.3 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:43242933 G>A maps to NM_021016.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:43233374 G>A maps to NM_021016.3 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:43698669 G>A maps to NM_002780.3 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:43698624 C>T maps to NM_002780.3 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:43708383 C>T maps to NM_002780.3 W28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:43702362 C>T maps to NM_002780.3 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:43702410 G>A maps to NM_002780.3 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:43702149 G>A maps to NM_002780.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:43699231 C>T maps to NM_002780.3 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:43680106 C>T maps to ENST00000270059 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr19:43679466 G>A maps to ENST00000270059 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:43689234 G>A maps to ENST00000270059 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr19:43680106 C>T maps to ENST00000270059 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr19:43679475 C>T maps to ENST00000270059 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:43680250 C>T maps to ENST00000270059 E253E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:43689183 C>T maps to ENST00000270059 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:43679499 C>T maps to ENST00000270059 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:43690518 G>A maps to ENST00000270059 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:43680250 C>T maps to ENST00000270059 E253E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:43689021 C>A maps to ENST00000270059 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:43680244 C>T maps to ENST00000270059 K255K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr19:43689252 C>T maps to ENST00000270059 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:43689045 G>A maps to ENST00000270059 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:43411959 C>T maps to NM_002782.3 R251R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DA-A1I2-06A-21D-A19A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:43420349 G>A maps to NM_002782.3 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:43414735 G>A maps to NM_002782.3 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:43420370 G>A maps to NM_002782.3 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:43414941 A>G maps to NM_002782.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:43411266 G>A maps to NM_002782.3 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr19:43411092 G>A maps to NM_002782.3 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:43421911 C>T maps to NM_002782.3 Q11Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:43406598 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr19:43420343 G>A maps to NM_002782.3 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:43412004 C>T maps to NM_002782.3 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr19:43411266 G>A maps to NM_002782.3 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:43411914 C>T maps to NM_002782.3 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr19:43411107 C>T maps to NM_002782.3 K402K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr19:43433849 G>A maps to NM_002783.2 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr19:43430057 C>T maps to NM_002783.2 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:43439692 C>T maps to NM_002783.2 *98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr19:43441195 C>T maps to NM_002783.2 Q11Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr19:43433849 G>A maps to NM_002783.2 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:43441216 G>A maps to NM_002783.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr19:43429958 C>T maps to NM_002783.2 K403K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:43433834 G>A maps to NM_002783.2 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:43430674 C>T maps to NM_002783.2 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:43430006 C>T maps to NM_002783.2 K387K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:43430024 G>A maps to NM_002783.2 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:43433762 C>T maps to NM_002783.2 W180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:43430818 C>T maps to NM_002783.2 E253E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:43430057 C>T maps to NM_002783.2 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:43430866 C>T maps to NM_002783.2 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:43439820 G>A maps to NM_002783.2 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:43441228 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:43430758 C>T maps to NM_002783.2 W273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr19:43430144 G>A maps to NM_002783.2 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr19:43259362 C>T maps to NM_182707.2 K255K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:43262327 G>A maps to NM_182707.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:43262157 G>A maps to NM_182707.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr19:43262391 G>A maps to NM_182707.2 N157N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr19:43258630 C>T maps to NM_182707.2 W366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:43268067 G>A maps to NM_182707.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:43262256 G>A maps to NM_182707.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:43262406 G>A maps to NM_182707.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr19:43259371 C>T maps to NM_182707.2 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:43259143 G>A maps to NM_182707.2 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:43269688 C>T maps to NM_182707.2 W15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:43259326 C>T maps to NM_182707.2 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr19:43269724 G>A maps to NM_182707.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:43268179 G>A maps to NM_182707.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr19:43268067 G>A maps to NM_182707.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr19:43258617 C>T maps to NM_182707.2 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr19:43268191 A>G maps to NM_182707.2 Y102Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr19:43258473 G>A maps to NM_182707.2 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr19:43258584 G>A maps to NM_182707.2 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr19:43259362 C>T maps to NM_182707.2 K255K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:43259248 C>T maps to NM_182707.2 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr19:43259418 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:43763156 G>A maps to NM_002784.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr19:43762546 G>A maps to NM_002784.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:43763092 T>A maps to NM_002784.3 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr19:43762486 C>T maps to NM_002784.3 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:43762486 C>T maps to NM_002784.3 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:43762486 C>T maps to NM_002784.3 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:43773532 C>T maps to NM_002784.3 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:43762573 G>A maps to NM_002784.3 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:43773538 C>T maps to NM_002784.3 W15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:43762594 G>A maps to NM_002784.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr19:43773550 C>T maps to NM_002784.3 Q11Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr19:43762528 C>T maps to NM_002784.3 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr19:43762546 G>A maps to NM_002784.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr19:43763093 C>T maps to NM_002784.3 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:43772254 C>T maps to NM_002784.3 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:43771945 G>A maps to NM_002784.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:43762486 C>T maps to NM_002784.3 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:15472666 G>A maps to NM_001128217.1 R314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr9:15468712 A>T maps to NM_001128217.1 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:15486015 C>T maps to NM_001128217.1 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr16:67943578 C>T maps to NM_006742.2 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:87060882 G>A maps to ENST00000276616 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr8:87076610 G>A maps to ENST00000276616 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:87060723 C>T maps to ENST00000276616 R375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:87081803 C>T maps to ENST00000276616 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:87060846 C>T maps to ENST00000276616 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr8:87076556 G>A maps to ENST00000276616 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr8:87076748 C>T maps to ENST00000276616 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr8:87076823 G>A maps to ENST00000276616 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr8:87076412 C>T maps to ENST00000276616 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:87076220 C>T maps to ENST00000276616 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:87076499 C>T maps to ENST00000276616 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr7:42966223 G>A maps to NM_002787.4 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr15:78837985 C>T maps to NM_002789.4 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:109954794 G>A maps to NM_002790.3 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr20:60712005 C>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:23713938 C>T maps to NM_144662.2 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr18:23713986 C>T maps to NM_144662.2 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr18:23713928 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr18:23731864 G>A maps to NM_144662.2 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr6:170852707 G>A maps to NM_002793.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr6:170862326 A>G maps to NM_002793.3 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr16:67969900 G>A maps to NM_002801.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr14:23512186 C>T maps to NM_001099780.1 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:23511880 C>T maps to NM_001099780.1 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:36074988 G>A maps to NM_002794.4 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:4701344 C>T maps to NM_002798.1 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr6:32810725 G>A maps to NM_148919.3 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr6:32810459 G>T maps to NM_148919.3 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:32811716 G>A maps to NM_148919.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:32827224 C>T maps to NM_002800.4 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr14:90730088 C>T maps to NM_002802.2 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:47446710 C>T maps to NM_002804.4 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr11:47446033 G>A maps to NM_002804.4 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:47447450 G>A maps to NM_002804.4 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr17:40729481 C>T maps to NM_016556.2 K44K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:40480234 C>T maps to NM_006503.2 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A197-06A-32D-A197-08 chr19:40480735 G>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr19:40480234 C>T maps to NM_006503.2 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:40480515 C>T maps to NM_006503.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:61908516 T>C maps to NM_002805.5 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:61908867 C>T maps to NM_002805.5 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:61907654 C>T maps to NM_002805.5 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr14:53173912 C>T maps to NM_002806.3 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr14:53184853 C>T maps to NM_002806.3 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr14:53185030 C>T maps to NM_002806.3 Q240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:231948294 C>T maps to NM_002807.3 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:231936973 C>T maps to NM_002807.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr2:232035368 C>T maps to NM_002807.3 I935I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:107331009 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr17:30806300 T>C maps to NM_002815.2 D315D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr17:65341904 G>A maps to NM_002816.3 H288H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:184026630 C>T maps to NM_002808.3 L894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:184021488 C>T maps to NM_002808.3 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:184026545 C>T maps to NM_002808.3 F865F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:184022169 C>G maps to NM_002808.3 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:184020521 C>T maps to NM_002808.3 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr3:184017646 G>A maps to NM_002808.3 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:184019347 C>T maps to NM_002808.3 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr17:38151307 C>T maps to NM_002809.2 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:38142925 C>T maps to NM_002809.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr17:38151307 C>T maps to NM_002809.2 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr17:38140724 C>T maps to NM_002809.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr1:151238481 C>T maps to ENST00000368881 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:123595595 A>C maps to NM_005047.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:64004322 G>A maps to ENST00000492933 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:74330841 G>C maps to NM_002811.3 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr16:74335513 C>A maps to NM_002811.3 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:122353784 C>T maps to NM_002813.4 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr12:122337654 C>A maps to NM_002813.4 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr12:122353784 C>T maps to NM_002813.4 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:122353803 C>T maps to NM_002813.4 Q200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:24607771 G>A maps to NM_176783.1 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:24613610 G>A maps to ENST00000429021 Q158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr17:40990767 C>T maps to NM_176863.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:54147373 G>A maps to NM_014614.2 L792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:54133981 G>A maps to NM_014614.2 I936I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:54101579 G>A maps to NM_014614.2 Q1666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:54148046 A>C maps to NM_014614.2 P747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:54128510 A>C maps to NM_014614.2 Y1087*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:54153115 G>A maps to NM_014614.2 F546F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:54153115 G>A maps to NM_014614.2 F546F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:54101547 G>A maps to NM_014614.2 F1676F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:54101511 C>T maps to NM_014614.2 W1688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr2:54159154 C>T maps to NM_014614.2 W378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:54153115 G>A maps to NM_014614.2 F546F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:54159123 A>G maps to NM_014614.2 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr20:1115874 C>T maps to NM_006814.3 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr21:40551855 C>T maps to NM_003720.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr13:20283703 G>C maps to NM_001042414.1 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26D-06A-11D-A19A-08 chr13:20279861 G>A maps to NM_001042414.1 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:56085029 G>A maps to NM_004577.3 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:56087372 G>A maps to NM_004577.3 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr7:56079529 G>A maps to NM_004577.3 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr1:109824519 C>T maps to ENST00000409138 E80E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:109824339 G>A maps to ENST00000409138 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr15:77324709 C>T maps to NM_003978.3 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:77310493 G>A maps to NM_003978.3 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:77317639 C>T maps to NM_003978.3 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr15:77310493 G>A maps to NM_003978.3 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr18:43577765 G>A maps to NM_024430.3 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:43591176 G>A maps to NM_024430.3 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:28476821 G>A maps to NM_001164721.1 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:28476527 G>A maps to NM_001164721.1 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:28477199 G>A maps to NM_001164721.1 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:28477118 G>A maps to NM_001164721.1 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:28477076 G>A maps to NM_001164721.1 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:28477267 G>A maps to NM_001164721.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr1:28476797 G>A maps to NM_001164721.1 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:28476902 G>A maps to NM_001164721.1 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:28477112 G>A maps to NM_001164721.1 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr1:28477475 C>T maps to NM_001164721.1 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:72333277 G>A maps to NM_001099666.1 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:72349109 G>C maps to NM_001099666.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:808652 C>T maps to NM_002819.4 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:808726 C>T maps to NM_002819.4 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr1:97236328 A>T maps to ENST00000370197 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:97250670 C>T maps to ENST00000370197 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:97236283 C>T maps to ENST00000370197 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr7:99032538 G>A maps to NM_001198879.1 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr7:99017658 C>T maps to NM_001198879.1 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:99022468 G>A maps to NM_001198879.1 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:99021526 G>A maps to NM_001198879.1 A646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:71634537 C>T maps to NM_024754.3 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:71627108 C>T maps to NM_024754.3 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:71631619 G>A did not map to a codon.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr5:71616251 C>A maps to NM_024754.3 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr5:71622532 G>A maps to NM_024754.3 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr2:86344203 C>T maps to NM_017952.5 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:86355107 C>T maps to NM_017952.5 Q381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:98220324 G>A maps to NM_000264.3 F1046F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:98218602 G>A maps to NM_000264.3 I1087I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr9:98231302 G>A maps to NM_000264.3 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr9:98209358 G>A maps to NM_000264.3 P1393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:98220342 G>A maps to NM_000264.3 F1040F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr9:98221921 G>A maps to NM_000264.3 V949V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:98209619 G>A maps to NM_000264.3 P1306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:98209631 G>A maps to NM_000264.3 P1302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:45294228 G>A maps to NM_003738.4 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:45295588 C>T maps to NM_003738.4 E309E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:45293592 G>A maps to NM_003738.4 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:45288248 G>A maps to NM_003738.4 P1150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:45293380 G>A maps to NM_003738.4 I688I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:45297673 G>A maps to NM_003738.4 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:45292282 G>A maps to NM_003738.4 F951F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:45288150 C>T maps to NM_003738.4 W1183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:45288155 G>A maps to NM_003738.4 P1181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr1:45294870 G>A maps to NM_003738.4 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:45292967 G>A maps to NM_003738.4 A795A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:45295393 G>A maps to NM_003738.4 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:23411971 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:23410834 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:23411554 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr23:23398357 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:23398034 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:23398121 T>G did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:23398123 A>G did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:23398261 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:23411621 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:23398357 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:23398302 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:23411268 A>T did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:23398130 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:23412059 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:23397802 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr23:23411488 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:23398357 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:23398128 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:23410681 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:23410744 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:23410954 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:23411137 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:23411680 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:23411706 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:23397737 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:23410851 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:23410680 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:11585236 C>T maps to NM_020780.1 F827F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:11561756 C>T maps to NM_020780.1 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:11589958 C>T maps to NM_020780.1 F1015F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:11589642 C>T maps to NM_020780.1 P943P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:11561676 C>T maps to NM_020780.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:11585299 C>G maps to NM_020780.1 S848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:11586829 C>T maps to NM_020780.1 A912A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:11579866 C>T maps to NM_020780.1 I710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:11580750 C>T maps to NM_020780.1 F736F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:11561951 C>T maps to NM_020780.1 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:11590962 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:11589624 C>T maps to NM_020780.1 F937F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:11589904 G>A maps to NM_020780.1 G997G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:11574470 G>A maps to NM_020780.1 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:11589928 G>A maps to NM_020780.1 V1005V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr1:11577548 C>T maps to NM_020780.1 F593F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:11562816 C>T maps to NM_020780.1 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr1:11595676 G>A maps to NM_020780.1 E1264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr1:11562835 C>T maps to NM_020780.1 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:11561453 G>A maps to NM_020780.1 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:11585236 C>T maps to NM_020780.1 F827F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:11586748 C>G maps to NM_020780.1 T885T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:11584080 C>T maps to NM_020780.1 P815P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr1:11574555 C>T maps to NM_020780.1 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:11562735 C>G maps to NM_020780.1 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:11580894 C>T maps to NM_020780.1 I784I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:11589615 G>A maps to NM_020780.1 K934K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:11596487 C>T maps to NM_020780.1 F1308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:11596499 C>T maps to NM_020780.1 I1312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:11595676 G>A maps to NM_020780.1 E1264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr1:11561795 C>T maps to NM_020780.1 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:11596668 C>T maps to NM_020780.1 L1369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:11561564 C>T maps to NM_020780.1 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr10:27687294 G>A maps to NM_001034842.3 I744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr10:27688143 G>A maps to NM_001034842.3 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr10:27702222 G>A maps to NM_001034842.3 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr10:27702396 G>A maps to NM_001034842.3 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr10:27702711 G>A maps to NM_001034842.3 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr10:27702537 G>A maps to NM_001034842.3 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr10:27687849 C>T maps to NM_001034842.3 W559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:27687744 G>A maps to NM_001034842.3 P594P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:27702555 G>A maps to NM_001034842.3 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:27702576 C>T maps to NM_001034842.3 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:27687294 G>A maps to NM_001034842.3 I744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr10:27703026 C>T maps to NM_001034842.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:27702573 C>T maps to NM_001034842.3 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr10:27687507 C>T maps to NM_001034842.3 R673R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:27702339 C>T maps to NM_001034842.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:27702627 G>A maps to NM_001034842.3 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:27702969 C>T maps to NM_001034842.3 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:27702993 C>T maps to NM_001034842.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr10:27702555 G>A maps to NM_001034842.3 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr10:27702639 C>T maps to NM_001034842.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:27702366 G>A maps to NM_001034842.3 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr10:27703026 C>T maps to NM_001034842.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr10:27702303 C>T maps to NM_001034842.3 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:27687294 G>A maps to NM_001034842.3 I744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:27702756 G>A maps to NM_001034842.3 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:27703020 G>A maps to NM_001034842.3 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:27702597 G>A maps to NM_001034842.3 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:42890984 C>T maps to NM_138296.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr6:42892000 G>A maps to NM_138296.2 E138E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr6:42890790 C>T maps to NM_138296.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr8:97299283 C>T maps to NM_014754.1 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:97332524 C>T maps to NM_014754.1 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51K-06A-11D-A25O-08 chr11:488239 C>T maps to NM_030783.1 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr11:479145 C>T maps to NM_030783.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr11:489423 C>T maps to NM_030783.1 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr10:89720740 C>T maps to NM_000314.4 Q298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr10:89720740 C>T maps to NM_000314.4 Q298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr10:89717740 G>T maps to NM_000314.4 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr10:89720875 G>C did not map to a codon.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr10:89711915 T>A maps to NM_000314.4 Y178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr10:89692774 C>T maps to NM_000314.4 Q87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr10:89720670 G>A maps to NM_000314.4 W274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:16547033 G>A maps to NM_030664.3 K238K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr14:52734847 C>T maps to NM_000953.2 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr14:52734900 C>T maps to NM_000953.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:52735293 C>T maps to NM_000953.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr14:52741657 C>T maps to NM_000953.2 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:139873731 C>T maps to ENST00000224167 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:139873743 G>A maps to ENST00000224167 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:139874653 G>A maps to ENST00000224167 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr14:52782084 C>T maps to NM_000956.3 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr14:52782018 G>A maps to NM_000956.3 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr14:52781511 C>T maps to NM_000956.3 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:52781634 G>A maps to NM_000956.3 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:52781676 G>A maps to NM_000956.3 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:52781481 C>T maps to NM_000956.3 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:71418598 C>T maps to NM_198718.1 K416K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:71418637 C>T maps to NM_198718.1 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:71318539 C>T maps to NM_198716.1 E369E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:71418616 G>A maps to NM_198718.1 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:71512660 G>A maps to ENST00000354608 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:40681541 C>T maps to NM_000958.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:40681211 C>T maps to NM_000958.2 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr9:132510953 G>A maps to NM_004878.4 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:132510953 G>A maps to NM_004878.4 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr9:130887689 G>A maps to NM_025072.5 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:78958571 C>T maps to NM_000959.3 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:78958514 C>T maps to NM_000959.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:78958514 C>T maps to NM_000959.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:78958950 C>T maps to NM_000959.3 R175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr1:79002161 C>T maps to NM_000959.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:78959015 G>A maps to NM_000959.3 W196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr1:78959093 C>T maps to NM_000959.3 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:78958661 C>T maps to NM_000959.3 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:117509536 C>T maps to NM_020440.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:117484383 C>T maps to NM_020440.2 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:117503967 G>A maps to NM_020440.2 A439A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr19:47126969 G>A maps to NM_000960.3 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:47124665 C>T maps to NM_000960.3 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:47124797 G>A maps to NM_000960.3 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:47124806 C>T maps to NM_000960.3 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr19:47124836 C>T maps to NM_000960.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:48130848 G>A maps to NM_000961.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr20:48124591 G>A maps to NM_000961.3 F456F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr20:48160849 G>A maps to NM_000961.3 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr14:74345863 C>T maps to NM_152444.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr14:74340787 C>T maps to NM_152444.2 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr9:125148725 G>A maps to NM_000962.2 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr9:125154660 G>A maps to NM_000962.2 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:125154474 G>A maps to NM_000962.2 K484K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:125152508 C>T maps to NM_000962.2 I443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:125152535 G>A maps to NM_000962.2 R452R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr9:125152607 C>T maps to NM_000962.2 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:125148746 C>T maps to NM_000962.2 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:125148989 C>T maps to NM_000962.2 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr9:125152475 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr9:125140265 G>A maps to NM_000962.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr9:125154654 G>A maps to NM_000962.2 W544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr9:125144004 G>A maps to NM_000962.2 K247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr9:125145865 C>T maps to NM_000962.2 Q281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:125140817 C>T maps to NM_000962.2 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:125143693 C>T maps to NM_000962.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:125140748 C>T maps to NM_000962.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:186648223 G>A maps to NM_000963.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr1:186645641 C>T maps to NM_000963.2 W309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr1:186643772 T>G maps to NM_000963.2 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr11:13514138 C>T maps to NM_000315.2 W54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr3:46939629 G>A maps to NM_000316.2 W164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr3:46937273 G>A maps to NM_000316.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:46944030 C>T maps to NM_000316.2 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:46943284 C>T maps to NM_000316.2 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:46944923 C>T maps to NM_000316.2 P520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:46935486 C>T maps to NM_000316.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:46943281 C>T maps to NM_000316.2 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:46937282 G>A maps to NM_000316.2 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr3:46944048 C>T maps to NM_000316.2 P415P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-OD-A75X-06A-12D-A32N-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr3:46944015 G>A maps to NM_000316.2 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr3:46939360 G>A maps to NM_000316.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr2:209302495 C>T maps to NM_005048.2 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:209309520 C>T maps to NM_005048.2 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:209353736 G>A maps to NM_005048.2 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr2:209302319 G>A maps to NM_005048.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr2:209302495 C>T maps to NM_005048.2 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:209345796 G>A maps to NM_005048.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr2:209302537 T>C maps to NM_005048.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:209302319 G>A maps to NM_005048.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr2:209358098 G>A maps to NM_005048.2 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:209308123 C>T maps to NM_005048.2 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:209309565 C>T maps to NM_005048.2 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:209353868 C>T maps to NM_005048.2 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr12:28116390 C>T maps to ENST00000354417 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:28116411 C>T maps to ENST00000354417 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:28116680 G>A maps to ENST00000354417 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr12:28116537 C>T maps to ENST00000354417 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr12:28116411 C>T maps to ENST00000354417 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:28116335 G>A maps to ENST00000354417 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:28116693 A>C maps to ENST00000354417 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr12:28116381 C>T maps to ENST00000354417 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr8:141799612 G>A maps to NM_005607.4 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr8:141874460 G>A maps to NM_005607.4 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:141675039 G>A maps to NM_005607.4 L996L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr8:27295361 C>T maps to NM_004103.3 A536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr8:27290974 C>T maps to NM_004103.3 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:27308327 G>A maps to NM_004103.3 K801K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr8:27311672 C>T maps to NM_004103.3 S866S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:27288475 C>T maps to NM_004103.3 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:27296604 C>T maps to NM_004103.3 D567D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:27300481 C>T maps to NM_004103.3 F710F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:27301784 C>T maps to NM_004103.3 F737F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr8:27255115 C>T maps to NM_004103.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr8:27288403 C>T maps to NM_004103.3 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:27296616 C>T maps to NM_004103.3 S571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr8:27278209 C>T maps to NM_004103.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:27289778 C>T maps to NM_004103.3 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:27315812 C>T maps to NM_004103.3 I939I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr8:27297853 C>T maps to NM_004103.3 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:62164988 C>T maps to NM_005975.2 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:62165015 C>T maps to NM_005975.2 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:62163969 G>A maps to NM_005975.2 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:43109922 C>T maps to NM_002821.3 Q645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:43107156 C>T maps to NM_002821.3 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr6:43109801 C>T maps to NM_002821.3 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr6:43098318 C>T maps to NM_002821.3 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:43109933 C>T maps to NM_002821.3 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr6:43098318 C>T maps to NM_002821.3 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr6:43126659 C>T maps to NM_002821.3 Q943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:43099756 C>T maps to NM_002821.3 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr6:43106992 C>T maps to NM_002821.3 A494A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr6:43096871 C>T maps to NM_002821.3 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:232577545 C>T maps to ENST00000409321 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr2:232576080 T>C maps to ENST00000409321 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr8:142437169 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:142441071 G>A maps to NM_032611.1 E150E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr9:96863936 G>A maps to ENST00000434261 V701V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr9:96860101 C>T maps to ENST00000434261 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr9:96863861 C>T maps to ENST00000434261 S676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:96827035 C>T maps to NM_177995.1 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:96860797 C>T maps to ENST00000434261 A650A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr15:65862520 G>A maps to NM_016395.2 W251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr15:65851052 C>T maps to NM_016395.2 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:21007079 T>G maps to NM_001010915.3 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr20:49195841 C>T maps to NM_002827.2 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr20:49197859 C>T maps to NM_002827.2 Q383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr20:49195138 C>T maps to NM_002827.2 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr12:112926861 C>T maps to ENST00000392596 I498I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr12:112940051 C>T maps to ENST00000392596 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:112893801 C>A maps to ENST00000392596 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr12:112926921 C>T maps to ENST00000392596 I518I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr12:112884097 C>T maps to ENST00000392596 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr7:77212885 A>C maps to NM_002835.3 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:77256823 G>T maps to NM_002835.3 E610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr7:77261683 T>C maps to NM_002835.3 D672D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:87705670 T>G maps to NM_080685.2 T2031T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr4:87728917 C>T maps to NM_080685.2 I2322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:87622697 C>T maps to NM_080685.2 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:87671905 C>T maps to NM_080685.2 L978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:87691039 C>T maps to NM_080685.2 L1541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:87610235 C>A maps to NM_080685.2 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr4:87696664 C>T maps to NM_080685.2 S1922S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr4:87693929 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:87556462 G>A maps to NM_080685.2 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:87730950 G>A maps to NM_080685.2 L2376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:87735634 C>T maps to NM_080685.2 V2468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:214556656 G>A maps to NM_005401.4 I847I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:214557430 G>A maps to NM_005401.4 Y589Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr1:214557828 G>A maps to NM_005401.4 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr1:214556991 G>A maps to NM_005401.4 Q736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr1:214556992 G>A maps to NM_005401.4 A735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:214567111 G>A maps to NM_005401.4 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:214576223 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr1:214571287 C>T maps to NM_005401.4 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:214625206 A>C maps to NM_005401.4 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:214557397 C>T maps to NM_005401.4 R600R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr1:214551322 G>A maps to NM_005401.4 T889T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:214549623 G>A maps to NM_005401.4 R949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:214556953 G>A maps to NM_005401.4 P748P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:214556971 G>A maps to NM_005401.4 A742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr18:12794450 C>T maps to NM_002828.2 K358K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr14:88945347 G>A maps to NM_007039.3 A809A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:88945805 G>A maps to NM_007039.3 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr14:88945371 G>A maps to NM_007039.3 L801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:114402004 G>A maps to NM_015967.5 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:114401650 G>A maps to NM_015967.5 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:114402025 C>G maps to NM_015967.5 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:114377566 C>T maps to NM_015967.5 W620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:114394647 C>T did not map to a codon.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:114414212 C>T maps to NM_015967.5 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr3:47453619 C>T maps to NM_015466.2 F1370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr3:47454614 C>T maps to NM_015466.2 T1617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr3:47454653 C>T maps to NM_015466.2 L1630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:47447871 C>T maps to NM_015466.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr3:47453655 G>A maps to NM_015466.2 R1382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr9:112166831 C>A maps to NM_002829.3 E617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr2:120702674 A>G maps to NM_002830.2 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr2:120702668 C>T maps to NM_002830.2 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:120720202 C>T maps to NM_002830.2 H764H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr11:18754862 C>T maps to NM_032781.3 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:18754141 G>A maps to NM_032781.3 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:18754871 G>A maps to NM_032781.3 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:18759451 C>T maps to NM_032781.3 K325K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:18750519 G>A maps to NM_032781.3 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:18751010 G>A maps to NM_032781.3 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:18751215 G>A maps to NM_032781.3 I493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:18762338 C>T maps to NM_032781.3 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:18763837 G>A maps to NM_032781.3 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:18764910 G>A maps to NM_032781.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr11:18765555 G>A maps to NM_032781.3 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr12:7063976 T>C maps to ENST00000416215 H114H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:7067171 C>T maps to ENST00000416215 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:7065715 G>A maps to ENST00000416215 E355E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:7065700 C>T maps to ENST00000416215 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:7069122 C>T maps to ENST00000416215 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:202128596 C>T maps to NM_080588.2 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:202127302 G>A maps to ENST00000309017 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:202128566 C>T maps to ENST00000309017 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:202123349 G>A maps to ENST00000309017 L295L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-FW-A3R5-06A-11D-A23B-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:202123388 C>T maps to ENST00000309017 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr15:75798233 G>A maps to NM_002833.2 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr15:75801284 G>A maps to NM_002833.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr15:75798233 G>A maps to NM_002833.2 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr15:75815514 G>A maps to NM_002833.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr15:75782617 G>A maps to NM_002833.2 N331N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr15:75816558 G>A maps to NM_002833.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr15:75798233 G>A maps to NM_002833.2 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr15:75763106 G>A maps to NM_002833.2 R425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr15:75798293 A>T maps to NM_002833.2 C230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:75761169 G>A maps to NM_002833.2 F574F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr20:2969050 G>A maps to NM_002836.3 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr20:3005128 C>T maps to NM_002836.3 V492V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:3002851 C>T maps to NM_002836.3 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:3003364 C>T maps to NM_002836.3 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr20:2944952 C>A maps to NM_002836.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:3005266 G>A maps to NM_002836.3 K538K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:3005227 C>T maps to NM_002836.3 I525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:3002767 C>T maps to NM_002836.3 D410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:2945771 C>T maps to NM_002836.3 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:70949860 G>A maps to NM_001109754.1 I1594I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:70932724 G>A maps to NM_001109754.1 R1950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:71029547 T>C maps to NM_001109754.1 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:71029627 G>A maps to NM_001109754.1 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr12:70964851 C>T maps to NM_001109754.1 T1108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr12:70988445 G>A maps to NM_001109754.1 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr12:70928674 G>A maps to NM_001109754.1 L2048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:70946639 T>A maps to NM_001109754.1 A1768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:70953340 C>T maps to NM_001109754.1 W1499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr12:71029685 G>A maps to NM_001109754.1 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr12:70949899 G>A maps to NM_001109754.1 C1581C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr12:70954676 C>T maps to NM_001109754.1 R1402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:70954553 C>T maps to NM_001109754.1 T1443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:70949818 C>T maps to NM_001109754.1 R1608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:70956756 C>T maps to NM_001109754.1 Q1345Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:70960269 G>A maps to NM_001109754.1 I1283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:70988417 G>A maps to NM_001109754.1 R449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr12:70918311 C>T maps to NM_001109754.1 R2188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:70954553 C>T maps to NM_001109754.1 T1443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:70949779 C>T maps to NM_001109754.1 L1621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:70953404 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr12:70946573 C>T maps to NM_001109754.1 K1790K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr12:70954595 G>A maps to NM_001109754.1 P1429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:70960356 G>A maps to NM_001109754.1 I1254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:71003005 G>A maps to NM_001109754.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:71029529 C>T maps to NM_001109754.1 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:70954520 C>T maps to NM_001109754.1 R1454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:70960287 C>T maps to NM_001109754.1 K1277K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:70949650 G>A maps to NM_001109754.1 D1664D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr12:70953165 G>A maps to NM_001109754.1 S1557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr12:70954505 C>T maps to NM_001109754.1 W1459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr12:70954553 C>T maps to NM_001109754.1 T1443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr12:70986320 G>T maps to NM_001109754.1 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr12:70990069 C>T maps to NM_001109754.1 E339E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:70932011 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:70933759 C>T maps to NM_001109754.1 R1879R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:70946573 C>T maps to NM_001109754.1 K1790K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:70953126 C>T maps to NM_001109754.1 R1570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:70956738 G>A maps to NM_001109754.1 D1351D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:70974909 G>A maps to NM_001109754.1 F828F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:71003107 C>T maps to NM_001109754.1 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr12:70954540 G>A maps to NM_001109754.1 Q1448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:71029682 G>A maps to NM_001109754.1 N73N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:70963485 C>T maps to NM_001109754.1 L1201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr12:71029511 C>T maps to NM_001109754.1 W130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:70988445 G>A maps to NM_001109754.1 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr12:70954520 C>T maps to NM_001109754.1 R1454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:198665997 C>T maps to ENST00000271610 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:198672481 C>T maps to ENST00000271610 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:198723532 C>T maps to ENST00000271610 F1215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:198725048 C>T maps to ENST00000271610 F1220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:198711128 C>T maps to ENST00000271610 F845F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:198719640 G>A maps to ENST00000271610 V1031V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:198703463 G>A maps to ENST00000271610 R729R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:198704323 G>A maps to ENST00000271610 K782K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:198685877 G>A maps to ENST00000271610 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:198668771 A>G maps to ENST00000271610 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr1:198685877 G>A maps to ENST00000271610 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:198665839 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr1:198691543 G>A did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:198721841 G>A maps to ENST00000271610 Q1150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr1:198711435 G>A maps to ENST00000271610 V879V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr1:198703490 G>A maps to ENST00000271610 R738R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:198687313 C>T maps to ENST00000271610 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:198713185 C>T maps to ENST00000271610 Q901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:198687358 T>C maps to ENST00000271610 V529V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr9:8465522 G>A maps to NM_002839.3 L1219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr9:8521496 G>A maps to NM_002839.3 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr9:8338945 C>T maps to NM_002839.3 R1785R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr9:8331619 T>C maps to NM_002839.3 E1832E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr9:8331705 G>A maps to NM_002839.3 Q1804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr9:8449746 C>T maps to NM_002839.3 R1322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:8523524 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr9:8341947 G>A maps to NM_002839.3 I1564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr9:8465570 G>A maps to NM_002839.3 F1203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:8319881 G>A maps to NM_002839.3 F1873F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:8500898 C>T maps to NM_002839.3 E661E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:8471024 C>T maps to NM_002839.3 W1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr9:8486101 C>T maps to NM_002839.3 E905E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:8471042 C>T maps to NM_002839.3 G1152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:8341691 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr9:8331705 G>A maps to NM_002839.3 Q1804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr9:8331706 G>A maps to NM_002839.3 F1803F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:8484183 C>T maps to NM_002839.3 G1116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr9:8518268 C>T maps to NM_002839.3 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:8389357 C>T maps to NM_002839.3 R1420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:8499748 C>T maps to NM_002839.3 Q740Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr9:8492970 G>A maps to NM_002839.3 I786I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:8501059 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr9:8460538 G>A maps to NM_002839.3 P1249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr9:8341931 A>G maps to NM_002839.3 L1570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr9:8460522 G>A maps to NM_002839.3 L1255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr9:8404585 C>T maps to NM_002839.3 A1387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr9:8341824 G>A maps to NM_002839.3 I1605I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr9:8486161 G>A maps to NM_002839.3 I885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr9:8499712 C>T maps to NM_002839.3 V752V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:8404585 C>T maps to NM_002839.3 A1387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:8449743 G>A maps to NM_002839.3 R1323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:8471042 C>T maps to NM_002839.3 G1152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:8486137 G>A maps to NM_002839.3 F893F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:8518117 G>A maps to NM_002839.3 Q425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:8331685 C>T maps to NM_002839.3 E1810E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:8341166 G>A maps to NM_002839.3 S1683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr9:8485972 A>G maps to NM_002839.3 N948N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr10:129871686 G>A maps to NM_006504.4 W517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr10:129868701 G>A maps to NM_006504.4 E427E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr10:129871680 G>A maps to NM_006504.4 W515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr10:129875948 C>T maps to NM_006504.4 I598I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr10:129867988 G>A maps to NM_006504.4 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:129859245 C>T maps to NM_006504.4 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:129861437 G>A maps to NM_006504.4 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:129875894 G>A maps to NM_006504.4 Q580Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr10:129868692 C>T maps to NM_006504.4 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:129868692 C>T maps to NM_006504.4 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:129846042 G>A maps to NM_006504.4 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:129866535 C>T maps to NM_006504.4 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr10:129869091 C>T maps to NM_006504.4 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:129847803 G>A maps to NM_006504.4 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:129875930 C>T maps to NM_006504.4 F592F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:44085234 C>T maps to NM_002840.3 L1641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:44071197 A>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:44057490 C>T maps to NM_002840.3 Q514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:44058186 A>T maps to NM_002840.3 T576T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:44035273 C>T maps to NM_002840.3 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr1:44086842 C>T maps to NM_002840.3 V1865V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:44087634 C>T maps to NM_002840.3 A1895A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:44070901 G>A maps to NM_002840.3 S1059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:44083120 C>T maps to NM_002840.3 I1359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr1:44071072 C>T maps to NM_002840.3 F1116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr1:44072624 C>T maps to NM_002840.3 I1281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr1:44064456 G>A maps to NM_002840.3 W729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:44070955 G>A maps to NM_002840.3 L1077L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:44019226 C>T maps to NM_002840.3 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:44069432 C>T maps to NM_002840.3 F870F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:44083473 C>T maps to NM_002840.3 I1421I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:44087625 C>T maps to NM_002840.3 Y1892Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:44069555 C>T maps to NM_002840.3 P911P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:44083234 C>T maps to NM_002840.3 I1397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:44083234 C>T maps to NM_002840.3 I1397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:61734564 C>T maps to NM_002841.3 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:62259507 A>T maps to NM_002841.3 K1152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:62204552 C>T maps to NM_002841.3 S728S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:61734582 C>T maps to NM_002841.3 H39H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:62142768 C>T maps to NM_002841.3 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:55715399 C>T maps to NM_002842.3 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:55697703 G>A maps to NM_002842.3 F889F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:55716712 C>T maps to NM_002842.3 E200E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:55693470 G>A maps to NM_002842.3 L1037L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:55718303 G>A maps to NM_002842.3 N35N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:55699490 C>T maps to NM_002842.3 R810R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr19:55708575 C>T maps to NM_002842.3 E633E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:48157813 C>T maps to NM_002843.3 V613V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:48177547 C>T maps to NM_002843.3 S1105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:128388687 G>A maps to ENST00000368210 F711F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr6:128294822 C>T maps to ENST00000368210 T1391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr6:128505787 G>A maps to ENST00000368210 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr6:128294274 G>A maps to ENST00000368210 F1405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr6:128294259 G>A maps to ENST00000368210 I1410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:128330312 G>A maps to ENST00000368210 I765I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:128304413 A>T maps to ENST00000368210 S1138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:128410982 C>T maps to ENST00000368210 K439K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:128316681 A>C maps to ENST00000368210 Y935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr6:128505718 G>A maps to ENST00000368210 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:128306882 G>A maps to ENST00000368210 P1096P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:128403648 G>A maps to ENST00000368210 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:128411003 G>A maps to ENST00000368210 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr6:128505769 G>A maps to ENST00000368210 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:128410901 C>T maps to ENST00000368210 K466K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr6:128294864 C>T maps to ENST00000368210 V1377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr6:128294822 C>T maps to ENST00000368210 T1391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:128306885 G>A maps to ENST00000368210 G1095G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr6:128410976 G>A maps to ENST00000368210 D441D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr6:128330303 G>A maps to ENST00000368210 L768L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr6:128304395 G>A maps to ENST00000368210 V1144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr18:8244166 G>A maps to NM_001105244.1 E804E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr18:8379257 C>T maps to NM_001105244.1 L1236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr18:8370886 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:7949228 C>T maps to NM_001105244.1 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:220167204 G>A maps to NM_002846.3 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr2:220164774 G>T maps to NM_002846.3 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr2:220155546 C>T did not map to a codon.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr2:220161166 G>A maps to NM_002846.3 F794F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:220167368 G>A maps to NM_002846.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:220167308 G>A maps to NM_002846.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:220166328 C>T maps to NM_002846.3 K369K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:220161809 C>T maps to NM_002846.3 K711K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:220156214 G>A maps to NM_002846.3 S902S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:220172256 C>T maps to NM_002846.3 Q63Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:220161175 G>A maps to NM_002846.3 I791I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:220166352 C>T maps to NM_002846.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:220161713 G>A maps to NM_002846.3 F743F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:220156202 G>A maps to NM_002846.3 I906I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr7:157903555 G>A maps to NM_002847.3 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:157691406 C>T maps to NM_002847.3 E582E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr7:157926649 C>T maps to NM_002847.3 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:157926382 G>A maps to NM_002847.3 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:157959758 G>A maps to NM_002847.3 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:157475509 G>A maps to NM_002847.3 I636I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:157475512 G>A maps to NM_002847.3 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:157874026 G>A maps to NM_002847.3 V562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr7:157926649 C>T maps to NM_002847.3 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr7:157370802 G>A maps to NM_002847.3 I842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:157341684 G>T maps to NM_002847.3 T977T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:157387989 C>T maps to NM_002847.3 R812R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:157926529 G>A maps to NM_002847.3 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:157959968 G>A maps to NM_002847.3 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:157926592 C>T maps to NM_002847.3 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr7:157931072 G>A maps to NM_002847.3 R349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:157926391 C>T maps to NM_002847.3 R511R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr7:157691391 C>T maps to NM_002847.3 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:157691391 C>T maps to NM_002847.3 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:157959901 G>A maps to NM_002847.3 Q211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:157341642 C>T maps to NM_002847.3 T991T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:157997861 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:157931187 G>A maps to NM_002847.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:157414156 C>T maps to NM_002847.3 K747K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr7:157926475 C>T maps to NM_002847.3 E483E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:157475584 G>A maps to NM_002847.3 D611D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:157926511 C>T maps to NM_002847.3 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:157931072 G>A maps to NM_002847.3 R349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:157959833 C>T maps to NM_002847.3 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr7:157475610 G>A maps to NM_002847.3 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr7:157387989 C>T maps to NM_002847.3 R812R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:157387947 G>A maps to NM_002847.3 T826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:157475443 T>G maps to NM_002847.3 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr12:15656963 C>T maps to NM_030667.1 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr12:15669712 G>A maps to NM_030667.1 K534K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:15704581 G>A maps to NM_030667.1 R845R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:15734656 C>T maps to NM_030667.1 A1059A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:15654908 C>T maps to NM_030667.1 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:15747887 C>T maps to NM_030667.1 I1188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:15677784 C>T maps to NM_030667.1 F643F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:15734689 G>A maps to NM_030667.1 E1070E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr12:15734638 C>T maps to NM_030667.1 F1053F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:15661698 C>T maps to NM_030667.1 Q488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:15718544 G>A maps to NM_030667.1 K910K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr12:15656911 G>A maps to NM_030667.1 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:71286611 G>A maps to NM_002849.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:71286617 G>A maps to NM_002849.2 Y66Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr12:71139614 G>A maps to NM_002849.2 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr12:71286689 G>A maps to NM_002849.2 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr12:71077942 C>T maps to NM_002849.2 V487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr12:71139838 G>A maps to NM_002849.2 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr12:71286482 G>A maps to NM_002849.2 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:71095057 C>T maps to NM_002849.2 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr12:71139734 G>C maps to NM_002849.2 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:5207950 C>A maps to NM_002850.3 P1920P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr19:5238960 G>A maps to NM_002850.3 T606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:5215580 G>A maps to NM_002850.3 P1374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:5245825 G>A maps to NM_002850.3 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:5229344 C>T maps to NM_002850.3 T786T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:5208025 G>A maps to NM_002850.3 I1895I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:5238957 G>A maps to NM_002850.3 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:5212121 G>A maps to NM_002850.3 Q1637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr19:5210797 G>A maps to NM_002850.3 I1751I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:5220312 G>A maps to NM_002850.3 F1169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr20:40979338 G>A maps to ENST00000373198 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr20:40944527 G>A maps to ENST00000373198 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr20:41419867 G>A maps to ENST00000373198 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr20:41076901 C>T maps to ENST00000373198 W506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr20:41419966 C>T maps to ENST00000373198 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr20:41306657 C>T maps to ENST00000373198 W334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr20:40827897 G>A maps to ENST00000373198 Q847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr20:40743880 C>T maps to ENST00000373198 E1041E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr20:40944409 G>A maps to ENST00000373198 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr20:41385113 G>A maps to ENST00000373198 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr20:40735439 G>A maps to ENST00000373198 L1148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr20:41306740 C>T maps to ENST00000373198 W306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:40770567 C>T maps to ENST00000373198 G941G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:41076951 G>A maps to ENST00000373198 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:40770579 C>T maps to ENST00000373198 K937K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:40713400 G>A maps to ENST00000373198 L1375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:40743862 G>A maps to ENST00000373198 V1047V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr20:40827880 G>A maps to ENST00000373198 F852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr20:41076901 C>T maps to ENST00000373198 W506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr20:41419836 G>A maps to ENST00000373198 Q162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:40944428 C>T maps to ENST00000373198 W691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:41385138 C>T maps to ENST00000373198 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr20:40727111 G>A maps to ENST00000373198 F1287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr20:41408888 C>T maps to ENST00000373198 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr20:41419867 G>A maps to ENST00000373198 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr20:40735464 A>T maps to ENST00000373198 R1139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:40727060 C>T maps to ENST00000373198 Q1304Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:40739031 G>A maps to ENST00000373198 F1087F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:40877385 G>A maps to ENST00000373198 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:41306626 G>A maps to ENST00000373198 N344N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:40827880 G>A maps to ENST00000373198 F852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr20:40739031 G>A maps to ENST00000373198 F1087F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr20:40944527 G>A maps to ENST00000373198 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr20:41400149 C>T maps to ENST00000373198 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr20:41101170 G>A maps to ENST00000373198 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr20:40747075 G>A maps to ENST00000373198 I1005I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:40747108 C>T maps to ENST00000373198 W994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr20:40747084 G>A maps to ENST00000373198 S1002S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr20:41306584 G>A maps to ENST00000373198 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr20:40770600 C>T maps to ENST00000373198 K930K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:40757459 G>A maps to ENST00000373198 S949S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr20:40710566 G>A maps to ENST00000373198 I1431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr20:41306745 G>A maps to ENST00000373198 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr20:40747135 C>T maps to ENST00000373198 P985P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr20:41420047 G>A maps to ENST00000373198 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr20:40733210 G>A maps to ENST00000373198 Q1202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:40979299 C>T maps to ENST00000373198 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr20:40790138 G>A maps to ENST00000373198 I867I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr20:41400104 C>T maps to ENST00000373198 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr20:40727102 G>A maps to ENST00000373198 N1290N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr20:40980865 C>T maps to ENST00000373198 G540G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr20:41419903 G>A maps to ENST00000373198 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr20:41101053 C>T maps to ENST00000373198 Q434Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr20:41076907 G>A maps to ENST00000373198 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr20:40733223 G>A maps to ENST00000373198 I1197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:40743952 C>T maps to ENST00000373198 V1017V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr20:41101143 G>A maps to ENST00000373198 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr20:40727168 G>A maps to ENST00000373198 F1268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr20:40827982 C>T maps to ENST00000373198 R818R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr20:40730817 G>A maps to ENST00000373198 F1242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr20:40735439 G>A maps to ENST00000373198 L1148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr20:40739127 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr20:41420005 G>A maps to ENST00000373198 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr20:40747057 C>T maps to ENST00000373198 L1011L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr20:40733210 G>A maps to ENST00000373198 Q1202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr20:40877448 C>T maps to ENST00000373198 Q749Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:40770639 G>A maps to ENST00000373198 A917A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr20:40739013 G>A maps to ENST00000373198 F1093F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:40710657 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:40714388 G>A maps to ENST00000373198 F1339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:40739001 C>T maps to ENST00000373198 P1097P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:40790000 C>T maps to ENST00000373198 E913E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:40944473 G>A maps to ENST00000373198 T676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:40979311 G>A maps to ENST00000373198 I607I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:40980865 C>T maps to ENST00000373198 G540G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:41306650 C>T maps to ENST00000373198 E336E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:41306737 G>A maps to ENST00000373198 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr20:41306713 G>A maps to ENST00000373198 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:40710584 G>A maps to ENST00000373198 I1425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:40980865 C>T maps to ENST00000373198 G540G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:41076943 G>A maps to ENST00000373198 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:41306695 G>A maps to ENST00000373198 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:40877448 C>T maps to ENST00000373198 Q749Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:41306698 G>A maps to ENST00000373198 I320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr20:40747129 C>T maps to ENST00000373198 Q987Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr20:40727111 G>A maps to ENST00000373198 F1287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr20:40770555 G>A maps to ENST00000373198 S945S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr20:41385270 C>T maps to ENST00000373198 W230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr20:40713347 C>T maps to ENST00000373198 R1392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr1:29647297 C>T maps to NM_005704.4 I1273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:29631290 C>T maps to NM_005704.4 F901F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr1:29611307 C>T maps to NM_005704.4 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr1:29647297 C>T maps to NM_005704.4 I1273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:29611348 C>T maps to NM_005704.4 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:29618380 G>A maps to NM_005704.4 P783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:29641913 C>T maps to NM_005704.4 I1096I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr1:29587200 C>T maps to NM_005704.4 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:29581880 C>T maps to NM_005704.4 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:29642575 C>T maps to NM_005704.4 I1152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:29651801 C>T maps to NM_005704.4 T1414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:29606569 C>T maps to NM_005704.4 A595A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:121684489 C>T maps to NM_002851.2 F1984F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr7:121651907 C>T maps to NM_002851.2 S936S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:121651529 C>T maps to NM_002851.2 I810I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:121651175 C>T maps to NM_002851.2 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:121698912 C>T maps to NM_002851.2 S2196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:121674424 C>T maps to NM_002851.2 I1759I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:121652069 C>T maps to NM_002851.2 L990L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:121693986 C>T maps to NM_002851.2 F2092F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:40556803 G>A maps to NM_012232.5 A358A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A2M6-06A-12D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr17:57775141 C>T maps to ENST00000409433 K67K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:57774889 C>T maps to ENST00000409433 Q151Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:57775239 G>A maps to ENST00000409433 R35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:57774864 G>A maps to ENST00000409433 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:57775024 G>T maps to ENST00000409433 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:57775087 G>A maps to ENST00000409433 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr4:37962315 C>T maps to NM_006607.2 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr4:37962066 G>A maps to NM_006607.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr4:37962246 G>A maps to NM_006607.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:37962102 C>T maps to NM_006607.2 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr16:1536506 G>A maps to NM_001013658.1 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:1537890 G>A maps to NM_001013658.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:1536521 G>A maps to NM_001013658.1 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr16:1536422 G>A maps to NM_001013658.1 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr16:1537731 G>A maps to NM_001013658.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr16:1537479 C>T maps to NM_001013658.1 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr16:1537416 C>T maps to NM_001013658.1 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:1535942 G>A maps to NM_001013658.1 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr16:1537383 C>T maps to NM_001013658.1 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr16:1537488 C>T maps to NM_001013658.1 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:1537824 C>T maps to NM_001013658.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:1536176 G>A maps to NM_001013658.1 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:1536467 G>A maps to NM_001013658.1 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:144900173 G>A maps to NM_078480.1 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:144900407 G>A maps to NM_078480.1 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:144899815 G>A maps to NM_078480.1 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:31441267 G>A maps to ENST00000373741 P562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:31532131 C>A maps to ENST00000373741 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:31447635 G>A maps to ENST00000373741 V492V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:31467991 G>A maps to ENST00000373741 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:31425182 G>A maps to ENST00000373741 A909A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:31406063 G>A maps to ENST00000373741 I1223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:20463138 G>A maps to ENST00000361078 S680S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:20458105 G>A maps to ENST00000361078 A794A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:139494290 C>T maps to NM_005859.4 N175N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:44924287 C>T maps to NM_033224.3 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr8:30889983 C>T maps to NM_013357.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:30854141 C>T maps to NM_001015508.1 Q312Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr8:30889974 G>A maps to NM_013357.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:132426449 C>T maps to NM_025215.5 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:132428094 C>T maps to NM_025215.5 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:132426288 C>T maps to NM_025215.5 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr2:61238932 C>T maps to NM_144709.2 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr2:61236122 G>A maps to NM_144709.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:61194635 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:61233691 C>T maps to NM_144709.2 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr11:125766074 A>G maps to NM_031307.3 N35N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:105121518 G>A maps to NM_019042.3 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr7:105135650 G>A maps to NM_019042.3 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:105105784 G>A maps to NM_019042.3 F534F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:44125509 G>A maps to NM_031292.3 Q593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:44148637 C>T maps to NM_031292.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:44148715 G>A maps to NM_031292.3 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:1246311 G>A maps to NM_153339.1 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:1244488 C>T maps to NM_153339.1 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:37211238 G>A maps to NM_002854.2 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:37213030 G>A maps to NM_002854.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:37213031 C>T maps to NM_002854.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:37209711 C>T maps to NM_002854.2 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:37211163 G>A maps to NM_002854.2 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:45153138 C>T maps to NM_006505.3 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:45153183 C>T maps to NM_006505.3 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:45150798 C>T maps to NM_006505.3 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:45157172 C>T maps to NM_006505.3 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:99818868 C>T maps to NM_024070.3 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:99817586 G>A maps to NM_024070.3 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:119549428 G>A maps to NM_002855.4 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:119510717 C>T maps to NM_203285.1 K336K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:119510621 G>A maps to NM_203285.1 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:119549140 G>A maps to NM_002855.4 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:119545889 G>A maps to NM_002855.4 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:119545950 G>A maps to NM_002855.4 N307N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr19:45377706 C>T maps to NM_001042724.1 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:45381852 C>T maps to NM_002856.2 I472I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:45368753 C>T maps to NM_001042724.1 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr19:45381726 C>T maps to NM_002856.2 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:45375206 C>T maps to NM_001042724.1 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:110852542 C>T maps to NM_015480.1 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:161049596 T>C maps to NM_030916.2 E74E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:161042563 G>A maps to NM_030916.2 Q474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr1:161047264 G>A maps to NM_030916.2 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr1:161044073 G>A maps to NM_030916.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:161047402 T>G maps to NM_030916.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:161046223 G>A maps to NM_030916.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:161043551 G>A maps to NM_030916.2 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:161047417 C>T maps to NM_030916.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:161044515 C>T maps to NM_030916.2 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:161049389 G>A maps to NM_030916.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr1:161044464 G>A maps to NM_030916.2 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:161044143 C>T maps to NM_030916.2 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:161042633 C>T maps to NM_030916.2 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:161047498 T>G maps to NM_030916.2 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr21:45548477 C>T maps to NM_005049.2 I852I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr21:45548194 C>T maps to NM_005049.2 S809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr21:45540341 C>T maps to NM_005049.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:159520834 G>A maps to NM_001130864.1 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:159520275 G>A maps to NM_001130864.1 R461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:134218945 C>T maps to NM_138499.3 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr10:134219017 C>T maps to NM_138499.3 H338H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr10:134219611 G>A maps to NM_138499.3 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr2:1647272 G>A maps to NM_012293.1 I1273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:1653136 C>T maps to NM_012293.1 T805T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:1651987 C>T maps to NM_012293.1 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:1643105 C>T maps to NM_012293.1 P1347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:1648499 G>A maps to NM_012293.1 I1211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:1653262 G>A maps to NM_012293.1 F763F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:1651960 G>A maps to NM_012293.1 I1197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:1652194 C>T maps to NM_012293.1 R1119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr2:1652488 G>A maps to NM_012293.1 I1021I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:1653322 C>T maps to NM_012293.1 T743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:1647275 C>T maps to NM_012293.1 R1272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:1677424 G>A maps to NM_012293.1 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr2:1652917 G>A maps to NM_012293.1 F878F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:1653403 G>A maps to NM_012293.1 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:1658191 G>A maps to NM_012293.1 T642T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:1670154 G>A maps to NM_012293.1 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr8:52320799 G>A maps to NM_144651.4 S1128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr8:52287173 C>T maps to NM_144651.4 R1225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr8:52321540 G>A maps to NM_144651.4 V881V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr8:52567256 C>T maps to NM_144651.4 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:52321171 G>A maps to NM_144651.4 I1004I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:52387679 C>T maps to NM_144651.4 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr8:52252212 G>A maps to NM_144651.4 Q1373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:52359681 G>A maps to NM_144651.4 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr8:52336258 G>A maps to NM_144651.4 F557F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr8:52323825 C>T maps to NM_144651.4 V682V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr8:52387577 G>A maps to NM_144651.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr8:52567283 C>T maps to NM_144651.4 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr8:52321801 G>A maps to NM_144651.4 T794T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:52384799 G>A maps to NM_144651.4 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:52321654 G>A maps to NM_144651.4 F843F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:52370067 G>A maps to NM_144651.4 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr8:52320916 G>A maps to NM_144651.4 S1089S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr8:52323831 G>A maps to NM_144651.4 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr8:52359641 G>A maps to NM_144651.4 Q483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr8:52321480 C>T maps to NM_144651.4 G901G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr8:52359636 G>A maps to NM_144651.4 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr8:52321171 G>A maps to NM_144651.4 I1004I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr8:52321549 C>T maps to NM_144651.4 V878V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr8:52232504 G>A maps to NM_144651.4 C1446C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:52320733 G>A maps to NM_144651.4 I1150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr8:52322008 C>T maps to NM_144651.4 A725A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:52284456 G>A maps to NM_144651.4 R1293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:52258421 C>T maps to NM_144651.4 K1329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:52321966 C>T maps to NM_144651.4 Q739Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:52322008 C>T maps to NM_144651.4 A725A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr8:52370109 G>A maps to NM_144651.4 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr8:52320685 C>T maps to NM_144651.4 K1166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr8:52339265 C>T maps to NM_144651.4 K526K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr3:58395264 C>T maps to NM_017771.3 Q439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:58368344 G>A maps to NM_017771.3 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:133272541 C>T maps to NM_018663.1 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:32298408 G>A maps to NM_007238.4 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:32298411 G>A maps to NM_007238.4 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:120652669 G>A maps to NM_001080855.1 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:36359600 G>A maps to NM_152990.3 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:79891107 G>A maps to ENST00000432920 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:79892615 G>A maps to ENST00000432920 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr8:144687914 G>A maps to NM_023078.3 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:144687953 G>A maps to NM_023078.3 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:191179127 C>T maps to NM_001083308.1 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:191179157 G>A maps to NM_001083308.1 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:191178965 A>T maps to NM_001083308.1 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:191179052 C>T maps to NM_001083308.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:191179242 T>A maps to NM_001083308.1 *98K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr20:25262701 G>A maps to NM_002862.3 K479K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr20:25277118 C>T maps to NM_002862.3 S831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr20:25252025 C>T maps to NM_002862.3 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:25257898 C>T maps to NM_002862.3 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:25255247 G>A maps to NM_002862.3 W183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr20:25274901 C>T maps to NM_002862.3 I762I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr20:25261733 C>T maps to NM_002862.3 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:25264766 C>T maps to NM_002862.3 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr20:25259079 C>T maps to NM_002862.3 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:51379767 C>T maps to NM_002863.4 R533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:51378725 G>A maps to NM_002863.4 F599F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:51390767 G>A maps to NM_002863.4 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr14:51382590 G>A maps to NM_002863.4 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:51376659 G>A maps to NM_002863.4 F710F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:51379770 G>A maps to NM_002863.4 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:51382067 G>A maps to NM_002863.4 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:51382208 C>T maps to NM_002863.4 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:51382662 G>A maps to NM_002863.4 F373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:51383416 G>A maps to NM_002863.4 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr14:51382067 G>A maps to NM_002863.4 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:64525788 G>A maps to NM_005609.2 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:64518026 C>T maps to NM_005609.2 Q666Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr11:64526157 A>G maps to NM_005609.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:64519429 G>A maps to NM_005609.2 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:64518905 G>A maps to NM_005609.2 I620I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:64522188 C>T maps to NM_005609.2 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr11:64522218 G>A maps to NM_005609.2 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr11:64525337 C>T maps to NM_005609.2 E191E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64514190 C>T maps to NM_005609.2 R823R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr11:64522182 G>A maps to NM_005609.2 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:55838928 G>A maps to NM_015617.1 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:154932028 G>A maps to NM_138300.3 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:154932049 G>A maps to NM_138300.3 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:154932007 G>A maps to NM_138300.3 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:154932193 G>A maps to NM_138300.3 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:154931773 G>A maps to NM_138300.3 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:158911969 G>A maps to NM_152501.3 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:158946489 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:158908247 G>A maps to NM_152501.3 Q109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:158908922 C>T maps to NM_152501.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:158908247 G>A maps to NM_152501.3 Q109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158911993 C>T maps to NM_152501.3 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:21614954 C>T maps to NM_024854.3 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:21598303 C>T maps to NM_024854.3 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:21614954 C>T maps to NM_024854.3 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr10:100148192 G>A maps to NM_032709.2 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr10:100152775 G>A maps to NM_032709.2 Q284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:100152728 G>A maps to NM_032709.2 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:100144779 G>A maps to NM_032709.2 A533A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:100144799 G>A maps to NM_032709.2 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr10:100148243 G>A maps to NM_032709.2 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:100157210 G>A maps to NM_032709.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:100159989 G>A maps to NM_032709.2 R114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:100152212 G>A maps to NM_032709.2 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:9346711 G>A maps to NM_002864.2 I405I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:9309929 G>A maps to NM_002864.2 L1131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr12:9348940 G>A maps to NM_002864.2 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:9333576 A>T did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr12:9309906 C>T maps to NM_002864.2 W1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr12:9317889 G>A maps to NM_002864.2 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:9349706 C>T maps to NM_002864.2 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr12:9317860 A>G maps to NM_002864.2 S787S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr12:9356429 C>T maps to NM_002864.2 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr12:9345242 G>A maps to NM_002864.2 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:9322154 G>A maps to NM_002864.2 T624T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr12:9307346 C>T maps to NM_002864.2 E1213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:9333680 G>A maps to NM_002864.2 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr12:9345242 G>A maps to NM_002864.2 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:9307217 G>A maps to NM_002864.2 S1256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:9333728 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:3145195 G>A maps to NM_014731.2 A642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr3:49139285 C>T maps to NM_005051.1 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:49139279 G>A maps to NM_005051.1 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr6:163984664 T>A maps to ENST00000361752 L289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:163876428 T>A maps to ENST00000361752 Y93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:163987772 C>T maps to ENST00000361752 R325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr6:163956049 C>T maps to ENST00000361752 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:37586814 C>T maps to NM_012413.3 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:46205095 C>T maps to NM_017659.3 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr16:29708518 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr9:133769067 C>T maps to NM_198180.1 W53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:122250648 C>T maps to NM_198179.2 K372K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr4:122301781 G>A maps to NM_198179.2 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr3:49083866 A>T maps to NM_198880.1 C554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:49114438 G>A maps to NM_198880.1 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr3:49095125 G>A maps to NM_198880.1 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:49068077 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr3:49114341 T>A maps to NM_198880.1 K37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:49094945 G>A maps to NM_198880.1 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr17:74273321 G>T maps to NM_032134.1 T1563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:74288613 G>A maps to NM_032134.1 Q566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr17:74278106 G>A maps to NM_032134.1 T1201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:74276754 G>A maps to NM_032134.1 L1315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:74288340 G>A maps to NM_032134.1 Q657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr17:74278088 G>A maps to NM_032134.1 I1207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr17:74288611 T>C maps to NM_032134.1 Q566Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:74283969 C>T maps to NM_032134.1 R1103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:74278175 G>A maps to NM_032134.1 I1178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:74288016 G>A maps to NM_032134.1 L765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:74274116 G>A maps to NM_032134.1 I1524I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr17:74288158 T>C maps to NM_032134.1 Q717Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:74287399 G>A maps to NM_032134.1 A970A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:74288614 G>A maps to NM_032134.1 V565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:74287111 G>A maps to NM_032134.1 F1066F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr17:74288491 G>A maps to NM_032134.1 V606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:74277016 G>A maps to NM_032134.1 G1261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:107096971 G>A maps to NM_018292.4 K151K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr11:32954768 C>T maps to NM_001076786.1 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:32956277 T>C maps to NM_001076786.1 G1029G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr11:32955371 A>G maps to NM_001076786.1 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr11:32954687 C>A maps to NM_001076786.1 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:32949634 C>T maps to NM_001076786.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:180163447 C>T maps to NM_002826.4 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:180165421 C>T maps to NM_002826.4 F498F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:180153077 C>A maps to NM_002826.4 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr1:180165580 C>T maps to NM_002826.4 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:180165991 C>T maps to NM_002826.4 A688A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:180151403 C>T maps to NM_002826.4 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:180151424 C>T maps to NM_002826.4 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:180151442 C>T maps to NM_002826.4 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:180165586 G>A maps to NM_002826.4 R553R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:180165988 G>A maps to NM_002826.4 E687E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr1:180158703 C>T maps to NM_002826.4 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:180165586 G>A maps to NM_002826.4 R553R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:180166057 C>T maps to NM_002826.4 I710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr9:139100771 G>A maps to NM_181701.3 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr9:139118625 G>T maps to NM_181701.3 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr9:139100612 G>A maps to NM_181701.3 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:139113754 G>A maps to NM_181701.3 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr9:139100717 G>A maps to NM_181701.3 F651F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:10823441 C>T maps to NM_031209.2 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:10823849 C>T maps to NM_031209.2 F372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:10823825 C>T maps to NM_031209.2 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:10823276 C>T maps to NM_031209.2 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:113784184 C>T maps to ENST00000485050 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr3:113786846 A>C maps to ENST00000485050 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:113795693 C>T maps to ENST00000485050 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:113804627 C>T maps to ENST00000485050 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:136433014 C>T maps to ENST00000409606 Q722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr2:136437804 C>T maps to ENST00000409606 F756F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:136473260 C>T maps to ENST00000409606 Q926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr2:136409325 C>T maps to ENST00000409606 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:57648708 G>A maps to ENST00000438036 L992L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:57651863 G>A maps to ENST00000438036 P838P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:57648849 G>A maps to ENST00000438036 T945T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:57677619 C>T maps to ENST00000438036 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr12:57650226 G>A maps to ENST00000438036 L891L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr20:42969930 G>A maps to NM_178491.2 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr15:66169673 C>T maps to ENST00000435304 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr19:8468309 C>T maps to NM_004218.3 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr8:37734743 G>A maps to NM_001002814.2 Q233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:37730432 G>A maps to NM_001002814.2 P629P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:37732412 G>A maps to NM_001002814.2 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:37732589 G>A maps to NM_001002814.2 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:37730498 G>A maps to NM_001002814.2 S607S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:37734738 G>A maps to NM_001002814.2 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:37730365 G>A maps to NM_001002814.2 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:37729976 G>A maps to NM_001002814.2 V781V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr8:37720448 G>A maps to NM_001002814.2 I1272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZH-06A-11D-A197-08 chr8:37729628 G>A maps to NM_001002814.2 V897V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:37732433 G>A maps to NM_001002814.2 D407D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr8:37730651 G>A maps to NM_001002814.2 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:37729304 G>A maps to NM_001002814.2 V1005V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr10:119768706 C>G maps to ENST00000369199 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr16:553030 C>T maps to NM_014700.3 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:570472 G>A maps to NM_014700.3 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:570754 G>A maps to NM_014700.3 E729E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:521376 C>T maps to NM_014700.3 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr17:29857405 C>T maps to NM_032932.3 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:29858711 C>T maps to NM_032932.3 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:29849019 C>T maps to NM_032932.3 N282N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:29844719 G>T maps to NM_032932.3 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr2:73315292 C>A maps to NM_015470.2 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:73303159 G>A maps to NM_015470.2 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:73315848 C>A maps to NM_015470.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:73302720 G>A maps to NM_015470.2 I630I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:73315383 C>T maps to NM_015470.2 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:73315551 C>T maps to NM_015470.2 E398E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:73315776 G>A maps to NM_015470.2 D323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:153957210 G>A maps to NM_002870.2 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:153955016 C>A maps to NM_002870.2 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:65417869 C>A did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr7:140125835 C>T maps to ENST00000275874 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:111176530 G>A maps to NM_017817.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr13:111176260 C>T maps to NM_017817.1 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:111176458 C>T maps to NM_017817.1 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr20:56934663 C>T maps to NM_020673.2 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr1:156038241 C>T maps to NM_020387.2 R141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:156038174 C>T maps to NM_020387.2 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr15:55522633 G>A maps to NM_183235.1 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:55497755 G>A maps to NM_183235.1 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr18:52544878 G>A maps to NM_004163.3 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr18:52546598 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr18:52556514 C>T maps to NM_004163.3 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr18:52551644 C>T maps to NM_004163.3 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr18:52556556 G>A maps to NM_004163.3 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr18:52555244 T>C maps to NM_004163.3 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr18:52546619 G>A maps to NM_004163.3 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr18:52544929 C>T maps to NM_004163.3 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr18:52551644 C>T maps to NM_004163.3 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr18:52556604 G>A maps to NM_004163.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr18:52556514 C>T maps to NM_004163.3 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr18:52546658 G>A maps to NM_004163.3 Q71Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:13378201 G>A maps to NM_004249.3 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:61496780 C>T maps to NM_002865.1 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr14:21931880 G>A maps to NM_032846.3 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:21930571 G>A maps to NM_032846.3 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr11:82693212 G>A maps to NM_014488.3 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:82698773 C>T maps to NM_014488.3 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr18:9859234 C>T maps to NM_006868.3 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:140375441 C>T maps to NM_031296.1 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:27043982 C>T maps to NM_001144943.1 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr17:27042486 G>A maps to NM_001144943.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr17:27042504 G>A maps to NM_001144943.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:27042227 G>T maps to NM_001144943.1 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:120536900 G>A maps to NM_006861.6 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:120536842 G>A maps to NM_006861.6 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:120536843 G>A maps to NM_006861.6 C114C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr12:120535156 C>T maps to NM_006861.6 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:23498190 C>T maps to NM_004914.2 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr17:72736953 C>T maps to NM_001006638.2 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:72739287 G>A maps to NM_001006638.2 Q89Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:72738418 G>A maps to NM_001006638.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr17:72739287 G>A maps to NM_001006638.2 Q89Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:72739296 C>T maps to NM_001006638.2 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:72736947 C>T maps to NM_001006638.2 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:107832710 A>G maps to NM_017516.1 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:154493498 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr23:154490182 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr23:154490183 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:154493471 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr19:18313541 G>A maps to NM_002866.4 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr19:18313451 C>T maps to NM_002866.4 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr1:52385652 C>T maps to NM_002867.3 K202K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:52442594 G>A maps to NM_002867.3 Y65Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:11448053 G>A maps to NM_004283.3 Q8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:135851206 A>G maps to NM_001172435.1 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:135888227 C>T maps to NM_001172435.1 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:135891592 C>T maps to NM_001172435.1 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:220363795 C>T maps to ENST00000358951 Q518Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:220340850 G>A maps to ENST00000358951 A991A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:220368695 G>A maps to ENST00000358951 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:220383831 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:220340694 G>A maps to ENST00000358951 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:220340699 C>A maps to ENST00000358951 E1008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:220375672 A>G maps to ENST00000358951 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:220386236 G>A maps to ENST00000358951 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:61672341 G>A maps to NM_013401.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:70189093 G>A maps to NM_175623.2 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:70206785 C>T maps to NM_175623.2 Q441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr12:70188970 C>T maps to NM_175623.2 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:70149250 C>T maps to NM_175623.2 D37D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr12:70178596 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:70206776 C>T maps to NM_175623.2 R438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:70188293 A>G maps to NM_175623.2 K244K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:102755028 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:102754974 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr23:102192923 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr23:102193016 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:102193022 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:102193058 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:102193022 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:102192850 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr17:80616412 G>A maps to NM_006822.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:80616564 G>A maps to NM_006822.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr17:80616412 G>A maps to NM_006822.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:677502 C>T maps to NM_021168.4 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr16:677561 C>T maps to NM_021168.4 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:675978 C>T maps to NM_021168.4 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:675939 G>T maps to NM_021168.4 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr23:69502085 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:69504463 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:69504150 A>G did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:128810151 G>A maps to NM_198490.1 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:229431639 C>T maps to NM_004578.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr1:229433228 C>T maps to NM_004578.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr19:41289900 C>T maps to ENST00000419646 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:41285940 C>T maps to ENST00000419646 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:41292840 C>T maps to ENST00000419646 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:20017216 C>T maps to NM_004162.4 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:19992419 C>T maps to NM_004162.4 N10N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:56385227 C>T maps to NM_002868.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:56385227 C>T maps to NM_002868.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr12:56385912 C>T maps to NM_002868.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:56380878 C>T maps to NM_002868.2 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:40280675 G>A maps to NM_201434.1 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:40278854 G>A maps to NM_201434.1 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:40280338 G>A maps to NM_201434.1 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:133557033 C>T maps to NM_016577.3 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:130738116 G>A maps to NM_032144.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:205739571 A>G maps to NM_003929.2 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:16238861 C>T maps to NM_005370.4 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:16238833 A>G did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:103080311 T>G did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:42462916 G>A maps to NM_006423.2 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr17:5212103 T>C maps to NM_004703.4 Y50Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr17:5286421 G>A maps to NM_004703.4 Q831Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr16:28925685 G>A maps to NM_024816.2 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:28917074 G>A maps to NM_024816.2 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:28917075 G>A maps to NM_024816.2 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr16:28925995 G>A maps to NM_024816.2 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:28925883 G>A maps to NM_024816.2 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr16:28935916 G>A maps to NM_024816.2 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:28925751 G>A maps to NM_024816.2 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:127990198 C>T maps to NM_005833.3 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:127975691 C>T maps to NM_005833.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr9:125865464 C>T maps to NM_012197.3 T1061T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr9:125760933 T>G maps to NM_012197.3 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr9:125852080 C>T maps to NM_012197.3 T823T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr9:125835865 G>A maps to NM_012197.3 K673K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:174219734 G>A maps to NM_014857.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:66270310 C>T maps to ENST00000451741 I552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:66240306 C>T maps to ENST00000451741 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:24739637 G>A maps to NM_182836.1 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr2:114391762 C>T maps to ENST00000409875 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:114398487 G>A maps to ENST00000409875 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr22:51208363 G>A maps to NM_001130923.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:120424950 G>A maps to NM_173825.3 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:120417365 C>T maps to NM_173825.3 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:120424950 G>A maps to NM_173825.3 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:100961489 G>A maps to NM_022777.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr7:6426905 C>T maps to NM_018890.3 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr22:37627400 G>A maps to NM_002872.3 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr22:37627424 G>A maps to NM_002872.3 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:37627424 G>A maps to NM_002872.3 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr5:34913670 G>A maps to NM_002853.3 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr5:34911750 C>A maps to NM_002853.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr5:68695976 C>T maps to NM_133339.1 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr5:68689178 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:68682006 G>A maps to NM_133339.1 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:68684931 C>T maps to NM_133339.1 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:68677777 G>A maps to NM_133339.1 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr3:8983220 G>A maps to NM_020165.3 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr3:8940726 C>T maps to NM_020165.3 Q391Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:117874125 A>G maps to NM_006265.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:117861237 G>A maps to NM_006265.2 Q551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr19:13059530 G>T maps to NM_005053.2 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:13058989 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:13059911 C>T maps to NM_005053.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:13059061 C>T maps to NM_005053.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:13063555 G>A maps to NM_005053.2 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr19:13063579 G>T maps to NM_005053.2 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:131915551 A>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr5:131931280 C>T maps to NM_005732.3 A662A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:131923621 C>T maps to NM_005732.3 Q298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:41020920 T>C maps to NM_002875.4 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:4662197 C>T maps to NM_001130862.1 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:4652968 C>T maps to NM_001130862.1 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:17698587 C>T maps to NM_001099218.2 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:17698905 G>A maps to NM_001099218.2 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr2:17698845 C>T maps to NM_001099218.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:17697102 C>T maps to NM_001099218.2 E860E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:17692160 G>A maps to NM_001099218.2 I1130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr2:17692133 C>T maps to NM_001099218.2 R1139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:17698254 A>T maps to NM_001099218.2 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:17698393 C>T maps to NM_001099218.2 W430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:17699325 G>A maps to NM_001099218.2 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr17:56787222 C>T maps to NM_058216.1 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr17:56811483 G>A maps to NM_058216.1 Q344Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:56809877 G>A maps to NM_058216.1 K333K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr14:68934941 C>T maps to NM_133509.3 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr17:33428001 C>T maps to NM_002878.3 Q319Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr17:33443909 G>A maps to NM_001142571.1 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr17:33433425 G>A maps to NM_002878.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:1023638 G>A maps to NM_134424.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr8:95384576 G>A maps to NM_012415.2 Q852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr8:95392467 A>G maps to NM_012415.2 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:95392416 A>G maps to NM_012415.2 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:95403848 G>A maps to NM_012415.2 F599F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr1:46726409 C>T maps to NM_003579.3 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:46736439 C>T maps to NM_003579.3 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:46733198 G>A maps to NM_003579.3 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:46733246 C>T maps to NM_003579.3 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:51679736 C>T maps to NM_015106.2 V929V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr3:51679643 C>T maps to NM_015106.2 F898F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr3:51694051 C>A maps to NM_015106.2 I1109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:51697237 C>T maps to NM_015106.2 S1402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:51673919 C>T maps to NM_015106.2 Y712Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:51675864 C>T maps to NM_015106.2 R778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:51697237 C>T maps to NM_015106.2 S1402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr11:67163817 G>A maps to NM_004584.2 Q273Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:67161031 C>T maps to NM_004584.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr7:4841434 C>T maps to NM_018059.4 T897T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr7:4917239 C>T maps to NM_018059.4 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:4845236 C>T maps to NM_018059.4 W750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:4839070 G>A maps to NM_018059.4 L1056L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:4839352 C>T maps to NM_018059.4 P1010P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:4839026 G>A maps to NM_018059.4 F1070F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr7:4839104 G>A maps to NM_018059.4 D1044D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:55948607 T>C maps to NM_001015885.1 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr20:55948793 G>C maps to NM_001015885.1 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:150211054 G>A maps to NM_139165.1 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr6:150342227 G>A maps to NM_130900.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr3:12632391 C>T maps to ENST00000415519 E445E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr3:12660031 C>T maps to ENST00000415519 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr3:12641888 G>T maps to ENST00000415519 S307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr3:12653552 C>A maps to ENST00000415519 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:12660109 G>A maps to ENST00000415519 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:36597718 C>T maps to NM_000448.2 S955S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr11:36596354 C>T maps to NM_000448.2 Q501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:36596621 C>T maps to NM_000448.2 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:36597232 C>T maps to NM_000448.2 S793S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:36596674 C>T maps to NM_000448.2 D607D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr11:36597824 C>T maps to NM_000448.2 L991L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:36594952 C>T maps to NM_000448.2 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:36595522 G>A maps to NM_000448.2 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:36595228 G>A maps to NM_000448.2 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:36596149 C>T maps to NM_000448.2 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:36597595 C>T maps to NM_000448.2 F914F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:155108416 C>G maps to NM_018845.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr1:155110690 C>T maps to NM_018845.3 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:36614458 G>A maps to NM_000536.3 C420C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:36615271 C>T maps to NM_000536.3 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:36615430 C>T maps to NM_000536.3 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:36614440 A>G maps to NM_000536.3 D426D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:36615271 C>T maps to NM_000536.3 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:36615117 G>A maps to NM_000536.3 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:36615271 C>T maps to NM_000536.3 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:36614164 C>T maps to NM_000536.3 K518K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:17700962 C>T maps to ENST00000395776 P1567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:17699090 G>A maps to ENST00000395776 E943E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:17700173 C>T maps to ENST00000395776 L1304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:17701562 C>T maps to ENST00000395776 G1767G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:17698095 C>T maps to ENST00000395776 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr17:17700191 C>T maps to ENST00000395776 F1310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr17:17700192 C>T maps to ENST00000395776 Q1311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr17:17701472 G>A maps to ENST00000395776 E1737E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr17:17699759 C>T maps to ENST00000395776 G1166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:17697185 C>T maps to ENST00000395776 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:17699040 C>T maps to ENST00000395776 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr17:17699231 G>A maps to ENST00000395776 E990E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr17:17700782 C>T maps to ENST00000395776 A1507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:17700533 C>T maps to ENST00000395776 F1424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:34823974 C>T maps to NM_001145521.1 I676I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:17819464 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr23:17818678 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:17819455 G>A did not map to a codon.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr23:17819062 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:17820123 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr23:17819063 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:17819281 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:17818678 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:17819391 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:17819511 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:17819665 G>C did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:17819703 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:17819690 G>A did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:17819690 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:17818800 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:17819274 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:17819534 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:17819928 C>T did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:17819306 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr2:121047314 C>T maps to NM_002881.2 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr2:121047206 C>T maps to NM_002881.2 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr18:9533712 C>T maps to NM_006788.3 H530H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr18:9533364 C>T maps to NM_006788.3 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr18:9522281 G>A maps to NM_006788.3 E276E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr18:9533742 C>A maps to NM_006788.3 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr14:36039820 A>G did not map to a codon.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr14:36041765 C>T maps to NM_194301.2 E1950E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:36096920 G>A maps to NM_194301.2 Q1572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr14:36244916 G>A maps to NM_194301.2 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr14:36207787 A>G maps to NM_194301.2 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:36125018 G>A maps to NM_194301.2 S1324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr14:36207733 G>A maps to NM_194301.2 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr14:36064992 T>C maps to NM_194301.2 V1846V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q3-06A-11D-A196-08 chr20:20483994 C>T maps to NM_020343.3 K1736K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:20505049 C>T maps to NM_020343.3 R1300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:20553674 G>A maps to NM_020343.3 I915I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr20:20527461 C>T maps to NM_020343.3 T1057T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr20:20527470 G>A maps to NM_020343.3 I1054I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr20:20493761 G>A maps to NM_020343.3 S1417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr20:37186984 C>T maps to NM_020336.2 S1140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr20:37168550 C>T maps to NM_020336.2 Q838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:37202876 C>T maps to NM_020336.2 A1409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:37154671 C>T maps to NM_020336.2 T679T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:37153555 T>C maps to NM_020336.2 F585F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr20:37199424 C>T maps to NM_020336.2 L1359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr20:37174900 C>G maps to NM_020336.2 L910L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr20:37146557 G>A maps to NM_020336.2 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr20:37154130 C>T maps to NM_020336.2 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:135977930 G>A maps to NM_006266.2 P647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr9:135984180 G>A maps to NM_006266.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:135985089 G>A maps to NM_006266.2 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr9:135977951 G>A maps to NM_006266.2 N640N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:135975711 G>A maps to NM_006266.2 L838L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr9:135977357 G>A maps to NM_006266.2 F726F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr9:129728187 C>A maps to NM_014636.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:129974487 C>T maps to NM_014636.2 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:178753572 C>T maps to NM_152663.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:178854322 G>A maps to NM_152663.3 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr20:32661651 C>T maps to NM_016732.1 Y119Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr20:32663679 G>A maps to NM_016732.1 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr8:85800010 G>A maps to NM_001100391.1 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:85774623 G>A maps to NM_001100391.1 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr8:85441711 C>T maps to NM_001100391.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:85799848 G>A maps to NM_001100391.1 K245K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:238820346 C>T maps to NM_005855.2 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:45222923 C>T maps to NM_005856.2 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:45222866 C>T maps to NM_005856.2 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:45222923 C>T maps to NM_005856.2 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr7:45222947 T>C maps to NM_005856.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:45222932 C>T maps to NM_005856.2 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:45222932 C>T maps to NM_005856.2 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr12:131359256 C>T maps to ENST00000392369 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr12:131357379 G>T did not map to a codon.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr22:20109897 C>T maps to NM_002882.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr16:67763684 G>T maps to NM_020850.1 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr16:67763669 G>A maps to NM_020850.1 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr16:67763670 G>A maps to NM_020850.1 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr16:67840346 C>T maps to NM_020850.1 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr16:67768906 C>T maps to NM_020850.1 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:67763905 G>A maps to NM_020850.1 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr5:170395318 C>T maps to NM_022897.3 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:170345782 C>T maps to NM_022897.3 Q341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:170667971 G>A maps to NM_022897.3 Q821Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr5:170338052 C>T maps to NM_022897.3 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr2:109383768 C>T maps to NM_006267.4 F2258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr2:109382769 G>A maps to NM_006267.4 Q1925Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:109381018 C>T maps to NM_006267.4 L1342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:109383801 C>T maps to NM_006267.4 F2269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr2:109379917 T>C maps to NM_006267.4 L975L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:109382421 A>C maps to NM_006267.4 P1809P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:109371667 C>T maps to NM_006267.4 Q807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:109347930 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:109378608 C>T maps to NM_006267.4 S885S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:109367804 C>T maps to NM_006267.4 I453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:109398751 C>T maps to NM_006267.4 Q2977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:5921217 G>A maps to NM_007322.2 R442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:5923821 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr19:5933470 G>A maps to NM_007322.2 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:36257607 C>T maps to NM_001161429.1 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:36271413 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:36257147 G>T maps to NM_001161429.1 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:36265060 C>T maps to NM_001161429.1 K185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr5:36270059 T>G maps to NM_001161429.1 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:36257173 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:36271372 C>T maps to NM_001161429.1 K44K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr9:6013111 A>G maps to NM_012416.2 V832V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr9:6013285 G>A maps to NM_012416.2 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:6013255 G>A maps to NM_012416.2 S784S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:13632703 G>A maps to NM_005493.2 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr6:13644841 G>A maps to NM_005493.2 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:13697092 G>A maps to NM_005493.2 R203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr22:41660751 G>A maps to NM_002883.2 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr22:41670627 G>A maps to NM_002883.2 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:41654017 G>A maps to NM_002883.2 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:112240079 C>T maps to NM_002884.2 C48C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr12:69050129 A>G maps to NM_015646.4 E123E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr12:69047971 C>T maps to NM_015646.4 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:21940144 G>A maps to NM_001145658.1 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:21940573 G>A maps to NM_001145658.1 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:21934822 G>A maps to NM_001145658.1 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:21940135 A>C maps to NM_001145658.1 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:21925998 C>T maps to NM_001145658.1 E652E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:21935402 C>A maps to NM_001145658.1 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:21928214 G>A maps to NM_001145658.1 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:21929376 C>T maps to NM_001145658.1 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U9-06A-11D-A32N-08 chr1:21940510 G>A maps to NM_001145658.1 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:2883592 G>A maps to NM_015085.4 K203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr17:2898643 C>T maps to NM_015085.4 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr17:2901633 G>A maps to NM_015085.4 Q388Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:2901636 C>T maps to NM_015085.4 V389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:2901654 G>A maps to NM_015085.4 E395E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:2901624 C>T maps to NM_015085.4 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:2923808 G>A maps to NM_015085.4 R557R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr17:2908718 C>T maps to NM_015085.4 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr17:2894667 G>A maps to NM_015085.4 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:2884529 C>T maps to NM_015085.4 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:2908727 C>T maps to NM_015085.4 F422F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr17:2923835 C>T maps to NM_015085.4 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:2901624 C>T maps to NM_015085.4 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr4:99363183 C>T maps to NM_001100426.1 V581V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:99363183 C>T maps to NM_001100426.1 V581V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr4:99325640 A>G maps to NM_001100426.1 E218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr4:99273741 T>C maps to NM_001100426.1 C118C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr13:98116527 C>T maps to NM_021033.6 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:152880781 C>T maps to NM_002886.2 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:152880700 G>A maps to NM_002886.2 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr9:134473698 T>A did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr9:134501591 G>A maps to NM_198679.1 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:134501765 A>T maps to NM_198679.1 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr9:134471739 G>A maps to NM_198679.1 V710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr9:134497233 G>A maps to NM_198679.1 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:134459919 G>A maps to NM_198679.1 F931F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr9:134464267 G>A maps to NM_198679.1 I823I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:134497251 G>A maps to NM_198679.1 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr9:134458020 C>T maps to NM_198679.1 S993S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20I-06A-11D-A196-08 chr4:160274752 T>A maps to NM_014247.2 A1241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:160277269 C>T maps to NM_014247.2 L1478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:160253699 C>T maps to NM_014247.2 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:160273927 G>A maps to NM_014247.2 S1158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:48141518 G>A maps to NM_001098531.2 D483D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:48142294 C>T maps to NM_001098531.2 K395K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr12:48134790 C>T maps to NM_001098531.2 V652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:48135320 G>C maps to NM_001098531.2 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr12:48133922 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr12:48134706 A>G maps to NM_001098531.2 S680S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:48133941 G>A maps to NM_001098531.2 S785S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:48133001 C>T maps to NM_001098531.2 W795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:48133932 C>T maps to NM_001098531.2 E788E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:48142633 G>A maps to NM_001098531.2 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:48145555 G>A maps to NM_001098531.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:173891898 C>T maps to NM_007023.3 Q824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:173882198 C>T maps to NM_007023.3 Q659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr2:173898661 G>A maps to NM_007023.3 K890K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:173879314 G>A maps to NM_007023.3 E594E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:173679041 G>A maps to NM_007023.3 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr2:173853539 C>T maps to NM_007023.3 D449D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:173787009 G>A maps to NM_007023.3 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:173916422 G>A maps to NM_007023.3 R988R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr2:173830403 C>T maps to NM_007023.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:173891400 G>A maps to NM_007023.3 W785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:22194145 G>A maps to ENST00000344041 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr7:22347998 T>C maps to ENST00000344041 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr7:22165255 G>A maps to ENST00000344041 V683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:22202139 G>A maps to ENST00000344041 Q282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:22348105 G>A maps to ENST00000344041 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:22190072 C>T maps to ENST00000344041 E461E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:130938998 G>A maps to ENST00000514667 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr5:130797420 G>A maps to ENST00000514667 F997F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-ER-A19P-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:130797666 G>A maps to ENST00000514667 A915A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:130883775 G>A maps to ENST00000514667 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:38340513 G>A maps to ENST00000456989 K215K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr17:38348925 C>T maps to ENST00000456989 F574F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:38349235 G>A maps to ENST00000456989 E600E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr17:38349178 C>T maps to ENST00000456989 D581D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:204320165 T>C maps to ENST00000374493 K484K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:204335009 G>A maps to ENST00000374493 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr2:204305455 G>A maps to ENST00000374493 F871F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:47470501 C>T maps to NM_005055.3 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:47469699 G>A maps to NM_005055.3 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr17:38512372 G>C maps to NM_001145301.2 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:25635172 C>G maps to NM_000965.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr3:25636061 T>A maps to NM_000965.3 L348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr12:53608013 G>A maps to NM_000966.4 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr12:53621299 C>T maps to NM_000966.4 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:53621184 G>A maps to NM_000966.4 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:158422675 C>T maps to NM_206963.1 W192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr7:150037539 C>T maps to NM_002889.3 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:150037221 C>T maps to NM_002889.3 W82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:150036167 C>T maps to NM_002889.3 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr7:150037220 T>A maps to NM_002889.3 K83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:63313694 G>A maps to NM_004585.3 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr11:63312102 C>T maps to NM_004585.3 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:63313724 C>T maps to NM_004585.3 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr5:167915682 T>A maps to NM_002887.3 L41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr5:167915735 C>T maps to NM_002887.3 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NF-06A-11D-A19A-08 chr5:167943886 C>T maps to NM_002887.3 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:167915659 C>T maps to NM_002887.3 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:88265151 G>A maps to NM_020320.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:88229409 G>C maps to NM_020320.3 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:141328324 C>T maps to ENST00000452898 S764S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:141328280 C>T maps to ENST00000452898 Q750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:141328726 G>T maps to ENST00000452898 G781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:141290289 C>T maps to ENST00000452898 R355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:141291999 C>T maps to ENST00000452898 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr13:114748763 G>A maps to ENST00000389544 S840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr13:114758000 G>A maps to ENST00000389544 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr13:114793395 C>A maps to ENST00000389544 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr13:114778679 G>A maps to ENST00000389544 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr13:114817545 G>A maps to ENST00000389544 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:114773082 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr12:113544914 C>T maps to NM_001193520.1 V549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:113553473 C>T maps to NM_001193520.1 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr12:113557191 C>T maps to NM_001193520.1 W162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:113543680 G>A maps to NM_001193520.1 V557V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:113565982 C>T maps to NM_001193520.1 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:113543542 G>T maps to NM_001193520.1 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:113552636 C>T maps to NM_001193520.1 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:113543662 G>A maps to NM_001193520.1 F563F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr12:113543631 G>A maps to NM_001193520.1 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr12:113553568 A>G maps to NM_001193520.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr12:113565626 G>C maps to NM_001193520.1 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:113553049 G>A maps to NM_001193520.1 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:113553506 G>A maps to NM_001193520.1 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:178427144 C>T maps to ENST00000263528 P895P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:178421658 C>T maps to ENST00000263528 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:178433444 C>T maps to ENST00000263528 S1084S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:178427384 C>T maps to ENST00000263528 S975S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:178442334 C>T maps to ENST00000263528 S1257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr19:15569351 G>A maps to NM_022904.1 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr19:15564262 G>A maps to NM_022904.1 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:15566919 G>A maps to NM_022904.1 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr19:15562671 C>T maps to NM_022904.1 R990R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:15574875 C>T maps to NM_022904.1 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:15569363 G>A maps to NM_022904.1 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr22:35943020 C>T maps to NM_014310.3 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr22:35947679 C>T maps to NM_014310.3 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr22:35947610 C>T maps to NM_014310.3 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:35947784 C>T maps to NM_014310.3 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr22:35943044 C>G maps to NM_014310.3 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr22:35947563 C>T maps to NM_014310.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr22:35947655 G>A maps to NM_014310.3 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr22:35943077 C>T maps to NM_014310.3 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr9:85640754 C>T maps to NM_152573.2 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr9:85619477 C>T maps to NM_152573.2 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr9:85627426 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr9:85619420 G>A maps to NM_152573.2 G398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:85613349 G>A maps to NM_152573.2 Q579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr9:85677353 G>A maps to NM_152573.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr9:85615843 C>T maps to NM_152573.2 Q468Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:85622404 G>A maps to NM_152573.2 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:43694428 C>T maps to ENST00000374459 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:82377912 G>A maps to NM_152545.1 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:82363474 C>T maps to NM_152545.1 K328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:82355090 C>G maps to NM_152545.1 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr4:82366917 C>T maps to NM_152545.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr5:179541541 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr5:179564878 G>A maps to NM_175062.3 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr5:179564661 G>A maps to NM_175062.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:179548089 C>G maps to NM_175062.3 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr5:179555478 G>A maps to NM_175062.3 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:179545792 G>A maps to NM_175062.3 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:179563497 G>A maps to NM_175062.3 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr5:179546358 G>A maps to NM_175062.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr5:179554671 C>T maps to NM_175062.3 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr15:79298658 C>T maps to NM_002891.4 T661T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:79320161 C>T maps to NM_002891.4 R434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr15:79298586 G>A maps to NM_002891.4 I685I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr15:79382666 C>T maps to NM_002891.4 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr15:79382828 C>T maps to NM_002891.4 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:79339137 G>A maps to NM_002891.4 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:79324608 G>A maps to NM_002891.4 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr15:79382678 G>A maps to NM_002891.4 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr15:79298705 G>A maps to NM_002891.4 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr15:79310210 A>G maps to NM_002891.4 F548F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr15:79350699 G>A maps to NM_002891.4 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr15:79291147 C>T maps to NM_002891.4 R938R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:79324608 G>A maps to NM_002891.4 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr15:79341873 G>T maps to NM_002891.4 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr15:79310165 G>A maps to NM_002891.4 I563I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr15:79324608 G>A maps to NM_002891.4 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr15:79350693 G>A maps to NM_002891.4 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr5:80409701 G>A maps to NM_006909.1 V811V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:80369073 G>A maps to NM_006909.1 Q230Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr5:80404840 T>C maps to NM_006909.1 G594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr5:80408638 C>A maps to NM_006909.1 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:80382719 C>T maps to NM_006909.1 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:80476055 C>T maps to NM_006909.1 R917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:80497237 G>A maps to NM_006909.1 R961R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr5:80382692 G>A maps to NM_006909.1 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr5:80256718 C>T maps to NM_006909.1 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr15:38852055 C>T maps to NM_005739.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr15:38808487 C>T maps to NM_005739.3 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:38800088 C>T maps to NM_005739.3 K360K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr15:38811571 G>A maps to NM_005739.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:38811523 G>A maps to NM_005739.3 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr15:38811550 C>T maps to NM_005739.3 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr15:38808487 C>T maps to NM_005739.3 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:64508457 C>T maps to ENST00000320253 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr11:64508457 C>T maps to ENST00000320253 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr11:64507143 C>T maps to ENST00000320253 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:64502687 C>T maps to ENST00000320253 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64504413 C>T maps to ENST00000320253 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64507628 G>A maps to ENST00000320253 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:64507260 G>A maps to ENST00000320253 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr2:33783889 C>T maps to NM_170672.2 V619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr2:33740223 G>A maps to NM_170672.2 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:33764264 G>A maps to NM_170672.2 R422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:33745624 G>A maps to NM_170672.2 W81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:33783991 G>A maps to NM_170672.2 W653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:33749040 G>A maps to NM_170672.2 W204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr2:33774769 G>A maps to NM_170672.2 Q498Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:33745022 C>T maps to NM_170672.2 R60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr2:33749031 C>T maps to NM_170672.2 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:33745631 G>A maps to NM_170672.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr19:38910510 G>A maps to ENST00000405332 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:38911766 C>G maps to ENST00000405332 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:38911591 C>T maps to ENST00000405332 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:38903605 G>A maps to ENST00000405332 F501F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:38903658 G>A maps to ENST00000405332 R484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:49227704 G>A maps to NM_017805.2 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:49230092 C>T maps to NM_017805.2 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:49230405 C>T maps to NM_017805.2 E627E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:49227691 G>A maps to NM_017805.2 L816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr19:49227674 C>T maps to NM_017805.2 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr19:49232748 G>A maps to NM_017805.2 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr22:29709931 G>A maps to NM_006477.3 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:34067431 G>A maps to NM_033315.3 W74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:34062226 C>T maps to NM_033315.3 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr13:27847286 C>T maps to NM_206827.1 Q129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:27847177 C>T maps to NM_206827.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:27847351 C>T maps to NM_206827.1 D150D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:65351727 C>T maps to NM_016563.2 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:65347593 C>T maps to NM_016563.2 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr15:65347554 G>A maps to NM_016563.2 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:50369287 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr20:4778691 G>A maps to NM_014737.2 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:4776515 G>A maps to NM_014737.2 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr20:4766925 G>A maps to NM_014737.2 Q288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr20:4773227 C>T maps to NM_014737.2 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr20:4771126 G>A maps to NM_014737.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr20:4768869 C>T maps to NM_014737.2 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr20:4776473 G>A maps to NM_014737.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr20:4776474 G>A maps to NM_014737.2 N91N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:65088620 C>T maps to NM_178169.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:65088587 T>C maps to NM_178169.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr10:45477988 C>T maps to NM_032023.3 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:45485152 C>T maps to NM_032023.3 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:45479472 G>A maps to NM_032023.3 K95K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:45484822 G>A maps to NM_032023.3 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr10:45465703 C>T maps to NM_032023.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:206681267 G>A maps to NM_182663.2 Q111Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:74453569 C>T maps to NM_201431.1 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr4:74441999 C>T maps to NM_201431.1 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr4:74447995 G>A maps to NM_201431.1 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:74442365 G>A maps to NM_201431.1 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:74477527 G>A maps to NM_201431.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr4:74450974 C>T maps to NM_201431.1 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:563472 C>T maps to NM_003475.3 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:563618 C>T maps to NM_003475.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:26218211 C>T maps to NM_001164747.1 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr12:86199394 G>A maps to NM_005447.3 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr12:86199463 G>A maps to NM_005447.3 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:86199211 G>A maps to NM_005447.3 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr12:86199301 C>T maps to NM_005447.3 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr12:86199697 C>T maps to NM_005447.3 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr12:86198968 C>T maps to NM_005447.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr12:86199301 C>T maps to NM_005447.3 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:10434206 G>A maps to NM_133452.2 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:10439629 G>A maps to NM_133452.2 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr19:10433931 C>A maps to NM_133452.2 G340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr19:10432266 G>A maps to NM_133452.2 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr19:10433947 G>A maps to NM_133452.2 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr19:10434110 G>A maps to NM_133452.2 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:10444150 G>A maps to NM_133452.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:10434092 G>A maps to NM_133452.2 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:65272916 G>A maps to ENST00000294428 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:65273009 G>A maps to ENST00000294428 Q511Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:65296647 A>T maps to ENST00000294428 K686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:65243730 C>T maps to ENST00000294428 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr1:65255082 C>T maps to ENST00000294428 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:56939652 C>T maps to NM_013435.2 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr13:48923090 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr13:49033821 A>C did not map to a codon.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr13:49027167 C>T maps to NM_000321.2 R579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr13:48955569 A>G maps to NM_000321.2 A562A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr13:48937000 C>T maps to NM_000321.2 Q257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr13:48953758 C>T maps to NM_000321.2 Y454Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr13:48953759 C>T maps to NM_000321.2 R455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr13:49027167 C>T maps to NM_000321.2 R579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr13:48934159 A>G maps to NM_000321.2 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr13:48923136 G>A maps to NM_000321.2 W195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr13:48936977 C>G maps to NM_000321.2 S249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr13:48955549 C>T maps to NM_000321.2 R556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr8:53580612 G>A maps to NM_014781.4 R381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr8:53586680 G>A maps to NM_014781.4 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr8:53596542 G>A maps to NM_014781.4 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr8:53580633 G>A maps to NM_014781.4 Q374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr8:53589058 G>A maps to NM_014781.4 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr8:53569133 C>T maps to NM_014781.4 Q1085Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:53558287 G>A maps to NM_014781.4 R1321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr8:53570447 G>A maps to NM_014781.4 S647S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr7:5105070 C>T maps to NM_021163.3 Q662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr7:5103440 T>C maps to NM_021163.3 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:5105063 C>T maps to NM_021163.3 V659V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr7:5104616 C>T maps to NM_021163.3 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:5096960 C>T maps to NM_021163.3 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:33135133 C>T maps to NM_005610.2 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:33134685 C>T maps to NM_005610.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:33134451 C>T maps to NM_005610.2 D199D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:33138434 G>A maps to NM_005610.2 W382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:205069146 G>A maps to NM_005057.3 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:205065951 G>A maps to NM_005057.3 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:205065951 G>A maps to NM_005057.3 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:205065990 G>A maps to NM_005057.3 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:205068927 G>A maps to NM_005057.3 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr16:24581763 C>T maps to NM_006910.4 V1251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:24582973 C>T maps to NM_006910.4 S1529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:24582319 C>T maps to NM_006910.4 I1311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr16:24581170 C>T maps to NM_006910.4 R1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr16:24567189 C>T maps to NM_006910.4 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr16:24574597 C>A maps to NM_006910.4 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr16:24583225 G>A maps to NM_006910.4 K1613K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:16870693 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr18:20529643 C>T maps to ENST00000360790 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:20570913 C>T maps to ENST00000360790 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:20570922 C>T maps to ENST00000360790 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr18:20572770 T>A maps to ENST00000360790 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr18:20576415 A>T maps to ENST00000360790 I673I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:28113152 C>T maps to NM_022128.1 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr2:28113190 G>A maps to NM_022128.1 Q8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr2:28113191 G>A maps to NM_022128.1 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr20:35668582 G>A maps to NM_002895.2 R626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr20:35668679 G>A maps to NM_002895.2 F593F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr16:53476710 G>A maps to NM_005611.3 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:53476716 C>T maps to NM_005611.3 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:47035919 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr23:47044468 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:47034425 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr23:47035966 G>C did not map to a codon.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr23:47039320 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:47045477 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:47045478 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr23:47041238 C>G did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:47039675 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:47041195 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr21:15599220 A>T maps to NM_144770.3 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr21:15592039 C>T maps to NM_144770.3 R85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr20:34241543 G>A maps to NM_001198838.1 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr20:34241215 G>A maps to NM_001198838.1 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr20:34242833 G>A maps to NM_001198838.1 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr20:34243229 G>A maps to NM_001198838.1 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:94746700 G>A maps to NM_203390.2 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:94746799 G>A maps to NM_203390.2 H613H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:66392363 C>T maps to NM_006328.3 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:110882212 G>A maps to NM_022768.4 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:51430284 C>T maps to NM_013286.4 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:155126595 C>T maps to NM_014892.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:155152087 G>T maps to NM_014892.3 E725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:155141448 C>T maps to NM_014892.3 Q592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr6:155143428 C>T maps to NM_014892.3 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr10:6157212 C>T maps to NM_001145547.1 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr10:6154271 G>A maps to NM_001145547.1 E268E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:125014197 G>A maps to NM_033117.3 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:125004170 G>A maps to NM_033117.3 R189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr12:114386827 G>A maps to NM_016196.3 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:114261085 G>A maps to NM_016196.3 I942I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:114358413 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:114385140 G>A maps to NM_016196.3 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr12:114380137 G>A maps to NM_016196.3 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:114395670 G>A maps to NM_016196.3 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:114282521 G>A maps to NM_016196.3 S912S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:114384268 G>A maps to NM_016196.3 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:114383674 G>A maps to NM_016196.3 I528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:114395760 A>T maps to NM_016196.3 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:114377952 G>A maps to NM_016196.3 R584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:114261085 G>A maps to NM_016196.3 I942I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:114386803 G>A maps to NM_016196.3 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr5:150078130 C>T maps to NM_018047.2 K67K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:150078148 G>A maps to NM_018047.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr14:23374320 G>A maps to NM_001077351.1 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr14:23374167 A>G maps to NM_001077351.1 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:23371419 G>A maps to NM_001077351.1 Q368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr14:23374143 A>G maps to NM_001077351.1 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:17291986 G>A maps to NM_001143942.1 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr14:73554748 C>T maps to NM_021239.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr14:73578359 C>T maps to NM_021239.2 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr13:79946062 G>A maps to ENST00000438737 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr5:145609351 C>T maps to NM_018989.1 Y156Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:145616975 C>T maps to NM_018989.1 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:145643194 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:145641170 C>T maps to NM_018989.1 N664N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr5:145616924 C>T maps to NM_018989.1 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr7:127958081 G>A maps to NM_018077.2 F547F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:127950945 G>A maps to NM_018077.2 T728T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:127953233 G>A maps to NM_018077.2 S713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:127961425 G>A maps to NM_018077.2 R486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:127961426 G>A maps to NM_018077.2 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:48433610 T>C did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:48433952 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr7:155504078 G>A maps to NM_053043.2 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr7:155530345 C>T maps to NM_053043.2 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:155567725 C>T maps to NM_053043.2 I1168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr7:155493558 C>T maps to NM_053043.2 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr1:235299068 G>A maps to NM_015014.2 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:34312575 G>A maps to NM_184234.1 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr23:106332041 T>A did not map to a codon.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr23:106312572 G>A did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:106312491 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr23:106359887 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:106331884 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr23:106331703 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:36123880 C>T maps to NM_024321.3 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr19:36124003 C>T maps to NM_024321.3 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:36125255 C>T maps to NM_024321.3 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:36125256 C>T maps to NM_024321.3 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr19:36128162 C>T maps to NM_024321.3 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:152107523 G>A maps to NM_198557.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:238726977 T>G maps to NM_001080504.2 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr2:238726608 C>T maps to NM_001080504.2 N350N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:238726809 C>T maps to NM_001080504.2 I417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:238726809 C>T maps to NM_001080504.2 I417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:178977482 C>T maps to ENST00000456670 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:178986072 T>C maps to ENST00000456670 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:178985967 C>T maps to ENST00000456670 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr2:178977542 C>T maps to ENST00000456670 C90C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:155719081 C>T maps to NM_144979.3 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:155718032 G>A maps to NM_144979.3 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr4:155719283 T>G maps to NM_144979.3 L158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:155719081 C>T maps to NM_144979.3 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:155719257 C>T maps to NM_144979.3 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr4:40440253 G>A maps to NM_001098634.1 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:40440316 G>A maps to NM_001098634.1 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr4:40440568 G>A maps to NM_001098634.1 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr4:40440439 C>T maps to NM_001098634.1 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr4:40427971 G>A maps to NM_001098634.1 F577F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr4:40440475 G>A maps to NM_001098634.1 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:40440319 G>A maps to NM_001098634.1 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:40440484 G>A maps to NM_001098634.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr4:40440408 G>A maps to NM_001098634.1 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr4:40440445 G>A maps to NM_001098634.1 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr4:40440589 G>A maps to NM_001098634.1 D107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:40440229 G>C maps to NM_001098634.1 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr4:40440364 G>A maps to NM_001098634.1 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:40440175 C>T maps to NM_001098634.1 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:40440304 C>T maps to NM_001098634.1 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:40440172 C>T maps to NM_001098634.1 K246K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr4:40440145 G>A maps to NM_001098634.1 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr11:66436568 G>A maps to NM_031492.2 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr3:50137971 C>T maps to NM_005778.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:50129559 G>A maps to NM_005778.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:50152982 C>T maps to NM_005778.2 R654R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:50155849 C>T maps to NM_005778.2 V803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:50155852 G>A maps to NM_005778.2 R804R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr3:50114527 C>T maps to NM_005777.2 R1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:50097164 C>A maps to NM_005777.2 A738A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:50005997 A>C maps to NM_005777.2 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr3:50103775 C>T maps to NM_005777.2 P928P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr3:50005388 C>T maps to NM_005777.2 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:50099459 C>T maps to NM_005777.2 P835P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr3:50009538 T>A maps to NM_005777.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:114273622 C>T maps to NM_016090.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr11:114276476 C>T maps to NM_016090.2 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:114278250 C>T maps to NM_016090.2 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:145507710 C>T maps to NM_005105.2 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr3:30032652 G>A maps to NM_001003793.2 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr3:29938926 C>T maps to NM_001003793.2 I283I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DA-A3F8-06A-11D-A20D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:29628665 G>A maps to NM_001003793.2 K123K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:135960093 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:135957685 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:135957686 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:135956520 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr23:135956421 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:135958761 G>C did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:135961215 G>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:129543262 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:129546524 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:129543257 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:89448462 G>A maps to NM_019610.5 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:7110494 G>A maps to NM_014469.4 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:7111097 G>A maps to NM_014469.4 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:7110383 C>T maps to NM_014469.4 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:7111037 G>A maps to NM_014469.4 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:7110455 C>T maps to NM_014469.4 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr11:7111037 G>A maps to NM_014469.4 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:7111151 C>T maps to NM_014469.4 D267D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:7110509 C>T maps to NM_014469.4 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:7111238 G>A maps to NM_014469.4 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:139181010 G>A maps to NM_004164.2 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr3:139180952 C>T did not map to a codon.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr3:139180953 C>T maps to NM_004164.2 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr10:48389017 C>T maps to NM_002900.2 E620E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr10:48389644 C>T maps to NM_002900.2 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:48389389 G>A maps to NM_002900.2 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:48390253 C>T maps to NM_002900.2 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr10:48387898 G>A maps to NM_002900.2 S993S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr10:48388900 C>T maps to NM_002900.2 Q659Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr10:48389029 G>A maps to NM_002900.2 I616I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr10:48390151 G>A maps to NM_002900.2 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr10:48389518 C>T maps to NM_002900.2 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:48390586 C>T maps to NM_002900.2 E97E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr10:48390151 G>A maps to NM_002900.2 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr10:48388675 G>A maps to NM_002900.2 F734F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:48385878 G>A maps to NM_002900.2 I1071I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:48390121 G>T maps to NM_002900.2 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:48382099 C>T maps to NM_002900.2 V1183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:48389275 T>C maps to NM_002900.2 Q534Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr10:48388699 G>A maps to NM_002900.2 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr10:48381931 C>T maps to NM_002900.2 R1239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:48390013 G>A maps to NM_002900.2 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr10:48388909 G>A maps to NM_002900.2 V656V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:48382024 C>T maps to NM_002900.2 G1208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:48388699 G>A maps to NM_002900.2 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:48388735 G>A maps to NM_002900.2 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:48389872 C>T maps to NM_002900.2 E335E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:48389176 C>T maps to NM_002900.2 E567E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:48381964 C>T maps to NM_002900.2 E1228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr10:48389173 G>A maps to NM_002900.2 I568I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr10:48387868 G>A maps to NM_002900.2 I1003I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr10:48390451 C>T maps to NM_002900.2 E142E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:48381937 C>T maps to NM_002900.2 V1237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:48388861 G>A maps to NM_002900.2 A672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:48389215 G>A maps to NM_002900.2 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:48390631 C>T maps to NM_002900.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:48382186 G>A maps to NM_002900.2 F1154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:48387922 C>T maps to NM_002900.2 L985L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:48390151 G>A maps to NM_002900.2 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr10:95360698 G>A maps to NM_006744.3 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:95360192 G>A maps to NM_006744.3 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr10:95360165 G>A maps to NM_006744.3 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:7280958 G>A maps to NM_031491.2 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:7280951 G>A maps to NM_031491.2 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:7280988 G>A maps to NM_031491.2 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:26431629 T>C maps to NM_005349.2 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:26417243 G>A maps to NM_005349.2 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr4:26417193 C>T maps to NM_005349.2 Q98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr20:43936798 C>T maps to NM_014276.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:43943150 A>C maps to NM_014276.2 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr20:43944837 C>T maps to NM_014276.2 C344C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr8:30407051 C>A maps to NM_001008711.1 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr8:30407078 C>T maps to NM_001008711.1 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr15:65040731 G>A maps to NM_194272.1 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:65040710 G>A maps to NM_194272.1 Y158Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr15:65041229 G>A maps to NM_194272.1 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr15:65041211 G>A maps to NM_194272.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:65042565 G>A maps to NM_194272.1 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:173933294 G>C maps to NM_172071.2 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:173915703 G>A maps to NM_172071.2 P957P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr21:35893824 G>A maps to NM_004414.5 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:46190988 G>A maps to ENST00000405162 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr6:46216546 G>A maps to ENST00000405162 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:46216486 C>T maps to ENST00000405162 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:50115836 G>A maps to NM_018191.3 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr13:50140793 G>A maps to NM_018191.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr13:49076947 G>A maps to NM_001268.2 I343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:28861845 C>T maps to NM_001048194.2 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:28861653 C>T maps to NM_001048194.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:28858690 C>T maps to NM_001048194.2 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:17755625 G>A maps to NM_018715.2 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:17749279 G>A maps to NM_018715.2 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:17752037 C>T maps to NM_018715.2 W174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:17743074 G>A maps to NM_018715.2 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr11:66613397 G>A maps to NM_005133.2 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:66613526 G>A maps to NM_005133.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:4844530 G>A maps to NM_005772.3 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr9:4826885 C>T maps to NM_005772.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:32124956 C>T maps to NM_002901.2 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:50031885 C>T maps to NM_020650.2 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr19:50040372 C>T maps to NM_020650.2 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr14:103173839 C>T maps to NM_015156.2 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr14:103167666 G>A maps to NM_015156.2 Q163Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr11:63680419 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr1:211462662 A>T maps to NM_001136223.1 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:211487013 C>T maps to NM_001136223.1 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:211451572 C>T maps to NM_001136223.1 Q211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:211451544 G>A maps to NM_001136223.1 Q201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:167666601 G>A maps to NM_052862.3 E247E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:167666670 G>A maps to NM_052862.3 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:167666898 G>A maps to NM_052862.3 K346K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:167654683 G>A maps to NM_052862.3 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr1:167666601 G>A maps to NM_052862.3 E247E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:167659302 G>A maps to NM_052862.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:167659341 G>A maps to NM_052862.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:167666688 G>A maps to NM_052862.3 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:9808254 C>T maps to NM_002903.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:211652398 G>A maps to NM_183059.2 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:211654712 C>T maps to NM_183059.2 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:31922530 G>A maps to ENST00000375425 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:31921901 G>A maps to ENST00000375425 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr8:74235015 C>T maps to NM_172037.3 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr8:74235027 C>T maps to NM_172037.3 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:68156953 G>A maps to NM_016026.3 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:68157130 G>A maps to NM_016026.3 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr14:68196001 C>T maps to NM_152443.2 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr14:68191300 T>C maps to NM_152443.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:68193770 C>T maps to NM_152443.2 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:55568047 G>A maps to NM_001145971.1 R105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:18736666 G>A maps to NM_020905.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:18736666 G>A maps to NM_020905.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:18736663 G>A maps to NM_020905.3 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:57348712 C>T maps to NM_003708.3 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr12:57351006 C>T maps to NM_003708.3 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr12:57351241 C>T maps to NM_003708.3 W2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:57348784 C>A maps to NM_003708.3 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:57348913 G>A maps to NM_003708.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:57346030 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr12:57346774 C>T did not map to a codon.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr12:57351141 C>T maps to NM_003708.3 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr12:57348853 C>T maps to NM_003708.3 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:57345839 G>A maps to NM_003708.3 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:56115530 G>A maps to NM_002905.3 W123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:10127868 C>T maps to NM_015725.2 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:10132292 A>G maps to NM_015725.2 K268K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:10129506 C>T maps to NM_015725.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr19:10129506 C>T maps to NM_015725.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:10127733 C>G maps to NM_015725.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr17:34247232 G>A maps to NM_145654.3 I237I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A3AC-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr17:34251716 C>T maps to NM_145654.3 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr11:110134694 G>A maps to ENST00000405097 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr11:110134695 G>A maps to ENST00000405097 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:110134899 G>A maps to ENST00000405097 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr14:24649107 C>A maps to NM_005132.2 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:24642194 C>T maps to NM_005132.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:24647298 G>A maps to NM_005132.2 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:24646964 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr9:36087793 C>T maps to NM_021111.2 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:36080600 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr9:36100426 C>T maps to NM_021111.2 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:36117062 C>T maps to NM_021111.2 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:36122897 C>T maps to NM_021111.2 V924V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:21636376 C>T maps to NM_032941.2 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:21624010 A>G maps to NM_032941.2 A563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:21652495 G>A maps to NM_032941.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr8:145738660 G>A maps to ENST00000428558 A801A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr17:73625543 C>T maps to NM_004259.5 K653K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:73625354 G>A maps to NM_004259.5 V716V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr17:73658636 G>A maps to NM_004259.5 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr17:73658684 G>A maps to NM_004259.5 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:73658914 G>A maps to NM_004259.5 Q139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr2:86491155 C>T maps to NM_022912.2 W38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:86479171 G>A maps to NM_022912.2 Q109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:86479187 G>A maps to NM_022912.2 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:86481849 C>T maps to NM_022912.2 K90K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr5:137776702 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:137780969 C>T maps to ENST00000378339 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:137780106 C>T maps to ENST00000378339 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr5:137780130 C>T maps to ENST00000378339 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:137780193 C>T maps to ENST00000378339 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:65379550 C>T maps to NM_001001330.2 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:21997707 G>A maps to NM_025232.2 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:21996457 G>A maps to NM_025232.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr8:21997707 G>A maps to NM_025232.2 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr8:21996205 G>A maps to NM_025232.2 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr19:1495356 C>T maps to ENST00000395479 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:1496321 G>A maps to ENST00000395479 W129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:79349983 G>A maps to NM_002909.4 W113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr2:79349160 C>T maps to NM_002909.4 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr2:79348793 G>A maps to NM_002909.4 W57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:79348010 C>T maps to NM_002909.4 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:79350285 G>A maps to NM_002909.4 W149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:79349190 G>A maps to NM_002909.4 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr2:79314714 G>A maps to NM_006507.3 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:79313630 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:79313492 C>T maps to NM_006507.3 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:79314690 G>A maps to NM_006507.3 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr2:79384406 C>T maps to NM_138937.2 W158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:79384419 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:79386513 G>A maps to NM_138937.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr2:79385860 C>T maps to NM_138937.2 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr2:79384758 C>T maps to NM_138937.2 W133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:79254931 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:79253890 C>T maps to NM_001008387.1 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:79255392 C>T maps to NM_001008387.1 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr2:79254179 C>T maps to NM_001008387.1 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr2:79255392 C>T maps to NM_001008387.1 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:120345645 C>T maps to NM_001159353.1 K70K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr1:120342461 G>A maps to NM_032044.3 N63N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:120345600 G>A maps to NM_001159353.1 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:120345525 G>A maps to NM_001159353.1 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:61149579 T>C maps to NM_002908.2 G590G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr2:61147182 C>G maps to NM_002908.2 Y287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:61149237 C>T maps to NM_002908.2 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:65425950 G>A maps to NM_021975.3 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:65423222 G>A maps to NM_021975.3 D323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr19:45528870 C>T maps to ENST00000221452 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:45537712 C>T maps to ENST00000221452 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr19:45515449 C>T maps to ENST00000221452 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:45506213 C>T maps to ENST00000221452 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:45537766 C>T maps to ENST00000221452 F445F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:45540981 C>T maps to ENST00000221452 F558F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr4:37650949 A>G maps to NM_001085399.1 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:141019573 G>A maps to NM_173828.4 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr5:141019703 G>T maps to NM_173828.4 G241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:103244905 C>T maps to ENST00000428762 W1011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr7:103338458 C>T maps to ENST00000428762 W328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr7:103202351 C>T maps to ENST00000428762 G1753G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr7:103205798 C>T maps to ENST00000428762 T1712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr7:103206797 T>C maps to ENST00000428762 Q1603Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr7:103243891 G>A maps to ENST00000428762 A1064A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:103206842 C>T maps to ENST00000428762 Q1588Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr7:103143593 C>T maps to ENST00000428762 W2786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr7:103194135 A>T maps to ENST00000428762 L1980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr7:103338350 G>A maps to ENST00000428762 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr7:103175776 G>A maps to ENST00000428762 L2445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr7:103301843 G>A maps to ENST00000428762 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr7:103216124 C>T maps to ENST00000428762 E1391E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:103234940 T>G did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:103322597 C>T maps to ENST00000428762 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:103474021 C>T maps to ENST00000428762 W145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr7:103207090 C>T maps to ENST00000428762 A1568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:103162525 C>T maps to ENST00000428762 G2537G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:103230098 C>T maps to ENST00000428762 G1363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:103338392 G>A maps to ENST00000428762 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr7:103197508 C>T maps to ENST00000428762 T1904T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:103236979 G>A maps to ENST00000428762 L1154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:103207117 G>A maps to ENST00000428762 I1559I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr7:103341445 A>G maps to ENST00000428762 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:103179573 G>A maps to ENST00000428762 F2377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:103275975 G>A maps to ENST00000428762 A787A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr7:103155839 G>A maps to ENST00000428762 R2637R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr7:103338392 G>A maps to ENST00000428762 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:103205750 G>A maps to ENST00000428762 I1728I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr7:103281033 G>A maps to ENST00000428762 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:103301970 C>T maps to ENST00000428762 W431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr7:103113259 C>T maps to ENST00000428762 *3461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr7:103143605 G>A maps to ENST00000428762 F2782F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:103234860 C>T maps to ENST00000428762 G1206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:103338392 G>A maps to ENST00000428762 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:103159894 G>A maps to ENST00000428762 F2579F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:103179741 C>T maps to ENST00000428762 T2321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr7:103130324 G>A maps to ENST00000428762 I3209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr7:103191668 C>T maps to ENST00000428762 A2049A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:103123408 C>T maps to ENST00000428762 R3397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:103155809 G>A maps to ENST00000428762 G2647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:103234329 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:103322675 A>T maps to ENST00000428762 Y392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:103557528 G>A maps to ENST00000428762 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:103236991 C>T maps to ENST00000428762 E1150E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:103322672 G>A maps to ENST00000428762 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr7:103162551 G>A maps to ENST00000428762 Q2529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:103236919 T>C maps to ENST00000428762 S1174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19T-06A-11D-A19A-08 chr7:103290822 G>A maps to ENST00000428762 R634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:103143605 G>A maps to ENST00000428762 F2782F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:103276701 G>A maps to ENST00000428762 F761F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr7:103629629 G>A maps to ENST00000428762 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:103185574 G>A maps to ENST00000428762 F2173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:103236979 G>C maps to ENST00000428762 L1154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:103270544 G>A maps to ENST00000428762 S848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr7:103557621 T>A maps to ENST00000428762 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr7:103338459 C>T maps to ENST00000428762 W328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr7:103368611 C>T maps to ENST00000428762 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:103137057 C>T maps to ENST00000428762 V3036V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:103143605 G>A maps to ENST00000428762 F2782F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:103143634 G>A maps to ENST00000428762 Q2773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:103629629 G>A maps to ENST00000428762 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:103155836 G>A maps to ENST00000428762 F2638F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:103276020 G>A maps to ENST00000428762 F772F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:103338392 G>A maps to ENST00000428762 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:103290784 C>T maps to ENST00000428762 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr7:103216013 G>A maps to ENST00000428762 F1428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr7:103214588 G>A maps to ENST00000428762 G1487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:73101834 C>T maps to NM_152222.1 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr20:30065649 C>T maps to NM_014012.4 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr20:30064319 C>T maps to NM_014012.4 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr14:23354166 C>T maps to NM_173527.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:204125924 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:204128573 G>A maps to NM_000537.3 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:204135391 C>T maps to NM_000537.3 W10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:204129780 C>G maps to NM_000537.3 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:204128681 C>T maps to NM_000537.3 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr1:204125359 G>A maps to NM_000537.3 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr1:204125923 C>T maps to NM_000537.3 E233E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:204129792 G>A maps to NM_000537.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:204128723 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:204124158 G>A maps to NM_000537.3 F402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:204129792 G>A maps to NM_000537.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:204125845 G>A maps to NM_000537.3 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr23:153206954 A>C did not map to a codon.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr23:153206980 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr23:153200956 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr23:153200957 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:27849683 C>T maps to NM_001029874.1 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:27849696 C>T maps to NM_001029874.1 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:150069034 C>T maps to NM_001099695.1 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:150069733 C>T maps to NM_001099695.1 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr7:150069907 G>A maps to NM_001099695.1 Q583Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150069244 C>T maps to NM_001099695.1 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150069301 C>T maps to NM_001099695.1 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:150069706 C>T maps to NM_001099695.1 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr23:16965204 C>A did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr23:17165541 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr23:17151999 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:17065575 T>G did not map to a codon.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr23:17165593 C>G did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:17153430 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:17065602 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr23:17151947 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:17072991 C>T did not map to a codon.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr23:17040293 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:17153396 C>T did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:17095491 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:8418826 C>A maps to NM_012102.3 L1256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:8418475 G>A maps to NM_012102.3 P1373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr1:8418511 G>A maps to NM_012102.3 P1361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:8674733 G>A maps to NM_012102.3 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:8421933 C>T maps to NM_012102.3 K635K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:8418850 G>A maps to NM_012102.3 P1248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:8425887 G>A maps to NM_012102.3 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:8420027 G>A maps to NM_012102.3 D1138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr1:8420554 G>A maps to NM_012102.3 P1004P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr1:8418475 G>A maps to NM_012102.3 P1373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:8418517 G>A maps to NM_012102.3 A1359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:8420713 G>A maps to NM_012102.3 L951L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr1:8424276 G>A maps to NM_012102.3 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:15264277 C>T maps to NM_032918.2 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:15264294 G>A maps to NM_032918.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr12:18234201 T>A maps to NM_024730.2 K181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:18234400 C>T maps to NM_024730.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:18234136 C>T maps to NM_024730.2 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr12:18234223 C>T maps to NM_024730.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr12:18234316 T>A maps to NM_024730.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:18237578 G>A maps to NM_024730.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr12:18234136 C>T maps to NM_024730.2 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr12:18234223 C>T maps to NM_024730.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr12:18234136 C>T maps to NM_024730.2 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr4:57777247 G>A maps to NM_005612.4 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr4:57796418 C>T maps to NM_005612.4 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr4:57797291 C>T maps to NM_005612.4 V756V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr4:57797292 C>T maps to NM_005612.4 Q757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr4:57798078 C>T maps to NM_005612.4 L1019L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr4:57798002 T>G maps to NM_005612.4 P993P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr10:43601939 C>T maps to NM_020975.4 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:43609982 C>T maps to NM_020975.4 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr10:43606731 C>T maps to NM_020975.4 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:43623686 G>A maps to NM_020975.4 A1105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:43604644 C>T maps to NM_020975.4 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr10:43622165 C>T maps to NM_020975.4 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:43623694 T>A maps to NM_020975.4 L1108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:43601822 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:43610162 C>T maps to NM_020975.4 S705S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr10:43617398 G>A maps to NM_020975.4 R912R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:43614994 C>T maps to NM_020975.4 I803I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr10:43595905 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:43596096 C>T maps to NM_020975.4 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:43615599 C>T maps to NM_020975.4 F893F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:43596086 G>A maps to NM_020975.4 W85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:43606782 C>T maps to NM_020975.4 I464I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:43609988 C>T maps to NM_020975.4 I647I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:108476002 G>A maps to NM_032579.2 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr3:108475996 G>A maps to NM_032579.2 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:108476020 G>A maps to NM_032579.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr3:108475927 G>A maps to NM_032579.2 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:108475403 G>A maps to NM_032579.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr3:108475981 C>T maps to NM_032579.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:108475996 G>A maps to NM_032579.2 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:108476005 G>A maps to NM_032579.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:108475945 G>A maps to NM_032579.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:85577172 G>A maps to NM_017750.3 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:85578055 G>A maps to NM_017750.3 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:100050809 G>A maps to NM_016316.2 I474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:100065958 G>A maps to NM_016316.2 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:100050845 G>A maps to NM_016316.2 N462N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:100055762 G>A maps to NM_016316.2 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:100058906 G>A maps to NM_016316.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:100038042 G>A maps to NM_016316.2 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:100022400 G>A maps to NM_016316.2 L928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:100022401 G>A maps to NM_016316.2 N927N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:100020939 T>G maps to NM_016316.2 G1004G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr2:100058828 C>T maps to NM_016316.2 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr6:111672891 G>A maps to NM_002912.3 I2429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr6:111696775 C>A maps to NM_002912.3 E928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr19:1827446 C>T maps to NM_020695.3 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:1817250 G>A maps to NM_020695.3 T1056T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:1821538 G>A maps to NM_020695.3 I791I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:1818750 G>C maps to NM_020695.3 P952P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:1826951 G>A maps to NM_020695.3 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:1820370 G>A maps to NM_020695.3 P806P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:1823745 G>A maps to NM_020695.3 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr4:39352970 G>A maps to ENST00000381897 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:39306455 G>C maps to ENST00000381897 T697T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:39304681 G>A maps to ENST00000381897 Q735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZU-06A-12D-A196-08 chr7:73646516 C>A maps to NM_181471.1 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr7:73668614 G>A maps to NM_181471.1 H33H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:186509531 C>G maps to NM_181573.2 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:186515358 T>A maps to NM_181573.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:118462716 C>T maps to NM_007370.4 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr17:33348623 A>T maps to NM_001017368.1 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr17:33343491 G>T maps to NM_001017368.1 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:33353482 G>A maps to NM_001017368.1 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:33348530 G>A maps to NM_001017368.1 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr17:80007606 G>A maps to NM_002917.1 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:29834863 G>A maps to NM_021026.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr22:29837972 T>C maps to NM_021026.2 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr22:29837867 C>T maps to NM_021026.2 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr22:29838059 G>A maps to NM_021026.2 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr22:29837591 G>A maps to NM_021026.2 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr22:29835097 G>A maps to NM_021026.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr22:29837576 T>A maps to NM_021026.2 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:29837732 G>A maps to NM_021026.2 W192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr22:32590398 G>A maps to NM_001098527.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:32587001 G>A maps to NM_001098527.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr22:32589189 A>G maps to NM_006605.3 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr22:32587082 G>A maps to NM_001098527.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:32756380 C>T maps to NM_001098535.1 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:32754261 G>A maps to NM_001098535.1 Q68Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr22:32756440 G>A maps to NM_001098535.1 W192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr22:32756275 C>T maps to NM_001098535.1 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:112671700 G>A maps to NM_001013734.2 *264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:112671434 C>T maps to NM_001013734.2 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:112671371 G>A maps to NM_001013734.2 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr6:112671700 G>A maps to NM_001013734.2 *264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:53159944 G>A maps to NM_052859.3 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:53133502 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:53159944 G>A maps to NM_052859.3 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:53155742 C>T maps to NM_052859.3 W177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr3:53155758 G>A maps to NM_052859.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:53138008 A>C maps to NM_052859.3 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:53155762 G>A maps to NM_052859.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr3:53126423 C>T maps to NM_052859.3 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:53157752 G>A maps to NM_052859.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:53157792 G>A maps to NM_052859.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:16411786 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:16475376 G>A maps to NM_015150.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:16358424 C>T maps to NM_015150.1 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr3:16450884 C>T maps to NM_015150.1 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:16475362 G>T maps to NM_015150.1 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:16475434 G>A maps to NM_015150.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:16535240 G>A maps to NM_015150.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:16419225 C>T maps to NM_015150.1 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr3:16419363 C>T maps to NM_015150.1 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:198460725 G>A maps to NM_144629.2 Q408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:176015318 G>A maps to NM_022457.5 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:176015347 C>A maps to NM_022457.5 E464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr16:74685905 A>G maps to NM_018124.3 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:74662524 G>A maps to NM_018124.3 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:14094354 G>A maps to NM_002918.4 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:14077498 G>A maps to NM_002918.4 G599G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:14074026 G>A maps to NM_002918.4 L877L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:14094342 G>A maps to NM_002918.4 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:14079478 G>A maps to NM_002918.4 Q544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:14077480 G>A maps to NM_002918.4 I605I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr19:6007047 G>A maps to NM_000635.3 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr19:6040209 G>A maps to NM_000635.3 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:6040131 G>A maps to NM_000635.3 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:6001898 G>A maps to NM_000635.3 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:6016273 C>T maps to NM_000635.3 W202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr19:6040080 G>A maps to NM_000635.3 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:6040143 G>A maps to NM_000635.3 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr9:3346737 C>T maps to NM_134428.1 Q48Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:3266284 G>A maps to NM_134428.1 R460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:3270455 G>A maps to NM_134428.1 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr9:3271118 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:106995095 G>A maps to ENST00000357881 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr12:107113833 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:107114652 C>T maps to ENST00000357881 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:107080871 G>A maps to ENST00000357881 E205E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr12:107080829 C>T maps to ENST00000357881 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZY-06A-11D-A197-08 chr12:107048023 G>A maps to ENST00000357881 E79E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:151315883 A>G maps to NM_000449.3 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:151314892 G>A maps to NM_000449.3 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:151315435 G>A maps to NM_000449.3 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr6:117198635 G>A maps to NM_173560.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr6:117216370 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr6:117232105 C>T maps to NM_173560.3 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:117246748 C>T maps to NM_173560.3 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:117248298 C>A maps to NM_173560.3 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:117244328 G>A maps to NM_173560.3 W499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:117201820 C>T maps to NM_173560.3 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:117201715 G>A maps to NM_173560.3 E130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:117246659 C>T maps to NM_173560.3 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:117248492 G>A maps to NM_173560.3 W730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr6:117248221 C>T maps to NM_173560.3 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F4-06A-12D-A25O-08 chr6:117246758 G>T maps to NM_173560.3 G608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr6:117243292 G>A maps to NM_173560.3 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:117243235 G>A maps to NM_173560.3 K453K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr6:117245848 C>T maps to NM_173560.3 R525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:56395810 G>A maps to NM_022841.5 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:56386043 A>T maps to NM_022841.5 P1294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr15:56387735 T>C maps to NM_022841.5 Q730Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr15:56386013 G>A maps to NM_022841.5 S1304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr15:56390308 G>A maps to NM_022841.5 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:56388239 G>A maps to NM_022841.5 P562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:19304784 C>T maps to NM_003721.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:19308363 C>T maps to NM_003721.2 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:19307805 C>T maps to NM_003721.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr19:19304880 C>T maps to NM_003721.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:101284527 C>T maps to NM_017819.2 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr4:100478545 G>A maps to NM_001134666.1 Q126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:100472065 G>A maps to NM_001134666.1 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:37762050 C>T maps to NM_144964.2 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr9:37777688 G>A maps to NM_144964.2 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr9:37762050 C>T maps to NM_144964.2 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr23:109694199 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:109694489 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:109694884 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:109696472 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:109697145 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr23:109696355 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:109694655 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr23:109693907 C>A did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr23:109695731 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:109694785 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:109696330 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:109695722 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:109695014 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:109696103 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:109698505 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:109697579 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:109694938 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:109696045 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr23:109694484 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:109694812 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:109695722 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:109696928 C>T did not map to a codon.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr23:109694430 C>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:71350021 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:71350718 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:71350310 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:71349748 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:71349822 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:71349760 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:183871707 C>T maps to NM_015149.3 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr1:183895275 C>T maps to NM_015149.3 A754A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:183711394 C>T maps to NM_015149.3 R35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:183895290 G>A maps to NM_015149.3 V759V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:183853957 C>T maps to NM_015149.3 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:33263310 G>A maps to NM_004761.3 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:11508177 G>A maps to NM_001161616.1 A620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr22:24034620 G>A maps to ENST00000382833 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr22:24034590 G>A maps to ENST00000382833 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:24036013 G>A maps to ENST00000382833 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr22:24035162 G>A maps to ENST00000382833 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:24036124 G>A maps to ENST00000382833 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr15:93595717 G>A maps to NM_020211.2 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:93588253 G>A maps to NM_020211.2 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr15:93588449 G>A maps to NM_020211.2 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:98115296 G>A maps to NM_001012761.2 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr23:46951460 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:46949286 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr5:73153510 C>T maps to NM_001080479.2 I607I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:73207293 G>A maps to NM_001080479.2 V1614V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:73181856 C>T maps to NM_001080479.2 L1080L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:73168938 C>T maps to NM_001080479.2 F894F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:73190267 C>T maps to NM_001080479.2 L1237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:73160697 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:73072344 C>T maps to NM_001080479.2 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:73072418 G>A maps to NM_001080479.2 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:73072452 G>T maps to NM_001080479.2 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:73168938 C>T maps to NM_001080479.2 F894F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr5:73205310 C>T maps to NM_001080479.2 L1412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:73045660 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:73045804 C>T maps to NM_001080479.2 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr5:73076499 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:73163755 C>T maps to NM_001080479.2 S736S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr5:73165999 G>A maps to NM_001080479.2 E844E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr9:35749252 G>A maps to ENST00000456972 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr9:35749252 G>A maps to ENST00000456972 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:35751720 C>T maps to ENST00000456972 N284N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:35750688 G>A maps to ENST00000456972 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:88125212 G>A maps to NM_001078170.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr2:88125212 G>A maps to NM_001078170.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr2:107040936 C>T maps to ENST00000304514 Q1162Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr2:107049700 G>T maps to ENST00000304514 S749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr2:107040301 C>T maps to ENST00000304514 W1374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr2:107084677 G>A maps to ENST00000304514 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:107041191 C>T maps to ENST00000304514 W1077*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:107032314 C>T maps to ENST00000304514 E1685E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:107042455 G>T maps to ENST00000304514 P898P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:107041239 A>T maps to ENST00000304514 Y1061*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr2:107041191 C>T maps to ENST00000304514 W1077*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr2:107050818 C>T maps to ENST00000304514 R690R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:107040780 T>G maps to ENST00000304514 T1214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:107073456 G>A maps to ENST00000304514 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:107040825 C>T maps to ENST00000304514 K1199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:107041553 T>A maps to ENST00000304514 K957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr2:107040816 C>T maps to ENST00000304514 L1202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:107041539 C>T maps to ENST00000304514 V961V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr2:108488435 C>T maps to NM_182588.2 Q1326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr2:108487715 A>T maps to NM_182588.2 K1086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr2:108487264 G>A maps to NM_182588.2 K935K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr2:108489193 G>A maps to NM_182588.2 L1578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:108488173 C>T maps to NM_182588.2 P1238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:108488608 G>A maps to NM_182588.2 K1383K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:108489193 G>A maps to NM_182588.2 L1578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:108488224 G>A maps to NM_182588.2 R1255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:108477283 G>A maps to NM_182588.2 W607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:108488580 G>A maps to NM_182588.2 W1374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr2:108499183 A>C maps to NM_182588.2 A1707A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:108475874 T>A maps to NM_182588.2 L500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:108488206 G>A maps to NM_182588.2 W1249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:108487684 G>A maps to NM_182588.2 R1075R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:108476198 G>A maps to NM_182588.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:108477286 G>A maps to NM_182588.2 K608K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr2:108489193 G>A maps to NM_182588.2 L1578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:108488581 G>A maps to NM_182588.2 W1374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:108487690 G>A maps to NM_182588.2 W1077*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:108487699 G>A maps to NM_182588.2 R1080R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:108488489 C>T maps to NM_182588.2 L1344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:108496544 C>T maps to NM_182588.2 V1682V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:113127769 G>A maps to NM_005054.2 S1761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr10:86007473 C>T maps to ENST00000358110 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:86007458 G>A maps to ENST00000358110 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr10:86012745 G>A maps to ENST00000358110 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:86014138 C>T maps to ENST00000358110 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:86018295 G>A maps to ENST00000358110 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:86008722 G>A maps to ENST00000358110 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:192545480 C>T maps to NM_002922.3 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr10:121275050 G>A maps to NM_001005339.1 H123H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr16:321456 G>A maps to NM_183337.1 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:320986 G>A maps to NM_183337.1 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr16:321420 C>T maps to NM_183337.1 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:321271 G>A maps to NM_183337.1 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr16:320593 C>T maps to NM_183337.1 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr16:321435 C>T maps to NM_183337.1 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr4:3425304 G>A maps to NM_198229.2 T1057T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:3318982 G>A maps to NM_198229.2 E362E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr4:3417784 C>T maps to NM_198229.2 A788A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:3318766 C>T maps to NM_198229.2 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:3319705 C>T maps to NM_198229.2 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr4:3318358 G>A maps to NM_198229.2 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:3319754 C>T maps to NM_198229.2 R620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr4:3441293 C>T maps to NM_198229.2 G1409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr5:176799072 C>T maps to ENST00000398128 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:176799012 G>A maps to ENST00000398128 Q547Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr5:176794827 T>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:176795903 C>T maps to ENST00000398128 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:182571241 G>A maps to NM_002928.3 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr1:182571102 C>A maps to NM_002928.3 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:153365069 A>G maps to NM_012419.4 C28C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr1:192153682 A>T maps to NM_130782.2 *236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr20:62705373 C>T maps to NM_005873.2 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr20:62705291 G>T maps to NM_005873.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:192335166 C>T maps to NM_001039152.3 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:192335064 C>T maps to NM_001039152.3 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr1:192335157 G>A maps to NM_001039152.3 K121K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:192321267 G>A maps to NM_001039152.3 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:192321318 C>T maps to NM_001039152.3 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr8:101092403 G>A maps to NM_015668.3 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr8:101076104 C>T maps to NM_015668.3 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr8:101014533 G>A maps to NM_015668.3 R896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr8:101105710 G>A maps to NM_015668.3 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:101092477 G>A maps to NM_015668.3 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:101075804 C>T maps to NM_015668.3 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:101076098 C>T maps to NM_015668.3 Q299Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:101076104 C>T maps to NM_015668.3 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:100990249 C>T maps to NM_015668.3 R1138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:101051254 C>T maps to NM_015668.3 W690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:101092442 C>T maps to NM_015668.3 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr9:116269665 G>A maps to NM_144488.4 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5KH-06A-11D-A27K-08 chr9:116303598 G>T did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr9:116224414 A>T maps to NM_144488.4 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:116269581 G>A maps to NM_144488.4 E367E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:116299109 C>A maps to NM_144488.4 S650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr9:116224471 C>T maps to NM_144488.4 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:163044238 C>T maps to NM_001102445.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:163042241 A>G maps to NM_001102445.2 E131E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr1:163117254 C>T maps to NM_003617.3 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:163131766 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:163122408 G>A maps to NM_003617.3 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:163138121 G>A maps to NM_003617.3 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:163172598 G>A maps to NM_003617.3 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:163122480 G>A maps to NM_003617.3 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:163122408 G>A maps to NM_003617.3 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr14:72936746 G>A maps to NM_004296.4 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:72976969 C>T maps to NM_004296.4 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr14:72926359 G>A maps to NM_004296.4 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr14:72936761 C>T maps to NM_004296.4 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:72939609 G>A maps to NM_004296.4 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr14:72944998 C>T maps to NM_004296.4 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr14:72939609 G>A maps to NM_004296.4 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr14:72939579 G>A maps to NM_004296.4 K179K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:72431579 C>T maps to NM_004296.4 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:72926359 G>A maps to NM_004296.4 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr14:72985151 G>A maps to NM_004296.4 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:241031931 G>A maps to ENST00000407727 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:240969601 C>T maps to ENST00000407727 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:241099901 G>A maps to ENST00000407727 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr1:241146406 C>T maps to ENST00000407727 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr1:241262020 T>C maps to ENST00000407727 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:240975258 G>A maps to ENST00000407727 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:240975258 G>A maps to ENST00000407727 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:240975333 C>T maps to ENST00000407727 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr1:240969441 G>A maps to ENST00000407727 Q423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:240969595 C>T maps to ENST00000407727 K371K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:240939510 C>T maps to NM_002924.4 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:240975258 G>A maps to ENST00000407727 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:240977012 C>T maps to ENST00000407727 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:240939510 C>T maps to NM_002924.4 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr5:63894251 G>A maps to NM_001029875.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr5:63890535 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr5:63871724 C>T maps to NM_001029875.1 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr5:63802465 G>A maps to NM_001029875.1 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:63871693 C>T maps to NM_001029875.1 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr5:63894230 G>A maps to NM_001029875.1 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:63890624 C>T maps to NM_001029875.1 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:63802465 G>A maps to NM_001029875.1 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:182616031 G>A maps to NM_033345.2 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:182635134 T>C maps to NM_033345.2 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:182635158 C>T maps to NM_033345.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:182617421 G>A maps to NM_033345.2 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:182616019 C>T maps to NM_033345.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:182617352 C>T maps to NM_033345.2 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr1:182616004 C>T maps to NM_033345.2 Q154Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:182615926 G>A maps to NM_033345.2 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr17:63154434 C>T maps to NM_003835.3 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr17:63193345 G>A maps to NM_003835.3 K321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:63149574 G>A maps to NM_003835.3 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr17:63173899 G>A maps to NM_003835.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr17:63193252 C>T maps to NM_003835.3 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:63221223 G>A maps to NM_003835.3 R504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:63206668 G>A maps to NM_003835.3 Q451Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr17:63157005 G>A maps to NM_003835.3 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr17:63206614 C>T maps to NM_003835.3 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr17:63156454 C>T maps to NM_003835.3 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:63221454 C>T maps to NM_003835.3 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:63157005 G>A maps to NM_003835.3 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:33167750 C>T maps to NM_207391.2 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:49582465 G>A maps to NM_000324.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:49583457 C>T maps to NM_000324.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:49586932 G>A maps to NM_000324.2 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr6:49578834 C>T maps to NM_000324.2 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:49585896 G>A maps to NM_000324.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr2:227729453 C>T maps to NM_001167608.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:75511492 G>A maps to NM_001040456.1 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr7:75511189 C>T maps to NM_001040456.1 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:75511309 C>T maps to NM_001040456.1 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:75517585 C>T maps to NM_001040456.1 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:75517489 G>A maps to NM_001040456.1 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:75513070 C>T maps to NM_001040456.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:29656400 C>T maps to NM_012265.1 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:29656821 G>A maps to NM_012265.1 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr16:112805 G>A maps to NM_022450.3 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr16:111684 G>A maps to NM_022450.3 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr16:114704 G>A maps to NM_022450.3 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr16:111687 G>A maps to NM_022450.3 F405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr16:111911 G>A maps to NM_022450.3 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:74475337 T>C maps to NM_024599.5 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr17:74473795 G>A maps to NM_024599.5 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr17:74470501 G>A maps to NM_024599.5 Q502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:74477579 C>T maps to NM_024599.5 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr17:74469097 G>A maps to NM_024599.5 F662F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:74470604 G>A maps to NM_024599.5 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:727793 G>A maps to NM_003961.1 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:726697 C>T maps to NM_003961.1 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr16:727044 G>A maps to NM_003961.1 K232K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr17:30616031 G>A maps to NM_138328.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:30648241 C>T maps to NM_138328.2 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr1:156351237 G>A maps to NM_020407.3 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr1:156351930 C>T maps to NM_020407.3 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:156351863 C>T maps to NM_020407.3 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:156347843 G>A maps to NM_020407.3 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:156351983 C>T maps to NM_020407.3 Y368Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:156351700 G>A maps to NM_020407.3 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:156351640 G>A maps to NM_020407.3 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:25747181 G>A maps to NM_020485.4 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:25718509 C>T maps to NM_020485.4 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:25735271 G>A maps to NM_020485.4 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:25747199 G>A maps to NM_020485.4 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:25712323 G>A maps to NM_020485.4 N317N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr15:90021106 G>A maps to NM_016321.1 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr15:90023567 G>A maps to NM_016321.1 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:90020812 G>A maps to NM_016321.1 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr15:90020400 C>T maps to NM_016321.1 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:151168656 A>G maps to NM_005614.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr12:49460442 G>A maps to NM_144593.1 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr3:129252473 C>T maps to NM_000539.3 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:129251201 C>T maps to NM_000539.3 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:129247890 C>T maps to NM_000539.3 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:129247884 C>T maps to NM_000539.3 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr3:129247596 T>C maps to NM_000539.3 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr3:129251488 C>T maps to NM_000539.3 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:129251557 C>T maps to NM_000539.3 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:129249779 G>A maps to NM_000539.3 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr3:49400012 G>A maps to NM_001664.2 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr2:20647243 G>A maps to NM_004040.2 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr2:20647336 C>T maps to NM_004040.2 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:62648350 G>A maps to NM_014836.4 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:62631392 G>A maps to NM_014836.4 F646F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr10:62631970 G>A maps to NM_014836.4 F631F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:62648612 G>A maps to NM_014836.4 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:62652647 G>A maps to NM_014836.4 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:62647982 C>T maps to NM_014836.4 K481K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:62648699 G>A maps to NM_014836.4 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr8:22864243 C>T maps to NM_001160036.1 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr8:22864684 G>A maps to NM_001160036.1 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr8:22864606 C>T maps to NM_001160036.1 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:22864606 C>T maps to NM_001160036.1 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:95116050 C>T maps to NM_014899.3 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr11:66834315 C>A maps to NM_014578.3 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:66834275 C>T maps to NM_014578.3 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr12:122218798 C>T maps to NM_019034.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr12:122218819 C>T maps to NM_019034.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:122219098 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr4:40245488 G>A maps to NM_004310.3 Q161Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr4:40245413 G>A maps to NM_004310.3 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr4:40245227 G>A maps to NM_004310.3 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44R-06A-41D-A25O-08 chr2:46770277 C>T maps to NM_012249.3 N31N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:30527973 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr17:30526560 C>T maps to NM_001033568.1 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:30533928 T>C maps to NM_001033568.1 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:30526554 C>T maps to NM_001033568.1 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr17:30536450 C>T maps to NM_001033568.1 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:720769 C>T maps to NM_138769.1 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr16:720125 C>T maps to NM_138769.1 R94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr16:723121 C>G maps to NM_138769.1 A574A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:720926 C>T maps to NM_138769.1 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:228879198 G>A maps to NM_021205.4 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:228873456 A>G maps to NM_021205.4 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:228871725 C>T maps to NM_021205.4 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr1:228879480 C>T maps to NM_021205.4 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:228879480 C>T maps to NM_021205.4 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:228879181 C>T maps to NM_021205.4 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:228873459 C>T maps to NM_021205.4 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:228879408 G>A maps to NM_021205.4 K233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:228879408 G>A maps to NM_021205.4 K233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr15:41166142 C>T maps to NM_133639.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:119246801 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr23:119249374 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:119249614 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:119249750 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr23:119293171 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:119293220 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:119211061 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:119293314 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:144464754 C>T maps to ENST00000422773 C673C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr8:144463851 C>T maps to ENST00000422773 V557V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr8:144464775 G>A maps to ENST00000422773 V680V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:144463857 C>T maps to ENST00000422773 I559I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:144461623 C>T maps to ENST00000422773 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:33512476 C>T maps to NM_033103.4 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:33493751 G>A maps to NM_033103.4 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:33512497 G>A maps to NM_033103.4 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:33486950 G>A maps to NM_033103.4 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:33482761 C>T maps to NM_033103.4 Q537Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:33503558 C>T maps to NM_033103.4 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:33503558 C>T maps to NM_033103.4 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:33517486 G>A maps to NM_033103.4 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr23:53457878 C>T did not map to a codon.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr23:53454996 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr23:53455527 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:53455433 G>A did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr22:45822018 C>T maps to NM_015653.3 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr22:45813719 T>C maps to NM_015653.3 D144D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:45813728 C>T maps to NM_015653.3 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr22:45813575 C>T maps to NM_015653.3 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:8148266 G>A maps to ENST00000309737 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:8132610 C>T maps to ENST00000309737 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:8132469 C>G maps to ENST00000309737 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:8159882 C>T maps to ENST00000309737 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr11:8159846 G>A maps to ENST00000309737 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:8132301 G>A maps to ENST00000309737 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:8148301 G>A maps to ENST00000309737 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:209909 C>T maps to NM_021932.4 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:107237703 C>T maps to ENST00000392837 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr12:107245346 C>T maps to ENST00000392837 F427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:107245346 C>T maps to ENST00000392837 F427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:107237691 C>T maps to ENST00000392837 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr17:12847455 C>T maps to NM_014859.4 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr17:12832320 G>A maps to NM_014859.4 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:12860055 C>T maps to NM_014859.4 F445F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr17:12812254 G>A maps to NM_014859.4 E80E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:12888154 G>A maps to NM_014859.4 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:12819327 G>A maps to NM_014859.4 E129E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:12823136 C>T maps to NM_014859.4 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr17:12832254 G>A maps to NM_014859.4 Q158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr17:12819291 G>A maps to NM_014859.4 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr17:12844380 C>T maps to NM_014859.4 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:38945126 G>A maps to ENST00000296782 I1583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr5:38975650 G>A maps to ENST00000296782 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:38964939 G>A maps to ENST00000296782 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:38959320 G>A maps to ENST00000296782 S718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr5:38950757 G>A maps to ENST00000296782 I1064I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr5:38958576 G>A maps to ENST00000296782 H796H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:38950814 G>A maps to ENST00000296782 F1045F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:38963058 G>A maps to ENST00000296782 D495D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:38955746 A>G maps to ENST00000296782 T853T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:152321016 A>G maps to NM_018151.4 E1661E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:152300066 T>A maps to NM_018151.4 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:152321760 C>T maps to NM_018151.4 S1909S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr2:152314360 C>T maps to NM_018151.4 S913S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:152319618 C>T maps to NM_018151.4 F1195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:152322469 C>T maps to NM_018151.4 Q2146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr2:152293788 C>T maps to NM_018151.4 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:152319618 C>T maps to NM_018151.4 F1195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:1549858 G>A maps to NM_031430.2 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr17:1552936 C>T maps to NM_031430.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr12:123983174 C>T maps to NM_178314.3 E239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr12:123900457 G>A maps to NM_145058.1 R206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:123915203 C>T maps to NM_145058.1 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr12:130898675 G>A maps to NM_015347.4 I882I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr12:130921581 C>T maps to NM_015347.4 R620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:130929738 G>A maps to NM_015347.4 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr12:130892273 G>A maps to NM_015347.4 V974V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:130935832 G>A maps to NM_015347.4 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr12:130919305 G>A maps to NM_015347.4 F725F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr12:130926558 G>A maps to NM_015347.4 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:130927161 G>A maps to NM_015347.4 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:130926843 G>A maps to NM_015347.4 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:130926675 C>T maps to NM_015347.4 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:130927092 G>A maps to NM_015347.4 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr12:130927092 G>A maps to NM_015347.4 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:130963464 G>A maps to NM_015347.4 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:130926777 C>T maps to NM_015347.4 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:130934773 C>T maps to NM_015347.4 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr12:130927161 G>A maps to NM_015347.4 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr22:20458067 G>A maps to NM_015672.1 F1078F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr22:20458667 C>T maps to NM_015672.1 E878E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr22:20458067 G>A maps to NM_015672.1 F1078F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:20458238 G>A maps to NM_015672.1 P1021P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr22:20457977 G>A maps to NM_015672.1 L1108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr22:20457899 C>T maps to NM_015672.1 K1134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:42880257 C>T maps to NM_173642.3 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:42865132 A>G maps to NM_173642.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:42880251 C>T maps to NM_173642.3 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:42865256 C>T maps to NM_173642.3 Q116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:42875707 C>T maps to NM_173642.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:42880389 G>A maps to NM_173642.3 Q307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:8926280 C>T maps to NM_020734.2 D354D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr12:8866623 G>A maps to NM_020734.2 E54E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr6:72678709 G>A maps to NM_014989.4 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr6:72889558 C>T maps to NM_014989.4 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:72596824 G>A maps to NM_014989.4 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:73110316 A>T maps to NM_014989.4 P1660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr6:73001642 C>T maps to NM_014989.4 H1248H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr6:72960097 A>C maps to NM_014989.4 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:72806822 C>T maps to NM_014989.4 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr8:105001568 T>G maps to NM_001100117.2 T988T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:105260929 C>T maps to NM_001100117.2 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:105263945 C>T maps to NM_001100117.2 F1316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:105257226 C>T maps to NM_001100117.2 R1140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr8:104897612 G>A maps to NM_001100117.2 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:104778597 G>A maps to NM_001100117.2 Q177Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:105263945 C>T maps to NM_001100117.2 F1316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr8:104928660 G>A maps to NM_001100117.2 W644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:105257165 G>A maps to NM_001100117.2 R1119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:105263336 C>T maps to NM_001100117.2 P1259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr8:104922428 G>A maps to NM_001100117.2 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:105001562 C>T maps to NM_001100117.2 T986T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:105263834 C>T maps to NM_001100117.2 I1279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr8:105260937 C>T maps to NM_001100117.2 F1162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:104927724 T>G maps to NM_001100117.2 V605V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:105026826 G>A maps to NM_001100117.2 K1106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr8:104987644 A>G maps to NM_001100117.2 S946S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:104922428 G>A maps to NM_001100117.2 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:105257213 G>A maps to NM_001100117.2 R1135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr8:104709349 G>A maps to NM_001100117.2 Q71Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr8:104897576 G>A maps to NM_001100117.2 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:104778669 G>A maps to NM_001100117.2 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:105257165 G>A maps to NM_001100117.2 R1119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr8:104948832 G>A maps to NM_001100117.2 W810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr1:41101625 G>A maps to NM_014747.2 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:41095018 G>A maps to NM_014747.2 D166D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:41092338 G>A maps to NM_014747.2 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr1:41101673 G>A maps to NM_014747.2 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr20:43385541 G>A maps to NM_182970.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr20:43386398 G>A maps to NM_182970.2 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr20:43399953 G>T maps to NM_182970.2 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr20:43385562 C>T maps to NM_182970.2 E189E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:43385537 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:43385613 G>A maps to NM_182970.2 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr20:43384942 A>T maps to NM_182970.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr11:66103266 G>A maps to NM_004292.2 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr11:66100730 G>A maps to NM_004292.2 Q625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:66099970 G>A maps to NM_004292.2 Q710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:66100812 G>A maps to NM_004292.2 T597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:66100135 G>A maps to NM_004292.2 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr20:19955745 C>T maps to ENST00000255006 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:19977360 C>T maps to ENST00000255006 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr20:19955649 G>A maps to ENST00000255006 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:19981478 C>T maps to ENST00000255006 R912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr20:19937297 G>A maps to ENST00000255006 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:93118035 C>T maps to NM_024832.3 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:93118950 C>T maps to NM_024832.3 A519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr14:93118860 C>T maps to NM_024832.3 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr14:93118767 C>T maps to NM_024832.3 V458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:93154368 G>A maps to NM_024832.3 A910A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:93154590 C>T maps to NM_024832.3 F984F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr14:93154410 C>T maps to NM_024832.3 F924F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr14:93154590 C>T maps to NM_024832.3 F984F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:93125794 C>T maps to NM_024832.3 S772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:33179270 C>T maps to NM_002931.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr6:33177793 G>A maps to NM_002931.3 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr19:39361342 G>A maps to NM_001195833.1 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:105187476 C>T maps to NM_021930.4 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr7:105187407 C>T maps to NM_021930.4 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr6:7405485 C>T maps to NM_031480.2 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr18:21044192 C>T maps to NM_003831.3 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:21053551 C>T maps to NM_003831.3 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr14:24808772 G>A maps to NM_006871.3 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:24808478 G>A maps to NM_006871.3 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr14:24808478 G>A maps to NM_006871.3 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr21:43176945 C>T maps to ENST00000352483 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr21:43187171 G>A maps to ENST00000352483 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr21:43161696 G>A maps to ENST00000352483 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr21:43161474 C>A maps to ENST00000352483 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr21:43166928 C>A maps to ENST00000352483 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr21:43162113 G>A maps to ENST00000352483 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:106144119 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:106144059 C>G did not map to a codon.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr23:106144089 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr1:155874166 G>A maps to ENST00000368322 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr18:40323526 C>T maps to NM_002930.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr18:40613800 G>A maps to NM_002930.2 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr18:40503607 G>A maps to NM_002930.2 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:40503538 G>A maps to NM_002930.2 Q142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr18:40503638 C>T maps to NM_002930.2 Q108Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:89755009 C>T maps to NM_000326.4 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:89760501 C>T maps to NM_000326.4 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:40656509 C>T maps to NM_012421.3 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr1:40702017 G>A maps to NM_012421.3 Q548Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr1:40704906 T>C maps to NM_012421.3 F1511F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:40688280 C>T maps to NM_012421.3 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:40702246 C>T maps to NM_012421.3 Q625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:40705608 C>T maps to NM_012421.3 V1745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:40702462 C>T maps to NM_012421.3 Q697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr1:40702788 C>T maps to NM_012421.3 F805F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:40656452 C>T maps to NM_012421.3 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:73812726 T>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:73811372 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:73812494 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:73811620 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:73812705 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:73814154 G>T did not map to a codon.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr23:73812409 G>A did not map to a codon.
Sequencing variant TCGA-GN-A26D-06A-11D-A19A-08 chr23:73811748 G>C did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:14139132 C>T maps to NM_080864.2 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44R-06A-41D-A25O-08 chr19:14141640 C>T maps to NM_080864.2 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:14141607 C>T maps to NM_080864.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:14139074 G>A maps to NM_080864.2 W20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr16:67688252 C>T maps to NM_001013838.1 D1080D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr16:67685654 G>A maps to NM_001013838.1 W832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr16:67690333 C>T maps to NM_001013838.1 S1274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:67681494 G>A maps to NM_001013838.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:67682023 C>T maps to NM_001013838.1 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr16:67682058 G>A maps to NM_001013838.1 W392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:67681485 G>A maps to NM_001013838.1 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:67686145 C>T maps to NM_001013838.1 A907A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr16:67681824 G>A maps to NM_001013838.1 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:86617212 T>C maps to NM_024945.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr6:151766441 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr6:151738424 G>A maps to NM_017909.2 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:86979110 C>T maps to NM_022780.3 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr5:177569656 G>A maps to NM_022762.3 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:177565239 G>A maps to NM_022762.3 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr5:177569980 G>A maps to NM_022762.3 E138E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:21269981 G>A maps to NM_198235.2 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:21270044 C>T maps to NM_198235.2 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:21269834 C>T maps to NM_198235.2 E131E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:21269992 G>A maps to NM_198235.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr14:20978696 C>T maps to ENST00000430083 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:20978884 C>T maps to ENST00000430083 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:21052492 C>T maps to NM_145250.3 Q47Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:21502417 G>A maps to NM_001012264.3 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr14:21424313 A>C maps to NM_002934.2 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:21359979 G>A maps to NM_002935.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr14:21167736 C>T maps to NM_194431.1 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr14:21025021 G>A maps to NM_001110361.1 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:21025084 C>T maps to NM_001110361.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:3599845 G>A maps to NM_002936.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:3595538 C>T maps to NM_002936.3 Q252Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr19:12923991 C>T maps to NM_006397.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:12924216 C>T maps to NM_006397.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:182551333 C>A maps to NM_021133.3 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:182555380 G>A maps to NM_021133.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:182550419 G>A maps to NM_021133.3 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:182555077 G>A maps to NM_021133.3 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:182555533 A>G maps to NM_021133.3 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:182544604 G>A maps to NM_021133.3 F716F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:182555608 G>A maps to NM_021133.3 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr5:31526643 G>A maps to NM_013235.4 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:31422942 G>A maps to NM_013235.4 L1124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr5:31405817 C>T maps to NM_013235.4 A1320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:31401631 G>A maps to NM_013235.4 I1344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:31526376 G>A maps to NM_013235.4 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr5:31410871 G>A maps to NM_013235.4 T1216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr5:31521269 G>A maps to NM_013235.4 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:31466344 G>A maps to NM_013235.4 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:31451647 G>A maps to NM_013235.4 L892L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr6:167352438 G>A maps to ENST00000428859 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr6:167343183 G>A maps to ENST00000428859 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:167352426 G>A maps to ENST00000428859 Y184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:167343099 G>A maps to ENST00000428859 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr12:49255803 G>A maps to NM_014470.3 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:49254899 G>A maps to NM_014470.3 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:151326665 A>G maps to NM_005168.3 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr12:120995134 T>C maps to ENST00000458409 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr12:120990330 C>T maps to ENST00000458409 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr12:121000872 G>A maps to ENST00000458409 K418K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr2:86831058 G>A maps to NM_005667.3 G655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr15:59359152 C>T maps to ENST00000434298 H519H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr17:19318162 G>A maps to NM_007148.4 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr17:19317817 G>A maps to NM_007148.4 Q311Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:19319211 G>A maps to NM_007148.4 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:19319265 C>T maps to NM_007148.4 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr13:98828563 C>T maps to NM_178861.4 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:71671825 C>T maps to NM_018320.4 H44H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr8:33406330 G>A maps to NM_024787.2 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr8:33406290 G>A maps to NM_024787.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr8:33416158 G>A maps to NM_024787.2 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:33416194 G>A maps to NM_024787.2 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:49738091 C>T maps to NM_022064.2 I409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr3:49740121 C>T maps to NM_022064.2 I562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr3:49753391 C>T maps to NM_022064.2 F1096F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr3:49749920 C>T maps to NM_022064.2 L836L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr3:49737766 C>T maps to NM_022064.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:49753850 C>T maps to NM_022064.2 P1147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:49751366 C>T maps to NM_022064.2 L954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:49753391 C>T maps to NM_022064.2 F1096F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:49738100 G>A maps to NM_022064.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:49736511 C>T maps to NM_022064.2 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:49743428 C>T maps to NM_022064.2 S773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr3:49737903 G>A did not map to a codon.
Sequencing variant TCGA-RP-A690-06A-11D-A30X-08 chr3:49735488 A>G maps to NM_022064.2 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:29645968 C>T maps to NM_017831.3 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:651690 C>T maps to ENST00000340092 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:106016361 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:106038898 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:105937257 T>G did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:106016277 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:106033471 C>G did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:105970250 C>T did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr23:106034422 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:105937240 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:105937346 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:106016287 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:106016213 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr5:179440118 C>T maps to NM_018434.4 W212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:122338702 G>A maps to NM_139175.1 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:122338480 G>A maps to NM_139175.1 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:122338651 C>T maps to NM_139175.1 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:29325794 G>A maps to NM_032322.3 E295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr17:29326073 C>T maps to NM_032322.3 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:125498513 T>G maps to NM_007218.3 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr8:125499401 A>G maps to NM_007218.3 A504A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr8:125498263 C>A maps to NM_007218.3 S125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:141359746 C>A maps to NM_183399.1 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:10555623 G>A maps to NM_016422.3 R28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr2:7160793 C>T maps to NM_014746.3 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:7137193 T>G did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:7154673 C>T maps to NM_014746.3 H75H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:7160715 C>T maps to NM_014746.3 C138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:18463532 C>T maps to NM_182757.3 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:18465261 G>A maps to NM_182757.3 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:158585992 G>A maps to NM_144726.2 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr5:158601154 T>C maps to NM_144726.2 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:158588570 T>G maps to NM_144726.2 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr6:127607949 T>G maps to ENST00000368314 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:122342399 C>A maps to NM_198085.1 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:122342648 G>A maps to NM_198085.1 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:122342003 G>A maps to NM_198085.1 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:122342351 G>C maps to NM_198085.1 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZU-06A-12D-A196-08 chr7:122342618 G>A maps to NM_198085.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr4:141789474 C>T maps to NM_020724.1 E419E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:142053479 C>T maps to NM_020724.1 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr4:142053554 G>A maps to NM_020724.1 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr4:142053623 G>A maps to NM_020724.1 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:141888926 G>A maps to NM_020724.1 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr4:141889013 G>A maps to NM_020724.1 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr16:2017794 G>A maps to NM_174903.4 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr18:59483680 G>A maps to NM_173557.2 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr18:59483489 G>A maps to NM_173557.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:59483291 G>A maps to NM_173557.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr18:59483681 G>A maps to NM_173557.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr18:59483372 C>T maps to NM_173557.2 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr18:59483342 G>A maps to NM_173557.2 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr18:59483099 C>T maps to NM_173557.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:59483291 G>A maps to NM_173557.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr18:59483666 C>T maps to NM_173557.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:74151702 C>T maps to NM_052916.2 E546E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:74151744 G>A maps to NM_052916.2 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr17:74163763 C>T maps to NM_052916.2 Q137Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:74163760 G>A maps to NM_052916.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:74208525 C>T maps to NM_052916.2 E42E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr21:30330850 G>A maps to NM_015565.2 I914I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr21:30338886 G>A maps to NM_015565.2 V688V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr21:30357189 G>A maps to NM_015565.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr21:30339414 G>A maps to NM_015565.2 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:30316197 G>A maps to NM_015565.2 S1383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr18:44013384 C>T maps to NM_152470.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr18:44013174 G>A maps to NM_152470.2 Q28Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr18:44030273 C>T maps to NM_152470.2 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:44013246 C>T maps to NM_152470.2 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:44015302 C>T maps to NM_152470.2 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr18:44030305 T>C maps to NM_152470.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr18:44030302 C>T maps to NM_152470.2 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr18:44013469 T>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:44015302 C>T maps to NM_152470.2 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:44030680 C>T maps to NM_152470.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:196215510 T>C maps to NM_152617.3 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:196199270 G>A maps to NM_152617.3 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:196199271 G>A maps to NM_152617.3 C378C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:196199337 G>A maps to NM_152617.3 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:74500680 C>T maps to NM_001098638.1 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr13:25356007 G>A maps to ENST00000381927 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr13:25433213 G>A maps to ENST00000381927 W1278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr13:25356013 G>A maps to ENST00000381927 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr13:25418067 G>A maps to ENST00000381927 K979K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr13:25373587 C>T maps to ENST00000381927 I485I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr13:25353860 C>T maps to ENST00000381927 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr13:25362209 G>A maps to ENST00000381927 E232E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr13:25435431 T>G maps to ENST00000381927 T1316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr13:25338386 C>T maps to ENST00000381927 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr13:25356079 C>A maps to ENST00000381927 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr13:25435509 C>T maps to ENST00000381927 L1342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr13:25433137 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr13:25439029 G>A maps to ENST00000381927 W1381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:42725191 G>A maps to NM_030954.3 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:154649357 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr4:154649399 G>A maps to ENST00000274068 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:154649451 C>T maps to ENST00000274068 W103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:154649468 C>T maps to ENST00000274068 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr4:154631607 G>A maps to ENST00000274068 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr2:85824240 C>T maps to NM_016494.3 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:13977772 C>T maps to NM_001165033.1 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:13977520 C>T maps to NM_001165033.1 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr6:13977475 G>A maps to NM_001165033.1 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr9:116060011 C>T maps to NM_145051.3 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:116059999 G>A maps to NM_145051.3 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr9:116060143 G>A maps to NM_145051.3 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr22:31600527 C>T maps to NM_152267.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:31600541 G>A maps to NM_152267.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:20141036 G>A maps to NM_019062.1 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:20140997 G>A maps to NM_019062.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:20141138 G>A maps to NM_019062.1 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:20141285 C>T maps to NM_019062.1 E103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr8:101282221 A>T maps to NM_183419.1 C301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:33402700 G>A maps to NM_153341.2 P635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:33404089 G>A maps to NM_153341.2 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:104309239 C>T maps to NM_019592.5 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:104303237 C>T maps to NM_019592.5 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:104302836 C>T maps to NM_019592.5 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr9:104319878 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:104312958 C>T maps to NM_019592.5 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr1:6273204 C>T maps to NM_207396.2 V538V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr9:140115217 G>A maps to NM_031297.3 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:140115070 G>A maps to NM_031297.3 D198D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr4:1107150 G>A maps to NM_001131034.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr17:78321974 G>A maps to NM_020914.4 A3329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr17:78350123 C>T maps to NM_020914.4 F4452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr17:78325562 C>T maps to NM_020914.4 S3470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr17:78319949 C>T maps to NM_020914.4 I2654I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr17:78320597 C>T maps to NM_020914.4 T2870T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr17:78363957 C>T maps to NM_020914.4 P5193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:78321566 C>T maps to NM_020914.4 P3193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr17:78321332 G>A maps to NM_020914.4 P3115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr17:78272243 G>A maps to NM_020914.4 W761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:78247197 C>T maps to NM_020914.4 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:78362452 A>G maps to NM_020914.4 E5037E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr17:78321959 G>T maps to NM_020914.4 L3324L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A29N-06A-12D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:78321752 C>T maps to NM_020914.4 F3255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:78268714 C>T maps to NM_020914.4 F605F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:78323703 C>T maps to NM_020914.4 V3411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:78337000 C>T maps to NM_020914.4 Q3868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:78318515 C>T maps to NM_020914.4 F2176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:78264461 C>T maps to NM_020914.4 I451I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-FS-A1ZZ-06A-11D-A197-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-FS-A1ZZ-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:78321851 C>T maps to NM_020914.4 P3288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr17:78318782 G>A maps to NM_020914.4 R2265R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-GF-A6C8-06A-12D-A30X-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr17:78326854 T>C maps to NM_020914.4 P3522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:117105017 G>A maps to NM_207343.2 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:117152756 C>T maps to NM_207343.2 Q495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr11:117150914 T>G maps to NM_207343.2 L362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr11:117152665 C>T maps to NM_207343.2 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44Q-06A-11D-A25O-08 chr22:30780393 G>A maps to NM_001017981.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr7:5680975 T>A maps to NM_207111.2 K731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:5662643 G>A maps to NM_207111.2 F873F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr7:5662591 G>A maps to NM_207111.2 L891L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:125379090 C>T maps to NM_152553.2 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr13:79189747 G>A maps to NM_024546.3 S716S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:79189747 G>A maps to NM_024546.3 S716S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr13:79191088 G>A maps to NM_024546.3 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr13:79213014 G>T maps to NM_024546.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:79190700 G>A maps to NM_024546.3 Q399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:45110433 T>C maps to ENST00000453887 D397D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:44878032 C>T maps to ENST00000453887 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:45091970 C>T maps to ENST00000453887 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:44877834 C>T maps to ENST00000453887 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:3915672 C>T maps to NM_001134338.1 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:219528913 G>A maps to NM_022453.2 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:219529153 G>A maps to NM_022453.2 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr2:219532829 G>A maps to NM_022453.2 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr14:24620798 C>T maps to NM_017999.4 Q615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:24618630 C>T maps to NM_017999.4 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr14:24618729 C>T maps to NM_017999.4 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:24621197 C>T maps to NM_017999.4 N709N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:24619979 C>T maps to NM_017999.4 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr14:24619940 C>T maps to NM_017999.4 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr12:121858579 C>T maps to NM_194271.1 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr12:121858570 C>T maps to NM_194271.1 N307N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr9:36390534 G>A maps to NM_022781.4 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:36390466 G>A maps to NM_022781.4 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:30043029 G>A maps to NM_025236.3 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr6:30043512 G>A maps to NM_025236.3 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr4:2515512 C>T maps to NM_002938.4 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr4:2514857 G>A maps to NM_002938.4 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:2515530 C>T maps to NM_002938.4 H186H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr16:30777522 C>T maps to NM_014771.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr16:30779945 C>T maps to NM_014771.2 A662A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:30779803 C>A maps to NM_014771.2 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr16:30783227 C>T maps to NM_014771.2 I887I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr16:30783228 C>T maps to NM_014771.2 Q888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr16:30785433 G>A maps to NM_014771.2 *1002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr16:30774531 C>T maps to NM_014771.2 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:56432330 G>A maps to NM_017763.4 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr17:56434904 A>T maps to NM_017763.4 P744P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr17:56435449 G>A maps to NM_017763.4 Q563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:56435834 G>A maps to NM_017763.4 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr17:56435717 G>A maps to NM_017763.4 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr17:56435407 G>A maps to NM_017763.4 Q577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:56436014 G>A maps to NM_017763.4 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:175957084 G>A maps to NM_014901.4 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr5:175958547 G>A maps to NM_014901.4 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr13:26788125 G>A maps to NM_005977.3 I631I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr13:26788620 C>T maps to NM_005977.3 R466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr13:26789090 G>A maps to NM_005977.3 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr6:37358612 G>A maps to NM_183078.2 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:37349113 C>T maps to NM_003958.3 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr6:37336895 C>T maps to NM_003958.3 Q293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:37328277 C>T maps to NM_003958.3 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:58034686 G>A maps to NM_016125.3 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr12:117271706 C>T maps to NM_001109903.1 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr12:117187909 C>T maps to NM_001109903.1 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr12:117273829 G>A maps to NM_001109903.1 Q366Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr12:117217065 C>T maps to NM_001109903.1 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:117187936 C>T maps to NM_001109903.1 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr12:117217092 C>T maps to NM_001109903.1 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:117191864 G>A maps to NM_001109903.1 K209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:117271694 C>T maps to NM_001109903.1 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:89559542 C>T maps to NM_003800.3 E345E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:502131 G>A maps to NM_203389.1 Q11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr10:90332735 G>A maps to NM_001031709.2 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr10:90034756 C>T maps to NM_018363.3 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr10:90074234 C>T maps to NM_001031709.2 W288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr10:90074235 C>T maps to NM_001031709.2 W288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr10:90074263 G>A maps to NM_001031709.2 Q279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr10:90034767 G>A maps to NM_018363.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr18:13742547 C>T maps to NM_003799.1 Q346*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D3-A5GO-06A-12D-A27K-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:694831 G>A maps to NM_018146.2 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:695283 T>A maps to NM_018146.2 L413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:695155 C>T maps to NM_018146.2 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:104093652 G>A maps to NM_017619.3 K484K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:201970809 C>T maps to NM_020216.3 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:201972422 C>T maps to NM_020216.3 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:201970810 C>T maps to NM_020216.3 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr1:201970887 C>T maps to NM_020216.3 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr1:201970857 C>T maps to NM_020216.3 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:241514989 C>T maps to NM_018226.3 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:241516376 C>T maps to NM_018226.3 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr2:241513565 C>T maps to NM_018226.3 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:241516007 C>T maps to NM_018226.3 L292L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D3-A2JL-06A-11D-A196-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-ER-A19M-06A-61D-A23B-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr16:2305680 G>A maps to ENST00000454671 Q141Q. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-FW-A3R5-06A-11D-A23B-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:78656093 G>A maps to NM_002941.3 L1511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr3:78766485 G>A maps to NM_002941.3 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:78734983 G>A maps to NM_002941.3 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:78710395 G>A maps to NM_002941.3 Q702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr3:78663873 G>A maps to NM_002941.3 A1453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr3:79174651 C>T maps to NM_002941.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:78695311 G>A maps to NM_002941.3 V956V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr3:78684947 G>A maps to NM_002941.3 I1116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:77599976 T>C maps to ENST00000332191 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr3:77684172 C>T maps to ENST00000332191 R1366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:77147246 G>A maps to ENST00000332191 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr3:77614212 G>A maps to ENST00000332191 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:77599979 C>T maps to ENST00000332191 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr3:77147192 C>T maps to ENST00000332191 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr3:77666721 C>T maps to ENST00000332191 L1118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:77147228 C>T maps to ENST00000332191 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:77612435 C>T maps to ENST00000332191 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr3:77684108 G>A maps to ENST00000332191 Q1344Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr3:77656952 G>A maps to ENST00000332191 G1047G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr3:77607239 G>T maps to ENST00000332191 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:77656967 G>A maps to ENST00000332191 K1052K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:77530251 C>T maps to ENST00000332191 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr3:77600110 T>A maps to ENST00000332191 L401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr3:77147225 C>T maps to ENST00000332191 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:77607173 G>A maps to ENST00000332191 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:77644300 C>T maps to ENST00000332191 Q898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr3:77626766 T>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:124744068 C>T maps to NM_022370.3 R630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:124745038 C>T maps to NM_022370.3 F702F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:124747938 C>T maps to NM_022370.3 T1031T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:124740917 C>T maps to NM_022370.3 Q348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:124750326 C>T maps to NM_022370.3 L1324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:124749732 C>T maps to NM_022370.3 L1283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:124740158 C>T maps to NM_022370.3 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:124743204 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:124750347 C>T maps to NM_022370.3 F1331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:124757689 G>A maps to NM_019055.5 S665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:124766555 C>T maps to NM_019055.5 E137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:124756537 G>A maps to NM_019055.5 S872S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr11:124761258 C>T maps to NM_019055.5 R628R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr11:124761447 C>T maps to NM_019055.5 W565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:124756396 G>A maps to NM_019055.5 F919F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr18:18586523 G>T maps to NM_005406.2 S558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr18:18539835 C>T maps to NM_005406.2 K1159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr18:18625311 G>A maps to NM_005406.2 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:11367398 G>A maps to NM_004850.3 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:11389843 G>A maps to NM_004850.3 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:11333967 G>A maps to NM_004850.3 V1208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:11376072 G>A maps to NM_004850.3 Q160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:11367398 G>A maps to NM_004850.3 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr9:114989799 G>A maps to NM_001163790.1 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:114989823 G>T maps to NM_001163790.1 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:114990731 G>A maps to NM_001163790.1 R390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr16:4847479 C>T maps to NM_024589.1 W282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:62380860 C>A maps to NM_000327.3 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:123699271 C>T maps to NM_017578.2 K19K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:125690938 G>A maps to NM_001012337.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr5:10442314 G>A maps to NM_031916.3 Q12Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr1:64515470 G>A maps to NM_005012.2 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:64608151 G>A maps to NM_005012.2 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:64515361 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:64605948 G>A maps to NM_005012.2 E256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:64474975 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:64605942 C>T maps to NM_005012.2 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:64643412 C>T maps to NM_005012.2 F563F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:64644096 C>T maps to NM_005012.2 F791F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:64644339 C>T maps to NM_005012.2 P872P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:64643821 G>T maps to NM_005012.2 E700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr9:94486933 C>T maps to NM_004560.2 K614K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CE-06A-11D-A19A-08 chr9:94486903 G>A maps to NM_004560.2 Y624Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr9:94499739 G>A maps to NM_004560.2 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr9:94538089 C>T maps to NM_004560.2 E36E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr9:94493195 C>T maps to NM_004560.2 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr9:94486684 G>A maps to NM_004560.2 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:94538028 G>A maps to NM_004560.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr9:94486978 G>A maps to NM_004560.2 I599I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr9:94486783 G>A maps to NM_004560.2 I664I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr9:94486999 G>A maps to NM_004560.2 F592F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr9:94487017 G>A maps to NM_004560.2 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:94493351 G>A maps to NM_004560.2 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr9:94499760 C>T maps to NM_004560.2 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr9:94499760 C>T maps to NM_004560.2 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr9:94487359 C>T maps to NM_004560.2 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr9:94488954 G>A maps to NM_004560.2 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr9:94493273 G>A maps to NM_004560.2 N367N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:94486954 G>A maps to NM_004560.2 S607S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:94486387 G>A maps to NM_004560.2 F796F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:60919494 G>A maps to NM_134260.2 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:60970871 C>T maps to NM_134261.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:60806937 G>A maps to NM_134260.2 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr15:60970871 C>T maps to NM_134261.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr9:77245240 C>T maps to ENST00000396204 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:77249569 G>A maps to ENST00000396204 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:77282746 G>A maps to ENST00000396204 K358K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:77257393 C>T maps to ENST00000396204 H111H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr9:77277466 G>A maps to ENST00000396204 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:77257717 C>T maps to ENST00000396204 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:77275560 C>G maps to ENST00000396204 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr9:77277427 C>T maps to ENST00000396204 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:77257577 C>T maps to ENST00000396204 Q173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:77282722 G>A maps to ENST00000396204 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:77286781 C>T maps to ENST00000396204 Q408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:77300425 G>C maps to ENST00000396204 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:77257729 C>T maps to ENST00000396204 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:151787049 C>T maps to ENST00000392697 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:151804201 C>T maps to NM_005060.3 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:151786027 G>A maps to ENST00000392697 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:151787563 C>T maps to ENST00000392697 E266E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:151787076 C>T maps to ENST00000392697 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:151780049 G>A maps to ENST00000392697 I539I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-ER-A19P-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:151789721 C>T maps to ENST00000392697 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:151804201 C>T maps to NM_005060.3 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr6:117678017 G>A maps to NM_002944.2 I1305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr6:117709078 G>A maps to NM_002944.2 F626F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:117632190 G>A maps to NM_002944.2 F2075F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr6:117724338 G>A maps to NM_002944.2 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr6:117710684 G>A maps to NM_002944.2 I529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr6:117709093 T>C maps to NM_002944.2 E621E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr6:117686902 C>T maps to NM_002944.2 G938G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:117662561 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:117662562 C>T maps to NM_002944.2 K1634K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:117718259 C>T maps to NM_002944.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:117687278 A>G maps to NM_002944.2 N924N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr6:117686902 C>T maps to NM_002944.2 G938G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:117674321 G>A maps to NM_002944.2 T1384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr6:117609789 C>T maps to NM_002944.2 R2303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr6:117710786 G>A maps to NM_002944.2 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:117730772 C>T maps to NM_002944.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:117679002 G>T maps to NM_002944.2 S1273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr6:117710684 G>A maps to NM_002944.2 I529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:117700223 C>T maps to NM_002944.2 Q865Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr6:117609819 G>A maps to NM_002944.2 G2293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr6:117686845 C>T maps to NM_002944.2 R957R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr6:117639382 C>T maps to NM_002944.2 K1991K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:117639385 C>T maps to NM_002944.2 E1990E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:117632190 G>A maps to NM_002944.2 F2075F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:117708142 G>A maps to NM_002944.2 I678I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr6:117609900 C>T maps to NM_002944.2 T2266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:55542843 C>T maps to NM_006269.1 F2134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr8:55537353 G>A maps to NM_006269.1 K304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr8:55537743 C>T maps to NM_006269.1 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr8:55534023 G>A maps to NM_006269.1 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr8:55539789 C>T maps to NM_006269.1 P1116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr8:55537464 A>T maps to NM_006269.1 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr8:55542156 C>T maps to NM_006269.1 D1905D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr8:55540309 C>T maps to NM_006269.1 Q1290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:55540719 G>A maps to NM_006269.1 R1426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:55541856 C>T maps to NM_006269.1 L1805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr8:55538457 G>A maps to NM_006269.1 K672K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr8:55533702 C>T maps to NM_006269.1 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr8:55533885 C>T maps to NM_006269.1 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr8:55539603 G>A maps to NM_006269.1 Q1054Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr8:55534056 C>A maps to NM_006269.1 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:55539816 C>T maps to NM_006269.1 S1125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:55540719 G>A maps to NM_006269.1 R1426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:55541394 C>T maps to NM_006269.1 T1651T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:55542525 G>A maps to NM_006269.1 L2028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr8:55542493 G>T maps to NM_006269.1 E2018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr8:55537821 G>A maps to NM_006269.1 K460K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr8:55534032 G>C maps to NM_006269.1 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:55538220 G>A maps to NM_006269.1 K593K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr8:55539178 C>T maps to NM_006269.1 Q913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr8:55538106 G>A maps to NM_006269.1 Q555Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr8:55533669 C>T maps to NM_006269.1 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:55542351 G>A maps to NM_006269.1 E1970E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr8:55540287 T>C maps to NM_006269.1 P1282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr8:55542624 C>T maps to NM_006269.1 I2061I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:55533780 C>T maps to NM_006269.1 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:55534688 C>T maps to NM_006269.1 Q210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:55537639 C>T maps to NM_006269.1 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:55540221 G>A maps to NM_006269.1 E1260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr8:55541964 C>T maps to NM_006269.1 T1841T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:55538364 A>G maps to NM_006269.1 R641R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:55540335 C>T maps to NM_006269.1 F1298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr8:55541532 G>A maps to NM_006269.1 Q1697Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr8:55540770 G>A maps to NM_006269.1 R1443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr8:55541856 C>T maps to NM_006269.1 L1805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr8:55537497 T>C maps to NM_006269.1 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr8:55541404 C>T maps to NM_006269.1 Q1655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr8:55542423 C>T maps to NM_006269.1 F1994F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:55541478 A>G maps to NM_006269.1 S1679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr8:55540335 C>T maps to NM_006269.1 F1298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr8:55538613 G>A maps to NM_006269.1 G724G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr8:55541973 G>A maps to NM_006269.1 K1844K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:55542051 C>T maps to NM_006269.1 S1870S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr8:55541829 G>A maps to NM_006269.1 T1796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:55534822 A>T maps to NM_006269.1 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:55537743 C>T maps to NM_006269.1 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:55538256 C>T maps to NM_006269.1 F605F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:55540726 C>T maps to NM_006269.1 Q1429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:55542279 C>T maps to NM_006269.1 F1946F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr8:55542054 T>C maps to NM_006269.1 F1871F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:55539936 G>A maps to NM_006269.1 E1165E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:55540335 C>T maps to NM_006269.1 F1298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:55540347 C>T maps to NM_006269.1 V1302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:55542279 C>T maps to NM_006269.1 F1946F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:55540719 G>A maps to NM_006269.1 R1426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr8:55538745 C>T maps to NM_006269.1 S768S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr8:55542279 C>T maps to NM_006269.1 F1946F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr8:10467848 T>C maps to NM_178857.5 Q1253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr8:10466090 C>T maps to NM_178857.5 E1839E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr8:10470536 G>A maps to NM_178857.5 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:10467098 G>A maps to NM_178857.5 S1503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:10480351 C>T maps to NM_178857.5 Q120Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:10469795 C>T maps to NM_178857.5 A604A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr8:10469090 C>T maps to NM_178857.5 R839R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:10470383 C>T maps to NM_178857.5 W408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr8:10465898 T>C maps to NM_178857.5 S1903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr8:10467029 C>T maps to NM_178857.5 T1526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:10469042 G>A maps to NM_178857.5 T855T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:10470275 C>T maps to NM_178857.5 G444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:10466651 C>T maps to NM_178857.5 E1652E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr8:10468037 C>T maps to NM_178857.5 T1190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr8:10469081 G>A maps to NM_178857.5 S842S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:10464761 G>A maps to NM_178857.5 S2282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:10469453 G>A maps to NM_178857.5 N718N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:10470220 C>A maps to NM_178857.5 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr8:10466675 C>T maps to NM_178857.5 G1644G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:10467707 C>T maps to NM_178857.5 E1300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:10467482 C>T maps to NM_178857.5 E1375E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:10466081 C>T maps to NM_178857.5 G1842G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:10470176 C>T maps to NM_178857.5 E477E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:10467497 C>T maps to NM_178857.5 E1370E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:10468595 C>T maps to NM_178857.5 G1004G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:10467863 C>T maps to NM_178857.5 G1248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:10480252 C>T maps to NM_178857.5 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr8:10469315 C>T maps to NM_178857.5 G764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr8:10465157 G>A maps to NM_178857.5 A2150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr8:10466594 G>A maps to NM_178857.5 S1671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr8:10465298 G>A maps to NM_178857.5 A2103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr8:10469462 G>A maps to NM_178857.5 A715A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr8:10470641 G>A maps to NM_178857.5 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr8:10464635 C>T maps to NM_178857.5 R2324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:10465834 G>A maps to NM_178857.5 L1925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:10465376 C>T maps to NM_178857.5 E2077E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:10467746 C>T maps to NM_178857.5 S1287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:10480585 C>T maps to NM_178857.5 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr8:10470145 G>A maps to NM_178857.5 Q488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:46719517 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:46713159 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:7676669 G>A maps to NM_002947.3 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:7676678 G>A maps to NM_002947.3 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr23:96140064 G>A did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:96139469 T>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:96140056 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:96139536 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr15:41814313 G>A maps to NM_015540.2 L959L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr15:41813124 G>A maps to NM_015540.2 L1087L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr15:41819161 G>A maps to NM_015540.2 P617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr15:41829308 C>T maps to NM_015540.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:41819266 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr15:41820201 G>A maps to NM_015540.2 D428D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr15:41812678 G>C maps to NM_015540.2 P1235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:41819638 G>A maps to NM_015540.2 A531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:41817241 G>A maps to NM_015540.2 A674A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr1:92789401 T>C maps to NM_024813.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:92798970 A>T maps to NM_024813.2 I493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:92798991 G>A maps to NM_024813.2 Q500Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:48062755 G>A maps to NM_024604.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:68905281 G>A maps to NM_000329.2 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:68904734 C>T maps to NM_000329.2 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:68905293 G>A maps to NM_000329.2 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:68905296 C>T maps to NM_000329.2 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:68910228 C>T maps to NM_000329.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:68897193 G>A maps to NM_000329.2 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:68905293 G>A maps to NM_000329.2 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:68910517 G>A maps to NM_000329.2 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:68912535 G>A maps to NM_000329.2 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:84961717 C>A maps to NM_025065.6 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:111345391 G>C maps to NM_032194.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr6:111346628 C>T maps to NM_032194.1 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:38128893 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:38150237 T>G did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:38129038 T>G did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:38147242 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr23:38132688 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:38156588 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:38146213 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:38150210 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:38150211 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:38128989 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:38146055 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr14:21790020 G>A maps to NM_020366.3 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr14:21792936 C>T maps to NM_020366.3 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr14:21794026 G>A maps to NM_020366.3 W802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr14:21794282 C>T maps to NM_020366.3 G887G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:21762903 C>T maps to NM_020366.3 R52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr14:21796671 G>A maps to NM_020366.3 K995K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr14:21796665 G>A maps to NM_020366.3 K993K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:21793122 A>C maps to NM_020366.3 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:21795947 G>A maps to NM_020366.3 K959K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:21789446 G>A maps to NM_020366.3 K499K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr14:21793426 G>A maps to NM_020366.3 W751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:53691511 G>A maps to NM_015272.2 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr16:53672323 C>A did not map to a codon.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr16:53679726 G>A maps to NM_015272.2 P831P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:113321159 C>T maps to NM_001143854.1 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr12:113303248 G>A maps to NM_001143854.1 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr12:113306308 G>A maps to NM_001143854.1 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:113266160 G>A maps to NM_001143854.1 W13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:113266161 G>A maps to NM_001143854.1 W13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:113321147 G>A maps to NM_001143854.1 W459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:113306308 G>A maps to NM_001143854.1 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:113333678 G>C did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr12:113333613 G>A maps to NM_001143854.1 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:113327842 G>A maps to NM_001143854.1 G526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:113285536 G>A maps to NM_001143854.1 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:113303251 G>A maps to NM_001143854.1 K88K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:113306317 G>A maps to NM_001143854.1 K176K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr17:169210 C>T maps to NM_006987.3 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:131579 C>T maps to NM_006987.3 K139K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr17:177277 C>T maps to NM_006987.3 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr2:89036099 C>T maps to NM_144563.2 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:89049513 C>T maps to NM_144563.2 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:89049514 C>T maps to NM_144563.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr2:89049588 C>T maps to NM_144563.2 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:153628231 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:153628952 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr23:153628211 A>T did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr23:153628212 T>C did not map to a codon.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr23:153628161 T>C did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr14:47120417 C>T maps to NM_080746.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr14:47120417 C>T maps to NM_080746.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:47120417 C>T maps to NM_080746.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr14:47120738 G>A maps to NM_080746.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr1:24022388 C>T maps to NM_000975.3 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr1:24022389 C>T maps to NM_000975.3 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:49995047 C>T maps to NM_012423.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:49993504 C>T maps to NM_012423.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr19:49993747 C>T maps to NM_012423.2 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:49994102 C>T maps to NM_012423.2 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr18:47014930 G>A maps to NM_001035006.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr18:47015806 G>A maps to NM_001035006.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:49119188 G>A maps to NM_000979.2 R146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr19:49120619 A>G maps to NM_000979.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:49119387 G>A maps to NM_000979.2 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:49120584 G>A maps to NM_000979.2 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr19:17972139 C>T maps to NM_000980.2 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:17972994 C>T maps to NM_000980.2 Y97Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:101399993 A>T maps to NM_000986.3 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:172395529 C>T maps to NM_016093.2 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:55899331 C>T maps to NM_001136135.1 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr22:39713524 G>A maps to NM_000967.3 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr22:39712779 C>T maps to NM_000967.3 K144K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr3:12880912 G>C maps to ENST00000273223 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:109546298 C>T maps to NM_033625.2 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr3:197680973 C>T maps to NM_000996.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr14:50085801 G>A maps to NM_001001.3 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:118923890 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:118923941 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr16:1996724 G>A maps to NM_005061.2 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:1997206 G>A maps to NM_005061.2 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr16:1997297 G>A maps to NM_005061.2 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr15:66792662 G>A maps to NM_000968.2 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:66793833 G>A maps to NM_000968.2 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:66795834 G>A maps to NM_000968.2 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:93298954 A>T maps to NM_000969.3 K5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:93303030 T>G maps to NM_000969.3 G182G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-FW-A3R5-06A-11D-A23B-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:93303019 C>T maps to NM_000969.3 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr12:112846076 G>A maps to NM_001024662.1 N101N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:112843767 G>A maps to NM_001024662.1 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr12:112846061 C>T maps to NM_001024662.1 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr12:112843835 G>A maps to NM_001024662.1 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:74204119 G>A maps to ENST00000396470 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr6:42851232 C>T maps to NM_198486.2 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr6:42853783 C>T maps to NM_198486.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr8:146017188 G>A maps to NM_000973.3 H83H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr8:146017430 G>C maps to NM_000973.3 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:146015847 C>A maps to NM_000973.3 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:146016824 G>A maps to NM_000973.3 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr4:39458101 G>A maps to NM_000661.4 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr4:39456225 G>A maps to NM_000661.4 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr3:128344385 G>A maps to NM_002950.3 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr3:128339277 G>A maps to NM_002950.3 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr20:35865052 C>T maps to NM_002951.3 I608I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:35854135 C>T maps to NM_002951.3 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr20:35833180 T>G maps to NM_002951.3 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:35812602 T>C maps to NM_002951.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr20:35835687 C>T maps to NM_002951.3 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:35838556 C>T maps to NM_002951.3 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:35860727 C>T maps to NM_002951.3 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:58296240 C>T maps to NM_007042.3 Q29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:58296100 C>T maps to NM_007042.3 N15N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:4996297 G>A maps to NM_006638.2 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:4996508 G>A maps to NM_006638.2 C235C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr6:4995313 A>T maps to NM_006638.2 *364K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr18:33610770 C>T maps to NM_018170.3 Q162Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:150430041 C>T maps to NM_015203.3 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:150443548 C>T maps to NM_015203.3 Q709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:150445224 C>T maps to NM_015203.3 F1267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:150337309 C>T maps to NM_015203.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:150445245 C>T maps to NM_015203.3 P1274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:150443484 A>G maps to NM_015203.3 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:150444237 C>T maps to NM_015203.3 F938F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:150445428 C>T maps to NM_015203.3 T1335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:150437133 G>T maps to NM_015203.3 E515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr1:150443425 C>T maps to NM_015203.3 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:150444873 C>T maps to NM_015203.3 S1150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:50000829 C>T maps to NM_001015.3 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:17096726 G>A maps to NM_001017.2 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr5:149826384 G>A maps to NM_005617.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:149826384 G>A maps to NM_005617.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:1440439 C>T maps to NM_001018.3 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q9-06A-11D-A19A-08 chr19:39924008 A>G maps to NM_001020.4 Y115Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr19:39924332 C>T maps to NM_001020.4 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:33244017 C>T maps to NM_022551.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:33244212 C>T maps to NM_022551.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr6:33243638 G>A maps to NM_022551.2 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr6:33243593 T>G maps to NM_022551.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr19:42373236 C>T maps to NM_001022.3 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr16:2012880 G>A maps to NM_002952.3 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:2012221 G>A maps to NM_002952.3 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr8:56985768 G>A maps to NM_001146227.1 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr20:60963366 T>G maps to NM_001024.3 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:81573551 C>A maps to NM_001025.4 G42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr11:75115749 C>T maps to NM_001005.3 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:75115201 T>C maps to NM_001005.3 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:152024150 C>T maps to NM_001006.3 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr24:2712176 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr24:22942836 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr24:22930723 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr24:22923204 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr24:22921929 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr24:22942836 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:58899605 C>T maps to NM_001009.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:58904808 G>A maps to NM_001009.3 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:26881655 G>A maps to NM_001006665.1 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:26887600 C>T maps to NM_001006665.1 H478H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:26898005 C>T maps to NM_001006665.1 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:26877900 C>T maps to NM_001006665.1 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:26877925 C>T maps to NM_001006665.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr1:26888048 G>A maps to NM_001006665.1 G504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr1:26885409 C>T maps to NM_001006665.1 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr1:26873440 C>T maps to NM_001006665.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:26877948 C>T maps to NM_001006665.1 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr6:166923789 G>A maps to ENST00000510118 H143H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:166912058 G>A maps to ENST00000510118 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr6:166944750 G>A maps to ENST00000510118 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:20174289 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:20252887 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:20206022 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:20181083 G>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:20181109 C>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr23:20211669 T>C did not map to a codon.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr23:20212369 C>T did not map to a codon.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr11:64138131 C>T maps to NM_003942.2 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:64138786 C>T maps to NM_003942.2 F718F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:64137217 C>T maps to NM_003942.2 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr11:64128626 C>T maps to NM_003942.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:64137229 C>T maps to NM_003942.2 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr23:83419361 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr23:83320108 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr23:83400548 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:83352834 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr23:83419354 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr23:83419355 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:83361436 A>G did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:83390149 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:83400518 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:83372092 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:83319408 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:83360881 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr23:83400548 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr23:83374902 C>G did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:83400544 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:83400548 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:83374993 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:83359607 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr23:83351246 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:83351311 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:83319311 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr23:83319311 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:83371239 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr23:83319401 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:83352840 C>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:83320118 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:83362657 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:83411175 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr23:83402012 G>A did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr23:83402022 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:83360864 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:83361967 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:83411175 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:83319289 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:83320118 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:83400548 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr11:67200854 C>T maps to NM_003952.2 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:213303011 G>C maps to NM_012424.3 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr1:213341252 C>T maps to NM_012424.3 Y296Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr1:213290685 T>C maps to NM_012424.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:213415275 C>T maps to NM_012424.3 F819F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr14:75376522 C>T maps to NM_031464.3 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:75376363 C>T maps to NM_031464.3 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr14:75377987 G>A maps to NM_031464.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:3624081 T>A maps to NM_001011.3 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:54710249 C>T maps to NM_001013.3 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:39449164 C>T maps to ENST00000443003 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:39449165 C>T maps to ENST00000443003 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:152129437 T>G did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr1:152127414 C>T maps to NM_001122965.1 E720E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr1:152128263 G>A maps to NM_001122965.1 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:152129265 C>T maps to NM_001122965.1 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr1:152130302 C>T maps to NM_001122965.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:152129382 G>A maps to NM_001122965.1 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr1:152127471 C>T maps to NM_001122965.1 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:152127504 C>T maps to NM_001122965.1 Q690Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:152128680 C>T maps to NM_001122965.1 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr17:78867522 G>A maps to NM_020761.2 A753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr17:78921038 G>A maps to NM_020761.2 W1051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr17:78899216 C>T maps to NM_020761.2 S952S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr17:78919515 C>T maps to NM_020761.2 V1025V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:78796093 C>T maps to NM_020761.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:78897295 C>T maps to NM_020761.2 S877S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:78919515 C>T maps to NM_020761.2 V1025V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr17:78820343 C>T maps to NM_020761.2 N428N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:78931466 C>T maps to NM_020761.2 L1138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:78933888 G>A maps to NM_020761.2 T1163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZY-06A-11D-A197-08 chr17:78882719 C>T maps to NM_020761.2 I837I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr15:40861739 C>T maps to NM_152260.1 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:40865982 C>T maps to NM_152260.1 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:9881916 C>T maps to NM_173659.3 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:9879873 G>A maps to NM_173659.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:126081382 G>A maps to NM_032795.2 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:126081383 G>A maps to NM_032795.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr2:219447743 C>T maps to NM_005444.1 H85H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:66957470 G>A maps to NM_004165.2 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:66957428 G>A maps to NM_004165.2 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr16:66956002 G>A maps to NM_004165.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr9:19049677 G>A maps to NM_006570.4 K7K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr23:55783667 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:55779872 G>A did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:55783758 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:39318075 G>A maps to NM_022157.2 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr19:50139923 G>A maps to NM_006270.3 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:14303158 G>A maps to NM_012250.5 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr20:17640671 G>A maps to ENST00000377813 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr20:17640801 G>A maps to ENST00000377813 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:17614115 G>A maps to ENST00000377813 L867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:17614116 G>A maps to ENST00000377813 V866V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:7229543 C>T maps to NM_001003699.3 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr6:7231148 C>T maps to NM_001003699.3 I939I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr6:7230383 C>T maps to NM_001003699.3 A684A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:7230848 T>C maps to NM_001003699.3 A839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:7231631 T>G maps to NM_001003699.3 A1100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:7231874 C>T maps to NM_001003699.3 I1181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr6:7229399 C>T maps to NM_001003699.3 D356D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr6:7231901 C>G maps to NM_001003699.3 T1190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:7231085 C>T maps to NM_001003699.3 S918S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr6:7231371 C>T maps to NM_001003699.3 L1014L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:7230452 C>T maps to NM_001003699.3 P707P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr6:7229426 C>T maps to NM_001003699.3 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr6:7230143 C>T maps to NM_001003699.3 A604A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr6:7231124 C>T maps to NM_001003699.3 S931S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr4:110763635 C>T maps to NM_006583.2 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:110763651 C>T maps to NM_006583.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr11:4153576 C>T maps to NM_001033.3 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:4139664 C>A maps to NM_001033.3 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:10263533 C>T maps to NM_001165931.1 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:10264845 G>A maps to NM_001165931.1 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr2:10263897 C>T maps to NM_001165931.1 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr8:103238241 G>A maps to NM_015713.4 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:103244403 T>C maps to NM_015713.4 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr16:15166833 G>A maps to NM_018427.3 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr21:45211306 C>T maps to NM_003683.5 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr21:45213218 C>T maps to NM_003683.5 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr21:45217383 C>T maps to NM_003683.5 H168H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr21:45215095 C>T maps to NM_003683.5 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:99148128 C>T maps to NM_015179.3 K299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:99126518 G>T maps to NM_015179.3 P1065P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:99126653 C>A maps to NM_015179.3 V1020V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr10:99126317 G>A maps to NM_015179.3 S1092S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:99141233 G>A maps to NM_015179.3 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:99153490 G>A maps to NM_015179.3 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr10:99126638 G>A maps to NM_015179.3 P1025P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr10:99126524 C>T maps to NM_015179.3 E1063E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr10:99130478 G>A maps to NM_015179.3 I859I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:218475768 C>T maps to NM_016052.3 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr21:45107443 C>T maps to NM_015056.2 Q397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr21:45107455 A>C maps to NM_015056.2 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr21:45096181 C>T maps to NM_015056.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr21:45094998 C>T maps to NM_015056.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr21:45089807 C>T maps to NM_015056.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr21:45094542 C>T maps to NM_015056.2 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr21:45107922 G>A maps to NM_015056.2 E556E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr22:42912124 G>A maps to NM_015703.4 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr22:42908927 G>A maps to NM_015703.4 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:51969226 G>A maps to NM_004704.3 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr3:51971265 G>A maps to NM_004704.3 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:51967752 G>A maps to NM_004704.3 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:51968489 G>A maps to NM_004704.3 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr3:51971238 G>A maps to NM_004704.3 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr3:51968671 G>A maps to NM_004704.3 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:51969368 G>A maps to NM_004704.3 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr23:18674877 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr23:18674878 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:18660156 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr23:18662559 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:18674774 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:48557288 C>T maps to NM_018346.1 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:48559708 C>T maps to NM_018346.1 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:48559765 C>T maps to NM_018346.1 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:48559687 C>T maps to NM_018346.1 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr17:48559549 C>T maps to NM_018346.1 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:48559732 C>T maps to NM_018346.1 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:7023634 G>A maps to NM_080657.4 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:114320370 G>A maps to NM_018364.3 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:114308957 G>A maps to NM_018364.3 Q685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr7:77402514 C>T maps to NM_198467.2 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZU-06A-12D-A196-08 chr7:77325803 C>T maps to NM_198467.2 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:15987430 G>A maps to NM_006511.1 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr11:77412869 C>T maps to NM_016578.3 K468K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:77387985 A>T maps to NM_016578.3 S1064S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:77411875 T>A maps to NM_016578.3 R800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr11:77409716 G>A maps to NM_016578.3 R844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:77458146 C>T maps to NM_016578.3 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:77411804 C>T maps to NM_016578.3 L823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:77402211 G>A maps to NM_016578.3 A964A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr11:77383159 G>A maps to NM_016578.3 S1226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:77412965 A>G maps to NM_016578.3 H436H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:77451870 G>T maps to NM_016578.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:77409716 G>A maps to NM_016578.3 R844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr11:77436739 G>A maps to NM_016578.3 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:77409716 G>A maps to NM_016578.3 R844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr16:11931673 G>T maps to NM_015659.2 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr21:43897452 G>A maps to NM_080860.2 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr21:43913093 G>A maps to NM_080860.2 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr21:43897467 C>T maps to NM_080860.2 W220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr21:43905787 C>T maps to NM_080860.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:5966179 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:5966148 C>T maps to NM_173565.3 E821E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:5967998 G>A maps to NM_173565.3 R754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr7:6797535 C>T maps to NM_173565.3 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:6820487 G>A maps to NM_173565.3 E526E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr7:6797550 C>T maps to NM_173565.3 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr7:6820505 C>T maps to NM_173565.3 A532A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr6:159403527 G>T maps to NM_031924.4 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr6:159398872 G>A maps to NM_031924.4 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:159420879 C>T maps to NM_031924.4 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:116943957 C>T maps to NM_001010892.2 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:116944107 G>A maps to NM_001010892.2 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr6:116938277 G>A maps to NM_001010892.2 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr6:116949432 T>C maps to NM_001010892.2 N521N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:116938430 G>A maps to NM_001010892.2 K215K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:46307761 G>A maps to NM_030785.3 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr19:46313905 C>T maps to NM_030785.3 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:46299342 G>A maps to NM_030785.3 I646I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:46307584 G>A maps to NM_030785.3 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:46307794 C>T maps to NM_030785.3 K456K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:46307917 G>A maps to NM_030785.3 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:46308181 G>A maps to NM_030785.3 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr19:46307995 C>T maps to NM_030785.3 E389E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:46308271 C>T maps to NM_030785.3 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:46307540 C>T maps to NM_030785.3 W541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr6:43623366 C>T maps to NM_152732.4 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr6:43623378 C>T maps to NM_152732.4 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:38078483 C>T maps to NM_001038633.2 Q245Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:38079493 C>T maps to NM_001038633.2 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:38078579 C>T maps to NM_001038633.2 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:38079994 G>A maps to NM_001038633.2 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:38078504 G>A maps to NM_001038633.2 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:38082189 G>A maps to NM_001038633.2 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z4-06A-11D-A197-08 chr1:38082348 T>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:38078450 T>C maps to NM_001038633.2 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:38078543 C>T maps to NM_001038633.2 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:108970356 G>A maps to NM_178565.4 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr8:108913383 G>A maps to NM_178565.4 N217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr8:108970341 C>T maps to NM_178565.4 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr8:109001380 G>A maps to NM_178565.4 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr6:127517110 C>T maps to ENST00000368317 Q260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:944608 C>T maps to NM_001029871.3 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:944608 C>T maps to NM_001029871.3 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:944707 C>T maps to NM_001029871.3 K155K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:57238584 T>G maps to NM_133368.1 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:57238575 C>T maps to NM_133368.1 I2I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:57269051 C>T maps to NM_133368.1 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr16:57272874 T>C maps to NM_133368.1 S573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr16:57238575 C>T maps to NM_133368.1 I2I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr3:158262012 G>A maps to NM_016625.2 K318K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:12945610 G>A maps to NM_031429.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:12939477 G>A maps to NM_031429.1 Q152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:12939478 G>A maps to NM_031429.1 C151C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:12939535 G>A maps to NM_031429.1 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr22:23476222 C>T maps to NM_014433.2 Q137Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr22:23401669 G>A maps to NM_014433.2 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr22:23401894 C>T maps to NM_014433.2 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr22:23406135 G>A maps to NM_014433.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr22:23403993 G>A maps to NM_014433.2 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr22:23401774 C>T maps to NM_014433.2 E304E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:23406207 C>T maps to NM_014433.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr20:62316916 C>T maps to ENST00000482936 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr20:62298827 C>T maps to ENST00000482936 C207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr20:62321442 C>T maps to ENST00000482936 F715F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:62324550 C>T maps to ENST00000482936 I969I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr20:62321442 C>T maps to ENST00000482936 F715F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr20:62298842 C>T maps to ENST00000482936 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr15:41749993 C>T maps to NM_015138.4 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr15:41745235 C>T maps to NM_015138.4 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:41769407 C>T maps to NM_015138.4 Q536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr2:74654712 G>A maps to NM_001015055.1 R365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:74657619 C>T maps to NM_001015055.1 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr10:64022543 G>A maps to NM_145307.2 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr10:63958146 A>G maps to NM_145307.2 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:63983056 G>A maps to NM_145307.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:64022524 C>T maps to NM_145307.2 W39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:64022543 G>A maps to NM_145307.2 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr14:101350951 G>A maps to NM_001134888.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr14:101350936 G>A maps to NM_001134888.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr14:101350960 C>T maps to NM_001134888.2 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr14:101348095 G>A maps to NM_001134888.2 A1010A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:101348053 C>T maps to NM_001134888.2 R1024R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:101348212 G>A maps to NM_001134888.2 V971V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr14:60194249 G>A maps to NM_021136.2 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr14:60212693 G>A maps to NM_021136.2 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:60193832 G>A maps to NM_021136.2 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:60212975 C>T maps to NM_021136.2 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:60193934 C>T maps to NM_021136.2 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:60063500 G>A maps to NM_021136.2 Q765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:60069929 C>T maps to NM_021136.2 Q743Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:60074100 G>A maps to NM_021136.2 A625A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:60212996 G>A maps to NM_021136.2 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:60212693 G>A maps to NM_021136.2 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr14:60194321 G>A maps to NM_021136.2 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr19:45996531 G>A maps to NM_005619.3 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:45997424 T>A maps to NM_005619.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:45997523 C>T maps to NM_005619.3 E238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:45997556 C>T maps to NM_005619.3 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr19:45992716 G>A maps to NM_005619.3 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:63486864 G>T maps to ENST00000377819 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:63486255 C>T maps to ENST00000377819 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr11:63488151 C>T maps to ENST00000377819 F726F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr2:55277310 C>T maps to NM_020532.4 E42E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr22:20230340 G>A maps to ENST00000425986 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:57235130 G>A maps to NM_178570.1 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr3:186915443 G>A maps to NM_153708.2 K47K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:187416462 G>C maps to NM_001004312.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:187416405 C>T maps to NM_001004312.2 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr3:46542109 C>T maps to NM_031440.1 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:46542358 C>T maps to NM_031440.1 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:46542364 G>A maps to NM_031440.1 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:46542034 G>A maps to NM_031440.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:46542316 G>A maps to NM_031440.1 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:46539608 G>A maps to NM_031440.1 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:46539574 G>A maps to NM_031440.1 W8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:187088771 C>T maps to NM_022147.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr18:67727213 T>C maps to NM_173630.3 K1604K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:67812979 A>G maps to NM_173630.3 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr18:67844066 G>A maps to NM_173630.3 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr18:67733127 G>A maps to NM_173630.3 Q1562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr18:67671410 G>A maps to NM_173630.3 L2219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:67776850 G>A maps to NM_173630.3 S1262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr18:67692057 G>A maps to NM_173630.3 V1950V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr18:67742645 A>G maps to NM_173630.3 C1502C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr18:67673640 C>T maps to NM_173630.3 W2167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:179028972 C>T maps to NM_025158.3 G614G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:179018723 G>A maps to NM_025158.3 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:71648890 C>T maps to NM_001037442.2 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:218940230 G>A maps to NM_198483.3 W339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:218940024 G>A maps to NM_198483.3 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:218940348 G>A maps to NM_198483.3 Q378Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr2:218940381 G>A maps to NM_198483.3 E389E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:41143108 C>T maps to NM_173079.2 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:41132592 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr17:41141500 T>G maps to NM_173079.2 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:41142436 T>A maps to NM_173079.2 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:12142406 C>T maps to NM_032167.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:12136781 G>A maps to NM_032167.2 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:12145989 C>T maps to NM_032167.2 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr16:12146073 C>T maps to NM_032167.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:12136844 C>T maps to NM_032167.2 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:12096891 C>T maps to NM_032167.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:87459343 G>A maps to NM_138290.2 *474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr7:87407148 C>T maps to NM_138290.2 N295N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr21:36206829 G>A maps to NM_001754.4 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr21:36171748 C>T maps to NM_001754.4 Q272Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr8:93017363 C>T maps to NM_175634.2 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr8:92999198 C>T maps to NM_175634.2 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:92999129 C>T maps to NM_175634.2 W354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr8:93003921 C>T maps to NM_175634.2 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:92988142 C>T maps to NM_175634.2 W446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr8:92998455 C>T maps to NM_175634.2 W392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:93088211 C>A maps to NM_175634.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:93003911 G>A maps to NM_175634.2 R316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr8:92982903 C>T maps to NM_175634.2 Q507Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr8:92988199 G>A maps to NM_175634.2 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr8:92983034 G>A maps to NM_175634.2 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:93029460 C>T maps to NM_175634.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr6:45459783 G>A maps to ENST00000359524 Q332Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr6:45480127 G>A maps to ENST00000359524 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr6:45390444 A>G maps to ENST00000359524 Q126Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:45514562 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:25229041 G>A maps to NM_001031680.2 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:155292769 A>C maps to NM_001105203.1 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:155291626 C>T maps to NM_001105203.1 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:155298060 C>T maps to NM_001105203.1 T845T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr9:35558457 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr9:35555192 C>T maps to NM_001135999.1 S717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:35555486 C>T maps to NM_001135999.1 P815P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:35547856 C>T maps to NM_001135999.1 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr9:35548089 G>A maps to NM_001135999.1 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr9:35547210 C>T maps to NM_001135999.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr9:35561050 C>T maps to NM_001135999.1 L1436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr3:127817731 T>C maps to NM_003707.2 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr3:127816273 G>A maps to NM_003707.2 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr19:49514510 C>T maps to NM_006666.1 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr19:49514511 C>T maps to NM_006666.1 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr19:49510597 C>T maps to NM_006666.1 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr19:49510598 C>T maps to NM_006666.1 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr6:116911442 C>T maps to NM_015952.2 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:116905894 C>T maps to NM_015952.2 Q49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr21:30380787 C>T maps to NM_016940.2 K74K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:95712207 C>T maps to NM_015485.4 H228H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr1:95699827 G>A maps to NM_015485.4 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:184572253 G>A maps to ENST00000326397 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr4:159526267 G>A maps to ENST00000440678 K174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr4:159554556 G>A maps to ENST00000440678 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr4:159533472 T>A maps to ENST00000440678 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr4:159572930 G>A maps to ENST00000440678 V693V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:159514631 G>A maps to ENST00000440678 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr4:159569786 C>T maps to ENST00000440678 F658F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr13:32355828 A>T maps to NM_130806.3 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr13:32376373 G>A maps to NM_130806.3 K699K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr13:32355861 C>T maps to NM_130806.3 C280C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr13:32376409 G>A maps to NM_130806.3 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr13:32376409 G>A maps to NM_130806.3 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr13:32366845 C>T maps to NM_130806.3 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr13:32367061 C>T maps to NM_130806.3 I541I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr13:32367142 G>A maps to NM_130806.3 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:32376298 G>A maps to NM_130806.3 W674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr13:32367001 C>T maps to NM_130806.3 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr13:32376409 G>A maps to NM_130806.3 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr13:32351581 C>T maps to NM_130806.3 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr13:32367142 G>A maps to NM_130806.3 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:33936923 C>T maps to NM_016568.3 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:33938077 G>A maps to NM_016568.3 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:33937951 C>T maps to NM_016568.3 Y369Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:155912018 G>A maps to NM_181885.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr9:137313634 C>T maps to NM_002957.4 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:137300901 C>T maps to NM_002957.4 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:165380212 G>A maps to NM_006917.4 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:165398041 G>A maps to NM_006917.4 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:165370562 G>A maps to NM_006917.4 I443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr1:165370607 G>A maps to NM_006917.4 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:165378826 G>A maps to NM_006917.4 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr3:133901897 G>A maps to ENST00000296084 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr3:133894461 A>T maps to ENST00000296084 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr19:38969089 C>T maps to NM_000540.2 N1490N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr19:38948138 C>T maps to NM_000540.2 V598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr19:39001301 C>T maps to NM_000540.2 I3001I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr19:39010013 G>C maps to NM_000540.2 L3393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr19:38989857 C>T maps to NM_000540.2 F2334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr19:38951098 C>T maps to NM_000540.2 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr19:38939030 C>T maps to NM_000540.2 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:38935282 G>A maps to NM_000540.2 W199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr19:38951131 G>A maps to NM_000540.2 K826K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr19:39023319 C>T maps to NM_000540.2 L3735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:38980007 A>G maps to NM_000540.2 A1913A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:39025367 G>A maps to NM_000540.2 Q3756Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr19:38956932 C>T maps to NM_000540.2 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr19:38980714 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:38980750 G>A maps to NM_000540.2 E1950E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:38997004 C>T maps to NM_000540.2 S2868S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:38976640 C>T maps to NM_000540.2 F1782F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:38976640 C>T maps to NM_000540.2 F1782F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr19:39023333 G>A maps to NM_000540.2 G3739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:38991497 C>T maps to NM_000540.2 F2494F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:39016075 C>T maps to NM_000540.2 I3520I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:39034005 G>A maps to NM_000540.2 R3903R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:39039041 C>T maps to NM_000540.2 S4088S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:39063863 G>A maps to NM_000540.2 L4682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:38959948 C>T maps to NM_000540.2 F1187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:38960044 G>A maps to NM_000540.2 Q1219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:39062678 G>A maps to NM_000540.2 G4589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:39038894 C>T maps to NM_000540.2 I4039I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:38990622 C>T maps to NM_000540.2 I2430I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:39023319 C>T maps to NM_000540.2 L3735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr19:38976535 C>T maps to NM_000540.2 F1747F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr19:38996453 G>A maps to NM_000540.2 E2803E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr19:39038921 G>A maps to NM_000540.2 V4048V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:38934822 C>T maps to NM_000540.2 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:38966002 G>A maps to NM_000540.2 P1402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:38976835 C>T maps to NM_000540.2 T1847T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:38951023 C>T maps to NM_000540.2 F790F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr19:38980828 C>T maps to NM_000540.2 R1976R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:39008005 G>A maps to NM_000540.2 G3231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:38976640 C>T maps to NM_000540.2 F1782F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:39008000 C>T maps to NM_000540.2 L3230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:38976640 C>T maps to NM_000540.2 F1782F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:38924498 C>T maps to NM_000540.2 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:38985035 C>T maps to NM_000540.2 Q2107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:39077170 C>T maps to NM_000540.2 F4992F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:38994999 G>A maps to NM_000540.2 K2689K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:38974063 G>A maps to NM_000540.2 V1614V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:39070656 C>T maps to NM_000540.2 S4800S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:39008050 G>A maps to NM_000540.2 L3246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:39034476 C>T maps to NM_000540.2 L3992L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr19:38989875 C>T maps to NM_000540.2 F2340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:38948852 G>A maps to NM_000540.2 G696G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:39075686 C>T maps to NM_000540.2 F4917F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr19:38949948 C>T maps to NM_000540.2 F777F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:39008293 G>T maps to NM_000540.2 L3327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr19:38983274 C>T maps to NM_000540.2 P2091P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YX-06A-11D-A197-08 chr19:39001157 C>T maps to NM_000540.2 R2985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr19:39025972 T>A maps to NM_000540.2 L3819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:38987053 C>T maps to NM_000540.2 I2223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:38996004 C>T maps to NM_000540.2 P2789P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr19:38958277 C>T maps to NM_000540.2 D1069D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:38996448 A>T maps to NM_000540.2 K2802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr19:39013912 C>T maps to NM_000540.2 S3468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr19:39070698 C>T maps to NM_000540.2 L4814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:38935267 C>T maps to NM_000540.2 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:38937178 C>T maps to NM_000540.2 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:38942415 C>T maps to NM_000540.2 Q379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:38949933 G>A maps to NM_000540.2 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:38954451 G>A maps to NM_000540.2 E916E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:38959745 C>T maps to NM_000540.2 S1174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:38959948 C>T maps to NM_000540.2 F1187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:38964207 G>A maps to NM_000540.2 E1319E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:38968366 G>A maps to NM_000540.2 R1437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:38983184 C>T maps to NM_000540.2 S2061S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:38993181 G>A maps to NM_000540.2 L2550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:39008128 C>T maps to NM_000540.2 I3272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:39019622 G>A maps to NM_000540.2 E3689E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:39023354 G>A maps to NM_000540.2 E3746E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:39039050 C>T maps to NM_000540.2 D4091D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:39066564 C>T maps to NM_000540.2 F4712F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:39068822 C>T maps to NM_000540.2 F4781F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr19:38995947 G>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:38939419 C>T maps to NM_000540.2 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:38964078 G>A maps to NM_000540.2 W1276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:38991629 G>A maps to NM_000540.2 T2538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr19:39051791 C>T maps to NM_000540.2 Q4108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr19:38997157 G>A maps to NM_000540.2 R2888R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:38948882 C>T maps to NM_000540.2 V706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:38994971 G>A maps to NM_000540.2 W2680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:38931479 C>T maps to NM_000540.2 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J6-06A-11D-A19A-08 chr1:237732503 C>T maps to NM_001035.2 V1161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:237780695 C>T maps to NM_001035.2 F1942F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:237777716 T>C maps to NM_001035.2 F1763F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:237802342 C>T maps to NM_001035.2 V2319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr1:237875103 C>T maps to NM_001035.2 F3430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:237880598 C>T maps to NM_001035.2 P3475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr1:237870468 C>T maps to NM_001035.2 A3267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:237947581 G>A maps to NM_001035.2 V4190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:237972277 C>T maps to NM_001035.2 F4792F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:237806679 C>T maps to NM_001035.2 S2425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr1:237895405 C>T maps to NM_001035.2 Q3666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:237872320 C>T maps to NM_001035.2 I3355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:237982469 C>T maps to NM_001035.2 V4856V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:237919622 G>A maps to NM_001035.2 Q3727Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:237947164 G>A maps to NM_001035.2 A4051A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:237875070 C>T maps to NM_001035.2 F3419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr1:237796903 C>T maps to NM_001035.2 A2194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:237969438 C>T maps to NM_001035.2 S4718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:237777611 C>T maps to NM_001035.2 P1728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:237806718 C>T maps to NM_001035.2 I2438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:237947467 C>T maps to NM_001035.2 I4152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:237947743 C>T maps to NM_001035.2 A4244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:237881820 G>A maps to NM_001035.2 K3518K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:237755153 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:237880619 C>T maps to NM_001035.2 A3482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:237880613 C>T maps to NM_001035.2 I3480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr1:237798219 G>A maps to NM_001035.2 L2240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:237780632 G>A maps to NM_001035.2 R1921R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:237957207 G>A maps to NM_001035.2 R4608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:237880637 C>T maps to NM_001035.2 L3488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:237982394 C>T maps to NM_001035.2 I4831I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr1:237774097 G>T maps to NM_001035.2 E1574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:237947467 C>T maps to NM_001035.2 I4152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:237778110 C>T maps to NM_001035.2 Q1895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:237801732 G>A maps to NM_001035.2 W2290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:237801733 G>A maps to NM_001035.2 W2290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr1:237580393 C>T maps to NM_001035.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:237982409 A>T maps to NM_001035.2 G4836G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr1:237791227 G>A maps to NM_001035.2 G2096G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr1:237794807 C>T maps to NM_001035.2 V2174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr1:237580393 C>T maps to NM_001035.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr1:237872837 G>T maps to NM_001035.2 E3401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:237617732 C>T maps to NM_001035.2 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:237947683 G>A maps to NM_001035.2 E4224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:237774181 C>T maps to NM_001035.2 Q1602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:237965206 C>T maps to NM_001035.2 F4714F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr1:237756849 C>T maps to NM_001035.2 F1450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr1:237955554 T>C maps to NM_001035.2 L4572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:237754052 G>A maps to NM_001035.2 P1307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:237754064 G>A maps to NM_001035.2 A1311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:237995875 C>T maps to NM_001035.2 Q4945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:237994813 G>A maps to NM_001035.2 L4919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:237617861 C>T maps to NM_001035.2 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:237753150 G>A maps to NM_001035.2 K1219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:237791146 G>A maps to NM_001035.2 W2069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:237863597 G>A maps to NM_001035.2 E3066E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:237936945 C>T maps to NM_001035.2 Q3925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:237947902 C>T maps to NM_001035.2 F4297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:237791305 C>T maps to NM_001035.2 S2122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:237796930 C>T maps to NM_001035.2 F2203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:237843766 T>A maps to NM_001035.2 P2969P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:237875070 C>T maps to NM_001035.2 F3419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:237955550 C>T maps to NM_001035.2 P4570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr1:237947260 C>T maps to NM_001035.2 F4083F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:237777680 C>T maps to NM_001035.2 I1751I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:237947149 G>A maps to NM_001035.2 R4046R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:237664158 C>T maps to NM_001035.2 I784I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:237921076 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr15:34113766 C>T maps to NM_001036.3 I3653I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr15:33927851 C>T maps to NM_001036.3 I1071I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr15:33954695 G>T maps to NM_001036.3 V1655V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr15:33952585 C>T maps to NM_001036.3 P1528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr15:34040352 G>A maps to NM_001036.3 L2676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr15:34042430 G>A maps to NM_001036.3 R2781R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr15:34153322 A>G maps to NM_001036.3 T4803T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:33955076 G>A maps to NM_001036.3 G1782G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr15:33962726 C>T maps to NM_001036.3 Q1944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr15:33858886 C>T maps to NM_001036.3 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr15:33873806 C>T maps to NM_001036.3 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr15:34078058 C>A maps to NM_001036.3 P3155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:33991976 C>T maps to NM_001036.3 Q2108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:34060900 C>T maps to NM_001036.3 S2916S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:34077983 C>T maps to NM_001036.3 V3130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:34150115 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:33765645 C>T maps to NM_001036.3 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:33872248 C>T maps to NM_001036.3 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr15:34130189 A>G maps to NM_001036.3 E4003E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:33855042 C>T maps to NM_001036.3 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:33916058 C>T maps to NM_001036.3 P803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:33988476 C>T maps to NM_001036.3 I1973I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:34015063 C>T maps to NM_001036.3 L2256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr15:33603282 C>T maps to NM_001036.3 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr15:33842362 G>A maps to NM_001036.3 W273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr15:34109107 G>A maps to NM_001036.3 W3516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:34150114 G>A maps to NM_001036.3 T4714T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr15:34105143 G>A maps to NM_001036.3 K3446K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:33858946 C>T maps to NM_001036.3 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr15:34080581 C>T maps to NM_001036.3 I3251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr15:34080524 G>A maps to NM_001036.3 E3232E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr15:34130702 G>A maps to NM_001036.3 K4174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr15:33858946 C>T maps to NM_001036.3 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr15:34130444 C>T maps to NM_001036.3 F4088F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr15:34040382 G>A maps to NM_001036.3 V2686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:34102738 C>T maps to NM_001036.3 I3362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr15:33961553 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr15:33842516 G>A maps to NM_001036.3 K324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr15:33858940 G>A maps to NM_001036.3 E403E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr15:33840329 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr15:33835880 G>A maps to NM_001036.3 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr15:33925185 G>A maps to NM_001036.3 L968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:33840369 C>T maps to NM_001036.3 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:33895341 C>T maps to NM_001036.3 F647F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:33895455 C>T maps to NM_001036.3 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:33920724 C>T maps to NM_001036.3 I876I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:33941322 C>T maps to NM_001036.3 V1343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:33991942 C>T maps to NM_001036.3 F2096F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:34014925 G>A maps to NM_001036.3 V2210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:34030706 G>A maps to NM_001036.3 W2524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:34111983 C>T maps to NM_001036.3 T3578T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:34129177 C>T maps to NM_001036.3 S3880S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:34129928 C>T maps to NM_001036.3 F3916F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr15:34047373 C>T maps to NM_001036.3 A2836A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:34150115 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:33954890 C>T maps to NM_001036.3 F1720F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:34129147 C>G maps to NM_001036.3 L3870L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr15:33927860 C>T maps to NM_001036.3 F1074F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr1:151958577 C>T maps to NM_002966.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:153346437 G>A maps to NM_005621.1 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:153587776 C>T maps to NM_020672.1 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:153587381 C>T maps to NM_020672.1 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:153580153 C>T maps to NM_080388.1 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr1:153580501 G>A maps to NM_080388.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:153533974 G>A maps to ENST00000368707 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:153520172 G>A maps to NM_002960.1 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:153507177 C>T maps to NM_014624.3 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:153507796 G>A maps to NM_014624.3 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:153431447 G>A maps to NM_002963.3 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:153430422 G>A maps to NM_002963.3 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:153431387 C>T maps to NM_002963.3 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:153431447 G>A maps to NM_002963.3 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:153390599 C>T maps to NM_176823.3 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:153390686 C>T maps to NM_176823.3 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:153391709 C>T maps to NM_176823.3 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:153391682 G>A maps to NM_176823.3 K68K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:153410685 G>A maps to NM_001045479.1 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:153410676 G>A maps to NM_001045479.1 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr1:153410700 C>T maps to NM_001045479.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:153410676 G>A maps to NM_001045479.1 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr1:153409575 C>T maps to NM_001045479.1 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr1:153409575 C>T maps to NM_001045479.1 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr1:153410685 G>A maps to NM_001045479.1 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr1:153409534 C>T maps to NM_001045479.1 *113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:153362984 C>T maps to NM_002964.4 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr1:153362719 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:153362719 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:153362972 G>A maps to NM_002964.4 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:153330860 G>A maps to NM_002965.3 Q34Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:153330851 C>T maps to NM_002965.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr1:153333205 C>T maps to NM_002965.3 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr23:16669153 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:6695748 G>A maps to NM_005980.2 K30K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:33318689 G>T maps to NM_022753.2 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:33292227 C>T maps to NM_022753.2 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr5:76171198 C>T maps to NM_130772.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:76173581 C>T maps to NM_130772.3 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr1:101705319 C>T maps to NM_001400.4 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr1:101705337 C>T maps to NM_001400.4 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr1:101705319 C>T maps to NM_001400.4 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:101705412 C>T maps to NM_001400.4 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:101705577 C>T maps to NM_001400.4 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:101705421 G>A maps to NM_001400.4 E294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr19:10335080 G>A maps to NM_004230.3 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:10334519 T>C maps to NM_004230.3 *354W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr9:91616627 G>A maps to NM_005226.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr9:91616747 C>T maps to NM_005226.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr9:91616903 C>T maps to NM_005226.2 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:91616642 G>A maps to NM_005226.2 W176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr9:91616370 C>T maps to NM_005226.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr9:91616966 C>T maps to NM_005226.2 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:91616822 G>A maps to NM_005226.2 E236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:91616900 C>T maps to NM_005226.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:91617110 C>T maps to NM_005226.2 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr19:3179146 C>T maps to NM_003775.3 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:3179083 C>T maps to NM_003775.3 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:10625117 G>A maps to NM_001166215.1 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:10625612 G>A maps to NM_001166215.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr11:18266984 C>T maps to NM_030754.4 W103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:18269486 G>A maps to NM_030754.4 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:18253191 G>A maps to NM_006512.3 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr11:18110952 G>A maps to NM_138421.2 Q232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr11:18105252 G>A maps to NM_138421.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr11:18101969 G>A maps to NM_138421.2 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:45748371 G>A maps to NM_014016.3 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr3:45779073 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:45773593 C>T maps to NM_014016.3 R351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr13:23914669 G>A maps to NM_014363.4 V1115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr13:23904400 G>A maps to NM_014363.4 Y4538Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr13:23913567 G>A maps to NM_014363.4 Q1483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:23905567 T>C maps to NM_014363.4 S4149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:23909098 T>G maps to NM_014363.4 P2972P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr13:23908552 G>A maps to NM_014363.4 P3154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr13:23912515 G>A maps to NM_014363.4 S1833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr13:23908709 A>T maps to NM_014363.4 L3102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr13:23906875 G>A maps to NM_014363.4 P3713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr13:23906646 G>A maps to NM_014363.4 Q3790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr13:23910789 G>A maps to NM_014363.4 Q2409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:23928005 G>A maps to NM_014363.4 F701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr13:23913631 A>C maps to NM_014363.4 T1461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr13:23929370 G>A maps to NM_014363.4 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr13:23907706 G>A maps to NM_014363.4 I3436I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr13:23928866 G>A maps to NM_014363.4 P628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr13:23907394 G>A maps to NM_014363.4 F3540F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr13:23908831 G>A maps to NM_014363.4 L3061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr13:23932609 G>A maps to NM_014363.4 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:47673088 C>T maps to NM_005500.2 C214C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:47653512 C>T maps to NM_005500.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr19:5668274 C>T maps to ENST00000433404 S909S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr19:5651067 C>T maps to ENST00000433404 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr19:5667858 C>A maps to ENST00000433404 S862S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr19:5653154 C>T maps to ENST00000433404 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr19:5667118 G>A maps to ENST00000433404 G799G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr19:5592768 G>A maps to NM_014649.2 H779H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr19:5587888 G>A maps to NM_014649.2 A876A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:5594005 C>T maps to NM_014649.2 E701E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:5590304 G>A maps to NM_014649.2 L837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:5610061 G>A maps to NM_014649.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:5594149 G>A maps to NM_014649.2 A653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:5590304 G>A maps to NM_014649.2 L837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:5612563 G>A maps to NM_014649.2 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:5610020 G>A maps to NM_014649.2 F427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:234238221 C>T maps to NM_000541.4 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr23:134989121 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:134994972 T>A did not map to a codon.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr23:134988649 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:134988656 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:134992271 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:134994478 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:134991024 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:134991025 C>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:134993769 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr23:134991835 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:134994547 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:134991099 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:134988264 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:134990380 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:134994495 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:134983802 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:134989113 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:134986724 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:134988270 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:134993769 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:134990693 G>A did not map to a codon.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr23:134987464 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:134993455 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:134992214 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr23:134987464 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:134990306 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr23:134989135 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:134992690 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:134990686 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:134991143 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:134992587 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:134993875 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:134991081 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:134990651 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:134993484 G>A did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:134993467 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr16:51172978 G>A maps to ENST00000251020 Q1052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr16:51173897 C>T maps to ENST00000251020 T745T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr16:51173663 G>A maps to ENST00000251020 N823N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr16:51171259 C>T maps to ENST00000251020 A1246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr16:51174710 C>T maps to ENST00000251020 E474E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr16:51173342 G>A maps to ENST00000251020 S930S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr16:51175385 C>T maps to ENST00000251020 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:51173228 C>T maps to ENST00000251020 G968G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:51173495 C>T maps to ENST00000251020 E879E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr16:51175507 G>A maps to ENST00000251020 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr16:51175193 C>T maps to ENST00000251020 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:51174182 G>A maps to ENST00000251020 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:51174818 C>T maps to ENST00000251020 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:51174058 G>A maps to ENST00000251020 Q692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:51171358 G>A maps to ENST00000251020 F1213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:51173297 C>T maps to ENST00000251020 E945E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr16:51171208 A>G maps to ENST00000251020 I1263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr16:51171345 G>A maps to ENST00000251020 Q1218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:51173576 G>A maps to ENST00000251020 S852S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr16:51171034 G>A maps to ENST00000251020 I1321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr16:51175808 C>T maps to ENST00000251020 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:51171259 C>T maps to ENST00000251020 A1246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr16:51174275 G>A maps to ENST00000251020 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:51174683 C>T maps to ENST00000251020 G483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:51175595 G>A maps to ENST00000251020 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:51175927 G>A maps to ENST00000251020 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr16:51173807 G>A maps to ENST00000251020 F775F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:51175913 G>A maps to ENST00000251020 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:51174416 C>T maps to ENST00000251020 T572T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:51174566 C>T maps to ENST00000251020 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr16:51172616 C>T maps to ENST00000251020 T1172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr16:51175595 G>A maps to ENST00000251020 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr16:51172856 G>A maps to ENST00000251020 F1092F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr16:51173534 C>T maps to ENST00000251020 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr16:51173933 G>A maps to ENST00000251020 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr16:51174410 C>T maps to ENST00000251020 E574E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr16:51174058 G>A maps to ENST00000251020 Q692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:51171298 G>A maps to ENST00000251020 F1233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:51172763 G>A maps to ENST00000251020 L1123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:51174242 G>A maps to ENST00000251020 V630V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:51174629 C>T maps to ENST00000251020 E501E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:51174767 C>T maps to ENST00000251020 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:51174905 G>A maps to ENST00000251020 I409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:51175976 G>A maps to ENST00000251020 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:51175391 G>A maps to ENST00000251020 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:51171034 G>A maps to ENST00000251020 I1321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:51171367 G>A maps to ENST00000251020 P1210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:51172966 G>A maps to ENST00000251020 L1056L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr16:51173969 C>T maps to ENST00000251020 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr14:21991059 G>A maps to NM_005407.1 P934P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:21992835 A>G maps to NM_005407.1 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr14:21991800 G>A maps to NM_005407.1 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:21991617 G>A maps to NM_005407.1 F748F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:21993630 G>A maps to NM_005407.1 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:21991827 G>A maps to NM_005407.1 F678F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr18:76753130 C>T maps to NM_171999.2 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr18:76754423 G>A maps to NM_171999.2 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr18:76755152 C>T maps to NM_171999.2 S1054S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr18:76754519 G>T maps to NM_171999.2 L843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr18:76754585 G>A maps to NM_171999.2 V865V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr18:76753361 C>T maps to NM_171999.2 F457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr18:76753691 C>T maps to NM_171999.2 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr18:76752539 G>A maps to NM_171999.2 Q183Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr18:76754600 G>A maps to NM_171999.2 G870G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr18:76757144 C>T maps to NM_171999.2 P1242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr18:76752137 G>A maps to NM_171999.2 E49E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr18:76752551 G>A maps to NM_171999.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:76754663 G>A maps to NM_171999.2 A891A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:76754681 C>G maps to NM_171999.2 S897S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr18:76753484 C>T maps to NM_171999.2 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr18:76754765 G>A maps to NM_171999.2 P925P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr18:76753211 C>T maps to NM_171999.2 F407F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr18:76754642 C>T maps to NM_171999.2 G884G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr18:76752242 G>A maps to NM_171999.2 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr18:76752614 G>A maps to NM_171999.2 Q208Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:76756928 G>A maps to NM_171999.2 A1170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:76757135 C>T maps to NM_171999.2 P1239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:76757168 C>T maps to NM_171999.2 L1250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr18:76752137 G>A maps to NM_171999.2 E49E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr18:76752272 C>T maps to NM_171999.2 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr18:76754897 G>A maps to NM_171999.2 R969R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr20:50408880 C>T maps to NM_020436.3 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr20:50407791 G>A maps to NM_020436.3 F410F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:50418920 G>A maps to NM_020436.3 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:50407221 G>A maps to NM_020436.3 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr20:50401094 G>A maps to NM_020436.3 I957I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr20:50407812 G>A maps to NM_020436.3 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr20:50406948 G>A maps to NM_020436.3 I691I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr20:50408715 G>A maps to NM_020436.3 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:861335 C>T maps to ENST00000443100 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:865650 C>T maps to ENST00000443100 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:879085 G>A maps to ENST00000443100 R566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:879130 G>A maps to ENST00000443100 E581E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr8:119391931 G>A maps to NM_207506.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr8:119593115 C>T maps to NM_207506.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr8:119391885 G>A maps to NM_207506.2 Q126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr8:119391886 G>A maps to NM_207506.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr8:119391883 C>T maps to NM_207506.2 Q126Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr8:119593127 G>A maps to NM_207506.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr8:119391805 G>A maps to NM_207506.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:119391793 G>A maps to NM_207506.2 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr8:119391904 G>A maps to NM_207506.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr17:48193395 C>T maps to NM_174920.2 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr17:48191658 C>A maps to NM_174920.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:48191777 C>T maps to NM_174920.2 E283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:130536381 A>G maps to ENST00000457563 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr6:130505277 G>A maps to ENST00000457563 H232H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr6:130465685 T>C maps to ENST00000457563 G538G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:130465868 C>T maps to ENST00000457563 R477R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:130505247 G>A maps to ENST00000457563 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:130530647 C>T maps to ENST00000457563 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr14:55168906 C>T maps to NM_015589.4 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr14:55251154 C>T maps to ENST00000251091 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr14:55168867 C>T maps to NM_015589.4 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr14:55251267 C>T maps to NM_015589.4 P685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:39871304 C>T maps to NM_018028.2 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr19:39847697 C>T maps to NM_018028.2 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:39867421 C>T maps to NM_018028.2 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:39866353 C>T maps to NM_018028.2 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:39866354 C>T maps to NM_018028.2 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:169642885 C>T maps to NM_182610.2 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:169644400 G>A maps to NM_182610.2 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:169644829 G>A maps to NM_182610.2 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr3:169637366 G>A maps to NM_182610.2 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr3:169656113 G>A maps to NM_182610.2 Q387Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:169644565 C>T maps to NM_182610.2 H172H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:169644745 C>T maps to NM_182610.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:169637339 C>T maps to NM_182610.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:169644814 C>T maps to NM_182610.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:169644953 C>T maps to NM_182610.2 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:169639115 G>A maps to NM_182610.2 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:169644413 C>T maps to NM_182610.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:169644427 C>T maps to NM_182610.2 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:169644532 G>A maps to NM_182610.2 Q161Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr3:169654228 C>T maps to NM_182610.2 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:169644769 G>A maps to NM_182610.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr3:169642891 G>A maps to NM_182610.2 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:76910585 C>T maps to ENST00000372690 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr7:92733973 C>T maps to NM_017654.3 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr7:92733357 G>A maps to NM_017654.3 R685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:92734270 G>A maps to NM_017654.3 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:92731570 G>A maps to NM_017654.3 P1280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:92731786 G>T maps to NM_017654.3 I1208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr7:92731441 G>A maps to NM_017654.3 F1323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr7:92732794 G>A maps to NM_017654.3 I872I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:92731216 G>A maps to NM_017654.3 I1398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:92731246 G>A maps to NM_017654.3 F1388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr7:92733978 C>A maps to NM_017654.3 E478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr7:92734351 C>T maps to NM_017654.3 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr7:92734675 C>T maps to NM_017654.3 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:92730706 C>T maps to NM_017654.3 E1568E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:92734351 C>T maps to NM_017654.3 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:92734951 C>T maps to NM_017654.3 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr7:92733844 C>T maps to NM_017654.3 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr7:92730948 T>A maps to NM_017654.3 R1488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr7:92734351 C>T maps to NM_017654.3 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:92733780 G>A maps to NM_017654.3 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr7:92734831 C>T maps to NM_017654.3 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:92734557 G>A maps to NM_017654.3 R285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr7:92731609 G>A maps to NM_017654.3 S1267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:92731164 G>A maps to NM_017654.3 R1416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr7:92765047 G>A maps to NM_152703.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr7:92762824 G>A maps to NM_152703.2 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr7:92760769 G>A maps to NM_152703.2 S1505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr7:92762824 G>A maps to NM_152703.2 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:92760957 G>A maps to NM_152703.2 Q1443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:92764285 C>T maps to NM_152703.2 W333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:92763133 C>T maps to NM_152703.2 K717K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:92762116 G>A maps to NM_152703.2 S1056S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr7:92764234 C>T maps to NM_152703.2 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:92763277 G>A maps to NM_152703.2 I669I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:92761053 G>A maps to NM_152703.2 R1411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:92761879 C>T maps to NM_152703.2 L1135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:92761186 G>A maps to NM_152703.2 F1366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:92764687 G>A maps to NM_152703.2 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:92765203 A>G maps to NM_152703.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr7:92762116 G>A maps to NM_152703.2 S1056S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr7:92762251 A>G maps to NM_152703.2 I1011I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr7:92762824 G>A maps to NM_152703.2 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr7:92761297 C>T maps to NM_152703.2 R1329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr7:92760907 G>A maps to NM_152703.2 F1459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:92761126 G>A maps to NM_152703.2 A1386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:92764207 C>T maps to NM_152703.2 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr7:92763772 C>T maps to NM_152703.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr20:35545196 A>G maps to NM_015474.3 D330D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr20:35526319 G>A maps to NM_015474.3 R551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr20:35579932 G>A maps to NM_015474.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr20:35575207 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr20:35526842 C>T maps to NM_015474.3 Q536Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:35547859 G>A maps to NM_015474.3 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:35526914 C>T maps to NM_015474.3 K512K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr20:35559247 G>A maps to NM_015474.3 H180H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:35563556 G>A maps to NM_015474.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:35532653 T>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr22:44371951 C>T maps to NM_015380.4 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr22:44386178 T>G maps to NM_015380.4 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr22:44372661 C>T maps to NM_015380.4 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr21:15870775 G>A maps to ENST00000285670 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:15873008 C>T maps to ENST00000285670 W271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:15893518 G>A maps to ENST00000285670 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr21:15884876 C>T maps to ENST00000285670 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr21:15858412 T>C maps to ENST00000285670 E382E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr21:15918570 T>C maps to NM_022136.3 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr21:15882642 G>A maps to ENST00000285670 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr21:15889308 A>G maps to ENST00000285670 N129N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZH-06A-11D-A197-08 chr21:15884825 C>T maps to ENST00000285670 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:128775340 G>A maps to NM_001145928.1 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:128747390 C>G maps to NM_001145928.1 G535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr2:128707887 G>A maps to NM_001145928.1 A865A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:128747282 G>A maps to NM_001145928.1 I571I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:128767934 G>A maps to NM_001145928.1 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:128699648 G>A maps to NM_001145928.1 V1061V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr2:128767934 G>A maps to NM_001145928.1 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:174292509 C>T maps to NM_003864.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:55741982 G>A maps to ENST00000443936 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:55750816 G>A maps to ENST00000443936 F631F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr22:50869684 C>T maps to ENST00000216061 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:50853015 C>T maps to ENST00000216061 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:50869675 C>T maps to ENST00000216061 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr22:50869684 C>T maps to ENST00000216061 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr22:50854525 G>C maps to ENST00000216061 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:50845249 C>T maps to ENST00000216061 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:50876644 C>T maps to ENST00000216061 Q628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr22:50877129 G>A maps to ENST00000216061 G689G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:50832477 C>T maps to ENST00000216061 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr22:50857294 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:68341636 C>T maps to NM_001164160.1 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:68315626 C>T maps to NM_001164160.1 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr11:68331882 C>T maps to NM_001164160.1 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr11:68331818 T>C maps to NM_001164160.1 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr11:68338521 T>A maps to NM_001164160.1 C431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:68337238 G>A maps to NM_001164160.1 W384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:68343462 C>T maps to NM_001164160.1 F499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:68312407 C>T maps to NM_001164160.1 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:68312408 C>T maps to NM_001164160.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:136578193 T>G maps to NM_007101.3 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr9:136573509 G>A maps to NM_007101.3 R457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:136599166 C>T maps to NM_007101.3 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr9:136597637 C>T maps to NM_007101.3 E139E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr9:136550344 G>A maps to NM_007101.3 T711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:136573514 C>T maps to NM_007101.3 W455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr9:136578246 C>T did not map to a codon.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr9:136536687 G>A maps to NM_007101.3 Y765Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr9:136584062 C>T maps to NM_007101.3 E339E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:136536720 C>T maps to NM_007101.3 A754A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:136568061 G>A maps to NM_007101.3 F548F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:136584083 C>T maps to NM_007101.3 E332E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:136597592 G>A maps to NM_007101.3 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr9:136595216 G>A maps to NM_007101.3 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr17:26711524 G>A maps to ENST00000379061 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr17:26711584 C>T maps to ENST00000379061 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:56182876 G>A maps to NM_033082.3 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:109777923 C>T maps to ENST00000369923 H280H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr1:109777938 C>T maps to ENST00000369923 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:109772076 T>C maps to ENST00000369923 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr1:109779137 C>A maps to ENST00000369923 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:109772064 C>T maps to ENST00000369923 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:109772142 C>T maps to ENST00000369923 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:109772143 C>T maps to ENST00000369923 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr19:39408362 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:65729298 G>A maps to NM_005146.4 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:65734963 C>T maps to NM_005146.4 R446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr12:108920196 C>T maps to NM_014706.3 E683E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr6:148865455 C>T maps to NM_015278.3 G950G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr6:148840833 C>T maps to NM_015278.3 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr6:148861625 C>T maps to NM_015278.3 Q715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr6:148865248 C>T maps to NM_015278.3 P881P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr6:148865641 C>T maps to NM_015278.3 P1012P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:128922471 G>C did not map to a codon.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr23:128922046 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:128924973 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:128922435 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:128926356 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:128926357 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:128914112 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr23:128926350 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr23:128926406 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr17:7529809 G>A maps to ENST00000380466 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr17:7530079 C>T maps to ENST00000380466 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:18393663 G>A maps to ENST00000332610 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr3:18390940 G>A maps to ENST00000332610 D705D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:18462345 G>A maps to ENST00000332610 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:18427890 C>T maps to ENST00000332610 Q475Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:18391066 G>A maps to ENST00000332610 P663P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:18436238 G>A maps to ENST00000332610 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:18458483 G>A maps to ENST00000332610 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr3:18436160 C>T maps to ENST00000332610 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:18391024 C>T maps to ENST00000332610 Q677Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:18393507 G>A maps to ENST00000332610 I587I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr3:18436238 G>A maps to ENST00000332610 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:200213696 G>A maps to NM_001172509.1 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:200137149 G>A maps to NM_001172509.1 F662F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:200137353 G>A maps to NM_001172509.1 S594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr2:200213621 C>T maps to NM_001172509.1 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr2:200136951 G>A maps to NM_001172509.1 A728A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:200137113 C>T maps to NM_001172509.1 G674G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:200213618 G>A maps to NM_001172509.1 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:200213591 G>A maps to NM_001172509.1 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:84349219 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:84363956 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:84363956 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:84363470 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr23:84362763 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:84362876 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr23:84363847 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:84362761 C>T did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:84362876 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:84362527 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:84363418 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:84363138 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:84363152 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr23:84362658 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr14:51107544 G>A maps to NM_021818.2 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:51132152 T>C maps to NM_021818.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:51132004 G>A maps to NM_021818.2 Q143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:66456123 G>A maps to NM_016038.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:50894659 T>G maps to ENST00000337034 S1427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr22:50886786 G>A maps to ENST00000337034 S1756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:50893736 G>A maps to ENST00000337034 F1500F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr22:50906052 G>A maps to ENST00000337034 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr22:50899590 G>A maps to ENST00000337034 F998F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr22:50900412 G>A maps to ENST00000337034 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr22:50903029 C>T maps to ENST00000337034 K533K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr22:50898061 G>A maps to ENST00000337034 V1185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr22:50893817 C>G maps to ENST00000337034 L1473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:50885666 C>T maps to ENST00000337034 V1872V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr11:9861154 G>A maps to NM_030962.3 F1115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:9838485 C>T maps to NM_030962.3 K1293K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr11:9989951 G>A maps to NM_030962.3 N512N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:9878063 G>A maps to NM_030962.3 L768L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:9853780 G>A maps to NM_030962.3 S1214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:28331719 C>T maps to NM_001024401.2 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr16:28331719 C>T maps to NM_001024401.2 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:28330370 C>T maps to NM_001024401.2 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:28331843 C>T maps to NM_001024401.2 Q293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:28331743 C>T maps to NM_001024401.2 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr16:28330370 C>T maps to NM_001024401.2 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:28331842 C>T maps to NM_001024401.2 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:28331764 C>T maps to NM_001024401.2 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:28331755 C>T maps to NM_001024401.2 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr16:28331719 C>T maps to NM_001024401.2 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr16:28330376 G>A maps to NM_001024401.2 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:28328885 G>A maps to NM_001024401.2 E58E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:28331752 C>T maps to NM_001024401.2 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:56041189 G>A maps to NM_001101401.2 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56042655 G>A maps to NM_001101401.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:56041189 G>A maps to NM_001101401.2 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr12:123782561 G>A maps to NM_001167856.1 I1334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:123815826 G>A maps to NM_001167856.1 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:123782684 T>A maps to NM_001167856.1 L1293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:123798170 A>G maps to NM_001167856.1 F1072F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:1119534 G>A maps to NM_014963.2 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr19:1119084 G>A maps to NM_014963.2 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:1123970 G>A maps to NM_014963.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:1127725 G>A maps to NM_014963.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:1127740 G>A maps to NM_014963.2 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr19:1127674 G>A maps to NM_014963.2 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:1119585 G>A maps to NM_014963.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:36018733 C>T maps to NM_001166034.1 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr19:36017566 C>T maps to NM_001166034.1 K539K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:166261449 C>T maps to NM_006745.3 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr4:166263023 C>T maps to NM_006745.3 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr4:166263023 C>T maps to NM_006745.3 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr17:39964116 G>A maps to NM_006455.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr17:39967157 G>T maps to NM_006455.2 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:39966000 G>A maps to NM_006455.2 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:39964116 G>A maps to NM_006455.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:50154704 C>T maps to NM_021228.2 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:50149387 C>T maps to NM_021228.2 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr19:50156273 C>T maps to NM_021228.2 F876F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:50148304 C>T maps to NM_021228.2 R8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:50156267 C>T maps to NM_021228.2 S874S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:50150025 C>T maps to NM_021228.2 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:50156132 G>A maps to NM_021228.2 R829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:50150028 C>T maps to NM_021228.2 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:50158108 C>G maps to NM_021228.2 G1200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:127762191 G>A maps to NM_173690.4 Q431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr5:77745825 C>T maps to NM_004866.4 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr15:75142925 G>A maps to NM_005697.3 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:155227152 G>A maps to NM_005698.2 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr1:155230208 C>T maps to NM_005698.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr1:155228652 G>A maps to NM_005698.2 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr1:155226533 G>A maps to NM_005698.2 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:155227092 G>T maps to NM_005698.2 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:155227152 G>A maps to NM_005698.2 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:1918276 C>T maps to NM_079834.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:1917762 C>T maps to NM_079834.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr19:1917807 C>T maps to NM_079834.2 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:75311161 T>C maps to ENST00000361900 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr15:75310791 G>A maps to ENST00000361900 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:75305140 G>A maps to ENST00000361900 W44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:75310763 G>A maps to ENST00000361900 W142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr15:75310791 G>A maps to ENST00000361900 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr15:75310851 C>G maps to ENST00000361900 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr15:75310791 G>A maps to ENST00000361900 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr6:28543317 C>T maps to NM_052923.1 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr6:28543644 G>A maps to NM_052923.1 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr6:28540236 C>T maps to NM_052923.1 W1143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr6:28543493 A>G maps to NM_052923.1 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr6:28539993 C>T maps to NM_052923.1 Q1224Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:28554170 G>A maps to NM_052923.1 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr6:28540104 T>C maps to NM_052923.1 E1187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:28542480 T>C maps to NM_052923.1 K667K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:28543485 C>T maps to NM_052923.1 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:28541391 C>T maps to NM_052923.1 Q758Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:28540404 G>A maps to NM_052923.1 P1087P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr6:28540299 C>T maps to NM_052923.1 K1122K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:28542959 G>A maps to NM_052923.1 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr6:28540743 A>G maps to NM_052923.1 A974A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr6:28541466 G>A maps to NM_052923.1 F733F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr6:28540377 C>T maps to NM_052923.1 V1096V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:28543584 C>T maps to NM_052923.1 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr6:28542959 G>A maps to NM_052923.1 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr6:28543644 G>A maps to NM_052923.1 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:28543476 C>T maps to NM_052923.1 K335K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:28542978 G>A maps to NM_052923.1 F501F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr6:28543644 G>A maps to NM_052923.1 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr6:28543043 G>A maps to NM_052923.1 R480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr6:28542978 G>A maps to NM_052923.1 F501F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:28540299 C>T maps to NM_052923.1 K1122K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:28540812 C>T maps to NM_052923.1 K951K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:28543008 G>A maps to NM_052923.1 N491N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr6:28541493 C>T maps to NM_052923.1 G724G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr6:28543602 C>T maps to NM_052923.1 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:47470025 G>A maps to NM_012235.2 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:47460942 C>T maps to NM_012235.2 E605E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr3:47462217 G>A maps to NM_012235.2 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:47467580 G>A maps to NM_012235.2 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr3:47462121 G>A maps to NM_012235.2 F495F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:76646475 G>A maps to ENST00000324767 I1287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:76643602 C>T maps to ENST00000324767 A1358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr15:77064214 A>T maps to ENST00000324767 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr8:27509100 C>T maps to NM_016240.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:27516853 C>T maps to NM_016240.2 F389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:27516388 C>T maps to NM_016240.2 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:27528507 C>A maps to NM_016240.2 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr8:27516430 C>T maps to NM_016240.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr8:27516580 C>T maps to NM_016240.2 H298H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:27516523 C>T maps to NM_016240.2 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:27845078 G>A maps to NM_173833.5 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:27764707 C>T maps to NM_173833.5 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr8:27823960 G>A maps to NM_173833.5 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:27729539 C>A maps to NM_173833.5 E467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr8:27729501 C>A maps to NM_173833.5 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr8:27779538 C>T maps to NM_173833.5 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr12:125298849 C>T maps to NM_005505.4 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:77087447 C>A maps to NM_005506.2 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr4:77100828 G>A maps to NM_005506.2 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:1538795 A>G maps to NM_003693.2 A583A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:1538486 G>A maps to NM_003693.2 G686G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:1548499 C>T maps to NM_003693.2 W45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr17:1538456 C>T maps to NM_003693.2 G696G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr17:1538474 C>T maps to NM_003693.2 T690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr22:20780063 G>A maps to NM_153334.4 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr22:20780369 G>A maps to NM_153334.4 A636A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr22:20783887 G>A maps to NM_153334.4 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr1:246887837 C>T maps to NM_016002.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:246907402 C>T maps to NM_016002.2 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:246930508 C>T maps to NM_016002.2 F399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr10:102116450 C>T maps to NM_005063.4 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr10:102108101 G>A maps to NM_005063.4 W103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr4:83582216 G>A maps to NM_024906.2 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:83602048 C>T maps to NM_001037582.2 W127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr4:83602041 C>T maps to NM_001037582.2 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr4:83719480 G>T maps to NM_001037582.2 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr13:78187058 C>T maps to NM_144777.2 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr13:78191758 A>T maps to NM_144777.2 K493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr13:78133980 C>T maps to NM_144777.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr13:78208579 G>A maps to NM_144777.2 E586E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr13:78187049 C>T maps to NM_144777.2 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr13:78176800 C>T maps to NM_144777.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr14:31107425 A>T maps to ENST00000311943 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr14:31204065 T>C did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr14:31191116 C>T maps to ENST00000311943 F596F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:31142535 C>T maps to ENST00000311943 R365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:31164035 C>T maps to ENST00000311943 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr14:31144255 T>G maps to ENST00000311943 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr4:54140029 C>T maps to NM_152540.3 W425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:54139994 G>A maps to NM_152540.3 Q437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:53773704 C>T maps to NM_152540.3 E587E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:224463673 G>A maps to NM_003469.4 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:224463013 C>T maps to NM_003469.4 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr2:224462446 G>A maps to NM_003469.4 I518I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr2:224462784 G>A maps to NM_003469.4 Q406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:224463502 G>A maps to NM_003469.4 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr2:224463208 C>T maps to NM_003469.4 E264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:224462719 T>G maps to NM_003469.4 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr15:51988144 G>A maps to NM_013243.3 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr15:51993376 A>G maps to NM_013243.3 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr15:51993415 A>G maps to NM_013243.3 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:51984447 G>A maps to NM_013243.3 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:51984483 A>G maps to NM_013243.3 E273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr15:51975627 C>T maps to NM_013243.3 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr15:51981459 G>A maps to NM_013243.3 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:51993385 G>A maps to NM_013243.3 K384K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr15:32935870 T>C maps to NM_001144757.1 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:61959675 G>A maps to NM_006552.1 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:61959681 C>G maps to NM_006552.1 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:62010788 T>G maps to NM_006551.3 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:62010914 C>T maps to NM_006551.3 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:62010825 C>T maps to NM_006551.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:62065101 A>T maps to NM_206998.1 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:62065007 A>G maps to NM_206998.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:62064999 C>T maps to NM_206998.1 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr11:61978008 G>A maps to NM_002407.2 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:35085112 G>A maps to NM_001025591.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:35085244 G>A maps to NM_001025591.2 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr6:25670231 C>T maps to NM_006998.3 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr6:25689423 C>T maps to NM_006998.3 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:25670231 C>T maps to NM_006998.3 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:25689430 C>T maps to NM_006998.3 Q187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:25665235 G>A maps to NM_006998.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:25670231 C>T maps to NM_006998.3 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:25689430 C>T maps to NM_006998.3 Q187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:25689715 G>T maps to NM_006998.3 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:25701496 G>A maps to NM_006998.3 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:25652672 C>T maps to NM_006998.3 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:159605540 G>A maps to NM_001197113.1 E423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr3:159606658 A>G maps to NM_001197113.1 K491K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:159609904 C>T maps to NM_001197113.1 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:159584070 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr7:12684209 G>A maps to NM_001112706.2 E587E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr7:12675747 A>T maps to NM_001112706.2 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:12692308 G>A maps to NM_001112706.2 W706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:12692309 G>A maps to NM_001112706.2 W706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr4:129913335 G>A maps to NM_144643.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:129864296 G>A maps to NM_144643.2 Q496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr4:129873955 G>A maps to NM_144643.2 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:129873955 G>A maps to NM_144643.2 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr2:238976787 C>T maps to NM_016510.4 F95F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-FS-A4FC-06A-11D-A24R-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:41494269 G>A maps to NM_001031694.2 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr1:41540947 G>A maps to NM_001031694.2 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:17768159 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:18260570 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:18265916 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:18323266 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:18323327 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:18342045 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:18264804 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:18338462 A>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:18259383 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:18260652 T>G did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:18259475 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:18283761 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:18283812 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:18276308 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:18343094 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:18264863 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:18264849 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:18278361 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr6:108042120 G>A maps to NM_198081.3 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:108042075 G>A maps to NM_198081.3 Y268Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr6:108067959 G>A maps to NM_198081.3 D140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:38802218 C>T maps to NM_006514.2 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr3:38750977 C>T maps to NM_006514.2 Q1424Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr3:38753669 G>A maps to NM_006514.2 Y1357Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr3:38768219 G>A maps to NM_006514.2 I988I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:38793754 T>C maps to NM_006514.2 Q570Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr3:38743381 G>A maps to NM_006514.2 F1535F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:38770293 G>A maps to NM_006514.2 I793I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr3:38748781 G>A maps to NM_006514.2 I1458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr3:38739355 C>T maps to NM_006514.2 L1785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr3:38781077 G>A maps to NM_006514.2 I736I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:38770338 C>T maps to NM_006514.2 K778K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr3:38760263 C>T maps to NM_006514.2 E1187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:38743464 G>A maps to NM_006514.2 L1508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr3:38753870 G>A maps to NM_006514.2 I1290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:38739880 G>A maps to NM_006514.2 I1610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:38793930 G>A maps to NM_006514.2 R512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr3:38781038 C>T maps to NM_006514.2 K749K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:38739448 C>T maps to NM_006514.2 E1754E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:38743471 C>T maps to NM_006514.2 T1505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:38739745 G>A maps to NM_006514.2 F1655F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:38791582 G>A maps to NM_006514.2 I616I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr3:38739952 C>T maps to NM_006514.2 L1586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:38798188 G>A maps to NM_006514.2 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr3:38748772 G>A maps to NM_006514.2 P1461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:38768375 G>A maps to NM_006514.2 C936C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:38768432 G>A maps to NM_006514.2 I917I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:38797419 G>A maps to NM_006514.2 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr3:38753714 G>A maps to NM_006514.2 F1342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:38753783 G>A maps to NM_006514.2 S1319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:38753897 G>A maps to NM_006514.2 I1281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:38768198 G>A maps to NM_006514.2 V995V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:38743501 C>T maps to NM_006514.2 V1495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:38739463 C>T maps to NM_006514.2 E1749E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:38743370 C>T maps to NM_006514.2 W1539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:38770272 G>A maps to NM_006514.2 V800V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:38770292 G>A maps to NM_006514.2 L794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:38748844 C>T maps to NM_006514.2 E1437E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr3:38768108 G>A maps to NM_006514.2 I1025I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr3:38760227 G>A maps to NM_006514.2 F1199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:38751001 G>A maps to NM_006514.2 V1416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:38768198 G>A maps to NM_006514.2 V995V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:38798278 G>A maps to NM_006514.2 I392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:38768111 C>T maps to NM_006514.2 V1024V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:38812822 G>A maps to NM_006514.2 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr3:38763769 G>A maps to NM_006514.2 I1162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:38755508 G>A maps to NM_006514.2 A1248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:38770041 C>T maps to NM_006514.2 G877G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:38760155 G>A maps to NM_006514.2 F1223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:38770122 C>T maps to NM_006514.2 W850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:38750977 C>T maps to NM_006514.2 Q1424Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:38755465 G>A maps to NM_006514.2 R1263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr3:38804993 A>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:38739952 C>T maps to NM_006514.2 L1586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:38752382 G>A maps to NM_006514.2 T1365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:38770287 G>A maps to NM_006514.2 A795A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:38797431 C>T maps to NM_006514.2 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr3:38783808 G>A maps to NM_006514.2 F693F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:38755465 G>A maps to NM_006514.2 R1263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:38763811 G>A maps to NM_006514.2 I1148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:38770080 G>A maps to NM_006514.2 S864S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:38770143 G>A maps to NM_006514.2 F843F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:38835384 C>T maps to NM_006514.2 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr3:38743471 C>T maps to NM_006514.2 T1505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:38753717 G>A maps to NM_006514.2 F1341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr3:38755547 C>T maps to NM_006514.2 A1235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr3:38753768 C>T maps to NM_006514.2 S1324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:38743414 G>A maps to NM_006514.2 V1524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:38739586 G>A maps to NM_006514.2 I1708I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr3:38783862 G>A maps to NM_006514.2 I675I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr3:38783934 C>T maps to NM_006514.2 W651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr3:38753882 G>A maps to NM_006514.2 L1286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38739232 C>T maps to NM_006514.2 E1826E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38739796 G>A maps to NM_006514.2 I1638I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38748772 G>A maps to NM_006514.2 P1461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38753714 G>A maps to NM_006514.2 F1342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38753834 G>A maps to NM_006514.2 L1302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38768369 G>A maps to NM_006514.2 F938F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38770068 G>A maps to NM_006514.2 I868I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38802869 C>T maps to NM_006514.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38830524 C>T maps to NM_006514.2 W131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38835303 G>A maps to NM_006514.2 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38835375 C>T maps to NM_006514.2 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr3:38739352 G>A maps to NM_006514.2 I1786I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:38760146 C>T maps to NM_006514.2 V1226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr3:38768111 C>T maps to NM_006514.2 V1024V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr3:38802764 G>A maps to NM_006514.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr3:38812792 C>T maps to NM_006514.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr3:38793943 G>A maps to NM_006514.2 F507F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:38797431 C>T maps to NM_006514.2 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr3:38760227 G>A maps to NM_006514.2 F1199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:38889189 G>A maps to ENST00000302328 F1457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:38945361 C>T maps to ENST00000302328 G612G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:38950507 G>A maps to ENST00000302328 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr3:38927620 G>A maps to ENST00000302328 R982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr3:38938440 G>A maps to ENST00000302328 C766C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:38892011 C>T maps to ENST00000302328 W1429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:38927708 C>T maps to ENST00000302328 E952E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:38968340 G>A maps to ENST00000302328 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:38889206 G>A maps to ENST00000302328 Q1452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr3:38938446 G>A maps to ENST00000302328 I764I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:38927693 C>T maps to ENST00000302328 T957T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr3:38908949 C>T did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:38926776 A>T did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:38926777 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:38908886 G>A maps to ENST00000302328 I1292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:38908898 G>A maps to ENST00000302328 F1288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr3:38949532 G>A maps to ENST00000302328 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr3:38951637 C>T maps to ENST00000302328 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:38892167 G>A maps to ENST00000302328 I1377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:38945565 G>A maps to ENST00000302328 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:38966957 G>A maps to ENST00000302328 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:38968340 G>A maps to ENST00000302328 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr3:38938386 T>G maps to ENST00000302328 S784S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:38938437 C>T maps to ENST00000302328 G767G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:38951637 C>T maps to ENST00000302328 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr3:38927693 C>T maps to ENST00000302328 T957T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:38889206 G>A maps to ENST00000302328 Q1452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:38941522 G>A maps to ENST00000302328 I628I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:38962690 C>T maps to ENST00000302328 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr3:38936361 G>A maps to ENST00000302328 Q833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:38936350 C>T maps to ENST00000302328 L836L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr3:38991748 C>T maps to ENST00000302328 K35K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr3:38968361 G>A maps to ENST00000302328 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr3:38991748 C>T maps to ENST00000302328 K35K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr3:38949447 G>A maps to ENST00000302328 Q489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:38888976 G>A maps to ENST00000302328 I1528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr3:38946681 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr3:38951577 G>A maps to ENST00000302328 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr3:38924753 G>A maps to ENST00000302328 I1063I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr3:38938700 A>G maps to ENST00000302328 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr3:38892128 T>C maps to ENST00000302328 Q1390Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:38968310 G>A maps to ENST00000302328 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr3:38938482 C>T maps to ENST00000302328 G752G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:38961475 C>T maps to ENST00000302328 K303K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:38945370 C>T maps to ENST00000302328 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:38888307 C>T maps to ENST00000302328 V1751V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:38946701 G>A maps to ENST00000302328 I528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:38950547 C>T maps to ENST00000302328 E413E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:38889189 G>A maps to ENST00000302328 F1457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:38949514 C>T maps to ENST00000302328 R466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:38888385 G>A maps to ENST00000302328 V1725V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr3:38962732 G>A maps to ENST00000302328 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr3:38962690 C>T maps to ENST00000302328 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr3:38949571 G>A maps to ENST00000302328 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:38991679 G>A maps to ENST00000302328 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:38908864 G>A maps to ENST00000302328 L1300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:38888976 G>A maps to ENST00000302328 I1528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:38889066 G>A maps to ENST00000302328 F1498F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:38921479 G>A maps to ENST00000302328 F1118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr3:38892218 G>A maps to ENST00000302328 F1360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38889213 C>T maps to ENST00000302328 L1449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38913776 C>T maps to ENST00000302328 V1134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38921527 G>A maps to ENST00000302328 I1102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38936374 C>T maps to ENST00000302328 R828R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38938644 G>A maps to ENST00000302328 V698V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38941513 G>A maps to ENST00000302328 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38968412 G>A maps to ENST00000302328 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:38908913 G>A maps to ENST00000302328 L1283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:38889090 C>T maps to ENST00000302328 L1490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr3:38936143 C>T maps to ENST00000302328 K905K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:166911170 G>A maps to NM_001165963.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:166870328 C>A maps to NM_001165963.1 T1210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:166868726 C>T maps to NM_001165963.1 K1257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:166900334 G>A maps to NM_001165963.1 S629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:166896100 G>A maps to NM_001165963.1 F807F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:166848846 G>A maps to NM_001165963.1 I1646I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:166848471 G>A maps to NM_001165963.1 I1771I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr2:166894333 G>A maps to NM_001165963.1 A966A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:166848837 C>T maps to NM_001165963.1 L1649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:166848492 G>A maps to NM_001165963.1 F1764F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr2:166892932 C>T maps to NM_001165963.1 R1018R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr2:166904163 C>T maps to NM_001165963.1 Q381Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:166894588 C>T maps to NM_001165963.1 K881K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr2:166911221 C>T maps to NM_001165963.1 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:166866245 G>A maps to NM_001165963.1 R1329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:166909410 C>T maps to NM_001165963.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:166900400 G>A maps to NM_001165963.1 S607S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:166905445 G>A maps to NM_001165963.1 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:166848474 G>A maps to NM_001165963.1 I1770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:166901654 G>A maps to NM_001165963.1 F520F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:166894360 C>T maps to NM_001165963.1 W957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:166848120 C>T maps to NM_001165963.1 Q1888Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:166909377 C>T maps to NM_001165963.1 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:166896091 G>A maps to NM_001165963.1 I810I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr2:166901654 G>A maps to NM_001165963.1 F520F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr2:166852530 G>A maps to NM_001165963.1 R1525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr2:166903432 G>A maps to NM_001165963.1 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:166848846 G>A maps to NM_001165963.1 I1646I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:166894573 G>A maps to NM_001165963.1 S886S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr2:166868756 C>T maps to NM_001165963.1 T1247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr2:166892866 C>T maps to NM_001165963.1 R1040R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr2:166892971 A>G maps to NM_001165963.1 D1005D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:166847760 C>T maps to NM_001165963.1 G2008G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:166893028 G>A maps to NM_001165963.1 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:166897920 G>A maps to NM_001165963.1 F745F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:166911221 C>T maps to NM_001165963.1 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr2:166894465 C>T maps to NM_001165963.1 K922K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:166848660 C>T maps to NM_001165963.1 E1708E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr2:166901552 C>T maps to NM_001165963.1 Q554Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr2:166892977 A>T maps to NM_001165963.1 T1003T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr19:35524521 C>T maps to NM_199037.3 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:35524581 C>T maps to NM_199037.3 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr2:166231232 C>T maps to NM_001040142.1 I1337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:166172018 C>T maps to NM_001040142.1 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:166152596 G>A maps to NM_001040142.1 K88K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:166201066 C>T maps to NM_001040142.1 L855L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr2:166165717 C>T maps to NM_001040143.1 R217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:166179727 C>T maps to NM_001040142.1 F578F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:166243484 G>A maps to NM_001040142.1 W1594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:166170156 G>A maps to NM_001040142.1 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:166245683 C>T maps to NM_001040142.1 L1790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:166229796 C>T maps to NM_001040142.1 S1304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr2:166231202 A>G maps to NM_001040142.1 V1327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:166188050 C>T maps to NM_001040142.1 F787F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr2:166210823 C>T maps to NM_001040142.1 I1014I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:166187933 G>A maps to NM_001040142.1 V748V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:166201288 C>T maps to NM_001040142.1 F929F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:166201294 C>T maps to NM_001040142.1 S931S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:166179937 G>A maps to NM_001040142.1 V648V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:166243506 G>A maps to NM_001040142.1 V1601V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr2:166179829 C>T maps to NM_001040142.1 F612F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr2:166201246 C>T maps to NM_001040142.1 S915S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:166170428 G>A maps to NM_001040142.1 G398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr2:166188000 T>C maps to NM_001040142.1 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:166172126 G>A maps to NM_001040142.1 Q510Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr2:166221773 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr2:166165232 C>T maps to NM_001040142.1 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr2:166166905 C>T maps to NM_001040142.1 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:166167070 C>T maps to NM_001040142.1 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:166229796 C>T maps to NM_001040142.1 S1304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:166246006 G>A maps to NM_001040142.1 T1897T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr2:166179958 C>A maps to NM_001040142.1 S655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:118037619 C>T maps to NM_004588.4 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:118037637 C>T maps to NM_004588.4 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:118039344 G>A maps to NM_004588.4 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:118037787 C>T maps to NM_004588.4 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr2:165987885 G>A maps to NM_006922.3 I811I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr2:165956895 G>A maps to NM_006922.3 Y1294Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr2:165984455 G>A maps to NM_006922.3 F1026F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr2:166003503 G>A maps to NM_006922.3 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr2:165952077 G>A maps to NM_006922.3 F1458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr2:165946983 G>A maps to NM_006922.3 T1893T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:165947757 G>A maps to NM_006922.3 I1635I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:166011108 G>A maps to NM_006922.3 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr2:165987909 G>A maps to NM_006922.3 F803F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:165948803 C>T maps to NM_006922.3 W1589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:166011075 C>T maps to NM_006922.3 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:166012312 G>A maps to NM_006922.3 R378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:165986540 C>T maps to NM_006922.3 W944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr2:165947681 G>A maps to NM_006922.3 L1661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr2:165986629 C>T maps to NM_006922.3 K914K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:166019275 G>A maps to NM_006922.3 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:165950985 A>G maps to NM_006922.3 F1478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr2:165953812 C>T maps to NM_006922.3 V1396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:166012312 G>A maps to NM_006922.3 R378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr2:166019264 G>A maps to NM_006922.3 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr2:166019312 C>T maps to NM_006922.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr2:165946962 C>T maps to NM_006922.3 E1900E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:166011150 C>T maps to NM_006922.3 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr2:166011150 C>T maps to NM_006922.3 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:166012312 G>A maps to NM_006922.3 R378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:166032862 G>A maps to NM_006922.3 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr2:166026968 C>T maps to NM_006922.3 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:165986572 G>A maps to NM_006922.3 F933F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:165947097 G>A maps to NM_006922.3 A1855A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:165984416 G>A maps to NM_006922.3 I1039I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr2:165984139 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr2:165948883 G>A maps to NM_006922.3 L1563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:165956886 G>A maps to NM_006922.3 L1297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:165987885 G>A maps to NM_006922.3 I811I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:123508997 G>A maps to NM_018400.3 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr11:123509024 C>T maps to NM_018400.3 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr11:123516297 G>A maps to NM_018400.3 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr11:123508985 G>A maps to NM_018400.3 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr11:123508997 G>A maps to NM_018400.3 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:123504886 C>T maps to NM_018400.3 E204E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:123513286 G>A maps to NM_018400.3 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:123516297 G>A maps to NM_018400.3 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr11:123516297 G>A maps to NM_018400.3 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:62045701 G>A maps to NM_000334.4 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr17:62045701 G>A maps to NM_000334.4 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr17:62020201 G>A maps to NM_000334.4 V1424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr17:62043902 C>T maps to NM_000334.4 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr17:62022095 G>A maps to NM_000334.4 S1283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:62041907 G>A maps to NM_000334.4 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:62034641 G>A maps to NM_000334.4 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:62019222 G>A maps to NM_000334.4 F1473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:62018439 G>A maps to NM_000334.4 I1734I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:62049185 G>A maps to NM_000334.4 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:62043467 G>A maps to NM_000334.4 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:62021183 C>T maps to NM_000334.4 T1313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:62022170 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:62036696 G>A maps to NM_000334.4 I649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr17:62050057 C>T maps to NM_000334.4 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:62019353 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr17:62045701 G>A maps to NM_000334.4 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:62018169 C>T maps to NM_000334.4 G1824G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:62018541 G>A maps to NM_000334.4 T1700T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:62018712 G>A maps to NM_000334.4 F1643F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:62018928 G>A maps to NM_000334.4 P1571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:62026816 C>T maps to NM_000334.4 E975E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:62036633 G>A maps to NM_000334.4 S670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:62041899 C>T maps to NM_000334.4 E460E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:62049185 G>A maps to NM_000334.4 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr17:62045641 G>A maps to NM_000334.4 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:118015843 G>A maps to NM_174934.3 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:118011947 G>A maps to NM_174934.3 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr3:38645367 C>T maps to NM_001099404.1 Q575Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr3:38603944 G>A maps to NM_001099404.1 L1308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr3:38674786 G>A maps to NM_001099404.1 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr3:38595872 G>A maps to NM_001099404.1 I1570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr3:38607965 C>T maps to NM_001099404.1 W1258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr3:38647495 C>T maps to NM_001099404.1 E428E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr3:38645289 G>A maps to NM_001099404.1 V601V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:38622850 G>A maps to NM_001099404.1 L933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr3:38627415 G>A maps to NM_001099404.1 F851F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr3:38627268 G>A maps to NM_001099404.1 I900I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:38592102 A>C maps to NM_001099404.1 S1920S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:38622532 G>C maps to NM_001099404.1 P1039P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr3:38592137 G>A maps to NM_001099404.1 Q1909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:38622598 C>T maps to NM_001099404.1 E1017E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:38618185 C>T maps to NM_001099404.1 Q1159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:38627268 G>A maps to NM_001099404.1 I900I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:38592468 C>T maps to NM_001099404.1 W1798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:38592525 C>T maps to NM_001099404.1 T1779T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:38622667 G>A maps to NM_001099404.1 A994A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr3:38647507 G>A maps to NM_001099404.1 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr3:38597167 C>T maps to NM_001099404.1 Q1507Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr3:38608040 C>T maps to NM_001099404.1 K1233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:38647554 G>A maps to NM_001099404.1 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:38647621 C>T maps to NM_001099404.1 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:38597961 G>A maps to NM_001099404.1 I1469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:38616820 G>A maps to NM_001099404.1 I1211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr3:38629052 C>T maps to NM_001099404.1 G758G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:38639246 G>A maps to NM_001099404.1 F745F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:38639420 C>T maps to NM_001099404.1 W687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr3:38622715 C>T maps to NM_001099404.1 W978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:38628983 C>T maps to NM_001099404.1 W781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:38671911 G>A maps to NM_001099404.1 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr3:38648228 G>A maps to NM_001099404.1 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:38592825 G>A maps to NM_001099404.1 F1679F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr3:38674786 G>A maps to NM_001099404.1 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:38622610 G>A maps to NM_001099404.1 P1013P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:38607911 G>A maps to NM_001099404.1 F1276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr3:38592723 C>T maps to NM_001099404.1 W1713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:38622517 G>A maps to NM_001099404.1 P1044P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr3:38662380 G>A maps to NM_001099404.1 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:38639246 G>A maps to NM_001099404.1 F745F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr3:38592489 G>A maps to NM_001099404.1 F1791F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr3:38646303 C>T maps to NM_001099404.1 R478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:38592576 G>A maps to NM_001099404.1 I1762I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:38627256 C>T maps to NM_001099404.1 W904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:38646228 G>A maps to NM_001099404.1 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:38622667 G>A maps to NM_001099404.1 A994A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr3:38663949 G>A maps to NM_001099404.1 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:38592954 C>T maps to NM_001099404.1 L1636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:38674558 C>T maps to NM_001099404.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38591832 C>T maps to NM_001099404.1 R2010R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38596016 G>A maps to NM_001099404.1 F1522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38607953 G>A maps to NM_001099404.1 G1262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38616850 G>A maps to NM_001099404.1 I1201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38620857 C>T maps to NM_001099404.1 W1119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38622529 C>T maps to NM_001099404.1 G1040G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38622673 G>A maps to NM_001099404.1 P992P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38627444 G>A maps to NM_001099404.1 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38639231 C>T maps to NM_001099404.1 Q750Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38647585 G>A maps to NM_001099404.1 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38655273 G>A maps to NM_198056.2 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr3:38639363 G>A maps to NM_001099404.1 I706I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:38646303 C>T maps to NM_001099404.1 R478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:38647621 C>T maps to NM_001099404.1 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:38663952 G>A maps to NM_001099404.1 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr3:38592576 G>A maps to NM_001099404.1 I1762I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:38622577 C>T maps to NM_001099404.1 K1024K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:167284378 C>T maps to NM_002976.2 R924R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:167298130 G>A maps to NM_002976.2 F644F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr2:167284357 T>C maps to NM_002976.2 V931V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr2:167298250 G>A maps to NM_002976.2 F604F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:167263127 G>A maps to NM_002976.2 S1337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:167322419 G>A maps to NM_002976.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:167262974 G>A maps to NM_002976.2 F1388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:167284354 C>T maps to NM_002976.2 E932E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:167262983 A>C maps to NM_002976.2 L1385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr2:167322435 G>A maps to NM_002976.2 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:167328849 G>A maps to NM_002976.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:167262488 G>A maps to NM_002976.2 F1550F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:167301439 A>G maps to NM_002976.2 N486N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:167262857 A>T maps to NM_002976.2 L1427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:167322342 C>T maps to NM_002976.2 E273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:167263156 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:167262446 G>A maps to NM_002976.2 L1564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr2:167334137 C>T maps to NM_002976.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr2:167263079 G>A maps to NM_002976.2 I1353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:167298169 G>A maps to NM_002976.2 V631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:167262831 C>T maps to NM_002976.2 W1436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:167279835 C>T maps to NM_002976.2 W987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:167298028 G>A maps to NM_002976.2 F678F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:167297986 G>A maps to NM_002976.2 T692T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:167322347 G>A maps to NM_002976.2 Q272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:167263082 C>T maps to NM_002976.2 R1352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr12:52168019 C>T maps to NM_014191.2 I1231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr12:52159696 C>G maps to NM_014191.2 V929V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:52200861 C>T maps to NM_014191.2 I1864I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr12:52159651 C>T maps to NM_014191.2 L914L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:52200888 C>T maps to NM_014191.2 F1873F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:52200417 C>T maps to NM_014191.2 N1716N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:52056747 G>A maps to NM_014191.2 E49E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:52200261 C>T maps to NM_014191.2 I1664I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:52200630 C>T maps to NM_014191.2 T1787T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr12:52056816 C>T maps to NM_014191.2 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:52162881 C>T maps to NM_014191.2 I1045I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr12:52200468 G>A maps to NM_014191.2 K1733K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:52200480 G>A maps to NM_014191.2 G1737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr12:52159762 C>T maps to NM_014191.2 A951A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr2:167133801 C>T maps to ENST00000303354 L856L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr2:167162384 G>A maps to ENST00000303354 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:167162389 T>A maps to ENST00000303354 K171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr2:167133822 G>A maps to ENST00000303354 S849S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:167085260 C>T maps to ENST00000303354 W1383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:167085290 G>A maps to ENST00000303354 A1373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr2:167108350 G>A maps to ENST00000303354 N1133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:167128971 G>A maps to ENST00000303354 S1097S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr2:167142980 G>A maps to ENST00000303354 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr2:167060516 G>A maps to ENST00000303354 F1575F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:167142944 C>T maps to ENST00000303354 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:167145069 G>A maps to ENST00000303354 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:167163560 C>T maps to ENST00000303354 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:167129169 C>T maps to ENST00000303354 L1031L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:167084227 A>T maps to ENST00000303354 T1405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:167083151 G>A maps to ENST00000303354 I1442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr2:167085479 G>A maps to ENST00000303354 V1310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:167108320 C>T maps to ENST00000303354 E1143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:167168109 A>G maps to ENST00000303354 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:167056192 G>A maps to ENST00000303354 F1653F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr2:167060471 G>A maps to ENST00000303354 S1590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:167160751 G>A maps to ENST00000303354 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:167133741 G>A maps to ENST00000303354 I876I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:167151134 G>A maps to ENST00000303354 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:167162324 C>T maps to ENST00000303354 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:167060675 G>A maps to ENST00000303354 I1522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:167149778 G>A maps to ENST00000303354 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr2:167138192 C>T maps to ENST00000303354 V701V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr2:167163560 C>T maps to ENST00000303354 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr2:167133615 G>A maps to ENST00000303354 F918F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:167055490 C>T maps to ENST00000303354 R1887R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:167142944 C>T maps to ENST00000303354 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:167162315 G>A maps to ENST00000303354 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr2:167055769 C>T maps to ENST00000303354 A1794A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr2:167138231 C>T maps to ENST00000303354 Q688Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:167056365 G>A maps to ENST00000303354 L1596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:167060582 C>T maps to ENST00000303354 V1553V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:167141088 C>T maps to ENST00000303354 G617G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:167162334 C>T maps to ENST00000303354 W189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:167060702 C>T maps to ENST00000303354 V1513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr2:167056228 G>A maps to ENST00000303354 S1641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:6463604 C>T maps to NM_001159576.1 W512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:6464563 G>A maps to NM_001159576.1 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:6457278 G>A maps to NM_001159576.1 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:6463682 C>T maps to NM_001159576.1 K486K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:6457949 G>A maps to NM_001159576.1 V583V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6457305 G>A maps to NM_001159576.1 F640F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6458117 C>T maps to NM_001159576.1 K576K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6471257 G>A maps to NM_001159576.1 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6483643 G>A maps to NM_001159576.1 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr16:23364158 G>T maps to ENST00000307331 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr16:23382665 C>T maps to ENST00000307331 F354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr16:23364244 G>A maps to ENST00000307331 W190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:23391950 C>T maps to ENST00000307331 A629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:23391490 G>C did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:23360096 C>T maps to ENST00000307331 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:23366795 G>A maps to ENST00000307331 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr16:23379176 G>A maps to ENST00000307331 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:23391947 G>A maps to ENST00000307331 E628E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr16:23364223 G>A maps to ENST00000307331 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:23366771 C>T maps to ENST00000307331 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:23364133 C>T maps to ENST00000307331 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr16:23379182 C>T maps to ENST00000307331 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr16:23379251 T>A maps to ENST00000307331 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:23387118 C>T maps to ENST00000307331 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr1:1226672 C>T maps to NM_001130413.2 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr1:1221514 C>T maps to NM_001130413.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:1222348 C>T maps to NM_001130413.2 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:23226756 G>A maps to NM_001039.3 Q639Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:23226031 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr16:23226576 C>T maps to NM_001039.3 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr16:23226480 C>T maps to NM_001039.3 I547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:23224184 C>T maps to NM_001039.3 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:23197753 C>T maps to NM_001039.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:23226448 C>T maps to NM_001039.3 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:23203734 G>A maps to NM_001039.3 Q227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:23224169 G>A maps to NM_001039.3 W462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:23205491 G>A maps to NM_001039.3 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:23208687 C>T maps to NM_001039.3 F339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:23226489 C>T maps to NM_001039.3 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:23197606 G>A maps to NM_001039.3 E5E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr16:23224032 C>T maps to NM_001039.3 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr16:23224033 C>T maps to NM_001039.3 Q444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:10590108 G>A maps to NM_004589.2 Q236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr1:53420477 T>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:53413729 G>A maps to NM_002979.4 Q59Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:53413750 T>C maps to NM_002979.4 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr17:55062797 C>T maps to NM_021626.2 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:55075780 C>A maps to NM_021626.2 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr17:55072875 C>T maps to NM_021626.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr17:55075816 A>T maps to NM_021626.2 R318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr17:55068476 C>T maps to NM_021626.2 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr8:144886746 G>A maps to NM_182706.3 Y1000Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr8:144874734 G>A maps to NM_182706.3 L1416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:144874995 G>A maps to NM_182706.3 S1353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr8:144890931 A>C maps to NM_182706.3 A654A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:144893231 G>A maps to NM_182706.3 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:144875013 G>A maps to NM_182706.3 A1347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:29963629 C>T maps to NM_001145514.1 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr7:30008608 C>T maps to NM_001145514.1 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:29976305 G>A maps to NM_001145514.1 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr7:29983620 C>T maps to NM_001145514.1 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:29976194 G>A maps to NM_001145514.1 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:29980385 C>T maps to NM_001145514.1 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr17:45915658 G>A maps to NM_138355.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:45917579 G>A maps to NM_138355.3 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr17:45915344 C>T maps to NM_138355.3 Q381Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:45915239 G>A maps to NM_138355.3 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:45918101 G>A maps to NM_138355.3 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr17:45916235 G>A maps to NM_138355.3 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr17:45916882 G>A maps to NM_138355.3 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr2:175263025 C>T maps to NM_024583.4 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:644917 G>A maps to NM_033129.3 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr2:120221716 G>A maps to NM_002980.2 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:120206319 G>A maps to NM_002980.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr2:120197773 G>A maps to NM_002980.2 H414H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr2:120236411 G>A maps to NM_002980.2 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:120221752 G>A maps to NM_002980.2 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:120252037 C>T maps to NM_002980.2 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:120197764 G>A maps to NM_002980.2 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr22:43735191 G>A maps to NM_173050.2 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr22:43687050 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr22:43617284 G>A maps to NM_173050.2 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:43619136 G>A maps to NM_173050.2 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr22:43654223 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr22:43735191 G>A maps to NM_173050.2 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr22:43616480 G>A maps to NM_173050.2 I554I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr22:43658762 G>T maps to NM_173050.2 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:43606196 G>A maps to NM_173050.2 S811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:43614357 G>A maps to NM_173050.2 V598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:43634856 C>T maps to NM_173050.2 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr11:9055211 G>A maps to ENST00000457346 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:9077349 G>A maps to ENST00000457346 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:9051440 G>A maps to ENST00000457346 T831T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:9090992 C>T maps to ENST00000457346 K189K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:9074718 G>A maps to ENST00000457346 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:9047336 G>A maps to ENST00000457346 T922T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:35212514 G>A maps to ENST00000394681 Q792Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr6:35212586 G>A maps to ENST00000394681 K816K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:35210858 G>A maps to ENST00000394681 K601K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:65306021 C>T maps to NM_020680.3 A804A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:65298128 C>T maps to NM_020680.3 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:65306006 C>T maps to NM_020680.3 P799P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:65294434 C>T maps to NM_020680.3 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:100691886 C>T maps to NM_017988.4 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:100708391 G>A maps to NM_017988.4 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:100717319 C>T maps to NM_017988.4 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:100707240 G>A maps to NM_017988.4 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:100711594 C>T maps to NM_017988.4 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr12:100717409 C>T maps to NM_017988.4 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:100717409 C>T maps to NM_017988.4 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr4:76896913 G>A maps to NM_018115.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr4:76878999 G>A maps to NM_018115.2 I526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:76891465 G>A maps to NM_018115.2 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:76878999 G>A maps to NM_018115.2 I526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr2:20402884 G>A maps to NM_001006946.1 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr2:20403830 G>A maps to NM_001006946.1 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:20404017 G>A maps to NM_001006946.1 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr2:20402565 G>A maps to NM_001006946.1 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:20403807 G>A maps to NM_001006946.1 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:20403771 G>A maps to NM_001006946.1 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr8:97614756 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:31347417 G>A maps to NM_014654.3 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr1:31349509 G>A maps to NM_014654.3 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:31347414 G>A maps to NM_014654.3 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:31349422 G>A maps to NM_014654.3 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:31349634 G>A maps to NM_014654.3 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr20:43956023 G>A maps to NM_002999.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:43956010 G>A maps to NM_002999.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr9:139301686 A>G maps to NM_001039707.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:139302277 C>T maps to NM_001039707.1 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:243589848 G>A maps to NM_006642.3 T658T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr22:21998283 C>T maps to NM_022044.2 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:21998343 C>T maps to NM_022044.2 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr1:1153954 G>A maps to NM_016176.3 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:1153969 G>A maps to NM_016176.3 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:1152972 G>A maps to NM_016176.3 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr1:1153002 G>A maps to NM_016176.3 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr5:235405 C>T maps to NM_004168.2 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr5:223655 G>A maps to NM_004168.2 K41K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:161332138 C>T maps to NM_003001.3 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:161332139 C>T maps to NM_003001.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr11:111965692 G>T maps to NM_003002.2 *160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr7:4247840 G>T maps to NM_152744.3 L1775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JB-06A-11D-A196-08 chr7:3998594 C>A maps to NM_152744.3 R395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr7:4050700 G>A maps to NM_152744.3 A745A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:4218207 C>T maps to NM_152744.3 V1696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:3861159 G>A maps to NM_152744.3 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:4014111 T>G maps to NM_152744.3 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:4091301 T>C maps to NM_152744.3 A917A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:4116723 C>T maps to NM_152744.3 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:4153706 C>T maps to NM_152744.3 S1208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr7:4051762 G>A maps to NM_152744.3 P772P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:4281440 C>T maps to NM_152744.3 T2049T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:4091445 C>T maps to NM_152744.3 V965V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:4169670 C>T maps to NM_152744.3 T1357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr7:4119179 G>A maps to NM_152744.3 G1096G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr7:4116639 C>T maps to NM_152744.3 I1007I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:3681620 G>A maps to NM_152744.3 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:4259902 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:4014039 G>A maps to NM_152744.3 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:4152924 C>T maps to NM_152744.3 R1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:3681647 G>A maps to NM_152744.3 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:3990603 G>T maps to NM_152744.3 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:4051786 G>A maps to NM_152744.3 R780R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:4008916 C>T maps to NM_152744.3 V525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr7:4153058 G>A maps to NM_152744.3 R1191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr7:4277375 C>T maps to NM_152744.3 V2030V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr7:4185358 C>T maps to NM_152744.3 Q1412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:4051762 G>A maps to NM_152744.3 P772P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:4260976 G>A maps to NM_152744.3 V1936V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:4119156 C>T maps to NM_152744.3 Q1089*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr7:4152975 C>A maps to NM_152744.3 R1164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr7:3658863 G>T maps to NM_152744.3 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:4185408 G>A maps to NM_152744.3 V1428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:4273010 G>A maps to NM_152744.3 A1984A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:4277402 G>A maps to NM_152744.3 K2039K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr7:4152924 C>T maps to NM_152744.3 R1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr7:4171978 C>T maps to NM_152744.3 L1384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:3658761 C>T maps to NM_152744.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:3658802 G>A maps to NM_152744.3 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:3681615 C>T maps to NM_152744.3 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:4150368 G>A maps to NM_152744.3 L1133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:4153781 G>A maps to NM_152744.3 L1233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:4153808 G>A maps to NM_152744.3 L1242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:4201466 C>T maps to NM_152744.3 S1593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:4249748 C>T maps to NM_152744.3 L1832L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:4277345 C>T maps to NM_152744.3 I2020I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:4281434 C>T maps to NM_152744.3 I2047I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:4247729 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:3861080 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:4304907 G>T maps to NM_152744.3 A2178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr17:71357856 C>T maps to NM_001144952.1 E1811E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr17:71387648 G>A maps to NM_001144952.1 F1309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr17:71380033 G>A maps to NM_001144952.1 A1562A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr17:71386489 C>T maps to NM_001144952.1 T1376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr17:71335028 G>A maps to NM_001144952.1 S2072S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr17:71346891 G>A maps to NM_001144952.1 F1932F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr17:71415333 C>T maps to NM_001144952.1 Q719Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:71410809 G>A maps to NM_001144952.1 F819F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:71431637 G>A maps to NM_001144952.1 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr17:71354239 G>A maps to NM_001144952.1 Y1857Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:71348735 C>T maps to NM_001144952.1 K1878K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr17:71364684 C>T maps to NM_001144952.1 K1676K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:71398250 C>T maps to NM_001144952.1 E838E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:71433890 G>A maps to NM_001144952.1 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:71334791 G>A maps to NM_001144952.1 Y2151Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr17:71364627 G>A maps to NM_001144952.1 A1695A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr17:71415363 G>A maps to NM_001144952.1 I709I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr17:71348645 G>A maps to NM_001144952.1 F1908F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:71394259 G>A maps to NM_001144952.1 Q1090*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:71433941 C>T maps to NM_001144952.1 K312K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr17:71419606 C>T maps to NM_001144952.1 R605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr17:71354290 G>A maps to NM_001144952.1 I1840I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr17:71354311 G>A maps to NM_001144952.1 I1833I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr2:192711432 C>T maps to NM_004657.5 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:192701140 G>A maps to NM_004657.5 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:192701119 C>T maps to NM_004657.5 E269E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:192701152 C>T maps to NM_004657.5 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr2:192700987 G>A maps to NM_004657.5 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:192701380 C>T maps to NM_004657.5 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:192701209 C>T maps to NM_004657.5 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:192700974 G>A maps to NM_004657.5 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:192700987 G>A maps to NM_004657.5 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:192701239 C>T maps to NM_004657.5 E229E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:192701218 C>T maps to NM_004657.5 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:192701140 G>A maps to NM_004657.5 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:192700855 C>T maps to NM_004657.5 E357E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:192700900 G>A maps to NM_004657.5 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:192701044 G>A maps to NM_004657.5 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:192701299 G>A maps to NM_004657.5 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:192711528 C>T maps to NM_004657.5 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:192700912 G>A maps to NM_004657.5 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr2:192700855 C>T maps to NM_004657.5 E357E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr8:57218205 T>C maps to NM_138969.2 K262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr8:57224832 G>A maps to NM_138969.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr8:57228734 A>G maps to NM_138969.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr8:57228864 G>A maps to NM_138969.2 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr8:57228678 C>T maps to NM_138969.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr8:57228801 C>T maps to NM_138969.2 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr8:57228678 C>T maps to NM_138969.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr8:57228801 C>T maps to NM_138969.2 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:57228678 C>T maps to NM_138969.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr16:82032904 C>T maps to NM_145168.2 K331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr16:82033759 G>A maps to NM_145168.2 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr16:82033080 G>A maps to NM_145168.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr16:82033435 C>T maps to NM_145168.2 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:82033000 G>A maps to NM_145168.2 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr16:82033576 G>A maps to NM_145168.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr16:82032970 G>A maps to NM_145168.2 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:82034427 G>A maps to NM_145168.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr16:82033702 C>T maps to NM_145168.2 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:82034439 C>T maps to NM_145168.2 K8K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:82033036 G>A maps to NM_145168.2 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:82034430 G>A maps to NM_145168.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:82032726 G>A maps to NM_145168.2 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:82033102 G>A maps to NM_145168.2 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr12:57317655 G>A maps to NM_148897.2 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:57324023 G>A maps to NM_148897.2 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:57323228 C>T maps to NM_148897.2 W223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr12:113836601 G>A maps to NM_006843.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr12:113835196 C>T maps to NM_006843.2 W142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr12:113835156 G>A maps to NM_006843.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:113831781 C>T maps to NM_006843.2 Q231Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr12:113873224 C>T maps to NM_138432.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr12:113866235 G>A maps to NM_138432.2 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:113875772 C>T maps to NM_138432.2 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:113865867 C>T maps to NM_138432.2 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:10357051 G>A maps to ENST00000343726 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr3:10353759 G>A maps to ENST00000343726 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:75210083 C>T maps to NM_001039573.2 S709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:75139695 G>A maps to NM_001039573.2 Q6Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr17:75190973 C>T maps to NM_001039573.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:75210015 C>T maps to NM_001039573.2 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr22:30806636 G>A maps to NM_012429.2 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr22:30812279 G>A maps to NM_012429.2 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr22:30860876 G>A maps to NM_174975.4 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr22:30864539 C>T maps to NM_174975.4 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr22:30864641 G>A maps to NM_174975.4 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr22:30860825 C>T maps to NM_174975.4 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr22:30867903 C>T maps to NM_174975.4 E14E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:30864655 G>A maps to NM_174975.4 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr22:30866011 G>A maps to NM_174975.4 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr22:30862998 G>A maps to NM_174975.4 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr22:30864569 G>A maps to NM_174975.4 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr22:30886141 C>T maps to NM_174977.3 E391E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr22:30886156 G>A maps to NM_174977.3 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr22:30891616 G>T maps to NM_174977.3 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr22:30887842 G>A maps to NM_174977.3 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:30888113 G>A maps to NM_174977.3 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr22:30887960 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr22:30887683 G>A maps to NM_174977.3 F319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr22:30888479 C>T maps to NM_174977.3 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr22:30891620 C>T maps to NM_174977.3 E61E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr22:30887677 C>T maps to NM_174977.3 K321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr22:30887876 G>A maps to NM_174977.3 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr22:30886108 G>A maps to NM_174977.3 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:30887888 C>T maps to NM_174977.3 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:30891357 G>A maps to NM_174977.3 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr16:5040862 C>T maps to NM_014692.1 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr16:5058630 G>A maps to NM_014692.1 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr16:5058534 C>T maps to NM_014692.1 A562A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr16:5064883 C>T maps to NM_014692.1 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:5053555 C>T maps to NM_014692.1 F428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:5057369 A>C maps to NM_014692.1 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr16:5053534 C>T maps to NM_014692.1 I421I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr16:5056030 C>T maps to NM_014692.1 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr16:5053558 C>T maps to NM_014692.1 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr16:5064877 G>A maps to NM_014692.1 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr9:139353681 G>A maps to NM_014866.1 F1771F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr9:139357389 G>A maps to NM_014866.1 L1614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr9:139370858 G>A maps to NM_014866.1 F403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:139372052 G>A maps to NM_014866.1 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:139341691 G>A maps to NM_014866.1 F2228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr9:139368509 G>C maps to NM_014866.1 L1186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr9:139370594 G>A maps to NM_014866.1 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr9:139345791 C>T maps to NM_014866.1 T2076T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr1:177905471 G>A maps to NM_033127.2 S844S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:177928085 A>G maps to NM_033127.2 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:177913707 G>A maps to NM_033127.2 I623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:177927476 G>A maps to NM_033127.2 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:177902402 G>A maps to NM_033127.2 T923T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:177901872 G>A maps to NM_033127.2 S964S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:177911163 G>A maps to NM_033127.2 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:177913746 G>A maps to NM_033127.2 F610F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:177906552 G>A maps to NM_033127.2 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:177911151 G>A maps to NM_033127.2 S635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:177935079 A>G maps to NM_033127.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr1:177930027 A>C maps to NM_033127.2 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:122942418 C>T maps to NM_012430.4 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:145109619 A>G maps to NM_004892.4 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:145109574 C>T maps to NM_004892.4 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:145109571 C>T maps to NM_004892.4 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:145115849 C>T maps to NM_004892.4 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:39555013 A>C maps to NM_006364.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr14:39543712 G>A maps to NM_006364.2 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:39508291 G>A maps to NM_006364.2 F717F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:39510024 G>A maps to NM_006364.2 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr20:18511377 C>T maps to NM_001172745.1 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:18529285 C>T maps to NM_001172745.1 Q593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:18511413 C>T maps to NM_001172745.1 F400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr20:18541302 A>G maps to NM_001172745.1 G741G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr20:18506572 G>A maps to NM_001172745.1 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr20:18505090 C>T maps to NM_001172745.1 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr20:18491676 T>A maps to NM_001172745.1 C66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:121675272 G>A maps to NM_007190.2 R472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:121675305 C>T maps to NM_007190.2 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:121652341 C>T maps to NM_007190.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:121692676 T>C maps to NM_007190.2 Y973Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr5:134044529 T>C maps to NM_021982.1 P893P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr5:134059306 C>T maps to NM_021982.1 F1038F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:134059339 C>T maps to NM_021982.1 F1049F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:134044442 G>C maps to NM_021982.1 R864R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:134041096 C>T maps to NM_021982.1 Q841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr4:110451529 C>T maps to NM_006323.2 G1054G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:110415978 C>T maps to NM_006323.2 N485N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr4:110442616 C>T maps to NM_006323.2 T781T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:110431224 G>A maps to NM_006323.2 K578K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:110447418 C>T maps to NM_006323.2 V943V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr4:110442724 C>T maps to NM_006323.2 S817S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:75520528 A>G maps to NM_198597.1 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:75519812 C>T maps to NM_198597.1 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:75530141 C>T maps to NM_198597.1 L989L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr10:75530501 G>A maps to NM_198597.1 K1030K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr4:119674000 G>A maps to ENST00000379735 I489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:119736659 G>A maps to ENST00000379735 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:119652549 C>T maps to ENST00000379735 W931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:119665154 G>T maps to ENST00000379735 Y662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr4:119727031 G>T maps to ENST00000379735 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr4:119661856 G>A maps to ENST00000379735 H734H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:119666173 G>A maps to ENST00000379735 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:83770028 G>A maps to ENST00000505472 P810P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:83748523 G>A maps to ENST00000505472 Q1128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr4:83765662 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:83772733 G>A maps to ENST00000505472 I726I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr4:83778122 G>A maps to ENST00000505472 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr10:102262130 G>A maps to NM_015490.3 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr10:102249885 G>A maps to NM_015490.3 G948G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:102248686 G>A maps to NM_015490.3 P1072P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr10:102256029 G>C maps to NM_015490.3 P765P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:102249867 G>A maps to NM_015490.3 T954T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:102257866 G>A maps to NM_015490.3 I594I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr10:102262190 C>T maps to NM_015490.3 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:102265161 T>A maps to NM_015490.3 K379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr10:102256890 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:102266173 C>T maps to NM_015490.3 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:102250604 G>A maps to NM_015490.3 T836T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr3:127786442 C>T maps to ENST00000464451 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr3:127786280 C>T maps to ENST00000464451 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:127783765 C>T maps to ENST00000464451 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:12191669 C>T maps to NM_018144.3 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr3:169700533 A>G maps to NM_003262.3 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr6:108218932 A>G maps to NM_007214.4 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr6:108230236 G>A maps to NM_007214.4 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr9:91949500 C>T maps to NM_024077.3 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:91964814 C>T maps to NM_024077.3 F621F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr15:49327568 G>A maps to NM_001193489.1 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:80280072 G>A maps to NM_003004.2 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:12984109 C>T maps to NM_001013437.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:82000022 G>A maps to NM_005065.4 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:81964265 G>A maps to NM_005065.4 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:13894460 G>A maps to NM_025229.1 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr20:13936760 T>C maps to NM_025229.1 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr4:25780744 G>A maps to NM_015187.3 I846I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr4:25760645 G>A maps to NM_015187.3 I1000I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:25803906 G>A maps to NM_015187.3 Q652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr4:25780744 G>A maps to NM_015187.3 I846I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:25823695 C>T maps to NM_015187.3 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:25836913 G>A maps to NM_015187.3 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr4:25806267 G>A maps to NM_015187.3 I557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr4:25789956 C>G maps to NM_015187.3 G702G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:25819832 G>A maps to NM_015187.3 F497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:25834645 G>A maps to NM_015187.3 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:169701993 G>A maps to NM_000450.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr1:169698339 G>A maps to NM_000450.2 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:169696610 C>T maps to NM_000450.2 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:169698417 G>A maps to NM_000450.2 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:169697229 C>T maps to NM_000450.2 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:169697039 G>A maps to NM_000450.2 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:169699597 C>T maps to NM_000450.2 W230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:169699598 C>T maps to NM_000450.2 W230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:169696640 A>G maps to NM_000450.2 V498V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr1:169699571 C>T did not map to a codon.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr1:169697313 G>A maps to NM_000450.2 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr1:169697247 G>A maps to NM_000450.2 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr1:169697036 C>T maps to NM_000450.2 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:169697229 C>T maps to NM_000450.2 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:169699696 C>T maps to NM_000450.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:169698417 G>A maps to NM_000450.2 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:169698399 G>A maps to NM_000450.2 F339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:169696961 C>T maps to NM_000450.2 E462E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:169697033 C>T maps to NM_000450.2 K438K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:169697036 C>T maps to NM_000450.2 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:169698760 G>A maps to NM_000450.2 Q257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr1:169702092 C>T maps to NM_000450.2 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:151340774 G>A maps to ENST00000435071 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:151340702 G>A maps to ENST00000435071 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr1:151338050 G>A maps to ENST00000435071 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:151341647 G>A maps to ENST00000435071 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:151339219 G>A maps to ENST00000435071 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:169672444 G>A maps to NM_000655.4 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:169670782 G>A maps to NM_000655.4 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:169676540 G>A maps to NM_000655.4 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr22:31501033 G>A maps to NM_080430.2 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr22:50649164 C>T maps to NM_031454.1 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr22:50649165 C>T maps to NM_031454.1 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:169572303 A>G maps to NM_003005.3 T555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr1:169582215 C>T maps to NM_003005.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:169586428 G>A maps to NM_003005.3 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:169586608 G>A maps to NM_003005.3 Y46Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:169582929 G>A maps to NM_003005.3 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:169564074 C>T maps to NM_003005.3 A714A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:169586416 G>A maps to NM_003005.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:169578855 G>A maps to NM_003005.3 Q407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:169565372 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:169586311 C>T maps to NM_003005.3 W145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:169562876 G>A maps to NM_003005.3 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:169586314 C>T maps to NM_003005.3 K144K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:169581509 T>C maps to NM_003005.3 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:109017753 C>T maps to ENST00000228463 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:109017753 C>T maps to ENST00000228463 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr15:101814676 G>A maps to NM_018445.4 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr3:150321205 C>T maps to NM_016275.3 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:150340892 G>A maps to NM_016275.3 K104K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr19:40009763 C>T maps to NM_182704.1 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:40009429 C>T maps to NM_182704.1 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr19:40009604 C>T maps to NM_182704.1 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:83592583 C>T maps to NM_006080.2 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr7:83640345 C>T maps to NM_006080.2 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:83758441 G>A maps to NM_006080.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr7:83689790 G>A maps to NM_006080.2 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr7:83689826 C>T maps to NM_006080.2 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:83764193 C>T maps to NM_006080.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:83689802 C>T maps to NM_006080.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:83591046 C>T maps to NM_006080.2 V652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:83631362 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:83634661 G>A maps to NM_006080.2 I451I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:83675643 G>A maps to NM_006080.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr7:83590695 C>T maps to NM_006080.2 R769R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr7:80427406 C>G did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:80418769 C>A maps to NM_006379.2 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr7:80427443 G>A maps to NM_006379.2 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:80374440 G>A maps to NM_006379.2 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr7:84666267 C>T maps to NM_152754.2 K376K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr7:84647597 G>A maps to NM_152754.2 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr7:84702397 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:84666345 G>A maps to NM_152754.2 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr7:84642161 C>T maps to NM_152754.2 R568R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr7:84710895 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr7:82997306 G>A maps to NM_012431.2 F641F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr7:83032081 G>A maps to NM_012431.2 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:83014732 C>T maps to NM_012431.2 K584K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:83032081 G>A maps to NM_012431.2 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:82997225 G>A maps to NM_012431.2 I668I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:83037699 A>G maps to NM_012431.2 D218D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr7:82997225 G>A maps to NM_012431.2 I668I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:83119492 G>A maps to NM_012431.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr7:83022000 G>A maps to NM_012431.2 Q513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:83014738 C>T maps to NM_012431.2 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:82997096 C>T maps to NM_012431.2 K711K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:82997078 G>A maps to NM_012431.2 I717I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:82997012 C>T maps to NM_012431.2 R739R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr7:83119495 G>A maps to NM_012431.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr7:83029391 G>A maps to NM_012431.2 R440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr7:83277753 C>G maps to NM_012431.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:82997177 C>T maps to NM_012431.2 K684K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:82997210 C>T maps to NM_012431.2 V673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:82997201 C>T maps to NM_012431.2 E676E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:83029527 G>A maps to NM_012431.2 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr3:50220646 C>T maps to NM_004186.3 D349D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:50220137 T>G maps to NM_004186.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:50225310 C>T maps to NM_004186.3 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:50220953 G>A maps to NM_004186.3 W397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:50224100 C>T maps to NM_004186.3 F623F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:50211349 C>T maps to NM_004186.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:50211350 C>T maps to NM_004186.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:50211680 C>T maps to NM_004186.3 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:50219774 C>T maps to NM_004186.3 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:50211367 C>T maps to NM_004186.3 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:50211674 G>A maps to NM_004186.3 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:50220637 G>A maps to NM_004186.3 Q346Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:50222237 C>T maps to NM_004186.3 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:50220960 C>T maps to NM_004186.3 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:50222930 G>A maps to NM_004186.3 E504E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr3:52474018 G>A maps to NM_020163.1 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:52476768 G>A maps to NM_020163.1 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:52475895 C>T maps to NM_020163.1 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:52476762 C>T maps to NM_020163.1 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr3:52472116 C>T maps to NM_020163.1 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:52475390 C>T maps to NM_020163.1 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:52475647 G>A maps to NM_020163.1 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:52472074 G>A maps to NM_020163.1 Y550Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:52472962 G>A maps to NM_020163.1 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:52475366 C>T maps to NM_020163.1 K242K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:52472065 G>A maps to NM_020163.1 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:52472086 G>A maps to NM_020163.1 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:52475668 C>T maps to NM_020163.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:156146226 C>T maps to NM_022367.3 I575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44Q-06A-11D-A25O-08 chr1:156132734 G>A maps to NM_022367.3 W328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:156146616 C>T maps to NM_022367.3 S705S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:156124464 G>A maps to NM_022367.3 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:156146721 G>A maps to NM_022367.3 K740K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:156142687 G>A maps to NM_022367.3 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:156145007 C>T maps to NM_022367.3 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:156128249 C>T maps to NM_022367.3 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:156128252 C>T maps to NM_022367.3 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr15:90764695 C>T maps to NM_198925.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr15:90760689 C>T maps to NM_198925.2 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:97527319 C>T maps to NM_017789.4 K556K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:97526998 G>A maps to NM_017789.4 A622A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:97530575 G>A maps to NM_017789.4 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:97532118 G>A maps to NM_017789.4 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr9:91994419 G>A maps to NM_006378.3 A596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:92006202 G>A maps to NM_006378.3 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:92008486 G>A maps to NM_006378.3 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr9:92002451 G>A maps to NM_006378.3 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr9:92002361 G>A maps to NM_006378.3 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:91994071 G>A maps to NM_006378.3 I712I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:92006330 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr2:74884744 G>A maps to NM_004263.3 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:74884996 T>C maps to NM_004263.3 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:74902715 C>T maps to NM_004263.3 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr2:74889938 A>C maps to NM_004263.3 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:74883760 G>A maps to NM_004263.3 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:74885032 C>T maps to NM_004263.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:74883772 C>T maps to NM_004263.3 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:74902994 C>T maps to NM_004263.3 F534F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:74902125 C>T maps to NM_004263.3 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:74884978 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:102739940 C>T maps to NM_017893.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:102740679 C>T maps to NM_017893.2 P523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr10:102738690 G>A maps to NM_017893.2 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr10:102740343 G>A maps to NM_017893.2 W454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:102743449 C>T maps to NM_017893.2 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:9063200 G>A maps to NM_003966.2 F772F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:9108304 G>A maps to NM_003966.2 Q674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:9190534 G>A maps to NM_003966.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:9154727 G>A maps to NM_003966.2 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:9380001 G>A maps to NM_003966.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:9154727 G>A maps to NM_003966.2 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr5:9043098 C>T maps to NM_003966.2 E1045E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr5:9052066 G>A maps to NM_003966.2 I921I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:9052062 G>A maps to NM_003966.2 L923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:9197354 G>A maps to NM_003966.2 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:9337874 G>A maps to NM_003966.2 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:9063101 C>T maps to NM_003966.2 R805R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr3:122629826 G>A maps to NM_001031702.2 L1053L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:122634724 C>T maps to NM_001031702.2 G567G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:122645327 C>T maps to NM_001031702.2 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr3:122645309 G>A maps to NM_001031702.2 Y355Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:122629770 C>T maps to NM_001031702.2 L1071L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:122642520 G>A maps to NM_001031702.2 Y405Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:122645393 C>T maps to NM_001031702.2 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:122629034 G>A maps to NM_001031702.2 F1137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:122645473 G>A maps to NM_001031702.2 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:122645474 G>A maps to NM_001031702.2 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:122646730 G>A maps to NM_001031702.2 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:122632265 G>A maps to NM_001031702.2 F762F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr3:122667437 G>A maps to NM_001031702.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:122631109 A>G maps to NM_001031702.2 R935R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:122642466 G>A maps to NM_001031702.2 F423F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr3:122680021 C>T maps to NM_001031702.2 W30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:122667506 G>A maps to NM_001031702.2 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:122646766 G>A maps to NM_001031702.2 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NF-06A-11D-A19A-08 chr3:122629052 G>A maps to NM_001031702.2 P1131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:122631746 G>A maps to NM_001031702.2 L890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:122632214 C>T maps to NM_001031702.2 W779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:122632265 G>A maps to NM_001031702.2 F762F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:122632736 G>A maps to NM_001031702.2 G700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:122634643 C>T maps to NM_001031702.2 W594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr3:122645327 C>T maps to NM_001031702.2 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:115783292 G>A maps to ENST00000257414 T720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:115783049 G>A maps to ENST00000257414 I801I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:115782557 G>A maps to ENST00000257414 S965S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:115782983 C>T maps to ENST00000257414 R823R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr5:115783139 G>A maps to ENST00000257414 A771A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:4558144 G>A maps to NM_032108.3 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:4548094 G>A maps to NM_032108.3 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:4554459 C>T maps to NM_032108.3 W237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr19:4550812 G>A maps to NM_032108.3 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:4544407 G>A maps to NM_032108.3 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:4554474 G>A maps to NM_032108.3 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:151110495 G>A maps to NM_001178061.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:151110474 G>A maps to NM_001178061.1 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:151108068 G>A maps to NM_001178061.1 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:151111939 G>A maps to NM_001178061.1 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:151109465 G>A maps to NM_001178061.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr1:151105667 C>A maps to NM_001178061.1 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr1:151112558 G>A maps to NM_001178061.1 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:151105852 G>A maps to NM_001178061.1 R666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:151105853 G>A maps to NM_001178061.1 H665H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:151108511 G>A maps to NM_001178061.1 Q412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:151108593 A>C maps to NM_001178061.1 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:151110474 G>A maps to NM_001178061.1 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:48060829 C>T maps to NM_153618.1 I606I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr15:48063525 C>T maps to NM_153618.1 V922V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr15:48052081 C>T maps to NM_153618.1 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:48055273 C>T maps to NM_153618.1 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr15:48058106 T>A maps to NM_153618.1 L490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr15:74708936 G>A maps to NM_003612.3 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr15:74711171 G>A maps to NM_003612.3 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr20:43836378 G>A maps to NM_003007.3 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr20:43836231 A>G maps to NM_003007.3 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr20:43835770 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr20:43836840 A>C maps to NM_003007.3 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr20:43851115 G>C maps to NM_003008.2 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:43851158 A>C maps to NM_003008.2 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:43850540 C>T maps to NM_003008.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:43851397 G>A maps to NM_003008.2 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr20:43851541 G>A maps to NM_003008.2 K423K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:43850449 C>T maps to NM_003008.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr20:43850422 A>T maps to NM_003008.2 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr20:43851397 G>A maps to NM_003008.2 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:48482618 G>A maps to ENST00000004980 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:48458934 C>T maps to ENST00000004980 K396K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:185330416 A>C maps to ENST00000427465 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:185337193 T>C maps to ENST00000427465 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr3:185307940 C>T maps to ENST00000427465 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:196612840 C>T maps to NM_152699.4 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr6:76412390 C>T maps to NM_015571.2 F773F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr6:76350408 C>T maps to NM_015571.2 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:76412654 G>A maps to NM_015571.2 V861V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:76369080 T>A maps to NM_015571.2 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:101136569 G>A maps to NM_020654.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr3:101090874 A>T maps to NM_020654.3 L258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:101086762 G>A maps to NM_020654.3 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:101060584 G>A maps to NM_020654.3 F715F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr15:72432497 C>T maps to NM_145204.3 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:72432141 C>T maps to NM_145204.3 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:72432137 C>T maps to NM_145204.3 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:72432291 C>T maps to NM_145204.3 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr10:13386799 G>A maps to NM_012247.4 Q51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr10:13386800 G>A maps to NM_012247.4 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:13380725 G>A maps to NM_012247.4 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr10:13380725 G>A maps to NM_012247.4 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr10:13380731 G>A maps to NM_012247.4 Y90Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr16:30455806 G>A maps to ENST00000478753 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr16:30455896 A>C maps to ENST00000478753 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:26140456 C>T maps to NM_020451.2 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:26138010 C>T maps to NM_020451.2 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:26135081 C>T maps to NM_020451.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:26131721 C>T maps to NM_020451.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr1:26131759 C>T maps to NM_020451.2 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr5:42801046 C>T maps to NM_001093726.1 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr5:42804835 G>A maps to NM_001093726.1 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr5:42808287 T>C maps to NM_001093726.1 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr5:42801130 C>T maps to NM_001093726.1 K309K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr5:42807011 G>A maps to NM_001093726.1 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:42801054 G>A maps to NM_001093726.1 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr5:42804832 G>A maps to NM_001093726.1 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr5:42808344 T>C maps to NM_001093726.1 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:42807044 G>A maps to NM_001093726.1 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:42807210 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr4:25125801 G>A maps to NM_016955.3 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr4:25125708 G>A maps to NM_016955.3 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr16:30392691 G>A maps to NM_052838.3 C136C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr2:110310774 G>A maps to ENST00000356688 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:110321940 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:77949799 A>G maps to ENST00000510515 E334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr4:77941742 C>T maps to ENST00000510515 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr4:77941689 C>T maps to ENST00000510515 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr16:4833546 G>A maps to NM_144605.3 N214N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:4833742 G>A maps to NM_144605.3 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr16:4829766 C>T maps to NM_144605.3 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr16:4834002 G>A maps to NM_144605.3 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:55863770 G>A maps to NM_207366.2 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:55874915 G>T maps to NM_207366.2 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:55874949 C>T maps to NM_207366.2 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:55872950 C>T maps to NM_207366.2 E373E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:55863728 G>A maps to NM_207366.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr7:55863611 C>T maps to NM_207366.2 K431K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:55914297 C>T maps to NM_207366.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:55863770 G>A maps to NM_207366.2 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:55873039 G>A maps to NM_207366.2 Q344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:55874925 G>A maps to NM_207366.2 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:55863611 C>T maps to NM_207366.2 K431K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:242285598 C>T maps to ENST00000391972 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr2:242289489 C>T maps to ENST00000391972 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:242285634 C>T maps to ENST00000391972 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr22:42383210 G>A maps to NM_145733.2 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:42377781 C>T maps to NM_145733.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr22:42383745 C>T maps to NM_145733.2 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr22:42377817 C>T maps to NM_145733.2 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr17:56599114 C>T maps to NM_004574.3 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr17:56604276 G>A maps to NM_004574.3 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr17:56598702 G>A maps to NM_004574.3 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr17:56599380 G>A maps to NM_004574.3 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:56599150 G>A maps to NM_004574.3 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:56599281 C>T maps to NM_080415.2 K262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr22:19707890 C>T maps to NM_002688.5 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr22:19707341 G>A maps to NM_002688.5 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:19707965 C>T maps to NM_002688.5 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:118763464 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:118784019 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:118783979 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:118786935 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:118771076 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:118783992 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:118786966 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr7:35872490 A>G maps to NM_001788.4 E49E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:132100088 G>A maps to NM_001098811.1 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr17:75398447 C>T maps to NM_001113491.1 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr17:75471896 T>G maps to NM_001113495.1 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr17:75471617 G>A maps to NM_001113495.1 W6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr17:75398633 C>T maps to NM_001113491.1 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:48282053 C>A maps to NM_003009.2 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr6:158541536 G>A maps to NM_032861.3 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:158565363 A>G maps to NM_032861.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr6:158534505 G>A maps to NM_032861.3 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr1:67895944 G>C maps to NM_001018067.1 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr11:18025993 G>A maps to NM_012139.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:18026016 G>A maps to NM_012139.2 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:42956257 G>A maps to NM_014509.3 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr6:122767980 G>A maps to NM_020755.2 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:31896634 C>T maps to NM_178865.4 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr20:43142582 G>A maps to NM_006811.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:43142615 G>A maps to NM_006811.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:43142582 G>A maps to NM_006811.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr20:43139984 G>A maps to NM_006811.2 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:44087898 C>T maps to ENST00000319327 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr15:44087629 G>A maps to ENST00000319327 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:79498770 G>A maps to NM_001174072.1 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:79498761 G>A maps to NM_001174072.1 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:79441965 G>A maps to NM_001174072.1 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:79441965 G>A maps to NM_001174072.1 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:94847251 G>A maps to NM_001127707.1 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr14:94845869 G>A maps to NM_001127707.1 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:94847296 G>A maps to NM_001127707.1 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:94849448 C>T maps to NM_001127707.1 Q42Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr14:94847428 G>A maps to NM_001127707.1 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr14:94754771 C>T maps to NM_001100607.1 K281K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr14:94756492 C>T maps to NM_001100607.1 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr14:94754894 C>T maps to NM_001100607.1 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:94756336 G>A maps to NM_001100607.1 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr14:94756563 G>A maps to NM_001100607.1 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr14:94756534 G>A maps to NM_001100607.1 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:94756498 G>A maps to NM_001100607.1 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:94756699 C>T maps to NM_001100607.1 K77K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:94756684 G>A maps to NM_001100607.1 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:94756231 C>T maps to NM_001100607.1 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr14:94756606 G>A maps to NM_001100607.1 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr14:94756471 G>A maps to NM_001100607.1 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:94754867 G>A maps to NM_001100607.1 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:94756285 C>T maps to NM_001100607.1 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr14:94912738 C>T maps to NM_001080451.1 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr14:94909131 C>T maps to NM_001080451.1 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:94912738 C>T maps to NM_001080451.1 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:94914508 C>T maps to NM_001080451.1 Q201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:94914804 G>A maps to NM_001080451.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr14:94912840 C>T maps to NM_001080451.1 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:94912696 C>T maps to NM_001080451.1 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr14:94914814 G>A maps to NM_001080451.1 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr14:94912909 C>T maps to NM_001080451.1 Q225Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr14:94912825 G>A maps to NM_001080451.1 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr14:94914514 G>A maps to NM_001080451.1 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr14:94964173 C>T maps to NM_173850.2 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr14:94962729 C>T maps to NM_173850.2 W295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:94955959 G>C maps to NM_173850.2 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr14:94964482 G>A maps to NM_173850.2 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:94962912 A>G maps to NM_173850.2 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr14:94964659 G>A maps to NM_173850.2 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:94962930 G>A maps to NM_173850.2 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr14:94964179 G>A maps to NM_173850.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr14:95088747 C>T maps to ENST00000393080 Q355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr14:95088729 C>T maps to ENST00000393080 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr14:95081353 C>T maps to ENST00000393080 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr14:95081239 G>A maps to ENST00000393080 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr14:95085772 C>T maps to ENST00000393080 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:95081290 G>A maps to ENST00000393080 Q196Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:95080918 C>T maps to ENST00000393080 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr14:95081347 G>A maps to ENST00000393080 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr14:95080939 G>A maps to ENST00000393080 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr14:95081290 G>A maps to ENST00000393080 Q196Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr14:95081242 G>A maps to ENST00000393080 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr14:95088719 G>A maps to ENST00000393080 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr14:95081329 G>A maps to ENST00000393080 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr14:95080885 G>A maps to ENST00000393080 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr14:95081347 G>A maps to ENST00000393080 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:95090039 G>A maps to ENST00000393080 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr14:95090105 G>A maps to ENST00000393080 Q434Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr14:95030283 C>T maps to NM_006215.2 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:95030379 G>A maps to NM_006215.2 K187K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr14:95029830 C>T maps to NM_006215.2 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:95030271 C>T maps to NM_006215.2 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr14:95030310 G>A maps to NM_006215.2 E164E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr14:95033312 G>A maps to NM_006215.2 W219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:95030175 G>A maps to NM_006215.2 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:95034465 G>A maps to NM_006215.2 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:95035856 C>T maps to NM_006215.2 F403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:95035922 G>A maps to NM_006215.2 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr14:95033517 G>A maps to NM_006215.2 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr14:95029968 G>A maps to NM_006215.2 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr14:95030427 G>A maps to NM_006215.2 K203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr14:95033574 G>A maps to NM_006215.2 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:95030025 G>A maps to NM_006215.2 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:95033490 C>T maps to NM_006215.2 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr14:95033382 G>A maps to NM_006215.2 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr14:95054238 G>A maps to NM_000624.4 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr14:95057106 C>T maps to NM_000624.4 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr14:95053710 C>T maps to NM_000624.4 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:95053902 C>T maps to NM_000624.4 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr14:95053710 C>T maps to NM_000624.4 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr14:95054318 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:95053896 C>T maps to NM_000624.4 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:95057220 C>T maps to NM_000624.4 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr14:95054271 C>T maps to NM_000624.4 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:95053749 C>T maps to NM_000624.4 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:95056387 G>A maps to NM_000624.4 E210E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:95057175 C>T maps to NM_000624.4 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:95058563 G>A maps to NM_000624.4 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr14:95057148 C>A maps to NM_000624.4 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:95053776 G>A maps to NM_000624.4 E26E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr14:94780400 G>A maps to NM_001756.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:94770781 G>A maps to NM_001756.3 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr14:94780715 G>A maps to NM_001756.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:94780691 A>G maps to NM_001756.3 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:94770799 G>A maps to NM_001756.3 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:94776281 C>T maps to NM_001756.3 E225E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:94780445 C>T maps to NM_001756.3 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr14:94776089 G>A maps to NM_001756.3 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:94776173 C>T maps to NM_001756.3 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:94772530 C>T maps to NM_001756.3 K303K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr14:94770781 G>A maps to NM_001756.3 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:94776125 G>A maps to NM_001756.3 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:94780658 G>A maps to NM_001756.3 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:94780766 G>A maps to NM_001756.3 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr23:105280694 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr23:105280881 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:105277522 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:105280495 A>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:105277517 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr23:105280704 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:105279184 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:105278307 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr23:105280481 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:105280644 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr23:105280840 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:105277499 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:105277505 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:105279278 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:105280592 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:105280657 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:105280807 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr23:105280604 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr23:105279361 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr23:105280806 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:105279123 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:105280811 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:105280470 C>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:105279177 T>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:105280896 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:105280676 C>T did not map to a codon.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr23:105280575 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:94933501 C>T maps to NM_175739.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr14:94929441 G>T maps to NM_175739.3 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:94935573 G>A maps to NM_175739.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr14:94931160 G>A maps to NM_175739.3 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr14:94935928 G>A maps to NM_175739.3 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr14:94929549 C>T maps to NM_175739.3 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:94929537 G>A maps to NM_175739.3 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:94933696 G>A maps to NM_175739.3 H235H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:94935628 G>A maps to NM_175739.3 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr14:94931058 G>A maps to NM_175739.3 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr14:94933528 G>A maps to NM_175739.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr14:94935964 G>A maps to NM_175739.3 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:2833937 G>A maps to NM_030666.2 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr18:61587098 C>T maps to NM_005024.1 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr18:61585197 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr18:61585197 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:61585239 C>T maps to NM_005024.1 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:61587118 G>A maps to NM_005024.1 W157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:61597339 G>A maps to NM_005024.1 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:61602271 C>T maps to NM_005024.1 N330N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr18:61597288 G>A maps to NM_005024.1 Q167Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr18:61597402 G>A maps to NM_005024.1 K205K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr18:61387271 G>A maps to NM_080475.2 K167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr18:61390506 G>A maps to NM_080475.2 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr18:61383354 G>A maps to NM_080475.2 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr18:61390572 C>T maps to NM_080475.2 F373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:61378628 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr18:61390599 G>A maps to NM_080475.2 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr18:61383298 C>T maps to NM_080475.2 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr18:61383348 G>A maps to NM_080475.2 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr18:61390599 G>A maps to NM_080475.2 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:61225608 C>T maps to ENST00000382768 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr18:61228352 G>A maps to ENST00000382768 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr18:61225607 C>T maps to ENST00000382768 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr18:61233847 G>A maps to ENST00000382768 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr18:61234210 C>T maps to ENST00000382768 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr18:61226938 C>T maps to ENST00000382768 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr18:61228355 G>A maps to ENST00000382768 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:61232796 C>T maps to ENST00000382768 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr18:61262348 G>A maps to NM_012397.3 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr18:61262318 C>T maps to NM_012397.3 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr18:61256065 G>A maps to NM_012397.3 E55E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:61262328 T>C maps to NM_012397.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr18:61259697 C>T maps to NM_012397.3 Y114Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr18:61264293 G>A maps to NM_012397.3 E291E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr18:61261697 A>G maps to NM_012397.3 E194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr18:61262318 C>T maps to NM_012397.3 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:61261587 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:61262369 C>T maps to NM_012397.3 D241D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:61264575 C>T maps to NM_012397.3 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr18:61262303 C>T maps to NM_012397.3 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr18:61570537 A>T maps to NM_001143818.1 *416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:61569061 G>A maps to NM_001143818.1 W208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr18:61565016 C>T maps to NM_001143818.1 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:61570517 C>T maps to NM_001143818.1 F409F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr18:61564404 G>A maps to NM_001143818.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:61562571 C>T maps to NM_001143818.1 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:61564392 G>A maps to NM_001143818.1 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:61570355 C>T maps to NM_001143818.1 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr18:61569049 C>T maps to NM_001143818.1 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:61569034 G>A maps to NM_001143818.1 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr18:61322950 G>A maps to NM_006919.2 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr18:61326680 C>T maps to NM_006919.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr18:61328074 G>A maps to NM_006919.2 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr18:61325750 C>T maps to NM_006919.2 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr18:61328389 T>A maps to NM_006919.2 K21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr18:61323244 C>T maps to NM_006919.2 Q273Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr18:61326698 G>A maps to NM_006919.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr18:61326643 G>A maps to NM_006919.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr18:61322956 G>A maps to NM_006919.2 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr18:61324063 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:61324205 G>A maps to NM_006919.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr18:61328396 C>T maps to NM_006919.2 Q18Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr18:61328407 G>A maps to NM_006919.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr18:61310799 G>A maps to NM_002974.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr18:61309020 G>A maps to NM_002974.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr18:61306490 C>T maps to NM_002974.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr18:61310694 C>T maps to NM_002974.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr18:61304982 G>A maps to NM_002974.2 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr18:61310739 C>T maps to NM_002974.2 E24E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr18:61308141 C>T maps to NM_002974.2 K145K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr18:61310721 G>A maps to NM_002974.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:61156596 G>A maps to NM_002639.4 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr6:2948627 G>A maps to ENST00000316782 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:2948777 G>A maps to ENST00000316782 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:2953286 T>C maps to ENST00000316782 K221K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr6:2948849 G>A maps to ENST00000316782 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr18:61468107 G>A maps to NM_001040147.1 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr18:61465847 G>A maps to NM_001040147.1 K155K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr18:61468137 G>A maps to NM_001040147.1 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr18:61471507 G>A maps to NM_001040147.1 W261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr18:61449740 C>T maps to NM_001040147.1 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr18:61449692 C>T maps to NM_001040147.1 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr18:61471569 G>T maps to NM_001040147.1 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr18:61468107 G>A maps to NM_001040147.1 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:61449755 C>T maps to NM_001040147.1 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr18:61471867 G>A maps to NM_001040147.1 *381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr18:61459656 G>T maps to NM_001040147.1 G67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr18:61471605 C>T maps to NM_001040147.1 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr18:61471867 G>A maps to NM_001040147.1 *381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:61463558 G>A maps to NM_001040147.1 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:61468131 G>A maps to NM_001040147.1 Q210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr18:61449713 C>T maps to NM_001040147.1 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr18:61654136 C>T maps to NM_198833.1 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr18:61654340 C>T maps to NM_198833.1 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr18:61654187 C>T maps to NM_198833.1 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:61645656 C>T maps to NM_198833.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr18:61654451 C>T maps to NM_198833.1 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr6:2900803 G>A maps to NM_004155.4 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:2890585 G>A maps to NM_004155.4 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr6:2890647 G>A maps to NM_004155.4 Q294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:2900695 G>A maps to NM_004155.4 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:2890585 G>A maps to NM_004155.4 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr1:173880993 G>A maps to NM_000488.3 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:173883915 C>T maps to NM_000488.3 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr22:21141179 G>A maps to NM_000185.3 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:100771898 A>C maps to NM_000602.3 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:100777117 C>T maps to NM_000602.3 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr2:224856568 C>T maps to NM_001136530.1 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:224849629 G>A maps to NM_001136530.1 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:224866464 G>A maps to NM_001136530.1 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:224866632 G>A maps to NM_001136530.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr13:51922374 C>T maps to NM_001101320.1 Q243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr13:51935964 G>A maps to NM_001101320.1 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr13:51918394 G>A maps to NM_001101320.1 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr17:1678350 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr17:1674329 G>A maps to NM_002615.4 E97E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr17:1657584 G>A maps to NM_000934.3 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:1651890 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:1649138 C>T maps to NM_000934.3 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:1650747 C>T maps to NM_000934.3 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:57373618 C>T maps to ENST00000403558 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:57379248 G>A maps to ENST00000403558 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr11:57367644 C>G maps to ENST00000403558 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr11:57367645 C>T maps to ENST00000403558 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:57381807 C>T maps to ENST00000403558 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:57381987 C>T maps to ENST00000403558 F522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:57379245 C>T maps to ENST00000403558 N405N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:57367837 C>T maps to ENST00000403558 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:57381936 C>T maps to ENST00000403558 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:75279854 C>T maps to NM_001235.2 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:75277831 C>T maps to NM_001235.2 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:167510405 G>A maps to NM_005025.4 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr3:167525034 C>T maps to NM_005025.4 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr3:167506978 C>T maps to NM_005025.4 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr3:167543098 C>T maps to NM_005025.4 F407F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:167510532 C>T maps to NM_005025.4 Q213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr3:167510376 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:167525097 C>T maps to NM_005025.4 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr3:167543104 A>G maps to NM_005025.4 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:167183028 C>T maps to NM_006217.3 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:167183360 G>A maps to NM_006217.3 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:167184984 G>A maps to NM_006217.3 Y112Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr3:167184855 T>C maps to NM_006217.3 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:167189610 G>A maps to NM_006217.3 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr3:167184987 G>A maps to NM_006217.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:167189519 G>A maps to NM_006217.3 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:167164252 C>T maps to NM_006217.3 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:167184963 C>T maps to NM_006217.3 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr3:167170816 T>A maps to NM_006217.3 K291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:167183118 G>A maps to NM_006217.3 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:64863942 G>A maps to NM_014755.2 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr2:64863654 G>A maps to NM_014755.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:40947744 G>A maps to NM_203344.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:210411351 C>A maps to NM_019605.3 S16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:210415345 T>C maps to NM_019605.3 D245D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:210414988 C>T maps to NM_019605.3 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:210414907 C>T maps to NM_019605.3 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:210414946 C>T maps to NM_019605.3 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:210415615 C>T maps to NM_019605.3 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr6:109319925 G>A maps to NM_014454.1 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:109319811 G>A maps to NM_014454.1 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr1:28605700 C>T maps to NM_031459.3 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:28607247 C>T maps to NM_031459.3 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:28605652 G>A maps to NM_031459.3 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:28595740 C>A maps to NM_031459.3 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr11:94918596 G>A maps to NM_144665.2 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:180056520 G>A maps to NM_178123.4 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr2:179979886 G>A maps to NM_178123.4 R582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:131455960 G>A maps to NM_001122821.1 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr18:42532418 C>T maps to NM_015559.2 F1038F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr18:42531896 G>A maps to NM_015559.2 T864T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:42533084 G>A maps to NM_015559.2 T1260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr18:42531491 G>A maps to NM_015559.2 R729R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr18:42531785 G>A maps to NM_015559.2 W827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr18:42532124 G>A maps to NM_015559.2 R940R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr18:42643131 C>T maps to NM_015559.2 I1420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr18:42618612 G>A maps to NM_015559.2 S1388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr18:42281736 C>T maps to NM_015559.2 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr18:42531221 G>A maps to NM_015559.2 E639E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr18:42530558 G>A maps to NM_015559.2 R418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr18:42531845 C>T maps to NM_015559.2 S847S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr18:42531059 G>A maps to NM_015559.2 K585K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr18:42532838 C>T maps to NM_015559.2 A1178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:42532995 C>T maps to NM_015559.2 L1231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr18:42530558 G>A maps to NM_015559.2 R418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr18:42531998 C>T maps to NM_015559.2 S898S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr18:42531572 G>A maps to NM_015559.2 P756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr18:42530951 C>T maps to NM_015559.2 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr18:42533291 C>T maps to NM_015559.2 S1329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:42281670 G>A maps to NM_015559.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr18:42281763 G>A maps to NM_015559.2 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr16:30991854 C>T maps to NM_014712.1 P1486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:30972805 C>T maps to NM_014712.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:30978284 C>T maps to NM_014712.1 S862S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr16:30995334 C>T maps to NM_014712.1 S1705S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr16:30982822 C>G maps to NM_014712.1 S1047S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr16:30976274 C>T maps to NM_014712.1 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr16:30972748 C>T maps to NM_014712.1 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:47164379 G>A maps to NM_014159.6 I582I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:47125361 G>A maps to NM_014159.6 L1970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:47162161 G>A maps to NM_014159.6 R1322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:47158224 G>A maps to NM_014159.6 R1492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr3:47098525 G>A maps to NM_014159.6 Q2250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:47163856 G>A maps to NM_014159.6 Q757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:47163475 G>A maps to NM_014159.6 Q884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr14:99924780 G>A maps to NM_032233.2 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr14:99879296 G>A maps to NM_032233.2 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr14:99871663 G>A maps to NM_032233.2 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr14:99865351 A>C maps to NM_032233.2 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr21:37418269 G>A maps to NM_017438.3 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr3:9486918 G>T maps to ENST00000407969 E478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:9489683 C>A maps to ENST00000407969 T718T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:140439175 G>A maps to NM_030648.2 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:123875205 C>T maps to NM_020382.3 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:123875267 C>A maps to NM_020382.3 S75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:123892186 C>T maps to NM_020382.3 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:150921899 C>T maps to NM_001145415.1 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr1:150921737 C>T maps to NM_001145415.1 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr13:50062648 T>C maps to NM_031915.2 D612D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr13:50065896 G>A maps to NM_031915.2 W691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr13:50055133 C>T maps to NM_031915.2 N358N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr13:50055133 C>T maps to NM_031915.2 N358N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:135204947 T>A maps to ENST00000372169 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr9:135158746 G>A maps to ENST00000372169 I2150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:135206522 G>A maps to ENST00000372169 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:135201740 G>A maps to ENST00000372169 F1748F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr9:135158695 G>A maps to ENST00000372169 F2167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:135139745 G>A maps to ENST00000372169 F2667F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:135206510 C>G maps to ENST00000372169 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:135140050 G>A maps to ENST00000372169 Q2566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:135145025 G>A maps to ENST00000372169 I2421I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:27308581 G>A maps to NM_178860.4 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:27306817 C>T maps to NM_178860.4 W246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr17:27296880 G>A maps to NM_178860.4 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr17:27285067 C>T maps to NM_178860.4 V733V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:27308884 G>A maps to NM_178860.4 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr17:27286791 C>T maps to NM_178860.4 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr17:27284992 C>T maps to NM_178860.4 W758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr17:27308494 G>A maps to NM_178860.4 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr17:27284986 C>T maps to NM_178860.4 E760E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:27287920 G>T maps to NM_178860.4 Y437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr22:26692963 C>T maps to NM_021115.4 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr22:26702041 G>A maps to NM_021115.4 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr22:26688978 G>A maps to NM_021115.4 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr22:26706635 G>A maps to NM_021115.4 R505R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr22:26736404 G>A maps to NM_021115.4 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr22:26688786 G>A maps to NM_021115.4 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr22:26688744 C>T maps to NM_021115.4 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr22:26736598 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:26707866 C>T maps to NM_021115.4 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr22:26688730 C>T maps to NM_021115.4 Q152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:26692916 C>T maps to NM_021115.4 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr22:26693008 G>A maps to NM_021115.4 Q375Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:26688909 G>A maps to NM_021115.4 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr22:26707731 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr22:26688843 G>A maps to NM_021115.4 K189K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr22:26709826 C>T maps to NM_021115.4 I658I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr22:26688663 G>A maps to NM_021115.4 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:26688486 C>T maps to NM_021115.4 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:26707776 G>A maps to NM_021115.4 G575G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:26761338 G>A maps to NM_021115.4 S867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr22:26706776 C>T maps to NM_021115.4 A552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:26707902 G>A maps to NM_021115.4 W617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr22:26692894 C>T maps to NM_021115.4 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr22:26747087 G>A maps to NM_021115.4 V826V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr22:26688825 C>T maps to NM_021115.4 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr22:26736482 G>A maps to NM_021115.4 G699G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:26688486 C>T maps to NM_021115.4 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:26688702 C>T maps to NM_021115.4 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:26690363 C>T maps to NM_021115.4 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:26694974 C>T maps to NM_021115.4 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:26747145 C>T maps to NM_021115.4 L846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr22:26688981 G>A maps to NM_021115.4 E235E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr22:26688564 C>T maps to NM_021115.4 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr16:29907122 C>T maps to NM_201575.2 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr16:29908155 C>T maps to NM_201575.2 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:29883582 G>A maps to NM_201575.2 F876F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:29906685 G>A maps to NM_201575.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr16:29906769 C>T maps to NM_201575.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr16:29891209 C>T maps to NM_201575.2 W516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:29908236 G>A maps to NM_201575.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr16:29909233 G>A maps to NM_201575.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr16:29909285 C>T maps to NM_201575.2 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:64533496 G>A maps to NM_201995.2 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr11:64537795 C>T maps to NM_201995.2 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr11:64532980 G>A maps to NM_201995.2 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr22:30735184 G>A maps to NM_005877.4 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:30742480 G>A maps to NM_005877.4 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:38450405 G>A maps to NM_006802.2 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:38435102 G>A maps to NM_006802.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr2:198288627 G>A maps to NM_012433.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr2:198264884 T>C maps to NM_012433.2 K969K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr2:198266519 G>A maps to NM_012433.2 I772I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr2:198273221 C>A maps to NM_012433.2 G330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:24290697 C>T maps to NM_016047.3 K104K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:65826342 C>T maps to NM_006842.2 Q337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:65828150 C>T maps to NM_006842.2 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:65827416 C>T maps to NM_006842.2 F522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr11:65826341 C>T maps to NM_006842.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr11:65822641 C>T maps to NM_006842.2 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:65829158 G>A maps to NM_006842.2 G594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:70605667 C>T maps to NM_012426.4 P1202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:70605709 C>T maps to NM_012426.4 A1216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr16:70562803 C>T maps to NM_012426.4 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr16:70595630 T>C maps to NM_012426.4 G744G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:70588472 C>T maps to NM_012426.4 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:70599144 C>T maps to NM_012426.4 Q881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr16:70605700 C>T maps to NM_012426.4 T1213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr16:70601420 C>T maps to NM_012426.4 L978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:70605011 C>T maps to NM_012426.4 F1141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:149895453 G>A maps to NM_005850.3 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:149895904 C>T maps to NM_005850.3 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:149899117 G>A maps to NM_005850.3 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:19389561 G>A maps to NM_172231.2 F524F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:19407921 T>C maps to NM_172231.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:19387761 G>A maps to NM_172231.2 N635N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:19420912 G>A maps to NM_172231.2 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr22:32014352 C>T maps to NM_001007467.1 P1226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr22:31998229 G>A maps to NM_001007467.1 W526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:31985557 C>T maps to NM_001007467.1 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr22:32009697 G>A maps to NM_001007467.1 R951R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr22:31942913 C>T maps to NM_001007467.1 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:52950198 G>A maps to NM_016329.3 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr3:52954616 A>G maps to NM_016329.3 D436D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:52941279 G>A maps to NM_016329.3 S712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:52955763 G>A maps to NM_016329.3 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:7262486 G>A maps to NM_001018039.1 R406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr10:7218090 G>A maps to NM_001018039.1 I615I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr10:7230607 G>A maps to NM_001018039.1 Q596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr10:7213003 C>T maps to NM_001018039.1 E810E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:7212937 G>A maps to NM_001018039.1 F832F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:7262418 G>A maps to NM_001018039.1 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr10:7213012 C>T maps to NM_001018039.1 T807T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr10:7218090 G>A maps to NM_001018039.1 I615I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:7262415 G>A maps to NM_001018039.1 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:27190434 G>A maps to NM_006142.3 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:35652631 G>A maps to NM_005066.2 T652T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:41122808 C>T maps to NM_003012.4 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:41122946 C>T maps to NM_003012.4 K228K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr8:41122982 C>T maps to NM_003012.4 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:154702800 C>T maps to NM_003013.2 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr4:154702752 G>A maps to NM_003013.2 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:37954008 C>T maps to ENST00000223214 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:37951817 G>A maps to ENST00000223214 R254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr7:37951872 C>T maps to ENST00000223214 E235E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr7:37953975 G>A maps to ENST00000223214 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:99527510 C>T maps to NM_003015.3 K238K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:70715709 C>T maps to NM_004768.3 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:70687415 G>T maps to NM_004768.3 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:65459652 C>T maps to NM_001077199.1 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:65460689 C>T maps to NM_001077199.1 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr19:19114992 G>T maps to NM_001017392.3 L971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr19:19120937 G>A maps to NM_001017392.3 L688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr19:19120955 G>A maps to NM_001017392.3 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr19:19106038 C>A maps to NM_001017392.3 L1014L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:19135662 G>A maps to NM_001017392.3 I498I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:19112430 G>A maps to NM_001017392.3 S994S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:19112481 G>A maps to NM_001017392.3 V977V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr19:19120952 G>A maps to NM_001017392.3 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19105984 G>A maps to NM_001017392.3 S1032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr21:33064135 G>A maps to NM_020706.2 S574S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr21:33057750 G>A maps to NM_020706.2 S752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr19:45563721 C>T maps to NM_007056.2 Y262Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:1714277 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr23:1718146 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:1712999 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr23:1712775 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:1719913 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:1719912 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr6:99849092 T>A maps to NM_032870.2 K581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr6:99860602 C>T maps to NM_032870.2 W34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:99856121 G>A maps to NM_032870.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr6:99851717 G>A maps to NM_032870.2 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:99848993 G>A maps to NM_032870.2 R614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:99848994 G>A maps to NM_032870.2 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr12:46339062 A>G maps to NM_004719.2 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:46320945 G>A maps to NM_004719.2 S846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:46320216 A>C maps to NM_004719.2 Y1089*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:46318573 G>A maps to NM_004719.2 P1281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:46320975 C>T maps to NM_004719.2 K836K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:46320977 T>A maps to NM_004719.2 K836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr6:36569553 C>T maps to NM_003017.4 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr1:29475056 C>A maps to NM_005626.4 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr14:70235599 C>T maps to NM_006925.3 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr20:42089645 C>T maps to NM_006275.5 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr20:42089158 C>T maps to NM_006275.5 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr20:42089212 C>A maps to NM_006275.5 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:38976767 G>A maps to NM_001031684.2 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr2:38977247 A>G maps to NM_001031684.2 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr2:38977331 G>A maps to NM_001031684.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:132209996 C>T maps to NM_004592.2 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr12:132237734 C>T maps to NM_004592.2 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:132238957 C>T maps to NM_004592.2 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr12:132198654 C>T maps to NM_004592.2 Y86Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr12:132209969 C>T maps to NM_004592.2 H209H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr12:120903444 G>A maps to NM_003769.2 R112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:166743717 G>A maps to NM_145169.1 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:30899846 G>A maps to NM_205854.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:30899507 G>A maps to NM_205854.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr6:30899539 C>A maps to NM_205854.2 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr14:36960450 G>A maps to NM_001101341.1 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr10:81373829 G>A maps to NM_001093770.2 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr10:81372116 G>A maps to NM_001093770.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:81373757 C>T maps to NM_001093770.2 Y227Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:81372945 G>A maps to NM_001093770.2 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:85894226 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:85892728 C>T maps to NM_198843.2 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr2:85892782 G>A maps to NM_198843.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr2:85892447 C>T maps to NM_198843.2 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr2:85892779 G>A maps to NM_198843.2 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:85893847 G>A maps to NM_198843.2 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr10:81697823 G>A maps to NM_003019.4 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:81697910 C>T maps to NM_003019.4 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:81702204 C>T maps to NM_003019.4 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:81702240 A>C maps to NM_003019.4 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr10:81700485 C>T maps to NM_003019.4 Q242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:81697940 G>A maps to NM_003019.4 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr10:81701172 C>T maps to NM_003019.4 K216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:81701770 G>A maps to NM_003019.4 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:81697725 C>T maps to NM_003019.4 W337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:81697928 G>A maps to NM_003019.4 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:81706229 C>T maps to NM_003019.4 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:81701761 T>C maps to NM_003019.4 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A6L9-06A-11D-A32N-08 chr5:174939194 C>T maps to NM_022754.5 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:174936155 C>T maps to NM_022754.5 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:174940516 G>A maps to NM_022754.5 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:104486482 C>T maps to NM_178858.4 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:104486896 C>T maps to NM_178858.4 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr10:104488271 C>T maps to NM_178858.4 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:102794525 G>A maps to NM_030971.3 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:102799290 C>T maps to NM_030971.3 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr10:102797184 G>A maps to NM_030971.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:120914642 G>A maps to NM_213649.1 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:120917535 G>A maps to NM_213649.1 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:120919251 G>A maps to NM_213649.1 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:120914602 G>A maps to NM_213649.1 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:120914603 G>A maps to NM_213649.1 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:73188367 G>A maps to NM_144579.2 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr2:73188367 G>A maps to NM_144579.2 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:73215455 G>A maps to NM_144579.2 Q186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:73228692 G>A maps to NM_144579.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:48246560 T>G maps to NM_000023.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:48247703 G>A maps to NM_000023.2 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:48247505 G>A maps to NM_000023.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:48245369 G>A maps to NM_000023.2 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:48245360 G>A maps to NM_000023.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr4:52894172 G>A maps to NM_000232.4 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:156074492 C>T maps to NM_000337.5 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr5:156184688 C>T maps to NM_000337.5 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:94218044 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:94248116 T>C maps to NM_001099401.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr13:23777973 C>T maps to NM_000231.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr13:23869575 A>G maps to NM_000231.2 E176E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr13:23778000 G>A maps to NM_000231.2 W56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr13:23853607 C>T maps to NM_000231.2 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr8:14412267 C>T maps to NM_139167.2 W69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr8:14022146 C>A maps to NM_139167.2 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr8:13965709 C>T maps to NM_139167.2 E194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:14095146 C>T maps to NM_139167.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:14412321 G>A maps to NM_139167.2 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr8:13959908 G>A maps to NM_139167.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr8:13965681 G>A maps to NM_139167.2 Q204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr8:13965682 G>A maps to NM_139167.2 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr8:13965703 C>T maps to NM_139167.2 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:13948014 G>A maps to NM_139167.2 Y292Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:14022122 C>T maps to NM_139167.2 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:14022145 G>A maps to NM_139167.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:14022149 C>T maps to NM_139167.2 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:14412246 G>A maps to NM_139167.2 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr8:13959929 C>T maps to NM_139167.2 K233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:153847441 G>A maps to NM_015595.3 Q401Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:153943784 C>T maps to NM_015595.3 I692I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:153840273 T>C maps to NM_015595.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:67108539 A>G maps to ENST00000237247 E96E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:134494410 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:134494411 C>T maps to NM_001143676.1 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr6:134491987 A>G maps to NM_001143676.1 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr6:134491573 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr6:134492023 G>A maps to NM_001143676.1 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr6:134493876 C>T maps to NM_001143676.1 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:134491531 G>A maps to NM_001143676.1 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:42977839 C>T maps to NM_032237.3 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:42199297 C>T maps to NM_016276.3 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr20:42213655 G>A maps to NM_016276.3 *428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:42204949 C>T maps to NM_016276.3 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr20:42198128 C>T maps to NM_016276.3 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr20:42204952 C>T maps to NM_016276.3 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:42196632 G>A maps to NM_016276.3 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr8:8234496 G>A maps to NM_001080826.1 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr8:8234124 C>T maps to NM_001080826.1 R598R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr8:8185813 C>A maps to NM_001080826.1 P826P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:8175942 G>A maps to NM_001080826.1 I1314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:8197129 C>T maps to NM_001080826.1 K726K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:8235321 G>A maps to NM_001080826.1 D199D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr8:8185690 C>T maps to NM_001080826.1 G867G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:8176518 G>A maps to NM_001080826.1 F1122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:8176167 G>A maps to NM_001080826.1 I1239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:8185534 G>A maps to NM_001080826.1 S919S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:8235326 G>A maps to NM_001080826.1 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr8:8197066 C>T maps to NM_001080826.1 R747R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:8176140 G>A maps to NM_001080826.1 F1248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:8176467 G>A maps to NM_001080826.1 I1139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:8234013 G>A maps to NM_001080826.1 C635C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:8235339 G>A maps to NM_001080826.1 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:8234054 T>G maps to NM_001080826.1 R622R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr15:77474241 T>C maps to NM_024776.2 E9E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:77472885 A>C maps to NM_024776.2 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:77425472 G>A maps to NM_024776.2 L1317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr15:77473383 G>A maps to NM_024776.2 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr15:77407409 G>A maps to NM_024776.2 S1443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr15:77406716 G>A maps to NM_024776.2 L1674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:77406533 G>A maps to NM_024776.2 S1735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:77406944 G>A maps to NM_024776.2 L1598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:77407037 G>A maps to NM_024776.2 D1567D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:77425643 G>A maps to NM_024776.2 P1260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr17:26938428 G>A maps to NM_001174103.1 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr17:26939358 C>A maps to NM_001174103.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:26941125 G>A maps to NM_001174103.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr10:52103733 G>A maps to ENST00000361543 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr10:52071151 T>C maps to ENST00000361543 Q261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr10:52066984 G>A maps to ENST00000361543 R393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:52067843 G>A maps to ENST00000361543 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:52103295 G>A maps to ENST00000361543 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:52103385 C>T maps to ENST00000361543 K169K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:52071082 C>T maps to ENST00000361543 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:52103436 G>A maps to ENST00000361543 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:52067876 C>T maps to ENST00000361543 W315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr10:52086979 G>A maps to ENST00000361543 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:52066964 G>A maps to ENST00000361543 F399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr4:108816867 C>T maps to NM_152621.5 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:20215771 C>T maps to NM_001012410.3 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:20225192 G>A maps to NM_001012410.3 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr2:201436530 C>T maps to NM_152524.5 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:201434610 C>T maps to NM_152524.5 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr2:201438005 C>T maps to NM_152524.5 S979S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr10:72633178 C>T maps to NM_003901.3 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:223386514 G>A maps to NM_152386.2 K136K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:223386574 G>A maps to NM_152386.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr17:78188093 G>A maps to NM_000199.3 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr17:78184568 G>A maps to NM_000199.3 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:78184799 G>A maps to NM_000199.3 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr22:25294018 G>A maps to NM_001039948.2 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr22:25294444 C>T maps to NM_001039948.2 L898L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr22:25294018 G>A maps to NM_001039948.2 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr22:25270421 G>A maps to NM_001039948.2 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr22:25294300 C>T maps to NM_001039948.2 F850F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr22:25313626 C>T maps to NM_001039948.2 I1032I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:25264406 C>T maps to NM_001039948.2 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:25320225 G>A maps to NM_001039948.2 L1144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr22:25264412 G>A maps to NM_001039948.2 K355K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr22:25294153 C>T maps to NM_001039948.2 P801P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr22:25315916 G>A maps to NM_001039948.2 L1105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr22:25272679 G>A maps to NM_001039948.2 E531E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr22:25294252 G>A maps to NM_001039948.2 Q834Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr22:25289462 C>T maps to NM_001039948.2 I667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:25294300 C>T maps to NM_001039948.2 F850F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr22:25294504 T>A maps to NM_001039948.2 S918S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:25275470 C>T maps to NM_001039948.2 I546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr22:25270529 G>A maps to NM_001039948.2 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr22:25297915 C>T maps to NM_001039948.2 I964I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr22:25280098 C>T maps to NM_001039948.2 D580D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:25264388 G>A maps to NM_001039948.2 Q347Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:25294156 G>A maps to NM_001039948.2 T802T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:25294369 G>A maps to NM_001039948.2 R873R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:25270514 C>T maps to NM_001039948.2 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:25294144 G>A maps to NM_001039948.2 R798R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr17:2266310 G>A maps to NM_014853.2 K185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:2264967 C>T maps to NM_014853.2 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr17:2274703 C>T maps to NM_014853.2 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:2279162 C>G maps to NM_014853.2 A826A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr22:40803433 T>A maps to NM_015705.4 Y462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:40803046 G>A maps to NM_015705.4 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr22:40803206 G>T maps to NM_015705.4 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:2762545 G>A maps to NM_003021.3 N198N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:65008882 G>A maps to NM_019072.2 Q37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr16:28880630 G>A maps to NM_001145795.1 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr16:28878038 C>T maps to NM_001145795.1 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:28883916 C>T maps to NM_001145795.1 S596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr16:28883931 C>T maps to NM_001145795.1 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:28883218 C>T maps to NM_001145795.1 I476I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr16:28877901 C>T maps to NM_001145795.1 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr16:28877984 C>T maps to NM_001145795.1 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr16:28883937 C>T maps to NM_001145795.1 H603H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:28883640 C>T maps to NM_001145795.1 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr16:28880340 C>T maps to NM_001145795.1 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr7:101950083 G>A maps to ENST00000306803 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr7:101952182 C>T maps to ENST00000306803 D306D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:111855963 C>T maps to NM_005475.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:123505235 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:123480513 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:123504070 C>T did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:123504072 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:162381716 T>C maps to NM_053282.4 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:162372561 G>A maps to NM_053282.4 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:156779575 G>A maps to NM_001161441.1 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:156777074 G>A maps to NM_001161441.1 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:6763732 G>A maps to NM_005490.2 D9D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:6754924 G>A maps to NM_005490.2 Q300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:6754925 G>A maps to NM_005490.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr19:6755165 G>A maps to NM_005490.2 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:6760962 G>A maps to NM_005490.2 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:6763720 T>C maps to NM_005490.2 Q13Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:6760878 G>A maps to NM_005490.2 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:6760923 C>T maps to NM_005490.2 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr19:6760956 A>C maps to NM_005490.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:6760923 C>T maps to NM_005490.2 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr9:130511644 G>A maps to NM_170600.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr9:130536636 G>A maps to NM_170600.2 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr9:130507001 C>T maps to NM_170600.2 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr9:130507373 G>A maps to NM_170600.2 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:130501159 C>T maps to NM_170600.2 T816T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:130504132 C>T maps to NM_170600.2 E674E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:130509441 G>A maps to NM_170600.2 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:130509542 G>A maps to NM_170600.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:130511629 G>A maps to NM_170600.2 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:130511740 G>A maps to NM_170600.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:82348390 A>G maps to NM_207372.2 K167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:82331304 C>T maps to NM_207372.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:21048470 G>A maps to ENST00000444387 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:21048470 G>A maps to ENST00000444387 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr1:21049314 C>T maps to ENST00000444387 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:21049397 G>A maps to ENST00000444387 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:21050576 G>A maps to ENST00000444387 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr15:78385033 G>A maps to NM_001101404.1 E36E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr15:78390919 C>T maps to NM_001101404.1 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr15:78393752 G>A maps to NM_001101404.1 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:78393353 G>A maps to NM_001101404.1 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:78393812 C>T maps to NM_001101404.1 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr21:40823922 C>T maps to NM_007341.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr21:40847107 C>T maps to NM_007341.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr21:40823880 G>A maps to NM_007341.2 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr21:40834458 G>A maps to NM_007341.2 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr21:40880955 T>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr21:40834350 C>T maps to NM_007341.2 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr21:40847110 C>T maps to NM_007341.2 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:80532514 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:80532662 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr23:80532637 T>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:26607281 C>T maps to ENST00000374243 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr22:38041402 C>T maps to NM_018957.3 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr22:38049818 C>T maps to NM_018957.3 S544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr22:38046167 C>G maps to NM_018957.3 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr22:38035853 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr4:2826381 C>T maps to NM_001145856.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:2831772 C>T maps to NM_001145856.1 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:2829022 C>T maps to NM_001145856.1 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr2:235950999 C>T maps to NM_014521.2 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:235962429 C>T maps to NM_014521.2 S954S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr2:235949970 C>T maps to NM_014521.2 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:235950771 C>T maps to NM_014521.2 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:235950336 T>C maps to NM_014521.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:235950648 C>T maps to NM_014521.2 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr2:235951887 G>A maps to NM_014521.2 V825V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr2:235943747 C>T maps to NM_014521.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:235949553 C>T maps to NM_014521.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr3:15311261 G>A maps to NM_004844.3 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr3:15300545 C>T maps to NM_004844.3 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:15297697 G>A maps to NM_004844.3 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:15297670 C>T maps to NM_004844.3 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:15303784 C>T maps to NM_004844.3 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr3:15372030 T>A maps to NM_004844.3 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:152069132 G>A maps to NM_001009555.3 Q395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr4:152053518 C>T maps to NM_001009555.3 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr4:152069193 C>T maps to NM_001009555.3 Q374Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:4361743 C>T maps to NM_003025.2 E320E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:4363407 G>A maps to NM_003025.2 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:4363868 G>A maps to NM_003025.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:4363869 G>A maps to NM_003025.2 H157H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:4364150 G>A maps to NM_003025.2 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:4365620 G>A maps to NM_003025.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr9:17795734 C>T maps to NM_003026.2 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr9:17791248 C>T maps to NM_003026.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:84287020 C>T maps to ENST00000434347 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:84245384 G>A maps to ENST00000434347 K180K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr15:84245342 G>A maps to ENST00000434347 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:84237341 C>T maps to ENST00000434347 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:84287020 C>T maps to ENST00000434347 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:131777079 G>A maps to ENST00000372554 N146N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr9:131774559 C>T maps to ENST00000372554 Q197Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr9:131777151 T>C maps to ENST00000372554 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr23:19854288 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:19610233 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:19568111 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:19564141 G>C did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:19713796 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:19560172 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:19713845 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:19713825 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:19564138 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:105361946 G>A maps to ENST00000369774 R1010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:105386855 C>T maps to ENST00000369774 K236K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:105362046 C>A maps to ENST00000369774 A976A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr10:105362472 G>A maps to ENST00000369774 T834T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr10:105372775 G>A maps to ENST00000369774 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:105361806 G>A maps to ENST00000369774 S1056S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:105362499 G>A maps to ENST00000369774 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr5:171766296 G>A maps to NM_001017995.2 A604A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr5:171765957 A>G maps to NM_001017995.2 D717D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:171773189 G>A maps to NM_001017995.2 Q380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr5:171765708 G>A maps to NM_001017995.2 V800V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:170028122 G>A maps to NM_020870.3 A791A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:170077707 G>A maps to NM_020870.3 Y172Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:170028272 G>A maps to NM_020870.3 T741T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr5:145442020 C>T maps to NM_152550.3 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:145439537 G>A maps to NM_152550.3 Q555Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr5:145393467 C>T maps to NM_152550.3 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:145393494 G>A maps to NM_152550.3 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:145428694 G>A maps to NM_152550.3 K403K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:145383697 C>T maps to NM_152550.3 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr5:145439657 C>T maps to NM_152550.3 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:145439501 C>T maps to NM_152550.3 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr5:145435567 C>T maps to NM_152550.3 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:145435593 G>A maps to NM_152550.3 W458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:145442096 C>T maps to NM_152550.3 Q675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr5:145379787 C>T maps to NM_152550.3 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:145379721 G>A maps to NM_152550.3 E160E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:145427420 G>A maps to NM_152550.3 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:145439618 C>T maps to NM_152550.3 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:145439657 C>T maps to NM_152550.3 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr2:110049071 C>T maps to NM_001099289.1 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:110049061 G>A maps to NM_001099289.1 K503K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:110049064 G>A maps to NM_001099289.1 G504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:110065722 C>T maps to NM_001099289.1 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:8216227 C>T maps to NM_018986.3 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr4:8221093 C>T maps to NM_018986.3 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr4:8229538 C>T maps to NM_018986.3 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr4:8237239 C>T maps to NM_018986.3 F1121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr4:8229238 C>T maps to NM_018986.3 N606N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr4:8229239 C>T maps to NM_018986.3 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:8229589 C>T maps to NM_018986.3 P723P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:8221200 G>A maps to NM_018986.3 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr4:8229892 C>T maps to NM_018986.3 I824I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr4:8229601 G>A maps to NM_018986.3 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr4:8229976 G>A maps to NM_018986.3 R852R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr4:8218682 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:8214497 C>T maps to NM_018986.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr4:8229466 G>A maps to NM_018986.3 E682E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr4:8242576 G>A maps to NM_018986.3 Q1302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr4:8217958 C>T maps to NM_018986.3 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:8229214 C>T maps to NM_018986.3 F598F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr4:8218843 C>T maps to NM_018986.3 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:8214428 C>T maps to NM_018986.3 D83D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr5:148407302 T>C maps to NM_024577.3 G664G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr5:148406771 G>A maps to NM_024577.3 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:148406504 C>T maps to NM_024577.3 L930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:148427495 G>A maps to NM_024577.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr5:148406202 C>T maps to NM_024577.3 R995R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:148407893 G>A maps to NM_024577.3 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr5:148407695 G>A maps to NM_024577.3 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr5:148388435 G>A maps to NM_024577.3 A1152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:148407131 G>A maps to NM_024577.3 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:51171751 G>A maps to ENST00000391814 I1163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:51171490 C>T maps to ENST00000391814 R1250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:51201136 C>T maps to ENST00000391814 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr19:51217084 G>A maps to ENST00000391814 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:51165626 G>A maps to ENST00000391814 P2035P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:51217120 G>A maps to ENST00000391814 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:51215335 C>T maps to ENST00000391814 K276K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:51170629 G>A maps to ENST00000391814 P1537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:51219588 C>T maps to ENST00000391814 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr19:51165350 G>A maps to ENST00000391814 F2127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:51218954 G>A maps to ENST00000391814 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr19:51220098 G>A maps to ENST00000391814 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:51215326 C>T maps to ENST00000391814 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:51205793 G>A maps to ENST00000391814 F559F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:51218984 G>A maps to ENST00000391814 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:51189595 G>A maps to ENST00000391814 I833I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr19:51200889 G>A maps to ENST00000391814 F631F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:51201151 G>A maps to ENST00000391814 F603F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:51205784 C>T maps to ENST00000391814 V562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:51215209 G>A maps to ENST00000391814 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:51220089 G>A maps to ENST00000391814 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:51192472 G>A maps to ENST00000391814 F676F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr11:70332560 C>T maps to ENST00000338508 E1273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr11:70332755 G>A maps to ENST00000338508 S1208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:70338448 T>C maps to ENST00000338508 S804S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr11:70319501 C>T maps to ENST00000338508 T1668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr11:70332968 G>A maps to ENST00000338508 S1137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr11:70331906 C>T maps to ENST00000338508 R1491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr11:70333466 G>A maps to ENST00000338508 F971F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:70333412 G>A maps to ENST00000338508 I989I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr11:70332944 C>T maps to ENST00000338508 R1145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:70506016 G>A maps to ENST00000338508 F660F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:70331924 G>A maps to ENST00000338508 I1485I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:70338454 C>T maps to ENST00000338508 A802A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:70332683 G>A maps to ENST00000338508 A1232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:70332128 G>A maps to ENST00000338508 I1417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr11:70333292 G>A maps to ENST00000338508 I1029I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:70331666 G>A maps to ENST00000338508 I1571I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:70332746 G>A maps to ENST00000338508 A1211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:70333232 G>A maps to ENST00000338508 I1049I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:70319105 G>A maps to ENST00000338508 A1800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr11:70331861 G>A maps to ENST00000338508 T1506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:70331435 G>A maps to ENST00000338508 S1648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:70333094 G>A maps to ENST00000338508 A1095A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:70332968 G>A maps to ENST00000338508 S1137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr11:70333196 C>T maps to ENST00000338508 R1061R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:70319450 C>T maps to ENST00000338508 Q1685Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:70331567 C>T maps to ENST00000338508 E1604E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:70331605 G>A maps to ENST00000338508 Q1592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:70331696 G>A maps to ENST00000338508 L1561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:70332824 C>T maps to ENST00000338508 A1185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:70332872 G>A maps to ENST00000338508 S1169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:70332926 G>A maps to ENST00000338508 F1151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:70333019 G>A maps to ENST00000338508 F1120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:70333556 C>T maps to ENST00000338508 E941E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:70332215 G>A maps to ENST00000338508 P1388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr22:51143465 C>T maps to NM_001080420.1 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr22:51143462 C>T maps to NM_001080420.1 R672R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr22:51160136 C>T maps to NM_001080420.1 S1308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr22:51160691 C>T maps to NM_001080420.1 P1493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:51143223 C>T maps to NM_001080420.1 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:51160457 C>T maps to NM_001080420.1 F1415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:37955926 C>T maps to NM_003028.2 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:37919850 G>A maps to NM_003028.2 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr9:37955893 G>A maps to NM_003028.2 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr9:37955977 G>A maps to NM_003028.2 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr17:7535031 C>T maps to NM_001040.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr17:7534094 C>T maps to NM_001040.3 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:7535055 C>T maps to NM_001040.3 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr17:7536266 G>A maps to NM_001040.3 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr17:7534036 G>A maps to NM_001040.3 E81E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr17:7535019 C>T maps to NM_001040.3 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:7534654 C>T maps to NM_001040.3 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:154942594 G>C maps to NM_001130040.1 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:154941261 C>A maps to NM_001130040.1 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr19:438990 G>A maps to NM_012435.2 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr19:425214 G>A maps to NM_012435.2 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:430693 G>A maps to NM_012435.2 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:436389 G>A maps to NM_012435.2 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr9:91653171 G>A maps to NM_016848.5 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr9:91686137 G>A maps to NM_016848.5 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr9:91667022 G>A maps to NM_016848.5 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:91661872 C>T maps to NM_016848.5 E333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr9:91686131 G>A maps to NM_016848.5 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr15:49176513 A>G maps to NM_203349.3 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:49160066 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:49118248 G>A maps to NM_203349.3 I604I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr15:49118323 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr15:49254921 G>A maps to NM_203349.3 N97N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:49160045 G>A maps to NM_203349.3 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr16:46638350 G>A maps to NM_024745.4 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:46617488 A>C maps to NM_024745.4 V544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr16:46638272 G>A maps to NM_024745.4 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:4283084 C>T maps to NM_020209.3 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:4283123 C>T maps to NM_020209.3 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr19:4288329 C>T maps to NM_020209.3 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:4290473 C>T maps to NM_020209.3 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr1:154474154 C>T maps to NM_001010846.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:154461710 C>T maps to NM_001010846.2 K280K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:154461713 G>A maps to NM_001010846.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:154461815 A>G maps to NM_001010846.2 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:154456750 C>T maps to NM_001010846.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr1:154461713 G>A maps to NM_001010846.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:154474133 G>A maps to NM_001010846.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:154459013 C>T maps to NM_001010846.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:154471639 G>A maps to NM_001010846.2 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr15:45470423 T>G maps to ENST00000437903 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr15:45467504 G>A maps to ENST00000437903 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr7:155599242 C>T maps to NM_000193.2 K103K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:155599041 G>A maps to NM_000193.2 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr7:155604657 C>T maps to NM_000193.2 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:155596397 C>T maps to NM_000193.2 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr13:26621160 G>A maps to NM_001007538.1 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:42403084 C>T maps to NM_001080505.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr4:42403191 C>T maps to NM_001080505.1 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:42403224 C>T maps to NM_001080505.1 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:201860622 C>T maps to NM_198149.2 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr3:48510877 C>T maps to NM_016479.3 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr19:41083313 A>G maps to NM_138392.3 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:41096314 C>T maps to NM_138392.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr19:41092698 C>T maps to NM_138392.3 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr19:41096182 C>T maps to NM_138392.3 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:41095039 C>T maps to NM_138392.3 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:41086711 C>T maps to NM_138392.3 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:41083491 C>T maps to NM_138392.3 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:41096726 C>T maps to NM_138392.3 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr17:18233962 G>A maps to NM_004169.3 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr12:57627353 C>T maps to NM_005412.5 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr12:57627813 C>T maps to NM_005412.5 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:112764467 C>T maps to NM_007373.3 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr23:591838 T>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:595509 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:595386 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:591780 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:595459 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:605214 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr3:157820544 A>G maps to NM_003030.4 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr3:157820622 T>C maps to NM_003030.4 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr17:3518751 C>T maps to NM_013276.2 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:3524681 G>C maps to NM_013276.2 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr17:3539423 G>A maps to NM_013276.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr6:146264610 G>A maps to ENST00000367503 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr6:146262941 G>A maps to ENST00000367503 I769I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:146276179 G>A maps to ENST00000367503 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr6:146214475 G>A maps to ENST00000367503 P1587P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:72799686 G>A maps to NM_018130.2 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr3:72799686 G>A maps to NM_018130.2 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr5:132158505 G>A maps to NM_001172700.1 F847F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr5:132159879 G>A maps to NM_001172700.1 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:132158505 G>A maps to NM_001172700.1 F847F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:132161205 G>A maps to NM_001172700.1 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:9863310 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:9900703 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:9900725 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:9863143 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr23:9862878 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr23:9905571 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr23:9914759 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr23:9864372 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr23:9905554 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:9900625 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr23:9863351 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:9914784 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:9907267 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:9863834 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr23:9912691 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:9862716 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:9900604 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:9907343 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:9864157 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:9900854 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:9864269 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:9864373 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr4:77661149 T>G maps to NM_020859.3 A608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr4:77661509 G>A maps to NM_020859.3 R728R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr4:77676126 C>T maps to NM_020859.3 S1497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr4:77660990 C>T maps to NM_020859.3 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:77661473 G>A maps to NM_020859.3 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr4:77660489 G>A maps to NM_020859.3 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr4:77691828 G>A maps to NM_020859.3 A1800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:77676342 C>T maps to NM_020859.3 P1569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr4:77631395 G>A maps to NM_020859.3 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:77660516 C>T maps to NM_020859.3 H397H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:77660021 C>T maps to NM_020859.3 Y232Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:77660214 G>T maps to NM_020859.3 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr4:77691978 C>T maps to NM_020859.3 S1850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:77661506 G>A maps to NM_020859.3 G727G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:77675820 C>T maps to NM_020859.3 T1395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:77661857 G>A maps to NM_020859.3 G844G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:77691933 G>A maps to NM_020859.3 R1835R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr4:77660117 C>T maps to NM_020859.3 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:77661443 G>A maps to NM_020859.3 R706R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:77677739 C>T maps to NM_020859.3 S1616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr4:77691816 C>T maps to NM_020859.3 T1796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr4:77675568 C>T maps to NM_020859.3 S1311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:77660735 A>T maps to NM_020859.3 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:77662358 G>A maps to NM_020859.3 L1011L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:77677850 G>A maps to NM_020859.3 K1653K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr4:77700218 C>T maps to NM_020859.3 F1960F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:50376199 T>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:50376391 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr23:50377763 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr23:50377609 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:50345781 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:50351017 C>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:50438891 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr23:50341288 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr23:50351040 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr23:50377588 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:50381251 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr23:50378445 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:50339750 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:50339751 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:50351073 A>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:50350550 A>G did not map to a codon.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr23:50351040 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr23:50345802 G>A did not map to a codon.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr23:50341480 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:50381219 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:50339779 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:50345792 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:50376883 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:50345691 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:50376914 C>T did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:50350843 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:164704952 G>A maps to NM_001041.3 L1724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr3:164793788 C>T maps to NM_001041.3 K4K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr3:164739069 G>A maps to NM_001041.3 I1067I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr3:164700822 G>A maps to NM_001041.3 D1738D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:164750405 G>A maps to NM_001041.3 I880I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:164727138 G>A maps to NM_001041.3 S1369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:164750356 G>A maps to NM_001041.3 Q897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:164755791 C>T maps to NM_001041.3 R774R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:164760924 T>G maps to NM_001041.3 T642T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:164783090 C>T maps to NM_001041.3 W255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:164785147 C>T maps to NM_001041.3 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr3:164772985 C>T maps to NM_001041.3 W503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:164739018 G>A maps to NM_001041.3 V1084V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:164757743 C>T maps to NM_001041.3 T725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:164777009 G>A maps to NM_001041.3 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr3:164780203 G>A maps to NM_001041.3 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr3:164735611 C>T maps to NM_001041.3 G1190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:164755722 G>A maps to NM_001041.3 I797I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:164764688 C>T maps to NM_001041.3 W609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:164716331 G>A maps to NM_001041.3 I1512I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:164724635 G>A maps to NM_001041.3 L1458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr3:164786914 G>A maps to NM_001041.3 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:164704956 A>G maps to NM_001041.3 G1722G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr3:164785147 C>T maps to NM_001041.3 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr3:164777009 G>A maps to NM_001041.3 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:164786527 G>T maps to NM_001041.3 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:164709178 G>A maps to NM_001041.3 I1690I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:164709980 C>T maps to NM_001041.3 W1656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:164780272 T>C did not map to a codon.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr3:164783090 C>T maps to NM_001041.3 W255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr3:164733005 C>A maps to NM_001041.3 G1302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:164732946 G>A maps to NM_001041.3 V1321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:164733802 G>A maps to NM_001041.3 F1275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr3:164783090 C>T maps to NM_001041.3 W255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:164714346 C>T maps to NM_001041.3 R1556R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:164737434 C>A maps to NM_001041.3 L1126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:164757743 C>T maps to NM_001041.3 T725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr3:164786619 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr11:124517266 A>G maps to NM_170601.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:124530643 G>A maps to NM_170601.3 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:124519594 G>A maps to NM_170601.3 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr13:46357544 C>T maps to NM_198849.2 E261E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr13:46357631 C>T maps to NM_198849.2 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr13:46357979 C>T maps to NM_198849.2 W116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr13:46357565 C>T maps to NM_198849.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr13:46357844 G>A maps to NM_198849.2 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr13:46357937 G>A maps to NM_198849.2 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr13:46357799 C>T maps to NM_198849.2 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr13:46357904 G>A maps to NM_198849.2 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:113302284 C>T maps to ENST00000393830 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr3:113300281 C>T maps to ENST00000393830 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr3:113346506 G>A maps to ENST00000393830 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:113342324 G>C maps to ENST00000393830 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:113304060 C>T maps to ENST00000393830 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:117066764 A>T maps to NM_001040455.1 K828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:117063025 C>T maps to NM_001040455.1 I643I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:117056930 G>A maps to NM_001040455.1 E318E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:117061418 C>A maps to NM_001040455.1 C566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr11:407815 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr11:408109 C>T maps to NM_021805.2 Q101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr20:3682121 G>A maps to NM_023068.3 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr20:3683949 G>A maps to NM_023068.3 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr20:3678688 C>T maps to NM_023068.3 V626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:3677341 G>A maps to NM_023068.3 S858S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:3683868 C>T maps to NM_023068.3 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr20:3675517 C>T maps to NM_023068.3 V912V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr20:3687267 G>A maps to NM_023068.3 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr20:3683844 G>A maps to NM_023068.3 N409N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:3684063 G>A maps to NM_023068.3 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr20:3677314 G>C maps to NM_023068.3 G867G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr20:3672568 G>A maps to NM_023068.3 I1437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr20:3679915 G>A maps to NM_023068.3 Y573Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:3683931 G>A maps to NM_023068.3 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr20:3680095 G>A maps to NM_023068.3 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr20:3687129 C>T maps to NM_023068.3 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NF-06A-11D-A19A-08 chr20:3674961 G>A maps to NM_023068.3 I1054I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:3687198 C>T maps to NM_023068.3 Q68Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr20:3673740 C>T maps to NM_023068.3 E1182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:3675457 C>T maps to NM_023068.3 R932R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:3677846 G>A maps to NM_023068.3 P755P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:3686421 C>T maps to NM_023068.3 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:3687252 C>T maps to NM_023068.3 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:3669800 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr19:51918567 C>T maps to NM_033130.4 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:51918464 G>A maps to NM_033130.4 Q434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:51918441 G>A maps to NM_033130.4 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:51914430 G>A maps to NM_033130.4 F672F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr19:51919317 C>T maps to NM_033130.4 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:51917724 G>A maps to NM_033130.4 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:51920719 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr19:51918075 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:51919419 G>A maps to NM_033130.4 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:51916983 G>A maps to NM_033130.4 V601V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:51914607 C>T maps to NM_033130.4 Q613Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:51920573 G>A maps to NM_033130.4 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:51917061 C>T maps to NM_033130.4 P575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:51919974 C>T maps to NM_033130.4 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:51918102 C>T maps to NM_033130.4 Q530Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:51914541 C>T maps to NM_033130.4 K635K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:51918216 G>A maps to NM_033130.4 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr19:51919938 G>C maps to NM_033130.4 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr19:50462038 C>T maps to NM_052884.2 Q408Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:50463541 G>A maps to NM_052884.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr19:50453289 G>A maps to NM_052884.2 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr19:50461730 C>T maps to NM_052884.2 W487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:50464037 C>T maps to NM_052884.2 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:50461795 G>A maps to NM_052884.2 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:50462011 G>A maps to NM_052884.2 D417D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr19:50453418 C>T maps to NM_052884.2 G635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr19:50462695 G>T maps to NM_052884.2 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:50455583 G>A maps to NM_052884.2 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:50461684 G>A maps to NM_052884.2 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr19:50463869 C>T maps to NM_052884.2 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:52002460 C>T maps to NM_053003.2 Q366Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr19:52004702 G>A maps to NM_053003.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:52002860 C>T maps to NM_053003.2 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr19:52002860 C>T maps to NM_053003.2 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:52002911 C>T maps to NM_053003.2 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:52003211 C>T maps to ENST00000441969 W108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:52003318 G>A maps to ENST00000441969 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:52001350 C>T maps to NM_053003.2 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:52002791 G>A maps to NM_053003.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:52004615 C>T maps to NM_053003.2 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr19:51995074 C>T maps to NM_053003.2 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:52002944 G>A maps to NM_053003.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr19:51995020 G>A maps to NM_053003.2 A554A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr19:52001406 G>A maps to NM_053003.2 Q424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:52002860 C>T maps to NM_053003.2 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr19:52001488 G>A maps to NM_053003.2 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:52001428 C>T maps to NM_053003.2 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:52003321 G>A maps to ENST00000441969 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:52000607 G>A maps to NM_053003.2 F499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr19:52000670 C>T maps to NM_053003.2 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr19:52001350 C>T maps to NM_053003.2 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:52000607 G>A maps to NM_053003.2 F499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:52004740 G>A maps to NM_053003.2 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr19:52002830 G>A maps to NM_053003.2 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr19:51994939 C>T maps to NM_053003.2 Q581Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:52003216 C>T maps to ENST00000441969 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr19:52147155 G>A maps to NM_001098612.1 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:52147227 G>A maps to NM_001098612.1 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:52149073 G>A maps to NM_001098612.1 Q221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:52147044 G>A maps to NM_001098612.1 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:52149195 C>T maps to NM_001098612.1 W180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr18:43422082 G>A maps to NM_213602.2 Q306Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr19:52131204 G>A maps to ENST00000222107 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:52130499 C>T maps to ENST00000222107 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr19:52131192 C>T maps to ENST00000222107 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr19:52129335 C>T maps to ENST00000222107 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:52131336 C>T maps to ENST00000222107 E249E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:52132743 G>A maps to ENST00000222107 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:52130824 C>T maps to ENST00000222107 W391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr19:52130493 C>T maps to ENST00000222107 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:52132749 G>A maps to ENST00000222107 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr19:52130741 G>A maps to ENST00000222107 Q419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr19:52130934 G>A maps to ENST00000222107 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:52130501 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:52129362 C>T maps to ENST00000222107 V462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:52131147 G>A maps to ENST00000222107 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:52131210 G>A maps to ENST00000222107 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:52115666 C>T maps to ENST00000222107 R491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr19:52031078 C>T maps to NM_001245.5 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr19:52033149 G>A maps to NM_001245.5 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:52033983 G>A maps to NM_001245.5 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:52034552 G>A maps to NM_001245.5 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:52034460 C>T maps to NM_001245.5 W127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:52033224 G>A maps to NM_001245.5 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:52033134 G>A maps to NM_001245.5 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:52033110 C>T maps to NM_001245.5 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:52034561 G>A maps to NM_001245.5 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:52023350 G>A maps to NM_001245.5 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr19:52031505 C>T maps to NM_001245.5 W338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:52034211 G>A maps to NM_001245.5 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:52033983 G>A maps to NM_001245.5 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr19:52023377 C>T maps to NM_001245.5 K440K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:52034097 G>A maps to NM_001245.5 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:52034561 G>A maps to NM_001245.5 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:52034579 C>T maps to NM_001245.5 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:51650071 C>T maps to NM_014385.2 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:51646021 G>A maps to NM_014385.2 W132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:51645724 C>T maps to NM_014385.2 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:51650086 C>T maps to NM_014385.2 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:51647819 C>T maps to NM_014385.2 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:51649260 C>T maps to NM_014385.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:51647724 C>T maps to NM_014385.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:51650567 C>T maps to NM_014385.2 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:51656402 C>T maps to NM_014385.2 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:51647924 C>T maps to NM_014385.2 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr19:51647744 G>A maps to NM_014385.2 W172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr19:51645697 G>A maps to NM_014385.2 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr19:51960799 C>T maps to NM_014442.2 Q216Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr19:51958828 C>T maps to NM_014442.2 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr19:51960474 C>T maps to NM_014442.2 W248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:51955836 G>A maps to NM_014442.2 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:51958837 C>T maps to NM_014442.2 W295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:51955725 T>C maps to NM_014442.2 E469E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:51955767 C>T maps to NM_014442.2 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:51958873 A>G maps to NM_014442.2 C283C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr19:51960829 G>A maps to NM_014442.2 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:51955845 C>T maps to NM_014442.2 K429K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:51957553 C>T maps to NM_014442.2 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:51960930 G>A maps to NM_014442.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:51960452 G>A maps to NM_014442.2 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:51955851 G>A maps to NM_014442.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr19:51631290 C>T maps to NM_014441.2 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:51628584 C>T maps to NM_014441.2 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr19:51631269 C>T maps to NM_014441.2 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:51631297 T>C did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:51633161 A>G maps to NM_014441.2 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:51628482 G>A maps to NM_014441.2 W84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:51630491 C>T maps to NM_014441.2 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:51633197 C>T maps to NM_014441.2 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:51629368 C>T maps to NM_014441.2 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr19:51630350 C>T maps to NM_014441.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:51628497 C>T maps to NM_014441.2 D89D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:51629088 G>A maps to NM_014441.2 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:51631290 C>T maps to NM_014441.2 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:51630440 C>T maps to NM_014441.2 N301N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:51629058 C>T maps to NM_014441.2 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:51630527 G>A maps to NM_014441.2 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr9:34637409 G>A maps to NM_005866.2 D53D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr21:44841616 G>A maps to NM_173354.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:44837538 G>A maps to NM_173354.3 A620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr21:44837514 G>A maps to NM_173354.3 F628F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr21:44837583 G>A maps to NM_173354.3 I605I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr21:44839250 G>A maps to NM_173354.3 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr21:44836900 G>A maps to NM_173354.3 G691G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr21:44837463 C>T maps to NM_173354.3 R645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr21:44840965 G>A maps to NM_173354.3 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr21:44836678 G>A maps to NM_173354.3 D765D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr21:44841137 G>A maps to NM_173354.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:111591307 C>T maps to NM_015191.1 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:111572219 C>T maps to NM_015191.1 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:116729132 G>A maps to ENST00000445177 I1009I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IB-06A-11D-A196-08 chr11:116728532 G>T maps to ENST00000445177 P1209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr11:116747030 G>A maps to ENST00000445177 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:116744292 G>A maps to ENST00000445177 G540G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:116729252 G>A maps to ENST00000445177 F969F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr11:116732560 G>A maps to ENST00000445177 Q764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:116728594 C>A maps to ENST00000445177 E1189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:116746667 G>A maps to ENST00000445177 R378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr11:116729108 C>T maps to ENST00000445177 R1017R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:116827672 C>T maps to ENST00000445177 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:116732035 G>C maps to ENST00000445177 P786P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr11:116729356 G>A maps to ENST00000445177 L935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:116731999 G>A maps to ENST00000445177 I798I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:115323134 G>A maps to NM_001102396.1 Q32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr5:138362516 G>A maps to ENST00000509534 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:138456733 G>A maps to ENST00000509534 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:138378347 G>A maps to ENST00000509534 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr5:138287559 G>A maps to ENST00000509534 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr5:138356954 G>A maps to ENST00000509534 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr12:56359779 T>A maps to NM_006928.3 K6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:56350934 G>A maps to NM_006928.3 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:56349272 C>T maps to NM_006928.3 V579V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr6:100895166 G>A maps to ENST00000262901 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr6:100897560 T>A maps to ENST00000262901 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:100841366 G>A maps to ENST00000262901 I522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:100841498 G>A maps to ENST00000262901 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:100896524 G>A maps to ENST00000262901 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:100895250 G>A maps to ENST00000262901 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr6:100838965 C>T maps to ENST00000262901 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr6:100841663 G>A maps to ENST00000262901 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr6:100841375 G>A maps to ENST00000262901 V519V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr6:100841463 C>T maps to ENST00000262901 W490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr6:100896509 C>T maps to ENST00000262901 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:100841513 C>T maps to ENST00000262901 E473E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:100897527 G>A maps to ENST00000262901 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr21:38098424 C>T maps to NM_005069.3 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr21:38117418 C>T maps to NM_005069.3 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr21:38098502 G>A maps to NM_005069.3 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr21:38095400 G>A maps to NM_005069.3 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr21:38114027 G>A maps to NM_005069.3 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:38098610 G>A maps to NM_005069.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr15:75694308 G>A maps to NM_001145357.1 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr15:75722575 G>A maps to NM_001145357.1 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr15:75684775 G>A maps to NM_001145357.1 F886F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr15:75693112 G>A maps to NM_001145357.1 Y565Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:16980668 C>T maps to NM_015260.1 P767P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:16989321 C>T maps to NM_015260.1 V1091V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:16977228 C>T maps to NM_015260.1 F588F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:16974543 C>T maps to NM_015260.1 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:16980350 C>T maps to NM_015260.1 I661I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:16980351 C>T maps to NM_015260.1 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr19:16962281 C>T maps to NM_015260.1 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:16977261 G>A maps to NM_015260.1 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:16974603 C>T maps to NM_015260.1 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr19:16942412 T>C maps to NM_015260.1 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr19:16974537 C>T maps to NM_015260.1 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:16962338 C>T maps to NM_015260.1 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:16977297 C>T maps to NM_015260.1 F611F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:16980626 C>T maps to NM_015260.1 A753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr11:65408625 C>T maps to NM_153253.29 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr11:65413394 G>A maps to NM_153253.29 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr11:65414472 G>A maps to NM_153253.29 A656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:65417934 G>A maps to NM_153253.29 Q989Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr14:72138057 C>T maps to NM_015556.1 I826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr14:72205784 G>A maps to NM_015556.1 E1774E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr14:72137928 C>T maps to NM_015556.1 F783F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:72137928 C>T maps to NM_015556.1 F783F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:72138207 C>T maps to NM_015556.1 C876C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:72137928 C>T maps to NM_015556.1 F783F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr14:72202090 G>A maps to NM_015556.1 Q1723Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:72202109 T>C did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:72137901 C>T maps to NM_015556.1 F774F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr14:72197009 C>A maps to NM_015556.1 S1639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:72152306 C>T maps to NM_015556.1 I1111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr14:72200465 C>T maps to NM_015556.1 L1670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr1:232629308 G>A maps to NM_020808.3 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr1:232600774 G>A maps to NM_020808.3 S877S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:232650683 G>A maps to NM_020808.3 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:232577036 G>A maps to NM_020808.3 H1214H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:232561464 G>A maps to NM_020808.3 S1500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:232600813 G>A maps to NM_020808.3 F864F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr1:232650695 G>A maps to NM_020808.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:232626745 G>A maps to NM_020808.3 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:232650683 G>A maps to NM_020808.3 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:232551300 G>A maps to NM_020808.3 L1567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:232581314 G>A maps to NM_020808.3 R1105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr1:232649918 G>A maps to NM_020808.3 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:38692514 C>T maps to NM_015073.1 V1666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:38572801 C>T maps to NM_015073.1 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr19:38572411 C>T maps to NM_015073.1 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:38609957 C>T maps to NM_015073.1 T768T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:38573728 C>T maps to NM_015073.1 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:38621190 C>T maps to NM_015073.1 L974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:38621202 C>T maps to NM_015073.1 G978G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:38610461 C>T maps to NM_015073.1 I936I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:38573503 G>A maps to NM_015073.1 E433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:38655243 C>T maps to NM_015073.1 S1302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:38609984 C>T maps to NM_015073.1 G777G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:38597183 C>T maps to NM_015073.1 S679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr19:38673291 A>T maps to NM_015073.1 K1448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:38590621 C>T maps to NM_015073.1 S562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:38573179 G>A maps to NM_015073.1 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:38609981 C>T maps to NM_015073.1 F776F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:38573728 C>T maps to NM_015073.1 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:38610500 G>A maps to NM_015073.1 R949R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:38655201 C>T maps to NM_015073.1 F1288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr19:38633302 C>T maps to NM_015073.1 S1162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:38652965 C>T maps to NM_015073.1 S1245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:38631904 C>T maps to NM_015073.1 P1075P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:1903151 C>T maps to ENST00000400068 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:1902296 C>T maps to ENST00000400068 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr20:1559236 G>A maps to NM_006065.3 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr20:1552568 C>T maps to NM_006065.3 W183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr20:1546881 G>A maps to NM_006065.3 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr20:1552408 C>T maps to NM_006065.3 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr20:1559293 G>A maps to NM_006065.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr20:1551703 G>A maps to NM_006065.3 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr20:1552567 C>T maps to NM_006065.3 W183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr20:1600547 G>A maps to NM_006065.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr20:1592243 G>A maps to NM_001135844.1 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr20:1551637 C>T maps to NM_006065.3 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:1584657 C>T maps to NM_001135844.1 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr20:1559044 C>T maps to NM_006065.3 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr20:1551703 G>A maps to NM_006065.3 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr20:1592123 G>A maps to NM_001135844.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:1551583 C>T maps to NM_006065.3 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:1551457 G>A maps to NM_006065.3 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:1552536 G>A maps to NM_006065.3 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:1552368 G>A maps to NM_006065.3 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr20:1458920 C>T maps to NM_001122962.1 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:1460519 G>A maps to NM_001122962.1 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr20:1460462 G>A maps to NM_001122962.1 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr20:1517810 C>T maps to ENST00000381621 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr20:1532559 C>T maps to ENST00000381621 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr20:1532445 G>A maps to ENST00000381621 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr20:1517840 G>A maps to ENST00000381621 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr20:1532541 C>T maps to ENST00000381621 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr20:1617023 C>T maps to NM_018556.3 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr20:1617023 C>T maps to NM_018556.3 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr20:1638336 G>A maps to NM_018556.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:1616840 G>A maps to NM_018556.3 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr20:1616213 G>A maps to NM_018556.3 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr20:1629934 G>A maps to NM_018556.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr20:1630034 C>T maps to NM_018556.3 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr20:1616063 C>T maps to NM_018556.3 W310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr20:1616064 C>T maps to NM_018556.3 W310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:1616171 C>T maps to NM_018556.3 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr20:1638345 G>A maps to NM_018556.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr20:1617023 C>T maps to NM_018556.3 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:1629809 G>A maps to NM_018556.3 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:1630006 G>A maps to NM_018556.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr20:1617041 C>T maps to NM_018556.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:69666590 C>T maps to NM_012238.4 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr10:69651311 G>A maps to NM_012238.4 K314K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:39371531 G>A maps to NM_012237.3 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:39379774 G>A maps to NM_012237.3 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr19:39380776 T>C maps to NM_012237.3 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:39384090 G>A maps to NM_012237.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:230547 C>A maps to NM_012239.5 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:233184 G>A maps to NM_012239.5 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:233183 G>A maps to NM_012239.5 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr12:120741432 G>A maps to NM_012240.2 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:120750396 C>T maps to NM_012240.2 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:120741693 C>T maps to NM_012240.2 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr6:13592076 C>T maps to NM_012241.3 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr6:13592121 C>T maps to NM_012241.3 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr19:4174811 G>A maps to NM_016539.2 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:4180900 G>A maps to NM_016539.2 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr19:4179204 G>A maps to NM_016539.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr17:79875932 C>T maps to NM_016538.2 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr9:35650623 G>A maps to NM_014450.2 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr9:35650536 C>T maps to NM_014450.2 W66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:35650596 G>A maps to NM_014450.2 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr14:105221988 C>T maps to NM_006427.3 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:45235790 C>T maps to NM_016932.4 E153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:45233326 G>A maps to NM_016932.4 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:45233466 G>A maps to NM_016932.4 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:45235712 G>A maps to NM_016932.4 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:45170037 G>A maps to NM_005413.3 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:61180412 C>T maps to NM_017420.4 G686G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:46269028 G>A maps to NM_175875.4 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr14:60976433 C>T maps to ENST00000381716 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:60977968 G>A maps to ENST00000381716 *306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr18:47918527 A>T maps to NM_145060.3 K227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr18:47911609 T>G maps to NM_145060.3 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr18:47908563 C>T maps to NM_145060.3 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:21732063 G>A maps to NM_145061.5 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr17:46239845 G>A maps to NM_003726.3 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr17:46247992 C>T maps to NM_003726.3 E285E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:46265268 C>T maps to NM_003726.3 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr17:46423351 C>T maps to NM_003726.3 Q65Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:26766565 G>A maps to NM_003930.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr1:2234764 C>T maps to NM_003036.3 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:2160543 C>T maps to NM_003036.3 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr3:170108971 T>A maps to NM_005414.3 L607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:170108170 C>T maps to NM_005414.3 I530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:170078769 C>T maps to NM_005414.3 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:170078454 C>T maps to NM_005414.3 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr3:170108029 T>C maps to NM_005414.3 N483N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:170079213 C>A maps to NM_005414.3 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:170108191 T>C maps to NM_005414.3 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr6:31929756 C>T maps to NM_006929.4 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr6:31931313 C>A maps to NM_006929.4 R510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr6:31933720 C>T maps to NM_006929.4 P711P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:31932029 C>T maps to NM_006929.4 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr6:31935790 C>T maps to NM_006929.4 T930T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:31932085 C>T maps to NM_006929.4 I646I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:31932100 C>T maps to NM_006929.4 F651F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:31930541 C>T maps to NM_006929.4 I421I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr6:31933651 C>T maps to NM_006929.4 T688T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr6:31927099 C>T maps to NM_006929.4 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr6:31935610 C>T maps to NM_006929.4 L901L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:31931243 C>T maps to NM_006929.4 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr5:54696146 C>T maps to NM_015360.4 V793V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:54618223 C>T maps to NM_015360.4 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:54649090 C>T maps to NM_015360.4 F509F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:54649091 C>T maps to NM_015360.4 R510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:54635984 G>T maps to NM_015360.4 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:54696092 C>T maps to NM_015360.4 P775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:54639207 C>T maps to NM_015360.4 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr5:133509698 C>T maps to NM_170679.2 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr8:134050864 G>A maps to NM_006748.3 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr8:134050771 G>A maps to NM_006748.3 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:134072417 C>T maps to NM_006748.3 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:134063088 G>A maps to NM_006748.3 R85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:134060147 C>T maps to NM_006748.3 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:134057255 G>A maps to NM_006748.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr20:35269707 G>A maps to NM_032214.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr20:35269708 A>C maps to NM_032214.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr13:78320733 A>C maps to ENST00000389459 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr13:78320655 G>A maps to ENST00000389459 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:78335024 C>T maps to ENST00000389459 R471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr1:160604529 G>A maps to NM_003037.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:160607056 C>T maps to NM_003037.2 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:160589592 C>T maps to NM_003037.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:160589631 C>T maps to NM_003037.2 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr1:160582292 G>A maps to NM_003037.2 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:160589592 C>T maps to NM_003037.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr1:160460018 T>A maps to NM_001184714.1 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:160460439 G>A maps to NM_001184714.1 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:160460439 G>A maps to NM_001184714.1 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:160465986 C>T maps to NM_001184714.1 Q82Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr1:160492958 G>A maps to NM_001184714.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:160465952 G>A maps to NM_001184714.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr1:160461133 G>A maps to NM_001184714.1 Q143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:160458916 C>T maps to NM_001184714.1 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:160465878 C>T maps to NM_001184714.1 K118K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:160460374 C>T maps to NM_001184714.1 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr1:160720136 C>T maps to NM_021181.3 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:160719701 G>A maps to NM_021181.3 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:160720128 C>T maps to NM_021181.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:160720137 C>T maps to NM_021181.3 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr1:160720151 C>T maps to NM_021181.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:160719869 G>A maps to NM_021181.3 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:159802888 G>A maps to NM_020125.2 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:159799848 C>T maps to NM_020125.2 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:159799842 C>T maps to NM_020125.2 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:159799815 C>T maps to NM_020125.2 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:159799843 C>T maps to NM_020125.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:159799773 C>T maps to NM_020125.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:159804974 G>A maps to NM_020125.2 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:159921543 G>A maps to NM_033438.3 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr1:159922211 G>A maps to NM_033438.3 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:159923198 G>A maps to NM_033438.3 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:159923180 C>T maps to NM_033438.3 E103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:159922085 A>G maps to NM_033438.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr1:159921543 G>A maps to NM_033438.3 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:159923228 G>A maps to NM_033438.3 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr14:70263653 G>A maps to NM_003049.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr14:70252858 G>A maps to NM_003049.3 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr14:70263758 G>A maps to NM_003049.3 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr13:103710710 G>A maps to NM_000452.2 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:103701738 G>A maps to NM_000452.2 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr13:103703704 G>A maps to NM_000452.2 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr13:103703782 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr13:103703761 G>A maps to NM_000452.2 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr13:103705038 G>A maps to NM_000452.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr13:103703677 T>C maps to NM_000452.2 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr13:103718587 C>T maps to NM_000452.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr13:103718365 G>A maps to NM_000452.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr13:103718359 G>A maps to NM_000452.2 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:153716273 C>A did not map to a codon.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr23:153716342 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:153716407 G>C did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr23:153717109 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:153716662 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:153716919 C>A did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:153716815 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:153716269 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:153716270 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:153715942 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:48490877 G>A maps to NM_152679.3 E412E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr4:48487026 G>A maps to NM_152679.3 W223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr4:48486094 C>T maps to NM_152679.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:48486969 C>T maps to NM_152679.3 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr8:82605899 G>A maps to NM_001010893.2 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr4:87746603 G>A maps to NM_197965.2 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:87744978 C>T maps to NM_197965.2 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr4:147204417 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:147179969 G>A maps to ENST00000507030 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:147227086 G>A maps to ENST00000507030 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:219254648 C>T maps to NM_000578.3 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:219254751 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:219251362 C>T maps to NM_000578.3 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:219254627 C>T maps to NM_000578.3 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:219249952 G>A maps to NM_000578.3 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:219249888 G>A maps to NM_000578.3 W98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:219249889 G>A maps to NM_000578.3 W98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:219254612 C>T maps to NM_000578.3 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:219256208 C>T maps to NM_000578.3 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr2:219257708 C>T maps to NM_000578.3 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:51390707 G>A maps to NM_001174125.1 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:51382182 G>A maps to NM_001174125.1 F566F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:51384697 A>G maps to NM_001174125.1 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:51384700 G>A maps to NM_001174125.1 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr15:48537067 A>G maps to NM_000338.2 E473E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr15:48591432 G>A maps to NM_000338.2 W1019*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:48539176 C>T maps to NM_000338.2 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:48539589 G>A maps to NM_000338.2 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:48541796 C>T maps to NM_000338.2 I570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:48499969 C>T maps to NM_000338.2 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr15:48539562 C>T maps to NM_000338.2 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:48500134 C>T maps to NM_000338.2 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:48500134 C>T maps to NM_000338.2 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:48524940 G>T maps to NM_000338.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:127471438 C>T maps to NM_001046.2 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:127516635 C>T maps to NM_001046.2 I1054I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:127477567 C>T maps to NM_001046.2 I556I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:127474323 C>T maps to NM_001046.2 R482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr5:127469918 C>T maps to NM_001046.2 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:56913533 C>T maps to NM_000339.2 C472C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:56906279 C>T maps to NM_000339.2 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:56906646 C>T maps to NM_000339.2 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:56904074 C>T maps to NM_000339.2 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr16:56899359 C>T maps to NM_000339.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:56917963 G>A maps to NM_000339.2 W558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:56928467 C>T maps to NM_000339.2 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr16:56928512 C>T maps to NM_000339.2 F873F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr16:56918051 G>A maps to NM_000339.2 W587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:56936404 G>A maps to NM_000339.2 T956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr16:56904020 C>T maps to NM_000339.2 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr16:56904074 C>T maps to NM_000339.2 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr16:56947239 C>T maps to NM_000339.2 L1006L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:56917977 C>T maps to NM_000339.2 Q563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:56916347 C>T maps to NM_000339.2 F536F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:67991874 G>A maps to NM_005072.4 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:67991875 G>A maps to NM_005072.4 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr16:67980932 G>A maps to NM_005072.4 S716S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr16:67991821 G>A maps to NM_005072.4 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr16:67981621 C>T maps to NM_005072.4 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr16:67985082 G>T maps to NM_005072.4 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr16:67991660 G>A maps to NM_005072.4 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr20:44664486 C>T maps to NM_001134771.1 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr20:44672272 G>A maps to NM_001134771.1 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr20:44681629 C>T maps to NM_001134771.1 A827A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr20:44665918 C>T maps to NM_001134771.1 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr20:44664158 A>G maps to NM_001134771.1 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr20:44670117 C>T maps to NM_001134771.1 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr20:44664486 C>T maps to NM_001134771.1 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:44672308 G>A maps to NM_001134771.1 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr20:44672557 C>T maps to NM_001134771.1 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr20:44673631 C>T maps to NM_001134771.1 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:44672557 C>T maps to NM_001134771.1 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:44676131 C>T maps to NM_001134771.1 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr20:44666018 C>T maps to NM_001134771.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:44664161 G>A maps to NM_001134771.1 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:44669130 G>A maps to NM_001134771.1 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:44673603 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:44673673 C>T maps to NM_001134771.1 V511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:44685807 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:44685808 G>A maps to NM_001134771.1 L1065L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:44685173 G>A maps to NM_001134771.1 E1050E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr20:44670090 C>T maps to NM_001134771.1 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr15:34544407 G>A maps to NM_133647.1 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr15:34547528 G>A maps to NM_133647.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr15:34546781 G>A maps to NM_133647.1 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr15:34536193 G>A maps to NM_133647.1 R675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr15:34536194 G>A maps to NM_133647.1 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr15:34529691 G>A maps to NM_133647.1 I954I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr15:34536214 G>A maps to NM_133647.1 R668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr15:34543177 A>G maps to NM_133647.1 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:34549923 G>A maps to NM_133647.1 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr5:1081725 G>A maps to NM_006598.2 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr5:1079555 G>A maps to NM_006598.2 I451I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr5:1064085 C>T maps to NM_006598.2 W871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:1076864 G>A maps to NM_006598.2 I564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:1075532 G>A maps to NM_006598.2 S640S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:1078004 C>T maps to NM_006598.2 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr3:124810370 C>T maps to NM_001195483.1 V611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr3:124837618 C>T maps to NM_001195483.1 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:124829173 G>A maps to NM_001195483.1 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:124826508 C>T maps to NM_001195483.1 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:124837627 G>A maps to NM_001195483.1 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:124839504 C>T maps to NM_001195483.1 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:124826484 G>A maps to NM_001195483.1 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr3:124826655 G>A maps to NM_001195483.1 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:124896668 G>A maps to NM_001195483.1 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:124802868 G>A maps to NM_001195483.1 I670I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr3:124807164 G>A maps to NM_001195483.1 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr3:124826445 C>T maps to NM_001195483.1 W528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:124802799 G>A maps to NM_001195483.1 F693F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:100456717 C>T maps to NM_020246.2 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:100456508 C>T maps to NM_020246.2 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:100458767 C>T maps to NM_020246.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:100458768 C>T maps to NM_020246.2 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr7:100454733 C>T maps to NM_020246.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr7:100454517 C>T maps to NM_020246.2 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr7:100460417 G>A maps to NM_020246.2 G609G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr7:100458767 C>T maps to NM_020246.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:122759152 G>A maps to NM_022444.3 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:122759253 G>A maps to NM_022444.3 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:122811946 A>G maps to NM_022444.3 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr7:122821053 G>A maps to NM_022444.3 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:122787232 G>A maps to NM_022444.3 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:122765623 A>G maps to NM_022444.3 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr7:122765665 G>A maps to NM_022444.3 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr7:122768995 G>A maps to NM_022444.3 Q346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:122811881 C>T maps to NM_022444.3 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:122787289 G>A maps to NM_022444.3 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:122808457 C>T maps to NM_022444.3 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:122839955 G>A maps to NM_022444.3 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr7:122774537 C>T maps to NM_022444.3 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr17:26818750 C>A maps to NM_001145975.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr17:26822812 C>T maps to NM_001145975.1 F532F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:26817326 C>T maps to NM_001145975.1 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr17:26800786 C>T maps to NM_001145975.1 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:26821450 G>A maps to NM_001145975.1 W459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:26822719 G>A maps to NM_001145975.1 Q501Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:26823499 C>T maps to NM_001145975.1 V550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:26820741 C>T maps to NM_001145975.1 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:26821418 G>A maps to NM_001145975.1 G448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr17:26816314 C>T maps to NM_001145975.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr20:45217803 G>A maps to NM_022829.5 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr20:45194891 G>A maps to NM_022829.5 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr20:45242259 G>A maps to NM_022829.5 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr20:45242181 G>A maps to NM_022829.5 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:45216771 G>A maps to NM_022829.5 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:45221074 C>T maps to NM_022829.5 W296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr20:45217887 C>T maps to NM_022829.5 W309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr20:45217888 C>T maps to NM_022829.5 W309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:45194879 G>A maps to NM_022829.5 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:45217841 G>A maps to NM_022829.5 R325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr20:45194870 C>T maps to NM_022829.5 E497E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr20:45188717 C>T maps to NM_022829.5 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr20:45195019 G>A maps to NM_022829.5 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr20:45221137 G>A maps to NM_022829.5 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:45242108 G>A maps to NM_022829.5 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr20:45194948 G>A maps to NM_022829.5 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:45216729 G>A maps to NM_022829.5 F363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr20:45221065 G>A maps to NM_022829.5 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:135366409 C>T maps to NM_012450.2 V594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:135384290 C>T maps to NM_012450.2 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:135386426 C>T did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr7:135392920 C>T maps to NM_012450.2 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:135378925 C>T maps to NM_012450.2 E359E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr7:135376073 C>T did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr17:6589654 C>T maps to NM_177550.3 V526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr17:6604349 C>T maps to NM_177550.3 W271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:6589526 T>G maps to NM_177550.3 *569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:6599088 G>A maps to NM_177550.3 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:6599223 C>T maps to NM_177550.3 K292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr17:6599121 C>T maps to NM_177550.3 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:6590865 G>A maps to NM_177550.3 H519H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:6594232 C>T maps to NM_177550.3 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:6594259 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:6599214 C>T maps to NM_177550.3 E295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:6606395 C>T maps to NM_177550.3 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr17:6596476 C>T maps to NM_177550.3 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:43316483 C>T maps to NM_001146037.1 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:43310377 C>T maps to NM_001146037.1 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:43319610 C>T maps to NM_001146037.1 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr18:43224012 G>A maps to NM_007163.3 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr18:43216984 C>T maps to NM_007163.3 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr18:43247924 G>A maps to NM_007163.3 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr18:43249459 C>T maps to NM_007163.3 P742P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr18:43219781 C>T maps to NM_007163.3 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr18:43221264 C>T maps to NM_007163.3 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:43217119 C>T maps to NM_007163.3 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:43247861 G>A maps to NM_007163.3 V594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr18:43221246 C>T maps to NM_007163.3 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr18:43246154 C>T maps to NM_007163.3 R510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr18:43262463 C>T maps to NM_007163.3 Q915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr18:43258958 G>A maps to NM_007163.3 L844L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr18:43224000 C>T maps to NM_007163.3 F409F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr18:43224001 C>T maps to NM_007163.3 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr18:43221222 C>T maps to NM_007163.3 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr18:43212335 C>T maps to NM_007163.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr18:43206998 C>T maps to NM_007163.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:43212398 C>T maps to NM_007163.3 Y202Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:43243748 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:43247945 C>T maps to NM_007163.3 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr18:43204724 G>A maps to NM_007163.3 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr18:43224000 C>T maps to NM_007163.3 F409F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr18:43243840 C>T maps to NM_007163.3 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr13:99354777 C>T maps to NM_005073.3 K474K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr13:99361878 C>T maps to NM_005073.3 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:99337052 C>T maps to NM_005073.3 E684E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr13:99337100 C>T maps to NM_005073.3 R668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr13:99340519 G>C maps to NM_005073.3 T555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:99378489 G>A maps to NM_005073.3 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr13:99356563 C>T maps to NM_005073.3 W465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr13:99368161 G>A maps to NM_005073.3 N231N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr3:121616253 C>T maps to NM_021082.3 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr3:121616253 C>T maps to NM_021082.3 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr3:121613395 C>T maps to NM_021082.3 R25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:121649723 C>T maps to NM_021082.3 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr3:121641930 C>T maps to NM_021082.3 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:121643823 C>T maps to NM_021082.3 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:121630465 C>T maps to NM_021082.3 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:121631882 C>T maps to NM_021082.3 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:121643802 C>T maps to NM_021082.3 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr3:121659736 C>T maps to NM_021082.3 I691I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:121634130 T>C maps to NM_021082.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:121615296 G>C maps to NM_021082.3 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:121613337 G>A maps to NM_021082.3 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:121630438 C>T maps to NM_021082.3 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:121643196 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:121659730 C>T maps to NM_021082.3 F689F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:121658221 G>A maps to NM_021082.3 W596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr11:60707010 C>T maps to NM_016582.2 W459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:60714146 G>A maps to NM_016582.2 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:60704702 C>T maps to NM_016582.2 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr11:60705348 C>T maps to NM_016582.2 K528K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:60714281 G>A maps to NM_016582.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:60705471 G>A maps to NM_016582.2 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:60705348 C>T maps to NM_016582.2 K528K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:60708633 C>T maps to NM_016582.2 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:60704806 G>A maps to NM_016582.2 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:60708741 G>A maps to NM_016582.2 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:60711214 C>T maps to NM_016582.2 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:129299605 G>A maps to ENST00000376744 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:111498711 G>A maps to NM_018593.4 E262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr10:91222167 G>A maps to NM_213606.3 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:91198440 C>T maps to NM_213606.3 Q316Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:91222194 C>T maps to NM_213606.3 W47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:91222221 C>T maps to NM_213606.3 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr10:91198934 C>A maps to NM_213606.3 G152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr10:91198575 C>T maps to NM_213606.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:91198419 G>A maps to NM_213606.3 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:91195976 G>A maps to NM_213606.3 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:6941639 C>T maps to NM_201566.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:6942020 C>T maps to NM_201566.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:6940076 C>T maps to NM_201566.2 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:6941597 C>T maps to NM_201566.2 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:230910665 A>T maps to NM_152527.4 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:230911258 G>A maps to NM_152527.4 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr2:230914546 G>A maps to NM_152527.4 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr2:230911304 C>T maps to NM_152527.4 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:230910950 G>A maps to NM_152527.4 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr2:230910503 G>A maps to NM_152527.4 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr2:230911217 G>A maps to NM_152527.4 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr2:230910821 G>A maps to NM_152527.4 I340I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:230910782 G>A maps to NM_152527.4 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr2:230911382 G>A maps to NM_152527.4 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:230910956 C>T maps to NM_152527.4 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:230910800 C>T maps to NM_152527.4 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:230911274 C>T maps to NM_152527.4 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr2:230914620 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:230911094 C>T maps to NM_152527.4 K249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:230923873 G>A maps to NM_152527.4 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:230911019 C>T maps to NM_152527.4 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:230911019 C>T maps to NM_152527.4 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr23:73744597 G>C did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:73749079 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:73751255 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:73749128 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:73740948 C>T did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:73641832 G>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr17:80196836 G>A maps to NM_001042423.1 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr17:80196791 C>T maps to NM_001042423.1 F446F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr17:80196776 G>A maps to NM_001042423.1 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr17:80195473 C>T maps to NM_001042423.1 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr17:80194102 G>A maps to NM_001042423.1 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:80193901 G>A maps to NM_001042423.1 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:80195263 G>A maps to NM_001042423.1 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:80195755 G>A maps to NM_001042423.1 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:110906414 G>C maps to NM_004696.1 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr17:73102103 T>A maps to ENST00000450736 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr17:73096888 C>T maps to ENST00000450736 F417F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:73096513 C>T maps to ENST00000450736 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:73096879 C>T maps to ENST00000450736 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr17:66267712 G>A maps to NM_004694.4 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:66267064 G>A maps to NM_004694.4 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:66267745 G>A maps to NM_004694.4 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:60165123 C>T maps to NM_004731.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:60098647 G>T maps to NM_004731.3 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:60168849 C>T maps to NM_004731.3 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr22:38478709 C>T maps to NM_013356.2 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:61432606 G>A maps to NM_194298.2 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr10:61444017 C>T maps to NM_194298.2 W11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:61413574 C>T maps to NM_194298.2 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr10:61413643 G>A maps to NM_194298.2 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:61413643 G>A maps to NM_194298.2 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:61414213 G>A maps to NM_194298.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr10:61413643 G>A maps to NM_194298.2 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:61413484 C>T maps to NM_194298.2 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr6:25811929 T>G maps to NM_005074.3 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr6:25799113 G>A maps to NM_005074.3 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:25801129 C>T maps to NM_005074.3 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr6:25799036 T>C maps to NM_005074.3 K460K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:25819946 C>T maps to NM_005074.3 W135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:25799086 G>A maps to NM_005074.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:25813130 G>A maps to NM_005074.3 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr6:25813337 G>T maps to NM_005074.3 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:25826823 G>A maps to NM_005074.3 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:25799050 G>A maps to NM_005074.3 Q456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:25813082 G>A maps to NM_005074.3 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:25799015 G>A maps to NM_005074.3 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:25813406 G>A maps to NM_005074.3 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:25917005 G>A maps to NM_005835.2 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr6:25924105 C>T maps to NM_005835.2 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:25916918 G>A maps to NM_005835.2 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr6:25917289 G>A maps to NM_005835.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:25914866 C>T maps to NM_005835.2 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:25923991 G>A maps to NM_005835.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:25917047 G>A maps to NM_005835.2 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:25921499 C>T maps to NM_005835.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr6:25862089 G>A maps to NM_001098486.1 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr6:25862607 C>T maps to NM_001098486.1 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:25862089 G>A maps to NM_001098486.1 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr6:25862218 G>A maps to NM_001098486.1 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:25862607 C>T maps to NM_001098486.1 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:25851001 G>A maps to NM_001098486.1 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:25770458 C>T maps to NM_005495.2 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:25773754 C>T maps to NM_005495.2 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:25776929 C>T maps to NM_005495.2 T365T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A2MJ-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:25769327 C>T maps to NM_005495.2 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr6:74351494 G>A maps to NM_012434.4 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr6:74351533 C>A maps to NM_012434.4 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:22380957 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:22399063 G>A maps to NM_020346.2 E509E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr11:22391619 C>T maps to NM_020346.2 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr11:22360115 A>T maps to NM_020346.2 K13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:22382447 G>A maps to NM_020346.2 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:22399009 T>C maps to NM_020346.2 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:22399264 G>A maps to NM_020346.2 K576K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:22363238 C>T maps to NM_020346.2 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:22382473 G>A maps to NM_020346.2 W202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:22399050 G>A maps to NM_020346.2 W505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:22396375 C>T maps to NM_020346.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:49935842 G>A maps to NM_020309.3 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:49933979 C>T maps to NM_020309.3 E493E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:49937913 C>T maps to NM_020309.3 W194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:49937003 C>T maps to NM_020309.3 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:49944627 G>A maps to NM_020309.3 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr12:100806614 C>A maps to NM_139319.2 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr12:100774535 G>A maps to NM_139319.2 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:100813678 G>A maps to NM_139319.2 G504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:100796199 G>A maps to NM_139319.2 E282E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:100774728 C>T maps to NM_139319.2 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr12:100806573 C>T maps to NM_139319.2 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:100784870 C>T maps to NM_139319.2 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:100751231 G>A maps to NM_139319.2 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr12:100813666 C>T maps to NM_139319.2 V500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:100813666 C>T maps to NM_139319.2 V500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr20:61598782 G>A maps to NM_022082.3 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:61595007 C>T maps to NM_022082.3 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr20:61595007 C>T maps to NM_022082.3 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr20:61595632 C>T maps to NM_022082.3 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:61594691 G>A maps to NM_022082.3 W232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:61595590 C>T maps to NM_022082.3 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:61596511 C>T maps to NM_022082.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr8:20004873 C>T maps to NM_001135691.2 K453K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:20022594 A>G maps to NM_001135691.2 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:20022404 G>A maps to NM_001135691.2 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr8:20030598 C>T maps to NM_001135691.2 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr8:20004825 G>A maps to NM_001135691.2 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr8:20005147 G>A maps to NM_001135691.2 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr8:20022597 G>A maps to NM_001135691.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr8:20036651 G>A maps to NM_001135691.2 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:20035988 G>A maps to NM_001135691.2 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr10:119027221 G>A maps to NM_003054.4 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr10:119026271 T>C maps to NM_003054.4 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr10:119003614 G>A maps to NM_003054.4 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:50820006 C>T maps to NM_003055.2 F407F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr10:50820021 C>T maps to NM_003055.2 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:50819729 G>A maps to NM_003055.2 W315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:50819631 C>T maps to NM_003055.2 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:50819611 C>T maps to NM_003055.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:50819706 C>T maps to NM_003055.2 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr21:46935715 G>A maps to NM_194255.1 S544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr21:46957801 G>A maps to NM_194255.1 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr21:46945829 C>A maps to NM_194255.1 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr21:46945796 G>A maps to NM_194255.1 I409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:169439358 G>A maps to NM_006996.2 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:169446659 G>A maps to NM_006996.2 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr1:169435089 T>C maps to NM_006996.2 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:169446428 G>A maps to NM_006996.2 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:169446467 A>G maps to NM_006996.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:228564172 T>C maps to NM_025243.3 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr2:228563526 G>A maps to NM_025243.3 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr2:228563863 G>A maps to NM_025243.3 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:228564157 G>A maps to NM_025243.3 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:228563863 G>A maps to NM_025243.3 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:4576649 C>T maps to NM_004170.5 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr9:4573942 G>A maps to NM_004170.5 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr9:4576754 C>T maps to NM_004170.5 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:4585527 C>T maps to NM_004170.5 T515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr9:4572295 C>G maps to NM_004170.5 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr11:35287298 C>T maps to NM_004171.3 R476R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr11:35336567 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:35336588 G>A maps to NM_004171.3 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr11:35333993 C>G maps to NM_004171.3 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr11:35333981 C>T maps to NM_004171.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:35287112 G>A maps to NM_004171.3 V538V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr5:36684073 G>A maps to NM_004172.4 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr5:36629558 C>T maps to NM_004172.4 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr5:36629591 C>T maps to NM_004172.4 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:36677049 G>A maps to NM_004172.4 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr5:36608579 C>T maps to NM_004172.4 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr2:65245732 C>T maps to NM_003038.4 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:65217268 C>T maps to NM_003038.4 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:47280487 G>A maps to NM_005628.2 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:47278982 G>A maps to NM_005628.2 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:47280250 G>A maps to NM_005628.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:15072962 G>A maps to NM_005071.1 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:15065068 G>A maps to NM_005071.1 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:15075148 C>T maps to NM_005071.1 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:15073118 G>A maps to NM_005071.1 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:15073079 G>A maps to NM_005071.1 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:15083647 C>T maps to NM_005071.1 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:15067484 C>T maps to NM_005071.1 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:15061144 G>A maps to NM_005071.1 I519I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:15072935 G>A maps to NM_005071.1 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr19:15075163 A>G maps to NM_005071.1 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15061168 C>T maps to NM_005071.1 G511G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15065097 G>A maps to NM_005071.1 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:15083548 G>A maps to NM_005071.1 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:53558434 G>A maps to NM_006671.4 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:53600041 G>A maps to NM_006671.4 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:53559149 G>A maps to NM_006671.4 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr1:53580623 G>A maps to NM_006671.4 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:53558446 G>A maps to NM_006671.4 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:53553854 G>A maps to NM_006671.4 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:53553806 G>A maps to NM_006671.4 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:53558263 G>A maps to NM_006671.4 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:53556324 G>A maps to NM_006671.4 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:53558272 G>A maps to NM_006671.4 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr1:53559149 G>A maps to NM_006671.4 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr1:53558272 G>A maps to NM_006671.4 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:53555536 G>A maps to NM_006671.4 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:53580494 C>T maps to NM_006671.4 K122K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:53580518 G>A maps to NM_006671.4 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:53608037 G>A maps to NM_006671.4 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:53555602 G>A maps to NM_006671.4 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:113416432 C>T maps to NM_005415.3 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:42294574 G>A maps to NM_006749.3 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:42294622 G>A maps to NM_006749.3 D469D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:42294757 G>A maps to NM_006749.3 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:42294927 C>A maps to NM_006749.3 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr8:42294859 G>A maps to NM_006749.3 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:42302215 G>A maps to NM_006749.3 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr6:160555049 C>T maps to NM_003057.2 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr6:160579577 C>T maps to NM_003057.2 Y543Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr6:160557601 C>G maps to NM_003057.2 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:160560702 C>T maps to NM_003057.2 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:160557580 T>A maps to NM_003057.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:160551161 G>A maps to NM_003057.2 W146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:160553262 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr11:63064783 A>C maps to NM_001039752.3 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr11:63072193 G>A maps to NM_001039752.3 R477R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr11:63071673 C>T maps to NM_001039752.3 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr11:63064843 C>T maps to NM_001039752.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:63069866 C>T maps to NM_001039752.3 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:63072301 C>T maps to NM_001039752.3 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:63057642 C>T maps to NM_001039752.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:63065040 G>A maps to NM_001039752.3 W224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:63069866 C>T maps to NM_001039752.3 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:63057906 C>T maps to NM_001039752.3 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:63064811 C>T maps to NM_001039752.3 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:63064897 C>T maps to NM_001039752.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:63067077 G>A maps to NM_001039752.3 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr11:63057912 C>T maps to NM_001039752.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:63069893 C>T maps to NM_001039752.3 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr11:63072304 C>T maps to NM_001039752.3 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:63057883 C>T maps to NM_001039752.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:63067080 C>T maps to NM_001039752.3 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:63059012 G>A maps to NM_001039752.3 W135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:63064843 C>T maps to NM_001039752.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr11:63064903 C>T maps to NM_001039752.3 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr11:63067087 C>T maps to NM_001039752.3 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:63069906 C>T maps to NM_001039752.3 R393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:63067086 C>T maps to NM_001039752.3 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:64326683 C>T maps to NM_018484.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr11:64326683 C>T maps to NM_018484.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr11:64323542 C>T maps to NM_018484.2 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:64336178 A>C maps to NM_018484.2 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:64326683 C>T maps to NM_018484.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr11:64323863 G>A maps to NM_018484.2 K131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:64337276 C>T maps to NM_018484.2 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64331851 G>A maps to NM_018484.2 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64335110 C>T maps to NM_018484.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:64326680 C>T maps to NM_018484.2 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr11:64359090 G>A maps to NM_144585.2 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr11:64360948 C>T maps to NM_144585.2 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:64359246 G>A maps to NM_144585.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:64359321 C>T maps to NM_144585.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:64368230 G>A maps to NM_144585.2 Q473Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:64360945 C>T maps to NM_144585.2 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr11:64359258 C>T maps to NM_144585.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:64366371 G>A maps to NM_144585.2 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr11:64367881 C>T maps to NM_144585.2 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:64359244 C>T maps to NM_144585.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:64366014 C>T maps to NM_144585.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64368269 C>T maps to NM_144585.2 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr11:64359216 C>T maps to NM_144585.2 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:64359240 C>T maps to NM_144585.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:38317579 C>T maps to NM_004256.3 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:38317121 C>T maps to NM_004256.3 H327H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:38316507 G>A maps to NM_004256.3 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr3:38307644 C>T maps to NM_004256.3 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38317408 C>T maps to NM_004256.3 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38317409 C>T maps to NM_004256.3 Q354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:38354489 G>A maps to NM_004803.3 W315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr3:38347826 C>T maps to NM_004803.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr3:38357862 C>T maps to NM_004803.3 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr3:38347783 C>T maps to NM_004803.3 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:38350535 C>T maps to NM_004803.3 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:38357868 C>T maps to NM_004803.3 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr3:38350535 C>T maps to NM_004803.3 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:38357109 G>A maps to NM_004803.3 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr3:38348009 A>T maps to NM_004803.3 K165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr3:38355223 C>A maps to NM_004803.3 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr3:38347900 C>T maps to NM_004803.3 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:38350535 C>T maps to NM_004803.3 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:38348791 C>T maps to NM_004803.3 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr3:38348770 G>A maps to NM_004803.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:38347570 G>A maps to NM_004803.3 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:38355424 C>T maps to NM_004803.3 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38357817 G>A maps to NM_004803.3 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:38355397 C>T maps to NM_004803.3 I448I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr1:116574188 C>T maps to NM_018420.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:116569583 C>T maps to NM_018420.2 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr6:110763783 G>A maps to NM_033125.2 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:110746123 C>T maps to NM_033125.2 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:110759940 G>A maps to NM_033125.2 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:110763834 C>T maps to NM_033125.2 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:110757098 G>A maps to NM_033125.2 G459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:110746096 C>T maps to NM_033125.2 R571R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:110763561 C>T maps to NM_033125.2 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr6:110746228 G>A maps to NM_033125.2 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr14:23817499 G>A maps to NM_020372.2 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:23816341 G>A maps to NM_020372.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:23817803 G>A maps to NM_020372.2 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr14:23817418 G>A maps to NM_020372.2 N263N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr11:2946300 C>T maps to NM_002555.5 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr11:2943698 C>T maps to NM_002555.5 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:2924712 C>T maps to NM_002555.5 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr11:2943375 G>T maps to NM_002555.5 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:2943676 C>T maps to NM_002555.5 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:160664670 A>C maps to NM_003058.3 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:160671583 G>A maps to NM_003058.3 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:160670396 C>T maps to NM_003058.3 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:160679734 G>A maps to NM_003058.3 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:160662506 G>A maps to NM_003058.3 F500F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:160677689 T>C maps to NM_003058.3 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:160679501 C>T maps to NM_003058.3 W96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:160638495 G>A maps to NM_003058.3 Q546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:160671647 C>T maps to NM_003058.3 W202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:160679774 C>T maps to NM_003058.3 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:160662515 C>T maps to NM_003058.3 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:160664718 G>A maps to NM_003058.3 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:160679777 G>A maps to NM_003058.3 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr6:160679717 G>A maps to NM_003058.3 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr6:160679690 G>A maps to NM_003058.3 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr6:160662617 C>T maps to NM_003058.3 R463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr11:64985140 C>T maps to ENST00000438990 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr11:64985155 C>T maps to ENST00000438990 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64981639 C>T maps to ENST00000438990 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:3298436 G>A maps to ENST00000436008 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:3410536 G>A maps to ENST00000436008 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr6:3287255 G>A maps to ENST00000436008 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr6:3289997 G>T maps to ENST00000436008 S438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr6:3284207 C>T maps to ENST00000436008 G535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr6:3284162 G>A maps to ENST00000436008 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr11:62997013 C>T maps to NM_199352.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr11:62933663 G>A maps to NM_199352.3 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr11:62984832 G>A maps to NM_199352.3 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:62948232 G>A maps to NM_199352.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:62931310 C>T maps to NM_199352.3 R543R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:62997105 G>A maps to NM_199352.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:62933730 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:62951204 C>T maps to NM_199352.3 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr11:62985074 G>A maps to NM_199352.3 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:62997055 G>A maps to NM_199352.3 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:62997028 G>A maps to NM_199352.3 Y32Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr11:62984907 C>T maps to NM_199352.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:62951204 C>T maps to NM_199352.3 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr11:62997099 G>A maps to NM_199352.3 Q9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:62933702 G>A maps to NM_199352.3 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr11:62985191 G>A maps to NM_199352.3 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr11:62948145 G>A maps to NM_199352.3 F352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:62933663 G>A maps to NM_199352.3 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:62931459 G>A maps to NM_199352.3 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:62984928 G>A maps to NM_199352.3 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr6:160864667 C>T maps to ENST00000392145 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr6:160828165 G>A maps to ENST00000392145 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:160829905 C>T maps to ENST00000392145 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:160831820 G>A maps to ENST00000392145 Q306Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:160828153 C>T maps to ENST00000392145 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr6:160829803 G>A maps to ENST00000392145 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:160829917 C>T maps to ENST00000392145 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q3-06A-11D-A196-08 chr5:131670425 G>T maps to NM_003059.2 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr5:131671622 C>T maps to NM_003059.2 N458N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:131647921 C>T maps to NM_003059.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26D-06A-11D-A19A-08 chr5:131630374 C>T maps to NM_003059.2 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr5:131719901 G>A maps to ENST00000435065 Q211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:131726459 C>T maps to ENST00000435065 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr5:131728257 C>T maps to ENST00000435065 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:131729428 C>T maps to ENST00000435065 I528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr11:62751135 C>T maps to NM_004790.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr11:62744810 G>A maps to NM_004790.3 I470I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:62747341 C>T maps to NM_004790.3 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr11:62751835 C>T maps to NM_004790.3 W109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:62749402 G>A maps to NM_004790.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:62751814 G>A maps to NM_004790.3 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr11:62747338 G>A maps to NM_004790.3 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:62748476 G>A maps to NM_004790.3 F339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:62751904 C>T maps to NM_004790.3 W86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr6:43269382 C>T maps to ENST00000372585 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr6:43270054 C>T maps to ENST00000372585 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr6:43267407 C>T maps to ENST00000372585 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr6:43271892 C>T maps to ENST00000372585 I501I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr6:43271916 C>T maps to ENST00000372585 A509A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:43268902 G>A maps to ENST00000372585 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:43271892 C>T maps to ENST00000372585 I501I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr6:43266440 G>A maps to ENST00000372585 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:62768247 A>C maps to ENST00000430500 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr11:62760987 C>T maps to ENST00000430500 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:62762116 G>A maps to ENST00000430500 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:62766403 G>A maps to ENST00000430500 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:62760969 C>T maps to ENST00000430500 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr11:62762218 G>A maps to ENST00000430500 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:62763569 G>A maps to ENST00000430500 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:62760975 G>A maps to ENST00000430500 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:62760936 C>T maps to ENST00000430500 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:62782325 G>A maps to ENST00000430500 N35N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:62760969 C>T maps to ENST00000430500 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:62766394 G>A maps to ENST00000430500 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr11:62760804 G>A maps to ENST00000430500 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr11:63141130 C>T maps to NM_080866.2 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr11:63137758 C>T maps to NM_080866.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr11:63137910 C>A maps to NM_080866.2 S128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr11:63143143 C>T maps to NM_080866.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:63141196 C>T maps to NM_080866.2 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:63173967 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:63149659 G>A maps to NM_080866.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr11:63137539 G>A maps to NM_080866.2 Q4Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:63141469 C>T maps to NM_080866.2 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr11:63149725 G>A maps to NM_080866.2 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr11:63141130 C>T maps to NM_080866.2 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:63141130 C>T maps to NM_080866.2 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:63174091 G>A maps to NM_080866.2 W399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:63174109 C>T maps to NM_080866.2 N405N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr11:63174022 G>A maps to NM_080866.2 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:63137656 C>T maps to NM_080866.2 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:63141519 C>T maps to NM_080866.2 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:63149659 G>A maps to NM_080866.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:63149731 C>T maps to NM_080866.2 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:63174097 G>A maps to NM_080866.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:63176291 C>T maps to NM_080866.2 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:63149687 C>T maps to NM_080866.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr5:138718904 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:4848511 G>A maps to NM_203327.1 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:220027108 G>A maps to NM_001144890.1 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr15:65943234 C>T maps to NM_004727.2 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr15:65931955 G>A maps to NM_004727.2 G656G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr9:19786752 G>A maps to NM_020344.2 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr9:19573378 G>A maps to NM_020344.2 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr9:19576973 C>T maps to NM_020344.2 K392K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:19786549 C>T maps to NM_020344.2 K105K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:19786146 G>A maps to NM_020344.2 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:19576955 C>T maps to NM_020344.2 E398E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:19786501 C>T maps to NM_020344.2 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr9:19786831 G>A maps to NM_020344.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:19786486 G>A maps to NM_020344.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr20:19664826 C>T maps to NM_020689.3 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr20:19634764 G>A maps to NM_020689.3 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr20:19261651 G>A maps to NM_020689.3 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr20:19677496 C>T maps to NM_020689.3 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr20:19665841 C>A maps to NM_020689.3 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:19261651 G>A maps to NM_020689.3 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:19566124 C>T maps to NM_020689.3 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:19666003 C>T maps to NM_020689.3 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr20:19566124 C>T maps to NM_020689.3 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr20:19674038 C>T maps to NM_020689.3 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr20:19677460 C>T maps to NM_020689.3 T504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr20:19677461 C>T maps to NM_020689.3 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr20:19701693 C>T maps to NM_020689.3 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr20:19673951 C>T maps to NM_020689.3 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr20:19665796 C>T maps to NM_020689.3 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr20:19662552 G>A maps to NM_020689.3 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:19665766 G>A maps to NM_020689.3 R362R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr20:19698203 C>T maps to NM_020689.3 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:19560690 C>T maps to NM_020689.3 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:19566124 C>T maps to NM_020689.3 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:19634719 C>T maps to NM_020689.3 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr20:19677496 C>T maps to NM_020689.3 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr20:19566130 C>T maps to NM_020689.3 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:92953041 G>A maps to NM_153646.3 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:92953124 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:92949072 C>T maps to NM_153646.3 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr14:92953116 G>A maps to NM_153646.3 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr14:92922944 C>T maps to NM_153646.3 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr14:92922827 G>A maps to NM_153646.3 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr12:113748107 G>A maps to NM_024959.2 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:113758211 G>A maps to NM_024959.2 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr12:113744324 G>A maps to NM_024959.2 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:113758888 G>A maps to NM_024959.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:113758479 G>A maps to NM_024959.2 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:19163959 C>T maps to NM_005984.2 Q265Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr17:79682554 C>T maps to ENST00000331531 D87D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:4841673 G>A maps to NM_003562.4 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr17:4842407 G>A maps to NM_003562.4 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr2:172700880 G>A maps to NM_003705.3 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr2:172666181 A>C maps to NM_003705.3 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:172725231 G>A maps to NM_003705.3 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:172644338 G>A maps to NM_003705.3 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr2:172683358 G>A maps to NM_003705.3 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:172644359 G>A maps to NM_003705.3 I561I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:95822396 G>A maps to NM_001160210.1 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:95813733 A>C maps to NM_001160210.1 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr7:95761115 G>A maps to NM_001160210.1 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:129480526 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:129499601 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:129506906 A>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:129483302 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr23:129474279 A>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:41379283 C>T maps to NM_014252.3 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr22:41173121 C>A maps to NM_006358.2 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr22:41190564 G>A maps to NM_006358.2 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr22:41175069 G>A maps to NM_006358.2 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:18072878 G>A maps to NM_031481.1 E275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr22:18069941 C>T maps to NM_031481.1 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr22:18064156 G>A maps to NM_031481.1 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr22:18072869 G>A maps to NM_031481.1 W272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr22:18070825 C>T maps to NM_031481.1 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr17:73282436 C>T maps to NM_021734.4 W79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:73279575 G>A maps to NM_021734.4 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr17:73269591 G>A maps to NM_021734.4 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr5:140682808 G>A maps to NM_031947.2 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:140683342 G>A maps to NM_031947.2 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:140683228 G>A maps to NM_031947.2 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:140683186 G>A maps to NM_031947.2 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:48896531 G>A maps to NM_000387.4 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr3:48900026 C>T maps to NM_000387.4 Q161Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:48921518 G>A maps to NM_000387.4 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:37180644 C>A maps to NM_030631.3 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:37180579 G>A maps to NM_030631.3 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:37153958 G>A maps to NM_030631.3 Q259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:37153962 G>A maps to NM_030631.3 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:6459552 C>T maps to NM_024103.2 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:6452424 C>T maps to NM_024103.2 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:6452336 G>A maps to NM_024103.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:6454084 G>A maps to NM_024103.2 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:108703824 G>A maps to NM_013386.3 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:108735131 G>A maps to NM_213651.1 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:108700164 C>T maps to NM_013386.3 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:108735131 G>A maps to NM_213651.1 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:66428149 C>T maps to NM_173471.3 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:46623598 C>T maps to NM_004277.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr6:46623670 C>T maps to NM_004277.3 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr10:101370956 G>A maps to NM_031212.3 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr10:101370911 G>A maps to NM_031212.3 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:98987794 C>T maps to NM_213611.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr4:128651762 G>A maps to NM_031291.2 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr4:128651822 C>T maps to NM_031291.2 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:128651717 G>A maps to NM_031291.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:128651717 G>A maps to NM_031291.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:128689926 G>A maps to NM_031291.2 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr4:128688338 C>T maps to NM_031291.2 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:9642360 C>T maps to NM_032315.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:9633420 T>C maps to NM_032315.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr1:9640068 C>T maps to NM_032315.2 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr1:16065801 C>T maps to NM_207348.1 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:16063162 C>T maps to NM_207348.1 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:16063163 C>T maps to NM_207348.1 R62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:16064661 T>A maps to NM_207348.1 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr17:8194750 A>T maps to NM_201520.1 L165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:23429013 C>T maps to NM_016612.2 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr8:23429208 C>T maps to NM_016612.2 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:23428989 C>T maps to NM_016612.2 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:39431044 C>T maps to NM_017875.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr17:42397639 G>A maps to NM_001143780.1 N296N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:42397636 G>A maps to NM_001143780.1 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr4:186066009 C>T maps to NM_001151.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:87476315 A>T maps to NM_018843.3 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr19:6432136 G>A maps to NM_173637.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:6433509 G>A maps to NM_173637.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:6433578 C>T maps to NM_173637.3 W42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr19:19217189 G>T maps to NM_178526.3 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19206956 C>T maps to NM_178526.3 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:156169796 C>T maps to NM_014655.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:156180107 C>T maps to NM_014655.2 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:156170036 C>T maps to NM_014655.2 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:65144346 G>A maps to NM_182556.2 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:65147373 G>A maps to NM_182556.2 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:118603856 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr23:1505545 C>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:1506174 C>T did not map to a codon.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr23:1508347 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr4:985080 C>T maps to NM_213613.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr4:982734 C>T maps to NM_213613.2 G664G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr12:58014158 G>T maps to NM_133489.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr12:58016844 C>T maps to NM_133489.2 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr12:58018665 G>C maps to NM_133489.2 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr12:58017648 C>T maps to NM_133489.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr17:78199643 G>A maps to NM_173626.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:78223001 C>T maps to NM_173626.3 I524I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:78195514 C>T maps to NM_173626.3 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:78220410 C>T maps to NM_173626.3 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:78196485 C>T maps to NM_173626.3 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:78211391 C>T maps to NM_173626.3 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr17:78195415 C>T maps to NM_173626.3 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:78223040 G>A maps to NM_173626.3 Q537Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr17:78221939 C>T maps to NM_173626.3 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr5:149361300 G>A maps to NM_000112.3 A715A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:149357661 C>T maps to NM_000112.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr5:149357871 T>C maps to NM_000112.3 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:149360586 C>T maps to NM_000112.3 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr7:107431495 G>A maps to NM_000111.2 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr7:107434304 C>T maps to NM_000111.2 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr7:107427285 C>T maps to NM_000111.2 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr7:107431669 C>T maps to NM_000111.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:107420172 C>T maps to NM_000111.2 K449K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:107416968 C>T maps to NM_000111.2 V535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:107430067 G>A maps to NM_000111.2 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:107430121 C>T maps to NM_000111.2 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:107431615 G>A maps to NM_000111.2 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr7:107415298 G>A maps to NM_000111.2 R566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr7:107432323 G>A maps to NM_000111.2 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr7:107340577 C>T maps to NM_000441.1 F555F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr7:107314678 C>T maps to NM_000441.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:107323768 C>T maps to NM_000441.1 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr7:107350631 C>T maps to NM_000441.1 S741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:107330681 G>A maps to NM_000441.1 Q421Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr7:103053509 G>A maps to ENST00000354356 Y114Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr7:103050936 G>A maps to ENST00000354356 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:103018140 T>G maps to ENST00000354356 R633R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr7:103029777 G>A maps to ENST00000354356 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr7:103050936 G>A maps to ENST00000354356 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:103029808 G>A maps to ENST00000354356 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:103032169 G>A maps to ENST00000354356 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:103032170 G>A maps to ENST00000354356 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:103061832 C>T maps to ENST00000354356 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr3:48668506 G>A maps to NM_022911.2 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:48669321 G>A maps to NM_022911.2 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:48667390 G>A maps to NM_022911.2 F481F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr3:48669204 G>A maps to NM_022911.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:48669453 G>A maps to NM_022911.2 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:48669453 G>A maps to NM_022911.2 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:48668506 G>A maps to NM_022911.2 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:48663734 G>A maps to NM_022911.2 T727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:48669749 G>A maps to NM_022911.2 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:48667521 G>A maps to NM_022911.2 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr8:92378860 G>A maps to NM_134266.1 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr8:92307924 G>A maps to NM_134266.1 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr8:92365222 G>A maps to NM_134266.1 W438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:92378824 G>A maps to NM_134266.1 V502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr8:92364063 C>T maps to NM_134266.1 F389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:92378857 C>T maps to NM_134266.1 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr8:92364063 C>T maps to NM_134266.1 F389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr8:92364075 C>T maps to NM_134266.1 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:92346638 G>A maps to NM_134266.1 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:92346620 G>A maps to NM_134266.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:92364063 C>T maps to NM_134266.1 F389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:35936668 G>A maps to NM_052961.3 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:35945085 C>T maps to NM_052961.3 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:35960328 C>T maps to NM_052961.3 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:35967772 G>A maps to NM_052961.3 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:35927553 G>A maps to NM_052961.3 F556F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr6:35967835 G>A maps to NM_052961.3 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:35960337 G>A maps to NM_052961.3 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr6:35943220 G>A maps to NM_052961.3 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:35923042 C>T maps to NM_052961.3 R706R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:35949968 G>A maps to NM_052961.3 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr6:35930376 G>A maps to NM_052961.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:205893548 G>A maps to NM_134325.2 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:205904825 G>A maps to NM_134325.2 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:205890813 G>A maps to NM_134325.2 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:205890903 G>A maps to NM_134325.2 T615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:205897029 C>T maps to NM_134325.2 Q367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:205892543 G>A maps to NM_134325.2 I526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:205902148 G>A maps to NM_134325.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:205892483 G>A maps to NM_134325.2 F546F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:205884231 G>A maps to NM_134325.2 L818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:205896724 G>A maps to NM_134325.2 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:205899139 G>A maps to NM_134325.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:205902071 C>T did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:205884130 G>A maps to NM_134325.2 S851S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr19:17597443 C>A maps to NM_198580.1 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:17612166 G>A maps to NM_198580.1 K574K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:17611208 G>A maps to NM_198580.1 Q443Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr15:50519204 C>T maps to NM_003645.3 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr15:50497526 T>G maps to NM_003645.3 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr15:50489847 G>A maps to NM_003645.3 W210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr15:50528280 C>T maps to NM_003645.3 T617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:50489751 C>T maps to NM_003645.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr15:50518183 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr15:50519258 G>A maps to NM_003645.3 K447K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr1:153749198 C>T maps to ENST00000271857 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr1:153748447 G>T maps to ENST00000271857 G287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:153751847 C>T maps to ENST00000271857 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr9:131115731 C>T maps to NM_005094.3 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr9:131105464 G>A maps to NM_005094.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:131118022 C>T maps to NM_005094.3 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:59022256 C>T maps to NM_012254.2 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:59012678 G>A maps to NM_012254.2 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:59012769 G>T maps to NM_012254.2 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:59010863 G>A maps to NM_012254.2 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:59023010 G>A maps to NM_012254.2 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:59010863 G>A maps to NM_012254.2 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:59022195 G>A maps to NM_012254.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:59010863 G>A maps to NM_012254.2 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:59010860 G>A maps to NM_012254.2 F555F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr19:59010863 G>A maps to NM_012254.2 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:59010863 G>A maps to NM_012254.2 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr19:59010863 G>A maps to NM_012254.2 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr5:128302294 C>T maps to NM_001017372.1 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr5:128302183 C>T maps to NM_001017372.1 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:128302183 C>T maps to NM_001017372.1 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:128320886 G>A maps to NM_001017372.1 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr5:128351717 C>T maps to NM_001017372.1 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:128351642 G>A maps to NM_001017372.1 W345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr5:128302183 C>T maps to NM_001017372.1 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:128320886 G>A maps to NM_001017372.1 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:128320901 T>G maps to NM_001017372.1 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr5:128351642 G>A maps to NM_001017372.1 W345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr5:128359347 T>C maps to NM_001017372.1 F400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:128359403 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr5:128302093 G>A maps to NM_001017372.1 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:128324425 G>C maps to NM_001017372.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:128359362 C>A maps to NM_001017372.1 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr5:128320838 G>A maps to NM_001017372.1 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr5:128326112 C>T maps to NM_001017372.1 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:128324335 G>A maps to NM_001017372.1 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:128362841 C>T maps to NM_001017372.1 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr15:85461753 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr15:85487806 C>T maps to NM_004213.3 V558V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr15:85478733 G>A maps to NM_004213.3 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:85461777 C>T maps to NM_004213.3 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr15:85461792 C>T maps to NM_004213.3 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:85438183 C>T maps to NM_004213.3 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:85438351 G>A maps to NM_004213.3 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:85447432 C>T maps to NM_004213.3 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:85478589 G>A maps to NM_004213.3 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr15:85486725 C>T maps to NM_004213.3 F544F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr15:85451965 G>A maps to NM_004213.3 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr15:85478640 C>T maps to NM_004213.3 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr15:85476407 G>A maps to NM_004213.3 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:85438258 C>T maps to NM_004213.3 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:85447411 C>T maps to NM_004213.3 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr15:85433757 C>T maps to NM_004213.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:85461765 C>T maps to NM_004213.3 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr15:85478741 G>A maps to NM_004213.3 W525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr15:45567647 G>A maps to NM_004212.3 K638K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr15:45556888 C>T maps to NM_004212.3 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr15:45555370 G>A maps to NM_004212.3 K125K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr15:45556156 C>T maps to NM_004212.3 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:45554282 C>T maps to NM_004212.3 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr15:45559946 G>A maps to NM_004212.3 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr15:45554215 G>A maps to NM_004212.3 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr15:45554281 C>T maps to NM_004212.3 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr15:45545628 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:45556875 G>A maps to NM_004212.3 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:45561667 C>T maps to NM_004212.3 Q501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr9:86900946 G>A maps to NM_022127.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr9:86920217 C>T maps to NM_022127.2 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:86909136 C>G maps to NM_022127.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:44197192 C>T maps to ENST00000313248 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:44198582 A>G maps to ENST00000313248 E320E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:44199763 C>T maps to ENST00000313248 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr6:44198552 C>T maps to ENST00000313248 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:44198552 C>T maps to ENST00000313248 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:66133651 G>A maps to NM_001532.2 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:66136997 G>A maps to NM_001532.2 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr11:66138780 C>T maps to NM_001532.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:66136561 G>A maps to NM_001532.2 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr10:73121806 C>T maps to NM_018344.5 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:73082807 C>T maps to NM_018344.5 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:73082808 C>T maps to NM_018344.5 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:73121974 C>T maps to NM_018344.5 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr10:73082714 G>A maps to NM_018344.5 W68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr10:73122115 C>T maps to NM_018344.5 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:73104006 C>A maps to NM_018344.5 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:5330755 G>A maps to NM_153247.2 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:5340249 C>T maps to NM_153247.2 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:5338732 C>T maps to NM_153247.2 Q333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr7:5334560 G>A maps to NM_153247.2 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr7:5331405 C>T maps to NM_153247.2 Y166Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr7:5331408 C>T maps to NM_153247.2 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:5340054 C>T maps to NM_153247.2 I404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:43395661 G>A maps to NM_006516.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr1:43396302 G>A maps to NM_006516.2 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:43393332 T>G maps to NM_006516.2 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:43395706 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:43393398 G>A maps to NM_006516.2 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:43396733 G>A maps to NM_006516.2 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr1:43395583 G>A maps to NM_006516.2 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:43394916 G>A maps to NM_006516.2 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr20:45353821 C>T maps to NM_030777.3 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr20:45354694 C>T maps to NM_030777.3 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr20:45354325 C>T maps to NM_030777.3 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr20:45354928 C>T maps to NM_030777.3 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr20:45353908 C>T maps to NM_030777.3 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:45354766 G>A maps to NM_030777.3 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr20:45353821 C>T maps to NM_030777.3 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:45353839 C>T maps to NM_030777.3 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr20:45354226 C>T maps to NM_030777.3 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:45353686 C>T maps to NM_030777.3 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:45354271 C>T maps to NM_030777.3 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr20:45353965 C>T maps to NM_030777.3 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr20:45353696 C>T maps to NM_030777.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:45354340 C>T maps to NM_030777.3 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:45354697 C>T maps to NM_030777.3 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr20:45354397 C>T maps to NM_030777.3 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr20:45354859 C>T maps to NM_030777.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr22:24226867 C>T maps to NM_030807.3 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr22:24219283 C>T maps to NM_030807.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr22:24226882 C>T maps to NM_030807.3 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:24210736 C>T maps to NM_030807.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:24226909 C>T maps to NM_030807.3 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr22:24217411 C>T maps to NM_030807.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr6:134349843 G>T maps to NM_145176.2 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:134349723 G>A maps to NM_145176.2 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr6:134312436 C>T maps to NM_145176.2 V570V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:40345069 A>T maps to NM_052885.3 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:7982502 G>A maps to NM_153449.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:7973828 G>A maps to NM_153449.2 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:7966932 C>T maps to NM_153449.2 K514K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:7966932 C>T maps to NM_153449.2 K514K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr12:7966956 C>T maps to NM_153449.2 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:7981300 C>T maps to NM_153449.2 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:7967019 G>A maps to NM_153449.2 I485I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr12:7984357 G>A maps to NM_153449.2 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr12:7982508 G>A maps to NM_153449.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:7985358 G>A maps to NM_153449.2 Q47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr3:170715715 G>A maps to NM_000340.1 F517F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:170716074 G>A maps to NM_000340.1 F427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr3:170724938 G>A maps to NM_000340.1 Q204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:170716011 G>A maps to NM_000340.1 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:170720367 G>A maps to NM_000340.1 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:8083864 G>A maps to NM_006931.2 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr12:8074053 C>T maps to NM_006931.2 E482E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:8075446 G>A maps to NM_006931.2 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr12:8074017 G>A maps to NM_006931.2 T494T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr17:7189831 C>T maps to NM_001042.2 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:7189139 G>A maps to NM_001042.2 Q413Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr17:7186856 C>T maps to NM_001042.2 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:7186889 C>T maps to NM_001042.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr20:62373357 C>T maps to NM_020062.3 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr20:62374128 C>T maps to NM_020062.3 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr20:62373327 C>T maps to NM_020062.3 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr20:62373916 C>T maps to NM_020062.3 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:9099903 G>A maps to NM_003039.2 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:9100216 G>A maps to NM_003039.2 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:9097824 G>A maps to NM_003039.2 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:9107681 C>T maps to NM_003039.2 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:9101859 G>A maps to NM_003039.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:9100180 G>A maps to NM_003039.2 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:9117526 G>A maps to NM_003039.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:9118219 G>A maps to NM_003039.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr1:9107786 C>T maps to NM_003039.2 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr9:136340103 G>A maps to NM_017585.3 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr9:136337265 G>A maps to NM_017585.3 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:136341395 G>A maps to NM_017585.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:9079266 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:9086356 C>T maps to NM_207420.2 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:9063373 C>T maps to NM_207420.2 K508K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:9063436 C>T maps to NM_207420.2 V487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:9083005 G>A maps to NM_207420.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:9085127 G>A maps to NM_207420.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:9078380 G>A maps to NM_207420.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:9073679 C>T maps to NM_207420.2 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr1:9079292 G>A maps to NM_207420.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:9064903 G>A maps to NM_207420.2 F409F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:9079355 G>A maps to NM_207420.2 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr9:130167831 C>T maps to NM_014580.3 F428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:130162256 C>T maps to NM_014580.3 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:130167265 C>T maps to NM_014580.3 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr9:130167181 C>T maps to NM_014580.3 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr9:130167744 G>A maps to NM_014580.3 E399E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr4:9892266 G>A maps to NM_020041.2 F394F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:9836516 G>A maps to NM_020041.2 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:9828062 G>A maps to NM_020041.2 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:9828092 C>T maps to NM_020041.2 R517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr4:9909969 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr4:9836603 C>T maps to NM_020041.2 E440E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr4:9982235 G>A maps to NM_020041.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr4:9892266 G>A maps to NM_020041.2 F394F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr4:9892284 A>G maps to NM_020041.2 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr4:9943609 C>T maps to NM_020041.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr1:220100430 G>A maps to NM_018713.2 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:220091756 G>A maps to NM_018713.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:220089195 G>A maps to NM_018713.2 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:26365704 C>T maps to NM_001004434.1 E355E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr2:27480114 C>T maps to NM_003459.4 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr2:27481678 C>T maps to NM_003459.4 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:27481639 G>A maps to NM_003459.4 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:27481726 C>T maps to NM_003459.4 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr2:27481642 G>A maps to NM_003459.4 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr15:45782996 G>A maps to NM_013309.4 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:68412344 C>T maps to NM_022902.2 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr5:68412401 G>A maps to NM_022902.2 Q418Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr2:32445305 C>T maps to NM_001193513.1 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr8:118170029 C>T maps to NM_173851.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:118159240 G>A maps to NM_173851.2 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:118170030 C>T maps to NM_173851.2 Q174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:118169948 C>T maps to NM_173851.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:118159387 C>T maps to NM_173851.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr8:118159336 G>A maps to NM_173851.2 W72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr8:118170029 C>T maps to NM_173851.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:118184904 A>G maps to NM_173851.2 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:118174003 C>T maps to NM_173851.2 C200C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:118183309 G>A maps to NM_173851.2 E289E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr8:118159207 G>A maps to NM_173851.2 Q29Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr8:118159342 C>T maps to NM_173851.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:118184919 G>A maps to NM_173851.2 *370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr8:118184838 G>A maps to NM_173851.2 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:118147625 C>T maps to NM_173851.2 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr4:42077754 T>G maps to NM_006345.3 V500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:42041010 C>T maps to NM_006345.3 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:42037346 C>T maps to NM_006345.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr20:37356405 G>A maps to NM_080552.2 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr20:37356630 C>T maps to NM_080552.2 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr20:37353723 G>A maps to NM_080552.2 W119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr20:37357062 C>T maps to NM_080552.2 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:37356288 C>T maps to NM_080552.2 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:37356728 G>A maps to NM_080552.2 W342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr20:37357135 C>T maps to NM_080552.2 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr3:155551304 G>A maps to NM_004733.3 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr3:155571018 A>T maps to NM_004733.3 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr3:155560231 G>A maps to NM_004733.3 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr3:155571627 C>T maps to NM_004733.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:155547506 G>A maps to NM_004733.3 N484N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:155560403 G>A maps to NM_004733.3 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr5:176813003 G>A maps to NM_003052.4 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:176823737 C>T maps to NM_003052.4 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:176823737 C>T maps to NM_003052.4 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr5:176821167 C>T maps to NM_003052.4 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:176812795 C>T maps to NM_003052.4 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr5:176820744 A>T maps to NM_003052.4 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:176812783 C>T maps to NM_003052.4 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:176813027 C>T maps to NM_003052.4 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:176820705 C>T maps to NM_003052.4 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:176824005 C>T maps to NM_003052.4 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr4:25673284 G>A maps to NM_006424.2 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr4:25673302 G>A maps to NM_006424.2 W336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr4:25674844 C>T maps to NM_006424.2 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr4:25675921 C>T maps to NM_006424.2 F407F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr4:25676181 C>T maps to NM_006424.2 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr4:25678061 G>A maps to NM_006424.2 Q588Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr4:25677758 C>T maps to NM_006424.2 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:25677758 C>T maps to NM_006424.2 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr4:25674772 C>T maps to NM_006424.2 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr4:25669532 C>T maps to NM_006424.2 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:25667804 G>A maps to NM_006424.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr4:25678049 G>A maps to NM_006424.2 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:25675987 C>T maps to NM_006424.2 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr4:25673326 G>A maps to NM_006424.2 K344K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:25678097 G>A maps to NM_006424.2 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr4:25678073 C>T maps to NM_006424.2 F592F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr4:25677917 C>T maps to NM_006424.2 I540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr9:140126204 G>A maps to NM_080877.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:140126548 G>A maps to NM_080877.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr23:48763719 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr23:48762210 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:112299692 T>C maps to NM_017945.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:8419893 G>A maps to NM_001142540.1 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:8417173 C>A maps to NM_001142540.1 G310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:8422705 G>A maps to NM_001142540.1 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr7:133979701 G>A maps to NM_032826.4 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr7:133981162 G>A maps to NM_032826.4 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr7:133986831 G>A maps to NM_032826.4 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr11:45832349 C>T maps to NM_018389.4 Q187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:45832765 G>A maps to NM_018389.4 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr20:44987130 G>A maps to NM_173179.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr20:44980725 G>A maps to NM_173179.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr20:44979442 C>A maps to NM_173179.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:44983826 G>A maps to NM_173179.2 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr20:44986400 G>A maps to NM_173179.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr9:99084311 G>A maps to NM_007001.2 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:99126775 G>A maps to NM_007001.2 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:137245230 C>T maps to NM_001008783.1 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr6:137245644 C>G maps to NM_001008783.1 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:16666130 G>A maps to NM_024881.4 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr1:1670359 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:1670427 G>A maps to NM_182838.2 Q131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:69140393 C>T maps to NM_018656.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:69145888 C>T maps to NM_018656.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr22:31042756 G>A maps to NM_001001479.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:31042954 C>T maps to NM_001001479.2 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr6:118556685 C>T maps to NM_001029858.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:118588246 C>T maps to NM_001029858.3 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr6:118475629 C>T maps to NM_001029858.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:118588183 C>T maps to NM_001029858.3 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr6:118588216 C>T maps to NM_001029858.3 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:118588246 C>T maps to NM_001029858.3 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr6:118598701 G>A maps to NM_001029858.3 W280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:107677458 C>T maps to NM_017515.4 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:107673740 G>A maps to NM_017515.4 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:107686521 G>A maps to NM_017515.4 R94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr1:234041334 C>T maps to NM_173508.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr1:234367361 G>A maps to NM_173508.2 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:234445035 C>T maps to NM_173508.2 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:234041367 G>A maps to NM_173508.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:234367361 G>A maps to NM_173508.2 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr1:234452463 C>T maps to NM_173508.2 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:234367229 C>A maps to NM_173508.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:234367367 C>T maps to NM_173508.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:234454585 C>T maps to NM_173508.2 I348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:234367361 G>A maps to NM_173508.2 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:234458821 C>T maps to NM_173508.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr1:234041331 G>A maps to NM_173508.2 Q37Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:234458811 C>T maps to NM_173508.2 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr1:234452364 C>T maps to NM_173508.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:234040832 C>T maps to NM_173508.2 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:234367232 G>A maps to NM_173508.2 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:234452364 C>T maps to NM_173508.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:234445035 C>T maps to NM_173508.2 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr1:234452367 C>T maps to NM_173508.2 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:234452442 G>A maps to NM_173508.2 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:234444845 G>A did not map to a codon.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:234444846 G>A maps to NM_173508.2 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr14:58063570 C>T maps to NM_001080455.1 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr14:58031068 C>A maps to NM_001080455.1 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr14:58047964 C>T maps to NM_001080455.1 W294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr14:58048033 C>T maps to NM_001080455.1 K271K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:58056037 G>A maps to NM_001080455.1 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr14:58060759 G>A maps to NM_001080455.1 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr14:58030954 C>T maps to NM_001080455.1 K488K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:58036611 G>A maps to NM_001080455.1 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:58055935 G>A maps to NM_001080455.1 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:58055998 G>A maps to NM_001080455.1 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr2:114501362 A>G maps to NM_025181.2 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr2:114486998 A>G maps to NM_025181.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:114483037 G>A maps to NM_025181.2 F389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr5:150838400 C>T maps to NM_078483.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:150867586 C>T maps to NM_078483.2 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:150867571 G>A maps to NM_078483.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:150856303 C>T maps to NM_078483.2 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr5:150858925 C>T maps to NM_078483.2 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr5:150722468 C>T maps to NM_181776.2 Q140Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:150718686 G>A maps to NM_181776.2 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr5:150704866 G>A maps to NM_181776.2 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr5:150696554 G>A maps to NM_181776.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr5:150718686 G>A maps to NM_181776.2 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:150696593 G>A maps to NM_181776.2 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr5:150714949 G>A maps to NM_181776.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr5:150726973 G>A maps to NM_181776.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:150712865 G>A maps to NM_181776.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:150696647 G>A maps to NM_181776.2 C394C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:150715009 G>A maps to NM_181776.2 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:150714976 C>T maps to NM_181776.2 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:150722483 G>A maps to NM_181776.2 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr5:150657222 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr5:150660742 A>G maps to NM_001145017.1 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr5:150672983 C>T maps to NM_001145017.1 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr5:150663627 G>A maps to NM_001145017.1 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr11:92881927 G>A maps to NM_152313.2 I430I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:92895882 G>C maps to NM_152313.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:92881963 G>A maps to NM_152313.2 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:92881866 G>A maps to NM_152313.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:92881867 G>A maps to NM_152313.2 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr21:44000467 T>G maps to NM_018964.3 *534G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:43982258 C>T maps to NM_018964.3 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr21:43988540 C>T maps to NM_018964.3 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr11:124947391 C>T maps to NM_198277.2 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr7:140045770 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:140051895 G>A maps to NM_207113.1 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr12:46591541 G>A maps to NM_030674.3 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:46591571 G>A maps to NM_030674.3 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr12:46598181 G>A maps to NM_030674.3 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr12:46623370 C>T maps to NM_030674.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr12:46591541 G>A maps to NM_030674.3 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:46601384 C>T maps to NM_030674.3 K136K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:46601354 C>T maps to NM_030674.3 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr12:46601348 G>A maps to NM_030674.3 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:46598323 G>A maps to NM_030674.3 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr12:46601348 G>A maps to NM_030674.3 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr12:46601354 C>T maps to NM_030674.3 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:46601348 G>A maps to NM_030674.3 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:46592407 C>T maps to NM_030674.3 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:46598181 G>A maps to NM_030674.3 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:46598344 G>A maps to NM_030674.3 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:46598181 G>A maps to NM_030674.3 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:46591501 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:46622946 G>A maps to NM_030674.3 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr12:46591600 C>T did not map to a codon.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr12:46623361 C>T maps to NM_030674.3 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr17:79226001 G>A maps to NM_001037984.1 S646S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr17:79249885 G>A maps to NM_001037984.1 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:79226132 G>A maps to NM_001037984.1 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr17:79226241 G>A maps to NM_001037984.1 A566A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:79256042 G>A maps to NM_001037984.1 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:79226966 C>A maps to NM_001037984.1 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:79225239 G>A maps to NM_138570.2 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:165802237 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:165802229 G>A maps to ENST00000409662 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr3:50255383 C>T maps to NM_006841.4 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:50256358 C>T maps to NM_006841.4 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:50254687 G>A maps to NM_006841.4 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:50255383 C>T maps to NM_006841.4 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr3:50256136 C>T maps to NM_006841.4 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:50252886 C>T maps to NM_006841.4 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:50253063 C>T maps to NM_006841.4 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr3:50256023 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr12:47178370 C>T maps to NM_018018.4 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:47173645 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:47181745 G>A maps to NM_018018.4 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:47181748 C>T maps to NM_018018.4 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:47162188 C>T maps to NM_018018.4 G482G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr12:47168900 G>A maps to NM_018018.4 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:48321363 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:48325380 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:48320619 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:48325350 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:48318135 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:48325461 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:48320626 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:48320627 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr14:61512122 C>T maps to NM_001172702.1 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr14:61497232 C>T maps to NM_001172702.1 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr16:58712282 G>A maps to NM_018231.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:58701363 G>A maps to NM_018231.1 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr16:84050127 G>A maps to NM_001080442.1 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr16:84075654 G>C maps to NM_001080442.1 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:84050229 G>A maps to NM_001080442.1 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr16:84070349 G>A maps to NM_001080442.1 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:84070370 G>A maps to NM_001080442.1 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr16:84050752 G>A maps to NM_001080442.1 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:84050172 G>A maps to NM_001080442.1 I371I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:84063100 G>A maps to NM_001080442.1 Q230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:84050172 G>A maps to NM_001080442.1 I371I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:84075594 G>A maps to NM_001080442.1 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr16:84050752 G>A maps to NM_001080442.1 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:54923756 G>A maps to NM_173514.2 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:54922344 G>A maps to NM_173514.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:153932927 G>A maps to NM_014437.3 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:153932813 G>A maps to NM_014437.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr2:196571436 C>T maps to NM_001127257.1 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:196544999 C>T maps to NM_001127257.1 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:196548521 C>T maps to NM_001127257.1 Q370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:196545681 C>T maps to NM_001127257.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:196571355 C>T maps to NM_001127257.1 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:196581389 C>T maps to NM_001127257.1 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr2:196592923 C>T maps to NM_001127257.1 Q730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:196599728 C>T maps to NM_001127257.1 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:71080985 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:70845856 G>A maps to NM_001159770.1 R180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:70845916 G>A maps to NM_001159770.1 Q160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr17:70644967 G>A maps to NM_001159770.1 D308D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr17:70644979 G>A maps to NM_001159770.1 Y304Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr10:18242234 C>T maps to NM_001145195.1 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:18270266 G>A maps to NM_001145195.1 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:18250703 G>A maps to NM_001145195.1 Q152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:18270239 G>A did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr10:18266934 C>T maps to NM_001145195.1 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr10:18276510 C>T maps to NM_001145195.1 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:18266906 G>A maps to NM_001145195.1 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:47436452 G>A maps to NM_001128225.2 K304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr11:47431914 C>T maps to NM_001128225.2 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr11:47431915 C>T maps to NM_001128225.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr8:22267570 C>T maps to NM_015359.4 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr8:22265864 G>T maps to NM_001135153.1 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:22275266 C>T maps to NM_001135153.1 I417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr14:21469566 G>A maps to NM_014579.3 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:2733090 G>A maps to NM_144564.4 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:145640662 G>A maps to NM_130849.2 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:145641265 C>T maps to NM_130849.2 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:145641388 G>A maps to NM_130849.2 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:145642041 C>T maps to NM_130849.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr8:145638190 G>A maps to NM_130849.2 I589I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr8:145638193 C>T maps to NM_130849.2 W588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr12:56630754 C>T maps to NM_001135195.1 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:56626550 G>A maps to NM_001135195.1 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr12:56625336 C>T maps to NM_001135195.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr12:56626589 G>A maps to NM_001135195.1 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr12:56629016 G>A maps to NM_001135195.1 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:56625138 C>T maps to NM_001135195.1 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr6:33169318 G>A maps to NM_006979.2 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr4:103188709 G>A maps to NM_001135146.1 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr4:103225506 G>A maps to NM_001135146.1 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:103189131 A>G maps to NM_001135146.1 N315N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:103228745 G>A maps to NM_001135146.1 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:103236960 G>A maps to NM_001135146.1 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:103188657 G>A maps to NM_001135146.1 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr2:44507906 G>A maps to NM_000341.3 W161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:44508526 T>C maps to NM_000341.3 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:44540972 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:44547675 G>A maps to NM_000341.3 T652T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:44508547 C>T maps to NM_000341.3 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr2:190439983 G>A maps to NM_014585.5 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:190430206 C>T maps to NM_014585.5 W211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:190428763 G>A maps to NM_014585.5 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr2:190444571 G>A maps to NM_014585.5 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:205764126 G>A maps to NM_173854.4 A409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr1:205779248 G>A maps to NM_173854.4 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:205764126 G>A maps to NM_173854.4 A409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:205760768 G>A maps to NM_173854.4 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:105280194 G>A maps to NM_032148.3 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:105282951 G>A maps to NM_032148.3 Q247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr12:105282899 C>T maps to NM_032148.3 W264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr12:105238261 G>A maps to NM_032148.3 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr3:125741704 G>A maps to NM_001008485.1 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr3:125752455 G>A maps to NM_001008485.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr3:125786894 C>T maps to NM_001008485.1 E56E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr3:125725966 C>T maps to NM_001008485.1 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:57256810 G>A maps to NM_003627.5 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr11:57254630 G>A maps to NM_003627.5 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:57256423 G>A maps to NM_003627.5 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:57268308 G>A maps to NM_003627.5 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr17:1494707 G>A maps to ENST00000382147 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:1478903 G>A maps to ENST00000382147 F572F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:1478957 C>T maps to ENST00000382147 Q554Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:57182184 G>A maps to ENST00000428603 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr9:108097937 C>T maps to NM_080546.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:108127886 C>T maps to NM_080546.3 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:10747057 C>T maps to NM_020428.3 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:10741780 C>T maps to NM_020428.3 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr19:10748930 C>T maps to NM_020428.3 H623H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:10747039 C>T maps to NM_020428.3 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr19:10738466 C>T maps to NM_020428.3 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr19:10748389 C>T maps to NM_020428.3 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:10742305 C>T maps to NM_020428.3 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:10747051 C>T maps to NM_020428.3 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:10747243 C>T maps to NM_020428.3 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr19:10738632 C>T maps to NM_020428.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr1:95310895 C>T maps to NM_001114106.1 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:95290161 T>C maps to NM_001114106.1 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:95290158 C>T maps to NM_001114106.1 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:31831495 G>A maps to NM_025257.2 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:31831496 G>A maps to NM_025257.2 S680S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:31838769 C>T maps to NM_025257.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:31833141 G>A maps to NM_025257.2 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr6:31839333 C>T maps to NM_025257.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr1:75707689 T>C maps to NM_152697.4 K176K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:75684293 G>A maps to NM_152697.4 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr1:75685025 G>A maps to NM_152697.4 F394F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:75685495 G>A maps to NM_152697.4 V389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:75672357 G>A maps to NM_152697.4 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:75766336 G>A maps to NM_152697.4 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:75672357 G>A maps to NM_152697.4 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:75677162 G>A maps to NM_152697.4 F679F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:75679470 C>G maps to NM_152697.4 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr1:75684344 G>A maps to NM_152697.4 I453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:75707704 C>T maps to NM_152697.4 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:75716950 G>A maps to NM_152697.4 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr1:75707704 C>T maps to NM_152697.4 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:75684293 G>A maps to NM_152697.4 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr1:75707704 C>T maps to NM_152697.4 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:75684322 A>G maps to NM_152697.4 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr1:75707704 C>T maps to NM_152697.4 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr1:75672357 G>A maps to NM_152697.4 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:75672357 G>A maps to NM_152697.4 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:75684293 G>A maps to NM_152697.4 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:75679467 G>A maps to NM_152697.4 A628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr1:75699689 C>T maps to NM_152697.4 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:8384475 G>A maps to ENST00000377479 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr1:8397903 C>T maps to ENST00000377479 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:8384544 G>A maps to ENST00000377479 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:8399556 C>T maps to ENST00000377479 I627I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr1:8390335 C>T maps to ENST00000377479 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr1:8390929 C>T maps to ENST00000377479 I493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:8390872 G>A maps to ENST00000377479 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:8390416 C>T maps to ENST00000377479 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:8390855 C>T maps to ENST00000377479 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr1:8395588 C>T maps to ENST00000377479 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:8390351 C>T maps to ENST00000377479 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:33964038 G>A maps to NM_016180.3 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q1-06A-21D-A196-08 chr1:205632105 C>G maps to NM_033102.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:205628559 G>A maps to NM_033102.2 I488I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:205631985 G>A maps to NM_033102.2 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr1:205628502 G>A maps to NM_033102.2 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr1:205632161 G>A maps to NM_033102.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:142222400 G>A maps to NM_001080431.1 S681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr8:142229075 G>A maps to NM_001080431.1 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr8:142229072 G>A maps to NM_001080431.1 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:142226066 G>A maps to NM_001080431.1 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:142228571 G>A maps to NM_001080431.1 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:142227243 G>A maps to NM_001080431.1 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:142227280 G>T maps to NM_001080431.1 S495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:142228772 G>T maps to NM_001080431.1 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:142228238 G>A maps to NM_001080431.1 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr8:142222445 G>A maps to NM_001080431.1 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:142231751 G>A maps to NM_001080431.1 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr8:142221564 C>T maps to NM_001080431.1 P791P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr8:142222459 G>A maps to NM_001080431.1 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr8:142222460 G>A maps to NM_001080431.1 F661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:142228517 G>A maps to NM_001080431.1 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:142231802 G>A maps to NM_001080431.1 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:142228672 G>A maps to NM_001080431.1 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:142231685 G>A maps to NM_001080431.1 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:142228853 C>T maps to NM_001080431.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr17:26726680 C>T maps to ENST00000440501 Q457Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:26732174 C>T maps to ENST00000440501 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:115652847 C>T maps to NM_033051.3 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr9:115652280 T>C maps to NM_033051.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr13:29287433 C>T maps to NM_001135919.1 W148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr13:29287570 G>A maps to NM_001135919.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:29287570 G>A maps to NM_001135919.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:29287357 G>A maps to NM_001135919.1 D173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr13:29278210 G>A maps to NM_001135919.1 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr17:19445734 C>T maps to ENST00000395585 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr17:19458544 C>T maps to ENST00000395585 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:19459314 C>T maps to ENST00000395585 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:19451410 C>T maps to ENST00000395585 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:19451382 G>A maps to ENST00000395585 W131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:19470506 C>T maps to ENST00000395585 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:19480769 G>A maps to ENST00000395585 R539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr17:19458974 G>A maps to ENST00000395585 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:19480670 G>A maps to ENST00000395585 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr17:19470491 C>T maps to ENST00000395585 G420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:19612070 C>T maps to NM_152908.3 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr17:19617250 C>T maps to NM_152908.3 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr17:42336710 G>A maps to NM_000342.3 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr17:42335161 C>T maps to NM_000342.3 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr17:42338084 C>T maps to NM_000342.3 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr17:42335104 G>A maps to NM_000342.3 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:42340063 G>A maps to NM_000342.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr17:42330612 G>A maps to NM_000342.3 T728T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:42333049 G>A maps to NM_000342.3 F597F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:42335537 C>T maps to NM_000342.3 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr17:42334864 G>A maps to NM_000342.3 I493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr17:42335498 G>A maps to NM_000342.3 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:42335104 G>A maps to NM_000342.3 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr17:42327840 C>G maps to NM_000342.3 V907V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr17:42338144 C>T maps to NM_000342.3 K69K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:42333049 G>A maps to NM_000342.3 F597F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:42335104 G>A maps to NM_000342.3 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:42337854 T>C maps to NM_000342.3 Q134Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr2:162834229 A>G did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:162820766 C>T maps to NM_001178015.1 G995G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr2:162627541 C>T maps to NM_001178015.1 H36H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr2:162730516 T>C did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:162661049 G>A maps to NM_001178015.1 K74K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:162719393 T>A maps to NM_001178015.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr2:162761338 C>T maps to NM_001178015.1 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr2:162761302 C>T maps to NM_001178015.1 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:162821559 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:162711575 A>G maps to NM_001178015.1 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:162719558 C>T maps to NM_001178015.1 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:162804209 C>T maps to NM_001178015.1 F746F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr2:162815019 T>G maps to NM_001178015.1 Y939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr2:162760522 G>A maps to NM_001178015.1 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:162696314 G>A maps to NM_001178015.1 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr20:3210285 G>A maps to NM_001174090.1 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr20:3208912 G>A maps to NM_001174090.1 I893I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:3214628 G>A maps to NM_001174090.1 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr20:3210285 G>A maps to NM_001174090.1 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr20:3214774 G>A maps to NM_001174090.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr20:3214213 C>A maps to NM_001174090.1 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:3209757 C>T maps to NM_001174090.1 V710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr20:3215508 G>A maps to NM_001174090.1 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:3210415 C>T maps to NM_001174090.1 W542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:3211822 G>A maps to NM_001174090.1 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr20:3211615 G>A maps to NM_001174090.1 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr20:3211213 G>A maps to NM_001174090.1 F497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr20:3215454 G>A maps to NM_001174090.1 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:27907939 C>T maps to NM_018158.2 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:150761398 C>T maps to NM_003040.3 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:150761398 C>T maps to NM_003040.3 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:150771340 C>T maps to NM_003040.3 F917F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:150773191 C>T maps to NM_003040.3 A1188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:150771817 C>T maps to NM_003040.3 V979V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr7:150771142 C>T maps to NM_003040.3 P851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr7:150761826 C>T maps to NM_003040.3 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr7:150769180 C>T maps to NM_003040.3 I831I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150768842 C>T maps to NM_003040.3 V753V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr2:220502343 G>A maps to NM_201574.2 E886E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:220505161 C>T maps to NM_201574.2 I1123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:220505216 C>T maps to NM_201574.2 L1142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:220502520 C>T maps to NM_201574.2 F945F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:220502521 C>T maps to NM_201574.2 L946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:220496988 C>T maps to NM_201574.2 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:220502337 C>T maps to NM_201574.2 P884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:220504209 C>T maps to NM_201574.2 I1037I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:220504251 C>T maps to NM_201574.2 F1051F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:220501403 C>T maps to NM_201574.2 F808F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr2:220504245 C>T maps to NM_201574.2 S1049S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:220500129 C>T maps to NM_201574.2 F655F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:220505161 C>T maps to NM_201574.2 I1123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr2:220500081 C>T maps to NM_201574.2 P639P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:220494143 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:220494886 C>T maps to NM_201574.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:220496783 C>T maps to NM_201574.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:220500078 C>T maps to NM_201574.2 I638I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:220501063 C>T maps to NM_201574.2 I771I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:220497035 G>A maps to NM_201574.2 W365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr4:72423452 C>T maps to NM_001098484.2 L930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:72397810 C>T maps to NM_001098484.2 I733I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:72222737 C>T maps to NM_001098484.2 D188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr4:72306346 C>T maps to NM_001098484.2 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:72120973 G>A maps to NM_001098484.2 K37K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:72399969 C>T maps to NM_001098484.2 F769F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr4:72263330 C>T maps to NM_001098484.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:74477520 G>A maps to NM_021196.3 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:74460588 C>T maps to NM_021196.3 L845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:74462302 G>A maps to NM_021196.3 S786S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:74477559 G>A maps to NM_021196.3 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr2:74460549 G>A maps to NM_021196.3 N858N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr2:74491355 G>A maps to NM_021196.3 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:74474337 G>A maps to NM_021196.3 I628I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:74492234 G>A maps to NM_021196.3 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:74480219 C>T maps to NM_021196.3 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:74492336 G>A maps to NM_021196.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:74475490 G>A maps to NM_021196.3 F592F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:74460663 G>A maps to NM_021196.3 F820F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:74480228 G>A maps to NM_021196.3 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:74489342 C>T maps to NM_021196.3 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr3:27427484 G>A maps to ENST00000454389 L1130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr3:27490214 T>C maps to ENST00000454389 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr3:27436501 G>A maps to ENST00000454389 I936I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr12:51864225 C>T maps to NM_001039960.1 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:51851148 C>T maps to NM_001039960.1 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr12:51882613 C>T maps to NM_001039960.1 V806V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:51888892 C>T maps to NM_001039960.1 F978F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr12:51888781 C>T maps to NM_001039960.1 F941F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:51863538 G>A maps to NM_001039960.1 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr12:51853748 C>T maps to NM_001039960.1 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:51883545 C>T maps to NM_001039960.1 I837I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr12:51888838 G>A maps to NM_001039960.1 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:51887519 C>T maps to NM_001039960.1 F911F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr12:51868968 G>A maps to NM_001039960.1 T717T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr12:51888847 C>T maps to NM_001039960.1 L963L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:51852421 G>A maps to NM_001039960.1 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:51863538 G>A maps to NM_001039960.1 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:51864297 C>T maps to NM_001039960.1 F549F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:51853829 C>T maps to NM_001039960.1 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr5:139741432 C>T maps to ENST00000507527 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:139740440 G>A maps to ENST00000507527 W116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:139751115 C>T maps to ENST00000507527 T883T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:139747450 C>T maps to ENST00000507527 A798A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:139748219 C>T maps to ENST00000507527 S825S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr5:139739895 G>A maps to ENST00000507527 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr5:139743727 G>A maps to ENST00000507527 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr22:32480930 G>A maps to NM_000343.3 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:32495187 G>A maps to NM_000343.3 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr22:32495247 C>T maps to NM_000343.3 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:32506126 G>A maps to NM_000343.3 W641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr22:32479097 G>A maps to NM_000343.3 Q207Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr22:32463991 C>T maps to NM_000343.3 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr22:32445928 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:32445997 G>A maps to NM_000343.3 W68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:32500793 C>T maps to NM_000343.3 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:18923081 G>A maps to NM_152351.3 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr17:18874356 G>A maps to NM_152351.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr17:18923668 C>T maps to NM_152351.3 F588F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr17:18862035 C>T maps to NM_152351.3 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:18923088 C>T maps to NM_152351.3 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr17:18923162 C>T maps to NM_152351.3 F532F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:18863934 C>T maps to NM_152351.3 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:24920275 G>A maps to NM_052944.2 Q503Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:24873929 G>A maps to NM_052944.2 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:24909296 G>A maps to NM_052944.2 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:24909425 C>T maps to NM_052944.2 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:24881265 C>T maps to NM_052944.2 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:24918041 G>A maps to NM_052944.2 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:24918475 G>A maps to NM_052944.2 K415K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr11:26714111 C>T maps to NM_178498.3 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:26708085 A>G maps to NM_178498.3 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr11:26720048 G>A maps to NM_178498.3 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr11:26714048 G>A maps to NM_178498.3 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr11:26742961 G>A maps to NM_178498.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr11:26743063 C>T maps to NM_178498.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:26694999 C>T maps to NM_178498.3 K552K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:26695002 C>T maps to NM_178498.3 K551K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:26718781 G>A maps to NM_178498.3 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:26725471 C>T maps to NM_178498.3 W183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:26743006 G>A maps to NM_178498.3 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:26743048 A>G maps to NM_178498.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:26743204 G>A maps to NM_178498.3 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr16:31498707 C>T maps to ENST00000431354 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr16:31500278 C>T maps to ENST00000431354 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr16:31501462 G>A maps to ENST00000431354 E568E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr16:31497117 G>A maps to ENST00000431354 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr16:31497552 C>T maps to ENST00000431354 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr16:31501825 G>A maps to ENST00000431354 V689V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:31498896 G>A maps to ENST00000431354 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr16:31500245 C>G maps to ENST00000431354 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:31497189 C>T maps to ENST00000431354 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:31498854 C>T maps to ENST00000431354 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr16:31497516 C>T maps to ENST00000431354 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr16:31497531 G>A maps to ENST00000431354 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr21:35467790 C>T maps to NM_006933.4 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr21:35468783 C>T maps to NM_006933.4 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:35469467 C>T maps to NM_006933.4 F657F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr21:35468342 C>T maps to NM_006933.4 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr22:32630982 A>G maps to NM_014227.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr22:32631045 G>A maps to NM_014227.2 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr22:32631036 G>A maps to NM_014227.2 Y236Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr22:32626958 G>A maps to NM_014227.2 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr22:32635078 T>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr22:32647780 G>A maps to NM_014227.2 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:32650158 G>A maps to NM_014227.2 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr19:17985482 G>A maps to NM_000453.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:17992852 G>A maps to NM_000453.2 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:18004595 C>T maps to NM_000453.2 F614F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:18004595 C>T maps to NM_000453.2 F614F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:17988808 C>T maps to NM_000453.2 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:18004535 C>T maps to NM_000453.2 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr19:17994488 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:18001773 G>A maps to NM_000453.2 K577K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr19:17985011 G>A maps to NM_000453.2 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:17986819 C>T maps to NM_000453.2 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:18004538 C>T maps to NM_000453.2 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:18004607 G>A maps to NM_000453.2 K618K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:27425704 G>A maps to NM_021095.2 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr2:27427418 G>A maps to NM_021095.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr2:27427330 G>A maps to NM_021095.2 Q335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:27425701 G>A maps to NM_021095.2 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:27430262 G>A maps to NM_021095.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:27427750 G>A maps to NM_021095.2 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr2:27427750 G>A maps to NM_021095.2 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:27423916 G>A maps to NM_021095.2 S571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:27427439 G>A maps to NM_021095.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr2:27427783 G>A maps to NM_021095.2 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr2:108626770 G>A maps to NM_021815.2 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr2:108608586 C>T maps to NM_021815.2 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr2:108609494 A>G maps to NM_021815.2 Q120Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr2:108624963 A>G maps to NM_021815.2 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:108627289 G>A maps to NM_021815.2 G572G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:108618399 C>T maps to NM_021815.2 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:108626827 C>T maps to NM_021815.2 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr2:108626959 C>T maps to NM_021815.2 Y462Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:108626704 C>T maps to NM_021815.2 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr2:108626905 C>T maps to NM_021815.2 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:108622611 G>A maps to NM_021815.2 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr2:108609539 G>A maps to NM_021815.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr2:108604736 C>T maps to NM_021815.2 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:101581229 G>A maps to NM_145913.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:101603314 G>A maps to NM_145913.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:101581280 G>A maps to NM_145913.3 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:101588902 C>T maps to NM_145913.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr12:101560290 G>A maps to NM_145913.3 Q503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr12:101581217 G>A maps to NM_145913.3 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:101603326 C>T maps to NM_145913.3 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:101584310 G>A maps to NM_145913.3 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:101587404 C>T maps to NM_145913.3 W230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr12:101560290 G>A maps to NM_145913.3 Q503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr12:101555773 C>T maps to NM_145913.3 G536G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:101551176 C>T maps to NM_145913.3 K571K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:101587520 G>A maps to NM_145913.3 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr1:48699390 C>T maps to NM_001135181.1 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:48694827 G>A maps to NM_001135181.1 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:48708152 C>A maps to NM_001135181.1 R593R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:48688461 G>A maps to NM_001135181.1 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:48688548 C>T maps to NM_001135181.1 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:48701515 G>A maps to NM_001135181.1 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:48690436 C>T maps to NM_001135181.1 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:48695052 G>A maps to NM_001135181.1 K167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:48699372 G>A maps to NM_001135181.1 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:48713042 G>A maps to NM_001135181.1 W650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr3:11078615 G>A maps to NM_003042.3 Q588Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr3:11078618 G>A maps to NM_003042.3 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:11059121 G>A maps to NM_003042.3 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:11064034 C>T maps to NM_003042.3 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:11067166 C>T maps to NM_003042.3 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:11059100 G>A maps to NM_003042.3 W68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:11067520 C>T maps to NM_003042.3 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr3:11061951 C>T maps to NM_003042.3 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr3:11067562 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr3:11059583 C>T maps to NM_003042.3 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:11059121 G>A maps to NM_003042.3 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr3:11059589 G>A maps to NM_003042.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:11068022 C>T maps to NM_003042.3 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:11067520 C>T maps to NM_003042.3 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:11059541 C>T maps to NM_003042.3 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:11059583 C>T maps to NM_003042.3 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:11060363 C>T maps to NM_003042.3 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:11067175 C>T maps to NM_003042.3 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:11067974 C>T maps to NM_003042.3 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:11078582 C>T maps to NM_003042.3 I577I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:11059100 G>A maps to NM_003042.3 W68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr3:10865068 G>A maps to NM_014229.1 E205E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr3:10916677 C>T maps to NM_014229.1 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr3:10971012 G>A maps to NM_014229.1 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:10970961 G>A maps to NM_014229.1 R436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:10980003 G>A maps to NM_014229.1 R605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:10865056 C>T maps to NM_014229.1 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:10861487 C>T maps to NM_014229.1 C161C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr3:10980039 G>A maps to NM_014229.1 K617K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr3:10967783 C>T maps to NM_014229.1 F405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr3:10861261 G>A maps to NM_014229.1 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:10885925 G>A maps to NM_014229.1 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:10916767 C>T maps to NM_014229.1 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:10974874 C>T maps to NM_014229.1 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr3:10975830 C>T maps to NM_014229.1 I518I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr12:307163 C>T maps to NM_003044.3 W284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr12:306645 G>A maps to NM_003044.3 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr12:305953 G>A maps to NM_003044.3 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:305415 C>T maps to NM_003044.3 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:301743 C>T maps to NM_003044.3 W534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr12:305971 G>A maps to NM_003044.3 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr12:304398 C>T maps to NM_003044.3 W474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr12:313841 G>A maps to NM_003044.3 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr12:369077 C>T maps to NM_016615.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr12:333659 G>A maps to NM_016615.3 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:344276 G>A maps to NM_016615.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr12:344335 G>A maps to NM_016615.3 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr12:352843 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr12:344335 G>A maps to NM_016615.3 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:351819 G>A maps to NM_016615.3 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr12:352916 C>A maps to NM_016615.3 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:335679 C>T maps to NM_016615.3 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:336798 G>A maps to NM_016615.3 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr12:335559 C>T maps to NM_016615.3 E352E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:333187 G>A maps to NM_016615.3 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:333250 G>A maps to NM_016615.3 Y406Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:333602 G>A maps to NM_016615.3 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:336756 G>C maps to NM_016615.3 Y303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:352968 G>A maps to NM_016615.3 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:346428 C>T maps to NM_016615.3 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr12:344273 C>T maps to NM_016615.3 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:352956 G>A maps to NM_016615.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:115586160 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr23:115577961 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:115582804 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:115582805 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:115584238 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:115590031 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:115590036 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr23:115574865 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr23:115586624 T>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:115588791 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:115590031 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:115588828 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:115586146 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:115585493 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:115590107 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr23:115590070 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr23:115568958 A>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:115584227 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:115573980 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:115574930 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:115573854 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:115576207 C>T did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:115569004 G>A did not map to a codon.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr23:115576097 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:115589993 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr12:85264377 G>A maps to NM_182767.4 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:49793484 G>A maps to NM_014037.2 S702S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:49812644 G>A maps to NM_014037.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:49797752 C>T maps to NM_014037.2 K429K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:49796616 G>A maps to NM_014037.2 F547F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr19:49797111 G>A maps to NM_014037.2 F530F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr1:110740759 C>T maps to NM_001010898.2 V626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:110740127 C>T maps to NM_001010898.2 F574F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:110740837 C>T maps to NM_001010898.2 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:110734610 C>T maps to NM_001010898.2 D294D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr1:110735143 C>T maps to NM_001010898.2 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:110741020 T>A maps to NM_001010898.2 Y713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:110717560 G>A maps to NM_001010898.2 K244K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:110735142 C>T maps to NM_001010898.2 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:110735143 C>T maps to NM_001010898.2 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:110740789 C>T maps to NM_001010898.2 F636F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:110717530 C>T maps to NM_001010898.2 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:110740789 C>T maps to NM_001010898.2 F636F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr1:110734653 T>C maps to NM_001010898.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:110740720 C>T maps to NM_001010898.2 F613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr5:1240660 G>A maps to NM_182632.2 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr5:1232388 C>T maps to NM_182632.2 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr5:1239662 T>C maps to NM_182632.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:1232355 C>T maps to NM_182632.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr5:1232887 C>T maps to NM_182632.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr5:1246070 C>T maps to NM_182632.2 Q589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:1232869 G>A maps to NM_182632.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:1239650 C>T maps to NM_182632.2 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:1242956 C>T maps to NM_182632.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:1232950 C>G maps to NM_182632.2 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:1244404 C>T maps to NM_182632.2 F471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:1232977 C>T maps to NM_182632.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:1244842 C>T maps to NM_182632.2 F539F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A2MC-06A-12D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:1235755 G>A maps to NM_182632.2 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:1243728 G>A maps to NM_182632.2 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:1239617 C>T maps to NM_182632.2 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr5:1240714 C>T maps to NM_182632.2 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr5:1232962 G>A maps to NM_182632.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:1235689 C>T maps to NM_182632.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:1240645 G>A maps to NM_182632.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:1243833 G>A maps to NM_182632.2 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:1246030 C>T maps to NM_182632.2 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:1232950 C>A maps to NM_182632.2 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:1239563 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr5:1212583 C>T maps to NM_001003841.2 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr5:1221331 C>G maps to NM_001003841.2 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:1219160 C>T maps to NM_001003841.2 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:1221376 C>T maps to NM_001003841.2 F550F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:1216765 C>T maps to NM_001003841.2 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr5:1219022 G>A maps to NM_001003841.2 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr5:1217041 C>T maps to NM_001003841.2 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr5:1214153 C>T maps to NM_001003841.2 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:1201908 C>T maps to NM_001003841.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:1221814 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr5:1214132 C>T maps to NM_001003841.2 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:1214132 C>T maps to NM_001003841.2 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:1213609 C>T maps to NM_001003841.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:1208885 C>T maps to NM_001003841.2 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:1208886 C>T maps to NM_001003841.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:1216762 G>A maps to NM_001003841.2 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:1213672 C>T maps to NM_001003841.2 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:1217050 C>T maps to NM_001003841.2 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:1221817 G>A maps to NM_001003841.2 E568E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:55719063 C>T maps to NM_001043.3 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr16:55735809 C>T maps to NM_001043.3 H598H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:55725861 C>T maps to NM_001043.3 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:55725870 C>T maps to NM_001043.3 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr16:55703513 C>T maps to NM_001043.3 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:55719147 C>T maps to NM_001043.3 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr16:55703513 C>T maps to NM_001043.3 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr16:55730156 C>T maps to NM_001043.3 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr16:55706063 C>T maps to NM_001043.3 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:55690818 C>T maps to NM_001043.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:55705874 C>T maps to NM_001043.3 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:45817381 C>T maps to NM_020208.3 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:45823575 G>A maps to NM_020208.3 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:45801375 C>T maps to NM_020208.3 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:45817372 G>A maps to NM_020208.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr3:45800493 C>T maps to NM_020208.3 R585R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr3:45804442 C>T maps to NM_020208.3 V475V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:45807203 G>A maps to NM_020208.3 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr3:45823680 G>A maps to NM_020208.3 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:45823674 C>T maps to NM_020208.3 E54E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:45812902 C>T maps to NM_020208.3 Q247Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr3:45807065 C>T maps to NM_020208.3 K422K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr3:45817402 G>A maps to NM_020208.3 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:45812824 C>T maps to NM_020208.3 Q273Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr3:45817381 C>T maps to NM_020208.3 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr3:45821515 G>A maps to NM_020208.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:45817279 G>A maps to NM_020208.3 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:45817351 C>T maps to NM_020208.3 Q161Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr3:45823707 G>A maps to NM_020208.3 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr5:1441596 G>A maps to NM_001044.4 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:1420809 C>T maps to NM_001044.4 W267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:1441510 C>T maps to NM_001044.4 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:1443051 G>A maps to NM_001044.4 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr5:1409198 G>T maps to NM_001044.4 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:1441549 G>A maps to NM_001044.4 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:1422074 C>G maps to NM_001044.4 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:1441489 G>A maps to NM_001044.4 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:1416265 G>A maps to NM_001044.4 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:1443231 C>T maps to NM_001044.4 K27K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:1443228 C>T maps to NM_001044.4 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr5:1422092 G>A maps to NM_001044.4 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr5:1422008 G>A maps to NM_001044.4 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr5:1414875 G>A maps to NM_001044.4 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr5:1441561 C>T maps to NM_001044.4 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr5:1421993 C>T maps to NM_001044.4 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:1403201 G>A maps to NM_001044.4 F534F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:1422038 G>A maps to NM_001044.4 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:1441597 G>A maps to NM_001044.4 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr17:28548745 C>T maps to ENST00000394821 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:28544282 C>T maps to ENST00000394821 Q288Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr17:28537619 G>A maps to ENST00000394821 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:28539842 G>A maps to ENST00000394821 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr17:28544222 G>A maps to ENST00000394821 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:28543188 G>A maps to ENST00000394821 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr17:28538365 G>A maps to ENST00000394821 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:28534795 C>T maps to ENST00000394821 W577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:28537604 G>A maps to ENST00000394821 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:28548731 C>T maps to ENST00000394821 W124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr17:28545830 G>A maps to ENST00000394821 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:28544291 C>T maps to ENST00000394821 K285K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q1-06A-21D-A196-08 chr11:20629079 G>T maps to NM_004211.3 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr11:20636270 G>A maps to NM_004211.3 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr11:20648306 C>T maps to NM_004211.3 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr11:20658821 C>T maps to NM_004211.3 F614F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr11:20673875 C>T maps to NM_004211.3 T704T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:20673884 T>A maps to NM_004211.3 S707S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr11:20676362 C>T maps to NM_004211.3 S781S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:20623210 G>A maps to NM_004211.3 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:20625866 G>A maps to NM_004211.3 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:20649546 C>T maps to NM_004211.3 Q473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:20648365 G>A maps to NM_004211.3 W458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:20652290 C>T maps to NM_004211.3 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:20628565 C>T maps to NM_004211.3 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:20648276 C>T maps to NM_004211.3 F428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:20628604 C>T maps to NM_004211.3 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:20625866 G>A maps to NM_004211.3 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:20622859 G>A maps to NM_004211.3 Q63Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:20676347 C>T maps to NM_004211.3 P776P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:20623093 G>A maps to NM_004211.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:20676293 G>A maps to NM_004211.3 W758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:20636223 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:20652290 C>T maps to NM_004211.3 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:20658725 C>T maps to NM_004211.3 T582T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:20676383 G>A maps to NM_004211.3 V788V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:20639369 C>A maps to NM_004211.3 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:20623060 G>A maps to NM_004211.3 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr3:14485186 G>A maps to NM_001134367.1 K15K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr3:14485160 C>T maps to NM_001134367.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:14485315 C>T maps to NM_001134367.1 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:14487282 C>T maps to NM_001134367.1 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr3:14513720 C>T maps to NM_001134367.1 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:14485348 C>T maps to NM_001134367.1 Y69Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:14489120 C>T maps to NM_001134367.1 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr5:149583588 C>T maps to NM_014228.3 I440I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:149576303 C>T maps to NM_014228.3 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:149578886 C>T maps to NM_014228.3 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr5:149585173 C>T maps to NM_014228.3 G563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:149583552 G>A maps to NM_014228.3 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr5:149589030 G>A maps to NM_014228.3 T588T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:149578865 C>T maps to NM_014228.3 C220C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr5:149576345 C>T maps to NM_014228.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:152959617 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:152956945 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:152956946 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:152958982 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:152954134 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:44466676 G>A maps to NM_201649.2 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:44476401 C>T maps to NM_201649.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:44467118 G>A maps to NM_201649.2 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:44475742 G>A maps to NM_201649.2 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:44467190 G>A maps to NM_201649.2 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:44468291 G>A maps to NM_201649.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:44467208 G>A maps to NM_201649.2 H424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr1:44463366 G>A maps to NM_201649.2 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:44468070 G>A maps to NM_201649.2 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:44468195 G>A maps to NM_201649.2 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:30096454 A>G maps to NM_003045.4 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr13:30091755 A>G maps to NM_003045.4 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr13:30088715 G>A maps to NM_003045.4 F597F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr19:33703817 G>A maps to NM_019849.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:33703435 A>C maps to NM_019849.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:33700388 C>T maps to NM_019849.2 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:33702228 G>A maps to NM_019849.2 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:33703781 G>A maps to NM_019849.2 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr4:139100446 G>A maps to ENST00000280612 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr4:139140445 A>T maps to ENST00000280612 Y240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr4:139101887 G>A maps to ENST00000280612 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:87226775 G>A maps to NM_138817.2 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:87241945 C>T maps to NM_138817.2 K187K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:87229821 G>A maps to NM_138817.2 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:87229698 C>T maps to NM_138817.2 K393K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:87242268 G>A maps to NM_138817.2 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr8:87242404 G>A maps to NM_138817.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr8:87242251 C>T maps to NM_138817.2 K85K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:87242491 C>T maps to NM_138817.2 E5E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr8:87242233 C>T maps to NM_138817.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr8:87242254 G>A maps to NM_138817.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:87229719 G>A maps to NM_138817.2 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:170198171 G>A maps to NM_020949.2 P633P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:170198579 C>T maps to NM_020949.2 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr3:170219036 G>A maps to NM_020949.2 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:170244710 G>A maps to NM_020949.2 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:170198804 G>A maps to NM_020949.2 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:170198339 G>A maps to NM_020949.2 F577F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:170198831 G>A maps to NM_020949.2 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr3:170198276 G>A maps to NM_020949.2 I598I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:170201137 G>T maps to NM_020949.2 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:170198228 C>T maps to NM_020949.2 V614V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F4-06A-12D-A25O-08 chr3:170216548 C>T maps to NM_020949.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:170198468 C>T maps to NM_020949.2 K534K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:170201209 G>A maps to NM_020949.2 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr8:17401051 C>T maps to NM_001164771.1 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr8:17396428 C>T maps to NM_001164771.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:17417986 C>T maps to NM_001164771.1 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:17419558 C>T maps to NM_001164771.1 F577F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr8:17401204 C>T maps to NM_001164771.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:17417986 C>T maps to NM_001164771.1 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:17417917 G>A maps to NM_001164771.1 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr8:17419558 C>T maps to NM_001164771.1 F577F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:17412147 C>T maps to NM_001164771.1 Q419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:17422639 G>A maps to NM_001164771.1 K694K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr8:17406286 G>A maps to NM_001164771.1 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:70146806 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:70148083 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:70146883 G>A did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:70146734 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:70145976 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:70147841 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr23:70148818 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr23:70149552 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr23:70148724 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:70148385 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:70149630 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:70145774 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:70147779 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:70147387 G>A did not map to a codon.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr23:70146005 G>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:70145691 G>A did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:70147133 G>A did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:70148083 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr22:21383445 G>A maps to NM_004173.2 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr22:21385909 C>T maps to NM_004173.2 K64K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr22:21384584 G>A maps to NM_004173.2 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr22:21386020 G>A maps to NM_004173.2 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr22:21384497 C>T maps to NM_004173.2 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:87873355 G>A maps to NM_003486.5 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr16:68308839 C>T maps to NM_003983.4 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr16:68338066 C>T maps to NM_032178.2 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:23282370 C>T maps to NM_001126106.1 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:23600756 G>A maps to NM_012244.2 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr14:23634536 G>A maps to NM_012244.2 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr19:33324148 C>T maps to NM_014270.4 W435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:33333130 C>T maps to NM_014270.4 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr19:33355125 G>A maps to NM_014270.4 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr19:33333196 G>A maps to NM_014270.4 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:33355125 G>A maps to NM_014270.4 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:33334772 G>A maps to NM_014270.4 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr19:33350845 G>A maps to NM_014270.4 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr2:40391996 G>A maps to NM_021097.2 F722F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:40405617 G>A maps to NM_021097.2 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr2:40397469 C>T maps to NM_021097.2 K663K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:40397448 C>T maps to NM_021097.2 P670P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:40342677 G>A maps to NM_021097.2 F879F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr2:40366763 G>A maps to NM_021097.2 F774F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:40655721 G>A maps to NM_021097.2 R567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:40366724 G>A maps to NM_021097.2 V787V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr2:40657095 G>A maps to NM_021097.2 Q109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr2:40366628 T>G maps to NM_021097.2 G819G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:40656541 C>T maps to NM_021097.2 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr2:40656658 C>T maps to NM_021097.2 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:40405572 G>A maps to NM_021097.2 F623F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:40655947 G>A maps to NM_021097.2 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:40342470 G>A maps to NM_021097.2 S948S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:40366816 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr2:40366763 G>A maps to NM_021097.2 F774F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr2:40366634 G>A maps to NM_021097.2 F817F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:40655983 G>A maps to NM_021097.2 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:40656112 C>T maps to NM_021097.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:40656475 C>T maps to NM_021097.2 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:40656880 G>A maps to NM_021097.2 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr2:40655947 G>A maps to NM_021097.2 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr2:40656790 C>T maps to NM_021097.2 W210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:40342455 G>A maps to NM_021097.2 L953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:40392047 G>A maps to NM_021097.2 I705I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:40656676 G>A maps to NM_021097.2 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:47969381 G>A maps to NM_015063.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:47935700 C>T maps to NM_015063.2 G704G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:47969381 G>A maps to NM_015063.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr19:47960800 G>A maps to NM_015063.2 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr19:47935676 C>A maps to NM_015063.2 G712G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:47940788 C>T maps to NM_015063.2 T680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:47940746 C>T maps to NM_015063.2 Q694Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:47941135 C>T maps to NM_015063.2 E660E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:47969129 G>A maps to NM_015063.2 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:47935670 C>T maps to NM_015063.2 R714R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr14:70634242 C>T maps to NM_183002.1 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr14:70634452 G>A maps to NM_183002.1 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr14:70633492 C>T maps to NM_183002.1 E549E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr14:70634272 C>T maps to NM_183002.1 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr14:70633879 C>T maps to NM_183002.1 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr14:70522524 G>A maps to NM_183002.1 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr14:70634560 C>T maps to NM_183002.1 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr14:70634875 G>A maps to NM_183002.1 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr14:70517803 G>A maps to NM_183002.1 I684I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr14:70634875 G>A maps to NM_183002.1 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:70633450 G>A maps to NM_183002.1 I563I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr14:70522525 G>A maps to NM_183002.1 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr14:70515649 G>A maps to NM_183002.1 P747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr14:70634889 G>A maps to NM_183002.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr14:70527577 C>T maps to NM_183002.1 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr14:70527655 C>T maps to NM_183002.1 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:70515730 C>T maps to NM_183002.1 G720G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr14:70634071 G>A maps to NM_183002.1 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:70634623 C>T maps to NM_183002.1 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr14:70530585 G>A maps to NM_033262.3 F615F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr14:70633873 C>A maps to NM_183002.1 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:70515730 C>T maps to NM_183002.1 G720G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:70633846 C>T maps to NM_183002.1 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr14:70634035 G>A maps to NM_183002.1 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr14:70515703 G>A maps to NM_183002.1 D729D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr14:70634317 G>A maps to NM_183002.1 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:70527655 C>T maps to NM_183002.1 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr14:70635067 G>A maps to NM_183002.1 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr14:70634451 G>A maps to NM_183002.1 Q230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr14:70633482 G>A maps to NM_183002.1 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:70634272 C>T maps to NM_183002.1 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:70633753 C>T maps to NM_183002.1 K462K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr14:70634092 C>T maps to NM_183002.1 K349K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr14:70634926 C>T maps to NM_183002.1 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr14:70517734 G>C maps to NM_183002.1 T707T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr14:70633855 G>A maps to NM_183002.1 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr14:70634131 C>T maps to NM_183002.1 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr14:70634941 C>T maps to NM_183002.1 E66E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr14:70634965 G>A maps to NM_183002.1 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:70530545 G>A maps to NM_033262.3 Q629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:70530585 G>A maps to NM_033262.3 F615F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:70634005 C>T maps to NM_183002.1 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr14:70515508 G>A maps to NM_183002.1 F794F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr14:70634002 C>T maps to NM_183002.1 K379K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr14:70633996 G>A maps to NM_183002.1 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:27434229 G>A maps to NM_003047.3 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:27436217 G>A maps to NM_003047.3 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:27432477 G>A maps to NM_003047.3 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:27440721 G>A maps to NM_003047.3 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:27436205 G>A maps to NM_003047.3 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:27436208 G>A maps to NM_003047.3 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr3:111936299 C>T maps to NM_183061.1 E593E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:111898497 C>T maps to NM_183061.1 K933K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:111901051 A>G maps to NM_183061.1 P859P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:111958782 G>A maps to NM_183061.1 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:111993776 G>A maps to NM_183061.1 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr3:111996614 G>A maps to NM_183061.1 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:111988877 G>A maps to NM_183061.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:111927150 C>T maps to NM_183061.1 V620V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:111887904 C>T maps to NM_183061.1 W1019*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:111918167 C>T maps to NM_183061.1 K841K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:111981907 G>A maps to NM_183061.1 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:111997700 G>A maps to NM_183061.1 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:173569288 G>A maps to NM_178527.3 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:173493149 G>A maps to NM_178527.3 I866I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr1:173503739 T>G maps to NM_178527.3 I619I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:173493233 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:173542433 T>C maps to NM_178527.3 E311E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:173526622 G>A maps to NM_178527.3 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:173470235 A>G maps to NM_178527.3 S1124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:173545849 C>T maps to NM_178527.3 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr1:173550992 G>A maps to NM_178527.3 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:173493113 G>A maps to NM_178527.3 F878F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:173493179 G>A maps to NM_178527.3 P856P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr1:173499163 T>A maps to NM_178527.3 A731A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:173542415 G>A maps to NM_178527.3 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:173552675 C>T maps to NM_178527.3 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:173556802 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:173556855 G>A maps to NM_178527.3 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr2:103299779 C>T maps to NM_003048.3 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:103274200 C>T maps to NM_003048.3 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:103322348 G>A maps to NM_003048.3 T674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:103324923 C>T maps to NM_003048.3 A805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:103299902 C>T maps to NM_003048.3 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr2:103300662 C>T maps to NM_003048.3 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:103281722 C>T maps to NM_003048.3 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:103236546 C>A maps to NM_003048.3 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:103318919 C>T maps to NM_003048.3 R602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:103274236 G>A maps to NM_003048.3 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:103281713 C>T maps to NM_003048.3 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr2:103236555 G>A maps to NM_003048.3 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:103236408 G>A maps to NM_003048.3 E34E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:103300792 C>T maps to NM_003048.3 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr2:103281749 C>T maps to NM_003048.3 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr2:103300653 C>T maps to NM_003048.3 D428D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:103300713 C>T maps to NM_003048.3 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:103274323 C>T maps to NM_003048.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:103299893 C>T maps to NM_003048.3 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:103236459 C>T maps to NM_003048.3 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:103322375 G>A maps to NM_003048.3 R683R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:103281629 C>T maps to NM_003048.3 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:103300776 C>T maps to NM_003048.3 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr2:103300681 C>T maps to NM_003048.3 R438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:103274170 C>T maps to NM_003048.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:103299893 C>T maps to NM_003048.3 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:103300776 C>T maps to NM_003048.3 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:103311563 G>A maps to NM_003048.3 W526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:103321103 G>A maps to NM_003048.3 R649R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:103274200 C>T maps to NM_003048.3 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:103236459 C>T maps to NM_003048.3 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:103274275 C>T maps to NM_003048.3 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr2:103281713 C>T maps to NM_003048.3 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr5:477529 G>A maps to NM_004174.2 I559I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:484714 G>A maps to NM_004174.2 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:488571 C>A maps to NM_004174.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr5:484711 G>A maps to NM_004174.2 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr5:475068 G>A maps to NM_004174.2 S810S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:484774 C>T maps to NM_004174.2 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr5:480073 G>A maps to NM_004174.2 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:482665 G>A maps to NM_004174.2 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:484801 G>A maps to NM_004174.2 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr2:103095454 C>T maps to NM_001011552.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:103148843 G>A maps to NM_001011552.3 R698R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:103121874 G>A maps to NM_001011552.3 W381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr2:103124626 C>T maps to NM_001011552.3 R430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:103121826 G>A maps to NM_001011552.3 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:103095586 G>A maps to NM_001011552.3 Q182Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:103121889 C>T maps to NM_001011552.3 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:103128687 C>T maps to NM_001011552.3 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:103120160 C>T maps to NM_001011552.3 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr2:103095602 C>T maps to NM_001011552.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:103125367 C>T maps to NM_001011552.3 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr2:103120071 C>T maps to NM_001011552.3 Q296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:103120100 C>T maps to NM_001011552.3 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:103149074 G>A maps to NM_001011552.3 S775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:103120154 C>T maps to NM_001011552.3 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:103136326 G>A maps to NM_001011552.3 R577R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr2:103120031 C>T maps to NM_001011552.3 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:103120031 C>T maps to NM_001011552.3 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:103124626 C>T maps to NM_001011552.3 R430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:103142728 G>A maps to NM_001011552.3 K654K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:103142758 G>A maps to NM_001011552.3 G664G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr16:67298299 G>T maps to NM_004594.2 E630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr16:67293839 G>A maps to NM_004594.2 P611P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr16:67289713 C>T maps to NM_004594.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr16:67298343 G>A maps to NM_004594.2 R644R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:67288958 C>T maps to NM_004594.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr16:67289374 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr16:67304816 G>T maps to NM_004594.2 E799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:67290925 C>T maps to NM_004594.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:135104755 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:135092657 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:135080652 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:135106571 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr23:135084285 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:135092719 C>T did not map to a codon.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr23:135092681 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr23:135126864 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:46521566 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:46508217 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:46539135 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:46532036 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:46491082 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:46472822 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:46466518 G>T did not map to a codon.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr23:46466516 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:46522064 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr20:48466141 C>T maps to ENST00000417961 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:48472031 C>T maps to ENST00000417961 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr3:143412149 C>G did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr3:143292978 G>A maps to NM_173653.3 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:143292978 G>A maps to NM_173653.3 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr3:143214260 C>T maps to NM_173653.3 E373E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:143186015 G>A maps to NM_173653.3 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr3:143371182 G>A maps to NM_173653.3 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:143186015 G>A maps to NM_173653.3 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:142985651 T>C maps to NM_173653.3 K610K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:142985653 T>A maps to NM_173653.3 K610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:143513906 G>A maps to NM_173653.3 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:143567109 G>A maps to NM_173653.3 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:143100922 C>T maps to NM_173653.3 E501E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:143412127 C>T maps to NM_173653.3 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr12:21422496 C>T maps to NM_134431.3 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:21445168 G>A maps to NM_134431.3 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:21457496 C>T maps to NM_134431.3 K151K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr12:21450416 G>A maps to NM_134431.3 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:21457424 G>A maps to NM_134431.3 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:21427407 G>A maps to NM_134431.3 T596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:21453303 C>T maps to NM_134431.3 K296K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr12:21453399 G>A maps to NM_134431.3 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr12:21446931 G>A maps to NM_134431.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:21422679 C>T maps to NM_134431.3 P605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr12:21427476 G>A maps to NM_134431.3 S573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr12:21349937 C>T maps to NM_006446.4 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:21331609 T>C maps to NM_006446.4 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr12:21370150 G>A maps to NM_006446.4 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr12:21349912 G>A maps to NM_006446.4 W254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:21370150 G>A maps to NM_006446.4 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:21294543 G>A maps to NM_006446.4 E12E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:21353448 C>T maps to NM_006446.4 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:21327589 C>T maps to NM_006446.4 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:21329769 C>T maps to NM_006446.4 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:21370126 C>T maps to NM_006446.4 C524C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr12:21329736 C>T maps to NM_006446.4 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:21054377 G>A maps to NM_019844.2 R614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr12:21051368 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr12:21032373 C>T maps to NM_019844.2 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr12:21036449 G>A maps to NM_019844.2 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:21032428 A>T maps to NM_019844.2 K399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr12:21036536 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr12:21011451 C>T maps to NM_019844.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:21028175 C>T maps to NM_019844.2 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:21028247 C>T maps to NM_019844.2 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr12:21054377 G>A maps to NM_019844.2 R614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:21028226 C>T maps to NM_019844.2 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:21036458 C>T maps to NM_019844.2 F535F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:21014013 C>T maps to NM_019844.2 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:21032497 C>T maps to NM_019844.2 Q422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:21036449 G>A maps to NM_019844.2 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:21036449 G>A maps to NM_019844.2 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr12:21036449 G>A maps to NM_019844.2 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr12:21032465 C>A maps to NM_019844.2 S411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:21032511 C>T maps to NM_019844.2 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr12:21015415 G>A maps to NM_019844.2 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:21051369 G>A maps to NM_019844.2 K561K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:21069000 C>T maps to NM_019844.2 F643F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:21069025 C>T maps to NM_019844.2 Q652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr12:21028359 C>T maps to NM_019844.2 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:20854349 C>T maps to NM_017435.4 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:20874894 C>T maps to NM_017435.4 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:20854340 G>A maps to NM_017435.4 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:20852581 T>G maps to NM_017435.4 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:20868208 T>C maps to NM_017435.4 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:20874852 G>A maps to NM_017435.4 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:20868115 C>T maps to NM_017435.4 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:20876069 C>T maps to NM_017435.4 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:20890039 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:20870064 G>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:20890124 C>A maps to NM_017435.4 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr12:20868115 C>T maps to NM_017435.4 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr12:20896268 C>T maps to NM_017435.4 A588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:20896277 C>T maps to NM_017435.4 I591I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr3:133667503 G>A maps to NM_005630.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr3:133674002 C>T maps to NM_005630.2 Q144Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:133666164 G>A maps to NM_005630.2 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr3:133674035 C>T maps to NM_005630.2 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:133667386 G>A maps to NM_005630.2 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr3:133666218 G>A maps to NM_005630.2 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:133667500 G>A maps to NM_005630.2 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:133661477 G>A maps to NM_005630.2 S532S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:133670171 G>A maps to NM_005630.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr3:133670153 C>T maps to NM_005630.2 W253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr3:133666257 C>T maps to NM_005630.2 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:74907660 C>T maps to NM_007256.4 Y512Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:74880714 C>T maps to NM_007256.4 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr11:74880347 C>T maps to NM_007256.4 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr11:74880729 C>T maps to NM_007256.4 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:74913985 C>T maps to NM_007256.4 Q602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:74873719 C>T maps to NM_007256.4 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:74915492 C>T maps to NM_007256.4 F666F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:74911426 C>T maps to NM_007256.4 I586I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:74911426 C>T maps to NM_007256.4 I586I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:74876914 C>T maps to NM_007256.4 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:74904477 C>T maps to NM_007256.4 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:74880392 C>T maps to NM_007256.4 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:74883532 C>T maps to NM_007256.4 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:74904518 C>T maps to NM_007256.4 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:74904305 C>T maps to NM_007256.4 F373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:74904575 C>T maps to NM_007256.4 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr15:92705992 C>T maps to NM_013272.3 I587I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr15:92706124 C>T maps to NM_013272.3 I631I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:92690347 C>T maps to NM_013272.3 I549I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:92669354 C>T maps to NM_013272.3 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:92638123 G>A maps to NM_013272.3 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr15:92669426 C>T maps to NM_013272.3 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:92706136 C>T maps to NM_013272.3 S635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr15:92647729 C>T maps to NM_013272.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr15:92459368 C>T maps to NM_013272.3 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr15:92459305 G>A maps to NM_013272.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr15:92706010 C>T maps to NM_013272.3 F593F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:92459284 C>T maps to NM_013272.3 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:92663746 C>T maps to NM_013272.3 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr20:61299386 C>A maps to NM_016354.3 I554I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr5:101572562 C>T maps to NM_180991.4 *725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr5:101593662 G>A maps to NM_180991.4 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr5:101592949 G>A maps to NM_180991.4 F446F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr5:101593779 C>T maps to NM_180991.4 K380K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr5:101597670 C>T maps to NM_180991.4 W322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:101572567 T>C maps to NM_180991.4 E723E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr5:101593754 G>A maps to NM_180991.4 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:101583014 G>A maps to NM_180991.4 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:101593662 G>A maps to NM_180991.4 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr8:70591848 C>T maps to NM_030958.2 R596R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr8:70667860 G>A maps to NM_030958.2 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:70744758 G>A maps to NM_030958.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:70667773 C>T maps to NM_030958.2 K381K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr8:70585397 A>T maps to NM_030958.2 I751I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr8:70744029 G>A maps to NM_030958.2 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:70591656 G>A maps to NM_030958.2 F660F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:70667683 C>T maps to NM_030958.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr8:70591626 G>A maps to NM_030958.2 I670I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr8:70585409 G>A maps to NM_030958.2 F747F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:70744058 G>A maps to NM_030958.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr8:70650302 G>A maps to NM_030958.2 I465I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr8:70585409 G>A maps to NM_030958.2 F747F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:70585409 G>A maps to NM_030958.2 F747F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:70591656 G>A maps to NM_030958.2 F660F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:70650416 C>T maps to NM_030958.2 R427R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr5:101748765 T>G maps to NM_173488.3 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:101813488 G>A maps to NM_173488.3 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr5:101795411 G>A maps to NM_173488.3 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr5:101726727 A>C maps to NM_173488.3 R612R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr5:101834542 G>A maps to NM_173488.3 F2F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr5:101774465 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:101748840 C>T maps to NM_173488.3 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:101834413 C>T maps to NM_173488.3 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr5:101709082 A>C maps to NM_173488.3 V711V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr5:101834497 C>T maps to NM_173488.3 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr5:101748840 C>T maps to NM_173488.3 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:101774461 G>A maps to NM_173488.3 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:101834347 C>T maps to NM_173488.3 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:101735365 C>T maps to NM_173488.3 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr5:101813565 C>T did not map to a codon.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr5:101834272 G>A maps to NM_173488.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr5:101834245 A>G maps to NM_173488.3 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:101816073 G>A maps to NM_173488.3 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr5:101834455 C>T maps to NM_173488.3 K31K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr5:101834449 C>T maps to NM_173488.3 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:101813496 G>A maps to NM_173488.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:101834205 G>A maps to NM_173488.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:101834533 G>A maps to NM_173488.3 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:101834542 G>A maps to NM_173488.3 F2F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr5:101834449 C>T maps to NM_173488.3 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:101834347 C>T maps to NM_173488.3 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr5:101794106 C>T maps to NM_173488.3 K370K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:33680061 G>A maps to NM_152270.3 F673F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr17:33690244 G>A maps to NM_152270.3 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr17:33690172 G>A maps to NM_152270.3 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:33680929 C>T maps to NM_152270.3 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr17:33679436 G>A maps to NM_152270.3 L882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr17:33690646 C>T maps to NM_152270.3 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr17:33680061 G>A maps to NM_152270.3 F673F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr17:33690139 C>T maps to NM_152270.3 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr17:33680004 C>T maps to NM_152270.3 K692K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:33690157 G>A maps to NM_152270.3 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:33680368 C>T maps to NM_152270.3 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:33749180 G>A maps to NM_018042.3 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:33747314 T>C maps to NM_018042.3 Q375Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr17:33738893 G>A maps to NM_018042.3 F400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:33749705 G>A maps to NM_018042.3 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:33806469 T>A maps to ENST00000361112 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr17:33802160 G>A maps to ENST00000361112 I545I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr17:33849308 C>T maps to ENST00000361112 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr17:33772552 G>C maps to NM_144682.5 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:33771892 C>T maps to NM_144682.5 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:33772623 G>A maps to NM_144682.5 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr17:33767880 A>C maps to NM_144682.5 V809V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:33772414 G>A maps to NM_144682.5 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr17:33586575 C>A maps to NM_144975.3 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr17:33586548 C>T maps to NM_144975.3 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr17:33585882 C>T maps to NM_144975.3 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:41483315 G>A maps to NM_144990.3 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:98825812 G>A maps to NM_003061.2 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr10:98763969 C>T maps to NM_003061.2 T1240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr10:98778823 G>A maps to NM_003061.2 C929C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:98760955 C>T maps to NM_003061.2 R1506R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:98764532 G>A maps to NM_003061.2 N1209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:98790524 G>A maps to NM_003061.2 S857S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:98808835 G>A maps to NM_003061.2 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:98764505 C>T maps to NM_003061.2 Q1218Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:98781150 G>A maps to NM_003061.2 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:98807586 C>T maps to NM_003061.2 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:98807583 C>T maps to NM_003061.2 E499E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:98819884 G>A maps to NM_003061.2 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr10:98802661 C>T maps to NM_003061.2 E720E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr10:98762107 G>A maps to NM_003061.2 C1391C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr10:98823947 G>A maps to NM_003061.2 N202N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr10:98803197 G>A maps to NM_003061.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr10:98763969 C>T maps to NM_003061.2 T1240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:98820539 C>T maps to NM_003061.2 Q266Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:98763930 G>A maps to NM_003061.2 A1253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:98807466 G>A maps to NM_003061.2 I538I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:98808817 G>A maps to NM_003061.2 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr10:98816190 G>A maps to NM_003061.2 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr4:20619118 G>A maps to ENST00000273739 L1411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr4:20611773 T>A maps to ENST00000273739 S1290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr4:20530689 C>T maps to ENST00000273739 I531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:20490459 C>T maps to ENST00000273739 N210N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr4:20525428 C>T maps to ENST00000273739 Q397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:20525789 C>T maps to ENST00000273739 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:20620553 C>T maps to ENST00000273739 F1517F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr4:20618794 G>A maps to ENST00000273739 R1383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:20525789 C>T maps to ENST00000273739 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr4:20620616 G>A maps to ENST00000273739 T1538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:20599937 C>T maps to ENST00000273739 D1217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:20611731 C>T maps to ENST00000273739 I1276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr4:20493456 C>T maps to ENST00000273739 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:20611719 G>A maps to ENST00000273739 G1272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr4:20620553 C>T maps to ENST00000273739 F1517F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:20591307 C>T maps to ENST00000273739 L1057L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr4:20525514 C>T maps to ENST00000273739 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:20525484 C>T maps to ENST00000273739 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:20493435 C>T maps to ENST00000273739 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr4:20493456 C>T maps to ENST00000273739 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr4:20525457 C>T maps to ENST00000273739 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr4:20493498 T>C maps to ENST00000273739 N301N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr4:20598127 C>T maps to ENST00000273739 I1150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:20255467 C>T maps to ENST00000273739 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr4:20598262 G>A maps to ENST00000273739 T1195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:20525738 C>T maps to ENST00000273739 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:20555587 C>T maps to ENST00000273739 Q912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:20541108 C>T maps to ENST00000273739 F630F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:20598262 G>A maps to ENST00000273739 T1195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr4:20598202 G>A maps to ENST00000273739 V1175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr5:168135016 C>T maps to NM_003062.2 V936V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr5:168189611 C>T maps to NM_003062.2 T514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr5:168250272 G>A maps to NM_003062.2 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr5:168098444 C>T maps to NM_003062.2 T1295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr5:168176486 G>A maps to NM_003062.2 F709F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:168123333 G>A maps to NM_003062.2 I1015I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:168244353 C>T maps to NM_003062.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:168093497 C>T maps to NM_003062.2 V1511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:168093668 G>A maps to NM_003062.2 V1454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr5:168176564 G>A maps to NM_003062.2 I683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr5:168098255 G>A maps to NM_003062.2 G1358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:168093532 G>A maps to NM_003062.2 Q1500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr5:168233536 G>A maps to NM_003062.2 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr5:168620508 G>A maps to NM_003062.2 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:168112874 G>A maps to NM_003062.2 D1124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:168123336 C>T maps to NM_003062.2 G1014G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:168176555 C>T maps to NM_003062.2 G686G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr5:168179970 G>A maps to NM_003062.2 S654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:168093494 C>T maps to NM_003062.2 E1512E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:168112739 C>T maps to NM_003062.2 V1169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:168176540 C>T maps to NM_003062.2 Q691Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:168180990 G>A maps to NM_003062.2 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:168199801 C>T maps to NM_003062.2 K481K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:168310313 C>T maps to NM_003062.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:168678405 C>T maps to NM_003062.2 K85K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:168678417 G>A maps to NM_003062.2 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:168678435 C>T maps to NM_003062.2 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:168098222 C>T maps to NM_003062.2 R1369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:168114081 C>T maps to NM_003062.2 E1072E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:168310310 G>A maps to NM_003062.2 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:168135004 G>A maps to NM_003062.2 R940R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:168151455 G>A maps to NM_003062.2 P768P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:168678441 G>A maps to NM_003062.2 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr5:168112874 G>A maps to NM_003062.2 D1124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:168180966 G>A maps to NM_003062.2 F577F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr13:84455096 G>A maps to NM_052910.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr13:84453716 G>A maps to NM_052910.1 I642I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr13:84454754 C>T maps to NM_052910.1 E296E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:84454471 G>A maps to NM_052910.1 R391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:84453716 G>A maps to NM_052910.1 I642I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr13:84453890 C>T maps to NM_052910.1 R584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr13:84454583 C>T maps to NM_052910.1 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr13:84454853 C>T maps to NM_052910.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr13:84454712 C>T maps to NM_052910.1 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr13:84455189 C>T maps to NM_052910.1 Q151Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr13:84455006 G>A maps to NM_052910.1 N212N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr13:84454499 G>A maps to NM_052910.1 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr13:84455420 G>A maps to NM_052910.1 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr13:84455195 G>A maps to NM_052910.1 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr13:84453941 C>T maps to NM_052910.1 K567K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:84453653 G>A maps to NM_052910.1 S663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:84454370 G>A maps to NM_052910.1 D424D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:84454439 G>A maps to NM_052910.1 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:84455120 G>A maps to NM_052910.1 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr13:84454484 C>T maps to NM_052910.1 K386K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr13:84454409 G>A maps to NM_052910.1 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr23:144906301 T>A did not map to a codon.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr23:144904693 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr23:144905880 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:144905617 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:144905506 A>G did not map to a codon.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr23:144905765 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr3:164905885 C>T maps to NM_014926.2 K911K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr3:164907673 G>A maps to NM_014926.2 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr3:164907634 G>A maps to NM_014926.2 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr3:164907016 C>T maps to NM_014926.2 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr3:164906326 C>T maps to NM_014926.2 V764V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr3:164907232 G>A maps to NM_014926.2 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:164906575 C>T maps to NM_014926.2 R681R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:164908086 G>A maps to NM_014926.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:164907790 C>T maps to NM_014926.2 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:164907331 C>T maps to NM_014926.2 W429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr3:164908060 G>A maps to NM_014926.2 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:164906935 C>T maps to NM_014926.2 E561E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:164908538 C>T maps to NM_014926.2 W27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr3:164907790 C>T maps to NM_014926.2 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:164905756 G>A maps to NM_014926.2 L954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr3:164906674 C>T maps to NM_014926.2 G648G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:164908492 C>T maps to NM_014926.2 E42E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:164907931 C>T maps to NM_014926.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr3:164905894 G>A maps to NM_014926.2 P908P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr3:164906263 C>T maps to NM_014926.2 P785P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr3:164907091 T>G maps to NM_014926.2 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr23:142717537 C>T did not map to a codon.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr23:142716832 G>A did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:142718883 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:142717441 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:142718345 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:142716503 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:142718197 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:142717585 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:142717285 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:142717674 T>G did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:142718599 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:142717911 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:142717102 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:142718334 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:142717896 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:142718462 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:142717155 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:142717195 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:142717705 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:142716476 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:142717255 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr23:142718197 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr23:142718917 G>A did not map to a codon.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr23:142718515 G>A did not map to a codon.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr23:142718516 G>A did not map to a codon.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr23:142718410 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr23:142717690 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:142717340 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr23:142718156 G>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr23:142717679 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:142716445 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:142717017 A>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:142717101 C>T did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr23:142716797 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:142717195 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:142716673 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:142716899 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:142717742 T>G did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:142718344 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr13:88328959 C>T maps to NM_015567.1 H439H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr13:88329679 C>T maps to NM_015567.1 F679F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr13:88329001 C>T maps to NM_015567.1 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:88328746 C>T maps to NM_015567.1 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr13:86369350 G>A maps to NM_032229.2 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr13:86368965 G>A maps to NM_032229.2 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr13:86368800 G>A maps to NM_032229.2 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:86369316 C>A maps to NM_032229.2 E443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr13:86370412 C>T maps to NM_032229.2 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:86369086 C>T maps to NM_032229.2 W519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr13:86370583 G>A maps to NM_032229.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr13:86370607 G>A maps to NM_032229.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr13:86369482 G>A maps to NM_032229.2 F387F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr13:86369305 G>A maps to NM_032229.2 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr13:86370193 C>T maps to NM_032229.2 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr13:86370169 C>T maps to NM_032229.2 K158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr13:86368315 C>T maps to NM_032229.2 R776R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr13:86368999 G>A maps to NM_032229.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:86368423 C>T maps to NM_032229.2 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:105778665 G>A maps to NM_014720.2 K1044K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr10:105778642 C>T maps to NM_014720.2 Q1037*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:105762726 T>G maps to NM_014720.2 T597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:57843837 C>T maps to ENST00000428312 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:57835522 C>T maps to ENST00000428312 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:59180639 G>A maps to NM_024755.2 H773H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:159834578 T>A maps to NM_006425.4 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:159841343 G>T maps to NM_006425.4 Y102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:159831821 G>A maps to NM_006425.4 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:143822686 G>A maps to NM_020427.2 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr4:146461203 C>T maps to NM_001003688.1 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr18:45374898 A>C maps to NM_001003652.2 L315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr18:45395779 G>A maps to NM_001003652.2 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr18:45395656 T>C maps to NM_001003652.2 E159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr15:67482831 C>T maps to NM_005902.3 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr15:67479752 C>T maps to NM_005902.3 Q354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr15:67473594 C>G maps to NM_005902.3 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr18:48604767 C>T maps to NM_005359.5 H530H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:135513138 C>T maps to NM_001001419.1 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr15:67073542 C>T maps to NM_005585.4 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:67073659 C>T maps to NM_005585.4 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr15:67073704 C>T maps to NM_005585.4 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr15:67073821 C>T maps to NM_005585.4 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr18:46468878 C>T maps to NM_005904.3 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:46474784 G>A maps to NM_005904.3 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:46447849 C>T maps to NM_005904.3 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:46447990 G>A maps to NM_005904.3 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr13:37453562 G>A maps to NM_001127217.2 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr13:37446897 G>A maps to NM_001127217.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr13:37427645 G>A maps to NM_001127217.2 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr13:37427603 G>A maps to NM_001127217.2 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr1:40881028 C>T maps to NM_022733.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:40881028 C>T maps to NM_022733.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IB-06A-11D-A196-08 chr23:128625999 C>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:128614695 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:128624165 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:128605255 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:128645871 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:128641928 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr23:128582285 T>C did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:128602860 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr23:128649885 C>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:128582374 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr23:128624132 G>T did not map to a codon.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr9:2123807 C>T maps to NM_003070.3 I1284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr9:2086992 C>T maps to NM_003070.3 F897F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr9:2039778 G>A maps to NM_003070.3 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:2123807 C>T maps to NM_003070.3 I1284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:2186139 C>T maps to NM_003070.3 A1502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr9:2084114 C>T maps to NM_003070.3 V815V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZU-06A-12D-A196-08 chr9:2161876 C>T maps to NM_003070.3 I1391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr9:2039610 C>T maps to NM_003070.3 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:2110320 C>T maps to NM_003070.3 F1120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:2161843 C>T maps to NM_003070.3 P1380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:2182193 C>T maps to NM_003070.3 V1471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:11123650 C>T maps to NM_001128849.1 S767S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:11113772 C>T maps to NM_001128849.1 I627I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:11094892 T>A maps to NM_001128849.1 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr19:11152221 C>T maps to NM_001128849.1 I1502I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr19:11134210 G>A maps to NM_001128849.1 E959E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:11097072 G>A maps to NM_001128849.1 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:11144842 C>T maps to NM_001128849.1 I1306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:11097626 C>T maps to NM_001128849.1 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr19:11105631 G>A maps to NM_001128849.1 K516K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr19:11101983 C>T maps to NM_001128849.1 R468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:11138480 G>C maps to NM_001128849.1 S1079S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr19:11145738 C>T maps to NM_001128849.1 F1367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:11134265 C>T maps to NM_001128849.1 R978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:11132564 C>T maps to NM_001128849.1 F927F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr19:11101965 C>T maps to NM_001128849.1 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr4:144445528 C>T maps to NM_003601.2 H143H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr4:95147327 C>T maps to NM_001128429.1 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:95197526 C>T maps to NM_001128429.1 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr4:95201807 C>T maps to NM_001128429.1 F830F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr4:95194770 C>T maps to NM_001128429.1 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:95147381 C>T maps to NM_001128429.1 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:95194800 C>T maps to NM_001128429.1 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:217297569 C>T maps to NM_014140.3 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:217297569 C>T maps to NM_014140.3 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:217279597 C>T maps to NM_014140.3 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:217297461 C>T maps to NM_014140.3 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:217279703 C>T maps to NM_014140.3 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:217347507 G>A maps to NM_014140.3 E891E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr22:24167500 G>A maps to NM_003073.3 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr22:24143199 C>T maps to NM_003073.3 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr22:24175873 C>T maps to NM_003073.3 Q368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr22:24167437 C>T maps to NM_003073.3 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:47755908 C>T maps to NM_003074.3 W263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:47703860 G>A maps to NM_003074.3 D707D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr12:56565109 G>A maps to NM_003075.3 F733F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:56561888 C>T maps to NM_003075.3 R904R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr12:56563688 G>A maps to NM_003075.3 R776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr12:56563689 G>A maps to NM_003075.3 P775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr12:56583178 G>A maps to NM_003075.3 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:56558216 G>A maps to NM_003075.3 N1146N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:56563638 C>T maps to NM_003075.3 E792E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr12:56575586 G>A maps to NM_003075.3 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr12:56558149 G>A maps to NM_003075.3 Q1169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr12:56565502 G>A maps to NM_003075.3 V684V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr12:50492782 G>A maps to NM_003076.4 *516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr12:50480089 C>T maps to NM_003076.4 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr12:50484050 C>T maps to NM_003076.4 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:61914856 G>A maps to NM_001098426.1 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr17:61914985 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr7:150945579 G>A maps to NM_001003801.1 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr7:150939004 G>A maps to NM_003078.3 D232D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr7:150939872 C>T maps to NM_003078.3 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr7:150937275 C>T maps to NM_003078.3 E352E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr17:38787945 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q1-06A-21D-A196-08 chr23:53438819 G>C did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:53436076 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr23:53436193 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:53440017 T>G did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:53421714 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr22:45802415 C>T maps to NM_148674.3 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr22:45785650 G>A maps to NM_148674.3 R558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr22:45798262 C>T maps to NM_148674.3 K268K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:45749992 C>T maps to NM_148674.3 K1046K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:45802442 C>T maps to NM_148674.3 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:45768121 G>A maps to NM_148674.3 T703T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:45798379 G>A maps to NM_148674.3 Y229Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr9:106892048 T>C maps to NM_001042550.1 L972L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr9:106901544 G>A maps to NM_001042550.1 K1181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr9:106882312 C>T maps to NM_001042550.1 R668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr3:160122244 C>T maps to NM_005496.3 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr3:160135740 G>A maps to NM_005496.3 K556K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:160118640 C>T maps to NM_005496.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr3:160150894 A>G maps to NM_005496.3 V1204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr9:72933760 G>T maps to NM_015110.3 E678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr9:72965374 C>T maps to NM_015110.3 F1051F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:17860179 C>T maps to ENST00000381272 R978R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q3-06A-11D-A196-08 chr18:2760727 C>T maps to NM_015295.2 N1475N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr18:2700606 T>C maps to NM_015295.2 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr18:2718388 A>T maps to NM_015295.2 A805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr18:2740735 C>T maps to NM_015295.2 Q1184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr18:2718180 T>C maps to NM_015295.2 I762I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr18:2732330 A>T maps to NM_015295.2 L1039L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:2769795 C>T maps to NM_015295.2 I1608I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:152857233 C>T maps to NM_030663.2 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:152856946 C>T maps to NM_030663.2 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr17:18167114 C>T maps to NM_148886.1 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:18167642 C>T maps to NM_148886.1 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:18167216 C>T maps to NM_148886.1 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:18167900 C>T maps to NM_148886.1 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr22:39909778 C>T maps to NM_019008.4 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:39908020 C>T maps to NM_019008.4 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr22:39907867 G>T maps to NM_019008.4 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr22:39910159 C>T maps to NM_019008.4 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:18219177 C>T maps to NM_144775.2 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:18220689 C>T maps to NM_144775.2 I529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:55826001 G>A maps to NM_001122964.1 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:55792096 G>A maps to NM_001122964.1 F672F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:55785910 C>T maps to NM_001122964.1 K818K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:18845579 G>A maps to ENST00000389467 P2837P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr16:18823441 C>A maps to ENST00000389467 R3544R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:18851079 G>A maps to ENST00000389467 L2295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr16:18823443 G>T maps to ENST00000389467 R3544R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr16:18828729 G>A maps to ENST00000389467 A3320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr1:156233338 C>T maps to NM_015327.2 S626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:156247023 G>A maps to NM_015327.2 H102H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr1:156236055 G>A maps to NM_015327.2 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:156222767 G>A maps to NM_015327.2 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:156237363 C>T maps to NM_015327.2 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:2075960 G>A maps to NM_017575.4 T1116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:2186921 C>T maps to NM_017575.4 R815R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:2203842 G>A maps to NM_017575.4 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:2090051 C>T maps to NM_017575.4 K1020K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr17:2202765 G>A maps to NM_017575.4 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr17:1968968 G>A maps to NM_017575.4 I1280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr17:2203326 G>A maps to NM_017575.4 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:183514305 C>T maps to ENST00000367537 P740P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:183515120 C>T maps to ENST00000367537 S794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:183498583 T>C maps to ENST00000367537 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:183521047 C>T maps to ENST00000367537 T1179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:128851576 C>T maps to NM_005631.4 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:128851577 C>T maps to NM_005631.4 Q635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:128846131 G>A maps to NM_005631.4 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr7:128850260 G>A maps to NM_005631.4 E508E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:128846077 C>T maps to NM_005631.4 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr14:70418949 C>T maps to NM_001034852.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr14:70418997 G>A maps to NM_001034852.1 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr14:70478207 G>A maps to NM_001034852.1 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:70461137 G>A maps to NM_001034852.1 W202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:70461187 A>C maps to NM_001034852.1 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:70489976 C>T maps to NM_001034852.1 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr14:70420161 G>A maps to NM_001034852.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr14:70420176 C>T maps to NM_001034852.1 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr14:70490066 G>A maps to NM_001034852.1 K398K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr14:70459158 G>A maps to NM_001034852.1 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:70420230 G>A maps to NM_001034852.1 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr6:168927077 G>A maps to NM_022138.2 K103K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:169008848 G>A maps to NM_022138.2 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:168947778 C>T maps to NM_022138.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:168927050 G>A maps to NM_022138.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:168947784 C>T maps to NM_022138.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr20:4162475 C>T maps to ENST00000443211 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr20:4168038 C>T maps to ENST00000443211 F581F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:4162830 C>T maps to ENST00000443211 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:6415774 C>T maps to NM_000543.4 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:6414573 G>A maps to NM_000543.4 W407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:6415809 C>T maps to NM_000543.4 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:109763177 G>T maps to NM_003080.2 G76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr16:68405280 C>T maps to NM_018667.3 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr16:68404908 G>A maps to NM_018667.3 Y392Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:68405553 G>A maps to NM_018667.3 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr16:68405013 C>T maps to NM_018667.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:68405115 G>A maps to NM_018667.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr16:68405628 C>T maps to NM_018667.3 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:68405007 G>A maps to NM_018667.3 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr16:68398947 G>A maps to NM_018667.3 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr16:68405049 G>A maps to NM_018667.3 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr16:68405895 G>A maps to NM_018667.3 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr16:68405850 C>T maps to NM_018667.3 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:68405280 C>T maps to NM_018667.3 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:68405286 C>T maps to NM_018667.3 Q266Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr16:68405877 G>A maps to NM_018667.3 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:130910666 G>A maps to NM_017951.4 I740I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr2:130929995 G>A maps to NM_017951.4 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:130914229 G>A maps to NM_017951.4 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:130912693 G>A maps to NM_017951.4 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:130910936 G>A maps to NM_017951.4 I699I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:130911457 G>A maps to NM_017951.4 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:130911969 G>A maps to NM_017951.4 F552F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:28285117 G>A maps to NM_014474.2 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:28282349 C>T maps to NM_014474.2 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:28282463 C>T maps to NM_014474.2 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:28285021 G>A maps to NM_014474.2 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:28285051 C>T maps to NM_014474.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:21761902 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:21761933 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:21761898 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr4:71232662 C>T maps to NM_012390.3 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:71232542 C>T maps to NM_012390.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:71232464 C>T maps to NM_012390.3 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:71232488 G>A maps to NM_012390.3 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr4:71255501 C>T maps to NM_006685.3 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr4:71255501 C>T maps to NM_006685.3 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:21997081 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:22002441 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:22010803 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:21996171 A>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:21985354 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:21996130 G>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:21995221 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:21996106 C>G did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr22:31486980 C>T maps to ENST00000454496 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:31486824 C>T maps to ENST00000454496 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr22:31493303 C>T maps to ENST00000454496 S798S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr22:31486980 C>T maps to ENST00000454496 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:31484000 C>T maps to ENST00000454496 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr22:31487241 C>T maps to ENST00000454496 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr11:57310132 G>A maps to ENST00000457912 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:57310519 G>A maps to ENST00000457912 E153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:57313407 G>A maps to ENST00000457912 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr11:57317530 G>A maps to ENST00000457912 Q495Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:57310660 G>A maps to ENST00000457912 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:57310132 G>A maps to ENST00000457912 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:4500471 G>A maps to NM_001114974.1 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:33076600 C>A maps to NM_018225.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:33048157 G>A maps to NM_018225.2 D463D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:54577460 A>C maps to NM_014311.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr7:98645494 G>A maps to NM_020429.2 Q348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:98643358 G>A maps to NM_020429.2 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:62579627 G>A maps to NM_022739.3 Q174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr17:62553785 G>A maps to NM_022739.3 F457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:88393053 C>T maps to NM_198274.3 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr2:88367502 C>T maps to NM_198274.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr2:88408039 C>T maps to NM_198274.3 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:88384002 G>A maps to NM_198274.3 E102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:88390634 C>T maps to NM_198274.3 N211N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:88390601 C>T maps to NM_198274.3 N200N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:88405848 G>A maps to NM_198274.3 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr2:88387407 G>A maps to NM_198274.3 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:88383987 G>A maps to NM_198274.3 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:88402626 G>A maps to NM_198274.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:88396128 C>T maps to NM_198274.3 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:214491426 C>T maps to NM_020197.2 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:214454716 C>T maps to NM_020197.2 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:214504345 C>T maps to NM_020197.2 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr1:246498674 G>A maps to NM_001167740.1 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr1:245927408 C>T maps to NM_001167740.1 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr1:246091331 G>A maps to NM_001167740.1 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:246078852 G>A maps to NM_001167740.1 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:245927441 G>A maps to NM_001167740.1 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:246027152 C>T maps to NM_001167740.1 W283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:246021952 G>T maps to NM_001167740.1 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:245912888 G>A maps to NM_001167740.1 C421C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:1686345 G>A maps to NM_052928.2 A748A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:1715305 G>A maps to NM_052928.2 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr17:1686375 A>G maps to NM_052928.2 V738V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr2:73446017 C>T maps to NM_006062.2 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr2:73449885 C>T maps to NM_006062.2 Q216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:73446038 C>T maps to NM_006062.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:73449920 C>T maps to NM_006062.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr8:49832488 G>A maps to NM_003068.3 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr8:49831425 G>A maps to NM_003068.3 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:49833767 G>A maps to NM_003068.3 Y19Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr16:88747754 G>A maps to NM_178310.3 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr16:88747684 G>A maps to NM_178310.3 Q172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr16:88747883 G>A maps to NM_178310.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:10273629 C>T maps to NM_003081.2 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:227947070 C>T maps to NM_053052.3 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:227935397 G>A maps to NM_053052.3 Q32Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:227968361 G>A maps to NM_053052.3 K461K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr1:227947010 G>A maps to NM_053052.3 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:227935647 C>T maps to NM_053052.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:227947187 T>C did not map to a codon.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr6:84292058 G>A maps to NM_014841.2 F677F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr6:84371228 C>T maps to NM_014841.2 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:84302255 C>T maps to NM_014841.2 V616V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr6:84284812 C>T maps to NM_014841.2 E786E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:84284827 C>T maps to NM_014841.2 Q781Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr6:84292024 G>A maps to NM_014841.2 Q689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:84292058 G>A maps to NM_014841.2 F677F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:84371228 C>T maps to NM_014841.2 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:84366584 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr19:7986930 C>T maps to NM_003083.3 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr19:7987026 G>A maps to NM_003083.3 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:7987170 G>A maps to NM_003083.3 K208K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr9:139272465 C>T maps to NM_003086.2 L1271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:139275290 G>A maps to NM_003086.2 I800I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr9:139272678 G>A maps to NM_003086.2 P1200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:139286444 G>A maps to NM_003086.2 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:139283018 G>A maps to NM_003086.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr9:139272357 G>A maps to NM_003086.2 A1307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr9:139290162 G>A maps to NM_003086.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:90647781 G>A maps to NM_001146055.1 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr5:121759070 G>A maps to ENST00000379533 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr5:121786527 G>A maps to ENST00000379533 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:121780310 G>A maps to ENST00000379533 K539K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr5:121761123 G>A maps to ENST00000379533 Q407Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr5:121787007 G>A maps to ENST00000379533 V869V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr5:121758665 G>A maps to ENST00000379533 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:121758578 G>A maps to ENST00000379533 W96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr5:121787061 G>A maps to ENST00000379533 K887K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr5:121759070 G>A maps to ENST00000379533 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:121787121 T>A maps to ENST00000379533 P907P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr5:121780262 G>A maps to ENST00000379533 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:121739510 G>A maps to ENST00000379533 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:121786521 G>A maps to ENST00000379533 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:121787001 G>A maps to ENST00000379533 E867E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr5:121739510 G>A maps to ENST00000379533 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:121787253 G>A maps to ENST00000379533 K951K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:121786926 C>A maps to ENST00000379533 P842P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr5:121739510 G>A maps to ENST00000379533 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:121759379 G>A maps to ENST00000379533 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:121758650 C>T maps to ENST00000379533 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr5:121780260 T>C maps to ENST00000379533 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:176053762 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:176056598 C>T maps to NM_003085.3 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr10:88718555 G>A maps to NM_003087.2 K34K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:88722410 G>A maps to NM_003087.2 E114E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr7:127326752 T>G maps to NM_014390.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:127341361 C>T maps to NM_014390.2 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:127729644 C>T maps to NM_014390.2 T841T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr7:127344915 C>T maps to NM_014390.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:127714630 C>T maps to NM_014390.2 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q1-06A-21D-A196-08 chr2:242011003 C>T maps to NM_001080437.1 G1201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr2:242007269 C>T maps to NM_001080437.1 T1034T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:242027812 T>G maps to NM_001080437.1 S1413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:241976318 G>A maps to NM_001080437.1 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:242002211 C>T maps to NM_001080437.1 I754I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:242004772 C>T maps to NM_001080437.1 I924I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:241973163 C>T maps to NM_001080437.1 Q172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:38003597 G>A maps to NM_024700.2 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:38005999 A>T maps to NM_024700.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:38005954 G>A maps to NM_024700.2 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A6L9-06A-11D-A32N-08 chr20:1286073 C>T maps to ENST00000381876 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr20:1285659 C>T maps to ENST00000381876 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr20:1281304 C>T maps to ENST00000381876 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:43389844 C>T maps to NM_017719.4 V698V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr3:43381974 C>T maps to NM_017719.4 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:43381974 C>T maps to NM_017719.4 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr3:43389430 C>T maps to NM_017719.4 F560F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr3:43381974 C>T maps to NM_017719.4 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:43388866 C>T maps to NM_017719.4 D372D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:43389193 G>A maps to NM_017719.4 K481K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:96955566 G>A maps to NM_014014.3 V970V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:96963389 G>A maps to NM_014014.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:96957527 G>A maps to NM_014014.3 A757A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr2:96944682 G>A maps to NM_014014.3 D1729D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:96964023 G>T maps to NM_014014.3 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:96964024 G>A maps to NM_014014.3 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr2:96950137 G>A maps to NM_014014.3 L1450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr2:96944040 G>A maps to NM_014014.3 I1848I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:96950134 G>A maps to NM_014014.3 F1451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:96950251 G>A maps to NM_014014.3 T1412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:96967352 C>G maps to NM_014014.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr2:96956090 G>A maps to NM_014014.3 I905I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:96953255 G>A maps to NM_014014.3 L1135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:96952163 G>A maps to NM_014014.3 P1296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:96961309 G>A maps to NM_014014.3 I586I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:96944688 G>A maps to NM_014014.3 H1727H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr2:70130360 C>T maps to NM_006857.1 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr2:70122295 G>A maps to NM_006857.1 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:123950398 C>G maps to NM_180699.2 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:123950371 C>T maps to NM_180699.2 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr1:31769574 C>T maps to ENST00000446633 K8K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:31754331 G>A maps to ENST00000446633 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:31762187 C>T maps to ENST00000446633 K148K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:31744310 G>A maps to ENST00000446633 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr6:7601662 C>T maps to NM_152551.3 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr6:7594067 C>A maps to NM_152551.3 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr19:41269490 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:41269565 C>T maps to NM_004596.4 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:41263306 C>T maps to NM_004596.4 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:41263307 C>T maps to NM_004596.4 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:41265427 C>T maps to NM_004596.4 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:41268891 C>T maps to NM_004596.4 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:2443765 G>A maps to ENST00000339610 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr20:2444464 A>G maps to ENST00000339610 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:2443864 G>A maps to ENST00000339610 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr20:16721489 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr6:34741274 C>T maps to ENST00000374017 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:34738119 C>T maps to ENST00000374017 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:203834232 C>A maps to NM_003094.2 S70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr15:25220560 C>T maps to NM_022805.2 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:25220524 G>A maps to NM_022805.2 K8K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:31996539 A>T maps to NM_003098.2 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:32005577 G>A maps to NM_003098.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr8:121644848 G>A maps to NM_021021.3 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr8:121706062 G>A maps to NM_021021.3 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr8:121587438 C>T maps to NM_021021.3 W341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:121644713 C>T maps to NM_021021.3 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:121823711 C>T maps to NM_021021.3 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr8:51705280 C>T maps to NM_018967.2 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr8:51314859 G>T maps to NM_018967.2 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr8:51571222 G>A maps to NM_018967.2 K346K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr8:51571223 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:51617287 C>T maps to NM_018967.2 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:51415351 G>A maps to NM_018967.2 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr8:51569551 G>A maps to NM_018967.2 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr8:51362268 C>T maps to NM_018967.2 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:51449362 G>A maps to NM_018967.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr2:1079205 G>A maps to NM_018968.3 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr2:1079205 G>A maps to NM_018968.3 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr2:1161239 C>T maps to NM_018968.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:1079205 G>A maps to NM_018968.3 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:1079274 G>A maps to NM_018968.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:1079274 G>A maps to NM_018968.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr2:1251211 T>A maps to NM_018968.3 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:1241661 G>A maps to NM_018968.3 W241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:1079241 C>T maps to NM_018968.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:1093937 G>A maps to NM_018968.3 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:1093938 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:1094082 C>T maps to NM_018968.3 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:1133455 T>C maps to NM_018968.3 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:1161304 T>C maps to NM_018968.3 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr2:1204871 C>T maps to NM_018968.3 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:1271288 C>T maps to NM_018968.3 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:1263173 G>A maps to NM_018968.3 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:1168826 C>T maps to NM_018968.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:1079274 G>A maps to NM_018968.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr2:1271343 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:1079205 G>A maps to NM_018968.3 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:1263152 C>T maps to NM_018968.3 F339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:1263212 G>A maps to NM_018968.3 K359K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr2:1133329 C>T maps to NM_018968.3 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:63638371 C>T maps to NM_001080537.1 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr3:63645455 C>T maps to NM_001080537.1 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:75890737 G>A maps to ENST00000371091 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr15:75890926 G>A maps to ENST00000371091 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:25213132 C>T maps to NM_022804.2 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:25207320 C>T maps to NM_022804.2 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr14:78205404 C>A did not map to a codon.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr15:64418363 G>A maps to NM_003099.3 E199E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr15:64410334 C>T maps to NM_003099.3 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr15:64410325 G>T maps to NM_003099.3 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:64404803 C>T maps to NM_003099.3 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:26404213 C>T maps to ENST00000446848 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:46190721 C>T maps to NM_152244.1 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:46196495 C>T maps to NM_152244.1 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr17:46196338 C>T maps to NM_152244.1 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr17:46198644 T>G maps to NM_152244.1 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:70281764 C>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr23:70281771 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:17915118 G>A maps to ENST00000417048 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr7:17843140 G>A maps to ENST00000417048 S757S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr6:86281875 C>T maps to NM_153816.3 K132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:64800006 C>T maps to NM_013306.4 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr11:64802340 C>T maps to NM_013306.4 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:64799641 C>T maps to NM_013306.4 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr11:64802569 C>T maps to NM_013306.4 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64803080 C>T maps to NM_013306.4 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YX-06A-11D-A197-08 chr8:82714664 C>T maps to NM_152836.2 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr2:27596118 C>T maps to NM_014748.2 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr11:130781575 G>A maps to NM_014758.2 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:130785159 G>A maps to NM_014758.2 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:130784895 G>A maps to NM_014758.2 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:122143970 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr16:50707907 G>A maps to NM_182854.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:50707820 G>A maps to NM_182854.2 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr16:50711413 C>T maps to NM_182854.2 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr16:50709815 C>T maps to NM_182854.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr16:50707820 G>A maps to NM_182854.2 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr16:50711341 G>A maps to NM_182854.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr16:50707514 C>T maps to NM_182854.2 E251E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:50707820 G>A maps to NM_182854.2 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr5:122343404 C>T maps to ENST00000395451 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr4:186272750 C>T maps to NM_031953.2 F654F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:151630868 C>A maps to ENST00000458013 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr1:151641026 G>A maps to ENST00000458013 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr16:12618695 C>T maps to NM_001080530.2 F387F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:12618695 C>T maps to NM_001080530.2 F387F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr9:115593150 C>T maps to NM_001012994.1 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:115580004 C>T maps to NM_001012994.1 D123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:101601093 C>T maps to NM_152628.3 Q364Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:101586158 T>C maps to NM_152628.3 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:101601143 G>A maps to NM_152628.3 Q348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:101608911 G>A maps to NM_152628.3 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:101609052 C>T maps to NM_152628.3 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:65617688 G>A maps to NM_152760.2 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr11:65618238 G>A maps to NM_152760.2 K172K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr11:65617483 G>T maps to NM_152760.2 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:65618232 G>C maps to NM_152760.2 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr15:75942336 C>T maps to NM_153271.1 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr15:75942804 G>A maps to NM_153271.1 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr15:75941868 C>T maps to NM_153271.1 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:75941880 C>T maps to NM_153271.1 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr20:17934737 G>A maps to NM_152227.1 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr20:17923791 G>A maps to NM_152227.1 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:17934725 A>G maps to NM_152227.1 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr20:17923825 G>A maps to NM_152227.1 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr14:35077235 G>A maps to NM_152233.2 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr14:35072580 G>A maps to NM_152233.2 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:2296550 G>A maps to NM_013321.2 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:2304087 G>A maps to NM_013321.2 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:2302894 G>A maps to NM_013321.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:2297375 G>A maps to NM_013321.2 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:2297429 C>T maps to NM_013321.2 Q308Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:2302929 G>A maps to NM_013321.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:2302894 G>A maps to NM_013321.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr6:158353275 C>T maps to NM_016224.3 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr6:158294153 G>A maps to NM_016224.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr6:158349732 C>T maps to NM_016224.3 G429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:179304711 G>A maps to NM_003101.4 K83K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr12:53509921 T>A maps to NM_003578.3 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr12:53517623 G>A maps to NM_003578.3 E495E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:53499365 G>A maps to NM_003578.3 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:53515094 G>A maps to NM_003578.3 W382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:53516947 C>T maps to NM_003578.3 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr12:53516962 C>T maps to NM_003578.3 F445F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:107954977 G>A maps to NM_018013.3 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:107955661 C>T maps to NM_018013.3 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:11348858 G>A maps to NM_003745.1 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:93968783 C>T maps to NM_003877.3 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:93968855 C>T maps to NM_003877.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr17:76354552 G>A maps to NM_003955.3 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:76354882 C>T maps to NM_003955.3 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr17:76354759 T>A maps to NM_003955.3 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr17:76354747 G>A maps to NM_003955.3 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:46986116 C>T maps to NM_144949.2 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:46985926 C>T maps to NM_144949.2 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr18:67993349 T>C maps to NM_004232.3 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr18:67992405 C>T maps to NM_004232.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:36521281 C>T maps to NM_014598.2 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr4:24801433 C>T maps to NM_003102.2 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:138588461 G>A maps to NM_001101677.1 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:138590848 C>T maps to NM_001101677.1 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:138587047 G>A maps to NM_001101677.1 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr9:138586221 G>A maps to NM_001012415.2 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr13:36764132 C>T maps to ENST00000511166 E274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr13:36776215 G>A maps to ENST00000511166 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr13:36748900 C>T maps to ENST00000511166 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr13:36748879 G>A maps to ENST00000511166 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr13:36776167 C>T maps to ENST00000511166 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:36776041 C>T maps to ENST00000511166 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr16:597653 G>A maps to NM_005632.2 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr16:602522 C>T maps to NM_005632.2 A910A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:596993 C>T maps to NM_005632.2 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:598007 C>T maps to NM_005632.2 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:601379 C>T maps to NM_005632.2 P715P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr16:597449 C>T maps to NM_005632.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr21:34926483 T>G maps to NM_138927.1 G1649G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr21:34922670 C>T maps to NM_138927.1 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr21:34945678 C>G maps to NM_138927.1 G2317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr21:34923546 G>A maps to NM_138927.1 S670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr21:34927500 T>C maps to NM_138927.1 P1988P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26D-06A-11D-A19A-08 chr21:34923345 T>C maps to NM_138927.1 A603A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:97078131 G>A maps to NM_001034954.1 L1252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:97096856 G>A maps to NM_001034954.1 H1020H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr10:97096853 G>A maps to NM_001034954.1 L1021L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:97192280 G>A maps to NM_001034954.1 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr4:186545031 G>A maps to ENST00000355634 F613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr4:186545427 G>A maps to ENST00000355634 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:186545031 G>A maps to ENST00000355634 F613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:186544449 C>T maps to ENST00000355634 R807R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:186545076 C>T maps to ENST00000355634 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr4:186545433 G>A maps to ENST00000355634 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr4:186545538 G>A maps to ENST00000355634 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr4:186545619 G>A maps to ENST00000355634 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZH-06A-11D-A197-08 chr4:186545334 C>T maps to ENST00000355634 E512E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:186545031 G>A maps to ENST00000355634 F613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:186545532 C>T maps to ENST00000355634 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr8:22429259 C>T maps to NM_005775.4 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:22424681 T>G maps to NM_005775.4 Y433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:22429331 C>T maps to NM_005775.4 T615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr8:22414246 C>T maps to NM_005775.4 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr10:108389026 G>A maps to NM_001013031.1 F865F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:108536384 A>C maps to NM_001013031.1 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr10:108338906 C>T maps to NM_001013031.1 Q1158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:108339230 G>A maps to NM_001013031.1 A1089A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:108339002 G>A maps to NM_001013031.1 I1126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:108377997 G>A maps to NM_001013031.1 F943F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:108389017 G>A maps to NM_001013031.1 T868T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr10:108469040 A>T maps to NM_001013031.1 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr4:7666116 C>T maps to NM_020777.2 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr4:7731379 C>T maps to NM_020777.2 L1017L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr4:7684477 G>A maps to NM_020777.2 G450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr4:7726902 G>A maps to NM_020777.2 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:7730137 C>T maps to NM_020777.2 T977T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr4:7736083 C>T maps to NM_020777.2 I1098I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr4:7705053 G>A maps to NM_020777.2 V572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:7714546 G>A maps to NM_020777.2 E652E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr10:106924129 G>A maps to NM_014978.1 W601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr10:106924130 G>A maps to NM_014978.1 W601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr10:107015512 G>A maps to NM_014978.1 L1097L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr10:106960903 G>A maps to NM_014978.1 R718R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:106737115 G>A maps to NM_014978.1 E273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:106916912 G>A maps to NM_014978.1 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:106916912 G>A maps to NM_014978.1 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:106865233 C>T maps to NM_014978.1 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:106937874 T>A maps to NM_014978.1 V651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr10:107006989 C>T maps to NM_014978.1 S1002S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr10:106737199 C>T maps to NM_014978.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr10:106959777 C>T maps to NM_014978.1 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr10:106960891 C>T maps to NM_014978.1 V714V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr10:106982970 C>T maps to NM_014978.1 T944T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:106959852 G>A maps to NM_014978.1 Q702Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr10:106983006 G>A maps to NM_014978.1 K956K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:106976716 C>T maps to NM_014978.1 I857I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:107005368 C>T maps to NM_014978.1 Q980*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:106974283 C>T maps to NM_014978.1 A820A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:107022244 C>T maps to NM_014978.1 V1200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:106927071 C>T maps to NM_014978.1 A622A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr10:106937898 G>A maps to NM_014978.1 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr10:106976803 G>A maps to NM_014978.1 A886A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr10:106982946 C>T maps to NM_014978.1 V936V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr10:107012636 G>A maps to NM_014978.1 R1070R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:106675689 G>A maps to NM_014978.1 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:106865266 C>T maps to NM_014978.1 F402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:106899193 C>T maps to NM_014978.1 R418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:106917008 G>A maps to NM_014978.1 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:106918651 C>T maps to NM_014978.1 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:106924103 C>T maps to NM_014978.1 F592F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:106970942 C>T maps to NM_014978.1 F770F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:107012558 C>T maps to NM_014978.1 I1044I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr10:107006989 C>T maps to NM_014978.1 S1002S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:106974265 G>A maps to NM_014978.1 Q814Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr10:107015521 G>A maps to NM_014978.1 G1100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr10:106899244 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:45353346 C>T maps to NM_003104.5 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr11:121414376 G>A maps to NM_003105.5 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:121491882 G>A maps to NM_003105.5 G2000G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:121358886 C>T maps to NM_003105.5 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr11:121358739 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:121358778 C>T maps to NM_003105.5 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr11:121348915 C>T maps to NM_003105.5 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr11:121384958 G>A maps to NM_003105.5 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr11:121414406 C>T maps to NM_003105.5 I612I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:121424682 C>T maps to NM_003105.5 S768S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:121428057 C>T maps to NM_003105.5 I869I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr11:121424793 C>T maps to NM_003105.5 S805S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:121491894 C>T maps to NM_003105.5 I2004I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:121348825 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:121498414 C>T maps to NM_003105.5 F2172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr11:121429473 C>T maps to NM_003105.5 I946I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr11:121358778 C>T maps to NM_003105.5 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:121340714 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:121416051 C>T maps to NM_003105.5 T655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:121490577 C>T maps to NM_003105.5 S1947S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:121414295 C>T maps to NM_003105.5 I575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr11:121414376 G>A maps to NM_003105.5 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr11:121393404 C>T maps to NM_003105.5 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:121477908 G>A maps to NM_003105.5 R1692R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:121425921 G>A maps to NM_003105.5 G822G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:121483500 G>A maps to NM_003105.5 R1793R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:121428099 C>T maps to NM_003105.5 L883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:121475025 C>T maps to NM_003105.5 A1548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:121367676 C>T maps to NM_003105.5 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:121428057 C>T maps to NM_003105.5 I869I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:121414343 G>A maps to NM_003105.5 G591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr11:121495831 C>T maps to NM_003105.5 I2070I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr11:121490523 G>A maps to NM_003105.5 P1929P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:121421347 G>A maps to NM_003105.5 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:121384871 C>T maps to NM_003105.5 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr11:121358838 C>T maps to NM_003105.5 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:121358775 G>A maps to NM_003105.5 W188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:121384952 G>A maps to NM_003105.5 E378E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:121391558 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:121414255 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:121414280 C>T maps to NM_003105.5 T570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:121414361 C>T maps to NM_003105.5 F597F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:121428051 C>T maps to NM_003105.5 L867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:121430235 C>T maps to NM_003105.5 I973I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:121485640 G>A maps to NM_003105.5 G1827G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:121492934 G>A maps to NM_003105.5 W2043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:121498411 C>T maps to NM_003105.5 A2171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:121498456 C>T maps to NM_003105.5 F2186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:121393341 C>T maps to NM_003105.5 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:121414292 C>T maps to NM_003105.5 F574F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr1:109870130 G>A maps to NM_002959.4 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:109869672 C>G maps to NM_002959.4 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:109870142 G>T maps to NM_002959.4 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:109883349 G>A maps to NM_002959.4 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:39285888 G>A maps to NM_005633.3 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr2:39234269 G>A maps to NM_005633.3 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr14:50655283 C>T maps to NM_006939.2 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:50626281 A>G maps to NM_006939.2 Y573Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:50600951 G>A maps to NM_006939.2 F988F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:50655307 G>A maps to NM_006939.2 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr14:50619803 G>A maps to NM_006939.2 F715F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:41836019 C>T maps to NM_025237.2 K30K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:16502463 G>A maps to ENST00000396652 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr13:112722184 G>A maps to NM_005986.2 Q71Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr13:112722043 C>T maps to NM_005986.2 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr22:38379616 G>A maps to NM_006941.3 Q59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr22:38369714 G>A maps to NM_006941.3 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr22:38369507 C>T maps to NM_006941.3 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr22:38369840 G>A maps to NM_006941.3 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:5833755 G>A maps to NM_003108.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:5832927 A>G maps to NM_003108.3 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr20:306915 G>A maps to NM_006943.2 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:204085648 C>T maps to ENST00000367206 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:204091517 C>T maps to ENST00000367206 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:204086785 C>T maps to ENST00000367206 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:137483784 G>A maps to NM_004189.2 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr20:62680638 G>A maps to NM_018419.2 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:181431044 G>A maps to NM_003106.2 Q299Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr13:95364221 G>A maps to NM_007084.2 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:139586694 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:139585905 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:139586096 C>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:139586739 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:139586874 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr5:157053482 G>A maps to NM_178424.1 N709N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:157065499 G>A maps to NM_178424.1 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr5:157065566 G>A maps to NM_178424.1 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:157078396 G>C maps to NM_178424.1 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr5:157065623 C>T maps to NM_178424.1 Q498Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:157065458 G>A maps to NM_178424.1 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:21595724 C>T maps to NM_003107.2 D320D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr12:23699315 T>A maps to NM_006940.4 K511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr12:23699248 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:23696304 G>A maps to NM_006940.4 V537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:24048855 G>A maps to NM_006940.4 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:16119220 G>A maps to NM_001145819.1 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:16071319 C>T maps to NM_001145819.1 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:16340163 G>A maps to NM_001145819.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr11:16036518 G>A maps to NM_001145819.1 V580V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:16071293 C>T maps to ENST00000352083 W453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:16071334 G>A maps to NM_001145819.1 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr11:16119234 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:10583913 G>A maps to ENST00000354846 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:70118997 G>A maps to NM_000346.3 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:53803250 T>C maps to NM_138473.2 H650H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:53775536 C>T maps to NM_138473.2 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr2:231331028 C>T maps to NM_001080391.1 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:231380222 T>G maps to NM_003113.3 Y836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr2:231380003 C>T maps to NM_003113.3 F763F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:231404076 C>T maps to NM_001080391.1 I730I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:231379973 C>T maps to NM_003113.3 I753I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:231036811 C>T maps to NM_080424.2 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:231067393 G>A maps to NM_080424.2 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:231036435 G>A maps to NM_080424.2 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:231102933 C>T maps to NM_007237.4 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:231159023 G>A maps to NM_007237.4 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr2:231155211 G>A maps to NM_007237.4 K586K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr2:231109742 G>A maps to NM_007237.4 K204K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr2:231155262 G>A maps to NM_007237.4 K603K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:231101812 C>T maps to NM_007237.4 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr2:231109749 G>T maps to NM_007237.4 G207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:231108485 G>T maps to NM_007237.4 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:231102956 C>T maps to NM_007237.4 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:231152661 G>A maps to NM_007237.4 Q567Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:231103040 G>A maps to NM_007237.4 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:231158984 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:231102933 C>T maps to NM_007237.4 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:231159023 G>A maps to NM_007237.4 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr2:231109787 T>G maps to NM_007237.4 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:231106163 T>G maps to NM_007237.4 L151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:231109736 C>T maps to NM_007237.4 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:231115756 C>T maps to NM_007237.4 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:231150512 G>A maps to NM_007237.4 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr2:231162143 G>A maps to NM_007237.4 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:231256844 C>T maps to NM_138402.4 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr2:231222633 C>T maps to NM_138402.4 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:231222633 C>T maps to NM_138402.4 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:231256844 C>T maps to NM_138402.4 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:231222633 C>T maps to NM_138402.4 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:231222520 C>T maps to NM_138402.4 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:231249969 G>A maps to NM_138402.4 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:231264924 G>A maps to NM_138402.4 E427E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:46002881 C>T maps to NM_003110.5 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:45994183 G>A maps to NM_003110.5 K249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:174820666 A>G maps to NM_003111.4 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr7:21516878 C>T maps to NM_003112.3 R621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:21469371 C>T maps to NM_003112.3 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr17:45925171 C>T maps to NM_199262.2 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr17:45925189 C>T maps to NM_199262.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:53722076 G>A maps to NM_001173467.1 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr12:53722749 C>T maps to NM_001173467.1 W159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:20825372 G>A maps to NM_182700.4 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr11:124545171 A>G maps to NM_017425.3 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:124545174 C>T maps to NM_017425.3 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr6:88773911 T>C maps to NM_030960.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr6:88768506 C>T maps to NM_030960.2 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr6:88757814 G>A maps to NM_030960.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:31324750 C>T maps to NM_173847.3 C201C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:49110474 G>A maps to NM_133498.2 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr8:101252999 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr8:101232633 C>T maps to NM_003114.3 Q555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:7308310 C>T maps to NM_058201.2 W109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr8:7308671 C>T maps to NM_016512.3 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr8:7320367 G>A maps to NM_058201.2 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr2:214878743 C>T maps to NM_024532.3 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:214972960 C>T maps to NM_024532.3 I523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr2:214794731 G>A maps to NM_024532.3 W421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:214794827 C>T maps to NM_024532.3 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:118558587 C>T maps to NM_206996.2 T1429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:118629341 G>A maps to NM_206996.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:118537049 C>T maps to NM_206996.2 W1719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:118629607 G>A maps to NM_206996.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr1:118624179 C>T maps to NM_206996.2 G616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr1:118584659 C>T maps to NM_206996.2 W940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr1:118539225 G>A maps to NM_206996.2 V1639V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:118509304 C>T maps to NM_206996.2 K2153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:118567965 G>A maps to NM_206996.2 H1268H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:118535127 T>G maps to NM_206996.2 I1774I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:118624092 C>T maps to NM_206996.2 Q645Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr1:118598527 C>T maps to NM_206996.2 L850L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:118558674 T>A maps to NM_206996.2 G1400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:118534049 G>A maps to NM_206996.2 L1821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:118548078 C>T maps to NM_206996.2 E1578E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:118565957 C>T maps to NM_206996.2 T1346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:118623748 C>T maps to NM_206996.2 K728K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:118516143 G>A maps to NM_206996.2 S2015S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:118583457 C>A maps to NM_206996.2 G1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:118624212 C>T maps to NM_206996.2 E605E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:118570915 G>A maps to NM_206996.2 F1237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:118558686 G>A maps to NM_206996.2 T1396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:118628632 C>T maps to NM_206996.2 W558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:118523896 A>T maps to NM_206996.2 P2000P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:118629580 G>A maps to NM_206996.2 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:118537121 G>A maps to NM_206996.2 F1695F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:118581975 C>T maps to NM_206996.2 E1086E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr1:118523995 C>T maps to NM_206996.2 Q1967Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr1:118550789 C>T maps to NM_206996.2 V1488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr1:118534049 G>T maps to NM_206996.2 L1821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr1:118567962 A>C maps to NM_206996.2 Y1269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:118539273 G>A maps to NM_206996.2 S1623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:118539255 C>T maps to NM_206996.2 K1629K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr1:118550792 C>T maps to NM_206996.2 Q1487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:118567983 G>A maps to NM_206996.2 Y1262Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:118629335 C>T maps to NM_206996.2 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:118657992 C>T maps to NM_206996.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:118598419 C>T maps to NM_206996.2 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:34208850 G>A maps to NM_003116.1 W407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:34206879 G>A maps to NM_003116.1 E251E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:26906831 A>G maps to NM_006461.3 L941L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:26910555 G>A maps to NM_006461.3 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr10:22680665 C>T maps to ENST00000376603 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr10:22700093 G>A maps to ENST00000376603 E559E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr10:22690106 G>A maps to ENST00000376603 K481K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr10:22653926 T>A maps to ENST00000376603 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:22676876 G>A maps to ENST00000376603 K344K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:4863177 G>A maps to NM_004890.2 Q151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:4863767 G>A maps to NM_004890.2 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:4864137 G>A maps to NM_004890.2 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr9:35811379 C>T maps to NM_001039592.1 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:35811391 G>A maps to NM_001039592.1 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr9:35811979 G>A maps to NM_001039592.1 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:49197822 G>A maps to ENST00000376407 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:49052261 G>A maps to ENST00000376407 I1191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr7:123594214 G>A maps to NM_001174046.1 K197K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:123593704 C>T maps to NM_001174046.1 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:123599722 G>A maps to NM_001174046.1 E410E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:123593836 C>T maps to NM_001174046.1 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:123594481 C>T maps to NM_001174046.1 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:123594487 T>G maps to NM_001174046.1 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:123594220 C>T maps to NM_001174046.1 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:123599998 C>T maps to NM_001174046.1 I502I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:123593842 C>T maps to NM_001174046.1 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:123594568 C>T maps to NM_001174046.1 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr7:123593737 C>T maps to NM_001174046.1 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr7:123593965 C>T maps to NM_001174046.1 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:123593737 C>T maps to NM_001174046.1 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:123594270 G>A maps to NM_001174046.1 W216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:123599965 C>T maps to NM_001174046.1 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:123599974 C>T maps to NM_001174046.1 F494F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr7:123594118 G>A maps to NM_001174046.1 K165K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:123599578 G>A maps to NM_001174046.1 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:123594007 G>A maps to NM_001174046.1 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:123594433 T>A maps to NM_001174046.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:140335735 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:140335747 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:140336563 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:140335799 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:140335766 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:140785719 C>T did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:140785719 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:140786536 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr23:140785800 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:140785707 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:140785711 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:140785744 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:140785747 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:140785744 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:140785650 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:144337234 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:144329144 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr23:142795560 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr23:142795379 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:142795503 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr23:142795397 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:142795240 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:142795188 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:142795214 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:142795543 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr23:142795494 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:142795382 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr23:142795151 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr23:142803706 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:142795201 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr23:142795240 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr23:142795318 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:142795251 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:142795340 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:142795590 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:142795592 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:142795418 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:142795458 G>A did not map to a codon.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr23:142795147 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr23:142596952 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:142596839 G>A did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:142596802 T>C did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:142596643 C>T did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:142596927 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr23:142596749 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:142605202 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:142596788 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:142605189 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:142596794 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:142605208 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:142596668 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:142605180 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:142596706 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:142596738 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr23:142596669 A>T did not map to a codon.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr23:52825607 C>T did not map to a codon.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr23:52825664 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:52825550 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:52825637 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:52826357 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr23:52825637 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:52825649 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:52826349 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:52825617 C>T did not map to a codon.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr23:52825575 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr23:52826384 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:52826359 C>G did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:88411473 C>T maps to NM_004684.4 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr4:88416265 A>T maps to NM_004684.4 L23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:88401666 C>T maps to NM_004684.4 K558K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:88411452 G>T maps to NM_004684.4 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:32352052 T>C maps to NM_014946.3 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr2:32368402 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr13:24876757 C>T maps to ENST00000424834 A1264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:24823823 C>T maps to ENST00000424834 D658D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:24861027 C>T maps to ENST00000424834 V906V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr13:24864926 C>T maps to ENST00000424834 I1032I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr3:172674551 C>T maps to NM_031955.5 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:172834996 C>T maps to NM_031955.5 W175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:172835236 C>T maps to NM_031955.5 K95K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr3:172607419 C>T maps to NM_031955.5 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr3:172694841 C>T maps to NM_031955.5 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:172835107 C>T maps to NM_031955.5 E138E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:172835377 C>T maps to NM_031955.5 K48K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:172674506 G>A maps to NM_031955.5 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:218036174 A>G maps to NM_138796.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:217955520 C>T maps to NM_138796.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:217856628 T>A maps to NM_138796.2 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr1:217947740 G>A maps to NM_138796.2 K195K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:217856676 C>T maps to NM_138796.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:217915316 G>A maps to NM_138796.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr1:217915407 C>T maps to NM_138796.2 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:217947878 G>A maps to NM_138796.2 Q241Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr1:217947743 A>G maps to NM_138796.2 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:52926997 C>T maps to NM_145263.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:52945032 C>T maps to NM_145263.2 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr4:52945914 G>A maps to NM_145263.2 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr4:52927008 C>T maps to NM_145263.2 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:52943112 C>T maps to NM_145263.2 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr4:52928426 G>A maps to NM_145263.2 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:52943175 C>T maps to NM_145263.2 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:52945986 C>T maps to NM_145263.2 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:133712401 G>A maps to NM_174927.1 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:133714481 A>G maps to NM_174927.1 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:48522671 C>T maps to NM_006038.3 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr17:48628142 C>T maps to NM_022827.2 Y416Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:48629524 C>T maps to NM_022827.2 P647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:48628456 G>A maps to NM_022827.2 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:48631789 C>T maps to NM_022827.2 A712A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:48631790 C>T maps to NM_022827.2 Q713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr17:48632648 C>T maps to NM_022827.2 V738V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:48631612 C>T maps to NM_022827.2 D653D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:48626510 C>T maps to NM_022827.2 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:48628956 C>T maps to NM_022827.2 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:48627928 C>A maps to NM_022827.2 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr17:48626276 C>T maps to NM_022827.2 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr17:48628175 C>T maps to NM_022827.2 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:48626318 C>T maps to NM_022827.2 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr17:48632594 C>T maps to NM_022827.2 I720I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:16736208 G>A maps to NM_198546.1 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:16736382 C>T maps to NM_198546.1 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:16736304 G>A maps to NM_198546.1 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:16748443 G>A maps to NM_198546.1 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:16735649 C>T maps to NM_198546.1 E212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:16736517 C>T maps to NM_198546.1 E55E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:89763813 G>A maps to NM_152339.3 A401A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr4:177113928 A>G maps to NM_144644.2 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr4:124235122 C>T maps to NM_145207.2 F862F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:123859364 T>C maps to NM_145207.2 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr4:124235189 C>T maps to NM_145207.2 Q885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:123855399 C>T maps to NM_145207.2 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr4:123868581 G>A maps to NM_145207.2 Q551Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr15:45694680 C>T maps to NM_024063.2 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr15:45706920 G>A maps to NM_024063.2 V529V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:45695523 C>T maps to NM_024063.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr15:45706828 A>T maps to NM_024063.2 K499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:48865301 G>A maps to NM_019073.2 Y167Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:48865251 G>C maps to NM_019073.2 S184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:48877183 G>A maps to NM_019073.2 H119H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:48865076 C>G maps to NM_019073.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr1:48861027 T>C did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:88893048 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:88904667 C>T maps to NM_018418.4 Q568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:88892805 A>G maps to NM_018418.4 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr14:88904657 C>T maps to NM_018418.4 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr14:88895798 C>T maps to NM_018418.4 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr14:88892793 C>T maps to NM_018418.4 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr15:97328250 C>T maps to NM_173499.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:97328247 G>A maps to NM_173499.3 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr15:97328296 C>T maps to NM_173499.3 Q90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr15:97328247 G>A maps to NM_173499.3 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:97328320 C>T maps to NM_173499.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:95011279 G>A maps to NM_031952.3 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:94994440 C>T maps to NM_031952.3 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:145095469 C>T maps to NM_198572.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:145095065 C>T maps to NM_198572.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:145095478 C>A maps to NM_198572.2 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:145095814 C>T maps to NM_198572.2 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:145094816 C>T maps to NM_198572.2 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr8:145096184 G>A maps to NM_198572.2 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:145094855 C>T maps to NM_198572.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:145095982 C>T maps to NM_198572.2 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr6:44344093 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:49888604 C>T maps to NM_023071.3 Q116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:49919797 C>T maps to NM_023071.3 N466N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr2:169727970 C>T maps to NM_020675.3 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:169732593 G>A maps to NM_020675.3 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr3:52741806 G>A maps to NM_014041.3 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:52741806 G>A maps to NM_014041.3 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:74676881 C>T maps to NM_014752.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr6:34512118 G>A maps to NM_012391.1 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:34508851 C>T maps to NM_012391.1 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr6:34511827 C>T maps to NM_012391.1 E135E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr6:34511860 G>A maps to NM_012391.1 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:34508833 C>T maps to NM_012391.1 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:29063174 C>A maps to NM_182756.3 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr2:29072764 G>A maps to NM_182756.3 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr2:29063267 G>A maps to NM_182756.3 Q261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr11:64940061 C>T maps to NM_001008778.1 Q168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:64938923 C>T maps to NM_001008778.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:64938872 C>T maps to NM_001008778.1 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:64938873 C>T maps to NM_001008778.1 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:44047166 C>T maps to NM_175064.2 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:99905579 G>A maps to NM_001004351.4 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:99917220 G>A maps to NM_001004351.4 E460E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr17:8658917 G>A maps to NM_001128076.1 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:8660619 G>A maps to NM_001128076.1 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:8656700 G>A maps to NM_001128076.1 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:35776357 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr5:35793319 C>T maps to NM_024867.3 F1538F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr5:35740308 C>T maps to NM_024867.3 S1090S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr5:35727870 G>A maps to NM_024867.3 Q1003Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:35654728 C>T maps to NM_024867.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:35705827 C>T maps to NM_024867.3 I861I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:35659284 C>T maps to NM_024867.3 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:35641691 G>A maps to NM_024867.3 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:35727906 G>A maps to NM_024867.3 V1015V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:35806879 G>A maps to NM_024867.3 R1694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:35814618 G>A maps to NM_024867.3 E1811E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:35659300 C>T maps to NM_024867.3 R387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:35641616 C>T maps to NM_024867.3 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:35740049 G>A maps to NM_024867.3 W1031*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr5:35667214 C>T maps to NM_024867.3 F403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr5:35814588 G>A maps to NM_024867.3 R1801R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr5:35793313 G>A maps to NM_024867.3 R1536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:35644626 G>A maps to NM_024867.3 K195K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr5:35774064 G>A maps to NM_024867.3 R1340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr5:35792538 C>T maps to NM_024867.3 T1515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:35759749 G>A maps to NM_024867.3 E1183E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr5:35792478 C>T maps to NM_024867.3 I1495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:35771754 A>G maps to NM_024867.3 E1282E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:35792539 C>T maps to NM_024867.3 Q1516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:35654683 C>T maps to NM_024867.3 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr5:35806837 G>A maps to NM_024867.3 E1680E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr5:35691303 T>C maps to NM_024867.3 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr5:35740048 G>A maps to NM_024867.3 W1031*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr5:35740049 G>A maps to NM_024867.3 W1031*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:35807312 T>C maps to NM_024867.3 F1779F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:35774064 G>A maps to NM_024867.3 R1340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:35691311 G>A maps to NM_024867.3 G566G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr2:220356952 C>T maps to NM_005876.4 F3194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr2:220349084 C>T maps to NM_005876.4 P2300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr2:220346118 C>T maps to NM_005876.4 F1821F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr2:220346119 C>T maps to NM_005876.4 L1822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:220355184 C>T maps to NM_005876.4 F2992F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr2:220334051 C>T maps to NM_005876.4 F1222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:220338337 C>T maps to NM_005876.4 V1420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:220312827 C>T maps to NM_005876.4 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:220342692 C>T maps to NM_005876.4 F1631F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:220355196 C>T maps to NM_005876.4 I2996I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr2:220337661 C>T maps to NM_005876.4 Q1331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:220350098 G>A maps to NM_005876.4 W2547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:220352922 C>T maps to NM_005876.4 P2583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:220354499 C>T maps to NM_005876.4 P2920P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr2:220355283 G>A maps to NM_005876.4 L3025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:220309381 G>A maps to NM_005876.4 E132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:220350092 C>T maps to NM_005876.4 L2545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:220356961 G>A maps to NM_005876.4 K3197K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:220354298 G>A maps to NM_005876.4 Q2853Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr2:220337665 G>A maps to NM_005876.4 W1332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr2:220331917 G>A maps to NM_005876.4 L968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:220333880 G>A maps to NM_005876.4 S1165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:220337665 G>A maps to NM_005876.4 W1332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:220348082 G>A maps to NM_005876.4 G1966G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:220348865 G>A maps to NM_005876.4 K2227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:220348928 C>T maps to NM_005876.4 I2248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:220332070 C>T maps to NM_005876.4 F1019F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr2:220342126 G>A maps to NM_005876.4 A1563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr2:220337673 C>T maps to NM_005876.4 L1335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr2:220338614 G>A maps to NM_005876.4 L1479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:220354499 C>T maps to NM_005876.4 P2920P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr17:7324239 C>T maps to NM_199339.2 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:7324545 C>T maps to NM_199339.2 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:16255608 T>C maps to NM_015001.2 L958L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr1:16257963 C>T maps to NM_015001.2 S1743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:16264443 C>T maps to NM_015001.2 I3549I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:16258958 C>A maps to NM_015001.2 S2075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:16255290 G>A maps to NM_015001.2 R852R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr1:16257609 G>A maps to NM_015001.2 E1625E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:16257459 C>T maps to NM_015001.2 S1575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr1:16258239 C>T maps to NM_015001.2 I1835I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:16255686 G>A maps to NM_015001.2 R984R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:16202811 C>T maps to NM_015001.2 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr1:16265265 G>A maps to NM_015001.2 E3586E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:16259359 C>T maps to NM_015001.2 Q2209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr1:16255329 G>A maps to NM_015001.2 E865E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:16237593 A>G did not map to a codon.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:16245991 C>A maps to NM_015001.2 R539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr1:16261539 G>T maps to NM_015001.2 G2935G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:16258176 G>A maps to NM_015001.2 K1814K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:16262682 C>T maps to NM_015001.2 P3316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:16258975 C>T maps to NM_015001.2 R2081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:16235855 C>T maps to NM_015001.2 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:16256616 C>T maps to NM_015001.2 V1294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:16256941 C>T maps to NM_015001.2 R1403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:16257607 G>T maps to NM_015001.2 E1625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr13:46287651 G>A maps to NM_152719.1 K164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr13:46287906 C>T maps to NM_152719.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr13:46287426 C>T maps to NM_152719.1 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:46287744 C>T maps to NM_152719.1 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr13:46287732 G>A maps to NM_152719.1 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr13:46276944 C>T maps to NM_152719.1 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr13:46287336 C>T maps to NM_152719.1 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr13:46287543 C>T maps to NM_152719.1 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr13:46287703 C>T maps to NM_152719.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr13:46288365 G>A maps to NM_152719.1 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr13:46287345 C>T maps to NM_152719.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:46287519 G>A maps to NM_152719.1 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:46288296 G>A maps to NM_152719.1 E379E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr13:46287414 G>A maps to NM_152719.1 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr13:46287543 C>T maps to NM_152719.1 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:69238673 A>G maps to NM_145658.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:69238781 G>A maps to NM_145658.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr15:44890913 T>C maps to NM_025137.3 R1269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:44903076 G>A maps to NM_025137.3 A1084A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr15:44918537 C>T maps to NM_025137.3 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr15:44898229 A>T maps to NM_025137.3 A1171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:44892687 G>A maps to NM_025137.3 I1221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:44865753 G>A maps to NM_025137.3 Q2066*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr13:36888535 A>G maps to NM_001142294.1 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr13:36909301 A>T maps to NM_001142294.1 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr15:65262490 G>A maps to NM_016630.3 D174D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr16:89603236 C>T maps to NM_199367.1 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:89590483 G>A maps to NM_003119.2 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr16:89598931 C>T maps to NM_003119.2 I404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr16:89597203 G>A maps to NM_003119.2 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr16:89598916 C>T maps to NM_003119.2 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:89619493 C>T maps to NM_003119.2 A629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:89619494 C>T maps to NM_003119.2 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr16:89620244 C>T maps to NM_003119.2 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr19:49131967 G>A maps to NM_020126.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:49132519 C>G maps to NM_020126.3 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr19:49132012 G>A maps to NM_020126.3 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:49132207 C>G maps to NM_020126.3 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:49132705 C>T maps to NM_020126.3 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr2:228884238 C>T maps to NM_001142644.1 W444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr2:228882590 C>T maps to NM_001142644.1 R993R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr2:228884528 G>A maps to NM_001142644.1 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:228882731 C>T maps to NM_001142644.1 A946A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:228883352 C>T maps to NM_001142644.1 K739K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:228883421 C>T maps to NM_001142644.1 V716V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr2:228882590 C>T maps to NM_001142644.1 R993R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr2:228881144 G>A maps to NM_001142644.1 A1475A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:228881600 G>A maps to NM_001142644.1 I1323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:228882731 C>T maps to NM_001142644.1 A946A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr2:228886514 C>T maps to NM_001142644.1 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:228882554 C>T maps to NM_001142644.1 R1005R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:228882626 C>T maps to NM_001142644.1 R981R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:228883064 C>T maps to NM_001142644.1 L835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr2:228882731 C>T maps to NM_001142644.1 A946A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:228882662 C>T maps to NM_001142644.1 L969L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:228883859 G>A maps to NM_001142644.1 V570V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr2:228884207 C>T maps to NM_001142644.1 Q454Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:228882107 C>T maps to NM_001142644.1 K1154K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:228883229 C>T maps to NM_001142644.1 T780T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:228882683 C>T maps to NM_001142644.1 W962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:228883991 C>T maps to NM_001142644.1 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:228884528 G>A maps to NM_001142644.1 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:228881912 C>T maps to NM_001142644.1 W1219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:228882224 A>C maps to NM_001142644.1 S1115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:228884840 A>T maps to NM_001142644.1 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:228882167 C>T maps to NM_001142644.1 V1134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:228884105 G>A maps to NM_001142644.1 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:228883991 C>T maps to NM_001142644.1 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr2:228886514 C>T maps to NM_001142644.1 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:228886514 C>T maps to NM_001142644.1 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:228890177 C>A maps to NM_001142644.1 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:228881726 G>A maps to NM_001142644.1 S1281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr2:228883976 C>T maps to NM_001142644.1 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:228883066 G>A maps to NM_001142644.1 L835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:228882344 C>T maps to NM_001142644.1 W1075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:228882548 C>T maps to NM_001142644.1 T1007T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr2:228846519 G>A maps to NM_001142644.1 F1672F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:228855763 C>T maps to NM_001142644.1 G1637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:228882329 G>A maps to NM_001142644.1 A1080A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:228883544 G>A maps to NM_001142644.1 I675I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr2:228883991 C>T maps to NM_001142644.1 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:228882623 C>T maps to NM_001142644.1 K982K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:228846564 G>A maps to NM_001142644.1 V1657V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:228886514 C>T maps to NM_001142644.1 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:228881213 G>A maps to NM_001142644.1 L1452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:228882608 C>T maps to NM_001142644.1 G987G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:228855856 C>T maps to NM_001142644.1 R1606R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:228884528 G>A maps to NM_001142644.1 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:228886430 C>T maps to NM_001142644.1 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr2:228886616 G>A maps to NM_001142644.1 N169N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr2:228884219 G>A maps to NM_001142644.1 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr2:228884837 C>T maps to NM_001142644.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr2:228886526 C>T maps to NM_001142644.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:228884063 A>G maps to NM_001142644.1 C502C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:228881534 C>T maps to NM_001142644.1 E1345E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:228882167 C>T maps to NM_001142644.1 V1134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:228882731 C>T maps to NM_001142644.1 A946A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:228884216 G>A maps to NM_001142644.1 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:228886490 C>T maps to NM_001142644.1 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:228860229 G>A maps to NM_001142644.1 S1543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:228883438 G>A maps to NM_001142644.1 Q711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:228883655 G>A maps to NM_001142644.1 D638D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:228884333 G>A maps to NM_001142644.1 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:228884798 C>T maps to NM_001142644.1 W257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:47376924 C>T maps to NM_001080547.1 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:47376852 C>T maps to NM_001080547.1 K247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr19:50926221 C>T maps to NM_003121.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:50926860 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr12:101880266 G>A maps to ENST00000299272 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr12:101876614 C>T maps to ENST00000299272 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:101876673 A>G maps to ENST00000299272 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:101880290 C>T maps to ENST00000299272 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:101880302 G>A maps to ENST00000299272 Q167Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr12:101880380 C>T maps to ENST00000299272 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:101880425 G>A maps to ENST00000299272 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:101880267 A>T maps to ENST00000299272 K156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr9:91090125 C>T maps to NM_006717.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:91041468 C>T maps to NM_006717.2 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr9:91077650 C>T maps to NM_006717.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:57162277 G>A did not map to a codon.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr23:57162289 G>A did not map to a codon.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr23:57146321 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:57021157 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:62570691 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:147661794 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr5:147549339 G>A maps to NM_001001325.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:57686734 G>A maps to ENST00000506738 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:33240223 G>A maps to NM_014471.1 W6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:147510859 G>A maps to NM_001127698.1 R1031R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:147449947 G>A maps to NM_001127698.1 K48K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:147486631 G>A maps to NM_001127698.1 R504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:147449989 A>G maps to NM_001127698.1 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr5:147466005 G>A maps to NM_001127698.1 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:147505303 C>T maps to NM_001127698.1 R950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr5:147480126 C>T maps to NM_001127698.1 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:147470748 C>T maps to NM_001127698.1 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:147481402 G>A maps to NM_001127698.1 E454E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:147480075 G>A maps to NM_001127698.1 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:147506638 T>G maps to NM_001127698.1 S1017S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr5:147593498 C>T maps to NM_205841.3 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:147582694 G>A maps to NM_205841.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr5:147594479 A>G maps to NM_205841.3 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:147692066 C>T maps to NM_032566.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:147693682 G>A maps to NM_032566.2 K36K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr5:147719229 G>A maps to NM_001040433.1 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:147716006 G>A maps to NM_001040433.1 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr20:44174434 G>A maps to NM_181502.1 H6H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:44174392 G>A maps to ENST00000396669 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:44171378 G>A maps to ENST00000396669 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr20:44174440 C>T maps to NM_181502.1 K4K. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-GN-A266-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr15:41146658 C>T maps to NM_181642.2 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr15:41146264 C>T maps to NM_181642.2 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr15:41145987 C>T maps to NM_181642.2 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr15:41145987 C>T maps to NM_181642.2 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A6L9-06A-11D-A32N-08 chr15:41148986 C>T maps to NM_181642.2 V468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:41146873 C>T maps to NM_181642.2 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr19:38779790 G>A maps to NM_021102.3 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr19:38782531 C>T maps to NM_021102.3 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr19:38780918 C>T maps to NM_021102.3 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:44352645 C>T maps to NM_178455.1 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr18:12464891 G>C maps to NM_001128626.1 V490V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:12546885 T>C maps to NM_001128626.1 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:89924776 C>T maps to NM_032451.1 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:89924857 C>T maps to NM_032451.1 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr16:89920914 C>T maps to NM_032451.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr16:29675912 C>T maps to NM_003123.3 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr16:28994598 C>T maps to NM_032038.2 Y436Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:28993230 C>T maps to NM_032038.2 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr16:28992875 C>G maps to NM_032038.2 S250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr16:28990564 C>T maps to NM_032038.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:28993230 C>T maps to NM_032038.2 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr16:28986624 C>T maps to NM_032038.2 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr17:4428421 G>A maps to NM_001124758.1 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr17:4435967 C>T maps to NM_001124758.1 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr17:4416545 C>T maps to NM_001124758.1 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:4437102 G>A maps to NM_001124758.1 E433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr17:4356415 C>T maps to NM_182538.4 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr17:4391137 G>A maps to NM_182538.4 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:4348462 G>A maps to NM_182538.4 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr17:4349485 C>T maps to NM_182538.4 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:4391182 G>A maps to NM_182538.4 E511E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:4337324 C>T maps to NM_182538.4 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:4348327 C>T maps to NM_182538.4 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:4356352 G>A maps to NM_182538.4 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:4348366 C>T maps to NM_182538.4 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:4389578 C>T maps to NM_182538.4 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:4389718 C>T maps to NM_182538.4 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr20:55910509 G>A maps to ENST00000371258 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr20:55918435 C>T maps to ENST00000371258 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr1:32280763 C>T maps to NM_144569.4 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:32280508 G>A maps to NM_144569.4 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:32258905 G>A maps to NM_144569.4 V886V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:32256709 G>A maps to NM_144569.4 Q1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:32280742 G>A maps to NM_144569.4 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:32265027 A>G maps to NM_144569.4 R614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:32259352 C>T maps to NM_144569.4 Q843Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:32279989 G>A maps to NM_144569.4 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:32279890 C>T maps to NM_144569.4 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr1:32264051 G>A maps to NM_144569.4 P673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:32279599 G>A maps to NM_144569.4 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr1:32266185 C>T maps to NM_144569.4 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:32259376 C>T maps to NM_144569.4 R835R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:32259442 C>T maps to NM_144569.4 G813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:32280439 C>T maps to NM_144569.4 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr5:136324195 G>A maps to NM_004598.3 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:136324195 G>A maps to NM_004598.3 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr5:136328178 G>A maps to NM_004598.3 Q234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:73822655 G>A maps to NM_014767.2 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr10:73822643 C>T maps to NM_014767.2 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:73822589 C>T maps to NM_014767.2 E401E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr10:73823965 G>A maps to NM_014767.2 Q321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr10:73826741 G>A maps to NM_014767.2 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr10:73822562 C>T maps to NM_014767.2 E410E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr10:73822655 G>A maps to NM_014767.2 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr4:167663151 G>A maps to NM_016950.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:167675731 G>A maps to NM_016950.2 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr4:167663157 C>T maps to NM_016950.2 K331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr4:167675731 G>A maps to NM_016950.2 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:168155140 G>A maps to NM_016950.2 R62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:167675875 G>A maps to NM_016950.2 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:167921567 G>A maps to NM_016950.2 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr4:167658744 G>A maps to NM_016950.2 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:14287091 G>A maps to NM_006108.2 T760T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr11:14284294 G>A maps to NM_006108.2 S677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:14101557 G>A maps to NM_006108.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:14277323 C>T maps to NM_006108.2 I407I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:14101551 C>T maps to NM_006108.2 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr11:14287199 G>A maps to NM_006108.2 K796K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:14101557 G>A maps to NM_006108.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr11:14279388 C>T maps to NM_006108.2 P478P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A3J5-06A-11D-A20D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:14284315 G>A maps to NM_006108.2 G684G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr4:1165155 C>T maps to NM_012445.3 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr17:47684677 G>A maps to NM_003563.3 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr17:47688702 G>A maps to NM_003563.3 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:139326592 A>T maps to NM_001001664.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:139308106 C>T maps to NM_001001664.2 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr4:88903753 G>A maps to NM_001040058.1 W217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr4:88902884 C>T maps to NM_001040058.1 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr4:88902847 C>T maps to NM_001040058.1 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:234969092 C>T maps to NM_006944.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:234959618 C>T maps to NM_006944.2 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:234969092 C>T maps to NM_006944.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:234967583 C>T maps to NM_006944.2 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:51012138 G>A maps to NM_032802.3 Q496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:2351459 C>T maps to NM_152988.2 F460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:2338836 C>T maps to NM_152988.2 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:2334632 C>T maps to NM_152988.2 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:2345249 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr19:2338752 C>T maps to NM_152988.2 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:2345311 C>T maps to NM_152988.2 F445F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr19:2338752 C>T maps to NM_152988.2 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:121206839 G>A maps to NM_139015.3 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:121205251 G>A maps to NM_139015.3 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:121206240 G>A maps to NM_139015.3 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr15:38614473 C>T maps to NM_152594.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr15:38643622 C>T maps to NM_152594.2 Q365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:38641714 C>T maps to NM_152594.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:38641715 C>T maps to NM_152594.2 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:38643765 C>T maps to NM_152594.2 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr2:65540934 C>T maps to NM_181784.2 E319E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:65540703 G>A maps to NM_181784.2 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:65543942 G>A maps to NM_181784.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:65541249 G>A maps to NM_181784.2 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:65541249 G>A maps to NM_181784.2 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr2:65561832 G>A maps to NM_181784.2 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr19:38882850 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:38881043 C>T maps to NM_001042522.1 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr1:152957879 G>A maps to NM_005987.3 Q58Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr1:153004997 C>T maps to NM_003125.2 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:153004922 C>T maps to NM_003125.2 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr1:153012732 C>T maps to NM_006945.4 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:153066137 C>T maps to NM_001024209.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:153066217 G>A maps to NM_001024209.2 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:153085053 C>T maps to NM_001014450.1 Q52Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:152975555 G>A maps to NM_005416.2 Q20Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:152975726 C>T maps to NM_005416.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr1:152975540 G>A maps to NM_005416.2 Q15Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr1:152975747 G>A maps to NM_005416.2 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:152975750 C>T maps to NM_005416.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr1:152975690 C>T maps to NM_005416.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr1:152975750 C>T maps to NM_005416.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr1:152975798 C>T maps to NM_005416.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:152944576 C>T maps to NM_173080.1 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:152944428 G>A maps to NM_173080.1 Q21Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:152944434 G>A maps to NM_173080.1 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:152944416 G>A maps to NM_173080.1 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:152944374 C>T maps to NM_173080.1 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:152944542 C>T maps to NM_173080.1 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:152944533 G>A maps to NM_173080.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr4:124323558 C>T maps to NM_199327.1 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:124323282 C>T maps to NM_199327.1 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr23:155004373 C>T did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:155004001 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:155003686 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:155004260 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:155004344 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr23:155004374 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr23:155004375 C>A did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr23:155003645 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr23:155003646 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr23:155004020 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr23:155004062 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:155003536 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:155004071 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:155004271 C>T did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr23:155003855 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:141694697 G>A maps to NM_030964.3 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr12:53470995 G>A maps to NM_032840.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:53470941 G>A maps to NM_032840.2 Q43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:53470965 G>A maps to NM_032840.2 R35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:53470948 G>A maps to NM_032840.2 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:53461986 G>A maps to NM_032840.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:56863216 G>A maps to NM_207344.3 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:55653011 G>A maps to NM_032681.3 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr11:55653185 G>A maps to NM_032681.3 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr11:55658833 G>A maps to NM_032681.3 W362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:55652969 C>T maps to NM_032681.3 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:9416027 C>T maps to NM_025106.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr1:9416477 C>T maps to NM_025106.3 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr16:1827772 G>A maps to NM_080861.3 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:140785534 C>T maps to NM_080862.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:140785548 C>T maps to NM_080862.1 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:140866078 C>T maps to NM_080862.1 Q264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:158615154 C>T maps to NM_003126.2 E1339E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:158613206 C>T maps to NM_003126.2 K1449K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr1:158617378 C>T maps to NM_003126.2 K1282K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:158632720 G>A maps to NM_003126.2 I745I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:158627412 G>A maps to NM_003126.2 R887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr1:158592976 A>G maps to NM_003126.2 T1972T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr1:158632603 G>A maps to NM_003126.2 T784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:158595956 G>A maps to NM_003126.2 F1963F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:158589112 C>T maps to NM_003126.2 Q2143Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:158617339 G>A maps to NM_003126.2 L1295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:158605764 G>A maps to NM_003126.2 I1790I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:158648240 G>A maps to NM_003126.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:158615103 G>A maps to NM_003126.2 I1356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:158617435 C>T maps to NM_003126.2 Q1263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:158585012 G>A maps to NM_003126.2 Q2261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:158637651 C>T maps to NM_003126.2 Q678Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:158585142 C>T maps to NM_003126.2 V2217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:158609734 C>T maps to NM_003126.2 G1600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:158614042 C>T maps to NM_003126.2 Q1446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:158637816 C>T maps to NM_003126.2 Q623Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:158612322 G>A maps to NM_003126.2 L1539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:158604383 C>T maps to NM_003126.2 K1838K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:158590057 G>A maps to NM_003126.2 Q2107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:158590058 G>A maps to NM_003126.2 D2106D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:158624529 C>T maps to NM_003126.2 Q969Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:158637747 C>T maps to NM_003126.2 E646E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:158612329 C>T maps to NM_003126.2 R1536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:158612260 G>A maps to NM_003126.2 I1559I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:158590153 G>A maps to NM_003126.2 L2075L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:158632566 G>A maps to NM_003126.2 L797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:158639498 C>T maps to NM_003126.2 G559G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:158651328 C>T maps to NM_003126.2 W173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:158622262 G>A maps to NM_003126.2 F1123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:158653283 C>T maps to NM_003126.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:158596767 C>T maps to NM_003126.2 E1898E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:158607857 G>A maps to NM_003126.2 F1718F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:158641234 C>T maps to NM_003126.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr1:158597468 G>A maps to NM_003126.2 V1870V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:158587378 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:158618310 G>A maps to NM_003126.2 P1234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:158624466 G>A maps to NM_003126.2 A990A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:158582657 G>A maps to NM_003126.2 F2361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:158609698 G>A maps to NM_003126.2 F1612F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr1:158596697 A>G maps to NM_003126.2 L1922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:158590250 C>T maps to NM_003126.2 E2042E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr1:158596731 G>T maps to NM_003126.2 T1910T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158581077 G>A maps to NM_003126.2 F2412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158587368 G>A maps to NM_003126.2 L2186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158589026 C>T maps to NM_003126.2 W2172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158607974 G>A maps to NM_003126.2 F1679F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158609380 C>T maps to NM_003126.2 L1657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158609716 G>A maps to NM_003126.2 A1606A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158614084 C>T maps to NM_003126.2 L1432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158618316 G>A maps to NM_003126.2 L1232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158623134 G>A maps to NM_003126.2 F1039F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158627484 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158637663 C>T maps to NM_003126.2 E674E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:158641159 G>A maps to NM_003126.2 A524A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:158632528 G>A maps to NM_003126.2 I809I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:158582687 G>A maps to NM_003126.2 I2351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:158582714 G>A maps to NM_003126.2 F2342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:158606493 C>T maps to NM_003126.2 Q1749Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:158637646 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:158618340 C>T maps to NM_003126.2 R1224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr1:158612244 G>A maps to NM_003126.2 L1565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:158636177 C>T maps to NM_003126.2 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:158637762 C>T maps to NM_003126.2 Q641Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr9:131395597 G>A maps to NM_001130438.2 S2473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr9:131329156 C>T maps to NM_001130438.2 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr9:131329157 C>T maps to NM_001130438.2 Q47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr9:131379951 C>T maps to NM_001130438.2 Y1797Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:131353853 C>T maps to NM_001130438.2 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr9:131370321 A>G maps to NM_001130438.2 E1446E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:131337033 C>T maps to NM_001130438.2 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:131339656 C>T maps to NM_001130438.2 D319D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:131375668 C>T maps to NM_001130438.2 L1685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr14:65239369 G>A maps to ENST00000389723 D1831D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr14:65260292 G>A maps to ENST00000389723 I700I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr14:65269005 T>C maps to ENST00000389723 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr14:65259725 G>A maps to ENST00000389723 V889V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr14:65236379 C>T maps to ENST00000389723 R1959R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr14:65253297 G>A maps to ENST00000389723 Q1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr14:65252633 G>A maps to ENST00000389723 S1203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr14:65262075 G>A maps to ENST00000389723 I545I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr14:65260451 G>A maps to ENST00000389723 F647F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr14:65240021 C>T maps to ENST00000389723 E1702E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr14:65262321 G>A maps to ENST00000389723 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr14:65253757 C>T maps to ENST00000389723 K979K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr14:65239537 C>T maps to ENST00000389723 W1775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr14:65261205 G>A maps to ENST00000389723 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:65260142 G>A maps to ENST00000389723 F750F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr14:65262070 C>T maps to ENST00000389723 W547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr14:65252633 G>A maps to ENST00000389723 S1203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr14:65271707 C>T maps to ENST00000389723 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr14:65266487 G>A maps to ENST00000389723 Y351Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr14:65270480 C>T maps to ENST00000389723 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:65262153 C>T maps to ENST00000389723 E519E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr14:65260424 C>T maps to ENST00000389723 W656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:65239435 C>T maps to ENST00000389723 T1809T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr14:65234494 C>T maps to ENST00000389723 G2039G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:65237847 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:65261236 C>A maps to ENST00000389723 G585G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:65268513 C>T maps to ENST00000389723 W206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr14:65252597 C>T maps to ENST00000389723 E1215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr14:65253508 C>T maps to ENST00000389723 G1062G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr14:65252477 C>T maps to ENST00000389723 L1255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr14:65253160 C>T maps to ENST00000389723 Q1178Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr14:65252492 C>T maps to ENST00000389723 K1250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:65239504 G>A maps to ENST00000389723 L1786L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:65241863 G>A maps to ENST00000389723 V1611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:65245922 G>A maps to ENST00000389723 D1509D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:65253697 C>T maps to ENST00000389723 R999R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:65260193 C>T maps to ENST00000389723 K733K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:65260292 G>A maps to ENST00000389723 I700I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:65263283 G>A maps to ENST00000389723 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:65264470 C>T maps to ENST00000389723 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:65264524 G>A maps to ENST00000389723 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr14:65253735 G>A maps to ENST00000389723 L987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr14:65260220 C>T maps to ENST00000389723 E724E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr14:65240078 C>G maps to ENST00000389723 A1683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:54886355 C>A maps to NM_003128.2 P2103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr2:54885065 C>T maps to NM_003128.2 S2042S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:54845317 T>C maps to NM_003128.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:54858273 C>T maps to NM_003128.2 A1030A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr2:54856481 G>A maps to NM_003128.2 K737K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:54856097 C>T maps to NM_003128.2 I609I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:54872556 C>T maps to NM_003128.2 I1487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr2:54873099 C>T maps to NM_003128.2 S1510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:54856250 C>T maps to NM_003128.2 I660I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:54856571 C>T maps to NM_003128.2 V767V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr2:54891738 C>T maps to NM_003128.2 A2190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:54853329 C>T maps to NM_003128.2 Q535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:54858618 G>A maps to NM_003128.2 Q1145Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr2:54850614 G>A did not map to a codon.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr2:54753597 C>T maps to NM_003128.2 Q15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:66454997 G>A maps to NM_006946.2 L2208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:66481866 G>A maps to NM_006946.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:66475055 G>A maps to NM_006946.2 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr11:66478104 G>A maps to NM_006946.2 Q341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:66455486 T>A maps to NM_006946.2 G2146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:66468094 G>A maps to NM_006946.2 R1159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:66472484 G>A maps to NM_006946.2 A754A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:66468227 C>T maps to NM_006946.2 V1114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr11:66475049 G>A maps to NM_006946.2 N530N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr11:66476447 G>A maps to NM_006946.2 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:66457314 C>T maps to NM_006946.2 G1970G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr11:66457359 C>T maps to NM_006946.2 E1955E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr19:41026058 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr19:41071418 G>A maps to NM_020971.2 Q2002Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:41009897 C>T maps to NM_020971.2 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:41072162 C>T maps to NM_020971.2 S2078S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:41008108 G>A maps to NM_020971.2 W324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr19:41066342 C>A maps to NM_025213.2 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:41072234 G>A maps to NM_020971.2 E2102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr19:41081459 C>T maps to NM_020971.2 S2560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr19:41000806 C>T maps to NM_020971.2 Y197Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:41056226 G>A maps to NM_020971.2 K1556K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr19:41066350 G>A maps to NM_025213.2 W662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:41000802 G>A did not map to a codon.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr19:41078017 G>A maps to NM_020971.2 G2471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:41008107 G>A maps to NM_020971.2 W324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:41008205 C>T maps to NM_020971.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:41010032 G>A maps to NM_020971.2 E553E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:41012156 C>T maps to NM_020971.2 S560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:41040072 G>A maps to NM_020971.2 E1394E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:41062004 G>A maps to NM_020971.2 R1700R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr15:42171477 G>A maps to ENST00000320955 F1054F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr15:42145865 G>A maps to ENST00000320955 T3298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr15:42154372 G>A maps to ENST00000320955 S2501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr15:42185569 C>T maps to ENST00000320955 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr15:42160314 G>A maps to ENST00000320955 L2053L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr15:42147786 G>A maps to ENST00000320955 Q3060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr15:42159819 G>A maps to ENST00000320955 A2076A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:42174340 G>A maps to ENST00000320955 Y750Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:42178053 G>A maps to ENST00000320955 Q467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr15:42178456 C>T maps to ENST00000320955 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr15:42143347 T>A maps to ENST00000320955 K3582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr15:42178456 C>T maps to ENST00000320955 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr15:42158680 C>T maps to ENST00000320955 W2164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr15:42170570 G>A maps to ENST00000320955 L1147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr15:42178129 G>A maps to ENST00000320955 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr15:42172062 C>T did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr15:42149845 C>T maps to ENST00000320955 E2763E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:42166141 G>A maps to ENST00000320955 I1597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr9:94800568 G>A maps to NM_006415.2 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:94800616 G>A maps to NM_006415.2 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:94809924 G>A maps to NM_006415.2 C318C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr14:78063593 G>A maps to NM_004863.2 R88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:78045299 G>A maps to NM_004863.2 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr14:77987880 G>A maps to NM_004863.2 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr14:78021665 C>A maps to NM_004863.2 G385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr20:13029696 C>T maps to NM_018327.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:13145492 G>A maps to NM_018327.2 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr20:13098254 C>T maps to NM_018327.2 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr20:13052902 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr20:13134659 A>G maps to NM_018327.2 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr20:13098185 C>T maps to NM_018327.2 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:13107245 G>A maps to NM_018327.2 V387V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:13107317 C>T maps to NM_018327.2 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:13029642 G>A maps to NM_018327.2 E56E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr20:13098174 C>T maps to NM_018327.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr20:13055014 C>T maps to NM_018327.2 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:13029624 C>T maps to NM_018327.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:13071779 G>A maps to NM_018327.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:13098372 G>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:18636785 C>A maps to NM_194285.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:18637313 G>A maps to NM_194285.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr5:79616183 C>T maps to NM_032567.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:79617098 G>A maps to NM_032567.3 Q355Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:79616891 A>T maps to NM_032567.3 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:79616858 G>A maps to NM_032567.3 Q275Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:79616712 C>T maps to NM_032567.3 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr5:79616894 C>T maps to NM_032567.3 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr5:79616162 C>T maps to NM_032567.3 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr8:126015509 C>T maps to NM_003129.3 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr8:126011773 C>T maps to NM_003129.3 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr15:45965881 G>A maps to NM_021199.2 W179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr15:45981325 C>T maps to NM_021199.2 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr15:45965917 C>T maps to NM_021199.2 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr15:45965899 C>T maps to NM_021199.2 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr15:45981392 C>T maps to NM_021199.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:45968357 G>A maps to NM_021199.2 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr3:142769798 C>T maps to NM_001080415.1 Q855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:142720496 T>C maps to NM_001080415.1 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:142741800 C>T maps to NM_001080415.1 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:45645517 G>A maps to NM_018079.4 I773I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:45829062 G>A maps to NM_018079.4 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:45774701 G>A maps to NM_018079.4 F575F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:45829062 G>A maps to NM_018079.4 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:45778354 G>A maps to NM_018079.4 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:45829062 G>A maps to NM_018079.4 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr20:36022651 C>T maps to ENST00000373558 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:36031724 C>T maps to ENST00000373558 F524F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr20:36022381 C>T maps to ENST00000373558 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr20:36031706 C>T maps to ENST00000373558 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:36030029 G>A maps to ENST00000373558 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr20:36031703 C>T maps to ENST00000373558 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U9-06A-11D-A32N-08 chr20:36028623 T>C maps to ENST00000373558 H328H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr16:30748989 C>T maps to NM_006662.2 L2543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:30721364 C>T maps to NM_006662.2 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:30748521 C>T maps to NM_006662.2 A2387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:30748968 C>T maps to NM_006662.2 I2536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:30744599 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:30740784 C>T maps to NM_006662.2 Q2007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:30740726 C>T maps to NM_006662.2 P1987P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:30736198 C>T maps to NM_006662.2 S1818S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr16:30740880 C>T maps to NM_006662.2 Q2039*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr16:30740726 C>T maps to NM_006662.2 P1987P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:30748992 C>A maps to NM_006662.2 P2544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:30749202 C>T maps to NM_006662.2 G2614G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr16:30748977 A>G maps to NM_006662.2 S2539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:30733926 C>T maps to NM_006662.2 L1250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr16:30732063 C>T maps to NM_006662.2 G1006G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr16:30747893 C>T maps to NM_006662.2 F2319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr16:30749823 C>T maps to NM_006662.2 P2821P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:30724929 C>T maps to NM_006662.2 F797F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr16:30740291 C>T maps to NM_006662.2 S1888S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr16:30747893 C>T maps to NM_006662.2 F2319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr17:36708982 C>T maps to NM_025248.2 G770G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr17:36700075 C>T maps to NM_025248.2 R1133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:36708268 G>A maps to NM_025248.2 F860F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr17:36707394 G>A maps to NM_025248.2 G986G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:76027101 G>A maps to NM_080744.1 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:6633925 C>T maps to NM_001047.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:6652029 C>T maps to NM_001047.2 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr5:6656242 C>T maps to NM_001047.2 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:31754405 G>A maps to NM_000348.3 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:31754398 G>A maps to NM_000348.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr2:31754492 G>A maps to NM_000348.3 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:31754405 G>A maps to NM_000348.3 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:31756537 G>A maps to NM_000348.3 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:31754405 G>A maps to NM_000348.3 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:31754405 G>A maps to NM_000348.3 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:31751289 T>C maps to NM_000348.3 K246K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr4:56230310 C>T maps to NM_024592.3 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:56225557 C>T maps to NM_024592.3 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr17:17719279 G>A maps to NM_001005291.2 A789A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:17721616 G>A maps to NM_001005291.2 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr22:42274096 C>T maps to NM_004599.2 H577H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr22:42293127 C>T maps to NM_004599.2 P856P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr22:42276871 C>T maps to NM_004599.2 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:42296417 C>T maps to NM_004599.2 S941S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr22:42280954 C>T maps to NM_004599.2 I716I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:42263102 C>T maps to NM_004599.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr22:42273333 C>T maps to NM_004599.2 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr22:42263285 T>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr22:42266927 C>T maps to NM_004599.2 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:42289182 C>T maps to NM_004599.2 S757S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:43144298 C>T maps to NM_003131.2 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:43146563 C>T maps to NM_003131.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:43146876 C>T maps to NM_003131.2 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr12:64519839 C>T maps to NM_020762.2 L770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:64521468 C>T maps to NM_020762.2 S835S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:64472793 C>T maps to NM_020762.2 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:64521664 C>T maps to NM_020762.2 P855P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:64521497 T>A maps to NM_020762.2 L845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:206632055 C>T maps to ENST00000414359 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:206634485 C>T maps to ENST00000414359 P902P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr1:206619606 C>T maps to ENST00000414359 G610G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:9068637 G>A maps to NM_014850.2 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:9055491 G>A maps to NM_014850.2 I616I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:9166410 G>A maps to NM_014850.2 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:9027439 G>A maps to NM_014850.2 P1021P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:9032336 C>T maps to NM_014850.2 A915A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:9068637 G>A maps to NM_014850.2 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:9166572 G>A maps to NM_014850.2 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:9055490 G>A maps to NM_014850.2 Q617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:9094803 G>A maps to NM_014850.2 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr3:9034641 G>A maps to NM_014850.2 Q836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:9055473 G>A maps to NM_014850.2 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr3:9027472 G>A maps to NM_014850.2 A1010A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr3:9032285 G>A maps to NM_014850.2 S932S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:9027574 C>T maps to NM_014850.2 R976R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:9094803 G>A maps to NM_014850.2 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr3:9055491 G>A maps to NM_014850.2 I616I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:9106079 C>T maps to NM_014850.2 K224K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:9034636 G>A maps to NM_014850.2 S837S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:9057340 G>A maps to NM_014850.2 R585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr10:70863759 C>T maps to NM_002727.2 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr7:87848224 G>A maps to NM_003130.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr16:4254573 G>A maps to ENST00000330063 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr16:4245656 G>A maps to ENST00000330063 F607F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr16:4242965 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr16:4254546 G>A maps to ENST00000330063 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:4242549 G>A maps to ENST00000330063 I780I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:4242774 C>T maps to ENST00000330063 R705R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:4253224 G>A maps to ENST00000330063 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr16:4254582 G>A maps to ENST00000330063 I476I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr16:4242621 C>T maps to ENST00000330063 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr16:4242576 G>A maps to ENST00000330063 I771I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:4245737 C>T maps to ENST00000330063 K580K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr16:4245656 G>A maps to ENST00000330063 F607F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:11118915 G>A maps to NM_003132.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr1:11115048 G>C maps to NM_003132.2 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr1:11115858 G>A maps to NM_003132.2 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:11116697 G>A maps to NM_003132.2 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:11116705 G>A maps to NM_003132.2 Q164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr20:62173645 C>T maps to NM_080823.2 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr20:62175631 C>T maps to NM_080823.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr20:62174756 C>T maps to NM_080823.2 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr20:62173660 G>A maps to NM_080823.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:62178549 G>A maps to NM_080823.2 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:62178648 G>A maps to NM_080823.2 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:112200421 C>T maps to NM_003135.1 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:74043999 G>A maps to NM_014230.2 Q377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:74060212 C>T maps to NM_014230.2 W135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr17:74060071 G>A maps to NM_014230.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:57350912 C>T maps to NM_006947.3 C323C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr1:225976979 G>A maps to NM_003133.5 K60K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:35837315 C>A maps to ENST00000361690 E468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr6:35838100 G>A maps to ENST00000361690 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:35825090 G>A maps to ENST00000361690 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:35840460 G>A maps to ENST00000361690 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr7:104782674 G>A maps to ENST00000336613 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr23:153049255 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:153048561 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:153050921 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr11:126136092 A>G maps to NM_003139.3 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr23:38037562 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:38020263 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:38033465 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr23:38079977 A>G did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:38019391 T>C did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:99922363 C>G did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:99921833 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:99920600 C>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:99922336 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:99917313 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:99919866 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:99919867 T>G did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:99917234 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr23:99920557 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:99917208 G>C did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:99901386 C>T did not map to a codon.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr23:99921876 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr23:99917308 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:99917270 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:99917295 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:99925833 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:99917353 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:99924354 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr22:26881995 C>T maps to NM_001013694.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:24996656 C>A maps to NM_005839.3 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:24979044 C>T maps to NM_005839.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr1:24975471 C>T maps to NM_005839.3 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr1:24998752 G>A maps to NM_005839.3 K897K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:24989169 C>T maps to NM_005839.3 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr16:2816168 C>T maps to NM_016333.3 T1880T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr16:2815607 A>C maps to NM_016333.3 S1693S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr16:2812814 C>T maps to NM_016333.3 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr16:2816696 C>T maps to NM_016333.3 S2056S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:2812250 T>C maps to NM_016333.3 R574R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:2817905 C>T maps to NM_016333.3 S2459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr16:2810466 C>T maps to NM_016333.3 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr16:2812403 T>C maps to NM_016333.3 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:2820364 C>T maps to NM_016333.3 P2678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:2813459 C>A maps to NM_016333.3 T977T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr16:2811980 C>T maps to NM_016333.3 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:2811635 C>T maps to NM_016333.3 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr16:2816258 A>G maps to NM_016333.3 R1910R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr16:2812214 C>T maps to NM_016333.3 S562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr16:2813975 C>T maps to NM_016333.3 D1149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:75877510 C>A maps to ENST00000388802 S80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr7:75912380 G>A maps to ENST00000388802 R565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr7:75877511 G>A maps to ENST00000388802 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr12:119554777 G>A maps to NM_194286.2 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:119592119 G>A maps to NM_194286.2 R488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:119583406 G>A maps to NM_194286.2 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr12:119540076 G>A maps to NM_194286.2 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr12:119594347 C>G maps to NM_194286.2 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:119568605 C>T maps to NM_194286.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:119554780 G>A maps to NM_194286.2 K135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr12:119540112 C>T maps to NM_194286.2 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:119540139 G>A maps to NM_194286.2 W77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:119588923 C>T maps to NM_194286.2 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr12:119592146 G>A maps to NM_194286.2 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr12:119592158 G>A maps to NM_194286.2 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:119583449 T>C maps to NM_194286.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:119583406 G>A maps to NM_194286.2 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr12:119583469 C>T maps to NM_194286.2 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:100484423 C>T maps to NM_015908.5 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:100482419 G>A maps to NM_015908.5 K334K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr7:100482172 G>A maps to NM_015908.5 Q314Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:100479838 C>T maps to NM_015908.5 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr20:629486 G>A maps to NM_080725.1 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr24:2655549 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr24:2655387 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:23612461 A>G maps to ENST00000415083 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr20:60737979 C>T maps to NM_198935.1 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:170664990 G>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:141443418 G>A maps to NM_003143.1 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:80785070 G>A maps to ENST00000380182 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr5:80770323 G>A maps to ENST00000380182 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:54706581 G>A maps to NM_145716.2 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:18538196 C>T maps to NM_032627.3 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:18542188 C>T maps to NM_032627.3 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr2:182766491 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:182767009 T>C maps to NM_001130445.1 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr2:182766877 T>C maps to NM_001130445.1 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr2:182763782 G>A maps to NM_001130445.1 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr2:182787024 T>A maps to NM_001130445.1 V1187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:182779944 T>C maps to NM_001130445.1 V526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:182781009 C>T maps to NM_001130445.1 F881F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:109186022 G>A maps to NM_001161330.1 S644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr12:109186493 G>A maps to NM_018984.3 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr12:109181952 G>A maps to NM_018984.3 F987F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:109181808 G>A maps to NM_018984.3 P1035P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr12:109186336 G>A maps to NM_018984.3 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr12:109201428 G>A maps to NM_018984.3 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr12:109186136 G>A maps to NM_018984.3 T606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:27958626 G>A maps to NM_033389.2 L1168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr17:27959544 G>A maps to NM_033389.2 Y862Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:27975268 C>T maps to NM_033389.2 W413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:28120913 C>T maps to NM_033389.2 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:27958397 G>A maps to NM_033389.2 Q1245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:27958623 G>A maps to NM_033389.2 S1169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:27963648 G>A maps to NM_033389.2 V506V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:27959826 C>A maps to NM_033389.2 L768L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:27963288 G>A maps to NM_033389.2 S626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:67076894 G>A maps to NM_017857.3 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:67075682 C>T maps to NM_017857.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:67077397 C>T maps to NM_017857.3 F456F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:67075029 C>T maps to NM_017857.3 Q205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr11:67077376 C>T maps to NM_017857.3 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:67079174 C>T maps to NM_017857.3 S599S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr9:140083668 C>A maps to NM_003731.2 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr7:149509387 C>T maps to NM_198455.2 S3265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr7:149486749 C>T maps to NM_198455.2 I1509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:149500847 C>T maps to NM_198455.2 S2723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr7:149502520 G>A maps to NM_198455.2 W2779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr7:149513088 G>A maps to NM_198455.2 G3667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr7:149473470 G>A maps to NM_198455.2 E29E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:149488687 G>A maps to NM_198455.2 W1714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:149475891 G>A maps to NM_198455.2 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr7:149489538 C>T maps to NM_198455.2 R1899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr7:149526050 G>A maps to NM_198455.2 G5041G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:149489748 G>A maps to NM_198455.2 R1936R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:149500611 C>T maps to NM_198455.2 P2672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:149474908 G>A maps to NM_198455.2 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:149483264 C>T maps to NM_198455.2 F1112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:149490418 G>A maps to NM_198455.2 E1966E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr7:149490700 C>T maps to NM_198455.2 A2026A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:149492393 C>T maps to NM_198455.2 L2096L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr7:149500561 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:149477971 C>T maps to NM_198455.2 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr7:149474279 C>T maps to NM_198455.2 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:149480747 G>A maps to NM_198455.2 R818R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:149489166 G>A maps to NM_198455.2 Q1805Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:149490517 C>T maps to NM_198455.2 C1999C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:149510821 C>T maps to NM_198455.2 D3372D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:149510822 C>T maps to NM_198455.2 L3373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr7:149500561 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr7:149519197 C>T maps to NM_198455.2 C4338C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:149480199 G>A maps to NM_198455.2 Q694Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr7:149474716 C>T maps to NM_198455.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr7:149518984 C>T maps to NM_198455.2 S4267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:149508019 C>T maps to NM_198455.2 P3141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr7:149492393 C>T maps to NM_198455.2 L2096L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:149474857 C>T maps to NM_198455.2 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:149493700 C>T maps to NM_198455.2 L2234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:149477865 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:149481112 G>A maps to NM_198455.2 G865G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:149482622 G>A maps to NM_198455.2 R1014R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:149494362 C>T maps to NM_198455.2 F2279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:149528222 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr6:7301719 G>A maps to ENST00000474597 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr6:7301713 G>A maps to ENST00000474597 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr6:7295625 G>A maps to ENST00000474597 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:155988122 G>A maps to ENST00000368312 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:155989873 G>A maps to ENST00000368312 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:155989820 G>A maps to ENST00000368312 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:155981609 G>A maps to ENST00000368312 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:153061896 T>C did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:153062942 A>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:153062006 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr11:57099630 G>A maps to NM_003146.2 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:57099699 G>A maps to NM_003146.2 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:65338925 C>T maps to NM_006396.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr14:38678810 C>T maps to NM_001049.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr14:38679226 C>T maps to NM_001049.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr14:38678614 C>T maps to NM_001049.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr14:38679445 G>A maps to NM_001049.2 W284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:38679289 C>T maps to NM_001049.2 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:38678771 C>T maps to NM_001049.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:38678932 C>T maps to NM_001049.2 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:38679710 C>T maps to NM_001049.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr17:71166471 G>A maps to NM_001050.2 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr17:71166294 C>T maps to NM_001050.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr17:71166318 C>T maps to NM_001050.2 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:71165805 G>A maps to NM_001050.2 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:71166024 G>A maps to NM_001050.2 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr17:71165664 C>A maps to NM_001050.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:71166147 C>T maps to NM_001050.2 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr22:37603701 G>A maps to NM_001051.2 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr22:37603033 C>T maps to NM_001051.2 W270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr22:37602744 C>T maps to NM_001051.2 K366K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:37602954 G>A maps to NM_001051.2 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:23016128 C>T maps to NM_001052.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr20:23016461 C>T maps to NM_001052.2 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr20:23016548 C>T maps to NM_001052.2 D143D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:23016467 C>T maps to NM_001052.2 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr16:1129822 C>T maps to NM_001053.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr16:1128876 C>T maps to NM_001053.3 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:1129185 C>T maps to NM_001053.3 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr16:1129539 C>T maps to NM_001053.3 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:1129701 G>A maps to NM_001053.3 Q278Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr16:1129539 C>T maps to NM_001053.3 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:1129932 C>T maps to NM_001053.3 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:1500229 G>C maps to NM_014188.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:48116698 C>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:48125807 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3BZ-06A-12D-A196-08 chr1:85136352 T>C maps to NM_001166417.1 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:85121525 G>A maps to NM_001166417.1 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr23:48214652 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr23:48214154 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr23:48206955 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr23:48208990 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:48206993 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:48209479 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:48214614 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr23:48214128 T>C did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:48206961 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:48213489 C>T did not map to a codon.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr23:48211543 G>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:48047156 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:48047101 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:48047089 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:48047098 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:48049606 C>T did not map to a codon.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr23:48053620 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:52682504 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:52677368 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:52681978 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr23:52681971 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:52681932 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:52682013 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:52682028 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:52681977 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:52682453 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:52677368 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr22:41252511 G>A maps to NM_003932.3 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr22:41252454 G>A maps to NM_003932.3 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr22:41223177 T>G maps to NM_003932.3 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr11:130064115 G>A maps to NM_021978.3 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr11:130079579 C>T maps to NM_021978.3 S810S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr11:130060505 C>T maps to NM_021978.3 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:130068469 G>A maps to NM_021978.3 G546G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr11:130059738 C>T maps to NM_021978.3 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:130066310 C>T maps to NM_021978.3 C397C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr11:130059762 C>T maps to NM_021978.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:130059684 C>T maps to NM_021978.3 H164H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:130060505 C>T maps to NM_021978.3 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr11:130078484 C>T maps to NM_021978.3 S725S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:130066488 C>T maps to NM_021978.3 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:53084991 C>T maps to NM_014682.2 Q143Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr8:53045642 C>T maps to NM_014682.2 K806K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:53045672 C>T maps to NM_014682.2 R796R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:53073992 G>A maps to NM_014682.2 F512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr8:53076591 G>A maps to NM_014682.2 Q452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr8:53084865 G>C maps to NM_014682.2 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr8:53062479 G>A maps to NM_014682.2 R622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:53071456 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr8:53073992 G>A maps to NM_014682.2 F512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr8:53045672 C>T maps to NM_014682.2 R796R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:53084430 G>A maps to NM_014682.2 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr8:53076591 G>A maps to NM_014682.2 Q452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr8:53084652 C>T maps to NM_014682.2 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr8:53038692 C>A maps to NM_014682.2 G892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:53084727 C>T maps to NM_014682.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:53074094 G>A maps to NM_014682.2 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:53074100 G>A maps to NM_014682.2 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:53073992 G>A maps to NM_014682.2 F512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr8:53028864 T>C maps to NM_014682.2 S991S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr8:53044606 C>T maps to NM_014682.2 W859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr8:53044607 C>T maps to NM_014682.2 W859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr8:53084517 C>A maps to NM_014682.2 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr8:53085018 C>T maps to NM_014682.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr8:134475674 G>A maps to NM_173344.2 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:134477115 C>T maps to NM_173344.2 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:134474153 G>A maps to NM_173344.2 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:70417113 G>A maps to NM_006927.3 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:70428922 G>C maps to NM_006927.3 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:70422340 G>A maps to NM_006927.3 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:44386158 C>T maps to NM_174963.2 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:44364863 C>T maps to NM_174963.2 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:86090552 G>A maps to NM_003896.3 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:86075165 A>T maps to NM_003896.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr3:98506933 C>T maps to ENST00000493584 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:98507297 C>A maps to ENST00000493584 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:98492774 C>T maps to ENST00000493584 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr3:98487367 C>T maps to ENST00000493584 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:8752656 G>A maps to NM_005418.3 H60H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr11:8732709 G>A maps to NM_005418.3 F747F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:186760641 C>T maps to NM_003032.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr3:186760839 C>T maps to NM_003032.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:186760694 C>T maps to NM_003032.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr3:186760985 G>A maps to NM_003032.2 W165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:107459713 C>T maps to NM_001142351.1 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:107460301 G>A maps to NM_001142351.1 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:107459755 C>T maps to NM_001142351.1 K226K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr2:107459536 G>A maps to NM_001142351.1 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:107423253 G>A maps to NM_001142351.1 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:107459875 C>T maps to NM_001142351.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:107459923 C>T maps to NM_001142351.1 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:107460078 T>A maps to NM_001142351.1 K119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:107423352 G>A maps to NM_001142351.1 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr2:107446575 G>A maps to NM_001142351.1 Q422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr2:107459539 G>A maps to NM_001142351.1 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:107423352 G>A maps to NM_001142351.1 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:107459539 G>A maps to NM_001142351.1 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:107459887 C>T maps to NM_001142351.1 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:107460391 G>A maps to NM_001142351.1 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr2:107423238 C>T maps to NM_001142351.1 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:107460340 G>T maps to NM_001142351.1 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:107449068 G>A maps to NM_001142351.1 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:107460136 C>T maps to NM_001142351.1 W99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr2:107459713 C>T maps to NM_001142351.1 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z4-06A-11D-A197-08 chr2:107423244 C>T maps to NM_001142351.1 Q493Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr2:107450537 C>T maps to NM_001142351.1 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:107459823 G>A maps to NM_001142351.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:107450549 C>T maps to NM_001142351.1 E332E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:107460298 G>A maps to NM_001142351.1 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:107460391 G>A maps to NM_001142351.1 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr2:107459653 G>A maps to NM_001142351.1 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr17:74621516 G>A maps to NM_018414.3 N566N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:74622735 C>T maps to NM_018414.3 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:74623608 G>A maps to NM_018414.3 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr17:74623616 G>A maps to NM_018414.3 Q294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZG-06A-11D-A197-08 chr17:74625600 C>T maps to NM_018414.3 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:74622450 C>T maps to NM_018414.3 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr17:74562236 G>A maps to NM_006456.2 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:76779671 G>A maps to NM_152996.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:76878048 G>A maps to NM_152996.2 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:76877776 C>T maps to NM_152996.2 R100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr9:130670703 G>A maps to NM_175039.3 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:130674662 G>A maps to NM_175039.3 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:77528731 C>T maps to NM_030965.1 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:77528659 G>A maps to NM_030965.1 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr1:77509908 G>A maps to NM_030965.1 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:77510079 G>A maps to NM_030965.1 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:77515942 G>A maps to NM_030965.1 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:77510199 C>T maps to NM_030965.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:77516014 C>T maps to NM_030965.1 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:77515941 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:130656949 G>A maps to NM_013443.3 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr9:130648990 G>A maps to NM_013443.3 Q297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:130649776 G>A maps to NM_013443.3 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr7:116862970 C>T maps to NM_021908.2 F565F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:116810932 C>T maps to ENST00000323984 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr7:116739826 T>C maps to ENST00000323984 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr7:116859150 C>T maps to ENST00000323984 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:113140609 A>T maps to NM_017744.4 L202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:113153618 C>A maps to NM_017744.4 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:113153604 G>A maps to NM_017744.4 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr1:113124628 G>A maps to NM_017744.4 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:113084620 G>A maps to NM_017744.4 A527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:22354545 G>A maps to NM_003034.3 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr15:92981672 C>T maps to NM_006011.3 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:92973278 G>A maps to NM_006011.3 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr15:92981676 C>T maps to NM_006011.3 R129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr15:92981768 C>T maps to NM_006011.3 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr15:92981813 G>A maps to NM_006011.3 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:92988027 C>T maps to NM_006011.3 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr18:55020145 G>A maps to NM_015879.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr18:55024563 C>T maps to NM_015879.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr18:55027445 C>T maps to NM_015879.2 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr18:55024224 C>T maps to NM_015879.2 H128H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr18:55020173 C>T maps to NM_015879.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:55021668 C>T maps to NM_015879.2 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:55024476 C>T maps to NM_015879.2 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr18:55024350 C>T maps to NM_015879.2 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr18:55027309 G>A maps to NM_015879.2 E315E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr18:55024482 C>T maps to NM_015879.2 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:100147741 G>A maps to NM_005668.4 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:100231368 G>A maps to NM_005668.4 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr5:100147715 C>T maps to NM_005668.4 K305K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:100147721 G>A maps to NM_005668.4 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:100147757 G>A maps to NM_005668.4 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:100231437 G>A maps to NM_005668.4 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:100147827 C>T maps to NM_005668.4 W268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:100222167 G>A maps to NM_005668.4 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr18:44260064 G>A maps to NM_013305.4 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:44260064 G>A maps to NM_013305.4 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:44260361 G>A maps to NM_013305.4 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr18:44266165 C>T maps to NM_013305.4 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr18:44266135 C>T did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr18:44260418 G>A maps to NM_013305.4 Y239Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr10:17363325 T>A maps to NM_001004470.1 K250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:17363163 G>A maps to NM_001004470.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:17369020 G>A maps to NM_001004470.1 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:52553305 G>A maps to NM_015136.2 A1687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:52554132 C>T maps to NM_015136.2 V1803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:52554680 G>A maps to NM_015136.2 L1891L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr3:52536091 G>A maps to NM_015136.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:52553574 C>T maps to NM_015136.2 L1744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:52539158 G>A maps to NM_015136.2 K506K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:52547981 C>T maps to NM_015136.2 F1144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr3:52557284 G>A maps to NM_015136.2 L2356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:52538151 G>A maps to NM_015136.2 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr3:52537849 C>T maps to NM_015136.2 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:52552737 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:52557705 G>A maps to NM_015136.2 W2443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:52529458 C>T maps to NM_015136.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:52529497 C>T maps to NM_015136.2 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:52538519 C>T maps to NM_015136.2 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:52541960 G>A maps to NM_015136.2 K689K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:52551895 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:52539754 G>A maps to NM_015136.2 V551V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr3:52542314 C>T maps to NM_015136.2 F725F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr3:52550414 G>A maps to NM_015136.2 G1396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:52548787 G>A maps to NM_015136.2 S1250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr3:52557921 G>T maps to NM_015136.2 A2477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr3:52555398 C>T maps to NM_015136.2 S1977S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr3:52547737 C>T maps to NM_015136.2 V1092V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr3:52554111 G>A maps to NM_015136.2 R1796R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:52536040 G>A maps to NM_015136.2 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:52540748 G>A maps to NM_015136.2 R624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:52548199 C>T maps to NM_015136.2 L1173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:52546962 G>A maps to NM_015136.2 P1049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr3:52550582 G>A maps to NM_015136.2 R1422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:52554221 C>T maps to NM_015136.2 A1805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr12:104071277 G>A maps to NM_017564.9 Q898Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr12:104084291 C>T maps to NM_017564.9 F1091F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr12:104138990 C>T maps to NM_017564.9 I2024I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr12:104089540 G>A maps to NM_017564.9 E1167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:104121067 C>T maps to NM_017564.9 V1625V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr12:104105273 G>A maps to NM_017564.9 G1438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr12:104084291 C>T maps to NM_017564.9 F1091F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:104155079 G>A maps to NM_017564.9 T2417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:104048355 C>T maps to NM_017564.9 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:104109591 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr12:104122763 C>T maps to NM_017564.9 S1691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr12:104142921 G>A maps to NM_017564.9 K2142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr12:103984797 C>T maps to NM_017564.9 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:104033935 C>T maps to NM_017564.9 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:104056727 C>T maps to NM_017564.9 V658V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:104089597 C>T maps to NM_017564.9 I1186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr12:104078801 C>T maps to NM_017564.9 S979S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr12:104142831 G>A maps to NM_017564.9 K2112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:104033935 C>T maps to NM_017564.9 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:104149489 C>T maps to NM_017564.9 F2327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:104046443 C>T maps to NM_017564.9 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:104089422 C>T maps to NM_017564.9 I1157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr12:104142807 G>A maps to NM_017564.9 T2104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr12:104046341 G>A maps to NM_017564.9 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:104048355 C>T maps to NM_017564.9 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr12:104056646 G>A maps to NM_017564.9 V631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:104077009 C>T maps to NM_017564.9 R945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr12:104067778 C>T maps to NM_017564.9 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr12:104086618 C>T maps to NM_017564.9 V1109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr12:104131518 G>A maps to NM_017564.9 L1886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:104131470 C>T maps to NM_017564.9 D1870D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:104138999 C>T maps to NM_017564.9 S2027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:103988232 G>A maps to NM_017564.9 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr12:104048397 C>T maps to NM_017564.9 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr12:104046377 G>A maps to NM_017564.9 V434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr12:104092977 C>T maps to NM_017564.9 F1229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr12:104081985 G>A maps to NM_017564.9 W1013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr12:104033935 C>T maps to NM_017564.9 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr12:104109614 C>T maps to NM_017564.9 N1520N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr12:104126944 G>A maps to NM_017564.9 V1815V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:104071292 G>A maps to NM_017564.9 G903G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:104081959 C>T maps to NM_017564.9 L1004L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:104099447 C>T maps to NM_017564.9 F1313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:104144427 C>T maps to NM_017564.9 P2170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr12:104054125 G>A maps to NM_017564.9 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr12:104121052 C>T maps to NM_017564.9 F1620F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr12:104081986 G>A maps to NM_017564.9 W1013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:104048346 G>A maps to NM_017564.9 K474K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:104084291 C>T maps to NM_017564.9 F1091F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:104149474 C>T maps to NM_017564.9 P2322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr12:104149444 G>A maps to NM_017564.9 G2312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr12:104121052 C>T maps to NM_017564.9 F1620F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr3:36570348 C>T maps to NM_003149.1 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:36587753 C>T maps to NM_003149.1 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:36422170 G>A maps to NM_003149.1 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:36545949 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:36570431 C>T maps to NM_003149.1 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:36422185 G>A maps to NM_003149.1 K17K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr3:36545918 C>T maps to NM_003149.1 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:36570341 G>A maps to NM_003149.1 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:36527668 C>T maps to NM_003149.1 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:37371267 C>T maps to NM_198993.3 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr12:57640631 G>A maps to NM_145064.1 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr12:57643377 G>A maps to NM_145064.1 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:57642488 G>A maps to NM_145064.1 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:136196178 G>A maps to NM_005862.2 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:136062735 G>A maps to NM_005862.2 P1128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr23:123190021 A>T did not map to a codon.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr23:123205125 T>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:123195716 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:123227932 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:123220439 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:123164886 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr23:123200073 T>G did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:123196816 C>A did not map to a codon.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr23:123205087 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr23:123181207 G>A did not map to a codon.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr23:123200027 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr7:99780443 C>T maps to NM_012447.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr7:99799823 C>T maps to NM_012447.2 L808L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A29S-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr7:99808748 C>T maps to NM_012447.2 P1118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr7:99801717 C>T maps to NM_012447.2 S925S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:99802320 G>A maps to NM_012447.2 R958R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A2MR-06A-11D-A196-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-EE-A2MR-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:99798110 C>T maps to NM_012447.2 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:99798111 C>T maps to NM_012447.2 Q603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr7:99802727 C>A maps to NM_012447.2 R1018R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:17726679 G>A maps to NM_003473.2 K44K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr10:17750893 C>T maps to NM_003473.2 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:74077594 C>T maps to NM_213622.1 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:74077594 C>T maps to NM_213622.1 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:90673099 C>T maps to NM_020799.2 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:68441173 G>A maps to NM_012108.2 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:68459021 G>A maps to NM_012108.2 K258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:68447022 C>T maps to NM_012108.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr4:68472053 G>A maps to NM_012108.2 K289K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:68424574 G>A maps to NM_012108.2 Q16Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A690-06A-11D-A30X-08 chr4:68424565 G>A maps to NM_012108.2 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:4333714 G>A maps to ENST00000314714 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:4328765 G>A maps to ENST00000314714 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:4328766 G>A maps to ENST00000314714 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:4327184 G>A maps to ENST00000314714 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:38003965 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:38005786 C>T maps to NM_000349.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:72468890 G>A maps to NM_006645.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr11:72492031 C>T maps to NM_006645.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:72466184 G>A maps to NM_006645.2 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:72466748 G>T maps to NM_006645.2 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:72466781 C>T maps to NM_006645.2 W198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr13:33681025 G>A maps to NM_178007.2 S1023S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr13:33701616 G>A maps to NM_178007.2 I597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr13:33681070 C>T maps to NM_178007.2 R1008R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr13:33700319 G>A maps to NM_178007.2 V652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr13:33760144 G>A maps to NM_178007.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr13:33700223 G>A maps to NM_178007.2 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr13:33681013 C>T maps to NM_178007.2 E1027E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr13:33704279 C>T maps to NM_178007.2 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr13:33684993 C>T maps to NM_178007.2 E878E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:33703676 C>T maps to NM_178007.2 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr13:33704222 G>T maps to NM_178007.2 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr13:33716452 C>T maps to NM_178007.2 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr13:33700217 C>T maps to NM_178007.2 Q686Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:37818593 C>T maps to NM_006804.3 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr17:37814035 C>A maps to NM_006804.3 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:110842034 C>A maps to NM_139164.1 G50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr5:110835778 C>T maps to NM_139164.1 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr5:110835664 C>T maps to NM_139164.1 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr18:51858171 G>A maps to NM_139171.1 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr18:51863621 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:51880871 C>T maps to NM_139171.1 W24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr18:51851241 G>A maps to NM_139171.1 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr2:96852637 G>A maps to NM_020151.3 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:96859048 G>A maps to NM_020151.3 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q9-06A-11D-A19A-08 chr23:67940174 A>C did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:67941948 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:67932801 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr23:67938433 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr23:67938117 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:67937432 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:67937433 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:67937558 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:67937559 T>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:67943916 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:67942406 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:67943841 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:67937722 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:67938307 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:67941579 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:67943845 C>T did not map to a codon.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr2:191841734 C>A maps to NM_007315.3 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:191844532 G>A maps to NM_007315.3 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:191872348 G>A maps to NM_007315.3 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr12:56749256 G>A maps to NM_005419.3 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:56737283 G>A maps to NM_005419.3 I815I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:56749511 G>A maps to NM_005419.3 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:56748281 G>C maps to NM_005419.3 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:56742737 G>A maps to NM_005419.3 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr17:40474351 G>A maps to NM_139276.2 F683F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr17:40498616 G>A maps to NM_139276.2 H81H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr17:40481781 G>A maps to NM_139276.2 D374D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr17:40475297 G>A maps to NM_139276.2 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:40485734 C>T maps to NM_139276.2 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:40498621 G>A maps to NM_139276.2 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr17:40489792 G>A maps to NM_139276.2 D211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr17:40478181 G>A maps to NM_139276.2 I439I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:40474512 C>G did not map to a codon.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr17:40483542 C>A maps to NM_139276.2 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:192012848 G>A maps to NM_003151.2 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:191905793 C>T maps to NM_003151.2 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:191897873 C>T maps to NM_003151.2 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:191937853 G>A maps to NM_003151.2 H145H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:192012913 G>A maps to NM_003151.2 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:191905874 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr2:191927507 C>T maps to NM_003151.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:40456591 C>T maps to NM_003152.3 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:40375411 G>A maps to NM_012448.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr17:40379651 G>A maps to NM_012448.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:57499066 G>A maps to NM_003153.4 Q290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:57499067 G>A maps to NM_003153.4 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr12:57502001 G>C maps to NM_003153.4 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr12:57501991 G>A maps to NM_003153.4 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:57492325 G>A maps to NM_003153.4 S707S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:57496102 G>A maps to NM_003153.4 H494H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr4:70864162 C>T maps to NM_003154.2 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr20:47741136 G>A maps to NM_001037328.1 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:47733731 G>A maps to NM_017453.2 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr20:47782546 G>T maps to NM_017453.2 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr20:47740944 A>G maps to NM_017453.2 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr20:47733716 C>T maps to NM_017453.2 Q526Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr8:74516059 G>A maps to NM_001164380.1 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr8:23711946 C>T maps to NM_003155.2 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr8:23708981 G>A maps to NM_003155.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr8:23709032 G>A maps to NM_003155.2 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr8:23708885 C>T maps to NM_003155.2 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr8:23702438 G>A maps to NM_003155.2 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:23702351 G>A maps to NM_003155.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr5:172744942 G>A maps to NM_003714.2 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr5:172755148 C>T maps to NM_003714.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr5:172752948 C>T maps to NM_003714.2 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:172750262 C>T maps to NM_003714.2 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:172745134 C>T maps to NM_003714.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr5:172750361 G>A maps to NM_003714.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:89789116 A>G maps to ENST00000433102 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr7:89861916 G>A maps to NM_152999.3 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr7:89856352 C>T maps to NM_152999.3 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr7:89861700 T>A maps to NM_152999.3 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:89854482 G>A maps to NM_152999.3 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:120003270 C>T maps to NM_182915.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:120005430 C>T maps to NM_182915.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:120003311 A>G maps to NM_182915.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:120003227 C>T maps to NM_182915.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr2:120003227 C>T maps to NM_182915.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr2:120020655 C>T maps to NM_182915.2 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:120005745 C>T maps to NM_182915.2 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:120003548 G>A maps to NM_182915.2 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:120003203 C>T maps to NM_182915.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr2:120003518 C>T maps to NM_182915.2 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr2:120003509 C>T maps to NM_182915.2 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr2:120005454 C>T maps to NM_182915.2 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr2:120012321 C>T maps to NM_182915.2 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:120003116 G>C maps to NM_182915.2 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:120005391 G>A maps to NM_182915.2 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:87913427 G>A maps to NM_024636.2 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:87908727 C>T maps to NM_024636.2 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:87912033 G>A maps to NM_024636.2 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:87912021 G>A maps to NM_024636.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:87912131 G>A maps to NM_024636.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:44076765 C>T maps to NM_001007532.2 Q41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr17:44076812 C>T maps to NM_001007532.2 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr1:47735458 G>T maps to NM_001048166.1 S821S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr1:47765656 G>A maps to NM_001048166.1 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:47753278 G>A maps to NM_001048166.1 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:47716975 G>A maps to NM_001048166.1 T1233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr1:47717464 C>A maps to NM_001048166.1 L1070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:4112755 C>T maps to NM_003156.3 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:4107738 C>T maps to NM_003156.3 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr11:4095771 G>T maps to NM_003156.3 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr11:4112671 C>T maps to NM_003156.3 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:4095773 G>A maps to NM_003156.3 E278E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr11:4080624 C>T maps to NM_003156.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:27024440 C>T maps to ENST00000382009 I783I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr5:171491789 G>A maps to NM_005990.3 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:171510057 G>A maps to NM_005990.3 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:171523555 G>A maps to NM_005990.3 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:171471912 G>A maps to NM_005990.3 F960F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr5:171481680 C>T maps to NM_005990.3 E848E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr5:171520702 G>A maps to NM_005990.3 Q423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr19:1218458 C>T maps to NM_000455.4 Q112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr2:220467230 C>T maps to NM_052902.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:220476725 C>T maps to NM_052902.2 F806F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:220467488 A>G maps to NM_052902.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:220466086 C>T maps to NM_052902.2 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr2:220480794 C>T maps to NM_052902.2 L1060L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:220471782 C>T maps to NM_052902.2 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:220476524 C>T maps to NM_052902.2 T779T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:220472775 C>T maps to NM_052902.2 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:220476455 C>T maps to NM_052902.2 V756V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:220466101 C>T maps to NM_052902.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:220472775 C>T maps to NM_052902.2 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:220472775 C>T maps to NM_052902.2 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr7:43664263 C>T maps to NM_004760.2 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:197004444 G>A maps to NM_004226.3 L245L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A181-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr13:99127537 G>A maps to NM_003576.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr13:99171520 G>T maps to NM_003576.3 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr13:99171630 G>A maps to NM_003576.3 Q59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr8:99608307 A>T maps to ENST00000354930 C286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:99718718 A>C maps to ENST00000354930 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr7:23808777 C>T maps to NM_031414.3 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr7:23775179 G>A maps to NM_031414.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:23802526 C>T maps to NM_031414.3 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:23826182 C>T maps to NM_031414.3 Y777Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr7:23823224 G>A maps to NM_031414.3 Q697Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:23810626 C>T maps to NM_031414.3 Q573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr7:23809347 C>T maps to NM_031414.3 V562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:23854761 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:23809267 C>T maps to NM_031414.3 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:23809323 C>T maps to NM_031414.3 I554I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:23811824 C>T maps to NM_031414.3 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:23871840 C>T maps to NM_031414.3 F972F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr7:23775374 G>A maps to NM_031414.3 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:23810744 T>C did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr7:23811824 C>T maps to NM_031414.3 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:23825110 C>T maps to NM_031414.3 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr5:146703478 G>A maps to NM_001112724.1 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:5458574 C>T maps to NM_018401.1 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:5418632 C>T maps to NM_018401.1 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr4:5448397 A>C did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr10:134021639 C>T maps to NM_173575.2 Q445Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:134059436 G>A maps to NM_173575.2 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:8486351 T>C maps to NM_030906.2 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:8486288 C>T maps to NM_030906.2 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:8435183 C>T maps to NM_030906.2 W401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:8478966 C>T maps to NM_030906.2 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:8494733 C>T maps to NM_030906.2 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:8476353 C>T maps to NM_030906.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:8478936 C>T maps to NM_030906.2 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:8486288 C>T maps to NM_030906.2 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr11:8486363 G>A maps to NM_030906.2 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:8486288 C>T maps to NM_030906.2 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr20:2083989 C>T maps to NM_080836.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr2:219563576 C>T maps to NM_015690.3 L1104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:219553454 C>T maps to NM_015690.3 I472I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:219559037 C>T maps to NM_015690.3 V796V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:219538445 C>T maps to NM_015690.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:219540913 C>T maps to NM_015690.3 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:219561299 C>T maps to NM_015690.3 I854I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr2:219558012 G>A maps to NM_015690.3 R698R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:219563401 C>T maps to NM_015690.3 P1045P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:219538349 C>T maps to NM_015690.3 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:219561889 C>T maps to NM_015690.3 S905S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr6:36464551 G>A maps to NM_007271.2 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:36464512 T>C maps to NM_007271.2 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:36483233 G>A maps to NM_007271.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:36483159 G>A maps to NM_007271.2 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr6:36492155 C>A maps to NM_007271.2 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:36492231 G>A maps to NM_007271.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr12:27465493 C>T maps to NM_015000.3 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr12:27467548 C>T maps to NM_015000.3 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:168986230 G>A maps to NM_013233.2 Q338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:168931711 G>A maps to NM_013233.2 H373H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:169023839 T>C maps to NM_013233.2 E133E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:43610523 C>T maps to NM_006282.2 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:36826900 C>T maps to ENST00000373130 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr1:36809728 G>A maps to ENST00000373130 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:36809041 G>A maps to ENST00000373130 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:36820959 G>A maps to ENST00000373130 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:36821031 G>A maps to ENST00000373130 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:36807397 G>A maps to ENST00000373130 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr8:80553688 C>T maps to NM_007029.3 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr8:80553664 G>A maps to NM_007029.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:80567197 C>T maps to NM_007029.3 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr20:62275111 C>T maps to NM_015894.2 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:62275111 C>T maps to NM_015894.2 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:62275186 G>A maps to NM_015894.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr20:62275252 G>A maps to NM_015894.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:62275219 G>A maps to NM_015894.2 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:27098663 C>T maps to NM_030795.2 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:27098617 G>A maps to NM_030795.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:27097514 G>A maps to NM_030795.2 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:27101226 C>T did not map to a codon.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr8:27099929 C>T maps to NM_030795.2 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr9:124111427 A>C maps to NM_004099.4 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr15:74280974 G>A maps to NM_004809.3 Q187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:74284492 G>A maps to NM_004809.3 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:74281508 G>A maps to NM_004809.3 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr9:35100990 G>A maps to NM_013442.1 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr9:35101909 G>A maps to NM_013442.1 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:39546731 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr13:39544383 A>G maps to NM_145286.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr13:39542551 C>T maps to NM_145286.2 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr13:39550877 G>A maps to NM_145286.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:48808113 C>T maps to NM_172311.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:48808300 C>T maps to NM_172311.2 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:48809548 C>T maps to NM_172311.2 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr2:48809274 C>T maps to NM_172311.2 I501I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:48808953 G>A maps to NM_172311.2 E394E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:48808113 C>T maps to NM_172311.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:48808332 G>A maps to NM_172311.2 W187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:48808563 C>T maps to NM_172311.2 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr2:48809493 C>T maps to NM_172311.2 V574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr14:81743842 G>A maps to NM_033104.2 F604F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr14:81744868 G>A maps to NM_033104.2 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:81862502 G>A maps to NM_033104.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:81745045 C>T maps to NM_033104.2 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:81837504 C>T maps to NM_033104.2 W133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:81744040 G>A maps to NM_033104.2 F538F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr14:81862460 G>A maps to NM_033104.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr14:81744728 C>T maps to NM_033104.2 W309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr14:81736941 G>A maps to NM_033104.2 F895F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:81743737 C>T maps to NM_033104.2 W639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:81743738 C>T maps to NM_033104.2 W639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:81744901 C>T maps to NM_033104.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr10:70645726 G>A maps to NM_001130161.2 V725V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr10:70645006 C>T maps to NM_001130161.2 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr10:70645891 C>T maps to NM_001130161.2 T780T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr10:70644202 C>T maps to NM_001130161.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:70644836 C>T maps to NM_001130161.2 R429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr10:70645750 T>C maps to NM_001130161.2 S733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:70644562 C>T maps to NM_001130161.2 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr10:70644562 C>T maps to NM_001130161.2 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr4:184930404 C>T maps to NM_020225.1 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:184930404 C>T maps to NM_020225.1 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr4:184938350 C>A maps to NM_020225.1 R899R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr4:184931614 C>T maps to NM_020225.1 Q542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:79980700 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:79980701 C>T maps to ENST00000392359 K12K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:74481543 G>A maps to ENST00000449139 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr15:74473252 C>T maps to ENST00000449139 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:74472507 C>T maps to ENST00000449139 W678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:74473121 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr15:74481579 G>A maps to ENST00000449139 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr15:74483559 G>A maps to ENST00000449139 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr15:74476281 G>A maps to ENST00000449139 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr15:74476272 C>T maps to ENST00000449139 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr15:74481510 G>A maps to ENST00000449139 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:134916781 C>T maps to NM_182489.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:202343135 C>T maps to NM_018571.5 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:16052847 G>A maps to ENST00000025399 K275K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr12:16050833 C>T maps to ENST00000025399 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:125901813 G>A maps to NM_018387.4 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr9:125909133 C>T maps to NM_018387.4 K446K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr15:43892248 G>A maps to NM_153700.2 V1716V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:43896245 C>T maps to NM_153700.2 K1441K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr15:43893647 C>T maps to NM_153700.2 V1549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:43893671 C>T maps to NM_153700.2 R1541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:43893737 G>A maps to NM_153700.2 P1519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:37105105 A>T maps to NM_003162.2 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:37085020 T>A maps to NM_003162.2 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:37076661 G>A maps to NM_003162.2 F760F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:37085035 C>T maps to NM_003162.2 E600E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr14:31424859 G>A maps to NM_001083893.1 N142N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr19:47241453 G>A maps to NM_001039877.1 Q143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr19:47241454 G>A maps to NM_001039877.1 N142N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:47226196 G>A maps to NM_001039877.1 V599V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:47225276 G>A maps to NM_001039877.1 A693A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:7175565 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr23:7243495 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:7171258 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:7171257 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:7171305 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:7267935 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:7177763 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:7177711 G>A did not map to a codon.
Sequencing variant TCGA-ER-A197-06A-32D-A197-08 chr23:7243498 A>G did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:7268098 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:7268243 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:7171325 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:125476269 C>T maps to NM_152713.3 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr11:125479395 C>T maps to NM_152713.3 I343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:125476197 C>T maps to NM_152713.3 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:125479473 C>T maps to NM_152713.3 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:125478119 C>T maps to NM_152713.3 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:125478008 C>T maps to NM_152713.3 V262V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D3-A3C1-06A-12D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr3:31661281 T>C maps to NM_178862.1 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr6:144508384 C>T maps to NM_003764.3 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:144507917 C>T maps to NM_003764.3 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr6:144508264 C>T maps to NM_003764.3 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr20:57244504 C>T maps to NM_001001433.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:102713376 T>G maps to NM_017919.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:93733939 C>T maps to NM_001001850.1 Q58Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:93733720 C>T maps to NM_001001850.1 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:31008831 G>T maps to NM_052874.3 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr16:31008891 G>A maps to NM_052874.3 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:31004165 G>A maps to NM_052874.3 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:31049833 C>T maps to NM_004604.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr16:31045632 C>T maps to NM_004604.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:31045632 C>T maps to NM_004604.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr11:62593011 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr11:62592568 G>A maps to NM_003164.3 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:62574949 G>A maps to NM_003164.3 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:180974551 C>T maps to NM_005819.4 W28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:180962548 G>A maps to NM_005819.4 Q105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZY-06A-11D-A197-08 chr1:180957436 G>A maps to NM_005819.4 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:130422358 C>T maps to NM_003165.3 Y99Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:7712100 C>T maps to ENST00000441779 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr19:7711205 C>T maps to ENST00000441779 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:7712641 C>T maps to ENST00000441779 F587F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:7709609 C>T maps to ENST00000441779 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:7703651 G>A maps to ENST00000441779 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:7709558 C>T maps to ENST00000441779 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:7712088 C>T maps to ENST00000441779 F509F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:109321927 C>T maps to NM_007269.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr1:109338902 C>T maps to NM_007269.2 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:53237184 C>T maps to NM_178509.5 I525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr17:53237184 C>T maps to NM_178509.5 I525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:53150370 C>T maps to NM_178509.5 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:147685155 C>T maps to NM_001127715.1 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr3:121100317 C>T maps to NM_014980.2 S866S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr3:120977926 C>T maps to NM_014980.2 Q624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr3:120976025 C>T maps to NM_014980.2 Q560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr3:120764301 T>C maps to NM_014980.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:120952508 C>T maps to NM_014980.2 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:121126222 G>A maps to NM_014980.2 R931R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:121001167 C>T maps to NM_014980.2 I722I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr3:120952496 G>A maps to NM_014980.2 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:121126316 C>T maps to NM_014980.2 L963L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:121100281 C>T maps to NM_014980.2 F854F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:120952508 C>T maps to NM_014980.2 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr3:120760549 C>T maps to NM_014980.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:120871406 G>A maps to NM_014980.2 E251E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:120876349 G>A did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr3:120977919 A>G maps to NM_014980.2 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:120998771 G>A maps to NM_014980.2 R693R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:121097678 C>T maps to NM_014980.2 R789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr3:120941993 C>T maps to NM_014980.2 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr12:10783713 G>A maps to NM_018423.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:10774548 G>A maps to NM_018423.2 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:10783812 G>A maps to NM_018423.2 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:10774521 G>A maps to NM_018423.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:10782193 C>T maps to NM_018423.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:10777293 G>A maps to NM_018423.2 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:10783683 G>A maps to NM_018423.2 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr14:53223322 C>T maps to NM_145251.3 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr7:75625830 A>G maps to NM_016086.2 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:75634722 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:75634641 G>A maps to NM_016086.2 D178D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:75651289 G>A maps to NM_016086.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr7:75630320 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:75634656 G>A maps to NM_016086.2 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:75643074 G>A maps to NM_016086.2 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr13:48542772 G>A maps to NM_003850.2 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr13:48575366 C>T maps to NM_003850.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr13:48523623 A>G maps to NM_003850.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:48571089 G>A maps to NM_003850.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr3:67579590 T>C maps to NM_003848.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:67570914 G>A maps to NM_003848.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:67570995 C>T maps to NM_003848.3 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:151599071 C>T maps to NM_033050.4 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:151598397 A>T maps to NM_033050.4 K23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:151599095 G>A maps to NM_033050.4 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:151598432 C>T maps to NM_033050.4 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:151598918 C>T maps to NM_033050.4 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:151598432 C>T maps to NM_033050.4 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr3:151598688 C>T maps to NM_033050.4 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr3:151598432 C>T maps to NM_033050.4 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr3:151598495 G>A maps to NM_033050.4 W55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr3:151598432 C>T maps to NM_033050.4 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:151598688 C>T maps to NM_033050.4 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr3:151597691 C>T maps to NM_033050.4 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:118827738 C>T maps to NM_022491.2 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr12:118827742 C>T maps to NM_022491.2 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:104378824 C>T maps to NM_001178133.1 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:104269021 C>T maps to NM_016169.3 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr8:70533445 A>G maps to NM_001128206.1 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr8:70536399 G>A maps to NM_001128206.1 V606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:70476233 G>A maps to NM_001128206.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr8:70513989 G>A maps to NM_001128206.1 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:70570766 T>G maps to NM_001128206.1 G871G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:70515486 C>T maps to NM_001128206.1 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:70541909 G>A maps to NM_001128206.1 W760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:70539471 C>T maps to NM_001128206.1 I626I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr8:70513986 G>A maps to NM_001128206.1 K328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:70501250 C>T maps to NM_001128206.1 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:70501325 G>A maps to NM_001128206.1 E228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr8:70517064 C>T maps to NM_001128206.1 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr20:46331286 C>T maps to NM_001161841.1 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr20:46313183 G>A maps to NM_001161841.1 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr20:46331340 G>A maps to NM_001161841.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr20:46365558 G>A maps to NM_001161841.1 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:46365615 G>A maps to NM_001161841.1 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:46365630 G>A maps to NM_001161841.1 H77H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:46365603 G>A maps to NM_001161841.1 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr16:28631440 G>A maps to NM_177536.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:28619820 G>A maps to NM_177529.1 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:28619844 G>A maps to NM_177529.1 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:28619680 G>A maps to NM_177529.1 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:28618162 G>A maps to NM_177529.1 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr16:28620092 C>G maps to NM_177529.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:28617509 G>A maps to NM_177529.1 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:28618126 G>A maps to NM_177529.1 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr16:28620050 G>T maps to NM_177529.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr16:28617509 G>A maps to NM_177529.1 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr16:28603629 G>C maps to NM_001054.3 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr16:28603668 C>T maps to NM_001054.3 K230K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr16:28603626 G>A maps to NM_001054.3 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr16:28603752 C>T maps to NM_001054.3 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr16:28607161 G>A maps to NM_001054.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:28603582 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr4:70592811 C>T maps to NM_014465.3 E295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:70615495 C>T maps to NM_014465.3 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:70620878 G>A maps to NM_014465.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:70599184 C>T maps to NM_014465.3 W181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr2:108917355 C>T maps to ENST00000437390 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:108910263 C>T maps to ENST00000437390 Y47Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:108910802 A>G maps to ENST00000437390 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:108917374 G>A maps to ENST00000437390 W134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr2:108863802 G>A maps to NM_001008743.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:108881764 G>A maps to NM_001008743.1 K291K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:108872050 C>T maps to NM_001008743.1 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:108881441 C>T maps to NM_001008743.1 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr2:108881315 C>T maps to NM_001008743.1 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr2:108881709 G>A maps to NM_001008743.1 W273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:108881279 G>A did not map to a codon.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr2:108875247 C>T maps to NM_001008743.1 H195H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr2:108868923 G>A maps to NM_001008743.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:108869897 G>A maps to NM_001008743.1 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:108872050 C>T maps to NM_001008743.1 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:109002724 C>T maps to NM_006588.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:108994909 G>A maps to NM_006588.2 W39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:108994819 T>C maps to NM_006588.2 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:108999956 C>T maps to NM_006588.2 D202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:108994897 G>A maps to NM_006588.2 W35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:108999908 G>A maps to NM_006588.2 W186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr4:70710059 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr4:70707807 C>T maps to NM_005420.2 W263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr4:70715275 G>A maps to NM_005420.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:70715263 C>T maps to NM_005420.2 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:70719949 C>T maps to NM_005420.2 W118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr4:70710023 G>A maps to NM_005420.2 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr4:70715153 C>T did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr4:70721060 G>A maps to NM_005420.2 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr19:48378070 C>T maps to NM_003167.3 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:48374807 C>T maps to NM_003167.3 W254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:48382322 G>A maps to NM_003167.3 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:49090501 C>T maps to NM_177973.1 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:49100165 C>T maps to NM_177973.1 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr19:49100030 C>T maps to NM_177973.1 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr19:49094966 C>T maps to NM_177973.1 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr22:44234846 C>T maps to NM_014351.3 K136K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr22:44258217 G>A maps to NM_014351.3 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:37406706 G>A maps to NM_001032377.1 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:37414599 C>T maps to NM_001032377.1 W32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:37406711 G>A maps to NM_001032377.1 R102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:37415609 G>A maps to NM_001032377.1 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr3:4452588 C>T maps to NM_182760.3 W305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr7:56136220 C>T maps to ENST00000395437 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr7:56136221 C>T maps to ENST00000395437 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr7:56140704 G>A maps to ENST00000395437 E102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr17:73164460 G>A maps to NM_006937.3 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:73170891 G>A maps to NM_006937.3 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr21:46226919 G>A maps to ENST00000411651 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:892477 C>T maps to ENST00000456758 F503F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr7:881720 G>A maps to ENST00000456758 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr7:909026 C>T maps to ENST00000456758 S863S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr7:881762 C>T maps to ENST00000456758 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:896020 C>A maps to ENST00000456758 T648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:892284 C>T maps to ENST00000456758 I486I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:893140 C>T maps to ENST00000456758 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr22:39147368 C>T maps to ENST00000405018 K44K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr22:39132376 C>T maps to ENST00000405018 T704T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr22:39138307 G>A maps to ENST00000405018 Q377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr22:39135879 G>A maps to ENST00000405018 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:48056918 C>T maps to NM_152782.3 Q76Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:48026964 G>A maps to NM_152782.3 R346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:48026964 G>A maps to NM_152782.3 R346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr20:31573550 G>A maps to NM_080675.3 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr20:31585461 C>T maps to NM_080675.3 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr20:31573679 G>A maps to NM_080675.3 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:31572945 G>A maps to NM_080675.3 Q315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr20:31585461 C>T maps to NM_080675.3 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr20:31571701 C>T maps to NM_080675.3 W346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr20:31583445 C>T maps to NM_080675.3 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:31577456 G>A maps to NM_080675.3 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:31585461 C>T maps to NM_080675.3 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr20:31590455 G>A maps to NM_080675.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr12:56397532 G>A maps to NM_001032387.1 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:56398468 C>T maps to NM_001032387.1 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr14:21836514 A>G maps to NM_007192.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr14:21836515 A>T maps to NM_007192.3 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr14:21821652 G>A maps to NM_007192.3 R998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr14:21821653 G>A maps to NM_007192.3 A997A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr14:21827666 G>A maps to NM_007192.3 D759D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr14:21830468 G>A maps to NM_007192.3 S560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:21834602 G>A maps to NM_007192.3 N347N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:21834650 G>A maps to NM_007192.3 D331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:21838551 G>A maps to NM_007192.3 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:21840062 G>A maps to NM_007192.3 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr14:21837439 G>A maps to NM_007192.3 D235D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:44929547 A>G maps to NM_181356.1 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr6:44929496 T>C maps to NM_181356.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr19:39963570 T>A did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:39963552 C>T maps to NM_003169.3 S713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:39962100 C>T maps to NM_003169.3 I594I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:39959787 C>T maps to NM_003169.3 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:39963959 C>T maps to NM_003169.3 P792P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr19:39964644 C>T maps to NM_003169.3 T845T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr19:39961135 C>T maps to NM_003169.3 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:39959431 C>T maps to NM_003169.3 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr19:39967005 C>T maps to NM_003169.3 N1077N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr19:39960880 C>T maps to NM_003169.3 F499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:39961135 C>T maps to NM_003169.3 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:39959962 C>T maps to NM_003169.3 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:39960880 C>T maps to NM_003169.3 F499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:39963691 C>T maps to NM_003169.3 A732A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr17:27024696 C>T maps to NM_003170.3 A1423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr17:27011696 C>T maps to NM_003170.3 Q775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:27001621 C>T maps to NM_003170.3 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr17:27008286 C>T maps to NM_003170.3 Q455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr17:27008960 C>T maps to NM_003170.3 R520R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr17:27017170 G>A maps to NM_003170.3 R1138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:27023943 C>T maps to NM_003170.3 D1351D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:27023944 C>T maps to NM_003170.3 Q1352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr17:27027481 C>A maps to NM_003170.3 S1586S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:27010010 C>T maps to NM_003170.3 A593A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr17:27003315 C>T maps to NM_003170.3 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:27005188 C>T maps to NM_003170.3 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:27026843 C>A maps to NM_003170.3 G1498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:27026844 C>T maps to NM_003170.3 Q1499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:27008340 C>T maps to NM_003170.3 R473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:27015131 G>A maps to NM_003170.3 R1010R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr17:27004734 C>T maps to NM_003170.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr17:27020796 C>T maps to NM_003170.3 F1239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr17:27010767 C>T maps to NM_003170.3 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:27876606 C>T maps to NM_014860.1 E330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr10:70945776 G>A maps to NM_003171.3 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:70954989 C>T maps to NM_003171.3 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:70954959 T>C maps to NM_003171.3 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:136227981 C>A maps to NM_017503.3 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr9:136200571 G>A maps to NM_006753.4 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr9:136201321 C>T maps to NM_006753.4 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:136199575 G>A maps to NM_006753.4 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr9:114825233 C>T maps to NM_022486.3 E611E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr9:114886618 C>T maps to NM_022486.3 E268E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr9:114840971 C>T maps to NM_022486.3 K533K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr9:114804187 A>C maps to NM_022486.3 A734A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:114874093 G>A maps to NM_022486.3 D337D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:24579501 C>T maps to NM_019601.3 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr22:24579588 C>T maps to NM_019601.3 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:24579085 G>A maps to NM_019601.3 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:24584089 G>A maps to NM_019601.3 P776P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:24580797 C>T maps to NM_019601.3 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:24580779 C>T maps to NM_019601.3 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr22:24579558 C>T maps to NM_019601.3 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr22:24583629 C>T maps to NM_019601.3 F661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr22:24579486 C>T maps to NM_019601.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:24581993 C>T maps to NM_019601.3 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:24583560 C>T maps to NM_019601.3 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr9:95846866 G>A maps to NM_145006.2 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:95838132 C>T maps to NM_145006.2 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:223441997 G>A maps to NM_017982.3 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr1:223396906 G>A maps to NM_017982.3 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:223465796 G>A maps to NM_017982.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:223408419 G>A maps to NM_001037175.2 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:223465811 G>A maps to NM_017982.3 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:223465898 G>A maps to NM_017982.3 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:223465961 G>A maps to NM_017982.3 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:223465991 C>T maps to NM_017982.3 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:223442006 G>A maps to NM_017982.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:223401021 G>A maps to NM_017982.3 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:223402593 G>A maps to NM_017982.3 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:223465937 C>T maps to NM_017982.3 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:33249378 G>A maps to NM_015551.1 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:33249378 G>A maps to NM_015551.1 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:48558700 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr11:67942630 T>G maps to NM_017635.3 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr11:67942592 C>T maps to NM_017635.3 K145K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr11:67925385 C>T maps to NM_017635.3 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:55854201 C>T maps to NM_032701.3 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:55854201 C>T maps to NM_032701.3 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr17:30325967 G>A maps to NM_015355.2 L722L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44Q-06A-11D-A25O-08 chr17:30325675 G>T did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:149878274 C>T maps to NM_014849.3 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr1:149885218 G>A maps to NM_014849.3 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:149879640 G>A maps to NM_014849.3 F499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr1:149882127 G>A maps to NM_014849.3 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:149885368 C>T maps to NM_014849.3 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:149880811 G>A maps to NM_014849.3 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:149879341 G>A maps to NM_014849.3 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:149885218 G>A maps to NM_014849.3 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:149883494 G>A maps to NM_014849.3 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:149878253 C>T maps to NM_014849.3 G611G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:149883446 G>A maps to NM_014849.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:149884828 G>A maps to NM_014849.3 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr1:149878223 C>T maps to NM_014849.3 K621K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr1:149877520 G>A maps to NM_014849.3 I652I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:91811790 G>A maps to NM_014848.4 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:91811826 G>A maps to NM_014848.4 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:91810783 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:91803599 C>T maps to NM_014848.4 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:91795652 G>A maps to NM_014848.4 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:91811790 G>A maps to NM_014848.4 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr15:91827350 C>T maps to NM_014848.4 F536F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr15:91795166 C>T maps to NM_014848.4 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:91795140 C>T maps to NM_014848.4 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:91795688 C>T maps to NM_014848.4 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:91795727 C>T maps to NM_014848.4 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:91809810 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:91769873 C>T maps to NM_014848.4 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr5:75591626 C>T maps to NM_014979.1 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr5:75597247 C>T maps to NM_014979.1 F626F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:75580985 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:75594627 G>A maps to NM_014979.1 G504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:75427892 C>T maps to NM_014979.1 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:75597322 G>A maps to NM_014979.1 W651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr5:75591653 C>T maps to NM_014979.1 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:75428042 C>T maps to NM_014979.1 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:75428042 C>T maps to NM_014979.1 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:75596678 C>T maps to NM_014979.1 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:75597271 C>T maps to NM_014979.1 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:75505559 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:75596659 G>A maps to NM_014979.1 W581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:75596680 G>A maps to NM_014979.1 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr5:75597229 G>A maps to NM_014979.1 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr9:113169590 C>T maps to ENST00000374463 W2766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr9:113192602 G>A maps to ENST00000374463 I1830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr9:113170151 G>A maps to ENST00000374463 A2579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr9:113166681 G>A maps to ENST00000374463 F3200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr9:113312237 C>T maps to ENST00000374463 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr9:113197545 G>A maps to ENST00000374463 I1624I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:113169002 G>A maps to ENST00000374463 F2962F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr9:113197560 C>T maps to ENST00000374463 V1619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr9:113312198 C>T maps to ENST00000374463 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:113194886 C>T maps to ENST00000374463 L1699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:113212421 G>A maps to ENST00000374463 T1340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:113168711 G>A maps to ENST00000374463 F3059F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:113173477 G>A maps to ENST00000374463 S2174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:113252032 G>A maps to ENST00000374463 F609F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr9:113194309 G>A maps to ENST00000374463 V1749V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr9:113228142 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:113194892 A>T maps to ENST00000374463 P1697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr9:113170145 G>A maps to ENST00000374463 I2581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:113170289 G>A maps to ENST00000374463 L2533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:113241923 C>T maps to ENST00000374463 L826L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr9:113170130 G>A maps to ENST00000374463 F2586F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr9:113198673 G>A maps to ENST00000374463 L1587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr9:113212403 G>A maps to ENST00000374463 V1346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:113170541 G>A maps to ENST00000374463 I2449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:113312204 G>A maps to ENST00000374463 T237T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-ER-A19H-06A-12D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr9:113163262 G>A maps to ENST00000374463 F3234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr9:113275227 G>A maps to ENST00000374463 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:113171162 T>G maps to ENST00000374463 G2242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:113208244 G>A maps to ENST00000374463 L1445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:113312258 G>A maps to ENST00000374463 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr9:113251993 G>A maps to ENST00000374463 I622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:113189869 C>T did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr9:113170145 G>A maps to ENST00000374463 I2581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr9:113170733 G>A maps to ENST00000374463 T2385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr10:29812461 T>C maps to NM_021738.2 G1027G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr10:29812908 T>A maps to NM_021738.2 S878S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr10:29813490 C>T maps to NM_021738.2 A832A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr10:29821660 G>A maps to NM_021738.2 T545T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:29747362 C>T maps to NM_021738.2 E2186E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr10:29840031 C>T maps to NM_021738.2 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:29839932 C>T maps to NM_021738.2 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:29773715 C>T maps to NM_021738.2 G1608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:29840138 G>A maps to NM_021738.2 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:109306378 G>A maps to NM_018711.2 Q474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:109313542 C>T maps to NM_018711.2 W339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr12:109309579 G>A maps to NM_018711.2 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:109309617 G>A maps to NM_018711.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr12:109306310 C>T maps to NM_018711.2 *496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:138341225 C>T maps to NM_001139456.1 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr7:138333804 G>A maps to NM_001139456.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr7:138305865 C>T maps to NM_001139456.1 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr7:138312111 G>A maps to NM_001139456.1 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:138305865 C>T maps to NM_001139456.1 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr7:138312159 C>T maps to NM_001139456.1 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr7:138341225 C>T maps to NM_001139456.1 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:138329482 C>T maps to NM_001139456.1 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:9746213 C>T maps to NM_015055.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr11:9771498 G>A maps to NM_015055.2 E580E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr23:16761837 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:16775303 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr8:110587740 G>A maps to NM_001099744.1 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:110587269 G>A maps to NM_001099744.1 V619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr8:110655053 G>A maps to NM_001099744.1 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:110592131 C>T maps to NM_001099744.1 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:110655121 G>A maps to NM_001099744.1 R22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr8:110631155 C>T maps to NM_001099744.1 K114K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:110588103 G>A maps to NM_001099744.1 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr10:135372832 C>T maps to NM_001143764.1 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:135369375 C>T maps to NM_001143764.1 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:135372835 G>A maps to NM_001143764.1 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:135369384 C>T maps to NM_001143764.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:135367794 C>T maps to NM_001143763.1 *319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:115537407 G>A maps to NM_003176.2 K931K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr1:115401175 G>A maps to NM_003176.2 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr1:115454126 T>C maps to NM_003176.2 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr1:115537359 G>A maps to NM_003176.2 R915R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:115453109 C>T maps to NM_003176.2 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:115401231 G>A maps to NM_003176.2 W119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:115523997 G>A maps to NM_003176.2 W808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr1:115487075 G>A maps to NM_003176.2 E681E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:115523955 G>T did not map to a codon.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr1:115401287 A>C maps to NM_003176.2 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:115524037 C>T maps to NM_003176.2 R822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:115399877 C>T maps to NM_003176.2 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:115420731 C>T maps to NM_003176.2 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:115487548 T>C maps to NM_003176.2 D700D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr20:58495427 C>A maps to NM_014258.2 G95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:58450425 C>T maps to NM_014258.2 W1083*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr20:58491600 G>A maps to NM_014258.2 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:58491600 G>A maps to NM_014258.2 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr6:10961743 G>A maps to NM_001040274.2 G789G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:10913149 C>T maps to NM_001040274.2 F354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr6:10926588 G>A maps to NM_001040274.2 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr6:10942728 C>T maps to NM_001040274.2 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:10894141 C>T maps to NM_001040274.2 Q41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:10930682 G>A maps to NM_001040274.2 Q523Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr6:10961627 G>A maps to NM_001040274.2 K782K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:10926588 G>A maps to NM_001040274.2 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:10928670 C>T maps to NM_001040274.2 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:10928655 C>T maps to NM_001040274.2 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:10894143 G>A maps to NM_001040274.2 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr6:10935385 T>G maps to NM_001040274.2 A593A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:15222494 C>T maps to NM_033025.4 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:85648236 C>T maps to NM_032184.1 R696R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:85656400 C>T maps to NM_032184.1 K260K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:85624433 C>G maps to NM_032184.1 *1195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:85634894 A>G maps to NM_032184.1 D895D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:85665965 C>T maps to NM_032184.1 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr9:93636490 C>T maps to NM_003177.5 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr9:93650843 G>C maps to NM_003177.5 R590R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr9:93650892 C>T maps to NM_003177.5 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr9:93606332 C>T maps to NM_003177.5 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:93640053 G>A maps to NM_003177.5 Q461Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr9:93637032 G>A maps to NM_003177.5 K361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr9:93626930 C>T maps to NM_003177.5 Q260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:93629423 G>A maps to NM_003177.5 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr19:46355637 G>A maps to NM_004819.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr19:46326659 G>A maps to NM_004819.2 F890F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr19:46355790 G>A maps to NM_004819.2 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:46345589 G>A maps to NM_004819.2 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:46318829 C>T maps to NM_004819.2 K1271K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:46332352 G>A maps to NM_004819.2 F620F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:46319748 G>A maps to NM_004819.2 P1115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:46318910 G>A maps to NM_004819.2 P1244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:46328539 G>A maps to NM_004819.2 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:46332448 G>A maps to NM_004819.2 I588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:46338423 G>A maps to NM_004819.2 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr19:46331156 G>A maps to NM_004819.2 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr23:47436012 G>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:47464660 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:47466580 C>T did not map to a codon.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr23:47434644 C>T did not map to a codon.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr23:47434645 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr23:47466363 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:47432302 C>G did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr23:47466578 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:47466348 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:12208796 C>T maps to NM_133625.3 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr3:12203092 C>T maps to NM_133625.3 H273H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:12192798 G>A maps to NM_133625.3 Q248Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:12208782 C>T maps to NM_133625.3 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr22:32914103 G>A maps to NM_003490.3 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:32937672 G>A maps to NM_003490.3 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr22:32929778 C>T maps to NM_003490.3 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr22:33402356 G>A maps to NM_003490.3 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr22:32909798 G>A maps to NM_003490.3 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:32914271 G>A maps to NM_003490.3 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr22:33265033 C>T maps to NM_003490.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:33260979 G>A maps to NM_003490.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:86324598 G>A maps to NM_006372.4 Q583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr6:86324794 G>A maps to NM_006372.4 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr6:152644638 G>A maps to NM_182961.2 I5297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr6:152771890 G>A maps to NM_182961.2 L1088L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr6:152737952 G>A maps to NM_182961.2 F1873F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr6:152708308 C>T maps to NM_182961.2 A2795A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr6:152473195 G>A maps to NM_182961.2 N8070N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr6:152639302 C>T maps to NM_182961.2 K5495K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51K-06A-11D-A25O-08 chr6:152694293 C>A maps to NM_182961.2 E3129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:152711440 G>A maps to NM_182961.2 I2717I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr6:152697631 G>A maps to NM_182961.2 R3070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:152675940 G>A maps to NM_182961.2 F3593F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:152725356 T>C maps to NM_182961.2 P2272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr6:152771803 C>T maps to NM_182961.2 R1117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:152737771 G>A maps to NM_182961.2 Q1934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:152740784 C>T maps to NM_182961.2 W1780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:152772237 G>A maps to NM_182961.2 R1044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:152831443 C>T maps to NM_182961.2 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:152841605 G>A maps to NM_182961.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:152718115 C>T maps to ENST00000341594 Q2489Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:152553249 C>T did not map to a codon.
Alternatively spliced codon TCGA-EE-A2GH-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:152563398 G>A maps to NM_182961.2 I6623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:152646289 G>A maps to NM_182961.2 R5196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:152708266 G>A maps to NM_182961.2 F2809F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:152712528 C>T maps to NM_182961.2 L2629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr6:152464811 G>A maps to NM_182961.2 I8355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr6:152565695 G>A maps to NM_182961.2 S6556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:152771869 C>T maps to NM_182961.2 R1095R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:152542122 G>A maps to NM_182961.2 Q7239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:152464811 G>A maps to NM_182961.2 I8355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:152644758 G>A maps to NM_182961.2 F5257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:152720789 G>A maps to NM_182961.2 Q2400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:152841652 T>A maps to NM_182961.2 K84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:152461225 G>A maps to NM_182961.2 L8439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:152631047 G>A maps to NM_182961.2 L5708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:152690745 G>A maps to NM_182961.2 L3171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:152457866 C>T maps to NM_182961.2 K8515K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr6:152553292 G>A maps to NM_182961.2 S6940S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:152552663 C>T maps to NM_182961.2 V6967V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr6:152668337 G>A maps to NM_182961.2 D3978D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:152708489 C>T maps to NM_182961.2 W2735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:152720829 T>G maps to NM_182961.2 I2386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:152755058 C>T maps to NM_182961.2 V1444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:152776590 C>T maps to NM_182961.2 G954G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:152646419 A>G maps to NM_182961.2 V5152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr6:152708212 A>T maps to NM_182961.2 V2827V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr6:152949424 G>A maps to NM_182961.2 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr6:152746628 T>C maps to NM_182961.2 Q1718Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr6:152576737 G>A maps to NM_182961.2 L6416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:152454551 C>G maps to NM_182961.2 L8620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr6:152708284 C>T maps to NM_182961.2 K2803K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:152737898 C>T maps to NM_182961.2 V1891V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F4-06A-12D-A25O-08 chr6:152623199 T>C did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr6:152469312 G>A maps to NM_182961.2 I8281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr6:152443612 G>A maps to NM_182961.2 F8784F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:152583268 G>A maps to NM_182961.2 S6290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:152737850 C>T maps to NM_182961.2 K1907K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:152768619 G>A maps to NM_182961.2 F1214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:152782812 G>A maps to NM_182961.2 H771H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:152831473 G>A maps to NM_182961.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:152847232 G>A maps to NM_182961.2 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr6:152688433 C>T maps to NM_182961.2 T3297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr6:152831379 G>A maps to NM_182961.2 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:152485375 G>A maps to NM_182961.2 I7904I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:152708302 G>A maps to NM_182961.2 S2797S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:152832156 G>A maps to NM_182961.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:152841598 T>A maps to NM_182961.2 R102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr6:152841608 G>A maps to NM_182961.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr6:152501269 C>T did not map to a codon.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr6:152686085 G>A maps to NM_182961.2 V3347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:152804246 C>T maps to NM_182961.2 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:152697584 G>A maps to NM_182961.2 I3085I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:152768688 C>T maps to NM_182961.2 L1191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr14:64496704 C>T maps to NM_182914.2 S2269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr14:64587766 C>T maps to NM_182914.2 F4382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr14:64468787 C>T maps to NM_182914.2 Q1259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr14:64692042 C>T maps to NM_182914.2 P6841P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr14:64494360 C>T maps to NM_182914.2 F2188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr14:64676295 G>A maps to NM_182914.2 E6180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr14:64465734 C>T maps to NM_182914.2 Q1153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:64408665 C>T maps to NM_182914.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:64460551 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:64520141 C>T maps to NM_182914.2 Q3171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:64461880 C>T maps to NM_182914.2 I967I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:64476783 C>T maps to NM_182914.2 L1560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:64593100 C>T maps to NM_182914.2 F4537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr14:64421517 A>G maps to NM_182914.2 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr14:64628972 C>T maps to NM_182914.2 P5426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:64453313 C>T maps to NM_182914.2 T764T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr14:64588806 G>A maps to NM_182914.2 Q4412Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:64519169 C>T maps to NM_182914.2 Q2847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:64612817 C>T maps to NM_182914.2 I5172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:64692072 C>T maps to NM_182914.2 L6851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr14:64547172 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr14:64484367 G>A maps to NM_182914.2 W1648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:64593100 C>T maps to NM_182914.2 F4537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:64630182 C>T maps to NM_182914.2 R5455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr14:64519573 C>T maps to NM_182914.2 I2981I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:64692099 C>T maps to NM_182914.2 P6860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr14:64604590 T>C maps to NM_182914.2 C4911C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr14:64529516 C>T maps to NM_182914.2 Y3372Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr14:64574243 C>T maps to NM_182914.2 S4176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr14:64519207 C>T maps to NM_182914.2 P2859P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:64461880 C>T maps to NM_182914.2 I967I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:64556356 C>T maps to NM_182914.2 I3912I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:64630176 C>T maps to NM_182914.2 L5453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:64681135 C>T maps to NM_182914.2 G6427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr14:64491656 G>A maps to NM_182914.2 R1956R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:33391260 G>A maps to NM_006772.2 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:33412330 C>T maps to NM_006772.2 I1173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:33410235 C>T maps to NM_006772.2 I767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:33400469 C>T maps to NM_006772.2 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:33406561 C>T maps to NM_006772.2 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:33405665 C>T maps to NM_006772.2 Y328Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr6:33408709 C>T maps to NM_006772.2 A627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:33406561 C>T maps to NM_006772.2 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:33402958 A>G maps to NM_006772.2 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:33408640 G>T maps to NM_006772.2 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr6:33414467 C>T maps to NM_006772.2 I1233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr22:39772069 C>T maps to NM_004711.4 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr22:39746023 G>A maps to NM_004711.4 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr22:39770346 C>T maps to NM_004711.4 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F4-06A-12D-A25O-08 chr22:39770400 C>T maps to NM_004711.4 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:39773622 C>T maps to NM_145731.3 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr17:76167052 C>T maps to NM_004710.3 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:2042727 G>A maps to NM_004209.5 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr19:48878999 C>T maps to NM_012451.3 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:48878891 C>T maps to NM_012451.3 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr19:48879391 C>T maps to NM_012451.3 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:48878948 C>T maps to NM_012451.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr21:34003880 C>T maps to NM_003895.3 R1421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr21:34045782 C>T maps to NM_003895.3 K570K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr21:34003736 G>A maps to NM_003895.3 F1469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr21:34022608 G>A maps to NM_003895.3 I1013I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr21:34018859 G>A maps to NM_003895.3 L1069L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:34018826 G>A maps to NM_003895.3 S1080S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr6:158497656 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr6:158502224 C>T maps to NM_003898.3 F884F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr6:158454696 C>T maps to NM_003898.3 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:158517143 C>T maps to NM_003898.3 D1413D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr6:158502224 C>T maps to NM_003898.3 F884F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:158485991 G>A maps to NM_003898.3 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:158514069 C>T maps to NM_003898.3 L1226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:158492714 C>T maps to NM_003898.3 F674F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr6:158483031 C>T maps to NM_003898.3 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:158484826 C>T maps to NM_003898.3 Q378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr6:158509710 G>A maps to NM_003898.3 K1121K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr6:158483100 G>A maps to NM_003898.3 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr6:158450040 G>A maps to NM_003898.3 W156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:158505105 C>T maps to NM_003898.3 L1036L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr15:99672947 C>T maps to ENST00000336292 T1460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr15:99672050 G>A maps to ENST00000336292 A1161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:99670730 C>T maps to ENST00000336292 A721A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr15:99670139 C>T maps to ENST00000336292 F524F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr15:99670305 C>T maps to ENST00000336292 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr15:99670364 G>A maps to ENST00000336292 V599V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:99669599 C>A maps to ENST00000336292 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr15:99671129 C>T maps to ENST00000336292 I854I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZY-06A-11D-A197-08 chr15:99669740 T>G maps to ENST00000336292 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:99670139 C>T maps to ENST00000336292 F524F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:150028985 C>T maps to NM_001166209.1 F627F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr4:119952971 C>T maps to NM_133477.2 A1014A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:119952506 G>A maps to NM_133477.2 V859V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:119979004 C>T maps to NM_133477.2 S1234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:119979004 C>T maps to NM_133477.2 S1234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr4:119978959 T>C maps to NM_133477.2 Y1219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr4:119948195 T>C maps to NM_133477.2 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr4:119952317 C>T maps to NM_133477.2 N796N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr4:119952980 G>A maps to NM_133477.2 T1017T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:119951735 C>T maps to NM_133477.2 P602P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr4:119979073 G>A maps to NM_133477.2 W1257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:119947922 C>T maps to NM_133477.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:119948252 G>A maps to NM_133477.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr4:119948129 C>T maps to NM_133477.2 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:119951153 C>G maps to NM_133477.2 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr4:119944593 C>T maps to NM_133477.2 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:119951747 C>T maps to NM_133477.2 T606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:119952827 G>A maps to NM_133477.2 K966K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:119952896 C>T maps to NM_133477.2 P989P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr4:119952867 C>T maps to NM_133477.2 Q980*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr4:119951996 G>A maps to NM_133477.2 R689R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr10:75407924 C>T maps to NM_001114133.1 A495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:75407492 C>A maps to NM_001114133.1 P639P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr10:75407026 G>A maps to NM_001114133.1 L795L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr10:75407603 C>T maps to NM_001114133.1 G602G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr10:75407477 C>T maps to NM_001114133.1 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr10:75408419 C>T maps to NM_001114133.1 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:75408263 C>T maps to NM_001114133.1 E382E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:75408419 C>T maps to NM_001114133.1 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:63466542 C>T maps to NM_001130003.1 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:63594955 C>T maps to NM_001130003.1 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr3:63542371 T>A maps to NM_001130003.1 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:35879045 G>A maps to NM_007247.4 L1314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:35902458 G>A maps to NM_007247.4 I939I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr17:35880721 G>A maps to NM_007247.4 S1232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:35898497 A>G maps to NM_007247.4 L1149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:35914039 G>A maps to NM_007247.4 F595F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:35900517 G>A maps to NM_007247.4 I1110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:35900498 G>A maps to NM_007247.4 L1117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:35928906 G>A maps to NM_007247.4 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr1:110019424 C>T maps to NM_001040709.1 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:110022027 G>A maps to NM_001040709.1 W226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:110022023 C>T maps to NM_001040709.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:110018315 C>T maps to NM_001040709.1 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:110022013 C>T maps to NM_001040709.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:110018216 C>T maps to NM_001040709.1 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:110018222 C>T maps to NM_001040709.1 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr12:79679642 G>A maps to NM_005639.2 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:79689859 G>A maps to NM_005639.2 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:79837865 G>A maps to NM_005639.2 K314K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:79679636 C>T maps to NM_005639.2 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr12:79679681 G>A maps to NM_005639.2 K94K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:79685897 C>T maps to NM_005639.2 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:79689862 C>T maps to NM_005639.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:79693273 G>A maps to NM_005639.2 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:79693174 G>A maps to NM_005639.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:79679693 G>A maps to NM_005639.2 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:79693273 G>A maps to NM_005639.2 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr12:79693240 C>T maps to NM_005639.2 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr12:79679738 G>A maps to NM_005639.2 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:79747292 G>A maps to NM_005639.2 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:79842817 C>T maps to NM_005639.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:33579074 G>A maps to NM_198992.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr12:33559963 C>T maps to NM_198992.3 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr12:33560107 G>A maps to NM_198992.3 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:33559963 C>T maps to NM_198992.3 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr12:33579302 G>A maps to NM_198992.3 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:33579245 C>T maps to NM_198992.3 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:33579404 G>A maps to NM_198992.3 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:33535330 C>T maps to NM_198992.3 E441E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:33532877 G>A maps to NM_198992.3 V463V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:33560281 G>A maps to NM_198992.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:33592343 G>A maps to NM_198992.3 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr12:33579197 C>T maps to NM_198992.3 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr12:33538202 G>A maps to NM_198992.3 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr12:33532765 C>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:33535402 C>T maps to NM_198992.3 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:33592442 C>T maps to NM_198992.3 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:33559744 T>C maps to NM_198992.3 K352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr12:33559747 C>T maps to NM_198992.3 W351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr12:33559762 C>T maps to NM_198992.3 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:33579149 G>A maps to NM_198992.3 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:33559748 C>T maps to NM_198992.3 W351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:33559957 C>T maps to NM_198992.3 K281K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:33579329 C>T maps to NM_198992.3 W84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr12:33559852 G>A maps to NM_198992.3 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:33579404 G>A maps to NM_198992.3 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:33529797 G>A maps to NM_198992.3 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:33535419 G>A maps to NM_198992.3 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr12:33560281 G>A maps to NM_198992.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr12:33592400 G>A maps to NM_198992.3 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:155851142 C>T maps to NM_152280.4 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:155837945 C>T maps to NM_152280.4 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:155838374 C>T maps to NM_152280.4 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:155837855 G>A maps to NM_152280.4 E45E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:155838371 G>A maps to NM_152280.4 K217K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:155851154 C>T maps to NM_152280.4 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:155851142 C>A maps to NM_152280.4 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr1:155838350 G>A maps to NM_152280.4 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:66807361 C>T maps to NM_001177880.1 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr11:66807331 C>T maps to NM_001177880.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:66812086 C>T maps to NM_001177880.1 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:66813296 C>T maps to NM_001177880.1 N347N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:66807445 C>T maps to NM_001177880.1 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr11:66807658 C>T maps to NM_001177880.1 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr11:45274136 G>A maps to NM_020826.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:45265863 C>T maps to NM_020826.2 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr11:45274136 G>A maps to NM_020826.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:45274136 G>A maps to NM_020826.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr11:45267997 G>A maps to NM_020826.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr11:45274136 G>A maps to NM_020826.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr11:45265887 G>A maps to NM_020826.2 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:45265662 C>T maps to NM_020826.2 W407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:45277286 G>A maps to NM_020826.2 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:210334236 T>A maps to NM_001146261.1 Y570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:210194390 C>T maps to NM_001146261.1 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:210334186 C>T maps to NM_001146261.1 Q554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr10:46969436 C>T maps to NM_031912.3 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:46967611 C>T maps to NM_031912.3 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:46967674 G>A maps to NM_031912.3 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:46965113 C>T maps to NM_031912.3 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr10:46967551 T>C maps to NM_031912.3 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr10:46969394 G>A maps to NM_031912.3 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:46967611 C>T maps to NM_031912.3 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:46969277 G>A maps to NM_031912.3 C61C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr10:46960013 C>T maps to NM_181519.2 Q376Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr10:46963858 C>A maps to NM_031912.3 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr10:46965843 G>A maps to NM_031912.3 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:62462917 C>T maps to NM_031914.2 Q61*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D9-A6EC-06A-11D-A30X-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr14:62567415 G>A maps to NM_031914.2 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr14:62536414 G>A maps to NM_031914.2 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:62567373 G>A maps to NM_031914.2 K629K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr14:62551074 C>T maps to NM_031914.2 F532F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr14:62567163 T>G maps to NM_031914.2 R559R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr14:62567415 G>A maps to NM_031914.2 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr14:62463104 G>A maps to NM_031914.2 W123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr14:62567121 A>G maps to NM_031914.2 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr14:62536399 C>T maps to NM_031914.2 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:62462973 G>A maps to NM_031914.2 E79E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:62547778 G>A maps to NM_031914.2 Q407Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:62547880 G>A maps to NM_031914.2 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr14:62551075 C>T maps to NM_031914.2 R533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:19278341 C>T maps to NM_016524.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr16:19195342 C>T maps to NM_016524.2 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr16:19278238 C>T maps to NM_016524.2 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr16:19236020 C>T maps to NM_016524.2 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:19195291 G>A maps to NM_016524.2 E258E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:19195303 C>T maps to NM_016524.2 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:19194955 G>A maps to NM_016524.2 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:202571505 C>T maps to NM_177402.4 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:202568429 C>T maps to NM_177402.4 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:202566019 G>A maps to NM_177402.4 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr1:202574756 C>T maps to NM_177402.4 K48K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:202568426 C>T maps to NM_177402.4 K324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr19:51135964 C>T maps to NM_001160329.1 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:51135760 C>T maps to NM_001160329.1 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr19:51132549 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:51132595 C>T maps to NM_001160329.1 Q412Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr19:51133394 C>T maps to NM_001160329.1 Q236Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr19:51135997 G>A maps to NM_001160329.1 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:51133250 C>T maps to NM_001160329.1 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:51133145 C>T maps to NM_001160329.1 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:51133406 G>A maps to NM_001160329.1 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr19:51140560 G>A maps to NM_001160329.1 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr18:40850359 G>A maps to NM_020783.3 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr18:40850434 G>A maps to NM_020783.3 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr18:40853625 T>C maps to NM_020783.3 E256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr18:40853628 C>T maps to NM_020783.3 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr18:40854288 C>T maps to NM_020783.3 W35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr18:40851749 G>A maps to NM_020783.3 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr18:40850563 C>T maps to NM_020783.3 K340K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:40853712 C>T maps to NM_020783.3 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:40850575 C>T maps to NM_020783.3 K336K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:40853802 C>T maps to NM_020783.3 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr18:40854289 C>T maps to NM_020783.3 W35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:55686337 G>A maps to NM_003180.2 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr19:55687184 C>T maps to NM_003180.2 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:55686018 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:55689656 C>T maps to NM_003180.2 K53K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:55689593 C>T maps to NM_003180.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr1:114680608 C>T maps to ENST00000369545 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:114641752 G>A maps to ENST00000369545 Q443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:114680413 G>C maps to ENST00000369545 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:114682400 C>T maps to ENST00000369545 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:114636409 A>C maps to ENST00000369545 *511G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:114641716 G>A maps to ENST00000369545 R455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr11:61295561 C>T maps to NM_004200.2 E149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr11:61318935 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr11:61291957 G>A maps to NM_004200.2 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:61290645 G>A maps to NM_004200.2 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:61290546 C>T maps to NM_004200.2 K369K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:61291906 G>A maps to NM_004200.2 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:61291962 G>A maps to NM_004200.2 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:1858223 G>A maps to NM_138567.3 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr11:1858456 C>T maps to NM_138567.3 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:1858492 C>T maps to NM_138567.3 H346H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr11:1858066 C>T maps to NM_138567.3 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:1856415 C>T maps to NM_138567.3 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:7335109 C>T maps to NM_175733.3 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr11:7441862 G>A maps to NM_175733.3 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:7334910 G>A maps to NM_175733.3 K261K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:7334793 G>A maps to NM_175733.3 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr11:7441751 G>A maps to NM_175733.3 E451E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr11:7439254 G>A maps to NM_175733.3 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:7334766 G>A maps to NM_175733.3 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:7324300 C>T maps to NM_175733.3 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr11:7324556 C>T maps to NM_175733.3 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:7335156 C>T maps to NM_175733.3 I343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:7334967 C>T maps to NM_175733.3 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr11:7335132 G>A maps to NM_175733.3 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:27679919 G>A maps to NM_001193308.1 W497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:27676942 G>A maps to NM_001193308.1 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:27679914 C>T maps to NM_001193308.1 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:85436749 C>T maps to ENST00000359152 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:85456744 G>A maps to NM_001162953.1 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:85468695 G>A maps to NM_001162953.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr11:85435887 G>A maps to ENST00000359152 L1062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:85459354 G>A maps to NM_001162953.1 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr11:85435741 C>T maps to ENST00000359152 K1110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr11:85407406 C>T maps to ENST00000359152 R1672R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:85448656 G>A maps to NM_001162953.1 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:159146557 G>A maps to ENST00000297239 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:159181673 G>A maps to ENST00000297239 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr6:159086618 G>A maps to ENST00000297239 W101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:159166609 C>T maps to ENST00000297239 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:99941717 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr23:99933441 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:99955921 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:99933418 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:99942166 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:99942167 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:99944876 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:99944857 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:99955943 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:99956462 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:99956509 G>A did not map to a codon.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr23:99956963 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:99936231 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:99934390 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:99945635 C>T did not map to a codon.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr23:99936256 A>G did not map to a codon.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr23:37969625 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:37965984 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:37979615 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:37984625 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr23:37979701 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:37913578 G>T did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:37893190 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:37913545 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr23:37893254 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:37935887 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr23:37969633 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:64900473 G>A maps to NM_172230.2 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:64897316 C>T maps to NM_172230.2 E493E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:64900542 G>A maps to NM_172230.2 H76H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr11:64900491 G>A maps to NM_172230.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64899784 G>A maps to NM_172230.2 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr6:166571955 G>A maps to NM_003181.2 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:166571985 G>A maps to NM_003181.2 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:166571847 G>A maps to NM_003181.2 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr6:166571829 C>T maps to NM_003181.2 W427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:132966170 G>A maps to NM_138327.1 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:132966494 G>A maps to NM_138327.1 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr6:132938530 A>G maps to NM_001033080.1 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:132939185 G>A maps to NM_001033080.1 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:132939275 G>A maps to NM_001033080.1 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr6:132939104 G>A maps to NM_001033080.1 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:132909850 G>A maps to NM_003967.2 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr6:132910107 G>A maps to NM_003967.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr6:132910108 G>A maps to NM_003967.2 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:132891894 C>T maps to NM_175067.1 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:132891843 C>T maps to NM_175067.1 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr6:132892409 G>A maps to NM_175067.1 W317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:132891929 G>A maps to NM_175067.1 W157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:132891669 C>T maps to NM_175067.1 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:132873960 C>T maps to NM_053278.1 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:132859925 G>T maps to NM_175057.3 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr22:39817843 C>T maps to NM_006116.2 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr22:39811540 C>T maps to NM_006116.2 N69N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:39824182 C>T maps to NM_006116.2 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:149691192 C>T maps to NM_015093.4 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:149720246 T>C maps to NM_015093.4 H622H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:149700079 T>C maps to NM_015093.4 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr23:30849650 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr17:47921471 C>T maps to NM_170685.2 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr8:38699874 C>T maps to ENST00000379931 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr8:38677794 C>T maps to ENST00000379931 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr8:38696040 C>T maps to ENST00000379931 T643T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:38700835 G>A maps to ENST00000379931 Q729Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr10:123970032 C>T maps to NM_206862.2 A2031A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr10:123987436 G>T maps to NM_206862.2 E2604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr10:123847036 C>T maps to NM_206862.2 A1674A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr10:123892198 C>T maps to NM_206862.2 S1883S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:123843115 G>A maps to NM_206862.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:123985897 G>A maps to NM_206862.2 P2542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr10:123845509 C>T maps to NM_206862.2 C1165C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:123844718 C>T maps to NM_206862.2 Q902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:123974920 G>A maps to NM_206862.2 V2433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:123970389 G>A maps to NM_206862.2 V2150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:123985960 C>T maps to NM_206862.2 P2563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:123842290 T>C maps to NM_206862.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:123845920 G>A maps to NM_206862.2 G1302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:123996968 C>T maps to NM_206862.2 I2729I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr10:123843517 G>A maps to NM_206862.2 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:123970632 G>A maps to NM_206862.2 R2231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:123844579 G>A maps to NM_206862.2 G855G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr10:123845833 G>A maps to NM_206862.2 E1273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:123842713 C>T maps to NM_206862.2 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr10:123781519 G>C maps to NM_206862.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr10:123971034 A>G maps to NM_206862.2 Q2365Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr10:123843337 C>T maps to NM_206862.2 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr10:123997040 C>T maps to NM_206862.2 I2753I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr10:123843106 G>A maps to NM_206862.2 K364K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:123842626 C>T maps to NM_206862.2 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:123843061 C>T maps to NM_206862.2 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:123845773 G>A maps to NM_206862.2 V1253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:123846091 G>A maps to NM_206862.2 G1359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:123970965 G>A maps to NM_206862.2 W2342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:123971139 C>T maps to NM_206862.2 I2400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:123987393 G>A maps to NM_206862.2 A2589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr10:123845569 C>T maps to NM_206862.2 H1185H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:123842554 G>A maps to NM_206862.2 K180K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:123970458 G>A maps to NM_206862.2 T2173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr10:123842581 C>T maps to NM_206862.2 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr10:123842257 G>A maps to NM_206862.2 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr10:123847991 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr4:1729446 C>T maps to NM_006342.1 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr4:1746529 C>T maps to NM_006342.1 Q808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr4:1742646 G>A maps to NM_006342.1 E719E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr4:1746492 C>T maps to NM_006342.1 A795A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:1746291 C>T maps to NM_006342.1 I757I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr4:1729698 C>T maps to NM_006342.1 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr4:1725499 C>T maps to NM_006342.1 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr4:1742602 C>T maps to NM_006342.1 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:1739027 C>T maps to NM_006342.1 F603F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:61685211 C>T maps to NM_016360.3 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:61685283 C>T maps to NM_016360.3 D272D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:61685284 C>T maps to NM_016360.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:75347737 G>A maps to NM_001058.3 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:75425979 T>C maps to NM_001058.3 Q27Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:75276561 G>A maps to NM_001058.3 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:75425990 G>A maps to NM_001058.3 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr2:75425895 C>T maps to NM_001058.3 W55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:75425859 C>T maps to NM_001058.3 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr2:75425859 C>T maps to NM_001058.3 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:75425709 G>A maps to NM_001058.3 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr10:71175908 G>A maps to NM_001057.2 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr10:71175866 G>A maps to NM_001057.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:71164840 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:71174783 G>A maps to NM_001057.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr4:104510904 G>A maps to NM_001059.2 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr4:104511030 G>A maps to NM_001059.2 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:104511151 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:104577452 G>A maps to NM_001059.2 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:104579460 G>A maps to NM_001059.2 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:104640508 C>T maps to NM_001059.2 W108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:104640703 T>C maps to NM_001059.2 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:104640631 G>A maps to NM_001059.2 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:104640603 G>A maps to NM_001059.2 Q77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr4:104511146 G>A maps to NM_001059.2 R364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:104511146 G>A maps to NM_001059.2 R364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr4:104640508 C>T maps to NM_001059.2 W108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:104577401 G>A maps to NM_001059.2 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:104640457 C>T maps to NM_001059.2 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:104640679 G>A maps to NM_001059.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:59042192 C>T maps to NM_002353.2 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:166845464 C>T maps to NM_053053.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:166831520 C>T maps to NM_053053.3 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:35783642 C>T maps to NM_001166105.1 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr17:35825628 C>T maps to NM_001166105.1 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr17:35827576 G>A maps to NM_001166105.1 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr4:7056213 C>T maps to NM_152293.2 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr4:7056684 C>T maps to NM_152293.2 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:7056042 C>T maps to NM_152293.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:9831434 G>A maps to NM_006354.2 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:9831592 G>A maps to NM_006354.2 R88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr3:9831605 G>A maps to NM_006354.2 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr3:9828997 G>A maps to NM_006354.2 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:70597601 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:70641223 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr23:70613283 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr23:70602451 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:70607246 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:70683686 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr23:70598118 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:70586252 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:70679468 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:70683699 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:70598117 T>C did not map to a codon.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr23:70608164 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr23:70587970 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:70586245 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:70601711 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:109607281 G>A maps to NM_005645.3 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr17:34171093 T>C maps to NM_139215.1 Y340Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:34171514 C>T maps to NM_139215.1 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr1:222753198 C>A maps to NM_005681.2 G103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:222737455 C>T maps to NM_005681.2 Q302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr2:10059865 T>G maps to NM_005680.2 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr2:10059866 C>T maps to NM_005680.2 Q495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:10059172 C>T maps to NM_005680.2 Y425Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr16:84212770 G>A maps to NM_005679.2 Q796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:84213038 G>A maps to NM_005679.2 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:84216903 G>A maps to NM_005679.2 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:84213269 G>A maps to NM_005679.2 T629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr16:84215593 G>A maps to NM_005679.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr16:84217324 G>A maps to NM_005679.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr9:32632763 G>A maps to NM_153809.2 F938F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr9:32634773 C>T maps to NM_153809.2 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:32630333 C>T maps to NM_153809.2 E1748E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:32631734 C>T maps to NM_153809.2 L1281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:32633141 C>T maps to NM_153809.2 G812G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:32634965 A>G maps to NM_153809.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr9:32634817 G>A maps to NM_153809.2 R254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:32634686 C>T maps to NM_153809.2 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr9:32633615 T>C maps to NM_153809.2 S654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:32632306 G>A maps to NM_153809.2 L1091L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr9:32631650 C>T maps to NM_153809.2 S1309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:32634113 G>T maps to NM_153809.2 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:32634944 C>T maps to NM_153809.2 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:32634977 C>T maps to NM_153809.2 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr9:32631677 G>A maps to NM_153809.2 L1300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:32630147 G>A maps to NM_153809.2 P1810P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:32633222 C>T maps to NM_153809.2 R785R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr9:32634314 G>A maps to NM_153809.2 F421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:32633684 G>A maps to NM_153809.2 I631I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr9:32631149 C>T maps to NM_153809.2 A1476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:32631359 G>A maps to NM_153809.2 S1406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:32631950 G>A maps to NM_153809.2 V1209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:32634068 G>A maps to NM_153809.2 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:32631764 C>T maps to NM_153809.2 K1271K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:32635016 G>A maps to NM_153809.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr9:32634731 C>T maps to NM_153809.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:120816118 T>G maps to NM_003184.3 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr8:120744175 G>A maps to NM_003184.3 S1196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr8:120816185 G>C maps to NM_003184.3 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:120809246 G>A maps to NM_003184.3 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr10:8006789 C>T maps to NM_031923.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr10:8006231 A>G maps to NM_031923.2 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:8006645 C>T maps to NM_031923.2 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr10:7866324 C>T maps to NM_031923.2 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:8051253 C>T maps to NM_031923.2 P843P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:7860671 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:8006909 G>T maps to NM_031923.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:8006978 C>T maps to NM_031923.2 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:8051145 C>T maps to NM_031923.2 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr20:60574055 G>A maps to NM_003185.3 L966L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:60585160 G>A maps to NM_003185.3 Q568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr18:23862008 G>A maps to ENST00000418698 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr18:23873454 C>T maps to ENST00000418698 Q603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:229730511 G>A maps to NM_014409.3 F434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:229738628 G>A maps to NM_014409.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:229730346 G>A maps to NM_014409.3 D489D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:229738376 G>A maps to NM_014409.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:229730169 G>A maps to NM_014409.3 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:229750145 G>A maps to NM_014409.3 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:229738199 G>A maps to NM_014409.3 A238A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A3AC-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr5:140699251 C>T maps to NM_005642.2 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:100532674 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:100548020 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:100531341 A>T did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:100532598 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:100548009 G>A did not map to a codon.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr23:100532668 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:100547831 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:100547832 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:100533047 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:100547998 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:100547998 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr23:100547821 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:100547860 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:42044896 G>A maps to NM_138572.2 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:42036227 C>T maps to NM_138572.2 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:42034063 C>T maps to NM_138572.2 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr5:68665290 G>C maps to NM_016283.4 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:68651549 G>A maps to NM_016283.4 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:77393564 T>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:77394418 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr6:159457476 C>T maps to NM_054114.3 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:159463276 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:159461761 G>A maps to NM_054114.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr6:159457251 C>T maps to NM_054114.3 Q601Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:159462466 C>T maps to NM_054114.3 K132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:159890197 G>A maps to ENST00000368096 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr3:111719726 C>T maps to NM_001008272.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr3:111730610 G>A maps to NM_001008272.1 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:47685577 C>T maps to ENST00000371883 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:47685394 C>T maps to ENST00000371883 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:47691494 G>T maps to ENST00000371883 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:47685724 C>T maps to ENST00000371883 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:47685757 G>A maps to ENST00000371883 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:108424935 C>T maps to NM_005421.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:764333 C>T maps to NM_006755.1 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr2:160027077 C>T maps to NM_033394.2 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:160031621 C>T maps to NM_033394.2 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:160076290 G>T maps to NM_033394.2 L1197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:160087159 C>T maps to NM_033394.2 S1741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:160035305 C>T maps to NM_033394.2 F714F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:160031579 C>T maps to NM_033394.2 D540D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:160035503 C>T maps to NM_033394.2 G780G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:160050862 C>T maps to NM_033394.2 G946G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:61497653 C>T maps to ENST00000389520 L1447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr17:61498503 C>T maps to ENST00000389520 Q1731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr17:61176545 C>T maps to ENST00000389520 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr17:61466796 C>T maps to ENST00000389520 F907F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr17:61498088 C>T maps to ENST00000389520 S1592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:61432353 C>T maps to ENST00000389520 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:61432353 C>T maps to ENST00000389520 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:61495702 C>T maps to ENST00000389520 A1327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:61498623 G>T maps to ENST00000389520 E1771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:61497944 C>T maps to ENST00000389520 S1544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:61498856 C>T maps to ENST00000389520 T1848T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:61498025 C>T maps to ENST00000389520 P1571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr17:27869899 C>T maps to NM_020791.2 R956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr17:27837967 C>T maps to NM_020791.2 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr17:27802790 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:27844578 C>T maps to NM_020791.2 R605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:27844551 C>T maps to NM_020791.2 Q596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:27857436 C>T maps to NM_020791.2 Q721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:29999174 C>T maps to NM_016151.2 I1194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:29998478 C>T maps to NM_016151.2 S962S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr16:29997948 C>T maps to NM_016151.2 Q786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F2-06A-11D-A20D-08 chr16:29998499 G>C maps to NM_016151.2 L969L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr16:29997606 C>T maps to NM_016151.2 Q672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr16:29993024 C>T maps to NM_016151.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:29994206 C>T maps to NM_016151.2 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:29990325 C>T maps to NM_016151.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr16:29998829 G>A maps to NM_016151.2 R1079R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:29994068 C>T maps to NM_016151.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:29998370 C>T maps to NM_016151.2 I926I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr16:29998715 T>A maps to NM_016151.2 V1041V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:29994969 C>A maps to NM_016151.2 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:29994970 C>T maps to NM_016151.2 R470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:29997795 C>T maps to NM_016151.2 Q735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:118598040 T>C maps to NM_016281.3 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:118598004 G>A maps to NM_016281.3 A766A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr6:32816428 C>T maps to NM_000593.5 Q582Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:32815347 A>T maps to NM_000593.5 A675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:32818753 G>A maps to NM_000593.5 F399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr6:32816877 C>T maps to NM_000593.5 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:32815320 G>A maps to NM_000593.5 F684F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:32800148 G>A maps to ENST00000452392 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr6:32803452 G>A maps to ENST00000452392 Q236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr6:32803453 G>A maps to ENST00000452392 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:32797737 G>A maps to ENST00000452392 F588F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:32805776 G>A maps to ENST00000452392 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr6:32805545 G>A maps to ENST00000452392 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr6:32798421 G>A maps to ENST00000452392 P478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr6:33272287 G>A maps to NM_172208.2 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:33281528 T>G maps to NM_172208.2 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr12:6562850 A>T maps to NM_018009.4 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:6566746 G>A maps to NM_018009.4 Q247Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:6562688 C>T maps to NM_018009.4 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:234534126 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:234527373 G>A maps to NM_005646.3 I1605I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:234565930 G>A maps to NM_005646.3 P837P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:234563100 G>A maps to NM_005646.3 N1095N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:234595031 G>A maps to NM_005646.3 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr1:234541778 G>A maps to NM_005646.3 R1287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:234564991 G>A maps to NM_005646.3 Q984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:234529413 G>A maps to NM_005646.3 I1471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr12:53898928 T>G maps to NM_134323.1 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr12:53895945 C>T maps to NM_134323.1 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr12:53898558 A>G maps to NM_134323.1 E191E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:38305207 G>A maps to ENST00000443402 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:38305121 C>T maps to ENST00000443402 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr7:38305100 C>T maps to ENST00000443402 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr5:33463924 C>T maps to ENST00000455217 Q668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:33463896 A>C maps to ENST00000455217 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:33462102 T>C maps to ENST00000455217 T607T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:33455742 C>T maps to ENST00000455217 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:33458687 C>T maps to ENST00000455217 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:33467053 C>T maps to ENST00000455217 R696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr5:33462243 C>T maps to ENST00000455217 R624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:150471437 C>T maps to NM_025150.3 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:150469025 C>T maps to NM_025150.3 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:150463096 C>T maps to NM_025150.3 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:150471387 C>T maps to NM_025150.3 Q473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:150471693 C>T maps to NM_025150.3 V514V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:150469305 C>T maps to NM_025150.3 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:150463974 C>T maps to NM_025150.3 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:150463975 C>T maps to NM_025150.3 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:150471470 C>T maps to NM_025150.3 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr15:102201985 G>A maps to NM_152334.2 I667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr15:102215838 G>A maps to NM_152334.2 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr15:102215870 G>A maps to NM_152334.2 Q574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:102241366 G>A maps to NM_152334.2 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:102242447 G>A maps to NM_152334.2 I405I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:6631137 C>T maps to NM_138697.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:6635391 C>T maps to NM_138697.3 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:6634779 G>A maps to NM_138697.3 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:6639205 T>G maps to NM_138697.3 T696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:6635451 G>A maps to NM_138697.3 Q420Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:6635452 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:6631004 C>T maps to NM_138697.3 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:6634814 G>A maps to NM_138697.3 W208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr1:6631073 G>A maps to NM_138697.3 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr1:6635076 G>A maps to NM_138697.3 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:6631077 C>T maps to NM_138697.3 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:6634899 G>A maps to NM_138697.3 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:19185995 G>A maps to NM_152232.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:19168235 G>A maps to NM_152232.2 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:19180907 C>T maps to NM_152232.2 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:19166131 G>A maps to NM_152232.2 F827F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr1:19185995 G>A maps to NM_152232.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:19166161 G>A maps to NM_152232.2 F817F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:19184013 G>A maps to NM_152232.2 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:19184085 G>A maps to NM_152232.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:19181354 C>T maps to NM_152232.2 W203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:19181225 G>A maps to NM_152232.2 N246N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:19183977 C>T maps to NM_152232.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:19168343 G>A maps to NM_152232.2 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:19175918 G>A maps to NM_152232.2 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:19166188 G>A maps to NM_152232.2 F808F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr1:19166647 G>A maps to NM_152232.2 I655I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr1:19168221 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:19168268 G>A maps to NM_152232.2 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:19176014 G>A maps to NM_152232.2 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:19183982 G>A maps to NM_152232.2 Q109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:19180730 G>A maps to NM_152232.2 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:19186079 C>T maps to NM_152232.2 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:1269723 G>A maps to NM_152228.1 R813R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:1268329 C>T maps to NM_152228.1 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr5:9629553 C>T maps to NM_019599.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr5:9630006 G>A maps to NM_019599.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:9629396 G>A maps to NM_019599.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:9630015 C>T maps to NM_019599.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:9629673 C>T maps to NM_019599.2 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr5:9629919 G>A maps to NM_019599.2 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:9629439 G>A maps to NM_019599.2 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr12:10978255 T>G maps to NM_023921.1 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:10978118 A>G maps to NM_023921.1 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr12:10978271 G>A maps to NM_023921.1 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr12:10978577 C>T maps to NM_023921.1 W97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:10978475 G>A maps to NM_023921.1 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:10978658 G>A maps to NM_023921.1 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr12:10978547 G>A maps to NM_023921.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:11061050 G>A maps to NM_023920.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr12:11061570 G>T maps to NM_023920.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:11091062 G>A maps to NM_023922.1 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr12:11091266 T>G maps to NM_023922.1 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:11091095 G>A maps to NM_023922.1 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:11091011 G>A maps to NM_023922.1 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr7:122635676 G>A maps to NM_016945.2 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:122635652 G>A maps to NM_016945.2 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:122635334 C>T maps to NM_016945.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr7:141464242 G>A maps to NM_016943.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr7:141464125 C>T maps to NM_016943.2 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr7:141464236 C>T maps to NM_016943.2 N93N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:141463991 C>T maps to NM_016943.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:141464374 C>T maps to NM_016943.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:141464173 T>C maps to NM_016943.2 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:141464516 C>T maps to NM_016943.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr12:11286735 G>A maps to NM_001097643.1 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:11183700 T>A maps to NM_176885.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr12:11183904 G>A maps to NM_176885.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr12:11183589 G>A maps to NM_176885.2 N115N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr7:141673168 G>A maps to NM_176817.4 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:141673372 C>T maps to NM_176817.4 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr7:141673384 G>A maps to NM_176817.4 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr7:141673246 G>A maps to NM_176817.4 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:141672709 G>A maps to NM_176817.4 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:141673384 G>A maps to NM_176817.4 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr7:141673384 G>A maps to NM_176817.4 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:141672871 G>A maps to NM_176817.4 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:141673291 G>A maps to NM_176817.4 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr7:141673075 C>T maps to NM_176817.4 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr7:141673372 C>T maps to NM_176817.4 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr7:141673291 G>A maps to NM_176817.4 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:141672637 C>A maps to NM_176817.4 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:141673291 G>A maps to NM_176817.4 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:141673384 G>A maps to NM_176817.4 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:141672579 A>G maps to NM_176817.4 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:141673246 G>A maps to NM_176817.4 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr7:141673372 C>T maps to NM_176817.4 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr7:141673117 G>A maps to NM_176817.4 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr7:141672907 G>T maps to NM_176817.4 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:141673384 G>A maps to NM_176817.4 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr7:141672724 G>A maps to NM_176817.4 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr7:141672667 G>A maps to NM_176817.4 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:141673351 C>T maps to NM_176817.4 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:142880666 T>C maps to NM_176881.2 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:142881206 C>T maps to NM_176881.2 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:142881020 C>T maps to NM_176881.2 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:142881492 C>T maps to NM_176881.2 R328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:142881443 G>A maps to NM_176881.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr7:142880576 C>T maps to NM_176881.2 C22C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:142880657 C>T maps to NM_176881.2 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:142881020 C>T maps to NM_176881.2 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:142881158 G>A maps to NM_176881.2 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr7:141479031 C>T maps to NM_016944.1 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr7:141479076 C>T maps to NM_016944.1 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:141478551 C>T maps to NM_016944.1 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:142919779 C>T maps to NM_176882.1 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:142919779 C>T maps to NM_176882.1 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:142919218 C>T maps to NM_176882.1 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:142919728 C>T maps to NM_176882.1 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:142919713 G>A maps to NM_176882.1 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:142919644 T>C maps to NM_176882.1 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:142919455 C>T maps to NM_176882.1 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:142919548 C>T maps to NM_176882.1 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr7:142919713 G>A maps to NM_176882.1 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr7:142920097 G>A maps to NM_176882.1 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:142919179 G>A maps to NM_176882.1 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:142919779 C>T maps to NM_176882.1 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr7:142920019 C>T maps to NM_176882.1 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:143175669 C>T maps to NM_176883.2 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr7:143175717 C>T maps to NM_176883.2 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:143175417 G>A maps to NM_176883.2 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:143175379 C>T maps to NM_176883.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr7:143175706 C>T maps to NM_176883.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:143175480 G>A maps to NM_176883.2 W172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr7:143175684 C>T maps to NM_176883.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr7:143175393 C>T maps to NM_176883.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:143175678 C>T maps to NM_176883.2 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:143175861 G>A maps to NM_176883.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr7:143175711 C>T maps to NM_176883.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:143175136 C>T maps to NM_176883.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:143175462 G>A maps to NM_176883.2 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:143175681 C>T maps to NM_176883.2 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:143175835 C>T maps to NM_176883.2 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:143175350 G>A maps to NM_176883.2 W129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:11339231 G>A maps to NM_181429.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr12:11339168 C>T maps to NM_181429.1 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:11338853 C>T maps to NM_181429.1 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr12:11244555 G>A maps to ENST00000422992 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:11214244 G>A maps to ENST00000422992 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr12:11214050 C>T maps to ENST00000422992 W281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr12:11214051 C>T maps to ENST00000422992 W281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:11214257 A>G maps to ENST00000422992 H212H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:141490304 C>T maps to NM_018980.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr7:141490886 C>T maps to NM_018980.2 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:141490490 C>T maps to NM_018980.2 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:141490331 C>T maps to NM_018980.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr7:141490772 C>T maps to NM_018980.2 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:141490277 C>T maps to NM_018980.2 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr7:141491018 C>T maps to NM_018980.2 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr7:141490925 C>T maps to NM_018980.2 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr7:141490304 C>T maps to NM_018980.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:11139090 C>T maps to NM_176890.2 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:11138915 G>A maps to NM_176890.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:143141174 C>T maps to NM_177437.1 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:143140805 C>T maps to NM_177437.1 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:143140826 G>A maps to NM_177437.1 Q94Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr7:143140775 C>T maps to NM_177437.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr7:143140934 C>T maps to NM_177437.1 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:143140670 G>A maps to NM_177437.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:143141012 C>T maps to NM_177437.1 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:143140972 G>A maps to NM_177437.1 W143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:143140925 C>T maps to NM_177437.1 H127H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:143140655 C>T maps to NM_177437.1 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:143140982 C>T maps to NM_177437.1 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:143140568 A>G maps to NM_177437.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:143140838 C>T maps to NM_177437.1 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:143140839 C>T maps to NM_177437.1 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr7:143140904 G>A maps to NM_177437.1 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr7:143141129 C>T maps to NM_177437.1 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr7:143140982 C>T maps to NM_177437.1 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr7:143141492 G>A maps to NM_177437.1 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:143141324 C>T maps to NM_177437.1 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:143141006 C>T maps to NM_177437.1 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:143141024 C>T maps to NM_177437.1 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:143140619 C>T maps to NM_177437.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:143141324 C>T maps to NM_177437.1 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:10954401 G>A maps to NM_023919.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:10954749 G>A maps to NM_023919.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr12:10954812 G>A maps to NM_023919.2 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr12:10954482 G>A maps to NM_023919.2 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:10954431 G>A maps to NM_023919.2 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:10958973 G>A maps to NM_023918.1 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:10962527 G>A maps to NM_023917.2 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr12:10962127 G>A maps to NM_023917.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:10962037 G>A maps to NM_023917.2 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:10962047 G>A maps to NM_023917.2 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:10962037 G>A maps to NM_023917.2 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:71602166 G>A maps to NM_000353.2 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr16:71604617 G>A maps to NM_000353.2 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr16:71604621 C>T maps to NM_000353.2 W291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:71602046 C>T maps to NM_000353.2 *455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:71602145 G>A maps to NM_000353.2 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr16:71602112 C>T maps to NM_000353.2 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr16:71606213 C>T maps to NM_000353.2 W194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:125531095 T>C maps to NM_032026.3 Q55Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:10312419 C>T maps to NM_014760.3 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:10320091 C>T maps to NM_014760.3 I697I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr3:10320600 G>A maps to NM_014760.3 P726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:10291129 C>T maps to NM_014760.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:10311960 C>T maps to NM_014760.3 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr3:10312399 C>T maps to NM_014760.3 Q512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:10291177 C>T maps to NM_014760.3 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:10291285 C>T maps to NM_014760.3 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:10312173 C>T maps to NM_014760.3 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:10312263 A>G maps to NM_014760.3 Q466Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr1:212977940 T>C maps to NM_001146171.1 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr7:27831770 C>T maps to ENST00000409980 R395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:27835783 C>A maps to ENST00000409980 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr7:27868342 G>A maps to ENST00000409980 K779K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:153649074 G>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr23:153649021 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:153640453 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr4:37903742 G>A maps to NM_015173.2 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr4:38119751 C>T maps to NM_015173.2 A967A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:38016500 C>T maps to NM_015173.2 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:38016230 C>T maps to NM_015173.2 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr4:38055921 C>T maps to NM_015173.2 T671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:38016170 C>T maps to NM_015173.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:38119796 C>T maps to NM_015173.2 F982F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr4:38051339 C>T maps to NM_015173.2 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:38023280 C>T maps to NM_015173.2 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr4:38051433 C>T maps to NM_015173.2 Q609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr4:37903865 C>T maps to NM_015173.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr4:38051327 G>A maps to NM_015173.2 S573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr4:38016290 C>T maps to NM_015173.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr22:30688369 G>A maps to ENST00000403477 Y514Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr22:30688390 G>A maps to ENST00000403477 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr22:30700558 G>A maps to ENST00000403477 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:30370637 G>A maps to NM_015527.3 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:67172874 G>A maps to NM_198517.2 K86K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:67172937 G>A maps to NM_198517.2 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:67174402 C>T maps to NM_198517.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:67177182 G>A maps to NM_198517.2 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:67174476 C>T maps to NM_198517.2 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr10:96201760 C>A maps to NM_015188.1 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr10:96201751 G>A maps to NM_015188.1 Q357Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:96267072 C>T maps to NM_015188.1 F523F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr9:131568244 C>T maps to NM_018201.3 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:7000917 C>T maps to NM_001113361.1 N384N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr4:7016245 G>A maps to NM_001113361.1 K573K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:72266707 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:72291719 C>T maps to NM_022771.4 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr17:77915896 G>A maps to NM_019020.2 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:77915870 G>A maps to NM_019020.2 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr17:77924269 G>A maps to NM_019020.2 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:77984428 G>A maps to NM_019020.2 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:50385370 C>T maps to NM_024682.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:50383659 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr4:26756567 G>A maps to NM_018317.2 *527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr4:26638891 C>T maps to NM_018317.2 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr4:26638891 C>T maps to NM_018317.2 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr4:26661293 C>T maps to NM_018317.2 Q186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:100995791 C>T maps to NM_018421.3 Q229Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:100971426 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:100995812 G>A maps to NM_018421.3 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr9:100983147 G>A maps to NM_018421.3 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr9:100975446 G>A maps to NM_018421.3 H476H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:420924 G>A maps to ENST00000246077 C270C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr15:74181415 C>T maps to NM_153356.1 Q329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:74174022 C>T maps to NM_153356.1 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:74177173 C>T maps to NM_153356.1 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr15:74178925 C>T maps to NM_153356.1 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr15:74180076 G>A maps to NM_153356.1 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:74174022 C>T maps to NM_153356.1 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr22:47393559 C>T maps to NM_014346.2 Q386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr22:47274573 C>T maps to NM_014346.2 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr22:47507456 C>G maps to NM_014346.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:47193356 C>T maps to NM_014346.2 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr6:37247199 G>A maps to NM_017772.2 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:37254827 C>T maps to NM_017772.2 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr6:37250667 G>A maps to NM_017772.2 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr3:100009430 C>T maps to ENST00000394144 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:2550411 C>T maps to ENST00000434757 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr16:2546499 C>T maps to ENST00000434757 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:2548286 C>T maps to ENST00000434757 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr16:2550411 C>T maps to ENST00000434757 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr16:2550330 C>T maps to ENST00000434757 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr16:2550411 C>T maps to ENST00000434757 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr16:2550411 C>T maps to ENST00000434757 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:2546535 C>T maps to ENST00000434757 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:2546845 C>T maps to ENST00000434757 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:48419063 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:48403395 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:48399768 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:48418939 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:48419013 C>T did not map to a codon.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr23:48418268 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:15643440 G>A maps to NM_178571.4 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:15641387 G>A maps to NM_178571.4 K92K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr17:15641668 A>C maps to NM_178571.4 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:18541688 G>A maps to NM_001039397.2 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr17:18541697 C>T maps to NM_001039397.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:28890220 C>T maps to NM_015594.2 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr17:28889908 G>A maps to NM_015594.2 K67K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr17:28887651 C>T maps to NM_015594.2 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr15:78316503 C>T maps to NM_144572.1 R488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:78295820 C>T maps to NM_144572.1 R800R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr15:78346415 G>A maps to NM_144572.1 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr13:75861124 G>A maps to ENST00000431480 L1235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:75861029 G>A maps to ENST00000431480 L1266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr13:75863084 G>A maps to ENST00000431480 L1217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:75900466 G>A maps to ENST00000431480 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:76055822 G>A maps to ENST00000431480 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr13:75863073 A>T maps to ENST00000431480 L1221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr13:75898446 G>A maps to ENST00000431480 F708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:17279727 G>A maps to NM_001134381.1 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:17333419 C>T maps to NM_001134381.1 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:17418069 G>A maps to NM_001134381.1 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:17226658 C>T maps to NM_001134381.1 Q620Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr6:13306759 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:101670714 G>A maps to NM_001102426.1 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:101706808 G>A maps to NM_001102426.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:101670581 G>A maps to NM_001102426.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:101656711 G>A maps to NM_001102426.1 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr23:106083957 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:106117027 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr23:106082651 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:106070457 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:106117149 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:106064138 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr23:106109208 T>C did not map to a codon.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr23:106069311 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr23:106069312 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:106066666 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr23:106108820 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:106109167 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr23:106093513 T>G did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:106116849 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:106116841 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:106083982 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:106111663 G>A did not map to a codon.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr23:106096798 T>G did not map to a codon.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr23:106070443 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr23:106083425 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZG-06A-11D-A197-08 chr23:106109034 T>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:106066549 G>A did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:106116850 C>T did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:106116851 C>T did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:106064219 A>G did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:106046202 G>C did not map to a codon.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr4:141600838 G>A maps to NM_015130.2 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr4:141578864 G>A maps to NM_015130.2 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr4:141600145 G>A maps to NM_015130.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr4:141600877 G>A maps to NM_015130.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:141600150 G>A maps to NM_015130.2 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr4:141590793 C>T maps to NM_015130.2 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:141592032 G>A maps to NM_015130.2 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:141600826 A>G maps to NM_015130.2 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:141543918 C>T maps to NM_015130.2 E1077E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:141590110 G>A maps to NM_015130.2 I516I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:141578691 G>A maps to NM_015130.2 T732T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:141600297 G>A maps to NM_015130.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr4:141543774 G>A maps to NM_015130.2 S1125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr4:141600150 G>A maps to NM_015130.2 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr4:141590808 G>A maps to NM_015130.2 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr4:141543666 G>A maps to NM_015130.2 S1161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:141583072 G>A maps to NM_015130.2 R593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:141600241 G>A maps to NM_015130.2 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:141600877 G>A maps to NM_015130.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr5:179306080 C>T maps to NM_198868.2 E511E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr5:179302140 G>A maps to NM_198868.2 F649F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr5:179320270 G>A maps to NM_198868.2 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:179306086 G>A maps to NM_198868.2 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr5:179315210 G>A maps to NM_198868.2 D382D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:179306097 G>A maps to NM_198868.2 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:179321404 G>A maps to NM_198868.2 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:179302074 G>A maps to NM_198868.2 F671F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr5:179303025 G>A maps to NM_198868.2 I598I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:179302047 G>A maps to NM_198868.2 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:179318396 G>A maps to NM_198868.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:76989168 G>A maps to NM_004607.2 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr19:36612444 C>T maps to NM_001281.2 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:36616632 C>T maps to NM_001281.2 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:186272335 G>A maps to NM_001134415.1 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:186276298 G>A maps to NM_001134415.1 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr3:186274414 G>A maps to NM_001134415.1 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:80763834 C>T maps to NM_005993.4 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr17:80772793 G>A maps to NM_005993.4 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:80847545 C>T maps to NM_005993.4 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr1:235543450 C>T maps to NM_003193.3 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr1:235599135 C>T maps to NM_003193.3 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:235600749 C>T maps to NM_003193.3 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr1:235577777 G>A maps to NM_003193.3 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr1:235600749 C>T maps to NM_003193.3 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:120957501 C>T maps to NM_152715.3 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr11:120925772 C>T maps to NM_152715.3 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:120924357 C>T maps to NM_152715.3 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr4:107037520 G>A maps to NM_001163436.1 I750I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:107114862 G>A maps to NM_001163436.1 F654F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr4:107016743 G>A maps to NM_001163436.1 F822F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr4:107114874 C>T maps to NM_001163436.1 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:107165817 G>A maps to NM_001163436.1 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:107037520 G>A maps to NM_001163436.1 I750I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:9622286 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr23:9660252 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:9665456 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:9659734 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr3:176755936 C>T maps to NM_024665.4 W357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:176768297 G>A maps to NM_024665.4 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr24:6938850 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr24:6948885 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr24:6942648 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr24:6932063 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr24:6955438 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr24:6932136 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr24:6939828 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr24:6948774 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr24:6954415 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr7:72985205 G>A maps to NM_012453.2 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr7:72985289 G>A maps to NM_012453.2 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr7:72985040 G>A maps to NM_012453.2 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr16:2028153 C>T maps to NM_006453.2 I689I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr16:2027059 C>T maps to NM_006453.2 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr16:2025692 C>T maps to NM_006453.2 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr16:2025693 C>T maps to NM_006453.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr16:2027164 C>T maps to NM_006453.2 F517F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:2025810 C>T maps to NM_006453.2 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:2026060 C>T maps to NM_006453.2 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:2024952 T>C maps to NM_006453.2 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U9-06A-11D-A32N-08 chr16:2028389 G>T maps to NM_006453.2 V737V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:170873695 C>T maps to NM_003194.4 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr14:55902630 G>A maps to NM_199047.2 N210N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr14:55903565 G>A maps to NM_199047.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr14:55902651 C>T maps to NM_199047.2 Q203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr14:55902609 C>T maps to NM_199047.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:55895619 G>A maps to NM_199047.2 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:55903340 G>A maps to NM_199047.2 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:162280632 C>T maps to NM_006593.2 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr2:162273043 G>A maps to NM_006593.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:162273211 C>T maps to NM_006593.2 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:162279981 C>T maps to NM_006593.2 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:162280206 C>T maps to NM_006593.2 F506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr7:45143015 G>A maps to ENST00000404564 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr7:45148638 G>A maps to ENST00000404564 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr7:45141669 C>A did not map to a codon.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr22:19753282 C>T maps to NM_080647.1 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:19770514 C>T maps to NM_005992.1 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:19752563 C>T maps to NM_080647.1 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:67399162 C>T maps to NM_005995.4 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:67402534 C>T maps to NM_005995.4 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:67400523 G>A maps to NM_005995.4 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:67402521 G>A maps to NM_005995.4 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr11:67401725 C>T maps to NM_005995.4 W161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:67402483 G>A maps to NM_005995.4 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:67402342 G>A maps to NM_005995.4 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:119427480 C>T maps to ENST00000369429 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:119469230 C>T maps to ENST00000369429 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr1:119469209 C>T maps to ENST00000369429 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:119427723 G>A maps to ENST00000369429 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:119427675 G>A maps to ENST00000369429 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:119427930 C>T maps to ENST00000369429 Q411Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:119427723 G>A maps to ENST00000369429 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:119427723 G>A maps to ENST00000369429 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:119428056 G>A maps to ENST00000369429 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:119427890 G>A maps to ENST00000369429 Q425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:119427731 G>A maps to ENST00000369429 Q478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:119466166 G>A maps to ENST00000369429 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:119466223 G>A maps to ENST00000369429 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr6:85448269 C>T maps to NM_001080508.1 W348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:85472278 G>A maps to NM_001080508.1 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr6:85472361 G>A maps to NM_001080508.1 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr6:85446744 G>A maps to NM_001080508.1 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr6:85446846 C>T maps to NM_001080508.1 V460V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:85470043 G>A maps to NM_001080508.1 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:85466568 C>T maps to NM_001080508.1 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:85466563 C>T maps to NM_001080508.1 W208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr1:168278022 G>A maps to NM_005149.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr1:168282098 G>A maps to NM_005149.2 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:168260457 C>T maps to NM_005149.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:168274351 C>T maps to NM_005149.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:168274387 G>A maps to NM_005149.2 Q290Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:168274396 C>T maps to NM_005149.2 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr1:168274381 C>T maps to NM_005149.2 H288H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr1:168274382 C>A maps to NM_005149.2 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:168282155 G>A maps to NM_005149.2 W421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:59481988 C>T maps to NM_005994.3 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr17:59485542 C>T maps to NM_005994.3 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:35244194 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:35280489 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:35280520 A>G maps to NM_001077653.2 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:35244177 G>A maps to NM_001077653.2 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:35288413 C>T maps to NM_001077653.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr7:35242109 G>A maps to NM_001077653.2 Q426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:35242182 G>A maps to NM_001077653.2 A401A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr7:35242161 C>T maps to NM_001077653.2 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr7:35280640 C>T maps to NM_001077653.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr17:45822321 C>T maps to NM_013351.1 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:45822584 C>T maps to NM_013351.1 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:45822197 C>T maps to NM_013351.1 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:79281234 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:79279630 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:79282800 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:79281234 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:79286390 G>C did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:79286391 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:79286044 C>G did not map to a codon.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr23:79282276 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:79282781 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:79286409 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:79286458 C>T did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:79286267 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:115112503 G>T maps to NM_016569.3 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr12:115114220 C>T maps to NM_016569.3 E332E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:115109848 G>A maps to NM_016569.3 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:59560339 C>T maps to ENST00000393853 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:59560747 G>A maps to ENST00000393853 R504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:59557285 C>T maps to ENST00000393853 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr17:59560723 C>A maps to ENST00000393853 R496R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr12:114841556 C>T maps to NM_000192.3 Q49Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr12:114793660 G>A maps to NM_000192.3 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr12:114832644 C>T maps to NM_000192.3 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:114793459 G>A maps to NM_000192.3 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:30102230 G>A maps to NM_004608.3 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:30097954 T>C maps to NM_004608.3 E325E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr19:3600596 G>A maps to NM_201636.2 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr19:3600065 G>A maps to NM_201636.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:3600422 G>A maps to NM_201636.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:3595811 G>A maps to NM_201636.2 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:3600302 G>A maps to NM_201636.2 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:139661905 C>T maps to NM_001166253.1 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr7:139715525 C>T maps to NM_001166253.1 F457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:139706934 G>A maps to NM_001166253.1 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:139655380 C>T maps to NM_001166253.1 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:139661794 C>T maps to NM_001166253.1 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:139653177 C>T maps to NM_001166253.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:139657445 C>T maps to NM_001166253.1 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:139657562 G>A maps to NM_001166253.1 E320E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:139717521 C>T maps to NM_001166253.1 F519F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:139719886 C>T maps to NM_001166253.1 I577I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr14:92251697 G>A maps to NM_001128596.1 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr14:92278800 C>T maps to NM_001128596.1 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr14:92249507 C>T maps to NM_001128596.1 W470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr14:92251697 G>A maps to NM_001128596.1 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr14:92251697 G>A maps to NM_001128596.1 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr14:92258806 C>T maps to NM_001128596.1 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:92278782 A>C maps to NM_001128596.1 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr14:92258767 G>A maps to NM_001128596.1 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:92258737 C>T maps to NM_001128596.1 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:92264693 C>T maps to NM_001128596.1 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr14:92268711 G>A maps to NM_001128596.1 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:92251507 G>A maps to NM_001128596.1 Q454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:92251508 G>A maps to NM_001128596.1 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:92251697 G>A maps to NM_001128596.1 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr14:92265363 C>T maps to NM_001128596.1 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr14:92268738 G>A maps to NM_001128596.1 R110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr14:92268711 G>A maps to NM_001128596.1 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:92251697 G>A maps to NM_001128596.1 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:92251697 G>A maps to NM_001128596.1 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr8:54912520 G>A maps to NM_006756.2 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:62698281 G>A maps to NM_003195.4 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:62701939 C>T maps to NM_003195.4 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:62701940 C>T maps to NM_003195.4 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:23743875 A>G maps to NM_003196.1 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:23724044 G>A maps to NM_003196.1 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:102884994 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:101382336 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:101382459 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:101382380 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:101382329 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:101381826 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:102864577 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:102864505 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:102864559 G>A did not map to a codon.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr23:102864582 C>T did not map to a codon.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr23:102864326 G>C did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:102864355 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr23:102528902 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr23:102528896 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:102529149 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:102529336 C>T did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:102529336 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:101396160 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:101396220 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:101395789 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:101396104 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:101396042 C>T did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:101395954 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr23:102586466 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:102508792 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:13681192 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr16:2827032 G>T maps to NM_207013.1 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:24078018 C>T maps to NM_003198.2 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:24078019 C>T maps to NM_003198.2 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:24080686 C>T maps to NM_003198.2 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr18:44560282 C>T maps to NM_016427.2 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr18:44560477 G>A maps to NM_016427.2 Y386Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr18:44560939 C>T maps to NM_016427.2 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr18:44560780 C>T maps to NM_016427.2 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr18:44561401 G>A maps to NM_016427.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr18:44560696 C>T maps to NM_016427.2 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr18:44560282 C>T maps to NM_016427.2 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr18:44560015 A>G maps to NM_016427.2 N540N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr18:44559499 G>A maps to NM_016427.2 P712P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr18:44559960 G>A maps to NM_016427.2 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr18:44560507 G>A maps to NM_016427.2 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr18:44560507 G>A maps to NM_016427.2 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr18:44561338 G>A maps to NM_016427.2 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:44560507 G>A maps to NM_016427.2 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:44559622 C>T maps to NM_016427.2 E671E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:44559838 C>T maps to NM_016427.2 Q599Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:44561401 G>A maps to NM_016427.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr18:44560609 G>A maps to NM_016427.2 N342N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:44561505 G>A maps to NM_016427.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr18:44559856 G>A maps to NM_016427.2 F593F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:44555073 T>C maps to NM_145653.3 K380K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr18:44555307 C>T maps to NM_145653.3 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr18:44549170 G>A maps to NM_145653.3 Y376Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:44549191 C>T maps to NM_145653.3 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:44555103 C>T maps to NM_145653.3 W370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr18:44555103 C>T maps to NM_145653.3 W370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr18:44554604 G>A maps to NM_145653.3 R537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr18:44555049 C>T maps to NM_145653.3 E388E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr18:44555148 C>T maps to NM_145653.3 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr18:44555148 C>T maps to NM_145653.3 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr18:44554573 T>C maps to NM_145653.3 *547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19T-06A-11D-A19A-08 chr18:44555262 G>A maps to NM_145653.3 N317N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:44555031 C>T maps to NM_145653.3 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr5:145872508 G>A maps to NM_006706.3 R713R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr5:145834771 T>A maps to NM_006706.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr5:145883446 C>T maps to NM_006706.3 R870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr5:145843327 C>T maps to NM_006706.3 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr10:133058651 G>T maps to NM_174937.3 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:133107538 C>T maps to NM_174937.3 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr10:132944874 C>T maps to NM_174937.3 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:57523363 C>T maps to NM_207036.1 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr6:31129288 C>T maps to NM_007109.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr6:31127305 C>T maps to NM_007109.2 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr22:42606415 G>A maps to NM_005650.1 Y1632Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr22:42605785 G>A maps to NM_005650.1 I1842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:42606537 G>A maps to NM_005650.1 Q1592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:42609802 G>A maps to NM_005650.1 G503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr22:42609175 A>G maps to NM_005650.1 S712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr22:42609367 A>G maps to NM_005650.1 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:42607228 G>A maps to NM_005650.1 S1361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr22:42606727 G>A maps to NM_005650.1 F1528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr22:42557353 C>T maps to NM_181492.1 W1937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:42607561 G>A maps to NM_005650.1 P1250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:134210669 G>A maps to NM_003206.3 E45E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:134210762 G>A maps to NM_003206.3 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:134210882 C>T maps to NM_003206.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:27372134 G>A maps to NM_175769.2 W45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr2:27373232 G>A maps to NM_175769.2 K155K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:27373112 G>A maps to NM_175769.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:27375591 C>T maps to NM_175769.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:27373151 C>T maps to NM_175769.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:89965177 C>T maps to NM_014972.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr16:89977543 C>T maps to NM_014972.2 N643N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:1615701 G>T maps to NM_003200.2 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr19:1632112 G>A maps to NM_003200.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr19:1625577 G>A maps to NM_003200.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr18:52899810 C>T maps to ENST00000398339 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:52896132 G>A maps to ENST00000398339 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr18:52946884 G>A maps to ENST00000398339 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr18:52899792 C>T maps to ENST00000398339 K634K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr18:52928711 C>T maps to ENST00000398339 G427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr18:52942942 C>T maps to ENST00000398339 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr18:52895575 C>T maps to ENST00000398339 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr18:52895476 C>T maps to ENST00000398339 S767S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr18:52946788 G>A maps to ENST00000398339 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr18:52901818 C>T maps to ENST00000398339 A584A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr5:133451022 G>A maps to ENST00000395029 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr2:85534769 G>A maps to NM_031283.2 K421K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr2:85531452 G>A maps to NM_031283.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:114905796 G>A maps to NM_030756.4 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr10:114925433 C>T maps to NM_030756.4 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:114905823 C>T maps to NM_030756.4 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr10:114925427 C>T maps to NM_030756.4 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:114925694 C>T maps to NM_030756.4 P585P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr20:61488952 C>G maps to NM_006602.2 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr20:61485472 G>A maps to NM_006602.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:152085440 A>G maps to NM_007113.2 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:152081678 G>A maps to NM_007113.2 F1338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr1:152080058 C>T maps to NM_007113.2 R1878R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:152081396 G>A maps to NM_007113.2 F1432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:152082158 C>T maps to NM_007113.2 Q1178Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:152081741 T>C maps to NM_007113.2 E1317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:152080058 C>T maps to NM_007113.2 R1878R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:152083877 C>T maps to NM_007113.2 E605E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:152083118 C>T maps to NM_007113.2 E858E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:152084927 C>T maps to NM_007113.2 K255K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:152083781 C>T maps to NM_007113.2 E637E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr1:152084954 C>T maps to NM_007113.2 W246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:152081231 G>A maps to NM_007113.2 F1487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:152081945 C>T maps to NM_007113.2 Q1249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:152059795 C>T maps to NM_001008536.1 W121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:152059795 C>T maps to NM_001008536.1 W121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:152060595 G>A maps to NM_001008536.1 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:152058963 C>T maps to NM_001008536.1 E398E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:152058540 G>A maps to NM_001008536.1 F539F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr1:152058876 C>T maps to NM_001008536.1 Q427Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:152058189 C>T maps to NM_001008536.1 Q656Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr1:152059397 G>A maps to NM_001008536.1 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:152057750 G>A maps to NM_001008536.1 Q803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:152058891 C>T maps to NM_001008536.1 Q422Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:152058540 G>A maps to NM_001008536.1 F539F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:152059113 C>T maps to NM_001008536.1 K348K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:152057628 G>A maps to NM_001008536.1 I843I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:152059152 T>C maps to NM_001008536.1 E335E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:152060505 C>T maps to NM_001008536.1 Q38Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:152058984 C>T maps to NM_001008536.1 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:152058006 C>T maps to NM_001008536.1 Q717Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:67815130 C>T maps to NM_006019.3 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:67809239 C>T maps to NM_006019.3 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:67811693 C>T maps to NM_006019.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:67815411 G>A maps to NM_006019.3 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:67816407 C>T maps to NM_006019.3 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:67816613 C>T maps to NM_006019.3 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:67815432 C>T maps to NM_006019.3 I516I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr11:67816661 G>A maps to NM_006019.3 W596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr11:67815267 G>A maps to NM_006019.3 W487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr11:67815268 G>A maps to NM_006019.3 W487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr14:96180331 G>A maps to NM_021966.2 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr14:96180331 G>A maps to NM_021966.2 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr14:96180289 G>A maps to NM_021966.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:96180331 G>A maps to NM_021966.2 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:96180331 G>A maps to NM_021966.2 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr14:96180340 C>T maps to NM_021966.2 W21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr14:96178733 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr14:96178664 G>A maps to NM_021966.2 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:96180376 C>T maps to NM_021966.2 E9E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr14:96157188 G>A maps to NM_004918.3 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:96157077 A>G maps to NM_004918.3 E56E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr14:96157637 C>T maps to NM_004918.3 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr14:96152839 C>T maps to NM_004918.3 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:96157627 C>T maps to NM_004918.3 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:96152911 C>T maps to NM_004918.3 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr11:59629045 G>A maps to NM_001062.3 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:31018984 C>T maps to NM_000355.3 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr22:31008904 C>T maps to NM_000355.3 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr22:31013450 C>T maps to NM_000355.3 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr22:31010334 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr22:31003344 C>T maps to NM_000355.3 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr5:149755306 C>T maps to ENST00000451292 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:149749137 C>T maps to ENST00000451292 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr5:149753760 C>T maps to ENST00000451292 Q299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:167790033 C>T maps to NM_004610.3 K192K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:33956524 C>T maps to NM_144659.5 K30K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:167592605 T>A maps to NM_001145121.1 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr6:167595343 C>T maps to NM_001145121.1 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:167590487 T>C maps to NM_001145121.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr6:167585679 C>T maps to NM_001145121.1 H16H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:167591984 G>A maps to NM_001145121.1 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:167595346 G>A maps to NM_001145121.1 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:35088803 C>A maps to NM_001093728.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:35088241 G>A maps to NM_001093728.1 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:35108536 C>T maps to NM_001093728.1 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:35087958 G>A maps to NM_001093728.1 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:33090373 C>T maps to NM_001145541.1 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr12:106740245 C>T maps to NM_152772.1 R500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:106715469 C>T maps to NM_152772.1 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:106717398 C>T maps to NM_152772.1 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:106740155 C>T maps to NM_152772.1 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:49449975 C>T maps to NM_022171.2 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr3:49449939 G>A maps to NM_022171.2 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr6:44253874 G>A maps to NM_182539.3 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr6:44253958 G>A maps to NM_182539.3 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:44250044 G>A maps to NM_182539.3 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:44249951 G>A maps to NM_182539.3 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr6:44255328 G>A maps to NM_182539.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:44253778 G>A maps to NM_182539.3 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:44253973 G>A maps to NM_182539.3 V191V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A3AB-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr6:44253958 G>A maps to NM_182539.3 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:44253736 G>A maps to NM_182539.3 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:44249921 G>A maps to NM_182539.3 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:44253757 G>A maps to NM_182539.3 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:67243088 T>C maps to NM_152665.2 N164N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr12:111085660 C>T maps to NM_001082538.2 A581A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:111057719 G>A maps to NM_001082538.2 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:111066587 C>T maps to NM_001082538.2 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:111057731 C>T maps to NM_001082538.2 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:111078276 C>T maps to NM_001082538.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr12:124171516 C>T maps to NM_024809.3 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:124191383 C>T maps to NM_024809.3 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:124163772 C>T maps to NM_024809.3 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:124192217 C>T maps to NM_024809.3 F684F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:124191311 C>T maps to NM_024809.3 T603T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:124181718 G>C maps to NM_024809.3 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:124180962 T>C maps to NM_024809.3 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr10:97446806 G>A maps to ENST00000371217 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:104376611 C>T maps to NM_003211.4 Q172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr12:104373735 T>C maps to NM_003211.4 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:104370809 C>T maps to NM_003211.4 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:104370701 C>T maps to NM_003211.4 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:46620794 G>A maps to NM_003212.3 Q54Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr3:46621316 G>A maps to NM_003212.3 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:46620720 G>A did not map to a codon.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr3:46620587 G>A maps to NM_003212.3 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:156832719 C>T maps to NM_005651.2 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:156830136 G>A maps to NM_005651.2 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:90446901 C>T maps to NM_018319.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr14:90458318 C>A maps to NM_018319.3 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr14:90450896 G>T maps to NM_018319.3 G308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:90485725 C>T maps to NM_018319.3 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr14:90450889 T>C maps to NM_018319.3 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr6:24653342 G>A maps to NM_016614.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q9-06A-11D-A19A-08 chr10:115980453 C>T maps to NM_198795.1 T874T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr10:115947898 G>A maps to NM_198795.1 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:115981143 G>A maps to NM_198795.1 T933T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr10:115964518 A>G maps to NM_198795.1 E388E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:115947781 G>A maps to NM_198795.1 K64K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:115973128 G>A maps to NM_198795.1 W619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:154516510 C>T maps to NM_001098475.1 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:154515249 G>A maps to NM_001098475.1 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:154492802 G>A maps to NM_001098475.1 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:154516555 C>T maps to NM_001098475.1 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:154516516 G>A maps to NM_001098475.1 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:154516516 G>A maps to NM_001098475.1 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:154516909 C>T maps to NM_001098475.1 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr13:61103107 C>T maps to NM_001146070.1 F583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q3-06A-11D-A196-08 chr1:179631267 G>T maps to ENST00000444136 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:179620093 C>T maps to ENST00000444136 I631I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:179631267 G>A maps to ENST00000444136 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:179659849 C>T maps to ENST00000444136 I960I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:179631384 G>A maps to ENST00000444136 K823K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:179609004 C>T maps to ENST00000444136 R518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:179604941 C>T maps to ENST00000444136 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr1:179603593 C>T maps to ENST00000444136 Q377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr1:179609004 C>T maps to ENST00000444136 R518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:179564868 G>A maps to ENST00000444136 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:179599909 T>C maps to ENST00000444136 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:179631297 G>A maps to ENST00000444136 W794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:179631264 C>T maps to ENST00000444136 C783C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:179659831 G>A maps to ENST00000444136 V954V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:179638489 C>T maps to ENST00000444136 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:179620141 C>T maps to ENST00000444136 F647F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:179638384 C>T maps to ENST00000444136 F902F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr1:179659831 G>A maps to ENST00000444136 V954V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:179620141 C>T maps to ENST00000444136 F647F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:179604914 C>T maps to ENST00000444136 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:179587747 C>T maps to ENST00000444136 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:179604893 C>T maps to ENST00000444136 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr6:46659158 T>C maps to NM_001010870.2 C1098C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr6:46660227 C>T maps to NM_001010870.2 Q1455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:46657202 C>T maps to NM_001010870.2 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:46656335 C>T maps to NM_001010870.2 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:46656731 T>C maps to NM_001010870.2 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:46663582 G>A maps to NM_001010870.2 L2024L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:46660691 A>G maps to NM_001010870.2 E1609E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:46665772 C>T maps to NM_001010870.2 N2070N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:46660325 T>A maps to NM_001010870.2 L1487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr9:100204112 C>T maps to NM_014290.2 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:100245159 C>T maps to NM_014290.2 I814I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:100235829 C>T maps to NM_014290.2 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr14:104492470 C>T maps to NM_153046.2 Q1007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr14:104460924 C>T maps to NM_153046.2 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr14:104460696 A>G maps to NM_153046.2 E403E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr14:104491923 G>A maps to NM_153046.2 W914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr14:104493224 C>T maps to NM_153046.2 V1077V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:104452582 G>A maps to NM_153046.2 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:104508524 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:151752544 G>A maps to NM_001083965.1 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:151754019 C>T maps to NM_001083965.1 E56E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:151747915 C>T maps to NM_001083965.1 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:151748674 G>A maps to NM_001083965.1 R372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:151748636 C>T maps to NM_001083965.1 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:151748674 G>A maps to NM_001083965.1 R372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:151748308 C>T maps to NM_001083965.1 R423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:151748983 G>A maps to NM_001083965.1 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr11:12923644 C>T maps to NM_021961.5 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:12958747 T>A maps to NM_021961.5 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:12901313 C>T maps to NM_021961.5 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:35454262 G>A maps to ENST00000357281 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr6:35454394 G>A maps to ENST00000357281 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr6:35443833 C>T maps to ENST00000357281 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:3120218 C>T maps to NM_003213.3 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr12:3131140 C>T maps to NM_003213.3 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr12:3103985 C>T maps to NM_003213.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A690-06A-11D-A30X-08 chr12:3103970 G>A maps to NM_003213.3 W13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:48147206 G>A maps to NM_003215.2 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr4:48147212 C>T maps to NM_003215.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr4:48173433 A>G maps to NM_003215.2 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr4:48143370 C>T did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr4:48170628 G>A maps to NM_003215.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:48169958 G>A maps to NM_003215.2 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr7:97854177 G>A maps to ENST00000379795 F877F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr7:97874277 C>T maps to ENST00000379795 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr7:97870246 G>A maps to ENST00000379795 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:97860613 G>A maps to ENST00000379795 A683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr7:97846713 G>A maps to ENST00000379795 P1164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:97852430 G>A maps to ENST00000379795 A935A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr7:97862207 G>A maps to ENST00000379795 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr7:97870502 G>A maps to ENST00000379795 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr14:102843270 C>T maps to NM_014844.3 N71N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr14:102881013 C>T maps to NM_014844.3 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:102964021 G>A maps to NM_014844.3 W1349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr14:102918803 C>T maps to NM_014844.3 P1160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr14:102963976 C>T maps to NM_014844.3 A1334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:102901337 C>T maps to NM_014844.3 V728V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:102916010 C>T maps to NM_014844.3 Q1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:102904438 C>T maps to NM_014844.3 C825C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr14:102901184 C>T maps to NM_014844.3 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:14676598 G>A maps to ENST00000436007 W296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr4:65147221 G>A maps to NM_001010874.4 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr4:65145873 C>T maps to NM_001010874.4 W336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr4:65180439 G>A maps to NM_001010874.4 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr4:65155461 G>A maps to NM_001010874.4 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:65145906 A>G maps to NM_001010874.4 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:65175597 G>A maps to NM_001010874.4 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:65194253 G>A maps to NM_001010874.4 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:65147236 G>A maps to NM_001010874.4 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:65145864 C>T maps to NM_001010874.4 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr4:65274967 G>A maps to NM_001010874.4 H34H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr11:120984326 C>T maps to NM_005422.2 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:120989021 C>T maps to NM_005422.2 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr11:121016361 C>T maps to NM_005422.2 G1214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr11:121028932 G>A maps to NM_005422.2 K1563K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:121008169 C>T maps to NM_005422.2 I994I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:121058702 C>T maps to NM_005422.2 I2054I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:121008415 C>T maps to NM_005422.2 P1076P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:121016634 C>T maps to NM_005422.2 P1305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:121059868 G>A maps to NM_005422.2 R2081R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:121058618 C>T maps to NM_005422.2 V2026V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:120980155 C>T maps to NM_005422.2 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr11:121008697 C>T maps to NM_005422.2 I1170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr11:121038779 C>T maps to NM_005422.2 I1868I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr11:121000697 C>T maps to NM_005422.2 R907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:121059868 G>A maps to NM_005422.2 R2081R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:121032792 C>T maps to NM_005422.2 A1662A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:120980002 C>T maps to NM_005422.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:120996387 C>T maps to NM_005422.2 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:121037447 C>T maps to NM_005422.2 Q1849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr11:120989021 C>T maps to NM_005422.2 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr11:120980166 G>A maps to NM_005422.2 W149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:120998803 C>T maps to NM_005422.2 F706F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr11:121008490 C>T maps to NM_005422.2 I1101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr11:121008169 C>T maps to NM_005422.2 I994I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:121061413 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:120979942 C>T maps to NM_005422.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr11:121016262 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr11:121037452 C>T maps to NM_005422.2 I1850I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:121060539 C>A maps to NM_005422.2 L2106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:121058573 C>T maps to NM_005422.2 I2011I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:121039496 G>A maps to NM_005422.2 T1954T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:121000612 G>A maps to NM_005422.2 W878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr11:121038914 G>A maps to NM_005422.2 K1913K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19T-06A-11D-A19A-08 chr11:120996243 G>A maps to NM_005422.2 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:121023743 C>T maps to NM_005422.2 I1420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr11:121023722 C>T maps to NM_005422.2 V1413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:120980042 C>T maps to NM_005422.2 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:120996130 C>T maps to NM_005422.2 Q442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:120998596 C>T maps to NM_005422.2 F637F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:121008490 C>T maps to NM_005422.2 I1101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:121016535 G>A maps to NM_005422.2 K1272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr11:120998979 G>A maps to NM_005422.2 W765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr11:120998596 C>T maps to NM_005422.2 F637F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:120979978 C>T maps to NM_005422.2 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:120984336 C>T maps to NM_005422.2 Q234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:114044338 C>T maps to NM_058222.1 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr10:114044416 T>C maps to NM_058222.1 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr9:27183466 G>A maps to NM_000459.3 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:27180343 G>A maps to NM_000459.3 Q336Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:27203052 G>A maps to NM_000459.3 E715E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr9:27158108 C>T maps to NM_000459.3 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:27172710 C>T maps to NM_000459.3 C242C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:27205035 G>A maps to NM_000459.3 R779R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:27228233 G>A maps to NM_000459.3 E1077E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:27169586 A>T maps to NM_000459.3 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr9:27206674 C>T maps to NM_000459.3 D820D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr9:27158126 G>A maps to NM_000459.3 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:27157862 C>T maps to NM_000459.3 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:27169627 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:27206693 C>T maps to NM_000459.3 Q827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr9:27168556 C>T maps to NM_000459.3 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr17:6718549 G>A maps to NM_053285.1 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:6718609 G>A maps to NM_053285.1 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:6722552 C>T maps to NM_053285.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr17:6718591 C>T maps to NM_053285.1 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:6716271 G>A maps to NM_053285.1 R244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:6704241 G>A maps to NM_053285.1 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:6716194 C>T maps to NM_053285.1 K269K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:36553080 C>T maps to NM_014466.2 H299H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:36553170 C>A maps to NM_014466.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr17:15234782 G>A maps to NM_031898.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:15212015 C>T maps to NM_031898.2 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr2:95542330 C>T maps to NM_144705.2 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:95540640 C>T maps to NM_144705.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:95537509 G>A maps to NM_144705.2 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:95540640 C>T maps to NM_144705.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:10788364 G>A maps to NM_144674.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr16:10721442 G>A maps to NM_144674.1 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr16:10788229 C>T maps to NM_144674.1 Q167Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr16:10788373 G>A maps to NM_144674.1 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:10788310 G>A maps to NM_144674.1 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr16:10788402 G>A maps to NM_144674.1 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:10769818 C>T maps to NM_144674.1 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:10788472 G>A maps to NM_144674.1 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:10729697 C>T maps to NM_144674.1 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr16:1551672 C>T maps to NM_016111.3 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr16:1551435 C>T maps to NM_016111.3 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr16:1545502 C>T maps to NM_016111.3 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:1551717 C>T maps to NM_016111.3 I472I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr16:1547052 C>T maps to NM_016111.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr16:1557341 C>T maps to NM_016111.3 F754F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr16:1544461 G>T maps to NM_016111.3 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr16:1552362 C>T maps to NM_016111.3 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr16:1544320 G>A maps to NM_016111.3 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr12:53452856 C>T maps to NM_170754.2 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:53452555 C>T maps to NM_170754.2 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr12:53452877 C>T maps to NM_170754.2 Q485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:53456000 C>T maps to NM_170754.2 I1213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:53454782 C>T maps to NM_170754.2 P1031P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr12:53449620 C>T maps to NM_170754.2 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr14:20876286 G>A maps to NM_007110.4 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr14:20876478 G>A maps to NM_007110.4 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr14:20846646 G>A maps to NM_007110.4 P1800P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:20846374 G>A maps to NM_007110.4 A1843A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr14:20851702 A>G maps to NM_007110.4 L1271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr14:20871926 C>T maps to NM_007110.4 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr14:20852663 G>A maps to NM_007110.4 Y1075Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr14:20851799 G>A maps to NM_007110.4 S1238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:20846356 G>A maps to NM_007110.4 A1849A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:20850796 G>A maps to NM_007110.4 F1375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:20851951 G>A maps to NM_007110.4 T1220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:58018240 G>A maps to NM_199046.2 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:58019363 C>T maps to NM_199046.2 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:69404471 G>A maps to NM_005652.3 Q210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr16:69404472 G>A maps to NM_005652.3 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr5:1293434 C>T maps to NM_198253.2 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:1254579 G>A maps to NM_198253.2 P1066P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr5:1272353 G>A maps to NM_198253.2 F776F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:1253878 C>T maps to NM_198253.2 P1121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:1264577 G>A maps to NM_198253.2 F928F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:1278770 C>T maps to NM_198253.2 K757K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:1260657 C>T maps to NM_198253.2 G967G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:1255501 G>A maps to NM_198253.2 L1019L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr5:1272320 C>T maps to NM_198253.2 R787R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr5:1255419 G>A maps to NM_198253.2 L1047L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr5:1280440 C>T maps to NM_198253.2 K594K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr5:1255462 G>A maps to NM_198253.2 F1032F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:1268708 G>T maps to NM_198253.2 I836I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:1268744 G>A maps to NM_198253.2 S824S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:1271265 G>A maps to NM_198253.2 F812F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:1272353 G>A maps to NM_198253.2 F776F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:1278758 G>A maps to NM_198253.2 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr5:1254493 G>C maps to NM_198253.2 S1095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr5:1253898 G>A maps to NM_198253.2 L1115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr7:115889118 C>T maps to NM_015641.2 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr12:117494654 G>A maps to ENST00000392545 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr9:35607611 G>A maps to NM_006285.2 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:35605819 C>T maps to NM_006285.2 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:45813621 G>A maps to NM_007170.2 D197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:45887401 G>A maps to NM_007170.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:45810871 G>A maps to NM_007170.2 R452R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:45813303 G>A maps to NM_007170.2 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:45813304 G>C maps to NM_007170.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr10:70406331 T>C maps to NM_030625.2 Y1282Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr10:70404864 C>T maps to NM_030625.2 F793F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:70446174 C>T maps to NM_030625.2 L1705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:70333187 C>T maps to NM_030625.2 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:70446315 C>T maps to NM_030625.2 P1752P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr10:70446315 C>T maps to NM_030625.2 P1752P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr10:70404930 T>C maps to NM_030625.2 H815H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:70446315 C>T maps to NM_030625.2 P1752P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:70332985 C>T maps to NM_030625.2 Y297Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr10:70405329 A>T maps to NM_030625.2 G948G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr10:70451264 C>T maps to NM_030625.2 H2035H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:70405455 C>T maps to NM_030625.2 S990S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:70441246 T>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:70446397 C>T maps to NM_030625.2 R1780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:106155815 C>T maps to ENST00000513237 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:106158122 G>A maps to ENST00000513237 K1029K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr4:106157387 C>T maps to ENST00000513237 P784P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr4:106157972 G>A maps to ENST00000513237 Q979Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr4:106156271 C>T maps to ENST00000513237 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:74307654 C>T maps to ENST00000409262 I779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr2:74328039 C>T maps to ENST00000409262 L1282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:74274087 G>A maps to ENST00000409262 K255K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:74274684 C>T maps to ENST00000409262 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr2:74275056 C>A maps to ENST00000409262 P578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr2:74327598 C>T maps to ENST00000409262 S1135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:74326588 C>T maps to ENST00000409262 L1059L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:74274261 G>A maps to ENST00000409262 W313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:74274555 C>T maps to ENST00000409262 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr2:74274396 C>T maps to ENST00000409262 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr2:74328186 G>A maps to ENST00000409262 E1331E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:74328066 C>T maps to ENST00000409262 P1291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr9:103092372 G>A maps to NM_017746.3 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:103088588 G>A maps to NM_017746.3 H658H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:103111463 A>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:43920618 C>T maps to NM_031451.4 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:43920618 C>T maps to NM_031451.4 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:43920618 C>T maps to NM_031451.4 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr19:43920261 C>T maps to NM_031451.4 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr23:69945157 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:69826838 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr23:69825275 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:69890231 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:69774521 T>C did not map to a codon.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr23:70073178 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr23:70093150 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:69849513 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:69945115 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr23:70099867 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:69844688 T>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr23:69843813 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:70026600 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:70080743 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:69871314 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:69871301 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:112041209 C>T maps to NM_031275.4 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:104464032 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr23:104464955 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr23:104464956 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:104464727 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr23:104463823 C>T did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:104464657 C>T did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr23:104464112 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:104463948 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:104464308 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr23:104464007 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:104464405 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr23:104464351 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:104464875 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr23:104463704 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr23:104463949 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:104464984 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:104463986 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:107224933 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:107224620 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:107224758 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr17:56664996 G>A maps to ENST00000240361 I917I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:56699099 G>A maps to ENST00000240361 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr17:56676728 G>A maps to ENST00000240361 S665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr17:56700249 C>T maps to ENST00000240361 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:56692690 C>T maps to ENST00000240361 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:56694919 G>A maps to ENST00000240361 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:56643153 C>T maps to ENST00000240361 T1352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr17:56676713 C>T maps to ENST00000240361 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr17:56700312 G>A maps to ENST00000240361 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:56650587 G>T maps to ENST00000240361 P1201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:56676452 G>A maps to ENST00000240361 I757I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:56663165 G>A maps to ENST00000240361 F1028F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:56663309 C>T maps to ENST00000240361 R980R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr8:30705723 G>A maps to NM_031271.3 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:30699537 G>A maps to NM_031271.3 S2332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:30703215 C>T maps to NM_031271.3 R1106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:30694898 C>T maps to NM_031271.3 K2584K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:30700698 G>A maps to NM_031271.3 S1945S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:30700974 G>A maps to NM_031271.3 D1853D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr8:30699873 C>T maps to NM_031271.3 R2220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr8:30703653 G>A maps to NM_031271.3 S960S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:30703035 G>A maps to NM_031271.3 P1166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr8:30704621 A>G maps to NM_031271.3 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:30702527 G>A maps to NM_031271.3 Q1336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr8:30701208 C>T maps to NM_031271.3 R1775R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr8:30703551 G>A maps to NM_031271.3 S994S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:30701384 G>A maps to NM_031271.3 R1717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr8:30700584 G>A maps to NM_031271.3 H1983H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:30702747 C>T maps to NM_031271.3 A1262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:30704349 C>T maps to NM_031271.3 G728G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:30705810 G>A maps to NM_031271.3 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:30699873 C>T maps to NM_031271.3 R2220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:30701331 T>G maps to NM_031271.3 P1734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr8:30701291 G>A maps to NM_031271.3 Q1748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr8:30700059 G>A maps to NM_031271.3 L2158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr17:80320466 G>A maps to NM_207459.3 W147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr17:80320085 C>T maps to NM_207459.3 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:80320136 C>T maps to NM_207459.3 C37C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:80320139 C>T maps to NM_207459.3 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:80320273 G>A maps to NM_207459.3 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:62290113 G>A maps to NM_018469.3 I488I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:62290857 G>A maps to NM_018469.3 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr17:62290230 G>A maps to NM_018469.3 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:71215822 G>A maps to NM_144582.2 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr3:51708475 C>T maps to NM_015926.4 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:51718649 G>A maps to NM_015926.4 K160K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:51718541 C>T maps to NM_015926.4 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr3:133475756 G>A maps to NM_001063.3 K258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr3:133474252 G>A maps to NM_001063.3 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr3:133494361 G>A maps to NM_001063.3 E591E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:133475777 C>T maps to NM_001063.3 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:133478169 C>T maps to NM_001063.3 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:133487005 C>T maps to NM_001063.3 F540F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:133474261 C>T maps to NM_001063.3 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr3:133478169 C>T maps to NM_001063.3 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr3:133497451 C>T maps to NM_001063.3 F695F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr3:133478160 C>T maps to NM_001063.3 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr3:133473406 C>T maps to NM_001063.3 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:133475155 C>T maps to NM_001063.3 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:133494305 C>T maps to NM_001063.3 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr6:10398685 G>T maps to ENST00000379613 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr6:10410439 G>A maps to ENST00000379613 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:10410430 G>A maps to ENST00000379613 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr6:50803972 C>T maps to ENST00000263046 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:50805738 C>T maps to ENST00000263046 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:50805685 A>C did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr6:50810879 C>T maps to ENST00000263046 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr6:50810880 C>T maps to ENST00000263046 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr6:50807983 C>T maps to ENST00000263046 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr20:55204607 G>A maps to NM_003222.3 W3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr20:55209214 G>A maps to NM_003222.3 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr20:55209304 C>T maps to NM_003222.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr20:55212795 A>G maps to NM_003222.3 K360K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr20:55211687 G>A maps to NM_003222.3 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:55206394 C>T maps to NM_003222.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr6:50681779 C>T maps to NM_172238.3 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:50740412 C>T maps to NM_172238.3 Q399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:50696948 G>A maps to NM_172238.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:50712952 G>A maps to NM_172238.3 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr16:4310096 G>A maps to NM_003223.2 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr16:4312326 G>A maps to NM_003223.2 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr16:4310168 G>A maps to NM_003223.2 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:51497943 G>A maps to NM_005653.4 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:51566124 G>T maps to NM_005653.4 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:51510134 C>T maps to NM_005653.4 W140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:51512485 G>A maps to NM_005653.4 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:51512410 G>A maps to NM_005653.4 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr2:121995288 G>A maps to NM_014553.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr2:121995289 G>A maps to NM_014553.2 H304H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:121991769 C>T maps to NM_014553.2 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:121989506 C>T maps to NM_014553.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:121989509 G>A maps to NM_014553.2 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr2:121989452 G>A maps to NM_014553.2 H430H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:122007185 C>T maps to NM_014553.2 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:122007206 G>A maps to NM_014553.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr13:114287494 C>T maps to NM_007111.4 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:114287578 C>T maps to NM_007111.4 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr13:114287485 C>T maps to NM_007111.4 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:132352017 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:132352078 A>C did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:132351759 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:132351974 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:132352066 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr23:132351833 C>T did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:132351791 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr23:48887751 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:48896762 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:48896773 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:48896848 A>C did not map to a codon.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr23:48887841 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr23:48887842 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr23:48887769 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:48896731 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr7:115624342 C>T maps to NM_012252.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr7:115614247 G>A maps to NM_012252.2 D81D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:115594655 C>T maps to NM_012252.2 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:115614310 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:115624495 G>A maps to ENST00000484212 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr21:43783453 G>A maps to NM_003225.2 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr21:43783484 C>T maps to NM_003225.2 Q39Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr21:43786598 G>A maps to NM_003225.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr21:43783427 G>A maps to NM_003225.2 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr21:43783427 G>A maps to NM_003225.2 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:100438852 C>T maps to NM_001007565.2 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr22:26895180 G>A maps to NM_012143.2 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr2:188361800 C>T maps to NM_006287.4 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:188368423 G>T maps to NM_006287.4 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:188332639 C>T maps to NM_006287.4 W216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:188349700 G>A maps to NM_006287.4 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr2:188361635 C>T maps to NM_006287.4 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr2:188361701 G>A maps to NM_006287.4 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:188349652 C>T maps to NM_006287.4 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:188361701 G>A maps to NM_006287.4 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:93519936 C>T maps to NM_006528.2 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr7:93516203 C>T maps to NM_006528.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:93518425 G>A maps to NM_006528.2 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr7:100238391 G>A maps to NM_003227.3 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr7:100225713 G>A maps to NM_003227.3 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:100225226 G>A maps to NM_003227.3 V580V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:100229755 G>A maps to NM_003227.3 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:100229758 G>A maps to NM_003227.3 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:100229529 G>A maps to NM_003227.3 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:195791240 G>A maps to NM_001128148.1 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:195798338 C>T maps to NM_001128148.1 K205K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr3:195794483 G>A maps to NM_001128148.1 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr8:134146995 C>T maps to NM_003235.4 L2755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:133923721 G>A maps to NM_003235.4 W1368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr8:133925382 C>T maps to NM_003235.4 F1417F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr8:133900397 C>T maps to NM_003235.4 F782F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr8:134144178 C>T maps to NM_003235.4 F2662F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr8:133919137 C>T maps to NM_003235.4 A1280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr8:134108472 C>T maps to NM_003235.4 F2476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr8:133899119 C>T maps to NM_003235.4 F501F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr8:134108578 C>T maps to NM_003235.4 Q2512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:134042138 C>T maps to NM_003235.4 I2370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr8:134125826 G>A maps to NM_003235.4 R2578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr8:133953645 C>T maps to NM_003235.4 Q1698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:134145863 C>T maps to NM_003235.4 S2716S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:133920582 C>T maps to NM_003235.4 Q1334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr8:133984963 C>T maps to NM_003235.4 P2059P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr8:134108505 C>T maps to NM_003235.4 F2487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr8:133900484 A>G maps to NM_003235.4 E811E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr8:133961051 C>A maps to NM_003235.4 P1755P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr8:134128867 C>A maps to NM_003235.4 I2590I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:133900622 C>T maps to NM_003235.4 P857P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr8:133923692 C>T maps to NM_003235.4 T1358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:133883779 G>A maps to NM_003235.4 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:133894780 C>T maps to NM_003235.4 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:133984068 G>A maps to NM_003235.4 A2002A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:134125724 G>A maps to NM_003235.4 Q2544Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:134125847 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:134144054 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:134034309 C>T maps to NM_003235.4 I2317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:133899329 C>T maps to NM_003235.4 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:133925406 C>T maps to NM_003235.4 L1425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr8:133978826 C>T maps to NM_003235.4 S1857S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:70742000 G>A maps to NM_003236.2 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:31485737 C>T maps to NM_001042454.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:31488839 C>T maps to NM_001042454.2 F443F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr16:31487869 C>T maps to NM_001042454.2 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr16:31487373 C>T maps to NM_001042454.2 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr16:31487388 T>C maps to NM_001042454.2 C257C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:31488638 C>T maps to NM_001042454.2 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr16:31485176 C>T maps to NM_001042454.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr14:76437467 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:76429780 C>T maps to NM_003239.2 K268K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr14:76429780 C>T maps to NM_003239.2 K268K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:135390406 G>T maps to NM_000358.2 G423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:135382141 C>T maps to NM_000358.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:101907093 T>C maps to NM_004612.2 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr9:101894866 A>T maps to NM_004612.2 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr3:30713310 C>T maps to NM_001024847.2 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:30713628 G>A maps to NM_001024847.2 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr3:30713877 C>T maps to NM_001024847.2 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:30713418 C>T maps to NM_001024847.2 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:92200471 G>A maps to NM_003243.4 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:92182151 G>A maps to NM_003243.4 S560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:92178030 C>T maps to NM_003243.4 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:92195498 C>A maps to NM_003243.4 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:105924668 C>T maps to NM_004257.4 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:105897098 G>A maps to NM_004257.4 H401H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr2:105883860 G>A maps to NM_004257.4 S854S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:105924377 G>A maps to NM_004257.4 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:105890129 G>A maps to NM_004257.4 F561F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:105883950 G>A maps to NM_004257.4 P824P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:105924122 G>A maps to NM_004257.4 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr18:3457418 G>A maps to NM_170695.2 K229K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr18:3452057 C>T maps to NM_170695.2 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr20:35207363 C>T maps to NM_021809.6 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr20:35219437 C>T maps to NM_021809.6 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:89177428 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:89177474 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:89177129 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:89177316 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:89177552 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr24:3447330 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr24:3447611 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr24:3447712 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q1-06A-21D-A196-08 chr14:24729190 G>T maps to NM_000359.2 Y277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr14:24730979 G>A maps to NM_000359.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:24729893 G>A maps to NM_000359.2 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:24723875 G>A maps to NM_000359.2 S694S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr14:24729712 G>A maps to NM_000359.2 Q234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:24718641 C>T maps to NM_000359.2 Q777Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr14:24724430 C>T maps to NM_000359.2 E558E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr14:24728446 G>A maps to NM_000359.2 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:24730967 G>A maps to NM_000359.2 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr14:24730946 G>A maps to NM_000359.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:36766764 G>A maps to NM_004613.2 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:36766713 C>T maps to NM_004613.2 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr20:36784483 G>A maps to NM_004613.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:36779352 C>T maps to NM_004613.2 W180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr20:36760876 G>A maps to NM_004613.2 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:36776476 G>A maps to NM_004613.2 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr20:36789987 C>T maps to NM_004613.2 E8E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr20:36779353 C>T maps to NM_004613.2 W180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:36760864 G>A maps to NM_004613.2 Y551Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr20:36760849 C>A maps to NM_004613.2 T556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:36767897 G>A maps to NM_004613.2 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr20:2290304 C>T maps to NM_003245.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr20:2297712 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:2291762 G>A maps to NM_003245.3 W176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr20:2312849 G>A maps to NM_003245.3 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr20:2315888 C>T maps to NM_003245.3 I590I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:2293602 C>T maps to NM_003245.3 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:2293546 G>T maps to NM_003245.3 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr20:2312717 G>A maps to NM_003245.3 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr20:2312687 G>A maps to NM_003245.3 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr20:2308916 C>T maps to NM_003245.3 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:2308865 C>T maps to NM_003245.3 D396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:2297847 C>T maps to NM_003245.3 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:2291058 G>A maps to NM_003245.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:2321100 G>A maps to NM_003245.3 K652K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:2290851 G>A maps to NM_003245.3 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:2297748 G>A maps to NM_003245.3 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:2297769 C>T maps to NM_003245.3 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:2321208 C>T maps to NM_003245.3 S688S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:2312849 G>A maps to NM_003245.3 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:2321169 C>T maps to NM_003245.3 F675F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr20:2308844 C>T maps to NM_003245.3 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:44945381 C>T maps to NM_003241.3 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:44943396 C>T maps to NM_003241.3 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr3:44951726 C>T maps to NM_003241.3 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr3:44926976 G>A maps to NM_003241.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:44955174 G>A maps to NM_003241.3 V671V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:44932093 G>A did not map to a codon.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr3:44926889 G>A maps to NM_003241.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr3:44948522 C>T maps to NM_003241.3 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:44926877 G>A maps to NM_003241.3 W27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:44945381 C>T maps to NM_003241.3 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:44951663 G>A maps to NM_003241.3 E470E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:44932132 G>A maps to NM_003241.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:44945375 G>A maps to NM_003241.3 W324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr15:43527772 G>A maps to NM_201631.3 F536F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr15:43552310 C>T maps to NM_201631.3 Q125Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:43527002 C>T maps to NM_201631.3 K613K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:43552265 G>A maps to NM_201631.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr15:43548858 T>C maps to NM_201631.3 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr15:43552316 G>A maps to NM_201631.3 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr15:43531463 C>T maps to NM_201631.3 W334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:43552442 G>A maps to NM_201631.3 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr15:43527778 G>A maps to NM_201631.3 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:43552310 C>T maps to NM_201631.3 Q125Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:43552379 C>T maps to NM_201631.3 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:43552274 G>A maps to NM_201631.3 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:43552322 G>A maps to NM_201631.3 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr15:43527964 G>A maps to NM_201631.3 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr20:2380982 C>T maps to NM_198994.2 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:2381051 C>T maps to NM_198994.2 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr20:2411159 C>T maps to NM_198994.2 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr20:2378578 C>T maps to NM_198994.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr20:2375242 G>A maps to NM_198994.2 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr20:2384302 C>T maps to NM_198994.2 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr20:2375915 A>C maps to NM_198994.2 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr20:2381042 G>A maps to NM_198994.2 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:2376065 C>T maps to NM_198994.2 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr20:2377256 G>A maps to NM_198994.2 W177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr20:2375098 G>A maps to NM_198994.2 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr20:2380988 C>A maps to NM_198994.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:2413240 C>T maps to NM_198994.2 F691F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:2413172 C>T maps to NM_198994.2 Q669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:2375858 C>T maps to NM_198994.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:2377215 C>T maps to NM_198994.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:2413243 G>A maps to NM_198994.2 P692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr15:43584242 T>A maps to NM_052955.2 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:43571344 G>A maps to NM_052955.2 I603I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr15:43577112 G>A maps to NM_052955.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:43585713 G>A maps to NM_052955.2 Y42Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:43574237 C>T maps to NM_052955.2 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr15:43568685 C>T maps to NM_052955.2 K700K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr15:43585096 G>A maps to NM_052955.2 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr15:43574781 C>T maps to NM_052955.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:43579607 C>T maps to NM_052955.2 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:43585108 G>A maps to NM_052955.2 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:43571823 C>T maps to NM_052955.2 K559K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr15:43571422 C>T maps to NM_052955.2 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:56723524 C>T maps to NM_024831.6 F743F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:2186472 C>T maps to NM_199292.2 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr11:2190933 G>A maps to NM_199292.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:2190957 C>T maps to NM_199292.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:2189796 G>A maps to NM_199292.2 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:2185558 G>A maps to NM_199292.2 I497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:2189823 C>T maps to NM_199292.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:57566461 C>T maps to NM_198976.1 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr2:43797553 G>A maps to ENST00000330266 H721H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr2:43779018 G>A maps to ENST00000330266 L953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:43625186 G>A maps to ENST00000330266 R1385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr2:43819105 G>A maps to ENST00000330266 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr2:43519315 G>A maps to ENST00000330266 Q1623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr2:43519316 G>A maps to ENST00000330266 P1622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:43768300 C>T maps to ENST00000330266 E1088E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:43625186 G>A maps to ENST00000330266 R1385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:43625190 G>A maps to ENST00000330266 T1383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:43778949 G>A maps to ENST00000330266 L976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:43804267 G>A maps to ENST00000330266 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:43625250 G>A maps to ENST00000330266 S1363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr16:67877152 A>G maps to NM_020457.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr12:72070869 C>T maps to NM_031435.3 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:242524125 G>A maps to NM_015963.5 F543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:242542424 G>A maps to NM_015963.5 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:242572422 G>A maps to NM_015963.5 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr2:242573100 C>T maps to NM_015963.5 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:242572545 G>A maps to NM_015963.5 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:242573388 G>A maps to NM_015963.5 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr2:242545738 G>A maps to NM_015963.5 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:76452306 G>A maps to NM_144721.4 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:36530863 G>A maps to NM_152658.2 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr4:83839809 A>T maps to NM_024672.4 V815V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr4:83839110 G>A maps to NM_024672.4 E582E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr20:23028830 G>A maps to NM_000361.2 F437F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A197-06A-32D-A197-08 chr20:23029064 G>A maps to NM_000361.2 D359D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:23029229 G>A maps to NM_000361.2 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr15:39881500 C>T maps to NM_003246.2 F624F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr15:39885303 C>T maps to NM_003246.2 F957F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr15:39874922 C>T maps to NM_003246.2 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:39875834 G>A maps to NM_003246.2 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:39886528 C>T maps to NM_003246.2 I1131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:39874922 C>T maps to NM_003246.2 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:39885655 G>A maps to NM_003246.2 R1018R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr15:39874526 C>T maps to NM_003246.2 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr15:39883390 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:39874628 G>A maps to NM_003246.2 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:39882121 C>T maps to NM_003246.2 G681G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr15:39886346 C>T maps to NM_003246.2 F1105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr15:39882058 C>T maps to NM_003246.2 N660N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:39885208 C>T maps to NM_003246.2 R926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr15:39874526 C>T maps to NM_003246.2 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr15:39875852 C>T maps to NM_003246.2 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr15:39885721 G>A maps to NM_003246.2 W1040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr15:39881266 C>T maps to NM_003246.2 Q585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr15:39882037 G>A maps to NM_003246.2 G653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr15:39885333 C>A maps to NM_003246.2 P967P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:39879653 C>T maps to NM_003246.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:39880360 G>A maps to NM_003246.2 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:39884770 G>A maps to NM_003246.2 L845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:39884992 G>A maps to NM_003246.2 K919K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:39885297 C>T maps to NM_003246.2 T955T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr15:39880261 G>A maps to NM_003246.2 W438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:39886528 C>T maps to NM_003246.2 I1131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr6:169628376 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:169648949 G>A maps to NM_003247.2 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:169648877 C>T maps to NM_003247.2 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr6:169648775 G>A maps to NM_003247.2 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:169648775 G>A maps to NM_003247.2 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:169648949 G>A maps to NM_003247.2 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr6:169648822 G>A maps to NM_003247.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:169623559 C>T maps to NM_003247.2 R928R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr6:169640625 G>C maps to NM_003247.2 S318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:169648793 G>A maps to NM_003247.2 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr6:169620353 C>T maps to NM_003247.2 L1150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:169623442 C>T maps to NM_003247.2 L967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:169648949 G>A maps to NM_003247.2 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:155173094 C>T maps to NM_007112.3 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:155167719 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:155171225 A>G maps to NM_007112.3 N437N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:155170708 C>T maps to NM_007112.3 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr1:155165883 C>T maps to NM_007112.3 A902A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr1:155175011 G>A maps to NM_007112.3 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:155172640 G>A maps to NM_007112.3 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr5:79355628 C>T maps to NM_003248.4 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:79354580 C>T maps to NM_003248.4 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:79375867 C>T maps to NM_003248.4 F884F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:79357627 G>A maps to NM_003248.4 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr5:79354081 C>T maps to NM_003248.4 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr5:79374010 G>A maps to NM_003248.4 G742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr5:79351698 C>T maps to NM_003248.4 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr5:79351608 C>T maps to NM_003248.4 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:79374016 C>T maps to NM_003248.4 A744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr5:79374022 C>T maps to NM_003248.4 I746I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr5:79374918 G>A maps to NM_003248.4 G783G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:79363878 C>T maps to NM_003248.4 N426N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:79375867 C>T maps to NM_003248.4 F884F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr5:79373992 G>A maps to NM_003248.4 V736V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:362367 C>T maps to NM_016585.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:372692 G>A maps to NM_016585.3 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:373503 G>A maps to NM_016585.3 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:375874 G>A maps to NM_016585.3 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:375931 G>A maps to NM_016585.3 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:151825968 G>A maps to NM_182578.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:151820662 G>A maps to NM_182578.3 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr6:128222008 G>A maps to NM_001164685.1 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr6:128134288 C>A maps to NM_001164685.1 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:128150660 C>T maps to NM_001164685.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:128176253 C>T maps to NM_001164685.1 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:128134489 T>A maps to NM_001164685.1 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:128151020 C>T maps to NM_001164685.1 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr6:128134111 C>T maps to NM_001164685.1 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr6:128134783 G>A maps to NM_001164685.1 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:128150660 C>T maps to NM_001164685.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:128134339 C>T maps to NM_001164685.1 E482E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:128150693 C>T maps to NM_001164685.1 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr6:128222008 G>A maps to NM_001164685.1 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:128135059 G>A maps to NM_001164685.1 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr6:128176298 A>G maps to NM_001164685.1 C42C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:128134384 G>A maps to NM_001164685.1 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:128150760 C>T maps to NM_001164685.1 W190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:128134111 C>T maps to NM_001164685.1 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:128135035 G>A maps to NM_001164685.1 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr6:128150693 C>T maps to NM_001164685.1 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:157161589 C>T maps to NM_017872.3 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr5:157158486 G>A maps to NM_017872.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr10:25312883 G>A maps to NM_024838.4 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr10:25312541 C>T maps to NM_024838.4 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:25313573 C>T maps to NM_024838.4 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr10:25313733 C>T maps to NM_024838.4 R528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr2:88474314 C>T maps to NM_018271.3 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:88472869 C>T maps to NM_018271.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:88472833 G>A maps to NM_018271.3 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:88482260 C>T maps to NM_018271.3 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr23:122801094 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:122754786 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:122820483 A>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:122769981 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr23:122830591 A>C did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:122747275 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr23:122778636 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:122756647 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:122756648 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr23:122754816 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:122758410 T>G did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:122760432 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:122756987 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr23:122754785 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:122753265 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:122758464 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:122747527 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr23:122755258 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:122756608 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:122759827 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:122759916 G>A did not map to a codon.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr5:175387025 G>A maps to NM_032361.2 D334D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr17:79846179 C>T maps to NM_005782.3 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:29927910 G>A maps to NM_003678.4 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr22:29921855 G>A maps to NM_003678.4 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr22:29940510 G>A maps to NM_003678.4 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:3077380 C>T maps to NM_024339.3 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:3077381 C>T maps to NM_024339.3 Q276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr16:3077241 C>T maps to NM_024339.3 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr16:3077226 C>T maps to NM_024339.3 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:3077235 C>T maps to NM_024339.3 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:63823681 G>A maps to NM_025075.2 Q108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44R-06A-41D-A25O-08 chr19:2811638 C>T maps to NM_003249.3 Y605Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:2811692 C>T maps to NM_003249.3 F623F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr3:184090873 C>G maps to NM_000460.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr3:184090582 G>A maps to NM_000460.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:184091367 C>T maps to NM_000460.2 E77E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr3:184091238 G>A maps to NM_000460.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr3:184090867 A>T maps to NM_000460.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr17:38233776 C>T maps to NM_003250.5 Y46Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr17:38240092 C>T maps to NM_003250.5 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr1:36755031 G>A maps to NM_005119.3 W471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:36758295 C>T maps to NM_005119.3 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:36754861 C>T maps to NM_005119.3 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr1:36748265 C>T maps to NM_005119.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr1:36748266 C>T maps to NM_005119.3 R35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:36752049 C>T maps to NM_005119.3 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr1:36752673 C>T maps to NM_005119.3 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:36748259 C>T maps to NM_005119.3 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:36748260 C>T maps to NM_005119.3 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:24169110 C>T maps to NM_001128177.1 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr3:24231673 G>A maps to NM_001128177.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr3:24185189 C>T maps to NM_001128177.1 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:24164461 G>A maps to NM_001128177.1 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:24185162 C>T maps to NM_001128177.1 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:24188210 C>A maps to NM_001128177.1 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:24185141 C>T maps to NM_001128177.1 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:24169110 C>T maps to NM_001128177.1 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:24231760 T>G maps to NM_001128177.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr11:77775334 G>A maps to NM_003251.2 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr13:52951767 G>A maps to NM_018676.3 S779S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr13:52952919 G>A maps to NM_018676.3 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr13:52952721 C>T maps to NM_018676.3 K461K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr15:71447213 C>T maps to NM_024817.2 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr15:71447237 C>T maps to NM_024817.2 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr15:72030341 G>A maps to NM_024817.2 G634G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr15:71433892 C>T maps to NM_024817.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr15:71534993 G>A maps to NM_024817.2 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr15:72057426 C>T maps to NM_024817.2 T886T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr15:71447213 C>T maps to NM_024817.2 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:72050248 G>A maps to NM_024817.2 A808A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:71953005 C>T maps to NM_024817.2 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr15:72039233 C>T maps to NM_024817.2 H698H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:71535176 C>T maps to NM_024817.2 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:72023548 G>A maps to NM_024817.2 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:72037538 G>A maps to NM_024817.2 E667E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr15:72057459 C>T maps to NM_024817.2 F897F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr15:71535230 G>A maps to NM_024817.2 Q236Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:11676524 C>T maps to ENST00000423059 W85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:11452337 C>T maps to ENST00000423059 E1209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:11446643 G>A maps to ENST00000423059 Q1319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:11676391 C>T maps to ENST00000423059 W129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:11676262 G>A maps to ENST00000423059 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr7:11416267 G>A maps to ENST00000423059 T1606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:11630228 C>T maps to ENST00000423059 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr7:11676190 G>A maps to ENST00000423059 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:11676355 C>T maps to ENST00000423059 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:11676535 C>T maps to ENST00000423059 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:11485934 C>T maps to ENST00000423059 K939K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr7:11676535 C>T maps to ENST00000423059 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr7:11676085 G>A maps to ENST00000423059 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:11485850 C>T maps to ENST00000423059 G967G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr7:11632978 G>A maps to ENST00000423059 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr7:11513998 G>A maps to ENST00000423059 I738I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:11468726 G>A maps to ENST00000423059 I1030I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:138163336 G>A maps to ENST00000272643 T885T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:138373879 C>T maps to ENST00000272643 L1190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr2:137872744 C>T maps to ENST00000272643 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:137990577 G>A maps to ENST00000272643 E675E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:138000071 C>T maps to ENST00000272643 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:138425404 C>T maps to ENST00000272643 F1574F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:138373800 G>A maps to ENST00000272643 L1163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr2:138421074 G>A maps to ENST00000272643 G1530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:138163336 G>A maps to ENST00000272643 T885T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:138169218 T>C maps to ENST00000272643 L912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:137814035 G>A maps to ENST00000272643 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:137917930 G>A maps to ENST00000272643 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:137872753 G>A maps to ENST00000272643 Q420Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:137988662 G>A maps to ENST00000272643 R591R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr2:138169378 C>T maps to ENST00000272643 R966*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:138425404 C>T maps to ENST00000272643 F1574F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:137852487 C>T maps to ENST00000272643 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr2:138208413 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr2:137917930 G>A maps to ENST00000272643 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr2:138425404 C>T maps to ENST00000272643 F1574F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:138421074 G>A maps to ENST00000272643 G1530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:138413198 C>T maps to ENST00000272643 I1361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:138400172 C>T maps to ENST00000272643 V1308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:137872822 C>T maps to ENST00000272643 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:137872823 C>T maps to ENST00000272643 Q444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr2:137917930 G>A maps to ENST00000272643 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:137814116 G>A maps to ENST00000272643 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:137814592 G>A maps to ENST00000272643 W248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr2:137917849 C>T maps to ENST00000272643 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:138414465 G>A maps to ENST00000272643 R1405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr2:138414697 G>A maps to ENST00000272643 W1451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:137814412 G>A maps to ENST00000272643 W188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr2:137852476 C>T maps to ENST00000272643 Q329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:138208521 C>T maps to ENST00000272643 R1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:137814592 G>A maps to ENST00000272643 W248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:138000128 G>A maps to ENST00000272643 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:138378198 G>A maps to ENST00000272643 Q1237Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:137872795 G>A maps to ENST00000272643 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:137917849 C>T maps to ENST00000272643 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr2:137928437 C>T maps to ENST00000272643 I551I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:137928413 C>T maps to ENST00000272643 Y543Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:138000128 G>A maps to ENST00000272643 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr2:138208521 C>T maps to ENST00000272643 R1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr2:137988737 C>T maps to ENST00000272643 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr2:138414489 G>A maps to ENST00000272643 E1413E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:138169324 C>T maps to ENST00000272643 R948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:137852487 C>T maps to ENST00000272643 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr2:137928434 G>A maps to ENST00000272643 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr2:137928320 G>A maps to ENST00000272643 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr2:138208521 C>T maps to ENST00000272643 R1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:137928482 G>A maps to ENST00000272643 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:137852556 G>A maps to ENST00000272643 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:138000128 G>A maps to ENST00000272643 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:138400169 G>A maps to ENST00000272643 W1307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:137814719 G>A maps to ENST00000272643 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:137872795 G>A maps to ENST00000272643 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:137988647 C>T maps to ENST00000272643 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:137990484 C>T maps to ENST00000272643 P644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr2:137814162 C>T maps to ENST00000272643 Q105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr2:138378222 G>A maps to ENST00000272643 V1245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:138375964 G>A maps to ENST00000272643 W1193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:39993246 G>A maps to NM_025264.4 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr2:39997186 C>T maps to NM_025264.4 W112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:39964114 G>A maps to NM_025264.4 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:9406784 C>T maps to NM_015453.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:9406785 C>T maps to NM_015453.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:9412784 C>A maps to NM_015453.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr11:119290150 G>A maps to NM_006288.3 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr11:119290156 G>A maps to NM_006288.3 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr11:134120207 G>T maps to NM_199298.1 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr2:70457968 G>A maps to NM_022173.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr10:121338306 A>G maps to NM_001033925.1 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:121336988 G>A maps to NM_001033925.1 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr21:32502612 G>A maps to NM_003253.2 S1321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr21:32624358 G>A maps to NM_003253.2 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr21:32639144 G>A maps to NM_003253.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr21:32575282 G>A maps to NM_003253.2 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr21:32502581 G>A maps to NM_003253.2 R1332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr21:32502581 G>A maps to NM_003253.2 R1332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr21:32598134 C>T maps to NM_003253.2 Q572Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr21:32582378 G>A maps to NM_003253.2 T790T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr21:32496852 G>A maps to NM_003253.2 A1431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr21:32624214 G>A maps to NM_003253.2 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr21:32519303 C>A maps to NM_003253.2 L1128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr21:32567600 G>A maps to NM_003253.2 I838I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:32526726 G>A maps to NM_003253.2 A1003A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A264-06A-11D-A196-08 chr21:32496903 A>G maps to NM_003253.2 Y1414Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr21:32496912 G>A maps to NM_003253.2 S1411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr21:32638799 C>T maps to NM_003253.2 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr21:32582489 G>A maps to NM_003253.2 N753N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:155451250 C>T maps to ENST00000456144 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:155458327 G>A maps to ENST00000456144 E404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr6:155469377 G>A maps to ENST00000456144 K646K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:155458690 G>A maps to ENST00000456144 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr6:155485619 C>T maps to ENST00000456144 S700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr6:155485620 C>T maps to ENST00000456144 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:155451410 C>T maps to ENST00000456144 Q352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:155569311 G>A maps to ENST00000456144 T1277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr6:155450803 C>T maps to ENST00000456144 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr6:155451256 G>A maps to ENST00000456144 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:155485631 G>A maps to ENST00000456144 G704G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr6:155451083 C>T maps to ENST00000456144 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr6:155571003 G>A maps to ENST00000456144 E1284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr6:155569308 G>A maps to ENST00000456144 L1276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:155450701 C>T maps to ENST00000456144 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:155485640 G>A maps to ENST00000456144 P707P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr6:155450983 C>T maps to ENST00000456144 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:155451112 C>T maps to ENST00000456144 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:4817135 G>A maps to NM_182919.2 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:4816466 G>A maps to NM_182919.2 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:4817963 G>A maps to NM_182919.2 N142N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr19:4817258 G>A maps to NM_182919.2 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:4817009 G>A maps to NM_182919.2 F460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr19:4817243 G>A maps to NM_182919.2 F382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr19:4816400 G>A maps to NM_182919.2 F663F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr1:43772658 C>T maps to NM_005424.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:43778084 C>T maps to NM_005424.2 F580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:43778222 C>T maps to NM_005424.2 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:43775075 G>A maps to NM_005424.2 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:43779025 C>T maps to NM_005424.2 F716F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:43772942 G>A maps to NM_005424.2 Q257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:43778084 C>T maps to NM_005424.2 F580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:43772658 C>T maps to NM_005424.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:43783009 C>T maps to NM_005424.2 F850F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:43777489 G>A maps to NM_005424.2 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:43779608 G>A maps to NM_005424.2 R793R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:43774699 C>T maps to NM_005424.2 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:43777488 C>A maps to NM_005424.2 S494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:43777746 G>A maps to NM_005424.2 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:43784949 G>A maps to NM_005424.2 E989E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:43783337 G>A maps to NM_005424.2 K908K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:43777468 G>A maps to NM_005424.2 Q487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr1:43783565 C>T maps to NM_005424.2 I915I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr1:43778231 C>T maps to NM_005424.2 G629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr1:43777680 C>T maps to NM_005424.2 N503N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:43773518 G>A maps to NM_005424.2 Q322Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:43783021 C>T maps to NM_005424.2 I854I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:134785607 G>A maps to NM_001099221.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:134785186 C>T maps to NM_001099221.1 W148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:134785467 G>A maps to NM_001099221.1 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr5:134785515 G>A maps to NM_001099221.1 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:90035003 C>T maps to NM_145715.2 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:65123329 G>A maps to NM_145719.2 K17K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:65123858 C>T maps to NM_145719.2 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:65124163 C>T maps to NM_145719.2 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr11:65124430 C>T maps to NM_145719.2 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr11:65123629 C>T maps to NM_145719.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:65124130 C>T maps to NM_145719.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:65123716 C>T maps to NM_145719.2 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr11:65124565 C>T maps to NM_145719.2 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:65124001 C>T maps to NM_145719.2 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:65123659 G>A maps to NM_145719.2 W127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr4:153691348 G>A maps to NM_145720.2 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr4:153691265 C>T maps to NM_145720.2 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:144680468 C>T maps to NM_032862.4 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:144681845 C>T maps to NM_032862.4 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:3349418 C>T maps to NM_033208.3 W399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:114014473 C>T maps to ENST00000481065 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:114026782 G>A maps to ENST00000481065 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr3:114014611 C>T maps to ENST00000481065 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:114014665 C>G maps to ENST00000481065 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:156378772 G>A maps to NM_138379.2 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr5:156349164 G>A maps to NM_138379.2 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:156381660 C>T maps to NM_138379.2 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:156381621 G>A maps to NM_138379.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:156381594 G>A maps to NM_138379.2 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:156375463 C>T maps to NM_138379.2 W269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr5:156381660 C>G maps to NM_138379.2 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:156378651 G>A maps to NM_138379.2 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:156381434 G>A maps to NM_138379.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:156375505 G>A maps to NM_138379.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:156378589 G>A maps to NM_138379.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr12:56826248 G>A maps to NM_003920.3 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr12:56814623 G>A maps to NM_003920.3 R1028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr12:56814624 G>A maps to NM_003920.3 I1027I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:56811924 G>A maps to NM_003920.3 S1149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:56822103 G>A maps to NM_003920.3 F498F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:56823951 G>A maps to NM_003920.3 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:56815552 A>G maps to NM_003920.3 L895L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr12:56827627 G>A maps to NM_003920.3 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:201934671 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr17:900466 C>T maps to NM_013337.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:902025 C>T maps to NM_013337.2 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:7997559 G>A maps to NM_006351.3 D313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:7998810 G>A maps to NM_006351.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr19:39971435 C>T maps to NM_001001563.1 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:39971591 C>T maps to NM_001001563.1 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:39976353 C>T maps to NM_001001563.1 C236C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:100601520 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:100601520 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:47442820 C>T did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:47444665 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:76851754 G>A maps to NM_003255.4 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:76867037 G>A maps to NM_003255.4 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:12198883 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr3:12200283 C>G maps to NM_003256.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:12195212 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:12195893 C>T maps to NM_003256.2 W137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:12195140 C>T maps to NM_003256.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr3:12195889 C>T maps to NM_003256.2 E138E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:54173467 C>T maps to NM_014464.3 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:54186100 C>T maps to NM_014464.3 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr6:54212255 C>T maps to NM_014464.3 N280N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:54208087 G>A maps to NM_014464.3 W230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:54208129 G>A maps to NM_014464.3 W244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:54173452 C>T maps to NM_014464.3 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr6:54173503 C>T maps to NM_014464.3 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr6:54254638 G>A maps to NM_014464.3 R449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr6:54212202 C>T maps to NM_014464.3 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:54219309 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:32050547 C>G maps to NM_022164.2 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:32050548 C>T maps to NM_022164.2 Q257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr1:32044856 C>T maps to NM_022164.2 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:32042973 C>T maps to NM_022164.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr14:24709493 T>C maps to NM_001099274.1 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr3:156395965 G>A maps to NM_015508.4 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:156422823 C>T maps to NM_015508.4 F626F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr3:156395963 C>T maps to NM_015508.4 Q160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:156395584 C>T maps to NM_015508.4 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:156395947 C>T maps to NM_015508.4 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr15:66633494 T>A maps to NM_017858.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr15:66641431 G>A maps to NM_017858.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:168160617 A>C maps to NM_152902.3 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:168153169 C>T maps to NM_152902.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:43472806 T>C maps to NM_001146016.1 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr15:30009028 G>A maps to NM_003257.3 Q1330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr15:30025311 G>A maps to NM_003257.3 I574I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:30026534 G>A maps to NM_003257.3 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:30010268 G>A maps to NM_003257.3 P1310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr15:30009038 G>A maps to NM_003257.3 I1326I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:30026559 G>A maps to NM_003257.3 I478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr9:71851100 G>T maps to NM_004817.3 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr9:71852824 C>T maps to NM_004817.3 G737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:71833265 C>T maps to NM_004817.3 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr19:3736219 G>A maps to NM_014428.1 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:3735608 C>T maps to NM_014428.1 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:3735566 G>A maps to NM_014428.1 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:3744027 C>T maps to NM_014428.1 I678I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:3746786 G>A maps to NM_014428.1 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr19:3743958 G>A maps to NM_014428.1 V655V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:3728612 G>A maps to NM_014428.1 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:3735876 G>A maps to NM_014428.1 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:3733818 G>A maps to NM_014428.1 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:3739120 C>T maps to NM_014428.1 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:3738584 G>A maps to NM_014428.1 R472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr19:3736222 G>A maps to NM_014428.1 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:3730079 C>T maps to NM_014428.1 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:3740729 C>T maps to NM_014428.1 Y637Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:3736192 C>T maps to NM_014428.1 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:3738602 C>T maps to NM_014428.1 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:3728435 G>A maps to NM_014428.1 E21E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:66545942 C>T maps to ENST00000299697 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:66545951 G>A maps to ENST00000299697 H281H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:66565281 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:66565282 C>T maps to ENST00000299697 Q167Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr16:66570868 G>A maps to ENST00000299697 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:53259837 C>T maps to ENST00000423516 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr3:53263299 G>A maps to ENST00000423516 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:53265453 G>A maps to ENST00000423516 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:153533722 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr23:153524337 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:153556203 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:153556242 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:153557974 G>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:153541043 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:153556194 C>T did not map to a codon.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr23:153553685 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr4:164394718 C>T maps to NM_032136.4 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr4:164394580 C>T maps to NM_032136.4 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr4:164393410 C>T maps to NM_032136.4 E492E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:164393467 G>A maps to NM_032136.4 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr4:164393086 C>T maps to NM_032136.4 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:164394220 C>T maps to NM_032136.4 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr4:164393818 C>T maps to NM_032136.4 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:164393862 G>A maps to NM_032136.4 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:164393655 G>A maps to NM_032136.4 Q411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:164394439 C>T maps to NM_032136.4 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:164394580 C>T maps to NM_032136.4 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr9:84231584 G>A maps to NM_005077.3 N247N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:84208113 G>A maps to NM_005077.3 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:84226686 G>A maps to NM_005077.3 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:3000674 C>T maps to NM_003260.4 W698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:3009614 G>A maps to NM_003260.4 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:3005909 G>A maps to NM_003260.4 I519I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:3005777 G>A maps to NM_003260.4 F563F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:3002401 G>A maps to NM_003260.4 Q666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:3009538 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr19:3011089 G>A maps to NM_003260.4 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:3006495 C>T maps to NM_003260.4 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:3009668 G>A maps to NM_003260.4 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr19:3009581 G>A maps to NM_003260.4 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr15:70348701 G>A maps to NM_005078.2 D424D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:70342441 G>A maps to NM_005078.2 I771I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr15:70368485 C>T maps to NM_005078.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr15:70347594 G>A maps to NM_005078.2 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr9:82188650 C>T maps to ENST00000376537 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr9:82267686 C>T maps to ENST00000376537 H190H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr9:82323514 C>T maps to ENST00000376537 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr9:82242320 G>A maps to ENST00000376537 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr9:82333687 T>C maps to ENST00000376537 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr9:82267551 C>T maps to ENST00000376537 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr9:82324554 C>T maps to ENST00000376537 H459H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:2991876 C>T maps to NM_001143986.1 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr19:2987152 G>A maps to NM_001143986.1 W153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr19:2991912 G>T maps to NM_001143986.1 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:2987366 C>T maps to NM_001143986.1 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:2989205 C>T maps to NM_001143986.1 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr2:171906376 G>T maps to ENST00000360843 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:60678056 C>T maps to ENST00000326270 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:60685475 C>T maps to ENST00000326270 F704F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr17:60678135 T>C maps to ENST00000326270 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZH-06A-11D-A197-08 chr17:60600508 A>C maps to ENST00000326270 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr17:60689770 T>C maps to ENST00000326270 L722L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:60631028 C>T maps to ENST00000326270 D211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr4:166996084 G>A maps to ENST00000507499 T771T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr4:166978334 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr4:166795172 G>A maps to ENST00000507499 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:166976292 C>T maps to ENST00000507499 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr4:166960488 A>G did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr4:166795118 C>T maps to ENST00000507499 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr4:166914028 T>A maps to ENST00000507499 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44Q-06A-11D-A25O-08 chr4:166981295 A>C maps to ENST00000507499 R678R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:166964466 C>T maps to ENST00000507499 Q474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:166964466 C>T maps to ENST00000507499 Q474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr4:166960591 T>A maps to ENST00000507499 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr4:167012278 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:166996155 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:166929122 G>A maps to ENST00000507499 E280E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:167020675 C>T maps to ENST00000507499 S991S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr4:166996084 G>A maps to ENST00000507499 T771T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:166916231 C>T maps to ENST00000507499 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr4:166929185 G>A maps to ENST00000507499 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:166964516 G>A maps to ENST00000507499 W490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:166976310 C>T maps to ENST00000507499 F559F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:166996153 A>G maps to ENST00000507499 E794E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:98180819 T>G did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr10:98129905 C>T maps to NM_012465.3 E943E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:98164992 A>T maps to NM_012465.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:98188496 T>G maps to NM_012465.3 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr10:98136547 C>T maps to NM_012465.3 V783V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:98155085 G>A maps to NM_012465.3 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:98155082 C>T maps to NM_012465.3 T529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:98188431 C>T maps to NM_012465.3 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:98155082 C>T maps to NM_012465.3 T529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:98188503 C>T maps to NM_012465.3 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr9:35710650 G>A maps to NM_006289.3 S1411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr9:35713964 G>T maps to NM_006289.3 P1078P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr9:35706000 G>A maps to NM_006289.3 V1823V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:35705809 G>A maps to NM_006289.3 F1850F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:35711665 G>A maps to NM_006289.3 R1269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:35700223 G>A maps to NM_006289.3 S2208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:35710877 G>A maps to NM_006289.3 V1373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr15:63128193 C>T maps to NM_015059.2 V2432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr15:63089459 G>A maps to NM_015059.2 T2031T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr15:63084958 C>T maps to NM_015059.2 I1952I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:63047732 C>T maps to NM_015059.2 V1493V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:63127943 C>T maps to NM_015059.2 S2379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr15:63102155 G>A maps to NM_015059.2 E2232E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr15:62989952 G>A maps to NM_015059.2 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr15:63127946 C>T maps to NM_015059.2 I2380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:63031707 C>T maps to NM_015059.2 F1283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:62986582 C>T maps to NM_015059.2 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:62994230 G>A maps to NM_015059.2 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr15:63000708 C>T maps to NM_015059.2 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:62994293 C>T maps to NM_015059.2 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:63092631 G>A maps to NM_015059.2 K2100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr15:63040585 G>A maps to NM_015059.2 L1354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr15:62949983 C>T maps to NM_015059.2 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr15:63011986 C>T maps to NM_015059.2 Q967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr15:63097860 G>A maps to NM_015059.2 T2180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr15:62989970 C>T maps to NM_015059.2 G459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:63047834 C>T maps to NM_015059.2 F1527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr15:63125821 A>G maps to NM_015059.2 Q2374Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr15:62993336 C>T maps to NM_015059.2 D540D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr4:38798179 C>T maps to NM_003263.3 W758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr4:38799294 T>C maps to NM_003263.3 E386E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:38799132 G>A maps to NM_003263.3 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr4:38800437 G>A maps to NM_003263.3 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr4:38777027 G>A maps to NM_030956.3 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr4:38775818 G>A maps to NM_030956.3 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr4:38774976 C>T maps to NM_030956.3 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:38774897 G>A maps to NM_030956.3 R772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:38776167 C>T maps to NM_030956.3 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr4:154626371 G>C maps to NM_003264.3 R771R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr4:154624817 G>A maps to NM_003264.3 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr4:154625606 G>A maps to NM_003264.3 K516K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:154626390 C>T maps to NM_003264.3 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr4:154626056 C>T maps to NM_003264.3 F666F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr4:154625967 A>C maps to NM_003264.3 R637R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:154626224 C>T maps to NM_003264.3 F722F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr4:154625663 C>T maps to NM_003264.3 F535F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:154625687 C>T maps to NM_003264.3 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:186997826 G>A maps to NM_003265.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:187005026 G>A maps to NM_003265.2 R729R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr4:187004843 C>T maps to NM_003265.2 I668I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr4:187004903 G>T maps to NM_003265.2 V688V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr4:187004729 C>T maps to NM_003265.2 F630F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:187004510 C>T maps to NM_003265.2 F557F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr4:187005260 C>T maps to NM_003265.2 I807I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:187004312 C>T maps to NM_003265.2 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr4:187003964 C>T maps to NM_003265.2 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr9:120476829 G>A maps to NM_138554.3 W808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr9:120476724 G>A maps to NM_138554.3 K773K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:120475003 C>T maps to NM_138554.3 Q200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:120476487 G>A maps to NM_138554.3 K694K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:120476799 G>A maps to NM_138554.3 E798E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr9:120475866 C>T maps to NM_138554.3 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:120475596 G>A maps to NM_138554.3 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr9:120476460 G>A maps to NM_138554.3 E685E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr9:120475239 G>A maps to NM_138554.3 E278E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:120470923 G>A maps to NM_138554.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:120475735 C>T maps to NM_138554.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr9:120474948 C>T maps to NM_138554.3 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr9:120475752 C>T maps to NM_138554.3 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr9:120476175 C>T maps to NM_138554.3 F590F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr9:120476809 C>T maps to NM_138554.3 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr9:120475866 C>T maps to NM_138554.3 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:120474837 C>T maps to NM_138554.3 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:120475395 C>T maps to NM_138554.3 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:120476040 C>T maps to NM_138554.3 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:120470977 C>T maps to NM_138554.3 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:120475866 C>T maps to NM_138554.3 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr9:120466776 G>A maps to NM_138554.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr1:223284363 A>G maps to NM_003268.5 C670C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:223284140 G>A maps to NM_003268.5 Q745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:223284969 G>A maps to NM_003268.5 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:223284111 G>A maps to NM_003268.5 I754I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:223285674 A>C maps to NM_003268.5 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:223285356 T>C maps to NM_003268.5 Q339Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:223285803 G>A maps to NM_003268.5 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:223285572 G>A maps to NM_003268.5 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr1:223286154 C>T maps to NM_003268.5 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:223285824 G>A maps to NM_003268.5 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr1:223285503 C>T maps to NM_003268.5 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:223283799 G>A maps to NM_003268.5 S858S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:223284894 G>A maps to NM_003268.5 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:223285896 G>A maps to NM_003268.5 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr4:38828712 C>T maps to NM_006068.3 V794V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr4:38829513 C>T maps to NM_006068.3 G527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr4:38828820 C>T maps to NM_006068.3 R758R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr4:38829057 G>A maps to NM_006068.3 V679V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr4:38830671 T>C maps to NM_006068.3 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:12905003 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr23:12904188 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:12905624 T>C did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:12906043 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:12904995 C>T did not map to a codon.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr23:12905614 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:12904971 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:12903931 C>G did not map to a codon.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr23:12906150 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:12904183 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:12904460 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:12904431 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr23:12904177 A>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:12906352 T>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr23:12905376 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:12906411 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr23:12905794 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:12906681 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:12905586 G>A did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:12906043 C>T did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:12906494 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:12937324 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:12939763 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr23:12939519 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:12937472 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:12939770 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr23:12939507 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:12939091 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:12938650 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:12939915 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:12939812 C>T did not map to a codon.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr23:12940064 A>T did not map to a codon.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr23:12937720 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr23:12939832 T>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:12939931 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr23:12939544 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:12938026 C>T did not map to a codon.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr23:12938040 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:52256779 G>A maps to ENST00000494383 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr3:52256089 G>A maps to ENST00000494383 L901L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr3:52255378 G>A maps to ENST00000494383 Q1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:102893962 G>A maps to NM_005521.3 K200K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:102849569 C>T maps to NM_001085398.1 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr5:170737322 G>A maps to NM_021025.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:170736467 C>T maps to NM_021025.2 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr8:38852863 G>A maps to NM_031940.3 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr8:38853912 G>A maps to NM_078473.2 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr15:102186925 A>G maps to ENST00000453041 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr3:149093294 T>C maps to ENST00000383054 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr3:149042779 G>A maps to NM_138786.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr3:149039265 C>T maps to NM_138786.3 *202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:149040219 G>A maps to NM_138786.3 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:149040163 C>T maps to NM_138786.3 W157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr3:196050868 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:196050786 G>A maps to NM_138461.2 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:196054332 G>A maps to NM_138461.2 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr2:228228544 T>C maps to NM_024795.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr2:228228517 C>T maps to NM_024795.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:149205419 G>A maps to NM_004617.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:4685922 C>T maps to NM_003963.2 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:4686322 G>A maps to NM_003963.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr17:4686322 G>A maps to NM_003963.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:83781588 C>T maps to NM_023003.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:83781638 C>T maps to NM_023003.3 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:83784672 C>T maps to NM_023003.3 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:19378880 T>G maps to NM_001001524.2 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:19381837 G>C maps to NM_001001524.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:19381049 G>A maps to NM_001001524.2 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:19379522 G>A maps to NM_001001524.2 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr11:64882835 C>T maps to NM_003273.2 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:64882810 G>A maps to NM_003273.2 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr12:27132717 C>T maps to NM_016551.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:27127113 A>G maps to NM_016551.2 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr12:27143380 A>C did not map to a codon.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr12:27148192 G>A maps to NM_016551.2 Q223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr8:105367187 C>T maps to NM_030788.2 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:105367187 C>T maps to NM_030788.2 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:105367280 C>T maps to NM_030788.2 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr8:105361685 C>T maps to NM_030788.2 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr8:105361670 C>T maps to NM_030788.2 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:105367187 C>T maps to NM_030788.2 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr8:105367304 C>G maps to NM_030788.2 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:105361649 G>A maps to NM_030788.2 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:105367391 G>A maps to NM_030788.2 R439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr8:105367172 C>T maps to NM_030788.2 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr8:105367116 C>T maps to NM_030788.2 Q348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:105361649 G>A maps to NM_030788.2 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:105368386 G>A maps to NM_030788.2 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr8:105361649 G>A maps to NM_030788.2 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:105367187 C>T maps to NM_030788.2 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr8:105361550 G>A maps to NM_030788.2 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:105361586 G>A maps to NM_030788.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr13:100207826 C>T maps to NM_004800.1 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr13:100207846 T>G maps to NM_004800.1 V566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr13:100211642 C>T maps to NM_004800.1 F593F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr13:100191741 C>T maps to NM_004800.1 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:98303925 G>A maps to NM_020123.3 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr20:30730861 C>T maps to NM_014742.3 Y202Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr20:30747793 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr20:30733134 C>T maps to NM_014742.3 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:30747904 G>T maps to NM_014742.3 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:30753237 G>A maps to NM_014742.3 K640K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr20:30747838 C>T maps to NM_014742.3 F538F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr20:30734615 C>T maps to NM_014742.3 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:30745676 C>T maps to NM_014742.3 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr12:50146758 C>T maps to NM_001098576.1 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr9:75387399 C>T maps to NM_138691.2 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr9:75369766 G>A maps to NM_138691.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr9:75445575 G>A maps to NM_138691.2 K746K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr9:75406914 T>A maps to NM_138691.2 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr9:75315532 G>A maps to NM_138691.2 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:75403344 C>T maps to NM_138691.2 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr20:2559847 G>A maps to NM_080751.2 W234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr20:2560641 G>A maps to NM_080751.2 W258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr20:2604919 G>A maps to NM_080751.2 G728G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr20:2591195 G>A maps to NM_080751.2 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr20:2604976 C>T maps to NM_080751.2 F747F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr20:2582802 C>T maps to NM_080751.2 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr20:2591072 C>T maps to NM_080751.2 I474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr20:2552824 G>A maps to NM_080751.2 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr20:2618211 C>T maps to NM_080751.2 A826A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:2573038 C>T maps to NM_080751.2 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:2592919 C>A maps to NM_080751.2 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr20:2604976 C>T maps to NM_080751.2 F747F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr20:2559847 G>A maps to NM_080751.2 W234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr20:2542548 C>T maps to NM_080751.2 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr20:2591081 C>T maps to NM_080751.2 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:2559841 C>T maps to NM_080751.2 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:2592878 C>T maps to NM_080751.2 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:2542536 G>A maps to NM_080751.2 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:2542542 C>T maps to NM_080751.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:2542543 C>T maps to NM_080751.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr20:2596820 G>A maps to NM_080751.2 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr20:2604976 C>T maps to NM_080751.2 F747F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr15:81636305 G>A maps to ENST00000454937 F533F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr15:81635618 C>T maps to ENST00000454937 W572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr15:81650575 G>A maps to ENST00000454937 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr15:81660593 C>T maps to ENST00000454937 E104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:81627095 C>T maps to ENST00000454937 G811G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:81636305 G>A maps to ENST00000454937 F533F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr15:81627284 C>T maps to ENST00000454937 K748K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:81625005 G>A maps to ENST00000454937 F1022F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:81644160 C>T maps to ENST00000454937 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr15:81633858 C>T maps to ENST00000454937 W572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr15:81627134 C>T maps to ENST00000454937 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr15:81633858 C>T maps to ENST00000454937 W572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr15:81650587 C>T maps to ENST00000454937 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:81648079 C>T maps to ENST00000454937 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:81654594 G>A maps to ENST00000454937 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:81654597 G>A maps to ENST00000454937 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr15:81637124 C>T maps to ENST00000454937 W500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr15:81666379 G>A maps to ENST00000454937 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr19:54666488 G>T maps to NM_001145303.1 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:54676764 C>T maps to NM_001145303.1 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:54673269 C>T maps to NM_001145303.1 W147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:54675775 A>G maps to NM_001145303.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:54675646 C>T maps to NM_001145303.1 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr16:19490829 C>T maps to NM_001105248.1 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr16:19451377 G>A maps to NM_001105248.1 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:19451431 C>T maps to NM_001105248.1 N24N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr16:19455459 C>T maps to NM_001105248.1 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:19471647 G>A maps to NM_001105248.1 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr16:19468036 C>T maps to NM_024780.4 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr16:19451449 G>A maps to NM_001105248.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:19475204 C>T maps to NM_001105248.1 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:19477444 C>T maps to NM_001105248.1 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr16:19471575 C>T maps to NM_001105248.1 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:19505675 G>A maps to NM_001105248.1 R973R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr16:19498600 C>T maps to NM_001105248.1 F842F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr16:19451377 G>A maps to NM_001105248.1 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr16:19452013 C>T maps to NM_001105248.1 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr16:19475336 C>T maps to NM_001105248.1 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:19452046 G>A maps to NM_001105248.1 E229E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:19505675 G>A maps to NM_001105248.1 R973R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:19460897 C>T maps to NM_001105248.1 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr16:19471641 G>A maps to NM_001105248.1 E378E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr16:19452004 C>T maps to NM_001105248.1 N215N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:19498639 C>T maps to NM_001105248.1 T855T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr16:19468183 G>A maps to NM_024780.4 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr16:19471575 C>T maps to NM_001105248.1 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:19485448 C>T maps to NM_001105248.1 F647F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:19490826 C>T maps to NM_001105248.1 S748S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:19498648 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:19490829 C>T maps to NM_001105248.1 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr16:19488760 G>A did not map to a codon.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr16:19485448 C>T maps to NM_001105248.1 F647F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr16:19485493 C>T maps to NM_001105248.1 F662F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr16:19460948 C>A maps to NM_001105248.1 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr16:19468121 C>T maps to NM_024780.4 Q32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:19475336 C>T maps to NM_001105248.1 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:19451866 C>T maps to NM_001105248.1 N169N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:19460864 G>A maps to NM_001105248.1 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:19483432 G>A maps to NM_001105248.1 Q602Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:19492694 C>T maps to NM_001105248.1 I757I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:19498516 C>T maps to NM_001105248.1 I814I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:19501773 C>T maps to NM_001105248.1 S877S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr16:19474631 G>A maps to NM_001105248.1 Q393Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr16:19488830 T>A maps to NM_001105248.1 S720S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr17:76120116 G>A maps to NM_007267.6 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:76117645 G>A maps to NM_007267.6 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:76115084 G>A maps to NM_007267.6 I618I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:76118721 G>A maps to NM_007267.6 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr16:19056265 C>T maps to NM_024847.3 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr16:19046996 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:19032951 G>A maps to NM_024847.3 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr16:19047030 G>A maps to NM_024847.3 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:19020602 G>A maps to NM_024847.3 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:19051669 G>A maps to NM_024847.3 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr16:19047022 C>T maps to NM_024847.3 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr16:19058494 G>A maps to NM_024847.3 W555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr16:19058498 C>T maps to NM_024847.3 I556I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:19033065 G>A maps to NM_024847.3 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr16:19034495 C>T maps to NM_024847.3 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr16:19032951 G>A maps to NM_024847.3 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr16:19051672 C>T maps to NM_024847.3 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:19073158 G>A maps to NM_024847.3 R722R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr16:19041652 C>T maps to NM_024847.3 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr16:19020500 C>T maps to NM_024847.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:19032966 G>A maps to NM_024847.3 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:19032966 G>A maps to NM_024847.3 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:76134512 C>T maps to NM_152468.4 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:76133841 C>T maps to NM_152468.4 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:76128476 C>T maps to NM_152468.4 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:129389267 G>A maps to NM_001017395.3 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:129389741 G>A maps to NM_001017395.3 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:129389207 G>A maps to NM_001017395.3 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:205238604 C>T maps to NM_014858.3 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:205210688 C>T maps to NM_014858.3 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:205241101 C>T maps to NM_014858.3 F660F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:205238337 C>T maps to NM_014858.3 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:94975609 C>T maps to NM_020698.2 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:94975783 G>A maps to NM_020698.2 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr12:94965245 G>A maps to NM_020698.2 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:94976050 G>A maps to NM_020698.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr12:94975963 G>A maps to NM_020698.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:165697265 G>A maps to NM_019026.3 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:40717076 C>T maps to NM_001008740.3 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:40713877 G>A maps to NM_001008740.3 W71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr1:40717247 G>A maps to NM_001008740.3 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr13:114193763 C>T maps to NM_017905.4 I544I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr13:114164665 C>T maps to NM_017905.4 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr13:114164615 C>T maps to NM_017905.4 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr13:114150192 C>T maps to NM_017905.4 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:114202623 C>T maps to NM_017905.4 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr1:20072025 G>A maps to NM_181719.4 Y292Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:20072115 G>A maps to NM_181719.4 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:20107097 G>A maps to NM_181719.4 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:20107098 G>A maps to NM_181719.4 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:20066334 G>A maps to NM_181719.4 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:20021022 G>A maps to NM_181719.4 F468F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr1:20107098 G>A maps to NM_181719.4 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:20107103 G>A maps to NM_181719.4 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr15:38233931 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr15:38243359 G>A maps to NM_152453.2 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr16:69056764 C>T maps to NM_024562.1 I959I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr16:68934431 G>A maps to NM_024562.1 Q491Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:68894225 C>T maps to NM_024562.1 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:68961553 C>T maps to NM_024562.1 I737I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr16:68894291 G>A maps to NM_024562.1 K200K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:68893949 C>T maps to NM_024562.1 N86N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr19:10943868 C>T maps to NM_006858.2 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr19:10943697 G>A maps to NM_006858.2 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:124081260 C>T maps to NM_006815.3 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr15:79614516 C>T maps to NM_007364.2 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr15:79614546 C>T maps to NM_007364.2 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr7:44619143 G>A maps to NM_182547.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:69385548 G>A maps to NM_144676.3 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr14:77812697 G>A maps to NM_213601.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MO-06A-11D-A21A-08 chr14:77809737 G>A maps to NM_213601.1 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr14:77808176 G>A maps to NM_213601.1 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:177020754 C>T maps to NM_017510.4 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr2:192863846 G>A maps to NM_016192.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr2:193056683 G>A maps to NM_016192.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:193059172 G>A maps to NM_016192.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:53798338 G>A maps to NM_001099640.1 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:53798371 C>T maps to NM_001099640.1 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:53798338 G>A maps to NM_001099640.1 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:53798110 C>T maps to NM_001099640.1 W107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr17:53798371 C>T maps to NM_001099640.1 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:42089456 G>A maps to NM_032376.2 Q205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:42090520 G>A maps to NM_032376.2 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr17:7339603 G>A maps to NM_178518.2 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:72832249 G>A maps to NM_017728.3 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr17:72815923 C>T maps to NM_017728.3 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:72832414 C>T maps to NM_017728.3 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:72832573 C>T maps to NM_017728.3 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr17:72832477 G>A maps to NM_017728.3 K381K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr17:72815908 C>T maps to NM_017728.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr17:72832786 C>T maps to NM_017728.3 F484F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:79287741 G>A maps to NM_178520.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:79288206 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr17:79287762 C>T maps to NM_178520.3 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr17:41365227 C>T maps to NM_145041.1 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:41365859 G>A maps to NM_145041.1 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr7:12269309 A>T maps to NM_018374.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:48359876 C>T maps to NM_001143842.1 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:48359716 C>T maps to NM_001143842.1 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr12:48361032 G>A maps to NM_001143842.1 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr3:133098854 C>A maps to NM_001136469.1 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:133099319 G>A maps to NM_001136469.1 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:133114706 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:133098600 C>T maps to NM_001136469.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr3:133114781 C>T maps to NM_001136469.1 F560F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:133098764 C>T maps to NM_001136469.1 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:133099442 G>A maps to NM_001136469.1 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:133099973 C>T maps to NM_001136469.1 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr3:133099841 C>T maps to NM_001136469.1 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr11:60687339 C>T maps to NM_024092.2 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:60689405 C>T maps to NM_024092.2 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:60689297 C>T maps to NM_024092.2 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr17:21102044 G>T maps to NM_003876.2 Y57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:52876859 C>T maps to ENST00000504329 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:52883817 G>A maps to ENST00000504329 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:52878871 G>A maps to ENST00000504329 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:50395885 T>C maps to NM_007024.4 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr12:44770457 T>C maps to NM_032256.1 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:44238709 C>T maps to NM_032256.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr12:108986009 G>A maps to NM_181724.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr12:108985649 C>T maps to NM_181724.2 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:108985565 C>T maps to NM_181724.2 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:108985775 G>A maps to NM_181724.2 Y128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr12:108985910 G>A maps to NM_181724.2 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr12:108985889 G>A maps to NM_181724.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:108985508 C>T maps to NM_181724.2 Q217Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:122213561 C>T maps to NM_001080825.2 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr12:122209432 C>T maps to NM_001080825.2 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:122181599 T>C maps to NM_001080825.2 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr1:43739004 T>C maps to NM_144626.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:43738873 T>C maps to NM_144626.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:96920667 G>A maps to NM_017849.3 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr4:4239571 G>A maps to ENST00000382753 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr7:98452870 G>A maps to NM_001134450.1 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr7:98453757 G>T maps to NM_001134450.1 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:98457845 G>A maps to NM_001134450.1 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr7:98457809 G>A maps to NM_001134450.1 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:98452870 G>A maps to NM_001134450.1 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:98457809 G>A maps to NM_001134450.1 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:98449089 G>A maps to NM_001134450.1 I320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:98457956 G>A maps to NM_001134450.1 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:98453742 G>C maps to NM_001134450.1 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr7:98449068 G>A maps to NM_001134450.1 Y327Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:98460835 G>A maps to NM_001134450.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:98452870 G>A maps to NM_001134450.1 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr7:98446274 G>A maps to NM_001134450.1 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr2:98373813 G>A maps to NM_015348.1 S1800S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:98408896 G>A maps to NM_015348.1 L1366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:98453575 G>A maps to NM_015348.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr2:98453575 G>A maps to NM_015348.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:98409002 G>A maps to NM_015348.1 S1330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:98392350 G>A maps to NM_015348.1 T1425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr2:98409919 C>T maps to NM_015348.1 P1161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:98453598 C>A maps to NM_015348.1 G249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:98453599 A>G maps to NM_015348.1 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:98421633 C>T maps to NM_015348.1 Q773Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:60699182 C>T maps to NM_017870.3 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr11:60699181 C>T maps to NM_017870.3 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:60702139 C>T maps to NM_017870.3 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr11:60702199 C>T maps to NM_017870.3 V601V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr11:60702136 C>T maps to NM_017870.3 H580H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:60701051 G>A maps to NM_017870.3 K466K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr11:60702776 G>A maps to NM_017870.3 T631T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr11:60702229 C>T maps to NM_017870.3 S611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr11:60704033 G>A maps to NM_017870.3 L910L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:60702166 C>T maps to NM_017870.3 D590D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:60704360 G>A maps to NM_017870.3 R1019R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:60701033 C>T maps to NM_017870.3 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:60696267 G>A maps to NM_017870.3 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr11:60698101 C>T maps to NM_017870.3 H329H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:60702235 G>A maps to NM_017870.3 E613E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:60696258 C>T maps to NM_017870.3 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr11:60703349 C>T maps to NM_017870.3 S682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:60694697 G>A maps to NM_017870.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:60703793 G>A maps to NM_017870.3 E830E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr12:125834238 C>T maps to NM_052907.2 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr12:126068458 C>T maps to NM_052907.2 V447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr12:126138586 G>A maps to NM_052907.2 G856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:126138589 G>A maps to NM_052907.2 K857K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr12:126128722 C>T maps to NM_052907.2 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:126138865 G>A maps to NM_052907.2 G949G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:126139081 G>A maps to NM_052907.2 R1021R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:126004122 G>A maps to NM_052907.2 E410E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:126004128 C>T maps to NM_052907.2 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:126138961 G>A maps to NM_052907.2 R981R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:125900130 C>T maps to NM_052907.2 D333D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:126128659 G>A maps to NM_052907.2 K487K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:126137132 C>T maps to NM_052907.2 I682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr12:125834403 G>A maps to NM_052907.2 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:126135360 C>T maps to NM_052907.2 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:125834400 T>G maps to NM_052907.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:126137105 G>A maps to NM_052907.2 Q673Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:126139204 G>A maps to NM_052907.2 G1062G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:125834328 C>T maps to NM_052907.2 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:126138646 G>A maps to NM_052907.2 G876G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:125834715 G>A maps to NM_052907.2 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:125834658 G>A maps to NM_052907.2 W238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:126137024 G>A maps to NM_052907.2 K646K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:125834064 G>A maps to NM_052907.2 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:126137057 C>T maps to NM_052907.2 I657I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:126139150 C>T maps to NM_052907.2 I1044I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr12:125834808 G>A maps to NM_052907.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr12:126004086 G>A maps to NM_052907.2 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr12:126138637 C>A maps to NM_052907.2 P873P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr12:125834064 G>A maps to NM_052907.2 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr12:126135438 C>T maps to NM_052907.2 I613I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr12:126138586 G>A maps to NM_052907.2 G856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:126128650 G>A maps to NM_052907.2 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:125834709 C>T maps to NM_052907.2 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:125834316 C>T maps to NM_052907.2 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:125834478 G>A maps to NM_052907.2 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:126137027 G>A maps to NM_052907.2 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:126137037 C>T maps to NM_052907.2 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:126138292 G>A maps to NM_052907.2 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:126138577 C>T maps to NM_052907.2 P853P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:126068434 G>A maps to NM_052907.2 K439K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr12:126128722 C>T maps to NM_052907.2 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr12:129558631 G>A maps to NM_133448.2 Q1030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr12:130185046 G>A maps to NM_133448.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:130015638 G>A maps to NM_133448.2 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr12:130184677 G>A maps to NM_133448.2 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr12:129558902 C>T maps to NM_133448.2 V939V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:129558524 G>A maps to NM_133448.2 I1065I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:129694172 C>T maps to NM_133448.2 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr12:130184902 C>T maps to NM_133448.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr12:129559454 G>A maps to NM_133448.2 I755I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr12:129558863 G>A maps to NM_133448.2 F952F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:129559535 C>T maps to NM_133448.2 G728G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:129822328 G>A maps to NM_133448.2 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:129822268 G>A maps to NM_133448.2 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:130184761 C>T maps to NM_133448.2 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr12:129694133 C>T maps to NM_133448.2 E458E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:129558593 C>T maps to NM_133448.2 R1042R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:129822268 G>A maps to NM_133448.2 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:129822268 G>A maps to NM_133448.2 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:129558470 C>G maps to NM_133448.2 G1083G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr12:130184599 C>T maps to NM_133448.2 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:130015695 G>A maps to NM_133448.2 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:129563267 G>A maps to NM_133448.2 I642I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:129822250 G>A maps to NM_133448.2 I409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:130185019 G>A maps to NM_133448.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr17:32953332 G>A maps to NM_207313.1 K85K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr17:32963171 C>T maps to NM_207313.1 I618I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr17:32964422 G>A maps to NM_207313.1 K709K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr17:32954074 A>C maps to NM_207313.1 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:32964614 C>T maps to NM_207313.1 V773V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:32956108 G>A maps to NM_207313.1 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr17:32959913 C>T maps to NM_207313.1 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:100863137 C>T maps to NM_032021.2 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr11:67235030 G>A maps to NM_025124.2 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:87029189 C>T maps to NM_022918.3 F363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:142983262 G>A maps to NM_153345.1 Q71Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:142983717 C>T maps to NM_153345.1 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr19:48845900 G>A maps to NM_018273.2 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:48863343 G>A maps to NM_018273.2 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:159158715 A>C maps to NM_018342.4 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:159161563 C>T maps to NM_018342.4 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr4:159162694 C>T maps to NM_018342.4 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr4:159136445 G>A maps to NM_018342.4 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr4:159162703 G>A maps to NM_018342.4 W282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr4:159133875 C>T maps to NM_018342.4 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr4:159154115 T>C maps to NM_018342.4 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:42818673 G>A maps to ENST00000406159 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr19:42818468 C>T maps to ENST00000406159 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr19:42819391 C>T maps to ENST00000406159 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:5739353 T>G maps to NM_152784.3 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr19:5757876 C>T maps to NM_152784.3 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:5748225 C>T maps to NM_152784.3 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:5763294 C>T maps to NM_152784.3 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:5766154 C>T maps to NM_152784.3 I516I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr19:5778626 G>A maps to NM_152784.3 R779R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr19:5751794 G>A maps to NM_152784.3 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:5778503 G>A maps to NM_152784.3 W738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:5746028 C>T maps to NM_152784.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:5757924 G>A maps to NM_152784.3 G450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:5759095 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:36038231 C>T maps to NM_032635.2 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr19:36230276 G>A maps to NM_024660.2 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr6:52546632 T>A maps to NM_014051.3 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr6:52541911 C>T maps to NM_014051.3 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:10751399 C>T maps to NM_030969.3 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:152058519 C>T maps to NM_001123228.1 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr3:152058687 C>T maps to NM_001123228.1 Q2Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr19:55828328 C>T maps to NM_001085488.1 K110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:55832371 G>A maps to NM_001085488.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:55828196 G>A maps to NM_001085488.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:55824349 G>A maps to NM_001085488.1 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:55832398 C>T maps to NM_001085488.1 W2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:83417286 C>T maps to NM_001080506.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr11:66062586 C>T maps to NM_153266.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr4:153573855 G>A maps to NM_152680.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:38995415 G>A maps to NM_024943.1 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:38995403 C>T maps to NM_024943.1 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:39000347 G>A maps to NM_024943.1 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:38995436 C>T maps to NM_024943.1 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:39000464 G>A maps to NM_024943.1 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:21172580 C>T maps to ENST00000451578 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:21181904 C>T maps to ENST00000451578 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:47549938 G>A maps to NM_017854.1 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:19243162 G>A maps to NM_017814.1 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19231956 G>A maps to NM_017814.1 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:19231574 C>A maps to NM_017814.1 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:87498843 G>A maps to NM_153354.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:87516401 G>A maps to NM_153354.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr2:135260540 G>A maps to NM_030923.4 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:135470806 G>A maps to NM_030923.4 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:135470836 C>T maps to NM_030923.4 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:135260555 G>A maps to NM_030923.4 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr23:109247306 C>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:109416617 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:109414664 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:109414665 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:112423806 C>T maps to NM_022484.4 Q358Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr7:112424595 G>A maps to NM_022484.4 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:112407698 T>G maps to NM_022484.4 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr2:216965154 C>T maps to NM_138390.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:62728451 C>T maps to NM_198276.2 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:72424223 G>C maps to NM_173490.6 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:138861081 G>A maps to NM_198282.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:138860758 G>A maps to NM_198282.2 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:72469264 C>T maps to NM_153217.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr5:72469696 G>A maps to ENST00000433849 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:72469288 C>T maps to NM_153217.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr4:941905 C>T maps to NM_032326.2 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr4:951686 C>T maps to NM_032326.2 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr4:941544 C>T maps to NM_032326.2 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr7:150499313 C>T maps to NM_018487.2 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:150499313 C>T maps to NM_018487.2 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:150500715 G>A maps to NM_018487.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:150499310 G>A maps to NM_018487.2 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr7:150499310 G>A maps to NM_018487.2 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr7:150499313 C>T maps to NM_018487.2 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr7:150501478 C>T maps to NM_018487.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr7:150498775 G>A maps to NM_018487.2 Q46Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150498667 C>T maps to NM_018487.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150499313 C>T maps to NM_018487.2 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:150493504 C>T maps to NM_014020.3 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:150491072 G>A maps to NM_014020.3 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:150488648 C>T maps to NM_014020.3 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:150489175 G>A maps to NM_014020.3 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:150488693 C>T maps to NM_014020.3 E246E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr7:150490295 G>A maps to NM_014020.3 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr7:150490295 G>A maps to NM_014020.3 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:150490223 C>T maps to NM_014020.3 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150489233 G>A maps to NM_014020.3 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:150490214 C>T maps to NM_014020.3 W187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr7:150488623 G>A maps to NM_014020.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr2:120438599 C>T maps to NM_030577.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:120438539 C>T maps to NM_030577.2 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:120438713 C>T maps to NM_030577.2 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr2:39931245 C>T maps to NM_152390.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:105063331 G>A maps to NM_207379.1 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr11:62556589 C>T maps to NM_199337.2 Y64Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr2:669633 C>A maps to NM_152834.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr2:677330 G>A maps to NM_152834.2 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr10:104231131 C>T maps to NM_024789.3 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:104232642 C>T maps to NM_024789.3 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:104230439 C>T maps to NM_024789.3 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:104230739 C>T maps to NM_024789.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr6:158957846 C>T maps to NM_020823.1 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:103378690 C>T maps to NM_144632.3 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:103414376 C>T maps to NM_144632.3 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:103431342 C>T maps to NM_144632.3 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:103414343 C>T maps to NM_144632.3 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:103431348 C>T maps to NM_144632.3 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:103378690 C>T maps to NM_144632.3 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:202987673 C>T maps to NM_001079809.1 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:202991990 C>T maps to NM_001079809.1 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr7:1586592 G>A maps to NM_001097620.1 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:1586623 C>T maps to NM_001097620.1 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:1595054 C>T maps to NM_001097620.1 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:1595099 G>A maps to NM_001097620.1 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr7:1586602 G>A maps to NM_001097620.1 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:1587387 C>T maps to NM_001097620.1 E334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr7:1594937 G>A maps to NM_001097620.1 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr22:38620790 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr22:38621497 G>A maps to NM_012264.4 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:38641965 G>A maps to NM_012264.4 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr22:38617541 G>A maps to NM_012264.4 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr22:38642013 G>A maps to NM_012264.4 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr22:38622799 C>T maps to NM_012264.4 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr23:148690450 T>C did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr16:8890249 G>A maps to NM_015421.3 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:153247740 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:153248285 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:48746164 G>A maps to NM_199203.2 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:48746164 G>A maps to NM_199203.2 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:48760117 G>A maps to NM_199203.2 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr20:48700665 C>T maps to NM_199203.2 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:72083431 C>T maps to NM_018279.3 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:72092797 C>T maps to NM_018279.3 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr12:72090353 G>A did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:55889381 C>T maps to NM_139172.1 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:55888982 C>T maps to NM_139172.1 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr4:166021900 G>A maps to NM_001100389.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:57458522 C>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:57453715 C>T maps to NM_001130963.1 E427E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:15470630 C>T maps to NM_001004320.1 W171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:15240948 A>G maps to NM_001004320.1 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr7:15584535 C>T maps to NM_001004320.1 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:19765244 G>A maps to NM_152774.3 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:19765250 G>A maps to NM_152774.3 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr7:19765298 G>A maps to NM_152774.3 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:19765280 A>C maps to NM_152774.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:220409513 G>A maps to NM_001005209.1 W22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:220412288 C>T maps to NM_001005209.1 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:220412342 G>A maps to NM_001005209.1 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:220412675 C>T maps to NM_001005209.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:26687821 C>T maps to ENST00000457710 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:26687782 C>T maps to ENST00000457710 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:26687797 C>T maps to ENST00000457710 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr9:74332990 G>A maps to NM_013390.2 R758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:74359986 G>A maps to NM_013390.2 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr9:74324375 G>A maps to NM_013390.2 V928V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:74319524 G>A maps to NM_013390.2 L1060L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr9:74312987 T>C maps to NM_013390.2 A1170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr9:74365181 A>G maps to NM_013390.2 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr9:74360013 G>A maps to NM_013390.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr9:74300160 G>A maps to NM_013390.2 V1368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr9:74337424 A>G maps to NM_013390.2 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr9:74332990 G>A maps to NM_013390.2 R758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:95660748 C>T maps to NM_001134658.1 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:95660811 C>T maps to NM_001134658.1 H221H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr6:130762227 C>T maps to NM_052913.2 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr6:130761677 G>A maps to NM_052913.2 K37K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:130762175 G>A maps to NM_052913.2 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr6:130762526 G>A maps to NM_052913.2 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:130762622 G>A maps to NM_052913.2 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr6:130761674 G>A maps to NM_052913.2 E36E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:130762607 G>A maps to NM_052913.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:130762385 G>A maps to NM_052913.2 K273K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:130762727 C>T maps to NM_052913.2 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:130762526 G>A maps to NM_052913.2 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:130762526 G>A maps to NM_052913.2 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:130762616 C>T maps to NM_052913.2 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr6:130762049 G>A maps to NM_052913.2 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:130762526 G>A maps to NM_052913.2 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr6:130761986 C>T maps to NM_052913.2 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr6:130761743 C>T maps to NM_052913.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr6:130761980 C>T maps to NM_052913.2 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:130762526 G>A maps to NM_052913.2 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr6:130763036 G>A maps to NM_052913.2 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:130761986 C>T maps to NM_052913.2 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr18:5891768 G>A maps to NM_001080209.1 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A197-06A-32D-A197-08 chr18:5891621 C>T maps to NM_001080209.1 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:5891894 G>A maps to NM_001080209.1 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:9661185 C>T maps to NM_001130924.2 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr1:9656999 C>T maps to NM_001130924.2 D106D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:9661296 C>T maps to NM_001130924.2 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr15:72690726 G>A maps to NM_001080462.1 K20K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr15:72691127 C>T maps to NM_001080462.1 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr15:72690729 G>A maps to NM_001080462.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr15:72699072 C>T maps to NM_001080462.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr15:72700032 G>A maps to NM_001080462.1 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr15:72691187 C>T maps to NM_001080462.1 Y92Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr15:72690747 G>A maps to NM_001080462.1 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:140099731 G>A maps to NM_053045.1 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:11453736 G>A maps to NM_198536.2 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:11456053 G>A maps to NM_198536.2 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr1:212538574 T>C maps to NM_001198862.1 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:190158105 C>A maps to NM_207316.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:190167525 G>A maps to NM_207316.1 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:190147431 G>A maps to NM_207316.1 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:190158178 C>T did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr3:190147384 C>T maps to NM_207316.1 *147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr16:67262720 A>G maps to NM_014187.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr7:129841881 G>A maps to NM_032842.3 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:129832561 G>A maps to NM_032842.3 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:25331386 C>T maps to ENST00000423535 W172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr22:25334155 C>T maps to ENST00000423535 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr22:25331524 G>A maps to ENST00000423535 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr22:25334155 C>T maps to ENST00000423535 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:138487708 C>T maps to ENST00000422794 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr7:138487771 G>A maps to ENST00000422794 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:138487708 C>T maps to ENST00000422794 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:27258869 C>T maps to NM_017727.4 Q224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:27258878 C>T maps to NM_017727.4 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:27263325 C>T maps to NM_017727.4 A635A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:27263280 C>T maps to NM_017727.4 F620F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:27262684 C>T maps to NM_017727.4 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:27257113 C>T maps to NM_017727.4 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr2:27262999 C>T maps to NM_017727.4 F575F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:27263259 G>A maps to NM_017727.4 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:27263260 A>C maps to NM_017727.4 R614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:37186743 G>A maps to NM_145316.3 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:37186563 G>A maps to NM_145316.3 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr6:37186389 G>A maps to NM_145316.3 H139H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:124967576 G>A maps to NM_001080546.1 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:124967603 G>A maps to NM_001080546.1 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:136573916 C>T maps to NM_025246.2 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr3:136573808 C>T maps to NM_025246.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:136573346 G>A maps to NM_025246.2 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:136573670 G>A maps to NM_025246.2 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:27660754 C>T maps to NM_032125.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr1:27661923 C>T maps to NM_032125.2 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr11:123753895 C>T maps to NM_001013743.1 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:123753895 C>T maps to NM_001013743.1 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:123755323 C>T maps to NM_001013743.1 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:123755221 G>A maps to NM_001013743.1 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:123753854 C>T maps to NM_001013743.1 W223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:123754797 G>A maps to NM_001013743.1 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:123755272 C>T maps to NM_001013743.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:123753849 G>A maps to NM_001013743.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr11:123754836 C>T maps to NM_001013743.1 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr11:123755221 G>A maps to NM_001013743.1 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:67940538 C>T maps to NM_182526.2 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:67940337 G>A maps to NM_182526.2 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr14:67940433 G>A maps to NM_182526.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr10:63170421 C>T maps to NM_178505.6 W255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr10:63170283 G>A maps to NM_178505.6 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:63188865 C>T maps to NM_178505.6 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr10:63188831 G>A maps to NM_178505.6 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr10:63170313 C>T maps to NM_178505.6 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:63188715 G>A maps to NM_178505.6 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:63173293 C>T did not map to a codon.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr10:63188781 G>A maps to NM_178505.6 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:15663085 A>C did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:15646195 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:15677153 T>C did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:15646126 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:15646185 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:15657811 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr6:75965892 G>A maps to NM_018247.3 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:75994288 G>A maps to NM_018247.3 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:41951390 C>T maps to NM_018126.2 N201N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:100349696 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:100349719 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:100349861 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:100349735 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:100349859 C>T did not map to a codon.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr23:100349605 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:100349771 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:120194595 C>T maps to NM_183240.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr2:120194856 C>T maps to NM_183240.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:120194826 C>T maps to NM_183240.2 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:120194502 C>T maps to NM_183240.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:120194568 G>T maps to NM_183240.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:120194766 C>T maps to NM_183240.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:120194766 C>T maps to NM_183240.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:120194517 C>T maps to NM_183240.2 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr19:16791363 C>T maps to NM_024074.1 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:16791315 C>T maps to NM_024074.1 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:16793316 T>A maps to NM_024074.1 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:16799019 C>T maps to NM_024074.1 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:16799064 C>T maps to NM_024074.1 N261N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr19:16799181 G>C maps to NM_024074.1 *300Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr19:16791327 C>T maps to NM_024074.1 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr9:108536264 A>G maps to NM_018112.1 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr9:108457006 C>T maps to NM_018112.1 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:119165875 G>A maps to NM_018266.1 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:32560426 C>T maps to NM_018056.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr1:32560458 C>T maps to NM_018056.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:12791286 T>C maps to ENST00000431022 Q17Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:12779253 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr3:12785411 C>T maps to ENST00000431022 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:9305014 G>A maps to NM_015012.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:9308056 G>A maps to NM_015012.2 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr3:44906593 C>T maps to NM_144638.1 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr3:14176300 C>T maps to NM_024334.2 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr3:14174405 C>T maps to NM_024334.2 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:14175298 C>T maps to NM_024334.2 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:194344018 G>A maps to NM_001166305.1 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:100277321 C>T maps to ENST00000403410 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:100277279 G>A maps to ENST00000403410 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr11:129722547 C>T maps to NM_138788.3 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr11:129725642 G>A maps to NM_138788.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:34648487 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:54269673 G>A maps to NM_018087.4 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:54284680 G>A maps to NM_018087.4 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:54258907 G>A maps to NM_018087.4 F543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:54258907 G>A maps to NM_018087.4 F543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:54272139 G>A maps to NM_018087.4 C314C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr12:64174928 A>T maps to NM_014254.1 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:64202715 C>T maps to NM_014254.1 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr12:64202700 G>A maps to NM_014254.1 K387K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:64173856 C>T maps to NM_014254.1 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:25669525 C>T maps to NM_014313.2 Y56Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:25679391 C>T maps to NM_014313.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:25669549 C>T maps to NM_014313.2 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:25669549 C>A maps to NM_014313.2 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:25679391 C>T maps to NM_014313.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:15545932 G>T maps to NM_018022.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr1:1849326 G>A maps to NM_178545.3 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr1:1849692 G>A maps to NM_178545.3 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr1:45120413 C>T maps to NM_024587.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:33360930 C>T maps to NM_033504.2 W190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:33366824 G>A maps to NM_033504.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr8:92032398 G>A maps to NM_018710.2 C116C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr8:92052893 G>A maps to NM_018710.2 Y28Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr1:95616879 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:95657411 A>G maps to NM_152487.2 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr1:95616887 C>T maps to NM_152487.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:95639397 G>A maps to NM_152487.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:25773354 C>T maps to NM_018202.4 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:25817908 G>A maps to NM_018202.4 R542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:25812148 C>T maps to NM_018202.4 I453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:25824872 C>T maps to NM_018202.4 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:25824875 C>T maps to NM_018202.4 P638P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:25784984 C>T maps to NM_018202.4 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:25812148 C>T maps to NM_018202.4 I453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:25824818 C>T maps to NM_018202.4 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:25784984 C>T maps to NM_018202.4 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:25784985 C>T maps to NM_018202.4 R253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:18726819 C>T maps to NM_012109.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:18729299 C>T maps to NM_012109.2 Q300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:18726819 C>T maps to NM_012109.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr19:18729194 C>T maps to NM_012109.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr19:18729232 C>T maps to NM_012109.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:18731331 C>T maps to NM_012109.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:18724758 C>T maps to NM_012109.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr15:43446959 C>T maps to NM_024956.3 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:226055586 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr1:226050547 G>A maps to NM_014698.2 D250D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:226050211 G>A maps to NM_014698.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr6:44120421 C>T maps to NM_018426.1 I643I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr6:44121497 C>T maps to NM_018426.1 I676I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr6:44121813 C>T maps to NM_018426.1 F705F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:44102476 C>T maps to NM_018426.1 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr6:44114649 C>T maps to NM_018426.1 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:44102467 C>T maps to NM_018426.1 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:44121906 C>A maps to NM_018426.1 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:44102467 C>T maps to NM_018426.1 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:44114595 C>T maps to NM_018426.1 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:44120385 C>T maps to NM_018426.1 F631F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:77702966 G>A maps to NM_020431.2 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:77723027 C>T maps to NM_020431.2 Q794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:77715664 G>A maps to NM_020431.2 T634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:77685306 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:77710774 C>T maps to NM_020431.2 A475A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:77710754 C>T maps to NM_020431.2 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr14:77703062 G>A maps to NM_020431.2 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr14:77705056 C>T maps to NM_020431.2 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr14:77709290 C>T maps to NM_020431.2 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr14:77718138 C>T maps to NM_020431.2 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr14:77710795 C>T maps to NM_020431.2 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr14:77723021 C>T maps to NM_020431.2 Q792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr14:77685233 G>A maps to NM_020431.2 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr14:77709245 G>A maps to NM_020431.2 W396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr14:77706029 C>T maps to NM_020431.2 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr14:77702976 C>T maps to NM_020431.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:77719700 C>T maps to NM_020431.2 S734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr8:29923606 G>T maps to NM_016127.4 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr8:29931524 G>A maps to NM_016127.4 D50D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr8:94809638 C>T maps to NM_153704.5 Q681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr8:94828613 C>T maps to NM_153704.5 I974I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr8:94827548 C>T maps to NM_153704.5 F927F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:94767231 C>T maps to NM_153704.5 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr8:94792927 C>T maps to NM_153704.5 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:94828613 C>T maps to NM_153704.5 I974I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr8:94809557 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:94793188 C>T maps to NM_153704.5 F319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:94822080 C>T maps to NM_153704.5 F910F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:94815879 C>T maps to NM_153704.5 R764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:56668904 C>A maps to ENST00000434581 G131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr8:133740182 C>T maps to ENST00000395406 K179K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:133734322 G>A maps to ENST00000395406 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr8:133769526 C>T maps to ENST00000395406 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:45430455 C>T maps to NM_001123376.1 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:45430326 G>A maps to NM_001123376.1 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:109796760 G>A maps to NM_153015.1 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:109796958 C>T maps to NM_153015.1 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr8:109796862 C>T maps to NM_153015.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr8:109797192 C>T maps to NM_153015.1 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:109796736 G>A maps to NM_153015.1 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr8:109796454 C>T maps to NM_153015.1 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr8:109797303 C>T maps to NM_153015.1 K8K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:156261253 G>T maps to NM_032323.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:700155 C>T maps to ENST00000449452 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:205053199 G>A maps to NM_203376.1 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:205053190 G>A maps to NM_203376.1 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr1:16073476 C>T maps to NM_001013641.1 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr15:34520783 C>T maps to NM_016454.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr15:42523437 G>A maps to ENST00000389834 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:112863615 C>A maps to NM_032824.2 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:112854727 G>C maps to NM_032824.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr17:7758980 G>A maps to NM_203411.1 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr17:7758454 C>T maps to NM_203411.1 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr3:48658388 G>A maps to NM_001008269.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr3:48658388 G>A maps to NM_001008269.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:48659054 C>A maps to NM_001008269.1 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr16:426577 C>T maps to NM_021259.2 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:426149 G>A maps to NM_021259.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:426583 G>A maps to NM_021259.2 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:427074 G>A maps to NM_021259.2 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:426754 G>A maps to NM_021259.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:35853797 C>T maps to NM_001042590.1 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:35847036 G>A maps to ENST00000360192 W653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:35853226 C>T maps to NM_001042590.1 F352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr9:35853226 C>T maps to NM_001042590.1 F352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:136389849 G>A maps to NM_001080483.2 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr9:136389885 C>T maps to NM_001080483.2 K27K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr9:136384007 G>A maps to NM_001080483.2 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr9:136385350 G>A maps to NM_001080483.2 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr9:136385349 G>A maps to NM_001080483.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:201104907 G>A maps to ENST00000421960 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr1:201113055 G>A maps to ENST00000421960 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:201115879 G>A maps to ENST00000421960 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr14:74876282 C>T maps to NM_001105579.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr14:74876342 C>T maps to NM_001105579.1 Q35Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr14:74874252 C>T maps to NM_001105579.1 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr14:74876108 C>T maps to NM_001105579.1 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:74874330 G>A maps to NM_001105579.1 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr14:74876441 C>T maps to NM_001105579.1 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:74874366 G>A maps to NM_001105579.1 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZY-06A-11D-A197-08 chr14:74874581 C>A maps to NM_001105579.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr14:74876060 C>T maps to NM_001105579.1 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:74874254 G>A maps to NM_001105579.1 Q234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:74876270 G>A maps to NM_001105579.1 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr20:24523949 C>T maps to NM_024893.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr20:24524125 G>A maps to NM_024893.1 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:24524173 C>T maps to NM_024893.1 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr20:24524131 C>T maps to NM_024893.1 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:24565547 G>A maps to NM_024893.1 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr20:24646001 G>A maps to NM_024893.1 K213K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr20:24524083 G>A maps to NM_024893.1 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:24565604 C>T maps to NM_024893.1 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:24523780 C>T maps to NM_024893.1 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:24524131 C>T maps to NM_024893.1 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr17:48356326 C>T maps to NM_153229.2 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr17:7258681 C>T maps to NM_198154.1 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr17:7259217 C>T maps to NM_198154.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:31261320 C>T maps to NM_015544.2 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr3:69088084 G>A maps to NM_007114.2 Q635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:69079078 C>T maps to NM_007114.2 Q827Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr3:46750655 G>A maps to NM_147196.2 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:46751176 G>A maps to NM_147196.2 *157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr19:4298301 G>A maps to NM_144615.2 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:4294603 G>A maps to NM_144615.2 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:4292703 G>A maps to NM_144615.2 C247C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:4292751 G>A maps to NM_144615.2 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:4294677 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr19:4294775 G>A maps to NM_144615.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:4298253 C>T maps to NM_144615.2 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:4292616 G>A maps to NM_144615.2 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:4292805 C>T maps to NM_144615.2 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:154736691 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:154774866 G>T did not map to a codon.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr9:100361934 G>T maps to NM_003275.3 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:100286523 C>T maps to NM_003275.3 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr15:52065921 C>T maps to NM_014548.3 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr15:52192438 C>T maps to NM_014547.4 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:98941582 C>T maps to NM_001032283.2 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:98928047 T>G maps to NM_003276.2 T671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:33135663 G>A maps to NM_001039770.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr3:33135201 G>A maps to NM_001039770.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr3:33135662 G>A maps to NM_001039770.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr4:68795739 C>T maps to NM_182606.3 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr4:68810233 C>T maps to NM_182606.3 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:68812210 C>T maps to NM_182606.3 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr4:68797745 C>T maps to NM_182606.3 K98K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:68810290 G>A maps to NM_182606.3 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:68795676 C>T maps to NM_182606.3 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr4:69095233 C>T maps to NM_182502.3 K229K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr4:69095233 C>T maps to NM_182502.3 K229K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:69097033 G>A maps to NM_182502.3 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr4:69100212 C>T maps to NM_182502.3 W146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr4:69093745 G>A maps to NM_182502.3 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:69097033 G>A maps to NM_182502.3 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr4:69101730 G>A maps to NM_182502.3 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr4:69094495 A>T maps to NM_182502.3 C351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:69101868 C>T maps to NM_182502.3 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:69093742 C>T maps to NM_182502.3 W379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr4:69095233 C>T maps to NM_182502.3 K229K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr4:69093697 C>T maps to NM_182502.3 K394K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:69101867 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:69095233 C>T maps to NM_182502.3 K229K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:69107479 C>T maps to NM_182502.3 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:68708277 C>T maps to NM_004262.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:68704003 G>A maps to NM_004262.2 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr4:68725320 C>T maps to NM_004262.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr4:69342024 C>T maps to NM_014058.3 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr4:69343095 C>T maps to NM_014058.3 N239N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr4:69334598 G>A maps to NM_014058.3 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:69337306 C>T maps to NM_014058.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:69327559 G>A maps to NM_014058.3 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr4:68939711 G>A maps to NM_207407.2 R100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr4:68939690 G>A maps to NM_207407.2 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr4:68930586 C>T maps to NM_207407.2 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr11:117779387 G>A maps to ENST00000413475 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:117779499 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:117779492 C>T maps to ENST00000413475 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:117784496 G>A maps to ENST00000413475 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr21:19685371 C>T maps to NM_002772.2 T685T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr21:19642393 G>A maps to NM_002772.2 F984F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr21:19715948 G>A maps to NM_002772.2 V434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:19726082 G>A maps to NM_002772.2 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr21:19713793 C>T maps to NM_002772.2 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr21:19744600 A>G maps to NM_002772.2 C191C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr21:19666681 G>A maps to NM_002772.2 P797P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:19725293 C>T maps to NM_002772.2 W366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:19770233 C>T maps to NM_002772.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr21:19653459 G>A maps to NM_002772.2 V855V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr21:42861440 C>T maps to NM_001135099.1 W143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr21:42845325 G>A maps to NM_001135099.1 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr21:42839717 T>C maps to NM_001135099.1 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr21:43802210 G>A maps to ENST00000380399 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr21:43808516 G>A maps to ENST00000380399 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr21:43796670 C>T maps to ENST00000380399 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr21:43795854 G>A maps to ENST00000380399 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19T-06A-11D-A19A-08 chr21:43802279 G>T maps to ENST00000380399 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:43802322 C>T maps to ENST00000380399 W352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr21:43795854 G>A maps to ENST00000380399 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr11:117988149 G>A maps to NM_019894.3 W428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:117965568 C>T maps to NM_019894.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:117973867 C>T maps to NM_019894.3 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr11:117965535 G>A maps to NM_019894.3 Q3Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr22:37491949 G>A maps to ENST00000381792 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr22:37462877 C>T maps to ENST00000381792 K768K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr22:37499388 C>T maps to ENST00000381792 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr22:37485789 G>A maps to ENST00000381792 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:37462937 C>T maps to ENST00000381792 E748E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:37467049 G>A maps to ENST00000381792 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr3:111795742 G>A maps to ENST00000443106 W647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr3:111769590 C>T maps to ENST00000443106 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:111799809 G>A maps to ENST00000443106 W792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr3:111785269 C>T maps to ENST00000443106 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:111795734 C>T maps to ENST00000443106 P644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr3:111785311 C>T maps to ENST00000443106 D531D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr3:111797601 C>T maps to ENST00000443106 S734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr3:111766781 C>T maps to ENST00000443106 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr19:2408431 C>T maps to NM_182973.1 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:2399191 G>C did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:2408440 C>T maps to NM_182973.1 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:2416538 G>A maps to NM_182973.1 T549T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:2413897 C>T maps to NM_182973.1 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:2413891 C>T maps to NM_182973.1 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:2415734 G>A maps to NM_182973.1 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:2408446 C>T maps to NM_182973.1 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:2403134 G>A maps to NM_182973.1 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:2408368 G>A maps to NM_182973.1 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:2422096 G>A maps to NM_182973.1 G766G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:2408368 G>A maps to NM_182973.1 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr19:2408368 G>A maps to NM_182973.1 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr19:2399054 C>T maps to NM_182973.1 H92H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr19:2408578 C>A maps to NM_182973.1 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:2410254 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:103219164 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:103219190 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:29725120 G>A maps to NM_001193451.1 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:29786247 G>A maps to NM_001193451.1 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr12:83359456 C>T maps to NM_152588.1 H601H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr12:83289649 C>T maps to NM_152588.1 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr12:83289709 G>A maps to NM_152588.1 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:88588802 C>T maps to NM_181783.3 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr13:101315307 G>A maps to NM_032813.2 Y154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr13:101315334 G>A maps to NM_032813.2 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr13:101289911 G>A maps to NM_032813.2 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr14:51716268 C>T maps to NM_030755.4 S191S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A2MI-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr14:51713809 T>C maps to NM_030755.4 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr11:57506651 C>T maps to NM_015959.3 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:57480206 G>A maps to NM_015959.3 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:57505830 C>T maps to NM_015959.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr18:66346768 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr20:7963023 G>A maps to NM_021156.2 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr20:7980461 G>A maps to NM_021156.2 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr9:117810805 G>A maps to NM_002160.2 L1529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr9:117810644 C>T maps to NM_002160.2 R1582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr9:117810647 C>T maps to NM_002160.2 Q1581Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr9:117852934 C>T maps to NM_002160.2 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr9:117826291 G>A maps to NM_002160.2 L1181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr9:117827166 C>A maps to NM_002160.2 V1082V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr9:117798449 C>T maps to NM_002160.2 T1861T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:117810800 G>A maps to NM_002160.2 P1530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:117786302 G>A maps to NM_002160.2 N2148N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:117853078 C>T maps to NM_002160.2 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:117846614 G>A maps to NM_002160.2 F668F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:117853252 G>A maps to NM_002160.2 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr9:117846626 C>A maps to NM_002160.2 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:117808905 G>A maps to NM_002160.2 F1636F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr9:117853195 C>T maps to NM_002160.2 Q34Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr9:117849553 T>C did not map to a codon.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr9:117836068 C>T maps to NM_002160.2 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr9:117819627 G>A maps to NM_002160.2 T1461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr9:117822078 A>G maps to NM_002160.2 P1412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:117788849 G>A maps to NM_002160.2 R2098R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:117853291 C>T maps to NM_002160.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:117786290 G>A maps to NM_002160.2 V2152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:117848530 C>T maps to NM_002160.2 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr9:117846692 G>A maps to NM_002160.2 A642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:31544542 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr6:31543637 C>T maps to NM_000594.2 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:31543538 C>T maps to NM_000594.2 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:31545301 C>T maps to NM_000594.2 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr17:26669338 C>T maps to NM_021137.4 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr17:26671536 C>T maps to NM_021137.4 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr14:103600050 C>T maps to NM_006291.2 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:103599730 G>A maps to NM_006291.2 V526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:103599775 G>A maps to NM_006291.2 K541K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:103601678 C>T maps to NM_006291.2 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:138197163 C>T maps to NM_006290.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr6:138196928 T>C maps to NM_006290.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:138192552 C>T maps to NM_006290.2 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr6:138199916 C>T maps to NM_006290.2 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:138202198 C>T maps to NM_006290.2 R706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:138200426 T>C maps to NM_006290.2 F615F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:152222711 C>T maps to NM_007115.3 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:152226540 G>A maps to NM_007115.3 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:118728889 G>A maps to NM_014350.2 E137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr5:118728850 C>T maps to NM_014350.2 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr19:4652030 G>A maps to NM_152362.2 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr15:51350461 G>A maps to NM_207381.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:51350236 G>A maps to NM_207381.2 H240H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr15:51350450 A>T maps to NM_207381.2 L169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:51350299 C>T maps to NM_207381.2 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr15:51350173 G>A maps to NM_207381.2 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr15:51397367 C>T maps to NM_207381.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:51350173 G>A maps to NM_207381.2 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:51350362 C>T maps to NM_207381.2 K198K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:51350413 C>T maps to NM_207381.2 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr8:23054696 C>T maps to NM_003844.3 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr8:23049443 C>T maps to NM_003844.3 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:23058221 G>A maps to NM_003844.3 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr8:23049350 C>T maps to NM_003844.3 R421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr8:23058221 G>A maps to NM_003844.3 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:23049398 C>T maps to NM_003844.3 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr8:23049377 C>T maps to NM_003844.3 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr8:23049443 C>T maps to NM_003844.3 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:23049443 C>T maps to NM_003844.3 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:23059355 G>A maps to NM_003844.3 D198D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:22884756 G>A maps to NM_003842.4 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:22960663 C>T maps to ENST00000356864 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:22974327 G>A maps to ENST00000356864 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr8:22972260 C>T maps to ENST00000356864 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:22969276 C>T maps to ENST00000356864 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:22972230 C>T maps to ENST00000356864 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:22995466 C>T maps to NM_003840.3 K359K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:23003352 G>A maps to NM_003840.3 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr18:60029003 G>A maps to NM_003839.2 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr18:60036028 G>A maps to NM_003839.2 K293K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr18:60036649 G>A maps to NM_003839.2 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr18:60036292 G>A maps to NM_003839.2 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr8:119938802 C>T maps to NM_002546.3 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr8:119938735 G>A maps to NM_002546.3 Q272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:119936638 G>A maps to NM_002546.3 Q394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr8:119936705 G>A maps to NM_002546.3 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:119938928 G>A maps to NM_002546.3 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:16852250 G>A maps to NM_012452.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:2492150 C>A maps to NM_003820.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr16:12061631 G>A maps to NM_001192.2 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:12060154 G>A maps to NM_001192.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:12059232 T>C maps to NM_001192.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:1140774 G>A maps to NM_004195.2 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:1140753 G>A maps to NM_004195.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:6438690 G>A maps to NM_001065.3 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:6443401 C>T maps to NM_001065.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6439001 G>A maps to NM_001065.3 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6440043 C>T maps to NM_001065.3 E200E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12253141 C>T maps to NM_001066.2 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr6:47253755 G>A maps to NM_014452.3 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr6:47221153 G>A maps to NM_014452.3 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:47251713 G>A maps to NM_014452.3 T401T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:47253755 G>A maps to NM_014452.3 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:47202493 G>A maps to NM_014452.3 F550F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:47202493 G>A maps to NM_014452.3 F550F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr6:47252043 G>A maps to NM_014452.3 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:47200575 A>T maps to NM_014452.3 I631I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:47202493 G>A maps to NM_014452.3 F550F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:47221099 G>A maps to NM_014452.3 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr6:47251986 C>T maps to NM_014452.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:6521580 G>A maps to ENST00000355862 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:6525500 C>G maps to ENST00000355862 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr1:6521676 G>A maps to ENST00000355862 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:6521697 G>A maps to ENST00000355862 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:6521817 G>A maps to ENST00000355862 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:6525593 G>A maps to ENST00000355862 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:1149453 G>A maps to NM_003327.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr1:1147430 C>T maps to NM_003327.3 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:1149456 G>A maps to NM_003327.3 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:1148073 G>A maps to NM_003327.3 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr20:62328224 C>T maps to ENST00000482936 L1338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr20:62328319 C>T maps to ENST00000482936 P1369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr1:12144567 T>G maps to NM_001243.3 Y37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:12144531 C>T maps to NM_001243.3 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:12144523 C>T maps to NM_001243.3 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:12170214 G>A maps to NM_001243.3 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:12170184 C>T maps to NM_001243.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:12175782 C>T maps to NM_001243.3 Q315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:8000003 G>A maps to NM_001561.5 N17N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:172224296 G>A maps to NM_003810.3 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:172224404 G>A maps to ENST00000382750 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:172224668 G>A maps to ENST00000382750 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr3:172241117 G>A maps to ENST00000382750 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr3:172227088 G>A maps to ENST00000382750 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr3:172224709 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:172224701 C>T maps to ENST00000382750 K142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:172241117 G>A maps to ENST00000382750 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr13:43175052 G>A maps to NM_003701.3 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr13:43148639 C>T maps to NM_003701.3 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr13:43148573 C>T maps to NM_003701.3 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr13:43180897 G>A maps to NM_003701.3 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr13:43180897 G>A maps to NM_003701.3 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr13:43181039 C>T maps to NM_003701.3 R314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:43181039 C>T maps to NM_003701.3 R314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr13:108922353 C>T maps to NM_006573.3 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr13:108955897 C>T maps to NM_006573.3 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr19:6665011 G>A maps to NM_003807.3 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:6667150 C>A maps to NM_003807.3 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr19:6665053 G>A maps to NM_003807.3 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:6665053 G>A maps to NM_003807.3 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:6665011 G>A maps to NM_003807.3 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:6664983 G>A maps to NM_003807.3 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr9:117553073 G>A maps to NM_005118.2 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr9:117553069 G>A maps to NM_005118.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr9:117553073 G>A maps to NM_005118.2 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:117552731 C>T maps to NM_005118.2 *252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:117552833 G>A maps to NM_005118.2 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr1:173010834 C>T maps to NM_005092.3 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:173010691 G>A maps to NM_005092.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:173013109 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:173176297 G>C maps to NM_003326.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr9:117666402 C>T maps to NM_001244.2 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr9:117666366 C>T maps to NM_001244.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr9:117692441 G>A maps to NM_001244.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr9:117666411 G>A maps to NM_001244.2 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:117666366 C>T maps to NM_001244.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:117666495 G>A maps to NM_001244.2 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:117692466 G>A maps to NM_001244.2 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr19:6535043 C>T maps to NM_003811.3 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr19:6534953 C>T maps to NM_003811.3 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:6534668 C>T maps to NM_003811.3 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:170805154 G>A maps to NM_015028.2 S954S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:170858196 C>T maps to NM_015028.2 E441E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:170825898 C>T maps to NM_015028.2 V779V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:170858229 C>T maps to NM_015028.2 Q430Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:170893072 C>T maps to NM_015028.2 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr3:170828505 G>A maps to NM_015028.2 R761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:170908525 C>T maps to NM_015028.2 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr3:170786635 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:170945974 G>A maps to NM_015028.2 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:170879093 C>T maps to NM_015028.2 E327E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:170828641 C>T maps to NM_015028.2 E715E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:170805229 G>A maps to NM_015028.2 L929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:170858235 C>T maps to NM_015028.2 E428E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:170906619 C>T maps to NM_015028.2 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr3:170846537 G>A maps to NM_015028.2 R580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr5:150439956 C>A did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr5:150436500 G>A maps to NM_006058.3 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:150416401 G>A maps to NM_006058.3 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:150436377 G>A maps to NM_006058.3 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:2744021 C>A maps to NM_024309.3 E418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr4:2747232 G>A maps to NM_024309.3 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr4:2749474 C>T maps to NM_024309.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:2746567 G>A maps to NM_024309.3 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr4:122062994 A>T maps to ENST00000509841 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr4:122059829 G>A maps to NM_001128843.1 Q299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:122068286 G>A maps to ENST00000509841 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr4:122078269 C>T maps to ENST00000509841 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:7290738 G>A maps to NM_003985.3 R480R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr17:7292013 G>A maps to NM_003985.3 K589K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:7290398 G>A maps to NM_003985.3 G441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr3:195611829 G>T maps to NM_001010938.1 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr3:195594768 G>A maps to NM_001010938.1 S863S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:195594449 G>A maps to NM_001010938.1 L970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr3:195605958 G>A maps to NM_001010938.1 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr8:9588485 C>T maps to NM_003747.2 R696R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:9610108 C>T maps to NM_003747.2 H1042H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:9623824 C>T maps to NM_003747.2 A1210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:57077189 C>A maps to NM_033396.2 E999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr11:57077226 G>A maps to NM_033396.2 F986F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:57076665 G>A maps to NM_033396.2 S1173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:57068485 A>C maps to NM_033396.2 A1667A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr11:57077265 C>T maps to NM_033396.2 Q973Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:57076695 G>A maps to NM_033396.2 D1163D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:57076758 C>T maps to NM_033396.2 K1142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr11:57068451 G>A maps to NM_033396.2 Q1679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr11:57076241 G>A maps to NM_033396.2 L1315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:57080340 G>A maps to NM_033396.2 T607T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:57069595 G>A maps to NM_033396.2 L1596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:93614873 G>A maps to NM_025235.3 V968V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr10:93582120 T>C did not map to a codon.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr10:93610974 C>T maps to NM_025235.3 I899I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:99848967 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr23:99849346 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:99854660 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:99849314 A>G did not map to a codon.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr23:99849347 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:175105030 G>A maps to NM_022093.1 R1127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr1:175097806 C>T maps to NM_022093.1 T1085T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:175086222 G>A maps to NM_022093.1 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:175046775 C>T maps to NM_022093.1 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:175046844 G>A maps to NM_022093.1 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr1:175046805 C>T maps to NM_022093.1 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:175046580 C>T maps to NM_022093.1 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:175063162 G>A maps to NM_022093.1 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:175087880 G>A maps to NM_022093.1 P857P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:175096175 C>T maps to NM_022093.1 I1000I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr1:175048470 C>T maps to NM_022093.1 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:175046760 G>A maps to NM_022093.1 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:175092599 G>A maps to NM_022093.1 W905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:175116170 G>A maps to NM_022093.1 K1288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:175049374 G>A maps to NM_022093.1 Q287Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:175066613 C>T maps to NM_022093.1 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:175046592 C>T maps to NM_022093.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:175105026 G>A maps to NM_022093.1 W1126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:175049338 G>A maps to NM_022093.1 E275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:175097241 C>T maps to NM_022093.1 S1040S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:175049372 C>T maps to NM_022093.1 Q287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr1:175052943 G>A maps to NM_022093.1 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr1:175097806 C>T maps to NM_022093.1 T1085T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr1:175105030 G>A maps to NM_022093.1 R1127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:175086183 C>T maps to NM_022093.1 T743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:175046793 G>A maps to NM_022093.1 E80E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:175046901 G>A maps to NM_022093.1 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:175048622 C>T maps to NM_022093.1 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:175063157 C>T maps to NM_022093.1 R453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:175063303 G>A maps to NM_022093.1 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:175063315 G>A maps to NM_022093.1 E505E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:175097743 C>T maps to NM_022093.1 F1064F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:175066577 G>A maps to NM_022093.1 V538V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:175054613 C>T maps to NM_022093.1 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:175096202 C>T maps to NM_022093.1 F1009F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:175067694 C>T maps to NM_022093.1 Q695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:52485482 C>T maps to NM_003280.2 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr3:52485803 C>T maps to NM_003280.2 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:52485520 G>A maps to NM_003280.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr3:52485776 G>A maps to NM_003280.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:52485317 G>A maps to NM_003280.2 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:201384367 G>A maps to ENST00000367312 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr1:201379533 C>T maps to ENST00000367312 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:1862277 G>A maps to ENST00000381906 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:1862074 G>A maps to ENST00000381906 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:1862717 G>A maps to ENST00000381906 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:1862397 G>A maps to ENST00000381906 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:1862726 C>T maps to ENST00000381906 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr19:55663276 C>T maps to ENST00000344887 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:74819006 C>T maps to NM_001112808.2 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:74737298 C>T maps to NM_001112808.2 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:74834751 C>T maps to NM_001112808.2 F557F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:74905257 C>T maps to NM_001112808.2 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:74957899 C>T maps to NM_001112808.2 F868F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:74715178 C>T maps to NM_001112808.2 Y163Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:74701795 G>A maps to NM_001112808.2 K118K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:75005953 G>A maps to NM_001112808.2 E897E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:201334318 G>A maps to ENST00000421663 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:201331123 C>T maps to ENST00000421663 Q212Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:201331114 C>T maps to ENST00000421663 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:201331105 C>T maps to ENST00000421663 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:201334339 G>A maps to ENST00000421663 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr1:201330442 G>A maps to ENST00000421663 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:201332428 G>A maps to ENST00000421663 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:201332528 C>T maps to ENST00000421663 E165E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:201333434 G>A maps to ENST00000421663 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr11:1955596 G>A maps to ENST00000397301 K145K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:1956112 C>T maps to ENST00000397301 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr11:1956058 G>A maps to ENST00000397301 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:1944289 G>A maps to ENST00000397301 E10E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:1955048 C>T maps to ENST00000397301 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:1956076 C>T maps to ENST00000397301 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr16:11361864 C>T maps to NM_005425.4 W135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:11361865 C>T maps to NM_005425.4 W135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr16:11362753 G>A maps to NM_005425.4 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr16:11362867 C>T maps to NM_005425.4 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:11361858 G>A maps to NM_005425.4 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:11363044 G>A maps to NM_005425.4 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:72189460 C>T maps to NM_002270.3 R692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr5:72178913 G>A maps to NM_002270.3 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:12822260 C>T maps to NM_001136196.1 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:12822414 G>A maps to NM_001136196.1 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:12826065 G>A maps to NM_001136196.1 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:12826134 G>A maps to NM_001136196.1 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:12814299 C>T maps to NM_001136196.1 E717E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:12822378 G>A maps to NM_001136196.1 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:128694743 C>T maps to ENST00000471166 K27K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:128615974 G>T maps to ENST00000471166 Y726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr1:175332877 G>A maps to NM_003285.2 F891F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:175372651 C>T maps to NM_003285.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr1:175355336 C>T maps to NM_003285.2 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:175375790 G>A maps to NM_003285.2 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr1:175362996 C>T maps to NM_003285.2 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr1:175332855 G>A maps to NM_003285.2 R899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:175331898 G>A maps to NM_003285.2 F918F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:175375844 C>T maps to NM_003285.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr1:175306678 G>A maps to NM_003285.2 D1173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr1:175375427 G>A maps to NM_003285.2 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:175375496 G>A maps to NM_003285.2 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:175375418 C>T maps to NM_003285.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr1:175292612 C>A did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:175328778 C>T maps to NM_003285.2 E981E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:175372435 C>T maps to NM_003285.2 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:175334167 G>A maps to NM_003285.2 P855P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:175355417 C>T maps to NM_003285.2 Q509Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:175323625 G>A maps to NM_003285.2 R1095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:175375427 G>A maps to NM_003285.2 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:175355429 G>A maps to NM_003285.2 D505D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:175332867 G>A maps to NM_003285.2 R895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:175372390 G>A maps to NM_003285.2 Y287Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:175332855 G>A maps to NM_003285.2 R899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:175323629 C>T maps to NM_003285.2 W1093*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:175331898 G>A maps to NM_003285.2 F918F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:175362945 G>A maps to NM_003285.2 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:175375808 G>A maps to NM_003285.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:175325581 G>A maps to NM_003285.2 I997I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:175360499 C>T maps to NM_003285.2 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:175375790 G>A maps to NM_003285.2 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:175299288 G>A maps to NM_003285.2 F1238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:175306815 C>G did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:175355174 G>A maps to NM_003285.2 F590F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:175304901 C>T maps to NM_003285.2 R1192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:175375604 C>T maps to NM_003285.2 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:175365851 C>T maps to NM_003285.2 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:175304862 C>T maps to NM_003285.2 E1205E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:175334293 C>T maps to NM_003285.2 E813E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:175365683 G>A maps to NM_003285.2 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr1:175365848 G>A maps to NM_003285.2 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:175355303 C>T maps to NM_003285.2 R547R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:175335251 G>A maps to NM_003285.2 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:175375478 G>A maps to NM_003285.2 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr1:175365881 C>T maps to NM_003285.2 W346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr7:5427387 G>A maps to NM_001080495.2 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:5410231 G>A maps to NM_001080495.2 F1331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr7:5352178 G>A maps to NM_001080495.2 F2781F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr7:5355674 G>A maps to NM_001080495.2 D2258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:5410822 G>A maps to NM_001080495.2 R1134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr7:5391579 C>T maps to NM_001080495.2 R1780R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr7:5348768 C>T maps to NM_001080495.2 Q2873Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:5391480 G>A maps to NM_001080495.2 F1813F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr7:5348975 G>A maps to NM_001080495.2 A2804A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:5355599 G>A maps to NM_001080495.2 D2283D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr7:5396873 G>A maps to NM_001080495.2 Q1623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:24829926 C>T maps to NM_014494.2 S1662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:24801471 C>T maps to NM_014494.2 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:24803028 G>A maps to NM_014494.2 W1022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr22:40662664 C>T maps to ENST00000454349 R825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr22:40681767 C>T maps to ENST00000454349 S1248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr22:40704565 G>T maps to ENST00000454349 G1405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr22:40708539 C>T maps to ENST00000454349 I1503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr22:40711446 C>T maps to ENST00000454349 P1627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr22:40719214 C>T maps to ENST00000454349 D1838D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr22:40662399 G>A maps to ENST00000454349 W736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:40708575 C>T maps to ENST00000454349 T1515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr22:40676047 C>A maps to ENST00000454349 L1118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr22:40662994 C>T maps to ENST00000454349 R935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:40719133 C>T maps to ENST00000454349 N1811N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:76075522 A>G maps to NM_001142640.1 Q1083Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:76094576 G>A maps to NM_001142640.1 W1523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr17:76063944 C>T maps to NM_001142640.1 Q904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr17:76045227 C>T maps to NM_001142640.1 Q29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr17:76045286 G>T maps to NM_001142640.1 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:76046246 C>T maps to NM_001142640.1 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:76089071 C>T maps to NM_001142640.1 S1340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:76098600 C>T maps to NM_001142640.1 L1552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:218674598 G>A maps to NM_022648.4 I1636I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:218682614 G>A maps to NM_022648.4 A1376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr2:218669214 G>A maps to NM_022648.4 S1725S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:218696247 G>A maps to NM_022648.4 A976A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:218682683 G>A maps to NM_022648.4 F1353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr2:218712974 G>A maps to NM_022648.4 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:218669220 G>A maps to NM_022648.4 F1723F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:218682839 G>A maps to NM_022648.4 G1301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:218683343 G>A maps to NM_022648.4 S1133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:218713598 G>A maps to NM_022648.4 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:218712398 G>A maps to NM_022648.4 F822F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:218683157 G>A maps to NM_022648.4 F1195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:218683157 G>A maps to NM_022648.4 F1195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:218669208 G>A maps to NM_022648.4 V1727V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr2:218682926 C>T maps to NM_022648.4 L1272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr2:218712962 G>A maps to NM_022648.4 V634V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:47409129 G>A maps to NM_022748.11 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr7:47408076 G>A maps to NM_022748.11 A722A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr7:47454704 G>A maps to NM_022748.11 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr7:47336689 C>G maps to NM_022748.11 L1222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:47408094 G>A maps to NM_022748.11 I716I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:47408376 G>A maps to NM_022748.11 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr7:47343142 G>A maps to NM_022748.11 P954P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:47454704 G>A maps to NM_022748.11 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr7:47454805 T>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:47454704 G>A maps to NM_022748.11 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr7:47342833 C>G maps to NM_022748.11 A1057A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr7:47385826 G>A maps to NM_022748.11 A803A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:47332456 G>A maps to NM_022748.11 A1273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr7:47479084 C>T maps to NM_022748.11 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr7:47408145 G>A maps to NM_022748.11 I699I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr17:38645015 C>A maps to NM_032865.5 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:38640798 G>A maps to NM_032865.5 R480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:38640745 C>T maps to NM_032865.5 Q497Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:38641185 G>A maps to NM_032865.5 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:38645132 G>A maps to NM_032865.5 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr17:38638426 G>A maps to NM_032865.5 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:38652455 G>A maps to NM_032865.5 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr17:38635927 C>T maps to NM_032865.5 R636R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr17:38643618 G>A maps to NM_032865.5 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:38645207 G>A maps to NM_032865.5 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:32023667 C>T maps to ENST00000375244 E2809E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr6:32015583 C>T maps to ENST00000375244 R3417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr6:32010369 G>A maps to ENST00000375244 I4024I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr6:32039860 G>A maps to ENST00000375244 I1632I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr6:32012984 C>G maps to ENST00000375244 S3575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr6:32052355 C>T maps to ENST00000375244 V1093V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr6:32011625 C>T maps to ENST00000375244 Q3810Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:32011619 G>A maps to ENST00000375244 L3812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:32020738 T>C maps to ENST00000375244 E2941E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:32029312 C>T maps to ENST00000375244 R2451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:32049990 A>G maps to ENST00000375244 F1186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr6:32013005 G>A maps to ENST00000375244 T3568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr6:32017242 G>A maps to ENST00000375244 T3187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:32012951 G>A maps to ENST00000375244 F3586F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:32057123 C>T maps to ENST00000375244 R797R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr6:32016247 G>A maps to ENST00000375244 R3313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr6:32016248 G>A maps to ENST00000375244 L3312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:32020698 G>A maps to ENST00000375244 L2955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:32012966 G>A maps to ENST00000375244 G3581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:32025964 C>T maps to ENST00000375244 A2565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:32041571 C>T maps to ENST00000375244 K1511K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:32029480 G>A maps to ENST00000375244 T2395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:32039785 G>A maps to ENST00000375244 V1657V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:32036659 C>T maps to ENST00000375244 V1947V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:32010300 G>A maps to ENST00000375244 F4047F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:32030249 C>T maps to ENST00000375244 K2284K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:32035615 G>A maps to ENST00000375244 F2122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:32052274 C>T maps to ENST00000375244 L1120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr6:32065630 C>T maps to ENST00000375244 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr6:32026069 C>T maps to ENST00000375244 V2530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:32047086 G>A maps to ENST00000375244 A1366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr6:32037988 C>T maps to ENST00000375244 L1731L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:32065144 C>T maps to ENST00000375244 W162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:32046846 C>T maps to ENST00000375244 G1446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:32037465 G>A maps to ENST00000375244 P1817P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:32037994 G>A maps to ENST00000375244 T1729T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:32012951 G>A maps to ENST00000375244 F3586F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:32020537 C>T maps to ENST00000375244 G3008G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:32026057 G>A maps to ENST00000375244 S2534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:32050068 G>A maps to ENST00000375244 P1160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:32016311 G>A maps to ENST00000375244 S3291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:32049951 C>T maps to ENST00000375244 R1199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:32017982 G>A maps to ENST00000375244 S3077S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr6:32030066 C>T maps to ENST00000375244 K2345K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr6:32049307 G>A maps to ENST00000375244 V1293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr6:32062966 C>T maps to ENST00000375244 E748E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:32032811 G>A maps to ENST00000375244 S2209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr6:32017224 G>A maps to ENST00000375244 F3193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr6:32023879 G>A maps to ENST00000375244 L2739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr6:32046930 A>G maps to ENST00000375244 V1418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr6:32047032 G>A maps to ENST00000375244 S1384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr6:32014231 A>T maps to ENST00000375244 A3442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:32037561 G>A maps to ENST00000375244 T1785T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr6:32037588 G>A maps to ENST00000375244 P1776P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr6:32029230 G>A maps to ENST00000375244 L2479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr6:32049834 G>A maps to ENST00000375244 P1238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr6:32036896 C>T maps to ENST00000375244 T1868T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr6:32036905 C>T maps to ENST00000375244 R1865R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr6:32049924 G>C maps to ENST00000375244 P1208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:32026087 G>A maps to ENST00000375244 L2524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:32065660 G>A maps to ENST00000375244 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr6:32053809 G>A maps to ENST00000375244 L955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:32015757 C>T maps to ENST00000375244 G3359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:32021303 C>T maps to ENST00000375244 Q2884Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:32037543 G>A maps to ENST00000375244 S1791S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:32041709 G>A maps to ENST00000375244 T1465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:32053652 G>A maps to ENST00000375244 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:32065161 A>T maps to ENST00000375244 C156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:32010357 C>T maps to ENST00000375244 R4028R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:32017110 C>T maps to ENST00000375244 K3231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr1:45807143 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr1:45807144 G>A maps to NM_025077.3 Q79Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:35717963 C>T maps to ENST00000451197 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr22:35719850 C>T maps to ENST00000451197 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:35728995 C>T maps to ENST00000451197 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr22:35719768 C>T maps to ENST00000451197 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr22:35729440 C>T maps to ENST00000451197 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CF-06A-11D-A196-08 chr17:52981123 C>T maps to NM_005486.2 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr17:53024633 G>A maps to NM_005486.2 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:52990071 C>T maps to NM_005486.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr17:53014063 C>T maps to NM_005486.2 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr17:17797058 G>A maps to NM_001082968.1 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:17766154 C>T maps to NM_001082968.1 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr17:17797058 G>A maps to NM_001082968.1 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:17751083 G>A maps to NM_001082968.1 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr17:17750953 G>A maps to NM_001082968.1 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr14:58869451 C>A maps to NM_207377.2 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr20:43571758 G>A maps to NM_006809.4 N307N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr19:45406308 C>T maps to NM_006114.2 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr19:45406290 T>C maps to NM_006114.2 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:161197991 C>T maps to NM_032174.4 H167H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:161198854 C>T maps to NM_032174.4 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr20:39750644 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr20:39750645 G>A maps to NM_003286.2 K682K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr20:39750786 A>G maps to NM_003286.2 T729T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:39741498 A>T maps to NM_003286.2 R462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:39729897 C>A maps to NM_003286.2 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr20:39741562 A>T maps to NM_003286.2 K484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:39742749 G>A maps to NM_003286.2 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr8:144408427 G>A maps to NM_052963.1 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:144391661 C>T maps to NM_052963.1 R585R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:144407675 G>A maps to NM_052963.1 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:144399902 G>A maps to NM_052963.1 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:144398198 G>A maps to NM_052963.1 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:144406177 G>A maps to NM_052963.1 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:144408460 G>A maps to NM_052963.1 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:38572722 C>T maps to ENST00000357601 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:38546330 G>A maps to ENST00000357601 V1488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:25665113 A>C maps to ENST00000264331 G873G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr3:25661494 A>T maps to ENST00000264331 L974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:25674065 G>A maps to ENST00000264331 N379N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr3:25675376 T>C maps to ENST00000264331 K327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:18181325 G>A maps to NM_004618.3 N830N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr17:18183947 G>A maps to NM_004618.3 F682F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:18183971 C>T maps to NM_004618.3 G674G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:18183972 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:18196104 A>G maps to NM_004618.3 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:18196149 G>A maps to NM_004618.3 R364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr17:18181277 G>A maps to NM_004618.3 F846F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr17:18205273 G>A maps to NM_004618.3 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:18181529 G>A maps to NM_004618.3 P762P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:18194299 G>A maps to NM_004618.3 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:22323142 G>A maps to NM_003935.3 Q196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr22:22314046 G>A maps to NM_003935.3 A572A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr22:22317152 G>A maps to NM_003935.3 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr22:22312878 G>A maps to NM_003935.3 R698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:22311704 G>A maps to NM_003935.3 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr22:22318361 C>T maps to NM_003935.3 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr3:133372318 T>A maps to NM_007027.3 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:133331238 G>A maps to NM_007027.3 F1343F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:32543664 G>A maps to NM_005802.4 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr9:132584973 G>A maps to ENST00000437532 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:179851813 C>T maps to ENST00000398836 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:179815643 G>A maps to NM_145034.4 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:130494318 G>A maps to NM_001085347.1 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr9:130495725 G>A maps to NM_001085347.1 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:179052081 C>T maps to NM_022371.3 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr8:59728226 C>T maps to NM_014729.2 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:59720341 C>T maps to NM_014729.2 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr8:59720329 C>T maps to NM_014729.2 R519R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr8:59727941 G>A maps to NM_014729.2 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:59851869 G>A maps to NM_014729.2 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr20:42682991 G>A maps to ENST00000348077 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr20:42635398 G>A maps to ENST00000348077 Q135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr20:42635278 G>A maps to ENST00000348077 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:42694455 C>T maps to ENST00000348077 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:42694575 C>T maps to ENST00000348077 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:42635365 C>T maps to ENST00000348077 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:42693415 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr20:42694606 C>T maps to ENST00000348077 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr20:42680181 C>T maps to ENST00000348077 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr20:42697298 C>T maps to ENST00000348077 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:42635224 G>A maps to ENST00000348077 E77E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:42682991 G>A maps to ENST00000348077 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:42680181 C>T maps to ENST00000348077 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr20:42635416 G>A maps to ENST00000348077 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr20:42682961 A>C maps to ENST00000348077 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr20:42679947 C>T maps to ENST00000348077 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:42683085 C>T maps to ENST00000348077 Q276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:42683153 G>A maps to ENST00000348077 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:42693478 G>A maps to ENST00000348077 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:52497938 C>T maps to ENST00000407228 Q105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr16:52473847 G>A maps to ENST00000407228 I340I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:52497914 G>A maps to ENST00000407228 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:52497887 G>A maps to ENST00000407228 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:52473799 G>A maps to ENST00000407228 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:52473640 C>T maps to ENST00000407228 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:52502447 C>T maps to ENST00000407228 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr14:21964742 C>T maps to NM_014828.2 N615N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr14:21961097 C>G maps to NM_014828.2 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr14:21960510 T>C maps to NM_014828.2 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr17:7576854 G>A maps to NM_001126112.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:7578369 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr17:7576864 A>T maps to NM_001126112.1 Y327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:7578290 T>G did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:7576896 G>A maps to NM_001126112.1 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr17:7574003 G>A maps to NM_001126112.1 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr17:7579311 C>T maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr17:7579309 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:7576896 G>A maps to NM_001126112.1 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr17:7578554 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:7578452 G>A maps to NM_001126112.1 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:128807488 G>A maps to ENST00000263583 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr11:128807689 G>A maps to NM_022112.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr15:43748438 G>A maps to NM_001141980.1 S789S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:43762100 G>A maps to NM_001141980.1 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr15:43748890 G>A maps to NM_001141980.1 R639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:43712806 A>T maps to NM_001141980.1 A1459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr15:43720297 G>A maps to NM_001141980.1 I1248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr15:43748831 G>A maps to NM_001141980.1 H658H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr15:43705503 G>A maps to NM_001141980.1 S1706S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:43784541 G>A maps to NM_001141980.1 H44H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:43773105 G>A maps to NM_001141980.1 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr15:43738696 T>G maps to NM_001141980.1 G976G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr15:43762073 G>A maps to NM_001141980.1 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr15:43783949 G>A maps to NM_001141980.1 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:43749274 G>A maps to NM_001141980.1 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr1:223988513 T>A did not map to a codon.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:223983954 C>T maps to NM_001031685.2 R762R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr1:223987609 C>T maps to NM_001031685.2 R492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:223991101 G>A maps to NM_001031685.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:224008964 G>A maps to NM_001031685.2 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:223989872 C>T maps to NM_001031685.2 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:223991035 G>A maps to NM_001031685.2 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr11:44958372 G>A maps to NM_006034.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr17:27896361 A>G maps to NM_138349.2 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:24305772 G>A maps to NM_147184.1 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr2:24300514 C>T maps to NM_147184.1 Q311Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:95952371 A>G maps to NM_033285.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:44005982 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr3:189526071 G>A maps to NM_003722.4 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:189612027 C>T maps to NM_003722.4 R594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:189526275 C>T maps to NM_003722.4 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr3:189612035 G>A maps to NM_003722.4 A596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:189584555 G>A maps to NM_003722.4 Q284Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:189608664 C>T maps to NM_003722.4 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:189586497 G>A maps to NM_003722.4 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:189607225 C>A maps to NM_003722.4 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:189455612 C>T maps to NM_003722.4 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr3:189526084 C>T maps to NM_003722.4 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr3:189582061 G>A maps to NM_003722.4 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:189607195 C>T maps to NM_003722.4 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:189608622 G>A maps to NM_003722.4 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:189612027 C>T maps to NM_003722.4 R594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:189526314 G>A maps to NM_003722.4 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:189456460 G>A maps to NM_003722.4 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr3:189611993 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:189585656 C>T maps to NM_003722.4 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:189582115 C>T maps to NM_003722.4 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr3:189526122 G>A maps to NM_003722.4 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr3:189612095 C>T maps to NM_003722.4 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:189455615 C>T maps to NM_003722.4 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZU-06A-12D-A196-08 chr3:189349360 C>A maps to NM_003722.4 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:189526071 G>A maps to NM_003722.4 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:189586377 C>T maps to NM_003722.4 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:189612185 C>T maps to NM_003722.4 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:189455531 C>T maps to NM_003722.4 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:189526083 C>T maps to NM_003722.4 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:189586378 C>T maps to NM_003722.4 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:189586384 C>T maps to NM_003722.4 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:189590652 G>A maps to NM_003722.4 R406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:189612095 C>T maps to NM_003722.4 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:189455615 C>T maps to NM_003722.4 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:189585719 G>A maps to NM_003722.4 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:189612203 C>T maps to NM_003722.4 F652F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr3:189586497 G>A maps to NM_003722.4 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr3:189455579 C>A maps to NM_003722.4 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:3638757 G>A maps to NM_005427.2 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr1:3599692 G>A maps to NM_005427.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr1:3640008 C>T maps to NM_005427.2 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:3638664 C>T maps to NM_005427.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:3638757 G>A maps to NM_005427.2 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr6:83075655 G>A maps to NM_006670.4 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr12:113724875 C>T maps to NM_001143819.1 V609V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:113723739 G>A maps to NM_001143819.1 V572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr12:113716032 G>A maps to NM_001143819.1 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:113729445 C>T maps to NM_001143819.1 S736S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr12:113717995 C>T maps to NM_001143819.1 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr11:68854620 C>T maps to NM_139075.3 P709P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:68825140 C>T maps to NM_139075.3 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:68839458 C>T maps to NM_139075.3 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr11:68822717 G>A maps to NM_139075.3 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:68835020 T>C maps to NM_139075.3 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:68839450 C>T maps to NM_139075.3 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:80965593 C>T maps to NM_001025252.1 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr8:80962684 G>A maps to NM_001025253.1 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:80965599 G>A maps to NM_001025252.1 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr6:125583981 G>A maps to NM_003287.2 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr6:125550370 G>A maps to NM_003287.2 Q81Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:6328867 A>G maps to NM_033516.5 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:6328915 G>A maps to NM_033516.5 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:6328915 G>A maps to NM_033516.5 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:18054889 C>T maps to ENST00000341556 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:72366379 C>T maps to ENST00000389376 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:72343388 C>T maps to ENST00000389376 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:72416258 C>T maps to ENST00000389376 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr12:72425075 C>T maps to ENST00000389376 D407D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:72338187 C>T maps to ENST00000389376 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:144245587 G>A maps to NM_022445.3 N203N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr7:144245644 G>A maps to NM_022445.3 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr7:144288586 G>A maps to NM_022445.3 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr7:144288533 C>T maps to NM_022445.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:144288521 G>A maps to NM_022445.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr15:63353403 C>T maps to ENST00000404484 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr15:63349294 A>T maps to ENST00000357980 K160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:63356338 C>T maps to ENST00000380364 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr15:63353403 C>T maps to ENST00000404484 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:35685460 G>A maps to ENST00000329305 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:35689739 G>C maps to ENST00000329305 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr9:35685756 G>A maps to ENST00000329305 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:154163751 C>T maps to ENST00000271850 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr1:154164464 C>T maps to ENST00000271850 Q10Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:154163757 C>T maps to ENST00000271850 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr19:16178514 G>A maps to NM_001145160.1 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr2:1437218 G>A maps to NM_000547.5 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr2:1480955 G>A maps to NM_000547.5 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr2:1480871 C>T maps to NM_000547.5 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:1481117 C>T maps to NM_000547.5 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:1488577 C>T maps to NM_000547.5 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:1488381 G>A maps to NM_000547.5 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr2:1497794 C>T maps to NM_000547.5 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:1544386 C>T maps to NM_000547.5 S880S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr2:1488423 G>A maps to NM_000547.5 Q465Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr2:1480955 G>A maps to NM_000547.5 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:1481043 C>T maps to NM_000547.5 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:1491746 G>A maps to NM_000547.5 R584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:1418233 C>T maps to NM_000547.5 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:1437350 G>A maps to NM_000547.5 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:1488504 C>T maps to NM_000547.5 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:1418266 C>T maps to NM_000547.5 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr2:1480904 C>T maps to NM_000547.5 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:1488369 C>T maps to NM_000547.5 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:1520667 C>T maps to NM_000547.5 L844L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:1457513 C>T maps to NM_000547.5 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:1491698 C>T maps to NM_000547.5 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:1488381 G>A maps to NM_000547.5 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:1499823 C>T maps to NM_000547.5 S690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:1507824 T>A maps to NM_000547.5 L831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr2:1481009 G>A maps to NM_000547.5 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr2:1418230 A>G maps to NM_000547.5 E17E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr2:1457567 C>T maps to NM_000547.5 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:1507795 C>T maps to NM_000547.5 F821F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:1437208 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:1437218 G>A maps to NM_000547.5 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:1488504 C>T maps to NM_000547.5 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:1507762 C>T maps to NM_000547.5 A810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:1546233 G>A maps to NM_000547.5 P930P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr2:1426871 G>A maps to NM_000547.5 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr2:1437329 G>A maps to NM_000547.5 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:6637258 G>A maps to ENST00000453338 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:6636488 G>A maps to ENST00000453338 G455G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:6635860 G>A maps to ENST00000453338 F545F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr11:6638090 C>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:6635911 G>A maps to ENST00000453338 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr13:103257168 C>T maps to ENST00000376052 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr13:103266515 C>T maps to ENST00000376052 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr13:103271109 G>T maps to ENST00000376052 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr13:103301255 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr13:103301836 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:677878 G>A maps to NM_007030.2 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr5:677983 G>A maps to NM_007030.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr5:666174 C>T maps to NM_007030.2 K125K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr16:67424843 G>A maps to NM_016140.2 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:67424130 G>A maps to NM_016140.2 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:186287931 G>A maps to NM_003292.2 F2199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:186313129 G>A maps to NM_003292.2 V1170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr1:186313129 G>A maps to NM_003292.2 V1170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:186316441 G>A maps to NM_003292.2 S975S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:186294971 A>G maps to NM_003292.2 T2012T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:186304567 G>A maps to NM_003292.2 Q1605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:186287895 A>C maps to NM_003292.2 V2211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:186332545 T>C maps to NM_003292.2 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:186292913 G>A maps to NM_003292.2 A2067A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:127298660 G>A maps to NM_001136053.1 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr3:189038587 C>T maps to NM_198485.3 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr3:188925304 G>A maps to NM_198485.3 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:188925382 G>A maps to NM_198485.3 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:188925301 G>A maps to NM_198485.3 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:188933082 G>A maps to NM_198485.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:188956521 G>A maps to NM_198485.3 K101K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:188956532 G>A maps to NM_198485.3 W105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr3:188925280 G>A maps to NM_198485.3 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr1:3542402 A>G maps to NM_182752.3 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr1:3542429 G>A maps to NM_182752.3 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:73957737 C>T maps to ENST00000409716 Q169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr9:140094257 G>A maps to NM_001128228.2 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:140093723 C>T maps to NM_001128228.2 R480R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr19:48306126 G>T maps to NM_198479.2 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr16:1291283 C>T maps to ENST00000461509 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:1291233 C>T maps to ENST00000461509 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:1279234 C>T maps to ENST00000445910 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:1279610 G>A maps to ENST00000445910 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr16:1306942 C>T maps to NM_012217.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr16:1306583 C>T maps to NM_012217.2 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:1306628 C>T maps to NM_012217.2 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:1272243 G>A maps to NM_012467.3 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:65705951 C>T maps to NM_003596.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:65706080 T>A maps to NM_003596.3 Y223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr7:65706179 C>T maps to NM_003596.3 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr22:26936873 C>T maps to NM_003595.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:26932424 G>A maps to NM_003595.3 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr22:26937077 G>A maps to NM_003595.3 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:26936879 C>T maps to NM_003595.3 E239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:26937529 G>A maps to NM_003595.3 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr21:10933873 C>T maps to NM_199261.2 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr21:10943003 G>A maps to NM_199261.2 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr21:10944678 C>T maps to NM_199261.2 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr21:10916457 A>C maps to NM_199261.2 Y396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr21:10934967 G>A maps to NM_199261.2 H275H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr21:10934954 G>A maps to NM_199261.2 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr21:10943003 G>A maps to NM_199261.2 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr21:10944705 G>A maps to NM_199261.2 Y176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr21:10952950 C>T maps to NM_199261.2 K82K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr21:10944678 C>T maps to NM_199261.2 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr21:10910312 G>A maps to NM_199261.2 F481F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr21:10951366 G>A maps to NM_199261.2 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr21:10933873 C>T maps to NM_199261.2 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr21:10933924 G>A maps to NM_199261.2 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr21:10934954 G>A maps to NM_199261.2 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr21:10916421 G>A maps to NM_199261.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr21:10914418 G>A maps to NM_199261.2 Q434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr21:10916421 G>A maps to NM_199261.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr21:10934954 G>A maps to NM_199261.2 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr21:10951281 G>A maps to NM_199261.2 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr21:10970042 T>A maps to NM_199261.2 K29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr21:10916421 G>A maps to NM_199261.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr21:10920106 G>A maps to NM_199261.2 Q383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr21:10934049 G>A maps to NM_199261.2 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr21:10914419 G>A maps to NM_199261.2 I433I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr21:10941910 G>A maps to NM_199261.2 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr21:10916421 G>A maps to NM_199261.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr21:10910327 C>T maps to NM_199261.2 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr21:10916472 C>T maps to NM_199261.2 K391K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr21:10916445 C>T maps to NM_199261.2 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr21:10951366 G>A maps to NM_199261.2 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:10906961 C>T maps to NM_199261.2 V533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:10910354 G>A maps to NM_199261.2 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:10941925 G>A maps to NM_199261.2 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:10951375 G>A maps to NM_199261.2 D112D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr21:10910306 C>T maps to NM_199261.2 S483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr21:10933879 G>A maps to NM_199261.2 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr21:10914442 C>G did not map to a codon.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr21:10916421 G>A maps to NM_199261.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr13:20006661 A>G maps to NM_199254.2 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr13:20048069 G>A maps to NM_199254.2 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr13:20024237 C>T maps to NM_199254.2 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr13:20000570 G>A maps to NM_199254.2 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr13:20039416 G>A maps to NM_199254.2 D218D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr13:20006664 G>A maps to NM_199254.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr13:20025322 G>A maps to NM_199254.2 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr13:20048193 G>A maps to NM_199254.2 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr13:20048069 G>A maps to NM_199254.2 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr20:30381721 C>T maps to ENST00000340513 I563I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr20:30381767 C>T maps to ENST00000340513 R579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr20:30385292 C>A maps to ENST00000340513 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr20:30380609 C>T maps to ENST00000340513 R532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr7:23555981 C>T maps to NM_013293.3 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:185638962 G>A maps to NM_004593.2 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr9:123673689 G>A maps to NM_001190945.1 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:123667327 G>A maps to NM_001190945.1 F407F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:123675968 G>A maps to NM_001190945.1 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr9:123667327 G>A maps to NM_001190945.1 F407F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:123676510 A>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:123671620 G>A maps to NM_001190945.1 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:123673734 C>T maps to NM_001190945.1 E254E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr9:139815662 C>T maps to ENST00000359662 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:139820208 C>T maps to ENST00000359662 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:139815662 C>T maps to ENST00000359662 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:103341983 G>A maps to NM_145725.2 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:103371841 C>T maps to NM_145725.2 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:103371730 C>T maps to NM_145725.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:239242626 G>A maps to NM_015650.3 K338K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:209950710 G>A maps to NM_025228.2 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:209936835 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr1:209955399 G>A did not map to a codon.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr1:209933494 C>A maps to NM_025228.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:209949038 G>A maps to NM_025228.2 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr1:209949039 G>T maps to NM_025228.2 E338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:209936437 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:209935879 A>G maps to NM_025228.2 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr1:209950782 C>T maps to NM_025228.2 C380C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr1:209933707 G>A maps to NM_025228.2 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr1:209933707 G>A maps to NM_025228.2 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:209950800 C>T maps to NM_025228.2 D386D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:209933533 G>A maps to NM_025228.2 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:209950791 G>A maps to NM_025228.2 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:209955416 G>A maps to NM_025228.2 W527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:209933707 G>A maps to NM_025228.2 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:27071153 C>T maps to NM_004295.3 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr1:211529806 C>T maps to ENST00000427925 Y125Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:211538795 C>T maps to ENST00000427925 Q270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr1:211545935 C>T maps to ENST00000427925 P533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:36511690 G>A maps to NM_145803.1 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr11:36516594 G>A maps to NM_145803.1 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:2225899 C>T maps to NM_032271.2 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:2223269 G>A maps to NM_032271.2 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:112579927 C>T maps to NM_006700.2 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr12:112578684 C>T maps to NM_006700.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:49866547 G>A maps to NM_005879.2 F466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:49878429 G>A maps to NM_005879.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr3:49877782 C>T maps to NM_005879.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:49866926 G>A maps to NM_005879.2 F417F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr3:42264730 G>A maps to NM_001042646.1 Q788Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:42264847 C>T maps to NM_001042646.1 V827V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr3:42230612 C>T maps to NM_001042646.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr3:42243951 G>C maps to NM_001042646.1 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:42242541 C>T maps to NM_001042646.1 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:42251703 C>T maps to NM_014965.3 I672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:42264535 C>T maps to NM_001042646.1 S723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr3:42244008 C>T maps to NM_001042646.1 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr3:42226208 C>T maps to NM_001042646.1 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr2:202248841 A>C maps to NM_015049.2 V687V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr2:202245709 G>A maps to NM_015049.2 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr2:202272228 G>A maps to NM_015049.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:202264131 G>A maps to NM_015049.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr4:118006336 G>A maps to NM_152402.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:118005808 C>T maps to NM_152402.2 Q247Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:118006360 C>T maps to NM_152402.2 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:118005532 C>T maps to NM_152402.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:52370482 G>A maps to NM_012288.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr3:36899475 G>A maps to NM_014831.2 F535F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr3:36893669 C>T maps to NM_014831.2 R1528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr3:36872538 C>T maps to NM_014831.2 V2801V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr3:36898704 G>A maps to NM_014831.2 I792I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:36873774 G>A maps to NM_014831.2 F2389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr3:36898029 C>T maps to NM_014831.2 V1017V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr3:36874581 C>T maps to NM_014831.2 V2120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:36893245 A>G maps to NM_014831.2 D1573D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:36899217 C>T maps to NM_014831.2 G621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr3:36898685 G>A maps to NM_014831.2 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr3:36873795 G>A maps to NM_014831.2 Y2382Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:36897936 C>T maps to NM_014831.2 K1048K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr3:36899217 C>T maps to NM_014831.2 G621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:36874176 G>A maps to NM_014831.2 S2255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:36899453 G>A maps to NM_014831.2 Q543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:36872702 C>A maps to NM_014831.2 E2747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:36875009 G>A maps to NM_014831.2 Q1978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:36880177 A>T maps to NM_014831.2 G1726G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:36896894 G>A maps to NM_014831.2 Q1396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:36873231 C>T maps to NM_014831.2 V2570V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr3:36872667 C>T maps to NM_014831.2 R2758R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr3:36872817 C>T maps to NM_014831.2 R2708R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:36872496 G>A maps to NM_014831.2 I2815I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:36897177 C>T maps to NM_014831.2 L1301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:36898641 C>T maps to NM_014831.2 K813K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:36872577 C>T maps to NM_014831.2 V2788V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:36896922 G>A maps to NM_014831.2 S1386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:36898680 C>T maps to NM_014831.2 K800K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:36871142 C>T maps to NM_014831.2 A2863A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:36872568 C>T maps to NM_014831.2 Q2791Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:36873708 G>A maps to NM_014831.2 L2411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:36898644 C>T maps to NM_014831.2 K812K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:36873993 C>T maps to NM_014831.2 R2316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr3:36898890 C>T maps to NM_014831.2 P730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:36873699 G>A maps to NM_014831.2 F2414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:36888714 G>A maps to NM_014831.2 L1626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr3:36873579 C>T maps to NM_014831.2 K2454K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:36896952 C>T maps to NM_014831.2 R1376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:36874140 G>A maps to NM_014831.2 I2267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr3:36899019 G>A maps to NM_014831.2 C687C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr3:36898458 G>A maps to NM_014831.2 I874I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:36898965 G>A maps to NM_014831.2 F705F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr3:36897033 G>A maps to NM_014831.2 S1349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:36898194 C>T maps to NM_014831.2 R962R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:36897003 G>A maps to NM_014831.2 S1359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:36874254 G>A maps to NM_014831.2 F2229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:36872802 C>T maps to NM_014831.2 G2713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr3:36873588 C>T maps to NM_014831.2 K2451K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr3:36874734 G>A maps to NM_014831.2 C2069C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr3:36872550 G>A maps to NM_014831.2 F2797F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:36873264 G>A maps to NM_014831.2 C2559C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:36873660 C>T maps to NM_014831.2 W2427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:36874347 G>A maps to NM_014831.2 F2198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:36884181 G>A maps to NM_014831.2 F1693F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:36893236 G>A maps to NM_014831.2 L1576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:36893669 C>T maps to NM_014831.2 R1528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:36893797 G>A maps to NM_014831.2 Q1486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:36897017 G>A maps to NM_014831.2 Q1355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:36897081 C>T maps to NM_014831.2 G1333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:36897585 G>A maps to NM_014831.2 F1165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:36898762 C>T maps to NM_014831.2 W773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:36873840 C>T maps to NM_014831.2 E2367E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:36874008 C>T maps to NM_014831.2 E2311E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:36874401 C>T maps to NM_014831.2 S2180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:36874635 C>T maps to NM_014831.2 L2102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:36880168 C>T maps to NM_014831.2 E1729E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr3:36897939 C>T maps to NM_014831.2 W1047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:36873936 C>T maps to NM_014831.2 R2335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:36897321 C>T maps to NM_014831.2 V1253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr16:3727656 G>T maps to NM_016292.2 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:3725372 G>A maps to NM_016292.2 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr21:45503143 C>T maps to NM_003274.4 T733T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr21:45483584 C>A maps to NM_003274.4 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:45518269 C>T maps to NM_003274.4 P1067P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr21:45483518 G>A maps to NM_003274.4 Q297Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr21:45523369 C>T maps to NM_003274.4 I1246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr21:45518269 C>T maps to NM_003274.4 P1067P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:45472165 C>T maps to NM_003274.4 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr21:45475629 C>T maps to NM_003274.4 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr21:45522839 C>T maps to NM_003274.4 S1176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr16:88926377 C>T maps to NM_016209.3 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:88925145 C>T maps to NM_016209.3 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:36603447 G>A maps to NM_014408.3 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:118889680 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr19:45668146 G>A maps to NM_024108.1 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:45668209 C>T maps to NM_024108.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr8:141445256 G>A maps to NM_031466.5 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr8:141231632 G>A maps to NM_031466.5 V925V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr8:141301105 G>A maps to NM_031466.5 R712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:140922486 C>T maps to NM_031466.5 E1054E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr8:141460941 A>C maps to NM_031466.5 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:141297806 G>A maps to NM_031466.5 F725F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr8:141301105 G>A maps to NM_031466.5 R712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr8:140922495 G>A maps to NM_031466.5 S1051S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr8:140744260 G>A maps to NM_031466.5 T1178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr8:141321399 G>A maps to NM_031466.5 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:141461202 C>T maps to NM_031466.5 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr8:141231632 G>A maps to NM_031466.5 V925V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:141370272 A>C maps to NM_031466.5 A555A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:141449222 G>A maps to NM_031466.5 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr8:141034146 G>C maps to NM_031466.5 Y960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr8:141321351 G>A maps to NM_031466.5 I637I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:108572543 G>A maps to NM_016388.2 Q127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr3:108572537 G>A maps to NM_016388.2 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:108568079 G>A maps to NM_016388.2 Q94Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr6:123673699 G>A maps to NM_006073.2 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr6:123542638 C>T maps to NM_006073.2 K681K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr11:118532426 C>T maps to ENST00000264029 W179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:118533870 C>T maps to ENST00000264029 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:41250187 C>T maps to NM_018643.2 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr6:41248703 G>A maps to NM_018643.2 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:41250361 C>T maps to NM_018643.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr6:41250297 G>A maps to NM_018643.2 Q81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr6:41254360 C>T maps to NM_018643.2 W11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:41129229 C>T maps to NM_018965.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr6:41129025 C>T maps to NM_018965.2 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr6:41121580 C>T maps to NM_178174.2 E97E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr6:41122008 G>A maps to NM_178174.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr6:41117416 C>T maps to NM_178174.2 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:41121768 G>A maps to NM_178174.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr6:41119030 C>T maps to NM_178174.2 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr6:41166096 G>A maps to ENST00000373108 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:41165970 C>T maps to ENST00000373108 Q143Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:41165885 G>A maps to ENST00000373108 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr6:41165886 G>A maps to ENST00000373108 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:41160569 G>A maps to ENST00000373108 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr6:41162266 G>A maps to ENST00000373108 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:41165886 G>A maps to ENST00000373108 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:41166045 C>T maps to ENST00000373108 R118R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D3-A3MU-06A-11D-A21A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr6:41204223 G>A maps to NM_198153.2 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:41204269 C>T maps to NM_198153.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:41204222 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr6:42204017 G>A maps to NM_033502.2 P997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr6:42227382 G>T maps to NM_033502.2 R655R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:42233511 G>A maps to NM_033502.2 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:42237005 C>T maps to NM_033502.2 W108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:42231057 G>A maps to NM_033502.2 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:42196394 C>T maps to NM_033502.2 K1097K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:42227386 C>T maps to NM_033502.2 K653K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:42236395 C>T maps to NM_033502.2 Q311Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:42211042 G>A maps to NM_033502.2 I934I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:42236590 C>T maps to NM_033502.2 Q246Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr6:42236209 G>A maps to NM_033502.2 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:42196397 G>A maps to NM_033502.2 F1096F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:42225910 G>A maps to NM_033502.2 V766V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:42236190 G>A maps to NM_033502.2 Q380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:42196220 G>A maps to NM_033502.2 P1155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:42227359 G>A maps to NM_033502.2 F662F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:48508521 C>T maps to NM_016381.3 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:72680646 A>G maps to NM_013381.2 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr12:73046805 C>T maps to NM_013381.2 L907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr12:73015510 G>A maps to NM_013381.2 W840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr12:72680607 C>T maps to NM_013381.2 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr12:73015525 G>A maps to NM_013381.2 R845R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:73046835 C>T maps to NM_013381.2 Q917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:73046125 C>T maps to NM_013381.2 I855I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr12:72936120 C>T maps to NM_013381.2 F546F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr12:72956809 C>T maps to NM_013381.2 Q633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:73015525 G>A maps to NM_013381.2 R845R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr12:73015525 G>A maps to NM_013381.2 R845R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr12:73056944 C>T maps to NM_013381.2 F1015F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:72969125 G>A maps to NM_013381.2 R696R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:72680598 G>A maps to NM_013381.2 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr12:72969050 T>C maps to NM_013381.2 T671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr12:73056944 C>T maps to NM_013381.2 F1015F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr12:73046173 C>T maps to NM_013381.2 F871F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:72969147 C>T maps to NM_013381.2 Q704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr12:73056944 C>T maps to NM_013381.2 F1015F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr12:73012703 G>A maps to NM_013381.2 E740E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:73046897 G>A maps to NM_013381.2 W937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr12:72969158 G>A maps to NM_013381.2 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:73046188 C>T maps to NM_013381.2 F876F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr12:72893288 G>A maps to NM_013381.2 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:72667226 G>A maps to NM_013381.2 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:73056941 T>C maps to NM_013381.2 L1014L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:73046897 G>A maps to NM_013381.2 W937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:72893402 C>T maps to NM_013381.2 I525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr8:110131306 C>T maps to NM_003301.4 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr8:110100286 G>A maps to NM_003301.4 K182K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:110131461 G>A maps to NM_003301.4 Q325Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:110131615 C>T maps to NM_003301.4 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr8:110131323 G>A maps to NM_003301.4 W279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr8:110100268 G>A maps to NM_003301.4 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:110100442 G>A maps to NM_003301.4 W234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:110100442 G>A maps to NM_003301.4 W234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:110100441 G>A maps to NM_003301.4 W234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr8:110131467 C>T maps to NM_003301.4 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr8:110131374 C>T maps to NM_003301.4 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr8:110131452 C>T maps to NM_003301.4 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr8:110131682 G>A maps to NM_003301.4 *399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr8:110100012 G>A maps to NM_003301.4 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr8:110100523 G>A maps to NM_003301.4 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr8:110100121 C>T maps to NM_003301.4 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:110131615 C>T maps to NM_003301.4 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr8:110100172 G>A maps to NM_003301.4 K144K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr8:110100523 G>A maps to NM_003301.4 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr8:126448442 C>T maps to NM_025195.2 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr8:126445566 C>T maps to NM_025195.2 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr2:12858522 A>T maps to NM_021643.3 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:12863678 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:368792 C>T maps to ENST00000422053 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr6:30128479 C>T maps to NM_006778.3 E52E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:30128311 G>A maps to NM_006778.3 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr6:30128512 G>A maps to NM_006778.3 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:30121958 G>A maps to NM_006778.3 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr6:30124758 G>A maps to NM_006778.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr6:30128350 C>T maps to NM_006778.3 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:30126364 G>A maps to NM_006778.3 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:228588892 C>T maps to NM_145214.2 K169K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:228582615 G>A maps to NM_145214.2 D399D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr1:228588736 C>T maps to NM_145214.2 Q221Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr1:228582666 G>A maps to NM_145214.2 F382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr9:100857227 G>A maps to NM_033219.1 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:100857248 G>A maps to NM_033219.1 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr9:100862239 C>T maps to NM_033219.1 Q170Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr9:100857209 C>T maps to NM_033219.1 K213K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:30136160 C>T maps to NM_033229.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:30134963 G>A maps to NM_033229.2 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:30140005 G>A maps to NM_033229.2 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr6:30136169 C>T maps to NM_033229.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:30136174 G>A maps to NM_033229.2 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr6:30136261 G>A maps to NM_033229.2 K221K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr6:30131815 C>T maps to NM_033229.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:30134963 G>A maps to NM_033229.2 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:30138785 G>A did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr6:30138388 C>T maps to NM_033229.2 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr17:15532108 G>A maps to NM_006470.3 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr17:15532009 C>T maps to NM_006470.3 K538K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr17:15539400 C>T maps to ENST00000455584 K280K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr17:18638496 G>A maps to NM_001037330.1 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:18638484 C>T maps to NM_001037330.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:228596849 C>T maps to NM_001134855.1 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:228596249 G>A maps to NM_016102.3 D362D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr1:228596849 C>T maps to NM_001134855.1 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:154216661 C>T maps to NM_015271.3 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:154197218 C>T maps to NM_015271.3 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr4:154197098 C>T maps to NM_015271.3 C90C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:154191563 A>G maps to NM_015271.3 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr11:4407075 G>A maps to NM_003141.3 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:4406759 G>A maps to NM_003141.3 Q395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:4411333 G>A maps to NM_003141.3 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr11:4411507 C>T maps to NM_003141.3 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:4406949 G>A maps to NM_003141.3 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:4410967 C>T maps to NM_003141.3 Q140Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:5729475 C>T maps to NM_006074.4 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:5730835 G>A maps to NM_006074.4 W485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr11:5719670 C>T maps to NM_006074.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr11:5719636 G>A maps to NM_006074.4 K204K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5730806 C>T maps to NM_006074.4 R476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5730826 C>T maps to NM_006074.4 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr11:5730874 C>T maps to NM_006074.4 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr5:64913953 G>A maps to NM_001656.3 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr5:64906723 G>A maps to NM_001656.3 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:138239557 C>T maps to NM_015905.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:138235854 C>T maps to NM_015905.2 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr7:138268671 C>T maps to NM_015905.2 S957S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:138235914 C>T maps to NM_015905.2 I417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:138239656 T>C maps to NM_015905.2 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:54969162 G>A maps to NM_005082.4 V597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr17:54990974 G>A maps to NM_005082.4 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:54972921 G>A maps to NM_005082.4 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr6:30164358 G>A maps to NM_003449.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr6:30166463 C>T maps to NM_003449.3 E139E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:30166565 G>A maps to NM_003449.3 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr6:30164462 G>A maps to NM_003449.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:30166829 G>A maps to NM_003449.3 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:28887959 G>A maps to NM_006510.4 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:28872104 G>A maps to NM_006510.4 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:28888010 G>A maps to NM_006510.4 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:28872398 G>A maps to NM_006510.4 I330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr6:28876587 G>A maps to NM_006510.4 Q306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr19:59061521 C>T maps to NM_005762.2 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr19:59059886 A>C maps to NM_005762.2 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr19:59060876 A>G maps to NM_005762.2 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr19:59059686 C>T maps to NM_005762.2 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr11:119993695 G>A maps to NM_012101.3 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr11:120008349 G>A maps to NM_012101.3 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr11:120008046 C>T maps to NM_012101.3 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:120008367 C>T maps to NM_012101.3 K124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr11:120008369 T>A maps to NM_012101.3 K124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:119991311 C>T maps to NM_012101.3 Q499Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:119986102 C>T maps to NM_012101.3 R549R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:120008529 G>A maps to NM_012101.3 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:119998142 C>T maps to NM_012101.3 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:119998048 G>A maps to NM_012101.3 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:6472140 G>A maps to NM_033278.2 A617A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr11:6477303 G>A maps to NM_033278.2 Q511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:6477300 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:6478606 G>A maps to NM_033278.2 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr11:6472625 G>A maps to NM_033278.2 R526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:6472638 G>A maps to NM_033278.2 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr11:6477533 G>A maps to NM_033278.2 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:6477914 G>A maps to NM_033278.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr11:6477848 C>T maps to NM_033278.2 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:6477539 G>A maps to NM_033278.2 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:6479041 G>A maps to NM_033278.2 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr6:30078326 C>T maps to NM_007028.3 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr6:30079498 G>A maps to NM_007028.3 Q147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:30080207 G>A maps to NM_007028.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr6:30071942 C>T maps to NM_007028.3 W320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:30076813 G>A maps to NM_007028.3 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:30078326 C>T maps to NM_007028.3 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr6:30079499 G>A maps to NM_007028.3 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr6:30071528 A>T maps to NM_007028.3 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:30075857 G>A maps to NM_007028.3 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr9:119461790 C>T maps to NM_012210.3 I590I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr1:114952901 G>A maps to NM_015906.3 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr1:114940388 A>G maps to NM_015906.3 L1089L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:114973460 C>A maps to NM_015906.3 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr1:115006055 G>A maps to NM_015906.3 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:114942114 G>A maps to NM_015906.3 V1028V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr11:5664746 C>T maps to NM_001003819.3 S779S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:5655113 G>A maps to NM_001003819.3 E522E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:5655032 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:5664812 C>T maps to NM_001003819.3 F801F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:5664746 C>T maps to NM_001003819.3 S779S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5655065 G>A maps to NM_001003819.3 K506K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5664386 G>A maps to NM_001003819.3 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5664530 G>A maps to NM_001003819.3 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:27145285 G>A maps to NM_171982.3 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr8:27145102 G>A maps to NM_171982.3 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:27145561 G>A maps to NM_171982.3 Y329Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr8:27151620 C>T maps to NM_171982.3 K246K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:27168521 G>A maps to NM_171982.3 N77N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr5:114462241 T>C maps to NM_018700.3 E715E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:114466464 G>A maps to NM_018700.3 I552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr17:57125122 G>A maps to NM_015294.3 Q530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:57134297 G>A maps to NM_015294.3 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:57094719 G>A maps to NM_015294.3 R775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:57168658 A>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:57168659 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:57134353 G>A maps to NM_015294.3 R361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr6:25983437 C>T maps to NM_006355.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:25973439 C>T maps to NM_006355.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr6:30309585 C>T maps to NM_021253.3 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:30298622 C>T maps to NM_021253.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr7:99490187 G>A maps to NM_033017.3 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:99506318 C>T maps to NM_033017.3 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:99489851 G>A maps to NM_033017.3 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:30105148 C>T maps to ENST00000376724 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr6:30114950 A>C maps to ENST00000376724 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr3:140407149 C>T maps to NM_152616.4 F542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:140407032 C>T maps to NM_152616.4 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:140401984 C>T maps to NM_152616.4 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:140407356 G>A maps to NM_152616.4 Q611Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:140406822 C>T maps to NM_152616.4 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:140409952 C>T maps to NM_152616.4 N668N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:140401660 C>T maps to NM_152616.4 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr11:35706841 C>T maps to NM_017583.4 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:35685315 T>C maps to NM_017583.4 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr11:35685279 C>T maps to NM_017583.4 H207H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr1:117654929 G>A maps to NM_025188.3 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:117658247 C>T maps to NM_025188.3 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:155154622 C>T maps to NM_025058.3 P628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:155156338 C>T maps to NM_025058.3 F651F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr1:155149756 G>A maps to NM_025058.3 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr1:155150686 A>T maps to NM_025058.3 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:155156497 C>T maps to NM_025058.3 F704F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:155148664 C>T maps to NM_025058.3 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr17:73870971 G>A maps to NM_033452.2 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:73872105 G>A maps to NM_033452.2 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:55032549 G>A maps to ENST00000357530 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:55032678 G>A maps to ENST00000357530 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:55036747 G>A maps to ENST00000357530 Q187Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:55032588 G>A maps to ENST00000357530 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:55032624 C>T maps to ENST00000357530 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:89537427 C>T maps to NM_020358.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:89531570 C>T maps to NM_020358.2 R362R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr11:5686458 G>A maps to NM_033034.2 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:5686227 C>T maps to NM_033034.2 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:72727132 G>A maps to NM_178125.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:72732988 C>T maps to NM_178125.2 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:72738545 G>A maps to NM_178125.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr7:72730582 G>A maps to NM_178125.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:72738611 C>T maps to NM_178125.2 Q58Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr2:27505712 G>A maps to NM_032546.3 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:27505661 G>A maps to NM_032546.3 E21E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:27528495 G>A maps to NM_032546.3 E260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:27528633 G>A maps to NM_032546.3 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr8:67047248 C>T maps to NM_184085.1 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr8:67062107 C>T maps to NM_184085.1 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr8:67040681 C>T maps to NM_184085.1 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:67047233 G>A maps to NM_184085.1 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr8:67039667 C>T maps to NM_184085.1 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr8:67039646 G>A maps to NM_184085.1 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr8:67047380 G>A maps to NM_184085.1 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr8:67040672 G>A maps to NM_184085.1 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr8:67049400 G>A maps to NM_184085.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:67039547 G>A maps to NM_184085.1 Q15Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:67064771 G>A maps to NM_184085.1 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:67066475 G>A maps to NM_184085.1 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr7:100730826 C>T maps to NM_030961.1 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr7:100731198 C>T maps to NM_030961.1 C202C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr7:100732119 G>A maps to NM_030961.1 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr7:100732536 C>T maps to NM_030961.1 F648F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:100730826 C>T maps to NM_030961.1 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:100730623 C>T maps to NM_030961.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:248039286 G>A maps to NM_015431.3 W319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:248028152 G>A maps to NM_015431.3 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr1:248039676 C>T maps to NM_015431.3 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr1:248039235 G>A maps to NM_015431.3 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr1:248039676 C>T maps to NM_015431.3 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:248028005 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248031354 G>A maps to NM_015431.3 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:248039285 G>A maps to NM_015431.3 W319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:5625834 C>T maps to NM_001003819.3 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:5626583 G>A maps to NM_001003819.3 E207E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:5632082 G>A maps to ENST00000380109 V362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:5632313 G>A maps to ENST00000380109 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:5631788 G>A maps to NM_001003819.3 W328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5626742 G>A maps to NM_001003819.3 E260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:165961961 G>A maps to NM_152620.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:165961310 C>T maps to NM_152620.2 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr4:165962308 G>A maps to NM_152620.2 W362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr4:165962459 C>T maps to NM_152620.2 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:165890965 C>T maps to NM_001012414.2 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr4:165890998 G>A maps to NM_001012414.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr1:33625296 C>G maps to NM_018207.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:33623902 G>A maps to NM_018207.2 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:33625344 C>T maps to NM_018207.2 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:33613050 G>A maps to NM_018207.2 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:26393829 G>A maps to NM_032588.2 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr17:73887945 G>A maps to NM_173547.2 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr1:231339622 C>T maps to NM_001004342.3 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:231342408 C>T maps to NM_001004342.3 V564V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:231339635 C>T maps to NM_001004342.3 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:231333209 C>T maps to NM_001004342.3 Q380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr1:231335967 G>A maps to NM_001004342.3 E446E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr1:231344873 C>T maps to NM_001004342.3 A667A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:4622012 G>A maps to NM_018073.5 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:4621529 G>A maps to NM_018073.5 I478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:4626488 G>A maps to NM_018073.5 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr11:4621724 G>A maps to NM_018073.5 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:4621925 G>A maps to NM_018073.5 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:45047123 C>T maps to NM_182985.3 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:45050925 G>A maps to NM_182985.3 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr15:45050925 G>A maps to NM_182985.3 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:45050877 C>T maps to NM_182985.3 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr15:45050850 C>T maps to NM_182985.3 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr5:180625699 C>T maps to NM_203293.1 K326K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:180622588 C>T maps to NM_203293.1 Q371Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr5:180622599 C>A maps to NM_203293.1 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr5:180625726 C>T maps to NM_203293.1 K317K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:180625717 G>T maps to NM_203293.1 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr3:32932225 T>G maps to NM_001039111.1 Y510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:32927433 C>T maps to NM_001039111.1 I343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr3:32932855 G>A maps to NM_001039111.1 R720R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:32933206 C>G maps to NM_001039111.1 G837G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr3:32859583 C>T maps to NM_001039111.1 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:32932693 G>A maps to NM_001039111.1 R666R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:32915323 C>T maps to NM_001039111.1 Y289Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:32933285 C>T maps to NM_001039111.1 R864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:32932741 C>T maps to NM_001039111.1 F682F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:32931958 C>T maps to NM_001039111.1 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:32932654 C>T maps to NM_001039111.1 F653F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:32932741 C>T maps to NM_001039111.1 F682F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:32932654 C>T maps to NM_001039111.1 F653F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:32932198 G>A maps to NM_001039111.1 K501K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:32931961 G>A maps to NM_001039111.1 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr3:32932555 C>T maps to NM_001039111.1 I620I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:32932624 C>T maps to NM_001039111.1 F643F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:32932586 C>T maps to NM_001039111.1 Q631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr3:32915399 C>T maps to NM_001039111.1 Q315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:32927475 G>A maps to NM_001039111.1 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:32932942 C>T maps to NM_001039111.1 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:31230828 G>T maps to NM_001008274.3 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:31234237 G>A maps to NM_001008274.3 W277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:31234159 C>T maps to NM_001008274.3 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:31230641 G>A maps to NM_001008274.3 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:31232215 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr7:75028288 G>A maps to ENST00000430211 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr10:104414851 C>T maps to NM_030912.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:104404679 C>T maps to NM_030912.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:51464870 C>T maps to ENST00000338969 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr4:189068081 G>A maps to NM_178556.3 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:189068456 C>T maps to NM_178556.3 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr4:189068222 C>T maps to NM_178556.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr4:189063464 C>T maps to NM_178556.3 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr4:189068195 G>A maps to NM_178556.3 K359K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:189060820 C>T maps to NM_178556.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:189068222 C>T maps to NM_178556.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:189060888 C>T maps to NM_178556.3 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:189060972 G>A maps to NM_178556.3 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:189068213 G>A maps to NM_178556.3 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr4:189061056 C>T maps to NM_178556.3 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:189068051 G>A maps to NM_178556.3 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr4:189068015 C>T maps to NM_178556.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:189068477 G>T maps to NM_178556.3 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:189068216 G>A maps to NM_178556.3 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:189063545 G>A maps to NM_178556.3 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr4:189068015 C>T maps to NM_178556.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr4:189061764 G>A maps to NM_178556.3 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr4:189068189 C>T maps to NM_178556.3 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:189065208 C>T maps to NM_178556.3 Q260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:189068246 C>T maps to NM_178556.3 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr4:189061020 G>A maps to NM_178556.3 K103K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr4:189064990 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:189022257 C>T maps to ENST00000326754 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:189022262 G>A maps to ENST00000326754 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:189020257 G>A maps to ENST00000326754 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr4:189012754 G>A maps to ENST00000326754 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:189012772 G>A maps to ENST00000326754 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:189026056 C>T maps to ENST00000326754 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:189012973 G>A maps to ENST00000326754 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:189022257 C>T maps to ENST00000326754 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr4:189012604 G>A maps to ENST00000326754 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr4:189020236 G>A maps to ENST00000326754 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:189012652 G>A maps to ENST00000326754 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:189020233 C>T maps to ENST00000326754 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:189022398 C>T maps to ENST00000326754 E47E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr4:189012766 C>T maps to ENST00000326754 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr4:189022317 G>A maps to ENST00000326754 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr5:14488281 C>T maps to NM_007118.2 R2515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr5:14369481 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:14488206 C>T maps to NM_007118.2 P2490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:14477056 C>T maps to NM_007118.2 S2046S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:14369568 T>A maps to NM_007118.2 S1051S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:14369625 C>T maps to NM_007118.2 F1070F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:14488203 C>T maps to NM_007118.2 I2489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:14387900 C>A maps to NM_007118.2 R1276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr5:14488290 C>T maps to NM_007118.2 A2518A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr5:14482698 C>T maps to NM_007118.2 I2158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr5:14304661 C>T maps to NM_007118.2 H487H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:14387672 C>T maps to NM_007118.2 L1233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:14508314 C>T maps to NM_007118.2 F3026F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:14336793 C>T maps to NM_007118.2 I668I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr5:14488215 C>T maps to NM_007118.2 P2493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:14367009 C>T maps to NM_007118.2 A932A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:14492704 C>T maps to NM_007118.2 S2554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:14498702 C>T maps to NM_007118.2 V2762V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:14508474 C>T maps to NM_007118.2 R3080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr5:14363863 G>A maps to NM_007118.2 W805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr22:38131087 G>A maps to NM_001039141.2 W1582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr22:38119693 C>T maps to NM_001039141.2 N377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr22:38121817 C>T maps to NM_001039141.2 F1085F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr22:38119354 G>A maps to NM_001039141.2 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:38121451 C>T maps to NM_001039141.2 S963S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr22:38121190 G>A maps to NM_001039141.2 E876E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:38120902 C>T maps to NM_001039141.2 T780T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr22:38121733 C>T maps to NM_001039141.2 P1057P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:38119784 C>T maps to NM_001039141.2 Q408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr22:38121279 G>A maps to NM_001039141.2 W906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr22:38122339 G>A maps to NM_001039141.2 G1259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr22:38153677 C>T maps to NM_001039141.2 L1916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr22:38120371 C>T maps to NM_001039141.2 A603A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr22:38120218 C>T maps to NM_001039141.2 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:38119319 C>T maps to NM_001039141.2 R253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:38121670 C>T maps to NM_001039141.2 D1036D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:38121881 C>T maps to NM_001039141.2 Q1107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr22:38130866 G>A maps to NM_001039141.2 K1508K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr22:38130440 C>T maps to NM_001039141.2 T1366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr22:38121704 G>T maps to NM_001039141.2 E1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr22:38121881 C>T maps to NM_001039141.2 Q1107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr22:38120386 C>T maps to NM_001039141.2 P608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr22:38150943 C>T maps to NM_001039141.2 L1814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:38120287 C>T maps to NM_001039141.2 P575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:38120833 C>T maps to NM_001039141.2 S757S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:38121502 C>T maps to NM_001039141.2 S980S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:38121862 C>T maps to NM_001039141.2 S1100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:38120920 C>T maps to NM_001039141.2 A786A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:6741256 G>T maps to ENST00000313244 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr19:6750052 G>A maps to ENST00000313244 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:6742980 C>T maps to ENST00000313244 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr14:92470029 G>A maps to NM_004239.3 F1430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:92484037 T>C maps to NM_004239.3 Q215Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr14:92441596 G>A maps to NM_004239.3 F1792F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U9-06A-11D-A32N-08 chr14:92461741 A>G maps to NM_004239.3 A1670A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr2:230636270 G>A maps to ENST00000389044 F1897F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr2:230652367 G>A maps to ENST00000389044 F1589F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:230660028 G>A maps to ENST00000389044 P1251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr2:230675851 C>T maps to ENST00000389044 E685E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:230661345 G>A maps to ENST00000389044 I1232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:230656936 C>A maps to ENST00000389044 G1356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr2:230654431 A>T maps to ENST00000389044 I1503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr5:901522 G>A maps to NM_004237.3 W171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr5:916027 G>A maps to NM_004237.3 E381E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:896821 C>T maps to NM_004237.3 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:917202 T>C maps to NM_004237.3 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:64701932 C>T maps to NM_016213.4 R317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr7:100466485 C>T maps to NM_003302.2 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:40310295 G>A maps to ENST00000316891 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr1:40310204 G>A maps to ENST00000316891 Q372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:40349010 G>A maps to ENST00000316891 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr19:13216332 G>A maps to NM_001136035.2 A557A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:13226253 C>T maps to NM_001136035.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:13220600 G>A maps to NM_001136035.2 H386H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr19:13226813 G>A maps to NM_001136035.2 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr6:126359915 C>T maps to NM_001031712.2 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:125463293 C>T maps to NM_017956.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr22:20102126 G>A maps to ENST00000439169 T401T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:100290672 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:100291998 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:100291973 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr23:100278592 A>G did not map to a codon.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr23:100292914 A>T did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr14:61446309 C>T maps to NM_020810.2 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr14:61446560 G>A maps to NM_020810.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:5923406 G>A maps to NM_015939.3 Y231Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr20:5927166 G>A maps to NM_015939.3 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:29074030 G>A maps to NM_017910.3 Q407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr22:46752824 C>T maps to NM_018006.4 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr22:46748034 C>T maps to NM_018006.4 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A197-06A-32D-A197-08 chr1:28904081 C>T maps to NM_017846.4 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:54954168 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:54951461 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr23:54956859 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:54956371 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr23:54956309 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:54949022 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:54957176 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:54951461 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:54956548 C>G did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:54957760 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:54952869 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:54955514 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:54955729 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr23:54957314 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:54957745 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:54957351 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:54951461 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:54955913 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:54956500 C>T did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr12:49721109 C>T maps to NM_005480.3 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:49723654 C>A maps to NM_005480.3 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:193045022 C>T maps to NM_004600.5 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:142455374 G>A maps to ENST00000476941 Q109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:142496492 C>T maps to ENST00000476941 R218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:142523419 G>A maps to ENST00000476941 W701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:142503748 C>T maps to ENST00000476941 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:122853842 G>A maps to NM_001130698.1 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr4:122831408 G>A maps to NM_001130698.1 F564F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:122833182 G>A maps to NM_001130698.1 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:122854175 G>A maps to NM_001130698.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr4:122820790 A>T maps to NM_001130698.1 I841I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:122835985 G>A maps to NM_001130698.1 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr4:122831396 C>T maps to NM_001130698.1 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:122854052 G>A maps to NM_001130698.1 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr4:122854148 C>T maps to NM_001130698.1 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:122854037 G>A maps to NM_001130698.1 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr4:122835991 G>A maps to NM_001130698.1 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr4:122835949 G>A maps to NM_001130698.1 I442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:122846349 C>T maps to NM_001130698.1 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:122836060 C>T maps to NM_001130698.1 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:122853692 C>T maps to NM_001130698.1 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:122853809 C>T maps to NM_001130698.1 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:122854193 G>A maps to NM_001130698.1 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:122854061 G>A maps to NM_001130698.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr4:122835985 G>A maps to NM_001130698.1 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr13:38211474 C>T maps to NM_003306.1 Q838Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr13:38237677 G>A maps to NM_003306.1 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr13:38213254 C>T maps to NM_003306.1 R716R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:38211735 G>A maps to NM_003306.1 F751F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr13:38225575 C>T maps to NM_003306.1 W635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr13:38211447 G>A maps to NM_003306.1 I847I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr13:38225437 C>T maps to NM_003306.1 K681K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:38211198 C>T maps to NM_003306.1 K930K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:38357146 G>A maps to NM_003306.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:38357416 G>A maps to NM_003306.1 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr13:38211282 C>T maps to NM_003306.1 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr13:38357407 C>T maps to NM_003306.1 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr13:38266445 C>T maps to NM_003306.1 Q308Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr13:38320169 G>A maps to NM_003306.1 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr13:38237700 G>A maps to NM_003306.1 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr13:38320462 G>A maps to NM_003306.1 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr13:38320169 G>A maps to NM_003306.1 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr13:38266405 T>G maps to NM_003306.1 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr13:38248493 C>T maps to NM_003306.1 W415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr13:38266367 G>A maps to NM_003306.1 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:38237608 C>T maps to NM_003306.1 T544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:38237700 G>A maps to NM_003306.1 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr13:38357221 C>T maps to NM_003306.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr13:38237761 G>A maps to NM_003306.1 I493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr13:38225593 G>A maps to NM_003306.1 D629D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr20:33592284 G>A maps to NM_015638.2 I675I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr20:33593573 G>A maps to NM_015638.2 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr23:111020193 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr23:111156001 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:111078214 G>T did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr23:111090630 T>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:111019940 G>A did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:111090649 A>T did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:111090376 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:111155754 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:111155755 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:111078195 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:111155629 C>T did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:111195413 C>T did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:111195504 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:111025180 G>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:111155589 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr23:111097217 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr23:111090481 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr23:111095587 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr23:111020102 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr23:111155740 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr23:111097262 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:111155952 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:111090434 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:111090414 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:111097281 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:111195329 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:111097060 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:111095550 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:111155952 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:111020050 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:111195441 C>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:111155952 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:111155742 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:111155952 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:111020230 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr23:111155628 C>T did not map to a codon.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr23:111155614 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr23:111090511 C>T did not map to a codon.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr23:111019566 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr23:111090557 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:111025245 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:111078148 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:111090582 T>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:111090595 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:111097298 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:111195316 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:111195389 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:111020118 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:111078261 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:111155559 G>A did not map to a codon.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr23:111020089 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:111090642 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:111090643 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr23:111025281 A>T did not map to a codon.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr23:111022255 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr11:101347110 C>T maps to NM_004621.5 Q555Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr11:101375405 C>T maps to NM_004621.5 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr11:101344499 C>T maps to NM_004621.5 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:101347221 G>A maps to NM_004621.5 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr11:101340232 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr11:101375174 C>T maps to NM_004621.5 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr11:101375366 G>A maps to NM_004621.5 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:101347197 C>T maps to NM_004621.5 W526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr11:101374913 C>T maps to NM_004621.5 Q262Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:101343008 C>T maps to NM_004621.5 V688V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr11:101347071 C>T maps to NM_004621.5 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr11:101374880 C>T maps to NM_004621.5 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr11:101375471 C>T maps to NM_004621.5 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:101344499 C>T maps to NM_004621.5 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:101359739 G>A maps to NM_004621.5 F407F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:101362288 T>A maps to NM_004621.5 K376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr11:101375291 G>A maps to NM_004621.5 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:101344484 G>A maps to NM_004621.5 P588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr11:101375455 G>A maps to NM_004621.5 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr5:135692529 G>A maps to NM_020389.2 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr5:135561736 C>T maps to NM_020389.2 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr5:135692538 G>A maps to NM_020389.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr5:135692571 G>A maps to NM_020389.2 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:135651455 C>T maps to NM_020389.2 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:135692538 G>A maps to NM_020389.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr5:135551957 G>A maps to NM_020389.2 I783I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:135587469 G>A maps to NM_020389.2 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:135692967 C>T maps to NM_020389.2 K36K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:135602061 G>A maps to NM_020389.2 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:135583172 G>A maps to NM_020389.2 N610N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:135583382 C>T maps to NM_020389.2 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr5:135583367 C>T maps to NM_020389.2 A545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:135561042 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:135692538 G>A maps to NM_020389.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr5:135692901 C>T maps to NM_020389.2 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:135587503 C>T maps to NM_020389.2 W471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr5:135693066 C>T maps to NM_020389.2 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:135602049 T>C maps to NM_020389.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:135583274 C>T maps to NM_020389.2 V576V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:135610432 G>A maps to NM_020389.2 F352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr5:135692622 G>A maps to NM_020389.2 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr5:135692997 G>A maps to NM_020389.2 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:135692877 G>A maps to NM_020389.2 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:135692538 G>A maps to NM_020389.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:135561027 C>T maps to NM_020389.2 Q759Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:135561039 C>T maps to NM_020389.2 K755K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:135587421 C>T maps to NM_020389.2 E498E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:135692568 G>A maps to NM_020389.2 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:135693066 C>T maps to NM_020389.2 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr5:135692373 G>A maps to NM_020389.2 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr5:135692712 G>A maps to NM_020389.2 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr5:135587469 G>A maps to NM_020389.2 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr15:31362262 G>A maps to NM_002420.4 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr15:31294924 G>A maps to NM_002420.4 F1304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr15:31358297 G>A maps to NM_002420.4 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr15:31332542 G>A maps to NM_002420.4 F676F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr15:31294702 G>A maps to NM_002420.4 S1378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr15:31294516 G>A maps to NM_002420.4 F1440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr15:31341577 T>A maps to NM_002420.4 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:31294507 G>A maps to NM_002420.4 S1443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:31323333 G>A maps to NM_002420.4 V971V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:31294042 G>A maps to NM_002420.4 S1598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr21:45845601 G>A maps to ENST00000397932 K1279K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr21:45855064 C>T maps to ENST00000397932 F1392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr21:45799002 C>T maps to ENST00000397932 Q380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr21:45815364 C>T maps to ENST00000397932 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr21:45860721 C>T maps to ENST00000397932 I1490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr21:45786737 G>A maps to ENST00000397932 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr21:45846586 G>A maps to ENST00000397932 R1330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr21:45773621 G>A maps to ENST00000397932 Q13Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr21:45802611 C>T maps to ENST00000397932 I409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr21:45786782 C>T maps to ENST00000397932 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr21:45799069 G>A maps to ENST00000397932 W402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr21:45861606 C>T maps to ENST00000397932 I1523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr21:45784066 C>T maps to ENST00000397932 Q109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:45773597 C>T maps to ENST00000397932 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:45786746 G>A maps to ENST00000397932 K178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:45833924 C>T maps to ENST00000397932 I1038I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:45861607 C>T maps to ENST00000397932 R1524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr21:45795867 C>T maps to ENST00000397932 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr21:45786746 G>A maps to ENST00000397932 K178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr21:45825901 C>T maps to ENST00000397932 I924I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr21:45817679 A>G maps to ENST00000397932 E661E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr21:45861639 C>T maps to ENST00000397932 L1534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr21:45844748 C>T maps to ENST00000397932 A1238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr21:45825122 C>T maps to ENST00000397932 F879F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr21:45799022 C>T maps to ENST00000397932 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr21:45833939 C>T maps to ENST00000397932 L1043L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr21:45784062 C>T maps to ENST00000397932 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr21:45798896 C>T maps to ENST00000397932 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr21:45811261 G>A maps to ENST00000397932 W516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr21:45861645 G>A maps to ENST00000397932 A1536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr21:45795834 G>A maps to ENST00000397932 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr21:45786722 G>A maps to ENST00000397932 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr21:45821719 C>T maps to ENST00000397932 S826S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr21:45837818 C>T maps to ENST00000397932 F1052F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr21:45843525 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr21:45821662 C>T maps to ENST00000397932 F807F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr21:45825904 C>T maps to ENST00000397932 I925I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr21:45838351 G>A maps to ENST00000397932 E1125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr21:45846544 G>A maps to ENST00000397932 T1316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr21:45786782 C>T maps to ENST00000397932 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr21:45844766 C>T maps to ENST00000397932 I1244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr21:45802617 G>A maps to ENST00000397932 R411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr21:45786767 G>A maps to ENST00000397932 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr21:45860700 G>A maps to ENST00000397932 R1483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr21:45833925 C>T maps to ENST00000397932 L1039L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:45799079 G>A maps to ENST00000397932 K405K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:45802611 C>T maps to ENST00000397932 I409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:45810907 G>A maps to ENST00000397932 K480K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:45837920 C>T maps to ENST00000397932 L1086L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:45844733 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:45861600 C>T maps to ENST00000397932 A1521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr21:45860757 G>A maps to ENST00000397932 Q1502Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr21:45798932 G>A maps to ENST00000397932 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr21:45819254 G>A maps to ENST00000397932 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr21:45811261 G>A maps to ENST00000397932 W516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr9:73477835 G>A maps to ENST00000419692 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr9:73457933 G>A maps to ENST00000419692 D203D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr9:73461500 G>A maps to ENST00000419692 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr9:73151405 C>T maps to ENST00000419692 R1495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr9:73461383 G>A maps to ENST00000419692 Q137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr9:73240409 C>T maps to ENST00000411705 W493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr9:73240415 G>A maps to ENST00000411705 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:73736186 C>T maps to NM_001007471.2 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr9:73255514 G>A maps to ENST00000419692 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr9:73461348 G>A maps to ENST00000419692 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:73167917 C>T maps to ENST00000419692 W1093*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr9:73151426 G>A maps to ENST00000419692 S1488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:73426097 A>G maps to ENST00000419692 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr9:73477937 G>A maps to ENST00000419692 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:73152143 C>T maps to ENST00000419692 S1249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:73442841 C>T maps to ENST00000419692 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:49703938 G>A maps to NM_017636.3 G950G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:49686034 C>T maps to NM_017636.3 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:49674905 C>T maps to NM_017636.3 C310C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:49691974 G>A maps to NM_017636.3 E607E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:49671178 C>T maps to NM_017636.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr19:49686005 C>T maps to NM_017636.3 Q479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr19:49703917 C>T maps to NM_017636.3 A943A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr19:49685890 C>T maps to NM_017636.3 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:49674629 C>T maps to NM_017636.3 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:49685890 C>T maps to NM_017636.3 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr19:49671515 G>A did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:49669381 C>T maps to NM_017636.3 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr11:2427988 G>A maps to ENST00000452833 V1053V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:2427955 G>A maps to ENST00000452833 F1064F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:2439582 G>A maps to ENST00000452833 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr11:2436410 G>A maps to ENST00000452833 F475F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:2444170 C>T maps to ENST00000452833 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:2443452 C>T maps to ENST00000452833 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:2444164 C>T maps to ENST00000452833 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:2441488 C>T maps to ENST00000452833 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:2441524 C>T maps to ENST00000452833 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr11:2443413 C>G maps to ENST00000452833 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:2438963 C>T maps to ENST00000452833 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:2429137 G>A maps to ENST00000452833 A931A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:2434410 C>T maps to ENST00000452833 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:2439450 C>T maps to ENST00000452833 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr11:2434127 C>T maps to ENST00000452833 G739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:2436005 C>T maps to ENST00000452833 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr11:2432705 G>A maps to ENST00000452833 A888A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr11:2444149 C>T maps to ENST00000452833 K39K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:2432909 G>A maps to ENST00000452833 A856A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:2437144 C>T maps to ENST00000452833 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:2442267 C>T maps to ENST00000452833 E153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:2444191 C>T maps to ENST00000452833 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr9:77343173 G>A maps to NM_017662.4 C1972C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr9:77455012 C>T maps to NM_017662.4 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:77400840 G>A maps to NM_017662.4 F956F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:77415334 G>A maps to NM_017662.4 A691A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr9:77400926 G>A maps to NM_017662.4 R928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr9:77365607 T>G maps to NM_017662.4 R1677R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr9:77448961 G>A maps to NM_017662.4 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr9:77407590 C>T maps to NM_017662.4 R829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:77339582 C>T maps to NM_017662.4 E2005E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:77457120 C>T maps to NM_017662.4 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr9:77435217 A>C did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr9:77455012 C>T maps to NM_017662.4 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:77353455 C>T maps to NM_017662.4 G1881G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:77415187 C>T maps to NM_017662.4 R740R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr9:77377028 G>A maps to NM_017662.4 Q1520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr9:77377005 G>A maps to NM_017662.4 I1527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr9:77353523 G>A maps to NM_017662.4 L1859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:77377920 C>T maps to NM_017662.4 L1222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:77378025 C>T maps to NM_017662.4 L1187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:77400933 G>A maps to NM_017662.4 F925F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:77415292 C>T maps to NM_017662.4 S705S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:77431652 G>A maps to NM_017662.4 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:77425748 G>A maps to NM_017662.4 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr9:77353395 C>T maps to NM_017662.4 E1901E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr9:77377179 C>T maps to NM_017662.4 K1469K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr9:77354857 G>A maps to NM_017662.4 S1756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr9:77354358 G>A maps to NM_017662.4 Q1832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr15:50899414 G>A maps to NM_017672.4 A897A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr15:50916398 G>A maps to NM_017672.4 F468F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr15:50931719 G>A maps to NM_017672.4 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr15:50884666 C>T maps to NM_017672.4 S1255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr15:50884348 G>A maps to NM_017672.4 S1361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr15:50925152 G>A maps to NM_017672.4 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr2:234847805 C>T maps to NM_024080.4 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:234873369 G>A maps to NM_024080.4 E616E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:234854558 G>A maps to NM_024080.4 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:234839311 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:234839326 T>C maps to NM_024080.4 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:234847722 C>T maps to NM_024080.4 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:234847757 C>T maps to NM_024080.4 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:234851301 G>A maps to NM_024080.4 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:234871951 C>T maps to NM_024080.4 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:234835193 G>A maps to NM_024080.4 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:234863776 C>T maps to NM_024080.4 A415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:234891806 C>T maps to NM_024080.4 F900F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:234858654 C>T maps to NM_024080.4 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:234878919 C>T maps to NM_024080.4 F735F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:234915530 G>A maps to NM_024080.4 W1055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:234863800 G>A maps to NM_024080.4 K423K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr8:116599331 G>A maps to NM_014112.2 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr8:116616458 G>A maps to NM_014112.2 F579F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr8:116616205 G>A maps to NM_014112.2 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:116599236 G>A maps to NM_014112.2 S897S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr8:116599242 G>A maps to NM_014112.2 S895S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr8:116616962 C>T maps to NM_014112.2 Q411Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:116599254 G>A maps to NM_014112.2 S891S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr8:116616575 G>A maps to NM_014112.2 F540F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr8:116632015 G>A maps to NM_014112.2 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:116426750 T>A maps to NM_014112.2 K1129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr17:3494393 C>T maps to ENST00000399756 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:3495395 G>A maps to ENST00000399756 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr17:3493666 G>A maps to ENST00000399756 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr17:16340148 G>A maps to NM_016113.4 E747E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr17:16330067 G>T maps to NM_016113.4 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:16340157 C>A maps to NM_016113.4 A750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:3458126 C>T maps to ENST00000381913 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:3458030 C>T maps to ENST00000381913 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:3424291 G>A maps to ENST00000381913 I595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:3447898 C>T maps to ENST00000381913 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr17:3436091 C>T maps to ENST00000381913 E308E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:3430212 G>A maps to ENST00000381913 A504A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr12:110246248 G>A maps to NM_021625.4 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr12:110246230 G>A maps to NM_021625.4 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr12:110252475 C>T maps to NM_021625.4 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr12:110222241 C>T maps to NM_021625.4 R779R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:110234353 G>A maps to NM_021625.4 I436I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:110238504 G>A maps to NM_021625.4 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:110246248 G>A maps to NM_021625.4 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:110232262 G>A maps to NM_021625.4 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr12:110232205 G>A maps to NM_021625.4 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:110240798 G>A maps to NM_021625.4 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:110230180 G>A maps to NM_021625.4 I626I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:110252388 G>A maps to NM_021625.4 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr12:110240829 G>A maps to NM_021625.4 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:110226282 G>A maps to NM_021625.4 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:110232226 G>A maps to NM_021625.4 F466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr7:142626631 C>T maps to NM_019841.4 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr7:142606681 G>A maps to NM_019841.4 F623F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr7:142609656 C>T maps to NM_019841.4 W593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:142630493 G>A maps to NM_019841.4 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:142609743 G>A maps to NM_019841.4 I564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:142609749 G>A maps to NM_019841.4 F562F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:142630543 G>A maps to NM_019841.4 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr7:142609821 G>C maps to NM_019841.4 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr7:142627510 G>A maps to NM_019841.4 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr7:142630470 C>T maps to NM_019841.4 W29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:142625245 C>T maps to NM_019841.4 E282E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:142627201 C>T maps to NM_019841.4 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr7:142625236 G>A maps to NM_019841.4 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:142609899 G>A maps to NM_019841.4 F512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:142625961 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:142605688 G>A maps to NM_019841.4 Y727Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:142609898 G>A maps to NM_019841.4 Q513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr7:142626215 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:142612702 C>T maps to NM_019841.4 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:142625941 G>A maps to NM_019841.4 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:142626168 G>A maps to NM_019841.4 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr7:142572878 G>A maps to NM_018646.2 V387V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:142572875 C>T maps to NM_018646.2 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr7:142569552 C>T maps to NM_018646.2 W695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:142572682 G>A maps to NM_018646.2 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:142575032 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:142569474 C>T maps to NM_018646.2 W721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:142572682 G>A maps to NM_018646.2 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr7:142575027 C>T maps to NM_018646.2 Q118Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:142573564 G>C maps to NM_018646.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:142573241 G>A maps to NM_018646.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:142574313 G>A maps to NM_018646.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr7:142575488 G>A maps to NM_018646.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:142573346 C>G maps to NM_018646.2 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:142569570 G>A maps to NM_018646.2 S689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:142571443 C>T maps to NM_018646.2 E515E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:142572321 G>A maps to NM_018646.2 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:142574199 G>A maps to NM_018646.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:142573597 G>A maps to NM_018646.2 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr7:98573801 C>T maps to ENST00000359863 L2617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr7:98608863 T>C maps to ENST00000359863 L3696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr7:98515104 C>T maps to ENST00000359863 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:98608811 G>A maps to ENST00000359863 L3678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:98550938 C>T maps to ENST00000359863 F1864F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr7:98609785 C>T maps to ENST00000359863 A3796A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr7:98535352 G>A maps to ENST00000359863 R1438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:98508851 C>T maps to ENST00000359863 V655V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:98547191 C>T maps to ENST00000359863 F1640F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr7:98547815 G>A maps to ENST00000359863 Q1748Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:98562330 C>T maps to ENST00000359863 S2296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:98551046 C>T maps to ENST00000359863 I1900I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:98592250 C>T maps to ENST00000359863 S3349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr7:98609127 C>T maps to ENST00000359863 V3755V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:98563400 C>T maps to ENST00000359863 F2346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:98606072 G>A maps to ENST00000359863 E3595E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr7:98565116 C>A maps to ENST00000359863 T2429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr7:98588088 T>C maps to ENST00000359863 L3205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:98495395 C>A maps to ENST00000359863 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:98576466 C>T maps to ENST00000359863 L2851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:98608763 C>T maps to ENST00000359863 A3662A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:98507908 C>T maps to ENST00000359863 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:98560039 C>T maps to ENST00000359863 S2266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:98581821 C>T maps to ENST00000359863 I3047I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:98533272 C>T maps to ENST00000359863 L1362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:98559062 C>T maps to ENST00000359863 L2216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:98506386 C>T maps to ENST00000359863 H384H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr7:98606063 C>T maps to ENST00000359863 S3592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:98565206 C>T maps to ENST00000359863 F2459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr7:98535298 C>T maps to ENST00000359863 V1420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr7:98524909 G>A maps to ENST00000359863 K1032K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr7:98557028 C>T maps to ENST00000359863 N2128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr7:98558886 C>T maps to ENST00000359863 Q2158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr7:98558954 C>T maps to ENST00000359863 V2180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr7:98558972 C>T maps to ENST00000359863 I2186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr7:98557091 C>T maps to ENST00000359863 F2149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr7:98559083 C>T maps to ENST00000359863 F2223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:98547863 C>T maps to ENST00000359863 F1764F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:98555692 C>T maps to ENST00000359863 F2100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:98592347 C>T maps to ENST00000359863 L3382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:98565206 C>T maps to ENST00000359863 F2459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr10:116732025 C>T maps to NM_139169.4 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr9:131071998 G>A maps to NM_015679.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr7:141955395 G>A maps to NM_001001317.2 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:141952184 A>T maps to NM_001001317.2 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:141955431 C>T maps to NM_001001317.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr7:141955401 G>A maps to NM_001001317.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:141952363 G>A maps to NM_001001317.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:141955413 G>A maps to NM_001001317.2 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:141955398 C>T maps to NM_001001317.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:141955401 G>A maps to NM_001001317.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:141954959 C>T maps to NM_001001317.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr7:141954929 G>A maps to NM_001001317.2 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr9:135777077 C>A maps to NM_000368.4 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr9:135781443 A>G maps to NM_000368.4 F507F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr9:135771900 G>C maps to NM_000368.4 A1072A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:135796753 G>A maps to NM_000368.4 R245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:135779088 G>A maps to NM_000368.4 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr9:135802641 G>A maps to NM_000368.4 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:135781418 G>A maps to NM_000368.4 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr9:135797352 C>T maps to NM_000368.4 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr9:135776202 G>A maps to NM_000368.4 Q842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr9:135776203 G>A maps to NM_000368.4 V841V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr16:2112523 C>T maps to NM_000548.3 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr16:2114418 C>T maps to NM_000548.3 I530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr16:2105493 C>A maps to NM_000548.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr16:2134314 C>T maps to NM_000548.3 S1364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:2100462 C>T maps to NM_000548.3 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:2129312 G>A maps to NM_000548.3 R1056R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr16:2115517 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr16:2121512 C>T maps to NM_000548.3 A614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr16:2105448 C>T maps to NM_000548.3 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:2129297 C>T maps to NM_000548.3 L1051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:2138109 C>T maps to NM_000548.3 F1710F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr16:2127661 G>A maps to NM_000548.3 K967K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr16:2110708 C>T maps to NM_000548.3 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr16:2129086 C>T maps to NM_000548.3 S1007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr3:150127274 C>T maps to NM_014779.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:150129005 C>T maps to NM_014779.2 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:106957889 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:106959953 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:100075451 G>A maps to NM_030935.3 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr7:100071976 G>A maps to NM_030935.3 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr7:100074962 G>A maps to NM_030935.3 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:54695979 C>T maps to NM_001077446.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr17:73517848 C>T maps to NM_207346.2 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:58180875 C>T maps to NM_001172696.1 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr2:99689497 C>T maps to NM_025244.2 E307E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr2:99695145 G>A maps to NM_025244.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr2:99614662 G>A maps to NM_025244.2 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:99681553 G>A maps to NM_025244.2 R418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr2:99651823 G>A maps to NM_025244.2 Q495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr11:65715021 G>A maps to NM_152762.2 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:65726389 G>A maps to NM_152762.2 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:65715115 A>T maps to NM_152762.2 K274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:65715015 G>A maps to NM_152762.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr11:65714784 G>A maps to NM_152762.2 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:65714718 C>T maps to NM_152762.2 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:65715222 G>A maps to NM_152762.2 K309K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr7:130364145 C>T maps to NM_052933.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr7:130353978 G>T maps to NM_052933.2 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:130044499 G>T maps to NM_018718.1 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:115576081 G>A maps to NM_000549.3 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:115576093 T>C maps to NM_000549.3 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr1:115576093 T>C maps to NM_000549.3 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr14:81554363 A>G maps to NM_000369.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr14:81610057 C>T maps to NM_000369.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr14:81610645 C>T maps to NM_000369.2 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:81554363 A>G maps to NM_000369.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:81534600 C>T maps to NM_000369.2 Y82Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr14:81610129 C>T maps to NM_000369.2 T576T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:81558907 C>T maps to NM_000369.2 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr14:81609960 G>A maps to NM_000369.2 W520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr14:81610189 C>T maps to NM_000369.2 I596I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr14:81610462 G>A maps to NM_000369.2 R687R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr14:81422134 C>T maps to NM_000369.2 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr14:81609649 C>T maps to NM_000369.2 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr14:81554306 G>A maps to NM_000369.2 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr18:72998240 C>T maps to NM_005786.4 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr18:72997586 G>A maps to NM_005786.4 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr18:72998543 C>T maps to NM_005786.4 N349N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:72999230 C>T maps to NM_005786.4 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr18:72997751 C>T maps to NM_005786.4 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr18:72998870 G>A maps to NM_005786.4 E458E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr18:72998519 G>A maps to NM_005786.4 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr18:73000565 G>A maps to NM_005786.4 L1023L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr18:73000568 C>T maps to NM_005786.4 I1024I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr20:51872849 C>T maps to NM_173485.5 F951F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr20:51872315 G>A maps to NM_173485.5 K773K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr20:51871553 T>G maps to NM_173485.5 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:51870557 G>A maps to NM_173485.5 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:51870755 G>A maps to NM_173485.5 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:51871683 C>T maps to NM_173485.5 Q563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:51872004 C>T maps to NM_173485.5 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:51873089 G>T maps to NM_173485.5 V1031V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:51870455 G>A maps to NM_173485.5 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr20:51871781 C>T maps to NM_173485.5 A595A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:51871841 G>A maps to NM_173485.5 G615G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr20:51870662 G>A maps to NM_173485.5 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr20:51870392 C>T maps to NM_173485.5 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr20:51871952 G>A maps to NM_173485.5 K652K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr20:51870104 C>T maps to NM_173485.5 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr20:51870435 C>T maps to NM_173485.5 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr20:51870548 G>A maps to NM_173485.5 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:51870680 C>T maps to NM_173485.5 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr20:51872801 C>T maps to NM_173485.5 F935F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr20:51872822 C>T maps to NM_173485.5 I942I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:51870773 G>A maps to NM_173485.5 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:51871502 G>A maps to NM_173485.5 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr20:51870953 G>T maps to NM_173485.5 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:51870455 G>A maps to NM_173485.5 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:51872147 C>T maps to NM_173485.5 S717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr20:51871100 C>T maps to NM_173485.5 Y368Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr20:51872072 C>T maps to NM_173485.5 I692I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr20:51871949 G>A maps to NM_173485.5 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr20:51870104 C>T maps to NM_173485.5 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr20:51871925 C>T maps to NM_173485.5 A643A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr20:51872132 C>T maps to NM_173485.5 P712P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr20:51872843 G>T maps to NM_173485.5 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr20:51871589 C>T maps to NM_173485.5 A531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:51871097 C>T maps to NM_173485.5 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:51871841 G>A maps to NM_173485.5 G615G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr20:51870959 G>A maps to NM_173485.5 K321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:51870596 G>A maps to NM_173485.5 Q200Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:51870680 C>T maps to NM_173485.5 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:51872999 G>A maps to NM_173485.5 R1001R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr20:51872768 C>T maps to NM_173485.5 P924P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr20:51870773 G>A maps to NM_173485.5 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:31768622 C>T maps to NM_020856.2 K692K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:31769132 G>A maps to NM_020856.2 I522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:31767938 C>T maps to NM_020856.2 G920G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr19:31768063 G>A maps to NM_020856.2 L879L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:31770323 G>A maps to NM_020856.2 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:31767826 G>A maps to NM_020856.2 R958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:31769156 C>T maps to NM_020856.2 E514E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr19:31770311 G>A maps to NM_020856.2 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:31768015 G>A maps to NM_020856.2 Q895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:31767605 G>A maps to NM_020856.2 S1031S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:31768238 G>A maps to NM_020856.2 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr19:31767602 G>A maps to NM_020856.2 S1032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:50248502 C>T maps to NM_021733.1 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:50248634 C>T maps to NM_021733.1 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:50247563 G>A maps to NM_021733.1 Q429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr19:50245168 G>A maps to NM_021733.1 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr19:50251365 C>T maps to NM_021733.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr19:50245249 G>A maps to NM_021733.1 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:50250055 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:50243068 G>A maps to NM_021733.1 T581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr19:50249809 C>T maps to NM_021733.1 W303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:50248616 C>T maps to NM_021733.1 Q343Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:50265440 G>A maps to NM_021733.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:50266480 C>T maps to NM_021733.1 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr11:76507463 C>T maps to NM_015516.3 N268N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr11:76507445 G>A maps to NM_015516.3 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:76506752 C>T maps to NM_015516.3 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:76507491 C>T maps to NM_015516.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr5:110411642 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:110407593 C>T maps to NM_033035.4 F2F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr8:143399924 G>A maps to ENST00000445818 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:143413153 G>A maps to ENST00000445818 Q262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr8:143365801 G>A maps to ENST00000445818 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:143412302 G>A maps to ENST00000445818 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr8:143425465 G>A maps to ENST00000445818 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr8:143436031 G>A maps to ENST00000445818 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:143310845 C>T maps to ENST00000445818 *515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr1:231673040 A>G maps to NM_005999.2 K68K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:67854816 C>T maps to ENST00000339830 R75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A264-06A-11D-A196-08 chr16:67860593 G>A did not map to a codon.
Sequencing variant TCGA-GN-A264-06A-11D-A196-08 chr16:67861432 G>T maps to ENST00000339830 E617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:46649918 C>T maps to NM_005727.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr17:79615125 C>T maps to NM_031945.3 N290N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr17:79615126 C>T maps to NM_031945.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr7:120450524 G>A maps to NM_012338.3 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:120446635 G>A maps to NM_012338.3 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr7:120478966 C>A did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr7:120480082 C>T maps to NM_012338.3 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:120446601 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:120455791 C>T maps to NM_012338.3 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr7:120446607 G>A maps to NM_012338.3 Q203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr7:16823043 C>T maps to NM_014399.3 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:16823073 G>A maps to NM_014399.3 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr7:16816728 C>T maps to NM_014399.3 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:16817502 C>T maps to NM_014399.3 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr10:71243541 C>T maps to NM_012339.3 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:71265941 C>T maps to NM_012339.3 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:11422831 C>T maps to NM_012466.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:11411965 G>A maps to NM_012466.2 W144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:11422891 G>A maps to NM_012466.2 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:11408879 G>A maps to NM_012466.2 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr5:176084569 C>T maps to NM_012171.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:176079892 C>T maps to NM_012171.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:176078636 G>A maps to NM_012171.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr11:44941528 G>A maps to ENST00000425677 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr11:44931323 C>T maps to ENST00000425677 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:44939537 C>T maps to ENST00000425677 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:44948235 G>A maps to ENST00000425677 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:115615568 C>T maps to NM_005725.4 K43K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:115615583 G>A maps to NM_005725.4 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr1:115604779 C>T maps to NM_005725.4 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr11:2339138 G>A maps to NM_139022.2 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr11:2337828 C>T maps to NM_139022.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:2334930 G>A maps to NM_139022.2 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:2335755 G>A maps to NM_139022.2 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:128801539 G>A maps to NM_178562.3 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr7:128801521 G>A maps to NM_178562.3 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:128807633 C>T maps to NM_178562.3 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:128802352 C>T maps to NM_178562.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:128802353 C>T maps to NM_178562.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:99885845 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:38525510 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr23:38525468 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:38420807 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr12:71523179 G>A maps to NM_004616.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:71533495 G>A maps to NM_004616.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr12:71537975 G>A maps to NM_004616.2 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr12:71531934 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:71526583 G>A maps to NM_004616.2 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr12:71533541 G>A maps to NM_004616.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:71519128 C>T maps to NM_004616.2 Q233Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:71531780 C>T maps to NM_004616.2 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:3387588 C>T maps to ENST00000407263 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:3388213 C>T maps to ENST00000407263 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr6:41011866 G>A maps to NM_001159726.1 K168K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr24:9305955 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr24:6115622 T>C did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr24:6114347 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr24:6115605 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr24:6114349 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr24:6115649 C>T did not map to a codon.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr24:6114316 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:116599703 C>T maps to NM_003309.3 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr6:116600048 A>T maps to NM_003309.3 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:53114854 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:53114470 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:53112162 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:53115419 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:53117108 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr23:53117120 A>T did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr23:53114504 T>G did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:53112064 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr8:98288962 G>A maps to NM_033512.2 N370N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:98288971 C>T maps to NM_033512.2 E367E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:98289598 C>T maps to NM_033512.2 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr2:54483132 G>A maps to NM_001003937.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr2:54482565 C>T maps to NM_001003937.2 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr2:54483114 C>T maps to NM_001003937.2 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:54483132 G>C maps to NM_001003937.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:2237873 G>A maps to NM_018128.4 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:54470859 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr23:54469870 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:54470528 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:3341911 G>A maps to ENST00000398659 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:3197798 G>A maps to ENST00000398659 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:3197849 G>A maps to ENST00000398659 C274C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:3341911 G>A maps to ENST00000398659 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr11:2424492 G>A maps to NM_005706.2 E210E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:2424459 C>T maps to NM_005706.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:2424760 G>T maps to NM_005706.2 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:2423940 C>T maps to NM_005706.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q7-06A-11D-A19A-08 chr5:112769723 C>T maps to NM_032028.3 W271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr5:112770047 C>T maps to NM_032028.3 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr5:112769747 G>A maps to NM_032028.3 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr5:112770496 G>A maps to NM_032028.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:112769798 C>T maps to NM_032028.3 K246K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:112769786 G>A maps to NM_032028.3 Y250Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:112770034 G>A maps to NM_032028.3 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr5:112769678 C>T maps to NM_032028.3 K286K. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DA-A1I1-06A-12D-A196-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-DA-A3F8-06A-11D-A20D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr22:19119040 C>T maps to NM_053006.4 I43I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A2MD-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr14:24677291 G>A maps to NM_001184739.1 E319E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:24675161 A>G maps to NM_001184739.1 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:19625777 G>A maps to NM_032037.2 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:37414701 C>T maps to NM_003312.4 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr22:37407109 G>A maps to NM_003312.4 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:37407091 G>A maps to NM_003312.4 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:37407091 G>A maps to NM_003312.4 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr8:144698812 G>A maps to NM_003313.3 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr8:144695447 C>T maps to NM_003313.3 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr8:144697043 G>A maps to NM_003313.3 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr8:144697043 G>A maps to NM_003313.3 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr9:100367788 C>T maps to NM_139246.4 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr9:100389827 G>T maps to NM_139246.4 S6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr6:43226928 C>T maps to NM_032538.1 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:43250682 G>A maps to NM_032538.1 E735E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:43251411 C>T maps to NM_032538.1 P978P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:43230739 C>T maps to NM_032538.1 I546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:43225647 C>T maps to NM_032538.1 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr6:43227375 G>A maps to NM_032538.1 R452R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:43251171 G>A maps to NM_032538.1 P898P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:43226871 C>T maps to NM_032538.1 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:43222807 C>T maps to NM_032538.1 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:43223479 G>A maps to NM_032538.1 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr6:43250472 C>T maps to NM_032538.1 S665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr6:43250670 G>A maps to NM_032538.1 G731G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:43226883 C>T maps to NM_032538.1 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:43214475 C>T maps to NM_032538.1 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:43251399 G>A maps to NM_032538.1 G974G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:43251171 G>T maps to NM_032538.1 P898P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr15:43045124 G>A maps to ENST00000263802 L1178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:43045246 G>A maps to ENST00000263802 Q1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:43086882 G>A maps to ENST00000263802 T718T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:43120224 G>A maps to ENST00000263802 N126N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:159463749 C>T maps to NM_003314.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:159492044 C>T maps to NM_003314.1 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr11:113210125 T>A maps to NM_017868.3 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:113210174 C>T maps to NM_017868.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:113196300 C>T maps to NM_017868.3 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:113209546 C>T maps to NM_017868.3 Q210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:113221963 C>T maps to NM_017868.3 F417F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:113233181 C>T maps to NM_017868.3 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr1:231044696 G>A maps to NM_024525.4 P793P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:231048464 C>A maps to NM_024525.4 T711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:231060653 G>A maps to NM_024525.4 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:231044744 G>A maps to NM_024525.4 I777I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:231056273 G>A maps to NM_024525.4 D655D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:180322050 C>T maps to NM_133462.3 N175N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr3:180322732 C>T maps to NM_133462.3 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:180327540 C>T maps to NM_133462.3 N508N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:3392197 C>T maps to NM_016030.5 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:3483042 C>T maps to NM_016030.5 S673S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:3391705 C>T maps to NM_016030.5 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr9:130489629 G>A maps to NM_144965.1 A550A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr9:130493173 G>A maps to NM_144965.1 K704K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:130479982 A>C maps to NM_144965.1 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:130486510 C>T maps to NM_144965.1 Q329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:130482668 C>T maps to NM_144965.1 Q218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr9:130480032 C>T maps to NM_144965.1 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr9:130489605 G>A maps to NM_144965.1 W542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:130479927 G>A maps to NM_144965.1 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr11:43471745 C>T maps to NM_018259.5 S967S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr11:43513658 C>T maps to NM_018259.5 I1080I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:43513658 C>T maps to NM_018259.5 I1080I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:43465730 C>T maps to NM_018259.5 G879G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:43418302 G>A maps to NM_018259.5 W236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr10:75059362 C>T maps to NM_145170.3 K509K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr10:75082750 G>A maps to NM_145170.3 Y364Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr10:75072322 G>A maps to NM_145170.3 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:75090991 C>T maps to NM_145170.3 E310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr10:75072272 C>T maps to NM_145170.3 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:75082780 C>T maps to NM_145170.3 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr10:75051661 G>A maps to NM_145170.3 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr10:75051169 G>A maps to NM_145170.3 R755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr10:75101168 G>A maps to NM_145170.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr10:75113452 G>A maps to NM_145170.3 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:15906111 C>A maps to NM_017775.2 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr3:39150694 C>T maps to ENST00000301819 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr3:39170392 G>A maps to ENST00000301819 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:39156155 C>T maps to ENST00000301819 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:39171797 C>T maps to ENST00000301819 S764S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:39172498 C>T maps to ENST00000301819 S833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:39162598 C>T maps to ENST00000301819 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:39169876 C>T maps to ENST00000301819 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:39162531 C>T maps to ENST00000301819 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr3:39166620 G>A maps to ENST00000301819 K395K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr3:39151625 C>T maps to ENST00000301819 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:39170380 C>T maps to ENST00000301819 I626I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:39174637 C>T maps to ENST00000301819 I894I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr2:166786249 G>A maps to NM_024753.3 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:166786257 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:166806198 G>A maps to NM_024753.3 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:166771802 G>A maps to NM_024753.3 A682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:166805993 G>A maps to NM_024753.3 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr2:166805993 G>A maps to NM_024753.3 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:166758372 C>T maps to NM_024753.3 Q872Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:55266611 G>A maps to NM_001114108.1 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:55266665 G>A maps to NM_001114108.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:55266737 G>A maps to NM_001114108.1 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr15:99768776 G>A maps to NM_022905.4 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:99740153 G>A maps to NM_022905.4 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:156555589 G>A maps to NM_001105669.2 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:156555556 C>T maps to NM_001105669.2 C503C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:156552954 G>A maps to NM_001105669.2 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:156554961 G>A maps to NM_001105669.2 Q465Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr17:40095263 A>G maps to ENST00000377543 K299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:40094954 G>A maps to ENST00000377543 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:40107250 C>T maps to ENST00000377543 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:40091481 C>T maps to ENST00000377543 Q43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr7:138853100 C>T maps to NM_024926.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr7:138854081 A>T maps to NM_024926.2 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:32865404 C>T maps to NM_017735.4 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr2:32983363 A>G maps to NM_017735.4 E486E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:32875263 C>T maps to NM_017735.4 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:32958979 G>A maps to NM_017735.4 W440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:32891780 C>T maps to NM_017735.4 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr4:147830394 C>T maps to ENST00000513335 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr4:147830292 C>T maps to ENST00000513335 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr4:147830271 G>A maps to ENST00000513335 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr4:147824777 C>T maps to ENST00000513335 K194K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr21:38462567 T>C maps to NM_003316.3 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr21:38569993 A>G maps to NM_003316.3 K1901K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr21:38539912 G>A maps to NM_003316.3 E1486E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr21:38524309 C>T maps to NM_003316.3 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr21:38516887 G>C maps to NM_003316.3 V612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr21:38525432 C>T maps to NM_003316.3 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr21:38538328 C>T maps to NM_003316.3 P1271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr21:38511015 T>C did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr21:38538328 C>T maps to NM_003316.3 P1271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr21:38467670 A>T maps to NM_003316.3 K237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr21:38568322 C>T maps to NM_003316.3 F1855F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr21:38525558 C>T maps to NM_003316.3 Q908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:178482355 G>A maps to NM_152275.3 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:178415795 G>A maps to NM_152517.2 R566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:74717473 C>T maps to NM_022492.4 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:74718726 C>T maps to NM_022492.4 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr2:74718708 C>T maps to NM_022492.4 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:74718669 C>T maps to NM_022492.4 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:74718696 G>A maps to NM_022492.4 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:74720227 C>A maps to NM_022492.4 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:74719541 C>T maps to NM_022492.4 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:74720194 C>T maps to NM_022492.4 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr8:109468134 T>A maps to NM_014673.3 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr8:109488125 C>T maps to NM_014673.3 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:109498749 C>T maps to NM_014673.3 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:118399447 G>A maps to NM_001080441.1 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr5:94863845 G>A maps to NM_014639.3 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:94814121 G>A maps to NM_014639.3 Q1413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:94814122 G>A maps to NM_014639.3 S1412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr5:94820511 G>A maps to NM_014639.3 S1323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:46669960 C>T maps to NM_017931.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:46685430 C>T maps to NM_017931.2 I405I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:51767298 C>T maps to ENST00000447632 W369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:51753900 C>T maps to ENST00000447632 Q590Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:51754554 C>T maps to ENST00000447632 E558E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:51777826 G>A maps to ENST00000447632 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr9:15192693 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr9:15203849 G>A maps to NM_152574.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr9:15190648 G>A maps to NM_152574.2 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:15185361 G>A maps to NM_152574.2 I510I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:21705461 G>A maps to NM_001135993.1 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr18:21649137 C>T maps to NM_001135993.1 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr18:21705488 C>T maps to NM_001135993.1 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:55188375 C>T maps to NM_004623.4 H166H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:55197278 C>T maps to NM_004623.4 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:20767021 G>A maps to NM_138376.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr14:20763899 G>A maps to NM_138376.2 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:20763872 C>T maps to NM_138376.2 E279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr2:47221584 C>T maps to ENST00000394850 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:47220594 C>T maps to ENST00000394850 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:47221611 C>T maps to ENST00000394850 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:47202211 C>T maps to ENST00000394850 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:47249062 C>T maps to ENST00000394850 F485F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:47221608 C>T maps to ENST00000394850 F319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:47221608 C>T maps to ENST00000394850 F319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:47300884 G>A maps to ENST00000394850 K824K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr2:47205992 C>T maps to ENST00000394850 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:47222298 C>T maps to ENST00000394850 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr14:91007885 G>A maps to NM_001010854.1 I786I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr14:91059965 G>A maps to NM_001010854.1 S657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:91044584 G>A maps to NM_001010854.1 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr14:89307482 C>T maps to NM_144596.2 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr14:89307836 C>T maps to NM_144596.2 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:62502995 C>T maps to NM_173810.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr11:62503007 C>T maps to NM_173810.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:62502995 C>T maps to NM_173810.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q3-06A-11D-A196-08 chr9:135273618 A>G maps to NM_007344.2 S562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr9:135277770 C>T maps to NM_007344.2 Q146Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr9:135273567 G>A maps to NM_007344.2 I579I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:117631541 C>T maps to NM_003594.3 A760A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:117618453 C>T maps to NM_003594.3 Y416Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:117617694 C>T maps to NM_003594.3 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:117633164 C>T maps to NM_003594.3 P836P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:117629056 C>T maps to NM_003594.3 I691I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr1:117635465 C>T maps to NM_003594.3 S973S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr22:43455515 G>A maps to NM_012263.4 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr1:1117764 C>T maps to NM_001130045.1 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:1120452 G>A maps to NM_001130045.1 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:1115636 C>T maps to NM_001130045.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:1117776 C>T maps to NM_001130045.1 Y289Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:1116177 C>T maps to NM_001130045.1 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr1:1118376 C>T maps to NM_001130045.1 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:1115514 C>T maps to NM_001130045.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:124751569 G>A maps to NM_001139442.1 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr9:124855613 G>A maps to NM_001139442.1 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:124752001 G>A maps to NM_001139442.1 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr22:43570366 G>A maps to NM_015140.3 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:43568524 G>A maps to NM_015140.3 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:43570581 G>A maps to NM_015140.3 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr22:43575961 G>A maps to NM_015140.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr15:90800927 C>T maps to ENST00000438251 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr6:167754578 T>C maps to NM_031949.4 C397C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr6:167753852 G>A maps to NM_031949.4 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:167754893 G>A maps to NM_031949.4 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr6:167755011 C>T maps to NM_031949.4 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:167753715 A>T maps to NM_031949.4 K110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:167754923 G>A maps to NM_031949.4 R512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:9877136 G>A maps to NM_001025930.3 A904A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr3:9867621 C>T maps to NM_001025930.3 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr3:9871027 G>A maps to NM_001025930.3 R644R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr3:9859351 G>A maps to NM_001025930.3 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr2:219614104 C>T maps to NM_014640.4 S910S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:219617634 A>T maps to NM_014640.4 P1042P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:219602992 C>T maps to NM_014640.4 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:219604795 C>T maps to NM_014640.4 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr2:219603139 C>T maps to NM_014640.4 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:219617874 C>T maps to NM_014640.4 F1075F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr14:76245980 C>T maps to NM_015072.4 F817F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:76330013 C>T maps to NM_015072.4 L1111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr17:46867330 C>T maps to NM_001130918.1 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51H-06A-12D-A25O-08 chr17:46863561 C>T maps to NM_001130918.1 Q575Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:46868952 G>A maps to NM_001130918.1 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr17:46846536 G>A maps to NM_001130918.1 L830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr17:46867348 C>T maps to NM_001130918.1 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr17:46862365 C>T maps to NM_001130918.1 S653S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-FW-A3R5-06A-11D-A23B-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:46868964 C>T maps to NM_001130918.1 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr17:46863591 C>T maps to NM_001130918.1 K565K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:46867381 G>A maps to NM_001130918.1 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr1:84412888 G>A maps to NM_024686.4 Q142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:84386788 G>A maps to NM_024686.4 R449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:84399431 G>A maps to NM_024686.4 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:84408172 C>T maps to NM_024686.4 K232K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:84415547 C>T maps to NM_024686.4 Q93Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr1:84383304 G>A maps to NM_024686.4 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr1:84408283 G>A maps to NM_024686.4 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr22:50483774 C>T maps to NM_001080447.1 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr22:50488559 C>T maps to NM_001080447.1 E56E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr22:50484294 C>T maps to NM_001080447.1 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr22:50483732 G>A maps to NM_001080447.1 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr22:50471707 G>A maps to NM_001080447.1 N402N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr22:50488592 G>A maps to NM_001080447.1 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:50472792 C>T maps to NM_001080447.1 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr22:50469153 C>T maps to NM_001080447.1 R636R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr20:30530769 A>G maps to NM_001008409.2 K422K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr20:30496447 C>T maps to NM_001008409.2 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:30507695 C>T maps to NM_001008409.2 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr20:30486299 C>T maps to NM_001008409.2 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:30486308 C>T maps to NM_001008409.2 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr20:30527067 C>T maps to NM_001008409.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr20:30530763 G>A maps to NM_001008409.2 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr20:30507727 G>A maps to NM_001008409.2 W189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:30507698 C>T maps to NM_001008409.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:30522559 G>A maps to NM_001008409.2 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:30496438 G>A maps to NM_001008409.2 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr20:30497646 C>T maps to NM_001008409.2 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr2:179457685 C>T maps to NM_133378.4 Q17152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr2:179584173 C>T maps to NM_133378.4 R6737R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:179576049 G>A maps to NM_133378.4 R8061*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:179584293 G>A maps to NM_133378.4 S6731S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:179602901 G>A maps to NM_133378.4 L3516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:179605173 G>A maps to NM_133437.3 I4091I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:179614006 G>A maps to ENST00000375038 Q4376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:179614007 G>A maps to ENST00000375038 H4375H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr2:179640908 G>A maps to NM_133378.4 I1894I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr2:179582772 G>A maps to NM_133378.4 S7076S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr2:179472296 C>T maps to NM_133378.4 W15138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr2:179596516 C>T maps to NM_133378.4 Q4451Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr2:179472559 C>A maps to NM_133378.4 E15084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr2:179665299 C>T maps to NM_133378.4 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:179567352 G>A maps to NM_133378.4 I8843I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:179600487 C>T maps to NM_133378.4 E3651E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:179616248 C>T maps to ENST00000375038 R3628R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:179641391 C>T maps to NM_133378.4 T1733T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr2:179572469 C>T maps to NM_133378.4 Q8364Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr2:179401090 A>G maps to NM_133378.4 L30893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr2:179498793 G>A maps to NM_133378.4 F11576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr2:179585273 G>A maps to NM_133378.4 R6495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr2:179644728 G>A maps to NM_133378.4 Q1243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr2:179585786 C>T maps to NM_133378.4 W6409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr2:179479460 G>A maps to NM_133378.4 L13692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr2:179544087 C>T maps to NM_133378.4 K9996K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:179613667 G>A maps to ENST00000375038 Q4489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:179439155 C>T maps to NM_133378.4 V21333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:179444549 C>T maps to NM_133378.4 L19890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:179599267 G>A maps to NM_133378.4 Q3851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr2:179638754 G>A maps to NM_133378.4 S2380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr2:179449971 C>T maps to NM_133378.4 W18932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:179615720 G>A maps to ENST00000375038 F3804F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:179634823 G>A maps to NM_133378.4 V2868V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:179410187 C>T maps to NM_133378.4 V29315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:179465767 C>T maps to NM_133378.4 W16053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:179465768 C>T maps to NM_133378.4 W16053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:179542555 C>T maps to NM_133378.4 E10117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:179587533 C>T maps to NM_133378.4 R6120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr2:179441490 C>T maps to NM_133378.4 W20592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:179411111 C>T maps to NM_133378.4 W29081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:179612363 T>C maps to ENST00000375038 K4923K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:179616449 G>A maps to ENST00000375038 H3561H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:179659140 T>C maps to NM_133378.4 Q461Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr2:179585786 C>T maps to NM_133378.4 W6409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr2:179654824 C>T maps to NM_133378.4 R606R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:179414372 G>A maps to NM_133378.4 F28124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:179434307 C>T maps to NM_133378.4 R22949R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:179486228 G>A maps to NM_133378.4 R12540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:179495905 C>T maps to NM_133378.4 K12055K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:179614088 G>A maps to ENST00000375038 I4348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr2:179569950 G>A maps to NM_133378.4 Q8608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr2:179407407 G>A maps to NM_133378.4 T29823T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr2:179427524 C>T maps to NM_133378.4 V25210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:179436059 G>A maps to NM_133378.4 I22365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:179438774 C>T maps to NM_133378.4 K21460K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:179465821 C>T maps to NM_133378.4 P16035P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:179474444 C>T maps to NM_133378.4 R14667R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:179482565 G>A maps to NM_133378.4 R13270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:179498799 C>T maps to NM_133378.4 L11574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:179534943 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:179567355 G>A maps to NM_133378.4 N8842N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:179615369 G>A maps to ENST00000375038 F3921F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:179665128 C>T maps to NM_133378.4 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr2:179640506 C>T maps to NM_133378.4 E2028E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr2:179590564 G>A maps to NM_133378.4 I5584I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr2:179585324 G>A maps to NM_133378.4 Q6478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr2:179579148 C>T maps to NM_133378.4 W7540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr2:179597845 G>A maps to NM_133378.4 R4109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:179612156 T>G maps to ENST00000375038 P4992P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr2:179612216 G>A maps to ENST00000375038 S4972S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr2:179466746 C>T maps to NM_133378.4 K15849K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:179410547 G>A maps to NM_133378.4 F29237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:179416816 A>G maps to NM_133378.4 T27702T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:179428658 A>C maps to NM_133378.4 A24832A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:179440322 C>T maps to NM_133378.4 E20944E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:179481672 C>T maps to NM_133378.4 T13413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:179497141 T>C did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:179514945 C>T maps to NM_133378.4 E10820E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:179553440 G>A maps to NM_133378.4 F9476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:179572400 C>T maps to NM_133378.4 K8387K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:179583187 C>T maps to NM_133378.4 E6971E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:179598551 T>C maps to NM_133378.4 Q3944Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:179612342 C>T maps to ENST00000375038 K4930K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:179616464 A>G maps to ENST00000375038 A3556A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:179634634 G>A maps to NM_133378.4 I2891I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:179642647 C>T maps to NM_133378.4 R1421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:179393048 T>A maps to NM_133378.4 K33209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:179428763 C>T maps to NM_133378.4 K24797K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:179606403 C>T maps to NM_133437.3 Q3681Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:179642596 G>A maps to NM_133378.4 S1438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr2:179438867 G>A maps to NM_133378.4 F21429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr2:179604663 G>A maps to NM_133437.3 I4261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr2:179611970 G>A maps to ENST00000375038 S5054S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr2:179576845 G>A maps to NM_133378.4 S7993S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr2:179583665 C>T maps to NM_133378.4 V6843V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr2:179584545 G>A maps to NM_133378.4 I6647I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr2:179392292 G>A maps to NM_133378.4 Q33286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:179437205 G>A maps to NM_133378.4 I21983I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:179455116 G>A maps to NM_133378.4 F17877F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:179621234 C>T maps to NM_133437.3 T3485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr2:179584974 C>T maps to NM_133378.4 V6554V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr2:179485338 C>T maps to NM_133378.4 R12735R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr2:179640770 C>T maps to NM_133378.4 R1940R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:179418388 C>T maps to NM_133378.4 W27213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:179432170 C>A maps to NM_133378.4 G23662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:179517254 C>T maps to NM_133378.4 P10585P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr2:179588784 T>C maps to NM_133378.4 V5823V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:179438573 C>T maps to NM_133378.4 R21527R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:179542555 C>T maps to NM_133378.4 E10117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:179585325 G>A maps to NM_133378.4 L6477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:179588244 C>T maps to NM_133378.4 L5950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:179597627 C>T maps to NM_133378.4 G4181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:179616236 C>T maps to ENST00000375038 R3632R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:179432378 T>C maps to NM_133378.4 E23592E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:179589254 G>A maps to NM_133378.4 V5705V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:179622509 C>T maps to NM_133432.3 G3433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:179631138 C>T maps to NM_133378.4 R3224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:179641766 T>C maps to NM_133378.4 G1608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr2:179436937 C>A maps to NM_133378.4 E22073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr2:179633574 G>T maps to NM_133378.4 G2996G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr2:179469026 C>T maps to NM_133378.4 W15561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:179395114 T>C maps to NM_133378.4 E32841E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:179417474 C>T maps to NM_133378.4 W27483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:179636168 G>A maps to NM_133378.4 Q2629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:179665386 G>A maps to NM_133378.4 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr2:179419595 G>A maps to NM_133378.4 I26962I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr2:179472788 G>A maps to NM_133378.4 I15007I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr2:179582005 G>A maps to NM_133378.4 I7241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr2:179582415 C>T maps to NM_133378.4 K7151K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr2:179665254 G>A maps to NM_133378.4 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20I-06A-11D-A196-08 chr2:179613494 G>A maps to ENST00000375038 D4546D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr2:179600388 G>A maps to NM_133378.4 L3684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr2:179576683 G>A maps to NM_133378.4 F8047F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr2:179590750 G>A maps to NM_133378.4 F5522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr2:179636109 G>A maps to NM_133378.4 S2648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr2:179404145 C>T maps to NM_133378.4 L30314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr2:179568877 G>A maps to NM_133378.4 I8829I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:179397748 C>T maps to NM_133378.4 K31963K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:179404418 C>T maps to NM_133378.4 R30223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:179404578 C>T maps to NM_133378.4 W30170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:179413973 G>A maps to NM_133378.4 F28225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:179431871 G>A maps to NM_133378.4 T23761T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:179438978 G>A maps to NM_133378.4 I21392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:179453499 C>T maps to NM_133378.4 W18416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:179454531 G>A maps to NM_133378.4 F18072F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:179495007 T>C maps to NM_133378.4 Q12179Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:179504808 G>A maps to NM_133378.4 L11016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:179566898 C>T maps to NM_133378.4 T8925T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:179583221 C>T maps to NM_133378.4 W6960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:179587192 G>A maps to NM_133378.4 R6197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:179587273 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:179589020 C>T maps to NM_133378.4 G5783G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:179594114 G>A maps to NM_133378.4 L5012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:179594164 G>A maps to NM_133378.4 R4996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:179604891 G>A maps to NM_133437.3 I4185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:179606591 G>A maps to NM_133437.3 Q3619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:179612957 G>A maps to ENST00000375038 S4725S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:179641160 C>T maps to NM_133378.4 R1810R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:179648796 C>T maps to NM_133378.4 K925K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:179411901 A>T maps to NM_133378.4 R28882R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:179425409 G>A maps to NM_133378.4 I25915I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:179444786 G>T maps to NM_133378.4 S19841S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:179452453 G>A maps to NM_133378.4 L18626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:179454201 C>T maps to NM_133378.4 G18182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:179458943 G>A maps to NM_133378.4 F16824F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:179577628 G>A maps to NM_133378.4 I7797I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:179581942 C>T maps to NM_133378.4 L7262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:179588211 C>T maps to NM_133378.4 G5961G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:179604237 C>T maps to NM_133437.3 E4403E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:179616046 G>A maps to ENST00000375038 L3696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:179632638 C>T maps to NM_133378.4 Q3106Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:179635379 C>T maps to NM_133378.4 L2713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr2:179440103 C>T maps to NM_133378.4 V21017V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr2:179560874 C>T maps to NM_133378.4 K9064K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr2:179584290 G>A maps to NM_133378.4 V6732V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr2:179441541 A>G maps to NM_133378.4 P20575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:179417695 C>T maps to NM_133378.4 K27409K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:179600730 G>A maps to NM_133378.4 F3570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:179605086 G>A maps to NM_133437.3 V4120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:179611641 C>T maps to ENST00000375038 W5164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:179621438 C>T maps to NM_133437.3 K3417K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:179647611 C>T maps to NM_133378.4 A1007A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:179648928 G>A maps to NM_133378.4 F881F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:179416537 C>T maps to NM_133378.4 K27795K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:179447839 C>T maps to NM_133378.4 W19329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:179574560 G>A maps to NM_133378.4 F8251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:179590352 G>A maps to NM_133378.4 L5616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:179599175 A>C maps to NM_133378.4 S3881S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:179610722 G>A maps to ENST00000375038 L5470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:179611799 G>A maps to ENST00000375038 P5111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:179613767 C>T maps to ENST00000375038 G4455G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:179634634 G>A maps to NM_133378.4 I2891I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr2:179542555 C>T maps to NM_133378.4 E10117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:179595649 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:179610422 G>A maps to ENST00000375038 F5570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:179483461 A>G maps to NM_133378.4 N13037N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr2:179432351 A>T maps to NM_133378.4 A23601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr2:179616022 A>G maps to ENST00000375038 L3704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:179481735 T>C maps to NM_133378.4 E13392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr2:179474942 G>A maps to NM_133378.4 L14536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr2:179603010 G>A maps to NM_133378.4 I3479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr2:179428406 A>G maps to NM_133378.4 D24916D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr2:179654824 C>T maps to NM_133378.4 R606R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:179478905 C>T maps to NM_133378.4 K13838K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:179497111 G>A maps to NM_133378.4 L11935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr2:179610805 G>A maps to ENST00000375038 R5443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr2:179641178 G>A maps to NM_133378.4 S1804S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr2:179583310 C>T maps to NM_133378.4 V6930V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:179611958 C>T maps to ENST00000375038 G5058G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr2:179615420 C>T maps to ENST00000375038 K3904K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:179425010 C>T maps to NM_133378.4 R26048R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:179440122 C>T maps to NM_133378.4 W21011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:179484482 G>A maps to NM_133378.4 Q12953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:179616308 A>G maps to ENST00000375038 Y3608Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr2:179589041 G>A maps to NM_133378.4 F5776F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:179480179 C>T maps to NM_133378.4 W13596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:179568945 G>A maps to NM_133378.4 R8807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:179579256 G>A maps to NM_133378.4 V7504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:179585897 A>G maps to NM_133378.4 A6372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:179594490 G>A maps to NM_133378.4 F4919F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr2:179597666 G>A maps to NM_133378.4 A4168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr2:179430716 C>T maps to NM_133378.4 K24146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr2:179458811 C>T maps to NM_133378.4 K16868K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:179484957 G>A maps to NM_133378.4 I12862I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:179584731 G>A maps to NM_133378.4 C6635C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:179605488 G>A maps to NM_133437.3 S3986S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:179631252 G>A maps to NM_133378.4 I3186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:179633409 A>G maps to NM_133378.4 L3051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:179640500 G>A maps to NM_133378.4 L2030L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:179641337 G>A maps to NM_133378.4 L1751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:179643719 A>T maps to NM_133378.4 T1363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:179666955 G>A maps to NM_133378.4 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:179395654 T>G maps to NM_133378.4 T32661T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:179554062 C>T maps to NM_133378.4 R9411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:179582271 G>A maps to NM_133378.4 S7199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:179583623 G>A maps to NM_133378.4 I6857I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:179399329 C>T maps to NM_133378.4 L31436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:179436311 C>T maps to NM_133378.4 R22281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:179453448 C>T maps to NM_133378.4 E18433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:179554062 C>T maps to NM_133378.4 R9411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:179574512 G>A maps to NM_133378.4 F8267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:179579722 G>A maps to NM_133378.4 I7486I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:179592957 G>A maps to NM_133378.4 C5287C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr2:179408102 G>A maps to NM_133378.4 V29631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr2:179603067 C>T maps to NM_133378.4 R3460R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:179404952 C>T maps to NM_133378.4 W30079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:179430747 C>T maps to NM_133378.4 W24136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:179458928 C>T maps to NM_133378.4 T16829T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:179473172 C>T maps to NM_133378.4 V14911V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:179585325 G>A maps to NM_133378.4 L6477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:179641268 G>A maps to NM_133378.4 I1774I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr2:179610842 C>T maps to ENST00000375038 V5430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr2:179431325 G>T maps to NM_133378.4 P23943P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:179435132 C>T maps to NM_133378.4 V22674V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:179497684 C>T maps to NM_133378.4 Q11823Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:179582510 T>A maps to NM_133378.4 R7120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:179416591 C>T maps to NM_133378.4 W27777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:179549654 C>T maps to NM_133378.4 K9600K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:179589233 C>T maps to NM_133378.4 P5712P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:179594213 C>T maps to NM_133378.4 T4979T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:179596690 A>G maps to NM_133378.4 P4393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:179636070 C>T maps to NM_133378.4 L2661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr2:179498296 G>A maps to NM_133378.4 F11695F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr2:179613356 G>A maps to ENST00000375038 F4592F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr2:179427422 G>A maps to NM_133378.4 A25244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr2:179494051 C>T maps to NM_133378.4 G12232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr2:179579149 C>T maps to NM_133378.4 W7540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr2:179599704 G>A maps to NM_133378.4 S3738S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:179544114 C>T maps to NM_133378.4 E9987E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:179584941 C>T maps to NM_133378.4 G6565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:179585866 G>A maps to NM_133378.4 Q6383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:179594267 C>T maps to NM_133378.4 L4961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:179640440 C>T maps to NM_133378.4 K2050K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr2:179430377 C>T maps to NM_133378.4 W24259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr2:179497427 G>T maps to NM_133378.4 P11867P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr2:179576809 C>T maps to NM_133378.4 T8005T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr2:179469521 G>A maps to NM_133378.4 T15530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:179568877 G>A maps to NM_133378.4 I8829I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:179664452 A>G maps to NM_133378.4 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:179665314 G>A maps to NM_133378.4 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:179469557 C>T maps to NM_133378.4 W15518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:179595811 G>A maps to NM_133378.4 G4616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:179611553 T>C maps to ENST00000375038 K5193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:179433242 A>T maps to NM_133378.4 V23304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:179454888 C>T maps to NM_133378.4 K17953K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:179616203 G>A maps to ENST00000375038 P3643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:179455276 C>T maps to NM_133378.4 W17824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:179576074 C>T maps to NM_133378.4 E8052E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:179590257 C>T maps to NM_133378.4 K5647K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr2:179634646 G>A maps to NM_133378.4 T2887T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:179486672 C>T maps to NM_133378.4 K12424K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:179569675 C>T maps to NM_133378.4 E8630E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:179592938 G>A maps to NM_133378.4 L5294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:179604552 C>T maps to NM_133437.3 L4298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:179633538 G>A maps to NM_133378.4 I3008I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr2:179593491 G>A maps to NM_133378.4 I5143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:179413262 C>T maps to NM_133378.4 R28462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:179433236 A>G maps to NM_133378.4 N23306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:179578870 G>A maps to NM_133378.4 S7594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:179583124 C>T maps to NM_133378.4 E6992E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:179648922 G>A maps to NM_133378.4 F883F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr2:179434589 G>A maps to NM_133378.4 F22855F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr2:179434751 G>A maps to NM_133378.4 L22801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr2:179449180 C>T maps to NM_133378.4 K19131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:179408276 G>A maps to NM_133378.4 I29573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:179438969 C>T maps to NM_133378.4 K21395K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:179480172 G>A maps to NM_133378.4 R13599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:179498036 C>T maps to NM_133378.4 V11753V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:179516192 G>A maps to NM_133378.4 A10744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:179621342 G>A maps to NM_133437.3 S3449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:179623867 C>T maps to NM_133378.4 K3382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:179631246 G>A maps to NM_133378.4 F3188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:179425151 A>G maps to NM_133378.4 L26001L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:179498631 C>T maps to NM_133378.4 L11630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:179638757 G>A maps to NM_133378.4 V2379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr2:179458553 C>T maps to NM_133378.4 E16923E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr2:179585768 G>A maps to NM_133378.4 F6415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr2:179621495 C>T maps to NM_133437.3 G3398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:179577950 C>T maps to NM_133378.4 R7726R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:179604786 C>T maps to NM_133437.3 Q4220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr2:179616449 G>A maps to ENST00000375038 H3561H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:179439959 C>T maps to NM_133378.4 L21065L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:179579779 C>T maps to NM_133378.4 G7467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:179583578 C>T maps to NM_133378.4 R6872R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:179632509 G>A maps to NM_133378.4 I3149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:179654824 C>T maps to NM_133378.4 R606R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:179473615 G>A maps to NM_133378.4 I14806I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:179495905 C>T maps to NM_133378.4 K12055K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:179498050 G>A maps to NM_133378.4 R11749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:179542395 C>A maps to NM_133378.4 E10171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:179584809 G>A maps to NM_133378.4 L6609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:179589041 G>A maps to NM_133378.4 F5776F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:179592434 A>G maps to NM_133378.4 L5380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:179606490 G>A maps to NM_133437.3 I3652I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr2:179579824 G>A maps to NM_133378.4 F7452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr2:179441824 C>T maps to NM_133378.4 K20511K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr2:179616236 C>T maps to ENST00000375038 R3632R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr2:179427845 C>T maps to NM_133378.4 E25103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr2:179497687 G>A maps to NM_133378.4 F11822F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr2:179622407 G>A maps to NM_133432.3 F3467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:179426123 T>C maps to NM_133378.4 E25677E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:179588001 C>T maps to NM_133378.4 G6000G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:179638820 G>A maps to NM_133378.4 I2358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr2:179427743 G>T maps to NM_133378.4 P25137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr2:179581843 A>G maps to NM_133378.4 C7295C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr2:179585786 C>T maps to NM_133378.4 W6409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr2:179659275 C>T maps to NM_133378.4 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr2:179436014 C>T maps to NM_133378.4 K22380K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr2:179412370 G>A maps to NM_133378.4 L28760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr2:179442497 C>T maps to NM_133378.4 S20317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr2:179460363 G>A maps to NM_133378.4 T16671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr2:179485032 G>A maps to NM_133378.4 F12837F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr2:179576683 G>A maps to NM_133378.4 F8047F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:179414405 G>C maps to NM_133378.4 A28113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:179655491 C>G maps to NM_133378.4 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr2:179400175 G>T maps to NM_133378.4 T31154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr2:179613607 G>A maps to ENST00000375038 L4509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr2:179474672 A>G maps to NM_133378.4 P14591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr2:179628973 G>A maps to NM_133378.4 I3348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr2:179455758 C>T maps to NM_133378.4 L17663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr2:179648853 G>A maps to NM_133378.4 I906I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr2:179588835 C>T maps to NM_133378.4 L5806L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:179472716 C>T maps to NM_133378.4 G15031G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:179542387 G>A maps to NM_133378.4 V10173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr2:179438159 A>G maps to NM_133378.4 T21665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:179485284 G>A maps to NM_133378.4 F12753F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:179495830 C>T maps to NM_133378.4 L12080L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:179495926 C>T maps to NM_133378.4 V12048V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:179582475 G>A maps to NM_133378.4 F7131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:179595649 A>G did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:179640776 G>A maps to NM_133378.4 V1938V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr2:179434604 G>A maps to NM_133378.4 T22850T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr2:179465821 C>T maps to NM_133378.4 P16035P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr2:179431634 G>A maps to NM_133378.4 N23840N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr2:179584143 C>T maps to NM_133378.4 L6747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr2:179622488 C>T maps to NM_133432.3 A3440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:179435843 G>A maps to NM_133378.4 D22437D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:179440964 G>A maps to NM_133378.4 I20730I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:179463873 G>A maps to NM_133378.4 F16314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:179592078 C>T maps to NM_133378.4 K5427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:179616026 C>T maps to ENST00000375038 V3702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:179622407 G>A maps to NM_133432.3 F3467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:179595316 C>T maps to NM_133378.4 L4737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:179615153 G>A maps to ENST00000375038 I3993I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:179423191 G>A maps to NM_133378.4 T26430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:179599319 G>A maps to NM_133378.4 F3833F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr2:179477897 C>T maps to NM_133378.4 K13978K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr2:179611970 G>A maps to ENST00000375038 S5054S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr2:179655530 T>C maps to NM_133378.4 V568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:179399167 C>T maps to NM_133378.4 R31490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:179501143 C>T maps to NM_133378.4 T11202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr2:179606493 G>A maps to NM_133437.3 F3651F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr2:179542584 G>A maps to NM_133378.4 L10108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr2:179546403 C>T maps to NM_133378.4 K9808K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr2:179589020 C>T maps to NM_133378.4 G5783G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr2:179612726 C>T maps to ENST00000375038 G4802G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:179428835 C>A maps to NM_133378.4 R24773R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:179431856 C>T maps to NM_133378.4 W23766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:179474028 G>A maps to NM_133378.4 V14768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:179498380 C>T maps to NM_133378.4 V11667V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:179517006 T>C maps to NM_133378.4 E10631E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:179590564 G>A maps to NM_133378.4 I5584I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:179596098 C>T maps to NM_133378.4 G4554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr2:179396514 G>A maps to NM_133378.4 R32375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr2:179475003 G>A maps to NM_133378.4 V14515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr2:179604774 C>T maps to NM_133437.3 L4224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr2:179635021 C>T maps to NM_133378.4 K2802K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr2:179433524 C>T maps to NM_133378.4 G23210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr2:179451421 G>A maps to NM_133378.4 I18834I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr2:179614556 T>G maps to ENST00000375038 V4192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr2:179410658 G>T maps to NM_133378.4 V29200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:179400745 C>T maps to NM_133378.4 G31008G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:179404388 C>T maps to NM_133378.4 G30233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:179449135 G>A maps to NM_133378.4 V19146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:179478623 G>A maps to NM_133378.4 I13894I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:179537422 C>T maps to NM_133378.4 K10297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:179585250 C>T maps to NM_133378.4 K6502K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:179606091 G>A maps to NM_133437.3 I3785I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:179611040 C>T maps to ENST00000375038 R5364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:179648922 G>A maps to NM_133378.4 F883F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr2:179426006 G>A maps to NM_133378.4 I25716I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr2:179440955 G>A maps to NM_133378.4 F20733F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr2:179596940 C>T maps to NM_133378.4 K4341K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr2:179650649 C>T maps to NM_133378.4 K765K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr2:179654824 C>T maps to NM_133378.4 R606R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr2:179597690 C>T maps to NM_133378.4 R4160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr2:179600703 C>T maps to NM_133378.4 V3579V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:179594511 G>A maps to NM_133378.4 F4912F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr2:179642030 C>T maps to NM_133378.4 Q1553Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179407829 C>T maps to NM_133378.4 E29722E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179429681 C>T maps to NM_133378.4 L24491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179436899 C>T maps to NM_133378.4 V22085V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179438750 C>T maps to NM_133378.4 K21468K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179474570 C>T maps to NM_133378.4 R14625R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179476171 C>T maps to NM_133378.4 V14360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179486594 C>T maps to NM_133378.4 A12450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179489357 C>T maps to NM_133378.4 V12315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179497988 G>A maps to NM_133378.4 H11769H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179499267 C>T maps to NM_133378.4 E11512E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179505289 C>T maps to NM_133378.4 R10999R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179510665 C>T maps to NM_133378.4 E10895E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179535005 C>T maps to NM_133378.4 K10474K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179535871 G>A maps to NM_133378.4 I10450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179552901 G>A maps to NM_133378.4 S9505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179567367 C>T maps to NM_133378.4 K8838K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179571362 G>A maps to NM_133378.4 F8502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179575644 C>T maps to NM_133378.4 G8149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179579280 C>T maps to NM_133378.4 K7496K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179580268 G>A maps to NM_133378.4 A7380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179582502 C>T maps to NM_133378.4 L7122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179583226 C>T maps to NM_133378.4 V6958V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179584155 G>A maps to NM_133378.4 F6743F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179588820 C>T maps to NM_133378.4 G5811G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179590248 C>T maps to NM_133378.4 V5650V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179591877 G>A maps to NM_133378.4 F5494F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179593735 C>T maps to NM_133378.4 V5099V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179594180 C>T maps to NM_133378.4 K4990K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179594267 C>T maps to NM_133378.4 L4961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179594904 G>A maps to NM_133378.4 A4830A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179595093 G>A maps to NM_133378.4 P4767P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179595334 G>A maps to NM_133378.4 F4731F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179596632 G>A maps to NM_133378.4 L4413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179599148 G>A maps to NM_133378.4 I3890I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179604075 G>A maps to NM_133437.3 S4457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179604198 C>T maps to NM_133437.3 E4416E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179604473 G>A maps to NM_133437.3 Q4325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179612644 G>A maps to ENST00000375038 L4830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179613866 T>A maps to ENST00000375038 P4422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179614235 C>T maps to ENST00000375038 W4299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179614316 G>A maps to ENST00000375038 S4272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179621170 G>A maps to NM_133437.3 Q3507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179631336 G>A maps to NM_133378.4 V3158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179633586 C>T maps to NM_133378.4 V2992V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179635142 C>T maps to NM_133378.4 V2792V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179639747 G>A maps to NM_133378.4 F2230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179640347 G>A maps to NM_133378.4 F2081F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179644777 C>T maps to NM_133378.4 R1226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179650430 G>A maps to NM_133378.4 V803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179659732 G>A maps to NM_133378.4 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179666961 C>T maps to NM_133378.4 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:179666988 G>A maps to NM_133378.4 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr2:179498589 T>C maps to NM_133378.4 K11644K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr2:179416810 C>T maps to NM_133378.4 W27704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr2:179495058 G>A maps to NM_133378.4 S12162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr2:179401240 C>T maps to NM_133378.4 V30843V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr2:179622643 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:179399746 G>A maps to NM_133378.4 S31297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:179431204 T>A maps to NM_133378.4 K23984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:179433872 G>A maps to NM_133378.4 I23094I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:179442497 C>T maps to NM_133378.4 S20317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:179458967 T>C maps to NM_133378.4 A16816A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:179481579 C>T maps to NM_133378.4 K13444K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:179577514 G>A maps to NM_133378.4 F7835F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:179577628 G>A maps to NM_133378.4 I7797I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:179579824 G>A maps to NM_133378.4 F7452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:179597015 G>A maps to NM_133378.4 A4316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:179598206 C>T maps to NM_133378.4 Q4027Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:179604840 C>T maps to NM_133437.3 Q4202Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:179612648 G>A maps to ENST00000375038 L4828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:179621213 G>A maps to NM_133437.3 F3492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:179629473 G>A maps to NM_133378.4 A3256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:179634790 C>T maps to NM_133378.4 V2879V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:179639093 C>T maps to NM_133378.4 W2299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:179641607 G>A maps to NM_133378.4 I1661I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:179659746 G>A maps to NM_133378.4 Q383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr2:179611550 C>T maps to ENST00000375038 R5194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr2:179611805 G>A maps to ENST00000375038 S5109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr2:179634463 C>T maps to NM_133378.4 S2948S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr2:179577950 C>T maps to NM_133378.4 R7726R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:179395822 G>A maps to NM_133378.4 A32605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:179426222 A>G maps to NM_133378.4 T25644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:179456834 C>T maps to NM_133378.4 K17364K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:179465821 C>T maps to NM_133378.4 P16035P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:179466860 G>A maps to NM_133378.4 F15811F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:179497391 G>A maps to NM_133378.4 I11879I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:179497711 C>T maps to NM_133378.4 L11814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:179569030 G>A maps to NM_133378.4 F8778F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:179590606 G>A maps to NM_133378.4 F5570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:179595337 G>A maps to NM_133378.4 A4730A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:179612524 C>A maps to ENST00000375038 E4870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:179614064 G>A maps to ENST00000375038 F4356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:179633553 C>T maps to NM_133378.4 K3003K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:179637974 G>A maps to NM_133378.4 I2572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:179638297 C>T maps to NM_133378.4 V2495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr2:179590744 A>G maps to NM_133378.4 P5524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr2:179615438 A>T maps to ENST00000375038 A3898A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr2:179434019 G>A maps to NM_133378.4 I23045I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr2:179642536 G>A maps to NM_133378.4 V1458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr2:179465713 C>T maps to NM_133378.4 V16071V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr2:179549402 G>A maps to NM_133378.4 L9632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr2:179584977 G>A maps to NM_133378.4 F6553F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:179427524 C>T maps to NM_133378.4 V25210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:179438978 G>A maps to NM_133378.4 I21392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:179441254 C>G did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:179449495 C>T maps to NM_133378.4 L19056L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:179453649 A>T maps to NM_133378.4 Y18366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:179574482 T>C maps to NM_133378.4 Q8277Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:179650463 C>T maps to NM_133378.4 K792K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr2:179410838 G>A maps to NM_133378.4 S29140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr2:179424737 C>T maps to NM_133378.4 G26139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr2:179599204 G>A maps to NM_133378.4 R3872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr2:179616566 C>A maps to ENST00000375038 P3522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:179641268 G>A maps to NM_133378.4 I1774I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:63978600 G>A maps to NM_000370.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:63978528 A>G maps to NM_000370.3 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q1-06A-21D-A196-08 chr20:43115233 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr20:43108796 G>A maps to NM_024331.3 W53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr20:43108797 G>A maps to NM_024331.3 W53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr20:43108899 C>T maps to NM_024331.3 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr19:54946738 G>A maps to ENST00000391739 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr19:54940484 G>C maps to ENST00000391739 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:54947050 C>T maps to ENST00000391739 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:72246426 C>T maps to NM_032646.5 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr17:72248443 C>T maps to NM_032646.5 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:72249959 C>T maps to NM_032646.5 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:72249255 C>T maps to NM_032646.5 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:2687679 C>T maps to NM_025250.2 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr7:2687221 G>A maps to NM_025250.2 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr7:2692624 G>A maps to NM_025250.2 W334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr7:2686503 G>A maps to NM_025250.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr7:2698039 C>T maps to NM_025250.2 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr11:8119364 G>A maps to NM_003320.4 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:8117064 C>T maps to NM_003320.4 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:8118893 C>T maps to NM_003320.4 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:8118268 G>A maps to NM_003320.4 E256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:8122527 C>T maps to NM_003320.4 I512I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:8060476 G>A maps to NM_003320.4 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:8122512 G>A maps to NM_003320.4 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:49579394 G>A maps to NM_006009.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:49579406 G>A maps to NM_006009.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr12:49522722 T>C did not map to a codon.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr12:49521860 C>T maps to NM_006082.2 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:49523141 G>A maps to NM_006082.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:49663312 C>T maps to NM_032704.3 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr12:49666154 C>T maps to NM_032704.3 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr12:49666879 G>A maps to NM_032704.3 W407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr13:19751591 G>A maps to NM_006001.1 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr13:19751675 G>A maps to NM_006001.1 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr13:19751420 G>A maps to NM_006001.1 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr13:19752418 G>A maps to NM_006001.1 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr13:19751675 G>A maps to NM_006001.1 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr13:19748107 C>T maps to NM_006001.1 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr13:19751120 G>A maps to NM_006001.1 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr13:19748200 C>T maps to NM_006001.1 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr13:19751120 G>A maps to NM_006001.1 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr13:19751363 C>T maps to NM_006001.1 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr13:19748239 C>T maps to NM_006001.1 Q372Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr13:19751627 G>A maps to NM_006001.1 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr13:19751675 G>A maps to NM_006001.1 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr13:19751282 C>T maps to NM_006001.1 K280K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr13:19751420 G>A maps to NM_006001.1 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr13:19753481 G>A maps to NM_006001.1 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:19748170 G>A maps to NM_006001.1 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:132238003 G>A maps to NM_080386.2 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr2:132237793 G>A maps to NM_080386.2 Q176Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr2:132238054 C>T maps to NM_080386.2 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:130951676 C>T maps to NM_207312.2 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:130951712 G>A maps to NM_207312.2 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:130951655 C>T maps to NM_207312.2 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr2:220115511 T>C maps to NM_006000.1 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr2:220115132 T>A maps to NM_006000.1 K430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:220116370 C>T maps to NM_006000.1 E97E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:220115709 G>A maps to NM_006000.1 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:18613674 C>T maps to NM_018943.2 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr22:18613812 G>A maps to NM_018943.2 E420E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:5435974 G>A maps to NM_024803.2 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr10:5437346 G>A maps to NM_024803.2 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr10:5435515 C>T maps to NM_024803.2 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr10:5435998 G>A maps to NM_024803.2 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:5435775 G>A maps to NM_024803.2 Q349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:5435977 G>A maps to NM_024803.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr10:5435974 G>A maps to NM_024803.2 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:30691564 C>T maps to NM_178014.2 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr20:57599798 G>A maps to NM_030773.3 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr20:57599798 G>A maps to NM_030773.3 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:57598952 G>A maps to NM_030773.3 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr6:3155865 G>A maps to NM_001069.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr6:3154831 G>T maps to NM_001069.2 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr9:140137800 G>T maps to NM_006088.5 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr16:90001824 C>T maps to ENST00000304984 S669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr16:90001225 G>T maps to ENST00000304984 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:90001539 C>T maps to ENST00000304984 H574H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:90002124 C>T maps to ENST00000304984 Y769Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr16:90002148 C>T maps to ENST00000304984 A777A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr19:6495963 G>A maps to NM_006087.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:6501322 G>A maps to NM_006087.2 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:6495471 G>A maps to NM_006087.2 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:6496109 G>A maps to NM_006087.2 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:6496197 C>G maps to NM_006087.2 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr18:12325477 C>T maps to NM_032525.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr18:12325367 G>T maps to NM_032525.1 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr18:12325642 C>T maps to NM_032525.1 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr18:12325111 G>A maps to NM_032525.1 E108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr10:93359 C>T maps to NM_177987.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr10:94561 G>A maps to NM_177987.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr10:93314 A>G maps to NM_177987.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:57958452 G>T maps to NM_016261.3 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr6:112393215 G>A maps to NM_016262.4 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:40766393 C>T maps to NM_001070.4 I320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:40766578 C>T maps to NM_001070.4 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:40762195 C>T maps to NM_001070.4 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:40766575 C>T maps to NM_001070.4 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr17:40817712 G>C maps to NM_016437.2 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:40811915 G>A maps to NM_016437.2 E38E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:40818498 C>T maps to NM_016437.2 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:40811957 C>T maps to NM_016437.2 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr17:40818628 A>G maps to NM_016437.2 E389E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr10:135098964 G>A maps to NM_006659.2 I630I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr10:135111498 G>A maps to NM_006659.2 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr10:135099032 G>A maps to NM_006659.2 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr10:135095759 G>A maps to NM_006659.2 A792A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr10:135103430 G>A maps to NM_006659.2 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:135098991 G>A maps to NM_006659.2 I621I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr10:135101770 G>A maps to NM_006659.2 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr10:135095783 G>A maps to NM_006659.2 T784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr13:113200060 G>A maps to NM_006322.4 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr13:113208440 C>T maps to NM_006322.4 W299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:113140351 G>A maps to NM_006322.4 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr13:113174229 G>A maps to NM_006322.4 I617I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr13:113158470 C>A maps to NM_006322.4 E728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr13:113176670 G>A maps to NM_006322.4 Q570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr13:113208408 G>A maps to NM_006322.4 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr15:43670088 T>C maps to ENST00000399460 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr15:43696744 G>A maps to ENST00000399460 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:43693967 C>A maps to ENST00000399460 R552R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr15:43663576 C>T maps to ENST00000399460 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:43668390 C>T maps to ENST00000399460 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:43670061 C>T maps to ENST00000399460 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr15:22853741 C>T maps to NM_052903.4 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr15:22851027 C>T maps to NM_052903.4 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr15:22868843 C>T maps to NM_052903.4 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr15:22846946 C>T maps to NM_052903.4 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr15:22846947 C>T maps to NM_052903.4 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:22861792 C>T maps to NM_052903.4 R605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr15:22864187 T>C maps to NM_052903.4 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr15:22853801 C>T maps to NM_052903.4 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr15:22867575 C>T maps to NM_052903.4 F884F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:22855191 C>T maps to NM_052903.4 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:22872488 C>T maps to NM_052903.4 S1006S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr15:22864222 C>T maps to NM_052903.4 F727F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr22:50667867 G>A maps to NM_020461.3 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr22:50660945 G>A maps to NM_020461.3 I782I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr22:50658707 G>A maps to NM_020461.3 T1360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr22:50658791 G>A maps to NM_020461.3 P1332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr22:50664312 C>T maps to NM_020461.3 E631E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr22:50664719 G>A maps to NM_020461.3 F563F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:50658826 G>A maps to NM_020461.3 L1321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr16:28855287 G>A maps to NM_003321.4 Q353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:28855356 G>A maps to NM_003321.4 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:28855797 G>A maps to NM_003321.4 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:28854469 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:151536459 C>T maps to NM_020127.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:151536460 C>T maps to NM_020127.2 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr6:35478662 C>T maps to NM_003322.3 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr6:35477634 C>T maps to NM_003322.3 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr6:35478644 G>A maps to NM_003322.3 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr6:35471585 G>A maps to NM_003322.3 N384N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr19:49385370 C>T maps to NM_003323.2 E455E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:49398411 C>T maps to NM_003323.2 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr19:49398287 G>A maps to NM_003323.2 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:49391245 G>A maps to NM_003323.2 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:49398324 G>A maps to NM_003323.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:3018743 C>T maps to NM_001160408.1 Q31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:3040400 C>T maps to NM_001160408.1 Q231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:3040253 C>T maps to NM_001160408.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr6:158923751 C>T maps to NM_020245.3 P1019P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:158924012 C>T maps to NM_020245.3 H1106H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:158882727 G>T maps to NM_020245.3 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:158900899 C>T maps to NM_020245.3 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr6:158923496 C>T maps to NM_020245.3 V934V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr6:158923850 C>T maps to NM_020245.3 S1052S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:15508317 C>T maps to NM_006765.2 Q141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr8:15517092 C>T maps to NM_006765.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:15508280 C>T maps to NM_006765.2 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr8:15519759 C>T maps to NM_006765.2 N221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr8:15398067 G>A maps to NM_006765.2 K43K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr8:15480758 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51K-06A-11D-A25O-08 chr17:1198819 C>T maps to NM_172367.2 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:1183546 G>A maps to NM_172367.2 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr17:1183459 G>A maps to NM_172367.2 Q55Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:62343573 C>T maps to NM_022830.2 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr11:62343078 G>T maps to NM_022830.2 A742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:62346322 C>T maps to NM_022830.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr3:52264890 G>A maps to ENST00000494383 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:52264924 G>A maps to ENST00000494383 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr3:52263097 G>A maps to NM_007284.3 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr7:19156581 G>A maps to NM_000474.3 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr7:19738073 G>A maps to NM_001002926.1 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr7:19748468 G>A maps to NM_001002926.1 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr18:9396350 G>A maps to NM_020648.5 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr4:48116366 C>T maps to NM_003328.2 K23K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr4:48078474 C>T maps to NM_003328.2 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:48076024 G>A maps to NM_003328.2 F428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:32657916 C>T maps to NM_175852.3 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:139576744 G>A maps to ENST00000358430 Q345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr6:139564175 C>T maps to ENST00000358430 E514E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr6:139564217 C>T maps to ENST00000358430 V500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:139609964 T>C maps to ENST00000358430 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr6:139563668 G>A maps to ENST00000358430 V683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:139564196 G>A maps to ENST00000358430 F507F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:16850828 A>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:16847823 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr22:36876737 G>A maps to NM_012473.3 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr22:36863859 C>A maps to NM_012473.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr22:36876790 G>A maps to NM_012473.3 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:11785401 G>A maps to ENST00000356957 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr16:11785737 G>A maps to ENST00000356957 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr16:11792182 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:11785895 G>A maps to ENST00000356957 Q411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr16:11830037 G>A maps to ENST00000356957 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr5:134229286 C>T maps to NM_024715.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:134223700 C>T maps to NM_024715.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr5:134223430 C>T maps to NM_024715.3 H50H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:52957603 C>T maps to NM_020784.2 W292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr14:52981632 G>A maps to NM_020784.2 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr14:52957678 G>A maps to NM_020784.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr14:52906027 C>A maps to NM_020784.2 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr14:52985898 C>A maps to NM_020784.2 G169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr18:9887000 G>A maps to NM_001098529.1 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr18:9887471 C>T maps to NM_001098529.1 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr18:9886877 C>T maps to NM_001098529.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:9887372 C>T maps to NM_001098529.1 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:9887523 G>T maps to NM_001098529.1 E350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr18:9887911 G>A maps to NM_001098529.1 W479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr18:9887912 G>A maps to NM_001098529.1 W479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr18:9886721 C>T maps to NM_001098529.1 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr18:9887843 G>A maps to NM_001098529.1 K456K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr18:9887777 C>T maps to NM_001098529.1 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr18:9886649 C>T maps to NM_001098529.1 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:9887507 C>T maps to NM_001098529.1 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:9887945 C>T maps to NM_001098529.1 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:37901709 G>A maps to NM_016616.4 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ME-06A-11D-A197-08 chr7:37901706 G>A maps to NM_016616.4 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:37907311 C>T maps to NM_016616.4 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:37916592 C>T maps to NM_016616.4 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:37916581 C>T maps to NM_016616.4 R323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr7:37927956 G>A maps to NM_016616.4 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr7:37916565 G>A maps to NM_016616.4 K317K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr7:37936582 C>T maps to NM_016616.4 I552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:37901643 C>T maps to NM_016616.4 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:37889892 C>T maps to NM_016616.4 Q9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:37916526 C>T maps to NM_016616.4 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr6:7904915 G>A maps to NM_030810.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr6:7904916 G>A maps to NM_030810.3 D101D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr3:138038352 G>A maps to ENST00000333911 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:138024932 C>T maps to ENST00000333911 Q183Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr3:138037004 G>A maps to ENST00000333911 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:138033207 G>C maps to ENST00000333911 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:138025308 C>T maps to ENST00000333911 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:113066796 T>G maps to NM_001003936.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr9:113096558 G>A maps to NM_001003936.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr2:99938560 G>A maps to NM_005783.3 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr18:54291640 G>A maps to NM_004786.2 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr18:54291640 G>A maps to NM_004786.2 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr12:104682757 C>G maps to NM_001093771.1 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr22:19865680 C>T maps to NM_006440.3 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr22:19906447 C>A maps to NM_006440.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr22:19865662 G>A maps to NM_006440.3 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr22:19898967 G>A maps to NM_006440.3 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr22:19918598 G>A maps to NM_006440.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:19865927 G>A maps to NM_006440.3 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:126291344 C>T maps to NM_001039783.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr3:126291209 G>A maps to NM_001039783.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:126291116 A>T maps to NM_001039783.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:10464892 G>A maps to NM_003331.4 V911V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr19:10476450 G>A maps to NM_003331.4 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr19:10467256 C>T maps to NM_003331.4 R868R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:10473090 G>A maps to NM_003331.4 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:10475315 G>A maps to NM_003331.4 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:10461602 G>A maps to NM_003331.4 S1157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:10475408 G>A maps to NM_003331.4 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:10465202 G>A maps to NM_003331.4 I900I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:10465271 G>A maps to NM_003331.4 V877V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:10476375 G>A maps to NM_003331.4 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr11:88911236 G>A maps to NM_000372.4 W39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr11:88911294 C>T maps to NM_000372.4 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:88911833 G>A maps to NM_000372.4 W238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr15:41861140 C>T maps to NM_006293.3 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr15:41854851 C>T maps to NM_006293.3 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr15:41861140 C>T maps to NM_006293.3 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr15:41859613 C>T maps to NM_006293.3 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:71903628 G>A maps to NM_173555.2 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr10:71905211 T>C maps to NM_173555.2 E377E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:71902466 G>A maps to NM_173555.2 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr7:66532273 C>T maps to NM_018264.2 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:66489954 C>T maps to NM_018264.2 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:66489984 T>A maps to NM_018264.2 I320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr7:66548428 C>T maps to NM_018264.2 N429N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr7:72178688 G>A maps to NM_001145440.1 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:72081674 G>A maps to NM_001145440.1 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:72159742 G>A maps to NM_001145440.1 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr1:75198981 G>A maps to NM_138467.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr19:36233528 G>A maps to NM_144987.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:36233573 G>A maps to NM_144987.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:56170675 C>T maps to NM_007279.2 D50D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:56170676 C>T maps to NM_007279.2 Q51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:56171938 C>T maps to NM_007279.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr15:70960838 G>A maps to NM_018003.2 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr15:70960301 T>C maps to NM_018003.2 L907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr15:70969479 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:70960073 T>C maps to NM_018003.2 V983V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr1:162536124 C>T maps to ENST00000367925 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:162567608 C>T maps to ENST00000367925 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:162567609 C>T maps to ENST00000367925 Q480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:47065791 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:47065787 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:47073811 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:47074245 G>C did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:47060943 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:34929647 C>T maps to NM_005499.2 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr19:34959990 T>C maps to NM_005499.2 D596D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr19:34921553 C>G maps to NM_005499.2 S71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr3:69111309 G>A maps to NM_003968.3 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr3:69111321 A>G maps to NM_003968.3 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:18685734 C>T maps to NM_003333.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr19:18684475 C>T maps to NM_003333.3 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:68500022 G>A maps to NM_018227.5 S650S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr4:68543346 G>A maps to NM_018227.5 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:68547870 G>A maps to NM_018227.5 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:49848489 C>T maps to NM_003335.2 W386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:138831521 G>A maps to NM_016172.2 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr9:138830122 G>A maps to NM_016172.2 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr13:99890807 G>A maps to NM_001144072.1 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr13:99966404 C>T maps to NM_001144072.1 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr9:33960856 C>T maps to NM_018449.2 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:33956123 G>A maps to NM_018449.2 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:154197656 C>T maps to NM_014847.3 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr1:154229840 C>T maps to NM_014847.3 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr1:154229840 C>T maps to NM_014847.3 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr1:154227724 C>A maps to NM_014847.3 T669T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:43864743 C>T maps to NM_018961.2 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr21:43838526 C>T maps to NM_018961.2 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr21:43838664 G>A maps to NM_018961.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr21:43838512 C>T maps to NM_018961.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr21:43829557 C>T maps to NM_018961.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr21:43838631 G>A maps to NM_018961.2 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr21:43833311 G>A maps to NM_018961.2 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr21:43838655 G>A maps to NM_018961.2 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr21:43862598 A>G maps to NM_018961.2 E508E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr21:43833248 C>T maps to NM_018961.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr21:43833574 C>T maps to NM_018961.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr21:43833206 C>T maps to NM_018961.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr21:43854999 G>A maps to NM_018961.2 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:122669680 C>T maps to NM_032873.4 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr11:122647761 G>A maps to NM_032873.4 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr17:16285328 T>C maps to NM_018955.2 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr17:16285496 A>G maps to NM_018955.2 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr17:16285559 T>C maps to NM_018955.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr12:125397414 G>A maps to NM_021009.5 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:125396517 G>A maps to NM_021009.5 H600H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:125397885 G>A maps to NM_021009.5 H144H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:125397651 T>C maps to NM_021009.5 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:125397804 G>C maps to NM_021009.5 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr12:125396451 G>A maps to NM_021009.5 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr6:29523698 C>T maps to NM_006398.3 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr6:29524028 C>T maps to NM_006398.3 K42K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:29523758 C>T maps to NM_006398.3 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:118708941 C>T did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr23:118709339 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr20:44444544 C>T maps to NM_007019.2 N158N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:44444314 C>T maps to NM_007019.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:44443051 C>T maps to NM_007019.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:83728786 G>A maps to NM_198920.1 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr6:83728795 G>A maps to NM_198920.1 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr6:83754239 G>A maps to NM_198920.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:83728786 G>A maps to NM_198920.1 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:60124589 C>T maps to NM_003338.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:103723738 G>A maps to NM_181890.1 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:43978037 C>T maps to NM_015983.3 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr3:23574052 C>T maps to NM_152653.3 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr3:23574053 C>T maps to NM_152653.3 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr3:23250195 C>T maps to NM_152653.3 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z4-06A-11D-A197-08 chr2:238940896 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:4192608 G>A maps to NM_003342.4 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr7:129497351 A>C maps to NM_003344.2 Y99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr16:1370211 C>T maps to NM_194259.1 Y87Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr16:1370211 C>T maps to NM_194259.1 Y87Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr1:1203264 G>A maps to NM_194315.1 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:1203255 C>T maps to NM_194315.1 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:1190810 G>A maps to NM_194315.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:57322015 G>A maps to NM_004223.3 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:57321972 C>A maps to NM_004223.3 G83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:59068130 G>A maps to NM_003969.3 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:93804627 C>T maps to NM_003348.3 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:93804642 C>T maps to NM_003348.3 W95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:142967601 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr23:142967208 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:142967433 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:142967325 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr23:142967307 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:142967225 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:142967307 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:142967458 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:142967417 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:142967525 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:142967492 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:74397133 G>A maps to NM_022066.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:74391898 G>A maps to NM_022066.3 A951A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:74387358 G>A maps to NM_022066.3 Q1182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr17:74395072 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:74392457 G>A maps to NM_022066.3 L854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:74401373 G>A maps to NM_022066.3 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:74401594 G>A maps to NM_022066.3 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr1:154524606 C>A maps to NM_017582.6 E310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:76175736 C>T maps to NM_173469.2 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:55913070 G>T maps to NM_014501.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:55913082 G>A maps to NM_014501.2 N130N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:64671362 G>A maps to ENST00000371077 W36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:64707406 G>A maps to ENST00000371077 W223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:48955639 G>T maps to NM_003350.2 G22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr8:74782502 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:74722758 G>A maps to NM_001001481.1 Q117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:46990248 C>T maps to NM_023079.4 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr15:25585359 G>A maps to NM_000462.2 I793I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:25585323 G>A maps to NM_000462.2 F805F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr12:109967760 C>T maps to NM_183415.1 A898A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:109939174 G>A did not map to a codon.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr12:109959292 C>T maps to NM_183415.1 I767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr12:109921394 C>T maps to NM_183415.1 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:109945400 C>T maps to NM_183415.1 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:109928860 C>T maps to NM_183415.1 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr12:109926453 G>A maps to NM_183415.1 W175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr12:109947475 C>T maps to NM_183415.1 F566F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:109971272 C>T maps to NM_183415.1 F975F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:109936078 C>T maps to NM_183415.1 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:109940942 C>T maps to NM_183415.1 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:109937498 C>T maps to NM_183415.1 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr7:156979614 C>T maps to NM_014671.2 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:156963047 C>T maps to NM_014671.2 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:156974993 C>T maps to NM_014671.2 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr7:156961789 C>T maps to NM_014671.2 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:156974993 C>T maps to NM_014671.2 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr7:156967665 G>A maps to NM_014671.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr7:156967648 C>T maps to NM_014671.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:157041159 C>T maps to NM_014671.2 A860A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr7:157000155 C>T maps to NM_014671.2 R495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr11:118257191 C>T maps to NM_004788.2 R825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:118267124 G>A maps to NM_004788.2 E1064E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:118245819 C>G maps to NM_004788.2 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:118267049 C>T maps to NM_004788.2 N1039N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:118255599 C>T maps to NM_004788.2 F791F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr11:118239487 C>T maps to NM_004788.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr11:118267124 G>A maps to NM_004788.2 E1064E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr11:118245633 G>A maps to NM_004788.2 K387K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:118243307 C>T maps to NM_004788.2 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr1:10239579 C>T maps to NM_001105562.2 P1269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:10161223 C>T maps to NM_001105562.2 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:10195089 C>T maps to NM_001105562.2 F690F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr1:10166365 C>T maps to NM_001105562.2 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:10155573 C>T maps to NM_001105562.2 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:10228226 C>T maps to NM_001105562.2 Q1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:10231362 C>T maps to NM_001105562.2 F1167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:23581892 G>A maps to ENST00000219638 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:11333956 C>T maps to NM_013319.2 D123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:11333957 C>T maps to NM_013319.2 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:11346121 C>T maps to NM_013319.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:11345968 C>T maps to NM_013319.2 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:11334046 C>T maps to NM_013319.2 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:11346121 C>T maps to NM_013319.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:11346013 C>T maps to NM_013319.2 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:11345803 C>T maps to NM_013319.2 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr13:30346296 G>A maps to NM_007106.3 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:110655203 G>A maps to NM_203412.1 K16K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:110655413 G>A maps to NM_203412.1 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr15:74738568 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr15:74743819 G>A maps to NM_201265.1 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr5:158697387 C>T maps to NM_145049.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:158699031 C>T maps to NM_145049.3 D150D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr16:4909161 T>C did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr16:4927089 C>T maps to NM_016936.3 S1081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:4927101 C>T maps to NM_016936.3 G1085G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:4910868 C>T maps to NM_016936.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:4909090 C>T maps to NM_016936.3 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr16:4927107 C>T maps to NM_016936.3 G1087G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:138943250 C>T maps to NM_173569.3 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:138978003 T>C maps to NM_173569.3 A1232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr7:138968701 T>C maps to NM_173569.3 A1017A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr7:138946271 C>T maps to NM_173569.3 Q394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr7:138958808 G>A maps to NM_173569.3 W654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr7:138967768 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr7:138968104 C>T maps to NM_173569.3 P818P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:138946033 G>A maps to NM_173569.3 K314K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr7:138946165 C>T maps to NM_173569.3 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr20:3102729 G>A maps to NM_014948.2 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:33481295 C>T maps to NM_001128161.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr3:33451018 A>T maps to NM_001128161.1 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr11:5530190 G>A maps to NM_017481.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr11:5529399 G>A maps to NM_017481.2 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr11:5530395 G>A maps to NM_017481.2 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:5529723 G>A maps to NM_017481.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:5529597 G>A maps to NM_017481.2 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:5530320 G>A maps to NM_017481.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr11:5529375 G>A maps to NM_017481.2 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:5529467 A>G maps to NM_017481.2 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:5529450 C>T maps to NM_017481.2 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:5529822 C>T maps to NM_017481.2 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr11:5529828 C>T maps to NM_017481.2 Q320Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr11:5529750 G>A maps to NM_017481.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5529495 C>T maps to NM_017481.2 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr1:156020297 A>C maps to NM_020131.3 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:156020206 G>A maps to NM_020131.3 Q206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr1:156013849 G>A maps to NM_020131.3 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:156018387 G>A maps to NM_020131.3 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr11:5537113 G>A maps to NM_145053.4 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr11:5537449 G>A maps to NM_145053.4 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:5536696 C>T maps to NM_145053.4 Q325Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr11:5537317 C>T maps to NM_145053.4 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:5537317 C>T maps to NM_145053.4 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:5536966 G>A maps to NM_145053.4 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr11:5537224 G>A maps to NM_145053.4 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5537101 G>A maps to NM_145053.4 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:5537224 G>A maps to NM_145053.4 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr11:5537407 C>T maps to NM_145053.4 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr15:43317038 C>T maps to NM_174916.2 G909G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr15:43339379 G>A maps to NM_174916.2 F549F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:43339379 G>A maps to NM_174916.2 F549F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr15:43367224 G>A maps to NM_174916.2 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr15:43347093 G>A maps to NM_174916.2 R429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:43318758 C>T maps to NM_174916.2 K845K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr15:43244480 G>A maps to NM_174916.2 F1667F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:43269029 C>T maps to NM_174916.2 W1418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr15:43340621 G>A maps to NM_174916.2 R503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr6:42585057 C>T maps to NM_015255.2 F421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:42627583 C>T maps to NM_015255.2 Q1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:42613321 T>G maps to NM_015255.2 P801P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:42637832 C>T maps to NM_015255.2 I1295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr6:42637844 G>A maps to NM_015255.2 E1299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:42615887 C>T maps to NM_015255.2 I814I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:42656115 C>T maps to NM_015255.2 I1672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr6:42656025 C>T maps to NM_015255.2 S1642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr6:42656026 C>T maps to NM_015255.2 Q1643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:42582839 T>C maps to NM_015255.2 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:42643910 T>C maps to NM_015255.2 L1457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:170871863 A>C maps to ENST00000442603 R1481R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:170897467 T>C maps to ENST00000442603 L1574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:19415263 G>A maps to ENST00000375267 L4807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:19415264 G>A maps to ENST00000375267 T4806T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr1:19407946 A>T maps to ENST00000375267 L5043L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:19500081 G>A maps to ENST00000375267 L1006L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr1:19518856 G>A maps to ENST00000375267 Q407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr1:19437237 G>A maps to ENST00000375267 L3964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr1:19441953 G>A maps to ENST00000375267 V3667V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:19446737 G>A maps to ENST00000375267 L3416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:19439232 C>T maps to ENST00000375267 L3862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:19433104 G>A maps to ENST00000375267 S4117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr1:19477068 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:19426926 G>A maps to ENST00000375267 N4388N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:19494555 G>A maps to ENST00000375267 L1288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:19430686 A>G maps to ENST00000375267 G4264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:19447896 G>A maps to ENST00000375267 F3309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:19525395 G>A maps to ENST00000375267 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:19433143 C>T maps to ENST00000375267 R4104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:19423028 G>A maps to ENST00000375267 R4502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr1:19477267 T>C maps to ENST00000375267 P2411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:19454737 G>A maps to ENST00000375267 S3026S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:19445391 G>A maps to ENST00000375267 T3505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:19449392 G>A maps to ENST00000375267 F3250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:19428055 G>A maps to ENST00000375267 T4327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:103269902 C>T maps to NM_015902.4 W2715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr8:103307738 G>A maps to NM_015902.4 F1278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:103291104 G>T maps to NM_015902.4 A2079A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr8:103311077 G>A maps to NM_015902.4 A1108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:103354799 A>G maps to NM_015902.4 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr8:103279189 G>A maps to NM_015902.4 S2469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:103323562 G>A maps to NM_015902.4 I860I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:103311160 G>A maps to NM_015902.4 R1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:103306289 T>A maps to NM_015902.4 T1414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr8:103271214 G>T maps to NM_015902.4 S2700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:103308006 G>A maps to NM_015902.4 L1223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr8:103316392 C>A maps to NM_015902.4 A944A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr14:93685664 C>G maps to NM_175748.3 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr14:93684978 C>T maps to NM_175748.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr5:171638917 G>A maps to NM_152277.2 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:171638902 G>A maps to NM_152277.2 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr5:171639157 G>A maps to NM_152277.2 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr17:42284845 C>T maps to NM_014233.2 E715E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:42288973 C>T maps to NM_014233.2 Q349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr11:62445418 C>T maps to NM_015853.3 K154K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:20517569 G>A maps to NM_152376.3 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:20517563 G>A maps to NM_152376.3 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr1:20517683 G>A maps to NM_152376.3 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:20517365 C>T maps to NM_152376.3 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:26620702 C>T maps to NM_183008.2 W184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:26620705 G>A maps to NM_183008.2 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:26620780 G>T maps to NM_183008.2 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:24199942 G>A maps to NM_181713.3 K95K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr8:59329507 C>T maps to NM_001077619.1 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr2:136505927 C>T maps to NM_014607.3 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr3:196098778 G>A maps to NM_015562.1 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:41262674 C>T maps to NM_004181.4 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:41262767 C>T maps to NM_004181.4 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr4:41262767 C>T maps to NM_004181.4 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr13:76134926 C>T maps to NM_006002.3 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:193018905 G>A maps to ENST00000367450 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr9:134405903 G>A maps to NM_031432.2 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr9:134404655 A>G maps to NM_031432.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr9:134404536 G>A maps to NM_031432.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:165859598 G>A maps to NM_012474.4 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr20:62577060 A>C maps to NM_017859.3 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr10:13275592 C>T maps to NM_145314.1 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:13264195 C>T maps to NM_145314.1 Q108Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr10:13275622 C>T maps to NM_145314.1 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr10:5415839 C>T maps to NM_053049.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:141483492 G>A maps to NM_021833.4 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr4:141489766 G>A maps to NM_021833.4 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:141489068 G>C maps to NM_021833.4 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:73688039 G>A maps to NM_003355.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:73687967 G>A maps to NM_003355.2 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:73686069 G>A maps to NM_003355.2 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:73715029 G>A maps to NM_003356.3 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:73716889 G>A maps to NM_003356.3 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr11:73717421 G>A maps to NM_003356.3 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr11:73716888 G>A maps to NM_003356.3 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:73715532 G>A maps to NM_003356.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr11:18579814 G>A maps to NM_001040697.1 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr11:18596939 C>T maps to NM_001040697.1 Q49Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:186329115 A>G maps to NM_018359.3 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr9:114695240 C>T maps to NM_003358.1 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr4:39510230 G>A maps to NM_003359.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr4:39523078 G>C maps to NM_003359.3 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr2:128877959 G>A maps to NM_020120.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:128918776 C>T maps to NM_020120.3 I920I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:128865524 C>T maps to NM_020120.3 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:128936107 C>A maps to NM_020120.3 S1260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr2:128870750 G>A maps to NM_020120.3 E205E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr2:128930206 G>A maps to NM_020120.3 K1055K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:128873891 C>T maps to NM_020120.3 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr13:96506701 G>A maps to NM_020121.3 R1346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr13:96536858 T>C maps to NM_020121.3 K1038K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr13:96578026 A>G maps to NM_020121.3 D734D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:96506590 A>G maps to NM_020121.3 L1383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr13:96508420 A>G maps to NM_020121.3 D1333D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr13:96553066 A>G maps to NM_020121.3 N876N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr2:64118255 A>G maps to NM_006759.3 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:234669286 G>A maps to NM_000463.2 K118K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr2:234676544 G>A maps to ENST00000373460 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:234677028 G>A maps to ENST00000373460 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr2:234680922 C>T maps to ENST00000373460 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:234669349 C>T maps to NM_000463.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:234669589 G>A maps to NM_000463.2 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr2:234676526 G>A maps to ENST00000373460 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:234669409 C>T maps to NM_000463.2 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:234681159 G>A maps to ENST00000373460 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr2:234681147 G>A maps to ENST00000373460 R513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:234669196 G>A maps to NM_000463.2 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:234545425 G>A maps to NM_019075.2 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr2:234545581 G>A maps to NM_019075.2 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:234545461 G>A maps to NM_019075.2 W98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:234545606 C>T maps to NM_019075.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr2:234545581 G>A maps to NM_019075.2 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:234545446 C>T maps to NM_019075.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:234546023 G>A did not map to a codon.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr2:234545245 G>A maps to NM_019075.2 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr2:234637996 C>T maps to NM_019093.2 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr2:234637996 C>T maps to NM_019093.2 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:234637840 G>A maps to NM_019093.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:234638434 C>T maps to NM_019093.2 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:234638182 G>A maps to NM_019093.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:234638206 C>T maps to NM_019093.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr2:234627472 A>T maps to NM_007120.2 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:234627963 G>A maps to NM_007120.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:234628149 T>C maps to NM_007120.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:234628095 G>A maps to NM_007120.2 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:234627834 C>T maps to NM_007120.2 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:234627555 G>A maps to NM_007120.2 K30K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44R-06A-41D-A25O-08 chr2:234622110 G>A maps to NM_019078.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr2:234622107 C>T maps to NM_019078.1 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:234622119 G>A maps to NM_019078.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr2:234621887 G>A maps to NM_019078.1 W84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:234622402 C>T maps to NM_019078.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:234602162 C>T maps to NM_001072.3 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:234602063 C>T maps to NM_001072.3 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:234602021 C>T maps to NM_001072.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:234602171 T>C maps to NM_001072.3 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr2:234602391 C>T maps to NM_001072.3 Q248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:234602468 C>T maps to NM_001072.3 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:234590829 C>T maps to NM_019077.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:234590738 G>A maps to NM_019077.2 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:234526964 G>A maps to NM_019076.4 K204K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:234526430 G>A maps to NM_019076.4 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:234526406 G>A maps to NM_019076.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:234526841 C>T maps to NM_019076.4 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:234580993 G>A maps to NM_021027.2 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:234580753 C>T maps to ENST00000373460 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:234581260 C>T maps to NM_021027.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:234581299 G>A maps to NM_021027.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:70513131 G>A maps to ENST00000514019 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:70512681 C>T maps to ENST00000514019 W227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:70513182 G>A maps to ENST00000514019 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr4:70460967 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:70455304 G>A maps to ENST00000514019 R623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:70464962 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr4:70513008 G>A maps to ENST00000514019 F118F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A3AA-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr4:70455221 G>A maps to ENST00000514019 F650F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr4:70455107 C>T maps to ENST00000514019 K688K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr4:70455304 G>A maps to ENST00000514019 R623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr4:70504642 C>T maps to ENST00000514019 W440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:70504956 G>A maps to ENST00000514019 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr4:70504812 G>A maps to ENST00000514019 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr4:70505017 C>T maps to ENST00000514019 W315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr4:69817355 G>A maps to NM_024743.3 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:69817322 C>T maps to NM_024743.3 E52E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr4:69817406 C>T maps to NM_024743.3 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:69796391 G>A maps to NM_024743.3 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr4:69795745 G>A maps to NM_024743.3 R457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr4:69796436 C>T maps to NM_024743.3 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:69816929 C>T maps to NM_024743.3 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr4:69798378 G>A maps to NM_024743.3 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr4:69795745 G>A maps to NM_024743.3 R457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:69817441 G>A maps to NM_024743.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr4:69798407 G>A maps to NM_024743.3 Q312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr4:69817430 G>A maps to NM_024743.3 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr4:69682405 C>T maps to NM_001075.4 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:69682276 A>G maps to NM_001075.4 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:69693116 G>A maps to NM_001075.4 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr4:69682354 C>T maps to NM_001075.4 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:69693176 G>A maps to NM_001075.4 K406K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:69696464 C>T maps to NM_001075.4 F485F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr4:69681840 G>A maps to NM_001075.4 W35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr4:69696494 C>T maps to NM_001075.4 F495F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:69682300 C>T maps to NM_001075.4 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr4:69692147 G>A maps to NM_001075.4 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr4:70079873 G>A maps to NM_001073.1 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr4:70070293 G>A maps to NM_001073.1 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:70080094 G>A maps to NM_001073.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr4:70080426 C>T maps to NM_001073.1 W5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr4:70066196 C>T maps to NM_001073.1 W517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:70078290 C>T maps to NM_001073.1 K290K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr4:70079873 G>A maps to NM_001073.1 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:70066427 C>T maps to NM_001073.1 E440E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:70071285 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr4:70071285 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:70079873 G>A maps to NM_001073.1 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr4:70079873 G>A maps to NM_001073.1 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr4:70066196 C>T maps to NM_001073.1 W517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr4:70080095 G>A maps to NM_001073.1 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr4:70066196 C>T maps to NM_001073.1 W517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr4:69433497 C>T maps to NM_001076.2 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr4:69433569 C>T maps to NM_001076.2 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr4:69535766 G>A maps to NM_001076.2 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51N-06A-11D-A25O-08 chr4:69520891 C>T maps to NM_001076.2 W338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr4:69533852 G>A maps to NM_001076.2 R260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr4:69403408 G>A maps to NM_001076.2 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr4:69434188 C>T maps to NM_001076.2 W5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr4:69536046 C>T maps to NM_001076.2 W97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:69512848 T>C maps to NM_001076.2 K522K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:69536327 C>T maps to NM_001076.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr4:69417556 G>A maps to NM_001076.2 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr4:69520827 G>A maps to NM_001076.2 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:69403477 C>T maps to NM_001076.2 W486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:69403525 G>A maps to NM_001076.2 R470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr4:69536261 C>T maps to NM_001076.2 K25K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr4:69434163 C>T maps to NM_001076.2 Q13Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:69536054 G>A maps to NM_001076.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr4:69512953 G>A maps to NM_001076.2 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr4:69535828 G>A maps to NM_001076.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:69535816 G>A maps to NM_001076.2 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:69403557 G>A maps to NM_001076.2 R460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr4:69433514 G>A maps to NM_001076.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:69535660 G>A maps to NM_001076.2 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:69519903 C>T maps to NM_001076.2 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr4:69512982 G>A maps to NM_001076.2 R478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:69519837 C>T maps to NM_001076.2 K410K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:69535703 C>T maps to NM_001076.2 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr4:69433497 C>T maps to NM_001076.2 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr4:69512956 C>T maps to NM_001076.2 W486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:69434188 C>T maps to NM_001076.2 W5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:69519924 G>A maps to NM_001076.2 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:69535790 C>T maps to NM_001076.2 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:69536063 C>T maps to NM_001076.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:69536327 C>T maps to NM_001076.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr4:69434043 C>T maps to NM_001076.2 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr4:69403557 G>A maps to NM_001076.2 R460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr4:70160311 C>T maps to NM_053039.1 R459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr4:70146487 C>T maps to NM_053039.1 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:70146427 C>T maps to NM_053039.1 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr4:70146245 C>T maps to NM_053039.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:70146562 C>T maps to NM_053039.1 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr4:70156463 G>A maps to NM_053039.1 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr4:70146415 C>T maps to NM_053039.1 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr4:70146658 C>T maps to NM_053039.1 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:70148319 C>T maps to NM_053039.1 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr4:70146619 G>A maps to NM_053039.1 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:70156379 G>A maps to NM_053039.1 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr4:70146231 G>A maps to NM_053039.1 W5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr4:70350972 C>T maps to NM_021139.2 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr4:70355165 G>A maps to NM_021139.2 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr4:70346576 C>T maps to NM_021139.2 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr4:70361117 G>A maps to NM_021139.2 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:70346363 C>T maps to NM_021139.2 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:70361012 G>A maps to NM_021139.2 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:70359452 G>A maps to NM_021139.2 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:70359494 C>T maps to NM_021139.2 W262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:70359505 G>A maps to NM_021139.2 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr4:70359505 G>A maps to NM_021139.2 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr4:70361320 C>A maps to NM_021139.2 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:70361565 C>T maps to NM_021139.2 W5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:70346420 G>A maps to NM_021139.2 F506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr4:70361498 C>T maps to NM_021139.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:70346552 G>A maps to NM_021139.2 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr4:70361387 G>A maps to NM_021139.2 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:70350972 C>T maps to NM_021139.2 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr4:70361201 G>A maps to NM_021139.2 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:69962702 C>T maps to NM_001074.2 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:69972912 G>A maps to NM_001074.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:69962300 G>A maps to NM_001074.2 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:69962504 C>T maps to NM_001074.2 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr4:69962507 C>T maps to NM_001074.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:35965769 G>A maps to NM_152404.3 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr5:35965874 G>A maps to NM_152404.3 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr5:35965694 C>T maps to NM_152404.3 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:35957326 C>T maps to NM_152404.3 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:35965727 C>T maps to NM_152404.3 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr5:35965628 C>T maps to NM_152404.3 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:35957326 C>T maps to NM_152404.3 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:35954471 C>T maps to NM_152404.3 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:35957388 C>A maps to NM_152404.3 G326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:35965925 C>T maps to NM_152404.3 K135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:35965643 G>A maps to NM_152404.3 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:35957317 C>T maps to NM_152404.3 V349V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A2MR-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:35954489 G>A maps to NM_152404.3 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr5:35957467 G>A maps to NM_152404.3 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr5:35991309 G>A maps to NM_152404.3 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:35955940 G>A maps to NM_152404.3 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr5:35957377 C>T maps to NM_152404.3 W329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr5:35991267 G>A maps to NM_152404.3 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:35965517 C>T maps to NM_152404.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:35957326 C>T maps to NM_152404.3 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr5:35957458 G>A maps to NM_152404.3 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr5:36049416 G>A maps to NM_174914.3 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr5:36039615 C>T maps to NM_174914.3 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr5:36039717 G>A maps to NM_174914.3 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr5:36049323 G>A maps to NM_174914.3 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr5:36049230 C>T maps to NM_174914.3 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr5:36037995 G>A maps to NM_174914.3 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:36049428 C>T maps to NM_174914.3 K135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr5:36049058 G>A maps to NM_174914.3 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:36039615 C>T maps to NM_174914.3 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:36035967 C>T maps to NM_174914.3 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr5:36039615 C>T maps to NM_174914.3 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr5:36035967 C>T maps to NM_174914.3 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr5:36052009 C>T maps to NM_174914.3 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:36035946 G>A maps to NM_174914.3 V475V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr5:36039783 A>G maps to NM_174914.3 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:36039615 C>T maps to NM_174914.3 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr5:36039615 C>T maps to NM_174914.3 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr5:36035823 C>T maps to NM_174914.3 G516G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr5:36049242 G>A maps to NM_174914.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:36035836 C>T maps to NM_174914.3 W512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:36036042 G>A maps to NM_174914.3 I443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:36049323 G>A maps to NM_174914.3 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr5:36035918 G>A maps to NM_174914.3 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr4:115585261 C>T maps to NM_003360.3 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr4:115544110 C>T maps to NM_003360.3 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:115544539 G>C maps to NM_003360.3 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr4:115544059 C>T maps to NM_003360.3 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr4:115544659 C>T maps to NM_003360.3 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:115544704 C>T maps to NM_003360.3 N223N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr4:115544402 C>T maps to NM_003360.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr1:162487889 A>G did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr19:4929250 C>T maps to ENST00000398240 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:4941584 C>T maps to ENST00000398240 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:4929268 C>T maps to ENST00000398240 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:4930756 G>A maps to ENST00000398240 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:34839358 A>T did not map to a codon.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr6:34831898 G>A maps to NM_017754.3 L1112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr6:34839368 C>T maps to NM_017754.3 I1330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:34823397 C>T maps to NM_017754.3 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:34789447 C>T maps to NM_017754.3 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:34826109 C>T maps to NM_017754.3 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr6:34825567 C>T maps to NM_017754.3 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:100491163 G>A maps to NM_015054.1 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr12:100453083 G>A maps to NM_015054.1 F657F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr12:100489540 G>A maps to NM_015054.1 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:100433463 G>A maps to NM_015054.1 V1395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:100451916 G>A maps to NM_015054.1 I1046I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr12:100453014 C>T maps to NM_015054.1 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr9:6460785 C>T maps to NM_152896.1 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr5:176332393 A>C maps to ENST00000377219 V684V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr5:176332390 G>A maps to ENST00000377219 S685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr5:176396035 A>G maps to ENST00000377219 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:150289956 C>T maps to NM_025218.2 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:150263262 C>T maps to NM_025217.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:150266535 G>A maps to NM_025217.2 K59K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:150266592 G>A maps to NM_025217.2 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:150385785 C>T maps to NM_024518.1 W231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:150387044 G>A maps to NM_024518.1 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr12:132403803 C>T maps to NM_003565.2 F853F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr12:132402022 C>T maps to NM_003565.2 S750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr12:132405685 G>A maps to NM_003565.2 E1001E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:132400953 C>T maps to NM_003565.2 S630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr12:132394838 G>A maps to NM_003565.2 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:132393303 C>T maps to NM_003565.2 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr12:132401070 C>T maps to NM_003565.2 P669P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:132394823 C>T maps to NM_003565.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:132399010 C>T maps to NM_003565.2 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:75130992 G>A maps to NM_001099436.1 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr3:41961248 G>A maps to NM_017886.2 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:41759337 G>A maps to NM_017886.2 I779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:41942228 G>A maps to NM_017886.2 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:41795884 G>A maps to NM_017886.2 N763N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr3:41961207 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:41759218 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:20359593 C>T maps to ENST00000424589 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr16:20352419 G>A maps to ENST00000424589 Q557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:20355392 G>A maps to ENST00000424589 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr16:20360448 G>A maps to ENST00000424589 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr16:20355392 G>A maps to ENST00000424589 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr21:43504230 G>A maps to NM_173568.3 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:43504284 C>T maps to NM_173568.3 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:43508456 C>T maps to NM_173568.3 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:43539309 C>T maps to NM_173568.3 I983I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:43543181 C>T maps to NM_173568.3 S1151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr21:43547328 C>T maps to NM_173568.3 I1297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr21:43547286 G>A maps to NM_173568.3 T1283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr21:43524198 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr21:43547862 C>T maps to NM_173568.3 S1332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr21:43533713 C>T maps to NM_173568.3 S840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr21:43504233 C>T maps to NM_173568.3 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr21:43508580 C>T maps to NM_173568.3 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr21:43531746 G>A maps to NM_173568.3 E805E. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A3J7-06A-11D-A20D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr21:43547340 C>T maps to NM_173568.3 F1301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr21:43531689 G>A maps to NM_173568.3 W786*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-FW-A3R5-06A-11D-A23B-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr21:43508591 T>C did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr21:43539231 C>T maps to NM_173568.3 S957S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr21:43543052 C>T maps to NM_173568.3 P1108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:124456748 C>T maps to NM_000373.3 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:124456811 C>T maps to NM_000373.3 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr17:26874677 A>G maps to NM_054035.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr17:26874713 G>A maps to NM_005148.3 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:121151119 C>T maps to NM_001080533.1 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr19:17756846 C>T maps to ENST00000428389 G794G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr19:17760344 C>T maps to ENST00000428389 R585R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr19:17759782 G>A maps to ENST00000428389 Q600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:17752323 G>A maps to ENST00000428389 V926V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:17780452 G>A maps to ENST00000428389 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:17756849 G>A maps to ENST00000428389 V793V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:17783267 C>T maps to ENST00000428389 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:17728549 G>A maps to ENST00000428389 L1595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:17741528 C>T maps to ENST00000428389 L1241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:17759753 G>A maps to ENST00000428389 A609A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:17741522 C>T maps to ENST00000428389 E1243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:17740066 G>A maps to ENST00000428389 S1333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:17752356 G>A maps to ENST00000428389 F915F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr19:17783261 C>T maps to ENST00000428389 W153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr19:17743613 C>T maps to ENST00000428389 K1223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr19:17752323 G>A maps to ENST00000428389 V926V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:17768935 G>A maps to ENST00000428389 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr9:35381638 C>T maps to ENST00000396787 Y789Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr9:35295813 C>T maps to ENST00000396787 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:35313968 C>T maps to ENST00000396787 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:35380571 C>T maps to ENST00000396787 F700F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr9:35398947 G>A maps to ENST00000396787 G1260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr15:54542545 C>T maps to ENST00000260323 L1118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr15:54307568 G>A maps to ENST00000260323 E823E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr15:54307356 C>T maps to ENST00000260323 Q753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr15:54306809 C>T maps to ENST00000260323 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr15:54847646 G>A maps to ENST00000260323 E1965E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:54306827 C>T maps to ENST00000260323 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:54307481 C>T maps to ENST00000260323 F794F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr15:54307554 C>T maps to ENST00000260323 L819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr15:54305840 T>C maps to ENST00000260323 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr15:54793034 C>T maps to ENST00000260323 F1720F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr15:54556411 G>A maps to ENST00000260323 Q1165Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:54919112 C>T maps to ENST00000260323 I2149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:54305219 G>A maps to ENST00000260323 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr15:54841849 C>T maps to ENST00000260323 F1946F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr15:54307469 G>A maps to ENST00000260323 K790K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr15:54625969 C>T maps to ENST00000260323 N1500N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr15:54542544 C>T maps to ENST00000260323 L1117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr15:54919181 G>A maps to ENST00000260323 L2172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr15:54527305 G>A maps to ENST00000260323 V1050V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr15:54825228 T>C maps to ENST00000260323 I1887I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:54542501 G>A maps to ENST00000260323 W1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr15:54556498 G>A maps to ENST00000260323 Q1194Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:54305504 G>A maps to ENST00000260323 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:54307229 G>A maps to ENST00000260323 E710E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr15:54307481 C>T maps to ENST00000260323 F794F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr15:54435819 C>T maps to ENST00000260323 R1004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr15:54817793 C>T maps to ENST00000260323 L1835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr15:54556558 G>A maps to ENST00000260323 G1214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:54786857 C>T maps to ENST00000260323 F1662F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:54847641 C>T maps to ENST00000260323 R1964*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr15:54860060 C>T maps to ENST00000260323 Q2008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr15:54586224 G>A maps to ENST00000260323 R1317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr15:54590051 G>A maps to ENST00000260323 L1344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr15:54707265 G>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr15:54306884 G>A maps to ENST00000260323 A595A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:54305291 G>A maps to ENST00000260323 K64K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:54305717 C>T maps to ENST00000260323 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:54306866 G>A maps to ENST00000260323 R589R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:54306917 G>A maps to ENST00000260323 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:54308036 C>T maps to ENST00000260323 A979A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:54435227 G>A maps to ENST00000260323 V999V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:54817802 C>T maps to ENST00000260323 V1838V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:54841885 G>A maps to ENST00000260323 L1958L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr15:54306725 C>T maps to ENST00000260323 F542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:54586114 C>T maps to ENST00000260323 R1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:73839596 G>A maps to ENST00000412096 Q41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:73839597 G>A maps to ENST00000412096 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:73832956 G>A maps to ENST00000412096 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr17:73831792 C>T maps to ENST00000412096 E554E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr17:73835951 C>T maps to ENST00000412096 Q341Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:73832316 G>A maps to ENST00000412096 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:91485795 A>T maps to NM_018671.3 K273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr15:91486169 C>T maps to NM_018671.3 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:91491903 C>T maps to NM_018671.3 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr15:91486205 C>T maps to NM_018671.3 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr15:91496168 C>T maps to NM_018671.3 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZH-06A-11D-A197-08 chr15:91496479 C>T maps to NM_018671.3 A839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr15:91491966 C>A maps to NM_018671.3 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:91492020 C>T maps to NM_018671.3 P625P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:33513329 T>C maps to NM_173167.2 L850L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr17:33504103 G>A maps to NM_173167.2 K700K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr17:33482340 G>A maps to NM_173167.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr17:33513464 C>T maps to NM_173167.2 L895L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr17:33501268 G>A maps to NM_173167.2 K615K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:33507613 C>T maps to NM_173167.2 I766I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:33503052 G>A maps to NM_173167.2 K677K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:33513463 C>T maps to NM_173167.2 I894I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:33513464 C>T maps to NM_173167.2 L895L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr17:33503016 G>A maps to NM_173167.2 K665K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:33482404 C>T maps to NM_173167.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:33482455 C>T maps to NM_173167.2 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:33475449 G>A maps to NM_173167.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr17:33510487 C>T maps to NM_173167.2 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr17:33482367 C>T maps to NM_173167.2 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr17:33477070 C>T maps to NM_173167.2 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:33507691 G>A maps to NM_173167.2 K792K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:176305268 C>T maps to NM_133369.2 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:176305339 C>T maps to NM_133369.2 S655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr5:176306859 C>T maps to NM_133369.2 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr5:176301535 C>T maps to NM_133369.2 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:176306742 C>T maps to NM_133369.2 S795S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:176304661 G>A maps to NM_133369.2 W531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr10:73058913 C>T maps to NM_170744.3 I906I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr10:73057760 C>T maps to NM_170744.3 I862I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr10:73044522 G>A maps to NM_170744.3 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr10:73046582 C>T maps to NM_170744.3 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr10:73046570 G>A maps to NM_170744.3 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:73051456 C>T maps to NM_170744.3 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:73055662 C>T maps to NM_170744.3 S757S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:73057802 G>A maps to NM_170744.3 R876R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:73051456 C>T maps to NM_170744.3 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:73056459 G>C maps to NM_170744.3 G817G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:73051438 C>T maps to NM_170744.3 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr10:73048346 G>A maps to NM_170744.3 W308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:73056339 C>T maps to NM_170744.3 I777I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr10:73051456 C>T maps to NM_170744.3 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr10:73053278 C>T maps to NM_170744.3 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:73053614 C>T maps to NM_170744.3 F700F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:73055575 G>A maps to NM_170744.3 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:73044543 G>A maps to NM_170744.3 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr10:73051546 C>T maps to NM_170744.3 C551C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr4:96091444 C>T maps to NM_003728.3 A830A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr4:96140240 C>T maps to NM_003728.3 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:96104134 C>T maps to NM_003728.3 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:96256714 G>A maps to NM_003728.3 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr4:96166143 A>G maps to NM_003728.3 C309C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr4:96140177 G>A maps to NM_003728.3 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:96137342 G>C maps to NM_003728.3 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:41002555 G>T maps to NM_173561.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr8:35542214 C>T maps to ENST00000416672 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:35608170 C>T maps to ENST00000416672 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr8:35647891 C>T maps to ENST00000416672 F896F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr8:35579779 C>T maps to ENST00000416672 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr8:35647875 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr8:35541066 G>A maps to ENST00000416672 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr8:35624457 G>A maps to ENST00000416672 Q789Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:35579896 C>T maps to ENST00000416672 F434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr8:35647891 C>T maps to ENST00000416672 F896F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr8:35425614 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr8:35406873 C>T maps to ENST00000416672 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr8:35647876 G>A maps to ENST00000416672 R891R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:35631863 C>T maps to ENST00000416672 F847F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:35631905 C>T maps to ENST00000416672 S861S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr8:35624479 C>T maps to ENST00000416672 L797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:35406840 C>T maps to ENST00000416672 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:35648032 C>T maps to ENST00000416672 S943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr8:35583955 C>T maps to ENST00000416672 I535I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:35425658 G>A maps to ENST00000416672 Q122Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:35606086 C>T maps to ENST00000416672 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr8:35647946 C>T maps to ENST00000416672 Q915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr6:167709568 C>T maps to NM_018974.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr6:167717443 C>T maps to NM_018974.3 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr6:167721270 G>A maps to NM_018974.3 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr6:167708177 C>T maps to NM_018974.3 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:167708162 C>T maps to NM_018974.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:167719429 C>T maps to NM_018974.3 Q290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr6:167719404 C>T maps to NM_018974.3 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr6:167709749 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:67770547 C>T maps to NM_030930.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr11:67770568 G>T maps to NM_030930.2 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:67766747 G>A maps to NM_030930.2 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:67765195 G>A maps to NM_030930.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:67766693 G>A maps to NM_030930.2 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr7:1273285 C>G maps to NM_001080461.1 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:1275592 C>T maps to NM_001080461.1 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:109537050 C>T maps to NM_080911.2 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr17:73818609 C>T maps to NM_001080419.1 F706F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr17:73805957 C>T maps to NM_001080419.1 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:73780867 C>T maps to NM_001080419.1 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr17:73815825 C>T maps to NM_001080419.1 F612F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr17:73815765 G>A maps to NM_001080419.1 E592E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr17:73780855 G>A maps to NM_001080419.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:73805987 C>T maps to NM_001080419.1 Y160Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:1453338 G>A maps to ENST00000508903 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr22:24896101 C>T maps to NM_016327.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr22:24921761 G>A maps to NM_016327.2 *385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr22:24916424 C>T maps to NM_016327.2 R288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr22:24919668 C>T maps to NM_016327.2 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr22:24916372 C>T maps to NM_016327.2 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr22:24919731 G>A maps to NM_016327.2 W354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:24911323 G>A maps to NM_016327.2 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J6-06A-11D-A19A-08 chr19:18960965 G>T maps to ENST00000418384 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:18975060 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:18971671 T>C maps to ENST00000418384 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:18971158 C>T maps to ENST00000418384 Q749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:18976860 C>T maps to ENST00000418384 Y1093Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr19:18968187 C>T maps to ENST00000418384 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:18960946 C>T maps to ENST00000418384 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr10:11973670 G>T maps to NM_015542.2 I1219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:12077173 C>T maps to NM_015542.2 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr10:12046532 G>T maps to NM_015542.2 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr10:12001226 G>A maps to NM_015542.2 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr10:12009395 C>A maps to NM_015542.2 G671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:118977162 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:118971940 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:118979220 G>C did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:118974616 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:118968881 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:118986780 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:118971901 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:118971902 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:118986798 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:36166863 C>T maps to NM_007000.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:36168792 G>A maps to NM_007000.2 W243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr3:118906806 G>A maps to NM_006952.3 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:118906806 G>A maps to NM_006952.3 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr22:45683228 C>T maps to NM_006953.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr22:45689116 C>T maps to NM_006953.3 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr22:45689149 C>T maps to NM_006953.3 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr22:45683287 C>T maps to NM_006953.3 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:45683228 C>T maps to NM_006953.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:45689188 C>T maps to NM_006953.3 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr7:76144447 C>T maps to NM_030570.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:76140981 G>A maps to ENST00000434948 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:76140313 C>T maps to NM_030570.2 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr7:48146551 G>T maps to NM_003364.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr7:48146545 C>T maps to NM_003364.2 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:158974352 C>T maps to NM_001135098.1 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:158978092 C>T maps to NM_001135098.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:74494207 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:74520768 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:74523297 T>C did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:74494157 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr20:33961985 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr20:33894522 C>G maps to NM_018244.4 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:33971915 G>A maps to NM_018244.4 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:48638485 C>T maps to NM_003365.2 W296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:48638486 C>T maps to NM_003365.2 W296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr3:48638437 G>A maps to NM_003365.2 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr16:21968751 A>G maps to NM_003366.2 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:229794914 C>T maps to NM_014777.2 I1482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:229771475 C>T maps to NM_014777.2 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:229773365 G>T maps to NM_014777.2 G1002G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:229794932 C>T maps to NM_014777.2 F1488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:229771704 C>T maps to NM_014777.2 Q449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:229773806 C>T maps to NM_014777.2 S1149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:229771091 G>A maps to NM_014777.2 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:229779424 G>A maps to NM_014777.2 W1260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr1:229771571 C>T maps to NM_014777.2 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:229773815 C>T maps to NM_014777.2 A1152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr1:229786998 C>T maps to NM_014777.2 I1389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:229771484 C>T maps to NM_014777.2 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:229772114 C>T maps to NM_014777.2 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:229772655 C>T maps to NM_014777.2 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr7:43917429 G>A maps to NM_001077663.1 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr7:43918338 G>A maps to NM_001077663.1 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:43918416 G>A maps to NM_001077663.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:43921515 G>A maps to NM_001077663.1 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr9:131151620 C>T maps to NM_001135947.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr3:126220113 C>T maps to NM_001165974.1 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:126226911 C>T maps to NM_001165974.1 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr3:126202262 C>T maps to NM_001165974.1 P673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr3:126224621 G>A maps to NM_001165974.1 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr3:126220113 C>T maps to NM_001165974.1 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:126216954 C>T maps to NM_001165974.1 Q519Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:126218906 C>T maps to NM_001165974.1 Q472Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr3:126207066 G>A maps to NM_001165974.1 A648A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr3:126218898 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:126226857 G>A maps to NM_001165974.1 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:126227300 C>T maps to NM_001165974.1 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:126224594 C>T maps to NM_001165974.1 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr3:126207040 C>T maps to NM_001165974.1 W657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr3:126224811 G>A maps to NM_001165974.1 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:126219671 C>T maps to NM_001165974.1 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:126208158 C>T maps to NM_001165974.1 R616R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:126219632 G>A maps to NM_001165974.1 F410F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:126219689 C>T maps to NM_001165974.1 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:126224648 G>A maps to NM_001165974.1 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:126226911 C>T maps to NM_001165974.1 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr1:45478859 T>G maps to NM_000374.4 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:127484703 G>A maps to NM_000375.2 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr10:127486658 G>A maps to NM_000375.2 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr19:17327012 C>T maps to NM_018467.3 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr19:17330492 G>A maps to NM_018467.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:161010422 G>A maps to NM_007122.3 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:161010422 G>A maps to NM_007122.3 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:161010634 C>G maps to NM_007122.3 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:161012644 C>T maps to NM_007122.3 E12E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr11:17517181 G>A maps to NM_153676.3 V863V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr11:17515899 C>T maps to NM_153676.3 R893R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:17542540 C>T maps to NM_153676.3 Q362Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:17552964 G>A maps to NM_153676.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:17553055 C>T maps to NM_153676.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr11:17531343 G>A maps to NM_153676.3 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:17523527 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:17533586 C>T maps to NM_153676.3 K425K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:17548863 G>A maps to NM_153676.3 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:17518321 C>T maps to NM_153676.3 K843K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:17519756 G>C maps to NM_153676.3 T814T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr11:17548357 C>G did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:17544344 C>T maps to NM_153676.3 Q335Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:17548833 G>A maps to NM_153676.3 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:72916231 G>A maps to NM_173477.2 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:72916141 A>G maps to NM_173477.2 N263N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr17:72916374 G>A maps to NM_173477.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:72916335 G>A maps to NM_173477.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr1:215848643 C>T maps to ENST00000366943 Q4203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:216062195 G>A maps to ENST00000366943 Q2599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr1:216380709 C>T maps to ENST00000366943 W1074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr1:215848793 G>T maps to ENST00000366943 A4153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:216017671 C>T maps to ENST00000366943 L3074L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr1:216173823 G>A maps to ENST00000366943 L2136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr1:215799197 C>T maps to ENST00000366943 E5202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:216017710 G>A maps to ENST00000366943 L3061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:215853562 T>A maps to ENST00000366943 V4074V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:216595567 G>A maps to ENST00000366943 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:215844526 C>T maps to ENST00000366943 L4640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:215848408 G>A maps to ENST00000366943 L4282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:215901521 C>T maps to ENST00000366943 W3972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:215933012 C>T maps to ENST00000366943 E3740E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:216073441 C>T maps to ENST00000366943 W2523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:215847602 C>T maps to ENST00000366943 V4550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:215823999 C>T maps to ENST00000366943 G4759G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:216052206 G>A maps to ENST00000366943 T2819T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:216424271 G>A maps to ENST00000366943 Q714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:215848524 C>T maps to ENST00000366943 W4243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:215916615 T>A maps to ENST00000366943 T3817T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:215847676 G>A maps to ENST00000366943 R4526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:215848418 G>A maps to ENST00000366943 P4278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:216073510 G>A maps to ENST00000366943 L2500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:215848394 G>A maps to ENST00000366943 I4286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:216062052 G>A maps to ENST00000366943 P2646P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:215808036 G>A maps to ENST00000366943 L5021L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:216061779 G>A maps to ENST00000366943 P2737P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr1:216496994 C>T maps to ENST00000366943 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:215955511 G>A maps to ENST00000366943 R3538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:215953203 C>T maps to ENST00000366943 R3640R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr1:216348771 G>A maps to ENST00000366943 I1483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr1:216040469 C>T maps to ENST00000366943 V2908V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr1:215823978 A>G maps to ENST00000366943 S4766S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr1:216251641 C>T maps to ENST00000366943 V1787V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr1:216260105 G>A maps to ENST00000366943 L1648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:215960036 C>T maps to ENST00000366943 G3454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:216062313 G>A maps to ENST00000366943 S2559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:216262376 G>A maps to ENST00000366943 I1621I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:215848205 G>A maps to ENST00000366943 I4349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:215807922 G>A maps to ENST00000366943 L5059L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:215820885 G>A maps to ENST00000366943 I4923I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:215848097 C>T maps to ENST00000366943 K4385K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:215848304 G>A maps to ENST00000366943 F4316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:215901704 C>T maps to ENST00000366943 E3911E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:215914767 C>T maps to ENST00000366943 W3887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:216348786 G>A maps to ENST00000366943 I1478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:216405293 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:216496928 G>A maps to ENST00000366943 F479F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:216497517 C>T maps to ENST00000366943 Q440Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:216595615 G>A maps to ENST00000366943 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:215916587 G>A maps to ENST00000366943 Q3827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:216420209 G>A maps to ENST00000366943 F842F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:215808040 C>T maps to ENST00000366943 L5019L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:215987168 C>T maps to ENST00000366943 L3216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:17367437 G>A maps to NM_031941.3 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr19:17370096 C>T did not map to a codon.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:17373417 G>A maps to NM_031941.3 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr19:17373465 C>T maps to NM_031941.3 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr19:17373624 C>T maps to NM_031941.3 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:17367357 G>A maps to NM_031941.3 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:17373660 C>T maps to NM_031941.3 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:17373399 C>T maps to NM_031941.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:17370459 G>A maps to NM_031941.3 Q284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:17374902 G>A maps to NM_031941.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:17373486 C>T maps to NM_031941.3 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr19:17370502 G>A maps to NM_031941.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:17370412 T>C maps to NM_031941.3 Q299Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:76695902 C>T maps to NM_003715.2 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:62911008 A>G maps to NM_003368.4 E386E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr16:84801963 G>A maps to NM_005153.2 E666E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:84792358 G>A maps to NM_005153.2 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr16:84806181 C>T maps to NM_005153.2 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:84778851 C>T maps to NM_005153.2 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:84797806 C>T maps to NM_005153.2 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr23:47102867 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:47104263 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr23:47103917 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr23:47106619 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:47104260 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:47102898 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr23:47101087 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:47106767 A>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:47100962 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:47099221 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr23:47098763 C>G did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:179483631 T>C maps to NM_003940.2 S803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr12:62783683 C>A maps to ENST00000280377 S587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr8:11994894 G>A maps to NM_201402.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr8:11995797 G>A maps to NM_201402.2 Q158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr8:11995135 C>T maps to NM_201402.2 W378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr8:11994697 C>T maps to NM_201402.2 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:11995286 C>T maps to NM_201402.2 W328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr8:11994904 G>A maps to NM_201402.2 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr8:11994677 C>T maps to NM_201402.2 *531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr22:18642942 G>T maps to NM_017414.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr22:18644646 G>A maps to NM_017414.3 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr22:18650085 C>T maps to NM_017414.3 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A197-06A-32D-A197-08 chr22:18650052 C>T maps to NM_017414.3 Y144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr3:49156455 T>C maps to ENST00000434032 K41K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr3:49146576 C>T maps to ENST00000434032 P1358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:49149152 A>G maps to ENST00000434032 G997G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr3:49146438 G>A maps to ENST00000434032 L1404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:49149410 G>A maps to ENST00000434032 L944L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr3:49148966 G>A maps to ENST00000434032 S1059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:49149062 A>C maps to ENST00000434032 L1027L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:49148459 G>A maps to ENST00000434032 A1154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:49149149 G>A maps to ENST00000434032 S998S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:49154917 G>A maps to ENST00000434032 H186H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:49151469 G>A maps to ENST00000434032 L818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:119243659 C>T maps to NM_004205.4 K177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:119243746 C>T maps to NM_004205.4 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:119228485 G>A maps to NM_004205.4 F494F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:119244028 G>A maps to NM_004205.4 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr9:132641891 C>T maps to NM_001008563.3 V851V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr9:132641903 C>T maps to NM_001008563.3 G855G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr9:132618590 C>T maps to NM_001008563.3 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr9:132637875 G>A maps to NM_001008563.3 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:132623220 C>T maps to NM_001008563.3 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:161133980 C>T maps to NM_012475.4 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:161133952 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr1:161130676 C>T maps to NM_012475.4 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:161130933 C>T maps to NM_012475.4 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:20907597 G>A maps to ENST00000455117 I552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr17:20921332 G>A maps to ENST00000455117 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:20921374 G>A maps to ENST00000455117 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr1:55548965 C>T maps to NM_015306.2 G2318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr1:55599780 G>A maps to NM_015306.2 Q1115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:55569673 G>A maps to NM_015306.2 R1634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:55569674 G>A maps to NM_015306.2 S1633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:55572981 G>A maps to NM_015306.2 I1564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:55547001 C>T maps to NM_015306.2 R2357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr21:17191159 C>T maps to ENST00000285681 Q359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr21:17191060 C>T maps to ENST00000285681 Q326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr23:132160350 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr23:132160052 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr23:132160127 A>C did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:132160169 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:132160570 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:132161856 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:132161549 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:132162060 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:132160488 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:132161802 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr23:132162237 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr23:132161994 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:132161262 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:132159887 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:132160519 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr23:132161157 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:132161795 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:132161644 C>G did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:132160264 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:132162209 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr23:132159789 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:132160350 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:132161703 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:132161739 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:132161740 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:132161987 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr23:132161248 G>A did not map to a codon.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr23:132160102 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:132161572 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:132160462 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:132160518 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr23:132161664 A>G did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:132160818 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:132162217 G>A did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:132160999 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:132159893 C>T did not map to a codon.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr23:132161509 G>A did not map to a codon.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr23:132160570 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr11:113677219 C>T maps to NM_020886.2 G797G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr11:113701609 G>A maps to NM_020886.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr11:113672310 G>A maps to NM_020886.2 I984I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr11:113673927 C>T maps to NM_020886.2 R938R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr11:113675654 G>A maps to NM_020886.2 P838P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:113679952 G>A maps to NM_020886.2 Q666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:57642371 C>T maps to NM_020903.2 Q777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr19:57642538 C>T maps to NM_020903.2 I832I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr19:57642766 C>T maps to NM_020903.2 I908I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:57641515 G>A maps to NM_020903.2 Q491Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:57640372 C>T maps to NM_020903.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:57642775 G>A maps to NM_020903.2 G911G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr19:57642236 G>T maps to NM_020903.2 E732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:57641001 G>A maps to NM_020903.2 W320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr19:57640196 C>T maps to NM_020903.2 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:57641410 C>T maps to NM_020903.2 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr19:57642766 C>T maps to NM_020903.2 I908I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:57640684 G>A maps to NM_020903.2 E214E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr19:57640196 C>T maps to NM_020903.2 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:57642175 C>T maps to NM_020903.2 S711S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:57641152 G>A maps to NM_020903.2 Q370Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:57642484 G>A maps to NM_020903.2 V814V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:57642598 C>T maps to NM_020903.2 A852A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr19:57641113 C>T maps to NM_020903.2 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:63850312 C>T maps to NM_006537.2 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr15:63855102 A>G maps to NM_006537.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:109509433 C>T maps to NM_032663.3 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr16:23099046 G>A maps to NM_020718.3 Q509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:23083399 G>A maps to NM_020718.3 S818S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:23080545 G>A maps to NM_020718.3 S960S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr16:23096192 G>A maps to NM_020718.3 T606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr16:23117766 G>A maps to NM_020718.3 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:23080254 G>A maps to NM_020718.3 S1057S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:23117571 G>A maps to NM_020718.3 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:58332544 G>A maps to NM_032582.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:58282962 G>A maps to NM_032582.3 L1032L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr17:58348780 C>T maps to NM_032582.3 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr17:58284460 G>A maps to NM_032582.3 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:78191400 G>A maps to NM_015017.3 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:78183732 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:78180376 G>A maps to NM_015017.3 R744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr2:61571001 G>A maps to NM_014709.3 L816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr2:61493251 C>T maps to NM_014709.3 K1828K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr2:61415731 T>C maps to NM_014709.3 P3382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:61597487 G>A maps to NM_014709.3 Q407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:77910658 C>T maps to NM_020798.2 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26D-06A-11D-A19A-08 chr11:77917003 G>T maps to NM_020798.2 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr17:76823354 G>A maps to NM_025090.3 Q221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:76802269 G>A maps to NM_025090.3 V728V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr17:76802332 G>A maps to NM_025090.3 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr17:76794552 G>A maps to NM_025090.3 F1107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:76799750 C>T maps to NM_025090.3 G842G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:76823412 G>A maps to NM_025090.3 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:76803430 C>T maps to NM_025090.3 G565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:219360673 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:219341664 G>A maps to NM_020935.2 C647C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:219423366 G>A maps to NM_020935.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:144135129 C>T maps to NM_032557.5 F667F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr4:144135967 A>T maps to NM_032557.5 K947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:144133487 T>A maps to NM_032557.5 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr2:85875081 C>T maps to NM_006590.2 D531D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr2:85850841 C>T maps to NM_006590.2 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr2:85866351 C>T maps to NM_006590.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:85848677 C>T maps to NM_006590.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:49321499 G>A maps to NM_003363.3 I820I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr3:49323651 G>A maps to NM_003363.3 T693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:49323747 C>T maps to NM_003363.3 E661E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:49362329 A>C maps to NM_003363.3 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:49321427 G>A maps to NM_003363.3 F844F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr2:234465631 G>A maps to NM_018218.2 R151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:234465578 G>A maps to NM_018218.2 D168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:234468558 G>A maps to NM_018218.2 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:234431967 G>A maps to NM_018218.2 I694I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr2:234386139 G>A maps to NM_018218.2 A1214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:234442223 G>A maps to NM_018218.2 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr2:234394514 G>A maps to NM_018218.2 S1113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:6196597 G>A maps to ENST00000404835 L1285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr7:6187441 C>T maps to ENST00000404835 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr7:6183808 C>T maps to ENST00000404835 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr17:9632018 C>G maps to NM_153210.3 G1028G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:9613337 C>T maps to NM_153210.3 R693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr17:9631770 C>T maps to NM_153210.3 R946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:9583585 G>A maps to NM_153210.3 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr17:9632243 G>A maps to NM_153210.3 Q1103Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr17:9632075 C>T maps to NM_153210.3 I1047I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:9615391 C>T maps to NM_153210.3 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:9580153 C>T maps to NM_153210.3 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr17:9632216 G>A maps to NM_153210.3 G1094G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr12:95926667 C>T maps to NM_032147.2 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr12:95927252 G>A maps to NM_032147.2 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:95918457 G>A maps to NM_032147.2 F577F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr12:95927371 G>A maps to NM_032147.2 Q221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:99894321 G>A maps to NM_001080481.1 D442D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:99885164 G>A maps to NM_001080481.1 S757S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr4:53494303 G>A maps to NM_022832.3 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr4:53468186 G>A maps to NM_022832.3 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:53494231 C>T maps to NM_022832.3 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:53476723 G>A maps to NM_022832.3 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr11:11919183 G>A maps to ENST00000399455 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:11951661 C>T maps to ENST00000399455 F537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr1:22055083 G>A maps to NM_032236.5 Q477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr6:41773650 G>A maps to ENST00000373009 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:41767677 T>C did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:41773947 C>G maps to ENST00000373009 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr12:6965271 C>T maps to NM_001098536.1 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:6968685 C>T maps to NM_001098536.1 Q371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:6973280 C>T maps to NM_001098536.1 P722P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr12:6975225 G>A maps to NM_001098536.1 Q854Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr12:6972452 C>T maps to NM_001098536.1 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr12:6965957 C>T maps to NM_001098536.1 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6966848 C>T maps to NM_001098536.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr15:50833251 G>A maps to ENST00000456636 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:55513530 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:55513531 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr4:120214167 G>A maps to NM_019050.2 Q1008Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr4:120194807 C>T maps to NM_019050.2 N732N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr4:120194808 C>T maps to NM_019050.2 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:120192590 C>T maps to NM_019050.2 R526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr4:120193171 A>G maps to NM_019050.2 K719K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr10:75289601 G>A maps to NM_152586.3 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr10:75276589 G>A maps to NM_152586.3 S1198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr10:75276255 G>A maps to NM_152586.3 Q1310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr10:75277246 C>A maps to NM_152586.3 G979G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr10:75289646 T>C maps to NM_152586.3 E617E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr10:75276289 C>T maps to NM_152586.3 E1298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:75290180 G>A maps to NM_152586.3 I516I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr17:5039146 C>T maps to NM_004505.2 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr17:5058736 C>T maps to NM_004505.2 F888F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr17:5042802 T>C maps to NM_004505.2 G444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:5041444 C>T maps to NM_004505.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr17:5049435 C>T maps to NM_004505.2 I762I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:5073876 C>T maps to NM_004505.2 L1207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:5042907 C>T maps to NM_004505.2 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr17:5042835 C>T maps to NM_004505.2 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:5076224 G>A maps to NM_004505.2 T1391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr17:5048749 C>T maps to NM_004505.2 F681F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:5036746 C>T maps to NM_004505.2 R96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr17:5048704 G>A maps to NM_004505.2 W666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:5036230 G>A maps to NM_004505.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:5042815 C>T maps to NM_004505.2 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr10:11505567 G>A maps to NM_001080491.2 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr10:11505372 G>A maps to NM_001080491.2 T535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr10:11505126 G>A maps to NM_001080491.2 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr16:8988991 G>A maps to NM_003470.2 Q979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44Q-06A-11D-A25O-08 chr16:8996278 G>A maps to NM_003470.2 R634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:8988679 G>A maps to NM_003470.2 I1024I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr16:8996002 G>A maps to NM_003470.2 F661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr16:9012977 G>A maps to NM_003470.2 H210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr16:9009192 G>A maps to NM_003470.2 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:8987934 G>A maps to NM_003470.2 L1077L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr15:50733666 A>T maps to NM_005154.3 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:50774162 A>C maps to NM_005154.3 V568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:50788175 C>T maps to NM_005154.3 F930F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr15:50786353 C>T maps to NM_005154.3 I845I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr15:50741604 C>T maps to NM_005154.3 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:41075483 T>C did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:41088903 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:41043858 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:41045826 C>T did not map to a codon.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr23:41000633 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:41048637 T>C did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:41069820 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr23:41043841 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:41029486 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:41029281 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:41055510 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:41007790 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:40982965 C>T did not map to a codon.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr23:40982968 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:41055567 C>G did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:41069762 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr23:41055613 T>G did not map to a codon.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr23:41057870 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:41075158 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:41069820 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:41055510 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:41084152 C>T did not map to a codon.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr24:14954329 A>T did not map to a codon.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr24:14954330 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr24:14923708 T>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr24:14928200 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr24:14902402 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr24:14954235 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr24:14889988 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr24:14848358 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr24:14968652 T>G did not map to a codon.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr24:14952449 A>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr24:14889986 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr24:14891491 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr24:14891492 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr13:31232500 T>C maps to NM_005800.4 L763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr13:31232916 G>A maps to NM_005800.4 K901K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:149262486 C>T maps to NM_005715.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr1:38484756 C>T maps to NM_016037.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:38489260 C>T maps to NM_016037.3 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:129058843 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:129060058 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:129060059 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:129045002 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:129053175 T>G did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:129053188 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:129059153 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:129063460 C>T did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:129045769 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr13:52604977 C>T maps to NM_021645.5 Q680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr13:52604412 C>T maps to NM_021645.5 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr13:52603380 C>T maps to NM_021645.5 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr13:52605075 C>T maps to NM_021645.5 F712F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr13:52605076 C>T maps to NM_021645.5 Q713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr13:52603377 C>T maps to NM_021645.5 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr13:52604613 C>T maps to NM_021645.5 N558N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr13:52603948 C>T maps to NM_021645.5 Q337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr13:52604667 C>T maps to NM_021645.5 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:72874888 G>A maps to NM_032175.2 K398K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr17:49371370 C>T maps to NM_016001.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr17:49374331 C>T maps to NM_016001.2 H551H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:101777418 G>A maps to NM_014503.2 R2676R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:101763608 C>T maps to NM_014503.2 D2165D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr12:101748766 C>T maps to NM_014503.2 S1755S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr12:101699780 C>T maps to NM_014503.2 Q624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr12:101679412 C>T maps to NM_014503.2 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr12:101759316 A>C maps to NM_014503.2 V2013V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:101763529 G>A maps to NM_014503.2 W2139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:101715374 C>T maps to NM_014503.2 A1003A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr12:101767223 C>T maps to NM_014503.2 A2308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr12:101750435 C>T maps to NM_014503.2 S1833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:101739388 C>T maps to NM_014503.2 Q1555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:101740230 C>T maps to NM_014503.2 I1583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr17:30202390 C>T maps to NM_018428.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr17:30192394 G>A maps to NM_018428.2 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:30226676 G>A maps to NM_018428.2 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr6:144759886 C>T maps to NM_007124.2 H416H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr6:144820409 G>A maps to NM_007124.2 Q1537Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:144835844 C>T maps to NM_007124.2 A1711A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:144774946 C>T maps to NM_007124.2 I742I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:144747580 C>T maps to NM_007124.2 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr6:144844168 G>A maps to NM_007124.2 L1917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:145160345 G>A maps to NM_007124.2 W3368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr6:144801042 C>T maps to NM_007124.2 A1144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr6:144780308 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:145095475 C>A maps to NM_007124.2 R2870R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:144852337 G>A maps to NM_007124.2 Q2019Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr6:144780341 C>A maps to NM_007124.2 P853P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr6:144835046 C>T maps to NM_007124.2 N1649N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:145069577 C>T maps to NM_007124.2 S2712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr6:144750810 C>T maps to NM_007124.2 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr6:144759928 C>T maps to NM_007124.2 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:7910878 C>T maps to NM_006786.3 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:7907880 C>T maps to NM_006786.3 W107*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-GF-A6C9-06A-11D-A30X-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:7912982 C>T maps to NM_006786.3 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:190986219 C>T maps to NM_198152.3 W115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:190994610 C>T maps to NM_198152.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:80332316 G>A maps to NM_018949.1 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr17:80332454 C>T maps to NM_018949.1 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F4-06A-12D-A25O-08 chr24:15469760 A>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr24:15417983 C>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr11:75715091 G>A maps to NM_003369.3 K290K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:75727928 C>T maps to NM_003369.3 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr2:106713259 G>A maps to ENST00000283148 Q354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr2:106721259 G>A maps to ENST00000283148 Q305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:106761703 G>A maps to ENST00000283148 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr2:106761805 G>A maps to ENST00000283148 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr23:47516643 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr23:47516984 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:47517188 G>A did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:47516987 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr16:70721904 G>A maps to NM_018052.3 Q759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr16:70778389 G>A maps to NM_018052.3 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:70731085 G>A maps to NM_018052.3 F637F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr16:70729522 C>T maps to NM_018052.3 G653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:70778437 G>A maps to NM_018052.3 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:7837361 G>A maps to NM_004781.3 W72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:171678873 C>T maps to NM_003762.4 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:155127811 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:155171568 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr23:155119164 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr23:155171723 C>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:155119252 A>T did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:155127841 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr23:155127819 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:155119158 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:155127866 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:155171640 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:155171641 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr23:155127883 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:116225053 C>T maps to NM_001172412.1 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:116206694 C>T maps to NM_001172412.1 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:116206469 C>T maps to NM_001172412.1 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr1:116228027 C>T maps to NM_001172412.1 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:116228078 G>A maps to NM_001172412.1 Q415Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:116206694 C>T maps to NM_001172412.1 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:116206790 C>T maps to NM_001172412.1 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:160389282 C>T maps to NM_020335.2 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:160393949 C>T maps to NM_020335.2 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr1:160385936 C>T maps to NM_020335.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:160389336 C>T maps to NM_020335.2 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:57009662 T>C maps to NM_004738.4 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr6:31747064 G>A maps to NM_006295.2 F1135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr6:31760654 G>A maps to NM_006295.2 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:31759514 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:31747780 G>A maps to NM_006295.2 V1025V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:31750957 C>T maps to NM_006295.2 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:31753446 G>A maps to NM_006295.2 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr6:31747259 G>A maps to NM_006295.2 I1114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr6:31762895 C>T maps to NM_006295.2 W33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr6:31747241 G>A maps to NM_006295.2 S1120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr6:31752240 G>A maps to NM_006295.2 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr6:31760051 C>T maps to NM_006295.2 E271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr6:31753401 G>A maps to NM_006295.2 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:31760543 A>G maps to NM_006295.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr6:31752210 G>A maps to NM_006295.2 F512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19L-06A-12D-A197-08 chr6:31759397 G>A maps to NM_006295.2 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr6:31747527 G>A maps to NM_006295.2 L1049L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr6:31749630 G>A maps to NM_006295.2 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:31746791 G>A maps to NM_006295.2 G1226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:31762880 G>A maps to NM_006295.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr6:31748801 G>A maps to NM_006295.2 S881S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:30890279 C>T maps to NM_001167734.1 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr6:30888876 C>T maps to NM_001167734.1 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr6:30889738 G>T maps to NM_001167734.1 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:30886610 G>A maps to NM_001167734.1 E361E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:30892177 C>T maps to NM_001167734.1 P868P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:30892177 C>T maps to NM_001167734.1 P868P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr6:30883521 G>A did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr6:30889744 C>T maps to NM_001167734.1 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr6:30892225 C>T maps to NM_001167734.1 A884A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:77244360 C>T maps to NM_014909.4 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr14:77242549 G>A maps to NM_014909.4 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:77229181 G>A maps to NM_014909.4 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:213134548 G>A maps to NM_001136474.1 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:213147298 C>T maps to NM_001136474.1 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:213134569 G>A maps to NM_001136474.1 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr16:4431849 G>A maps to NM_138440.2 E324E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr16:4431024 C>T maps to NM_138440.2 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr16:78005766 G>A maps to NM_020927.1 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr16:77859207 G>A maps to NM_020927.1 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:77918576 T>C maps to NM_020927.1 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:77822713 G>A maps to NM_020927.1 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr16:77859225 C>T maps to NM_020927.1 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr16:77850853 G>A maps to NM_020927.1 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr16:78011528 G>A maps to NM_020927.1 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:77918617 G>A maps to NM_020927.1 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:77859273 C>T maps to NM_020927.1 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr16:77896787 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr16:77910296 G>A maps to NM_020927.1 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:77910296 G>A maps to NM_020927.1 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:77918641 G>A maps to NM_020927.1 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:77859273 C>T maps to NM_020927.1 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr16:77918560 C>T maps to NM_020927.1 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:77910347 C>T maps to NM_020927.1 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr16:77850829 C>T maps to NM_020927.1 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:77910347 C>T maps to NM_020927.1 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:77918524 G>A maps to NM_020927.1 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:78005817 C>T maps to NM_020927.1 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr19:6820741 C>T maps to NM_005428.2 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:6822340 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:6828172 C>T maps to NM_005428.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr19:6820741 C>T maps to NM_005428.2 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr19:6825339 C>T maps to NM_005428.2 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr19:6825393 G>A maps to NM_005428.2 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:6820741 C>T maps to NM_005428.2 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:6828178 C>T maps to NM_005428.2 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr19:6832124 C>T maps to NM_005428.2 I474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:6828175 T>C maps to NM_005428.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:6821680 A>C maps to NM_005428.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:6825387 C>T maps to NM_005428.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:6828893 G>A maps to NM_005428.2 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:6853067 G>A maps to NM_005428.2 K770K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:6820765 C>T maps to NM_005428.2 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr19:6854015 C>T maps to NM_005428.2 D797D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr19:6820786 C>T maps to NM_005428.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:6832145 C>T maps to NM_005428.2 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:6833263 C>T maps to NM_005428.2 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:6833917 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr19:6836569 C>T maps to NM_005428.2 N635N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:6833725 C>T maps to NM_005428.2 F571F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr19:6825345 G>A maps to NM_005428.2 K252K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:136637128 C>T maps to NM_001134398.1 K725K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr9:136641193 G>A maps to NM_001134398.1 I658I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr9:136654405 G>A maps to NM_001134398.1 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr9:136650973 C>A maps to NM_001134398.1 G486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr1:108311103 G>A maps to NM_006113.4 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:108292185 G>A maps to NM_006113.4 I430I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr1:108303474 C>T maps to NM_006113.4 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:108152552 C>T maps to NM_006113.4 W672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:108507320 C>T maps to NM_006113.4 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr10:118896003 C>T maps to NM_001112704.1 Q136Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:118896120 C>T maps to NM_001112704.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:118891746 G>A maps to NM_199131.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:71160138 C>T maps to NM_012476.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:71160079 C>T maps to NM_012476.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:154456710 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:154464602 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr1:101186047 C>T maps to NM_001078.3 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr1:101197030 C>T maps to NM_001078.3 F494F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:101186047 C>T maps to NM_001078.3 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr1:101186266 A>G maps to NM_001078.3 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:101190258 C>T maps to NM_001078.3 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:101186047 C>T maps to NM_001078.3 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:101194909 G>A maps to NM_001078.3 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:101197030 C>T maps to NM_001078.3 F494F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:101186047 C>T maps to NM_001078.3 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:101198080 C>T maps to NM_001078.3 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:101186080 G>A maps to NM_001078.3 Q38Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:101185424 G>A maps to NM_001078.3 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:82808127 C>T maps to NM_004385.4 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr5:82835115 G>A maps to NM_004385.4 W2098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:82868368 G>A maps to NM_004385.4 K3290K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr5:82838035 C>T maps to NM_004385.4 L3072L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr5:82838004 C>T maps to NM_004385.4 S3061S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr5:82815861 C>T maps to NM_004385.4 V579V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr5:82836396 G>A maps to NM_004385.4 R2525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr5:82833504 C>T maps to NM_004385.4 A1561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr5:82837737 A>C maps to NM_004385.4 T2972T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr5:82833327 C>T maps to NM_004385.4 P1502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr5:82817592 T>C maps to NM_004385.4 P1156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:82786187 C>T maps to NM_004385.4 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:82833075 C>T maps to NM_004385.4 T1418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr5:82876183 G>A maps to NM_004385.4 K3374K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:82785995 T>C maps to NM_004385.4 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:82807961 C>T maps to NM_004385.4 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:82815174 G>A maps to NM_004385.4 E350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:82834002 G>A maps to NM_004385.4 E1727E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:82834818 C>T maps to NM_004385.4 F1999F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:82835439 C>T maps to NM_004385.4 F2206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:82836318 C>T maps to NM_004385.4 S2499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:82837305 C>T maps to NM_004385.4 P2828P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:82850795 G>A maps to NM_004385.4 W3225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr5:82816725 G>A maps to NM_004385.4 E867E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr5:82833264 G>A maps to NM_004385.4 W1481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:75849866 A>G maps to NM_014000.2 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr9:35061053 G>A maps to NM_007126.3 A439A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr9:35066717 T>C maps to NM_007126.3 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr8:67547092 G>A maps to NM_025054.4 A1104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr8:67577417 G>A maps to NM_025054.4 F592F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr8:67578461 C>T maps to NM_025054.4 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:67547157 G>A maps to NM_025054.4 R1083*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr8:67547091 G>A maps to NM_025054.4 Q1105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:67578797 G>A maps to NM_025054.4 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:7811697 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:7811739 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:8138245 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr23:6451805 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:6451785 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:8434286 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:8434312 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr5:133316435 G>A maps to NM_003374.2 Q179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr10:76990716 G>A maps to NM_001184783.1 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr8:42259488 C>T maps to ENST00000417062 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:48251325 C>T maps to NM_001017535.1 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:48240509 G>A maps to NM_001017535.1 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:48240512 G>A maps to NM_001017535.1 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:43745273 C>T maps to NM_001025366.2 Q243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr6:43745228 C>T maps to NM_001025366.2 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr6:43752295 G>A maps to NM_001025366.2 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr11:64005047 A>C maps to NM_003377.3 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr4:177605172 C>T maps to NM_005429.2 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr4:177609038 C>T maps to NM_005429.2 W249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr4:177608434 G>A maps to NM_005429.2 Q351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr4:177650814 C>T maps to NM_005429.2 W78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr4:177650813 C>T maps to NM_005429.2 W78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr4:177648940 G>A maps to NM_005429.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr4:177609039 C>T maps to NM_005429.2 W249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:135053635 C>T maps to NM_014468.2 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr3:157188162 C>T maps to NM_001167912.1 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr3:157178021 C>T maps to NM_001167912.1 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr3:157178090 G>A maps to NM_001167912.1 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr3:157178108 G>A maps to NM_001167912.1 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:56051965 G>A maps to NM_007146.2 H478H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:95676126 C>T maps to NM_017599.3 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:95681521 C>T maps to NM_017599.3 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr12:95694280 G>A maps to NM_017599.3 Q724Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3BZ-06A-12D-A196-08 chr7:100807584 C>G maps to NM_003378.3 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr23:135638622 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr23:135618247 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:135618347 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:135631093 G>A did not map to a codon.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr23:135618347 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:135618327 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:135618347 G>A did not map to a codon.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr23:135630984 C>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:135618371 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:117589529 T>C maps to NM_182645.2 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:117589583 G>A maps to NM_182645.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:117586979 C>T maps to NM_182645.2 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr3:87027685 G>A maps to NM_016206.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr3:87018238 G>A maps to NM_016206.2 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr3:87039869 A>T maps to NM_016206.2 Y8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:86996197 C>T maps to NM_016206.2 K319K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:86996205 G>A maps to NM_016206.2 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:10188297 T>C maps to NM_000551.2 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr3:10183809 C>T maps to NM_000551.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr3:10183810 G>T maps to NM_000551.2 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:10191546 C>T maps to NM_000551.2 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr3:10191496 C>T maps to NM_000551.2 Q164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr1:156268785 G>A maps to NM_001004319.2 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr2:219305464 G>A maps to NM_007127.2 V750V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr2:219295544 G>A maps to NM_007127.2 W349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr2:219295452 C>T maps to NM_007127.2 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:219294103 C>T maps to NM_007127.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr2:219289046 C>T maps to NM_007127.2 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:219299274 G>A maps to NM_007127.2 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:219296839 C>T maps to NM_007127.2 D425D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr2:219289046 C>T maps to NM_007127.2 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:219292990 C>T maps to NM_007127.2 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:219290450 C>T maps to NM_007127.2 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:219292963 G>A maps to NM_007127.2 W157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:219292990 C>T maps to NM_007127.2 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:219297643 C>T maps to NM_007127.2 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:219292981 G>A maps to NM_007127.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr2:219299364 C>T maps to NM_007127.2 F539F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:219299355 G>A maps to NM_007127.2 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:38035942 C>T maps to NM_015873.3 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr3:38038578 C>T maps to NM_015873.3 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:38040891 C>T maps to NM_015873.3 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:38044759 C>T maps to NM_015873.3 F587F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:38035810 G>A maps to NM_015873.3 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr3:38043242 G>A maps to NM_015873.3 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:38048181 C>T maps to NM_015873.3 A816A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:38045832 C>T maps to NM_015873.3 F631F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr10:17271960 G>A maps to NM_003380.3 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr10:17277175 C>T maps to NM_003380.3 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:153075348 T>A maps to NM_003381.2 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:153077364 G>A maps to NM_003381.2 K144K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:153073395 T>G maps to NM_003381.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr6:153076433 C>T maps to NM_003381.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:153076442 C>T maps to NM_003381.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:77919710 G>A maps to ENST00000445370 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr14:77902195 G>A maps to ENST00000445370 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:77896032 G>A maps to ENST00000445370 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr14:77908907 G>A maps to ENST00000445370 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:77919702 G>A maps to ENST00000445370 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr14:77893964 C>T maps to ENST00000445370 K518K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr14:77919711 G>A maps to ENST00000445370 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr14:77910663 G>A maps to ENST00000445370 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:77910636 G>A maps to ENST00000445370 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr3:42572421 G>A maps to NM_004624.3 W263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr3:42572389 G>A maps to NM_004624.3 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr3:42573336 G>A maps to NM_004624.3 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr3:42572996 C>T maps to NM_004624.3 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:42576496 C>T maps to NM_004624.3 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:42577766 G>A maps to NM_004624.3 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr7:158851212 C>T maps to ENST00000402066 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:158829452 C>T maps to ENST00000402066 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr7:158896489 G>A maps to ENST00000402066 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:158902548 G>A maps to ENST00000402066 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:158827271 G>A maps to ENST00000402066 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:158896489 G>A maps to ENST00000402066 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr7:158829467 G>A maps to ENST00000402066 F382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr2:37035853 C>T maps to NM_053276.3 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:37028482 G>A maps to NM_053276.3 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:37028482 G>A maps to NM_053276.3 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:36982173 G>A maps to NM_053276.3 W129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:37041341 G>A maps to NM_053276.3 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:37028482 G>A maps to NM_053276.3 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:37002148 C>T maps to NM_053276.3 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:37035814 C>T maps to NM_053276.3 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr2:37041324 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:37036009 C>T maps to NM_053276.3 F595F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:37036108 C>T maps to NM_053276.3 A628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:36982189 C>T maps to NM_053276.3 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:2641452 T>C maps to NM_003383.3 C134C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr9:2647524 A>G maps to NM_003383.3 G585G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:2647567 C>T maps to NM_003383.3 Q600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:5908850 C>T maps to NM_001017921.3 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:4688689 C>T maps to NM_182566.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:57967428 G>A maps to NM_020633.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:53762332 G>A maps to NM_173856.2 W235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:53762620 C>T maps to NM_173856.2 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:53762806 G>A maps to NM_173856.2 R393R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:53761936 G>A maps to NM_173856.2 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:53762569 C>T maps to NM_173856.2 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr19:53762533 T>C maps to NM_173856.2 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:53762277 G>A maps to NM_173856.2 W217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:53762527 G>A maps to NM_173856.2 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:53761936 G>A maps to NM_173856.2 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:53762791 C>T maps to NM_173856.2 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr19:53770606 G>A maps to NM_173857.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:53770021 C>T maps to NM_173857.2 W299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr19:53770582 C>T maps to NM_173857.2 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:53770582 C>T maps to NM_173857.2 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:53770582 C>T maps to NM_173857.2 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr19:53770867 C>T maps to NM_173857.2 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:53770252 G>A maps to NM_173857.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr19:53770207 G>A maps to NM_173857.2 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:247420410 G>A maps to NM_173858.1 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr6:133032870 C>T maps to NM_004666.2 W106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:133035072 C>T maps to NM_004666.2 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:133070845 A>G maps to NM_004665.2 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:133078616 G>A maps to NM_004665.2 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:133078616 G>A maps to NM_004665.2 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:55560111 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr7:55588790 G>A maps to NM_030796.3 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:55560107 G>A maps to NM_030796.3 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:55565346 G>A maps to NM_030796.3 C50C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr7:55560101 C>T maps to NM_030796.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:51458161 G>A maps to ENST00000273612 I754I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr3:51440679 G>A maps to ENST00000273612 F1454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr3:51440666 C>A maps to ENST00000273612 E1459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr3:51475838 G>T maps to ENST00000273612 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:51456308 G>A maps to ENST00000273612 F1086F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr22:22599667 C>T maps to NM_007128.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr22:22599457 C>T maps to NM_007128.2 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr22:24095101 C>T maps to ENST00000405618 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:118951814 C>T maps to NM_021729.4 Q817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:79917930 C>T maps to ENST00000376646 Q1305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr9:79843090 A>G maps to ENST00000376646 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:79932583 C>T maps to ENST00000376646 I1642I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr9:79932604 G>A maps to ENST00000376646 L1649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:79959076 C>T maps to ENST00000376646 P2345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr9:79890466 C>T maps to ENST00000376646 Q856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:79959073 C>T maps to ENST00000376646 I2344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr9:79933215 C>T maps to ENST00000376646 T1674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr9:79852916 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:79983000 C>T maps to ENST00000376646 F2835F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26D-06A-11D-A19A-08 chr9:79898508 C>T maps to ENST00000376646 N1094N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr8:100871676 G>A maps to NM_017890.3 G3696G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr8:100654472 G>A maps to NM_017890.3 G1910G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr8:100568702 C>T maps to NM_017890.3 R1616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr8:100887878 G>A maps to NM_017890.3 R4018R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr8:100133712 T>A maps to NM_181661.2 *416K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr8:100887878 G>A maps to NM_017890.3 R4018R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr8:100115223 C>T maps to NM_017890.3 N152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:100844829 G>A maps to NM_017890.3 Q3213Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr8:100887728 C>A maps to NM_017890.3 A3968A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr8:100287444 C>T maps to NM_017890.3 I929I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr8:100874046 G>T maps to NM_017890.3 R3721R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:100454725 G>A maps to NM_017890.3 W1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr8:100865744 C>T maps to NM_017890.3 D3401D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:100847424 G>A maps to NM_017890.3 R3230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr8:100654160 G>A maps to NM_017890.3 V1806V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr8:100831745 G>T maps to NM_017890.3 E2935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:100847490 T>C maps to NM_017890.3 S3252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr8:100844871 C>T maps to NM_017890.3 F3227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr8:100865924 G>A maps to NM_017890.3 K3461K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr8:100168820 G>A maps to NM_017890.3 R686R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr8:100847494 C>T maps to NM_017890.3 R3254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr8:100515154 C>T maps to NM_017890.3 F1378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr8:100673580 G>A did not map to a codon.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr8:100729537 G>A maps to NM_017890.3 G2223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr8:100108601 A>T maps to NM_017890.3 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:100796697 C>T maps to NM_017890.3 S2670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:100887644 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:100520085 C>T maps to NM_017890.3 R1416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:100844859 G>A maps to NM_017890.3 R3223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr8:100789095 C>T maps to NM_017890.3 T2472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr15:62283974 C>T maps to NM_020821.2 R460R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:62167113 A>G maps to NM_020821.2 L3459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:62182391 G>A maps to NM_020821.2 Q3105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:62165567 A>G maps to NM_020821.2 V3485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr15:62212313 G>A maps to NM_020821.2 L2477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr15:62209762 C>T maps to NM_020821.2 W2611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr15:62208095 G>A maps to NM_020821.2 F2727F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:62219478 G>A maps to NM_020821.2 I2109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:62254086 G>A maps to NM_020821.2 F1203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr15:62165534 C>T maps to NM_020821.2 K3496K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr15:62255040 G>A maps to NM_020821.2 S1114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr15:62241654 G>A maps to NM_020821.2 I1582I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:62239437 G>A maps to NM_020821.2 V1610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:12343418 C>T maps to NM_015378.2 Q1754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr1:12336377 T>G maps to NM_015378.2 T911T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr1:12359374 G>A maps to NM_015378.2 G2050G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr1:12353694 C>T maps to NM_015378.2 F1989F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr1:12316508 C>T maps to NM_015378.2 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr1:12337850 G>A maps to NM_015378.2 L1402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:12461713 C>T maps to NM_015378.2 L3946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:12374282 G>A maps to NM_015378.2 Q2349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:12337808 C>T maps to NM_015378.2 I1388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr1:12433864 C>T maps to NM_015378.2 L3623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr1:12368578 G>A maps to NM_015378.2 K2177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:12331141 C>T maps to NM_015378.2 I688I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:12374213 C>T maps to NM_015378.2 S2326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:12368587 G>A maps to NM_015378.2 E2180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr1:12321144 G>T maps to NM_015378.2 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:12409242 C>T maps to NM_015378.2 I3081I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr1:12317069 C>T maps to NM_015378.2 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr1:12460272 C>T maps to NM_015378.2 F3890F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:12337994 C>T maps to NM_015378.2 S1450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr1:12433879 A>G maps to NM_015378.2 S3628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr1:12364651 C>T maps to NM_015378.2 S2102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr1:12359294 C>T maps to NM_015378.2 L2024L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12343257 T>A maps to NM_015378.2 L1700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12343363 C>T maps to NM_015378.2 V1735V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12343663 C>T maps to NM_015378.2 I1835I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12353604 C>T maps to NM_015378.2 L1959L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:12364651 C>T maps to NM_015378.2 S2102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr1:12339580 C>T maps to NM_015378.2 T1492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:12389937 C>T maps to NM_015378.2 F2750F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr20:2843463 C>T maps to NM_022575.2 F405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr20:2841210 C>T maps to NM_022575.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr20:2843502 C>T maps to NM_022575.2 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr20:2843502 C>T maps to NM_022575.2 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr20:2843502 C>T maps to NM_022575.2 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr20:2840754 C>T maps to NM_022575.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:2846047 C>T maps to NM_022575.2 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:2842727 C>T maps to NM_022575.2 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:2841186 C>T maps to NM_022575.2 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:41191360 C>T maps to NM_020857.2 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr15:41192377 G>A maps to NM_020857.2 E454E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:41191636 C>T maps to NM_020857.2 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr15:41192209 C>T maps to NM_020857.2 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr15:41195019 C>T maps to NM_020857.2 F801F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr15:41191789 C>T maps to NM_020857.2 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr15:41188269 C>T maps to NM_020857.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr15:41192239 C>T maps to NM_020857.2 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr15:41192875 G>A maps to NM_020857.2 R620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr2:86756386 G>T maps to ENST00000439940 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:40928267 C>T maps to NM_032353.2 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:40926709 G>A maps to NM_032353.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr10:70925796 G>A did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:134113051 C>T maps to NM_052875.3 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:134114856 C>T maps to NM_052875.3 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr8:145649392 G>A maps to NM_183057.1 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr8:145650163 G>A maps to NM_183057.1 D113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr8:145649476 G>A maps to NM_183057.1 H165H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr8:145649347 G>A maps to NM_183057.1 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:122716888 G>A maps to NM_022916.4 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:122717443 G>A maps to NM_022916.4 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr12:122729244 G>A maps to NM_022916.4 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr12:122716936 G>A maps to NM_022916.4 F549F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:122750877 G>A maps to NM_022916.4 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:91543791 C>G maps to NM_018668.3 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:91560206 G>T maps to NM_018668.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr16:46695715 G>A maps to NM_018206.4 Q709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr16:46715296 G>A maps to NM_018206.4 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr16:46697008 C>T maps to NM_018206.4 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr16:46706385 T>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:46717500 G>A maps to NM_018206.4 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr16:46705720 G>A maps to NM_018206.4 Q474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr12:123351713 C>T maps to NM_024667.2 Q269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr12:123351824 G>A maps to NM_024667.2 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:73085384 G>A maps to NM_001077621.1 E145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:73085399 C>T maps to NM_001077621.1 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr15:42453968 G>A maps to ENST00000348544 V832V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr15:42483349 G>A maps to ENST00000348544 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr15:42458802 G>A maps to ENST00000348544 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr15:42479528 G>A maps to ENST00000348544 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr15:42458374 G>A maps to ENST00000348544 F565F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr15:42476895 C>T maps to ENST00000348544 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr15:42453929 G>A maps to ENST00000348544 I845I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:42458404 G>A maps to ENST00000348544 F555F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:42458806 G>A maps to ENST00000348544 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:42459060 G>A maps to ENST00000348544 C487C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr7:38812205 G>A maps to NM_014396.3 I348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr7:38783014 G>A maps to NM_014396.3 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr7:38857458 G>A maps to NM_014396.3 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr7:38781670 G>A maps to NM_014396.3 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:38857458 G>A maps to NM_014396.3 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:38783139 G>A maps to NM_014396.3 R662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:38783140 G>A maps to NM_014396.3 S661S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr7:38797963 G>A maps to NM_014396.3 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:38766520 G>A maps to NM_014396.3 P824P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:150049781 C>T maps to NM_007259.3 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:150054810 G>A maps to NM_007259.3 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:150065670 C>T maps to NM_007259.3 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:150116886 T>C maps to NM_007259.3 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr16:69354182 C>T maps to NM_013245.2 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr16:69352603 A>G maps to NM_013245.2 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr18:61064418 G>A maps to NM_004869.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr18:61064419 G>A maps to NM_004869.3 H313H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr18:61060687 C>T maps to NM_004869.3 W396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr6:33232153 G>A maps to NM_022553.4 H507H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr6:33231635 G>A maps to NM_022553.4 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:602611 C>T maps to NM_001128159.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr2:64160856 G>A maps to NM_016516.2 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:64147047 C>A maps to NM_016516.2 G711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:64160886 G>A maps to NM_016516.2 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr2:64208966 C>T maps to NM_016516.2 W64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr1:151156849 G>A maps to ENST00000354473 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:151149260 G>A maps to ENST00000354473 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:151149320 T>C maps to ENST00000354473 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:184577777 G>A maps to ENST00000437079 K383K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:184689488 C>T maps to ENST00000437079 T1123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr3:184769773 C>T maps to ENST00000437079 F1416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr3:184632795 C>T maps to ENST00000437079 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:184580815 C>T maps to ENST00000437079 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr3:184769773 C>T maps to ENST00000437079 F1416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr14:97347543 A>G maps to NM_003384.2 *397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr19:50482440 G>A maps to NM_016440.3 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:50504103 G>A maps to NM_016440.3 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:50511002 G>A maps to NM_016440.3 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:107316582 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:107310286 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr23:107320490 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:107315999 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:107310194 A>G did not map to a codon.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr23:107301307 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:107310233 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr12:118511786 G>A maps to NM_019086.5 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr12:118533380 G>A maps to NM_019086.5 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr12:118517277 G>A maps to NM_019086.5 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:118511609 G>A maps to NM_019086.5 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr11:124622006 G>A maps to NM_014312.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:124617445 G>A maps to NM_014312.3 L323L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A2GH-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:124619676 C>T maps to NM_014312.3 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:124618585 G>A maps to NM_014312.3 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr11:124617496 G>A maps to NM_014312.3 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr11:124621324 G>A maps to NM_014312.3 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr11:124620742 G>A maps to NM_014312.3 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr23:65259821 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:65252516 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr1:159827670 G>A maps to NM_001013661.1 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:17773478 G>A maps to NM_003385.4 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr2:17773475 C>T maps to NM_003385.4 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:17773485 C>T maps to NM_003385.4 Q49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr19:54545421 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:54545552 G>A maps to NM_198481.3 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr19:54544313 C>T maps to NM_198481.3 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr7:54612387 G>A maps to ENST00000404951 Q51Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr7:54610431 G>A maps to ENST00000404951 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr7:54610461 C>T maps to ENST00000404951 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:54612429 C>T maps to ENST00000404951 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:54612447 C>T maps to ENST00000404951 D71D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:54610434 C>T maps to ENST00000404951 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:54612429 C>T maps to ENST00000404951 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:54612348 G>A maps to ENST00000404951 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:54617531 G>A maps to ENST00000404951 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:54617552 C>T maps to ENST00000404951 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:36560174 G>A maps to NM_080607.2 W87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr20:25056958 G>A maps to NM_014588.4 Q346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr14:74711924 C>T maps to NM_182894.2 H171H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr14:74726429 C>T maps to NM_182894.2 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr14:74707910 C>T maps to NM_182894.2 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:74711966 G>A maps to NM_182894.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr6:142468496 C>T maps to NM_016485.3 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr6:142490803 C>A maps to NM_016485.3 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr1:117699391 G>A maps to NM_024626.2 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr1:117695782 C>T maps to NM_024626.2 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:117699532 G>A maps to NM_024626.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:117699244 G>A maps to NM_024626.2 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr10:114224328 C>T maps to NM_145206.2 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr10:114575102 C>T maps to NM_145206.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr17:26696732 C>T maps to NM_000638.3 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:26694949 C>T maps to NM_000638.3 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr17:26695043 C>T maps to NM_000638.3 W339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr17:26696363 G>A maps to NM_000638.3 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr17:26696552 C>T maps to NM_000638.3 K168K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr1:1374539 C>T maps to NM_022834.4 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:1372757 C>T maps to NM_022834.4 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:1374644 C>T maps to NM_022834.4 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr10:116045914 C>T maps to NM_198496.1 D405D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr10:116049009 C>T maps to NM_198496.1 A628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr10:116032618 G>A maps to NM_198496.1 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr10:116014794 C>T maps to NM_198496.1 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:116032654 G>A maps to NM_198496.1 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:116038529 G>A maps to NM_198496.1 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:116048976 C>T maps to NM_198496.1 I617I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr10:116049072 C>T maps to NM_198496.1 A649A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr10:116049156 G>A maps to NM_198496.1 R677R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:116048880 G>A maps to NM_198496.1 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:116037786 C>T maps to NM_198496.1 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:116046220 C>T maps to NM_198496.1 F507F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:116049294 C>T maps to NM_198496.1 P723P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr16:22157564 G>A maps to NM_173615.3 V913V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr16:22130236 G>A maps to NM_173615.3 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr16:22132293 C>T maps to NM_173615.3 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr16:22132859 C>T maps to NM_173615.3 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr16:22132417 C>T maps to NM_173615.3 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr16:22132862 G>A maps to NM_173615.3 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr16:22122258 C>T maps to NM_173615.3 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:22130332 C>T maps to NM_173615.3 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:22149820 G>A maps to NM_173615.3 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr2:98779419 C>T maps to NM_144992.4 D365D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr2:98928667 C>T maps to NM_144992.4 A1247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr2:98851192 C>T maps to NM_144992.4 S797S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:98744844 G>A maps to NM_144992.4 K282K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:98928407 C>T maps to NM_144992.4 L1216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr2:98914415 C>T maps to NM_144992.4 F1068F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:98846578 C>T maps to NM_144992.4 V739V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:98809360 G>A maps to NM_144992.4 R489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr2:98804457 C>T maps to NM_144992.4 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:98744709 C>T maps to NM_144992.4 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:98737761 G>A maps to NM_144992.4 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:98744760 C>T maps to NM_144992.4 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr11:123988942 C>T maps to NM_014622.4 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr11:123989324 C>G maps to NM_014622.4 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr11:124016026 G>A maps to NM_014622.4 E746E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr11:124016070 G>T did not map to a codon.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr11:123993679 A>G maps to NM_014622.4 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr11:124013186 C>T maps to NM_014622.4 Q688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:124007758 C>T maps to NM_014622.4 Q555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:124005659 C>T maps to NM_014622.4 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:123988954 G>A maps to NM_014622.4 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:124007366 C>A maps to NM_014622.4 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr11:124006948 C>T maps to NM_014622.4 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:123989366 C>T maps to NM_014622.4 C199C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr7:49842314 A>T maps to NM_198570.3 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr7:49842380 G>A maps to NM_198570.3 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:49951681 G>A maps to NM_198570.3 K293K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:215440492 G>A maps to NM_001080500.2 W206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr2:215440510 G>A maps to NM_001080500.2 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2ND-06A-11D-A196-08 chr2:215279276 G>A maps to NM_001080500.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:215440420 G>A maps to NM_001080500.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr2:215279276 G>A maps to NM_001080500.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr11:61032490 C>T maps to NM_152718.2 R692R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:61026239 G>A maps to NM_152718.2 T925T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr11:61026778 G>A maps to NM_152718.2 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:61026611 G>A maps to NM_152718.2 L801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr11:61026431 G>A maps to NM_152718.2 S861S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr11:61058814 G>A maps to NM_152718.2 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr11:61048114 C>T maps to NM_152718.2 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:61034972 G>A maps to NM_152718.2 F642F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr11:61026746 G>A maps to NM_152718.2 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:6061574 G>A maps to NM_000552.3 H2699H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:6128269 G>A maps to NM_000552.3 F1438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:6132875 G>A maps to NM_000552.3 F1100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr12:6140678 G>A maps to NM_000552.3 P917P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:6125314 G>A maps to NM_000552.3 L1799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr12:6232350 G>A maps to NM_000552.3 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr12:6127714 G>A maps to NM_000552.3 I1623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr12:6125315 G>A maps to NM_000552.3 I1798I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:6125983 G>A maps to NM_000552.3 F1702F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr12:6230459 G>A maps to NM_000552.3 R34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr12:6230460 G>A maps to NM_000552.3 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr12:6135212 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M8-06A-12D-A196-08 chr12:6103337 G>A maps to NM_000552.3 F2096F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:6103304 C>T maps to NM_000552.3 W2107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:6103061 C>T maps to NM_000552.3 G2188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:6167150 C>T maps to NM_000552.3 Q531Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr12:6105272 C>T maps to NM_000552.3 V1986V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:6076678 C>T maps to NM_000552.3 R2620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:6220132 C>T maps to NM_000552.3 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:6090950 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:6090951 C>T maps to NM_000552.3 K2429K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr12:6094762 G>A maps to NM_000552.3 V2289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr12:6091092 G>A maps to NM_000552.3 T2382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6078443 G>A maps to NM_000552.3 V2554V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6128443 G>A maps to NM_000552.3 I1380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:6181519 G>A maps to NM_000552.3 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:6128269 G>A maps to NM_000552.3 F1438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr12:6174304 G>A maps to NM_000552.3 Q431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:28884944 C>T maps to NM_016628.3 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:88260188 G>A maps to ENST00000342368 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr10:88260222 G>A maps to ENST00000342368 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr10:88206200 G>A maps to ENST00000342368 F1125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:88277457 G>A maps to ENST00000342368 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr14:100820168 G>A maps to NM_173701.1 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:100820806 G>A maps to NM_173701.1 H173H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:100813128 G>A maps to NM_173701.1 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr1:119575596 T>C maps to NM_015836.3 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr1:119619092 G>A maps to NM_015836.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:48542279 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr23:48542296 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:48546826 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:48546476 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:48545241 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:48547049 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr23:48545241 G>A did not map to a codon.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr23:48547270 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:48542352 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:27736450 G>A maps to NM_006990.2 H358H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:27736192 G>A maps to NM_006990.2 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr13:27255346 C>T maps to NM_006646.5 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:27259903 C>T maps to NM_006646.5 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr13:27256851 G>A maps to NM_006646.5 Q364Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr13:27250708 C>T maps to NM_006646.5 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr13:27216517 C>T maps to NM_006646.5 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr13:27216449 C>A maps to NM_006646.5 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:123346375 G>A maps to NM_003941.2 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:123332412 G>A maps to NM_003941.2 I445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr7:123334877 A>G maps to NM_003941.2 C239C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr2:74686870 G>A maps to ENST00000393972 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr12:14941980 G>A maps to NM_016312.2 R466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr12:14943564 G>A maps to NM_016312.2 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:14952595 G>T maps to NM_016312.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr12:14947651 A>T maps to NM_016312.2 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:73843625 G>A maps to NM_012478.3 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:73844681 G>A maps to NM_012478.3 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr22:42415350 C>T maps to NM_152613.2 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:42415332 G>A maps to NM_152613.2 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:102612715 T>C did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:102612854 G>A did not map to a codon.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr23:102612728 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr7:70885918 C>T maps to NM_022479.1 Q264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr7:70800542 C>T maps to NM_022479.1 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr7:70853226 G>A maps to NM_022479.1 K143K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr7:71177001 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr7:71177105 G>A maps to NM_022479.1 W591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr7:71036296 C>T maps to NM_022479.1 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:71130577 G>A maps to NM_022479.1 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:71175906 C>T maps to NM_022479.1 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:71175771 C>T maps to NM_022479.1 F509F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:70597850 C>T maps to NM_022479.1 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:71036308 G>A maps to NM_022479.1 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr7:71175772 C>T maps to NM_022479.1 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr7:70886088 C>T maps to NM_022479.1 I320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:71177028 G>A maps to NM_022479.1 T565T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr7:70853290 C>T maps to NM_022479.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr7:70853301 C>T maps to NM_022479.1 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr7:71036308 G>A maps to NM_022479.1 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr7:71175762 G>A maps to NM_022479.1 K506K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr7:70597976 C>T maps to NM_022479.1 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:70880875 G>A maps to NM_022479.1 E197E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:71036317 C>T maps to NM_022479.1 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:71135090 G>A maps to NM_022479.1 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:70880945 C>T maps to NM_022479.1 Q221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:70885929 G>A maps to NM_022479.1 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:70886082 C>T maps to NM_022479.1 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:70853358 C>T maps to NM_022479.1 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr7:73100983 C>T maps to ENST00000423497 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:73249192 G>C maps to NM_152559.2 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr7:73279580 C>T maps to NM_182504.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:73279354 C>T maps to NM_182504.3 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr7:73279528 G>A maps to NM_182504.3 Q93Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:73279444 C>T maps to NM_182504.3 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:73279938 C>T maps to NM_182504.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr7:73280103 C>T maps to NM_182504.3 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr13:52313269 C>T maps to NM_052950.3 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr4:85731478 G>A maps to NM_014991.4 R636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr4:85654606 C>T maps to NM_014991.4 K2383K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr4:85599426 G>A maps to NM_014991.4 R3385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr4:85617206 T>C maps to NM_014991.4 Q2939Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr4:85674876 G>A maps to NM_014991.4 P1904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr4:85696088 G>A maps to NM_014991.4 I1546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:85664946 G>A maps to NM_014991.4 S1993S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:85694048 G>A maps to NM_014991.4 T1596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr4:85731299 T>G maps to NM_014991.4 A695A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr4:85742678 G>A maps to NM_014991.4 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr4:85660250 C>T maps to NM_014991.4 L2162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr4:85612912 G>A maps to NM_014991.4 I3025I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr4:85672725 G>A maps to NM_014991.4 F1961F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr4:85676490 G>A maps to NM_014991.4 V1829V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:85663059 G>A maps to NM_014991.4 L2030L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:85696066 G>A maps to NM_014991.4 R1554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:85674966 G>A maps to NM_014991.4 F1874F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr4:85676481 G>A maps to NM_014991.4 I1832I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr4:85642711 A>T maps to NM_014991.4 P2485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:55453879 G>A maps to NM_007086.3 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr4:10105518 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:10079018 G>A maps to NM_017491.3 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:122665386 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:122664261 C>T maps to NM_018117.11 G1044G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:122665479 C>T maps to NM_018117.11 L1128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr10:122625191 T>C maps to NM_018117.11 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:122626201 C>T maps to NM_018117.11 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr10:122618231 T>C maps to NM_018117.11 N92N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr10:122648693 C>T maps to NM_018117.11 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:203759325 C>T maps to NM_018256.3 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51K-06A-11D-A25O-08 chr23:48458074 C>G did not map to a codon.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr23:48457987 G>A did not map to a codon.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr23:48463395 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:48463291 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:48458947 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:9536283 C>T maps to NM_145054.4 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr17:9497521 G>A maps to NM_145054.4 W140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:9538774 G>A maps to NM_145054.4 K458K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr17:9538849 G>A maps to NM_145054.4 G483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:9515754 G>A maps to NM_145054.4 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr17:9515787 C>T maps to NM_145054.4 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr4:177098789 G>A maps to NM_170710.4 T1278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr4:177041198 G>A maps to NM_170710.4 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr4:177067187 T>A maps to NM_170710.4 V548V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr4:177069352 G>A maps to NM_170710.4 V612V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A2A1-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr4:177100681 G>A maps to NM_170710.4 V1307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr4:177056374 G>A maps to NM_170710.4 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:177063140 C>T maps to NM_170710.4 R508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:177098681 T>G maps to NM_170710.4 T1242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:990243 C>T maps to NM_024100.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:990988 C>T maps to NM_024100.3 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:990988 C>T maps to NM_024100.3 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr4:39276557 G>A maps to NM_025132.3 K1232K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr4:39276557 G>A maps to NM_025132.3 K1232K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr4:39255579 C>A maps to NM_025132.3 S977S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr4:39219725 G>C did not map to a codon.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr4:39278648 T>C maps to NM_025132.3 D1242D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:39245968 C>T maps to NM_025132.3 V841V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr14:102675406 C>T maps to ENST00000454394 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:102675508 C>T maps to ENST00000454394 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr16:737698 C>T maps to ENST00000248142 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr16:734757 G>A maps to ENST00000248142 C913C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr16:737046 G>A maps to ENST00000248142 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr14:100996329 C>T maps to NM_001161476.1 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:100934476 C>T maps to NM_001161476.1 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr14:100847980 C>T maps to NM_001161476.1 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr14:100992259 C>T maps to NM_001161476.1 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr14:100995454 C>T maps to NM_001161476.1 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:100847881 C>T maps to NM_001161476.1 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr14:100934431 G>A maps to NM_001161476.1 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr6:170033159 G>A maps to NM_182552.3 I702I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr1:118499810 C>T maps to NM_006784.2 F858F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr1:118494989 C>T maps to NM_006784.2 Q659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:118485128 C>T maps to NM_006784.2 I353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:118499762 C>T maps to NM_006784.2 F842F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:118477253 C>T maps to NM_006784.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:118497969 G>A maps to NM_006784.2 G814G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr9:116083795 G>A maps to NM_001012361.2 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr9:116085414 G>A maps to NM_001012361.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr2:128528456 T>G maps to NM_018383.4 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr2:128467266 C>A maps to NM_018383.4 G1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:128525861 G>A maps to NM_018383.4 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:128477218 G>A maps to NM_018383.4 Q794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:128474765 G>A maps to NM_018383.4 P944P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr2:128477300 C>T maps to NM_018383.4 G766G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr2:128471434 G>T maps to NM_018383.4 P1010P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr9:131418972 G>A maps to NM_052844.3 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr9:131398015 C>T maps to NM_052844.3 W245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr2:20166596 C>T maps to NM_001006657.1 W361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:20114006 G>A maps to NM_001006657.1 I1062I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr2:20169254 G>A maps to NM_001006657.1 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:20135989 G>A maps to NM_001006657.1 R813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr5:110446898 C>T maps to NM_139281.2 F602F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:110459594 A>T maps to NM_139281.2 A803A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr5:110428012 G>A maps to NM_139281.2 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr10:1126376 C>A maps to ENST00000416775 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr9:127618182 G>A maps to NM_001045476.1 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr21:44282450 G>A maps to NM_018669.4 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr21:44283680 G>A maps to NM_018669.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:76736640 T>C maps to NM_018268.2 E293E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:76729000 G>A maps to NM_018268.2 Q447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3BZ-06A-12D-A196-08 chr2:29152467 A>T maps to NM_015131.1 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IB-06A-11D-A196-08 chr23:117526643 A>C did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:117576578 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:117527159 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:117527160 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:117576556 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:117532376 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:117529211 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:117526914 T>G did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:117528103 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:117529211 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:117531025 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:117566801 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr23:48934104 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:48934104 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr17:80575212 A>G maps to NM_019613.3 H255H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr17:80579640 G>A maps to NM_019613.3 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:80579640 G>A maps to NM_019613.3 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr6:33247112 C>T maps to NM_005452.5 K591K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:109544853 G>A maps to NM_001142550.1 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:109525356 A>G maps to NM_001142550.1 L722L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:109529263 G>A maps to NM_001142550.1 I610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:39133153 C>A maps to NM_020839.2 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr3:39108072 A>G maps to NM_020839.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr3:39135451 T>C maps to NM_020839.2 S611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr3:39093554 G>A maps to NM_020839.2 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr3:167272580 C>T maps to NM_178824.3 W219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr3:167254742 G>A maps to NM_178824.3 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr3:167249023 G>A maps to NM_178824.3 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:167245781 C>T maps to NM_178824.3 K458K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:167246849 C>T maps to NM_178824.3 W447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr3:167319956 G>A maps to NM_178824.3 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:167245787 G>A maps to NM_178824.3 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:167277917 G>A maps to NM_178824.3 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr3:167248901 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:167293759 C>T maps to NM_178824.3 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr3:167249032 T>C maps to NM_178824.3 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:167319986 G>A maps to NM_178824.3 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:167196683 C>T maps to NM_178824.3 V692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr3:167218037 C>T maps to NM_178824.3 V626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:167272580 C>T maps to NM_178824.3 W219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr3:167217995 C>T maps to NM_178824.3 R640R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:137007495 C>T maps to NM_052821.3 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:113115565 G>A maps to NM_001164496.1 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr3:113135414 G>A maps to NM_001164496.1 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr3:113138962 G>A maps to NM_001164496.1 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:113120438 A>G maps to NM_001164496.1 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:113114707 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:113138931 G>A maps to NM_001164496.1 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr3:196281399 G>A maps to NM_182627.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:140048689 C>T maps to NM_017706.4 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr16:74949782 C>T maps to NM_030581.3 R403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:74972116 G>A maps to NM_030581.3 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:74922120 G>A maps to NM_030581.3 P764P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:122134327 G>A maps to NM_019069.3 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr3:49050181 C>T maps to NM_018031.3 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:49051111 G>A maps to NM_018031.3 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:49052331 G>T maps to NM_018031.3 E1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:49049242 C>T maps to NM_018031.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:158723147 C>T maps to NM_018051.4 L830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:158704363 C>A maps to NM_018051.4 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:158663942 C>T maps to NM_018051.4 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr15:78580680 G>A maps to NM_025234.1 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr19:36577616 G>A maps to NM_001083961.1 R557R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:36558740 A>T maps to NM_001083961.1 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:36593009 C>T maps to NM_001083961.1 F1059F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:36590353 C>T maps to NM_001083961.1 Y858Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:36581412 C>T maps to NM_001083961.1 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:36558768 C>T maps to NM_001083961.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:36591687 C>T maps to NM_001083961.1 S926S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr19:36592979 C>A maps to NM_001083961.1 S1049S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:36591690 C>T maps to NM_001083961.1 F927F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr19:36594428 C>T maps to NM_001083961.1 S1233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr19:36583617 G>A maps to NM_001083961.1 P746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr19:36593924 C>T maps to NM_001083961.1 G1137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:36590395 C>T maps to NM_001083961.1 P872P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:85570254 C>T maps to NM_145172.3 Q510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:241886653 G>A maps to NM_144625.4 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:43663222 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:43651026 G>A maps to NM_001195831.1 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:43649359 C>T maps to NM_001195831.1 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:43675703 C>T maps to NM_152498.3 I682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:43675658 C>T maps to NM_152498.3 T667T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:43649365 G>A maps to NM_001195831.1 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr1:43649359 C>T maps to NM_001195831.1 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr1:43647460 G>A maps to NM_001195831.1 W138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:43649260 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:122361868 G>A maps to NM_144668.4 K240K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr12:122361857 C>T maps to NM_144668.4 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr12:122396264 G>A maps to NM_144668.4 K606K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr12:122437758 C>T maps to NM_144668.4 I1048I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr12:122437828 C>T maps to NM_144668.4 L1072L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr12:122439496 C>T maps to NM_144668.4 S1110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr12:122398589 C>T maps to NM_144668.4 R745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr8:124096405 C>T maps to NM_145647.3 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr8:124105883 C>T maps to NM_145647.3 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr8:124138818 C>T maps to NM_145647.3 F592F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:124105835 C>T maps to NM_145647.3 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:228786134 G>A maps to NM_178821.1 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr2:228786204 C>T maps to NM_178821.1 Q381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:228770951 G>A maps to NM_178821.1 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr2:228750133 T>A maps to NM_178821.1 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:228783511 C>T maps to NM_178821.1 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:228762941 G>A maps to NM_178821.1 W162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr2:228767755 G>A maps to NM_178821.1 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr18:54363638 C>T maps to NM_015285.2 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr18:54444025 C>T maps to NM_015285.2 V954V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr18:54349977 C>T maps to NM_015285.2 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr18:54694329 G>A maps to NM_015285.2 A1455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:54363638 C>T maps to NM_015285.2 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr5:37725135 T>A maps to NM_018034.2 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:37396569 A>C maps to NM_018034.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr5:37396596 C>T maps to NM_018034.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr15:53998205 A>T maps to NM_182758.2 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr15:53908077 G>A maps to NM_182758.2 S775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr15:53901720 G>A maps to NM_182758.2 Q981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr15:53998214 G>T maps to NM_182758.2 Y337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr15:53998202 G>A maps to NM_182758.2 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr15:53908381 C>T maps to NM_182758.2 W674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr15:54025313 C>T maps to NM_182758.2 W11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:53907759 C>T maps to NM_182758.2 Q881Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:53997400 G>A maps to NM_182758.2 Q378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:54015096 C>T maps to NM_182758.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:54025253 C>T maps to NM_182758.2 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr2:190334869 C>T maps to NM_032168.1 Q630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr2:190328663 C>T maps to NM_032168.1 Q364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:190327288 C>T maps to NM_032168.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr15:44153569 C>T maps to NM_024908.3 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr15:44150934 T>C maps to NM_024908.3 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:111983919 G>A maps to NM_024102.2 Q321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr1:67301340 C>T maps to NM_024763.4 R567R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:67299707 G>A maps to NM_024763.4 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:67356858 C>T maps to NM_024763.4 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr1:3551599 C>T maps to NM_017818.3 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:3548159 G>A maps to NM_017818.3 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr1:3551762 G>A maps to NM_017818.3 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:3566509 C>T maps to NM_017818.3 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:1631645 C>T maps to NM_001163809.1 P1131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:1637214 C>T maps to NM_001163809.1 S1628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr17:1637433 C>T maps to NM_001163809.1 F1701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr9:140458907 G>A maps to NM_138778.2 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:140450029 C>T maps to NM_138778.2 W340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr9:140459358 G>A maps to NM_138778.2 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:140468792 G>A maps to NM_138778.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr19:33647372 C>T maps to NM_173479.3 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr19:33647269 C>T maps to NM_173479.3 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:33639703 C>T maps to NM_173479.3 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:33639709 C>T maps to NM_173479.3 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:33623140 C>T maps to NM_173479.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:33623338 C>T maps to NM_173479.3 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:33639751 C>T maps to NM_173479.3 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:64066609 G>A maps to NM_080666.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr16:706314 C>T maps to NM_145294.4 P660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr16:716716 G>A maps to NM_145294.4 W1643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:711460 C>T maps to NM_145294.4 A1211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:716969 C>T maps to NM_145294.4 L1690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr16:708547 C>T maps to NM_145294.4 P930P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:709106 C>T maps to NM_145294.4 A1011A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr16:706314 C>G maps to NM_145294.4 P660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr16:716083 C>T maps to NM_145294.4 P1523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:705078 C>T maps to NM_145294.4 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr7:134891949 G>A maps to NM_014149.3 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr7:134871867 G>A maps to NM_014149.3 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:68368838 C>T maps to NM_138458.2 W168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:68368839 C>T maps to NM_138458.2 W168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:68364490 G>A maps to NM_138458.2 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr15:90280910 G>A maps to NM_020212.1 W572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr15:90281395 G>A maps to NM_020212.1 R630R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:90246317 C>T maps to NM_020212.1 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr15:90244976 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr15:90280817 C>T maps to NM_020212.1 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr15:90281314 C>T maps to NM_020212.1 I603I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr15:90281357 C>T maps to NM_020212.1 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr15:90280817 C>T maps to NM_020212.1 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr15:90245105 C>T maps to NM_020212.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:90255327 C>T maps to NM_020212.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:90276306 C>T maps to NM_020212.1 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr2:160139343 G>T maps to NM_001128212.1 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:27631590 C>T maps to ENST00000319394 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr1:27618753 C>T maps to ENST00000319394 D176D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:27631506 C>T maps to ENST00000319394 I553I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr1:27618876 C>T maps to ENST00000319394 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:27630175 C>T maps to ENST00000319394 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr7:141414187 G>A maps to NM_001105558.1 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr7:141423003 G>A maps to NM_001105558.1 K317K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:141420791 G>A maps to NM_001105558.1 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:141408848 A>G maps to NM_001105558.1 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr7:141416067 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:141408671 C>T maps to NM_001105558.1 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:141408672 C>T maps to NM_001105558.1 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr7:141408662 G>A maps to NM_001105558.1 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:84360500 G>A maps to NM_021197.2 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:84360530 G>A maps to NM_021197.2 Q216Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr16:84351932 C>T maps to NM_021197.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr20:44258499 G>A maps to NM_080753.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr20:44259521 C>T maps to NM_080753.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr20:44313573 G>T maps to NM_172131.2 P55P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D3-A5GO-06A-12D-A27K-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr20:44314547 C>T maps to NM_172006.2 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr20:44313537 G>A maps to NM_172131.2 F67F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A3J7-06A-11D-A20D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:44333609 C>T maps to NM_172131.2 R7R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-GN-A266-06A-11D-A197-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-QB-A6FS-06A-11D-A30X-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr20:44279155 C>T maps to NM_147197.2 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:44279215 C>T maps to NM_147197.2 W8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr20:44278036 C>T maps to NM_147197.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:44278036 C>T maps to NM_147197.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr20:43752534 C>T maps to NM_080869.1 W96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:43752763 C>T maps to NM_080869.1 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr20:44416616 C>T maps to NM_080614.1 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:44416580 G>A maps to NM_080614.1 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:43739056 G>A maps to ENST00000307971 C117C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr20:44168016 C>T maps to ENST00000372665 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr20:44167998 C>T maps to ENST00000372665 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q1-06A-21D-A196-08 chr20:44184400 G>A maps to NM_130896.2 C128C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr20:44190780 C>T maps to NM_130896.2 W35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:44180688 C>T maps to NM_130896.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr20:44181841 G>A maps to NM_130896.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:44190809 G>A maps to NM_130896.2 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr20:44237381 C>T maps to NM_147198.2 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:44237333 C>T maps to NM_147198.2 W69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr20:44238796 G>A maps to NM_147198.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr16:683312 G>A maps to NM_053284.2 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr16:681327 G>A maps to NM_053284.2 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:48917680 G>A maps to NM_175575.5 W344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:48917518 G>A maps to NM_175575.5 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:48917686 C>T maps to NM_175575.5 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr4:6303255 C>T maps to NM_006005.3 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr4:6303927 C>T maps to NM_006005.3 I802I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr4:6304173 C>T maps to NM_006005.3 F884F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr4:6303918 C>A maps to NM_006005.3 T799T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:6303030 C>T maps to NM_006005.3 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:6303633 C>T maps to NM_006005.3 F704F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:6279304 C>T maps to NM_006005.3 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr4:6303831 C>T maps to NM_006005.3 F770F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr4:6288871 C>T maps to NM_006005.3 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr4:6296780 C>T maps to NM_006005.3 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr4:6296912 G>A maps to NM_006005.3 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr4:6304158 C>T maps to NM_006005.3 F879F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr4:6304152 C>T maps to NM_006005.3 F877F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr4:6302763 C>T maps to NM_006005.3 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr4:1919899 C>T maps to NM_133335.3 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr4:1920067 C>T maps to NM_133335.3 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:1957748 C>T maps to NM_133335.3 P905P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:1961226 C>T maps to NM_133335.3 I1005I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr4:1957787 C>T maps to NM_133335.3 F918F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr8:38133952 C>T maps to NM_023034.1 K1311K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:38187042 G>A maps to NM_023034.1 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr8:38205260 C>A maps to NM_023034.1 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:38157052 G>A maps to NM_023034.1 S889S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:38187399 G>A maps to NM_023034.1 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr4:1993355 G>A maps to NM_005663.3 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr4:2010584 C>T maps to NM_005663.3 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:56297253 G>A maps to NM_032345.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:56295661 G>A maps to NM_032345.2 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr12:65462649 C>T maps to NM_007191.4 Q144Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr2:175446110 G>A maps to NM_003387.4 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr17:38430096 C>T maps to NM_133264.4 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:38416911 C>T maps to NM_133264.4 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:38421225 T>C maps to NM_133264.4 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:38433419 C>A maps to NM_133264.4 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr17:38416831 C>T maps to NM_133264.4 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:29924036 C>T maps to NM_001080529.1 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:66431802 G>A maps to NM_017983.5 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:5254223 C>T maps to NM_015610.3 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr8:134232968 C>A maps to NM_003882.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr8:134239796 G>A maps to NM_003882.2 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr8:134237762 T>C maps to NM_003882.2 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:134239811 C>T maps to NM_003882.2 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr8:134237663 G>A maps to NM_003882.2 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:134225126 G>A maps to NM_003882.2 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr8:134239781 C>T maps to NM_003882.2 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr8:134232938 A>C maps to NM_003882.2 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr20:43355791 G>A maps to NM_003881.2 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr20:43348737 G>A maps to NM_003881.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr20:43348728 C>T maps to NM_003881.2 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:43355770 C>T maps to NM_003881.2 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:112386126 G>A maps to NM_198239.1 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr6:112386016 C>T maps to NM_198239.1 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:15547878 G>A maps to ENST00000389282 F778F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr19:15538021 T>G maps to ENST00000389282 P1141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:15547764 G>A maps to ENST00000389282 T816T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr19:15535022 G>A maps to ENST00000389282 F1589F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:15558986 G>A maps to ENST00000389282 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:15547869 C>T maps to ENST00000389282 R781R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr19:15535022 G>A maps to ENST00000389282 F1589F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:15547701 G>A maps to ENST00000389282 F837F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:15535060 G>A maps to ENST00000389282 L1577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:15535061 G>A maps to ENST00000389282 S1576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:15535022 G>A maps to ENST00000389282 F1589F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:68591929 G>A maps to NM_024911.6 T535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:68603576 G>A maps to NM_024911.6 Q468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:68619309 G>A maps to NM_024911.6 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr12:978197 C>T maps to NM_001184985.1 F1102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr12:988836 C>T maps to NM_018979.3 F824F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr12:1006707 C>T maps to NM_001184985.1 T2363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr12:1005394 C>T maps to NM_001184985.1 I2174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:992578 C>T maps to NM_001184985.1 L1430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr12:968443 C>T maps to NM_001184985.1 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr12:989019 C>T maps to NM_018979.3 I885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:977789 A>T maps to NM_001184985.1 V966V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:990931 C>T maps to NM_001184985.1 T1322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr12:1005637 G>A maps to NM_001184985.1 K2255K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr12:968515 A>G maps to NM_001184985.1 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr12:995045 C>T maps to NM_001184985.1 I1952I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr12:988836 C>T maps to NM_018979.3 F824F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr12:994622 C>T maps to NM_001184985.1 S1811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr12:939187 C>T maps to NM_001184985.1 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:993926 C>T maps to NM_001184985.1 P1579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:994958 C>T maps to NM_001184985.1 F1923F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr9:95992138 G>A maps to ENST00000297954 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:96021604 T>C maps to ENST00000297954 P925P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:96079799 A>G did not map to a codon.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr9:96055254 C>T maps to ENST00000297954 F1873F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:96009841 C>T maps to ENST00000297954 F520F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:96051604 C>T maps to ENST00000297954 V1560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:96051805 G>A maps to ENST00000297954 G1627G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:96051796 C>T maps to ENST00000297954 P1624P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr9:96055404 G>A maps to ENST00000297954 S1923S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr9:96051718 C>T maps to ENST00000297954 Y1598Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr9:96051719 C>T maps to ENST00000297954 Q1599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr9:96051721 G>A maps to ENST00000297954 Q1599Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:96025958 C>T maps to ENST00000297954 S1174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:96051382 C>T maps to ENST00000297954 L1486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:96055275 C>T maps to ENST00000297954 F1880F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr9:96021331 C>T maps to ENST00000297954 F834F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr23:54359610 C>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:54264796 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr23:54275253 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:54324654 T>C did not map to a codon.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr23:54264843 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr23:54263501 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr23:54263820 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:54275962 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:54263407 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:54275314 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:54259291 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr23:54275667 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:54337639 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:54319340 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:54224977 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:54337605 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:54337719 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:54259281 G>C did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:54337719 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr23:54263450 T>C did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:54275340 G>A did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:54324688 T>A did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:54324689 T>A did not map to a codon.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr17:40947895 G>A maps to NM_032387.4 K1092K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:40936446 G>A maps to NM_032387.4 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:40947898 A>G maps to NM_032387.4 E1093E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr17:40934876 G>A maps to NM_032387.4 W240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr17:40933267 C>T maps to NM_032387.4 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr17:40939480 C>T maps to NM_032387.4 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:40937370 G>A maps to NM_032387.4 E449E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr17:40932964 C>T maps to NM_032387.4 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:40939865 C>T maps to NM_032387.4 P604P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:40935958 C>T maps to NM_032387.4 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr17:40940742 C>A maps to NM_032387.4 T695T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A264-06A-11D-A196-08 chr17:40947832 T>G maps to NM_032387.4 A1071A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr17:40940388 C>T maps to NM_032387.4 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr17:40947498 G>A maps to NM_032387.4 R994R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:49373259 G>A maps to NM_005430.3 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr2:219754736 C>T maps to NM_025216.2 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:219757815 C>T maps to NM_025216.2 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr2:219747083 G>A maps to NM_025216.2 W105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr2:219746918 C>T maps to NM_025216.2 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:219754736 C>T maps to NM_025216.2 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:49361920 G>A maps to NM_003394.3 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr12:49360219 C>T maps to NM_003394.3 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr12:49359896 C>T maps to NM_003394.3 W384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:75902837 G>A maps to NM_004626.2 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr11:75902749 G>A maps to NM_004626.2 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:75902849 G>A maps to NM_004626.2 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:120965492 G>A maps to ENST00000414945 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr7:120979032 G>A maps to NM_057168.1 K244K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:120965495 G>A maps to ENST00000414945 E14E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:120979047 G>A maps to NM_057168.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:116955181 C>T maps to NM_003391.2 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr7:116960675 C>T maps to NM_003391.2 W85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:116955220 C>T maps to NM_003391.2 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr7:116937681 G>A maps to NM_003391.2 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:116955217 G>A maps to NM_003391.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr7:116918400 A>C maps to NM_003391.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:116955340 G>A maps to NM_003391.2 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr1:113010170 C>T maps to NM_004185.3 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:113058975 G>A maps to NM_024494.2 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:113059741 G>C did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:44845943 C>T maps to NM_030753.3 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:228238549 C>T maps to ENST00000366753 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:228210553 G>A maps to ENST00000366753 W86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr1:228238561 G>A maps to ENST00000366753 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr1:228238405 C>T maps to ENST00000366753 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:228246895 C>T maps to ENST00000366753 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr1:228238594 C>T maps to ENST00000366753 N184N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:228210583 C>T maps to ENST00000366753 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr1:228246796 C>T maps to ENST00000366753 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:55508460 G>A maps to NM_003392.3 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr3:55504140 C>T maps to NM_003392.3 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:55508523 C>T maps to NM_003392.3 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr12:1748982 G>A maps to NM_032642.2 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:1748940 C>T maps to NM_032642.2 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr12:1755351 C>T maps to NM_032642.2 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:1742017 G>A maps to NM_032642.2 W92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:1755003 C>T maps to NM_032642.2 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:1755117 G>A maps to NM_032642.2 K260K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr2:219735748 G>A maps to NM_006522.3 W27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr3:13860506 G>A maps to NM_004625.3 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr3:13916510 G>A maps to NM_004625.3 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:13916591 C>G maps to NM_004625.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:13916495 C>T maps to NM_004625.3 W82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:13896033 G>A maps to NM_004625.3 R189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:13860803 C>T maps to NM_004625.3 K229K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr3:13916495 C>T maps to NM_004625.3 W82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr3:13860458 C>T maps to NM_004625.3 E344E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr3:13860501 C>T maps to NM_004625.3 W330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr3:13896033 G>A maps to NM_004625.3 R189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr3:13896034 G>A maps to NM_004625.3 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr3:13860791 G>A maps to NM_004625.3 N233N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr22:46346010 C>T maps to NM_058238.2 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:46372611 C>T maps to NM_058238.2 W8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:46327169 C>T maps to NM_058238.2 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:137426536 G>A maps to NM_058244.2 Q277Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr5:137424722 C>T maps to NM_058244.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr10:102222942 T>C maps to NM_003393.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr10:102239734 C>T maps to NM_003393.3 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr10:102222963 C>T maps to NM_003393.3 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr10:102238823 C>T maps to NM_003393.3 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr1:228109608 G>A maps to NM_003395.2 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:228109677 G>A maps to NM_003395.2 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:228112042 C>T maps to NM_003395.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr1:228109362 G>A maps to NM_003395.2 N318N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:228111919 G>A maps to NM_003395.2 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:44950041 G>A maps to NM_003396.1 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr17:44953981 C>T maps to NM_003396.1 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr17:44950056 C>T maps to NM_003396.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:44953630 G>A maps to NM_003396.1 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr17:44954019 G>A maps to NM_003396.1 W337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:44949960 G>A maps to NM_003396.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:7605006 C>T maps to NM_018081.2 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:7604070 C>T maps to NM_018081.2 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr17:7605063 C>T maps to NM_018081.2 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:7604845 C>T maps to NM_018081.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr21:40762754 G>A maps to NM_004627.4 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr8:30942716 C>T maps to NM_000553.4 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:30999283 C>T maps to NM_000553.4 L1076L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:31015035 C>T maps to NM_000553.4 P1324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:31024697 C>T maps to NM_000553.4 I1381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr8:30948413 C>T maps to NM_000553.4 I595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr8:30948372 C>T maps to NM_000553.4 Q582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:30999097 T>C maps to NM_000553.4 I1040I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr8:30916763 C>T maps to NM_000553.4 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:30948419 C>T maps to NM_000553.4 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:31015024 C>T maps to NM_000553.4 R1321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr6:2784556 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:2779538 T>C maps to NM_020135.2 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr6:2766620 C>G maps to NM_020135.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:25630395 C>T maps to NM_015626.8 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr17:5998537 C>T maps to NM_015253.1 Q282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:6012931 C>T maps to NM_015253.1 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:5984157 G>A maps to NM_015253.1 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr12:108589749 G>A maps to ENST00000261400 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr12:108600112 C>T maps to ENST00000261400 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr12:108589839 G>A maps to ENST00000261400 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:108642089 G>A maps to ENST00000261400 T576T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr12:108641990 C>T maps to ENST00000261400 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr12:108589758 G>A maps to ENST00000261400 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:108604065 G>A maps to ENST00000261400 Q222Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:108600112 C>T maps to ENST00000261400 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr12:108618588 C>T maps to ENST00000261400 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr12:108589749 G>A maps to ENST00000261400 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:108618543 C>T maps to ENST00000261400 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:108626547 C>T maps to ENST00000261400 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:32414221 C>T maps to NM_024426.4 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:34991053 C>T maps to ENST00000270288 S615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:34984005 C>T maps to ENST00000270288 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr5:167882459 C>T maps to NM_001161661.1 R920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr5:167850762 C>T maps to NM_001161661.1 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:167855771 C>T maps to NM_001161661.1 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr5:167882443 C>T maps to NM_001161661.1 S914S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr5:167868775 G>A maps to NM_001161661.1 K790K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr5:167849094 C>T maps to NM_001161661.1 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:167882374 C>T maps to NM_001161661.1 T891T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:167882443 C>T maps to NM_001161661.1 S914S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:167812346 C>T maps to NM_001161661.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr5:167882455 T>C maps to NM_001161661.1 F918F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr5:167891787 C>T maps to NM_001161661.1 L997L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:167882459 C>T maps to NM_001161661.1 R920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr4:184182239 C>T maps to ENST00000448232 F488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:184233504 C>T maps to ENST00000448232 S1156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:10098132 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr23:10098133 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:10096185 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr23:10062314 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:10046891 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:10058884 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:10092358 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr23:10085461 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:10094264 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr23:10085261 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr23:10085395 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:10084536 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr23:10085441 C>T did not map to a codon.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr23:10085348 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:78458946 C>T maps to NM_016373.1 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:87410598 T>A maps to NM_007013.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:87392991 C>T maps to NM_007013.3 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr16:69951743 C>T maps to NM_007014.3 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr16:69965787 C>T maps to NM_007014.3 I559I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr16:69965484 T>C did not map to a codon.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr16:69875993 C>A maps to NM_007014.3 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:69965069 C>T maps to NM_007014.3 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:69965482 G>A maps to NM_007014.3 Q531Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:69969856 C>T maps to NM_007014.3 D648D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:69969796 C>T maps to NM_007014.3 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr16:69970274 G>A maps to NM_007014.3 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr3:149290663 G>A maps to NM_001168278.1 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:149290771 G>A maps to NM_001168278.1 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:149375081 G>A maps to NM_001168278.1 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:149290714 G>A maps to NM_001168278.1 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:7692251 G>A maps to NM_020196.2 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr19:7687454 G>A maps to NM_020196.2 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:7689289 G>A maps to NM_020196.2 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr19:7685758 G>A maps to NM_020196.2 T648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:7691125 C>A maps to NM_020196.2 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr19:7692251 G>A maps to NM_020196.2 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr19:7687731 C>T maps to NM_020196.2 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:52893846 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:52893805 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:52896098 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:52896106 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr23:52893827 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:52842236 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:52842165 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:168549307 G>A maps to NM_002995.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:168549307 G>A maps to NM_002995.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:46063268 C>T maps to NM_005283.2 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:46063226 G>A maps to NM_005283.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:46062857 G>A maps to NM_005283.2 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr3:46062674 G>A maps to NM_005283.2 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr3:46062446 G>A maps to NM_005283.2 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:46062464 G>A maps to NM_005283.2 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:46062950 G>A maps to NM_005283.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr3:46063139 G>A maps to NM_005283.2 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr2:31562438 G>A maps to NM_000379.3 I1230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr2:31596795 G>A maps to NM_000379.3 F543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:31591430 T>C maps to NM_000379.3 E692E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:31572900 C>T maps to NM_000379.3 E940E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr2:31565047 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:31595131 G>A maps to NM_000379.3 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:31589780 C>T maps to NM_000379.3 G759G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr2:31591448 C>T maps to NM_000379.3 V686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr2:31600049 G>A maps to NM_000379.3 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:31604541 G>A maps to NM_000379.3 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:31573068 G>A maps to NM_000379.3 F884F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr2:31611134 C>T maps to NM_000379.3 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:31591448 C>T maps to NM_000379.3 V686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:31570492 G>A maps to NM_000379.3 I1057I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:31598274 G>A maps to NM_000379.3 Q525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:31598299 G>A maps to NM_000379.3 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:31572667 C>T maps to NM_000379.3 G951G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:31593226 C>T maps to NM_000379.3 K658K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:31587101 G>A maps to NM_000379.3 F851F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr2:31609292 C>T maps to NM_000379.3 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:31570498 C>T maps to NM_000379.3 L1055L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:31588337 G>A maps to NM_000379.3 F843F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr2:31588406 G>T maps to NM_000379.3 T820T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr2:31571175 C>T maps to NM_000379.3 G1035G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr2:31589777 C>T maps to NM_000379.3 E760E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:31572556 G>A maps to NM_000379.3 F988F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:31588336 G>A maps to NM_000379.3 L844L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:31593295 G>A maps to NM_000379.3 F635F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:31624190 G>A maps to NM_000379.3 H67H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:31599965 G>A maps to NM_000379.3 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr2:31602785 G>A maps to NM_000379.3 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:31598278 G>A maps to NM_000379.3 V523V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:31637490 C>T maps to NM_000379.3 K14K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:31595188 G>A maps to NM_000379.3 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:31596750 G>A maps to NM_000379.3 V558V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr2:31605980 C>T maps to NM_000379.3 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr23:123022524 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr23:123022525 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:123034362 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:39226214 G>A maps to NM_194293.2 F1574F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr3:39229652 G>A maps to NM_194293.2 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr3:39227899 G>A maps to NM_194293.2 Q1013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr3:39228701 G>A maps to NM_194293.2 I745I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44R-06A-41D-A25O-08 chr3:39225749 C>T maps to NM_194293.2 V1729V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:39227455 G>A maps to NM_194293.2 Q1161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:39225635 G>C maps to NM_194293.2 T1767T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr3:39230810 G>A maps to NM_194293.2 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:39226589 G>T maps to NM_194293.2 P1449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:39230045 C>T maps to NM_194293.2 E297E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:39230252 C>T maps to NM_194293.2 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:39227006 C>T maps to NM_194293.2 K1310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr3:39228014 G>A maps to NM_194293.2 P974P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:39229894 G>A maps to NM_194293.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr3:39227519 C>T maps to NM_194293.2 Q1139Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:39229745 G>A maps to NM_194293.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:39229316 C>T maps to NM_194293.2 Q540Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:39226979 G>A maps to NM_194293.2 P1319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr3:39226214 G>A maps to NM_194293.2 F1574F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr3:39227579 C>T maps to NM_194293.2 K1119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:39227429 C>T maps to NM_194293.2 R1169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:39230876 C>T maps to NM_194293.2 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr2:168100389 A>T maps to NM_152381.5 K830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr2:168107876 C>T maps to NM_152381.5 F3325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:167759997 C>T maps to NM_152381.5 F2F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:168099977 G>A maps to NM_152381.5 V692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr2:168105893 G>A maps to NM_152381.5 R2664R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:168102788 G>A maps to NM_152381.5 E1629E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr2:168106667 G>A maps to NM_152381.5 Q2922Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:168106706 G>A maps to NM_152381.5 R2935R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr2:168099104 C>T maps to NM_152381.5 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr2:168102533 G>A maps to NM_152381.5 K1544K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:168100349 T>A maps to NM_152381.5 P816P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr2:168105434 G>A maps to NM_152381.5 R2511R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr2:168115071 G>A maps to ENST00000420519 E705E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr2:168103757 G>A maps to NM_152381.5 V1952V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:168105731 C>A maps to NM_152381.5 P2610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:168106364 A>G maps to NM_152381.5 K2821K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr2:168108158 C>T maps to NM_152381.5 F3419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:168099962 G>A maps to NM_152381.5 G687G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:168103907 G>A maps to NM_152381.5 G2002G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:167992423 G>A maps to NM_152381.5 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:168102897 C>T maps to NM_152381.5 L1666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr2:168102635 G>A maps to NM_152381.5 G1578G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:168101570 C>T maps to NM_152381.5 I1223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr2:168104645 G>A maps to NM_152381.5 L2248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:168104645 G>A maps to NM_152381.5 L2248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:168104645 G>A maps to NM_152381.5 L2248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:168103797 C>T maps to NM_152381.5 Q1966*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr2:168107876 C>T maps to NM_152381.5 F3325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:168107273 C>T maps to NM_152381.5 I3124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:168099638 G>A maps to NM_152381.5 W579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:168102689 G>A maps to NM_152381.5 Q1596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr2:168099251 A>G maps to NM_152381.5 E450E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr2:168106202 T>A maps to NM_152381.5 A2767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:168101888 G>A maps to NM_152381.5 G1329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:168107795 G>A maps to NM_152381.5 K3298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr2:168103355 G>A maps to NM_152381.5 K1818K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:168115110 T>C maps to ENST00000420519 V718V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr2:168101651 G>A maps to NM_152381.5 K1250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr2:168107342 G>A maps to NM_152381.5 K3147K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:168105968 G>A maps to NM_152381.5 Q2689Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:168102836 T>C maps to NM_152381.5 T1645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr2:168100166 A>G maps to NM_152381.5 K755K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr2:168103546 G>A maps to NM_152381.5 W1882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr2:168100211 A>C maps to NM_152381.5 A770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19H-06A-12D-A196-08 chr2:168101759 G>A maps to NM_152381.5 E1286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr2:167760324 C>T maps to NM_152381.5 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr2:168107876 C>T maps to NM_152381.5 F3325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:167760033 G>A maps to NM_152381.5 Q14Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr2:168101943 C>T maps to NM_152381.5 R1348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:168106509 C>T maps to NM_152381.5 Q2870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr2:168102350 G>A maps to NM_152381.5 Q1483Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:168099317 C>T maps to NM_152381.5 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:168099641 C>T maps to NM_152381.5 I580I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:168099725 C>T maps to NM_152381.5 I608I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:168105524 G>A maps to NM_152381.5 K2541K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr2:168100496 G>A maps to NM_152381.5 E865E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:168107492 C>T maps to NM_152381.5 I3197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:168103355 G>A maps to NM_152381.5 K1818K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:168107876 C>T maps to NM_152381.5 F3325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:168102398 C>T maps to NM_152381.5 F1499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr2:168105434 G>A maps to NM_152381.5 R2511R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr23:37586968 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr23:37545248 T>G did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr23:37545384 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:37587524 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:37545255 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:37587600 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr22:17280778 G>A maps to NM_175878.3 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr22:17288657 C>T maps to NM_175878.3 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr22:17280796 G>A maps to NM_175878.3 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr22:17264937 G>A maps to NM_175878.3 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:17280820 C>T maps to NM_175878.3 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:17280820 C>T maps to NM_175878.3 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr22:17288876 G>A maps to NM_175878.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr22:17264923 C>T maps to NM_175878.3 W322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:17288675 C>T maps to NM_175878.3 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:17288699 G>A maps to NM_175878.3 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:17288906 C>T maps to NM_175878.3 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr22:17288711 G>A maps to NM_175878.3 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr8:56436521 C>T maps to NM_052898.1 F563F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr8:56436557 G>A maps to NM_052898.1 V575V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr8:56436206 C>T maps to NM_052898.1 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr8:56436146 G>A maps to NM_052898.1 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:56436023 C>T maps to NM_052898.1 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr8:56015500 C>T maps to NM_052898.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:56436023 C>T maps to NM_052898.1 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr8:56436479 C>T maps to NM_052898.1 I549I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr8:56436753 C>T maps to NM_052898.1 Q641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr8:56436608 A>G maps to NM_052898.1 E592E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:56435930 C>T maps to NM_052898.1 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:56436557 G>A maps to NM_052898.1 V575V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr8:56436224 C>T maps to NM_052898.1 I464I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:56435965 G>A maps to NM_052898.1 W378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr8:56270243 C>T maps to NM_052898.1 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:56270364 C>T maps to NM_052898.1 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:56435861 C>T maps to NM_052898.1 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:56436482 C>T maps to NM_052898.1 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:56436521 C>T maps to NM_052898.1 F563F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr8:56436023 C>T maps to NM_052898.1 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:6681181 G>A maps to NM_207411.4 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr8:6679432 G>A maps to NM_207411.4 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:6682705 G>A maps to NM_207411.4 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr8:6690261 G>A maps to NM_207411.4 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr8:6690363 G>A maps to NM_207411.4 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:6679507 G>A maps to NM_207411.4 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr8:10756349 C>T maps to NM_173683.3 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr8:10756187 C>T maps to NM_173683.3 W400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr8:11058467 G>A maps to NM_173683.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr8:10756046 C>T maps to NM_173683.3 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr8:10756376 G>A maps to NM_173683.3 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:10756220 G>A maps to NM_173683.3 F389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:11058137 G>A maps to NM_173683.3 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr8:10756181 G>A maps to NM_173683.3 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:10755866 G>A maps to NM_173683.3 I507I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr8:10756148 C>T maps to NM_173683.3 W413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr8:10782165 C>T maps to NM_173683.3 K313K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:10782216 G>A maps to NM_173683.3 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:10755511 G>A maps to NM_173683.3 R626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:10756349 C>T maps to NM_173683.3 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:10755743 C>T maps to NM_173683.3 T548T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr8:10782297 C>T maps to NM_173683.3 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr8:10756103 G>A maps to NM_173683.3 F428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:10755638 G>A maps to NM_173683.3 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:10756115 G>A maps to NM_173683.3 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:10782144 G>A maps to NM_173683.3 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr8:10755494 G>A maps to NM_173683.3 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr8:10755743 C>T maps to NM_173683.3 T548T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr20:30584503 T>C maps to NM_001011718.1 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr20:30584971 G>A maps to NM_001011718.1 R484R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:30556334 C>A maps to NM_001011718.1 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr20:30585109 G>A maps to NM_001011718.1 K530K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr20:30584443 C>T maps to NM_001011718.1 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:30584827 C>T maps to NM_001011718.1 Y436Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr20:30585091 G>A maps to NM_001011718.1 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr20:30585010 C>T maps to NM_001011718.1 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr20:30584689 C>T maps to NM_001011718.1 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:30584329 C>T maps to NM_001011718.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:30585175 G>A maps to NM_001011718.1 E552E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:30584563 G>A maps to NM_001011718.1 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr20:30584362 G>A maps to NM_001011718.1 Q281Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:28290031 G>A maps to NM_018053.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr8:71619233 C>T maps to NM_001011720.1 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr8:71619188 G>A maps to NM_001011720.1 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr8:71619233 C>T maps to NM_001011720.1 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:71619374 G>A maps to NM_001011720.1 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:71646646 C>T maps to NM_001011720.1 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:100169469 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:100169470 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:100169976 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr23:100169664 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr23:100169881 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:100182977 G>A did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:100182963 A>G did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:100177946 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:14214554 A>G maps to NM_004628.4 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:14190063 G>A maps to NM_004628.4 P806P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:111667469 G>A maps to NM_020383.3 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:111642288 G>A maps to NM_020383.3 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:111635350 G>A maps to NM_020383.3 V442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:111631565 G>A maps to NM_020383.3 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr23:128880633 T>A did not map to a codon.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr23:128877992 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:128879216 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr23:128873231 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:128887158 T>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:128901580 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:128880612 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:128902302 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr23:128887196 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:128896700 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr22:41277927 C>T maps to NM_022098.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr22:41310301 C>T maps to NM_022098.2 I343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr22:41277847 G>T maps to NM_022098.2 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr2:61709609 A>G maps to NM_003400.3 S959S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr2:61719316 G>C maps to NM_003400.3 V580V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr13:21436884 G>A maps to NM_022459.4 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr13:21371180 G>A maps to NM_022459.4 Q780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr13:21357875 G>A maps to NM_022459.4 L1147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr13:21362746 G>A maps to NM_022459.4 T975T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr13:21382647 C>T maps to NM_022459.4 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr13:21417935 G>A maps to NM_022459.4 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr13:21417144 G>A maps to NM_022459.4 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr6:43536446 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr6:43536447 C>T maps to NM_020750.2 K216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr6:43517300 C>G maps to NM_020750.2 R595R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr6:43514468 G>A maps to NM_020750.2 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr16:28118942 G>A maps to NM_015171.2 I799I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr16:28123300 G>A maps to NM_015171.2 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr16:28117462 G>A maps to NM_015171.2 I895I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr16:28146631 G>A maps to NM_015171.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr16:28128739 A>G maps to NM_015171.2 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:28115989 G>A maps to NM_015171.2 L941L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:28157509 A>G maps to NM_015171.2 G413G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:28146596 G>A maps to NM_015171.2 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr16:28181101 G>A maps to NM_015171.2 D178D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr16:28112886 G>A maps to NM_015171.2 V1056V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:28118870 G>A maps to NM_015171.2 A823A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr16:28188546 A>G maps to NM_015171.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr8:21856776 C>T maps to ENST00000434536 F877F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr8:21861514 A>G maps to ENST00000434536 R1057R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr8:21842175 C>T maps to ENST00000434536 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:21862529 C>T maps to ENST00000434536 F1074F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr8:21846588 C>T maps to ENST00000434536 S630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr12:64813916 C>A maps to NM_007235.3 S186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr12:64815125 C>T maps to NM_007235.3 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr12:64833071 C>T maps to NM_007235.3 Q928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr12:64828637 C>T maps to NM_007235.3 F878F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr12:64828324 C>T maps to NM_007235.3 Q831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr12:64815031 C>T maps to NM_007235.3 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:180794455 C>T maps to NM_004736.3 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:180756944 C>T maps to NM_004736.3 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:44058893 G>A maps to NM_006297.2 N106N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:44065133 C>T maps to NM_006297.2 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:44057649 G>A maps to NM_006297.2 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:152345843 G>A maps to NM_005431.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr14:104174865 G>A maps to NM_005432.3 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr5:82400779 C>T maps to NM_022406.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr2:217001834 C>T maps to NM_021141.3 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr22:42033663 C>T maps to NM_001469.3 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:58340856 C>T maps to NM_033276.2 Q105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr12:58345575 C>T maps to NM_033276.2 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:58350597 C>T maps to NM_033276.2 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr3:142037515 G>A maps to NM_019001.3 F1512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:142089448 G>A maps to NM_019001.3 Q1028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr3:142137707 G>A maps to NM_019001.3 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr3:142090132 G>A maps to NM_019001.3 Q1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:142030474 G>A maps to NM_019001.3 Q1667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr20:21335487 C>T maps to NM_012255.3 Y666Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr20:21311264 C>T maps to NM_012255.3 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr20:21369915 T>G maps to NM_012255.3 Y931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr20:21335473 C>T maps to NM_012255.3 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr11:74554478 C>T maps to NM_182969.1 W715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:38442460 C>T maps to NM_005108.3 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr3:38407205 C>A maps to NM_005108.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr16:17211548 G>A maps to NM_022166.3 F837F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr16:17221573 G>A maps to NM_022166.3 V724V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr16:17232250 G>A maps to NM_022166.3 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:17211548 G>A maps to NM_022166.3 F837F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr16:17211548 G>A maps to NM_022166.3 F837F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:17235192 G>A maps to NM_022166.3 F468F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:17353331 C>T maps to NM_022166.3 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:17228496 G>A maps to NM_022166.3 Y620Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:17235222 G>A maps to NM_022166.3 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr16:17221564 G>A maps to NM_022166.3 I727I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr16:17221564 G>A maps to NM_022166.3 I727I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:17228394 G>A maps to NM_022166.3 S654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:17235030 G>A maps to NM_022166.3 S522S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:17294425 C>T maps to NM_022166.3 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:17353253 G>A maps to NM_022166.3 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:17353331 C>T maps to NM_022166.3 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:17232271 G>A maps to NM_022166.3 I568I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr11:102033192 C>T maps to NM_001130145.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:33276316 G>A maps to NM_003680.3 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr1:33282818 C>T maps to NM_003680.3 E9E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:33276294 G>A maps to NM_003680.3 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A44R-06A-41D-A25O-08 chr1:33276307 T>C maps to NM_003680.3 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:33245803 G>A maps to NM_003680.3 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:33252004 G>A maps to NM_003680.3 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:33282827 G>A maps to NM_003680.3 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr12:32908767 C>T maps to NM_001040436.1 W14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr12:32908049 G>T maps to NM_001040436.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr12:32908664 G>A maps to NM_001040436.1 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:43162380 C>T maps to NM_004559.3 D141D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr17:7193842 G>A maps to NM_015982.3 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr22:21982730 G>A maps to NM_001017964.1 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:183521772 A>C did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:183472088 T>G maps to NM_018023.4 V442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:183491519 C>A maps to NM_018023.4 S769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:183480000 C>T maps to NM_018023.4 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr3:183480000 C>T maps to NM_018023.4 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr3:183469916 G>A maps to NM_018023.4 Q342Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:183446549 C>G maps to NM_018023.4 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:183521815 C>T maps to NM_018023.4 I1208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr12:69764526 C>A maps to NM_006530.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:69756578 C>T maps to NM_006530.2 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:743026 G>A maps to NM_005433.3 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr18:756665 G>A maps to NM_005433.3 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:66052984 G>A maps to ENST00000376904 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr11:66055102 C>T maps to ENST00000376904 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr19:38798127 G>A maps to NM_001039672.2 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:38799965 G>A maps to NM_001039672.2 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:38798388 G>A maps to NM_001039672.2 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:38799697 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:54344368 G>A maps to NM_018982.4 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr1:54344368 G>A maps to NM_018982.4 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr6:43480048 G>A maps to ENST00000506469 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr4:44624577 G>A maps to NM_182592.2 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:44626724 G>A maps to NM_182592.2 N191N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr4:44652081 G>A maps to NM_182592.2 Y36Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:44652015 A>T maps to NM_182592.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr4:44638056 T>A maps to NM_182592.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr4:44624577 G>A maps to NM_182592.2 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:44624496 C>T maps to NM_182592.2 Q259Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:44624559 G>A maps to NM_182592.2 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:44626786 G>A maps to NM_182592.2 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr19:19645889 C>T maps to NM_198537.3 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr19:19640256 G>A maps to NM_198537.3 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr19:19646387 C>T maps to NM_198537.3 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr19:19646237 C>T maps to NM_198537.3 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:19646357 C>T maps to NM_198537.3 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:19648221 C>T maps to NM_198537.3 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:19645928 C>T maps to NM_198537.3 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr7:44247781 G>A maps to NM_006555.3 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr14:75276308 G>A maps to NM_019589.2 W1583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr14:75248255 C>T maps to NM_019589.2 Q504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr14:75266094 C>T maps to NM_019589.2 F1365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:75296003 C>T maps to NM_019589.2 P2084P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:75276306 C>T maps to NM_019589.2 L1582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr14:75266106 T>G maps to NM_019589.2 G1369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:75265467 A>C maps to NM_019589.2 G1156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr14:75265468 C>T maps to NM_019589.2 L1157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr14:75247203 C>T maps to NM_019589.2 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr14:75265375 C>T maps to NM_019589.2 R1126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr14:75264454 C>T maps to NM_019589.2 Q819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr14:75302089 C>T maps to NM_019589.2 A2139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr14:75283734 C>T maps to NM_019589.2 I1929I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:75266119 C>T maps to NM_019589.2 R1374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr14:75278335 C>T maps to NM_019589.2 R1748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr14:75269375 T>A maps to NM_019589.2 Y1506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr10:27422980 G>A maps to NM_139312.1 N311N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr10:27408324 A>G maps to NM_139312.1 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:27404986 A>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr10:27434372 G>A maps to NM_139312.1 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:207222586 G>A maps to NM_018566.3 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr22:22065003 G>A maps to NM_013313.3 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr22:22057766 C>T maps to NM_013313.3 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr22:22057767 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr17:57430799 C>T maps to NM_001005404.3 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr17:57430800 C>T maps to NM_001005404.3 Q11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:57413471 C>T maps to NM_145008.2 K122K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr2:30379531 C>T maps to NM_001127399.1 F5F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D3-A3C7-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr2:135738521 C>T maps to NM_025052.3 G1263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:135741290 G>A maps to NM_025052.3 I1059I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:135738419 T>A maps to NM_025052.3 A1297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:135738473 G>A maps to NM_025052.3 I1279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr2:135745451 C>T maps to NM_025052.3 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:135741362 C>T maps to NM_025052.3 R1035R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr2:135744914 C>T maps to NM_025052.3 K509K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr2:135745328 C>T maps to NM_025052.3 K371K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr2:135745406 C>T maps to NM_025052.3 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:135756461 G>A maps to NM_025052.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr2:135738809 C>T maps to NM_025052.3 T1167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:135757540 G>A maps to NM_025052.3 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:135779311 G>A maps to NM_025052.3 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:69188608 G>A maps to NM_001031732.2 Q487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr4:69185918 G>A maps to NM_001031732.2 R536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:112888985 C>T maps to NM_022828.3 F599F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:112915281 G>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr5:112915295 C>T maps to NM_022828.3 P1086P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr5:112868586 C>T maps to NM_022828.3 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:112929052 C>A maps to NM_022828.3 P1422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:112903484 G>A maps to NM_022828.3 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:112868722 C>T maps to NM_022828.3 Q275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr20:61833878 C>T maps to NM_017798.3 K471K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr20:61833776 G>A maps to NM_017798.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr20:61834135 G>A maps to NM_017798.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:61834442 G>A maps to NM_017798.3 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:61834931 G>A maps to NM_017798.3 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr1:29070134 G>A maps to NM_016258.2 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:29064828 C>T maps to NM_016258.2 Y37Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr1:29069260 T>A maps to NM_016258.2 L160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr20:43532689 C>T maps to NM_139323.2 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:75959205 C>A maps to NM_012479.3 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:75959022 G>A maps to NM_012479.3 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr7:75959289 C>T maps to NM_012479.3 Q116Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:9728292 C>T did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr1:155630056 G>A maps to ENST00000368339 I686I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:155640127 G>A maps to ENST00000368339 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr1:155658731 C>T maps to NM_139118.2 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:155630086 G>A maps to ENST00000368339 A676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:21875418 A>C did not map to a codon.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr23:21875138 G>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:21875651 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:21874646 C>T did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:21875396 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:74078122 T>C maps to NM_180990.3 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr17:74075562 G>A maps to NM_180990.3 Q47Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr17:74077798 G>A maps to NM_180990.3 Q281Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr18:72913568 A>C maps to NM_175907.4 Y312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr18:72914261 A>T maps to NM_175907.4 Y81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr18:72913799 C>T maps to NM_175907.4 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr2:174131183 C>T maps to NM_016653.2 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr2:174096939 C>T maps to NM_016653.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr2:174047579 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr2:174104178 G>A maps to NM_016653.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr2:174047582 A>G maps to NM_016653.2 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:174074497 C>T maps to NM_016653.2 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:174055895 C>T maps to NM_016653.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr7:100350304 C>T maps to ENST00000349350 I859I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:100350346 C>T maps to ENST00000349350 I873I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:100358105 C>T maps to ENST00000349350 F1263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr7:100349626 C>T maps to ENST00000349350 P633P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:100392955 C>T maps to ENST00000349350 Q2755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr7:100350220 C>T maps to ENST00000349350 T831T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr7:100373012 C>T maps to ENST00000349350 L1948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr7:100371396 C>T maps to ENST00000349350 S1896S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:100349968 C>T maps to ENST00000349350 I747I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:100371094 C>T maps to ENST00000349350 D1871D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr7:100349563 C>T maps to ENST00000349350 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr7:100348401 C>T maps to ENST00000349350 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:100349899 C>T maps to ENST00000349350 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr7:100350499 G>A maps to ENST00000349350 T924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:100349605 C>T maps to ENST00000349350 P626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:100350286 C>A maps to ENST00000349350 S853S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr7:100350388 C>T maps to ENST00000349350 I887I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr7:100361533 A>G maps to ENST00000349350 P1364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:100383690 G>A maps to ENST00000349350 G2302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:100350646 G>A maps to ENST00000349350 T973T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:100389759 C>T maps to ENST00000349350 S2567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr7:100350463 A>G maps to ENST00000349350 K912K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr7:100365542 G>A maps to ENST00000349350 T1650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:100350388 C>T maps to ENST00000349350 I887I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:100365542 G>A maps to ENST00000349350 T1650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr7:100391744 G>A maps to ENST00000349350 W2663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:100373428 G>A maps to ENST00000349350 L2055L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr7:100348353 C>T maps to ENST00000349350 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr7:100369600 C>T maps to ENST00000349350 Q1795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr7:100361700 T>G maps to ENST00000349350 L1383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr7:100364798 C>T maps to ENST00000349350 I1593I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr7:100373158 G>A maps to ENST00000349350 T1996T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:100348285 C>T maps to ENST00000349350 Q430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:100382453 C>T maps to ENST00000349350 S2277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr7:100333341 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:100349593 C>T maps to ENST00000349350 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:100349740 C>T maps to ENST00000349350 S671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:100350328 C>T maps to ENST00000349350 S867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:100373311 C>T maps to ENST00000349350 P2016P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:100349947 C>T maps to ENST00000349350 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:100371411 C>T maps to ENST00000349350 I1901I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:100382393 G>A maps to ENST00000349350 V2257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr7:100390093 C>T maps to ENST00000349350 S2593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:98351916 G>A maps to NM_001079.3 K429K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:98354001 G>A maps to NM_001079.3 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr4:48495019 C>A maps to NM_175619.1 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr3:167000193 G>A maps to ENST00000307529 R696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr3:166960417 C>T maps to ENST00000307529 K756K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:167016197 G>A maps to ENST00000307529 Q592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr3:167023493 C>T maps to ENST00000307529 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr3:166960339 G>A maps to ENST00000307529 F782F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr3:167045832 G>A maps to ENST00000307529 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:166960339 G>A maps to ENST00000307529 F782F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:167031834 G>A maps to ENST00000307529 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:167023634 C>T maps to ENST00000307529 K507K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:166960381 G>A maps to ENST00000307529 F768F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:166958580 T>A maps to ENST00000307529 *840Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:167045757 C>T maps to ENST00000307529 K278K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:167051692 C>T maps to ENST00000307529 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:167077759 C>T maps to ENST00000307529 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr3:166958681 G>A maps to ENST00000307529 Q807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr3:167023634 C>T maps to ENST00000307529 K507K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:2407141 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr23:2408250 G>A did not map to a codon.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr23:2408251 G>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:2406847 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr23:2406909 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:2408598 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:2406967 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:2408526 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:2406783 G>T did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:2408223 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:2408224 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr23:2406964 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr23:2407160 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr23:2407647 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr23:2408216 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr23:2406966 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:2408287 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:2408545 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:2408223 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr3:111312496 C>T maps to NM_024508.3 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:111312973 C>T maps to NM_024508.3 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr3:111312559 C>T maps to NM_024508.3 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr3:111312559 C>T maps to NM_024508.3 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:111313021 C>T maps to NM_024508.3 E9E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr22:50278161 C>T maps to NM_014838.2 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr22:50279634 G>A maps to NM_014838.2 V775V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr22:50280696 C>T maps to NM_014838.2 V1129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr22:50277354 C>T maps to NM_014838.2 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr20:56190613 T>G maps to NM_030776.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr20:56189955 C>T maps to NM_030776.2 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr20:56186786 G>A maps to NM_030776.2 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr20:56191423 G>A maps to NM_030776.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:56179742 G>A maps to NM_030776.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr20:56191462 G>A maps to NM_030776.2 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr20:56185226 C>T maps to NM_030776.2 E357E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:56189955 C>T maps to NM_030776.2 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr14:64988362 C>T maps to NM_001123329.1 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr14:64989824 C>T maps to NM_001123329.1 R535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZG-06A-11D-A197-08 chr14:64988482 T>A maps to NM_001123329.1 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:81412129 C>T maps to NM_001105539.1 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr3:101378853 G>A maps to NM_014415.3 Q607*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-GF-A6C9-06A-11D-A30X-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr6:31867756 C>T maps to NM_181842.2 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr6:31868368 G>A maps to NM_181842.2 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr6:31868443 C>A maps to NM_181842.2 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr11:113934492 C>T maps to NM_001018011.1 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:114027097 C>T maps to NM_001018011.1 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr11:114121186 C>T maps to NM_001018011.1 S644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr11:113934822 G>A maps to NM_001018011.1 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr11:113934213 C>T maps to NM_001018011.1 H64H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr11:114112907 C>T maps to NM_001018011.1 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr11:113934558 C>T maps to NM_001018011.1 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:113934507 C>T maps to NM_001018011.1 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:113934795 G>A maps to NM_001018011.1 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26D-06A-11D-A19A-08 chr11:113934444 G>T maps to NM_001018011.1 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr1:16270309 G>A maps to ENST00000375733 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr6:151687338 C>A maps to NM_020861.1 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:151686699 A>G maps to NM_020861.1 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:151686990 G>A maps to NM_020861.1 Q404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr6:151686991 G>A maps to NM_020861.1 N403N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:151687576 G>A maps to NM_020861.1 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:151687920 G>A maps to NM_020861.1 R94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr6:151687609 G>A maps to NM_020861.1 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr3:114057947 C>T maps to NM_001164342.1 T710T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:114070717 G>A maps to NM_001164342.1 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:114069130 G>A maps to NM_001164342.1 F598F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:114069568 G>A maps to NM_001164342.1 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:114069352 G>A maps to NM_001164342.1 F524F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:114069465 G>A maps to NM_001164342.1 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:114069778 G>A maps to NM_001164342.1 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:114069373 C>G maps to NM_001164342.1 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:114058094 G>A maps to NM_001164342.1 S661S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:114070413 G>A maps to NM_001164342.1 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:33283415 G>A maps to NM_001145338.1 I426I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr6:33284381 G>A maps to NM_001145338.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:33283838 G>A maps to NM_001145338.1 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr6:33284312 G>A maps to NM_001145338.1 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr14:64954351 G>A maps to NM_006977.2 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr9:125681460 G>A maps to NM_020924.2 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr9:125681565 G>A maps to NM_020924.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr11:62520116 C>T maps to NM_024784.3 Q390Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:62520740 C>T maps to NM_024784.3 K182K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:36206301 C>T maps to NM_014383.1 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr19:36205767 G>A maps to NM_014383.1 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:119388444 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:119388969 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:119389152 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr23:119388865 T>C did not map to a codon.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr23:119389022 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:119388432 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr9:129642548 C>T maps to ENST00000319119 Q291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr9:129642868 C>T maps to ENST00000319119 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:129641833 A>G maps to ENST00000319119 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:129641744 C>T maps to ENST00000319119 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr1:173839908 G>A maps to NM_001122770.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr3:141164019 G>A maps to NM_001080412.2 Q930Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr3:141163287 C>T maps to NM_001080412.2 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:141163938 C>T maps to NM_001080412.2 F903F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr12:57397309 G>A maps to NM_014830.2 F464F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr12:57397507 G>A maps to NM_014830.2 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr12:57396571 C>T maps to NM_014830.2 P710P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr12:57396832 G>A maps to NM_014830.2 H623H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr12:57398535 G>A maps to NM_014830.2 Q56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr17:7366746 C>T maps to NM_020899.3 K518K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr17:7365456 G>A maps to NM_020899.3 L948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr17:7365774 G>A maps to NM_020899.3 S842S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr17:7366121 G>A maps to NM_020899.3 R727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr17:7366122 G>A maps to NM_020899.3 H726H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:22835216 C>T maps to NM_014870.3 F564F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:22852822 C>T maps to NM_014870.3 L1218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:22817085 C>T maps to NM_014870.3 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr1:22838355 C>T maps to NM_014870.3 D730D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr1:22837754 G>A maps to NM_014870.3 P639P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr1:22852822 C>T maps to NM_014870.3 L1218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:22852805 C>T maps to NM_014870.3 Q1213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr1:22850921 C>T maps to NM_014870.3 A1170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr1:22817076 T>C maps to NM_014870.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr1:197168952 A>G maps to NM_194314.2 C217C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr1:197159927 G>A maps to NM_194314.2 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr9:129594916 T>A maps to NM_014007.3 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:59028056 G>A maps to NM_032792.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A197-06A-32D-A197-08 chr19:59028284 C>T maps to NM_032792.2 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr19:59028742 G>A maps to NM_032792.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr20:62384101 G>A maps to NM_025224.2 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr20:62421498 C>T maps to NM_025224.2 K204K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr20:62421987 G>A maps to NM_025224.2 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr20:62421378 A>C maps to NM_025224.2 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr20:62407229 G>A maps to NM_025224.2 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr20:62407157 G>C maps to NM_025224.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr20:62421759 G>A maps to NM_025224.2 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr20:62421279 C>T maps to NM_025224.2 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:62378354 C>T maps to NM_025224.2 K566K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:42705341 C>T maps to NM_145166.3 I597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:6649217 C>T maps to NM_005341.2 V671V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:6649218 C>T maps to NM_005341.2 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr1:6640875 C>T maps to NM_005341.2 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr4:4322406 C>T maps to NM_145291.3 V554V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr9:37440576 T>A maps to NM_014872.2 K658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr19:4054984 G>A maps to NM_015898.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:154988032 C>T maps to ENST00000417934 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr1:154987921 C>T maps to ENST00000417934 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:154987937 C>T maps to ENST00000417934 Q302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr1:154987747 C>T maps to ENST00000417934 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:154987312 C>T maps to ENST00000417934 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr18:45555813 G>A maps to NM_001039360.2 F559F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr18:45555831 C>T maps to NM_001039360.2 E553E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr18:45567076 C>T maps to NM_001039360.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:45566545 C>T maps to NM_001039360.2 K311K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:45556062 C>T maps to NM_001039360.2 R476R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:45567247 G>A maps to NM_001039360.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr18:45555834 C>T maps to NM_001039360.2 E552E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr18:45566725 G>A maps to NM_001039360.2 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:45566608 C>T maps to NM_001039360.2 K290K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr18:45567100 G>A maps to NM_001039360.2 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr18:45566736 A>G maps to NM_001039360.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr18:45567247 G>A maps to NM_001039360.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr18:45566848 G>A maps to NM_001039360.2 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr18:45566761 G>A maps to NM_001039360.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:45555786 C>T maps to NM_001039360.2 R568R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:45556203 G>A maps to NM_001039360.2 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:45566347 C>T maps to NM_001039360.2 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:45567205 G>A maps to NM_001039360.2 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr18:45567094 C>T maps to NM_001039360.2 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr18:45567265 C>T maps to NM_001039360.2 Q71Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:33065968 T>C maps to NM_001040441.1 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr1:33060667 G>A maps to NM_001040441.1 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr6:33423698 C>T maps to NM_152735.3 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:33423926 G>A maps to NM_152735.3 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr6:33423953 A>G maps to NM_152735.3 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr12:56515569 C>T maps to NM_032786.1 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr12:56514648 T>C maps to NM_032786.1 D101D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr12:56515461 A>C maps to NM_032786.1 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr1:203820192 C>T maps to NM_014827.4 V705V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr1:203786248 C>A maps to NM_014827.4 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:37945971 C>T maps to NM_025079.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:64721992 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:64708987 G>C did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:64717043 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:64722767 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:64719061 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:64721965 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:64722080 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:64708955 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr23:64722320 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr23:64722945 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:64708942 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:64718907 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr23:64722307 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr11:110030083 C>T maps to NM_033390.1 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:110035849 C>T maps to NM_033390.1 F680F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr6:149795613 C>T maps to NM_207360.2 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr6:149777833 C>T maps to NM_207360.2 Q216Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr6:149773794 C>T maps to NM_207360.2 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:46543276 G>A maps to ENST00000242848 A1134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr13:46543264 G>A maps to ENST00000242848 S1138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr13:46542937 T>C maps to ENST00000242848 R1247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr13:46543899 G>A maps to ENST00000242848 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr14:89068305 A>C maps to NM_024824.4 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr14:89061144 C>T maps to NM_207662.3 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr14:89061315 A>T maps to NM_207662.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr14:89068391 C>T maps to NM_024824.4 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr16:88696902 C>T maps to ENST00000452588 D883D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr16:88643602 G>A maps to ENST00000452588 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr16:88664700 C>T maps to ENST00000452588 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr16:88643950 C>T maps to ENST00000452588 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:88695233 C>T maps to ENST00000452588 A870A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:144522250 G>A maps to NM_015117.2 P925P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr8:144621038 G>A maps to NM_015117.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr8:144550574 G>A maps to NM_015117.2 P694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr8:144621038 G>A maps to NM_015117.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:144620342 G>A maps to NM_015117.2 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr8:144620567 A>G maps to NM_015117.2 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr8:144550583 G>A maps to NM_015117.2 I691I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr19:47569966 C>T maps to NM_015168.1 K1186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr19:47570722 C>T maps to NM_015168.1 E934E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:47570506 G>A maps to NM_015168.1 P1006P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:47570287 G>A maps to NM_015168.1 D1079D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:47571033 G>A maps to NM_015168.1 R831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr19:47569894 G>A maps to NM_015168.1 T1210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:47570821 G>A maps to NM_015168.1 P901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:47569795 G>A maps to NM_015168.1 P1243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:47569951 G>A maps to NM_015168.1 V1191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:47570692 G>A maps to NM_015168.1 L944L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr19:47569795 G>A maps to NM_015168.1 P1243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:47569693 G>A maps to NM_015168.1 A1277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr19:47575046 G>A maps to NM_015168.1 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr2:113089500 C>T maps to NM_198581.2 N1002N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:113080359 C>T maps to NM_198581.2 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr16:11846619 G>A maps to NM_014153.3 S877S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr16:11859512 A>C maps to NM_014153.3 Y517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr16:11873126 C>G maps to NM_014153.3 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr16:11862318 G>A maps to NM_014153.3 F404F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr22:41738567 C>T maps to ENST00000351589 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr22:41735170 G>A maps to ENST00000351589 E280E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr22:41753381 T>C maps to ENST00000351589 G977G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr22:41742085 C>T maps to ENST00000351589 T529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr22:41747574 C>T maps to ENST00000351589 H669H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr22:41744139 C>T maps to ENST00000351589 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr22:41735041 C>T maps to ENST00000351589 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:41745270 C>T maps to ENST00000351589 I654I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr22:41742205 C>T maps to ENST00000351589 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr22:41742067 G>A maps to ENST00000351589 E523E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr22:41721579 C>T maps to ENST00000351589 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr22:41735932 C>T maps to ENST00000351589 I326I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:41735092 C>T maps to ENST00000351589 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:41735887 C>T maps to ENST00000351589 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr7:138764564 C>T maps to ENST00000464606 K374K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr7:138758703 G>A maps to ENST00000464606 S712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr7:138738766 G>A maps to ENST00000464606 F876F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:138732567 G>A maps to ENST00000464606 S949S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr7:138774395 G>A maps to ENST00000464606 Q140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:138732423 G>A maps to ENST00000464606 S997S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:138764795 G>A maps to ENST00000464606 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U9-06A-11D-A32N-08 chr7:138738781 A>C maps to ENST00000464606 A871A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr7:129662209 G>A maps to NM_016478.3 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr7:129679331 G>A maps to NM_016478.3 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr7:129658542 G>A maps to NM_016478.3 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr7:129691110 G>A maps to NM_016478.3 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr23:64141833 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:64138968 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr23:64140110 G>A did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:64139045 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:64139033 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:64141750 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr23:64138924 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr23:64139035 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:64140042 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:64138975 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:64139970 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:64141825 C>T did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:64139976 C>T did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:64140042 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:132342494 C>T maps to ENST00000509437 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr1:52902463 C>T maps to NM_001009881.2 E1375E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr1:52956468 T>C maps to NM_001009881.2 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:52941064 G>A maps to NM_001009881.2 F722F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr23:117960055 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr23:117959951 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:117960200 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:117960249 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:117959334 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr23:117960019 C>G did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:117959786 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr23:117959675 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:117960367 G>A did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:117960161 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:117960037 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:73524205 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:73524121 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:73524112 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:73524284 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:73524276 A>G did not map to a codon.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr23:73524128 G>A did not map to a codon.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr23:73524564 G>C did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr16:87453454 A>G maps to NM_015144.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:87445383 G>A maps to NM_015144.2 G844G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr16:87451257 A>C maps to NM_015144.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr16:87448143 C>T maps to NM_015144.2 E356E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr16:87445887 C>T maps to NM_015144.2 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr16:87445428 G>A maps to NM_015144.2 P829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:87445461 G>A maps to NM_015144.2 S818S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:111698022 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:111698281 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:111698522 T>C did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:111698177 C>T did not map to a codon.
Sequencing variant TCGA-EB-A5SH-06A-11D-A30X-08 chr23:111698454 C>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr23:111698716 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr23:111698679 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:111698218 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:111698245 A>T did not map to a codon.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr23:111698652 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr23:111697978 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:111698177 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:111698665 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:111697970 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:111698177 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:103359105 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr23:103358980 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr23:103358981 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:103359772 G>C did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr18:60241434 C>T maps to NM_017742.4 P707P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:60241836 C>T maps to NM_017742.4 I841I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:81192457 G>A maps to NM_153367.3 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr20:279330 G>A maps to NM_033089.6 R368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr4:25316962 C>T maps to NM_024936.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:25335044 C>T maps to NM_024936.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr4:25314460 C>T maps to NM_024936.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr4:25314442 C>T maps to NM_024936.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr4:25366776 G>A maps to NM_024936.2 K465K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr4:25366777 A>C maps to NM_024936.2 R466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr23:77913862 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:77913640 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:77912864 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:77913709 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr23:77912606 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:77913439 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:77913325 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:77913326 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:77913244 G>A did not map to a codon.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr23:77912523 G>A did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:77912665 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:77913740 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:77913209 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:77913436 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:77913355 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr23:77912604 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:77912857 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:77912860 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:77912711 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:77912767 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:77913530 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr23:77913450 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:77913700 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:77913439 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:77913818 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr23:77912993 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:77913355 G>A did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr23:77912993 G>A did not map to a codon.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr23:77913322 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr9:88916314 G>A maps to NM_024617.3 I1432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr9:88918035 G>A maps to NM_024617.3 I1353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:37126578 C>T maps to NM_032226.2 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr9:37126553 C>T maps to NM_032226.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr9:37126553 C>T maps to NM_032226.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr9:37349403 C>T maps to NM_032226.2 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr12:122964751 G>A maps to NM_017612.2 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:122958466 G>A maps to NM_017612.2 V567V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:80604377 A>G did not map to a codon.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr7:100004334 G>A maps to NM_017984.3 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:100002673 G>A maps to NM_017984.3 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr7:100002656 C>T maps to NM_017984.3 E410E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr7:100007118 C>T maps to NM_017984.3 W267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr7:100017417 C>T maps to NM_017984.3 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr7:100017405 C>T maps to NM_017984.3 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:100004370 G>A maps to NM_017984.3 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr3:28454675 G>A maps to NM_001040432.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr3:28557086 T>C maps to NM_001040432.1 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:28476732 C>T maps to NM_001040432.1 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:28476732 C>T maps to NM_001040432.1 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr3:28562495 G>A maps to NM_001040432.1 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr2:207174294 G>A maps to NM_020923.1 Q1681Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr2:207174274 C>T maps to NM_020923.1 R1675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr2:207173454 G>A maps to NM_020923.1 K1401K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr2:207173256 C>T maps to NM_020923.1 I1335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr2:207174951 C>T maps to NM_020923.1 V1900V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:207170115 C>T maps to NM_020923.1 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:207170307 C>A maps to NM_020923.1 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr2:207172737 G>A maps to NM_020923.1 L1162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr2:207175071 G>A maps to NM_020923.1 A1940A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr2:207175878 G>A maps to NM_020923.1 E2209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr2:207170214 C>T maps to NM_020923.1 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:207170235 G>A maps to NM_020923.1 K328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:207172521 G>A maps to NM_020923.1 A1090A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:207171930 G>A maps to NM_020923.1 K893K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:207173184 G>A maps to NM_020923.1 R1311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:207175677 G>A maps to NM_020923.1 K2142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr2:207171066 G>A maps to NM_020923.1 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:207161984 C>T maps to NM_020923.1 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr2:207171030 T>A maps to NM_020923.1 V593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr2:207175170 A>G maps to NM_020923.1 S1973S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr2:207174648 G>A maps to NM_020923.1 R1799R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr2:207173256 C>T maps to NM_020923.1 I1335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:207174648 G>A maps to NM_020923.1 R1799R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:207174672 C>A maps to NM_020923.1 V1807V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:207175677 G>A maps to NM_020923.1 K2142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr2:207171012 T>A maps to NM_020923.1 V587V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr16:67432186 G>A maps to NM_013304.2 H285H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr16:67432756 G>A maps to NM_013304.2 N207N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:67440213 G>A maps to NM_013304.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr5:840727 G>A maps to NM_024786.2 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:843766 G>A maps to NM_024786.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr11:19197387 C>T maps to NM_019028.2 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr6:158074586 C>G maps to NM_024630.2 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:157963676 C>T maps to NM_024630.2 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr6:158014137 C>T maps to NM_024630.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr6:158093790 C>T maps to NM_024630.2 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr6:158066849 C>T maps to NM_024630.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr6:158066792 C>T maps to NM_024630.2 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U9-06A-11D-A32N-08 chr6:158093952 G>A maps to NM_024630.2 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr23:74651288 G>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:74644605 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:74636997 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:74648913 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:74641820 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr23:74641750 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FB-06A-11D-A25O-08 chr23:74648946 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:74641767 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:74644532 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:74644534 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:74698745 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr10:99211644 G>T maps to NM_198046.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr12:77158081 G>A maps to NM_015336.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr12:77203528 A>G maps to NM_015336.2 K145K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:27177658 C>T maps to NM_032283.2 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:27177625 G>A maps to NM_032283.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr1:27175148 C>T maps to NM_032283.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr3:195938159 C>T maps to NM_001039617.1 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr8:17063205 C>A maps to NM_016353.4 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:17063271 C>T maps to NM_016353.4 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr8:17053074 G>A maps to NM_016353.4 Q105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr9:14639980 G>A maps to NM_178566.4 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr3:113677248 C>T maps to NM_173570.3 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:113672616 C>T maps to NM_173570.3 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:66307074 G>A maps to NM_207340.1 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:66311201 G>A maps to NM_207340.1 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:45000781 G>A maps to NM_016598.2 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr3:44986748 G>A maps to NM_016598.2 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr3:45000622 G>A maps to NM_016598.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr3:45000900 G>A maps to NM_016598.2 R10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:44974643 G>A maps to NM_016598.2 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:6624749 C>T maps to NM_018106.3 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr10:114190593 G>A maps to NM_022494.1 Q404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:85010781 C>A maps to NM_001145548.1 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr16:85024131 G>A maps to NM_001145548.1 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr22:20128402 G>A maps to NM_013373.3 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr22:20129010 C>T maps to NM_013373.3 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr22:20128177 C>T maps to NM_013373.3 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr22:20128178 C>T maps to NM_013373.3 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr22:20132775 C>T maps to NM_013373.3 P717P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr22:20130715 A>G maps to NM_013373.3 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr22:20128798 C>T maps to NM_013373.3 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr22:20130628 C>T maps to NM_013373.3 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:20129010 C>T maps to NM_013373.3 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:20130760 C>T maps to NM_013373.3 P536P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr23:128946753 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:128975807 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr23:128963075 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:128975786 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr10:31799742 C>T maps to NM_001174096.1 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:31749964 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:31810845 C>T maps to NM_001174096.1 I862I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:31809274 C>T maps to NM_001174096.1 Q339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:31810518 C>T maps to NM_001174096.1 I753I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:31816044 G>A maps to NM_001174096.1 E1077E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr10:31809945 C>T maps to NM_001174096.1 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr10:31810668 C>T maps to NM_001174096.1 I803I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr10:31810668 C>T maps to NM_001174096.1 I803I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:31815837 G>A maps to NM_001174096.1 S1008S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr10:31810767 G>A maps to NM_001174096.1 T836T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:31750137 G>A maps to NM_001174096.1 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:31810842 G>A maps to NM_001174096.1 V861V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr10:31809255 G>A maps to NM_001174096.1 K332K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:31812997 C>T maps to NM_001174096.1 F914F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr10:31809559 C>T maps to NM_001174096.1 Q434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C1-06A-12D-A196-08 chr2:145161623 G>A maps to NM_014795.3 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr2:145158835 G>A maps to NM_014795.3 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:145158811 G>A maps to NM_014795.3 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:145147182 G>A maps to NM_014795.3 F1160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr2:145157132 G>A maps to NM_014795.3 Q541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr9:131515759 G>A maps to NM_006336.2 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:131513065 C>A maps to NM_006336.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:131515788 A>G maps to NM_006336.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:1195109 G>A maps to ENST00000401903 H87H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr6:38029438 C>T maps to NM_021943.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:38029438 C>T maps to NM_021943.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr15:80429861 C>T maps to NM_019006.2 H173H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:80429957 C>T maps to NM_019006.2 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr8:135649737 G>A maps to NM_020863.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr8:135614395 C>T maps to NM_020863.3 E522E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr8:135614560 G>A maps to NM_020863.3 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr8:135614002 G>A maps to NM_020863.3 P653P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:135545107 C>T maps to NM_020863.3 G1028G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr8:135614508 G>A maps to NM_020863.3 Q485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:135649737 G>A maps to NM_020863.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:135614440 G>A maps to NM_020863.3 I507I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr8:135649737 G>A maps to NM_020863.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:135614508 G>A maps to NM_020863.3 Q485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr8:135600606 G>A maps to NM_020863.3 L865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr8:135649715 C>A maps to NM_020863.3 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:135613909 G>A maps to NM_020863.3 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr8:135490919 C>T maps to NM_020863.3 Q1179Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:135649737 G>A maps to NM_020863.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr12:72032284 T>C maps to NM_144982.4 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr12:72057129 T>C maps to NM_144982.4 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:72050881 G>A maps to NM_144982.4 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr12:72024625 T>A maps to NM_144982.4 T1193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:72036312 G>A maps to NM_144982.4 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:72028044 C>T maps to NM_144982.4 K800K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:72057146 G>A maps to NM_144982.4 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr16:72829864 C>T maps to NM_006885.3 W2239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr16:72991842 G>A maps to NM_006885.3 S734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:72829320 A>G maps to NM_006885.3 N2420N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr16:72992930 G>A maps to NM_006885.3 R372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:72993162 G>A maps to NM_006885.3 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr16:72991911 G>A maps to NM_006885.3 P711P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:72993057 G>A maps to NM_006885.3 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:72829896 G>A maps to NM_006885.3 P2228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:72830484 C>T maps to NM_006885.3 L2032L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:72992846 G>A maps to NM_006885.3 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:72821662 G>A maps to NM_006885.3 V3504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr16:72827742 C>T maps to NM_006885.3 Q2946Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:72993645 G>A maps to NM_006885.3 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr16:72822403 G>A maps to NM_006885.3 P3257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:72829476 G>A maps to NM_006885.3 S2368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:72993645 G>A maps to NM_006885.3 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:72827202 G>A maps to NM_006885.3 L3126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:72829101 G>A maps to NM_006885.3 P2493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr16:72827190 G>A maps to NM_006885.3 N3130N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:72829797 G>A maps to NM_006885.3 F2261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:72830292 G>A maps to NM_006885.3 I2096I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr16:72821893 G>A maps to NM_006885.3 T3427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr16:72821200 G>A maps to NM_006885.3 D3658D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr16:72923657 G>A maps to NM_006885.3 T1140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr16:72830829 C>T maps to NM_006885.3 E1917E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:72993642 G>A maps to NM_006885.3 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:72993645 G>A maps to NM_006885.3 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:72827913 C>T maps to NM_006885.3 R2889R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:72828489 C>T maps to NM_006885.3 R2697R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr8:77767757 T>A maps to NM_024721.4 S2867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr8:77766896 G>A maps to NM_024721.4 R2580R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:77763548 C>T maps to NM_024721.4 P1464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr8:77767139 G>A maps to NM_024721.4 R2661R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr8:77765555 G>A maps to NM_024721.4 R2133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr8:77617117 C>T maps to NM_024721.4 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:77765585 C>T maps to NM_024721.4 I2143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr8:77766842 G>A maps to NM_024721.4 Q2562Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr8:77767502 G>A maps to NM_024721.4 E2782E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:77616913 C>T maps to NM_024721.4 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:77767953 C>T maps to NM_024721.4 R2933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:77776233 C>T maps to NM_024721.4 F3428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:77617117 C>T maps to NM_024721.4 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:77617513 G>A maps to NM_024721.4 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:77763206 G>A maps to NM_024721.4 P1350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr8:77616955 C>T maps to NM_024721.4 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr8:77616556 G>A maps to NM_024721.4 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr8:77766065 G>A maps to NM_024721.4 R2303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr8:77763758 C>T maps to NM_024721.4 F1534F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:77616715 C>T maps to NM_024721.4 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:77766989 G>A maps to NM_024721.4 T2611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr8:77766740 C>T maps to NM_024721.4 F2528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:77763758 C>T maps to NM_024721.4 F1534F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:77776536 C>T maps to NM_024721.4 I3529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr8:77768291 G>A maps to NM_024721.4 R3045R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr8:77768198 G>A maps to NM_024721.4 V3014V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:77761884 C>T maps to NM_024721.4 L1261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr8:77764004 C>T maps to NM_024721.4 L1616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr8:77767502 G>A maps to NM_024721.4 E2782E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr8:77776233 C>T maps to NM_024721.4 F3428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:77766119 C>T maps to NM_024721.4 F2321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:77690487 T>A maps to NM_024721.4 Y1046*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr8:77764724 G>A maps to NM_024721.4 K1856K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:77766602 C>T maps to NM_024721.4 L2482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:77616857 C>T maps to NM_024721.4 Q179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:77616715 C>T maps to NM_024721.4 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:77765849 G>A maps to NM_024721.4 T2231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr8:77767766 C>T maps to NM_024721.4 S2870S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr8:77767727 G>A maps to NM_024721.4 T2857T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr8:77775474 C>T maps to NM_024721.4 S3175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr8:77619889 G>A maps to NM_024721.4 A900A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr8:77765585 C>T maps to NM_024721.4 I2143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr8:77617252 G>A maps to NM_024721.4 Q310Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr8:77618161 C>T maps to NM_024721.4 I613I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr8:77766794 G>A maps to NM_024721.4 L2546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr8:77776233 C>T maps to NM_024721.4 F3428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:77764946 G>A maps to NM_024721.4 K1930K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr8:77765792 C>T maps to NM_024721.4 P2212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr8:77618669 C>T maps to NM_024721.4 R783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr8:77618317 G>A maps to NM_024721.4 E665E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr8:77768483 C>T maps to NM_024721.4 L3109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr8:77764221 C>T maps to NM_024721.4 Q1689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr8:77616448 G>A maps to NM_024721.4 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:77618197 G>A maps to NM_024721.4 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:77619946 C>T maps to NM_024721.4 A919A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:77762533 C>T maps to NM_024721.4 A1300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:77764841 C>T maps to NM_024721.4 I1895I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:77766119 C>T maps to NM_024721.4 F2321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:77766836 C>T maps to NM_024721.4 P2560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:77767331 G>A maps to NM_024721.4 Q2725Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:77768151 C>T maps to NM_024721.4 Q2999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr8:77764748 G>A maps to NM_024721.4 K1864K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr8:77775546 G>A maps to NM_024721.4 V3199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr8:77765900 C>T maps to NM_024721.4 N2248N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr8:77776233 C>T maps to NM_024721.4 F3428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:75203604 C>T maps to NM_153688.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr15:42743289 T>A maps to NM_022473.1 K371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr15:42742290 G>A maps to NM_022473.1 Q704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr15:42717187 G>A maps to NM_022473.1 G1655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr15:42743512 A>C maps to NM_022473.1 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr15:42742954 G>A maps to NM_022473.1 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr15:42743007 G>A maps to NM_022473.1 Q465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr15:42744096 G>A maps to NM_022473.1 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr15:42743104 G>A maps to NM_022473.1 C432C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:44833295 G>A maps to ENST00000412927 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19O-06A-11D-A197-08 chr19:44834030 G>A maps to ENST00000412927 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:36853082 G>A maps to NM_020917.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F4-06A-12D-A25O-08 chr19:36832162 G>A maps to NM_020917.2 Q189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr19:36831764 G>A maps to NM_020917.2 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr18:5291480 A>G maps to NM_003409.3 N242N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr18:5292011 G>A maps to NM_003409.3 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr5:178358835 T>C maps to NM_030613.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr5:178358889 C>A maps to NM_030613.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr5:178359120 C>T maps to NM_030613.2 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr5:178358895 C>T maps to NM_030613.2 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:57065935 C>T maps to NM_020828.1 C594C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:57066539 C>T maps to NM_020828.1 Q796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr19:57060390 A>G maps to NM_020828.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr19:57065548 A>G maps to NM_020828.1 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:57059203 C>T maps to NM_020828.1 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr19:57065332 T>C maps to NM_020828.1 H393H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:57051082 C>T maps to NM_020828.1 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:57065578 C>T maps to NM_020828.1 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr17:4995974 C>T maps to NM_153018.2 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr17:4995530 G>A maps to NM_153018.2 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr17:4995164 C>T maps to NM_153018.2 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr17:4995165 C>T maps to NM_153018.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr17:4995743 G>A maps to NM_153018.2 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:4995351 C>T maps to NM_153018.2 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr19:38127132 C>T maps to NM_014898.2 W103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr19:38126523 G>A maps to NM_014898.2 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr14:69256855 G>A maps to NM_004926.2 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr14:69257038 G>A maps to NM_004926.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:69256435 G>A maps to NM_004926.2 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr2:43451459 A>T maps to NM_006887.4 *495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr9:115805765 C>A maps to NM_003408.1 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr9:115805517 G>T maps to NM_003408.1 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr9:115806072 G>C maps to NM_003408.1 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr8:144332303 G>A maps to NM_173832.3 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr8:144332162 C>T maps to NM_173832.3 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr8:144332412 C>T maps to NM_173832.3 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:144332510 C>T maps to NM_173832.3 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr8:144332051 C>T maps to NM_173832.3 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr8:144332570 C>T maps to NM_173832.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:144332486 C>T maps to NM_173832.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:144332486 C>T maps to NM_173832.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr4:188924629 G>A maps to NM_174900.3 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr4:188924722 G>A maps to NM_174900.3 K254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr4:188924785 C>T maps to NM_174900.3 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr4:188924848 C>T maps to NM_174900.3 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr4:188924638 C>T maps to NM_174900.3 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr4:188924668 C>T maps to NM_174900.3 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:188924638 C>T maps to NM_174900.3 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr4:188924638 C>T maps to NM_174900.3 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr4:188924155 G>A maps to NM_174900.3 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr4:188924785 C>T maps to NM_174900.3 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr4:188924149 C>T maps to NM_174900.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZU-06A-12D-A196-08 chr4:188924149 C>T maps to NM_174900.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr4:188924560 G>A maps to NM_174900.3 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:188924293 C>T maps to NM_174900.3 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:188924638 C>T maps to NM_174900.3 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:188924798 C>T maps to NM_174900.3 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr4:188924866 G>A maps to NM_174900.3 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr6:29640507 C>T maps to NM_001109809.2 R460R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr6:29640456 C>T maps to NM_001109809.2 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:29640906 G>A maps to NM_001109809.2 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29W-06A-11D-A196-08 chr6:29643800 G>A maps to NM_001109809.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr6:29641431 G>A maps to NM_001109809.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:29640525 G>A maps to NM_001109809.2 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:29641170 G>A maps to NM_001109809.2 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:29640420 G>A maps to NM_001109809.2 V489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:29641335 G>A maps to NM_001109809.2 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:29640974 G>A maps to NM_001109809.2 Q305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr20:50701677 G>A maps to NM_199427.2 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:50769920 G>A maps to NM_018197.2 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr20:50701143 G>A maps to NM_199427.2 V630V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr20:50769308 G>A maps to NM_018197.2 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr20:50769632 G>A maps to NM_018197.2 C366C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:50768816 G>A maps to NM_018197.2 I638I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr20:50701608 C>T maps to NM_199427.2 Q475Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr20:50701140 G>A maps to NM_199427.2 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr20:50769428 G>A maps to NM_018197.2 F434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:50776818 G>A maps to NM_018197.2 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:50701518 G>A maps to NM_199427.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr19:36884605 G>A maps to NM_133466.2 H212H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr19:36883942 T>G maps to NM_133466.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:36884176 G>A maps to NM_133466.2 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr19:36883765 G>A maps to NM_133466.2 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr16:68597631 C>T maps to NM_133458.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr16:68598372 C>T maps to NM_133458.2 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:58380310 C>T maps to NM_053023.4 Q329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr11:64854055 C>T maps to NM_006782.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr11:64854469 C>T maps to NM_006782.3 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr11:64853933 C>A maps to NM_006782.3 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr11:64854199 G>A maps to NM_006782.3 E139E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr8:106813371 G>C maps to NM_012082.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr8:106815699 C>T maps to NM_012082.3 N1130N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr8:106814061 C>T maps to NM_012082.3 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr8:106811100 C>T maps to NM_012082.3 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr8:106815087 C>T maps to NM_012082.3 S926S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr8:106813479 A>G maps to NM_012082.3 K390K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr8:106646526 G>A maps to NM_012082.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr8:106814061 C>T maps to NM_012082.3 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:106813293 C>T maps to NM_012082.3 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:106814319 G>A maps to NM_012082.3 V670V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:106815543 G>A maps to NM_012082.3 W1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:106814466 G>A maps to NM_012082.3 K719K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr8:106811100 C>T maps to NM_012082.3 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr8:106813866 G>A maps to NM_012082.3 K519K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr8:106814922 C>T maps to NM_012082.3 A871A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr8:106815486 G>A maps to NM_012082.3 Q1059Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr8:106815663 G>A maps to NM_012082.3 G1118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr8:106813461 C>T maps to NM_012082.3 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr8:106814721 G>A maps to NM_012082.3 T804T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr8:106813399 C>T maps to NM_012082.3 R364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:106814061 C>T maps to NM_012082.3 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr8:106815663 G>A maps to NM_012082.3 G1118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr8:106811111 C>T maps to NM_012082.3 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr8:106813293 C>T maps to NM_012082.3 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:106814319 G>A maps to NM_012082.3 V670V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr8:106810991 G>A maps to NM_012082.3 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr8:106815663 G>A maps to NM_012082.3 G1118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:106431438 C>T maps to NM_012082.3 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:106813461 C>T maps to NM_012082.3 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:106813467 C>T maps to NM_012082.3 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr8:106813830 C>T maps to NM_012082.3 I507I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr8:106813584 G>A maps to NM_012082.3 K425K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr8:106815453 G>A maps to NM_012082.3 L1048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:32417813 A>G maps to NM_016107.3 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr5:32400222 A>C maps to NM_016107.3 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr5:32415290 G>A maps to NM_016107.3 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr5:32387753 G>A maps to NM_016107.3 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:32415221 G>A maps to NM_016107.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:3813863 T>A maps to NM_015174.1 I732I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:3823357 C>A maps to NM_015174.1 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr19:3834899 C>T maps to NM_015174.1 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr19:3821399 C>T maps to NM_015174.1 R523R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:3827612 C>T maps to NM_015174.1 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:3823360 C>T maps to NM_015174.1 W418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr23:24229352 T>G did not map to a codon.
Sequencing variant TCGA-EE-A17Z-06A-11D-A196-08 chr23:24229386 C>G did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:24228473 A>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:24229002 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:24229454 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr23:24228974 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:24227092 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:24229280 A>T did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:24197772 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr23:24229335 A>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:24226483 T>C did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:24229430 C>T did not map to a codon.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr23:24228974 C>T did not map to a codon.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr23:24229437 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr24:2847287 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr24:2847344 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr14:73490958 C>T maps to NM_021260.2 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A6L9-06A-11D-A32N-08 chr14:73464798 C>T maps to NM_021260.2 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr14:73464861 C>T maps to NM_021260.2 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:73490865 A>C maps to NM_021260.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr14:73490735 G>A maps to NM_021260.2 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr5:79747352 C>T maps to NM_014733.3 L1144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr5:79744197 G>A maps to NM_014733.3 L1026L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:79730010 C>T maps to NM_014733.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:79768610 C>A maps to NM_014733.3 T1352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:15116338 G>A maps to NM_022340.2 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr3:15126323 G>A maps to NM_022340.2 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:15124053 G>A maps to NM_022340.2 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr3:15115942 G>A maps to NM_022340.2 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr3:15115606 G>A maps to NM_022340.2 F679F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr14:68250148 G>A maps to NM_015346.3 S1240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr14:68251079 G>A maps to NM_015346.3 L1199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr14:68250147 G>T maps to NM_015346.3 R1241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr14:68242763 G>A maps to NM_015346.3 P1678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr14:68250124 G>A maps to NM_015346.3 S1248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr14:68248108 G>A maps to NM_015346.3 Q1504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr14:68221862 G>A maps to NM_015346.3 D2297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr14:68274241 G>A maps to NM_015346.3 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:68244847 G>A maps to NM_015346.3 L1598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:68250148 G>A maps to NM_015346.3 S1240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr14:68264869 G>A maps to NM_015346.3 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:99517445 C>T maps to NM_001002261.3 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:99512937 C>T maps to NM_001002261.3 F352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr4:2306446 G>A maps to NM_020972.2 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr4:2275813 G>A maps to NM_020972.2 I727I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr4:2307181 G>A maps to NM_020972.2 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr4:2306677 G>A maps to NM_020972.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr4:2355695 C>T maps to NM_020972.2 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr4:2321949 C>T maps to NM_020972.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr4:2274993 C>T maps to NM_020972.2 T743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:2306248 G>A maps to NM_020972.2 A606A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:52759345 C>T maps to NM_004799.2 R1083*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:52732462 G>C maps to NM_004799.2 V805V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr16:2880725 C>T maps to NM_145252.2 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr16:2881919 C>T maps to NM_145252.2 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr16:2881911 C>T maps to NM_145252.2 Q127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:2882007 C>T maps to NM_145252.2 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:2881805 G>A maps to NM_145252.2 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr16:2882096 G>A maps to NM_145252.2 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:10416139 G>A maps to NM_001103167.1 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr19:10418985 C>T maps to NM_001103167.1 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:10418886 G>A maps to NM_001103167.1 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:10418877 C>T maps to NM_001103167.1 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:10419189 G>A maps to NM_001103167.1 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:62367162 G>A maps to NM_032527.4 E496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr20:62339958 C>T maps to NM_032527.4 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:62366599 C>T maps to NM_032527.4 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:62364576 C>T maps to NM_032527.4 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr8:124268123 G>A maps to NM_007222.3 D21D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr8:124267361 C>T maps to NM_007222.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr8:124267421 T>A maps to NM_007222.3 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr8:124267424 T>A maps to NM_007222.3 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr8:123964127 C>T maps to NM_014943.3 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:123963830 A>G maps to NM_014943.3 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr8:123964577 G>A maps to NM_014943.3 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr8:123964610 G>A maps to NM_014943.3 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:123965045 G>A maps to NM_014943.3 K432K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:123965553 C>T maps to NM_014943.3 Q602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:123965210 C>T maps to NM_014943.3 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:123963869 T>C maps to NM_014943.3 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr8:123965270 C>T maps to NM_014943.3 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr8:123965414 C>T maps to NM_014943.3 T555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr20:39832650 G>A maps to NM_015035.3 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr20:39833196 G>A maps to NM_015035.3 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr20:39832377 G>A maps to NM_015035.3 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr20:39831810 G>A maps to NM_015035.3 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr20:39831444 A>C maps to NM_015035.3 G704G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr3:147128381 G>A maps to NM_003412.3 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr3:147130317 C>T maps to NM_003412.3 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr3:147128810 C>T maps to NM_003412.3 C304C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr13:100634890 G>A maps to NM_007129.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr13:100635373 C>T maps to NM_007129.2 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr13:100637611 C>T maps to NM_007129.2 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr23:136649460 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:136649780 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:136649895 A>G did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:136649795 G>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:136649319 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr3:147113819 G>A maps to NM_001168379.1 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:147113687 C>T maps to NM_001168379.1 K251K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr19:58101700 G>A maps to NM_001010879.2 K174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:58101379 T>C maps to NM_001010879.2 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:57286150 G>A maps to NM_001146326.1 Q497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:57286595 C>T maps to NM_001146326.1 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr19:57301314 G>A maps to NM_001146326.1 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:57286271 C>T maps to NM_001146326.1 R456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:57286130 G>A maps to NM_001146326.1 F503F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:57286720 G>A maps to NM_001146326.1 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:57286742 C>T maps to NM_001146326.1 K299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:57290805 G>A maps to NM_001146326.1 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:57293411 G>A maps to NM_001146326.1 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr19:57646627 C>T maps to NM_052882.1 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:57648247 G>A maps to NM_052882.1 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:57649927 G>A maps to NM_052882.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:57646552 G>A maps to NM_052882.1 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:57646986 G>A maps to NM_052882.1 Q240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr19:57646453 C>T maps to NM_052882.1 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:57646504 G>A maps to NM_052882.1 F400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:57646756 G>A maps to NM_052882.1 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:57646786 G>A maps to NM_052882.1 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:57648288 T>A maps to NM_052882.1 K65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr19:57647170 T>C maps to NM_052882.1 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:57649930 G>A maps to NM_052882.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr19:57647092 G>A maps to NM_052882.1 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:57646681 C>T maps to NM_052882.1 E341E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr7:99627571 C>T maps to NM_003439.1 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr16:25268073 T>C maps to NM_001012981.4 K125K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:25251333 G>A maps to NM_001012981.4 R903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr16:25251874 C>T maps to NM_001012981.4 Q722Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr16:25258412 G>A maps to NM_001012981.4 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:25258336 G>A maps to NM_001012981.4 R394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:25258226 G>A maps to NM_001012981.4 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:25251333 G>A maps to NM_001012981.4 R903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr16:25258262 G>A maps to NM_001012981.4 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:25251823 C>T maps to NM_001012981.4 Q739Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr6:28333992 C>T maps to NM_024493.2 G516G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr6:28327542 C>T maps to NM_024493.2 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr6:28333680 C>T maps to NM_024493.2 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr6:28327563 C>T maps to NM_024493.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:28333368 C>T maps to NM_024493.2 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr6:28213460 G>A maps to NM_019110.3 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr6:28213226 A>G maps to NM_019110.3 N435N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr6:28217579 G>A maps to NM_019110.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr7:99129799 C>T maps to NM_014569.3 L816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr7:99129031 G>A maps to NM_014569.3 Q560Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:99123979 C>T maps to NM_014569.3 F439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr7:99117480 C>T maps to NM_014569.3 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:99124000 C>T maps to NM_014569.3 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr7:99123973 G>A maps to NM_014569.3 K437K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr23:101138612 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:101138891 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:101139699 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:101159206 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr23:101139486 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:101141651 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr23:101153002 C>G did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:101139512 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr23:101152858 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr23:101139524 T>G did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr8:40532384 G>A maps to NM_024645.2 Q139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr8:40625171 G>A maps to NM_024645.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:40554829 G>A maps to NM_024645.2 Q95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr8:40554829 G>A maps to NM_024645.2 Q95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr10:81060554 C>T maps to NM_020338.3 P625P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:81060672 C>T maps to NM_020338.3 Q665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr10:81061874 C>T maps to NM_020338.3 F677F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:81051953 C>T maps to NM_020338.3 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr10:81070874 C>A maps to NM_020338.3 P1010P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:81050843 C>T maps to NM_020338.3 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:81053202 C>T maps to NM_020338.3 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr7:44805829 C>T maps to NM_031449.3 T770T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:44805790 C>T maps to NM_031449.3 F757F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:44801180 C>T maps to NM_031449.3 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:44806153 C>T maps to NM_031449.3 G849G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr7:44797514 C>G maps to NM_031449.3 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr7:44806174 G>A maps to NM_031449.3 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr7:44805844 C>T maps to NM_031449.3 T775T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr7:44805811 C>T maps to NM_031449.3 T764T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:44795865 C>T maps to NM_031449.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr7:44801500 C>T maps to NM_031449.3 C531C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:44800028 C>T maps to NM_031449.3 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:44804026 C>T maps to NM_031449.3 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:40726602 G>A maps to NM_005857.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr1:35580023 C>T maps to NM_024772.3 L865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:35580521 C>T maps to NM_024772.3 R1031*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:35563144 A>C maps to NM_024772.3 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr23:70470391 C>A did not map to a codon.
Sequencing variant TCGA-D9-A149-06A-11D-A196-08 chr23:70469395 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr23:70464711 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:70466337 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:70468054 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:70465568 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr23:70468048 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr23:70467679 C>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:70466456 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:70472695 G>A did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:70472588 G>A did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:70472589 G>A did not map to a codon.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr23:70472881 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:35864597 C>T maps to NM_005095.2 F1129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr1:35873738 C>T maps to NM_005095.2 Y1309Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:35884162 C>T maps to NM_005095.2 L1477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:35881163 C>T maps to NM_005095.2 F1386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr1:35852765 C>T maps to NM_005095.2 Q667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:35881160 C>T maps to NM_005095.2 F1385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr1:35870709 G>A maps to NM_005095.2 L1205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr13:20411945 C>T maps to NM_001142684.1 K296K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr1:35452992 G>A maps to NM_007167.3 F1230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr1:35477574 G>A maps to NM_007167.3 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:35477492 G>A maps to NM_007167.3 Q354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:35452992 G>A maps to NM_007167.3 F1230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:35476562 C>T maps to NM_007167.3 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:35453184 G>A maps to NM_007167.3 F1166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:50380625 C>T maps to NM_015896.2 K174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr1:42905607 G>A maps to NM_032257.4 H171H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:42905640 G>A maps to NM_032257.4 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr17:4646700 C>T maps to NM_001136046.1 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr17:4646596 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr17:4648002 G>A maps to NM_001136046.1 R589R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr17:4646616 C>T maps to NM_001136046.1 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr17:4648216 G>A maps to NM_001136046.1 R630R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:4643875 C>T maps to NM_001136046.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr17:4644106 C>T maps to NM_001136046.1 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:4645011 G>A maps to NM_001136046.1 W243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr17:4646596 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:4649112 G>A did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr17:4647080 C>T maps to NM_001136046.1 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr10:75187945 G>A maps to NM_001024593.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:75187440 G>A maps to NM_001024593.1 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:75186373 G>A maps to NM_001024593.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:75187482 G>A maps to NM_001024593.1 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr10:75185683 C>T maps to NM_001024593.1 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:75184445 G>A maps to NM_001024593.1 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr10:75185908 G>A maps to NM_001024593.1 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr9:140477020 G>A maps to NM_138462.2 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr9:140477021 G>A maps to NM_138462.2 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr20:45853042 C>T maps to ENST00000471951 W1062*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr20:45850066 G>A maps to ENST00000471951 S1106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr20:45850048 C>T maps to ENST00000471951 S1112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr20:45916028 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:45878180 G>A maps to ENST00000471951 R543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr20:45853153 G>A maps to ENST00000471951 I1025I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr20:45867748 G>A maps to ENST00000471951 T807T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr12:133732653 C>T maps to NM_015394.4 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr12:133732821 C>T maps to NM_015394.4 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr19:21909496 G>A maps to NM_173531.3 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:21909538 G>A maps to NM_173531.3 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:21910165 G>A maps to NM_173531.3 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr19:19788776 C>T maps to NM_033204.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr19:19790499 C>T maps to NM_033204.2 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr7:64168625 C>T maps to NM_016220.3 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr7:64169006 C>T maps to NM_016220.3 P775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr7:64168502 C>T maps to NM_016220.3 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:64152333 C>T maps to NM_016220.3 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr19:48785632 G>C maps to NM_153608.1 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr7:64439186 G>A maps to NM_015852.3 C254C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr7:6731971 G>A maps to ENST00000330442 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr7:6730688 T>A maps to ENST00000330442 S685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr7:6730592 G>A maps to ENST00000330442 P717P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A1A1-06A-11D-A197-08 chr7:6737361 A>G maps to ENST00000330442 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9677161 G>A maps to NM_001008727.2 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:247320140 G>A maps to NM_003431.2 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr19:58945208 C>T maps to NM_003433.3 W534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:58945163 C>T maps to NM_003433.3 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:58945976 G>A maps to NM_003433.3 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr20:18296037 C>T maps to ENST00000401790 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:58578607 G>A maps to NM_007134.1 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr19:58578649 G>A maps to NM_007134.1 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr19:58579099 G>A maps to NM_007134.1 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:58579462 C>T maps to NM_007134.1 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr19:58578658 C>T maps to NM_007134.1 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:58579609 C>T maps to NM_007134.1 S610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr19:58579312 C>T maps to NM_007134.1 I511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr19:58578216 G>A maps to NM_007134.1 W146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr19:58579603 G>A maps to NM_007134.1 G608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:58579075 G>A maps to NM_007134.1 K432K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:58578376 C>T maps to NM_007134.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr19:58578847 G>A maps to NM_007134.1 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr19:12297720 C>T maps to NM_003437.3 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:12298479 C>T maps to NM_003437.3 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:12298666 C>T maps to NM_003437.3 R492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr7:64292120 C>T maps to ENST00000307355 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr19:19822282 G>A maps to NM_021030.2 R603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:19822874 G>A maps to NM_021030.2 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:19822583 G>A maps to NM_021030.2 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19822198 G>A maps to NM_021030.2 R631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19822366 G>A maps to NM_021030.2 R575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:19822385 G>A maps to NM_021030.2 F568F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:19822450 G>A maps to NM_021030.2 R547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr2:219510928 G>A maps to NM_001105537.1 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr2:219513366 G>A maps to NM_001105537.1 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr2:219508130 G>A maps to NM_001105537.1 S1036S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr2:219508457 T>A maps to NM_001105537.1 P927P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr2:219508925 G>A maps to NM_001105537.1 S771S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr2:219508925 G>A maps to NM_001105537.1 S771S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr2:219507866 G>A maps to NM_001105537.1 I1124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr2:219507637 G>A maps to NM_001105537.1 Q1201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr2:219507626 G>A maps to NM_001105537.1 F1204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr11:9537776 C>T maps to NM_003442.5 A518A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr11:9522698 C>T maps to NM_003442.5 I343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr11:9537806 G>A maps to NM_003442.5 Q528Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:9517923 A>G maps to NM_003442.5 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr11:9494242 T>C maps to NM_003442.5 N44N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr11:9530247 C>T maps to NM_003442.5 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:36727854 C>A maps to NM_007145.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr3:124998088 G>A maps to NM_021964.2 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:124952123 G>A maps to NM_021964.2 N482N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:124951259 G>A maps to NM_021964.2 P770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:124998088 G>A maps to NM_021964.2 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:58213272 C>T maps to NM_001085384.1 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:44500380 C>T maps to NM_003445.2 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr19:44501511 C>T maps to NM_003445.2 D501D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:47272936 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr23:47269688 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr23:47271914 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr23:47272120 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:47272112 G>A did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:47272783 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:47272814 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:47272620 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr23:47269704 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:47272289 C>T did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr8:146156456 G>A maps to NM_006958.2 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:146157161 G>A maps to NM_006958.2 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr8:146156158 A>G maps to NM_006958.2 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr8:146171580 G>A maps to NM_006958.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:146156153 G>A maps to NM_006958.2 I673I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr8:146156842 G>A maps to NM_006958.2 Q444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:53577485 A>G maps to NM_001102603.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr19:53571745 G>A maps to NM_001102603.1 Q681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:53571902 C>T maps to NM_001102603.1 K628K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr19:53572367 G>A maps to NM_001102603.1 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr19:53572826 C>T maps to NM_001102603.1 K320K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr6:28056992 T>C maps to NM_003447.3 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr6:28056770 G>A maps to NM_003447.3 K327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr6:28053999 T>C maps to NM_003447.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr3:44612221 C>T maps to NM_018651.2 D540D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr3:44598664 C>T maps to NM_018651.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:44612309 C>T maps to NM_018651.2 Q570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr9:97062697 G>A maps to NM_194320.2 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr9:97062187 C>T maps to NM_194320.2 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42K-06A-11D-A24R-08 chr9:97062124 T>C maps to NM_194320.2 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:57932644 C>T maps to NM_006959.2 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr16:3454461 G>T maps to NM_003450.2 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr16:3454463 G>A maps to NM_003450.2 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:3454457 C>T maps to NM_003450.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:52091389 C>T maps to NM_007147.2 F602F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:9491816 C>T maps to NM_001172651.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:9492218 C>T maps to NM_001172651.1 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:9491885 C>T maps to NM_001172651.1 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr17:11886656 T>G maps to NM_144680.2 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr17:11881675 G>A maps to NM_144680.2 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr17:11895894 G>A maps to NM_144680.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:11881711 G>A maps to NM_144680.2 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:11881771 G>A maps to NM_144680.2 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr19:44981859 G>A maps to NM_013256.3 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr19:44981503 G>A maps to NM_013256.3 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:44981194 G>A maps to NM_013256.3 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:44981614 G>A maps to NM_013256.3 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:47836084 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr23:47837100 T>C did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr23:47842374 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:47836031 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:47836835 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:47842374 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:47837014 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr23:47836114 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr23:47835804 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:47836429 T>G did not map to a codon.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr6:27419240 G>A maps to NM_007149.2 N699N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr6:27420653 C>T maps to NM_007149.2 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr6:27419891 G>A maps to NM_007149.2 A482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr6:27424694 G>A maps to NM_007149.2 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:152128331 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr23:152100263 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr23:152100264 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:152085688 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr23:152100319 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr23:152128321 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr9:104170613 T>C maps to NM_003452.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr9:104170391 C>T maps to NM_003452.2 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr9:104170391 C>T maps to NM_003452.2 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr9:104171025 C>T maps to NM_003452.2 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:71510035 G>A maps to NM_006961.3 H138H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr16:71509171 G>T maps to NM_006961.3 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr6:28119711 C>T maps to NM_006298.2 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:28119654 C>T maps to NM_006298.2 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:28121692 C>T maps to NM_006298.2 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr11:3381178 G>A maps to NM_001130520.1 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr11:3381133 G>A maps to NM_001130520.1 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:3381463 G>A maps to NM_001130520.1 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr11:3380509 T>C maps to NM_001130520.1 K576K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr11:3380422 G>A maps to NM_001130520.1 P605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr3:44684904 C>T maps to NM_006991.3 P761P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr3:44684196 C>T maps to NM_006991.3 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr3:44684451 T>C maps to NM_006991.3 I610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:44673610 G>T maps to NM_006991.3 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:44684448 C>T maps to NM_006991.3 F609F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:95847388 C>T maps to ENST00000453539 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:95847019 C>T maps to ENST00000453539 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:95847395 C>A maps to ENST00000453539 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:95845935 C>T maps to ENST00000453539 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:95847019 C>T maps to ENST00000453539 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:95847142 C>T maps to ENST00000453539 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:95847289 C>T maps to ENST00000453539 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:12243695 G>A maps to NM_021143.2 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr16:3274587 A>C maps to NM_198088.2 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr16:3273905 G>T maps to NM_198088.2 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:3274128 G>A maps to NM_198088.2 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:3274281 G>A maps to NM_198088.2 Y266Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr16:3274320 A>C maps to NM_198088.2 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:123600425 G>A maps to NM_003455.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr11:123597628 A>C maps to NM_003455.2 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:123596827 G>A maps to NM_003455.2 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr16:3165540 G>A maps to NM_001042428.1 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:3165420 G>A maps to NM_001042428.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:3170013 C>T maps to NM_001042428.1 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:3170235 C>T maps to NM_001042428.1 I525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr16:3168904 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr16:3169263 C>T maps to NM_001042428.1 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:3166462 C>T maps to NM_001042428.1 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr16:3169791 C>T maps to NM_001042428.1 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr17:30687932 T>C maps to ENST00000394679 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr17:30694882 C>T maps to ENST00000394679 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr17:30696709 C>T maps to ENST00000394679 Q476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:22154823 T>C maps to NM_007153.3 E1004E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr19:22156452 G>A maps to NM_007153.3 G461G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr19:22171660 C>T maps to NM_007153.3 W18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:22156926 A>G maps to NM_007153.3 H303H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr19:22155342 C>T maps to NM_007153.3 K831K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:22170021 G>A maps to NM_007153.3 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:22170084 G>A maps to NM_007153.3 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr19:22157609 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr19:22154361 A>G maps to NM_007153.3 Y1158Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:22156653 C>T maps to NM_007153.3 E394E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:22157588 G>A maps to NM_007153.3 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:22170084 G>A maps to NM_007153.3 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:22171597 G>A maps to NM_007153.3 N39N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr19:22157022 G>A maps to NM_007153.3 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr19:22156317 G>A maps to NM_007153.3 F506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr19:22157550 G>A maps to NM_007153.3 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:22156770 G>A maps to NM_007153.3 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:22155093 C>T maps to NM_007153.3 E914E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:22156614 A>G maps to NM_007153.3 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr19:22171612 T>C maps to NM_007153.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:22156956 G>A maps to NM_007153.3 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:22171588 G>A maps to NM_007153.3 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:22155546 G>A maps to NM_007153.3 T763T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:58146082 C>T maps to NM_006385.3 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr19:58152516 C>T maps to NM_006385.3 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr19:58153068 C>T maps to NM_006385.3 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:58153434 C>T maps to NM_006385.3 H540H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:58144752 C>T maps to NM_006385.3 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr7:148947311 G>A maps to NM_012256.3 E29E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr7:148950956 C>T maps to NM_012256.3 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:148951427 C>T maps to NM_012256.3 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:148951058 G>A maps to NM_012256.3 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:148947809 C>T maps to NM_012256.3 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr7:148947572 C>T maps to NM_012256.3 N116N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:148950695 C>T maps to NM_012256.3 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr16:3187370 G>A maps to NM_001134655.1 Q30Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:3190891 C>T maps to NM_001134655.1 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr16:3187496 C>G maps to NM_001134655.1 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr16:3188444 C>A maps to NM_001134655.1 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:7022596 C>T maps to NM_013249.2 W106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr11:7022745 G>A maps to NM_013249.2 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr11:7022703 C>T maps to NM_013249.2 W70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr11:6977046 G>A maps to NM_013250.2 W280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr11:6953619 G>A maps to NM_013250.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr11:6977309 C>T maps to NM_013250.2 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:6964833 G>A maps to NM_013250.2 W225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:6964834 G>A maps to NM_013250.2 W225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr11:6953790 C>T maps to NM_013250.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr11:6977074 C>T maps to NM_013250.2 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:6953542 C>T maps to NM_013250.2 R14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:6964813 G>A maps to NM_013250.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr11:6977605 C>T maps to NM_013250.2 N466N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr11:6977590 C>T maps to NM_013250.2 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr11:6977341 C>T maps to NM_013250.2 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr20:52198099 A>G maps to NM_006526.2 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J9-06A-11D-A196-08 chr20:52198558 G>A maps to NM_006526.2 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EG-06A-12D-A32N-08 chr20:52193784 A>C maps to NM_006526.2 Y506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr20:52193136 T>C maps to NM_006526.2 P722P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MN-06A-11D-A197-08 chr20:52198036 G>A maps to NM_006526.2 D443D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:52192386 G>A maps to NM_006526.2 F972F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr20:52192398 G>A maps to NM_006526.2 P968P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr20:52198477 G>A maps to NM_006526.2 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr10:45499061 C>T maps to NM_006963.4 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr10:45499484 C>T maps to NM_006963.4 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr19:44469184 C>T maps to NM_013359.2 Y55Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:44471348 G>A maps to NM_013359.2 K565K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr19:44471066 C>T maps to NM_013359.2 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr19:44536204 C>T maps to NM_001129996.1 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:44536183 T>G maps to NM_001129996.1 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr19:44537122 G>A maps to NM_001129996.1 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:44536708 C>T maps to NM_001129996.1 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr19:44564657 G>T maps to NM_013361.4 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:44610558 C>T maps to NM_013398.2 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr19:44610702 C>T maps to NM_013398.2 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:44611149 G>A maps to NM_013398.2 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:44611035 C>T maps to NM_013398.2 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr19:44604988 C>T maps to NM_013398.2 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:44611650 C>T maps to NM_013398.2 H446H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GH-06A-11D-A196-08 chr19:44636488 G>A maps to ENST00000421176 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:44636365 C>T maps to ENST00000421176 V511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr19:44680392 G>A maps to NM_001032372.1 Q326Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr19:44681406 C>T maps to NM_001032372.1 V664V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:44679804 C>T maps to NM_001032372.1 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr19:44680329 A>G maps to NM_001032372.1 E305E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:44676254 C>T maps to NM_001032372.1 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr19:44679945 C>T maps to NM_001032372.1 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr19:44679946 C>T maps to NM_001032372.1 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:44739314 C>T maps to NM_182490.1 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr19:44739803 C>T maps to NM_182490.1 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr19:44933773 G>A maps to NM_014518.2 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr19:44933323 G>A maps to NM_014518.2 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr19:44934487 G>A maps to NM_014518.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:44936433 G>A maps to NM_014518.2 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:44933668 C>T maps to NM_014518.2 G429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr19:44934486 G>A maps to NM_014518.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:44933092 G>A maps to NM_014518.2 V621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:44933887 C>T maps to NM_014518.2 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:44933266 C>T maps to NM_014518.2 Q563Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:44934631 G>A maps to NM_014518.2 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr19:44933578 C>T maps to NM_014518.2 K459K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:44932909 C>T maps to NM_014518.2 K682K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:44933551 C>T maps to NM_014518.2 K468K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:44936406 C>T maps to NM_014518.2 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GL-06A-11D-A196-08 chr16:71482268 G>A maps to NM_145911.1 I553I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr16:71482511 C>T maps to NM_145911.1 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:71482643 G>A maps to NM_145911.1 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr16:71483539 G>A maps to NM_145911.1 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:71483462 G>A maps to NM_145911.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:71483627 C>T maps to NM_145911.1 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:71482250 G>A maps to NM_145911.1 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:44515001 C>T maps to NM_006300.3 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:44777859 G>A maps to NM_181756.1 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:44777200 A>C maps to NM_181756.1 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:44777835 C>T maps to NM_181756.1 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr19:44770457 C>T maps to NM_181756.1 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr19:44770434 C>T maps to NM_181756.1 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5KH-06A-11D-A27K-08 chr19:44661953 C>T maps to NM_006630.2 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:44660891 C>T maps to NM_006630.2 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:44661599 C>T maps to NM_006630.2 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:44793188 G>A maps to NM_004234.4 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:44791541 G>A maps to NM_004234.4 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:44791595 G>A maps to NM_004234.4 F664F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:44791514 G>A maps to NM_004234.4 G691G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr18:74611015 C>T maps to NM_007345.3 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr18:74637499 C>T maps to NM_007345.3 A1337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr18:74639997 G>A maps to NM_007345.3 Q1508Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr18:74592080 C>T maps to NM_007345.3 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:74639408 C>A maps to NM_007345.3 T1448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr18:74631829 T>C maps to NM_007345.3 L1123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr18:74620485 G>A maps to NM_007345.3 G834G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr18:74625729 G>A maps to NM_007345.3 K977K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr18:74672777 A>T maps to NM_007345.3 K1794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:74593461 C>T maps to NM_007345.3 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:74640033 T>A maps to NM_007345.3 S1520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr1:244218068 C>T maps to NM_205768.2 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:244218221 C>T maps to NM_205768.2 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr1:244217610 C>T maps to NM_205768.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:244218165 C>T maps to NM_205768.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:244217907 C>T maps to NM_205768.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr10:44053047 C>T maps to NM_001099284.1 W160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr10:44052972 C>T maps to NM_001099284.1 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr10:44052779 G>A maps to NM_001099284.1 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr10:44053481 G>A maps to NM_001099284.1 R16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr10:44052771 G>A maps to NM_001099284.1 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr10:44053481 G>A maps to NM_001099284.1 R16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:44052375 G>A maps to NM_001099284.1 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:44053362 G>A maps to NM_001099284.1 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr10:38126602 G>A maps to NM_021045.1 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:38120919 G>A maps to NM_021045.1 Q455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr10:38121733 G>A maps to NM_021045.1 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:38121874 G>A maps to NM_021045.1 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr10:38121310 G>A maps to NM_021045.1 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:38121199 G>A maps to NM_021045.1 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr10:38121757 G>C maps to NM_021045.1 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr10:38120866 G>A maps to NM_021045.1 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr10:38121733 G>A maps to NM_021045.1 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:38121118 G>A maps to NM_021045.1 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:38127003 G>A maps to NM_021045.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr10:38241318 G>A maps to NM_145011.2 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr10:38242044 G>A maps to NM_145011.2 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:38245985 C>T maps to NM_145011.2 W67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr8:145947331 A>T maps to NM_138367.1 Y571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr8:145947690 G>A maps to NM_138367.1 R452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr8:145947979 C>T maps to NM_138367.1 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:145947970 G>A maps to NM_138367.1 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:19989411 C>T maps to NM_021047.2 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:20002847 C>T maps to ENST00000427401 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:24310481 C>T maps to NM_203282.2 I560I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:24309788 A>G maps to NM_203282.2 K329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:24310229 C>A maps to NM_203282.2 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:24309758 G>A maps to NM_203282.2 K319K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:24310184 C>T maps to NM_203282.2 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:58453233 C>T maps to NM_005773.2 Q314Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:58452657 G>A maps to NM_005773.2 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:58453671 G>A maps to NM_005773.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:22271406 C>T maps to NM_033468.2 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr19:22272153 G>A maps to NM_033468.2 K534K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:22255732 C>T maps to NM_033468.2 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:22270896 G>A maps to NM_033468.2 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:22255735 G>A maps to NM_033468.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:22255651 G>A maps to NM_033468.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:22271919 G>A maps to NM_033468.2 E456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr11:116655589 C>T maps to NM_003904.3 Q267Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr11:116656544 C>T maps to NM_003904.3 K183K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:116652936 C>A maps to NM_003904.3 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:37005501 G>A maps to NM_001166038.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:37005708 G>A maps to NM_001166038.1 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr19:57724216 C>T maps to NM_003417.4 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:57723538 C>T maps to NM_003417.4 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:57716816 G>A maps to NM_003417.4 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3ET-06A-11D-A20D-08 chr19:57724046 C>A maps to NM_003417.4 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:57723296 C>T maps to NM_003417.4 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr19:9524604 G>A maps to NM_006631.2 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:31926037 T>C maps to NM_003414.4 C156C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr16:31926232 T>G maps to NM_003414.4 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:31926742 T>A maps to NM_003414.4 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr16:31896569 C>T maps to NM_003414.4 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr16:31927747 C>T maps to NM_003414.4 N726N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr12:133764607 C>T maps to NM_001165881.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:64388278 A>G maps to NM_021148.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:64363778 C>T maps to NM_021148.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr7:64389037 C>T maps to NM_021148.2 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:58723653 T>C maps to NM_133502.1 D368D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr19:58722936 C>A maps to NM_133502.1 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:58718330 C>T maps to NM_133502.1 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr19:58718258 C>T maps to NM_133502.1 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:58718408 G>A maps to NM_133502.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr19:58718354 C>A maps to NM_133502.1 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:58723827 C>T maps to NM_133502.1 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:58724358 C>T maps to NM_133502.1 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr23:152612744 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr23:152612853 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr23:152612985 C>A did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:152612964 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr23:152612328 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr23:152612329 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:152612509 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr16:89789071 C>T maps to NM_001113525.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr16:89789746 C>T maps to NM_001113525.1 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:89789188 C>T maps to NM_001113525.1 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:89790007 C>T maps to NM_001113525.1 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:111927123 C>T maps to NM_021994.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:111935965 C>T maps to NM_021994.2 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr19:53303921 G>A maps to NM_006969.3 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:53303921 G>A maps to NM_006969.3 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr19:53303921 G>A maps to NM_006969.3 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:53304428 G>A maps to NM_006969.3 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:53304761 G>C maps to NM_006969.3 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr22:22869885 C>T maps to NM_080740.3 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr22:22868459 G>A maps to NM_080740.3 Q499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr22:22868568 C>T maps to NM_080740.3 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr22:22869804 C>T maps to NM_080740.3 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr22:22869153 G>A maps to NM_080740.3 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr22:22869717 G>A maps to NM_080740.3 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr22:22842469 T>C maps to NM_080764.2 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr23:129370207 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:129373650 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:129349847 A>G did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:129377576 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29X-06A-11D-A196-08 chr23:129343676 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr23:129377801 T>C did not map to a codon.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr23:129370282 A>G did not map to a codon.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr15:56993091 G>A maps to NM_001002844.1 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr1:200377282 G>A maps to NM_012482.3 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr7:148907713 C>T maps to NM_003575.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:148921667 C>T maps to NM_003575.2 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:148903909 C>T maps to NM_003575.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:44351946 T>C maps to NM_181845.1 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr19:44352210 C>T maps to NM_181845.1 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:44351244 C>T maps to NM_181845.1 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr19:44591031 C>T maps to NM_001037813.2 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr19:44590446 C>T maps to NM_001037813.2 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:44589981 C>T maps to NM_001037813.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr19:44586178 C>T maps to NM_001037813.2 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:44585251 C>T maps to NM_001037813.2 R34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr19:44891167 G>A maps to NM_152354.3 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:44890981 C>T maps to NM_152354.3 Q475Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:44891923 G>A maps to NM_152354.3 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr19:44891167 G>A maps to NM_152354.3 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr19:44891896 G>A maps to NM_152354.3 Y170Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:44892238 C>T maps to NM_152354.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:44890837 C>T maps to NM_152354.3 R523R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:44890981 C>T maps to NM_152354.3 Q475Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr17:15619829 C>T maps to NM_020652.2 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr17:18566005 G>A maps to NM_001145045.1 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr17:16467099 G>A maps to NM_020653.2 Q181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr17:16466514 G>A maps to NM_020653.2 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr17:16467091 G>A maps to NM_020653.2 D183D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr17:16470904 G>A maps to NM_020653.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr6:87964628 T>C maps to NM_015021.1 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:87967603 T>A maps to NM_015021.1 P1419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr6:87970414 T>C maps to NM_015021.1 P2356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr6:87970645 A>T maps to NM_015021.1 S2433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr6:87967171 C>T maps to NM_015021.1 F1275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:87969863 C>T maps to NM_015021.1 R2173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr6:87970906 C>T maps to NM_015021.1 C2520C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr6:87968875 C>T maps to NM_015021.1 G1843G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr21:43411720 G>A maps to NM_020727.4 S828S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr21:43412938 G>A maps to NM_020727.4 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr21:43412713 T>C maps to NM_020727.4 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr21:43413583 A>G maps to NM_020727.4 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr21:43413313 T>C maps to NM_020727.4 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:45579359 C>T maps to NM_145288.1 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:99669599 C>T maps to NM_032924.3 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:35434811 A>G maps to NM_001099438.1 K315K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:35435021 C>T maps to NM_001099438.1 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr5:150275723 C>T maps to NM_001172831.1 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr5:150278037 G>A maps to NM_001172831.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:150282704 G>A maps to NM_001172831.1 Q21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:150282705 G>A maps to NM_001172831.1 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr5:150282705 G>A maps to NM_001172831.1 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr5:150275612 C>T maps to NM_001172831.1 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:150275444 G>A maps to NM_001172831.1 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:57868607 C>T maps to ENST00000391705 G504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:57868433 C>T maps to ENST00000391705 F446F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:57868826 T>C maps to ENST00000391705 P577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr19:57867734 C>T maps to ENST00000391705 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr19:57867740 G>A maps to ENST00000391705 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:57868277 C>T maps to ENST00000391705 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr6:28971361 A>G maps to NM_001010877.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr6:28967303 C>T maps to NM_001010877.2 K90K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr6:28963142 G>A maps to NM_001010877.2 R546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr6:28963461 C>T maps to NM_001010877.2 R439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr6:28962846 C>T maps to NM_001010877.2 G644G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:9270854 C>T maps to NM_020933.4 D178D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:9270815 C>T maps to NM_020933.4 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:9271286 C>T maps to NM_020933.4 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:9267378 C>T maps to NM_020933.4 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:9271049 C>T maps to NM_020933.4 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9271433 C>T maps to NM_020933.4 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr6:43323409 G>A maps to NM_014345.2 P554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:43305006 G>A maps to NM_014345.2 S2243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr6:43306629 A>G maps to NM_014345.2 S1702S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:43308572 A>T maps to NM_014345.2 S1150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr6:43325229 G>A maps to NM_014345.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:43322557 G>A maps to NM_014345.2 I838I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr6:43308623 G>A maps to NM_014345.2 I1133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr6:43322650 G>A maps to NM_014345.2 T807T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:43325360 G>A maps to NM_014345.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr16:58030948 G>A maps to NM_020807.1 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:58030885 G>A maps to NM_020807.1 F428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:58031773 G>A maps to NM_020807.1 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr19:53432251 G>A maps to NM_203307.2 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr6:28294164 G>A maps to NM_030899.4 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr6:28297378 G>A maps to NM_030899.4 R28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:58982656 C>T maps to NM_014347.2 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:58983382 C>T maps to NM_014347.2 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:58966910 G>A maps to NM_207395.2 Q200Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:58966928 C>T maps to NM_207395.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:58967012 C>T maps to NM_207395.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:58966694 C>T maps to NM_207395.2 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr19:58967342 C>T maps to NM_207395.2 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr1:90473072 C>T maps to NM_182976.2 Q127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:58640555 G>A maps to NM_024620.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr19:58640039 G>A maps to NM_024620.3 H277H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:58639466 G>A maps to NM_024620.3 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:54074910 C>T maps to NM_001079907.1 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr19:54080989 C>T maps to NM_001079907.1 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:54080402 C>T maps to NM_001079907.1 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:54080950 C>G maps to NM_001079907.1 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr19:54074871 C>T maps to NM_001079907.1 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:54081121 G>A maps to NM_001079907.1 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:54080362 G>A maps to NM_001079907.1 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:54080584 A>G maps to NM_001079907.1 K257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:54074955 G>A maps to NM_001079907.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZR-06A-21D-A197-08 chr19:54080113 C>T maps to NM_001079907.1 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54080194 G>A maps to NM_001079907.1 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:54080818 C>T maps to NM_001079907.1 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:14826997 G>A maps to NM_032433.2 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr19:14806396 C>T maps to NM_032433.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:14826949 T>C maps to NM_032433.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr20:45131164 C>T maps to NM_018102.3 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr20:45133363 G>A maps to NM_018102.3 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr20:45130645 C>T maps to NM_018102.3 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:45131227 A>G maps to NM_018102.3 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:45130972 G>A maps to NM_018102.3 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr20:45130981 C>T maps to NM_018102.3 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr20:45131368 C>T maps to NM_018102.3 Q203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr20:45132919 C>T maps to NM_018102.3 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:45130735 G>A maps to NM_018102.3 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr20:44590752 G>A maps to NM_022095.3 Y534Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr20:44581016 G>A maps to NM_022095.3 S986S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr20:44598276 G>A maps to NM_022095.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr20:44581338 G>A maps to NM_022095.3 P904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr20:44589152 G>A maps to NM_022095.3 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:44587923 G>A maps to NM_022095.3 F723F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:44589350 G>A maps to NM_022095.3 F562F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:44598276 G>A maps to NM_022095.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr20:44596942 G>A maps to NM_022095.3 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr20:25657188 G>A maps to NM_015655.2 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr20:25656123 G>A maps to NM_015655.2 F600F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr10:38345157 C>T maps to NM_006954.1 F702F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr10:38344719 C>T maps to NM_006954.1 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:38344755 C>T maps to NM_006954.1 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr10:38343567 C>T maps to NM_006954.1 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr10:38344752 C>T maps to NM_006954.1 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:38345343 C>T maps to NM_006954.1 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr10:43089381 C>T maps to NM_006955.1 W339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr10:43088696 G>A maps to NM_006955.1 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr10:43088543 G>A maps to NM_006955.1 F618F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:43089566 A>G maps to NM_006955.1 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr8:145998668 C>T maps to NM_030580.3 R555R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr8:145999520 C>T maps to NM_030580.3 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr8:145999286 G>A maps to NM_030580.3 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr8:145999921 C>A maps to NM_030580.3 G138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr20:32369171 C>T maps to ENST00000375200 F566F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr20:32379196 T>G maps to ENST00000375200 T813T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr20:32378972 A>T maps to ENST00000375200 K739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:32344961 C>T maps to ENST00000375200 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr20:32379013 C>T maps to ENST00000375200 A752A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr20:32349677 G>T maps to ENST00000375200 E347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:32371623 C>T maps to ENST00000375200 F602F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:32378890 C>T maps to ENST00000375200 F711F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr20:32354732 G>A maps to ENST00000375200 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr20:2473351 G>A maps to NM_024325.4 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr20:2464181 A>G maps to NM_024325.4 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr20:2464421 G>A maps to NM_024325.4 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr20:2463908 G>A maps to NM_024325.4 V566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:2464163 A>G maps to NM_024325.4 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:2464817 G>A maps to NM_024325.4 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr19:37368889 C>T maps to NM_003419.3 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr5:176471520 C>T maps to ENST00000503039 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr5:176471496 G>A maps to ENST00000503039 K185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr5:176491536 C>G maps to ENST00000503039 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr19:53644385 T>A maps to NM_001172674.1 G566G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:53644231 G>A maps to NM_001172674.1 R618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:53644355 G>C maps to NM_001172674.1 G576G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr19:53644910 G>A maps to NM_001172674.1 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J6-06A-11D-A19A-08 chr3:44692708 G>A maps to NM_003420.3 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr3:44700265 C>T maps to NM_003420.3 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr5:178139263 G>A maps to NM_005649.2 Q539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr5:178139114 G>A maps to NM_005649.2 N588N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:178140386 C>T maps to NM_005649.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr5:178139425 G>A maps to NM_005649.2 Q485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr5:178310556 C>T maps to NM_058230.2 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr5:178311019 C>T maps to NM_058230.2 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr5:178309839 G>A maps to NM_058230.2 E129E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:178507031 C>T maps to NM_014594.1 F533F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr5:178506290 C>T maps to NM_014594.1 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr5:178506846 C>T maps to NM_014594.1 Q472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr5:178506098 G>A maps to NM_014594.1 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr5:178506356 C>T maps to NM_014594.1 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr5:178506062 C>T maps to NM_014594.1 Y210Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:7584436 C>T maps to NM_018083.4 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:7584403 C>T maps to NM_018083.4 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:33764607 G>A maps to NM_152493.2 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr10:64136686 G>A maps to NM_199451.2 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:64135993 G>A maps to NM_199451.2 Q14Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:64148313 C>T maps to NM_199451.2 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr10:64159340 C>T maps to NM_014951.2 F339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr10:64159310 A>T maps to NM_014951.2 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr10:64135999 C>T maps to NM_199451.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr10:64219503 G>A maps to NM_199451.2 W310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr5:71756609 G>A maps to NM_152625.1 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr5:71756237 C>T maps to NM_152625.1 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr5:71752398 C>T maps to NM_152625.1 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr5:71756213 G>A maps to NM_152625.1 C370C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr5:71756159 C>T maps to NM_152625.1 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:71756756 G>A maps to NM_152625.1 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr5:71756975 G>A maps to NM_152625.1 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr5:71756365 G>A maps to NM_152625.1 Q320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr5:71756149 G>A maps to NM_152625.1 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr5:71739687 C>T maps to NM_152625.1 R710R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:71740107 C>T maps to NM_152625.1 R570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:71756183 C>T maps to NM_152625.1 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr5:71740005 G>A maps to NM_152625.1 F604F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:99160470 G>A maps to NM_153695.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:38406387 C>T maps to NM_003421.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:37118319 C>T maps to NM_032825.3 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:37118319 C>T maps to NM_032825.3 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:37101640 C>T maps to NM_032825.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr19:37117983 C>T maps to NM_032825.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:37100897 C>T maps to NM_032825.3 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr12:6787561 G>A maps to NM_001135734.1 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr12:6782497 G>A maps to NM_001135734.1 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr12:54767879 G>A maps to NM_001130967.1 R100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr12:54767880 G>A maps to NM_001130967.1 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19C-06A-11D-A196-08 chr12:54764794 C>T maps to NM_001130967.1 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JG-06A-11D-A196-08 chr2:180348095 C>T maps to NM_152520.4 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr2:180311375 C>T maps to NM_152520.4 K264K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr2:180409646 G>T maps to NM_152520.4 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr2:180348095 C>T maps to NM_152520.4 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:180309665 C>T maps to NM_152520.4 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr2:180348095 C>T maps to NM_152520.4 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr2:180383311 G>A maps to NM_152520.4 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:180634296 C>T maps to NM_152520.4 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:180634323 G>A maps to NM_152520.4 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr2:180634401 C>T maps to NM_152520.4 E27E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr3:21462774 C>T maps to NM_024697.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr3:21478615 G>A maps to NM_024697.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr3:21467106 G>A maps to NM_024697.2 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr3:21552410 T>C maps to NM_024697.2 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:21466983 C>T maps to NM_024697.2 Q284Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr3:21552419 C>T maps to NM_024697.2 K124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr3:21462747 G>T maps to NM_024697.2 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr3:21467031 G>A maps to NM_024697.2 H268H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19B-06A-11D-A196-08 chr3:21606176 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr3:21465517 C>T maps to NM_024697.2 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:21552452 G>A maps to NM_024697.2 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:21606134 C>T maps to NM_024697.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr3:21462821 G>A maps to NM_024697.2 R358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr6:27368997 G>A maps to NM_001076781.1 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr6:27368373 G>A maps to NM_001076781.1 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:27368310 C>T maps to NM_001076781.1 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr7:99091874 G>A maps to NM_032164.2 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr8:28210824 G>A maps to NM_018660.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr8:28218599 G>A maps to NM_018660.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr18:32949370 G>A maps to NM_145756.2 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr18:32948371 C>T maps to NM_145756.2 K315K. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D3-A2JG-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:32834139 C>T maps to NM_001166012.1 Q253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:148875974 A>T maps to NM_170686.2 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:148876607 C>T maps to NM_170686.2 F548F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr7:148876643 C>T maps to NM_170686.2 I560I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:148876610 C>T maps to NM_170686.2 I549I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:44384216 C>T maps to ENST00000324394 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr19:44377702 C>T maps to ENST00000324394 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr18:72346736 C>T maps to NM_017757.2 L1254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr18:72589275 C>T maps to NM_017757.2 F1667F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr18:72347195 C>T maps to NM_017757.2 S1407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr18:72775832 C>G maps to NM_017757.2 A2052A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr18:72347585 C>T maps to NM_017757.2 N1537N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:72775157 C>T maps to NM_017757.2 F1827F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr18:72344765 C>T maps to NM_017757.2 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr18:72353072 C>T maps to NM_017757.2 V1599V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZT-06A-11D-A197-08 chr18:72345995 C>T maps to NM_017757.2 S1007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:72346769 C>T maps to NM_017757.2 L1265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:72775172 C>T maps to NM_017757.2 S1832S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr18:72589158 T>C maps to NM_017757.2 F1628F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr18:72343355 C>T maps to NM_017757.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr11:46726806 C>A maps to NM_024741.2 T519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr11:46726863 A>G maps to NM_024741.2 E538E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UL-06A-11D-A30X-08 chr11:46726602 C>A maps to NM_024741.2 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr11:46727244 G>A maps to NM_024741.2 E665E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr23:47307744 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr23:47307855 G>A did not map to a codon.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr23:47308212 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:47308034 T>G did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:47308117 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:47308280 T>A did not map to a codon.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr23:47307897 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:47306863 G>C did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:47307367 G>A did not map to a codon.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr23:47307903 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr14:74388823 C>T maps to NM_021188.1 N395N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr14:74360501 C>T maps to NM_021188.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:8576705 G>A maps to NM_001146175.1 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:8576744 G>A maps to NM_001146175.1 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr19:53612594 G>A maps to NM_001164309.1 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:53613027 C>T maps to NM_001164309.1 K90K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:53619641 C>T maps to NM_001164309.1 W20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:53612706 G>A maps to NM_001164309.1 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:53612706 G>A maps to NM_001164309.1 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr19:53612706 G>A maps to NM_001164309.1 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:58084160 G>A maps to NM_017879.1 R371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:58420697 A>G maps to NM_152475.2 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:58420217 C>T maps to NM_152475.2 K476K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:58438693 A>T maps to NM_133460.1 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:58437892 G>A maps to NM_133460.1 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:58437562 G>A maps to NM_133460.1 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:58437877 C>T maps to NM_133460.1 Q557Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:58438239 G>A maps to NM_133460.1 R437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:58439035 G>A maps to NM_133460.1 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:58005428 C>T maps to NM_001098491.1 R503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:58004509 C>T maps to NM_001098491.1 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:37619716 C>T maps to NM_144689.3 I608I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U9-06A-11D-A32N-08 chr19:37619737 T>C maps to NM_144689.3 Y615Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr16:49671829 G>A maps to NM_015069.2 C411C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr16:49671454 G>A maps to NM_015069.2 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:49671484 G>A maps to NM_015069.2 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:49764730 G>A maps to NM_015069.2 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:49671904 G>A maps to NM_015069.2 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:49672681 G>A maps to NM_015069.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr16:49672450 G>T maps to NM_015069.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr16:49671910 C>T maps to NM_015069.2 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr16:49671484 G>A maps to NM_015069.2 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:49671055 C>T maps to NM_015069.2 E669E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:49671595 G>A maps to NM_015069.2 F489F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:49671745 C>T maps to NM_015069.2 Q439Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr16:49671202 G>A maps to NM_015069.2 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr16:49670601 G>A maps to NM_015069.2 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr16:49670602 G>A maps to NM_015069.2 I820I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:49671868 C>T maps to NM_015069.2 R398R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr16:49670893 G>A maps to NM_015069.2 T723T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr16:49764691 G>A maps to NM_015069.2 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr16:49669969 G>A maps to NM_015069.2 S1031S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:49557645 G>A maps to NM_015069.2 F1238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:49670530 C>T maps to NM_015069.2 G844G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:49671964 G>A maps to NM_015069.2 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:49823407 C>T maps to NM_015069.2 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr7:148801945 G>A maps to NM_001001661.2 F339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:148800739 A>G maps to NM_001001661.2 I741I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr7:148801021 G>A maps to NM_001001661.2 F647F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr7:148801971 G>A maps to NM_001001661.2 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr7:148802029 G>A maps to NM_001001661.2 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr7:148801357 G>A maps to NM_001001661.2 F535F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:148815383 G>A maps to NM_001001661.2 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:148801240 C>T maps to NM_001001661.2 R574R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:9646887 G>A maps to NM_024106.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:9639685 G>A maps to NM_024106.1 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr19:9639547 A>G maps to NM_024106.1 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:21712582 C>T maps to NM_001001415.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:21713413 C>T maps to NM_001001415.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:21712510 C>T maps to NM_001001415.2 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:21719571 C>T maps to NM_001001415.2 N239N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:21719140 C>T maps to NM_001001415.2 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:21719374 C>T maps to NM_001001415.2 Q174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:21720270 G>A maps to NM_001001415.2 R472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:21992019 A>G maps to NM_003423.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:21990846 G>A maps to NM_003423.2 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:21240106 C>T maps to NM_025189.3 H331H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:21366593 C>T maps to NM_133473.2 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr19:21365843 C>T maps to NM_133473.2 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:52537164 T>C maps to NM_014650.2 Q589Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:52538276 G>A maps to NM_014650.2 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:12128745 T>A maps to NM_001080411.1 K49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr1:23688641 G>A maps to NM_001077195.1 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr1:23688593 G>A maps to NM_001077195.1 F427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr1:23688770 C>T maps to NM_001077195.1 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr1:23688770 C>T maps to NM_001077195.1 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr10:31137581 G>A maps to NM_182755.2 G584G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr10:31137869 G>A maps to NM_182755.2 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr10:31137986 G>A maps to NM_182755.2 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr10:31134407 G>A maps to NM_182755.2 Q657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr10:31138273 G>A maps to NM_182755.2 Q354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr10:31138997 G>A maps to NM_182755.2 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:31137779 G>A maps to NM_182755.2 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:31134207 A>T maps to NM_182755.2 C723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr10:31138046 G>A maps to NM_182755.2 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:31139023 G>A maps to NM_182755.2 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:11978399 C>T maps to NM_152262.2 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:11978879 G>A maps to NM_152262.2 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:11977054 C>T maps to NM_152262.2 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:11979243 C>T maps to NM_152262.2 R454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:12383431 G>A maps to NM_001164276.1 F594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J3-06A-11D-A20D-08 chr19:12384184 G>A maps to NM_001164276.1 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:12384535 G>A maps to NM_001164276.1 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:11942464 C>T maps to NM_152357.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr19:11942548 T>C maps to NM_152357.2 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr19:11891142 C>T maps to NM_152355.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr19:11892312 C>T maps to NM_152355.2 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:11891922 C>T maps to NM_152355.2 F428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:11888538 C>T maps to NM_152355.2 N39N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:12460847 T>C maps to NM_030824.2 E517E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:12461072 G>A maps to NM_030824.2 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr19:12463892 G>A maps to NM_030824.2 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr19:12541137 A>C maps to NM_005815.4 Y616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr19:12543218 G>A maps to NM_005815.4 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:12541953 T>C maps to NM_005815.4 K344K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:56671149 C>T maps to NM_018337.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr3:44492899 G>A maps to NM_181489.5 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr3:44491011 A>C maps to NM_181489.5 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr3:44488419 G>A maps to NM_181489.5 Q915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:44488447 G>A maps to NM_181489.5 F905F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:44488120 G>A maps to NM_181489.5 T1014T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr3:44492362 G>A maps to NM_181489.5 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:58988734 G>A maps to NM_017908.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:58988659 C>T maps to NM_017908.2 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr19:58989496 C>T maps to NM_017908.2 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr23:134494270 C>T did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:134483137 C>T did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr23:134483106 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr23:134494126 T>A did not map to a codon.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr23:134483195 G>A did not map to a codon.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr23:134483188 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:44418360 G>A maps to NM_003425.3 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:44418225 G>A maps to NM_003425.3 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr6:57012295 C>T maps to NM_001031623.2 T471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr6:57012418 C>T maps to NM_001031623.2 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr6:56999598 C>T maps to NM_001031623.2 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr6:57012013 C>T maps to NM_001031623.2 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr6:57017091 C>T maps to NM_001031623.2 F942F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z7-06A-11D-A197-08 chr6:57012154 T>C maps to NM_001031623.2 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:57013054 C>T maps to NM_001031623.2 C724C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:57013069 C>T maps to NM_001031623.2 I729I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr6:57006230 C>T maps to NM_001031623.2 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr5:178391809 C>T maps to NM_182594.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr5:178392061 A>G maps to NM_182594.2 R219R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A20C-06A-11D-A196-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr5:178392083 C>T maps to NM_182594.2 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr5:178391918 C>T maps to NM_182594.2 Q172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr5:178392826 G>A maps to NM_182594.2 E474E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr19:57803141 C>T maps to NM_006635.3 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:37129926 G>A maps to NM_153257.2 P440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr9:109691313 C>T maps to NM_021224.4 P1707P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr9:109689831 G>A maps to NM_021224.4 Q1213Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr9:109687518 C>A maps to NM_021224.4 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:109692837 C>T maps to NM_021224.4 I1960I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr9:109701388 G>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:109734355 G>A maps to NM_021224.4 R2166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr9:109691427 C>T maps to NM_021224.4 I1745I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr9:109686528 C>T maps to NM_021224.4 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr9:109690164 C>T maps to NM_021224.4 P1324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NG-06A-11D-A196-08 chr9:109688886 C>T maps to NM_021224.4 F898F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr9:109773145 C>T maps to NM_021224.4 H2452H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr9:109746500 C>T maps to NM_021224.4 S2289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:109686777 C>T maps to NM_021224.4 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:109688976 G>A maps to NM_021224.4 R928R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr7:149467601 G>A maps to NM_207336.1 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:149468109 G>A maps to NM_207336.1 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:53352421 C>T maps to NM_001008801.1 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:53344538 G>A maps to NM_001008801.1 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:53345198 G>A maps to NM_001008801.1 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:53352343 G>A maps to NM_001008801.1 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:53345104 G>A maps to NM_001008801.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:57085764 T>C maps to NM_001001668.3 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:57088183 C>T maps to NM_001001668.3 D129D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:57089347 C>T maps to NM_001001668.3 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr19:57088459 C>T maps to NM_001001668.3 D221D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:57088522 C>T maps to NM_001001668.3 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:57088759 C>T maps to NM_001001668.3 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:57089546 C>T maps to NM_001001668.3 Q584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:57029917 G>A maps to NM_020813.2 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:57035810 G>A maps to NM_020813.2 W125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:57037298 T>C maps to NM_020813.2 H621H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr19:50549409 C>T maps to NM_015428.1 T570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:50550096 A>G maps to NM_015428.1 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr19:50548281 C>T maps to NM_015428.1 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:50548182 C>T maps to NM_015428.1 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:50548689 C>T maps to NM_015428.1 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr5:121487945 C>T maps to NM_207317.1 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr5:121488488 C>T maps to NM_207317.1 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:121488170 G>A maps to NM_207317.1 Q162Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr5:121488632 G>A maps to NM_207317.1 Q316Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr5:121488389 C>T maps to NM_207317.1 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr5:121487966 C>T maps to NM_207317.1 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr5:121488494 G>A maps to NM_207317.1 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr7:57188458 G>A maps to NM_033273.1 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:57188065 G>A maps to NM_033273.1 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:57188146 G>A maps to NM_033273.1 C325C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:57194383 C>T maps to NM_033273.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:57193791 G>A maps to NM_033273.1 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:57194389 G>A maps to NM_033273.1 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:57187684 G>A maps to NM_033273.1 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:57188491 C>T maps to NM_033273.1 E210E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:30410151 C>T maps to ENST00000495929 A656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:30409821 C>T maps to ENST00000495929 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr16:30409509 C>T maps to ENST00000495929 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr19:52817501 T>C maps to NM_144684.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:52825825 C>G maps to NM_144684.2 G441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:52824895 C>T maps to NM_144684.2 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr19:52825754 C>T maps to NM_144684.2 R418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:52825503 G>A maps to NM_144684.2 W334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:52825348 C>T maps to NM_144684.2 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:52825555 C>T maps to NM_144684.2 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr9:114296128 G>A maps to NM_133464.2 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr9:114296141 C>T maps to NM_133464.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:114289974 C>T maps to NM_133464.2 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr9:95609958 G>A maps to NM_031486.1 N370N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr9:95608526 G>A maps to NM_031486.1 Q848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:95608713 G>A maps to NM_031486.1 F785F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr9:95609031 G>A maps to NM_031486.1 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:44112243 C>T maps to NM_145312.3 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr10:44112357 G>A maps to NM_145312.3 Q289Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr19:20296820 G>A maps to NM_052852.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:20307998 G>A maps to NM_052852.2 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:20278138 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3C6-06A-12D-A196-08 chr10:48370852 G>A maps to NM_153034.2 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr10:48370804 G>A maps to NM_153034.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr10:48371336 C>T maps to NM_153034.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr10:48371142 G>A maps to NM_153034.2 W204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr10:48371347 C>T maps to NM_153034.2 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:48370690 G>A maps to NM_153034.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:12693673 T>G maps to NM_020714.2 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr19:12691588 G>A maps to NM_020714.2 R434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:12692195 G>A maps to NM_020714.2 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr19:22847001 C>T maps to NM_020855.2 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:22846621 C>T maps to NM_020855.2 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:22846810 C>T maps to NM_020855.2 Q114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:21606447 C>T maps to NM_001076678.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:21607542 C>T maps to NM_001076678.2 F694F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr19:21606297 C>T maps to NM_001076678.2 Y279Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:21588585 C>T maps to NM_001076678.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr1:247464420 G>A maps to NM_032752.1 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr1:247473034 G>A maps to NM_032752.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr1:247464519 G>A maps to NM_032752.1 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr1:247464519 G>A maps to NM_032752.1 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr1:247473701 G>A maps to NM_032752.1 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:247464519 G>A maps to NM_032752.1 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:247463991 G>A maps to NM_032752.1 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:58868095 G>A maps to NM_198458.1 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:58867537 G>A maps to NM_198458.1 H488H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr19:58868413 G>A maps to NM_198458.1 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr7:99221678 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr7:99221765 G>A maps to NM_145115.2 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr7:99226910 C>T maps to NM_145115.2 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr16:4812274 G>A maps to NM_021646.1 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr16:4815778 G>A maps to NM_021646.1 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr16:4815910 C>T maps to NM_021646.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr3:44776380 T>C maps to NM_145044.2 H156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr3:44776023 T>C maps to NM_145044.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:44776470 A>T maps to NM_145044.2 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr3:44776089 C>T maps to NM_145044.2 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr3:44763571 C>T maps to NM_033210.4 C421C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr3:44763127 G>C maps to NM_033210.4 G273G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EE-A180-06A-11D-A21A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr10:77159217 G>A maps to NM_032772.4 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A6L9-06A-11D-A32N-08 chr19:19905396 A>C maps to NM_001099269.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr19:19905426 T>C maps to NM_001099269.2 K423K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr19:32845424 C>T maps to NM_014910.4 T563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr19:32843886 T>C maps to NM_014910.4 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:32873628 G>T maps to NM_014910.4 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr9:99521508 G>A maps to NM_014930.1 Q535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr9:99522715 G>A maps to NM_014930.1 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr10:135122931 G>A maps to NM_145806.2 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr10:135123717 C>T maps to NM_145806.2 D160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:27844027 C>T maps to NM_032434.2 F468F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:27844027 C>T maps to NM_032434.2 F468F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr20:62599267 G>A maps to NM_020713.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr20:62599258 G>A maps to NM_020713.1 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:62595508 G>A maps to NM_020713.1 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:62592679 G>A maps to NM_020713.1 I803I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr2:95815989 G>A maps to NM_032788.1 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:95815452 G>A maps to NM_032788.1 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr18:74074485 G>T maps to ENST00000443185 T1153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr18:74154767 G>A maps to ENST00000443185 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr18:74091180 G>A maps to ENST00000443185 A963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr18:74091180 G>A maps to ENST00000443185 A963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr18:74153873 G>A maps to ENST00000443185 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr18:74154875 G>A maps to ENST00000443185 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr18:74091636 G>A maps to ENST00000443185 S811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr18:74091510 G>A maps to ENST00000443185 P853P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr18:74154914 G>A maps to ENST00000443185 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:74082500 G>A maps to ENST00000443185 S1138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:74090858 C>T maps to ENST00000443185 A1070A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:74092230 G>A maps to ENST00000443185 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:74154188 G>A maps to ENST00000443185 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr18:74091528 G>A maps to ENST00000443185 S847S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr8:146032999 C>T maps to NM_213605.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr10:97916861 C>T maps to NM_014803.3 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr10:97917320 C>T maps to NM_014803.3 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr4:10446347 T>C maps to NM_053042.2 A535A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr4:10445684 G>A maps to NM_053042.2 T756T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr4:10445435 G>A maps to NM_053042.2 I839I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:10447214 G>A maps to NM_053042.2 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr4:10447099 G>A maps to NM_053042.2 Q285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr4:10447781 A>G maps to NM_053042.2 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr4:10445216 C>T maps to NM_053042.2 K912K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:10446014 G>A maps to NM_053042.2 V646V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr18:14124376 C>T maps to NM_145287.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr18:14105179 G>A maps to NM_145287.3 I453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr18:14106163 C>T maps to NM_145287.3 Q125Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr18:14124358 G>A maps to NM_145287.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr18:22804971 G>A maps to NM_015461.2 S970S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr18:22804971 G>A maps to NM_015461.2 S970S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr18:22804659 G>A maps to NM_015461.2 F1074F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr18:22807208 C>A maps to NM_015461.2 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr18:22806711 G>A maps to NM_015461.2 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr18:22807110 G>A maps to NM_015461.2 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr18:22804494 C>A maps to NM_015461.2 G1129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:22806108 G>A maps to NM_015461.2 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr18:22804971 G>A maps to NM_015461.2 S970S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:56113486 C>T maps to NM_153219.2 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:42729904 C>T maps to NM_133444.1 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NC-06A-11D-A197-08 chr19:42729577 C>T maps to NM_133444.1 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr19:42730351 G>A maps to NM_133444.1 R599R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:37880079 C>T maps to NM_032453.1 Q377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr19:37880054 C>T maps to NM_032453.1 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:37879796 C>T maps to NM_032453.1 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:37880219 C>T maps to NM_032453.1 F423F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:52918722 C>T maps to NM_032423.2 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr19:37037967 T>G maps to NM_001145649.1 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr19:37038204 C>A maps to NM_001145649.1 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr19:37038280 G>A maps to NM_001145649.1 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr19:58117969 C>T maps to NM_020880.3 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:58118494 C>T maps to NM_020880.3 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:58118506 G>A maps to NM_020880.3 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:58118647 C>T maps to NM_020880.3 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:58118648 C>T maps to NM_020880.3 Q586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:58115673 C>T maps to NM_020880.3 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:58118246 C>T maps to NM_020880.3 R452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:58117411 C>T maps to NM_020880.3 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr18:56586121 T>C maps to NM_018181.4 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr18:56586313 C>T maps to NM_018181.4 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr18:56587507 C>T maps to NM_018181.4 S663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr18:56587471 G>A maps to NM_018181.4 K651K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr18:56606835 C>T maps to NM_018181.4 I896I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr19:52941471 G>A maps to NM_001143939.1 Q266Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:52941579 G>A maps to NM_001143939.1 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr19:52941171 C>T maps to NM_001143939.1 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:52942137 C>T maps to NM_001143939.1 F488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:52942419 G>A maps to NM_001143939.1 R582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr19:52941669 C>T maps to NM_001143939.1 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:52942227 G>A maps to NM_001143939.1 Q518Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:31039267 C>T maps to NM_014717.1 F914F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr19:30935656 C>T maps to NM_014717.1 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr19:30935758 C>T maps to NM_014717.1 Y430Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr19:30934657 C>T maps to NM_014717.1 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:30936526 C>T maps to NM_014717.1 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:31039846 C>T maps to NM_014717.1 F1107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr19:31039165 C>T maps to NM_014717.1 V880V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr19:31039363 C>T maps to NM_014717.1 S946S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:31040257 C>T maps to NM_014717.1 P1244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:30934864 C>T maps to NM_014717.1 C132C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:31038980 C>T maps to NM_014717.1 Q819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:31039384 T>C maps to NM_014717.1 D953D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:30936196 G>A maps to NM_014717.1 Q576Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:31025853 G>A maps to NM_014717.1 G757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:31039510 G>A maps to NM_014717.1 Q995Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr19:31039423 G>A maps to NM_014717.1 R966R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:30934618 C>T maps to NM_014717.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:31039972 C>T maps to NM_014717.1 I1149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr19:30934834 C>T maps to NM_014717.1 D122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:31039261 G>A maps to NM_014717.1 V912V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr19:30935917 G>A maps to NM_014717.1 G483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:30934681 C>T maps to NM_014717.1 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:31039451 C>T maps to NM_014717.1 L976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:30936213 T>A maps to NM_014717.1 L582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr19:30935917 G>A maps to NM_014717.1 G483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:30935491 G>A maps to NM_014717.1 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:31040113 C>T maps to NM_014717.1 A1196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:31038980 C>T maps to NM_014717.1 Q819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:31039042 G>A maps to NM_014717.1 R839R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr19:30934606 C>T maps to NM_014717.1 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:30934636 C>T maps to NM_014717.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F8-06A-11D-A25O-08 chr19:31039381 G>A maps to NM_014717.1 V952V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:30935683 C>T maps to NM_014717.1 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:30935869 G>A maps to NM_014717.1 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:30935935 G>A maps to NM_014717.1 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:31040236 T>A maps to NM_014717.1 G1237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:30936568 C>T maps to NM_014717.1 V700V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:31039021 C>T maps to NM_014717.1 F832F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:30934507 G>A maps to NM_014717.1 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:38103017 T>G maps to NM_152606.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr19:38104025 C>T maps to NM_152606.3 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:57840032 G>T maps to NM_213598.3 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr19:58773672 G>A maps to NM_014480.2 Q567Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr19:58773810 C>T maps to NM_014480.2 F613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr19:40521504 C>T maps to NM_178544.3 P776P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:40512004 C>T maps to NM_178544.3 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:57911019 G>A maps to NM_001172773.1 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:57910225 C>T maps to NM_001172773.1 Q203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:58046567 C>T maps to ENST00000376233 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:58048917 C>T maps to ENST00000376233 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:58049490 C>T maps to ENST00000376233 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:58059143 G>A maps to NM_001039654.1 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:58198864 C>T maps to ENST00000356715 R408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:58199595 C>T maps to ENST00000356715 S651S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr19:58199109 C>A maps to ENST00000356715 I489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:58320091 G>A maps to NM_024762.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:2833847 C>T maps to NM_001102651.1 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:2853296 C>T maps to NM_152791.4 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5SG-06A-11D-A30X-08 chr19:2853484 C>T maps to NM_152791.4 H474H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:2853796 C>T maps to NM_152791.4 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:2853212 C>T maps to NM_152791.4 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:2853904 G>A maps to NM_152791.4 Q614Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:2853193 C>T maps to NM_152791.4 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr19:2873585 C>T maps to NM_024967.1 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:2877343 C>T maps to NM_024967.1 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:2878056 G>A maps to NM_024967.1 E367E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:2876089 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:2877834 G>A maps to NM_024967.1 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:2878083 G>A maps to NM_024967.1 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:2877897 C>T maps to NM_024967.1 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:2873573 C>T maps to NM_024967.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:2873516 G>A maps to NM_024967.1 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr19:2877582 G>A maps to NM_024967.1 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:2873620 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:2878140 G>A maps to NM_024967.1 E395E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:2877927 C>T maps to NM_024967.1 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:2877741 G>A maps to NM_024967.1 K262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:7076402 C>T maps to NM_024341.2 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr19:8921957 C>T maps to NM_144693.1 *403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr19:8922406 G>A maps to NM_144693.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr19:8931967 G>A maps to NM_144693.1 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:8922238 C>T maps to NM_144693.1 Q309Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr19:8922346 G>A maps to NM_144693.1 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:8931903 G>A maps to NM_144693.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:8922430 G>A maps to NM_144693.1 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:8931967 G>A maps to NM_144693.1 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr19:8922208 G>A maps to NM_144693.1 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:8931946 G>A maps to NM_144693.1 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr19:9453707 C>T maps to NM_032497.1 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:9452378 C>T maps to NM_032497.1 N84N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr19:9577474 G>A maps to NM_152476.2 D716D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr19:9578368 G>A maps to NM_152476.2 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr19:9578938 G>A maps to NM_152476.2 C228C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:9578712 G>A maps to NM_152476.2 Q304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr19:9577720 C>T maps to NM_152476.2 G634G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:9580357 G>A maps to NM_152476.2 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr19:9585961 G>A maps to NM_152476.2 Q10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:9584929 C>T maps to NM_152476.2 Q34Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:9578224 C>T maps to NM_152476.2 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:9581122 C>T maps to NM_152476.2 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:9581122 C>T maps to NM_152476.2 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:9579813 A>G maps to NM_152476.2 N193N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:9578869 G>A maps to NM_152476.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:9585961 G>A maps to NM_152476.2 Q10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr19:9579840 G>A maps to NM_152476.2 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:9577648 A>T maps to NM_152476.2 C658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:9579863 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr19:9579858 C>T maps to NM_152476.2 W178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9577795 G>A maps to NM_152476.2 F609F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9578101 C>T maps to NM_152476.2 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9578781 G>A maps to NM_152476.2 Q281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:9581066 C>T did not map to a codon.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr19:9578749 G>A maps to NM_152476.2 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JN-06A-11D-A196-08 chr19:9724726 C>T maps to NM_152289.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:9724726 C>T maps to NM_152289.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29P-06A-11D-A197-08 chr19:9764377 G>A maps to NM_001130032.1 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:9768811 C>T did not map to a codon.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:12430285 G>A maps to NM_145276.2 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:12430397 C>T maps to NM_145276.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr19:12430405 G>A maps to NM_145276.2 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr19:12638116 G>A maps to NM_144976.3 R269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I2-06A-21D-A19A-08 chr19:12638474 G>A maps to NM_144976.3 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr19:12637886 G>A maps to NM_144976.3 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:12638051 G>A maps to NM_144976.3 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:36940498 T>G maps to NM_001145343.1 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr19:37210564 A>G maps to ENST00000423498 E312E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:37211305 C>T maps to ENST00000423498 S559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:37210765 C>T maps to ENST00000423498 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr19:37440579 C>T maps to NM_198539.2 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr19:37441923 C>T maps to NM_198539.2 F623F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:37440438 C>T maps to NM_198539.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr19:37440438 C>T maps to NM_198539.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr19:37905193 T>C maps to NM_152484.2 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:37904620 G>A maps to NM_152484.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:37904470 G>A maps to NM_152484.2 F363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:37917217 A>G maps to NM_152484.2 D26D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:37904032 G>A maps to NM_152484.2 F509F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:37905285 G>A maps to NM_152484.2 Q92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:37904944 C>T maps to NM_152484.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr19:2917839 C>T maps to NM_173480.2 F407F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:38057120 C>T maps to NM_016536.3 W70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr8:125989787 C>T maps to NM_152412.2 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr8:125989877 C>T maps to NM_152412.2 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr8:125989826 T>C maps to NM_152412.2 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr8:125989922 C>T maps to NM_152412.2 T471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:125989805 G>A maps to NM_152412.2 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:38229710 C>T maps to NM_001172690.1 G560G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:38229710 C>T maps to NM_001172690.1 G560G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:38229536 G>A maps to NM_001172690.1 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:42583792 C>T maps to ENST00000222339 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:42584104 G>A maps to ENST00000222339 E539E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:42583204 C>A maps to ENST00000222339 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:52375985 G>A maps to NM_032679.2 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr19:52376885 G>A maps to NM_032679.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr19:52376080 C>A maps to NM_032679.2 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:52376321 G>A maps to NM_032679.2 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:52381753 G>A maps to NM_032679.2 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:53014260 G>A maps to NM_001099694.1 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:53015109 C>T maps to NM_001099694.1 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:53014272 C>T maps to NM_001099694.1 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr19:53014518 C>T maps to NM_001099694.1 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr19:53014212 C>T maps to NM_001099694.1 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:53008017 G>A maps to NM_001099694.1 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:53014272 C>T maps to NM_001099694.1 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:53015055 G>A maps to NM_001099694.1 K474K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:53015325 G>A maps to NM_001099694.1 E564E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:53015025 C>T maps to NM_001099694.1 F464F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr19:56090015 G>C maps to NM_152600.2 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:56090039 G>A maps to NM_152600.2 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56090168 G>A maps to NM_152600.2 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr19:56156050 C>T maps to NM_016535.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr19:56896236 C>T maps to NM_144690.1 K183K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr19:56896335 G>A maps to NM_144690.1 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:56895387 G>A maps to NM_144690.1 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:56895603 G>A maps to NM_144690.1 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:56895747 C>T maps to NM_144690.1 K346K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:58929093 C>T maps to NM_173548.1 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:58928496 C>T maps to NM_173548.1 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr19:58928728 C>T maps to NM_173548.1 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr19:37643894 G>A maps to ENST00000356958 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:37642628 C>T maps to ENST00000356958 G724G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:37643681 C>T maps to ENST00000356958 Q373Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:37643777 G>A maps to ENST00000356958 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr19:37644011 G>A maps to ENST00000356958 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr19:37643287 G>A maps to ENST00000356958 Q505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:37642535 G>A maps to ENST00000356958 F755F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:37643783 G>A maps to ENST00000356958 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:37644019 G>A maps to ENST00000356958 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:37644218 G>A maps to ENST00000356958 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:37643777 G>A maps to ENST00000356958 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr19:37644194 G>A maps to ENST00000356958 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:37644470 G>A maps to ENST00000356958 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr19:37677418 G>A maps to NM_152279.3 N340N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr19:37676995 G>A maps to NM_152279.3 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:37676239 C>T maps to NM_152279.3 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:37677597 G>A maps to NM_152279.3 Q281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:37677181 G>A maps to NM_152279.3 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:37676169 G>A maps to NM_152279.3 Q757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:37678108 G>A maps to NM_152279.3 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr19:37680974 G>A maps to NM_152279.3 N50N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:37677769 G>A maps to NM_152279.3 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:37697980 G>A maps to NM_152279.3 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr19:58290771 C>T maps to NM_017652.2 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:58290785 C>T maps to NM_017652.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr19:58288008 G>T maps to NM_017652.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:58370727 T>C maps to NM_032828.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:58367557 C>T maps to NM_032828.2 Y40Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr15:85334078 G>A maps to NM_014630.2 E788E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr15:85326895 G>A maps to NM_014630.2 K330K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr15:85327837 C>T maps to NM_014630.2 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr15:85341192 C>T maps to NM_014630.2 F831F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr15:85327174 G>A maps to NM_014630.2 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr15:85341835 C>T maps to NM_014630.2 P918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:85326412 C>T maps to NM_014630.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr15:85341985 C>T maps to NM_014630.2 A968A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:85327597 C>T maps to NM_014630.2 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:85327799 C>T maps to NM_014630.2 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:85327813 C>T maps to NM_014630.2 A636A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:85326274 C>T maps to NM_014630.2 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr17:5085337 A>T maps to NM_032530.1 C738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr17:5087257 G>A maps to NM_032530.1 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr17:5085352 C>T maps to NM_032530.1 E733E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr17:5087374 G>A maps to NM_032530.1 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr17:5086141 G>A maps to NM_032530.1 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr17:5085532 G>A maps to NM_032530.1 I673I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:5086308 G>A maps to NM_032530.1 Q415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:5087335 G>A maps to NM_032530.1 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr17:5085328 G>A maps to NM_032530.1 T741T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr4:59414 G>A maps to NM_182524.2 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr4:59327 C>T maps to NM_182524.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr4:60036 A>T maps to NM_182524.2 K73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr4:59432 G>A maps to NM_182524.2 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr4:59441 C>T maps to NM_182524.2 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JL-06A-11D-A196-08 chr8:195561 C>T maps to NM_001042416.1 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:192970 C>T maps to NM_001042416.1 Q33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:3486990 C>T maps to NM_152457.1 K236K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr16:3487538 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr16:2049608 G>A maps to ENST00000431526 P647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr16:2049599 G>A maps to ENST00000431526 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:2049617 C>T maps to ENST00000431526 R644R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr16:2050130 G>A maps to ENST00000431526 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:2050211 G>A maps to ENST00000431526 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:2049524 G>A maps to ENST00000431526 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:2050067 G>A maps to ENST00000431526 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr19:35251393 G>A maps to NM_001007248.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:35251314 G>A maps to NM_001007248.2 Q131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:35250154 G>A maps to NM_001007248.2 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:35250982 A>G maps to NM_001007248.2 D241D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr19:35258236 G>A maps to NM_001007248.2 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:35251314 G>A maps to NM_001007248.2 Q131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:53270330 G>A maps to NM_198457.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr19:53269235 G>A maps to NM_198457.2 F591F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:53269037 C>T maps to NM_198457.2 R657R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:53268875 G>A maps to NM_198457.2 H711H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:53269439 C>T maps to NM_198457.2 E523E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr12:133502372 G>A maps to NM_001164715.1 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:58490385 G>A maps to NM_025027.3 A554A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:58490540 G>A maps to NM_025027.3 Q503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:58490820 G>A maps to NM_025027.3 F409F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:58500039 C>T maps to NM_025027.3 W76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:58511241 G>A maps to NM_025027.3 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:58491077 G>A maps to NM_025027.3 Q324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr19:58490715 C>T maps to NM_025027.3 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:38190770 G>A maps to NM_032689.4 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:38190443 G>A maps to NM_032689.4 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:38189015 G>A maps to NM_032689.4 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:38200708 G>A maps to NM_032689.4 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:38189498 C>T maps to NM_032689.4 G511G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J7-06A-11D-A196-08 chr5:123984195 G>A maps to NM_020747.2 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr5:123983747 G>A maps to NM_020747.2 Q777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr5:123977035 G>A maps to NM_020747.2 S1453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6E9-06A-12D-A30X-08 chr15:64791705 G>T maps to NM_015042.1 G30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr15:64968299 T>C maps to NM_015042.1 L1083L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr15:64967428 C>G maps to NM_015042.1 A792A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr15:64968416 C>A maps to NM_015042.1 R1122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr15:64968227 C>T maps to NM_015042.1 L1059L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr15:64791938 C>T maps to NM_015042.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr15:64972382 G>A did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr15:64967026 C>T maps to NM_015042.1 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr19:52857507 C>T maps to NM_001161425.1 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr19:53208330 G>A maps to NM_001161500.1 F659F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:53208330 G>A maps to NM_001161500.1 F659F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr19:53209791 G>A maps to NM_001161500.1 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr19:52447894 C>T maps to NM_001031721.3 N253N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr19:52448380 C>T maps to NM_001031721.3 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:52448548 C>T maps to NM_001031721.3 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr19:52447375 C>T maps to NM_001031721.3 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:52519473 T>C maps to NM_025040.3 E459E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr19:52521668 G>A maps to NM_025040.3 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:52521632 G>A maps to NM_025040.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:52521669 G>A maps to NM_025040.3 N31N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29Q-06A-11D-A197-08 chr19:52497836 G>A maps to ENST00000354939 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A0-06A-11D-A196-08 chr19:52496213 C>T maps to ENST00000354939 E716E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:52505119 G>A maps to ENST00000354939 R62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19E-06A-11D-A197-08 chr19:52497017 G>A maps to ENST00000354939 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19Q-06A-11D-A197-08 chr19:52496597 T>C maps to ENST00000354939 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:52497353 G>A maps to ENST00000354939 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:52619837 G>A maps to NM_178523.3 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:52618570 G>A maps to NM_178523.3 Q616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr19:52619036 G>A maps to NM_178523.3 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr19:52619218 G>A maps to NM_178523.3 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr19:52618799 A>G maps to NM_178523.3 H539H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr9:116812056 C>T maps to ENST00000374126 I825I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr9:116812002 C>T maps to ENST00000374126 I807I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr9:116812252 C>T maps to ENST00000374126 Q891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr9:116812372 C>T maps to ENST00000374126 L931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr9:116770805 C>T maps to ENST00000374126 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr3:40528402 C>T maps to NM_001145082.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr3:40523355 C>T maps to NM_001145082.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr3:40529674 C>T maps to NM_001145082.2 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:40529674 C>T maps to NM_001145082.2 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr3:40558203 C>T maps to NM_175888.2 F373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr3:40571736 C>T maps to NM_001098414.1 H63H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:40574104 C>T maps to NM_001098414.1 Q282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr5:16451854 G>A maps to NM_033414.2 Q449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr5:16451854 G>A maps to NM_033414.2 Q449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr5:16453242 G>A maps to NM_033414.2 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr8:144732968 C>T maps to NM_014789.3 H309H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr8:144733463 C>T maps to NM_014789.3 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr8:144732243 C>T maps to NM_014789.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr8:144733648 T>A maps to NM_014789.3 L536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:16525964 G>A maps to NM_020787.3 I745I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr17:16527670 T>G maps to NM_020787.3 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr17:16527374 G>A maps to NM_020787.3 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr17:16527593 G>A maps to NM_020787.3 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:12256663 T>C maps to ENST00000439556 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:12256822 T>C maps to ENST00000439556 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr19:20829088 G>A maps to NM_001076675.2 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr19:20808397 G>A maps to NM_001076675.2 F95F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EE-A2MD-06A-11D-A197-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:20808004 C>T maps to NM_001076675.2 E226E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:20829175 G>A maps to NM_001076675.2 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:20829124 C>T maps to NM_001076675.2 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:20807500 C>T maps to NM_001076675.2 E394E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:20807785 G>T maps to NM_001076675.2 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:11725376 C>T maps to NM_145295.3 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr19:55992907 C>T maps to NM_033113.2 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr19:55992908 C>T maps to NM_033113.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:55994797 C>T maps to NM_033113.2 P742P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr19:55993030 C>T maps to NM_033113.2 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr16:30794742 G>A maps to NM_001080417.1 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr16:30793709 G>A maps to NM_001080417.1 Q647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZU-06A-12D-A196-08 chr16:30794343 G>A maps to NM_001080417.1 C435C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:30794043 G>A maps to NM_001080417.1 I535I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr23:47918857 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:47918759 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:47918760 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr23:47918540 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:47918961 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:47918962 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr23:47918843 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:47918213 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:47919158 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZJ-06A-12D-A197-08 chr23:47919834 A>T did not map to a codon.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr23:47918589 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:71576995 C>T maps to NM_014497.3 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr2:71576894 C>T maps to NM_014497.3 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:71591275 C>T maps to NM_014497.3 S537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr2:71655767 C>T maps to NM_014497.3 F1879F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:71576267 C>T maps to NM_014497.3 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr2:71591242 C>T maps to NM_014497.3 C526C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr2:71576657 C>T maps to NM_014497.3 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr2:71591281 C>T maps to NM_014497.3 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr3:179051055 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr12:48736791 G>A maps to NM_152320.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr1:40947507 C>T maps to NM_198494.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr1:40928600 C>T maps to NM_023070.2 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr1:40928285 C>T maps to NM_023070.2 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:40928259 C>T maps to NM_023070.2 Q202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:40922630 C>T maps to NM_023070.2 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J4-06A-11D-A20D-08 chr1:91403150 G>A maps to NM_201269.1 I1193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr1:91405829 G>A maps to NM_201269.1 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51F-06A-11D-A25O-08 chr23:22291978 C>T did not map to a codon.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr23:22291888 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:22291920 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr23:22291567 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:22292215 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:22291288 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:22292035 C>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:22292285 G>A did not map to a codon.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr23:22291916 C>T did not map to a codon.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr23:22292061 G>A did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr16:31087779 T>C maps to NM_014699.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr16:31091382 G>A maps to NM_014699.3 K1246K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr16:31087995 C>T maps to NM_014699.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:31090314 C>T maps to NM_014699.3 F890F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr16:31091617 C>T maps to NM_014699.3 Q1325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr16:31089711 C>T maps to NM_014699.3 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:31092306 A>C maps to NM_014699.3 T1554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr16:31088661 G>A maps to NM_014699.3 E339E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr16:31089889 C>T maps to NM_014699.3 Q749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr16:31092699 C>T maps to NM_014699.3 S1685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr16:31092342 C>T maps to NM_014699.3 F1566F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr16:31091181 G>A maps to NM_014699.3 G1179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr16:31089325 G>T maps to NM_014699.3 E561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr16:31088166 G>A maps to NM_014699.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr1:182026902 G>A maps to NM_001009992.1 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:182025597 G>A maps to NM_001009992.1 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:182025606 G>A maps to NM_001009992.1 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:182025747 G>A maps to NM_001009992.1 H466H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr19:52394232 T>A maps to NM_023074.3 K386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr17:47394240 G>A maps to NM_014897.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr17:47394652 A>G maps to NM_014897.2 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr19:11609135 G>A maps to NM_138783.3 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr19:11606795 G>A maps to NM_138783.3 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr19:11596513 G>A maps to NM_138783.3 F509F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U8-06A-11D-A32N-08 chr19:11594517 G>A maps to NM_138783.3 H609H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr3:88189573 A>T maps to NM_018293.2 K372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:88189137 C>G maps to NM_018293.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29T-06A-11D-A197-08 chr7:99169342 C>T maps to NM_001083956.1 Q57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:99169386 T>A maps to NM_001083956.1 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr9:40774473 C>A maps to NM_033160.5 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:40772475 C>T maps to NM_033160.5 T933T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr9:40772610 C>T maps to NM_033160.5 G888G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JE-06A-11D-A20D-08 chr9:40773138 T>C maps to NM_033160.5 K712K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr9:40772825 G>A maps to NM_033160.5 Q817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr9:40774548 G>A maps to NM_033160.5 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:44635927 G>A maps to NM_173658.1 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr3:42956296 G>A maps to NM_001134656.1 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr3:42956671 C>T maps to NM_001134656.1 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AD-06A-11D-A196-08 chr3:42956120 C>T maps to NM_001134656.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr3:42956041 C>T maps to NM_001134656.1 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:42956098 C>T maps to NM_001134656.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr12:124497311 C>T maps to NM_152437.1 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr12:124496839 G>A maps to NM_152437.1 W50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:53669478 G>A maps to NM_024733.3 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:53669100 G>A maps to NM_024733.3 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:53678752 C>T maps to NM_024733.3 Q29Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr19:53668428 G>A maps to NM_024733.3 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:53667725 G>A maps to NM_024733.3 R673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A5DY-06A-11D-A30X-08 chr19:53668998 G>A maps to NM_024733.3 N248N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:53678727 A>G maps to NM_024733.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr19:56952565 G>A maps to ENST00000342634 R728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr19:56952653 A>T maps to ENST00000342634 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:56953382 C>T maps to ENST00000342634 E455E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:56953340 C>T maps to ENST00000342634 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:56973721 C>T maps to ENST00000342634 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:56953163 G>A maps to ENST00000342634 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:56973709 G>T maps to ENST00000342634 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56953493 G>A maps to ENST00000342634 F418F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D3-A2J8-06A-11D-A196-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-D3-A51T-06A-11D-A25O-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr16:31075147 G>A maps to NM_001172669.1 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr16:31072477 C>A maps to NM_001172669.1 E614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr16:31072631 C>T maps to NM_001172669.1 P562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr1:247264611 G>A maps to NM_024804.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:247265088 G>A maps to NM_024804.2 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr1:247201302 G>A maps to NM_033213.3 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GL-06A-11D-A27K-08 chr1:247201646 G>A maps to NM_033213.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr1:247201206 A>G maps to NM_033213.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr1:247200867 G>A maps to NM_033213.3 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19S-06A-11D-A196-08 chr1:247202173 T>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr1:247200783 G>A maps to NM_033213.3 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:247202115 G>A maps to NM_033213.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:58234582 C>T maps to ENST00000335820 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:58231850 A>T maps to NM_024833.2 *535K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr1:249141904 C>T maps to NM_024836.1 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr1:249142579 C>T maps to NM_024836.1 C369C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:46388339 G>A did not map to a codon.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr23:46359366 A>G did not map to a codon.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:23837301 G>A maps to NM_138330.2 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:23836474 T>C maps to NM_138330.2 G420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:23836762 G>A maps to NM_138330.2 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:22364140 T>C maps to NM_001001411.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:22363198 C>T maps to NM_001001411.2 K440K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:22363786 C>T maps to NM_001001411.2 K244K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:22363618 C>T maps to NM_001001411.2 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr19:22364329 G>A maps to NM_001001411.2 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:22362850 A>T maps to NM_001001411.2 T556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr19:22362961 G>A maps to NM_001001411.2 I519I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:22362967 G>A maps to NM_001001411.2 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:22375877 G>A maps to NM_001001411.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:22363476 G>A maps to NM_001001411.2 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr19:22363812 G>A maps to NM_001001411.2 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:22363954 C>T maps to NM_001001411.2 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:22363936 C>T maps to NM_001001411.2 E194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr19:22364053 G>A maps to NM_001001411.2 H155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr19:22363801 G>A maps to NM_001001411.2 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr19:53740998 G>A maps to NM_182609.2 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr19:53741667 A>C maps to NM_182609.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:53754790 G>A maps to NM_182609.2 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GB-06A-11D-A197-08 chr19:53747072 G>A maps to NM_182609.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:53741051 G>A maps to NM_182609.2 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:227843246 C>T maps to NM_178549.3 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A4EO-06A-12D-A24R-08 chr1:227843162 C>T maps to NM_178549.3 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr7:63726688 C>T maps to NM_153363.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr7:63726943 C>T maps to NM_153363.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:63726505 C>T maps to NM_153363.2 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:63726871 G>A maps to NM_153363.2 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:63726289 C>T maps to NM_153363.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A267-06A-21D-A196-08 chr7:63727141 G>A maps to NM_153363.2 E377E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr19:23937643 C>T maps to NM_138286.2 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A6L9-06A-11D-A32N-08 chr19:23926950 T>C maps to NM_138286.2 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:23926752 G>A maps to NM_138286.2 P533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:23938317 G>A maps to NM_138286.2 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:23938329 C>T maps to NM_138286.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:23926505 T>A maps to NM_138286.2 K616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:23937628 G>A maps to NM_138286.2 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:20117128 C>T maps to NM_033196.2 E394E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr19:20135110 C>T maps to NM_033196.2 Q26Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:20117875 G>A maps to NM_033196.2 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:20117308 G>A maps to NM_033196.2 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YN-06A-11D-A23B-08 chr19:20117857 C>T maps to NM_033196.2 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:20117431 C>A maps to NM_033196.2 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:20117875 G>A maps to NM_033196.2 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A3OT-06A-23D-A23B-08 chr19:20117515 G>A maps to NM_033196.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr1:26691130 G>A maps to ENST00000436292 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr1:26694969 G>A maps to ENST00000436292 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr1:26691376 G>A maps to ENST00000436292 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr1:26691025 G>A maps to ENST00000436292 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:26691382 G>A maps to ENST00000436292 H218H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:26691667 G>A maps to ENST00000436292 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:26689561 C>T maps to ENST00000436292 Q366Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr1:26694126 C>T maps to ENST00000436292 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr1:41012516 C>T maps to NM_152373.3 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:41012345 C>T maps to NM_152373.3 H117H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr1:41006292 C>T maps to NM_152373.3 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr1:151261176 A>G maps to NM_020832.1 G763G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr16:30581395 G>A maps to NM_145271.3 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:30581395 G>A maps to NM_145271.3 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:249151505 G>A maps to NM_001136036.2 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:247150634 G>A maps to NM_020394.3 Y394Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr1:247151497 G>A maps to NM_020394.3 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr1:247151498 G>A maps to NM_020394.3 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr1:247151423 C>A maps to NM_020394.3 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:247151347 G>A maps to NM_020394.3 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr1:247151441 C>T maps to NM_020394.3 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr8:144378411 C>T maps to NM_030895.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr8:144378534 C>T maps to NM_030895.2 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:120165657 G>A maps to NM_001080470.1 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr19:9407284 G>A maps to NM_198535.1 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:9406612 G>A maps to NM_198535.1 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr19:9406188 G>A maps to NM_198535.1 R631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:9406741 G>A maps to NM_198535.1 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:9407452 G>A maps to NM_198535.1 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr8:146066809 G>A maps to ENST00000446747 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr22:24086712 G>A maps to NM_021916.2 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr22:24086676 G>A maps to NM_021916.2 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr22:24086046 G>A maps to NM_021916.2 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:12060845 G>A maps to NM_144566.1 K669K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:12058371 C>T maps to NM_144566.1 N78N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MH-06A-11D-A197-08 chr19:12060221 T>A maps to NM_144566.1 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19N-06A-11D-A197-08 chr19:12059186 G>A maps to NM_144566.1 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:53085899 C>T maps to NM_001172655.1 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:53086148 C>T maps to NM_001172655.1 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr8:81582745 G>A maps to NM_001033723.2 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr12:8329764 A>G maps to NM_001004328.2 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr12:8329983 C>T maps to NM_001004328.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr12:8330137 C>T maps to NM_001004328.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr8:102212259 A>T maps to NM_016096.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr8:144773286 G>A maps to NM_173831.3 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:21476171 G>A maps to NM_021269.2 Y532Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:21477442 G>A maps to NM_021269.2 Q109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:21476498 T>C maps to NM_021269.2 E423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:12574841 G>A maps to ENST00000428311 R632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:12576516 C>T maps to ENST00000428311 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr19:12576105 G>A maps to ENST00000428311 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:12575349 G>A maps to ENST00000428311 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:12575849 G>A maps to ENST00000428311 R296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:12576269 G>A maps to ENST00000428311 R156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:57133716 C>T maps to NM_021216.4 F354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:57133359 C>T maps to NM_021216.4 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr19:57133779 C>T maps to NM_021216.4 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:57133998 C>T maps to NM_021216.4 I448I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:57134053 C>T maps to NM_021216.4 R467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr15:90610491 G>A maps to NM_198526.2 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr15:90610515 C>T maps to NM_198526.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr15:90611619 C>T maps to NM_198526.2 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q3-06A-11D-A196-08 chr23:84526176 A>G did not map to a codon.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr23:84510571 C>T did not map to a codon.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr23:84520131 G>A did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:84526096 C>T did not map to a codon.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr23:84526217 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:84502581 G>A did not map to a codon.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:84520254 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:84526288 C>T did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:84526393 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:84526826 T>C did not map to a codon.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:84525119 G>A did not map to a codon.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr23:84525728 C>T did not map to a codon.
Sequencing variant TCGA-EB-A44Q-06A-11D-A25O-08 chr23:84525722 T>G did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:84526384 C>T did not map to a codon.
Sequencing variant TCGA-EE-A17Y-06A-11D-A196-08 chr23:84526006 G>A did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:84510302 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr23:84526399 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr23:84526399 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr23:84520195 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:84526435 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr23:84526690 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:84526399 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr23:84502637 C>T did not map to a codon.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr23:84526504 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr23:84520259 C>T did not map to a codon.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr23:84525691 G>A did not map to a codon.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr23:84526325 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr23:84510571 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr23:84526084 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr23:84526623 A>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZU-06A-12D-A196-08 chr23:84526575 G>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:84526399 C>T did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:84526584 A>T did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:84510500 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:84520206 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:84523311 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr23:84526468 C>T did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:84520254 G>A did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:84525025 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr7:56007332 C>T maps to NM_182633.1 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr7:56007167 C>T maps to NM_182633.1 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:56007623 C>T maps to NM_182633.1 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZS-06A-12D-A197-08 chr7:56006849 G>A maps to NM_182633.1 K148K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:55990880 C>T maps to NM_182633.1 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TV-06A-11D-A23B-08 chr7:56007350 C>T maps to NM_182633.1 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MV-06A-11D-A21A-08 chr19:21300027 C>T maps to NM_182515.3 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:21299950 C>T maps to NM_182515.3 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr19:21300876 A>G maps to NM_182515.3 K469K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NE-06A-21D-A196-08 chr19:21300564 G>A maps to NM_182515.3 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q4-06A-11D-A196-08 chr7:57510014 C>T maps to NM_001159279.1 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr7:57522257 G>A maps to NM_001159279.1 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:57528638 C>T maps to NM_001159279.1 Q158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr7:57529180 C>T maps to NM_001159279.1 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:57529219 C>T maps to NM_001159279.1 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr7:57522869 C>T maps to NM_001159279.1 H86H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A199-06A-11D-A197-08 chr7:57522874 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:57529186 G>A maps to NM_001159279.1 K340K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:57529547 G>T maps to NM_001159279.1 E461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr4:435915 G>A maps to NM_133474.2 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:436611 C>T maps to NM_133474.2 R548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr4:289908 G>A maps to ENST00000419098 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:265952 G>A maps to ENST00000419098 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr4:266375 C>T maps to ENST00000419098 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr4:289847 A>G maps to ENST00000419098 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:63796755 C>T maps to NM_001170905.1 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:63809131 C>T maps to NM_001170905.1 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:20736518 G>A maps to NM_001159293.1 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:20736554 C>T maps to NM_001159293.1 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:20727910 C>T maps to NM_001159293.1 E366E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr19:20728762 G>A maps to NM_001159293.1 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr22:20760066 C>T maps to NM_003426.2 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr22:20760717 C>T maps to NM_003426.2 I465I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr22:20760621 C>T maps to NM_003426.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr22:20759961 C>T maps to NM_003426.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:20760276 C>T maps to NM_003426.2 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr22:20760870 C>T maps to NM_003426.2 I516I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr22:20760870 C>T maps to NM_003426.2 I516I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr7:149171708 G>A maps to NM_001163474.1 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr7:149172260 G>A maps to NM_001163474.1 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MF-06A-11D-A21A-08 chr7:149191300 G>A maps to NM_001163474.1 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr7:149172481 G>A maps to NM_001163474.1 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr7:149191333 G>A maps to NM_001163474.1 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr7:149172350 C>T maps to NM_001163474.1 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:57955632 C>T maps to NM_001023561.2 Q373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:57955355 A>G maps to NM_001023561.2 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr19:57956042 G>A maps to NM_001023561.2 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:57956102 T>C maps to NM_001023561.2 H529H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:80788494 C>T maps to NM_024702.2 R565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr17:80790093 G>T maps to NM_024702.2 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr17:80789223 G>A maps to NM_024702.2 D369D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr16:3367221 C>T maps to NM_153028.2 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I5-06A-11D-A197-08 chr23:134426374 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr23:134424997 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MK-06A-11D-A196-08 chr23:134421365 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr23:134421468 G>A did not map to a codon.
Sequencing variant TCGA-FS-A1YY-06A-11D-A197-08 chr23:134421643 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr23:134427837 A>G did not map to a codon.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr23:134427865 G>A did not map to a codon.
Sequencing variant TCGA-D3-A2JP-06A-11D-A19A-08 chr6:35258482 C>T maps to NM_003427.3 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr6:35261548 C>T maps to NM_003427.3 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr6:35259166 C>T maps to NM_003427.3 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:53952799 C>T maps to NM_001008401.3 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr19:53959620 C>T maps to NM_001008401.3 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:53958447 C>T maps to NM_001008401.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:12089446 C>T maps to NM_001012753.1 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:52785398 C>T maps to NM_001010851.2 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:30536227 G>A maps to NM_024671.3 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:30536877 G>A maps to NM_024671.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr16:30536352 C>A maps to NM_024671.3 E370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:30536500 G>A maps to NM_024671.3 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr16:30536827 G>A maps to NM_024671.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr16:30536913 T>A maps to NM_024671.3 K183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:30536386 G>A maps to NM_024671.3 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr19:2933774 G>A maps to NM_021217.2 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:2936549 G>A maps to NM_021217.2 Q95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:2936610 G>A maps to NM_021217.2 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:57984884 G>A maps to NM_001024596.2 I409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19J-06A-11D-A196-08 chr19:57984992 A>T maps to NM_001024596.2 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr19:58016026 G>A maps to NM_198542.1 Q12Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20F-06A-21D-A196-08 chr19:58018620 T>G maps to NM_198542.1 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:58016718 G>A maps to NM_198542.1 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr15:90902175 G>A maps to NM_001004309.2 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr15:90897933 C>T maps to NM_001004309.2 H14H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr7:150095104 C>T maps to NM_173680.3 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3EV-06A-11D-A20D-08 chr7:150094915 C>T maps to NM_173680.3 N449N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr7:150093760 G>A maps to NM_173680.3 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr19:58265664 C>T maps to NM_173632.3 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q1-06A-21D-A196-08 chr7:149128938 G>T maps to ENST00000440594 C809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr7:149133840 G>A maps to ENST00000440594 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:149152684 G>A maps to ENST00000440594 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr7:149152509 G>A maps to ENST00000440594 Q202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr7:149152756 G>A maps to ENST00000440594 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A195-06A-11D-A196-08 chr7:149128997 G>A maps to ENST00000440594 Q790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:149129187 G>A maps to ENST00000440594 P726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr7:149129697 G>A maps to ENST00000440594 F556F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr7:149153028 G>A maps to ENST00000440594 R29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr16:89294741 C>T maps to NM_182531.2 F654F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:89293787 C>T maps to NM_182531.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr16:89294609 C>T maps to NM_182531.2 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr16:89289674 G>A maps to NM_182531.2 E76E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:89293397 C>T maps to NM_182531.2 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:40540275 G>A maps to NM_001005851.2 F830F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr19:40540275 G>A maps to NM_001005851.2 F830F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NF-06A-11D-A19A-08 chr19:40540451 G>A maps to NM_001005851.2 Q772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:40540617 G>A maps to NM_001005851.2 Y716Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:40541301 A>G maps to NM_001005851.2 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:38160066 T>G maps to NM_152605.3 *328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:38160476 G>T maps to NM_152605.3 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr19:38160383 G>A maps to NM_152605.3 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr9:99581464 G>A maps to NM_001001662.1 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr9:99580356 G>A maps to NM_001001662.1 Q650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:56133907 C>A maps to NM_203374.1 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:30596533 C>T maps to NM_152458.6 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:30594027 G>A maps to NM_152458.6 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:148767727 G>A maps to NM_152411.3 N712N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr7:148769368 G>A maps to NM_152411.3 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr7:148769368 G>A maps to NM_152411.3 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr7:148768477 G>A maps to NM_152411.3 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr7:148769494 G>A maps to NM_152411.3 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr7:148769062 G>A maps to NM_152411.3 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:148767688 G>A maps to NM_152411.3 I725I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:148767553 G>A maps to NM_152411.3 L770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr7:148768945 G>T maps to NM_152411.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr7:148768084 G>A maps to NM_152411.3 F593F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:56600429 G>A maps to NM_001002836.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr19:56599601 C>T maps to NM_001002836.2 E313E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr7:99084288 G>A maps to NM_213603.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr9:130197475 C>T maps to NM_007135.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr9:130206773 C>A maps to NM_007135.2 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr19:37309762 G>A maps to NM_206894.2 R495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MP-06A-11D-A197-08 chr19:37314680 G>A maps to NM_206894.2 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:12738684 C>T maps to NM_153358.2 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:12739545 C>T maps to NM_153358.2 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:12738594 C>T maps to NM_153358.2 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:12739938 C>T maps to NM_153358.2 A532A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:12740040 C>T maps to NM_153358.2 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51E-06A-11D-A25O-08 chr19:35450230 G>A maps to NM_175872.4 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29G-06A-12D-A196-08 chr19:35449030 G>A maps to NM_175872.4 T576T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JB-06A-11D-A21A-08 chr19:35450200 G>A maps to NM_175872.4 N186N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:35449720 G>A maps to NM_175872.4 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:35450245 G>A maps to NM_175872.4 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A262-06A-11D-A196-08 chr19:35450179 G>A maps to NM_175872.4 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr19:35449465 G>A maps to NM_175872.4 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:35449302 A>G maps to NM_175872.4 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:38028150 C>T maps to NM_001013659.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:38024237 C>T maps to NM_001013659.2 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:38024234 G>A maps to NM_001013659.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:38028069 G>A maps to NM_001013659.2 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:12501360 T>C maps to NM_001080821.2 G617G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr19:12503427 C>T maps to NM_001080821.2 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr19:12502344 G>A maps to NM_001080821.2 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:12502326 G>A maps to NM_001080821.2 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:58806334 C>T maps to NM_021089.2 H387H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:58797123 G>A maps to NM_021089.2 Q36Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr3:113955852 G>A maps to NM_007136.3 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr3:113955645 G>A maps to NM_007136.3 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr3:113955648 G>A maps to NM_007136.3 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr3:113955132 C>T maps to NM_007136.3 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr3:113955474 G>A maps to NM_007136.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr7:127013994 A>T maps to NM_176814.3 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr2:185802258 G>A maps to NM_194250.1 G712G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JD-06A-11D-A19A-08 chr2:185798352 G>A maps to NM_194250.1 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:185798352 G>A maps to NM_194250.1 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr2:185800740 G>A maps to NM_194250.1 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr2:185802723 G>A maps to NM_194250.1 R867R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr2:185802687 G>A maps to NM_194250.1 E855E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr2:185801484 C>T maps to NM_194250.1 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:185801065 C>T maps to NM_194250.1 Q315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr2:185802430 C>T maps to NM_194250.1 R770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr2:185800848 G>A maps to NM_194250.1 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr2:185802567 A>G maps to NM_194250.1 K815K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr2:185801539 C>T maps to NM_194250.1 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z3-06A-11D-A23B-08 chr2:185800758 C>T maps to NM_194250.1 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:185803344 C>T maps to NM_194250.1 L1074L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HW-06A-11D-A19A-08 chr2:185801920 A>T maps to NM_194250.1 K600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:185731148 A>T maps to NM_194250.1 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:185801391 G>A maps to NM_194250.1 E423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:185803674 C>T maps to NM_194250.1 F1184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:185802646 T>C maps to NM_194250.1 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr2:185803416 C>T maps to NM_194250.1 I1098I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr2:185798343 G>A maps to NM_194250.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GT-06A-12D-A197-08 chr2:185803136 T>G maps to NM_194250.1 L1005*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr2:185801340 G>A maps to NM_194250.1 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr2:185802717 C>T maps to NM_194250.1 I865I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr2:185800527 C>T maps to NM_194250.1 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MQ-06A-11D-A197-08 chr2:185731166 C>T maps to NM_194250.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:185800782 G>A maps to NM_194250.1 K220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr2:185802481 C>T maps to NM_194250.1 R787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:185800579 C>T maps to NM_194250.1 Q153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr2:185802717 C>T maps to NM_194250.1 I865I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr2:185802979 C>T maps to NM_194250.1 Q953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr2:185803389 C>T maps to NM_194250.1 S1089S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr2:185802717 C>T maps to NM_194250.1 I865I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZY-06A-11D-A197-08 chr2:185798352 G>A maps to NM_194250.1 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr2:185801067 A>G maps to NM_194250.1 Q315Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:185801490 C>T maps to NM_194250.1 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:185801862 A>C maps to NM_194250.1 I580I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:185802258 G>A maps to NM_194250.1 G712G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr2:185803596 G>A maps to NM_194250.1 G1158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr2:185803560 C>T maps to NM_194250.1 L1146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:185798362 C>T maps to NM_194250.1 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr2:185798431 C>T maps to NM_194250.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr2:185802780 C>T maps to NM_194250.1 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr2:185801361 G>A maps to NM_194250.1 K413K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:88963432 G>A maps to NM_181646.2 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr7:88965859 C>T maps to NM_181646.2 A1188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr7:88963945 G>A maps to NM_181646.2 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr7:88965298 G>A maps to NM_181646.2 T1001T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr7:88966267 C>T maps to NM_181646.2 C1324C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr7:88965961 C>T maps to NM_181646.2 S1222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:88962862 C>T maps to NM_181646.2 H189H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:88963819 G>A maps to NM_181646.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr7:88965934 C>T maps to NM_181646.2 F1213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr7:88963762 G>A maps to NM_181646.2 K489K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr19:53058232 C>T maps to NM_001039886.3 F688F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:53058508 C>T maps to NM_001039886.3 Y780Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr19:53056969 C>T maps to NM_001039886.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:53057080 C>T maps to NM_001039886.3 C304C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:53058064 C>T maps to NM_001039886.3 F632F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr23:47755314 G>A did not map to a codon.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr23:47775350 C>G did not map to a codon.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr23:47775141 C>T did not map to a codon.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr23:47747397 G>A did not map to a codon.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr23:47775618 C>T did not map to a codon.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr23:47775870 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr23:47774357 A>G did not map to a codon.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr23:47775929 C>T did not map to a codon.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr23:47776022 C>T did not map to a codon.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr23:47774408 G>A did not map to a codon.
Sequencing variant TCGA-FS-A4FD-06A-11D-A25O-08 chr23:47774918 C>T did not map to a codon.
Sequencing variant TCGA-GN-A26A-06A-11D-A19A-08 chr23:47775072 C>T did not map to a codon.
Sequencing variant TCGA-GN-A4U7-06A-21D-A32N-08 chr23:47774788 T>C did not map to a codon.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:53994193 C>T maps to NM_001004301.3 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:53994439 G>A maps to NM_001004301.3 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr19:53994073 C>T maps to NM_001004301.3 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:53994185 C>T maps to NM_001004301.3 Q234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:53994064 G>A maps to NM_001004301.3 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr19:53994185 C>T maps to NM_001004301.3 Q234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:53993858 C>T maps to NM_001004301.3 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:53994931 C>T maps to NM_001004301.3 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr19:58386283 T>C maps to NM_001144989.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19F-06A-11D-A196-08 chr19:58384954 C>T maps to NM_001144989.1 E601E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:53454808 G>A maps to NM_001031665.1 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CB-06A-11D-A196-08 chr19:53456033 A>G maps to NM_001031665.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:53453641 G>A maps to NM_001031665.1 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr19:53454450 G>A maps to NM_001031665.1 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AA-06A-11D-A196-08 chr19:53453515 A>G maps to NM_001031665.1 A504A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr19:53454820 G>A maps to NM_001031665.1 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr16:71895749 G>A maps to ENST00000425432 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr19:11832641 G>A maps to NM_001080493.2 F569F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr19:11833390 G>A maps to NM_001080493.2 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:11833306 G>A maps to NM_001080493.2 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr4:146824017 G>A maps to ENST00000508784 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr4:146824008 G>A maps to ENST00000508784 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:146824218 G>A maps to ENST00000508784 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr4:146824296 C>T maps to ENST00000508784 E38E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr4:146807226 G>A maps to ENST00000508784 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr4:146700652 C>T maps to ENST00000508784 K798K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr4:146823948 G>A maps to ENST00000508784 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr4:146686876 C>T maps to ENST00000508784 K958K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr4:146686279 C>T maps to ENST00000508784 T1030T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr4:146686843 G>A maps to ENST00000508784 S969S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr4:146823837 C>T maps to ENST00000508784 W191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr4:146807043 G>A maps to ENST00000508784 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr4:146824065 G>A maps to ENST00000508784 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr4:146823930 G>A maps to ENST00000508784 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr13:115090945 A>G maps to NM_032436.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr13:115090795 C>T maps to NM_032436.2 F493F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr13:115090555 C>T maps to NM_032436.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr13:115089778 G>T maps to NM_032436.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZP-06A-11D-A197-08 chr13:115089508 C>T maps to NM_032436.2 C64C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr13:115090015 C>T maps to NM_032436.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:37406119 G>A maps to NM_001171979.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C3-06A-12D-A19A-08 chr19:53116512 C>T maps to NM_018300.3 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:53117712 C>T maps to NM_018300.3 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr19:53116287 C>T maps to NM_018300.3 K510K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr17:33289448 C>T maps to NM_052857.3 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr20:57767264 G>A maps to NM_178457.1 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr20:57769664 G>A maps to NM_178457.1 E1197E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr20:57766235 C>T maps to NM_178457.1 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr20:57829602 G>A maps to NM_178457.1 R1613R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr20:57766886 C>T maps to NM_178457.1 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr20:57768374 C>T maps to NM_178457.1 P767P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr20:57781968 G>A maps to NM_178457.1 G1295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr20:57768482 G>A maps to NM_178457.1 Q803Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:57769064 C>T maps to NM_178457.1 S997S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr20:57766490 G>A maps to NM_178457.1 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr20:57767198 G>A maps to NM_178457.1 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr20:57766724 G>A maps to NM_178457.1 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr20:57829626 C>T maps to NM_178457.1 I1621I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr20:57769220 G>A maps to NM_178457.1 R1049R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr20:57828096 A>G maps to NM_178457.1 E1364E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr20:57768584 G>A maps to NM_178457.1 E837E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr20:57766565 G>A maps to NM_178457.1 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr20:57829281 G>A maps to NM_178457.1 Q1506Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr20:57766994 G>C maps to NM_178457.1 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr20:57768440 C>T maps to NM_178457.1 A789A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr20:57768887 C>T maps to NM_178457.1 S938S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr20:57767357 G>A maps to NM_178457.1 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr20:57767777 G>A maps to NM_178457.1 E568E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr20:57766215 C>T maps to NM_178457.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:57766580 G>A maps to NM_178457.1 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr20:57829326 G>A maps to NM_178457.1 G1521G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr20:57768767 G>A maps to NM_178457.1 G898G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:57769145 G>A maps to NM_178457.1 G1024G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr20:57828168 G>A maps to NM_178457.1 R1388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:57766403 C>T maps to NM_178457.1 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:57767402 C>T maps to NM_178457.1 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:57768539 G>A maps to NM_178457.1 R822R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr20:57829572 C>T maps to NM_178457.1 V1603V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr20:57771037 A>T maps to NM_178457.1 K1285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr20:57768674 G>A maps to NM_178457.1 G867G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2J8-06A-11D-A196-08 chr19:57176173 G>A maps to NM_001005850.1 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:57175183 C>T maps to NM_001005850.1 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:57176530 T>G maps to NM_001005850.1 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:57175150 C>T maps to NM_001005850.1 K494K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr19:57176461 T>C maps to NM_001005850.1 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F3-06A-11D-A20D-08 chr19:57175891 G>T maps to NM_001005850.1 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:57175231 G>A maps to NM_001005850.1 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:57175705 G>A maps to NM_001005850.1 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr19:57175855 C>T maps to NM_001005850.1 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr19:57175431 G>A maps to NM_001005850.1 Q401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J7-06A-11D-A20D-08 chr19:57175741 C>T maps to NM_001005850.1 E297E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JA-06A-11D-A20D-08 chr19:57176041 G>A maps to NM_001005850.1 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:57176371 C>T maps to NM_001005850.1 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr19:57175273 G>A maps to NM_001005850.1 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3I3-06A-11D-A21A-08 chr19:57175213 G>A maps to NM_001005850.1 C473C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:57176209 G>A maps to NM_001005850.1 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr19:52659921 G>A maps to NM_001102657.1 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr19:52663787 G>A maps to NM_001102657.1 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr14:102793130 C>T maps to NM_018335.3 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr14:102802154 C>T maps to NM_018335.3 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr19:52569367 T>C maps to NM_001136499.1 R589R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MC-06A-12D-A197-08 chr19:52569736 G>A maps to NM_001136499.1 F466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:52568890 G>A maps to NM_001136499.1 S748S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:52569400 G>A maps to NM_001136499.1 F578F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:12186403 C>T maps to NM_001136501.1 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:12187890 T>C maps to NM_001136501.1 V652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:12184859 C>T maps to NM_001136501.1 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:12184910 T>A maps to NM_001136501.1 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr19:53854515 C>T maps to NM_138374.1 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IA-06A-11D-A196-08 chr19:53855349 G>A maps to NM_138374.1 K474K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:53854515 C>T maps to NM_138374.1 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GP-06A-11D-A197-08 chr19:53856126 C>T maps to NM_138374.1 S733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:53854719 T>A maps to NM_138374.1 C264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr19:53854515 C>T maps to NM_138374.1 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr19:53856225 G>A maps to NM_138374.1 R766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19D-06A-11D-A197-08 chr19:53855688 C>T maps to NM_138374.1 V587V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:53855829 T>C maps to NM_138374.1 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GU-06A-11D-A27K-08 chr19:9874042 C>T maps to NM_001077624.1 Q19Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr19:9869116 G>A maps to NM_001077624.1 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JH-06A-11D-A196-08 chr19:21131568 C>T maps to NM_003429.4 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr19:21117842 C>T maps to NM_003429.4 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:32031755 G>A maps to NM_001137674.1 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:32031893 C>T maps to NM_001137674.1 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr7:149558189 C>T maps to NM_001099220.1 F647F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr7:149544995 C>T maps to NM_001099220.1 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr7:149558090 C>T maps to NM_001099220.1 I614I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A148-06A-11D-A19A-08 chr7:149543276 C>T maps to NM_001099220.1 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr7:149558489 C>T maps to NM_001099220.1 D747D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr7:149558498 C>T maps to NM_001099220.1 I750I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A193-06A-12D-A197-08 chr7:149559257 C>T maps to NM_001099220.1 L1003L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U3-06A-11D-A32N-08 chr7:149557667 C>T maps to NM_001099220.1 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:12155423 G>A maps to NM_001080404.1 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:12155096 C>T maps to NM_001080404.1 G420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:12155159 C>T maps to NM_001080404.1 K399K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr19:20215169 C>T maps to NM_007138.1 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A3Z1-06A-11D-A23B-08 chr19:20229661 C>T maps to ENST00000427401 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:20216028 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr19:20215133 G>A maps to NM_007138.1 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:20229880 G>A maps to NM_007138.1 E506E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr19:20215082 C>T maps to NM_007138.1 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr19:20228854 G>A maps to NM_007138.1 K164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZM-06A-12D-A197-08 chr19:20215082 C>T maps to NM_007138.1 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr19:20215073 C>T maps to NM_007138.1 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:20229964 G>A maps to NM_007138.1 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:20216064 C>T maps to NM_007138.1 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr19:20228765 C>T maps to NM_007138.1 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MU-06A-11D-A21A-08 chr19:23544274 G>A maps to NM_003430.2 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29H-06A-12D-A197-08 chr19:23542933 T>C maps to NM_003430.2 Q949Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GJ-06A-11D-A196-08 chr19:23542381 G>A maps to NM_003430.2 P1133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MT-06A-11D-A197-08 chr19:23544817 G>A maps to NM_003430.2 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr19:23542333 A>G maps to NM_003430.2 L1149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr19:23542294 G>A maps to NM_003430.2 I1162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:64864214 C>T maps to NM_152626.2 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AH-06A-11D-A196-08 chr19:20044199 C>T maps to NM_031218.3 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29B-06A-11D-A197-08 chr19:22575762 G>A maps to NM_001098626.1 Q92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:22574524 G>A maps to NM_001098626.1 H504H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:22574743 C>T maps to NM_001098626.1 E431E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr19:22574358 T>A maps to NM_001098626.1 K560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:22574491 C>T maps to NM_001098626.1 E515E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:22586274 G>A maps to NM_001098626.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:22941276 C>T maps to ENST00000397104 E387E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr19:22942274 G>A maps to ENST00000397104 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:22940850 G>A maps to ENST00000397104 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3CF-06A-11D-A196-08 chr19:22941561 G>A maps to ENST00000397104 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr19:22940895 G>A maps to ENST00000397104 F514F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr19:22941606 G>A maps to ENST00000397104 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr19:22939792 C>T maps to ENST00000397104 R846R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51T-06A-11D-A25O-08 chr19:22951143 C>T maps to ENST00000397104 W84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GN-06A-11D-A27K-08 chr19:22940631 C>T maps to ENST00000397104 R602R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:22951110 G>A maps to ENST00000397104 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GS-06A-11D-A27K-08 chr19:22941864 C>T maps to ENST00000397104 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr19:22941813 G>A maps to ENST00000397104 H208H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:22940940 C>T maps to ENST00000397104 E499E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A182-06A-11D-A196-08 chr19:22940631 C>T maps to ENST00000397104 R602R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29C-06A-21D-A197-08 chr19:22941690 G>A maps to ENST00000397104 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:22939281 C>T maps to ENST00000397104 R963R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:22941483 G>A maps to ENST00000397104 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr19:22941108 C>T maps to ENST00000397104 K443K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr19:22939431 C>T maps to ENST00000397104 E913E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M7-06A-11D-A197-08 chr19:22939263 C>T maps to ENST00000397104 K969K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JH-06A-11D-A21A-08 chr19:22939425 C>T maps to ENST00000397104 P915P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr19:22939099 C>T maps to ENST00000397104 G1007G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:22940044 C>T maps to ENST00000397104 R762R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr19:22939099 C>T maps to ENST00000397104 G1007G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZK-06A-11D-A197-08 chr19:22951110 G>A maps to ENST00000397104 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZW-06A-12D-A197-08 chr19:22940943 C>T maps to ENST00000397104 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:22940436 C>T maps to ENST00000397104 E667E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:22940538 C>T maps to ENST00000397104 E633E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:22941459 T>C maps to ENST00000397104 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:22940044 C>T maps to ENST00000397104 R762R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr19:22951143 C>T maps to ENST00000397104 W84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr19:22939009 G>A maps to ENST00000397104 P1037P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I8-06A-11D-A197-08 chr20:47881378 G>A maps to NM_021035.2 T675T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr20:47863845 G>A maps to NM_021035.2 A1905A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A185-06A-11D-A196-08 chr20:47865096 C>T maps to NM_021035.2 R1488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GC-06A-11D-A197-08 chr20:47865893 G>A maps to NM_021035.2 R1223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GU-06A-11D-A196-08 chr20:47881294 G>A maps to NM_021035.2 F703F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr20:47886752 G>A maps to NM_021035.2 F532F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr20:47864961 T>G maps to NM_021035.2 R1533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z3-06A-11D-A197-08 chr20:47866188 C>T maps to NM_021035.2 E1124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZQ-06A-11D-A197-08 chr20:47881324 G>A maps to NM_021035.2 T693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr20:47887208 G>A maps to NM_021035.2 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr20:47864577 C>T maps to NM_021035.2 Q1661Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr7:100865993 C>T maps to NM_006349.2 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:100865981 C>T maps to NM_006349.2 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19W-06A-41D-A23B-08 chr16:75127482 C>T maps to ENST00000320619 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr22:29446317 C>T maps to NM_032173.2 Q617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr22:29446916 C>T maps to NM_032173.2 T816T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr22:29445491 C>T maps to NM_032173.2 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A6-06A-11D-A197-08 chr22:29445935 C>T maps to NM_032173.2 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A69P-06A-21D-A30X-08 chr22:29446434 C>T maps to NM_032173.2 Q656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr22:29446880 C>T maps to NM_032173.2 F804F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C8-06A-12D-A19A-08 chr19:5456308 C>T maps to NM_181710.3 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr19:5456080 C>T maps to NM_181710.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr19:5456122 C>T maps to NM_181710.3 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29S-06A-11D-A197-08 chr19:5455957 C>T maps to NM_181710.3 N152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr19:5456626 C>T maps to NM_181710.3 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A198-06A-11D-A196-08 chr19:5456593 C>T maps to NM_181710.3 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:5456608 C>T maps to NM_181710.3 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:5456122 C>T maps to NM_181710.3 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:5456291 C>T maps to NM_181710.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:5456548 C>T maps to NM_181710.3 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:5456632 G>A maps to NM_181710.3 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr11:60635113 G>A maps to NM_207341.2 W27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr11:60642653 C>T maps to NM_207341.2 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr11:60637856 C>A maps to NM_207341.2 C245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:60638742 C>T maps to NM_207341.2 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr11:60638743 C>T maps to NM_207341.2 Q357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr11:60637230 C>A maps to NM_207341.2 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:60637185 C>T maps to NM_207341.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr11:60641148 C>T maps to NM_207341.2 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr16:21216881 C>T maps to NM_003460.1 W184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1IC-06A-11D-A197-08 chr16:21221023 C>T maps to NM_003460.1 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr16:21215353 C>T maps to NM_003460.1 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr16:21213433 C>T maps to NM_003460.1 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr16:21210172 G>T maps to NM_003460.1 A646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:21213293 C>T maps to NM_003460.1 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:21215694 G>A maps to NM_003460.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr16:21221023 C>T maps to NM_003460.1 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:21213472 C>T maps to NM_003460.1 G413G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr16:21218164 G>A maps to NM_003460.1 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr16:21211162 G>A maps to NM_003460.1 F577F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr16:21221023 C>T maps to NM_003460.1 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr16:21210906 G>A maps to NM_003460.1 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:21208824 C>T maps to NM_003460.1 E738E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:21211171 C>T maps to NM_003460.1 Q574Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr16:21222688 G>A maps to NM_003460.1 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr16:21222688 G>A maps to NM_003460.1 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:76054469 G>A maps to NM_001110354.1 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr7:76062958 C>T maps to NM_001110354.1 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr7:76062785 G>A did not map to a codon.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr7:76062805 G>A maps to NM_001110354.1 K185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr1:238050114 C>T maps to NM_021186.3 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:238053476 C>T did not map to a codon.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr1:238049116 G>A maps to NM_021186.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr1:238048096 G>A maps to NM_021186.3 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:238045825 G>A maps to NM_021186.3 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr1:238050805 C>T maps to NM_021186.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr1:238053212 C>T maps to NM_021186.3 K118K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A694-06A-11D-A30X-08 chr1:238048737 G>A maps to NM_021186.3 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HV-06A-21D-A196-08 chr7:50121475 G>A maps to NM_007009.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr7:50121402 G>A maps to NM_007009.2 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M6-06A-12D-A197-08 chr7:50097583 C>A did not map to a codon.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr7:50057910 A>C maps to NM_007009.2 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr17:38029372 C>T maps to NM_199321.2 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JW-06A-11D-A19A-08 chr17:38027042 G>A maps to NM_199321.2 W72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr17:38031604 T>C maps to NM_199321.2 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GM-06B-11D-A196-08 chr17:38028655 C>T maps to NM_199321.2 C180C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr17:38031535 G>A maps to NM_199321.2 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:38027072 G>A did not map to a codon.
Sequencing variant TCGA-D3-A1Q8-06A-11D-A19A-08 chr3:102196381 C>T maps to NM_175056.1 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JO-06A-11D-A196-08 chr3:102171805 G>A maps to NM_175056.1 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr3:102175134 C>T maps to NM_175056.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I1-06A-12D-A196-08 chr3:102171835 C>T maps to NM_175056.1 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr3:102183089 C>T maps to NM_175056.1 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr3:102187900 G>A maps to NM_175056.1 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr3:102189257 G>A maps to NM_175056.1 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:102183089 C>T maps to NM_175056.1 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr3:102189275 G>A maps to NM_175056.1 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr3:102189290 C>T maps to NM_175056.1 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MI-06A-11D-A197-08 chr3:102183089 C>T maps to NM_175056.1 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr3:102187819 C>T maps to NM_175056.1 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr3:102196368 C>T maps to NM_175056.1 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J8-06A-11D-A20D-08 chr3:102196335 G>A maps to NM_175056.1 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr3:102187966 C>T maps to NM_175056.1 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr3:102196386 C>T maps to NM_175056.1 C407C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr3:102183089 C>T maps to NM_175056.1 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3TU-06A-11D-A23B-08 chr3:102183089 C>T maps to NM_175056.1 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr3:102195859 G>A maps to NM_175056.1 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:126670316 T>A maps to NM_017580.2 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr10:126670317 C>T maps to NM_017580.2 Q490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:71530792 G>A maps to NM_203350.2 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr1:71544350 G>A maps to NM_203350.2 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr2:135982013 C>T maps to NM_032143.2 R744R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr2:136026660 C>T maps to NM_032143.2 W419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr2:135988469 G>A maps to NM_032143.2 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29N-06A-12D-A197-08 chr2:135966508 G>A maps to NM_032143.2 D845D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr2:136023175 G>A maps to NM_032143.2 F489F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr23:15827341 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr23:15833822 C>A did not map to a codon.
Sequencing variant TCGA-D3-A2JA-06A-11D-A196-08 chr19:58565008 C>T maps to NM_182572.3 Q273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3C7-06A-11D-A196-08 chr19:58549233 C>T maps to NM_182572.3 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:58549278 C>T maps to NM_182572.3 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EA-06A-11D-A30X-08 chr19:58563961 G>A maps to NM_182572.3 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr19:58563901 C>T maps to NM_182572.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:58565235 G>A maps to NM_182572.3 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EB-A5UN-06A-11D-A30X-08 chr19:58564950 G>A maps to NM_182572.3 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr19:58565115 C>T maps to NM_182572.3 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:58565250 G>A maps to NM_182572.3 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MM-06A-11D-A196-08 chr19:58565250 G>A maps to NM_182572.3 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:58565235 G>A maps to NM_182572.3 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:58551860 C>T maps to NM_182572.3 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A2NH-06A-11D-A196-08 chr19:58551913 T>G did not map to a codon.
Sequencing variant TCGA-FS-A1ZF-06A-12D-A197-08 chr19:58564833 G>A maps to NM_182572.3 W214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F9-06A-11D-A24R-08 chr19:58563907 G>A maps to NM_182572.3 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:58551860 C>T maps to NM_182572.3 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A693-06A-13D-A30X-08 chr19:58565085 G>A maps to NM_182572.3 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr16:3139825 G>A maps to NM_032805.1 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3ML-06A-11D-A21A-08 chr16:3140305 G>A maps to NM_032805.1 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr16:3139412 G>A maps to NM_032805.1 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I4-06A-11D-A196-08 chr16:3140468 G>A maps to NM_032805.1 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr16:3139277 C>T maps to NM_032805.1 Q664Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr16:3142077 C>T maps to NM_032805.1 Q157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:3139598 C>T maps to NM_032805.1 G557G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr16:3140195 G>A maps to NM_032805.1 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr16:3141589 C>T maps to NM_032805.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AG-06A-31D-A196-08 chr16:3141586 G>T maps to NM_032805.1 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:3139135 G>A maps to NM_032805.1 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:3139547 C>T maps to NM_032805.1 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr16:3142166 G>A maps to NM_032805.1 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr16:3140060 C>T maps to NM_032805.1 Q403Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr19:58596471 C>T maps to NM_001145542.1 R427R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29A-06A-12D-A196-08 chr19:58596360 G>A maps to NM_001145542.1 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr19:58601586 G>A maps to NM_001145542.1 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr19:58596342 G>A maps to NM_001145542.1 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A3PL-06A-11D-A23B-08 chr19:58598279 G>A maps to NM_001145542.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:58598336 C>T maps to NM_001145542.1 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F8-06A-11D-A20D-08 chr15:85147259 C>T maps to NM_181877.3 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19M-06A-61D-A23B-08 chr15:85164688 C>T maps to NM_181877.3 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr15:85165084 G>A maps to NM_181877.3 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:33960889 G>A maps to NM_145238.3 T982T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr1:33945116 C>T maps to NM_145238.3 C76C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr1:33944949 C>T maps to NM_145238.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A1-06A-11D-A197-08 chr1:33955155 C>T maps to NM_145238.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A2-06A-11D-A196-08 chr1:33956859 C>T maps to NM_145238.3 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GO-06A-11D-A196-08 chr1:33954733 C>T maps to NM_145238.3 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr1:33960691 C>T maps to NM_145238.3 S916S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F0-06A-11D-A24R-08 chr1:33958970 C>T maps to NM_145238.3 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:99654712 C>T maps to NM_145914.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr7:99654868 C>T maps to NM_145914.2 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29R-06A-11D-A197-08 chr7:99654907 C>T maps to NM_145914.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr7:99654751 G>A maps to NM_145914.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr6:28403788 C>T maps to NM_001012455.1 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr6:28403866 G>A maps to NM_001012455.1 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A3MR-06A-11D-A21A-08 chr15:43656347 G>A maps to NM_152455.3 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr15:43654011 G>A maps to NM_152455.3 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr15:43662000 G>A maps to NM_152455.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GR-06A-11D-A27K-08 chr19:58187824 G>A maps to NM_152677.2 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:58189532 G>A did not map to a codon.
Sequencing variant TCGA-EE-A181-06A-11D-A196-08 chr19:58190017 C>T maps to NM_152677.2 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:58189570 G>A maps to NM_152677.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MD-06A-11D-A197-08 chr19:58187626 G>A maps to NM_152677.2 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MJ-06A-11D-A197-08 chr19:58190185 C>T maps to NM_152677.2 Y405Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr19:58187716 C>T maps to NM_152677.2 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr19:58190038 G>C maps to NM_152677.2 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A4U4-06A-11D-A32N-08 chr19:58189625 C>T maps to NM_152677.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:58189730 C>T maps to NM_152677.2 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A5GO-06A-12D-A27K-08 chr19:56733417 C>T maps to NM_024303.1 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr19:56733669 C>T maps to NM_024303.1 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20H-06A-11D-A197-08 chr19:56735101 G>A maps to NM_024303.1 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29L-06A-12D-A196-08 chr19:56733492 T>A maps to NM_024303.1 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A42L-06A-11D-A24R-08 chr19:56733255 G>A maps to NM_024303.1 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56733071 G>A maps to NM_024303.1 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr19:56736205 A>G maps to NM_024303.1 H70H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RP-A695-06A-11D-A30X-08 chr19:56736226 C>T maps to NM_024303.1 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51G-06A-11D-A25O-08 chr19:56701423 G>A maps to NM_001080456.2 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51J-06A-11D-A25O-08 chr19:56701921 C>T maps to NM_001080456.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr19:56701915 T>C maps to NM_001080456.2 E256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr19:56702305 G>A maps to NM_001080456.2 N213N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29E-06A-11D-A197-08 chr19:56704271 G>A maps to NM_001080456.2 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GI-06A-11D-A196-08 chr19:56704103 C>T maps to NM_001080456.2 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2ML-06A-11D-A197-08 chr19:56701795 G>A maps to NM_001080456.2 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr19:56703299 C>T maps to NM_001080456.2 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:56701339 G>A maps to NM_001080456.2 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4FC-06A-11D-A24R-08 chr19:56704157 C>T maps to NM_001080456.2 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56701423 G>A maps to NM_001080456.2 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr19:56701921 C>T maps to NM_001080456.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C9-06A-11D-A30X-08 chr19:56702278 C>T maps to NM_001080456.2 E222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QB-A6FS-06A-11D-A30X-08 chr19:56702266 C>T maps to NM_001080456.2 K226K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JC-06A-11D-A19A-08 chr20:44511762 C>T maps to NM_080603.4 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr20:44511959 C>T maps to NM_080603.4 H243H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QA-06A-11D-A196-08 chr2:187694549 C>T maps to NM_182521.2 K333K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr2:187693427 C>T maps to NM_182521.2 W395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I0-06A-11D-A20D-08 chr2:187693412 C>T maps to NM_182521.2 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A17X-06A-11D-A197-08 chr2:187702043 C>T maps to NM_182521.2 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A180-06A-11D-A21A-08 chr2:187703836 G>A maps to NM_182521.2 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2A5-06A-11D-A197-08 chr2:187693193 G>A maps to NM_182521.2 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GR-06A-11D-A197-08 chr2:187702046 C>T maps to NM_182521.2 E243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AB-06A-11D-A196-08 chr2:187692815 C>T maps to NM_182521.2 G599G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr2:187698693 G>A maps to NM_182521.2 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1I7-06A-22D-A197-08 chr20:44506199 C>T maps to NM_080752.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr20:44505976 C>T maps to NM_080752.3 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZC-06A-11D-A197-08 chr20:44505616 T>C maps to NM_080752.3 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZE-06A-11D-A197-08 chr20:44505868 C>T maps to NM_080752.3 H224H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A265-06A-21D-A197-08 chr20:44486601 C>T maps to NM_080752.3 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A1JX-06A-11D-A19A-08 chr19:13915789 C>T maps to NM_023072.2 H180H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29D-06A-11D-A197-08 chr19:13941254 G>A maps to NM_023072.2 A787A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GE-06A-11D-A196-08 chr19:13941134 G>A maps to NM_023072.2 R747R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19G-06A-11D-A196-08 chr19:13928121 C>T maps to NM_023072.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A4F5-06A-11D-A25O-08 chr19:13941281 G>A maps to NM_023072.2 A796A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q5-06A-11D-A196-08 chr1:45500098 G>A maps to NM_020883.1 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2M5-06A-12D-A197-08 chr1:45485810 C>T maps to NM_020883.1 R874R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr1:45484179 C>T maps to NM_020883.1 Q1168Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MG-06A-11D-A197-08 chr1:45486443 G>A maps to NM_020883.1 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AC-06A-11D-A196-08 chr1:45524427 G>A maps to NM_020883.1 R369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FR-A44A-06A-11D-A24R-08 chr1:45486443 G>A maps to NM_020883.1 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1YW-06A-11D-A197-08 chr1:45484194 G>A maps to NM_020883.1 I1163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZD-06A-11D-A197-08 chr1:45506070 C>T maps to NM_020883.1 Q583Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:45671755 G>A maps to NM_020883.1 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:116973220 G>A maps to NM_145062.2 Q366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1Q6-06A-11D-A196-08 chr6:116973221 G>A maps to NM_145062.2 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A183-06A-11D-A196-08 chr6:116966921 G>A maps to NM_145062.2 Y548Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr11:113608317 G>A maps to NM_004724.2 V664V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GS-06A-12D-A197-08 chr11:113604493 G>A maps to NM_004724.2 S754S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3J5-06A-11D-A20D-08 chr11:113607478 G>A maps to NM_004724.2 P694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr11:113614567 G>A maps to NM_004724.2 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29V-06A-12D-A197-08 chr15:66811270 G>A maps to NM_017975.3 K125K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20B-06A-11D-A196-08 chr23:57936239 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2GD-06A-11D-A196-08 chr23:57935504 G>A did not map to a codon.
Sequencing variant TCGA-ER-A19A-06A-21D-A197-08 chr23:57934540 A>C did not map to a codon.
Sequencing variant TCGA-FR-A3YO-06A-11D-A23B-08 chr23:57936630 G>A did not map to a codon.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr23:57619840 T>A did not map to a codon.
Sequencing variant TCGA-FS-A1ZZ-06A-11D-A197-08 chr23:57619479 C>T did not map to a codon.
Sequencing variant TCGA-DA-A3F5-06A-11D-A20D-08 chr3:126191116 G>C maps to NM_025112.4 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AE-06A-11D-A196-08 chr3:126180809 G>A maps to NM_025112.4 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr1:53267619 C>T maps to NM_024646.2 Q539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A20C-06A-11D-A196-08 chr1:53262456 G>A did not map to a codon.
Sequencing variant TCGA-EE-A3JI-06A-11D-A21A-08 chr1:53245583 G>A maps to NM_024646.2 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZB-06A-12D-A197-08 chr1:53267768 C>T maps to NM_024646.2 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FW-A3R5-06A-11D-A23B-08 chr1:53236938 C>T maps to NM_024646.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr1:53282221 C>T maps to NM_024646.2 F655F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JF-06A-11D-A196-08 chr7:143079410 C>T maps to NM_001010972.1 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D9-A6EC-06A-11D-A30X-08 chr7:143078777 C>T maps to NM_001010972.1 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1ZA-06A-11D-A197-08 chr7:143080384 C>T maps to NM_001010972.1 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr7:143080288 C>T maps to NM_001010972.1 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A1QB-06A-11D-A19A-08 chr17:3916867 G>A maps to NM_015113.3 V2818V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A51R-06A-11D-A25O-08 chr17:4005635 G>A maps to NM_015113.3 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DA-A1HY-06A-11D-A19A-08 chr17:3970483 G>A maps to NM_015113.3 S1376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A184-06A-11D-A196-08 chr17:3947526 C>A maps to NM_015113.3 G2053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A29M-06A-11D-A196-08 chr17:3990780 G>A maps to NM_015113.3 F763F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2GN-06A-11D-A196-08 chr17:3967728 G>A maps to NM_015113.3 P1548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MR-06A-11D-A196-08 chr17:3969753 G>A maps to NM_015113.3 N1412N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MS-06A-11D-A197-08 chr17:3924425 G>A maps to NM_015113.3 F2467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A2MU-06A-21D-A196-08 chr17:3922982 G>A maps to NM_015113.3 F2495F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3AF-06A-11D-A196-08 chr17:3920856 G>A maps to NM_015113.3 V2603V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EE-A3JD-06A-11D-A20D-08 chr17:3937373 G>A maps to NM_015113.3 S2173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ER-A19P-06A-11D-A196-08 chr17:3999944 G>C maps to NM_015113.3 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FS-A1Z0-06A-11D-A197-08 chr17:4020304 G>A maps to NM_015113.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GF-A6C8-06A-12D-A30X-08 chr17:3999941 T>C maps to NM_015113.3 G575G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:3974194 G>T maps to NM_015113.3 P1286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A266-06A-11D-A197-08 chr17:3977636 G>A maps to NM_015113.3 T1164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GN-A268-06A-11D-A196-08 chr17:4015960 G>A maps to NM_015113.3 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OD-A75X-06A-12D-A32N-08 chr17:3990780 G>A maps to NM_015113.3 F763F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D3-A2JK-06A-11D-A196-08 chr1:78098793 G>A maps to NM_015534.4 S82S. Only missense variants will be evaluated by CHASM.
